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Chelating adsorption with variable stoichiometry: Separation of nickel and zinc in concentrated sulfate solution

机译:化学计量比可变的螯合吸附:浓硫酸盐溶液中镍和锌的分离

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摘要

A new approach is proposed for modeling of metal uptake data in chelating ion exchangers and adsorbents. In contrast to conventional equilibrium models assuming a constant stoichiometry for the surface complex, a step-wise reaction scheme is used in analogy with complex formation in bulk solution. The model is tested against equilibrium and dynamic uptake data, and the results are compared with those obtained using a conventional isotherm model. Nickel removal from ZnSO4 solutions using a commercial chelating adsorbent is used as test case. According to the results, the observed decrease in nickel uptake with increasing zinc concentration can be explained much better using the proposed model than with conventional isotherm models. Model parameters estimated from single-metal equilibrium data predict the behavior of batch and fixed-bed systems up to zinc concentrations of 2.2 mol/L with Zn/Ni mole ratio of about 10(4). (C) 2015 Elsevier B.V. All rights reserved.
机译:提出了一种用于螯合离子交换剂和吸附剂中金属吸收数据建模的新方法。与假定表面配合物化学计量恒定的常规平衡模型相反,采用逐步反应方案与在本体溶液中形成配合物类似。针对平衡和动态摄取数据对模型进行测试,并将结果与​​使用常规等温线模型获得的结果进行比较。使用商业螯合吸附剂从ZnSO4溶液中去除镍用作测试案例。根据结果​​,与常规等温线模型相比,使用建议的模型可以更好地解释观察到的镍吸收量随锌浓度的增加而降低的情况。从单金属平衡数据估算的模型参数可预测间歇式和固定床系统的行为,锌浓度最高为2.2 mol / L,且锌/镍摩尔比约为10(4)。 (C)2015 Elsevier B.V.保留所有权利。

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