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Aqueous reduction of cobalto-cobaltic oxides in ammoniacal medium using ammonium sulphite as the reductant

机译:使用亚硫酸铵作为还原剂在氨性介质中水还原钴-钴氧化物

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Studies have been carried out on aqueous reduction of cobalto-cobaltic oxide in ammoniacal medium using ammonium sulphite as the reductant. The various parameters studied include agitation speed, leaching time, ammonia and ammonium sulphite concentrations. The kinetics of dissolution follow a surface-controlled model. The order of reactions with respect to both ammonia and ammonium sulphite were found to be first order. The XRD patterns and TG-DTA traces of the original cobalto-cobaltic oxide and a typical leach residue were identical, showing that the reaction is surface-controlled and no preferential dissolution of Co(II) or Co(III) takes place. It was observed that on cooling and storing leach solutions obtained at 391 K using ammonia more concentrated than 4.5 and 0.23 M ammonium sulphite resulted in precipitation of a crystalline compound which showed distinct lines in the XRD pattern but did not correspond to any known compound of Co. The chemical analysis, TG-DTA and FTIR analysis suggest the compound to be Co(NH_3)_4S_2O_6 centre dot 2H_2O.
机译:已经进行了使用亚硫酸铵作为还原剂在氨性介质中水还原钴-钴氧化物的研究。研究的各种参数包括搅拌速度,浸出时间,氨和亚硫酸铵浓度。溶解动力学遵循表面控制模型。发现关于氨和亚硫酸铵的反应顺序是一阶的。原始钴-钴氧化物和典型浸出残渣的XRD图谱和TG-DTA痕迹相同,表明该反应是表面受控的,不会发生Co(II)或Co(III)的优先溶解。观察到,在冷却和储存在391 K下使用浓度比4.5和0.23 M亚硫酸铵更浓的氨水得到的浸出溶液时,导致结晶化合物沉淀,该结晶化合物在XRD图谱中显示出鲜明的线条,但与任何已知的Co化合物都不对应。化学分析,TG-DTA和FTIR分析表明该化合物为Co(NH_3)_4S_2O_6中心点2H_2O。

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