|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Chemical characteristics of PM_(2.5) during a typical haze episode in Guangzhou显示文摘The chemical characteristics(water-soluble ions and carbonaceous species) of PM2.5 in Guangzhou were measured during a typical haze episode.Most of the chemical species in PM2.5 showed significant difference between normal and haze days.The highest contributors to PM2.5 were organic carbon(OC),nitrate,and sulfate in haze days and were OC,sulfate,and elemental carbon(EC) in normal days.The concentrations of secondary species such as,NO3-,SO42-,and NH4+ in haze days were 6.5,3.9,and 5.3 times higher than those in normal days,respectively,while primary species(EC,Ca2+,K+) show similar increase from normal to haze days by a factor about 2.2-2.4.OC/EC ratio ranged from 2.8 to 6.2 with an average of 4.7 and the estimation on a minimum OC/EC ratio showed that SOC(secondary organic carbon) accounted more than 36.6% for the total organic carbon in haze days.The significantly increase in the secondary species(SOC,NO3-,SO42-,and NH4+),especially in NO3-,caused the worst air quality in this region.Simultaneously,the result illustrated that the serious air pollution in haze episodes was strongly correlated with the meteorological conditions.During the sampling periods,air pollution and visibility had a good relationship with the air mass transport distance;the shorter air masses transport distance,the worse air quality and visibility in Guangzhou,indicating the strong domination of local sources contributing to haze formation.High concentration of the secondary aerosol in haze episodes was likely due to the higher oxidation rates of sulfur and nitrogen species. | TAN Jihua DUAN Jingchun HE Kebin MA Yongliang DUAN Fengkui CHEN Yuan FU Jiamo | 2009 | Journal of Environmental Sciences2009，21，6： | 71 |
| 2 | Size distributions and sources of elements in particulate matter at curbside,urban and rural sites in Beijing显示文摘Size distributions of 29 elements in aerosols collected at urban,rural and curbside sites in Beijing were studied.High levels of Mn,Ni,As,Cd and Pb indicate the pollution of toxic heavy metals cannot be neglected in Beijing.Principal component analysis (PCA) indicates 4 sources of combustion emission,crust related sources,traffic related sources and volatile species from coal combustion.The elements can be roughly divided into 3 groups by size distribution and enrichment factors method (EFs).Group 1 elements are crust related and mainly found within coarse mode including Al,Mg,Ca,Sc,Ti,Fe,Sr,Zr and Ba;Group 2 elements are fossil fuel related and mostly concentrated in accumulation mode including S,As,Se,Ag,Cd,Tl and Pb;Group 3 elements are multi-source related and show multi-mode distribution including Be,Na,K,Cr,Mn,Co,Ni,Cu,Zn,Ga,Mo,Sn and Sb.The EFs of Be,S,Cr,Co,Ni,Cu,Ga,Se,Mo,Ag,Cd,Sb,Tl and Pb show higher values in winter than in summer indicating sources of coal combustion for heating in winter.The abundance of Cu and Sb in coarse mode is about 2-6 times higher at curbside site than at urban site indicating their traffic sources.Coal burning may be the major source of Pb in Beijing since the phase out of leaded gasoline,as the EFs of Pb are comparable at both urban and curbside sites,and about two times higher in winter than that in summer. | Jingchun Duan Jihua Tan Shulan Wang Jimin Hao Fahe Chai | 2012 | Journal of Environmental Sciences2012，24，1： | 67 |
