首页> 外文期刊>American Journal of Analytical Chemistry >Flame Atomic Absorption Spectrometric Determination of Trace Amounts of Zinc and Thallium in Different Matrixes after Solid Phase Extraction on Modified Multiwalled Carbon Nanotubes
【24h】

Flame Atomic Absorption Spectrometric Determination of Trace Amounts of Zinc and Thallium in Different Matrixes after Solid Phase Extraction on Modified Multiwalled Carbon Nanotubes

机译:改性多壁碳纳米管固相萃取后火焰原子吸收光谱法测定不同基质中痕量锌和hall

获取原文
           

摘要

The potential of modified multiwallcd carbon nanotubes, as a solid-phase extraction sorbent for the simultaneous separation and preconcentration of zinc and thallium has been investigated. Zinc and thallium were adsorbed quantitatively onto modified multiwalled carbon nanotubes in the pH range of 3 - 6.5. Parameters influencing the simultaneous preconcentration of Zn(II) and Tl(I) ions such as pH of the sample, sample and eluent flow rate, type and volume of elution solution and interfering ions, have been examined and optimized. Linearity was maintained between 0.1 to 20.0 μg?mL–1 for thallium and 20.0 ng?mL–1 to 5.0 μg?mL–1 for zinc in the final solution. The defection limits based on three times the standard deviation of the blank signal (n = 8) for thallium and zinc were 5.1 and 1.4 ng?mL–1, respectively. Seven replicate determination of a mixture of 5.0 and 0.2 μg?mL–1 of thallium and zinc in the final solution gave a mean absorbance of 0.085 and 0.074 with relative standard deviation 1.5% and 1.7%, respectively. The method has been applied for the determination of trace amounts of zinc and thallium in biological and water sample with satisfactory results.
机译:研究了改性多壁碳纳米管作为固相萃取吸附剂同时分离和预富集锌和th的潜力。在3-6.5的pH范围内,锌和th被定量吸附在改性的多壁碳纳米管上。已经检查并优化了影响Zn(II)和Tl(I)离子同时预富集的参数,例如样品的pH值,样品和洗脱液的流速,洗脱液的类型和体积以及干扰离子。在最终溶液中,th的线性保持在0.1至20.0μg?mL–1之间,锌保持在20.0 ng?mL–1至5.0μg?mL–1之间。根据fection和锌的空白信号标准偏差(n = 8)的三倍得出的缺陷极限分别为5.1和1.4 ng?mL–1。对最终溶液中的determination和锌的5.0和0.2μg?mL–1的混合物进行七次重复测定,得出平均吸光度为0.085和0.074,相对标准偏差分别为1.5%和1.7%。该方法用于生物和水样中痕量锌和al的测定,结果令人满意。

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