...
首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Ferric ion induced enhancement of ultraviolet vapour generation coupled with atomic fluorescence spectrometry for the determination of ultratrace inorganic arsenic in surface water
【24h】

Ferric ion induced enhancement of ultraviolet vapour generation coupled with atomic fluorescence spectrometry for the determination of ultratrace inorganic arsenic in surface water

机译:铁离子诱导的紫外蒸气产生的增强结合原子荧光光谱法测定地表水中的超痕量无机砷

获取原文
获取原文并翻译 | 示例
           

摘要

A novel method of ultraviolet vapour generation (UVG) coupled with atomic fluorescence spectrometry (AFS) was developed for the determination of ultratrace inorganic arsenic (iAs) in surface water. In this work, different ferric species were utilised for the first time as an enhancement reagent for the ultraviolet vapour generation of As(III), and their UVG efficiencies for volatile species of arsenic were investigated. 15 mg L-1 of ferric chloride provided the greatest enhancement of approximately 10-fold, using 20% acetic acid combined with 4% formic acid with 30 s ultraviolet irradiation at 200 mL min(-1) Ar/H-2 flow rate. Under the optimised conditions, the linear range was 1.0 mu g L-1-100.0 mu g L-1, and the spiked recoveries were 92%-98%. The limit of detection was 0.05 mu g L-1 for iAs, and the relative standard deviation (RSD) value of the repeated measurements was 2.0% (n = 11). This method was successfully applied to the determination of ultratrace iAs in tap water, river water, and lake water samples using 0.2% H2SO4 (v : v) as the sample preserver. The obtained values for the water samples of certified reference materials (CRMs) including GSB-Z50004-200431, GBW08605 and GBW(E)080390 were all within the certified ranges.
机译:建立了一种新的紫外蒸气发生法(UVG)与原子荧光光谱法(AFS)结合用于测定地表水中超痕量无机砷(iAs)的方法。在这项工作中,首次将不同的三价铁物种用作产生As(III)紫外线蒸气的增强剂,并研究了它们对砷的挥发性物种的UVG效率。在200 mL min(-1)Ar / H-2流速下,使用20%的乙酸和4%的甲酸在30 s的紫外线照射下结合使用,15 mg L-1的氯化铁的最大增强作用约为10倍。在最佳条件下,线性范围为1.0μgL-1-100.0μgL-1,加标回收率为92%-98%。 iAs的检出限为0.05μg L-1,重复测量的相对标准偏差(RSD)值为2.0%(n = 11)。该方法已成功用于以0.2%H2SO4(v:v)作为样品保存剂的自来水,河水和湖水样品中超痕量iAs的测定。包括GSB-Z50004-200431,GBW08605和GBW(E)080390在内的认证参考物质(CRM)的水样品获得的值均在认证范围内。

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