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中国机动车怠速排放的一次颗粒物及其二次有机气溶胶形成。

Primary particulate emissions and secondary organic aerosol (SOA) formation from idling diesel vehicle exhaust in China.

机构信息

State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; University of Chinese Academy of Sciences, Beijing 100049, China.

State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China.

出版信息

Sci Total Environ. 2017 Sep 1;593-594:462-469. doi: 10.1016/j.scitotenv.2017.03.088. Epub 2017 Mar 27.

Abstract

In China diesel vehicles dominate the primary emission of particulate matters from on-road vehicles, and they might also contribute substantially to the formation of secondary organic aerosols (SOA). In this study tailpipe exhaust of three typical in-use diesel vehicles under warm idling conditions was introduced directly into an indoor smog chamber with a 30m Teflon reactor to characterize primary emissions and SOA formation during photo-oxidation. The emission factors of primary organic aerosol (POA) and black carbon (BC) for the three types of Chinese diesel vehicles ranged 0.18-0.91 and 0.15-0.51gkg-fuel, respectively; and the SOA production factors ranged 0.50-1.8gkg-fuel and SOA/POA ratios ranged 0.7-3.7 with an average of 2.2. The fuel-based POA emission factors and SOA production factors from this study for idling diesel vehicle exhaust were 1-3 orders of magnitude higher than those reported in previous studies for idling gasoline vehicle exhaust. The emission factors for total particle numbers were 0.65-4.0×10particleskg-fuel, and particles with diameters less than 50nm dominated in total particle numbers. Traditional C-C precursor non-methane hydrocarbons (NMHCs) could only explain less than 3% of the SOA formed during aging and contribution from other precursors including intermediate volatile organic compounds (IVOC) needs further investigation.

摘要

在中国,柴油车主导了道路车辆的颗粒物一次排放,并且它们可能对二次有机气溶胶(SOA)的形成也有很大贡献。在这项研究中,三种典型的在用柴油车在暖怠速条件下的排气管尾气被直接引入一个室内烟雾箱中,使用一个 30m 的聚四氟乙烯(Teflon)反应器来对光氧化过程中的一次排放和 SOA 形成进行特征描述。这三种类型的中国柴油车的一次有机气溶胶(POA)和黑碳(BC)的排放因子分别为 0.18-0.91 和 0.15-0.51gkg-燃料;SOA 生成因子范围为 0.50-1.8gkg-燃料,SOA/POA 比值范围为 0.7-3.7,平均值为 2.2。与之前关于怠速汽油车尾气的研究相比,本研究中怠速柴油车尾气的燃料基 POA 排放因子和 SOA 生成因子高出 1-3 个数量级。总颗粒物数的排放因子为 0.65-4.0×10 个颗粒 kg-燃料,并且粒径小于 50nm 的颗粒在总颗粒物数中占主导地位。传统的 C-C 前体非甲烷烃(NMHCs)只能解释老化过程中形成的 SOA 的不到 3%,需要进一步研究其他前体物(包括中间挥发性有机化合物(IVOC))的贡献。

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