| 3 | Size distribution, characteristics and sources of heavy metals in haze episod in Beijing显示文摘Size segragated samples were collected during high polluted winter haze days in 2006 in Beijing, China. Twenty nine elements and 9 water soluble ions were determined. Heavy metals of Zn, Pb, Mn, Cu, As, Cr, Ni, V and Cd were deeply studied considering their toxic efect on human being. Among these heavy metals, the levels of Mn, As and Cd exceeded the reference values of National Ambient Air Quality Standard(GB3095-2012) and guidelines of World Health Organization. By estimation, high percentage of atmospheric heavy metals in PM2.5indicates it is an efective way to control atmospheric heavy metals by PM2.5controlling. Pb, Cd, and Zn show mostly in accumulation mode, V, Mn and Cu exist mostly in both coarse and accumulation modes, and Ni and Cr exist in all of the three modes. Considering the health efect, the breakthrough rates of atmospheric heavy metals into pulmonary alveoli are: Pb(62.1%) > As(58.1%) > Cd(57.9%) > Zn(57.7%) > Cu(55.8%) > Ni(53.5%) > Cr(52.2%) > Mn(49.2%) > V(43.5%). Positive matrix factorization method was applied for source apportionment of studied heavy metals combined with some marker elements and ions such as K, As, SO4 2 etc., and four factors(dust, vehicle, aged and transportation, unknown) are identified and the size distribution contribution of them to atmospheric heavy metals are discussed. | Jingchun Duan Jihua Tan Jiming Hao Fahe Chai | 2014 | Journal of Environmental Sciences2014，26，1： | 26 |
| 4 | Gas-to-particle conversion of atmospheric ammonia and sampling artifacts of ammonium in spring of Beijing显示文摘PM2.5 and gaseous pollutants(SO2,HNO2,HNO3,HCl,and NH3) were simultaneously collected by Partisol- Model 2300 Sequential Speciation Sampler with denuder-filter pack system in the spring of 2013 in Beijing.Water-soluble inorganic ions and gaseous pollutants were measured by Ion Chromatography.Results showed that the concentrations of NH3,NH+ 4and PM2.5 had similar diurnal variation trends and their concentrations were higher at night than in daytime.The results of gas-to-particle conversion revealed that [NH3]:[NH+4] ratio was usually higher than 1; however,it was less than 1 and the concentration of NH+4 increased significantly during the haze episode,indicating that NH3 played an important role in the formation of fine particle.Research on the sampling artifacts suggested that the volatilization loss of NH+4 was prevalent in the traditional single filter-based sampling.The excess loss of HNO3 and HCl resulted from ammonium-poor aerosols and semivolatile inorganic species had severe losses in the clean day,whereas the mass of NH+ 4was usually overestimated during the single filter-based sampling due to the positive artifacts.Correlation analysis was used to evaluate the influence of meteorological conditions on the volatilization loss of NH+4.It was found that the average relative humidity and temperature had great effects on the loss of NH+4.The loss of NH+4 was significantly under high temperature and low humidity,and tended to increase with the increasing of absorption of gaseous pollutants by denuder.The total mass of volatile loss of NH+4,NO- 3and Cl- could not be ignored and its maximum value was 12.17 μg m-3.Therefore it is important to compensate sampling artifacts for semivolatile inorganic species. | WEI LianFang DUAN JingChun TAN JiHua MA YongLiang HE KeBin WANG ShuXiao HUANG XiaoFeng ZHANG YuanXun | 2015 | Science China Earth Sciences2015，58，3： | 11 |
| 5 | Sources, evolution and impacts of EC and OC in snow on sea ice: a measurement study in Barrow, Alaska显示文摘Based on the field measurements in Barrow, Alaska within the period of April-May 2015, we investigate the sources and variations of elemental carbon(EC) and organic carbon(OC) in the surface layer of snowpack on sea ice, and estimate their effects on the sea ice albedo. Results show that the snow OC in Barrow are from natural sources(e.g. terrestrial higher plants and micro-organisms) mainly, as well as biomass burning(e.g. forest fires and straw combustion) as an important part. Both EC and OC can accumulate at the