Atmospheric impact of isoprene-derived Criegee intermediates and isoprene hydroxy hydroperoxide on sulfate aerosol formation in the Asian region

IF 3.8 Q2 ENVIRONMENTAL SCIENCES
Hiroo Hata , Shoma Hoshino , Michiya Fujita , Kenichi Tonokura
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引用次数: 0

Abstract

This study revealed the importance of two isoprene-derived pathways in the formation of sulfate aerosol (SO42−(p)), which are related to the gas-phase reactions of Criegee intermediates (CIs) and liquid-phase reactions of isoprene hydroxy hydroperoxide (ISOPOOH), in the atmosphere in the Asian region, using the community multiscale air quality (CMAQ) modeling system. The results showed that the incorporation of both isoprene-derived CIs and ISOPOOH chemistry increased the SO42−(p) concentration in specific domains of Asia, particularly isoprene hotspots, with up to 1% of the total SO42−(p) concentration compared to that obtained by the basic chemical transport model. The impact of ISOPOOH to SO42−(p) formation exhibited a more localized pattern compared to that of CIs, attributed to the tendency of ISOPOOH to condense in low-NO regions. SO42−(p) formation from CIs affected the compositions of nitrate (NO3), ammonium (NH4+), and secondary organic aerosols (SOA) in the particle phase, and in most of the analyzed sites, those compositions increased from 0.5% to 2.5%. In contrast, SO42−(p) formation from ISOPOOH exhibits a negative impact on SOA, resulting in a potential reduction of up to 5% due to the loss of SOA precursor by incorporating the ISOPOOH uptake reaction. The sensitivity analysis results showed that most of the SO42−(p) was generated by the gas-phase reaction of SO2 with OH; however, the CIs and ISOPOOH also affected the SO42−(p) formation more than the liquid-phase SO42−(p) formations by H2O2, O3, O2, etc.

异戊二烯衍生的Criegee中间体和羟基过氧化异戊二烯对亚洲地区硫酸盐气溶胶形成的大气影响
本研究使用社区多尺度空气质量(CMAQ)建模系统揭示了亚洲地区大气中两种异戊二烯衍生途径在硫酸盐气溶胶(SO42-(p))形成中的重要性,这两种途径与克里格中间体(CI)的气相反应和异戊二烯羟基氢过氧化物(ISOPOOH)的液相反应有关。结果表明,异戊二烯衍生的CI和ISOPOOH化学的结合增加了亚洲特定地区,特别是异戊二烯热点地区的SO42−(p)浓度,与基本化学传输模型相比,SO42−的总浓度高达1%。与CI相比,ISOPOOH对SO42-(p)形成的影响表现出更局部化的模式,这归因于ISOPOOH在低NO区域浓缩的趋势。CI形成的SO42−(p)影响了颗粒相中硝酸盐(NO3−)、铵(NH4+)和二次有机气溶胶(SOA)的组成,在大多数分析地点,这些组成从0.5%增加到2.5%。相反,ISOPOOH形成的SO42-(p)对SOA表现出负面影响,由于通过结合ISOPOOH吸收反应损失SOA前体,导致高达5%的潜在减少。灵敏度分析结果表明,SO42-(p)大部分是由SO2与OH的气相反应产生的;然而,与H2O2、O3、O2等液相SO42-(p)的形成相比,CI和ISOPOOH对SO42--(p)形成的影响更大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Atmospheric Environment: X
Atmospheric Environment: X Environmental Science-Environmental Science (all)
CiteScore
8.00
自引率
0.00%
发文量
47
审稿时长
12 weeks
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