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Atmospheric chlorine chemistry in southeast Texas: Impacts on ozone formation and control

机译:德克萨斯州东南部的大气氯化学:对臭氧形成和控制的影响

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Recent evidence has demonstrated that chlorine radical chemistry can enhance tropospheric hydrocarbon oxidation and has the potential to enhance ozone formation in urban atmospheres. To assess these effects quantitatively, an August-September 2000 photochemical episode in southeast Texas was simulated using the comprehensive air quality model, with extensions (CAMx). During this episode, ambient measurements of a unique marker of atmospheric chlorine chemistry, 1-chloro-3-methyl-3butene-2-one (CMBO), were made and model performance was assessed by comparing modeled and observed CMBO mixing ratios. The model predicted ambient CMBO mixing ratios within the uncertainty limits associated with the emissions inventory, so the model was used to assess the impacts of chlorine chemistry on ozone formation. Based on the current emissions inventory, chlorine emissions have the potential to enhance 1-h-averaged ozone mixing ratios by 70 ppb, in very localized areas, during morning hours. Over wider areas, and at times of day when peak ozone concentrations are observed, the impacts of chlorine emissions on ozone concentrations are typically less than 10 ppb. Chlorine emissions also influenced changes in ozone concentrations due to hydrocarbon and NO, emission controls.
机译:最近的证据表明,氯自由基化学可以增强对流层碳氢化合物的氧化,并具有增强城市大气中臭氧形成的潜力。为了定量评估这些影响,使用扩展的综合空气质量模型(CAMx)模拟了德克萨斯州东南部2000年8月至9月的光化学事件。在这一事件中,对大气中氯化学的唯一标记1-氯-3-甲基-3丁烯-2-酮(CMBO)进行了环境测量,并通过比较建模和观察到的CMBO混合比来评估模型性能。该模型预测了与排放清单相关的不确定性范围内的环境CMBO混合比,因此该模型用于评估氯化学对臭氧形成的影响。根据当前的排放清单,在很早的局部地区,氯气的排放有可能使1小时平均臭氧混合比提高70 ppb。在更广阔的地区,以及每天观察到最高臭氧浓度的时间,氯排放量对臭氧浓度的影响通常小于10 ppb。由于碳氢化合物和NO的排放控制,氯的排放还影响了臭氧浓度的变化。

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