首页> 外文期刊>Analytical Letters >Spectrophotometric Determination of Gold in Water and Ore with 2-Carboxyl-1-Naphthalthiorhodanine
【24h】

Spectrophotometric Determination of Gold in Water and Ore with 2-Carboxyl-1-Naphthalthiorhodanine

机译:2-羧-1-萘二硫代罗丹宁分光光度法测定水中和矿石中的金

获取原文
获取原文并翻译 | 示例
       

摘要

This paper reports on the synthesis of a new chromogenic reagent,2-carboxyl-1-naphthalthiorhodanine (CNTR).A high sensitive,selective,and rapid method for the determination of gold based on the rapid reaction of gold with CNTR and the solid phase extraction of the colored chelate with a reversed phase polymer-based C_(18) cartridge was developed.In the presence of 0.05-0.5 mol L~(-1) of phosphoric acid solution and emulsifier-OP medium,CNTR reacts with gold to form a red chelate of a molar ratio 1:3 (gold to CNTR).This chelate was enriched by the solid phase extraction with a polymer-based C_(18) cartridge and the retained chelate was eluted from the cartridge with dimethyl formamide (DMF).The enrichment factor of 100 was achieved.In the DMF medium,the molar absorptivity of the chelate is 1.35 x 10~5L mol~(-1) cm~(-1) at 540 nm.Beer's law is obeyed in the range of 0.01 approx 2 mu gmL~(-1) in the measured solution.The relative standard deviation for 11 replicates sample of 0.5 mu g L~(-1) level is 2.05%.The detection limit,based on three times the standard deviation is 0.02 mu g L~(-1) in the original sample.This method was applied to the determination of gold in water and ore with good results.
机译:本文报道了一种新的生色试剂2-羧基-1-萘硫基罗丹宁(CNTR)的合成。一种基于金与CNTR和固相的快速反应的高灵敏,选择性高的测定金的方法开发了反相聚合物基C_(18)柱对有色螯合物的萃取方法。在0.05-0.5 mol L〜(-1)磷酸溶液和乳化剂-OP介质存在下,CNTR与金反应形成摩尔比为1:3的红色螯合物(金与CNTR)。该螯合物通过使用基于聚合物的C_(18)柱进行固相萃取而富集,并使用二甲基甲酰胺(DMF)从柱中洗脱保留的螯合物达到了100的富集系数。在DMF介质中,螯合物的摩尔吸光度在540 nm下为1.35 x 10〜5L mol〜(-1)cm〜(-1)。被测溶液中的0.01约2μgmL〜(-1).11个重复样品的相对标准偏差为0.5μgL〜( -1)含量为2.05%。基于原样品三倍标准偏差0.02μg L〜(-1)的检出限,该方法用于水和矿石中金的测定,结果良好。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号