首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Investigation of Galaxolide degradation products generated under oxidative and irradiation processes by liquid chromatography/hybrid quadrupole time-of-flight mass spectrometry and comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry
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Investigation of Galaxolide degradation products generated under oxidative and irradiation processes by liquid chromatography/hybrid quadrupole time-of-flight mass spectrometry and comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry

机译:液相色谱/混合四极杆飞行时间质谱和综合二维气相色谱/飞行时间质谱研究氧化和辐照过程中生成的Galaxolide降解产物

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摘要

RATIONALE Polycyclic musks have become a concern due to their bioaccumulation potential and ecotoxicological effects. The HHCB transformation product (TP) (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl-cyclopenta[γ]- 2-benzopyran; HHCB-lactone) is the most stable intermediate generated and it is frequently detected in river waters. The aim of this work was the identification of relevant TPs generated from UV irradiation and ozone treatments. METHODS Identification of HHCB TPs was carried out by liquid chromatography/hybrid quadrupole time-of-flight mass spectrometry (LC/ESI-QTOF-MS) and two-dimensional gas chromatography/electron impact time-of-flight mass spectrometry (GC×GC-EI-TOF-MS). With LC/ESI-QTOF-MS, TPs were characterized by means of mass accuracy in both full-scan and MS/MS modes through information-dependent acquisition (IDA) and direct injection on-column. With stir bar sorptive extraction (SBSE)-GC×GC-EI-TOF-MS, identification was based on the enhanced separation capacity and screening of unknowns through the acquisition of full-range mass spectra. RESULTS The effectiveness of these complementary techniques allowed a detailed evaluation of the main TPs. Eighteen TPs were elucidated based on mass accuracy, in both full-scan and MS/MS modes using LC/ESI-QTOF-MS with mass errors below 5 ppm and 10 ppm (mostly), respectively. Most of the TPs had not been analytically identified in previous studies. Separation of the enantiomeric species (R) and (S) of HHCB-lactone, and the identification of other relevant TPs, was performed using SBSE-GC×GC-EI- TOF-MS. CONCLUSIONS LC/ESI-QTOF-MS and GC×GC-EI-TOF-MS analysis provides the best alternative for TP identification of chemicals of concern, which have a wide range of polarities and isobaric compounds. A prediction of PBT (persistence, bioaccumulation and toxicity) using the PBT Profiler program suggested a classification of 'very persistent' and 'very toxic' for most of the TPs identified.
机译:理性多环麝香由于其生物蓄积潜力和生态毒理作用而备受关注。 HHCB转化产物(TP)(1,3,4,6,7,8-六氢-4,6,6,7,8,8-六甲基-环戊[γ] -2-苯并吡喃; HHCB-内酯)为生成的最稳定的中间体,经常在河水中发现。这项工作的目的是确定由紫外线照射和臭氧处理产生的相关总磷。方法采用液相色谱/混合四极杆飞行时间质谱(LC / ESI-QTOF-MS)和二维气相色谱/电子碰撞飞行时间质谱(GC×GC)进行HHCB TPs的鉴定-EI-TOF-MS)。使用LC / ESI-QTOF-MS,通过信息相关采集(IDA)和柱上直接进样,在全扫描和MS / MS模式下通过质量精度来表征TP。使用搅拌棒吸附萃取(SBSE)-GC×GC-EI-TOF-MS进行鉴定,是基于增强的分离能力并通过全范围质谱的采集来筛选未知物质。结果这些互补技术的有效性允许对主要TP进行详细评估。基于质量准确度,在使用LC / ESI-QTOF-MS的全扫描和MS / MS模式下,根据质量精度阐明了18种TP,质量误差分别低于5 ppm和10 ppm(大部分)。在先前的研究中尚未对大多数TP进行分析鉴定。使用SBSE-GC×GC-EI-TOF-MS进行HHCB-内酯的对映异构体(R)和(S)的分离,以及其他相关TP的鉴定。结论LC / ESI-QTOF-MS和GC×GC-EI-TOF-MS分析为TP鉴定相关化学物质提供了最佳选择,这些化学物质具有多种极性和同量异位化合物。使用PBT Profiler程序对PBT(持久性,生物蓄积性和毒性)的预测建议对大多数已鉴定的TP进行“非常持久”和“非常有毒”的分类。

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