0000000000206758

AUTHOR

Junji Cao

showing 9 related works from this author

PM2.5-bound oxygenated PAHs, nitro-PAHs and parent-PAHs from the atmosphere of a Chinese megacity: Seasonal variation, sources and cancer risk assess…

2014

Polycyclic aromatic compounds (PACs) in air particulate matter contribute considerably to the health risk of air pollution. The objectives of this study were to assess the occurrence and variation in concentrations and sources of PM2.5 bound PACs [Oxygenated PAHs (OPAHs) nitro PAHs and parent PAHs] sampled from the atmosphere of a typical Chinese megacity (Xi'an) to study the influence of meteorological conditions on PACs and to estimate the lifetime excess cancer risk to the residents of Xi'an (from inhalation of PM2.5 bound PACs). To achieve these objectives we sampled 24 h PM2.5 aerosols (once in every 6days from 5 July 2008 to 8 August 2009) from the atmosphere of Xi'an and measured the…

Environmental Engineering010504 meteorology & atmospheric sciencesAtmospheric pressureOpahbiologyAir pollution010501 environmental sciencesParticulatesSeasonalitybiology.organism_classificationmedicine.disease_causemedicine.disease01 natural sciencesPollutionMegacity13. Climate actionCancer risk assessmentEnvironmental chemistry11. SustainabilitymedicineEnvironmental ChemistryEnvironmental scienceCancer riskWaste Management and Disposal0105 earth and related environmental sciencesScience of The Total Environment
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Determination of alkylamines in atmospheric aerosol particles: a comparison of gas chromatography–mass spectrometry and ion chromatography approaches

2014

Abstract. In recent years low molecular weight alkylamines have been recognized to play an important role in particle formation and growth in the lower atmosphere. However, major uncertainties are associated with their atmospheric processes, sources and sinks, mostly due to the lack of ambient measurements and the difficulties in accurate quantification of alkylamines at trace level. In this study, we present the evaluation and optimization of two analytical approaches, i.e., gas chromatography–mass spectrometry (GC-MS) and ion chromatography (IC), for the determination of alkylamines in aerosol particles. Alkylamines were converted to carbamates through derivatization with isobutyl chlorof…

Atmospheric ScienceIon chromatographyAnalytical chemistryMass spectrometrychemistryammoniachemistry.chemical_compoundColumn chromatographyaliphatic-aminesderivatizationlcsh:TA170-171phaseDerivatizationDetection limitChromatographyChemistrylcsh:TA715-787lcsh:Earthwork. Foundationsaromatic-aminesAerosollcsh:Environmental engineering13. Climate actionReagentnanoparticleschemical-compositionGas chromatography–mass spectrometryseasonal-variationsecondary organic aerosol
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UHPLC-Orbitrap mass spectrometric characterization of organic aerosol from a central European city (Mainz, Germany) and a Chinese megacity (Beijing)

2018

Abstract Fine urban aerosol particles with aerodynamic equivalent dimeter ≤2.5 μm (PM2.5) were collected in Mainz (a city within the Rhine-Main area, the third largest metropolitan region in Germany) and Beijing (Chinese megacity). A solvent mixture of acetonitrile-water was used to extract the organic aerosol fraction (OA) from the particle samples. The extracts were analyzed by an ultrahigh resolution mass spectrometer (UHRMS) Orbitrap coupled with ultra-high-performance liquid chromatography (UHPLC) both in the negative and positive ion mode. The number of compounds observed in Beijing is a factor of 2–10 higher compared to Mainz. The clear differences on chemical composition of OA in th…

chemistry.chemical_classificationAtmospheric ScienceDegree of unsaturation010504 meteorology & atmospheric sciencesPolycyclic aromatic hydrocarbonAromaticity010501 environmental sciencesOrbitrapMass spectrometry01 natural scienceslaw.inventionAerosolchemistryBeijinglawEnvironmental chemistryChemical composition0105 earth and related environmental sciencesGeneral Environmental ScienceAtmospheric Environment
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Severe Pollution in China Amplified by Atmospheric Moisture

2017

AbstractIn recent years, severe haze events often occurred in China, causing serious environmental problems. The mechanisms responsible for the haze formation, however, are still not well understood, hindering the forecast and mitigation of haze pollution. Our study of the 2012–13 winter haze events in Beijing shows that atmospheric water vapour plays a critical role in enhancing the heavy haze events. Under weak solar radiation and stagnant moist meteorological conditions in winter, air pollutants and water vapour accumulate in a shallow planetary boundary layer (PBL). A positive feedback cycle is triggered resulting in the formation of heavy haze: (1) the dispersal of water vapour is cons…

Haze010504 meteorology & atmospheric sciencesPlanetary boundary layerIMPACTlcsh:MedicineAEROSOL OPTICAL-PROPERTIES010501 environmental sciencesXINKENAtmospheric sciences01 natural sciencesArticlePollution in ChinaPLANETARY BOUNDARY-LAYERPARTICLESRelative humiditylcsh:ScienceHAZE0105 earth and related environmental sciencesMultidisciplinaryAtmospheric moistureAIRlcsh:RParticulatesPEARL RIVER-DELTAAerosolCLIMATEMODEL13. Climate actionEnvironmental sciencelcsh:QWater vaporScientific Reports
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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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