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Quantification,morphology and source of humic acid,kerogen and black carbon in offshore marine sediments from Xiamen Gulf,China

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Journal of Environmental Sciences 2013年第2期25卷 287-294页

作者： Yanting chen Jinping Zhao Liqian Yin jinsheng chen Dongxing Yuan Key Laboratory of Urban Environment and Health Institute of Urban EnvironmentChinese Academy of Sciences Environmental Science and Engineering Department Huaqiao University Guangdong Environmental Monitoring Center State Key Laboratory of Marine Environmental Science Xiamen University

Three types of macromolecular organic matters （MOMs）, i.e. humic acid （HA）, kerogen＋black carbon （KB）, and black carbon （BC） were extracted from marine sediments of Xiamen Gulf, southeast of China. The chemical composition, morphological property and source of the three extractions were characterized by elemental analyzer/isotope ratio mass spectrometry （EA/IRMS） and scanning electron microscope （SEM）. The results showed that KB was the predominant fraction in MOMs, which accounted for 61.79%-89.15% of the total organic content （TOC）, while HA consisted less than 5%. The relative high contents of kerogen and BC, and low contents of HA in the samples indicated that anthropogenic input might be the major source of organic matter in marine sediments near the industrial regions. The characterization of SEM, not only revealed morphological properties of the three fractions, but also allowed a better understanding of the source of MOMs. The δ 13 C values of the three fractions suggested that materials from terrestrial C 3 plants were predominant. Furthermore, the anthropogenic activities, such as the discharge of sewage, coal and biomass combustion from industry nearby and agricultural practices within drainage basin of the Jiulong River, were remarkably contributed to the variations in δ 13 C values of MOMs in the offshore marine sediments.

关键词： macromolecular organic matters elemental analyzer/isotope ratio mass spectrometry scanning electron microscope offshore marine sediment Xiamen

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Characterization of polycyclic aromatic hydrocarbons and gas/particle partitioning in a coastal city, Xiamen, Southeast China

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Journal of Environmental Sciences 2010年第7期22卷 1014-1022页

作者： Jinping Zhao Fuwang Zhang jinsheng chen Ya Xu Key Laboratory of Urban Environment and Health Institute of Urban Environment Chinese Academy of Sciences Xiamen 361021 China Graduate School of Chinese Academy of Sciences Beijing 100049 China

An intensive sampling program had been undertaken in autumn （October, 2008） and winter （December, 2008 and January, 2009） at urban （Xiamen University and Xianyue residential area）, suburban （Institute of Urban Environment）, industrial area （Lulian Hotel） and background （Tingxi Reservoir） in Xiamen, Fujian Province, to characterize the atmospheric concentration and gas-particle phase partitioning of PAHs. The average concentration of total PAHs in winter was almost 1.7 times higher than those in autumn. The log scale plot of Kp versus sub-cooled liquid vapor pressure （PL^0） for all the data of autumn and winter season samples gave significantly different slopes. The slope for the winter samples （-0.72） was steeper than that for the autumn samples （-0.58）. The partitioning results indicated that slope values varied depending on characteristics of specific site, source region and meteorological conditions which play important roles in the partitioning of PAHs. In addition, local emission sources had a stronger effect on partitioning results than long-transported polluted plume. The sources of PAHs in five sampling sites in Xiamen also have been discussed initially. Diagnostic ratios showed that the primary source of PAHs in urban, suburban and industrial area was from vehicle exhausts. While emission from petrochemical factory and power plant was another main contributor to industrial area.

关键词： PAHs gaseous/particulate partitioning diagnostic ratio Xiamen

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Chemical compositions of PM_(2.5) aerosol during haze periods in the mountainous city of Yong'an, China

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Journal of Environmental Sciences 2012年第7期24卷 1225-1233页

作者： LiqianYin Zhenchuan Niu Xiaoqiu chen jinsheng chen Lingling Xu Fuwang Zhang Key Laboratory of Urban Environment and Health Institute of Urban EnvironmentChinese Academy of SciencesXiamen 361021China Environmental Monitoring Center of Fujian Fuzhou 350003China Graduate School of Chinese Academy of Sciences Beijing 100049China

