To investigate the secondary formation and pollution sources of atmospheric particles in urban Beijing,PM2.5 and its chemical components were collected and determined by URG-9000 D ambient ion monitor(AIM) from March ...To investigate the secondary formation and pollution sources of atmospheric particles in urban Beijing,PM2.5 and its chemical components were collected and determined by URG-9000 D ambient ion monitor(AIM) from March 2016 to January 2017.Among water-soluble ions(WSIs), NO3-,SO42- and NH4+(SNA) had the largest proportion(77.8%) with the total concentration of 23.8 μg/m3.Moreover,as fine particle pollution worsened,the NO3-,SO4<sup>2- and NH4+ concentrations increased basically,which revealed that secondary aerosols were the main cause of particle pollution in Beijing.Furthermore,the particle neutralization ratio(1.1),the ammonia to sulfate molar ratio(3.4) and the nitrate to sulfate molar ratio(2.2) showed that secondary aerosols are under ammonium-rich conditions with the main chemical forms of NH4 NO3 and(NH4)2 SO4,and vehicle emission could be the main anthropogenic source of secondary aerosols in Beijing.Source analysis further indicated that secondary aerosols,solid fuel combustion,dust and marine aerosol were the principal pollution sources of PM2.5,accounting for about 46.1%,22.4% and 13.0%,respectively,and Inner Mongolia and Hebei Provinces could be considered as the main potential sources of PM2.5 in urban Beijing.In addition,secondary formation process was closely related with gaseous precursor emission amounts(SO2,NO2,NH3 and HONG),atmospheric ozone concentration(O3),meteorological conditions(temperature and relative humidity) and particle components.Sensitive analysis of the thermodynamic equilibrium model(ISORROPIA Ⅱ)revealed that controlling total nitrate(TN) is the effective measure to mitigate fine particle pollution in Beijing.展开更多
To investigate particle characteristics and find an effective measure to control severe particle pollution,year-round observation of size-segregated inorganic aerosols was conducted in Beijing fromJanuary to December,...To investigate particle characteristics and find an effective measure to control severe particle pollution,year-round observation of size-segregated inorganic aerosols was conducted in Beijing fromJanuary to December,2016.The sampled atmospheric particles all presented bimodal size distribution at four pollution levels(clear,slight pollution,moderate pollution and severe pollution),and peak values appeared at the size range of 0.7-2.1μmand>9.0μm,respectively.As dominant particle compositions,NO_(3)^(-),SO_(4)^(2-),and NH_(4)^(+)in four pollution levels all showed significant peaks in fine mode,especially at the size range of 1.1-2.1μm.Secondary inorganic aerosols accounted for about 67.6%(36.3%(secondary sulfates)+31.3%(secondary nitrates))of the total sources of fine particles in urban Beijing.Severe pollution of fine particles was mainly caused by the air masses transported from nearby western and southern areas,which are industrial and densely populated region,respectively.Sensitivity tests further revealed that the control measures focusing on ammonium emission reduction was the most effective for particle pollution mitigation,and fine particles all showed nonlinear responses after reducing ammonium,nitrate,and sulfate concentrations,with the fitting curves of y=-120.8x-306.1x^(2)+290.2x^(3),y=-43.5x-67.8x^(2),and y=-25.8x-110.4x^(2)+7.6x^(3),respectively(y and x present fine particle mass variation(μg/m3)and concentration reduction ratio(CRR)/100(dimensionless)).Overall,our study presents useful information for understanding the characteristics of atmospheric inorganic aerosols in urban Beijing,as well as offers policy makers with effective measure for mitigating particle pollution.展开更多
