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Understanding the sources and formation processes of fine particulate matter (PM) is crucial for improving urban air quality and public health. This study provides a real-time analysis of PM-bound water-soluble organic carbon (WSOC) and related carbonaceous species during winter, spring, and summer periods in 2023-2024, aiming to identify their major sources in central Los Angeles. Using advanced online monitoring equipment, including a Sunset Laboratory EC/OC analyzer and a custom-developed setup including a total organic carbon (TOC) analyzer coupled with a particle collection system, we obtained hourly measurements of organic carbon (OC), its fractions (OC-OC, based on volatility), elemental carbon (EC), and WSOC. Positive matrix factorization (PMF) identified three principal PM sources: vehicular emissions, secondary organic carbon (SOC) formation influenced by nighttime aqueous-phase chemical processes, and SOC formation driven by daytime photochemical reactions. Vehicular emissions dominated EC levels, accounting for 86-95% across seasons. This factor also had high contributions from nitrogen oxides (NOₓ) (75-82%), vehicle counts (approximately 85%), and OC (51-83%), reflecting the persistent influence of traffic emissions. Nighttime SOC formation was significant in winter, with WSOC and OC contributing 58% and 40% to this factor. In contrast, daytime photochemical SOC formation was prominent in summer, with WSOC and OC contributing 63% and 47%, and ozone loading up to 89%, reflecting increased photochemical activity. Spring exhibited a mix of aqueous and photochemical SOC formation, with similar contributions from WSOC (38-35%) and OC (35-33%), reflecting the transitional season's mixed SOC formation mechanisms. Diurnal profiles revealed that primary emissions peaked during morning rush hours, while secondary formation processes elevated OC levels at night in winter and during afternoons in summer. The EC tracer method corroborated these findings by estimating primary and secondary organic carbon levels, highlighting significant seasonal and diurnal variations in carbonaceous aerosols. These results emphasize the need for targeted strategies addressing both primary emissions and the precursors of secondary aerosol formation, to improve air quality in Los Angeles.
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http://dx.doi.org/10.1016/j.atmosenv.2025.121084 | DOI Listing |
Anal Chim Acta
November 2025
Department of chemistry and Biochemistry, University of Texas at Arlington, Arlington, TX, USA. Electronic address:
Background: Carbonate esters are polar aprotic solvents that can be used to replace polar solvents: methanol, acetonitrile, or even apolar solvents in the mobile phases for liquid chromatography. Dimethyl, diethyl, and propylene carbonates (DMC, DEC, and PC) are not fully soluble in water.
Results: Twelve volume phase diagrams of water, the three carbonates, and methanol, ethanol, propanol, and acetonitrile were determined.
Int J Biol Macromol
September 2025
Faculty of Agronomy and Agricultural Sciences, University of Dschang, PO. Box 222, Dschang, Cameroon.
Dissolved organic matter (DOM) plays a key role in grassland carbon biogeochemistry and shows sensitivity to global climate change, particularly nitrogen (N) deposition. We investigated the soil DOM molecular composition by UV-Vis and fluorescence spectroscopy, and FT-ICR MS through a N addition experiment (CK, N5, N10, N20, and N40 [0, 5, 10, 20, and 40 g N m-2 year-1, respectively]) in a desert steppe of northwest China. Moderate N inputs (N5-N20) caused a dose-dependent increase in DOM content (9.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Nanning Normal University, Guangxi Key Laboratory of Natural Polymer Chemistry and Physics, Nanning 530100, PR China. Electronic address:
Electrochemical depolymerization of lignin to produce low molecular weight aromatic compounds is characterized by mild conditions and low carbon emissions. However, using non-metallic catalysts for this process faces challenges in terms of selectivity and activity. This study found that high-melting-point organic salts - tetra-n-butyl tetrafluoroborate (TBABF), can function simultaneously as a catalyst and oxidant at room temperature and in air, effectively catalyzing the CO bond cleavage in lignin.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
State Key Laboratory of Green Biomanufacturing, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.; Key Laboratory of Industrial Biocatalysis, Ministry of Education, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.; Ordos Laboratory, Inner
Currently, electrocatalytic conversion of carbon dioxide into higher-value compounds is a promising approach. However, developing a stable and efficient catalyst with high selectivity for specific products remains a major challenge. Herein, we constructed a bismuth-based metal-organic framework (Bi-MOF) as a catalyst for the catalytic production of formic acid from carbon dioxide, to which different ratios of tin metal elements were doped.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (Beijing), Changping, 102249, China. Electronic address:
Carbon-based catalysts with free-standing structure are essential for rechargeable zinc-air battery as electrodes, which can avoid the side effects brought by organic binder. However, the current preparation methods still can be improved for faster preparation process and morphology control. In this study, we reported a fabrication strategy of self-standing carbon catalyst loaded with CoFe nanoparticles and carbon nanotube as air electrodes for liquid rechargeable zinc-air battery.
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