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Coprecipitation metal powder catalysts from

Inorganic precursors are much cheaper and easier to handle than metal alkoxides. Therefore the industrial production of oxide powders for ceramics and catalysts is mainly based on the precipitation or coprecipitation of inorganic salts from aqueous solutions. Gibbsite, Al(OH)3, (see Aluminum Inorganic Chemistry) is precipitated from aluminate solutions. Ti02 powders are made via the controlled hydrolysis of titanium salts. Stabilized zirconia is coprecipitated from aqueous solutions of zirconium oxychloride, ZrOC, and yttrium nitrate, YlKOsjs. [Pg.4503]

Mixed oxides can also be reduced to the mixed metal catalysts by hydrogen reduction. Such oxides have been prepared by sodium nitrate fusion of mixed metal salts, primarily those of the noble metals, following the procedure used for the prepeiration of Adams catalyst, platinum oxide. 31-136 Non-noble metal alloy powders are prepared by heating mixed nitrates, carbonates or hydroxides in air to convert them to the mixed oxides which are then reduced. The hydroxides can be prepared by coprecipitation from a mixed metal salt solution. ... [Pg.256]


See other pages where Coprecipitation metal powder catalysts from is mentioned: [Pg.16]    [Pg.613]    [Pg.124]    [Pg.294]    [Pg.82]    [Pg.594]    [Pg.1462]    [Pg.123]   
See also in sourсe #XX -- [ Pg.230 ]




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