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Corrosion of monel metal in photographic solutions

โœ Scribed by J.I. Crabtree; G.E. Matthews


Publisher
Elsevier Science
Year
1924
Tongue
English
Weight
135 KB
Volume
198
Category
Article
ISSN
0016-0032

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โœฆ Synopsis


CRITICAL consideration of the sensitometric, microscopic, and physico-chemical aspects of the subject. Neither of the simple assumptions that rate of development is determined primarily ( I ) by the rate of chemical reaction between the silver halide and the reducer, or (2) by the diffusion processes involved, is adequate to account for the sensitometric data available. A tentative hypothesis of the mechanism of the development process is based on the assumption of selective adsorption of the reducing agent by the silver halide grains.

This adsorption may be assumed to be followed by an intramolecular oxidation-reduction reaction, which is catalyzed by the latent image. The r6le of alkalies in development is intimately related to the action of the hydroxyl ion, which probably exercises a determinative influence upon the equilibrium between the polar (strongly adsorbed) and non-polar (less active) tautomeric modification of the reducing agent.

CORROSION OF MONEL METAL IN

PHOTOGRAPHIC SOLUTIONS.


๐Ÿ“œ SIMILAR VOLUMES


Cyclic voltammetry of monel 400 in lithi
โœ D.D. MacDonald ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 560 KB

The electrochemistry of Monel400 in 1 mole/kg-' LiOH solution at 25, 125 and 250ยฐC has been investigated using the technique of cyclic voltammetry. The general electrochemical hehaviour is found to most closely approximate to that of the major component, nickel, although expansion of the current sca