首页> 外文OA文献 >Speciation analysis of arsenic compounds by capillary electrophoresis on-line coupled with inductively coupled plasma mass spectrometry using a novel interface
【2h】

Speciation analysis of arsenic compounds by capillary electrophoresis on-line coupled with inductively coupled plasma mass spectrometry using a novel interface

机译:新型界面介导的毛细管电泳-电感耦合等离子体质谱在线分析砷化合物的形态

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this work, a capillary electrophoresis (CE) coupled with inductively coupled plasma mass spectrometer (ICP-MS) system was developed for the simultaneous determination of ten arsenic compounds including arsenite, arsenate, monomethylarsonic acid, dimethylarsinic acid, arsenobetaine, arsenocholine, 3-nitro-4-hydroxyphenylarsonic acid, o-Arsanilic acid, p-ureidophenylarsonic acid, and 4-nitrophenylarsonic acid. The CE-ICP-MS system was hyphenated by a novel and high efficient interface which was directly used as the nebulizer. The separation was achieved on a 100 cm length x 50 mu m ID fused-silica capillary. Analytical conditions such as electrophoretic buffer composition, concentration and pH value, separation voltage, methanol concentration in the sheath flow liquid and sample injection time were optimized. Baseline separation of the ten arsenic species was achieved using an electrophoretic buffer consisting of 12 mM NaH2PO4 and 8 mM HBO3 at pH 9.20 with an applied voltage of +30 kV. The detection limits of the ten arsenic compounds ranged from 0.9 to 3.0 ng As g(-1), corresponding to absolute detection limits in the range of 19-65 fg As and the relative standard deviations (RSD, n = 5) were below 1.5%, 5.7% and 4.8% for migration time, peak height and peak area, respectively. This method was successfully applied to determine various arsenicals in two certified reference materials (TORT-2 and DORM-3) and environmental samples such as ground water samples, herbal plants and chicken meat. (C) 2013 Elsevier B.V. All rights reserved.
机译:在这项工作中,开发了毛细管电泳(CE)和电感耦合等离子体质谱仪(ICP-MS)系统,用于同时测定十种砷化合物,包括亚砷酸盐,砷酸盐,一甲基砷酸,二甲基砷酸,砷甜菜碱,砷胆碱,3-硝基-4-羟基苯基亚磺酸,邻芳基茴香酸,对-脲基苯基亚磺酸和4-硝基苯基亚磺酸。 CE-ICP-MS系统通过新颖而高效的界面进行了连接,该界面直接用作雾化器。分离是在100 cm长x 50μmID的熔融石英毛细管上完成的。优化了电泳缓冲液组成,浓度和pH值,分离电压,鞘流液中甲醇浓度和样品注入时间等分析条件。使用电泳缓冲液实现十种砷物质的基线分离,该电泳缓冲液由pH值为9.20的12 mM NaH2PO4和8 mM HBO3组成,施加电压为+30 kV。十种砷化合物的检出限为0.9至3.0 ng As g(-1),对应于19-65 fg As的绝对检出限,相对标准偏差(RSD,n = 5)低于1.5迁移时间,峰高和峰面积分别为%,5.7%和4.8%。该方法已成功应用于两种认证参考物质(TORT-2和DORM-3)和环境样品(如地下水样品,草药植物和鸡肉)中的各种砷含量测定。 (C)2013 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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