CM 100 120 Mechanics
CM 100 120 Mechanics
CM 100 120 Mechanics
Contents
Figures
Contents H
2 Cleaning
2.1 Cleaning equipment and materials...................................................... 2-1
2.1.1 Instruments .......................................................................................... 2-1
2.1.2 Consumables ....................................................................................... 2-2
2.1.3 Chemicals ............................................................................................ 2-2
2.1.4 Danger Classification and Safety advice.............................................. 2-3
2.2 Cleaning process ................................................................................ 2-4
2.3 Emission Chamber And Gun Insulator................................................ 2-8
2.4 Wehnelt cylinder and anode................................................................ 2-9
2.5 Gun airlock ........................................................................................ 2-10
2.6 Objective lens pole pieces ................................................................ 2-10
2.7 Goniometer Stage .............................................................................. 2-11
2.7.1 CS CompuStage .................................................................................2-11
2.7.1 Right-hand ear ....................................................................................2-11
2.7.2 Left-hand ear.......................................................................................2-11
2.7.3 Frequency of cleaning.........................................................................2-11
2.8 Anti-contamination device ................................................................. 2-12
2.9 Vacuum lining tube (upper lens section) ........................................... 2-12
2.10 Vacuum lining tube (lower lens section) ............................................ 2-12
2.11 Camera airlock .................................................................................. 2-13
2.12 Fixed diaphragms.............................................................................. 2-13
2.13 Adjustable diaphragms...................................................................... 2-14
2.13.1 Condenser lens diaphragms .............................................................. 2-14
2.13.2 Objective lens diaphragms................................................................. 2-14
2.13.3 S.A. Diaphragms ................................................................................ 2-14
2.13.4 Diaphragm cleaning methods ............................................................ 2-14
2.14 Diaphragm holders............................................................................ 2-15
2.15 Projection chamber viewing windows ............................................... 2-15
2.16 Lens housings and desk ................................................................... 2-15
2.17 Exposure measurement system........................................................ 2-16
2.17.1 The SCA board .................................................................................. 2-16
2.17.2 The vacuum feed-through .................................................................. 2-16
2.17.3 Fluorescent screens........................................................................... 2-17
2.18 Penning gauge .................................................................................. 2-17
3 Preventive maintenance
3.1 Preventive maintenance for users....................................................... 3-1
3.1.1 Changing filaments .............................................................................. 3-1
3.1.2 Treatment of the specimen holder and goniometer airlock .................. 3-1
3.1.3 Camera systems and fluorescent screens ........................................... 3-2
3.2 6-Monthly maintenance....................................................................... 3-2
3.2.1 Emission chamber and gun.................................................................. 3-2
3.2.2 Diaphragms and liner tubes ................................................................. 3-3
Contents
Figures
Contents (cont’d) H
Contents (cont’d) H
Contents (cont’d) H
Contents (cont’d) H
Contents (cont’d) H
Contents (cont’d) H
Contents (cont’d) H
7 List of O-rings
7.1 Special O-rings and miscellaneous vacuum parts ............................... 7-4
7.2 Manufacturers of em accessories........................................................ 7-5
8 Mechanical drawings
9 Spare parts
9.1 Abbreviations ....................................................................................... 9-1
9.2 Miscellaneous spare parts ................................................................... 9-1
9.3 Cross section of microscope column ................................................... 9-2
9.4 Rear view............................................................................................. 9-2
9.5 Cross section of base plate (CM10) .................................................... 9-3
Contents
Figures
Contents (cont’d) H
List of Illustrations H
8 Mechanical drawings
801 Cross section of the microscope column ................................................... 8-1
802 Rear view ................................................................................................... 8-2
802A Rear view for CM120 BioFilter only ........................................................... 8-3
803A Cross setion baseplate (CM10) ................................................................. 8-4
803B Cross section baseplate (CM10(0)/CM12(0), from April 1992 onwards .... 8-5
Contents
Figures
1 Introduction H
NOTE: To find a particular item, first look it up in the contents list, then find
the page number given.
Contents
Figures
2 Cleaning H
2.1.1 Instruments
The following instruments are required:
• Ultrasonic cleaner
• Ultrasonic vapour degreaser (if available)
• Storage bottles (1 litre size)
• Beakers, EM liner tube size and smaller
• Petri dishes
• Stereo light microscope (magn. 5x to 50x)
• Tweezers
• IR heating lamps
• EM special tools (removal of liner tube and diaphragms)
Contents
Figures
2.1.2 Consumables H
The following consumables are required:
• Rubber gloves
• Safety goggles
• Lint-free clothes
• Lint-free gloves
• Dust-free tissue paper
• Grease-free cotton wool
• Wooden spills
• Aluminium foil
• “Gas Jet Duster” spray can
2.1.3 Chemicals
The following chemicals are required:
• De-ionized or distilled water
• Ethanol - C2H5OH
• Ethanol Pro-Analysis (99.8% pure) - C2H5OH
• KOH (Potassium Hydroxide) or NaOH (Sodium Hydroxide)
• EXTRAN - MA02 (neutral cleaning fluid)
• CIF
Danger Classification:
R11 : Highly inflammable
R35 : Causes severe burns
Safety advice:
S2 : Keep out of reach of children
S7 : Keep stored under sealed conditions
S16 : Keep away from igniters
Do not smoke
S26 : On contact with the eyes, rinse profusely with water
S37/39 : Wear protective gloves and facial protection devices
Code of practice
• Do not open the column unless it is really necessary, but check the
performance regularly; see 4 “Performance check/fault finding”.
• Always work in a clean and ventilated room
• Use a clean working table with good illumination
• Wear lint-free clothes
• Always wear clean gloves when handling “vacuum” parts
• Always use CLEAN solvents
• Before mounting, inspect parts under a light microscope
• Be sure that special tools are clean before use and packed after use in
aluminium foil
• Do not mix materials of different compositions in the cleaning baths
• Strip the assemblies as far as possible
• Pack items in aluminium foil after cleaning
• Collect all cleaning items and have them on site before opening column
• Vacuum parts that can not be remounted immediately should be wrapped
in aluminium foil and kept under an infrared lamp.
Contents
Figures
Phase 1:
Heavily polluted metal parts:
Rub cleaning must be done using “CIF”, a household fine abrasive. Rinse in
water.
Phase 2:
Less polluted metal parts and parts coming from phase 1:
Ultrasonically cleaned for 5 min. in a 5% dilution of “EXTRAN MO2” in water.
Raising the temperature increases the effect. This soap solution binds the dirt
and removes it from the surface of the part. Rinsing is done in distilled water;
raising the water temperature increases the effect.
Phase 3:
O-rings, synthetic materials and assemblies (which cannot be stripped
down in the field) start their cleaning sequence from this point.
Ultrasonic cleaning in Ethanol for 5 min. at 20°C, to remove the water.
Rinse in a new clean bath of Ethanol for 2 min.
Ethanol is highly flammable, do not use open flames, or smoke while cleaning.
Phase 4:
This phase must be skipped for O-rings and synthetic materials.
Ultrasonic cleaning in Ethanol - pro analysis (99.8% pure), to be sure all water
and traces left by Ethanol in phase 3 are removed.
Rinse for 2 min. in a new bath with Ethanol p/a.
If available, an ultrasonic vapour degreaser can be used.
Phase 5:
The parts must be dried with the aid of two 150W Infra Red lamps
(INFRAPHIL). To reach a temperature of 80°C, heating by the IR lamps must
be maintained for a minimum of 15 min., or, for heavy items and the emission
chamber, for 2 hours or more. If available, a vacuum oven can be used and set
to 80°C.
When mounted in the microscope and external heating is applied, the
temperature must kept under 100°C, otherwise damage to encapsulated items
will occur.
O-rings must not become warmer than 70 °C and can best be dried in air.
Parts should only be handled after they have cooled down below 50°C.
Spray the part with a gas jet duster, to remove any dust particles or fibres
before inspection.
After inspection under a light microscope, mount the parts directly in the
Electron Microscope and spray with the gas jet duster again before closing the
microscope.
If parts are not mounted but stored, pack them in aluminium foil
Contents
Figures
. H
Phase 1 Phase 2
Pole pieces
Wehnelt Ultrasonic Rinsing Ultrasonic Rinsing
Anode cleaning in tap water cleaning
30 min. 5 min. 5 min.
2) Distilled water
NaOH 6% dilution in distilled water Extran: 5% dilution
3)
or KOH 6% dilution in distilled water in distilled water 4)
1)
Cif: household fine abrasive
2)
NaOH: Sodium Hydroxide
3)
KOH: Potassium Hydroxide
2) 3)
R: 35 S: 2-26-37/39
4)
Extran: Industrial soap (neutral) for cleaning instruments
- Extran MA02 - (non reactive cleaning fluid)
- Raised water temperature increases the effect
EM9612
Ultrasonic Mounting
Ultrasonic Rinsing Rinsing Drying Inspection
cleaning in
cleaning
microscope
5 min. 2 min. 2 min. 2 min. 15 min. - 2 hr; Under light microscope
Ethanol 5) Ethanol p/a Ethanol p/a
Ethanol 5) IR lamps
Ultrasonic
cleaning Vapour
2 min. 1 min.
Ethanol p/a Ethanol p/a
5) Ethanol p/a: C H OH
Ethanol: C H OH 2 5
2 5
R: 11 S: 7-16 R: 11 S: 7-16
EM9612
Beaker
Liner tube
+ 300mm
_
Water/soap for
optimal Ultrasonic
transmission Cleaning fluid
Infraphil
IR lamps
EM8852
CAUTION! Never touch with bare hands any parts of the emission
chamber/gun that are located in UHV areas.
CAUTION! The Wehnelt cap 125, 126 (and anode 175) must be
absolutely free of scratches to avoid HT instability.
Frequency of cleaning:
• Insert cap 89: whenever a new filament is fitted;
• Wehnelt cap and anode: check cleanliness whenever a new filament is
fitted and clean as necessary, but clean at least once every five new
filaments.
Contents
Figures
O-rings 46 and 58, the operation shaft 39 and the interior of the air cylinder 64
should be cleaned when the airlock movement becomes stiff. Check for
damage and clean using a tissue dipped in cyclohexane.
Lightly grease O-rings 58, 48 and 46 with Fomblin RT15 Grease.
Frequency of cleaning:
Check operation every year (see 4.2 “Checking the airlock pumping times” and
4.3 “Tracing vacuum leaks in the column”), clean as necessary.
NOTE: For dismantling of the gun airlock see 5.8 “Removing, dismantling
& remounting of the gun airlock valve, gun centring coil or the x-
ray diaphragm”.
Clean as follows:
Check residual astigmatism (see 4.10 “Objective lens astigmatism”) every six
months and clean as necessary.
Clean pole pieces as necessary.
NOTE: For removal of the pole pieces see 5.11.1 “The upper objective
pole piece” and 5.23.1 “The lower objective pole piece”.
Contents
Figures
2.7.1 CS CompuStage
The specimen airlock can become contaminated due to dust and dirt particles
floating in during airlock operation, therefore check that the final vacuum
without the holder is equal to the vacuum with the holder.
If not, remove the CompuStage, open and dismantle the airlock; see
5.15.1 “CS Dismantling the airlock”.
Clean O-Ring 154, Figure 808A and lightly grease it with Fomblin RT 15.
If the vacuum improves with the airlock closed, check the O-Ring on the holder.
Clean it thoroughly and grease lightly with Fomblin RT 15.
Clean as follows:
• Remove the cold trap (see 5.18 “Removal, dismantling & assembly of the
anti-contamination device & pre-vacuum valve”);
• Clean the cold trap by rubbing with cotton wool wrapped on a wooden spill
and dipped in trichloroethylene or cyclohexane;
• Clean the cold trap for 3 minutes using an ultrasonic cleaner and
cyclohexane;
• Dry thoroughly using an oven (max. 70 °C) or infra-red lamp.
Frequency of cleaning:
Whenever the objective pole pieces are cleaned.
Frequency of cleaning:
Check the airlock every six months for smooth operation - clean if necessary.
Clean as follows:
• Rub with cotton wool wrapped on a wooden spill and dipped in
cyclohexane or trichloroethylene;
• If this is not successful use fine grain polishing paste or household cleaning
fluid e.g. Soft scrub or Jif;
• Wash thoroughly under hot running water;
• Clean in ultrasonic cleaner for 3 minutes using cyclohexane;
• Dry thoroughly in oven (max. 100 °C) or under infra-red lamp;
• Check cleanliness and sharpness of aperture using a light microscope;
• Remount (see 5.11 “Removing & replacing the upper objective pole piece
& the fixed diaphragms in the upper lens section” and 5.23 “Removing &
replacing the lower objective pole piece & the fixed diaphragms of the
lower lens section”.).
Frequency of cleaning:
• Diaphragms in upper objective pole piece: at the same time as the
objective lens pole pieces are cleaned;
• Other fixed diaphragms in lining tubes: according to result of visual
inspection.
See also 3.2.2 “Diaphragms and liner tubes”.
Contents
Figures
Method 1: Heat each diaphragm (held in the special tweezers with platinum
points) in a clean gas flame until white hot.
Take care that the diaphragms are not melted or stick to the
tweezers.
Dust + perspiration,
Coffee, tea, etc. Water and standard detergents
Contents
Figures
NOTE: To identify which item is causing the problem see Vol. 2, Sect.
3.5.2.
Frequency of cleaning:
When the meter for the exposure time already gives a value when the high
tension is still switched off, or when the measured values of the large screen
and the small screen are not within specification.
Clean as follows:
• Unscrew the shielding of the SCA board from the microscope.
• Remove the batteries from the holders (check if the batteries have the
correct voltage).
• Unsolder the input wires on the SCA board, X8 and X12 and remove
connectors X9 and X11.
• Unscrew the SCA board from its shielding.
• Clean the board with a soft brush and alcohol on both sides.
• Reassemble and remount the unit.
soldered
Contents
Clean as follows: H
• Remove the feed-through from the projection chamber.
• Unsolder the cable on the SCA board (X8 and X12).
• Dismantle the unit.
• Unsolder the wires on the feed-through.
• Clean all the parts of the unit in alcohol (not in an ultrasonic cleaner!).
• Reassemble the unit.
Be sure that:
• the mantle of the coaxial cables is removed from the inner wire for approx.
5 mm.
• the rubber sleeve is clean and mounted according to Figure 2-5.
• after soldering there is no solder resin left on the insulation of the inner
wires.
• the wire that is marked brown is connected to the large screen.
• the wire that is marked red is connected to the small screen.
Clean as follows:
• Carefully remove the screens.
• Clean the teflon insulators in alcohol.
• Carefully remount the screens.
3 Preventive maintenance H
Colour change to brown is caused by X-rays, this does not affect the quality
of the insulator. See also 2.3 “Emission Chamber And Gun Insulator”.
• Clean the anode 175, Figure 804 and the X-ray diaphragm 9 on top of the
upper membrane assembly 4-11, Figure 805.
Discolouration of the anode is mostly not caused by contamination but by
heating.
• The 20 ml of Santovac oil for the insulator should be heated and pre-dried
before use.
• Check level of oil in HT plug of the HT generator. It should fully surround
the plastic body of the HT cable.
NOTE: The X-ray diaphragm may be made visible using the gun shift
controls.
Contents
Figures
CM100:
– Select vacuum page and press “col air” softkey: If P3 increases, V3 is
leaky;
CM120:
– Select vacuum page and press “gun air” softkey: If IGP increases, V7
or V5 are leaky. If P3 increases, V6 is leaky.
CM100/CM120:
– Select vacuum page and press “cam air” softkey: If IGP increases, V4
or V6 are leaky;
– IGP should have the same value with and without the holder present;
– During specimen removal IGP should not increase by more than 20
units.
• Check colour and level of oil in OD pump. If oil is discoloured brown, the
pump must be cleaned and filled with new oil (60 ml Santovac 5);
• If a service visit or call is paid to a customer who uses large quantities of
photographic material, he should be advised to use the gas ballast of the
pre-vacuum pump for 2/3 days.
If, in spite of this measure, the right pressure is not reached, the pre-
vacuum pump oil should be replaced;
• Monitor the variation of P3 when the buffer pressure is rising.
When using a hot pump, the P3 pressure should not increase when the
buffer pressure rises from 13.3 Pa to 46.7 Pa (use T exposure time to
attain this level);
• Monitor the variation of P3 when using cameras and flu-screens;
• Check pumping times (see 4 “Performance check/fault finding”);
• Check leak rate (see Sect. 4.2 “Checking the airlock pumping times”);
• Check ultimate vacuum (see 4.1 “Checking the pumping speed”).
Contents
Figures
3.2.4 Pneumatics H
• Check pneumatic control valves for hissing sound;
• Check blow-off line for presence of water;
• Lubricate gun valve V7 with 1 drop of pneumatic oil;
• If present, check switching pressures of the compressor unit;
• Drain water from compressor-buffer vessel.
3.2.6 Electronics
• Check stabilities electrically or by an electron-optical method (diffraction
point and focus drift);
• Check condenser systems;
• Check magnifications, camera lengths and focus system optically;
• Check beam tilt/deflection system;
• Check all coil currents (display page);
• Check exposure meter modes, camera ratios, emulsion factor, camera and
numbering system (camera page);
• Check display monitor;
• Check pushbuttons, lamps and shaft encoders.
• Check batteries of Ram Combi Board.
3.2.7 CS CompuStage
• Clean the conical part of the specimen holders with chamois leather or lens
paper;
• Replace O-Ring on specimen holder and grease lightly with FOMBLIN;
• Clean or renew airlock seals of CompuStage and pre-vacuum valve if IGP
vacuum tests are unsatisfactory;
• Check the proper working of the pole hit protection;
• Ensure that the specimen is not in mid-position;
• Insert stop 505, Figure 808A (as a dummy holder);
• Short this stop to ground, check that the beep signal is activated, and that
the specimen is moved for about a second towards mid-position;
• Check that the Alpha, Z, X and Y, end stops work properly.
NOTE: This can best be done during a homing procedure while checking
the LED’s on the GDB board.
Contents
Figures
• Check if all specimen axes can be moved over their full range without any H
obstruction;
• Check if the vacuum with and without holder is the same;
• Check all specifications as given in Section 4.15CS;
• Release the drive rod and manually check if the Y movement has no stiff
points; if so lightly grease the balls 231, Figure 808A.
Procedure:
• Start the vacuum system (cold start);
• Select vacuum page;
• Normal pre-vacuum cycle will be performed;
• After about 30 min. the HV valve opens;
• At a P3 reading of approx. 62, V4 opens and IGP is switched on;
• One minute later valve V6 will close;
• Ten hours after the cold start the ultimate IGP indication must be less than
27 (approx. 7 x 10-5 Pa);
When using the anti-contamination device, the ultimate pressure is approx.
2.6 x 10-5 Pa (= IGP indication of 15).
NOTE: 1. The pumping times given below are only valid for microscopes
which are in regular use. These times may be greatly extended
after installation or repair.
2. The pumping times given below are only valid for microscopes
which are in regular use. These times may be greatly extended
after installation or repair.
3. To overcome heating up of an older IGP at its starting vacuum,
ensure that the IGP is switched on when the P3 pressure is
about 40 scale divisions.
*This time depends strongly on how well the plates and the plate container
Figures
NOTE: This check must be carried out before any vacuum leak test,
because the valves form an integral part of the vacuum test.
4.3.1.4 Check the leak rate of the emission chamber (not for CM100)
NOTE: The leak test for column and IGP can also be carried out for the
emission chamber. However, V5 and V7 must then be closed.
• Start the vacuum system and wait until the column is evacuated. Note the
final reading of the IGP.
– Admit air into the column and lift the upper part of the column.
– Close the holes on top of the objective stage and the UHV valve block
using test pieces 37 and 61, Figure 818.
– Start pumping again.
