气溶胶
铵
分馏
氨
大气(单位)
化学
氮气
环境化学
动能
同位素分馏
大气科学
气象学
色谱法
生物化学
有机化学
地质学
物理
量子力学
作者
Mengna Gu,Yang C. Zeng,Wendell W. Walters,Qian Sun,Yunting Fang,Yuepeng Pan
标识
DOI:10.1021/acs.est.4c09103
摘要
Abstract Aerosol ammonium (NH4+) is a critical component of particulate matter that affects air pollution, climate, and human health. Isotope-based source apportionment of NH4+ is essential for ammonia (NH3) mitigation but the role of kinetic vs equilibrium controls on nitrogen isotope (δ15N) fractionation between NH3 and NH4+ remains unresolved. Based on concurrent measurements of NH3 and NH4+ in winter Beijing, we observed that the difference of δ15N between NH3 and NH4+ on clean days (3.3 ± 13.3‰) was significantly lower than that during polluted periods (30.2 ± 11.8‰). This difference signified incomplete equilibrium fractionation and that kinetic fractionation may have occurred between NH3 and NH4+, especially during clean days. Assuming that kinetic and equilibrium fractionation occurred successively, the contribution of nonagricultural emissions to NH4+ was apportioned to 60.3 ± 12.8%, higher than that of 50.4 ± 17.7% considering only equilibrium fractionation. These results indicate that the source apportionment of NH4+ considering only equilibrium fractionation in the conventional scenario would underestimate the contribution of nonagricultural emissions by 16.4% (up to 33.1% on clean days). Our analysis highlighted the importance in considering both kinetic and equilibrium fractionation scenarios to improve the precision of NH4+ source apportionment by using nitrogen isotopes.
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