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双柱定性气相色谱电子捕获检测器测定上海市饮用水中微量碘化物
引用本文:韦霄,张亚英,张东,王霞,盛英杰,张晶,郭帅,郑唯韡,陈鑫,屈卫东.双柱定性气相色谱电子捕获检测器测定上海市饮用水中微量碘化物[J].中华预防医学杂志,2010,44(1):591-595.
作者姓名:韦霄  张亚英  张东  王霞  盛英杰  张晶  郭帅  郑唯韡  陈鑫  屈卫东
作者单位:200032,上海,复旦大学公共卫生学院公共卫生安全教育部重点实验室;广西壮族自治区疾病预防控制中心艾滋病性病防制科;上海市杨浦区疾病预防控制中心环境与职业卫生科;城市水资源开发利用(南方)国家工程研究中心总工室;复旦大学公共卫生学院公共卫生安全教育部重点实验室,上海,200032;上海市杨浦区疾病预防控制中心中心实验室;
基金项目:国家科技支撑计划国家高技术研究发展计划(863计划)国家自然科学基金上海市教育委员会曙光计划上海市公共卫生优秀学科带头人培养计划
摘    要:Objective To modify and optimize gas chromatographic conditions, qualitative and quantitative method on the base of the actual national standard detection method for drinking water on testing iodide with gas chromatography, and detect iodide in drinking water of Shanghai.Methods Iodobutanone derivative was identified by gas chromatography/mass spectrometry, then two capillary columns coupled to electron capture detector were made by qualitative and quantitative analysis.Finally, 100 ml water samples were collected respectively from raw water and finished water of three plants in which water sources were Yangtse river, Huangpu river, and inner river respectively and detected by this developed method.Results The results of mass spectrometry showed that iodide would form iodobutanone which could generate 1-iodo-2-butanone and 3-iodo-2-butanone isomers by derivatization.The data of qualitative analysis by two capillary columns revealed that iodobutanone was separated completely and the total time of chromatogram separation was 19.33 min.3-iodo-2-butanone with the high response value was selected to quantitatively analyse.The linear range was 1 - 100 μg/L,and the coefficient of determination (r2) was 0.9997.The limit of detection was 13 ng/L.Recoveries were between 97.68% and 104.37% ,and relative standard deviations were between 2.14% and 4.41%.The results of iodide detected by this method in raw water and finished water in three plants in Shanghai showed that the ranking of iodide's concentration in raw water was Huangpu river (15.14 μg/L) > inner river (6.97 μg/L) > Yangtse river (3.55 μg/L).The level of iodide in finished water of plant 1 (3.55 μg/L and 5.92 μg/L for raw and finished water respectively) and 3 ( 6.97 μg/L and 9.62 μg/L for raw and finished water respectively) increased slightly except for plant 2( 15.14 μg/L and 1.81 μg/L for raw and finished water respectively).The relative standard deviations of all water samples measured in duplicate were less than 9.73%.Conclusion The improved method possesses higher degree of sensitivity and accuracy of qualitative and quantitative analysis than actual national standard detection method, and it is fit for trace analysis of iodide in water.

关 键 词:碘化物    色谱法  气相        

Determination of trace iodide in drinking water in Shanghai by two columns and gas chromatography with electron capture detection
WEI Xiao,ZHANG Ya-ying,ZHANG Dong,WANG Xia,SHENG Ying-jie,ZHANG Jing,GUO Shuai,ZHENG Wei-wei,CHEN Xin,QU Wei-dong.Determination of trace iodide in drinking water in Shanghai by two columns and gas chromatography with electron capture detection[J].Chinese Journal of Preventive Medicine,2010,44(1):591-595.
Authors:WEI Xiao  ZHANG Ya-ying  ZHANG Dong  WANG Xia  SHENG Ying-jie  ZHANG Jing  GUO Shuai  ZHENG Wei-wei  CHEN Xin  QU Wei-dong
Abstract:
Keywords:IodidesChromatography  gasWater
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