Chemical composition and sources of amines in PM2.5 in an urban site of PRD, China.

Atmospheric amines have attracted increasing attention due to their significant impact on new particle formation, particle hygroscopicity and particle optical properties. In this study, four low-molecule-weight amines were detected from PM 2.5 filter samples collected at an urban site of Pearl River Delta (PRD) region of China in 2018 autumn. During the campaign, the mass concentrations of ambient particulate methylamine (MA, CH 3 NH 2), dimethylamine (DMA, (CH 3) 2 NH), trimethylamine (TMA, (CH 3) 3 N), and diethylamine (DEA, (C 2 H 5) 2 NH) were quantified at daily or 12-h resolution using an optimized Ion Chromatograph (IC) method. The total measured amine concentration was 297 ± 209 ng/m3, which can account for 0.76 ± 0.33% of PM 2.5 mass concentrations. The particulate amines in PRD urban area were dominated by MA (243 ± 179 ng/m3), accounting for over 80% of total amines, then followed by DMA (49 ± 30 ng/m3, 16.5%), TMA (4 ± 2 ng/m3) and DEA (1 ± 1 ng/m3). Based on the correlation analysis, MA and DMA mainly presented as nitrate and sulfate salts. We speculate the amines tend to react with gas-phase HNO 3 or particle-phase nitrate to form particulate amine salts via local process in Guangzhou. As the relative humidity (RH) increased, enhanced partitioning of amine towards the particle phase was observed. Using approach of multiple linear regression, 71% of the particulate amines in PRD urban site could be explained by acid-base process and the rest by primary emissions from combustion sources (29%). • Particulate amines in urban PRD were quantified using an optimized IC method. • Methylamine was the most abundant amine, followed by dimethylamine. • Methylamine and dimethylamine mainly presented as nitrate and sulfate salts. • Enhanced RH facilitated the partitioning of amine towards particle phase. • Acid-base process dominated the amine formation, the left by combustion source. [ABSTRACT FROM AUTHOR]