Haze phenomena were found to have an increasing tendency in recent years in Yong＇an, a mountainous industrial city located in the center part of Fujian Province, China. Atmospheric fine particles （PM2.5） in the urban area during haze periods in three seasons （spring, autumn and winter） from 2007 to 2008 were collected, and the mass concentrations and chemical compositions （seventeen elements, water soluble inorganic ions （WSIIs） and carbonaceous species） of PM2.5 were determined. PM2.5 mass concentrations did not show a distinct difference among the three seasons. The carbonaceous species organic carbon （OC） and elemental carbon （EC） constituted up to 19.2%-30.4% of the PM2.5 mass during sampling periods, while WSIIs made up 25.3%-52.5% of the PM2.5 mass. The major ions in PM2.5 were SO42-, NO3- and NH4~, while the major elements were Si, K, Pb, Zn, Ca and A1. The experimental results （from data based on three haze periods with a 10-day sampling length for each period） showed that the crustal element species was the most abundant component of PM2.5 in spring, and the secondary ions species （SO42-, NO3-, NH4＋, etc.） was the most abundant component in PM2.5 in autumn and winter. This indicated that dust was the primary pollution source for PM2.5 in spring and combustion and traffic emissions could be the main pollution sources for PM2.5 in autumn and winter. Generally, coal combustion and traffic emissions were considered to be the most prominent pollution sources for this city on haze days.

关键词： PM2.5 haze metal elements water soluble inorganic ions carbonaceous species Yong'an City

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Pollution characteristics of organic and elemental carbon in PM_(2.5) in Xiamen,China

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Journal of Environmental Sciences 2011年第8期23卷 1342-1349页

作者： Fuwang Zhang Jinping Zhao jinsheng chen Ya Xu Lingling Xu Key Lab of Urban Environment and Health Institute of Urban Environment Chinese Academy of Sciences Xiamen 361021 China. Graduate University of Chinese Academy of Sciences Beijing 100049 China

Xiamen, located on the southeastern coastal line of China, is undergoing rapid urbanization and industrialization, so its air quality has a trend of degradation. However, studies on level, temporal and spatial changes of fine particles （PM2.5） and their carbonaceous fractions are scarce. In this article, abundance, sources, seasonal and spatial variations, distribution of organic carbon （OC） and elemental carbon （EC） in PM2.5, were studied at suburban, urban and industrial sites in Xiamen during four season-representative months in 2009-2010. PM2.5 samples were collected with middle volume sampler and were analyzed for OC and EC with thermal optical transmittance （TOT） method. Results showed that the annual average PM2.5 concentrations were 63.88-74.80 Ixg/m3 at three sites. While OC and EC concentrations were in the range of 15.81-19.73 [xg/m3 and 2.74-3.49 ~tg/m3, respectively, and clearly presented the summer minima and winter maxima in this study. The carbonaceous aerosol accounted for 42.8%-47.3% of the mass of PMzs. The annual average of secondary organic carbon （SOC） concentrations in Xiamen were 9.23-11.36 ~g/m3, accounting for approximately 56% of OC. Strong correlations between OC and EC was found in spring （R2 = 0.50） and autumn （R2 = 0.73）, suggesting that there were similar emission and transport processes for carbonaceous aerosols in these two seasons, while weak correlations were found in summer （R2 = 0.33） and winter （R2 = 0.41）. The OCI＇EC ratios in PM2.5 varied from 2.1 to 8.7 with an annual average of 5.7, indicating that vehicle exhaust, coal smoke and biomass burning were main source apportionments of carbonaceous fractions in Xiamen.