– If the IGP reading is now better, the leak is in the upper part of the
column.
If the reading remains the same, the leak is in the IGP, the specimen
stage or the lower column.
Contents
Figures
Now remove the specimen stage from the column and close the hole in the H
getter pump using a test piece (not delivered) and the top of the UHV valve
block using test piece 61, Figure 818.
The IGP can now be tested alone as described in test 4.3.2.a.
• If it is found that the upper column section is leaking, the following tests
may help to locate the appropriate section:
– Remove the four screws fixing the emission chamber to the column to
reduce the pressure on the upper membrane.
If the vacuum reading decreases (i.e. vacuum better), the upper
membrane is leaking;
– Open the column between the upper lens section and the emission
chamber;
– Place a rubber stop on top of membrane 11, Figure 805.
– Close the hole on the top of the UHV valve block using test piece 61,
Figure 818;
– Start the pumping system;
– If IGP reading is now better the leak is in the emission chamber or the
indium sealing on top of the upper membrane;
– If no change in IGP reading, switch off the IGP (remove the plug IGP
X8);
– Partially slacken the four fixing screws of the membrane block.
If P3 reading increases (vacuum worse), the lower indium seal on
valve block V7 is leaking and must be renewed.
• If P3 reading decreases (vacuum better), the lower membrane of the valve
is probably leaking; reducing the pressure on the membrane reduces the
leak.
Some tips to help locate very small leaks:
After the pumping sequence is completed and valve V6 is closed, close valve
V4 manually. If the IGP indication increases (vacuum worse), O-ring 70,
Figure 810 at the bottom of the lining tube is leaking.
Before checking the stability of the electron beam, the microscope must have
been switched on for at least 60 minutes with all covers fitted.
Contents
Figures
If the dark current or rate of micro-discharges is too high, the emission chamber
and gun must be cleaned; these should be completely free of dust and dirt. The
dust may best be removed using a vacuum cleaner with a clean nozzle. Also
check that the oil in the gun is dry and clean.
the screen does not move, the presence of dirt above the diaphragm is H
indicated. If the image remained stationary, but moved when the
diaphragm is withdrawn, the presence of dirt underneath the
diaphragm is indicated;
– Repeat the objective and condenser adjustable diaphragms.
– Reverse in turn the diffraction, intermediate, projector 1 and projector 2
lens currents. If the dirt is above the lens with reversed current, there
will be a displacement; if not, the dirt is underneath that lens.
Ensure that:
• The specimen holder and specimen are clean;
• The column is correctly aligned;
• The objective diaphragm is out of the beam;
Select a spot size of 1 micron, and adjust the Intensity control to obtain correct
illumination.
Check the stability by observing Fresnel fringes at maximum magnification
using a perforated carbon film specimen.
Overfocus the edge of a hole.
The setting should be maintained for at least one minute; if not, check:
• HT stability (by observing the diffraction point - see 4.4 “Stability of the
electron beam (all HT settings)”);
• Objective lens current stability (see Electronics manual);
• That the filament is not saturated (this could cause slow fluctuations of the
HT and, therefore, focus instability).
diaphragm. H
(See 5.17.3 “Adjustments”.
Factors affecting image sharpness (see 4.8 “Image sharpness”) may also
affect contrast.
The following tests can be used to ascertain the cause of specimen drift:
• Allow 60 minutes for the microscope and 5 minutes for the HT to stabilize;
• Insert an empty single tilt holder that has been properly cleaned;
• Focus the edge of the hole in the specimen holder on the screen; the
image must remain stationary;
If the edge of the hole exhibits a constant drift in one direction the cause is
either contamination build-up or drift caused by the stage movement.
Observation of the diametrically opposite side of the hole will confirm which
phenomenon is present.
In the case of contamination build-up, the direction of apparent drift will
reverse. However, if the cause is stage movement, it will be in the same
direction.
If the image does, in fact, remain stationary, image drift can be attributed to the
specimen. Check this by observing the bar of an empty grid.
Specimen drift is influenced by the following:
Contents
To make sure that the spring ring is correctly adjusted, the following test is
suggested:
• Place an empty grid on the specimen holder and try to move it with the aid
of a needle;
• While observing the holder under a light microscope it can be easily
checked whether the grid is sufficiently tightly clamped.
Additionally, the specimen holder must be perfectly clean. Check this by
imaging the periphery of the 2 mm hole in the holder on the screen.
• Adjust focus until the overfocused part of the hole is in focus (the rest of the
Figures
hole is now underfocused). Read the defocus value on the data display H
monitor. and check that it is:
< 1.50 µm (CM120), or < 2.00 µm (CM100).
The astigmatism of a microscope that is in operation may not exceed twice the
inherent astigmatism value of clean pole pieces. If this level is exceeded, the
pole pieces require cleaning.
NOTE: 1. The pole pieces of the objective lens have an inherent astigmatism
of less than 0.75 µm (CM100 BioTWIN, CM120, CM120 BioTWIN),
or 1.00 µm (CM100).
2. Apart from the objective lens pole pieces, the following
components may give rise to astigmatism:
The objective diaphragm, its holder, the specimen, the
specimen holder and the fixed diaphragm in the objective lens.
3. If the astigmatism increases substantially above its original
value, one or more of the above components will need to be
cleaned.
4.12.1 Introduction
The rate of contamination is largely dependent on the use and initial
cleanliness of the microscope and specimen.
Before contamination measurements are made, ensure that there are no
vacuum leaks in the column (see 4.3.1 “Checking the vacuum tightness without
opening the column”).
If the column has been opened, especially in the vicinity of the specimen, it
must be pumped for at least one day* before proceeding, so as to reduce the
contamination rate to the previous level.
NOTE: The pumping time depends largely on the time during which the
column was open, and the ambient conditions (humidity, etc.) at
that time.
The contamination rate will gradually reduce to a lower level (≤
100 Å/min.) depending on the use of the microscope.
4.12.2 General
Use gold shadowed perforated carbon specimen 5322 397 60034.
• Initial settings:
– HT: max.
– Emission current: 10 µA (LaB6 and Tungsten)
– Spot size: 1
– Condenser diaphr.: max. or out of the beam
– Anti-cont. device: not cooled down
• Remove water vapour from the test location as
follows:
Select location 1 as indicated in the figure and allow 1
the beam to remove the water vapour for 10 2
minutes.
4.12.3 Procedure
• Select maximum magnification and focus image;
• Select a hole in the specimen that falls within the frame of the camera and
take a picture at 2 seconds exposure time. Focus the spot and during 1
minute, ensure that the spot centre is kept on the edge of the
contamination growth;
Contents
• Enlarge the picture to a magnification of 2 x 106 (1 mm = 0.5 nm) and measure the H
contamination growth;
This may not exceed 20 mm/min (= 10 nm/min).
4.12.4.1 Introduction
Baking out the column can be a means to speed up the conditioning of the UHV
system. Baking out is only recommended when the column has been opened
for a long time, or large vacuum parts, such as the liner tube, have been
cleaned or replaced.
Current (A)
Lens CM100/120
Cond. 1 1.46
Cond. 2 1.55
TWIN 0
Obj. 2.95
Diffr. 1.16
Int. 1.30
Proj. 1 1.19
Proj. 2 1.45
For water procedure from April 1992 onwards the following must also be
carried out (see Figure 814A):
Close valve V22 manually.
Contents
Figures
The electrical control units MRU and PBH, and the ODP are still supplied with H
water.
NOTE: For the water systems from April 1992 onwards, do not forget to
open V22 after baking out.
Manual stage
To run the motor continuously proceed as follows:
• Adjust the specimen translation rods X and Y to mid-position
• Adjust the specimen to eucentric height
• Remove the specimen holder
• Remove the cover of the right-hand ear 130, Figure 808
• Remove the microswitch 120, Figure 808. Cover the opening of the
microswitch using tape to avoid losing the ball 36, Figure 808 and the
pressure pin 119, Figure 808
• Remove the tilt axis limitation screws 113, Figure 808
• Manually check that the goniometer can be tilted over 360° without
obstructions.
• Switch on the tilt motor and let it run clockwise at half the speed.
• Check that the motor runs properly over 360° and is not obstructed.
• Now proceed with the normal bake-out procedure.
• After bake-out
During cooling down of the column let the motor run counter-clockwise for
at least one hour.
• Do not forget to remount the EDAX detector and IGP interlock MC-X8.
CompuStage
During bake-out the bearing scale may deform causing uncontrolled
movements during tilt. Via HELP DESK a Remote Control program can be
obtained to assist in the bake-out. The function of this program is to run the tilt
motor in intervals during bake-out.
The use of the program will be described in the accompanying README file.
• After bake-out replace the EDAX detector and replace the IGP interlock
MC-X8.
Contents
Figures
4.13.1 General
(Figure 4-1)
4.13.1.3 Tilt
The tilt is the imaginary line which can be drawn between the centre of the
ball bearing G, the centre of the hemispherical ball bearing B, and when
the goniometer is aligned, the electron optical axis. Tilt can only be
adjusted during tilt axis alignment with Allen screw D.
perpendicular to the tilt axis so that during tilt the tube T and thus the
Figures
With the specimen tilted, Y movement takes place in the tilted plane and Z
movement takes place perpendicular to the tilted plane.
Y-MOVEMENT
(HEIGHT)
A NE
A1 PL
EN
IM
EC
∆h C1 SP
C
T1
A TIL
T AX
SP IS
C2 EC
∆h IM C1
AX E
IS N
A2 C
C2
A1 / A2
T1
EM1472
A
CENTRE OF THE MAIN SCREEN
ELECTRON
E
OPTICAL AXIS AN
PL
N
I ME
EC
SP
SP
EC
IM
∆h A2 EN
AX
C2 T2 IS
C1
T2 C
A1
C2
TILT A C1
XIS
A2
EM1473
T2
A
T2
A1
CENTRE OF THE MAIN SCREEN
∆h1
A
C
A2 SP
E CIM
R EN
∆h2 ∆h T1 AX
C2 C1 IS
A1 C
C2
TILT C1
AX IS
T3
EM1475
T3
4.13.2 Specifications
4.13.2.1 Overall
The stage movements are checked on the main screen at a magnification of
120,000x and at maximum High Tension.
NOTE: All specifications marked with an asterisk (*) are only valid for
goniometers with the single tilt holder included in the delivery.
1. The total possible displacement of the specimen both along the tilt axis (X)
and at right angles to the tilt axis (Y) amounts to 2.0 mm, i.e. the total
specimen traverse is 2.0 mm x 2.0 mm in the tilted plane.
2. If the specimen is moved to and fro over an arbitrary distance with one of
the specimen translation controls, the displacement at right angles to the
line of displacement should not exceed 4 cm when using the X movement
and 2 cm when using the Y movement.
3. If the specimen is moved to and fro over a distance of 8 cm with one of the
specimen translation controls and then over a distance of 8 cm with the
Contents
Possible causes
Symptom Left-hand ear Right-hand ear
(see Figure 809) (See Figure 808)
Displacement at right angles to the line of dis- 3 2
placement of the left-hand specimen move- 2
ment
Displacement at right angles to the line of dis- 5
placement of the right-hand specimen move-
ment
Displacement during tilting 1 1, 3
Displacement in the direction of the left-hand 5, 1, 2 2, 1
specimen movement during tilting
Displacement when reversing the tilt angle 1, 2, 6
Jumping image when tilting manually 1 1, 5, 2, 3
Scratching sound during motor drive tilt 4
Specimen translation mechanism slips before 4 4
the end positions are reached
Image drift O-ring on the holder 318, Figure 808 is too dry;
Specimen is not properly fixed to the grid;
Grid is not properly fixed to the specimen holder;
Cold trap touches the specimen or diaphragm
holder;
Broken floating rod sapphire or specimen holder
sapphire;
Grease or dirt on: floating rod sapphire, the
specimen holder sapphire, the hemispherical
ball, or their bearing surfaces;
Grease or dirt on; pole pieces, objective dia-
phragm, or specimen holder;
Right-hand ear not properly secured by tighten-
ing the four Allen screws 209, Figure 808.
Excessive cooling water temperature changes.
Excessive room temperature changes.
2. Pressure rod assy. a.damaged sapphire Check sapphire and bearing cup with a
55 b.damaged bearing cup magnifying glass.
3. Lever, 8 a. Pivots or bearings are damaged Readjust pivots See 5.16.3 “Adjustments”
or released
4.Specimen transla- a.Dirt or grease in the slip coupling See Sect. 5.16.3 “Adjustments”.
tion mechanism
5.Central axis of the a.The central axis of the left-hand Readjust each time the left-hand ear is
left-hand ear ear is not properly aligned w.r.t. the removed from the goniometer stage. See
tilt axis also 5.16.3 “Adjustments”.
Vacuum leak with holder in the Check the O-ring 318 on the holder.
goniometer Check the O-ring 8, Figure 808.
Vacuum leak with holder in and out Check O-rings 8, 9, Figure 808.
4.13.1 CS Introduction
The CompuStage consists of four basic elements:
• Hardware (called the goniometer including motors and measuring system);
• The objective stage;
• Control electronics GNCB, GDB and SCB;
• Software: present on the GNCB as a PROM (also called firmware);
present on the Memory Mother Board (MMB) as PROM (from version 10.0
onwards).
All axes on the goniometer are motor-driven. The motors are controlled by a
microcontroller located on the GoNiometer Controller Board (GNCB). Also on
this board is software to control the motors and to measure the actual
specimen position.
The X, Y and Z motors are controlled via a joystick. The alpha-tilt and beta-tilt
motors are driven via potentiometers on the Left-Hand Panel. To control the
beta-tilt motor, a foot switch must first be activated.
All items located on the goniometer are described in this manual.
The block diagram is explained in the Electronics manual, Volume 1, Chapter
11CS.
The control electronics are described in the Electronics, Volume 3, Chapter
3.28.
The software is not described, although the calibration procedure is described
in Sect. 4.13.3CS.
The error messages are described in the Electronics, Volume 1, Section
1.12.2.
If the goniometer has been serviced, or in the event of problems, test software
may be needed to locate the cause of the fault. This test software will be made
available during service training courses at the supply centre. For a description
of the test see also the CMxxx CompuStage Test and Diagnostic Software
manual, code no. 4822 870 15459.
Contents
Figures
4.13.2.3 Y movement
The Y movement is the next movement on top of the Z movement, this means
that the Y movement takes place in the tilted plane and the actual height plane.
The Y motor 16 drives via a reduction a worm-wheel which in turn drives a
Contents
donator. The output of the donator is connected via a fixing block to a driving
Figures
axle. The driving axle moves the X support and thus the specimen hence and H
forth. Two anti-backlash springs 34 ensure that the X support is always in
contact with its driving rod. On the other side of the X support is mounted a
measuring system 28 that senses (via a ruler illuminated by a led) all
movements in the Y direction. The measuring system controls the movement
and keeps track of the Y position.
4.13.2.4 X movement
The X movement is the next movement mounted on top of the Y movement,
this means that the X movement takes place in the tilted plane, the actual
height plane, and the given Y traverse.
Via a reduction, the X motor 18 drives a worm-wheel which in turn drives a
donator. The output of the donator is connected via a fixing block to a driving
rod 9. The driving axle moves the X lever 7, of which the other side controls via
two pins 6 the inner floating tube. Two backlash springs 8 ensure that the X
lever is always in contact with its driving rod. The movement is transferred via
the inner floating tube to the holder which rests in the intermediate bearing cup
48. To avoid the use of a dynamic O-Ring a bellows construction 47 has been
made. On the X lever a measuring system is mounted that senses (via a ruler
illuminated by a led) all movements in the X direction. The measuring system
controls the movement and keeps track of the X position.
7 8 9 10 16 17 18 19 20 24
4 56
X (axial)
13
25
26
14
15 Y (lateral)
29 28 27
36 30
37 34
38 35
39 33
α tilt
48 47 46 45 44 40
41
Z (height)
42
EM6576A
H
EO AXIS
C1 = CENTRE OF HEMISPHERE
CC = CENTRE OF TILT AXIS BEARING
SPECIMEN
PLANE
HEMISPHERE -X
C1
TILT AXIS BEARING
α1
CC
Ideal situation: No displacement
+X
α2
+Z (EPDEPD)
-X
+X (EPD)
NO DISPLACEMENT -Y
+Y (EPD) EM6572-1
-Z
EO AXIS
HC C1 = CENTRE OF HEMISPHERE
CC = CENTRE OF TILT AXIS BEARING
α2’ HC = HEIGHT PLANE CORRECT
∆h HF HF = HEIGHT PLANE FAULTY
α1’
HEMISPHERE
TILT AXIS BEARING
SPECIMEN
C1
PLANE
-Z CC HOLDER AXIS Height error: Equal displacement
-Y
TILT
-X
+X
+Z (EPD) in both directions
AXIS (EPD) α1
-Z
ADJUST HEIGHT TO C3
EO AXIS
C1 = CENTRE OF HEMISPHERE
α1’ CC = CENTRE CORRECT
SPECIMEN CF = CENTRE FAULT
∆t PLANE
C1 CC
∆t TILT / HOLDER AXIS
CF -X
+X (EPD)
+Z (EPD)
Tilt error: Equal displacement
ADJUST
TILT AXIS SCREW
α1
-Y onr direction
TO CC
-Z
EO AXIS
HC C1 = CENTRE OF HEMISPHERE
CC = CENTRE CORRECT
α1’ ∆h HF CF = CENTRE FAULT
HC = HEIGHT PLANE CORRECT
HF = HEIGHT PLANE FAULTY
α2’
∆t
SPECIMEN
PLANE
HEMISPHERE TILT AXIS BEARING
C1 CC
HOLDER AXIS
∆t
-X Combined error: Unequal displacement
+X (EPD)
ADJUST
TILT AXIS
CF
-X +Z (EPD) in both directions
SCREW TO CC +X (EPD)
TILT AXIS ∆h
-Y
α1
0° TILT → α2’ - TILT C3
α2’ - TILT → α1’+ TILT ∆t
ADJUST HEIGHT TO C3
CAUTION! This safe entry switch does not work for holders with a sapphire
on the tip, or for third party holders. See also 4.13.5 “CS Holder
safe entry lock”, Safe entry lock.
NOTE: If a beta tilt holder is inserted, the holder will be automatically calibrated
while it is in the park position. During homing, the electrical zero-position
of the feedback potentiometer is read out and used as a reference for
mid-position of the holder. The holder should not be inserted if the red
led is lit.
Slow speed
Position at
start-up Full speed
Return to mid-position
SES SES
CAUTION! Never press the reset AB key as this will reset the holder to a
software calculated mid-position.
This procedure is only applicable to the Double tilt holder and must be followed
if the previous step was not successful.
• Press the Enabled softkey to disable the goniometer (If not yet done);
NOTE: This procedure is the same as when switching the microscope on and
off. See also 4.13.3 “Trouble shooting”.
NOTE: If the motor cannot be moved using the battery, e.g. because it is
mechanically obstructed, the column must be opened in order to safely
retract the holder.
Visible part
2 mm 1 x 4 mm 4.5 mm 7 mm
As can be seen from Figure 4-8, the holder identification switch can be set as
follows:
SELECT
Select means that the operator has to select the holder each time from the list
on the Data monitor. Terminate the selection with the softkey “Ready”.
NON-SELECT
Non-select means that the operator does not need to select a holder. In
practice this means that only a single tilt holder will fit in both SuperTWIN and
Contents
Figures
TWIN microscopes. H
The safety switches do not prevent or detect any unwanted insertion of holders
with a sapphire on their tip, or of third party holders.
CAUTION! If these holders are inserted, the O-Ring on the holder must be
replaced by one of size 2 x 8.5 mm.
94, Figure 818 Fixing tool to clamp the upper Y support. The tool is needed,
e.g., when removing the CompuStage from the objective
stage. After clamping, Z and Y movement is no longer
possible.
