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作 者:王小红[1] 董社英[1,2] 张帅鹏[2] 黄贵琦 黄廷林[1]
机构地区:[1]西安建筑科技大学环境与市政工程学院,西安710055 [2]西安建筑科技大学理学院,西安710055
出 处:《分析试验室》2015年第8期878-881,共4页Chinese Journal of Analysis Laboratory
基 金:国家自然科学基金(50830303);国家科技支撑计划(2012BAC04B02);陕西省科技统筹创新工程计划投资项目(2011KTCG03-07)资助
摘 要:建立了超声辅助-分散液相微萃取/高效液相色谱测定沉积物中双酚A,四溴双酚A,四溴双酚A双烯丙基醚,四溴双酚A双(2,3-二溴丙基)醚的方法。对萃取剂与分散剂的种类与用量、超声时间、盐效应及p H等萃取条件进行了优化。在优化的条件下,此方法的线性范围为0.1~100 mg/L,线性相关系数(r)为0.9996~0.9999。样品平均回收率为83%~91%,相对标准偏差为1.8%~4.9%。检出限(S/N=3)为0.01~0.15μg/L。方法可用于实际水库沉积物中双酚A及其衍生物的测定。A method of ultrasound-dispersive liquid-liquid microextraction( US-DLLME) combined with highperformance liquid chromatography( HPLC) has been developed for rapid determination of bisphenol A( BPA),tetrabromobisphenol A( TBBPA), TBBPA-bis( allyl ether)( TBBPA-BAE) and TBBPA-bis( 2,3-dibromopropyl ether)( TBBPA-BDBPE) in sediment. Experimental conditions of DLLME such as the type of extraction solvents and dispersive solvents,their volume,ultrasonic time,p H and ionic strength of the sediment samples were optimized. The results showed that analytes had linear responses between 0. 1 and 100 mg/L,with linear correlation coefficient( r) of 0. 9996 ~ 0. 9999. The limits of detection were 0. 08,0. 01,0.10,0. 15 μg/L,respectively. The average recoveries of spiked sediment samples were 83% ~ 91%,and the relative standard deviations were 1. 8% ~ 4. 9%. The developed method is simple and environmentally friendly for the determination of bisphenol A and its main derivatives in sediment samples.
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