Surfaces and Interfaces, Journal Year: 2024, Volume and Issue: 55, P. 105493 - 105493
Published: Nov. 25, 2024
Language: Английский
Surfaces and Interfaces, Journal Year: 2024, Volume and Issue: 55, P. 105493 - 105493
Published: Nov. 25, 2024
Language: Английский
Journal of Geophysical Research Atmospheres, Journal Year: 2023, Volume and Issue: 128(14)
Published: July 9, 2023
Abstract Amines affect particle formation, aerosol acidity, nitrogen cycle, and climate change. However, little is known about the temporal spatial differences in composition, source, formation process of amines fine particulate matter (PM 2.5 ) different regions China. Seven (amine salts) were investigated PM collected Yangtze River Delta (YRD, Shanghai Nanjing), Pearl (PRD, Guangzhou), northern China (Xi'an Haerbin), background (Puding) areas winter 2017–2018. Methylamine was dominant amine species at YRD, China, sites, while diethylamine dominated PRD site; moreover, mass concentration fraction lowest site. These results could be attributed to changes sources atmospheric processes. Further, coal combustion biomass burning found important contributors cities winter. The contribution weakened other urban sites. In contrast, abundance site largely controlled by biogenic sources. Acid‐base chemistry displacement mechanism tightly associated with salts all particular, degradation hydroxyl radical (•OH) significant Nanjing, Guangzhou, Xi'an, Haerbin insignificant photochemical sites can explained differentiated sources, meteorological conditions, •OH levels. Overall, our findings deepen understanding origins processes amines.
Language: Английский
Citations
26Atmospheric Environment, Journal Year: 2025, Volume and Issue: unknown, P. 121071 - 121071
Published: Jan. 1, 2025
Language: Английский
Citations
1Atmospheric chemistry and physics, Journal Year: 2024, Volume and Issue: 24(18), P. 10531 - 10542
Published: Sept. 23, 2024
Abstract. Amines and aminiums play an important role in particle formation, liquid-phase reactions, climate change have attracted considerable attention over the years. Here, we investigated concentrations compositions of PM2.5 11 Chinese cities during winter, focusing on characteristics polluted days key factors influencing aminium outbreak. Monomethylaminium was dominant species most cities, except Taiyuan Guangzhou, followed by dimethylaminium. Diethylaminium dominated total Guangzhou. Thus, main amine sources Guangzhou were significantly different from those other cities. The (TAs) increased days, while relatively weak outbreaks occurred Xi'an Beijing. Additionally, TAs Beijing insignificantly correlated with major acidic aerosol components, opposite pattern observed nine acid–base chemistry associated formation all Based sensitivity analysis : ammonium ratio to changes, as well excluding effects relative humidity atmospheric oxidation, proposed possibility competitive uptake ammonia versus amines aerosols or displacement (constraining outbreaks). Overall, this study deepens understanding spatiotemporal differences characteristic China. However, particles form relevant require further mechanistic research.
Language: Английский
Citations
4Atmosphere, Journal Year: 2025, Volume and Issue: 16(1), P. 98 - 98
Published: Jan. 17, 2025
Oxalic acid is the most abundant low-molecular-weight dicarboxylic in atmosphere, and it plays a crucial role formation of new particles cloud condensation nuclei. However, observational studies have focused on particulate oxalate, leaving significant knowledge gap oxalic vapor. This study investigated concentrations vapor oxalate PM2.5 at rural tropical coastal island site south China across different seasons, based semi-continuous measurements using an Ambient Ion Monitor-Ion Chromatograph (AIM-IC) system. We replaced default 25 μL sampling loop AIM-IC with 250 loop, improving ability to distinguish signal from noise. The data revealed clear seasonal patterns dependent daytime nighttime vapor, benefiting high signal-to-noise ratios. Specifically, were 0.059 ± 0.15 μg m−3 February April 2023, exhibiting consistent diurnal variations similar those O3, likely driven by photochemical reactions. These values decreased 0.021 0.07 November December higher related dark chemistry processes, amplified accumulation due low mixing layer height. comparable but exhibited (3–7)-day variations, superimposed fluctuations varying degrees. Additionally, thermodynamic equilibrium calculations performed data, independent size distributions upwind marine atmosphere analyzed support findings.
Language: Английский
Citations
0Aerosol Science and Engineering, Journal Year: 2025, Volume and Issue: unknown
Published: March 6, 2025
Language: Английский
Citations
0Journal of Hazardous Materials, Journal Year: 2025, Volume and Issue: unknown, P. 137999 - 137999
Published: March 1, 2025
Language: Английский
Citations
0ACS Earth and Space Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: March 29, 2025
Language: Английский
Citations
0Atmosphere, Journal Year: 2025, Volume and Issue: 16(5), P. 546 - 546
Published: May 5, 2025
Eulerian observations of chemical species at fixed positions in a flow field are known to violate conservation laws, while tracking moving air parcels practically unfeasible. often cause positive correlations between the reactants and products atmosphere, which frequently misinterpreted as evidence related conversion. This dilemma has motivated innovative trials. The perturbation technique, widely used mathematical physical studies, offers potential solution. Combining with techniques may compensate for this weakness, making approach particularly valuable studying gas–aerosol partitioning semi-volatile particulate ambient air. As an example, we examined combination through adiabatic-expansion-induced study dimethylamine (DMA) trimethylamine (TMA) size-segregated atmospheric particles ranging from 10 μm 0.056 μm, coupled downstream observations, were performed coastal marine atmospheres using commercial sampler (Nano-MOUDI-II, MSP, Shoreview, MN, USA), followed by offline analysis. results revealed that DMA generally tended evaporate during observational periods, enhanced perturbations occasionally led co-formation DMAHNO3 NH4NO3. However, gaseous TMA apparently underwent gas–particle condensation reach equilibrium air, resulting formation non-ionized particulates. thermodynamic analysis further supported observed was primarily determined rather than ionic TMAH+.
Language: Английский
Citations
0ACS Earth and Space Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: May 19, 2025
Language: Английский
Citations
0Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(42), P. 28866 - 28873
Published: Oct. 8, 2024
The hydrolysis of imines has long been assumed to be their main atmospheric fate, based on early studies in the field organic chemistry. However, mechanism and kinetics remain unclear. Here, an advanced Born-Oppenheimer molecular dynamics method was employed investigate noncatalyzed at air-water interface by selecting CH
Language: Английский
Citations
3