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首页> 外文期刊>Atmospheric chemistry and physics >New insight into the spatiotemporal variability and source apportionments of Csub1/sub–Csub4/sub alkyl nitrates in Hong Kong
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New insight into the spatiotemporal variability and source apportionments of Csub1/sub–Csub4/sub alkyl nitrates in Hong Kong

机译:香港C 1 –C 4 烷基硝酸盐的时空变异和来源分配的新见解

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Csub1/sub–Csub4/sub alkyl nitrates (RONOsub2/sub) were measured concurrently at a mountain site, Tai Mo Shan (TMS), and an urban site, Tsuen Wan (TW), at the base of the same mountain in Hong Kong from September to November?2010. Although the levels of parent hydrocarbons were much lower at TMS (ip/i??&??0.05), similar alkyl nitrate levels were found at both sites regardless of the elevation difference, suggesting various source contributions of alkyl nitrates at the two sites. Prior to using a positive matrix factorization (PMF) model, the data at TW were divided into "meso" and "non-meso" scenarios for the investigation of source apportionments with the influence of mesoscale circulation and regional transport, respectively. Secondary formation was the prominent contributor of alkyl nitrates in the meso scenario (60?±?2?%, 60.2?±?1.2?pptv), followed by biomass burning and oceanic emissions, while biomass burning and secondary formation made comparable contributions to alkyl nitrates in the non-meso scenario, highlighting the strong emissions of biomass burning in the inland Pearl River delta (PRD) region. In contrast to TW, the alkyl nitrate levels measured at TMS mainly resulted from the photooxidation of the parent hydrocarbons at TW during mesoscale circulation, i.e., valley breezes, corresponding to 52–86?% of the alkyl nitrate levels at TMS. Furthermore, regional transport from the inland PRD region made significant contributions to the levels of alkyl nitrates (~??58–82?%) at TMS in the non-meso scenario, resulting in similar levels of alkyl nitrates observed at the two sites. The simulation of secondary formation pathways using a photochemical box model found that the reaction of alkyl peroxy radicals (ROsub2/sub) with nitric oxide (NO) dominated the formation of RONOsub2/sub at both sites, and the formation of alkyl nitrates contributed negatively to Osub3/sub production, with average reduction rates of 4.1 and 4.7?pptv?pptvsup?1/sup at TMS and TW, respectively.
机译:在山地,大帽山(TMS)和市区同时测量C 1 –C 4 烷基硝酸盐(RONO 2 ) 2010年9月至11月在香港同一座山的基地荃湾(TW)。尽管在TMS上母体烃的含量要低得多(> 0.05),但无论海拔高低,在两个位点都发现了相似的硝酸烷基酯含量,表明烷基的各种来源贡献这两个地点的硝酸盐。在使用正矩阵分解(PMF)模型之前,将TW的数据分为“中观”和“非中观”两种情况,以研究受中尺度环流和区域运输影响的源分配。次生形成是中观情景中烷基硝酸盐的主要贡献者(60%±2%,60.2%±1.2%pptv),其次是生物质燃烧和海洋排放,而生物质燃烧和次级形成对烷基甲烷的贡献相当。非中观情景下的硝酸盐,突出了内陆珠江三角洲(PRD)地区燃烧的大量生物质。与TW相反,在TMS处测得的硝酸烷基酯含量主要来自中尺度循环过程中TW母体烃的光氧化作用,即山谷微风,相当于TMS处硝酸烷基酯含量的52–86%。此外,在非中观情景下,来自内陆珠三角地区的区域运输对TMS处的硝酸烷基酯水平也有显着贡献(〜58-82%),导致在两个地点观测到的硝酸烷基酯水平相似。利用光化学盒模型对次生形成途径的模拟发现,烷基过氧自由基(RO 2 )与一氧化氮(NO)的反应主导了RONO 2 的形成。两个位点以及硝酸烷基酯的形成对O 3 的产生均产生负面影响,TMS和TW的平均还原率分别为4.1和4.7?pptv?pptv ?1

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