95, Figure 818 Vacuum dummy. This tool can be used to check if there is a
leak in the goniometer. It can also be used during service
work on the CompuStage to ensure that the column vacuum
is maintained.
96, Figure 818 Support on which the goniometer must be mounted when
doing maintenance work on the CompuStage.
Note:It is strongly advised to support the floating rod once it is
removed from the hemispherical bearing cup, if it is
necessary to test any of the movements. This can best be
done using a soft polythene foam around the floating rod.
96B, Figure 818 Plastic ring to be mounted between the CompuStage block
16, Figure 808A and the supports on 96, Figure 818.
46, Figure 818 Key to remove the crown nut 121, Figure 807A.
Note:The key is delivered as a part of the goniometer tool kit
5322 695 14509.
47, Figure 818 Tool to remove the hemispherical bearing cup 132,
Figure 807B from the goniometer stage.
Note:The tool can be ordered under ordering code 5322 395
90197 or is also a part of the goniometer tool kit 5222 695
14509.
Contents
Figures
Alpha tracking error Check that the alpha EPD 10 is activated before a mechanical H
end stop is touched.
Check that the full tilt range is between + and – 80 degrees. See
also Section 4.14.4 “CS Alpha tilt limit stops”.
Readjust the alpha tilt drive see Section 4.14.10 “CS Adjust-
ment of the tilt motor drive” (not for first series).
Check that there is no mechanical obstruction, e.g.:
- from the covers or cover plates.
- from the ty-rap on the Z motor.
- from the front cap touching the encoders.
- upper or lower end stop jammed.
Temperature of MBG rack is too high. Leave front cover out.
Z tracking error Check that the Z opto coupler 284 is activated before a
mechanical end stop is touched, e.g.:
- lever touching the SIB 1 board;
- lever touching the opto coupler;
Check that the height range is between + 0.375 and –
0.375 mm. See also Section 4.14.5 “CS Z limit stops”
Gearwheels have too little play over their full range.
Upper or lower end stop (232 and 255) jammed, or passed the
lower end stop one turn.
Grubscrews to set the Y clamping block are too tight so that the
clamping block can not pivot.
Y tracking error Check that the Y EPD 298 is activated before a mechanical end
. stop is touched.
. Check that the full Y range is between + and – 1 mm. See also
. 4.14.6 “CS Y limit adjustments”
. Interchange the X and Y donators.
. Too much friction of the X support on the balls of the Z lever
. Measuring system is mechanically obstructed or electrically not
. working.
. Y driving rod not properly clamped.
. Front cover touches the measuring system.
. Braided wires form an obstruction.
Y travel errors Manual Double tilt, Rotation, Reflection Diffr holders need a
special tapered cover. (4022 185 40432).
X tracking error Check that the X EPD 59 is activated before a mechanical end
stop is touched.
Check that the full X range is between + and – 1 mm. See also
4.14.7 “CS X limit adjustments”.
Interchange the X and Y donators.
Measuring system is mechanically obstructed or electrically not
working.
X driving rod not properly clamped.
Braided wires form an obstruction.
Display value changes during Too much play on the balls 34, 37 Figure 808A.
an airlock cycle
Encoder error (alpha, beta, X, Check the wiring of the encoder that caused the error message.
Y, Z)
Contents
Figures
High Resolution problems Hinged bearing 190, Figure 808A does not give sufficient pres- H
. sure. V groove not properly adjusted.
. X lever bearings 34, 36, Figure 808A have too much play.
At 60 degrees Holder not sufficiently clamped in the floating rod.
Anti back-lash springs 96, Figure 808A not strong enough.
Double tilt Holder moves errat- Error in software version 10.
ically Proceed with special extraction procedure. See section
4.13.3 “CS Calibration procedure”.
Pole hit error Move the failing axis around the point where the pole hit
appears. Check that at that moment the 2 volt is grounded. This
can safest be done by inserting the dummy holder 503,
Figure 808A.
Due to wear, the metal tip of the measuring system can cause a
pole hit. Order new sapphire tip via help desk.
Springs of the Y driving rod are connected to ground.
Braided wires are connected to ground.
Protection eccentric 314, Figure 808A is incorrectly adjusted.
Third party holders are connected to ground via external elec-
tronics.
When touching the CompuStage the pole hit appears. Com-
puStage is grounded due to charging of operator.
Vacuum leaks during speci- Re-adjust protection pin 314, Figure 808A. Manually keep pres-
men retraction sure on the cover 138, Figure 808A while retracting .
Vacuum leaks during air inlet Re-adjust the air inlet pressure to max 0.1 bar overpressure.
Optical Axis
Position at EPD
start-up Full speed
Mid-position
If during calibration the end stop is found before the EPD, the result will be the error
message “Tracking error”
Contents
Figures
H
Errors after calibration
Optical Axis
Slow speed
Position at
start-up Full speed
SES SES
Mid-position
As can be seen the SES (Software end stop) is outside the mechanical end
stop away from the EPD. If after calibration the specimen is moved towards this
end stop, the result will be the error message “Tracking error or Unexpected
end of stroke”.
Optical Axis
Position at
start-up Full speed
EPD
SES SES
Mid position
Adjustable end stops
As can be seen the EPD is adjusted far away from the end stop. If after
calibration the specimen is moved near towards this end stop and a new
calibration is started from this position, the result will be the error message
“Tracking error”. This problem can be cured by manually moving the specimen
towards mid position and readjusting the EPD. (Often the Z EPD).
Contents
Figures
Vacuum leak with holder out of the goniometer Check O-Ring 54, Figure 808A. (or 6 in
(vacuum OK with holder inside) Figure 4-11. below)
Vacuum leak with holder in the goniometer (vac- Check the O-Ring on the holder (9 in Fig.
uum OK with holder retracted) below).
Check the O-Rings 2, 3, 4, 5, 11,12 in Fig.
below).
Check O-Rings 124, 226, 188, Figure 808A. (or
10, 7, 8 in Fig. below)
Vacuum leak with holder in and out Check O-Rings 125, 120, Figure 807A. (or 1, 2
in Fig. below)
If the vacuum leak is less with holder in while Check pre-vacuum valve and O-Ring 37,
simultaneously pumping the lines Figure 807A. (or 6 in Fig. below)
11 V8
4
12
3
Bearing Cup
5
2
1
6
Airlock Ball
6
1
2
5
3
4
Inner Objective Block
H
Airlock ball open
12
11 V8
4
12
3
Bearing Cup
5
2 Air In
1 8
6 Airlock Ball
9 Holder
6
8
1
2 10
5
3
4
11 V8
4
12
3
Bearing Cup
5
2
1
Airlock Tool
1
2
5
3
4
removing.
Figures
4.14 CS adjustments H
CAUTION! This adjustment should be carried out after dismantling the V-groove
assembly, or the airlock assembly. It is of vital importance that the
eccentric bush 98 and eccentric screw 78 turn simultaneously,
otherwise screw 78 may be damaged.
NOTE: To facilitate the adjustment remove the knob from the single-tilt holder as
follows:
Remove the Allen key 14 and take out key 15;
Via the key hole push out the cap 8;
Remove the screw 10 and take out the complete cap.
• Readjust with the eccentric screw 78 the V groove assembly height. The
specimen holder will centre the V groove in the Y direction so take care that
the Allen key does not apply too much force in the Y direction. The
adjustment is optimal when the V groove lifts the holder 20 µ m. When this
is the case the loop error in the X direction will be a minimum.
NOTE: Ensure that the eccentric screw 78 is adjusted so that the indication lines
on the eccentric point towards the column (so as to avoid touching the
front cover 138 when mounted).
NOTE: Check that after the adjustment the grubscrew 6 does not touch the walls
of the recess.
8
7
6
5
4
9
10
14
15
16
17
18
19
20 EM6628
NOTE: Ensure that the cover cap 138, Figure 808A is pushed towards the
column while retracting the holder.
Contents
Figures
NOTE: The adjustment of the limit stop 310 must be such that pin 347 strikes it
fully and cannot slip off and jam.
NOTE: The limit stop is only activated after completing a full turn (70 µm) of the
gearwheel 254. So that the eucentric position can only be adjusted (with
respect to calibrating position) in steps of 70 µm.
If not within the above limits, note the value and sign of the displayed value and
adjust the Z limit stops as follows:
• Calculate the number of Z movement revolutions required to bring the Z
Contents
Figures
axis in line with the eucentric axis = display value noted divided by 70 µm, H
rounded off to a whole number of revolutions;
• Release grubscrew 263 and adjust pin 255 so as to create mechanical
clearance;
• Move the Z towards the opto-switch using the joystick until the display
reads the maximum possible negative value;
• Press softkey “Enabled”;
• Mark the position of gearwheel 259, and manually turn this gearwheel the
exact number of revolutions calculated above (negative number = turn
counter-clockwise; positive number = turn clockwise).
• Adjust pin 255 so that if gearwheel 259 is now turned further in the same
direction, pin 253 fully “stops” pin 255, but if gearwheel 259 is turned in the
reverse direction, pin 253 just “clears” pin 255.
• When the adjustment is satisfactory, tighten grubscrew 263 and carry out
the calibration procedure.
NOTE: After readjusting the end stop the EPD 284, Figure 808A will need
readjustment too.
NOTE: This adjustment is only necessary when the complete goniometer has
been dismantled.
• Insert a single tilt holder in the goniometer. The holder must not contain a
specimen;
• Set the magnification to about 200x;
• Move the holder to its maximum negative limit using the joystick;
• Note the distance between the edge of the hole in the holder and the centre
of the screen;
• Move the holder to its maximum positive limit using the joystick;
• Note the distance between the edge of the hole in the holder and the centre
of the screen;
• If present release grubscrew 317A and adjust grubscrew 317 until the
distances just noted are equal. See figure following.
NOTE: Each time the grubscrew is adjusted, the calibration procedure must be
carried out.
The position of the Y driving rod is not important as the system is
calibrated from the mechanical limit close to the EPD.
Screen Screen
Screen centre
Image of the hole centre centre
in the holder
-1000 µm +1000 µm -1000 µm +1000 µm -1000 µm +1000 µm
NOTE: This adjustment is only necessary when the complete goniometer has
been dismantled.
• Insert a single tilt holder in the goniometer. The holder must not contain a
specimen;
• Set the magnification to about 200x;
• Move the holder to its maximum negative limit using the joystick;
• Note the distance between the edge of the hole in the holder and the centre
of the screen;
• Move the holder to its maximum positive limit using the joystick;
• Note the distance between the edge of the hole in the holder and the centre
of the screen;
• Release grubscrew 118 and adjust the end limit pin 124 until the distances
just noted are equal. See figure following.
NOTE: Each time the end limit pin is adjusted, the calibration procedure must
be carried out.
After readjusting the end stop the EPD 121, Figure 808A will need
readjusted too.
The position of the X driving rod is not important as the system is
calibrated from the mechanical limit close to the EPD.
H
Added as a pass gauge
EM7730
• Release screw 506 and remove the transport holder 503 from its bracket
507;
• Insert the transport holder 503 in the goniometer;
• Release the four screws 137 and accurately centre the front plate around
the holder.
NOTE: After fixing the front plate check that the holder does not touch the ring,
using the X joypad movement.
• Remove the X motor. See also 5.15.4 “CS Removal of the X motor
assembly”;
• Adjust grubscrew 81 until it just does not touch bush 199;
• Remount the X motor and check that the X movement does not suffer from
“lassoing”. See also 4.15.1 “CS Test procedure”.
NOTE: This adjustment is necessary when the alpha tilt causes tracking errors
but is not obstructed.
CAUTION! The grubscrews should just not touch the cover on top of the donator,
Contents
so that the clamping block can turn freely around its axis.
Figures
NOTE: All height and tilt errors will generally cause displacements in the same
direction as when using the Y movement. Errors in the direction of the X
movement must be due to the O-rings 119, 120, 125 in the bearing cup
or in the Y drive rod (old type)
• Tilt the specimen to +45°, 0°, -45° (or to the maximum allowed tilt angle for that H
pole piece configuration). Note the movement of the selected feature;
• Tilt again (or to the maximum allowed tilt angle for that pole piece
configuration). Bring the selected feature halfway back to the centre of the
screen with the tilt axis alignment screw, 350 Figure 808A;
• Bring the feature back to the centre of the screen using the X - Y joypad
controls;
• Repeat steps 3 to 8 until a minimal displacement occurs when tilting to +45° or -
45° (or to the maximum allowed tilt angle for that pole piece configuration) at a
magnification of 120,000x.
Z- Movement
Total travel : ≥ 0.75 mm
Step resolution : ≤ 36 nm
Maximum speed : ≥ 10 µm/sec.
Reproducibility : ≤ 0.5 µm
Read out resolution on CRT : 0.01 µm
Measurement resolution : ≤ 7 nm
– Ambient conditions: H
NOTE: For more diagnostic details see also 4.9 “Image drift (For CompuStage)”.
4.15.1.2 Z Movement
Travel:
Settings:Magnification about 50 kx.
Alpha tilt on 0 degrees and X and Y in mid-position.
Move the Z-movement to its maximum positive height and check that the
reading on the screen is +375 µm. Repeat this for the maximum negative
height; the reading must now be -375 µm.
• Split the column between the objective lens and the condenser lens (see
5.10 “Opening & closing the column above the specimen stage to gain
access to the specimen chamber”);
• First remove the objective diaphragm holder 140, Figure 807A, then its
mechanism (see 5.17.1 “Dismantling procedure”);
• Set the fixing plate 155 as low as possible. (For SuperTWIN set plate 155
as high as possible);
• Remount the diaphragm mechanism and set it in the highest position using
the play in the screw holes;
• Place a piece of lens paper on the lower pole piece. Carefully remount the
diaphragm holder. Now shift the diaphragm mechanism downwards until
the lens paper is just not touched.
Remove the lens paper and check that for all four (three) diaphragm
positions the holder just does not touch the pole piece.
NOTE: The height difference between the first and last diaphragms should be
within 50 µm.
NOTE: As the 7-position diaphragm holder is nearer to the lower pole, the
position of the aperture cannot be used as a reference for the TWIN
current adjustment. Use as a reference in alignment step 014 a TWIN
current of 95% of its maximum. See also Section 4.14.2 “CS Adjustment
of the X and Y motors on their gear-wheels”.
centred with the fine axial displacement knob. If not, replace grubscrew 69
Figures
in one of the other holes and repeat the check until satisfactory; H
• Release the lateral displacement knob. Now check that all four diaphragms
can be centred. If not, unscrew grubscrew 78 a little and try again. Repeat
until satisfactory.
NOTE: If requested select conical so that the central beam can be rotated over a
fixed angle for 360 degrees to find the optimum angle for visibility of
graphite fringes. For CM100 this is mostly at the 10 o’clock direction
NOTE: For BioTWIN magnetic fields must be: horizontal < 185 nTesla
vertical < 440 nTesla
The conditions are the same as described above, but follow the procedure
below:
0.34 nm point-to-point
• Only axial illumination.
• Select normal M mode.
• Select a suitable thin carbon particle, containing a band of high contrast,
located close to a grid bar to avoid drift.
Increase magnification to maximum, where lattice spacings, if present in
the selected part of the specimen, should be visible through the binocular.
Adjust the objective lens current for optimum visibility of the graphite
fringes, which occur at approx. 50-75 nm under-focus.
• Adjust "INTENSITY" to give an exposure time of 2 seconds, and make an
exposure.
• Develop the plates/film and make enlargements with a final magnification
of two million.
• Special attention should be paid to the rotation alignment accuracy.
If no beam tilt was necessary to achieve 0.34 nm lines in all directions, this
test can be considered as a valid point-to-point resolution test.
0.50 nm point-to-point
• Only axial illumination.
• Select normal M mode.
• Select a suitable thin carbon layer, close to a grid bar to avoid drift.
• Adjust "INTENSITY" to give an exposure time of 2 seconds.
• Increase magnification to maximum, Correct astigmatism. Adjust the
Contents
objective lens current for minimum contrast, Select focus step 2 and make
Figures
0.5nm
0.5nm
EM6915
4.16.3.2 Procedure
• Spot size position 2, intensity slightly over-focus.
• Ensure that the condenser astigmatism is properly corrected.
• Correct objective astigmatism on the grain structure of the specimen.
Highly accurate correction is necessary for obtaining a good micrograph.
• Select a suitable particle.
• Increase the magnification to maximum where lattice spacings, if present in
the selected part of the specimen, should be visible through the binocular.
• Adjust the objective lens for optimum visibility of the 0.23 nm Au lattice in
two directions. See Figure 4-13.
Contents
Figures
a’
H
For 0.1 nm
For
4 a 0.09 nm
1
For For
0.2 nm 0.14 nm
d’ d b b’
Central beam
3 c 2
c’ EM6347A
NOTE: - The step marked with an asterisk should not be performed when
doing the 0.2 nm axial resolution test.
- When the sample is first bombarded by electrons, there will be
some disturbance caused by localized heating of the sample.
The beam should then be left on a particular area for a short
time to thermally stabilize the sample before micrographs are
taken.
- If 0.14 nm lines in a certain direction cannot be found, use a
diffraction spot opposite to the one used before. So, e.g. instead
of spot 1, use spot 3 (see also previous Figure), or instead of
using spot a’, use spot c’, etc.
CRYSTAL AXIS
CRYSTAL
AXIS
CRYSTAL
0.14 nm 0.14 nm
90°
90°
0.204 nm
(0.10 nm orientation 0.204 nm (0.10 nm orientation
in same direction) in same direction)
45°
45°
NOTE: For detectors above the specimen the gold layer should be facing
upwards.
Resolution is proved when the specified distance can be found between the
edges of two separated gold particles.
System setup for STEM resolution (BF/DF detector only) not for CM100
- Test specimen : Gold-shadowed latex balls, Agar S128B,
5322 695 14566
- Select 120 kV : 45 minutes stabilized.
- Select C2 Aperture : 50 µm
- Set emission to : Tungsten : 60 to 80 µA
LaB6 : 10 to 20 µA
- Anti-contamination device : Cooled down for at least 45 minutes and
refilled before the test is started.
- Select spot size : 6 to 7
NOTE: The microscope must be properly aligned before starting the resolution
procedure.
Also it is advised to check the specimen in the TEM mode to see if the
particles are near to each other. If not, select another part or heat the
specimen (Large C2 aperture, high emission current) to make the
particles “grow”.
Procedure
• Select a magnification of 200,000 x (130,000 on photo-monitor) and make
an SA image
Line time 10 ms and lines/frame 288 or 576.
• Select Full frame mode . Select a line time of 55 ms. Select 1152 lines/
frame. Program these settings for EXP 1.
• The exposed (polaroid) film should show details with a separation of 0.13
mm (130,000 x 1 nm).
Contents
Figures
NOTE: The microscope must be properly aligned before starting the resolution
procedure.
Also it is advised to check the specimen in the TEM mode to see if the
particles are near to each other. If not, select another part or heat the
specimen (large C2 aperture, high emission current) to make the
particles “grow”.
Procedure
• Select a magnification of 75,000 x (50,000 on photo-monitor) and make an
SA image
Line time 10 ms and lines/frame 288 or 576.
• Select Full frame mode .Select a line time of 55 ms. Select 1152 lines/
frame. Program these settings for EXP 1.
• The exposed (polaroid) film should show details with a separation of:
SED 0.125 mm = (50,000 x 2.5 nm)
BSD 0.200 mm = (50,000 x 4.0 nm).
Position number
Aperture
Type
1 2 3 4
SA Not standard
SA Not standard
Contents
Figures
Position number H
Aperture
Type
1 2 3 4
Test conditions:
beam current used
X-ray leakage = x permissible X-ray leakage
max. beam current
20 µA 1 µSv = 0.2 µSv
X-Ray leak LaB6 x
100 µA
• Emission: Tungsten, 100 µA; LaB6, 30 µA;
• Select maximum high tension;
• Select a C2 aperture of 150 µm;
• Select spot size 1 and 8;
• Create the worst operating conditions to generate X-rays.
