期刊文献+

盐酸胍与溴化十六烷基吡啶从碱性氰化液中萃取Au(I) 被引量:2

Extraction of Au(I) from Alkaline Cyanide Solution with Guanidine Hydrochloride-Hexadecylpyridine Bromide
下载PDF
导出
摘要 以正戊醇为稀释剂,考察了盐酸胍与溴化十六烷基吡啶总浓度为0.06mol/L时,体系对Au(I)的协萃效应.结果表明,在整个浓度组成范围内均有协萃效应(协萃效应系数R>1),且有机相中盐酸胍与溴化十六烷基吡啶的浓度分别为0.05和0.01mol/L时,Au(I)的协萃系数为13.98.考察了平衡时间、相比、待萃液pH值及Au(I)浓度对Au(I)协同萃取性能的影响.对盐酸胍与溴化十六烷基吡啶萃取Au(I)的可能机理进行了分析.分别用Na2SO3和KSCN为反萃剂反萃Au(I),KSCN的反萃性能明显比Na2SO3好,KSCN浓度为12g/L、反萃时间30min、相比A/O=1时,Au(I)的反萃率为98.5%. The effects of concentrations of guanidine hydrochloride (GC1) and hexadecylpyridine bromide (RBr) served as extracting reagents on the performance of Au(I) extraction fxom cyanide solution were investigated when n-pentanol acted as diluting reagent. The synergic extraction effects of Au(I) were examined with GC1 and RBr at the total concentration of 0.06 mol/L. The results show that synergic extraction effects are obvious within the whole concentration composition range of GC1-RBr (synergic extraction coefficient R〉I), and when GC1 and RBr concentrations are 0.05 and 0.01 tool/L, the synergic extracting coefficient is 13.98. The effects of equilibrium time, phase ratio O/A, pH value and Au(I) concentration in the aqueous phase on the extraction rate of Au(I) were investigated by the synergic extraction system. The possible extraction mechanism of Au(I) with GC1 and RBr was analysed. Au(I) was stripped respectively by NaESO3 solution and KSCN solution, and KSCN was more excellent than NaESO3 on stripping of Au(I). The stripping rate of Au(I) was 98.5% when KSCN concentration was 12 girl and stripping time 30 rnin and phase ratio A/O 1.
出处 《过程工程学报》 EI CAS CSCD 北大核心 2008年第4期741-745,共5页 The Chinese Journal of Process Engineering
基金 安徽省高等学校青年教师科研基金资助项目(编号:2005jql137)
关键词 盐酸胍 溴化十六烷基吡啶 碱性氰化液 萃取 Au(I) guanidine hydrochloride hexadecylpyridine bromide alkaline cyanide solution extraction Au(I)
  • 相关文献

参考文献13

二级参考文献47

共引文献46

同被引文献19

  • 1潘路,鲍霞,魏亦军,储昭荣.盐酸胍从碱性氰化液中萃取金及机理研究[J].矿冶工程,2006,26(5):61-64. 被引量:7
  • 2沈兴海,李改玲,高宏成.醇对萃取有机相中形成微乳液的影响[J].北京大学学报(自然科学版),1997,33(2):153-157. 被引量:5
  • 3KOKYA T A, FARHADI K. Optimization of dispersiveliquid-liquid microextraction for the selectivedetermination of trace amounts of palladium by flameatomic absorption spectroscopy[J]. Journal of hazardousmaterials, 2009, 169(1): 726-733. 被引量:1
  • 4SAAVEDRA R, SOTO C, YANEZ J, et al. Determinationof Pd(11) content in catalysts and tap water samples viaphotoacoustic spectroscopy analysis of Pd(11)-3-[2′-thiazolylazo]-2,6-diaminopyridine complex on solidphase[J]. Journal of hazardous materials, 2009, 167(1):970-975. 被引量:1
  • 5FONTAS C, SALVADO V, HIDALGO M. Selectiveenrichment of palladium from spent automotive catalystsby using a liquid membrane system[J]. Journal ofmembrane science, 2003, 223(1): 39-48. 被引量:1
  • 6MARINHO R S, AFONSO J C, Cunha J W S D.Recovery of platinum from spent catalysts by liquidliquidextraction in chloride medium[J]. Journal ofhazardous materials, 2010, 179(1): 488-494. 被引量:1
  • 7PAN L. Solvent extraction and separation of palladium(11)and platinum(IV) from hydrochloric acid medium withdibutyl sulfoxide[J]. Minerals engineering, 2009, 22(15):1271-1276. 被引量:1
  • 8周扬,李学玲,顾烁玥,杨项军.用N503/TBP从碱性氰化液中萃取低浓度金[J].中国有色金属学报,2009,19(7):1345-1349. 被引量:9
  • 9杨得岭,宁朋歌,曹宏斌,张懿.伯胺N_(1923)络合萃取苯酚[J].过程工程学报,2012,12(4):569-575. 被引量:13
  • 10杨新周,杨子仙,胡秋芬,李学娇,郝志云.钯分离富集方法研究进展[J].云南化工,2013,40(1):30-35. 被引量:14

引证文献2

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部