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Source apportionment of volatile organic compounds in the northwest Indo-Gangetic Plain using a positive matrix factorization model

机译:使用正矩阵分解模型,西北地区难以膨胀平原中挥发性有机化合物的源分摊

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In this study we undertook quantitative source apportionment for 32 volatile organic compounds (VOCs) measured at a suburban site in the densely populated northwest Indo-Gangetic Plain using the US EPA PMF 5.0 model. Six sources were resolved by the PMF model. In descending order of their contribution to the total VOC burden these are “biofuel use and waste disposal” (23.2%), “wheat-residue burning”(22.4%), “cars” (16.2%), “mixed daytime sources”(15.7%) “industrial emissions and solvent use”(11.8%), and “two-wheelers” (8.6%). Wheat-residue burning is the largest contributor to the total ozone formation potential (32.4%). For the emerging contaminant isocyanic acid, photochemical formation from precursors (37%) and wheat-residue burning (25%) were the largest contributors to human exposure. Wheat-residue burning was also the single largest source of the photochemical precursors of isocyanic acid, namely, formamide, acetamide and propanamide, indicating that this source must be most urgently targeted to reduce human concentration exposure to isocyanic acid in the month of May. Our results highlight that for accurate air quality forecasting and modeling it is essential that emissions are attributed only to the months in which the activity actually occurs. This is important for emissions from crop residue burning, which occur in May and from mid-October to the end of November. The SOA formation potential is dominated by cars (36.9%) and two-wheelers (21.1%), which also jointly account for 47% of the human class I carcinogen benzene in the PMF model. This stands in stark contrast to various emission inventories which estimate only a minor contribution of the transport sector to the benzene exposure (~10%) and consider residential biofuel use, agricultural residue burning and industry to be more important benzene sources. Overall it appears that none of the emission inventories represent the regional emissions in an ideal manner. Our PMF solution suggests that transport sector emissions may be underestimated by GAINSv5.0 and EDGARv4.3.2 and overestimated by REASv2.1, while the combined effect of residential biofuel use and waste disposal emissions as well as the VOC burden associated with solvent use and industrial sources may be overestimated by all emission inventories. The agricultural waste burning emissions of some of the detected compound groups (ketones, aldehydes and acids) appear to be missing in the EDGARv4.3.2 inventory.
机译:在这项研究中,我们使用美国EPA PMF 5.0模型对郊区群落的郊区站点测量的32种挥发性有机化合物(VOC)进行定量源分配。 PMF模型解决了六个来源。他们对他们对总体负担的贡献的贡献顺序这些是“生物燃料使用和废物处理”(23.2%),“小麦 - 残留燃烧”(22.4%),“汽车”(16.2%),“混合的日间来源”( 15.7%)“工业排放和溶剂使用”(11.8%)和“两轮车”(8.6%)。小麦 - 残留燃烧是总臭氧形成电位(32.4%)的最大贡献者。对于新出现的污染物异氰酸,来自前体的光化学形成(37%)和小麦 - 残留物燃烧(25%)是人类暴露的最大贡献者。小麦 - 残留物燃烧也是异氰酸的光化学前体的最大源,即甲酰胺,乙酰胺和丙酰胺,表明该来源最迫切地靶向,以减少5月份的人群浓度暴露于异氰酸对异氰酸的影响。我们的结果突出显示,对于准确的空气质量预测和建模,排放归因于实际发生的活动。这对于农作物残留燃烧的排放是重要的,这可能在5月和10月中旬到11月底。 SOA形成电位由汽车(36.9%)和两轮车(21.1%)主导,这也共同占PMF模型中的47%的人类癌苯。这与各种排放清单呈现出鲜明对比,这估计了运输部门对苯曝光(〜10%)的轻微贡献,并考虑住宅生物燃料使用,农业残留燃烧和工业更重要的苯来源。总的来说,似乎没有任何排放库存以理想的方式代表区域排放。我们的PMF解决方案表明,通过Gainsv5.0和Edgarv4.3.2和Edv2.1高估,综合消费使用和废物处理排放以及与溶剂使用和工业相关的VOC负担的综合效果,可以低估运输部门排放和EDV2.1的综合效应以及与溶剂使用和工业相关的VOC负担的综合影响源可能受到所有排放清单的估量。 Edgarv4.3.2库存中,一些检测到的复合组(酮,醛和酸)的农业废物燃烧排放似乎缺失。

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