In the suburbs of Kitakyushu,Japan,the inorganic aerosol mass concentration(IAM)was about 32.7μg/m^(3),with the aerosol pH of 3.3.To study the thermodynamics of aerosol when its individual components'concentratio...In the suburbs of Kitakyushu,Japan,the inorganic aerosol mass concentration(IAM)was about 32.7μg/m^(3),with the aerosol pH of 3.3.To study the thermodynamics of aerosol when its individual components'concentration is reduced,sensitive tests were performed using the ISORROPIAⅡmodel,in which the seven control species—TNaCl,TNH_(4)^(+),TSO_(4)^(2-),TNO_(3)^(-),TMg^(2+),TK^(+),and TCa^(2+)—were taken into account.IAM and inorganic aerosol pH after reducing TNaCl,TNO_(3)^(-),TMg^(2+),TK^(+),and TCa^(2+)responded linearly(0%≤concentration reduction ratio(CRR)≤100%,with the exception of 100%in TNaCl);the nonlinear variations of these two parameters could be observed by controlling TNH_(4)^(+)and TSO_(4)^(2-).Unexpected aerosol behavior occurred at 100%reduction of TNaCl,which was caused by the sudden increase of NO_(3)^(-),NH_(4)^(+),and aerosol liquid water content(ALWC);the increase of IAM was also observed after controlling TSO_(4)^(2-)(60%≤CRR≤100%)and TCa^(2+)(0%≤CRR≤100%),which was mainly related to the variation of ALWC driven by the response of CaSO_(4).Multiple regression analysis showed that ALWC was statistically and strongly related to the variations of NO_(3)^(-),Cl-,SO_(4)^(2-),HSO_(4)^(-),HNO_(3),and NH_(3)(P<0.05),with regression coefficients of 1.68,5.23,1.83,2.81,0.34,and 0.57,respectively.The highest coefficient(5.23)was found for Cl^(-),revealing that sea salts significantly influenced particle responses.Overall,this study comprehensively investigated aerosol characteristics and inner responses for the reduction of components,which is of great significance for a better understanding of atmospheric chemistry in Kitakyushu,Japan.展开更多
基金supported by the National Research Program for key issues in air pollution control(No.DQGG0304-05)the Fundamental Research Funds for Central Public Welfare Scientific Research Institutes of China(No.2016YSKY-025)+7 种基金the National Department Public Benefit Research Foundation(No.201109005)the National Natural Science Foundation of China(Nos.41205093,41305124,and 21976106)the Opening Project of Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention(No.FDLAP18005)the National Key Research and Development Program of Ministry of Science and Technology of China(No.2016YFE0112200)supported by Science Foundation of Shandong Jianzhu University(No.XNBS1824)Shandong Key Research and Development Program(No.2019GSF109064)the supports from the Co-Innovation Center for Green Building of Shandong Province(No.X18027Z)the Introduction and Cultivation Plan for Young Innovative Talents of Colleges and Universities by the Education Department of Shandong Province(Serial No.142,2019)
文摘To investigate the secondary formation and pollution sources of atmospheric particles in urban Beijing,PM2.5 and its chemical components were collected and determined by URG-9000 D ambient ion monitor(AIM) from March 2016 to January 2017.Among water-soluble ions(WSIs), NO3-,SO42- and NH4+(SNA) had the largest proportion(77.8%) with the total concentration of 23.8 μg/m3.Moreover,as fine particle pollution worsened,the NO3-,SO4<sup>2- and NH4+ concentrations increased basically,which revealed that secondary aerosols were the main cause of particle pollution in Beijing.Furthermore,the particle neutralization ratio(1.1),the ammonia to sulfate molar ratio(3.4) and the nitrate to sulfate molar ratio(2.2) showed that secondary aerosols are under ammonium-rich conditions with the main chemical forms of NH4 NO3 and(NH4)2 SO4,and vehicle emission could be the main anthropogenic source of secondary aerosols in Beijing.Source analysis further indicated that secondary aerosols,solid fuel combustion,dust and marine aerosol were the principal pollution sources of PM2.5,accounting for about 46.1%,22.4% and 13.0%,respectively,and Inner Mongolia and Hebei Provinces could be considered as the main potential sources of PM2.5 in urban Beijing.In addition,secondary formation process was closely related with gaseous precursor emission amounts(SO2,NO2,NH3 and HONG),atmospheric ozone concentration(O3),meteorological conditions(temperature and relative humidity) and particle components.Sensitive analysis of the thermodynamic equilibrium model(ISORROPIA Ⅱ)revealed that controlling total nitrate(TN) is the effective measure to mitigate fine particle pollution in Beijing.
