...
首页> 外文期刊>Microchimica Acta >Determination of trace molybdenum in biological and water samples by graphite furnace atomic absorption spectrometry after separation and preconcentration on immobilized titanium dioxide nanoparticles
【24h】

Determination of trace molybdenum in biological and water samples by graphite furnace atomic absorption spectrometry after separation and preconcentration on immobilized titanium dioxide nanoparticles

机译:固定化二氧化钛纳米颗粒分离富集-石墨炉原子吸收光谱法测定生物和水样中痕量钼。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A new method has been developed for the determination of trace molybdenum based on separation and preconcentration with TiO2 nanoparticles immobilized on silica gel (immobilized TiO2 nanoparticles) prior to its determination by graphite furnace atomic absorption spectrometry (GFAAS). The optimum experimental parameters for preconcentration of molybdenum, such as pH of the sample, sample flow rate and volume, eluent and interfering ions, have been investigated. Molybdenum can be quantitatively retained by immobilized TiO2 nanoparticles at pH 1.0 and separated from the metal cations in the solution, then eluted completely with 0.5 mol L−1 NaOH. The detection limit of this method for Mo was 0.6 ng L−1 with an enrichment factor of 100, and the relative standard deviation (RSD) was 3.4% at the 10 ng mL−1 Mo level. The method has been applied to the determination of trace amounts of Mo in biological and water samples with satisfactory results. Keywords Immobilized titanium dioxide nanoparticles - Preconcentration - Molybdenum - Graphite furnace atomic absorption spectrometry
机译:通过固定化硅胶上固定的TiO 2 纳米颗粒(固定化的TiO 2 纳米颗粒)的分离和富集,开发了一种测定痕量钼的新方法。石墨炉原子吸收光谱法(GFAAS)。已研究了钼的预浓缩的最佳实验参数,例如样品的pH,样品的流速和体积,洗脱液和干扰离子。固定化的pH <1.0的TiO 2 纳米颗粒可以定量保留钼,并与溶液中的金属阳离子分离,然后用0.5 mol L -1 NaOH完全洗脱。该方法对Mo的检出限为0.6 ng L -1 ,富集系数为100,在10 ng mL -1 <时的相对标准偏差(RSD)为3.4%。 / sup> Mo水平。该方法已用于生物和水样中痕量钼的测定,结果令人满意。固定化二氧化钛纳米粒子预富集钼石墨炉原子吸收光谱法。

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