Preparation technique

The conventional technique frequently used for the preparation of SECM tips is largely based on the fabrication technique for disk-shaped microelectrodes, which have been described in the literature (1-3). The procedures [Pg.75]

Reduction of the size of SECM probes is important, since the resolution of SECM depends strongly on the size of tip used. In order to achieve this goal, one has to thin down the diameter of commercially available metal wires by electrochemical etching or by pulling in glass capillary as described below. Further coating and exposing steps are then necessary, as in the case of unetched wires, to expose only the electrode surface. One method for the [Pg.76]

or Pt-Ir Alloy. A 1 to 2 cm long Pt or Pt-Ir (80-20%) wire (125 or 250 yarn diameter) is sharpened by electrochemical etching in a solution containing saturated CaCl2 (60% by volume), H20 (36%), and concentrated [Pg.78]

2 The SECM approach curve obtained with a polished submicrometer-sized tip over a polished Pt substrate. The thin line shows the theoretical curve computed for disk-shaped 380 nm radius tip. (Reprinted with permission from Ref. 9. Copyright 1997 American Chemical Society.) [Pg.80]

Self-Assembled Spherical Gold Micro electrodes [Pg.81]

The gases used in C/ C measurements are CO2 and recently CO during pyrolysis applications. For CO2 the following preparation methods exist [Pg.48]

Carbonates are reacted with 100% phosphoric acid at temperatures between 20 and 90°C (depending on the type of carbonate) to liberate CO2 (see also oxygen ). [Pg.48]

As the commonly used international reference standard PDB has been exhausted for several decades, there is a need for introducing new standards. Even though several different standards are in use today, the international standard the 5-values are referred to remains to be the PDB-standard (Table 2.2). [Pg.49]

The two main terrestrial carbon reservoirs, organic matter and sedimentary carbonates, have distinctly different isotopic characteristics because of the operation of two different reaction mechanisms [Pg.49]

Isotope equilibrium exchange reactions within the inorganic carbon system atmospheric CO2 - dissolved bicarbonate - solid carbonate lead to an emich-ment of 13C in carbonates. [Pg.49]

Polyurethane is prepared by the rearrangement polymerisation method. The polymer chains are formed as in addition polymerisation, but the mechanics are similar to condensation polymerisation. Many of the plant seed oils mentioned in Chapter 2 have successfully been used to synthesise [Pg.158]

Polyurethane formation is a highly exothermic process. Polyurethane synthesis is a laboratory process which is mainly carried out by the solution polymerisation technique. The most common solvents used for this purpose [Pg.160]

In another approach, soybean oil fatty acid derivatives are carbonated in supercritical carbon dioxide which is then converted to polyurethane by reaction with primary amines such as ethylenediamine, hexamethylene-diamine and tris(2-aminoethyl)amine. This technique avoids the use of isocyanates (usually phosgene, a deadly poisonous gas which is used to obtain isocyanate) and the resultant polyurethane networks exhibited Tg values of approximately 34°C, 18°C and 43°C, respectively for the above amines. [Pg.161]

Using this technique, a large variety of polyurethanes have been prepared from different vegetable oils. Natural polyols like castor oil (generally trifunctional) are directly reacted with diisocyanates to obtain branched polyurethanes, although it is difficult to control the reactivity. However, bifunctional castor oil can be polymerised with diisocyanates in the presence of suitable chain extenders and catalysts to produce polyurethanes in a more controlled manner (Fig. 6.4). A castor oil polyol-based polyurethane network can also be prepared from epoxy terminated polyurethane pre-polymer with 1,6-hexamethylene diamine. Epoxy terminated pre-polymer is obtained by the reaction of glycidol and isocyanate terminated polyurethane pre-polymer of castor oil polyol, poly(ethylene glycol) (PEG) and 1,6-hexamethylene diisocyanate. [Pg.161]

Vegetable oil-based polyols obtained by epoxidation are treated with diisocyanates in the presence of a suitable chain extender and catalyst to obtain polyurethanes (Fig. 6.5). Polyurethanes have been prepared from olive, peanut, canola, corn, soybean, safflower and sunflower oil by the conventional epoxidation process, followed by treatment of the polyols of the epoxies with diphenylmethane diisocyanate. Polyurethane resins may also be obtained by the treatment of soybean polyols (which are obtained by methanolysis of epoxidised soybean oil with isocyanates at a temperature of 50°C) or from epoxidised linseed oil with TDI using xylene as the solvent. [Pg.161]