This can be done as follows:
– Obstruct the beam (focussed and non-focussed) to create horizontal
back-scattered electrons (and thus also X-rays) in the direction of the
suspected weak spot.
– Move the focussed beam to create vertical X-Rays directed towards
Contents
the suspected weak spot (e.g. a slit in the projection chamber bottom).
Figures
NOTE: * The “gun air” key cannot be activated after performing these steps.
NOTE: From version 10.0 onwards a “gun air” and “col. air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
5.3.1 Procedure
(for microscopes according to Figure 815B)
• Remove the cover at rear of microscope to gain access to water blow-off
device;
• Remove the compressed air fast coupling 6 from its normal position. This
process opens microswitch contacts S37 to switch off the microscope.
CAUTION! Check that the compressed air pressure is higher than the water
pressure.
• Now open, in turn, valves V24, V25, to drain the water from each branch
Figures
separately. Open valves V24 and V25 and now blow off the two branches H
together;
– Air will now flow into the column water hoses to blow off the cooling
water. This will take a few seconds. When there is a large amount of air
leaving the drain outlet (together with the water still flowing through the
pumping system), replace the air hose coupling in its normal position.
• Close non-return valve V26;
– Close valves V24, V25
– Reinsert the fast coupling 6 in its original position
• Carefully remove the appropriate water hoses ensuring that remaining
water cannot drip into any part of the microscope;
• If it is required to keep the pumping system switched on (not applicable for
CM100), proceed as follows:
– Switch on the microscope
– Operate the lifting mechanism in order to interrupt the lens supply (via
S34, lenses interlock);
– Press the bake-out switch P/A13-S2.
5.3.2 Procedure
(for microscopes according to Figure 815C)
• Remove the cover at the rear of the microscope to gain access to the water
blow-off device;
• Close valve V22;
• Check that the compressed air pressure is higher than the water pressure;
• Remove the air-hose coupling 8 from its normal position. This process
opens microswitch S37 to switch off the microscope;
• Connect fast coupling 8 into blow-off position 14. Compressed air will now
flow into the column water-hoses to blow-off the remaining cooling water.
This will take a few seconds. When there is a large amount of air leaving
the drain outlet, together with the water still flowing through the pumping
system, replace the air hose coupling in its normal position.
• close valve V21;
• Carefully remove the appropriate water hoses ensuring that remaining
water cannot drip into any part of the microscope;
If it is required to keep the pumping system of the microscope switched on, the microscope may
be switched on after blowing off the water. The following additional steps have to be taken:
• Interrupt the lens supply by disconnecting S34 (gun-lift switch);
• Switch on the microscope.
CAUTION! Do not forget to open valves V21 and V22 again after the draining
procedure.
Contents
Figures
NOTE: Any broken seals must be removed and replaced by new ones.
5.4.2.1 Tool C
Used to prepare indium seals. Indium wire of the correct thickness should be
wound around the appropriate part of the tool and cut with a scalpel or razor
blade with the blade in line with the forming tool (see Figure 5-1).
Contents
Figures
NOTE: Item D has two diameters and can also be used on top of the membrane
assy. 11, Figure 805.
5.4.2.4 Tool F
A guide bush to prevent damage to the objective pole pieces when using tool
B.
CAUTION! To remove the indium from the upper and lower objective pieces, use
also guide bush 5F.
Take care that no small indium particles fall into the gun airlock; use
tools 5D or 5E; Do not use any sharp tools that may cause damage to
the seat of a seal.
• Using tool 5C cut a piece of indium wire of the correct length and diameter;
• Clean the wire in an ultrasonic cleaner;
• Handle the cleaned wire with gloves - or with fingers well washed with
cyclohexane - and place the wire into its correct seating. Gently press into
position with the appropriate tool 5A or 5B.
CAUTION! Do not touch nuts 85 (covered with rubber hoods). See also
5.7 “Emission chamber: removal, assembly & alignment”
CAUTION! Take care that the porcelain does not touch the emission chamber as
this may cause HT instabilities.
NOTE: Gradually tighten the three screws 90 by equal amounts in turn. Ensure
that they are fully tightened.
• First carry out the procedures described in the previous two sections;
• Remove the plug from the gun tilt coils (DCB X1, X2) and free the cable.
Also release the plug to S33 and the safety earth connections;
• Release the 4 screws 200. Now the complete emission chamber can be
lifted from the column to be dismantled on a clean working table as follows:
a. Remove the lead protection elbow 226 by releasing the four screws
189;
b. Release the 3 screws 192 and take away the vacuum tube 193
between the emission chamber and the U.H.V. valve block;
c. Remove the gun tilt/gun shift coil by releasing screw 206;
d. Remove the 3 screws 184 and take away the lead ring;
Contents
e. Remove the three screws 179 and lift the emission chamber from its
Figures
housing 195. H
Reassembly and remounting is done in the reversed order, but take the
following notes into account:
– First fix the emission chamber back on top of the membrane block.
NOTE: Don't forget to remove the old indium seal 10, Figure 805 and
replace it by a new one, 0.7 mm dia., length 36 mm approx. Use
tools 5B, C and D, Figure 818.
• Remount the vacuum connection 193 and fix it to the emission chamber.
• Slacken the three screws 215;
• Adjust screws 225 until the play between the block 4, Figure 821 and the
ring 209 is minimal. Lock this position with the nuts 217;
• Now tighten the screws 215 to fix the O-ring 210;
• Mount the lead shields 226, 186. Take care that once these shields are
fitted the play between them is a minimum.
• Split the column between the objective and condenser lenses, see
5.2 “Admitting N2 to the column” and 5.10 “Opening & closing the column
above the specimen stage to gain access to the specimen chamber”.
• Lay 3 spacers, 18 mm 70, Figure 818 (not delivered), on the outer rim of
the objective stage and lower the condenser section until it is just above
the spacers;
• Adjust the 3 nuts 85 such that the bottom of the condenser lens is level with
the 3 spacers within 0.1 mm. Secure with the top nut 85 and perform the
same test again.
NOTE: If the rotation alignment cannot be done within the end controls, proceed
as follows:
- Release the screws 58, Figure 806;
- Release the screws 90, Figure 804 and proceed as if to lift the gun;
- Gently rock the upper part of the column w.r.t. the goniometer
stage;
- Lower the gun lifting device again and release screw 30;
- Tighten screws 58, Figure 806. Fasten screws 90 then screw
30.
Contents
Figures
CAUTION! Before the column is opened check that screws 90, Figure 804 are
tight.
• Admit air to the gun chamber and column, see 5.2 “Admitting N2 to the
column”;
• Place the gun lifting arm 14, Figure 804 in the hole one position higher to
locate the lifted part of the column;
• Remove the 4 Allen screws 200, Figure 804. By turning the lifting
mechanism clockwise, raise the emission chamber until it is well clear of
the lead block 1. Replace the gun lifting arm 14, Figure 804 and swing out
the column.
CAUTION! Check that the cables and hoses going to the emission chamber are
not obstructed.
– Pull out the bellows assembly 41 and the attached seating assembly H
from valve block 14;
– If necessary, the valve seating assembly can be dismantled after
removing circlip 26. Take care not to lose the four balls 20.
The condenser and diffraction diaphragm mechanisms are similar to that of the
objective diaphragm mechanism. Therefore, references in the text following are
made to the exploded view of Figure 807 showing the objective diaphragm
mechanism in detail.
• Remove the diaphragm holder 16, Figure 806 (for condenser diaphragm)
or 89, Figure 810 (for the diffraction diaphragm);
• Unscrew the three screws 15, Figure 806 (for condenser diaphragm) or 79,
Figure 810 (for the diffraction diaphragm). Now turn the complete
diaphragm mechanism counter-clockwise without pulling it.
NOTE: Take care not to lose the lead shielding 28, Figure 806 (for condenser
diaphragm) or 8, Figure 810 (for diffraction diaphragm).
• Remove grubscrew 76 and take out the plunger rod limiter 74.
Reassemble in the reversed order.
CAUTION! Before the column is opened check that screws 90, 200 Figure 804
are tight, and enure that the SED has been removed (see Section
5.20.2 “Secondary electron detector”).
• Place the gun lifting arm 14, Figure 804 in the upper position. Turn the
Figures
lifting mechanism clockwise and raise the column until the pole piece is H
well clear of the goniometer. Remove the gun lifting arm 14, Figure 804,
then swing out the column.
CAUTION! Check that the air/water hoses and cables to the column are not
obstructed. If the pneumatic hose to V7 is too short, press the “gun
air” softkey and release the hose.
NOTE: This frees the indium in the pole piece from the vacuum lining tube.
• Remove O-ring 27 and unscrew fixing nut 26 using tool 6, Figure 818: pole
piece 25 can now be removed;
• If a back-scatter detector is present, the diaphragm assembly 23 can now
be removed from the pole piece 25 using tool 62, Figure 818
Remount in the reversed order. Do not forget diaphragms 22, and the indium
seal 24, dia 0.7 mm, length 36 mm approx. See also Sect. 5.4 “Location and
replacement of indium seals”.
NOTE: Before fixing the pole piece 25, mount tool 28, Figure 818 underneath
the cover 10, Figure 806. Slide pin 29 into the hole of the pole piece and
tighten the pole piece.
The pole piece is now aligned to accept the SED.
lining tube 27. Release the grip and remove the fixed C1 diaphragm 36. H
NOTE: Place the diaphragms in a clean closed glass container. Inspect them
and clean if necessary.
• To fit the diaphragms follow the reversed procedure and do not forget the
indium seal in the pole piece: dia. 0.7 mm 24, Figure 807, length 36 mm
approx. See also 5.4 “Location and replacement of indium seals”.
NOTE: Do not forget to drain the water from the column (see 5.3 “Draining
water from the column”).
NOTE: This frees the indium in the pole piece from the vacuum lining tube.
• Remove O-ring 27, Figure 807 and unscrew the pole piece fixing nut 22,
Figure 807 using the tool 6, Figure 818. Take care that the diaphragm 22
does not drop.
• Remove the water hoses, water pillars and lens current plugs, MC-X1, X2,
X3.
Remove the alignment coil plugs X5 of DCB-3, 4, 5;
• Release the three screws 18, Figure 807 until the lens section rests on the
three screws 57.
• Release the three screws 57 while manually supporting the upper lens
section (about 5 kg).
CAUTION! When remounting the upper objective lens housing, great care must
be taken not to damage the fragile supports 42. These supports are
present in instruments delivered from Oct. 1990 onwards.
CAUTION! Never release centring plate 15, Figure 807 as this is factory
aligned.
Contents
Figures
• Unscrew the three screws 15. Now turn the complete diaphragm H
mechanism counterclockwise without pulling it.
• Remove the two screws 38 and plate 39. Now pull out the vacuum liner
tube 27 with its fixed diaphragms.
• To remove the C1/C2 lens assembly proceed as follows:
– Close the column and open it again between the emission chamber
and V7 (screws 200, Figure 804) - see also 5.8 “Removing,
dismantling & remounting of the gun airlock valve, gun centring coil or
the x-ray diaphragm”.
– Remove the lead shield 1, Figure 805.
– Now remove the four cheese-headed screws 13, Figure 805.
– Disconnect the electrical plug from S7 and the compressed air hose
55. Now the complete valve V7 can be removed. For dismantling of V7
see 5.8 “Removing, dismantling & remounting of the gun airlock valve,
gun centring coil or the x-ray diaphragm”.
• Remove the three locking plates 5. Screw the two knurled screws 7, Figure 818
into two of the four holes of pole piece 8 and remove the C1/C2 lens assembly.
CAUTION! When reassembling the upper column half, the lining tube must
always be fixed and centred first at the upper objective pole piece
with V7 not yet mounted, otherwise the lining tube may be seriously
damaged.
NOTE: Check that screws 90, 200, Figure 804, and 58 Figure 806 are fully
tightened.
CAUTION! Remove the SED before splitting the column (For TWIN only).
• Using the lifting mechanism lift the goniometer stage until it is just free of
the pole piece (about 15 mm).
CAUTION! Check that the air/water hoses and cables to the column are not
obstructed.
If the pneumatic hose to V7 is too short press “gun air” softkey and release the
hose.
• Lay three spacers (70, Figure 818, not delivered) on the outer mantle and
lower the column again.
• Release screws 58, Figure 806, lift the upper lens section and swing it out;
• The complete goniometer stage can now be removed (weight approx. 25
kg) and if necessary dismantled on a clean workbench.
CAUTION! Remove the SED before splitting the column (For TWIN only).
• Release the screws 58, Figure 806; lift the upper lens section and swing it
out;
NOTE: Check that the air/water hoses and cables to the column are not
obstructed.
• Lay three spacers (70 Figure 818, not delivered) on the outer mantle 100,
Figure 810 and lower the column again.
• Release screws 58, Figure 806, lift the upper lens section and swing it out;
• The complete goniometer stage can now be removed (weight approx. 25
kg) and if necessary dismantled on a clean workbench.
CAUTION! The X and Y levers must never be moved manually with their driving
rods 56, 300 Figure 808A fixed. This is only allowed with the driving
rods released.
Contents
Figures
• Remove the small front plate 138 by releasing the 4 screws 137.
NOTE: Take care not to lose the actual current holder identification slot 91, 92 or
93, Figure 808A.
• Select the Vacuum page and press the softkey “Column Air”.
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
The pressure of the Nitrogen when letting air into the column should
never be higher than 0.1 bar overpressure.
CAUTION! If service work has to be done on the CompuStage, either remove the
cables from the GDB or disable the GNCB via the CompuStage
control page, to prevent unwanted movement of the motor.
• Remove the rear cover 113. Figure 808B, using screws 112, Figure 807B;
• Release the screws 44, Figure 807B and remove the bracket 118.
Figure 807B;
• Mount the special tool 94, CompuStage tools (Figure 818), to fix the X, Y
and Z movements. The four screws 94a fix the tool to the X support 35, and
the 4 screws 94b are used to clamp the total assembly to the Z bracket
244;
• Release the Allen screw 126, Figure 807B of the upper wedge 40,
Contents
Figures
• Release the Allen screw 350 several turns (releasing the pressure on the H
spring 15). Release screw 14 two turns; Figure 808A
• Remove the cable guide 61, Figure 807B from its support 49, Figure 807B;
• Remove the 4 screws 115, Figure 807B fixing the CompuStage. Note the
position of the washers 116;
• Carefully remove the complete Computage and mount it on the support
delivered 96, CompuStage tools (Figure 818). Fix the CompuStage with the
screws 115. In order to prevent damage to the specially treated surface on
the CompuStage an extra synthetic ring must be added between the
screws 96A and the CompuStage.
NOTE: The inner O-Rings 119, 120, 125 in the hemispherical bearing scale can
now best be removed and greased, as otherwise the hemispherical
bearing scale can be easily contaminated.
O-Ring 119, Figure 807B has been replaced with a special O-Ring that
no longer has the manufacturing marks on the sealing surface. When
replacing one of the O-Rings 119, 120 or 125, O-Ring kit 5322 695
15975 can best be ordered. This kit contains specially selected O-Rings
119, 120 and 125.
Contents
Figures
NOTE: When assembling, slide the bush 156 over the airlock assembly,
ensuring that pin 158 slides in the groove;
Mount the O-Ring carrier 155 and airlock O-Ring 154 on top of the
airlock assembly 159.
Check that the airlock ball 157 can rotate smoothly over 90 degrees
when closing the airlock and that the O-Ring is just lifted up when the
airlock is fully closed.
If this is not correct, the nut 160 must be readjusted until the O-Ring 154
is just lifted up, but at the same time the pins of the airlock ball 158 can
move freely over the full range in the groove of sliding bush 156.
Lightly grease the airlock O-Ring 154, prior to assembling.
Completely tighten the four screws 225 when the airlock is fully open.
NOTE: The decoding rod 4, Figure 5-2 of the measuring system must move
freely in its support. After moving the rod it must return smoothly.
Potentiometer 9, Figure 5-2, on the measuring system is factory adjusted
and should not be touched.
• Led 16, Figure 5-2 can be replaced but care must be taken that only the top
screws 15, Figure 5-2 are removed.
CAUTION! Screws 5, Figure 5-2, should never be removed as they are factory
aligned and there is no field alignment procedure.
Contents
Figures
• Carefully unscrew measuring tip 4, Figure 5-2, from the ruler axle and shift H
out the ruler axle so that it can be cleaned.
15 16
4
5
14
6
7
11
8
10
9
EM6587
57581
NOTE: The decoding rod 4, Figure 5-2 of the measuring system must move
freely in its support. After moving the rod it must return smoothly.
The potentiometer 9, Figure 5-2 on the measuring system is a factory
adjustment and should not be touched.
Led 16, Figure 5-2 can be replaced but care must be taken that only the
top screws 15, Figure 5-2 are removed.
CAUTION! The screws 14, Figure 5-2 should never be removed as they are
factory aligned and there is no field alignment procedure.
Carefully unscrew measuring tip 4, Figure 5-2 from the ruler axis and shift out
the ruler axis so that it can be cleaned.
Contents
Figures
NOTE: If the motor is defective, it is advised to remove the motor only and to
leave the gearwheel reduction in position. Otherwise, adjustment of the
motor worm and the gearwheel of the donator must be remade.
CAUTION! Do not attempt to manually move the driving rod 56 when it is still
fixed, as otherwise the rod 56 or its clamp 63 will be damaged.
NOTE: Turn the pressure screw 67 exactly two turns again when tightening or
apply a force of 17 N using a torque meter. Fix the grubscrew 65.
NOTE: If the motor is defective it is advised to remove the motor only and to
leave the gearwheel reduction in position. Otherwise adjustment of the
motor worm and the gearwheel of the donator must be remade.
CAUTION! Do not attempt to move the driving rod 300 by hand while it is still
fixed, as otherwise the rod 300 or its clamp 296 will be damaged.
Contents
Figures
NOTE: Turn the pressure screw 297 exactly two turns again when tightening or H
apply a force of 17 N using a torque meter. Fix the grubscrew 294.
NOTE: This assembly can best be removed and mounted when the goniometer
is still attached to the stage. If this is not the case, and the Z motor must
be dismantled with the X and Y motors still present, take care not to
damage the balls 32.
Do not turn the screw ring on the decoder, and ensure that the dot on the
ring is always opposite to the double dot on the housing.
From January 1995 the CompuStages are delivered with the holder
height adjustment bracket 279 in the heavy holder position.
NOTE: The screws M4 x 16 must be remounted in the rear holes so that they do
not touch the gearwheel 259.
• Release the grubscrew 275 to remove the gearwheel 278 from the motor
276;
• Release the two springs 239;
• Unscrew the four screws 277 and remove the complete Z-motor assembly
241;
NOTE: Be careful to manually support the floating rod assembly as at this point
it is no longer supported.
• Remove the SIB1 board using screws 272, 273. Take care not to lose the
spacers 266, 269;
• Remove the SIB2 board using screws 248, 249. Take care not to lose the
spacers 246, 250;
• Remove the bracket 244 using the four screws 245, 251, 265;
Contents
Figures
NOTE: The screws 228, 236 must be tightened until the play of the Z-lever is
such that the lever just does not drop under its own weight.
NOTE: The floating rod can only be removed when the goniometer is removed
from the column. Further it is assumed that the X, Y, driving axles are
completely removed (see also Sections 5.15.4 “CS Removal of the X
motor assembly”. to 5.15.5 “CS Removal of the Y motor
assembly”).
• Remove (if mounted) the fixing tool 94, CompuStage tools (Figure 818)
from the floating rod assembly;
• Remove the braided (Litz) wires using the four screws 168;
NOTE: When assembling, the braided wires must be free from ground (2V) as
otherwise the pole hit protection is always active.