snow surface with snow melt. The variations in EC and OC and liquid water content in the snow layer are well consistent during the snow-melting period. A higher rate of snow melt implied a more efficient enrichment of EC and OC. In the last phase of snow melt, the concentration increased to a maximum of 16.2 ng/g for EC and 128 ng/g for OC, which is ~10 times larger than those before snow melt onset. Except for the dominant influence of melt amplification mechanism, the variation in concentrations of EC and OC could be disturbed by the air temperature fluctuation and snowfall. Our study indicates that the lightabsorbing impurities contributed 1.6%-5.1% to the reduction in sea ice albedo with melt during the measurement period. The significant period oflight-absorbing impurities influencing on sea ice albedo begins with the rapid melting of overlying snow and ends before the melt ponds formed widely, which lasted for about 10 days in Barrow, 2015. | Tingfeng Dou Cunde Xiao Zhiheng Du J. J. Schauer Hong Ren Baozhu Ge Aihong Xie Jihua Tan Pingqing Fu Yuanxun Zhang | 2017 | Science Bulletin2017，62，22： | 6 |
| 6 | Source apportionment of VOCs in a typical medium-sized city in North China Plain and implications on control policy显示文摘Characteristics of atmospheric VOCs(volatile organic compounds) have been extensively studied in megacities in China, however, they are scarcely investigated in medium/smallsized cities in North China Plain(NCP).A comprehensive research on possible sources of VOCs was conducted in a medium-sized city of NCP, from May to September 2019.A total of 143 canister samples of 8 sites in Xuchang city were collected, and 57 VOC species were detected.The average VOC concentrations were 42.6 ± 31.6 μg/m3, with 53.7 ± 31.0 μg/m3 and 32.1 ± 27.8 μg/m^(3), in the morning and afternoon, respectively.Alkenes and aromatics contributed 80% of the total ozone formation potential(OFP).Aromatics accounted for more than 95% of secondary organic aerosol potential(SOAP).VOCs were dominated by the local emission with significant transport from the southeast direction.PMF analysis extracted 6 sources, which were combustion(33.1%), LPG usage(19.3%), vehicular exhaust & fuel evaporation(15.8%), solvent usage(15.2%), industrial(9.11%) and biogenic(7.51%), respectively and they contributed 33.4%, 17.6%, 12.9%, 18.6%, 9.28% and 8.22% to the OFP, respectively.Combustion and LPG usage were the dominant VOC sources;and combustion, solvent usage and LPG usage were the main sources of OFP in Xuchang city, which were different to megacities in China with a high contribution from vehicular exhaust, solvent usage and industry,suggesting specific control strategies on VOCs need to be implemented in medium-sized city such as Xuchang city. | Juanjuan Qin Xiaobo Wang Yanrong Yang Yuanyuan Qin Shaoxuan Shi Peihua Xu Rongzhi Chen Xueming Zhou Jihua Tan Xinming Wang | 2021 | Journal of Environmental Sciences2021，33，9： | 6 |
| 7 | Excitation-emission matrix (EEM) fluorescence spectroscopy for characterization of organic matter in membrane bioreactors: Principles, methods and applications显示文摘The membrane bioreactor(MBR)technology is a rising star for wastewater treatment.The pollutant elimination and membrane fouling performances of MBRs are essentially related to the dissolved organic matter(DOM)in the system.Three-dimensional excitation-emission matrix(3D-EEM)fluorescence spectroscopy,a powerful tool for the rapid and sensitive characterization of DOM,has been extensively applied in MBR studies;however,only a limited portion of the EEM fingerprinting information was utilized.This paper revisits the principles and methods of fluorescence EEM,and reviews the recent progress in applying EEM to characterize DOM in MBR studies.We systematically introduced the information extracted