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使用中柴油车尾气的一次排放和二次有机气溶胶形成:怠速和巡航模式的比较。

Primary emissions and secondary organic aerosol formation from in-use diesel vehicle exhaust: Comparison between idling and cruise mode.

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.

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.

出版信息

Sci Total Environ. 2020 Jan 10;699:134357. doi: 10.1016/j.scitotenv.2019.134357. Epub 2019 Sep 7.

Abstract

Diesel vehicle exhaust is an important source of carbonaceous aerosols, especially in developing countries, like China. Driving condition impacts diesel vehicle emissions, yet its influence needs further understanding especially on secondary organic aerosol (SOA) formation. In this study tailpipe exhaust from an in-use light duty diesel vehicle at idling and driving speeds of 20 and 40 km h was introduced respectively into a 30 m indoor smog chamber to investigate primary emissions and SOA formation during photo-oxidation. The emission factors of SO at 20 and 40 km h were higher than those at idling, whereas the emission factors of aromatic hydrocarbons (AHs), polycyclic aromatic hydrocarbons (PAHs) and oxygenated volatile organic compounds (OVOCs) decreased when driving speeds increased. The emission factors of black carbon (BC) and primary organic aerosol (POA) at idling were comparable to those at 20 and 40 km h. The SOA production factors were 0.41 ± 0.09 g kg-fuel at idling, approximately 2.5 times as high as those at 20 km h (0.16 ± 0.09 g kg-fuel) or 40 km h (0.17 ± 0.09 g kg-fuel). Total carbonaceous aerosols, including BC, POA and SOA, from diesel vehicles at 20 and 40 km h were 60-75% of those at idling, due largely to a reduction in SOA production. Measured AHs and PAHs altogether were estimated to explain <10% of SOA production, and eight major OVOCs could contribute 8.4-23% of SOA production. A preliminary comparison was further made for the same diesel vehicle at idling using diesel oils upgraded from China 3 to China 5 standard. The emission factors of total particle numbers decreased by 38% owing to less nuclei mode particles, which was probably caused by the reducing fuel sulfur content; the emission factors of BC were almost unchanged, the POA emission factors and SOA production factors however decreased by 72% and 37%.

摘要

柴油车尾气是碳质气溶胶的一个重要来源,尤其是在中国等发展中国家。驾驶条件会影响柴油车的排放,但对二次有机气溶胶(SOA)形成的影响需要进一步了解。本研究在一个 30 米长的室内烟雾箱中分别引入怠速和 20、40km/h 行驶速度下的在用轻型柴油车的排气管尾气,以研究光氧化过程中的一次排放和 SOA 形成。20 和 40km/h 行驶速度下的 SO 排放因子高于怠速时的排放因子,而芳香烃(AHs)、多环芳烃(PAHs)和含氧挥发性有机化合物(OVOCs)的排放因子随着行驶速度的增加而降低。怠速时的黑碳(BC)和一次有机气溶胶(POA)排放因子与 20 和 40km/h 时的排放因子相当。SOA 生成因子在怠速时为 0.41±0.09g/kg-燃料,约为 20km/h(0.16±0.09g/kg-燃料)或 40km/h(0.17±0.09g/kg-燃料)的 2.5 倍。20 和 40km/h 时,柴油车总碳质气溶胶(包括 BC、POA 和 SOA)的生成量约为怠速时的 60-75%,这主要是由于 SOA 生成量的减少。测量的 AHs 和 PAHs 加起来估计只占 SOA 生成量的<10%,而 8 种主要的 OVOCs 可以贡献 8.4-23%的 SOA 生成量。进一步对同一辆在怠速时使用从中国 3 号升级到 5 号标准的柴油油的柴油车进行了初步比较。由于核模态颗粒较少,总颗粒数的排放因子降低了 38%,这可能是由于燃料含硫量降低所致;BC 的排放因子几乎不变,而 POA 的排放因子和 SOA 的生成因子则分别降低了 72%和 37%。

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