Contents
Figures
• Remove the screws 50 and remove the airlock EPD from connector SIB2-
X2, take care not to damage the spring 47;
• Now carefully remove the complete floating assembly;
• Assembly is done in the reversed order.
NOTE: It is assumed that all steps of Section 5.15.8CS have been carried out.
• Remove the screws 50 and remove the EPD 48. If still connected remove it
from SIB2-X2;
• Remove the Y axis driving rod 300, this can best be done as follows:
– Pull the Y driving rod (with teflon ring to isolate it from ground) away
from its bearing position and tilt it 90 degrees to release the spring
pressure;
– Remove the two springs 303: the two pins 86, 88 will now fall out;
NOTE: When assembling, first insert the springs 303 in their recesses, then
insert the pins 86, 88 in the holes. Ensure that the cut out edge of the
EPD actuator 302 is as indicated in the exploded view (Figure 808A).
• If not yet done, remove the X measuring system guiding plate 115 with
screws 116;
• Remove the X axis driving rod 56, this can best be done as follows:
– Pull the X axis driving rod away from its bearing position and tilt it 90
degrees to release the spring pressure;
– Remove the two springs 57, the two pins 40 will now fall out.
NOTE: When assembling, first insert the springs 57 in the recesses, then insert
the pins 40.
• Remove the springs 197, 214, and remove the protection clip 196, 210.
Carefully remove the two pressure pins 195, 215;
NOTE: When assembling take care that the pins are clean, not damaged and
that they fit correctly in their mating conical slots as shown below.
Contents
Figures
EM6577 (detail)
NOTE: For dismantling and assembly of the X-motor support, see Section
5.15.10 “CS Dismantling & assembly of X motor support”.
• Release the spring supports 198, 209, as otherwise the inner floating tube
194 can not be removed;
• Remove the four screws 166 and take out the C-shaped isolation plates
167. Gently bend the braided wires away and remove plates 170;
• Carefully slide tube 200 away from the inner floating tube.
NOTE: The tube must slide out in parallel with its outer mantle as otherwise the
phosphor bronze bearing assembly 190 and the small bearings 207, 218
may be damaged.
CAUTION! Prior to removing the bellow, a marker line must be made (if not yet
factory done).
• Insert a small screwdriver between the rim of the inner floating tube 194
and the outer mantle. When just open, gently pull the floating inner tube
194 out of its mantle 176;
NOTE: When assembling take care that the angle between the two marker lines
is as accurate as possible. The final check for the accuracy of the
adjustment of the inner floating tube 194 and its mantle 176 is done after
mounting the tube 200. The two spring supports 198, 209 must then fit in
the middle of their recesses in tube 200, as shown below.
Contents
Figures
EM6580 (detail)
CAUTION! PUSH OUT the eccentric screw 78 and eccentric bush 98. Now the
V-shaped bearing will come out.
• Remove the four screws 106, 114 and remove the bearing supports 107.
NOTE: Take care not to lose spring 38 and balls 34, 37.
When assembling ensure that the marker lines of bushes 30, 44 and the
X motor support 35 correspond.
- Set lever 28 in the middle of the recess in the X support 35
(accuracy within 0.1 mm);
- First secure the bush 30 using the grubscrews 36, secondly
secure the long bush 44 using the grubscrews 39.
Contents
Figures
CAUTION! Do not turn the screw ring on the decoder and ensure that the dot on
the ring is always opposite to the double dot on the housing.
NOTE: When assembling, take care that the tilt assembly is mounted rigidly
against its recess, so that the tilt axis assembly does not move during tilt.
NOTE: When assembling, take care that the shoulders of the worm wheel axle
339 butt up against the inside surfaces of the bearings 338, 344.
The adjustment of the tilt motor drive is described in Section 4.14.10CS.
NOTE: The pressure bearing can only be removed when the goniometer is
removed from the column. Further it is assumed that all three goniometer
driving axes X, Y, Z are completely removed and that the floating rod has
been removed. See also Sections 5.15.2CS to 5.15.8CS.
• Remove screws 4 and remove the cableform 6 with the two tyraps 5;
• Remove the three screws 3 and take out the three spacers 8;
• Remove the three screws 306 and take out the C-shaped gearwheel 309;
• Remove the two screws 134 and take out the bracket 136;
• Remove the six screws 20 and take out pressure plate 19;
• If not yet done, remove the alpha EPD connector from the TSI board; H
• Heat the housing 16 using heating lamps. If necessary also cool down
bearing 18 using liquid nitrogen. Now the X, Y, Z support 24 together with
pressure bearings 18 can be removed;
• Remove pressure ring 17 using a crown key 59/62 mm (not supplied)
• Heat the pressure bearings 18 using heating lamps. If necessary also cool
down the housing 24 using liquid nitrogen. Now the pressure bearings 18
can be removed from the X, Y, Z support 24;
NOTE: Using a marker pen, mark the back-to-back sides of the pressure
bearing 18.
NOTE: When releasing the ball take care not to lose the two spacers 5.
NOTE: To remove the right-hand ear from the goniometer, see 5.14.1 “CS
Removal of the CompuStage”.
NOTE: To assemble the specimen airlock, see Sect. 5.15.2 “CS Removal of
the X measuring system”.
NOTE: The complete floating rod airlock assembly can now be removed from
the tilt mechanism together with the service tool 44,Figure 818.
Take care that locking pin 31 passes through the slot.
• The pushing and pulling lever 59, 195 can be removed after releasing
locking screws 65-190 and unscrewing the pivots 70, 196;
• If necessary the ball bearing 66 can be pushed from the housing with an
Allen key through the central hole;
• Release the three springs 208 threaded bush 50 and threaded ring 47;
• Remove the screws 199. Pull out bush 198. Now release the crown nut 205
and remove the special pressure ball bearing 204.
CAUTION! Note the position of both bearing halves with respect to each other as
it is a back-to-back type of bearing.
NOTE: Take care not to damage pin 19, or the groove in the airlock conducting
bush 24.Punch dimple on the airlock conducting bush 24 such that the
screw 25 is kept in place.
and apply an oil with a viscosity that ensures minimum play between the H
threads but allows them to run smoothly,
• If necessary clean housing 42 thoroughly and apply a grease with a
viscosity such that the play is a minimum between the housing 42 and bush
50 but allows smooth upward and downward movement,
• Mount the threaded ring 47 with threaded bush 50 and check that key 55
fits without play in the keyway. If not, the key can be splayed out such that
it fits with no play. Fasten the three springs 208;
• Mount the levers 59 and 195 such that when the three holes on the bush
198 form an isosceles triangle with the APEX pointing downwards, the
pulling or contra lever is at the left-hand side and the pushing lever is at the
right-hand side. See Figure 5-5.
• Adjust the pivots 70-196 until the levers 59 and 195 are free of play and
lock them with the locking screws 65-190;
• Insert the airlock assembly in the right-hand-ear. Ensure that pin 31 passes
through the slot, and that after fitting it is in the direction of the pulling or
contra lever 195. Make sure that the whole airlock assembly is under
spring pressure. Fix the airlock assembly with respect to housing 42, using
service tool 44, 44b, Figure 818;
• Mount the ball 36 (2.5 mm dia.) behind lever 35;
• If necessary clean the gear ring 110 with, e.g. a brush (dirt would result in
vibrations during tilting);
Position the gear ring such that the length of spring 63 when mounted is
equal, and check that the holes in the holding plate 114 are in line with the
3 holes in the rotating part and the 6 holes in the gear ring;
NOTE: Take care that the bearing shoes 57, 61 are correctly positioned. Secure
them by turning threaded ring 47 so that the threaded bush 50 is moved
Contents
• Mount the housing 109 and fix it with four screws 216; H
• Fit the holding plate 114 with the 9 screws 3x118 + 6x135;
• Mount the locking plate 126 and tighten the crown nut 129 with service tool
42, Figure 818. Check that the fixing tools 44, 44b, Figure 818 keep the
floating rod in position. See Caution! of Sect. 5.15.1 “CS Dismantling the
airlock”.a;
• Remount the spring 116 and screw 117 and set the height adjustment to
mid-position;
• Mount pressure rod 119 to operate microswitch 120. Fix and adjust
microswitch 120 and check that it is operated when the holder is
introduced;
• Fit the specimen translation movement in such a way that the gearwheel
156 smoothly engages the threaded ring 47 with minimum play.
CAUTION! As long as the special tool 44 Figure 818 is present the right-hand
ear movement is blocked
The slip coupling 167, 168 should be without grease and should be
adjusted such that there is no play and that the coupling only slips in the
end positions;
• Refit the tilt motor drive 175-186 and adjust the eccentric bushes 97-104
until both gearwheels match. At the end stops the gearwheel should
automatically be lifted to prevent the cable from becoming twisted;
• Now the complete R.H. ear can be mounted on the stage. But first check
that bearing shell 5 and hemispherical bearing 14 are not scratched and
are absolutely clean, that the shell 5 is properly tightened in the stage with
locking nut 6, and that both O-rings 8, 9 are clean and lightly greased with
Fomblin RT15. See also 5.14.2 “CS Removal of the hemispherical bearing
scale”.
Contents
Figures
5.15.3 Adjustments H
NOTE: All height and tilt errors will generally cause displacements in the same
direction as when using the Y translation movement. Errors in the
direction of the X translation movement must be compensated by
centring the left-hand ear w.r.t. the right-hand ear; see
5.16.3 “Adjustments”.e.
• Bring the feature back to the centre of the screen using the specimen H
translation control knobs;
• Repeat steps 3 to 8 until a minimal displacement occurs when tilting between the
end stops, at a magnification of 120.000x.
Negative tilt angles are set similarly on the opposite side of the casing.
2 2
1 1
NOTE: Before removing the left-hand ear, allow for the fact that it is centred with
respect to the right-hand ear and that centring may take some time.
NOTE: This can best be done by lifting up lever 39 and at the same time pushing
down lever 8 so that maximum clearance is present to shift the ball of
bellows 55 through the slot in lever 39.
NOTE: Before reassembly thoroughly clean all items normally located in the
ultra-high vacuum side of the ear.
NOTE: When mounting the left-hand ear, push it towards the upper left side.
5.16.3 Adjustments
EM4759
• Turn the nuts until the dished washers are half compressed. Release the
other 2 screws 30;
• Before starting centring adjustment, check that the L.H. ear is positioned
towards the upper left-hand side.
• The right-hand top screw 53 will influence mostly the tilt error in the
direction of the right-hand movement. However, it will also have a small
influence on the tilt error in the direction of the left-hand movement.
• The bottom-left screw 53 will influence mostly the tilt error in the direction of
the left-hand movement. However, it will also have a small influence on the
tilt error in the direction of the right-hand movement.
• The top left-hand screw must only be used if the previous adjustments
were insufficient.
• Tighten all three screws once the adjustment has been completed.
Contents
Figures
• Remove grubscrew 76 and take out plunger rod limiter 74. Now the plunger
bearing can be removed with screw 75.
NOTE: All moving parts outside the vacuum should be greased with Alvania 2
(not delivered) except ball bearing 66; this should be greased with Tellus
27.
When remounting check that plate 48 is as far down as possible (upwards for
SuperTWIN pole pieces).
Also check that the diaphragm holder is just above the pole piece (0.1 mm
higher).
NOTE: For the SuperTWIN, a thinner diaphragm holder tip 86 is supplied. Also,
the three diaphragm holder tip must be mounted when an EDAX is used.
Contents
Figures
5.17.3 Adjustments H
NOTE: The height difference between the first and last diaphragms should be
within 50 µm.
• For CM100: the top of the objective holder must be set 74.2 +0.005 mm
lower than the upper rim of the goniometer.
25.64
30° Objective diaphragm holder
10
10 5.015
28.4
NOTE: If the alignment tool becomes too warm it will not fit in the CompuStage;
• Remove the objective diaphragm holder and remount the holder tip;
• Remount the objective diaphragm holder.
Measuring pin
4
Test flange 2 1 2
5
28.43 mm
41.83 mm
6
41.83 mm
Cryo shields
28.43 mm
7
8
2 1 2
Direction of Direction of Anti-
BSD port contamination device
Fig. 5-9 BioTWIN alignment of the cryoshields and obj. diaphragm holder
in one of the other holes and repeat the check until satisfactory;
Figures
• Release the lateral displacement knob. Now check that all four diaphragms H
can be centred. If not, unscrew grubscrew 78 a little and try again. Repeat
until satisfactory.
NOTE: This option is not compatible with the presence of the SuperTWIN, SED
or EDAX.
• Open the column above the goniometer stage; see also 5.10 “Opening &
closing the column above the specimen stage to gain access to the
Contents
specimen chamber”;
Figures
NOTE: The height of flange 15, must be adjusted so that it is in the middle of the
octagonal housing.
• Mount the complete cryo diaphragm mechanism 1, and secure with the
three Allen screws 2, (M4 x 30);
• Insert the Cryo diaphragm holder 4, in the Cryo diaphragm mechanism.
Use the diaphragm coarse movement to withdraw the holder as far as
possible from the optical axis;
• Remove the existing cold trap and carefully mount the newly delivered cryo
cold trap 5. Screw the cooling strip 7, to the sandwich cryo shields 8, and
hand-tighten the screw item 9, (M2 x 3). Now carefully insert the sandwich
cryo shields 8, and mount them on the insulated cryo diaphragm holder 4.
Use the cryo diaphragm coarse movement to insert the holder as far as
possible. Adjust the sandwich cryo shields so that they are in parallel with
the lower objective pole piece. The sandwich cryo shields must be as near
to optical axis as possible. Now the sandwich cryo shields 8, must be
secured with screw 9, (M2 x 3).
NOTE: The cold trap 5 is 1 mm concentric w.r.t. the lower pole piece.
Contents
Figures
Cooling Device
EM6289
• Now fix the cooling strip 7. This is the connection between the sandwich
cryo shields 8 and cold trap 5. The cooling strip must be fixed to the newly
delivered cold trap 5, with screw 6.
(M2.5 x 4);
• Centre the largest hole with respect to the hole in the lower pole piece
using the fine lateral and axial adjustment knobs of the cryo diaphragm
mechanism;
• Use the eccentric and the objective diaphragm coarse movement, to insert
the holder as far as possible;
• Move the cryo diaphragm holder using the coarse knob fully over its axial
range and check that there is no mechanical obstruction;
• Move the cryo diaphragm holder using the fine adjustment and check that
there is no obstruction;
• Close the column and make an image;
• Check that both holes in the sandwich cryo shields can be centred when
both cooled and not cooled.
Contents
Figures
NOTE: Only possible if the goniometer stage is removed from the column. See
5.13 “Removing & remounting the complete goniometer stage”
• Unscrew the four screws 36 and pull out the complete vacuum pipe 30 with
lead shield 29;
• Remount in the reversed order.
5.20.1.1 Removal
• Admit air to the column; see 5.2 “Admitting N2 to the column”.
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• Remove the two screws 363. Now the lead shield 516 can be removed.
• Remove the two screws 361 and the distance pieces 367. Now remove the
complete detector assembly 360 from the objective stage.
NOTE: Take care not to lose the four insulating bushes 366;
5.20.1.3 Mounting H
• Remount in the reversed order but observe the following points:
– An extra spacer may be added behind the O-ring 359 to ensure proper
centring;
– Check by measuring the resistance, between the backscatter 360 and
the column earth, that the detector is free from the column earth and
not touching the upper pole piece;
– Switch on the HT and make an image of the hole in the backscatter
detector assembly (low magnification). The hole must be
approximately in the centre of the screen: if not, small adjustments can
be made by releasing or fixing screws 361, and distance pieces 367.
CAUTION! Take great care, the detector glass rod 134 (Figure 824) can
easily be damaged!
5.20.2.1 Removal
1. Admit air to the column. See 5.2 “Admitting N2 to the column”
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
2. Remove the four screws 303 (Figure 807). Now remove the complete
assembly 300 (Figure 807) from the objective stage.
If a CompuStage is present, proceed with the next two steps (See
Figure 807A):
• Mark the position of the eccentric 313 with respect to the objective housing;
• Remove the eccentric 313 and take out O-Ring 314.
Further dismantling of the SED (Figure 824
• Remove the 4 screws 140, retract the complete assembly 118 to 144;
• Remove the two screws 113; take out the plastic block 144 and lead bush
118;
• Release the three screws 139 so that O-Ring 124 no longer secures the
glass rod;
• Release the three screws 137 and carefully retract the teflon insulator bush
129 together with the complete glass rod.
• Unscrew the metal tip 136 and taking extreme care, pull away the glass rod
from the teflon insulator bush 129;
• Remove the 4 screws fixing the HT feed-through 125 and pull out the
Contents
complete feed-through;
Figures
Assembly H
• Assembly is done in the reversed order. However the following points must
be observed:
The glass rod must be mounted fully in its metal bush 130, so that the 10
kV is conducted to the scintillator.
The glass rod must be adjusted such that it is within the level with the
plastic block 144. Once adjusted, tighten the three screws 139 so that the
glass rod is secured.
5.20.2.2 Mounting
1. Before mounting the SED assembly, be sure that the pole pieces 25
(Figure 807) are correctly mounted. If not, See 5.11.1 “The upper objective
pole piece”.
2. Mount the eccentric 313 in the same position as found;
3. Carefully insert the detector in the hole in the pole piece. Equally tighten
the four screws 303 (Figure 807);
4. Mount the lead shields 510, 512 using screws 513;
5. Check the resolution as described in Sect. 4.16.6 (Only for TWIN).
5.21 EDAX
(Figure 807)
• Admit air to the column, see 5.2 “Admitting N2 to the column”;
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
NOTE: For a Supertwin with the EDAX mounted, the objective diaphragm holder
tip, item 86 with three diaphragms, must be present. This limitation is not
present for the 7-position objective diaphragm holder.
NOTE: Before the column is opened check that screws 90-200, Figure 804 and
58, Figure 806 are tight.
Contents
Figures
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
Remove clamp 33, that fixes the ion getter pump to the objective vacuum
flange;
Remove vacuum seal 35.
• For CM100: Release the knurled knob 108, Figure 810 and remove the
fixing rods 105, 106, 107, Figure 810 and cover plate 104, Figure 810.
• Free the specimen translation rods (unscrew grubscrew 203).
• Free the cable VDB-X12 and the cable between right and left-hand ears,
X1.
• Release screws 78, Figure 810.
• Place the gun lifting arm 14, Figure 804 in the upper position. Turn the
lifting mechanism clockwise to raise the column until the pole piece is well
clear of the goniometer stage, then remove the gun lifting arm and swing
out the column.
CAUTION! Check that the air/water hoses and cables to the column are not
obstructed.If the pneumatic hose to V7 is too short press “gun air”
softkey and release the hose.
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
NOTE: The pole piece is now freed from the lower lining tube.
• Remove the O-ring 137 and unscrew ring 136 using tool 6, Figure 818.
Pole piece 135 can now be removed.
Remount in the reversed order. Do not forget the indium seal 0.7 mm dia.,
length 36 mm approx. See also 5.4 “Location and replacement of indium
Contents
seals”.
Figures
• Push the grip and insert tool 4, Figure 818 as far as possible.
• Release the grip and remove the fixed diffraction diaphragm 3.
• Push the grip and insert tool 4, Figure 818 as far as possible. Release the
grip and remove the long fixed intermediate diaphragm 5 (not for CM100).
NOTE: Place the diaphragms in a clean, closed glass container. Inspect them
and clean if necessary.
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• Remove the Instrument key, insert the service key, select the manual page
and open V4;
• Take out the front window 227, Fig. 812, the side window 250, Fig. 812 and
raise both screens;
• Remove the beam stop needle out of the beam.
