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Analyses of diurnal patterns of PM10 in the downtown of Pudong, Shanghai have been performed in this study at different daily ozone maximum concentrations (O(3,max)) from May to October, 2010. In order to evaluate secondary aerosol formation at different ozone levels, CO was used as a tracer for primary aerosol, and 0(3, max) was used as an index for photochemical activity. Results show that along with increasing of O3 concentration, the concentration of primary and secondary aerosol was increased respectively from 0. 036 to 0.044 mg x m(-3) and from 0.018 to 0.055 mg x m(-3). The ratio of secondary to primary aerosol was increased from 49.8% to 124.5%. Furthermore, along with the increase of O(3, max) the forming time of O(3,max) and secondary aerosol was changed respectively from 13:00 to 14:00 and from 11:00-20:00 to 09:00-20:00. At the same time, the chemical composition of PM2.5 was different at different photochemical levels. PM(2.5) was composed of 12.0% organic carbon (OC), 18.7% sulfate (SO4(2-1)), 13.1% nitrate (NO3-) and 4.5% element carbon (EC) when O(3, max) was < 0.10 mg x m(-3) and PM2.5 was composed of 20.0% organic carbon (OC), 22.9% sulfate, 23.1% nitrate and 4.7% element carbon (EC) with O(3, max) > 0. 20 mg x m(-3). These results approved that the photochemical reactivity promoted the production of SO4(2-), NO3- and OC.
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Sci Total Environ
December 2024
Department of Atmospheric Science, School of Environmental Studies, China University of Geosciences, Wuhan 430074, China; Research Centre for Complex Air Pollution of Hubei Province, Wuhan 430074, China. Electronic address:
Atmospheric oxidation capacity (AOC) reflects the potential of the atmosphere in converting primary pollutants into secondary aerosols and ozone (O). In this study, the AOC at an urban supersite in Wuhan, a megacity in central China, was quantified by considering the reactions of volatile organic compounds (VOCs) and carbon monoxide (CO) with atmospheric oxidants (OH, NO, O, and Cl). Photochemical loss of total VOCs (13.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2025
Department of Chemical Engineering, California Institute of Technology, Pasadena, CA 91106.
Aerosol light absorption has been widely considered as a contributing factor to the worsening of particulate pollution in large urban areas, primarily through its role in stabilizing the planetary boundary layer (PBL). Here, we report that absorption-dominated aerosol-radiation interaction can decrease near-surface fine particulate matter concentrations ([PM]) at a large-scale during wintertime haze events. A "warm bubble" effect by the significant heating rate of absorbing aerosols above the PBL top generates a secondary circulation, enhancing the upward motion (downward motion) and the convergence (divergence) in polluted (relatively clean) areas, with a net effect of lowering near-surface [PM].
View Article and Find Full Text PDFPleura Peritoneum
December 2024
Odense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.
Objectives: Pressurized IntraThoracic Aerosol Chemotherapy (PITAC) is a minimally invasive cancer-directed therapy for patients with malignant pleural effusion (MPE) and/or pleural metastasis (PLM). PITAC is based on Pressurized IntraPeritoneal Aerosol Chemotherapy, which has proven to be safe and feasible. Since 2012, 47 PITACs have been published, and prospective data on feasibility, safety and potential local response are lacking.
View Article and Find Full Text PDFEnviron Pollut
December 2024
Department of Physics - Università degli Studi di Milano and INFN, Milan, Italy. Electronic address:
C measurements on the carbonaceous fractions of atmospheric aerosol are an important tool for source apportionment. In this paper, a C-based source apportionment study was carried out on samples collected during winter 2021 at an urban background site in the Po Valley, one of the main pollution hot-spot areas in Europe. The samples were prepared using MISSMARPLE (MIlan Small-SaMple Automated Radiocarbon Preparation LinE for atmospheric aerosol), a recently developed sample preparation line for C measurements on atmospheric aerosol carbon fractions, specifically targeting small samples (about 50 μgC).
View Article and Find Full Text PDFSci Total Environ
December 2024
Department of Public Health Sciences, University of Rochester, School of Medicine and Dentistry, Rochester, NY, USA; Institute for a Sustainable Environment, Clarkson University, Potsdam, NY, USA.
Advanced receptor models can leverage the information derived from optical and chemical variables as input by a variety of instruments at different time resolutions to extract the source specific absorption Ångström exponent (AAE) from aerosol absorption. The multilinear engine (ME-2), a Positive Matrix Factorization (PMF) solver, serves as a proficient tool for performing such analyses, thereby overcoming the constraints imposed by the assumptions in current optical source apportionment methods such as the Aethalometer approach since the use of a-priori AAE values introduces additional uncertainty into the results of optical methods. Comprehensive PM chemical speciation datasets, and aerosol absorption coefficients (b, λ) at seven wavelengths measured by an Aethalometer (AE33), were used in multi-time source apportionment (MT-PMF).
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