配备颗粒过滤器的符合欧洲 6d 排放标准的汽油车排放的二次气溶胶的形成†。

IF 2.8 Q3 ENVIRONMENTAL SCIENCES Environmental science: atmospheres Pub Date : 2024-06-04 DOI:10.1039/D3EA00165B
Andreas Paul, Zheng Fang, Patrick Martens, Arya Mukherjee, Gert Jakobi, Mika Ihalainen, Miika Kortelainen, Markus Somero, Pasi Yli-Pirilä, Thorsten Hohaus, Hendryk Czech, Markus Kalberer, Olli Sippula, Yinon Rudich, Ralf Zimmermann and Astrid Kiendler-Scharr
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引用次数: 0

摘要

最新的欧洲法规--欧 6d 排放标准--要求所有汽油直喷(GDI)汽车使用三元催化器(TWC)和汽油微粒过滤器(GPF)作为尾气后处理装置。这些后处理方法旨在减少氮氧化物和一次颗粒物的排放。然而,对于出厂时配备了 GPF 的符合欧洲 6d 标准的 GDI 汽车排放的挥发性有机化合物(VOC)所形成的二次有机气溶胶(SOA),目前尚未进行研究。因此,为了探索 SOA 的形成和 GPF 的影响,我们对符合欧洲 6d 标准的 GDI 汽车在 4 种不同的稳定状态速度(怠速(0 km h-1)、50、80 和 100 km h-1)下的尾气进行了表征。尾气在光化学排放老化流管反应器(PEAR)中通过与 OH 自由基的反应进行氧化,氧化作用相当于 2.2 天的大气日氧化作用。研究发现,在所有调查的车速下,GPF 都能完全去除大于 10 纳米的原生颗粒。然而,氧化后会形成大量 SOA,在 50 km h-1 时,每千克燃料消耗形成 SOA 的可能性最大。经测定,SOA 的主要前体是甲苯、二甲苯和三甲苯,它们在所有行驶速度下形成的 SOA 中至少占 50%。此外,在所有行驶条件下,排气中都能观察到大量的氨气(NH3)排放,老化后形成硝酸铵(NH4NO3)。NH4NO3 的形成进一步促进了 OH 氧化后有机气相产物的共缩合,从而进一步提高了 SOA 的质量。
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Formation of secondary aerosol from emissions of a Euro 6d-compliant gasoline vehicle with a particle filter†

The most recent European regulation, the Euro 6d emission standard, requires all gasoline direct injection (GDI) vehicles to use both a three-way catalyst (TWC) and a gasoline particle filter (GPF) as exhaust aftertreatment. These aftertreatment methods are aimed at reducing NOx and primary particle emissions. However, the formation of secondary organic aerosols (SOAs) from the volatile organic compound (VOC) emissions of a Euro 6d compliant GDI vehicle, factory equipped with a GPF is not yet investigated. Therefore, to explore the SOA formation and effects of the GPF, the exhaust of a Euro 6d compliant GDI vehicle was characterized at 4 different steady state speeds, idling (0 km h−1), 50, 80 and 100 km h−1. The exhaust was oxidised in a photochemical emission aging flow tube reactor (PEAR) by reactions with OH radicals equivalent of 2.2 days of atmospheric day time oxidation. It was found that the GPF completely removes primary particles larger than 10 nm, at all investigated vehicle speeds. However, significant SOA was formed after oxidation, with the highest SOA formation potential per kg fuel consumed at 50 km h−1. The main SOA precursors were determined to be toluene, xylene and trimethyl-benzene which were found to account for at least 50% of SOA formed at all driving speeds. Furthermore, high emissions of ammonia (NH3) could be observed in the exhaust under all driving conditions which resulted in the subsequent formation of ammonium nitrate (NH4NO3) after aging. The formation of NH4NO3 additionally facilitated the co-condensation of organic gas phase products after OH oxidation enhancing SOA mass even further.

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Back cover Environmental Science: Atmospheres five years on Photodegradation of naphthalene-derived particle oxidation products. Back cover Estimation of neighborhood scale PM2.5 impacts in rural towns in the Purepecha region of Mexico.
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