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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
摘要点击 2079  全文点击 1014  投稿时间:2015-03-09  修订日期:2015-05-20
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中文关键词  搅拌棒吸附萃取  邻苯二甲酸酯  气质联用  海水  痕量  胶州湾
英文关键词  stir bar sorptive extraction (SBSE)  phthalic acid esters (PAEs)  gas chromatograph mass spectrometer (GC-MS)  sea water  trace amount  Jiaozhou Bay
作者单位E-mail
高晨晨 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 gaocc1990@126.com 
李锋民 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 lifengmin@ouc.edu.cn 
卢伦 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  
孙玥 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  
中文摘要
      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0.25~174.42ng·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.
英文摘要
      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.

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