4.7 Article

Solvent extraction of silver from nitric acid solutions by calix[4]arene amide derivatives

期刊

SEPARATION AND PURIFICATION TECHNOLOGY
卷 61, 期 3, 页码 366-374

出版社

ELSEVIER
DOI: 10.1016/j.seppur.2007.11.011

关键词

calixarene; solvent extraction; silver recovery; nitric acid; two-phase electrowinning; stripping

向作者/读者索取更多资源

Solvent extraction experiments were carried out to recover silver from nitric acid solutions using as the extractants calix[4]arene tetramide (LBC) and its thio-analogue (THIO) dissolved in dichloromethane. The stoichiometry of the formation of the silver-calixarene complex differs depending on the used extractant. It was shown that one silver ion reacts with a single molecule of LBC, while two silver ions are extracted with a single THTO molecule. Very high percent extractions (>90% with LBC and >99% with THIO) were achieved with both extractants by just adding surplus extractant (THIO: 0.6 mol/mol Ag+ and LBC: 1.4-1.5 mol/mol Ag+). Based on equilibrium data, the extraction isotherm relationship and the extraction constant K-ex for each extractant were derived. The extraction results show that THIO is an efficient extractant extracting silver either from acid or from neutral solutions with the same efficiency. Nitric acid, in the concentration range from 0 to 0.1 mol dm(-3), strongly affects the extraction capability of LBC in less acidic solutions, reducing the percent extraction down to 40%. LBC extracts both silver and sodium collectively and with the same efficiency. The selectivity coefficient has a value close to unity (beta approximate to 1). THIO has demonstrated extremely high selectivity for silver over sodium in a mixture. Stripping of silver was performed by two-phase electrowinning from the loaded organic phase, thereby achieving a high stripping degree (50-90%) and reasonably high current efficiency (60-90%). The calixarenes did not change their extraction features during the electrowinning process and can be reused for extraction many times. (C) 2007 Elsevier B.V All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据