0000000000416893

AUTHOR

Chunshui Lin

showing 7 related works from this author

Supplementary material to "Measurement report: Large contribution of biomass burning and aqueous-phase processes to the wintertime secondary…

2022

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Measurement report of the change of PM2.5 composition during the COVID-19 lockdown in urban Xi'an: Enhanced secondary formation and oxidation

2021

Enhanced secondary aerosol formation was observed during the COVID-19 lockdown in Xi'an, especially for polluted episodes. More oxidized‑oxygenated organic aerosol (MO-OOA) and sulfate showed the dominant enhancements, especially in large particle-mode. Meanwhile, relative humidity (RH) showed a positive promotion on the formation of sulfate and MO-OOA during the lockdown, but had no obvious correlation with less oxidized‑oxygenated organic aerosol (LO-OOA) or nitrate. Organosulfurs (OS) displayed a higher contribution (~58%) than inorganic sulfate to total sulfate enhancement in the polluted episode during the lockdown. Although the total nitrate (TN) decreased during the lockdown ascribin…

Environmental Engineering010504 meteorology & atmospheric sciencesCoronavirus disease 2019 (COVID-19)Chemistry010501 environmental sciences01 natural sciencesPollutionInorganic sulfateAerosolchemistry.chemical_compoundNitrateEnvironmental chemistryEnvironmental ChemistryHaze pollutionRelative humidityComposition (visual arts)SulfateWaste Management and Disposal0105 earth and related environmental sciencesScience of The Total Environment
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Brown Carbon Aerosol in Urban Xi'an, Northwest China: The Composition and Light Absorption Properties.

2018

Light-absorbing organic carbon (i.e., brown carbon or BrC) in the atmospheric aerosol has significant contribution to light absorption and radiative forcing. However, the link between BrC optical properties and chemical composition remains poorly constrained. In this study, we combine spectrophotometric measurements and chemical analyses of BrC samples collected from July 2008 to June 2009 in urban Xi'an, Northwest China. Elevated BrC was observed in winter (5 times higher than in summer), largely due to increased emissions from wintertime domestic biomass burning. The light absorption coefficient of methanol-soluble BrC at 365 nm (on average approximately twice that of water-soluble BrC) w…

Angstrom exponentChina010504 meteorology & atmospheric sciencesSOLUBLE ORGANIC-CARBONchemistry.chemical_element010501 environmental sciences01 natural sciencesEnvironmental ChemistryWATERPolycyclic Aromatic HydrocarbonsAbsorption (electromagnetic radiation)Chemical composition0105 earth and related environmental sciencesTotal organic carbonAerosolsAir PollutantsANGSTROM EXPONENTGeneral ChemistryCarbon blackOPTICAL-PROPERTIESRadiative forcingCarbonAerosolSOLAR-RADIATIONchemistrySOURCE APPORTIONMENTEnvironmental chemistryBLACK CARBONEnvironmental scienceFINE PARTICULATE MATTERSOUTHEASTERN UNITED-STATESCarbonBIOMASS-BURNING EMISSIONSEnvironmental sciencetechnology
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Effects of NH3 and alkaline metals on the formation of particulate sulfate and nitrate in wintertime Beijing

2020

Sulfate and nitrate from secondary reactions remain as the most abundant inorganic species in atmospheric particle matter (PM). Their formation is initiated by oxidation (either in gas phase or particle phase), followed by neutralization reaction primarily by NH3, or by other alkaline species such as alkaline metal ions if available. The different roles of NH3 and metal ions in neutralizing H2SO4 or HNO3, however, are seldom investigated. Here we conducted semi-continuous measurements of SO4 2−, NO3 −, NH4 +, and their gaseous precursors, as well as alkaline metal ions (Na+, K+, Ca2+, and Mg2+) in wintertime Beijing. Analysis of aerosol acidity (estimated from a thermodynamic model) indicat…

inorganic chemicalsEnvironmental Engineering010504 meteorology & atmospheric sciencesMetal ions in aqueous solutionEVOLUTION PROCESSESSEASONAL-VARIATIONchemistry.chemical_element010501 environmental sciencesNitrate01 natural scienceschemistry.chemical_compoundAmmoniaNitrateEnvironmental ChemistryWATERSulfateWaste Management and Disposal0105 earth and related environmental sciencesSECONDARY INORGANIC AEROSOLAMMONIAChemistryACIDIC GASESMASS-SPECTROMETRYParticulatesAlkali metalPollutionSulfurNitrogenSulfatePEARL RIVER-DELTASULFUR-DIOXIDEEnvironmental chemistryHAZE EVENTSAlkaline metalsThe Science of the Total Environment
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Determination of n-alkanes, PAHs and hopanes in atmospheric aerosol: evaluation and comparison of thermal desorption GC-MS and solvent extraction GC-…

2019

Organic aerosol (OA) constitutes a large fraction of fine particulate matter (PM) in the urban air. However, the chemical nature and sources of OA are not well constrained. Quantitative analysis of OA is essential for understanding the sources and atmospheric evolution of fine PM, which requires accurate quantification of some organic compounds (e.g., markers). In this study, two analytical approaches, i.e., thermal desorption (TD) gas chromatography-mass spectrometry (GC-MS) and solvent extract (SE) GC-MS were evaluated for the determination of n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and hopanes in ambient aerosol. For the SE approach, the recovery obtained is 89.3–101.5&…

Detection limitEnvironmental chemistryThermal desorptionEnvironmental scienceCoal combustion productsFraction (chemistry)Repeatability010501 environmental sciencesGas chromatography–mass spectrometryMass spectrometry01 natural sciences0105 earth and related environmental sciencesAerosol
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Contrasting sources and processes of particulate species in haze days with low and high relative humidity in winter time Beijing

2020

Abstract. Although there are many studies of particulate matter (PM) pollution in Beijing, the sources and processes of secondary PM species during haze periods remain unclear. Limited studies have investigated the PM formation in highly-polluted environments under low and high relative humidity (RH) conditions. Herein, we present a systematic comparison of species in submicron particles (PM1) in wintertime Beijing (29 December 2014 to 28 February 2015) for clean periods and pollution periods under low and high RH conditions. PM1 species were measured with an aerosol chemical species monitor (ACSM) and an aethalometer. Sources and processes for organic aerosol (OA) were resolved by positive…

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Organosulfates in atmospheric aerosol: synthesis and quantitative analysis of pm<sub>2.5</sub> from xi'an, northwestern c…

2018

Abstract. The sources, formation mechanism and amount of organosulfates (OS) in atmospheric aerosol are not yet well understood, partly due to the lack of authentic standards for quantification. In this study, we report an improved robust procedure for the synthesis of organosulfates with different functional groups. Nine authentic organosulfate standards were synthesized and four standards (benzyl sulfate, phenyl sulfate, glycolic acid sulfate, and hydroxyacetone sulfate) were used to quantify their ambient concentrations. The authentic standards and ambient aerosol samples were analyzed using an optimized ultra performance liquid chromatography–electrospray ionization-tandem mass spectrom…

Atmospheric Scienceparticulate organosulfates010504 meteorology & atmospheric sciences010501 environmental sciences01 natural scienceschemistry.chemical_compoundambient aerosolhaze eventsSulfateGlycolic acid0105 earth and related environmental sciencesDetection limitTotal organic carbondicarboxylic-acidsHydroxyacetonemass-spectrometryAerosolaromatic organosulfateschemistryEnvironmental chemistrychemical-compositionarctic aerosolsisopreneQuantitative analysis (chemistry)secondary organic aerosolOrganosulfate
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