A second technique has also been developed to manipulate the magnetization of individual dots this technique is based on the use of write heads developed by Headway Inc. The array of dots is mounted on a piezoelectric stage, which allows displacement of the sample over an area of 120 xmx 120 p.m. The head is in contact with the surface of the sample. A write current of 30 mA was used in the writer. An example of controlled writing of a line of dots is shown in Fig. 5.3-41 [3.123]. [Pg.1063]

Various strategies have been developed for the manufacture of nanostructured materials. They follow essentially two approaches [Pg.1063]

Many preparation techniques are very specific to one particular type of material for instance, many different chemical and physical techniques are used to produce porous sUicon. Hence, we list andhriefly describe below only the most common and generic methods for the [Pg.1063]

Block and graft copolymer micellar systems are generally produced by one of the following two procedures. [Pg.191]

In the first technique, the copolymer is dissolved molecularly in a common solvent, for example that is good for both types of blocks, and then the conditions such as temperature or composition of the solvent, are changed in the way that requires formation of micelles. This is commonly achieved by adding gradually a selective precipitant of one of the block type, eventually followed by stripping the common solvent. An alternative that is often recommended is the dialysis technique by which the common solvent is gradually replaced by the selective solvent. [Pg.191]

In a second technique, a soHd sample of the copolymer is directly dissolved in a selective solvent the micellar solution is let to anneal by standing and/or the annealing process is made by thermal treatment. [Pg.191]

From our own experience, and also from literature, it appeared with both of these techniques, that depending on the copolymer system, an equilibrium situation is not necessarily reached, especially if the core-forming polymer has a high glass transition temperature (Tg). In this case, for example with PS-PEO and PEO-PS-PEO di- and triblock copolymers so-called frozen micelles are formed. [Pg.191]

According to Munk [113] micelle formation by direct dissolution in a selective solvent is in general not very suitable. In fact the resulting micelles will depend on the initial two-phase morphology of the bulk sample as well as on the interactive properties of the selective solvent with respect to the polymer microphases in presence. In order to reach an equilibrium, it would be necessary that the selective solvent also swells quite extensively the insoluble block, which is almost impossible with amphiphilic block in an aqueous medium. [Pg.191]

The main preparative techniques used to make all seven trifluoromethyl-quiaoline isomers iaclude copper-assisted coupliag of the haloquiaoliae with trifluoromethyl iodide (112) quiaoliaecarboxyhc acid with sulfur tetrafluoride—hydrogea fluoride (434,445) and aminoben2otrifluoride and glycerol... [Pg.338]

Other Asymmetric Membrane Preparation Techniques. A number of other methods of preparing membranes have been reported i the literature and are used on a small scale. Table 1 provides a brief summary of these techniques. [Pg.69]

Table 1. Less Widely Used Membrane Preparation Techniques...

Esterification is generally carried out by refluxing the reaction mixture until the carboxyHc acid has reacted with the alcohol and the water has been spHt off. The water or the ester is removed from the equiUbrium by distillation. The choice of the esterification process to obtain a maximum yield is dependent on many factors, ie, no single process has universal appHcabiUty. Although extensive preparative techniques have been reviewed elsewhere (7,68), the methods given ia this section are representative of both laboratory and plant-scale techniques used ia batch esterifications. [Pg.382]

TLC can be used as an analytical technique, or as a guide to establishing conditions for column chromatography or as a preparative technique in its own right. [Pg.18]

Artifacts may be introduced from the environment or through preparative techniques. When assessing individual tiny particles of material, the risk of loss or contamination is high, so that samples of this nature are handled and prepared for examination in a clean bench or a cleanroom (class 100 or better). [Pg.67]

K. C. Thompson-Russell and J. W. Edington. Electron Microscope Specimen Preparation Techniques in Materials Science. Monographs in Practical Electron Microscopy, No. 5- Philips Technical Library, Eindhoven Delaware, 1977. [Pg.115]

It should be noted that for TEM at accelerating voltages of 100-400 keV the specimen thickness must be of the order of 10-100 nm which requires dedicated preparation techniques [2.173, 2.176, 2.178]. [Pg.51]

