二甲胺
甲胺
成核
硫酸
硝酸
化学
星团(航天器)
三元运算
动力学
氨
无机化学
物理化学
结晶学
物理
有机化学
量子力学
计算机科学
程序设计语言
作者
Fukang Qiao,Rongjie Zhang,Qiaojing Zhao,Fangfang Ma,Jingwen Chen,Hong‐Bin Xie
出处
期刊:Atmosphere
[Multidisciplinary Digital Publishing Institute]
日期:2024-04-10
卷期号:15 (4): 467-467
被引量:6
标识
DOI:10.3390/atmos15040467
摘要
Nitric acid (NA) has recently been found to enhance sulfuric acid (SA)-driven new particle formation (NPF) at low temperatures (≤240 K). However, studies on the role of NA in atmospheric NPF remain limited. Herein, we explored the enhancement effect of NA on binary SA–methylamine (MA) nucleation by investigating the mechanism and kinetics of (NA)x(SA)y(MA)z (0 ≤ x, 0 ≤ y, x + y ≤ 3, 0 ≤ z ≤ 3) clusters using quantum chemical calculations and cluster dynamics simulations. We found that the mixed ternary NA-SA-MA clusters have lower evaporation rates compared to the corresponding NA-SA–dimethylamine (DMA) and NA-SA–ammonia (A) clusters, indicating the stronger binding ability of NA with respect to SA-MA clusters. At atmospheric conditions (T ≥ 278.15 K), NA can enhance the cluster formation rate of SA-MA by about six orders of magnitude, demonstrating a surprisingly high enhancing potential. Moreover, NA acts as an important participant in the cluster growth pathways of the NA-SA-MA system, as opposed to the “bridging” role of NA in the previously studied NA-SA-A system. This study proposes the first case of NA efficiently enhancing SA–amine nucleation at ambient temperature, suggesting a larger impact of NA in atmospheric NPF than previously expected.
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