• Use tool 3, Figure 818 (the side with the long pin) together with extender
3A, Figure 818 to unscrew the complete differential and projector
diaphragms. If only diaphragm 71 is released, reverse the tool so that the
short pin faces upwards, once the tool mates, turn it through 90° and pull
out diaphragm 74.
Now diaphragm 72 can be unscrewed from diaphragm 71
NOTE: O-ring 70 can only be removed after the lower lining tube is pulled out via
the diffraction lens - see next section.
Place the diaphragms in a clean, closed glass container.
Inspect them and clean if necessary.
Contents
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• Open the column underneath the specimen stage; see 5.22 “Opening &
closing the column underneath the specimen stage”.;
• Remove hose pillars 32, 35, the lens current plugs MC-X4, X5, X6 and the
alignment coil plugs CSP-X2, X3, X4 and DCB8-X5;
• Remove the three screws 119, Figure 807 approx. 2 mm. Screw the three
knurled screws 7, Figure 818 in the other three threaded holes of the same
diameter;
• Remove O-ring 137, Figure 807 and unscrew ring 136, Figure 807 using
tool 6, Figure 818. Pole piece 135, Figure 807 can now be removed;
• Completely release screws 119, Figure 807. Now the complete lower
objective lens section can be removed from the column for further
dismantling:
CAUTION! When remounting the lower objective lens housing, great care must
be taken not to damage the fragile supports 113. These supports are
present in instruments delivered from Oct. 1990 onwards.
• Remove the two screws 49. Take out block 47. Now pull out the vacuum
liner tube 7 with fixed diaphragms 1 to 5. Now spring 6 can be pushed back
when all diaphragms are removed;
• Remove the centring ring 15 (screws 14);
• Remove the diffraction/intermediate lens assembly using the two knurled
knobs 7 Figure 818.
NOTE: when dismantling the D&I lens assembly take care not to lose the teflon
bush 62.
Contents
Figures
– Remove the four screws 28 and take out the intermediate lower lens
pole piece plate 26 with the intermediate lens coil 25 attached;
– If the intermediate lens coil has to be removed, unscrew the three
screws 27;
– To reach the diffraction lens coil 18, remove the four screws 17 and the
pole piece plate 16. Mark the correct position of the pole piece plate;
– To remove the coil 18, first remove the three screws 31;
– The pole piece assembly may be removed after unscrewing the four
screws 23 and removing ring 24.
When remounting the coils, care should be taken that they do not make any
contact with either the housing 20 or the pole piece 21.
– Check that the lens plug and waterpipes fit without any mechanical
Figures
obstruction. H
• Remove the shutter coil 50. Feed the cable and the attached plug through
the hole.
Remove the ring 54;
• Remove the 2 lens plugs MC-X7, X8 and remove the four hose pillars 117;
• Lower the column until the goniometer fits the outer mantle 100;
• Fit the 4 screws 78. Remove the 5 screws 374, Fig. 812 and lift the
complete column;
• Release the two screws 72, Figure 811;
• Pull out the complete beamstop assembly;
• Unscrew the four screws 64, Figure 811;
• Release the compressed air hose 5, Figure 811 and the 4 screws 64,
Figure 811.
• Lower the column again until the lower lens section fits the projection
chamber;
• Release the 4 screws 78 and lift the column with the goniometer stage
again;
• Use the two knurled knobs 7 Figure 818 and lift out the projector lenses.
Projector 1 and 2 lenses dismantling and assembly
– Remove the four screws 110 and the pole piece carrier 67.
– Remove the four screws 60; this separates the pole piece carrier 56
(with coil 57) from the pole piece carrier 59;
– The proj. 1 coil 57 can now be removed from the pole piece carrier by
removing the three screws 55. Take care not to drop the lead shield 61;
– The proj. 2 coil can now be removed from the pole piece 59 by
removing the three screws 58.
When remounting the coils, care should be taken that the coils do not touch
either the housing or the pole assembly. Proceed as follows:
– Remount lead shield 61. Place the coil 57 in the pole piece carrier 56,
note the position of water and electrical connections;
– Introduce a slip of paper (0.15 mm) between the coil and the pole piece
and another between the coil and the housing;
Fix the coil 57 to the pole piece plate 56 using screws 55 and remove
the spacers.
– Place the coil 64 in the housing 67, note the position of water and
electrical connections;
NOTE: Make sure that the coil is not making contact with either the housing or
the pole piece by introducing paper spacers;
Contents
Figures
NOTE: Check that screws 90-200, Figure 806 and 78 Figure 810 are fully
tightened.
• Admit air to the column and projection chamber (see 5.2 “Admitting N2 to
the column”)
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
Remove clamp 33, that fixes the ion getter pump to the objective vacuum
flange. Remove the vacuum seal 35.
• For CM100: Release the knurled knob 108, Figure 810; remove the fixing
rods 105, 106, 107, Figure 810 and the covers 104, Figure 810;
• Free the specimen translation rods (unscrew grubscrew 203).
• Release the 5 screws 196, Fig. 812.
• Place the gun lifting arm 14, Figure 804 in the upper position. Turn the
lifting mechanism clockwise until the projection chamber and the valve
block are well clear, then swing out the column.
CAUTION! Check that the air/water hoses and cables to the column are not
obstructed.
If the pneumatic hose to V7 is too short press “gun air” softkey and
release the hose (CM120 only).
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• Remove the 4 screws 64 and take out the complete V4 valve assembly;
Contents
Figures
• Disconnect the compressed air hose 5; Remove the 3 screws 4 and the H
cylinder housing 3;
• Remove nut 8 and cylinder piston 13.
• Remove the two screws 20, the flange assembly 24 including O-rings 18
and 25, bushes 17, 26 and O-ring 27;
• Remove circlip 15; remove washer 16 and bush 17, remove and check O-
ring 18;
• Release shaft 45 from the notch in bracket of plate 47;
• The shaft assembly 37, 39 with valve seating assembly 29 and spring
assembly 30 can now be removed;
• The valve seating can be dismantled if necessary after removing circlip 59.
Take care not to lose any of the small items, especially balls 38 (4 mm).
The beam stop assembly 65 to 79 inc. can be removed from valve V4 body by
pulling out the assembly after loosening the fixing screws 72.
To fit a new needle, insert it in bush 67. Mount the spring ring 68.
The beam stop should be adjusted to intercept the central part of the electron
beam; consequently the shadow image of the needle should be in the centre of
the screen. The axial position can be adjusted by screwing knob 77 in or out on
shaft 70, and the lateral position can be adjusted by rotating bush 76 after
loosening screws 72.
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• Remove the high tension cable plug 207 from the getter pump 101, the
earth lead, and safety plug X8.
• Remove clamp 147;
• Remove clamp 33, Figure 807 that fixes the ion getter pump to the objective
vacuum flange.
Remove the vacuum seal 35,Figure 807.
• Remove the two screws 4 and two screws 7, Figure 801, and remove the
IGP.
Each replacement ion getter pump is shipped sealed under vacuum. To admit
air into the pump, the metal tube seal on one of the flanges has to be carefully
cut using shears, NOT a saw blade, otherwise metal particles will enter the
pump.
NOTE: All water and air hoses should be at the left-hand side of the pump
(looking from the rear of the microscope). The pump should be
positioned so that the two flanges to fit to the goniometer and valve V5
(not for CM100) are correctly aligned.
• Insert the vacuum seal 35, Figure 807; Fix clamp 33, Figure 807 that fixes
the ion getter pump to the objective vacuum flange.
• Remount and tighten clamp 147;
• Due to mechanical pump tolerances, it may be necessary to readjust the
height of the ion getter pump. If so, slacken screws 5, 6, Figure 802 until
the surfaces of the valve V5 (CM120) or elbow (CM100) and the IGP mate
properly.
The connection to the goniometer will always fit because of its bellows
construction.
• Reconnect the HT plug 207 to the ion getter pump socket. Do not forget to
fit the interlock plug X8;
• Reconnect the earth lead.
Contents
Figures
NOTE: From version 10.0 onwards a “gun air” and “col air” can only be done by
pressing “vac func” first. This frees the “gun air” and “col air” softkeys.
• •Unscrew the ring 205, fixing the HT feed-through and carefully remove the
feed-through, 204, from the IGP 101.
NOTE: Using a tool (shown in figure following) makes removal of the feed-
through much easier. This tool is not supplied as standard and must be
produced locally when necessary.
3.5 (8x)
x) (2
45°
30
10 (2x)
Ø 22
Ø 34
x) (8
45°
=
240
ALL DIMENSIONS
IN mm
40 6
EM2581
MATERIAL: MILD STEEL
5.29.2 Removal & assembly of the small & large viewing screen
mechanisms
(Figure 812A)
• Remove the two screws 53 and 54.
• Now remove levers 66 and 115 by unscrewing 55 and 57, respectively.
• Remove cover 87.
• Remove circlip 85 and take out O-ring 80; take care not to drop ball 59.
Figures
NOTE: Grease (e.g. fingerprints) on the teflon insulator 106 or solder resin on
the insulation of the threaded rods 109 can cause small leakage currents
– these can influence the values of the exposure time readout on the
data screen. Therefore all parts of the feed-through must be thoroughly
cleaned in alcohol (not in an ultrasonic cleaner). See also Sect. 2.17.2.
5.29.5 Adjustments H
Check the position and sharpness of the displayed information as follows:
• Make the film display continuous by selecting the alignment page, pressing
softkey “service calibration” and pressing “segm disp” softkey;
• Move the plate to the working position by interchanging the pneumatic
hoses Y20-1 and Y20-0.
NOTE: If the projection chamber is not under vacuum the housing 277 must be
pushed towards the projection chamber.
The test pattern is reversed with respect to a normal film display. If the
four lines for the film text editor are not needed the film text pattern can
be shifted more outwards, to obscure less film.
• If the numbering is not in the right place, shift the image by adjusting screw
289. If the image is not sharp, release nuts 306 and shift the display until
the image is sharp.
NOTE: The brightness adjustment of the film display is done on the “cam init”
page with softkey “data int”.
Do not forget to reconnect the hoses to Y20-1 and Y20-0.
Just before the end of transport, the rear of the plate falls on the guide plate
185, Figure 812A.
When the transport slide 28 to 46 is in the end position, pin 189, Figure 812A
presses against rod 40, which in turn presses on the brackets 30, releasing the
front of the plate.
The plate now rests horizontally on platform 185, Figure 812A and can be
exposed after a delay of 5 s. (8 s. for SuperTWIN).
After exposure, transport slide 46 retracts the plate over guiding platform 185,
Figure 812A and the exposed plate falls into magazine (G), Figure 802.
NOTE: If the plate camera is ordered as an option and is being installed for the
first time, the following additional steps must be carried out:
• Remove the flange that is in place of the plate exchange holder 163;
• Remove the cover in place of the plate container;
• Insert the SDD unit in position MBCR X5;
• Remove the flange in place of the film display and mount the complete film
display with the three screws 260;
• Mount the flat cable between SDD X5 and the film display;
• Insert the jumper on the SDB MBCL X15 A2.
NOTE: Do not forget to switch off and on again to read the new options into the
system.
• Mount the pneumatic valves Y20.1 and Y20.0 and connect the electrical
Contents
wiring and pneumatic hoses according to Figure 816, Figure 817 and 422
Figures
(Electronics). H
Dismantling and assembly procedure:
• Let air into the projection chamber. See 5.2 “Admitting N2 to the column”;
• If present, remove the film container;
• Remove the side window 250 and remove the plate 185 (screws 181);
• Remove the table top by releasing the 6 screws fitting in the spacers 27,
Figure 802A;
• Remove the left-hand panel;
• Remove the support 178, Figure 807 for the left-hand specimen
movement;
• Remove the 4 screws 233, cover plate 231 and lead plate 232 and 182;
• Release the two nuts 7 fixing the thin threaded rods 26 and remove the
complete plate camera drive 2 to 45. Dismantling is carried out according
to Figure 812A;
Remove the lead shielding 46, 47 by removing the two screws 162;
• Remove the plate exchange holder 163 by releasing the two screws 161,
165;
• Assembly is carried out in the reverse order.
Ensure that the plate 185 is positioned correctly; this can be checked by
manually transporting the first plate.
5.30.3 Adjustments
Check that the distance between the flange 39 and the piston 27 is 23.5 ± 0.1
mm when the piston is in the neutral position. However, the thickness of the
camera house 163, is 18 ± 0.2 mm. This can be subtracted from the 23.5 ± 0.1
mm to check the size without removing the pneumatic drive. If these
dimensions are incorrect, the piston can be adjusted by screw 4, Figure 812A
(sealed with Loctite). See also cross section of plate camera drive.
Adjust the magnetic switch 41 so that the distance between the switch 41, and
the flange is 13.5 mm. See also cross section of plate camera drive.
Check the height of the two pins 164. Their height with respect to the surface in
which they are pressed must be 10.45 mm. These pins together with guiding
pins 157, will determine the position of the magazine in the camera housing
163. If they are not pressed down completely they can be tapped in carefully.
Check if the guiding pins 157 are also pressed down completely into the
camera housing. The part of the pin on which the magazine rests, must also be
10.45 mm above the surface in which it is pressed. This ensures that the
magazine is perfectly horizontal, and properly locked in the camera housing. If
they are not pressed down completely they can be carefully tapped in.
Check if the (empty) magazine can be inserted into and removed from the
camera housing without any noticeable force. If some force is still necessary,
the slide 46, Figure 813 has to be adjusted with respect to its frame, so that the
brass part on the rear of the slide can lock easily on the transport piston. This
can be done by turning both grubscrews 45, Figure 813 counterclockwise
equally until the magazine can be inserted into the camera housing without
force.
Contents
Figures
Check if slide 46, Figure 813, can run freely in the frame. If not, mechanically H
adjust slide rails 25 and 26, Figure 813. Do not use any grease.
Press 40, Figure 813 to check if the plate release brackets 30 function without
any obstruction.
NOTE: These brackets are not of the same dimensions as the ones for the 36
plates magazine.
Remove the exposed film magazine, and the top of the unexposed film
magazine.
Put the empty frame into the camera housing. The frame must rest on pins 164
and on the spring load of spring 16, Figure 813. The spring 16, Figure 813 is
lifted by 39 to release the slide. If this is not working properly, the spring will
scratch the piston 27 and become deformed. The spring force can be
increased, if necessary, by loosening screws 14, Figure 813, and tilting the
plastic block against the spring force. The force on both sides of the spring
must be equal, so the spring is horizontal with respect to the frame.
Check if the film holders are transported into the projection chamber without
any obstruction.
If not, readjust plate 185 to the correct height.
Check the plate camera operation with a full magazine, taking both single
exposures and a series of exposures.
of the three way valve V23. In the bake-out position the remaining water can be H
removed from the column using the compressed air connection S37. After H
blowing off the water, manual valve V26 must be closed. See also Sections
4.12.4 “Baking out device” and 5.3 “Draining water from the column”.
NOTE: Up until 1988 only one water branch was used for the column.
CAUTION! The flow in the water branches can only be correctly adjusted when
using as many flow meters as there are branches. This is because
the adjustment of the Watts regulator of one branch influences the
flow in all the other branches.
Switch off the microscope and drain the water from the column (see
5.3 “Draining water from the column”).
Connect as many flow meters as there are branches and adjust the Watts
regulators of each branch until each branch has 42 l/hr (0.7 l/min.).
NOTE: For a CM100/120 with only a water branch to the column (up to 1988),
the flow in this branch must be adjusted to 60 l/hr (1.0 l/min.).
CAUTION! Removing one of the Barry mounts may cause toppling over of the
column/ base plate, therefore the base plate must be supported.
POSITION 1 POSITION 2
A
2
2
3
5
4
3
6
4
7
EM6141A EM5355
Assembly H
NOTE: Take great care mounting the scintillator. Prism 58 should not touch the
fluorescent screen. The distance from the bottom of the scintillator to the
metal ring 34 should be approx. 30 mm.
The 35mm camera film transport mechanism is located on top of the projection
chamber.
5.34A.1 Mounting
• Remove cover 204, Figure 812A and mount the transport mechanism in its
place;
• Connect the plug to the socket on the MS panel X9;
• Loading of the camera, and its operation, are described in the microscope
Operating Instructions.
NOTE: When the 35mm camera is mounted, be sure that jumper A3 is placed
on the System Definition Board. The SDB is mounted in position MBCL-
X15, see Electronics, Sect. 3.10.6.
5.35 BioFilter H
NOTE: For the BioFilter Gatan has made a CDROM especially for Service. This
CDROM is called BioFilter Service, currently Revision 1. This CDROM is
intended for service engineers only and will be handed out on trainings
only. The CDROM comprises the mechanical and electrical drawings of
the Filter. Also the installation instructions for the Filter are located here.
The files are in Adobe PDF (Portable Document Format), which can be
read using the Adobe Acrobat reader on multiple platforms (reader files
are located on the CDROM).
NOTE: Switching the cooler to heating will reduce the waiting time. Make sure
the temperature of the peltier element is above 10 °C before letting air
into the projection chamber. Normal minumum waiting time is 30
minutes. This can be checked using the GetTemperature script in the
custom menu item of the Digital MicroGraph software on the MacIntosh
computer.
1
EM7728
NOTE: The water does not have to be switched off. The connections are made
via fast couplings.
• Remove the cover of the CCD camera by loosening the 4 screws M2.5.
NOTE: Before the camera is let up to air, make sure that the compressed air
connections are removed from the gate valve (See Figure 814E). Now
the gate valve stays in the opened position.
• Remove the 3 screws 1, M2.5. Now the CCD camera can be removed. H
CAUTION! Do not blow on, or brush the phosphor, because it is very sensitive.
• If the phosphor screen has to be removed, loosen the two Philips screws
and remove the clamping fork. Take care that the grounding wire does not
scratch the phosphor.
– Carefully slide the screen away. Clean the surface with Alcohol.
– Put a drop of immmersion oil (the bottle is marked MSC to SCINT)on
the scintillator surface.
NOTE: Make sure that there are no air bubles visible in oil.
– Replace the phosphor screen and retighten the two Philips screws.
• Mounting is done in the reversed order.
NOTE: Cooling down the camera takes also approx. 30 minutes. This can be
checked using the GetTemperature script in the custom menu item of the
Digital MicroGraph software on the MacIntosh computer.
NOTE: Do not forget to reconnect the gate valve compressed air hoses.
NOTE: Before the camera is let up to air, make sure that the compressed air
connections are removed from the gate valve (See Figure 814E). Now
the gate valve stays in the opened position.
NOTE: For the vacuum sequence and electrical operation see Electronics
Manual, Volume 1, Sect. 1.8.
Rotary pump - Change oil once a year (see6.2.2 “The rotary pre-
vacuum pump”.d, oil changing);
Exhaust filter p.v. pump - Drain oil, as determined by experience (see
6.2.2 “The rotary pre-vacuum pump”.e, Exhaust
filter);
Oil diffusion pump - Check pumping speed once a year (see
6.3.2 “Checking the pumping speed of the OD
pump”). Replace oil if discoloured or charred (see
6.2.3 “High vacuum pump unit”.b, Fluid changing);
Penning gauge - Check the operation every 6 months.
Clean if necessary (see 6.2.4 “Penning gauge”);
Pirani gauge - Check the operation every 6 months. Clean if
necessary (see6.2.6 “Pirani gauges”);
Pneumatic valve - Check operation once a year. Change the seals
every two years (see 6.2.5 “Pre-vacuum valves V1
and V2”), lubricate with “Fomblin RT15”;
Electromagnetic valves - Check operation every 6 months (see 6.2.9 “Valves
V8, V10, V11 and V12”). These valves should not
be lubricated but kept clean;
Ion Getter Pump - Check performance (see microscope column, Sect.
4.1 “Checking the pumping speed”.). See also
Sect. 6.2.7 “Ion getter pump”.e, Fault finding.
