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在光化学老化过程中,怠速和巡航汽油车的一次排放与二次有机气溶胶形成的比较。

Comparison between idling and cruising gasoline vehicles in primary emissions and secondary organic aerosol formation during photochemical ageing.

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; Center for Excellence in Regional Atmospheric Environment, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, 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. 2020 Jun 20;722:137934. doi: 10.1016/j.scitotenv.2020.137934. Epub 2020 Mar 14.

Abstract

Driving conditions are among the important factors determining gasoline vehicle emissions, yet their relation with exhaust-derived secondary pollutants is poorly understood. Here, we introduced exhaust from a gasoline vehicle under hot idling and cruising conditions into an indoor smog chamber by using a chassis dynamometer and investigated the formation of secondary organic aerosols (SOA) during photochemical ageing under light after characterizing the primary emission of non-methane hydrocarbons (NMHCs), nitrogen oxide (NO) and primary organic aerosol (POA) in the dark. When compared to emission factors (EFs) at idling, during cruising at 20 km h or 40 km h, the EFs of NMHCs decreased by more than an order of magnitude, while the EFs of NO were more than doubled, resulting in a large drop in the NMHC-to-NO ratios. The percentages of reactive alkenes and aromatic hydrocarbons also decreased from idling to cruising at 20 km h to that at 40 km h. The emission factor of benzene, a carcinogenic compound, decreased more than 10 times from ~0.35 g kg-fuel at idling to ~0.03 g kg-fuel during cruising. During photochemical ageing of exhaust, substantial SOA was formed, and the SOA/POA ratios decreased from 52 to 92 at idling to 4-14 during cruising. Traditional aromatics could explain 30-64% of the measured SOA at idling but less than 15% of the measured SOA during cruising. Our results highlight that traffic congestion would greatly promote the emission of reactive volatile organic compounds and carcinogenic benzene from gasoline vehicles and also show that NMHCs as a target in gasoline vehicle emission tests cannot effectively represent the SOA and ozone formation potentials of the partially oxidized hydrocarbons from poorly functioning converters.

摘要

驾驶条件是决定汽油车排放的重要因素之一,但人们对其与尾气衍生的二次污染物的关系知之甚少。在这里,我们使用底盘测功机将热怠速和巡航条件下的汽油车尾气引入室内烟雾箱,并在黑暗中对非甲烷烃 (NMHC)、氮氧化物 (NO) 和一次有机气溶胶 (POA) 的原始排放进行了特征描述,然后在光照下研究了光化学老化过程中二次有机气溶胶 (SOA) 的形成。与怠速时的排放因子 (EF) 相比,在 20km/h 和 40km/h 巡航时,NMHC 的 EF 降低了一个数量级以上,而 NO 的 EF 则增加了一倍以上,导致 NMHC-NO 比值大幅下降。从怠速到 20km/h 巡航,再到 40km/h 巡航,反应性烯烃和芳香烃的比例也有所下降。一种致癌化合物苯的排放因子从怠速时的约 0.35g/kg 燃料降低到巡航时的约 0.03g/kg 燃料,降低了 10 多倍。在尾气的光化学老化过程中,大量 SOA 形成,SOA/POA 比值从怠速时的 52 下降到巡航时的 4-14。传统芳烃可解释怠速时测量的 SOA 的 30-64%,但只能解释巡航时测量的 SOA 的 15%以下。我们的研究结果表明,交通拥堵将大大促进汽油车中活性挥发性有机化合物和致癌苯的排放,同时还表明,在部分氧化的 NMHCs 不能有效代表汽油车排放测试中作为目标的 SOA 和臭氧形成潜力较差的转化器。

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