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Rates and regimes of photochemical ozone production over Central East China in June 2006: a box model analysis using comprehensive measurements of ozone precursors

机译:2006年6月中国中部东部地区光化学臭氧产生的速率和方式:使用臭氧前体的全面测量进行的盒模型分析

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摘要

An observation-based box model approach was undertaken to estimateconcentrations of OH, HO, and RO radicals and the netphotochemical production rate of ozone at the top of Mount Tai, located inthe middle of Central East China, in June 2006. The model calculation wasconstrained by the measurements of O, HO, CO, NO, NO,hydrocarbon, HCHO, and CHCHO concentrations, and temperature and values. The net production rate of ozone was estimated to be 6.4 ppb has a 6-h average (09:00–15:00 CST), suggesting 58±37 ppb ofozone is produced in one day. Thus the daytime buildup of ozone recorded atthe mountain top as ~23 ppb on average is likely affected by in situphotochemistry as well as by the upward transport of polluted air mass inthe daytime. On days with high ozone concentrations (hourly values exceeding100 ppb at least once), in situ photochemistry was more active than it wason low ozone days, suggesting that in situ photochemistry is an importantfactor controlling ozone concentrations. Sensitivity model runs for whichdifferent NO and hydrocarbon concentrations were assumed suggestedthat the ozone production occurred normally under NO-limitedconditions, with some exceptional periods (undervolatile-organic-compound-limited conditions) in which there was freshpollution. We also examined the possible influence of the heterogeneous lossof gaseous HO radicals in contact with aerosol particle surfaces onthe rate and regimes of ozone production.
机译:2006年6月,在中国中部东部的泰山顶部,采用基于观测的盒模型方法来估计OH,HO和RO自由基的浓度以及臭氧的净光化学生产率。模型计算受到以下条件的约束测量O,HO,CO,NO,NO,碳氢化合物,HCHO和CHCHO的浓度以及温度和值。臭氧的净生产率估计为6.4 ppb,平均6小时(美国标准时间09:00–15:00),这意味着一天中会产生58±37 ppb的臭氧。因此,白天在山顶记录的平均臭氧量约为23 ppb,这可能受原位光化学反应以及白天被污染的空气向上输送的影响。在臭氧浓度高的日子(每小时至少超过100 ppb的值),原位光化学比低臭氧日的活性更高,这表明原位光化学是控制臭氧浓度的重要因素。假设不同的NO和碳氢化合物浓度的敏感性模型运行表明,臭氧生产通常在NO限制的条件下发生,并且在某些例外时期(在挥发性有机化合物限制的条件下)出现新鲜污染。我们还研究了气态HO自由基与气溶胶颗粒表面接触的不均匀损失对臭氧产生速率和产生机制的可能影响。

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