In addition to the pumping speed and pumping time checks for the different
airlock operations, it is necessary to ensure that the UHV valves (V4, V5, V6,
and V7) are good enough to prevent inter-vacuum leaks. If the seating of these
valves are inadequate, the pumping cycle can be disturbed during an airlock
cycle if IGP pressure increases above 2.6 x 10-2 Pa (IGP = 65).
On operating one of the airlock systems the change in vacuum reading due to
leakage may not exceed +1 unit as shown on the P3 display, or +3 units as
shown on the IGP display.
If the change in vacuum reading is greater than allowed, the valve should be
dismantled and cleaned.
Contents
Figures
Air is let into the pre-vacuum lines by opening valve V1 using the service key
and the manual page. Air can also be admitted into the pre-vacuum lines by
removing Pirani P2.
NOTE: When the pump is functioning correctly, the level of oil in the sight glass
will drop when the pump is switched on. During normal operation, the oil
level must always be visible in the sight glass.
6.2.2.6 Specification
Edwards Leybold
Type : E2M8 Trivac D8B
Ultimate vacuum : 2.6 x 10 Pa without gas ballast; 1.066 x 10-2 Pa
-2
6.2.3.1 Removing the high vacuum pump unit from the desk
• Admit air into the pumping system as described in 6.2.1. and switch off the
microscope;
• Remove connectors from PVG X5, X6, VDB X8-X10 and MS X7;
• Ensure that the pump is cold;
• Close the water inlet and disconnect the water hoses 187, 192 to the OD
pump inlet and outlet;
• Remove the PVP from the desk (see 6.2.2 “The rotary pre-vacuum
pump”.c). Also remove the hose 330 between manifold 320 and block 334
and disconnect the polyflo hose 370 from manifold 320;
• Close the compressed air valve and disconnect the compressed air hoses
Contents
• Remove clamp 155 between the backing outlet 145 and the buffer tank at H
the ODP end;
• Put a support under the ODP and unscrew the eight nuts 186 fixing the
pump assembly to the column;
• Move the vacuum system out of the desk.
NOTE: Reassembly of the vacuum unit can be carried out in the reversed order.
Check that seals 128, 129,Figure 820B (or for older systems seal 185,
Figure 820A) are clean.
6.2.3.3 Dismantling H
• Warm the fluid for a few minutes to assist draining;
• Switch off the pump heater and disconnect plug MS X7;
• Remove the high vacuum pump unit from the desk as described in 6.2.3.a;
• Remove Co-seal 128, 129 (or for older systems 185, Figure 820A) and, if
necessary, remove screws 135 and take out O-ring 134. For older systems
remove screw 133 and O-ring 135, Figure 820A.
• Remove V3 pneumatic valve driver assy. This should be done as follows:
– Remove the circlips 47, 55;
– Remove plate 48, release Allen screw 44, remove lever 40;
– Unscrew Allen screws 36;
• Unscrew the valve seating 130 from the high vacuum valve shaft 127,
releasing screws 126;
• Remove the high vacuum valve shaft from the pump;
• Release the Allen screw 125; strip 124 and baffle cap 118 can now be
removed from the pump interior;
• Remove the spring 119;
• Insert the extractor tool 117 in the M5 extraction hole located in the first
stage jet cap 120, then carefully withdraw the complete interior jet
assembly from the pump body.
• Wash the pump interior, the backing tube/ condenser and the jet assembly
in “GENKLENE” or other suitable solvent (trichloroethylene);
• Remove all traces of solvent by washing the components with acetone
then remove the acetone by baking to 75 °C or passing warm, dry air over
the components;
• Examine the valve seal 131 (or for older systems 130, Figure 820A) and
the O-ring seals 128, 129 (or for older systems 185, Figure 820A) on the
valve spindle and renew these if they show signs of wear, damage, or
deterioration. Lightly coat replacement seals with Fomblin RT15 grade oil
during assembly.
NOTE: Co-seals 128, 129 (or for older systems 185, Figure 820A) must never
be cleaned with solvent, use a dry (lint-free) cloth or paper tissue. If
removal of solvent from an elastomer is necessary, light baking under
rough vacuum is advised.
Contents
Figures
6.2.3.5 Reassembly H
(Figure 820B)
• Insert the jet assembly into the pump body and position it on the base,
aligning the jet with the backing tube and the slot in the base of the jet
assembly with the pin in the base. Position the spring 119 on the top of the
jet assembly;
• Insert the baffle cap into the pump, easing it through the valve bore.
Assemble the baffle cap 118 and the retainer strip 124 and secure the strip
with the retaining screw 125;
• Refill the pump with clean pump fluid (see fluid changing, 6.2.3 “High
vacuum pump unit”.b);
• Remount the HV valve shaft 127 in the pump;
• Mount the HV valve seating 130 on its shaft 127 using allen screws 126;
• Remount the pneumatic valve driver assembly as follows:
– Fix Allen screws 36;
– Remount plate 58, lever 40, plate 48 and fix circlips 47, 55;
• Mount co-seals 128, 129 (or for older systems 185, Figure 820A);
• Remount the high-vacuum unit under the desk as follows:
– tighten nuts 186 so that the OD pump is supported;
– switch on pumping system and pump down to a P1 readout of 30;
– retighten nuts 186, but ensure that rings 183, 185 can just be moved.
• Reconnect the buffer tank at point H with clamp 155 and screw 156.
See also Sect.6.2.3 “High vacuum pump unit”.a;
• Reconnect the cooling water and compressed air hoses;
• Remake the electrical connections.
NOTE: Further dismantling is not advised as all threads are secured with Loctite.
• When reassembling the cylinder, all O-rings must be lightly lubricated with
Fomblin RT 15.
NOTE: If seals must be replaced, please order the spare part kit for the
pneumatic cylinder (see parts list). For mechanical defects the complete
cylinder should be replaced. Take care that after assembly the
microswitch is activated.
6.2.4.2 Maintenance
The gauge head normally requires regular maintenance, e.g. twice per year. To
do this, or if the penning gauge reading is unstable or if it is suspected that the
gauge head is not functioning correctly, remove and dismantle the head for
inspection.
6.2.4.3 Dismantling
• Admit air into the pumping system, see Sect. 6.2.1 “Admitting air into the
pumping system”;
• Release the clamping ring 176 and remove the gauge head;
• While holding the gauge in the vertical plane with the electrical connection
end uppermost, unscrew the knurled nut 189 to remove the end cap and
cable 190;
Contents
Figures
• Carefully lift out the PTFE insulator 188 and O-ring 187; H
• Invert the gauge head to remove the compression spring 186, cathode
electrodes 180, 184, 185 and baffle;
• The anode assembly may be dismantled by unscrewing the brass thumb
nut 189 and withdrawing the anode and O-ring 187 from the vacuum side
of the teflon insulator.
6.2.4.4 Cleaning
Contamination may be removed by cleaning in KOH solution. Stubborn
deposits on the steel anode pin and the cathode cups (including the peripheries
of the holes) should be removed with fine emery paper. However, if the anode
surface becomes rough, e.g. after cleaning, it is advised to order a new one.
Finally, wash the cleaned items three or four times with cyclohexane and dry.
NOTE: It is important that the anode pin should not be distorted during this
process. Make sure that the central hole in each cathode cup through
which the anode pin is positioned has no encrustation, as this produces
instability.
6.2.4.5 Assembly
• Replace the baffle, cathode cups and spring;
• Insert the anode with the unlubricated O-ring into the PTFE insulator and
tighten the thumb nut just sufficiently to compress the O-ring;
• Visually check the axial alignment of the anode and adjust if necessary;
• Locate the PTFE insulator and the unlubricated O-ring in the body and
replace the end cap and nut;
• Position the gauge on its mounting block 99 and fix it with coupling 176.
valve pad is attached. The spring loaded shaft operates in anti-friction (“Oilite”) H
bushes housed in the pneumatic cylinder and in the bearing assembly. Shaft
sealing is by means of double O-ring seals fitted in the bearing assembly and
the inter-seal space is vented to atmosphere. The cylinder body is also
separately sealed by means of O-rings. A bracket fitted to the top face of the
cylinder body is provided for mounting the microswitch.
6.2.5.2 Maintenance
The valves have been designed for long term trouble-free life and the valve
actuating mechanism incorporates self-lubricating, anti-wear materials, hence
maintenance requirements are minimal.
NOTE: Elastomer O-ring seals have proved reliable for a service life greater
than 100.000 cycles under vacuum conditions. However, for optimum,
leak-free service and to conform with “planned maintenance
requirements”, it is recommended that the O-rings are changed at
25.000 cycles or every two years, as convenient.
NOTE: All O-rings must be lightly lubricated with Fomblin RT15 prior to
assembly.
2. To renew the cylinder body (upper and lower) O-ring seals 254-284:
Insert a 2.5 mm dia. steel pin in the hole provided in the valve shaft to
prevent rotation. Using a suitable peg spanner, carefully unscrew the valve
pad* 305 from the shaft 280. Remove the spring 288 and then withdraw the
bearing housing 285 and the piston assembly 280 from the cylinder body.
To gain access to the O-ring seals in the bearing housing and in the
cylinder body, first remove the bearings 252, 284. The upper and lower
body O-rings 254-287 may now be removed and replacement O-rings
fitted.
CAUTION! Do not exert excessive force when screwing home the valve on the
shaft as distortion of the shaft may occur.
6.2.6.1 Description
The gauge head has a single 12 micron tungsten filament mounted on a teflon
plug inserted into a stainless steel body tube to form a vacuum seal. This
filament is connected to the vacuum system and its temperature (= resistance)
is a measure of the pressure. A second filament on the outside of the gauge
head envelope is exposed to normal air and compensates for ambient
temperature fluctuations so as to ensure accuracy of measurement. Further
details are found in Sect. 3.11.
6.2.6.2 Maintenance
Considerable care has been taken in the design and manufacture of the
filament assembly to provide a robust structure capable of long reliable
performance. However, since the filament is of quite fine wire only 12 micron in
diameter, damage can occur if it is subjected to excessive mechanical shock or
vibration. Drift of the operating characteristics of the gauge head may occur if it
is operated in an atmosphere that causes contamination of the tungsten
filament. Since such contamination usually results from oil or grease vapours, it
can generally be removed by washing out with acetone (i.e. fill with solvent and
shake; do not damage the filament). After cleaning, wash with cyclohexane and
dry.
NOTE: When remounted, check the full scale adjustment (see Sect. 3.11.6 of
Electronics manual, Vol. 3).
Magnetic field
a b c d e f
Titanium
cathode
Stainless
steel
anode
Titanium
cathode
hydrogen. This hydrogen is not readily adsorbed through the film of oxide, thus H
large quantities of water present should be pumped out before using the ion
getter pump. Similarly, organic substances in the system in any large quantity,
e.g. freon gas, may poison the cathode surface. The method of dealing with
this is to enhance the sputtering rate by pumping argon for a short time, thus
exposing a clean titanium surface.
6.2.7.3 Cleaning
The performance of the ion getter pump is intrinsic in its design provided the
internal components of the pump remain clean. However, oil vapours may
accidentally arrive inside the pump from other parts of the system. Also, after
many months of operation, titanium films may build up inside the pump to an
extent which affects the ultimate vacuum, due to increased outgassing. If
essential, cleaning of the pump interior can be undertaken locally but, if known
to be contaminated, the pump should be replaced. When installing a new pump
ensure that it is not open to the atmosphere for any longer than is absolutely
necessary. Also check the cleanliness of the HT feed-through, as titanium
flakes may fall down into this area, causing instability and possible short-circuit
of the pump. Two procedures for improving the internal cleanliness of the pump
are outlined below (to be carried out only if unavoidable):
• Argon discharge cleaning
This procedure is recommended for improving the performance which has
been impaired by the occurrence of poisoned areas on the cathode
surfaces. To achieve this leak argon into the ion getter pump to a pressure
of about 0.13 Pa and run the pump under these conditions for a few
minutes. Due to the high sputtering rate of titanium for argon, a fresh
titanium layer is exposed and the performance improved.
• Chemical cleaning
Flakes of sputtered titanium and hydrocarbon contamination may be
removed by washing the interior of the pump thoroughly using a non-ionic
detergent. This must be followed by a tap water rinse then a deionized
water rinse. Gentle baking to about 100 °C in air will be sufficient to dry the
pump.
Slow starting which causes 1. Leak in system Trace leak and rectify
difficult starting and limits ulti- 2. Cathode surfaces are contami- Send to Eindhoven for replace-
mate pressure to above nated by organic material. ment.
1.33x10-4 Pa.
3. Insufficient inert gas by the oil Check tripping point (see 3.11).
4. Ion getter pump has been left Prolong the roughing cycle and
open to atmospheric pressure for use argon discharge cleaning if
an excessive time in humid atmo- necessary (see Cleaning).
sphere and a large quantity of
water vapour has been absorbed
in the cathodes.
Pressure Bursts Occur Flaking of sputtered deposits occurs. Clean pump as described under
“Cleaning”.
Leakage currents result in Field emission or resistive leakage Apply 10-14 kV a.c. at 20 to 30
accuracy of pump as a pres- due to whiskers. mA to burn off whiskers
sure indicating device to be - if this fails, clean the pump as
impaired described in “Cleaning”.
NOTE: From March 1993 onwards, air pressure is only used for opening the
valve. So only one air pressure hose will be connected to each valve.
The magnetic valves Y5.0 and Y6.0 on the column support will be
removed.
end being vacuum brazed to a stainless steel disk and the lower end to the
Figures
stainless steel valve pad into which the stainless steel valve shaft is screwed. H
The O-ring sealed, pneumatic piston is swaged to the shaft stem which
operates in anti-friction (“Oilite”) bushes inserted in the air cylinder body and in
the bearing housing. The air cylinder is separately sealed by O-rings which are
retained by the bushes. A bracket is provided (but not used) for mounting the
microswitch which can be actuated by the tapered valve shaft for remote
indication of “valve open/closed” position.
6.2.8.2 Maintenance
The valves have been designed for long term trouble-free life and the valve
actuating mechanism incorporates self-lubricating, anti-wear materials, hence
maintenance requirements are minimal.
NOTE: Elastomer O-ring seals have proved reliable for a service life greater
than 100,000 cycles under vacuum conditions. However, for optimum
leak-free service and to conform with “planned maintenance”
requirements, it is recommended that O-rings are changed at 25,000
cycles or every two years, as convenient. If the bellows assembly is
damaged, or if the seating is scored or defective, the complete valve
should be replaced.
In the following text, the numbers given refer to V6, while numbers in brackets
refer to V5.
i) To renew the valve pad O-rings 84 (149):
1. Disconnect the air supply to the valve. Remove the four socket screws 16
(170) from the cylinder body 14 (163) then detach the body. Withdraw the
valve actuating mechanism 12 (160) complete with bearing housing and
bellows assembly from the valve block 86 (57)
2. Detach the O-ring seal 84 (149) from the valve pad.
3. Examine the cylinder body and the pneumatic piston O-rings 11 (161) and
renew if damaged or deteriorated.
NOTE: With the exception of the pad seal 84 (149) and O-ring seal 85 (144), all
O-rings must be lightly lubricated with Fomblin RT15 prior to assembly.
CAUTION! Do not exert excessive force when screwing home the bellows
assembly on the shaft as distortion of the shaft may occur.
Contents
Figures
Technical data:
Type : Herion 0246 9202051
Function : 2/2 solenoid valve closed when de-energized
Voltage : 24 V (-10% to +15%); 7 W
NOTE: See also 4.1 “Checking the pumping speed” for Ion getter pump
performance and airlock recovery times.
Important: For fault finding see also 6.2.3 “High vacuum pump unit”.i.
NOTE: The vacuum system can only be operated in the manual mode when the
service key is present.
7 List of O-rings H
This section contains a list of the O-rings which the user of the microscope is
advised to keep on stock.
It is advisable to replenish the stock of O-rings in good time to avoid
unnecessary delays when such parts have to be replaced.
The hardness is 60 shore.
It is important to know the difference between Buna and Viton rings, as the
characteristics of these two types are very different and one should not be
substituted for the other.
If an O-ring has been removed from a package and its type is not known, this
can easily be determined by the fact that a Buna ring floats in cyclohexane,
whereas a Viton ring will sink.
