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首页> 外文期刊>Atmospheric environment >Nighttime aqueous-phase secondary organic aerosols in Los Angeles and its implication for fine particulate matter composition and oxidative potential
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Nighttime aqueous-phase secondary organic aerosols in Los Angeles and its implication for fine particulate matter composition and oxidative potential

机译:洛杉矶夜间水相二次有机气溶胶及其对细颗粒物组成和氧化电位的影响

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摘要

Recent investigations suggest that aqueous phase oxidation of hydrophilic organic compounds can be a significant source of secondary organic aerosols (SOA) in the atmosphere. Here we investigate the possibility of nighttime aqueous phase formation of SOA in Los Angeles during winter, through examination of trends in fine particulate matter (PM2.5) carbonaceous content during two contrasting seasons. Distinctive winter and summer trends were observed for the diurnal variation of organic carbon (OC) and secondary organic carbon (SOC), with elevated levels during the nighttime in winter, suggesting an enhanced formation of SOA during that period. The nighttime ratio of SOC to OC was positively associated with the relative humidity (RH) at high RH levels (above 70%), which is when the liquid water content of the ambient aerosol would be high and could facilitate dissolution of hydrophilic primary organic compounds into the aqueous phase. Time -integrated collection and analysis of wintertime particles at three time periods of the day (morning, 6:00 a.m.-9:00 a.m.; afternoon, 11:00 a.m.-3:00 p.m.; night, 8:00 p.m. -4:00 a.m.) revealed higher levels of water soluble organic carbon (WSOC) and organic acids during the night and afternoon periods compared to the morning period, indicating that the SOA formation in winter continues throughout the nighttime. Furthermore, diurnal trends in concentrations of semi-volatile organic compounds (SVOCs) from primary emissions showed that partitioning of SVOCs from the gas to the particle phase due to the decreased nighttime temperatures cannot explain the substantial OC and SOC increase at night. The oxidative potential of the collected particles (quantified using a biological macrophage -based reactive oxygen species assay, in addition to the dithiothreitol assay) was comparable during afternoon and nighttime periods, but higher (by at least 30%) compared to the morning period, suggesting that SOA formation processes possibly enhance the toxicity of the ambient particles compared to mobile -source dominated primary emissions in the Los Angeles area. (C) 2016 Elsevier Ltd. All rights reserved.
机译:最近的研究表明,亲水性有机化合物的水相氧化可能是大气中次要有机气溶胶(SOA)的重要来源。在这里,我们通过检查两个对比季节中细颗粒物(PM2.5)含碳量的趋势,研究了冬季冬季洛杉矶夜间水相形成的可能性。观察到冬季和夏季的明显趋势是有机碳(OC)和次要有机碳(SOC)的昼夜变化,冬季夜间水平升高,这表明该时期SOA的形成增加。在高RH水平(高于70%)时,SOC与OC的夜间比率与相对湿度(RH)呈正相关,此时环境气溶胶中的液态水含量很高,并且可以促进亲水性伯有机化合物的溶解进入水相。在一天的三个时间段(早晨6:00 AM-9:00 AM;下午11:00 AM-3:00 PM;晚上8:00 PM -4:时间整合)收集和分析冬季颗粒凌晨00点),与早晨相比,夜间和下午的水溶性有机碳(WSOC)和有机酸含量较高,这表明冬季的SOA形成贯穿整个夜间。此外,来自一次排放的半挥发性有机化合物(SVOC)浓度的昼夜趋势表明,由于夜间温度降低,SVOC从气相到颗粒相的分配无法解释夜间OC和SOC的大幅增加。在下午和夜间,收集到的颗粒的氧化电位(除了使用二硫苏糖醇分析外,还使用基于生物巨噬细胞的活性氧物种分析进行了定量),但与早晨相比更高(至少高出30%),这表明与洛杉矶地区以移动源为主的一次排放相比,SOA的形成过程可能会增强环境颗粒的毒性。 (C)2016 Elsevier Ltd.保留所有权利。

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