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含氧中挥发性有机化合物对汽油车排放物二次有机气溶胶形成的贡献被掩盖。

Obscured Contribution of Oxygenated Intermediate-Volatility Organic Compounds to Secondary Organic Aerosol Formation from Gasoline Vehicle Emissions.

机构信息

State Environmental Protection Key Laboratory of Formation and Prevention of Urban Air Pollution Complex, Shanghai Academy of Environmental Sciences, Shanghai 200233, China.

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518000, China.

出版信息

Environ Sci Technol. 2024 Jun 18;58(24):10652-10663. doi: 10.1021/acs.est.3c08536. Epub 2024 Jun 3.

Abstract

Secondary organic aerosol (SOA) formation from gasoline vehicles spanning a wide range of emission types was investigated using an oxidation flow reactor (OFR) by conducting chassis dynamometer tests. Aided by advanced mass spectrometric techniques, SOA precursors, including volatile organic compounds (VOCs) and intermediate/semivolatile organic compounds (I/SVOCs), were comprehensively characterized. The reconstructed SOA produced from the speciated VOCs and I/SVOCs can explain 69% of the SOA measured downstream of an OFR upon 0.5-3 days' OH exposure. While VOCs can only explain 10% of total SOA production, the contribution from I/SVOCs is 59%, with oxygenated I/SVOCs (O-I/SVOCs) taking up 20% of that contribution. O-I/SVOCs (e.g., benzylic or aliphatic aldehydes and ketones), as an obscured source, account for 16% of total nonmethane organic gas (NMOG) emission. More importantly, with the improvement in emission standards, the NMOG is effectively mitigated by 35% from China 4 to China 6, which is predominantly attributed to the decrease of VOCs. Real-time measurements of different NMOG components as well as SOA production further reveal that the current emission control measures, such as advances in engine and three-way catalytic converter (TWC) techniques, are effective in reducing the "light" SOA precursors (i.e., single-ring aromatics) but not for the I/SVOC emissions. Our results also highlight greater effects of O-I/SVOCs to SOA formation than previously observed and the urgent need for further investigation into their origins, i.e., incomplete combustion, lubricating oil, etc., which requires improvements in real-time molecular-level characterization of I/SVOC molecules and in turn will benefit the future design of control measures.

摘要

采用底盘测功机试验,利用氧化流动反应器(OFR)研究了涵盖广泛排放类型的汽油车二次有机气溶胶(SOA)的形成。借助先进的质谱技术,全面表征了 SOA 前体,包括挥发性有机化合物(VOCs)和中间/半挥发性有机化合物(I/SVOCs)。在 0.5-3 天 OH 暴露后,通过OFR 下游测量得到的 SOA 中,经特定分类的 VOCs 和 I/SVOCs 重建的 SOA 可以解释 69%。而 VOCs 只能解释总 SOA 生成量的 10%,I/SVOCs 的贡献为 59%,其中含氧 I/SVOCs(O-I/SVOCs)占该贡献的 20%。O-I/SVOCs(例如,苯甲基或脂肪族醛和酮)作为隐蔽源,占总非甲烷有机气体(NMOG)排放量的 16%。更重要的是,随着排放标准的提高,从国四到国六,NMOG 有效降低了 35%,这主要归因于 VOCs 的减少。不同 NMOG 成分和 SOA 生成的实时测量进一步表明,当前的排放控制措施,如发动机和三元催化转化器(TWC)技术的进步,有效降低了“轻”SOA 前体(即单环芳烃)的排放,但对 I/SVOC 排放的控制效果不明显。我们的研究结果还突出表明,O-I/SVOCs 对 SOA 形成的影响比之前观察到的更大,迫切需要进一步研究其来源,例如不完全燃烧、润滑油等,这需要提高对 I/SVOC 分子的实时分子水平的特征描述,并最终有利于未来控制措施的设计。

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