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超声辅助提取—固相萃取—同位素稀释高效液相色谱串联质谱测定室内灰尘中5种有机磷酸酯阻燃剂
Determination of Five Organophosphate Flame Retardants in Indoor Dust using Ultrasound Assisted Extraction-Solid Phase Extraction-Isotopic Dilution High Performance Liquid Chromatography-tandem Mass Spectrometry
【摘要】 目的建立灰尘中磷酸三苯酯(TPHP)、磷酸三甲苯酯(TCP)、磷酸三(2-氯乙基)酯(TCEP)、磷酸三(2-氯丙基)酯(TCPP)和磷酸三(1,3-二氯异丙基)酯(TDCPP) 5种有机磷酸酯阻燃剂的超声辅助提取—固相萃取(UAE-SPE)—同位素稀释高效液相色谱—串联质谱(HPLC-MS-MS)检测方法。方法取室内灰尘50 mg,加入3 m L乙酸乙酯丙酮溶液(3+2,V+V),涡旋1 min,超声5 min,3 500 r/min离心5 min,取上层清液,循环3次,合并上清液,将合并上清液氮吹至近干,3 m L正己烷复溶,CNWBOND NH2固相萃取柱(6 m L乙酸乙酯,6 m L正己烷活化)富集净化,3 m L乙酸乙酯洗脱2次,氮气吹干,1 m L乙腈水溶液(1+1,V+V)定容,过0. 22μm尼龙滤膜,以0. 1%甲酸溶液和0. 1%甲酸乙腈溶液为流动相,ACQUITY UPLC4HSS T3色谱柱(150 mm×2. 1 mm,1. 8μm)梯度洗脱分离,电喷雾离子源正离子模式(ESI+),多反应监测(MRM)模式检测。结果 5种有机磷阻燃剂在(6. 0~500)μg/L范围内线性关系良好,其相关系数均>0. 999,检出限范围(1. 8~36. 0) ng/g,定量限范围(5. 9~120. 0) ng/g,回收率范围75. 0%~116. 7%,精密度(RSD)范围2. 3%~9. 7%。结论该方法操作快速可靠,适用于室内灰尘中5种有机磷酸酯阻燃剂的同时测定。
【Abstract】 Objectives To develop a method for the determination of five organophosphate flame retardants,triphenyl phosphate( TPHP),tritotyl phosphate( TCP),tris-( 2-chloroethyl) phosphate( TCEP),tris-( 2-chloropropyl) phosphate( TCPP) and tris-( 1,3-dichloropropyl) phosphate( TDCPP),in indoor dust using Ultrasound Assisted Extraction-Solid Phase Extraction( UAE-SPE)-High Performance Liquid Chromatography-tandem Mass Spectrometry( HPLC-MS-MS). Methods Add 3 m L ethyl acetate-acetone( 3 + 2,V + V) into the dust sample( 50 mg). After 1 min vortex,5 min ultrasound,and 5 min centrifugation at 3 500 r/min,and the operation was repeated three times. The supernatant of each time was combined and concentrated to near dryness using nitrogen,reconstituted to 3 m L using n-hexane,enriched and purified through CNWBOND NH2 solid phase extraction column( conditioned with 6 m L ethyl acetate,6 m L n-hexane),eluted using 3 m L ethyl acetate twice,dried using nitrogen,adjusted to a constant volume using 1 m L acetonitrile-water( 1+1,V+V) and filtered with 0. 22 μm nylon filter. The five organophosphate flame retardants were eluted and separated in gradient using ACQUITY UPLC HSS T3 column( 150 mm × 2. 1 mm,1. 8 μm) with 0. 1% formic acid solution and acetonitrile solution of 0. 1% formic acid as mobile phase,then determined under positive ion mode of Electrospray Ionization( ESI+) and Multiple Reaction Monitoring( MRM) mode. Results The five organophosphate flame retardants showed a good linearity in the range of( 0. 5-500) μg/L,and the correlation coefficients were more than 0. 999. The limit of detection was in the range of( 1. 8-36. 0) ng/g,and the limit of quantification was in the range of( 5. 9-120. 0) ng/g. The recovery was in the range of 75. 0%-116. 7% with the relative standard deviations( RSD) of 2. 3%-9. 7%. Conclusions The method is fast and reliable,which is suitable for simultaneous determination of five organophosphate flame retardants in indoor dust.
【Key words】 organophosphate flame retardants; indoor dust; ultrasound assisted extraction; solid phase extraction; high performance liquid chromatography-tandem mass spectrometry;
- 【文献出处】 环境卫生学杂志 ,Journal of Environmental Hygiene , 编辑部邮箱 ,2020年01期
- 【分类号】X831;O657.63
- 【被引频次】2
- 【下载频次】237