摘要
建立了液-液萃取-气相色谱法同时测定地表水中17种硝基苯类和氯苯类化合物的方法。水中的硝基苯类和氯苯类化合物用乙酸乙酯/正己烷(2∶1,体积比)混合溶剂提取,经DB-35ms色谱柱分离后用ECD检测。方法灵敏度高,萃取定容后即可进样分析,无需进行高倍浓缩,17种化合物分离良好,检测灵敏度高,水中检出限为0.03~0.08μg/L,比饮用水源地限值低1~4个数量级。本法在40.0~400μg/L浓度范围内线性相关性良好,方法相对标准偏差为1.4%~5.2%,实际样品加标回收率为96.3%~106%。
A liquid-liquid extraction-gas chromatography method was established to simultaneously determination for 17 kinds of nitrobenzene-compounds and chlorobenzene-compounds in ground water.A mixed solvent ethyl acetate/n-hexane(2∶ 1,V/V) was used.The 17 compounds were separated by a DB-35ms capillary column and quantitative results were acquired by electron capture detector(ECD).The phase ratio of water to organic solvent was 10∶ 1.The extracts could be analyzed directly with no concentration.The present method has a good linearity ranged from 40.0μg/L to 400μg/L.The relative standard deviations(RSD) of parallel determination are between 1.41% to 5.18%.The spiked recoveries come to be 96.3%~106%.The method determination limits show to be 0.03~0.08μg/L,which are 1~4 orders of magnitude lower than the control limits of GB 3838-2002.
出处
《中国环境监测》
CAS
CSCD
北大核心
2011年第B10期19-23,共5页
Environmental Monitoring in China
基金
国家"水体污染控制与治理"重大科技专项(2009ZX07527)
关键词
液-液萃取
硝基苯类
氯苯类
气相色谱法
ECD
Liquid-liquid extraction
Nitrobenzene-compounds
Chlorobenzene-compounds
Gas chromatography
ECD