Perraud Véronique, Horne Jeremy R, Martinez Andrew S, Kalinowski Jaroslaw, Meinardi Simone, Dawson Matthew L, Wingen Lisa M, Dabdub Donald, Blake Donald R, Gerber R Benny, Finlayson-Pitts Barbara J
Department of Chemistry, University of California Irvine, Irvine, CA 92697;
Department of Mechanical & Aerospace Engineering, University of California Irvine, Irvine, CA 92697;
Proc Natl Acad Sci U S A. 2015 Nov 3;112(44):13514-9. doi: 10.1073/pnas.1510743112. Epub 2015 Oct 19.
Sulfuric acid (H2SO4), formed from oxidation of sulfur dioxide (SO2) emitted during fossil fuel combustion, is a major precursor of new airborne particles, which have well-documented detrimental effects on health, air quality, and climate. Another precursor is methanesulfonic acid (MSA), produced simultaneously with SO2 during the atmospheric oxidation of organosulfur compounds (OSCs), such as dimethyl sulfide. In the present work, a multidisciplinary approach is used to examine how contributions of H2SO4 and MSA to particle formation will change in a large coastal urban area as anthropogenic fossil fuel emissions of SO2 decline. The 3-dimensional University of California Irvine-California Institute of Technology airshed model is used to compare atmospheric concentrations of gas phase MSA, H2SO4, and SO2 under current emissions of fossil fuel-associated SO2 and a best-case futuristic scenario with zero fossil fuel sulfur emissions. Model additions include results from (i) quantum chemical calculations that clarify the previously uncertain gas phase mechanism of formation of MSA and (ii) a combination of published and experimental estimates of OSC emissions, such as those from marine, agricultural, and urban processes, which include pet waste and human breath. Results show that in the zero anthropogenic SO2 emissions case, particle formation potential from H2SO4 will drop by about two orders of magnitude compared with the current situation. However, particles will continue to be generated from the oxidation of natural and anthropogenic sources of OSCs, with contributions from MSA and H2SO4 of a similar order of magnitude. This could be particularly important in agricultural areas where there are significant sources of OSCs.
硫酸(H₂SO₄)由化石燃料燃烧过程中排放的二氧化硫(SO₂)氧化形成,是新生成的空气中颗粒物的主要前体,这些颗粒物对健康、空气质量和气候具有已被充分证明的有害影响。另一种前体是甲磺酸(MSA),它在有机硫化合物(OSCs)如二甲基硫的大气氧化过程中与SO₂同时产生。在本研究中,采用多学科方法来研究在一个大型沿海城市地区,随着人为源化石燃料SO₂排放量的下降,H₂SO₄和MSA对颗粒物形成的贡献将如何变化。利用三维的加利福尼亚大学欧文分校 - 加利福尼亚理工学院大气污染模型,比较在当前与化石燃料相关的SO₂排放情况下以及在化石燃料硫排放为零的最佳未来情景下,气相MSA、H₂SO₄和SO₂的大气浓度。模型补充内容包括:(i)量子化学计算结果,该结果阐明了此前不确定的MSA气相形成机制;(ii)已发表的和实验估计的OSC排放数据的组合,如来自海洋、农业和城市过程(包括宠物粪便和人类呼吸)的排放数据。结果表明,在人为SO₂排放为零的情况下,与当前情况相比,H₂SO₄导致的颗粒物形成潜力将下降约两个数量级。然而,天然和人为来源的OSC氧化仍将继续产生颗粒物,MSA和H₂SO₄的贡献处于相似的数量级。这在存在大量OSC来源的农业地区可能尤为重要。