0000000000315942

AUTHOR

Yong Jie Li

showing 7 related works from this author

Measurement report: PM<sub>2.5</sub>-bound nitrated aromatic compounds in Xi'an, Northwest China – seasonal variations an…

2021

Abstract. Nitrated aromatic compounds (NACs) are a group of key chromophores for brown carbon (light-absorbing organic carbon, i.e., BrC) aerosol, which affects radiative forcing. The chemical composition and sources of NACs and their contributions to BrC absorption, however, are still not well understood. In this study, PM 2.5 -bound NACs in Xi'an, Northwest China, were investigated for 112 daily PM 2.5 filter samples from 2015 to 2016. Both the total concentrations and contributions from individual species of NACs show distinct seasonal variations. The seasonally averaged concentrations of NACs are 2.1 (spring), 1.1 (summer), 12.9 (fall), and 56 ng m −3 (winter). Thereinto, 4-nitrophenol …

Total organic carbonAtmospheric Science010504 meteorology & atmospheric sciencesChemistryCoal combustion productschemistry.chemical_element010501 environmental sciencesRadiative forcing01 natural sciencesAerosolEnvironmental chemistryComposition (visual arts)Absorption (electromagnetic radiation)Chemical compositionCarbon0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Water-Insoluble Organics Dominate Brown Carbon in Wintertime Urban Aerosol of China: Chemical Characteristics and Optical Properties.

2020

The chromophores responsible for light absorption in atmospheric brown carbon (BrC) are not well characterized, which hinders our understanding of BrC chemistry, the links with optical properties, and accurate model representations of BrC to global climate and atmospheric oxidative capacity. In this study, the light absorption properties and chromophore composition of three BrC fractions of different polarities were characterized for urban aerosol collected in Xi'an and Beijing in winter 2013-2014. These three BrC fractions show large differences in light absorption and chromophore composition, but the chromophores responsible for light absorption are similar in Xi'an and Beijing. Water-ins…

AerosolsChinaOpahbiologyChemistryWaterAromaticityGeneral Chemistry010501 environmental sciencesWater insolubleChromophorebiology.organism_classification01 natural sciencesCarbonAerosolEnvironmental chemistryBeijingEnvironmental ChemistryComposition (visual arts)Absorption (electromagnetic radiation)Brown carbon0105 earth and related environmental sciencesEnvironmental MonitoringEnvironmental sciencetechnology
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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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One-year characterization of organic aerosol markers in urban Beijing: Seasonal variation and spatiotemporal comparison

2020

Abstract Organic aerosol (OA) is a major component of fine particulate matter (PM); however, only 10%–30% of OA have been identified as individual compounds, and some are used as markers to trace the sources and formation mechanisms of OA. The temporal and spatial coverage of these OA markers nonetheless remain inadequately characterized. This study presents a year-long measurement of 92 organic markers in PM2.5 samples collected at an urban site in Beijing from 2014 to 2015. Saccharides were the most abundant (340.1 ng m−3) species detected, followed by phthalic acids (283.4 ng m−3). In summer, high proportions (8%–24%) of phthalic acids, n-alkanes, fatty acids, and n-alcohols indicate dom…

PollutionEnvironmental Engineering010504 meteorology & atmospheric sciencesmedia_common.quotation_subjectBiogenic emissionsAir pollutionCoal combustion products010501 environmental sciencesSeasonalitymedicine.disease_causemedicine.disease01 natural sciencesPollutionHopanoidsAerosolBeijingEnvironmental chemistrymedicineEnvironmental ChemistryEnvironmental scienceWaste Management and Disposal0105 earth and related environmental sciencesmedia_commonScience 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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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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