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流动注射在线分离富集-火焰原子吸收光谱法测定环境水样中Cr(Ⅲ)和Cr(Ⅵ)的形态
引用本文:康维钧,梁淑轩,哈婧,申世刚,孙汉文. 流动注射在线分离富集-火焰原子吸收光谱法测定环境水样中Cr(Ⅲ)和Cr(Ⅵ)的形态[J]. 光谱学与光谱分析, 2003, 23(3): 572-575
作者姓名:康维钧  梁淑轩  哈婧  申世刚  孙汉文
作者单位:河北大学化学与环境科学学院,河北,保定,071002
基金项目:河北省自然科学基金资助课题 (编号 :2 0 31 1 0 )
摘    要:采用单阀阴离子和阳离子交换树脂微柱并联 ,两柱交替采样逆向洗脱流动注射在线分离富集环境水样中Cr(Ⅲ )和Cr(Ⅵ ) ,分别用 15 %HNO3和 8%NH4 NO3洗脱 ,火焰原子吸收光谱法直接检测。富集 1min时Cr(Ⅲ )和Cr(Ⅵ )的特征浓度分别为 :1 5 0 μg·L- 1 和 1 39μg·L- 1 ,Cr(Ⅲ )和Cr(Ⅵ )检出限 (3σ)分别为 1 0 3μg·L- 1 和 0 5 4 μg·L- 1 ;相对标准偏差 (10 μg·L- 1 )分别为 :3 4 1%和 1 80 % ,分析样品加标回收率在 93 5 %~ 10 7 5 %之间。

关 键 词:流动注射  火焰原子吸收光谱法  铬(Ⅲ)  铬(Ⅵ)
文章编号:1000-0593(2003)03-0572-04
修稿时间:2002-07-29

Determination of Chromium(Ⅲ) and Chromium(Ⅵ) in Water Using Flow Injection On-line Preconcentration and Separation with Flame Absorption Spectrometric Detection
KANG Wei-jun,LIANG Shu-xuan,HA Jing,SHEN Shi-gang and SUN Han-wen College of Chemistry and Environmental Science,Hebei University,Baoding ,China. Determination of Chromium(Ⅲ) and Chromium(Ⅵ) in Water Using Flow Injection On-line Preconcentration and Separation with Flame Absorption Spectrometric Detection[J]. Spectroscopy and Spectral Analysis, 2003, 23(3): 572-575
Authors:KANG Wei-jun  LIANG Shu-xuan  HA Jing  SHEN Shi-gang  SUN Han-wen College of Chemistry  Environmental Science  Hebei University  Baoding   China
Affiliation:College of Chemistry and Environmental Science, Hebei University, Baoding 071002, China.
Abstract:A rapid and sensitive method for the sequential determination of Cr(III) and Cr(VI) in water samples based on flow injection on-line preconcentration and separation with two-microcolumn system-flame atomic absorption spectrometry has been developed. The Cr(III) and Cr(VI) in water samples were respectively retained in a microcolum with cation exchange resin and in a microcolumn with anion exchange resin and were eluted directly by 15% HNO3 and 8% NH4NO3, respectively. The characteristic concentrations (pre-concentration time of 1 min) for Cr(III) and Cr(VI) were 1.50 micrograms.L-1 and 1.39 micrograms.L-1, respectively, The relative standard deviations at 10 micrograms.L-1 level were 3.41% and 1.80%, and the corresponding detection limits (3 sigma) were 1.03 micrograms.L-1 and 0.54 microgram.L-1, respectively. The satisfactory recovery of 93.48%-107.5% could be obtained from water samples.
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