Lei Yao

Reactions of Atmospheric Particulate Stabilized Criegee Intermediates Lead to High-Molecular-Weight Aerosol Components

Aging of organic aerosol particles is one of the most poorly understood topics in atmospheric aerosol research. Here, we used an aerosol flow tube together with an iodide-adduct high-resolution time-of-flight chemical-ionization mass spectrometer equipped with a Filter Inlet for Gases and AEROsols (FIGAERO-HRToF-CIMS) to investigate heterogeneous ozonolysis of oleic acid (OL), developing a comprehensive oxidation mechanism with observed products. In addition to the well-known first-generation C9 products including nonanal, nonanoic acid, azelaic acid, and 9-oxononanoic acid, the iodide-adduct chemical ionization permitted unambiguous determination of a large number of high-molecular-weight particulate products up to 670 Da with minimum amounts of fragmentation. These high-molecular-weight products are characterized by a fairly uniform carbon oxidation state but stepwise addition of a carbon backbone moiety, and hence continuous decrease in the volatility. Our results demonstrate that heterogeneous oxidation of organic aerosols has a significant effect on the physiochemical properties of organic aerosols and that reactions of particulate SCIs from ozonolysis of an unsaturated particulate species represent a previously underappreciated mechanism that lead to formation of high-molecular-weight particulate products that are stable under typical atmospheric conditions.

Uptake of Gaseous Alkylamides by Suspended Sulfuric Acid Particles: Formation of Ammonium/Aminium Salts

Amides represent an important class of nitrogen-containing compounds in the atmosphere that can in theory interact with atmospheric acidic particles and contribute to secondary aerosol formation. In this study, uptake coefficients (γ) of six alkylamides (C1 to C3) by suspended sulfuric acid particles were measured using an aerosol flow tube coupled to a high resolution time-of-flight chemical ionization mass spectrometer (HRToF-CIMS). At 293 K and < 3% relative humidity (RH), the measured uptake coefficients for six alkylamides were in the range of (4.8-23) × 10-2. A negative dependence upon RH was observed for both N-methylformamide and N,N-dimethylformamide, likely due to decreased mass accommodation coefficients (α) at lower acidities. A negative temperature dependence was observed for N,N-dimethylformamide under < 3% RH, also consistent with the mass accommodation-controlled uptake processes. Chemical analysis of reacted sulfuric acid particles indicates that alkylamides hydrolyzed in the presence of water molecules to form ammonium or aminium. Our results suggest that multiphase uptake of amides will contribute to growth of atmospheric acidic particles and alter their chemical composition.

Atmospheric new particle formation from sulfuric acid and amines in a Chinese megacity

A puzzle of new particles Atmospheric particulates can be produced by emissions or form de novo. New particle formation usually occurs in relatively clean air. This is because preexisting particles in the atmosphere will scavenge the precursors of new particles and suppress their formation. However, observations in some heavily polluted megacities have revealed substantial rates of new particle formation despite the heavy loads of ambient aerosols. Yao et al. investigated new particle formation in Shanghai and describe the conditions that make this process possible. The findings will help inform policy decisions about how to reduce air pollution in these types of environments. Science, this issue p. 278 Atmospheric new particle formation in heavily polluted cities can occur in certain chemical environments. Atmospheric new particle formation (NPF) is an important global phenomenon that is nevertheless sensitive to ambient conditions. According to both observation and theoretical arguments, NPF usually requires a relatively high sulfuric acid (H2SO4) concentration to promote the formation of new particles and a low preexisting aerosol loading to minimize the sink of new particles. We investigated NPF in Shanghai and were able to observe both precursor vapors (H2SO4) and initial clusters at a molecular level in a megacity. High NPF rates were observed to coincide with several familiar markers suggestive of H2SO4–dimethylamine (DMA)–water (H2O) nucleation, including sulfuric acid dimers and H2SO4-DMA clusters. In a cluster kinetics simulation, the observed concentration of sulfuric acid was high enough to explain the particle growth to ~3 nanometers under the very high condensation sink, whereas the subsequent higher growth rate beyond this size is believed to result from the added contribution of condensing organic species. These findings will help in understanding urban NPF and its air quality and climate effects, as well as in formulating policies to mitigate secondary particle formation in China.

Chemical Characteristics of Organic Aerosols in Shanghai: A Study by Ultrahigh‐Performance Liquid Chromatography Coupled With Orbitrap Mass Spectrometry

PM2.5 filter samples were collected in July and October 2014 and January and April 2015 in urban Shanghai, and analyzed using ultra-high-performance liquid chromatography (UHPLC) coupled to Orbitrap mass spectrometry (MS). The measured chromatogram-mass spectra were processed by a non-target screening approach to identify significant signals. In total, 810-1510 chemical formulas of organic compounds in the negative polarity (ESI-) and 860-1790 in the positive polarity (ESI+), respectively, were determined. The chemical characteristics of organic aerosols (OAs) in Shanghai varied among different months and between daytime and nighttime. In the January samples, organics were generally richer in terms of both number and abundance, whereas those in the July samples were far lower. More CHO- (compounds containing only carbon, hydrogen, and oxygen and detected in ESI-) and CHOS- (sulfur-containing organics) were found in the daytime samples, suggesting a photochemical source, whereas CHONS- (nitrogen- and sulfur-containing organics) were more abundant in the nighttime samples, due to nocturnal nitrate radical chemistry. A significant number of mono- and polycyclic aromatic compounds, and nitrogen- and sulfur-containing heterocyclic compounds were detected in all samples, indicating that biomass burning and fossil fuel combustion made important contributions to the OAs in urban Shanghai. Additionally, precursor-product pair analysis indicates that the epoxide pathway is an important formation route for organosulfates observed in Shanghai. Moreover, a similar analysis suggests that 35-57% of nitrogen-containing compounds detected in ESI+ could be formed through reactions between ammonia and carbonyls. Our study presents a comprehensive overview of OAs in urban Shanghai, which helps to understand their characteristics and sources.