Modification of this process for "black" chromium plating has been proposed. Current interruption and sulfate-free chromic acid with fluoride or complex fluoride catalyst have been used. Some practical of this process should be make trial for several changes in parameter in order feel confidence on produce black color of chrome deposit. For other color of chromium deposit should use different bath chemicals solution rather than chemicals for black color deposit. For color chrome deposit should find other kind bath solution that can produce color chrome deposit like for decorative chrome deposit. The method to produce color chrome deposit can be in two stage, for example by first plating using nickel plating than the subsequent plating using chrome plating, or the first layer use copper substance that the subsequent layer use chrome plating.
Trivalent Chromium Baths
Historically, trivalent chromium baths have been the first and favorite approach to chrome plating, but they have always failed to match the reproducibility and dependability of chromic acid solutions, as has already been discussed in the section on theory.
The United States Bureau of Mines developed a process for the electroplating of pure chrome to meta from the ore from ferrochromium. Using a mixed bivalent and trivalent chromium sulfate solution, but the process has not been adopted successfully to plating purposes. A two-compartment cell is used at the Union Carbide Corporation, Marietta, Ohio, plant, and continuous operation on a large scale seems necessary for good result. In another review of the operation that low efficiencies always prevail during the startup of a cell.
Success was very limited in effort to utilize such baths for electroplating. A chromium ammonium chloride solution was used for brush plating. Better results in brush plating were obtained with Gregory's salt, ammonium chromium oxalat.
More recently there has been an effort to commercially the use of chromium chloride solution in or containing, organic solvent. The deposits are darker than those from chromic acid solution, and some chlorine gas is generally evolve at the anode. Only decorative deposits are being considered.
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