| Literature DB >> 36196118 |
Runlong Cai1,2, Rujing Yin1, Chao Yan2,3, Dongsen Yang4, Chenjuan Deng1, Lubna Dada2,5, Juha Kangasluoma2, Jenni Kontkanen2, Roope Halonen6, Yan Ma4, Xiuhui Zhang7, Pauli Paasonen2, Tuukka Petäjä2, Veli-Matti Kerminen2, Yongchun Liu3, Federico Bianchi2, Jun Zheng4, Lin Wang8, Jiming Hao1, James N Smith9, Neil M Donahue10,11, Markku Kulmala2, Douglas R Worsnop2,12, Jingkun Jiang1.
Abstract
Transformation of low-volatility gaseous precursors to new particles affects aerosol number concentration, cloud formation and hence the climate. The clustering of acid and base molecules is a major mechanism driving fast nucleation and initial growth of new particles in the atmosphere. However, the acid-base cluster composition, measured using state-of-the-art mass spectrometers, cannot explain the measured high formation rate of new particles. Here we present strong evidence for the existence of base molecules such as amines in the smallest atmospheric sulfuric acid clusters prior to their detection by mass spectrometers. We demonstrate that forming (H2SO4)1(amine)1 is the rate-limiting step in atmospheric H2SO4-amine nucleation and the uptake of (H2SO4)1(amine)1 is a major pathway for the initial growth of H2SO4 clusters. The proposed mechanism is very consistent with measured new particle formation in urban Beijing, in which dimethylamine is the key base for H2SO4 nucleation while other bases such as ammonia may contribute to the growth of larger clusters. Our findings further underline the fact that strong amines, even at low concentrations and when undetected in the smallest clusters, can be crucial to particle formation in the planetary boundary layer.Entities:
Keywords: acid-base nucleation; aerosol; new particle formation; polluted urban environment
Year: 2022 PMID: 36196118 PMCID: PMC9522409 DOI: 10.1093/nsr/nwac137
Source DB: PubMed Journal: Natl Sci Rev ISSN: 2053-714X Impact factor: 23.178