from EEM by considering the fluorescence peak location/intensity,wavelength regional distribution,and spectral deconvolution(giving fluorescent component loadings/scores),and discussed how to use the information to interpret the chemical compositions,physiochemical properties,biological activities,membrane retention/fouling behaviors,and migration/transformation fates of DOM in MBR systems.In addition to conventional EEM indicators,novel fluorescent parameters are summarized for potential use,including quantum yield,Stokes shift,excited energy state,and fluorescence lifetime.The current limitations of EEM-based DOM characterization are also discussed,with possible measures proposed to improve applications in MBR monitoring. | Jinlan Yu Kang Xiao Wenchao Xue Yue-xiao Shen Jihua Tan Shuai Liang Yanfen Wang Xia Huang | 2020 | Frontiers of Environmental Science & Engineering2020，14，2： | 3 |
| 8 | Concentration, sources and ozone formation potential of volatile organic compounds (VOCs) during ozone episode in Beijing显示文摘 | Jingchun Duan Jihua Tan Liu Yang Shan Wu Jimin Hao | 2007 | Atmospheric Research2007，，1： | 3 |
| 9 | Concentration, sources and ozone formation potential of volatile organic compounds (VOCs) during ozone episode in Beijing显示文摘 | Jingchun Duan Jihua Tan Liu Yang Shan Wu Jimin Hao | 2007 | Atmospheric Research2007，，1： | 2 |
| 10 | Roadside, Urban, and Rural comparison of size distribution characteristics of PAHs and carbonaceous components of Beijing, China显示文摘 | Jingchun Duan Jihua Tan Shulan Wang Fahe Chai Kebin He Jimin Hao | 2013 | Journal of Atmospheric Chemistry2013，，4： | 2 |
| 11 | Sources and characteristics of carbonaceous aerosol in two largest cities in Pearl River Delta Region, China显示文摘 | Jingchun Duan Jihua Tan Dingxi Cheng Xinhui Bi Wenjing Deng Guoying Sheng Jiamo Fu M.H. Wong | 2006 | Atmospheric Environment2006，，14： | 2 |
| 12 | Seasonal variation on size distribution and concentration of PAHs in Guangzhou city, China 显示文摘 | Duan Jingchun Bi Xinhui Tan Jihua | 2007 | Chemosphere2007，67，3： | 1 |
| 13 | Roadside, Urban, and Rural comparison of size distribution characteristics of PAHs and carbonaceous components of Beijing, China显示文摘 | Jingchun Duan Jihua Tan Shulan Wang Fahe Chai Kebin He Jimin Hao | 2013 | Journal of Atmospheric Chemistry2013，，4： | 1 |
| 14 | Chemicalcharacteristics of haze during summer and winter in Guangzhou显示文摘 | TAN Jihua DUAN Jingchun CHEN Duohong | 2009 | Atmos Res2009，94，2： | 1 |
| 15 | Sources and characteristics of carbonaceous aerosol in two largest cities in Pearl River Delta Region, China显示文摘 | Jingchun Duan Jihua Tan Dingxi Cheng Xinhui Bi Wenjing Deng Guoying Sheng Jiamo Fu M.H. Wong | 2006 | Atmospheric Environment2006，，14： | 1 |
| 16 | DGPS-based vehicle-to-vehicle coopera- tive collision warning: engineering feasibility viewpoints 显示文摘 | Tan Huanshue Huang Jihua | 2006 | IEEE Xrans on Intelligent Transportation Systems2006，7，4： | 1 |
| 17 | Characteristics of atmospheric non-methane hydrocarbons during high PM 10 episodes and normal days in Foshan, China显示文摘 | Songjun Guo Jihua Tan Yongliang Ma Fumo Yang Yongchan Yu Jiewen Wang | 2011 | Atmospheric Research2011，，3： | 1 |
| 18 | Chemical characteristics of haze during summer and winter in Guangzhou显示文摘 | Tan Jihua Duan Jingchun Chen Duohong | 2009 | Atmospheric Research2009，94，2： | 1 |
| 19 | Concentra tion,sources and ozone formation potential of volatile organic compounds (VOCs) during ozone episode in Beiiing显示文摘 | DUAN Jingchun TAN Jihua LIU Yang | 2008 | Atmospheric Research2008，88，1： | 1 |
| 20 | Seasonal varia- tion of particulate polyeyclic aromatic hydrocarbons associated with PM10 in Guangzhou, China显示文摘 | TAN Jihua BI Xinhui DUAN Jingeun | 2006 | Atmospheric Research2006，80，4： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员