印度东北部生物质燃烧期间(2003-2017)痕量气体(VOCs和NOx)排放估算及其反应性

IF 3 4区 地球科学 Q2 ENVIRONMENTAL SCIENCES
Kunal Bali, Amit Kumar, Sapna Chourasiya
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引用次数: 5

摘要

该研究分析了印度东北地区(NER) 3月(2003-2017年)生物质燃烧期间的火灾辐射功率(FRP)的时空分布和痕量气体[挥发性有机化合物(VOCs)和氮氧化物(NOx)]的估计及其反应性。从全球火灾同化系统中检索了玻璃钢的再分析数据以及微量气体的排放率。结果显示,平均FRP估计为0.37 Wm?在研究区域的7个邦中,米佐拉姆邦的值最高,为0.16 Wm?2。从时间上看,2006年和2010年的FRP相对较高,而2017年最低。基于frp的VOCs和NOx排放估算值分别为431和69.5?mg/m2/day,与观察到的FRP一致。各VOCs类群中,含氧种类最多(约56%),其次为烯烃类、烷烃类、芳烃类和生物源类。利用丙烯当量法和最大增量法对VOCs的光化学反应活性进行了估算,结果表明含氧组分对化学反应活性的贡献最大。根据MIR量表,臭氧(O3)形成的前十大主要贡献物质依次为甲醛、乙醛、乙烯、丙烯、甲苯、丁烷、异戊二烯、甲醇、戊烯和己烷,约占总臭氧形成的97%。我们还使用VOCs/NOx比值研究了臭氧形成机制,这表明臭氧形成可能对NER的voc敏感。本研究结果可用于了解生物质燃烧过程中基于frp的痕量气体排放,并为减少O3污染制定有效的预防措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Emission estimates of trace gases (VOCs and NOx) and their reactivity during biomass burning period (2003–2017) over Northeast India

Emission estimates of trace gases (VOCs and NOx) and their reactivity during biomass burning period (2003–2017) over Northeast India

The study analysed spatio-temporal distribution of fire radiative power (FRP) and estimates of trace gases [volatile organic compounds (VOCs) and nitrogen oxides (NOx)] along with their reactivity during biomass burning period of March (2003–2017) over the northeast region (NER), India. Reanalysis data of FRP along with emission rates of trace gases have been retrieved from Global Fire Assimilation System. Results showed that average FRP was estimated to be 0.37 Wm?2 with the highest value in Mizoram (0.16 Wm?2) among 7-states of the study region. Temporally, relatively higher FRP occurred during the year of 2006 and 2010 while lowest in 2017. FRP-based VOCs and NOx emission estimates were 431 and 69.5?mg/m2/day, respectively which are consistent with observed FRP. Among different groups of VOCs, oxygenated species were the largest group (~56%) estimated followed by alkenes, alkanes, aromatics, and biogenic. Photochemical reactivities of VOCs were estimated using propylene-equivalent and maximum incremental reactivity methods which showed oxygenated species had the highest contributions in chemical reactivity. Based on the MIR scale, the top ten leading contributor species for ozone (O3) formation were in descending order of formaldehyde, acetaldehyde, ethene, propene, toluene, butane, isoprene, methanol, pentene, and hexane which accounted for approximately 97% of total ozone formation. We also examined the ozone formation regime using VOCs/NOx ratios which indicated that O3 formation was likely to be VOC-sensitive over NER. Our results could be used for the understanding of FRP-based trace gas emissions during biomass burning and to establish effective preventive measures for reduction in O3 pollution.

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来源期刊
Journal of Atmospheric Chemistry
Journal of Atmospheric Chemistry 地学-环境科学
CiteScore
4.60
自引率
5.00%
发文量
16
审稿时长
7.5 months
期刊介绍: The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics: Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only. The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere. Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere. Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.
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