Water-soluble precursors for nanometric calcium tungstate (CaWO 4 ) were prepared from calcium 2-hydroxycarboxylate salts. The precursors decompose as low as 425 8C to yield nanocrystalline scheelite. Supported CaWO 4 in a convenient form for water treatment processes was prepared by impregnation of high surface area catalyst support pellets with an aqueous solution of a single-source precursor followed by drying and calcining. Both the powder and supported nanocrystalline forms of CaWO 4 underwent ion-exchange reaction with aqueous lead ions whereby Ca 2 + was released and Pb 2 + was adsorbed to produce crystalline stolzite (PbWO 4 ). Electron microscopy demonstrated that little morphological change of the particles occurred upon reaction with excess Pb 2 + . The process appears to occur via an ion-exchange route. The nonlinear pseudo first-order kinetic model gave the best fit for both the powder and supported forms of CaWO 4 , allowing the kinetic results from the two materials to be directly compared to each other. Supporting of CaWO 4 improves the kinetics at higher Ca-WO 4 :Pb 2 + ratios while at lower ratios diffusion of the Pb 2 + ions into the porous pellets likely becomes the controlling factor and the powder form uptakes Pb 2 + faster. The molar capacity of the material for Pb 2 + uptake improved from 70 % to 100 % upon supporting the CaWO 4 . The novel ion-exchange materials were demonstrated to be useful for the purification of industrial wastewaters and juice.
Results and DiscussionThe calcium salts of the 2-hydroxyacids, gluconic and a-hydroxybutyric acid, readily react with tungstic acid, H 2 WO 4 , in reflux- [a] Dr.