关键词： fine particle carbonaceous aerosol organic carbon elemental carbon Xiamen

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Effects of calcination temperature on physicochemical property and activity of CuSO4/TiO2 ammonia-selective catalytic reduction catalysts

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Journal of Environmental Sciences 2020年第5期32卷 237-245页

作者： Yanke Yu Jiali Zhang Changwei chen Chi He Jifa Miao Huirong Li jinsheng chen Department of Environmental Science and Engineering School of Energy and Power EngineeringXi’an Jiaotong UniversityXi'an 710049China Department of Chemical Engineering Columbia UniversityNew York 10027USA College of Geology and Environment Xi’an University of Science and TechnologyXi’an 710054China National Engineering Laboratory for VOCs Pollution Control Material and Technology University of Chinese Academy of SciencesBeijing 101408China Center for Excellence in Regional Atmospheric Environment Institute of Urban EnvironmentChinese Academy of SciencesXiamen 361021China

CuSO4/TiO2 catalysts with high catalytic activity and excellent resistant to SO2 and H2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by *** performance of catalysts is largely affected by calcination ***,effects of calcination temperature on physicochemical property and catalytic activity of CuSO4/TiO2 catalysts were investigated in *** samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH3,temperature-programmed reduction of H2 and in situ diffuse reflectance infrared Fourier transform *** revealed that high calcination temperature had three main effects on the ***,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface ***,decomposition of CuSO4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface ***,CuO from the decomposition of CuSO4 changed surface reducibility of the catalyst and favored the process of NH3 oxidation to nitrogen oxides(NOx).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃)decreased largely.

关键词： Calcination temperature Sulfate catalyst Selective catalytic reduction of nitrogen oxides by NH3 Surface acidity NH3 oxidation

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Excellent alkali resistance of Fe,Ce and sulfates co-modified V_(2)O_(5)-WO_(3)/TiO_(2) catalyst for selective catalytic reduction of NO_(x) with NH_(3)

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Journal of Rare Earths 2024年第9期42卷 1682-1692,I0002页

作者： Biyi Huang Xianfang Yi Jianyi Zhang Yuqiu Liu Yanting chen jinsheng chen Jinxiu Wang Center for Excellence in Regional Atmospheric Environment and Key Lab of Urban Environment and HealthInstitute of Urban EnvironmentChinese Academy of SciencesXiamen361021China College of Resources and Environment Fujian Agriculture and Forestry UniversityFuzhou350002China Fujian Key Laboratory of Atmospheric Ozone Pollution Prevention Institute of Urban EnvironmentChinese Academy of SciencesXiamen361021China University of Chinese Academy of Sciences Beijing100049China

Improving the alkali resistance of catalysts for selective catalytic reduction of NO_(x) with NH_(3) is still a *** this work,the co-modification with Fe,Ce and sulfates on V_(2)O_(5)-WO_(3)/TiO_(2) catalysts(denoted as xSFeCeVWTi) significantly enhances its alkali resistance with K element as a representative.A series of xSFeCeVWTi catalysts was synthesized by wet impregnation with designed 0.05Fe/V, 1.5Ce/V and different S/V molar ratios *** NO_(x) conversion and K resistance of xSFeCeVWTi catalysts increase with the increase of loading amounts of sulfates but no longer further increase as the sulfates load is excessive to block the pores of catalysts and hinder the adsorption of *** optimal modified catalyst in about 2.2S/V actual loading ratio,corresponding to 10.5SFeCeVWTi sample,shows over 99.0%NO_(x) conversion and N_(2) selectivity at 300-400℃ after *** interaction between Fe,Ce and V improves its redox ability but slightly weakens surface acidity,while the proper amount of sulfate species enriches surface Br?nsted acid sites but attenuates its redox ***,a balance of redox capacity and surface acidity,caused by Fe,Ce and sulfate co-modification,contributes to the excellent K resistance of 10.5SFeCeVWTi ***,the change of physicochemical properties influences the reaction mechanism which follows the Eley-Rideal mechanism on *** *** results show that the co-modification with Fe,Ce and sulfates is a good way to improve the alkali tolerance of V_(2)O_(5)-WO_(3)/TiO_(2) catalyst in industrial applications.

