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十甲基环五硅氧烷(D)在实验室生成气溶胶和环境气溶胶中产生的二次有机气溶胶的分离与检测进展

Advances in the Separation and Detection of Secondary Organic Aerosol Produced by Decamethylcyclopentasiloxane (D) in Laboratory-Generated and Ambient Aerosol.

作者信息

Meepage Jeewani N, Welker Josie K, Meyer Claire M, Mohammadi Saeideh, Stanier Charles O, Stone Elizabeth A

机构信息

Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States.

Department of Chemical and Biochemical Engineering, University of Iowa, Iowa City, Iowa 52242, United States.

出版信息

ACS EST Air. 2024 Mar 27;1(5):365-375. doi: 10.1021/acsestair.3c00073. eCollection 2024 May 10.

Abstract

Decamethylcyclopentasiloxane (D), a common ingredient in many personal care products (PCPs), undergoes oxidation in the atmosphere, leading to the formation of secondary organic aerosol (SOA). Yet, the specific contributions of D-derived SOA on ambient fine particulate matter (PM) have not been characterized. This study addresses this knowledge gap by introducing a new analytical method to advance the molecular characterization of oxidized D and its detection in ambient aerosol. The newly developed reversed phase liquid chromatography method, in conjunction with high-resolution mass spectrometry, separates and detects D oxidation products, enabling new insights into their molecular and isomeric composition. Application of this method to laboratory-generated SOA and urban PM in New York City expands the number of D oxidation products observed in ambient aerosol and informs a list of molecular candidates to track D-derived SOA in the atmosphere. An oxidation series was observed in which one or more methyl groups in D (CHOSi) is replaced by a hydroxyl group, which indicates the presence of multistep oxidation products in ambient PM. Because of their specificity to PCPs and demonstrated detectability in ambient PM, several oxidation products are proposed as molecular tracers for D-derived SOA and may prove useful in assessing the impact of PCPs-derived SOA in the atmosphere.

摘要

十甲基环五硅氧烷(D)是许多个人护理产品(PCP)中的常见成分,它在大气中会发生氧化,导致二次有机气溶胶(SOA)的形成。然而,源自D的SOA对环境细颗粒物(PM)的具体贡献尚未得到明确。本研究通过引入一种新的分析方法来填补这一知识空白,以推进对氧化D的分子表征及其在环境气溶胶中的检测。新开发的反相液相色谱法与高分辨率质谱联用,可分离并检测D的氧化产物,从而对其分子和异构体组成有新的认识。将该方法应用于实验室生成的SOA和纽约市的城市PM,增加了在环境气溶胶中观察到的D氧化产物的数量,并为追踪大气中源自D的SOA的分子候选物清单提供了信息。观察到一个氧化系列,其中D(CHOSi)中的一个或多个甲基被羟基取代,这表明环境PM中存在多步氧化产物。由于它们对PCP的特异性以及在环境PM中已证明的可检测性,几种氧化产物被提议作为源自D的SOA的分子示踪剂,可能有助于评估PCP衍生的SOA对大气的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5af4/11091883/f8c3b31cd1d0/ea3c00073_0001.jpg

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