| Literature DB >> 32984431 |
Haotian Zheng1,2,3, Shaojie Song3, Golam Sarwar4, Masao Gen5, Shuxiao Wang1,2,3, Dian Ding1,2, Xing Chang1,2, Shuping Zhang1, Jia Xing1,2, Yele Sun6, Dongsheng Ji7, Chak K Chan8, Jian Gao9, Michael B McElroy3.
Abstract
Nitrate and sulfate are two key components of airborne particulate matter (PM). While multiple formation mechanisms have been proposed for sulfate, current air quality models commonly underestimate its concentrations and mass fractions during northern China winter haze events. On the other hand, current models usually overestimate the mass fractions of nitrate. Very recently, laboratory studies have proposed that nitrous acid (N(III)) produced by particulate nitrate photolysis can oxidize sulfur dioxide to produce sulfate. Here, for the first time, we parameterize this heterogeneous mechanism into the state-of-the-art Community Multi-scale Air Quality (CMAQ) model and quantify its contributions to sulfate formation. We find that the significance of this mechanism mainly depends on the enhancement effects (by 1-3 orders of magnitude as suggested by the available experimental studies) of nitrate photolysis rate constant ( J NO 3 - ) in aerosol liquid water compared to that in the gas phase. Comparisons between model simulations and in-situ observations in Beijing suggest that this pathway can explain about 15% (assuming an enhancement factor (EF) of 10) to 65% (assuming EF = 100) of the model-observation gaps in sulfate concentrations during winter haze. Our study strongly calls for future research on reducing the uncertainty in EF.Entities:
Year: 2020 PMID: 32984431 PMCID: PMC7510950 DOI: 10.1021/acs.estlett.0c00368
Source DB: PubMed Journal: Environ Sci Technol Lett