Literature DB >> 30096673

Impacts of potential HONO sources on the concentrations of oxidants and secondary organic aerosols in the Beijing-Tianjin-Hebei region of China.

Jingwei Zhang1, Junling An2, Yu Qu3, Xingang Liu4, Yong Chen3.   

Abstract

We first coupled indoor emissions and biomass burning emissions into the WRF-Chem model besides the other four potential HONO sources (i.e., traffic emissions, soil emissions, and heterogeneous reactions on aerosol and ground surfaces). Eight simulations were performed in the Beijing-Tianjin-Hebei region (BTH) of China in August of 2006. The results indicated that traffic emissions and heterogeneous reactions on ground and aerosol surfaces were the key sources of HONO at night, accounting for ~41%, ~27% and ~20% of the nighttime simulated HONO concentrations, respectively. The two heterogeneous reactions were the main contributors during the day, accounting for ~66% (ground surfaces) and ~19% (aerosol surfaces) of the daytime simulated HONO concentrations. The indoor emission source could be the second largest contributor during nighttime and led to a maximum hourly enhancement of 0.59 and 0.76 ppb at the central urban sites of Beijing and Tianjin, respectively. The six potential HONO sources enhanced the monthly meridional-mean concentrations of O3, OH and HO2 by 5-44%, 5~>150% and 5~>200%, respectively, leading to an enhancement of 1-3 μg m-3 in the monthly averaged concentrations of secondary organic aerosol (SOA), and that of 10-35 μg m-3 in the largest hourly concentrations of SOA within 1000 m above the ground in the BTH. The major precursors of the enhanced SOA were Xylenes, Toluene and BIGALK (lumped alkanes C > 3). The inclusion of the six potential HONO sources in the WRF-Chem model considerably improved the HONO simulations at both urban and suburban sites compared with the corresponding observations. The above results suggested that the six potential HONO sources significantly enhanced the atmospheric oxidation capacity and thus accelerated SOA chemical aging in the BTH of China, leading to large enhancements in the hourly SOA concentrations and aggravating haze events in this region.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  HONO; Heterogeneous reaction; Indoor source; SOA; WRF-Chem

Year:  2018        PMID: 30096673     DOI: 10.1016/j.scitotenv.2018.08.030

Source DB:  PubMed          Journal:  Sci Total Environ        ISSN: 0048-9697            Impact factor:   7.963


  3 in total

1.  Surface Charge Measurements with Scanning Ion Conductance Microscopy Provide Insights into Nitrous Acid Speciation at the Kaolin Mineral-Air Interface.

Authors:  Cheng Zhu; Gargi Jagdale; Adrien Gandolfo; Kristen Alanis; Rebecca Abney; Lushan Zhou; David Bish; Jonathan D Raff; Lane A Baker
Journal:  Environ Sci Technol       Date:  2021-08-27       Impact factor: 11.357

2.  Improving the representation of HONO chemistry in CMAQ and examining its impact on haze over China.

Authors:  Shuping Zhang; Golam Sarwar; Jia Xing; Biwu Chu; Chaoyang Xue; Arunachalam Sarav; Dian Ding; Haotian Zheng; Yujing Mu; Fengkui Duan; Tao Ma; Hong He
Journal:  Atmos Chem Phys       Date:  2021-10-22       Impact factor: 7.197

3.  Characteristics of HONO and its impact on O3 formation in the Seoul Metropolitan Area during the Korea-US Air Quality Study.

Authors:  Junsu Gil; Jeonghwan Kim; Meehye Lee; Gangwoong Lee; Joonyeong An; Dongsoo Lee; Jinsang Jung; Seogju Cho; Andrew Whitehill; James Szykman; Jeonghoon Lee
Journal:  Atmos Environ (1994)       Date:  2021       Impact factor: 4.798

  3 in total

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