基金supported by the Three-dimensional Comprehensive Observation Research Program for O3 and PM2.5 Compound Pollution in Key Areas in Summer 2021(No.DQGG2021101)the National Research Program for key issues in air pollution control(No.DQGG0304-05)+3 种基金and the National Natural Science Foundation of China(Nos.41205093,21976106,42075182)supported by the Opening Project of Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention(No.FDLAP19006)the CoInnovation Center for Green Building of Shandong Province(No.X18027Z)the Introduction and Cultivation Plan for Young Innovative Talents of Colleges and Universities by the Education Department of Shandong Province(No.142,2019)
文摘To investigate particle characteristics and find an effective measure to control severe particle pollution,year-round observation of size-segregated inorganic aerosols was conducted in Beijing fromJanuary to December,2016.The sampled atmospheric particles all presented bimodal size distribution at four pollution levels(clear,slight pollution,moderate pollution and severe pollution),and peak values appeared at the size range of 0.7-2.1μmand>9.0μm,respectively.As dominant particle compositions,NO_(3)^(-),SO_(4)^(2-),and NH_(4)^(+)in four pollution levels all showed significant peaks in fine mode,especially at the size range of 1.1-2.1μm.Secondary inorganic aerosols accounted for about 67.6%(36.3%(secondary sulfates)+31.3%(secondary nitrates))of the total sources of fine particles in urban Beijing.Severe pollution of fine particles was mainly caused by the air masses transported from nearby western and southern areas,which are industrial and densely populated region,respectively.Sensitivity tests further revealed that the control measures focusing on ammonium emission reduction was the most effective for particle pollution mitigation,and fine particles all showed nonlinear responses after reducing ammonium,nitrate,and sulfate concentrations,with the fitting curves of y=-120.8x-306.1x^(2)+290.2x^(3),y=-43.5x-67.8x^(2),and y=-25.8x-110.4x^(2)+7.6x^(3),respectively(y and x present fine particle mass variation(μg/m3)and concentration reduction ratio(CRR)/100(dimensionless)).Overall,our study presents useful information for understanding the characteristics of atmospheric inorganic aerosols in urban Beijing,as well as offers policy makers with effective measure for mitigating particle pollution.
文摘In the suburbs of Kitakyushu,Japan,the inorganic aerosol mass concentration(IAM)was about 32.7μg/m^(3),with the aerosol pH of 3.3.To study the thermodynamics of aerosol when its individual components'concentration is reduced,sensitive tests were performed using the ISORROPIAⅡmodel,in which the seven control species—TNaCl,TNH_(4)^(+),TSO_(4)^(2-),TNO_(3)^(-),TMg^(2+),TK^(+),and TCa^(2+)—were taken into account.IAM and inorganic aerosol pH after reducing TNaCl,TNO_(3)^(-),TMg^(2+),TK^(+),and TCa^(2+)responded linearly(0%≤concentration reduction ratio(CRR)≤100%,with the exception of 100%in TNaCl);the nonlinear variations of these two parameters could be observed by controlling TNH_(4)^(+)and TSO_(4)^(2-).Unexpected aerosol behavior occurred at 100%reduction of TNaCl,which was caused by the sudden increase of NO_(3)^(-),NH_(4)^(+),and aerosol liquid water content(ALWC);the increase of IAM was also observed after controlling TSO_(4)^(2-)(60%≤CRR≤100%)and TCa^(2+)(0%≤CRR≤100%),which was mainly related to the variation of ALWC driven by the response of CaSO_(4).Multiple regression analysis showed that ALWC was statistically and strongly related to the variations of NO_(3)^(-),Cl-,SO_(4)^(2-),HSO_(4)^(-),HNO_(3),and NH_(3)(P<0.05),with regression coefficients of 1.68,5.23,1.83,2.81,0.34,and 0.57,respectively.The highest coefficient(5.23)was found for Cl^(-),revealing that sea salts significantly influenced particle responses.Overall,this study comprehensively investigated aerosol characteristics and inner responses for the reduction of components,which is of great significance for a better understanding of atmospheric chemistry in Kitakyushu,Japan.
