首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Determination of Bismuth by Electrothermal Atomic Absorption Spectrometry using Single Drop Micro Extraction in Real Samples
【24h】

Determination of Bismuth by Electrothermal Atomic Absorption Spectrometry using Single Drop Micro Extraction in Real Samples

机译:样品中单滴微萃取的电热原子吸收光谱法测定铋

获取原文
获取原文并翻译 | 示例
       

摘要

A novel and extremely sensitive method for extraction and determination of bismuth in aqueous samples by liquid phase micro extraction (LPME) combined with electrothermal atomic absorption spectrometry using a new ligand is described. In this method Bi~(3+) in pH 6 during 20 min extraction time at 20 °C is reacted with S-methyl-3-salicylidene dithiocarbazate dissolved in 4 μL of chloroform micro drop. After extraction, the micro drop was retracted and directly transferred into a graphite tube coated by palladium and tungsten with co-injection of tartaric acid as chemical modifier. In this investigation the type of organic solvent, volume of organic solvent, pH, temperature and extraction time were optimized. Using 10 mL sample solution an enrichment factor of 100 was obtained. The detection limit was calculated to be 19 pg mL~(-1) based on 3S_b and relative standard deviation for five replicate analysis of 0.5 ng mL~(-1) Br~(3+ was 4.8 %. The calibration curve was liner in the range of 19 pg mL~(-1) to 2.4 ng mL~(-1) with a sensitivity of 4.0 pg mL~(-1). This method was used for determination of bismuth in tap water, waste water, sea water, soil and reliability of the method was evaluated using two reference materials.
机译:描述了一种新颖且极其灵敏的方法,该方法通过液相微萃取(LPME)结合使用新配体的电热原子吸收光谱法来萃取和测定水性样品中的铋。在该方法中,在20°C的萃取时间内20分钟内,pH 6的Bi〜(3+)与溶解在4μL氯仿微滴中的S-甲基-3-水杨基二硫代氨基甲酸酯反应。萃取后,将微滴缩回并直接转移到涂有钯和钨的石墨管中,同时注入酒石酸作为化学改性剂。在这项研究中,对有机溶剂的类型,有机溶剂的体积,pH,温度和萃取时间进行了优化。使用10 mL样品溶液,可获得100的富集系数。根据3S_b计算出的检出限为19 pg mL〜(-1),相对于0.5 ng mL〜(-1)Br〜(3+)的五次重复分析的相对标准偏差为4.8%。测定灵敏度为4.0 pg mL〜(-1)的范围为19 pg mL〜(-1)至2.4 ng mL〜(-1)。该方法用于自来水,废水和海水中铋的测定,土壤和方法的可靠性使用两种参考材料进行了评估。

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