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东莞工业集中区夏季臭氧污染与非污染期间VOCs组分特征及其来源
摘要点击 1889  全文点击 506  投稿时间:2021-11-28  修订日期:2022-01-28
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中文关键词  在线监测  芳香烃  烷烃  臭氧生成潜势(OFP)  溶剂源
英文关键词  online measurement  aromatics  alkane  ozone formation potential (OFP)  solvent source
作者单位E-mail
周振 广东省东莞生态环境监测站, 东莞 523009 61810955@qq.com 
肖林海 暨南大学环境与气候研究院, 广州 511443  
费蕾蕾 生态环境部华南环境科学研究所, 广州 510655 feileilei@scies.org 
余纬 广东省东莞生态环境监测站, 东莞 523009  
林满 广东省东莞生态环境监测站, 东莞 523009  
黄筠钧 暨南大学环境与气候研究院, 广州 511443  
张智胜 生态环境部华南环境科学研究所, 广州 510655  
陶俊 暨南大学环境与气候研究院, 广州 511443
生态环境部华南环境科学研究所, 广州 510655 
 
中文摘要
      为探讨东莞典型工业区夏季大气挥发性有机物(VOCs)污染特征及来源,于2020年夏季在厚街镇对大气环境中56种VOCs开展了在线观测,并同步收集了臭氧(O3)、氮氧化物(NOx)和一氧化碳(CO)等气体污染物浓度和气象因子等资料,在此基础上分析了VOCs总体积分数和主要物种体积分数特征,进一步估算了主要VOCs物种对臭氧生成潜势的贡献和不同臭氧浓度下VOCs的主要污染源贡献率.结果表明,观测期间56种VOCs的体积分数平均值为53.1×10-9,其中φ(芳香烃)、φ(烷烃)、φ(烯烃)和φ(炔烃)分别为24.7×10-9、23.7×10-9、3.9×10-9和0.7×10-9.与非臭氧污染期间相比,臭氧污染期间φ(芳香烃)、φ(烷烃)、φ(烯烃)和φ(炔烃)分别上升约10%、43%、38%和98%.无论是臭氧污染还是非臭氧污染期间,芳香烃对臭氧生成潜势的贡献率均最大,其次为烷烃、烯烃和炔烃.整个夏季观测期间,溶剂源、液化石油气泄漏、化石燃料燃烧源和油气挥发源对VOCs的贡献率分别为60%±20%、16%±11%、15%±11%和9%±6%;臭氧污染期间,溶剂源的贡献率下降到44%,而液化石油气泄漏和油气挥发源的贡献率分别上升到21%和16%.
英文摘要
      To investigate the characteristics and sources of atmospheric volatile organic compounds (VOCs) in a typical industrial zone in Dongguan, 56 VOCs species were continuously measured in Houjie Town of Dongguan in summer of 2020. In addition, mass concentrations of O3, NOx, and CO and meteorological data were synchronously collected. Then, characteristics of total VOCs and major species, the contributions of major VOCs species to ozone formation potential (OFP), and source apportionment of VOCs under the different ozone concentrations were discussed. The mean mixing ratio of VOCs was 53.1×10-9 including aromatics (24.7×10-9), alkanes (23.7×10-9), alkenes (3.9×10-9), and alkynes (0.7×10-9). The mean mixing ratios of aromatics, alkanes, alkenes, and alkynes increased approximately 10%, 43%, 38%, and 98% during the period of ozone pollution, respectively, compared with those during the period of non-ozone pollution. Aromatics contributed the most to OFP during the periods of both ozone pollution and non-ozone pollution, followed by alkanes, alkenes, and alkynes. Solvent sources, liquefied petroleum gas (LPG) leakage, fossil fuel combustion, and hydrocarbon volatilization were resolved using the PMF model, which accounted for 60%±20%, 16%±11%, 15%±11%, and 9%±6% of total VOCs, respectively. During the period of ozone pollution, the contribution of solvent sources to the total VOCs decreased to 44%, whereas that of LPG leakage and hydrocarbon volatilization increased to 21% and 16%, respectively.

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