Cao Xu-Liang
Food Research Division, Bureau of Chemical Safety, Food Directorate, Health Canada, 251 Frederick Banting Driveway, AL 2203D, Ottawa, Ontario K1A 0L2, Canada.
J Chromatogr A. 2008 Jan 18;1178(1-2):231-8. doi: 10.1016/j.chroma.2007.11.095. Epub 2007 Dec 3.
The performance of three fibres for the headspace solid-phase microextraction (SPME) of di-2-ethylhexyl adipate (DEHA) and eight phthalates in water was investigated systematically under different extraction conditions. Good responses on the 65 microm polydimethylsiloxane/divinylbenzene (PDMS/DVB) SPME fibre were observed for DEHA and all phthalates. The polydimethylsiloxane (PDMS) SPME fibre had very poor responses for the lighter and slightly polar phthalates, dimethyl phthalate (DMP) and diethyl phthalate (DEP), while the divinylbenzene/carboxen/polydimethylsiloxane (DVB/CAR/PDMS) SPME fibre had very poor responses for the heavier and non-polar adipate and phthalates. The salt (NaCl) was found to increase the partitioning of DMP, DEP, diisobutyl phthalate (DiBP), di-n-butyl phthalate, and benzyl butyl phthalate (BBP) from water into the headspace, while partitioning of heavier adipate and phthalates from water into headspace was suppressed when the concentration of NaCl was above 10%. The automated headspace SPME methods were developed and validated under two different salting conditions (30% NaCl for DMP, DEP and BBP, and 10% for DEHA, DiBP, DBP, di-n-hexyl phthalate (DHP), di-2-ethylhexyl phthalate (DEHP), and di-n-octyl phthalate (DOP)). Linearity with R(2) values better than 0.9949 was observed for DEHA and eight phthalates over the range from 0.1 to 20 microg L(-1). Method detection limits ranged from 0.003 microg L(-1) for DOP to 0.085 microg L(-1) for BBP. Good repeatability was observed for DEHA and most phthalates with relative standard deviation (RSD) values less than 10%. The methods were used to analyse bottled water samples for DEHA and eight phthalates. DMP, DHP, BBP, DEHA and DOP were not detected in any samples. Concentrations of the other phthalates were low (around sub-ppb) except for DBP in the water from a polycarbonate bottle at 1.72 microg L(-1).
系统研究了三种纤维在不同萃取条件下对水中己二酸二(2-乙基己基)酯(DEHA)和八种邻苯二甲酸酯进行顶空固相微萃取(SPME)的性能。对于DEHA和所有邻苯二甲酸酯,在65微米聚二甲基硅氧烷/二乙烯基苯(PDMS/DVB)SPME纤维上观察到良好的响应。聚二甲基硅氧烷(PDMS)SPME纤维对较轻且略带极性的邻苯二甲酸酯邻苯二甲酸二甲酯(DMP)和邻苯二甲酸二乙酯(DEP)响应非常差,而二乙烯基苯/碳分子筛/聚二甲基硅氧烷(DVB/CAR/PDMS)SPME纤维对较重且非极性的己二酸酯和邻苯二甲酸酯响应非常差。发现盐(NaCl)可增加DMP、DEP、邻苯二甲酸二异丁酯(DiBP)、邻苯二甲酸二正丁酯和邻苯二甲酸苄基丁酯(BBP)从水到顶空的分配,而当NaCl浓度高于10%时,较重的己二酸酯和邻苯二甲酸酯从水到顶空的分配受到抑制。在两种不同的加盐条件下(30%NaCl用于DMP、DEP和BBP,10%用于DEHA、DiBP、DBP、邻苯二甲酸二正己酯(DHP)、邻苯二甲酸二(2-乙基己基)酯(DEHP)和邻苯二甲酸二正辛酯(DOP))开发并验证了自动顶空SPME方法。在0.1至20微克/升的范围内,DEHA和八种邻苯二甲酸酯的线性相关系数(R²)值优于0.9949。方法检测限范围从DOP的0.003微克/升到BBP的0.085微克/升。对于DEHA和大多数邻苯二甲酸酯,观察到良好的重复性,相对标准偏差(RSD)值小于10%。这些方法用于分析瓶装水样品中的DEHA和八种邻苯二甲酸酯。在任何样品中均未检测到DMP、DHP、BBP、DEHA和DOP。除了聚碳酸酯瓶水中的DBP浓度为1.72微克/升外,其他邻苯二甲酸酯的浓度都很低(约为亚纳克/升)。