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Cobalt apatite

In mineral-reagent systems, surface precipitation has been proposed as another mechanism for chemisorption. The solubility product for precipitation and the activities of the species at the solid-liquid interface determine the surface precipitation process. Under appropriate electrochemical conditions, the activity of certain species can be higher in the interfacial region than that in the bulk solution and such a redistribution can lead to many reactions. For example, the sharp increase in adsorption of the calcium species on silica around pH 11 has been shown to be due to surface precipitation (Somasundaran and Anan-thapadmanabhan, 1985 Xiao, 1990). Similar correlations have been obtained for cobalt-silica, alumina-dodecylsulfonate, calcite/apatite/dolomite-fatty acid, francolite-oleate and tenorite-salicylaldoxime systems. The chemical state of the surfactant in the solution can also affect adsorption (Somasundaran and Ananthapadmanabhan, 1985). [Pg.81]

Grisafe DA, Hummel FA (1970) Crystal chemistry and color in apatites containing cobalt, nickel and rare-earth ions. Am Mineral 55 1131-1145... [Pg.44]


See other pages where Cobalt apatite is mentioned: [Pg.66]    [Pg.529]    [Pg.66]    [Pg.529]    [Pg.381]    [Pg.62]    [Pg.453]    [Pg.691]    [Pg.285]    [Pg.687]    [Pg.498]   
See also in sourсe #XX -- [ Pg.529 ]




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