关键词： SCR CeO_(2) Fe_(2)O_(3) SO_(4)^(2-) K resistance K poisoning

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Aerosol light absorption in a coastal city in Southeast China:Temporal variations and implications for brown carbon

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Journal of Environmental Sciences 2019年第6期31卷 257-266页

作者： Yuqing Qiu Xin Wu Yanru Zhang Lingling Xu Youwei Hong jinsheng chen Xiaoqiu chen Junjun Deng Center for Excellence in Regional Atmospheric Environment Institute of Urban Environment Chinese Academy of Sciences Key Laboratory of Urban Environment and Health Institute of Urban Environment Chinese Academy of Sciences University of Chinese Academy of Sciences Fujian Environmental Monitoring Station Institute of Surface-Earth System Science Tianjin University

Light-absorbing carbonaceous aerosols including black carbon(BC) and brown carbon(BrC)play significant roles in atmospheric radiative properties. One-year measurements of aerosol light absorption at multi-wavelength were continuously conducted in Xiamen,southeast of China in 2014 to determine the light absorption properties including absorption coefficients(σabs) and absorption ?ngstr?m exponent(AAE) in the coastal *** absorptions of BC and BrC with their contributions to total light absorption were further quantified. Mean σabsat 370 nm and 880 nm were 56.6 ± 34.3 and 16.5 ± 11.2 Mm-1,respectively. σabspresented a double-peaks diurnal pattern with the maximum in the morning and the minimum in the afternoon. σabswas low in warm seasons and high in cold seasons. AAE ranged from 0.26 to 2.58 with the annual mean of 1.46, implying that both fossil fuel combustion and biomass burning influenced aerosol optical properties. σabsof BrC at 370 nm was 24.0 ± 5.7 Mm-1, contributing 42% to the total absorption. The highest AAE(1.52 ± 0.02) and largest BrC contributions(47% ± 4%) in winter suggested the significant influence of biomass burning on aerosol light absorption. Long-distance air masses passing through North China Plain and the Yangtze River Delta led to high AAE and BrC contributions. High AAE value of 1.46 in July indicated that long-range transport of the air pollutants from intense biomass burning in Southeast Asia would affect aerosol light absorption in Southeast China. The study will improve the understanding of light absorption properties of aerosols and the optical impacts of BrC in China.

关键词： Light absorption Brown carbon Black carbon Absorption Angstrom exponent Biomass burning Western Taiwan Strait

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regeneration of thermally deactivated commercial V-W-Ti catalysts

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Frontiers of Chemical Science and Engineering 2012年第1期6卷 38-46页

作者： Xuesong SHANG Jianrong LI Xiaowei YU jinsheng chen Chi HE Key Laboratory of Urban Environment and Health Institute of Urban EnvironmentChinese Academy of SciencesXiamen 361021China College of Chemical Engineering Huaqiao UniversityXiamen 361021China

An effective method for the regeneration of thermally deactivated commercial monolith SCR catalysts was investigated. Two types of regenerated solutions, namely NH4C1 （l mol/L） and dilute H2SO4 （0.5 tool/L）, were employed to treat the used catalyst. The effects of temperature and the regeneration process on the structural and textural properties of the catalysts were determined by X-ray diffraction, scanning electron microscopy, N2 adsorption/desorption, elemental analysis and Fourier transform infrared spectroscopy. The results suggest that the anatase phase of the used catalyst is maintained after exposure to high temperatures. Some of the catalytic activity was restored after regeneration. The catalyst regenerated by aqueous NH4C1 had a higher activity than that of the catalyst treated by dilute H2SO4. The main reason is that the NH3 generated from the decomposition of NH4C1 at high temperatures can be adsorbed onto the catalyst which promotes the reaction. The aggregated V205 were partially re-dispersed during the regeneration process, and the intrinsic oxidation of ammonia with high concentrations of O2 is a factorthat suppresses the catalytic activity.

关键词： V2O5-WO3/TiO2 catalysts thermal deactiva-tion regeneration NH4C1 dilute H2SO4 solution

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Chemical characteristics of PM_(2.5) during haze episodes in the urban of Fuzhou,China

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Particuology 2013年第3期11卷 264-272页

作者： Fuwang Zhang Lingling Xu jinsheng chen Xiaoqiu chen Zhenchuan Niu Tong Lei Chunming Li Jinping Zhao Key Lab of Urban Environment and Health Institute of Urban EnvironmentChinese Academy of Sciences Graduate University of Chinese Academy of Sciences Environmental Monitoring Center of Fujian Environmental Monitoring Center of Guangdong

