Contributions of primary sources to submicron organic aerosols in Delni, India

被引:3
|
作者
Bhandari, Sahil [1 ,2 ]
Arub, Zainab [3 ]
Habib, Gazala [3 ]
Apte, Joshua S. [4 ,5 ]
Ruiz, Lea Hildebrandt [1 ]
机构
[1] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
[2] Univ British Columbia, Dept Mech Engn, Vancouver, BC, Canada
[3] Indian Inst Technol Delhi, Dept Civil Engn, New Delhi, India
[4] Univ Calif Berkeley, Dept Civil & Environm Engn, Berkeley, CA 94704 USA
[5] Univ Calif Berkeley, Sch Publ Hlth, Berkeley, CA 94704 USA
基金
美国国家科学基金会;
关键词
POSITIVE MATRIX FACTORIZATION; MUNICIPAL SOLID-WASTE; SOURCE APPORTIONMENT; PARTICULATE MATTER; AIR-POLLUTION; NEW-DELHI; CHEMICAL-COMPOSITION; MULTILINEAR ENGINE; MASS-SPECTROMETRY; PRIMARY EMISSIONS;
D O I
10.5194/acp-22-13631-2022
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Delhi, India, experiences extremely high concentrations of primary organic aerosol (POA). Few prior source apportionment studies on Delhi have captured the influence of biomass burning organic aerosol (BBOA) and cooking organic aerosol (COA) on POA. In a companion paper, we develop a new method to conduct source apportionment resolved by time of day using the underlying approach of positive matrix factorization (PMF). We call this approach "time-of-day PMF" and statistically demonstrate the improvements of this approach over traditional PMF. Here, we quantify the contributions of BBOA, COA, and hydrocarbon-like organic aerosol (HOA) by applying positive matrix factorization (PMF) resolved by time of day on two seasons (winter and monsoon seasons of 2017) using organic aerosol measurements from an aerosol chemical speciation monitor (ACSM). We deploy the EPA PMF tool with the underlying Multilinear Engine (ME-2) as the PMF solver. We also conduct detailed uncertainty analysis for statistical validation of our results. HOA is a major constituent of POA in both winter and the monsoon. In addition to HOA, COA is found to be a major constituent of POA in the monsoon, and BBOA is found to be a major constituent of POA in the winter. Neither COA nor the different types of BBOA were resolved in the seasonal (not time-resolved) analysis. The COA mass spectra (MS) profiles are consistent with mass spectral profiles from Delhi and around the world, particularly resembling MS of heated cooking oils with a high m/z 41. The BBOA MS have a very prominent m/z 29 in addition to the characteristic peak at m/z 60, consistent with previous MS observed in Delhi and from wood burning sources. In addition to separating the POA, our technique also captures changes in MS profiles with the time of day, a unique feature among source apportionment approaches available. In addition to the primary factors, we separate two to three oxygenated organic aerosol (OOA) components. When all factors are recombined to total POA and OOA, our results are consistent with seasonal PMF analysis conducted using EPA PMF. Results from this work can be used to better design policies that target relevant primary sources of organic aerosols in Delhi.
引用
收藏
页码:13631 / 13657
页数:27
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