EM4267
Figures
9. EBTEC Corporation H
120 Shoemaker Lane
P.O. Box 465
AGAWAM Mass 01001 USA
Telephone: 413-786-0393
Telex: 95-5343
10. Materials Science North/West Ltd.
North West House, Beverly Avenue
Poulton-le-Fylde,
Lancashire
England
Telephone: 0253-88 40 38
Contents
Figures
8 Mechanical drawings H
Spare parts
Contents
H
Spare parts
Contents
Spare parts
V30
*
BioFilter
84 mm
Photo multiplier
Screw
(4 x)
Spare parts
H
Contents
Figures
Spare parts
H
Contents
Figures
Cross section baseplate (CM10(0)/CM12(0), from April 1992 onwards Fig. 803B
Contents 8-6 50129 060427 CM 100/120 Mechanics
Figures
H
Spare parts 27
28
99 100
101
103 184
29
104
98 180
11
12 30 97 179
94 105
31
13 33 90 178
89 106
177 186
107 187
88 188
108 189 190
32 192
87 193
108
86
34 85 110
176
35 84
114
175
36
115
174
37
26 83 116
38 172
80
3 117
25 39
226
40 118 194
4 41 A
119 169
120 168 A
5 42 79
225
6 43 78 167 C
1 0 9 8 224
2 C
7
121
77 166 A C C 195 219
122 165 218
123 164 A
45 76 217
7 24 160
8 159 216
124
46 215
9 158
157 214
75 125 156
48 B 210
155
154 B
126 209
145
10 49 127
74 B 200 208
FOR TRANSPORT 144 B
23
ONLY 22 143 203 EM4608C
21 S34 142
20 141
19 68 69
50 140
67 139
18 66 70
17 64 138
65
51 59
58 60
14 16 56 137
57
15 204
205
135 206
134
130 207
129
H
Contents
Figures
3
Spare parts
4
8
ITEM 9 NOT 9
FOR CM200/300
10
11
1
109*
105*
106* 40
110*
107*
108*
13 ONLY FOR CM 100/120
12
3 14
ONLY FOR CM 200 40
4 100
5 42 40A
ONLY FOR
15 ONLY FOR CM 200
16
CM 300
6 17
7 104
18
8 19
9 48 54
20 55
10 38
11 13 39
12 23 41
14 24
40
25 61 62
26 43
27 44 73
45 46 72 70 71
ONLY 28
47
FOR 29
49
50
30 53
CM100 30 56
57
32 32 ONLY FOR CM 200 58
59
6063
33 64
33
65
34 34 66
ONLY FOR CM 200
35
35
ONLY FOR CM 300 67 68 69
NOTE: ITEMS SHOWN WITH * ARE
36 36 FOR CM200FEG AND CM300 FEG ONLY EM4609C
37 37
H
Contents
Figures
109 12 59
106107108 58 CM200
105 13 57
11 56
SEE ALSO GONIOMETER 55
STAGE 14 81.5
15 54
66.5
SEE ALSO 50
118 17 49
FIG.805 48
118 22 18
19
20 47
119
46
45
16 44
21 41
42
1
24 2
FROM OCT 1990
3
43
25 4
5
6
9X ONWARDS
7
8 172.5
9
33 CM100/120
26
37
27 81.5
40 66.5
39
28
38
36
35
31 ONLY CM200
34
30 EM4610G
29
H
Contents
Figures
H
Spare parts
Contents
H
FOR UPPER LENS: ALIGNMENT MARK 7 6 5 4 3
FACING DOWNWARDS
8 97 401
96
ALIGNMENT MARK 97
Spare parts 94
90
9 10
89 403
14 88 402
15 400
12 16 87
11 17 86
85
FOR STANDARD 18
19
24 20 A B
79 78 77
A B
A B
80
25
76
75
74
26
27
28
FOR FOR UT
STANDARD 29
30
34
31
Note: FOR DETAILS OF ALL PORTS
SEE FIG. 807B
CM200 ONLY
311 312 35 73
510 32
300 313 314
304
358
303 72 359
360
513 71
512
103 361
CM200 ONLY 104 36 365 CM100/120 ONLY
105 37 366
301 302 367
106 38
107 315
NOT FOR CM300 109 108 39
110 363
40 ALIGNMENT MARK
41
115 113 44
64 65 66 67 68 69 70
121
122 114 45
516
116 CM200 ONLY
124 117118 FOR LOWER LENS: ALIGNMENT MARK
125 120 123 FACING UPWARDS
126
129 NOT FOR UT 14 X 2
127
130 46 60
128
132131 47
62
48
133 61
144
134 49
135 50 FOR
136 54 STANDARD
137 55
138 56
139 57
140
143
NOTE: FOR FIXING THE DIAPHRAGM TO THE 58
OBJECTIVE STAGE SEE FIG. 807B
59 EM6814
5 29 28 27 26
207
206 33 14A
4 35
197
219 36 14C 14B
196 38
198 199 49
200
51 68
204 61 67
34 69
205 53 81 73 71
37 47 52 60
54 64 66
48 73A
46 56 59 71A
195 * = NOT FOR CM100 70
39 40 44 45 55 58 72
* 41 81A
190 189 188 187 186 185 48A 65
194 57
48B
*
CM100 ONLY 42
43 74
(4x) 75
*
CM200UT ONLY
76
CM200 ONLY 129 128 126 77
* 125 141 78
127 124 120 142
130 119 79
184 118
117
180 135 80
147 136 116
179 84
178 115 114 86
137 133 108
131 110 P 85
177 151
148 132 123
176 149 122 90
138 121 109
172 152 94 87 92
150
175 139 95 91
154 88
153 140 112 113A 113 96
CM200UT ONLY 174 155
156 97
171 89
170 144 CM200 ONLY
161 105 104
169
162 145 107
106 101 100 99 98
157 View on Arrow P
220 224 225
146
158 163 Detail of special O-Ring 120, Fig. 807B EM6575B
168 Z sensor
166 CM120 BIO TWIN
159
167 CM200 ONLY Manufacturing ridge
(greatly exaggerated)
CM200UT ONLY
160
165 164
Hemispherical bearing
H
Contents
Figures
H
Contents
Figures
X support
121 131
125 132 128
M 133
122
317A
Q Measuring
System Y
299
298
292
G
312
293 K
EM6580C
DETAIL B
Y-axle
296 300
H
Contents
Figures
EM6577
Spare parts
H
Contents
Figures
Spare parts 4 5 6 7 8
9 10
16 15 14
EM6566A
17
H
Contents
Figures
H
Spare parts 4
5
6
10
14
15
16 28
19
26
25 20
18 46
29
30 44
45
34 35 36 38 37 39 40 EM6899
Contents
Spare parts
H
Contents
Figures
H
Spare parts ONLY CM200
140
141
1
126
2
3 50
CM120/200 4 ONLY 120
5
6 54
7
8
55
46
49
CM100 49A
dia 4.1 x 6 x 31
52 56
125
52A
ONLY 48
dia 4.1 x 6 x 27 119 118
CM200 45 61 120
9 47 124
10 51 57
14 117
62
53 58 116
15 59 115
60
16
17 64 1 111
2
3
4
5
6
9X 112
7
8
9
137
18 66
136 138 139 113
67
CM120 68
69
68 70
69 114
19 44 74
70 110
40 ONLY
74 75 CM100/120
20 71 76
ONLY
dia 4.1 x 6 x 30 72 109 77
CM200
39 73
21 38
37
36 108
23 134
35
135
24 34
33
106 CM100
32
107
131 105
78
31 104
25 132
100
130
133 99
CM200 ONLY 92 ONLY
26 CM200 CM200
30
91
29
95 96
27 90
CM100
28
79 89
84
80
Spare parts 28
29
30 40
43
44
45
46
47
34
35
48
79
78
49 77
36
37 50 76
38 75
53 74
39 54
55 52 73
72
56
(FROM MARCH 1989
5 ONWARDS) 25
24
19 70
18
69 ONLY FOR CM120
6 11
7
9 67 68
66
65 76
4
64
ONLY FOR CM100
63
27
16 25 59 60
14 20 62
10 58
17 61 (ONLY FOR CM200) EM4614C
15 57
13
8
3
H
Contents
Figures
Spare parts
H
Contents
Figures
1 18 (2x)
Spare parts
17
16
10
11
12
13
14
EM7731
199 58751
15
Contents
Spare parts
38
10
37 24
25
17 26
1 18
ONLY
2 19
FOR CM300
3 14
16
4
15
5
6 28
29
7
14
31
32
33
20
A
36
27
(Ø 48 h7)
30
20.85
35
34
39
EM6517A
(199 38421)
FOCUS PLANE ONLY FOR CM300 ONLY FOR CM300
H
Contents
Figures
Spare parts
39 38 36 35 34 2
3
100 4
44 43 40 37
33 30 5
101
6
7
102
29 28
103
8
45 25
46
26 9
49
C
10 11 14
50 24
AB
51
C
52 23
57
58 20
59 19 18 A
B
60
15
53 16
54
17
55
EM2750B
56
H
Contents
Figures
Exchange unit plate film and plate film cassette Fig. 813
Contents 8-24 50129 060427 CM 100/120 Mechanics
Figures
H
H
Contents
Figures
Spare parts
Water and air connections, circuit diagram (up to Oct 1998) Fig. 814A
CM 100/120 Mechanics 50129 060427 8-25
Contents
Figures
H
Spare parts +24V
VDB
R3
COLUMN
X9-14
C1
C2 S34
COLUMN
OBJ. 1
SEPARATION
X9-15
OBJ. 2
DIFF
X81 VDB
INT
X32 X82
P1
P2 MS-X5-5 X17-9
0.7 l/min.
0.7 l/min.
0.7 l/min.
S39 X78
** X10-5
0.7 l/min.
S40 P/A13
6 6 MAINS
10
** PANEL
3 1
BAKE OUT
S37
compr. air 2
X10-4
X17-26
X77
blow - off MS-X5-4 X33
V21
5 9 X11-1
V22
6 LNSOFF
X203-13
0.7 l.
X202-1 RHP
0.7 l.
MRU PBH
MBCL-X34
LPR 7021
6 314 V7
*
113
0.7 l.
ODP 0.7 l.
4 CUROFF
SUPPLY
FAST COUPLING
310 REF-X14
COUPLING
DRAIN EM5107C
Fig. 814B Water and air connections, circuit diagram (up to Oct 1998)
Contents
Figures
H
1 No number
2 678.06050.2, Pressure on red line
means gate is closed.
3 Make sure the lens 2 cable is
connected to the filter before
mounting to the microscope as
afterwards it is very difficult.
4 Location of plugs can be swapped.
Spare parts
4
to GIB, slit GIB, magnet
GIB, VSM lower
to GIB, lens 3
GIB, focus 4
to camera control
unit, camera
transparent hose
to camera control,
camera air
(transparent)
(female)
GIB, slit (white label)
(male)
ODP 3-0 (red label) 1
(male)
ODP 3-1 (black label) 2
GIB, lens 2 3
Blue GIB, lens 1
label
To water out
(Water)
Green
Blue
Blue label Black To GIB, AN/SOL
label
(Green label) Blue Red
APERTURE
SELECTOR
GIF multiscan
flow camera unit
meter (679.07070.0)
10 - 15 l/h
to water in
(transparent)
EM7455
H
TO MICROSCOPE
WATER OUT
Length appr. 90 cm
Blue label
FROM FILTER (Female)
COOLING WATER
Green label
(Male) Filter
TO FILTER
COOLING WATER
20
15
10
2
5
20 C
l/h
TO MICROSCOPE
WATER SUPPLY
10 - 15 l/hour
EM7457
Coming
from CM
V3-1
(Black)
Open
V3 valve
Diffusion
pump
Camera
To Gate valve chamber
From CM
(Red) V3-0
Close
To compressed
air system
(Red)
Gate valve closed
To TV camera
controller (Black)
(Black)
(Transparent)
(Transparent) (Transparent)
To GIB slit To AN/SOL GIB
(White)
To slit To slit GIB
EM7456
Contents
4
Spare parts ONLY FOR CM12
8 9 10 14
WATER WATER
A INLET OUTLET
5
6
V26
S37
7 15 16
RETURN
FROM
COLUMN
V23
R 17 - 18 - 19
29 28 27 20
S32 TO
COLUMN
P A
A
ODP TO ELECTRICAL V22
UNITS
P
RETURN
EL. UNITS
RETURN
ODP
A A
EM4617A
PRESSED
AIR
A
26 25 TO ODP 24
H
Contents
Figures
Water and air connections, mechanical (upto Oct. 1988) Fig. 815A
Contents 8-30 50129 060427 CM 100/120 Mechanics
Figures
H
H
Contents
Figures
A 68 69
DRAWN ROTATED
67
V23 V24
MCR
LEVEL
CM200UT V30
VIEW A 54 COND. 1
160 & CM300 160
150 150 60 60 60 60
P 7
ONLY
50 50 50 50
DIFF.
50 49
100 100 40 40 40 40
61 62 5
30 30 30 30
63 64 65 66 V34 S37 8
50 50 20 20 20 20
INT.
10 10
B 10 10
COND. 2
20 20
10 15
5 5 5 5
PROJ. 2 9
55 56 57 58 59 60 FROM
AIR SUPPLY BLOCK
36
AIR
SUPPLY DIFF. 14
N2 GAS BLOCK V21
15 BLOW OFF
20
VIEW B V22
46 TO BLOW OFF
40 CM200UT 26
& CM300
ONLY ODP
71
TO WALL WATER
72
FROM ZEM 28
VIEW P 35
ODP
TO ZEM
73 WATER IN
34 CM200UT
& CM300 29 - 30 - 33
74 ONLY
72
75 TO LEVELLING SYSTEM
EM6489B
EMISSION Y5.0 * **
CHAMBER V11 Y11
3 AIR DAMPER
V33.2 V33.1
V5
UHV VALVE *
*
Y5.1 * Removed from March 1993
onwards
V10
V7 S7
GUN VALVE * Y10 *
Y7 *
**
2 AIR DAMPER
V32.2 V32.1
IGP
Y6.0
HV
VALVE V6
GONIOMETER
SPECIMEN Y8
V9 HOLDER Y6.1
M3 **
V8 1 AIR DAMPER
V4 V31.2 V31.1
PROJECTOR VALVE
Y4
V34
PROJ. V30*
CHAMBER
V20 S20
Y20.1
PL. CAMERA
Y12 SUPPLY BLOCK
V12 Y20.0
COMPRESSED
HV AIR SUPPLY
V3 S3 S3’
VALVE
Y3.0
BUFFER S32
Adjust
M1 to 4 bar
ODP Added from
March 1993 Y3.1
onwards
NOTE: .0 = REST POSITION
PV BUFFER V1 S1 S37 .1 = WORK POSITION
VALVE = NOT FOR CM100
Y1 *
* * = UNTIL AUG. 1989
BLOW OFF
V2 S2
PV VALVE EM4618B
M2 M PVP PROJ. Y2
CHAMBER
H
Contents
Figures
gun lift
Gun lo X2
DCB2 X5 X M3
PENNING LHT/P X1 X
MC X1
+ 1 5
C1 4
2 PBH A1 X1 X
MC X2
+ 1 2 column
C2 3 separation
2
BEAM DEFL. lo X3 S34
FBDR X5 option for STEM VDB X9 X
DCB3 X5 X
up X4
DCB4 X5 X
BEAM DEFL. UNIT TWIN X5 IGP
DCB5 X5 X PV valve
Y10
VDB X20 X
air inlet gun
X8
Y11 VDB X21 X
COND. STIGM. X7
DCB7 X5 X
X3 IGP SUPPLY
MC X3
1
OBJ. 1 5
+ 2 PBH A2 X1 X
MC X4
2
OBJ. 2 4 SPECIMEN VDB X12 X
+ 1 PV valve AIRLOCK
Y8
IMAGE
CSP X2 X
DEFL.
MC X5
1 4
DIFF.
2 + 5 PBH A3 X1 X
MC X6
2 3
INT.
1 + 2
SCA MC X7
1 + 5
PROJ. 1 4
2 PBH A4 X1 X
MC X8
1 + 2
PROJ. 2 3
2
MS X9 X HV valve gun
OPTS option for CM10 Y6.1
proj. valve VDB X9 X
SMALL SCREEN
Y4
VDB X14 X
OPTS LARGE SCREEN 400mm HV valve not for CM10
Y5.0
BUFFER
cable 0.382
cable 0.912 bake out VDB X24/25 X
Y23 not for CM10
PVG X5 X
P2
PVP MS X7 X
6
9
15
31
A B 12 71
3A C
4A
73
D E F 11 72
3 7 8
10
Spare parts 4 5
16 16A 32
28
13 14
73A
29
23
19A
17 18
30
25 26 27 33 34 35 36
19B 20 21 22 24 51
48
37 49 55 56
61
42 43 45 46 68
50
60 38 74 75 76
54
52 53
39
64 69
41 47A 57 58
40 77
59
44 44A
47 65
84 83 82 81 70 92 (3x) 93
63 90
62 78
96F 66
79 80
94A
44B 91
96E 96G 96D 85 67
94 95 92A
96B SF6
NOTE: ITEMS ARE NOT DRAWN TO SCALE 107
96A 96C HT TANK or
94B 106 EMISSION
CHAMBER
TOOLS FOR UT
N2
105
94D 109
98 99 100 108
SPECIAL TOOLS FOR 101 104
94C EM4619E
COMPUSTAGE PVP
96E 102 103
96G
H
Contents
Figures
V11 V10
Spare parts NITROGEN / AIR INLET +24V
FOR GUN AIRLOCK OR
COLUMN + IGP
+24V
MC
V7
GUN AIRLOCK
S7 V5
NOT FOR CM10
NOT FOR CM10
V6
S35 V9 ION GETTER PUMP
HV GAUGE V12
PROJECTION CHAMBER
V8 P4 NITROGEN / AIR INLET
SPECIMEN
HOLDER DIFFERENTIAL DIAPHRAGM
+24V +24V
200 µ
PENNING
GAUGE
V4 P3
CAMERA AIRLOCK
S30
OVERHEAT PROT. BUFFER
TANK
± 25 l
CLIXON (70 °C)
ODP
S31 V1 V2
OIL TEMP. PV VALVE BUFFER PV VALVE COLUMN
EXHAUST ROTARY
FILTER PV PUMP 220V
650W
S1 S2
EM4517A
PIRANI
GAUGE
P2
H
Contents
Figures
Spare parts
H
Contents
Figures
ODP and pre vacuum valves (from June 90 onwards) Fig. 820A
Contents CM 100/120 Mechanics 50129 060427 8-37
Figures
H
Spare parts
H
Contents
Figures
ODP and pre vacuum valves (from 1994 onwards) Fig. 820B
Contents 8-38 50129 060427 CM 100/120 Mechanics
Figures
H
Spare parts
H
Contents
Figures
Spare parts
H
Contents
Figures
Spare parts
H
Contents
Figures
Spare parts
X - RAY PROTECTION
GLUED
0 TOGETHER
-0.2
55
4.6
DETAIL B 8 YW
4
118 TOP VIEW
5 BK
OR
9
6 17
RD
7 16 GN
117 14
18 BN
116 15
20
115
19
106 107 108 109
114 25
SEE DETAIL B
26
D 27 DETAIL C
64 59 28
58 57 56 29
55 54
49 34
30
89 35
98 96 94
105 104 99 97 65 48 36
95 88 37
87
38
66
86 67 SEE DETAIL A 47
85
39
46
84
79 VIEW D
78 68 45
BD/DF BD/DF FARADAY CUP
NEAR AXIS ON AXIS
77 OR YW RD
A NEAR AXIS SYSTEM SUITABLE FOR DF-X1 DF-X3 DF-X5
76 1000 x 1000 PIXEL CAMERA’S HAS
THE TEXT “SLOWSCAN” ENGRAVED. 44
DF-X2 DF-X4 DF-X6
GN BN BK
EM5832A
(197 96832)
75
74
69
PMT
H
Contents
Figures
H
Spare parts STORE AND OPERATE
THIS MATERIAL IN
DARKNESS ONLY.
42
41
40
4
39
5
38
X6
A PRE AMP.
37 BROWN 3
32 16 X5 6
15 GREEN
31
12
11
14 7
BROWN X10
TO EARTH RAIL
30 GREEN X9 X6
29 X5
28
PMT
27
8
PMT
22 9
21
20
X1
19
18
17 EM5833
H
Spare parts
SOLDERING CONNECTION
OF DF DETECTOR
4
BROWN YELLOW
5
DF - X4 DF - X3
DF-X1 DF-X3
DF-X5
7 8
DF-X2
DF-X4 DF-X6
ON AXIS DF PRE AMPL.
(SSA - 3)
SIGNAL X9
EARTH X11
PROJ.
CHAMBER
EM5831A
9 Spare parts H
9.1 Abbreviations
Abbreviations for screw types in parts lists:
Scr. Screw Stl. Stainless
Cyl. Cylindrical St. Steel
Skt. Socket (Allen) Cr. Chrome
Rd. Round Br. Brass
Hv. Heavy Ni. Nickel
Csk. Countersunk Zn. Zinc
Al. Aluminium Mo. Molybdenum
NOTE: When a new table top is ordered new stickers must be ordered as well.
Stickers are delivered containing the maximum text. If the full text is not
needed, leave out the unwanted part of the sticker. E.g., for a CM 300
FEG the combination CM 200 FEG and CM 300 must be ordered and
locally assembled.
9.8 Valve V7
Figure 805
NOTE: For some CM100/120 microscopes a teflon ring 62 has been added to
ensure a better pressure on the indium seal of the lower pole piece. This
was necessary because of the build up of tolerances in the lower lens
section.
74 Special screw
75 O-ring Viton 2.62 x 7.59 ISO 109 5322 530 54332
As from October 1991 onwards, two types of film magazines are in existence,
viz.:
CAUTION! The new 56-plates magazines are physically different from the 36-
plates magazine and cannot be upgraded or modified in the field.
- The 56-film holders must be loaded only in the 56
unexposed plates magazine
- The 36-film holders must be loaded only in the 36
unexposed plates magazine
NOTE: For using the film holders and magazines, see the Operating Manual
section on Photography.
N2:
N2 filter grade 0.3 µm 5322 480 20066
External supply hoses:
Water supply hose 6 mm 5322 530 20591 Length as stated
Water supply hose 8 mm 5322 530 20598 Length as stated
Water supply hose 10 mm 5322 530 20592 Length as stated
Water supply hose 15 mm 5322 530 24152 Length as stated
Hose clamp 14 mm max. 4822 401 10257
Hose clamp 20 mm max. 4822 401 10492
Hose clamp 25 mm max.
NOTE: The tools listed below are not necessarily supplied as standard items
with the microscope.
must run on the SYNTHETIC oil with ordering code 4022 268 00653. (1 L) H
144 O-ring Viton Special 3.53 x 60.33 5322 530 50885 Edw.H021-26-164
Figures
214 O-ring Viton 1.78 x 1.78 ISO 004 5322 530 54026
215 O-ring Viton 1.78 x 2.90 ISO 006 5322 530 54028
218 Allen screw M3 x 16
225 Nut M1.4
226 O-ring Viton 1.27 x 1.07 5322 530 51051
Electrical
C001 Capacitor film 10 nF, 400 V 5322 121 42919
R001 High voltage resistor 10 M 4822 110 72214
Contents
Figures