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Aluminum chromium reduction

Appendix D presents the U.S. EPA data on a full-scale treatment of aluminum forming waste-water by chromium reduction, chemical precipitation, and sedimentation clarification. Chromium reduction, as described in detail by Wang, Hung and Shammas,9 is an important step prior to... [Pg.217]

Full Scale Treatment of Aluminum Forming Wastewater by Chromium Reduction, Chemical Precipitation, and Sedimentation Clarification... [Pg.228]

Aluminum metal is also used to produce other metals. The Goldschmidt process is a method of preparing a metal by reduction of its oxide with powdered aluminum. Chromium metal is obtained this way the reaction is highly exothermic, because of the large negative heat of formation of AI2O3 ... [Pg.917]

Chromium Metal by Pyrometallurgical Reduction. The principal pyrometaHurgical process for commercial chromium metal is the reduction of Cr202 by aluminum. [Pg.116]

Chromium oxide is mixed with aluminum powder, placed in a refractory-lined vessel, and ignited with barium peroxide and magnesium powder. The reaction is exothermic and self-sustaining. Chromium metal of 97—99% purity is obtained, the chief impurities being aluminum, iron, and silicon (Table 4). Commercial chromium metal may also be produced from the oxide by reduction with silicon in an electric-arc furnace. [Pg.116]

Chemical precipitation is used in porcelain enameling to precipitate dissolved metals and phosphates. Chemical precipitation can be utilized to permit removal of metal ions such as iron, lead, tin, copper, zinc, cadmium, aluminum, mercury, manganese, cobalt, antimony, arsenic, beryllium, molybdenum, and trivalent chromium. Removal efficiency can approach 100% for the reduction of heavy metal ions. Porcelain enameling plants commonly use lime, caustic, and carbonate for chemical precipitation and pH adjustment. Coagulants used in the industry include alum, ferric chloride, ferric sulfate, and polymers.10-12... [Pg.329]

Chemical reduction is used to transform a toxic substance with a higher valence to a nontoxic or less-toxic substance with lower valence. The most promising application is the reduction of hexava-lent chromium to trivalent chromium. This method is also applicable to other multivalent metals such as lead and mercury. Commonly used chemical agents for this purpose are sulfite salts, sulfur dioxide, and base metals (e.g., iron and aluminum).22 24... [Pg.625]

Chromite, Fe(Cr02)2 (which can also be written as l e(>Cr2C)3), is the principal ore containing chromium. After obtaining the oxide, chromium is prepared by the reduction of Cr203 with aluminum or... [Pg.381]

Chromium metal is produced hy thermal reduction of chromium(III) oxide, Cr203 by aluminum, silicon or carbon. The starting material in all these thermal reduction processes are Cr203 which is obtained from the natural ore chromite after the removal of iron oxide and other impurities. In the aluminum reduction process, the oxide is mixed with A1 powder and ignited in a refractory-lined vessel. The heat of reaction is sufficient to sustain the reaction at the required high temperature. Chromium obtained is about 98% pure, containing traces of carbon, sulfur and nitrogen. [Pg.218]

The process can be used to treat dissolved metals and is commonly used in groundwater treatment for the reduction and precipitation of hexavalent chromium, as well as in the oxidation of cyanide wastes (at concentrations up to 10%). Other potential applications of electrochemical treatment include remediation of arsenic, cadmium, molybdenum, aluminum, zinc,... [Pg.529]

We believe that catalysis occurs by formation of a complex between acetaldehyde, peracetic acid, and the metal ion in the 3+ oxidation state. The metal ion could be acting as a superacid as for peracetic acid decomposition, although oxidation-reduction reactions within the complex cannot be ruled out. Here again, we have found a disturbing lack of catalytic activity of other trivalent metals (aluminum, iron, and chromium). Simple acid catalysis is not as effective as proved when using p-toluenesulfonic acid and acetyl borate. This indicates that at least more than one coordination position is needed to obtain a complex of the proper configuration. [Pg.378]


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