Since then, TXRE has become the standard tool for surface and subsurface microanalysis [4.7-4.11]. In 1983 Becker reported the angular dependence of X-ray fluorescence intensities in the range of total reflection [4.12]. Recent demands have set the pace of further development in the field of TXRE - improved detection limits [4.13] in combination with subtle surface preparation techniques [4.14, 4.15], analyte concentrations extended even to ultratraces (pg) of light elements, e. g. A1 [4.16], spe-dation of different chemical states [4.17], and novel optical arrangements [4.18] and X-ray sources [4.19, 4.20]. [Pg.181]

SERS is usually restricted to specially prepared "active" surfaces. A broad range of other surfaces also becomes accessible to SERS spectroscopy after special preparation techniques ... [Pg.256]

Additional suggested resources for the reader include introductory articles on scanning probe techniques for materials properties measurement [82,83J. A comprehensive manual describing various surface preparation techniques, experimental procedures and instrumentation is also a good resource [84J, although the more recent modulation based techniques are not covered. Key textbooks include Johnson s on contact mechanics [51J and Israelachvili s on surface forces [18J, as well as a treatment of JKR/DMT issues by Maugis [85J. [Pg.206]

Wegman, R.F., Surface Preparation Techniques for Adhesive Bonding. Noyes Publications, Park Ridge, NJ, 1989. [Pg.1005]

It has been reported that SWCNTs form in the soot generated in the arc-discharge chamber when metal catalysts are present. This preparation technique was published almost concurrently by two groups [2,3]. Thus lijima and Ichihasi [2], employing an Fe catalyst and a mixture of CH4 (10 Torr) and Ar (40 Torr), obtained ca. 1 nm diameter SWCNTs, whereas Bethune et al. [3] produced ca. [Pg.144]

If cyclic ketones are monosubstituted in the a-position, their rates of reaction decrease as compared to the rate for the parent ketone (9,41). More highly substituted ketones (e.g., diisobutyl ketone, diisopropyl ketone) can be caused to react using newer preparative techniques (39,43,44, see Section VII). Monosubstituted acetones often can give selfcondensation products, but the recent literature (13,39,43) contains reports of the successful formation of the enamines of methyl ketones. [Pg.63]

Centrifugation can be used either as a preparative technique for separating and purifying macromolecules and cellular components or as an analytical technique to characterize the hydrodynamic properties of macromolecules such as proteins and nucleic acids. [Pg.157]

Although on-line sample preparation cannot be regarded as being traditional multidimensional chromatography, the principles of the latter have been employed in the development of many on-line sample preparation techniques, including supercritical fluid extraction (SFE)-GC, SPME, thermal desorption and other on-line extraction methods. As with multidimensional chromatography, the principle is to obtain a portion of the required selectivity by using an additional separation device prior to the main analytical column. [Pg.427]

In this chapter a number of the preparative techniques used in the resolution of enantiomers is presented. Some of these techniques will be developed more fully in following chapters. [Pg.2]

There are circumstances in which it is not possible to obtain the required enantiomer at manufacturing scale either by synthesis or isolation, e.g. because of difficulties with scale-up or failure to obtain material in a suitable physical form for pharmaceutical manufacture. In such cases, all the experimental results available should be described and the reason for the failure given. Likewise, if enantiomeric material could not be obtained for preclinical and clinical studies (see below), this should also be discussed. Advances in preparative techniques should eventually make this scenario less common. [Pg.324]

Although most solutions satisfy the three-component criterion they have usually been established by empirical methods and their compositions can be found by referring to tables on a recipe-book basis Many have been extensively explored by metallographers in search of improved preparation techniques, notably for electron microscopy . ... [Pg.301]

Recent advances in fabricating novel metal oxide electrodes have been made by exploiting hydrothermal preparation techniques [93, 94], An example is... [Pg.306]

In the analysis of polymer surfaces and interfaces there has been tremendous progress in recent years. This is to a large extent due to the development of surface- and interface-sensitive analytical techniques which previously had not been applied to polymers. It is thus possible to achieve molecular resolution both for the free polymer surface and for buried interfaces between polymers. In addition, suitable sample preparation techniques are available and extremely homogeneous and smooth polymer thin films can be prepared. They may be put together to investigate the interface between polymers. [Pg.394]

Reactions such as these are of interest in themselves. Beyond that, one can use the pulse radiolysis experiment as a preparative technique for other species. Thus, the reactions of numerous aliphatic, carbon-centered radicals have been evaluated.22 If one employs a reasonably high concentration of solute, say 0.1-1 M CH3OH, the formation of CH2OH is complete within the electron pulse. Following that, reactions such as the following can be studied ... [Pg.269]

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