Exposed area

Dichromated Resists. The first compositions widely used as photoresists combine a photosensitive dichromate salt (usually ammonium dichromate) with a water-soluble polymer of biologic origin such as gelatin, egg albumin (proteins), or gum arabic (a starch). Later, synthetic polymers such as poly(vinyl alcohol) also were used (11,12). Irradiation with uv light (X in the range of 360—380 nm using, for example, a carbon arc lamp) leads to photoinitiated oxidation of the polymer and reduction of dichromate to Ct(III). The photoinduced chemistry renders exposed areas insoluble in aqueous developing solutions. The photochemical mechanism of dichromate sensitization of PVA (summarized in Fig. 3) has been studied in detail (13). [Pg.115]

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. [Pg.118]

Care ought to be taken in handling acetic acid to avoid spillage or otherwise breathing vapors. Wash any exposed areas with large amounts of water. Once the odor of acetic acid vapors is noticeable, the area should be abandoned immediately. The U.S. threshold limit value for acetic acid is 10 ppm (25 mg/m ). Similar values prevail in Germany (75). [Pg.70]

Hydrogen chloride in air can also be a phytotoxicant (88). Tomatoes, sugar beets, and fmit trees of the Pmnus family are sensitive to HCl in air. Exposure of concentrated hydrochloric acid to the skin can cause chemical bums or dermatitis. Whereas the irritation is noticed readily, the acid can be water flushed from the exposed area. Copious use of miming water is the only recommended safety procedure for any external exposure. Ingestion is seldom a problem because hydrochloric acid is a normal constituent of the stomach juices. If significant quantities are accidentally swallowed, it can be neutrali2ed by antacids. [Pg.449]

Fig. 13. Single-sheet diffusion transfer plate (a) stmcture (b) upon exposure to light (c) development and (d) washing off and finish. In (a) the plate is first coated with a receiver layer of small (<5 nm) catalytic sites. The photographic layer is a spectrally sensitized silver haUde emulsion. In (c) the exposed areas develop as silver metal. Unexposed areas diffuse down to the receiver layer and form the printing image. In (d) the emulsion is washed off, revealing...

Because perspiration and bathing are commonly associated with sun exposure, the need to determine the SPE after bathing or long after appHcation to the body site is important. In use, the quantity of screen appHed and its uniform distribution over the exposed area control the achieved SPE. Methods for assessing the water-resistant or waterproof qualities of sunscreen products have been estabflshed by the EDA. [Pg.297]

Steel coated with tin (tinplate) is used to make food containers. Tin is more noble than steel therefore, well-aerated solutions will galvanically accelerate attack of the steel at exposed areas. The comparative absence of air within food containers aids in preserving the tin as well as the food. Also the reversible potential which the tin-iron couple undergoes in organic acids serves to protect exposed steel in food containers. [Pg.2424]

Aluminum coatings on steel will perform in a manner similar to zinc coatings. Aluminum has good resistance to many atmospheres in addition, being anodic to steel, it will galvanically protect exposed areas. Aluminum-coated steel products are quite serviceable under high-temperature conditions, for which gooa oxidation resistance is required. [Pg.2424]

All specimens should be measured carefully to permit accurate calculation of the exposed areas. An area calculation accurate to plus or minus I percent is usually adequate. [Pg.2425]

Short-time tests also can give misleading results on alloys that form passive films, such as stainless steels. With Borderline conditions, a prolonged test may be needed to permit breakdown of the passive film and subsequently more rapid attack. Consequently, tests run for long periods are considerably more reahstic than those conducted for short durations. This statement must be quahfied by stating that corrosion should not proceed to the point at which the original specimen size or the exposed area is drastic y reduced or the metal is perforated. [Pg.2427]

S Exposed area of the metal under consideration is small compared with the area of the metal with which it is coupled. [Pg.361]

Most galvanic corrosion processes are sensitive to the relatively exposed areas of the noble (cathode) and active (anode) metals. The corrosion rate of the active metal is proportional to the area of exposed noble metal divided by the area of exposed active metal. A favorable area ratio (large anode, small cathode) can permit the coupling of dissimilar metals. An unfavorable area ratio (large cathode, small anode) of the same two metals in the same environment can be costly. [Pg.361]

When possible, avoid coupling materials having widely dissimilar galvanic potentials. If this cannot he avoided, make use of favorable area ratios by giving the active metal a large exposed area relative to the noble metal. For example, copper or copper-based alloy tubes may be joined to a steel tube sheet. Because of the favorable area ratio in this case, a relatively inexpensive steel tube sheet may be intentionally substituted for a bronze or a brass tube sheet if thickness specifications allow for a small amount of galvanic corrosion of the steel. [Pg.364]

The impressed current method with metal oxide-coated niobium anodes is usually employed for internal protection (see Section 7.2.3). In smaller tanks, galvanic anodes of zinc can also be used. Potential control should be provided to avoid unacceptably negative potentials. Pure zinc electrodes serve as monitoring and control electrodes in exposed areas which have to be anodically cleaned in the course of operation. Ag-AgCl electrodes are used to check these reference electrodes. [Pg.468]

Here,. Ai(X) is the partial SASA of atom i (which depends on the solute configuration X), and Yi is an atomic free energy per unit area associated with atom i. We refer to those models as full SASA. Because it is so simple, this approach is widely used in computations on biomolecules [96-98]. Variations of the solvent-exposed area models are the shell model of Scheraga [99,100], the excluded-volume model of Colonna-Cesari and Sander [101,102], and the Gaussian model of Lazaridis and Karplus [103]. Full SASA models have been used for investigating the thermal denaturation of proteins [103] and to examine protein-protein association [104]. [Pg.147]

The rate of evolution of a toxie or flammable vapour from a liquid (e.g. in an open vessel, from a spillage or as a spray) is direetly related to the exposed area. Therefore, the rate of vapour formation from solvent-impregnated rag, from solvent-based films spread over a large area, from foams or from mists ean be many times greater than that from bulk liquid. [Pg.52]

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