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Modeling the Concentrations of Gas-Phase Toxic Organic Air Pollutants: Direct Emissions and Atmospheric Formation

机译:模拟气相有毒有机空气污染物的浓度:直接排放和大气形成

摘要

An Eulerian photochemical air quality model is describedudfor the prediction of the atmospheric transport andudchemical reactions of gas-phase toxic organic air pollutants. Model performance was examined in the Los Angeles, CA, area over the period August 27-28, 1987. The organic compounds were drawn from a list of 189 species selected for control as hazardous air pollutants in the Clean Air Act amendments of 1990. The species considered include benzene, various alkylbenzenes, phenol, cresols, 1,3- butadiene, acrolein, formaldehyde, acetaldehyde, andudperchloroethylene among others. It is found that photochemical generation contributes significantly to form-aldehyde, acetaldehyde, acetone, and acrolein concentrations for the 2-day period studied. Phenol concentrations are dominated by direct emissions, despite the existence of a pathway for atmospheric formation from benzene oxidation. The finding that photochemical productionudcan be a major contributor to the total concentrations ofudsome toxic organic species implies that control programsudfor those species must consider more than just directudemissions.
机译:描述了一个欧拉光化学空气质量模型,以预测气相有毒有机空气污染物的大气迁移和化学反应。 1987年8月27日至28日在加利福尼亚州洛杉矶地区检查了模型性能。该有机化合物选自1990年《清洁空气法》修正案中作为控制有害空气污染物的189种物种。所考虑的物种包括苯,各种烷基苯,苯酚,甲酚,1,3-丁二烯,丙烯醛,甲醛,乙醛和过氯乙烯等。发现在所研究的2天时间内,光化学生成对甲醛,乙醛,丙酮和丙烯醛的浓度有显着贡献。尽管存在由苯氧化形成大气的途径,但苯酚的浓度仍以直接排放为主。光化学生产可能是造成udmed有毒有机物总浓度的主要因素,这一发现表明这些物种的控制程序所考虑的不仅仅是直接排放。

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