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高效液相色谱-电喷雾质谱法测定环境大气中的六溴环十二烷
引用本文:李岩,王龙星,朱秀华,高媛,陈吉平. 高效液相色谱-电喷雾质谱法测定环境大气中的六溴环十二烷[J]. 色谱, 2017, 35(10): 1080-1085. DOI: 10.3724/SP.J.1123.2017.06026
作者姓名:李岩  王龙星  朱秀华  高媛  陈吉平
作者单位:1. 大连交通大学环境与化学工程学院, 辽宁 大连 116028;2. 中国科学院大连化学物理研究所, 辽宁 大连 116023
基金项目:国家自然科学基金项目(21577009).
摘    要:优化了环境大气样品前处理步骤中复合硅胶柱的净化条件,建立了高效液相色谱-电喷雾-质谱(HPLC-ESIMS)测定环境大气中六溴环十二烷(hexabromocyclododecanes,HBCDs)的分析方法。样品经正己烷提取后,采用复合硅胶柱净化,以50 mL正己烷和100 mL正己烷-二氯甲烷(9∶1,v/v)为淋洗液,以180 mL正己烷-二氯甲烷(4∶1,v/v)为洗脱液。采用UF-ODS柱(150 mm×2.1 mm,3.0μm),以乙腈-甲醇-水为流动相进行梯度洗脱,在电喷雾负离子源、选择离子监测(SIM)模式下检测。在优化的条件下,α-HBCD、β-HBCD和γ-HBCD能很好地分离,在1~100μg/L范围内,α-HBCD、β-HBCD和γ-HBCD与进样内标D_(18)-γ-HBCD峰面积的比值与对应的质量浓度均具有良好的线性关系,相关系数(R)≥0.998 8。α-HBCD、β-HBCD和γ-HBCD的仪器检出限(S/N=3)分别为0.4、0.5和0.4μg/L;定量限(S/N=10)分别为1.4、1.6和1.3μg/L;方法检出限(MDL)分别为0.13、0.17和0.13pg/m~3(n=5);实际样品的加标回收率为74.8%~95.8%。该法灵敏度高,选择性好,可以满足大气样品中HBCDs的监测和分析需求。

关 键 词:高效液相色谱-电喷雾-质谱  六溴环十二烷  大气
收稿时间:2017-06-27

Determination of hexabromocyclododecanes in ambient air by high performance liquid chromatography- electrospray ionization-mass spectrometry
LI Yan,WANG Longxing,ZHU Xiuhua,GAO Yuan,CHEN Jiping. Determination of hexabromocyclododecanes in ambient air by high performance liquid chromatography- electrospray ionization-mass spectrometry[J]. Chinese journal of chromatography, 2017, 35(10): 1080-1085. DOI: 10.3724/SP.J.1123.2017.06026
Authors:LI Yan  WANG Longxing  ZHU Xiuhua  GAO Yuan  CHEN Jiping
Affiliation:1. School of Environmental and Chemical Engineering, Dalian Jiaotong University, Dalian 116028, China;2. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
Abstract:A high performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS) method was developed for the determination of hexabromocyclododecanes (HBCDs) in ambient air samples. The samples were extracted by Soxhlet extractor with hexane, then purified on the composite gel column. At first, the interfering substances were rinsed with 50 mL hexane and 100 mL hexane-dichloromethane (9:1, v/v), then 180 mL hexane -dichloromethane (4:1, v/v) was used to elute the targets. The compounds were separated by gradient elution with acetonitrile-methanol-water as mobile phases on a UF-ODS column (150 mm×2.1 mm, 3.0 μm). Electrospray ionization negative ion source and selective ion monitoring (SIM) mode were adopted in MS detection. The results showed that α -HBCD, β -HBCD and γ -HBCD could be well separated, and the chromatographic peak area ratio of α -HBCD, β -HBCD and γ -HBCD to internal standard D18- γ -HBCD with their concentrations had a good linear relationship, with the correlation coefficients (R) ≥ 0.9988. The limits of detection (LODs, S/N=3) of α -HBCD, β -HBCD and γ -HBCD were 0.4, 0.5 and 0.4 μg/L, respectively. The limits of quantification (LOQs, S/N=10) were 1.4, 1.6 and 1.3 μg/L, respectively. The method detection limits (MDL) were 0.13, 0.17 and 0.13 pg/m3 (n=5), respectively. The recoveries of HBCDs spiked in the actual air samples were in the range of 74.8%-95.8%. It is demonstrated that the method has high sensitivity and good selectivity, and can meet the requirement of monitoring and analyzing HBCDs in air samples.
Keywords:high performance liquid chromatography-electrospray ionization-mass spectrometry (HPLC-ESI-MS)  hexabromocyclododecanes (HBCDs)  air
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