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搅拌棒吸附萃取-气相色谱-质谱联用测定海水中邻苯二甲酸酯
引用本文:高晨晨,李锋民,卢伦,孙玥.搅拌棒吸附萃取-气相色谱-质谱联用测定海水中邻苯二甲酸酯[J].环境科学,2015,36(10):3906-3912.
作者姓名:高晨晨  李锋民  卢伦  孙玥
作者单位:中国海洋大学环境科学与工程学院, 海洋环境与生态教育部重点实验室, 青岛 266100;中国海洋大学环境科学与工程学院, 海洋环境与生态教育部重点实验室, 青岛 266100;中国海洋大学环境科学与工程学院, 海洋环境与生态教育部重点实验室, 青岛 266100;中国海洋大学环境科学与工程学院, 海洋环境与生态教育部重点实验室, 青岛 266100
基金项目:国家自然科学基金项目(51378480);国家重点基础研究发展规划(973)项目(2015CB453301);国家自然科学基金委员会-山东省人民政府联合资助海洋科学研究中心项目(U1406403);海洋公益性行业科研专项(201305003)
摘    要:为了测定海水中痕量邻苯二甲酸酯,构建并优化了搅拌棒吸附萃取-气相色谱-质谱联用方法.选取邻苯二甲酸二甲酯、邻苯二甲酸二乙酯、邻苯二甲酸二丁酯、邻苯二甲酸丁基苄基酯、邻苯二甲酸二(2-乙基己基)酯和邻苯二甲酸二辛酯这6种邻苯二甲酸酯作为研究对象,优化了萃取时间和解析时间等5种因素,通过回收率和相对标准偏差等对SBSE-GC-MS方法进行验证.结果表明,最佳萃取时间为2 h,最佳甲醇添加量为10%,最佳氯化钠添加量为5%,最佳解析时间为50 min,最佳解析溶剂为甲醇∶乙腈=4∶1(体积比).6种邻苯二甲酸酯的峰面积和质量浓度线性对应关系良好,相关性系数均大于0.997,检出限在0.25~174.42 ng·L-1之间,不同质量浓度的回收率均在56.97%~124.22%之间,相对标准偏差在0.41%~14.39%之间.在建立方法的基础上,测定了胶州湾主要河流入海口的样品,结果表明所有采样点均检出邻苯二甲酸酯,邻苯二甲酸二乙酯检出率为100%,质量浓度较大的污染物为邻苯二甲酸二丁酯、邻苯二甲酸丁基苄基酯、邻苯二甲酸二(2-乙基己基)酯和邻苯二甲酸二辛酯.

关 键 词:搅拌棒吸附萃取  邻苯二甲酸酯  气质联用  海水  痕量  胶州湾
收稿时间:3/9/2015 12:00:00 AM
修稿时间:2015/5/20 0:00:00

Application of Stir Bar Sorptive Extraction and Gas Chromatograph Mass Spectrometer to the Phthalic Acid Esters Analysis in Seawater
GAO Chen-chen,LI Feng-min,LU Lun and SUN Yue.Application of Stir Bar Sorptive Extraction and Gas Chromatograph Mass Spectrometer to the Phthalic Acid Esters Analysis in Seawater[J].Chinese Journal of Environmental Science,2015,36(10):3906-3912.
Authors:GAO Chen-chen  LI Feng-min  LU Lun and SUN Yue
Institution:Key Laboratory of Marine Environment and Ecology, Ministry of Education, College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100, China;Key Laboratory of Marine Environment and Ecology, Ministry of Education, College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100, China;Key Laboratory of Marine Environment and Ecology, Ministry of Education, College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100, China;Key Laboratory of Marine Environment and Ecology, Ministry of Education, College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100, China
Abstract:For the determination of trace amounts of phthalic acid esters (PAEs) in complex seawater matrix, a stir bar sorptive extraction gas chromatography mass spectrometry (SBSE-GC-MS) method was established.Dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), butyl benzyl phthalate (BBP), dibutyl phthalate (2-ethylhexyl) phthalate (DEHP) and dioctyl phthalate (DOP) were selected as study objects.The effects of extraction time, amount of methanol, amount of sodium chloride, desorption time and desorption solvent were optimized.The method of SBSE-GC-MS was validated through recoveries and relative standard deviation.The optimal extraction time was 2 h.The optimal methanol content was 10%.The optimal sodium chloride content was 5%.The optimal desorption time was 50 min.The optimal desorption solvent was the mixture of methanol to acetonitrile (4:1, volume: volume).The linear relationship between the peak area and the concentration of PAEs was relevant.The correlation coefficients were greater than 0.997.The detection limits were between 0.25 and 174.42 ng·L-1.The recoveries of different concentrations were between 56.97% and 124.22%.The relative standard deviations were between 0.41% and 14.39%.On the basis of the method, several estuaries water sample of Jiaozhou Bay were detected.DEP was detected in all samples, and the concentration of BBP, DEHP and DOP were much higher than the rest.
Keywords:stir bar sorptive extraction (SBSE)  phthalic acid esters (PAEs)  gas chromatograph mass spectrometer (GC-MS)  sea water  trace amount  Jiaozhou Bay
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