Sarrión M N, Santos F J, Moyano E, Galceran M T
Departament de Química Analítica, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028-Barcelona, Spain.
Rapid Commun Mass Spectrom. 2003;17(1):39-48. doi: 10.1002/rcm.873.
Liquid chromatography with atmospheric pressure chemical ionisation mass spectrometry (LC/APCI-MS), using negative ion detection in a triple quadrupole instrument, was used for the determination of chlorophenols (CPs) in environmental samples. In-source collision-induced dissociation (CID) was compared with MS/MS fragmentation. In general, less fragmentation was observed in MS/MS as compared with in-source CID, with the latter providing more intense fragment ions due to chemical ionisation. Under MS/MS conditions M - H - HCl was the main fragment ion observed for all compounds except for pentachlorophenol, which showed no fragmentation. For multiple reaction monitoring (MRM) acquisition mode, the transition from M - H to M - H - HCl was selected, leading to detection limits down to 0.3 ng injected. Direct and headspace-solid-phase microextraction (HS-SPME) were used as preconcentration procedures for the analysis of CPs in wood and in industrially contaminated soils. CPs were quantified by standard addition, which led to good reproducibility (RSD between 4 and 11%) in both SIM and MRM modes, and detection limits down to ng/g. The combination of MS/MS and in-source CID allowed confirmation of the presence of CPs in environmental samples.
采用大气压化学电离质谱联用(LC/APCI-MS),在三重四极杆仪器中使用负离子检测,用于测定环境样品中的氯酚(CPs)。将源内碰撞诱导解离(CID)与MS/MS碎裂进行了比较。一般来说,与源内CID相比,MS/MS中观察到的碎裂较少,由于化学电离,后者提供了更强的碎片离子。在MS/MS条件下,除五氯酚外,所有化合物观察到的主要碎片离子为M - H - HCl,五氯酚未显示碎裂。对于多反应监测(MRM)采集模式,选择了从M - H到M - H - HCl的跃迁,使得进样检测限低至0.3 ng。直接和顶空固相微萃取(HS-SPME)用作预浓缩程序,用于分析木材和工业污染土壤中的CPs。CPs通过标准加入法定量,在SIM和MRM模式下均具有良好的重现性(相对标准偏差在4%至11%之间),检测限低至ng/g。MS/MS和源内CID的结合可确认环境样品中CPs的存在。