...
首页> 外文期刊>Analytica chimica acta >Simplified method for the Re-Os dating of molybdenite using acid digestion and isotope dilution ICP-MS
【24h】

Simplified method for the Re-Os dating of molybdenite using acid digestion and isotope dilution ICP-MS

机译:酸消解和同位素稀释ICP-MS简化辉钼矿Re-Os定年的方法

获取原文
获取原文并翻译 | 示例
           

摘要

An anlaytical method was developed for Os-Re dating of molybdenite. The method is based on determination of Os and Re concentrations in molybdenite by isotope dilution inductively-coupled plasma mass spectrometry (ID-ICP-MS0). Sample digestion and sample/spike equilibration were achieved by a two-stage autoclave-based procedure using a mixture of nitric and sulphuric acids. Os was separated from the sample diges by modified single-stage distillation of osmium tetraoxide (OsO_4) using elevated temperature and on-line addition of hydrogen peroxide. OsO_4(g) was trapped in a mixture of 0.05% thiourea in 0.05 M sodium hydroxide. An anion-exchange column was used to separate Re from excess Mo in the solution remaining after distillation. Os and Re isotope ratio measurements were performed by single-collector, double focusing inductively-coupled plasma mass spectrometry (ICP-MS) with on-line mass-bias correction. Typical instrumental precision was in the range 0.02-0.2% relative standard deviation (R.S.D.) depending on the analyte concentrations. Notorious Os memory effects in the ICP-MS introduction system were eliminated using 5% ammonia solution, both as matrix for final dilution of the trap mixture as well as for washing between the samples. The reproducibility of the entire analytical procedure was accessed by replicate dating of two molybdenite standards and three polybdenite separates, and was found to be in the range 0.87-1.52% R.S.D.Though accuracy of the method is limited by difficulties in evaluating exact concentration of Os in spike solution, ages obtained in the course of these work agrees well wit previously published data.
机译:开发了一种用于辉钼矿Os-Re定年的分析方法。该方法基于同位素稀释电感耦合等离子体质谱法(ID-ICP-MS0)测定辉钼矿中Os和Re的浓度。样品的消解和样品/加标的平衡是通过使用硝酸和硫酸的混合物,通过基于高压釜的两阶段程序实现的。通过使用高温和在线添加过氧化氢对四氧化(OsO_4)进行改良的单级蒸馏,从样品中分离出Os。将OsO_4(g)捕集在0.05%的氢氧化钠中的0.05%硫脲的混合物中。使用阴离子交换柱将蒸馏后剩余溶液中的Re与过量Mo分离。 Os和Re同位素比的测量是通过单收集器,双聚焦感应耦合等离子体质谱(ICP-MS)和在线质量偏差校正进行的。仪器的典型精度取决于分析物浓度,相对标准偏差(R.S.D.)在0.02-0.2%的范围内。 ICP-MS引入系统中使用5%的氨水消除了臭名昭著的Os记忆效应,既用作最终稀释捕集阱混合物的基质,又用于样品之间的洗涤。通过重复测定两种辉钼矿标准品和三种辉钼矿分离物的质量,可以得到整个分析过程的重现性,其RSD范围为0.87-1.52%。尽管该方法的准确性受到评估准确的Os浓度困难的限制。峰值解决方案,在这些工作过程中获得的年龄与以前发布的数据非常吻合。

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