首页> 外文会议>2001 TMS (The Minerals, Metals amp; Materials Society) Annual Meeting, Feb 11-15, 2001, New Orleans, Louisana >SILVER ION EXTRACTION REACTIONS BY DIBUTYLTHIOUREA (DBT) OR DISULFIRAM(DSF) FROM CONCENTRATED CHLORIDE SOLUTIONS
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SILVER ION EXTRACTION REACTIONS BY DIBUTYLTHIOUREA (DBT) OR DISULFIRAM(DSF) FROM CONCENTRATED CHLORIDE SOLUTIONS

机译:浓氯化物溶液中丁二酸(DBT)或二硫化物(DSF)萃取银离子的反应

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Investigation on profitable ways to recover significant quantities of silver remaining dissolved in highly concentrated chloride solutions frequently pass through the development of solvent extraction (SX) routes. In this work, the general pathways involving Ag(I) extraction by dibutylthiourea (DBT) or tetraethylthiuram disulfide (disulfiram, DSF), from concentrated acidic chloride solutions, are investigated. With this purpose, the dependence of Ag(I) distribution coefficient on ligand and chloride concentrations has been analysed. Furthermore, in order to check whether there is some protonation at any site of DBT or DSF after contact with adequate chloride phases, ~1H NMR has also been used. The collected spectroscopic data suggest that anionic Ag(I) extraction reactions are not likely to occur. Based on the overall results achieved, proposals for the most probable Ag(I) extraction reactions are made.
机译:对回收可溶解在高浓度氯化物溶液中的大量剩余银的有利方法的研究通常通过溶剂萃取(SX)路线的开发来进行。在这项工作中,研究了从浓酸性氯化物溶液中通过二丁基硫脲(DBT)或四乙基秋兰姆二硫化物(disulfiram,DSF)提取Ag(I)的一般途径。为此目的,已经分析了Ag(I)分布系数对配体和氯化物浓度的依赖性。此外,为了检查在与适当的氯化物相接触后DBT或DSF的任何部位是否存在质子化,还使用了〜1H NMR。收集的光谱数据表明,阴离子Ag(I)提取反应不太可能发生。基于获得的总体结果,提出了最可能的Ag(I)提取反应的建议。

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