Derwent Richard
a rdscientific , Newbury , Berkshire , United Kingdom.
J Air Waste Manag Assoc. 2017 Jul;67(7):789-796. doi: 10.1080/10962247.2017.1292969. Epub 2017 Feb 22.
The intercomparison of seven chemical mechanisms for their suitability for air quality policy formulation and assessment is described. Box modeling techniques were employed using 44 sets of background environmental conditions covering North America to constrain the chemical development of the longer lived species. The selected mechanisms were modified to enable an unbiased assessment of the adequacy of the parameterizations of photochemical ozone production from volatile organic compound (VOC) oxidation in the presence of NO. Photochemical ozone production rates responded differently to 30% NO and VOC reductions with the different mechanisms, despite the striking similarities between the base-case ozone production rates. The 30% reductions in NO and VOCs also produced changes in OH. The responses in OH to 30% reductions in NO and VOCs appeared to be more sensitive to mechanism choice, compared with the responses in the photochemical ozone production rates. Although 30% NO reductions generally led to decreases in OH, 30% reductions in VOCs led to increases in OH, irrespective of mechanism choice and background environmental conditions. The different mechanisms therefore gave different OH responses to NO and VOC reductions and so would give different responses in terms of changes in the fate and behavior of air toxics, acidification and eutrophication, and fine particle formation compared with others, in response to ozone control strategies. Policymakers need to understand that there are likely to be inherent differences in the responses to ozone control strategies between different mechanisms, depending on background environmental conditions and the extents of NO and VOC reductions under consideration.
The purpose of this paper is to compare predicted ozone responses to NO and VOC reductions with seven chemical mechanisms under North American conditions. The good agreement found between the tested mechanisms should provide some support for their application in the air quality models used for policymaking.
描述了七种化学机制在空气质量政策制定和评估适用性方面的相互比较。采用箱式模型技术,利用涵盖北美的44组背景环境条件来限制寿命较长物种的化学发展。对选定的机制进行了修改,以便在存在一氧化氮(NO)的情况下,对挥发性有机化合物(VOC)氧化产生光化学臭氧的参数化的充分性进行无偏评估。尽管基准情况下的臭氧产生率有显著相似之处,但不同机制下光化学臭氧产生率对NO和VOC减少30%的反应不同。NO和VOC减少30%也导致了羟基自由基(OH)的变化。与光化学臭氧产生率的反应相比,OH对NO和VOC减少30%的反应似乎对机制选择更为敏感。尽管一般来说,NO减少30%会导致OH减少,但VOC减少30%会导致OH增加,与机制选择和背景环境条件无关。因此,不同的机制对NO和VOC减少的OH反应不同,所以在空气有毒物质的归宿和行为、酸化和富营养化以及细颗粒物形成的变化方面,与其他机制相比,对臭氧控制策略会有不同的反应。政策制定者需要明白,根据背景环境条件以及所考虑的NO和VOC减少程度,不同机制对臭氧控制策略的反应可能存在固有差异。
本文的目的是比较在北美条件下,七种化学机制对NO和VOC减少的预测臭氧反应。在测试机制之间发现的良好一致性应为它们在用于政策制定的空气质量模型中的应用提供一些支持。