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利用超高分辨质谱对港口环境大气颗粒态有机硫酸盐进行分子特征分析:交通排放的鉴定。

Molecular characterization of atmospheric particulate organosulfates in a port environment using ultrahigh resolution mass spectrometry: Identification of traffic emissions.

机构信息

State Key Laboratory of Plateau Ecology and Agriculture, College of Eco-environmental Engineering, Qinghai University, Xining 810016, China; State Key Joint Laboratory of ESPC, State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex, School of the Environment, Tsinghua University, Beijing 100084, China.

State Key Joint Laboratory of ESPC, State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex, School of the Environment, Tsinghua University, Beijing 100084, China.

出版信息

J Hazard Mater. 2021 Oct 5;419:126431. doi: 10.1016/j.jhazmat.2021.126431. Epub 2021 Jun 18.

Abstract

Organosulfates (OSs) are an important component of atmospheric organic aerosol (OA) and are widespread in various environments. However, the OSs generated from anthropogenic emissions are poorly understood. In this study, the molecular compositions of OSs from atmospheric PM samples collected during a winter measurement campaign (SEISO-Bohai) at Jingtang Harbor were characterized via ultrahigh resolution mass spectrometry (UHRMS). The changes of port OS compositions were observed in episodes of complete haze pollution. As the pollution aggravated, the relative abundances of OSs were apparently increased, and the molecule compositions became more complex, primarily driven by the oxidation and fragmentation processes. Potential OS precursors from traffic emissions were identified based on an optimized "OS precursor map" developed in the previous study. OSs characterized by high molecular weights and low degrees of both unsaturation and oxidization were suggested to mainly derive from secondary reactions of intermediate volatile organic compounds (IVOCs) emitted by traffic sources. These OSs were primarily detected in clean-day samples, followed by decreasing with the pollution process. In addition, our study also finds that ship emissions may further facilitated OS productions under haze pollution conditions.

摘要

有机硫酸盐(OSs)是大气有机气溶胶(OA)的重要组成部分,广泛存在于各种环境中。然而,人为排放产生的 OSs 还了解甚少。本研究通过超高效分辨率质谱(UHRMS)对在京唐港冬季测量活动(SEISO-Bohai)期间采集的大气 PM 样品中的 OSs 的分子组成进行了表征。在完全霾污染的爆发期间观察到港口 OS 组成的变化。随着污染的加剧,OSs 的相对丰度明显增加,分子组成变得更加复杂,主要是由氧化和碎片化过程驱动的。根据先前研究中开发的优化的“OS 前体图谱”,确定了来自交通排放的潜在 OS 前体。具有高分子量、不饱和度和氧化度较低的 OSs 被认为主要源自交通源排放的中间挥发性有机化合物(IVOCs)的二次反应。这些 OSs 主要在清洁日样品中检测到,然后随着污染过程的进行而减少。此外,我们的研究还发现,在霾污染条件下,船舶排放可能进一步促进了 OS 的产生。

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