Atmospheric fine particles （PM2.5） were collected in this study with middle volume samplers in Fuzhou, China, during both normal days and haze days in summer （September 2007） and winter （january 2008）. The concentrations, distributions, and sources of polycyclic aromatic hydrocarbons （PAHs）, organic carbon （OC）, elemental carbon （EC）, and water soluble inorganic ions （WSIls） were determinated. The results showed that the concentrations of PM2.s, PAHs, OC, EC, and WSIIs were in the orders of haze 〉 normal and winter〉 summer. The dominant PAHs of PM2.s in Fuzhou were Fluo, Pyr, Chr, BbF, BkF, BaP, BghiP, and IcdP, which represented about 80.0% of the total PAHs during different sampling periods. The BaPeq concentrations of ^-~PAHs were 0.78, 0.99, 1.22, and 2.43 ng/m3 in summer normal, summer haze, winter normal, and winter haze, respectively. Secondary pollutants （SO42 , NO3 , NH4＊, and OC） were the major chemical compositions of PM2.5, accounting for 69.0%, 55.1%, 63.4%, and 64.9% of PM2.s mass in summer normal, summer haze, winter normal, and winter haze, respectively. Correspondingly, secondary organic carbon （SOC） in Fuzhou accounted for 20.1%, 48.6%, 24.5%, and 50.5% of OC. The average values of nitrogen oxidation ratio （NOR） and sulfur oxidation ratio （SOR） were higher in haze days （0.08 and 0.27） than in normal days （0.05 and 0.22）. Higher OC/EC ratios were also found in haze days （5.0） than in normal days （3.3）. Correlation analysis demonstrated that visibility had positive correlations with wind speed, and neg- ative correlations with relative humidity and major air pollutants. Overall, the enrichments of PM2.5, OC, EC, SO42 ,andNO3 promoted haze formation. Furthermore, the diagnostic ratios of IcdP/（IcdP ＋ BghiP）, lcdP/BghiP, OC/EC, and NO3 /SO42 indicated that vehicle exhaust and coal consumption were the main sources of pollutants in Fuzhou.

关键词： Fine particles Haze Polycyclic aromatic hydrocarbons Organic carbon Elemental carbon Water soluble inorganic ions

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Sources appointment and health risks of PM_(2.5)-bound trace elements in a coastal city of southeastern China

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Journal of Environmental Sciences 2024年第4期138卷 561-571页

作者： Ziyi Lin Xiaolong Fan Gaojie chen Youwei Hong Mengren Li Lingling Xu Baoye Hu chen Yang Yanting chen Zhiqian Shao jinsheng chen Center for Excellence in Regional Atmospheric Environment Institute of Urban EnvironmentChinese Academy of SciencesXiamen 361021China Key Lab of Urban Environment and Health Institute of Urban EnvironmentChinese Academy ofSciencesXiamen 361021China University of Chinese Academy of Sciences Beijing 100049China Minnan Normal University Zhangzhou 363000China

To gain a comprehensive understanding of sources and health risks of trace elements in an area of China with high population densities and low PM_(2.5)concentrations,15 trace elements(Al,K,Ca,Ti,V,Cr,Mn,Fe,Ni,Cu,Zn,As,Sn,Ba,Pb)in PM_(2.5)were monitored from December 2020 to November 2021 in a representative city,*** concentrations of trace elements in Xiamen displayed an obvious seasonal variation and were dominated by K,Fe,Al,Ca and *** on Positive Matrix Factorization analysis,source appointment revealed that the major sources of trace elements in Xiamen were traffic,dust,biomass and firework combustion,industrial manufacture and shipping *** to health risk assessment combined with the source appointment results,it indicated that the average noncarcinogenic risk was below the threshold and cancer risk of four hazardous metals(Cr,Ni,As,Pb)exceeded the threshold(10^(-6)).Traffic-related source had almost half amount of contribution to the health risk induced by PM_(2.5)-bound trace *** the dust transport period or Spring Festival period,the health risks exceeded an acceptable threshold even an order of magnitude higher,suggesting that the serious health risks still existed in low PM_(2.5)environment at certain *** risk assessment reminded that the health risk reduction in PM_(2.5)at southeastern China should prioritize traffic-related hazardous trace elements and highlighted the importance of controlling vehicles emissions in the future.

关键词： PM_(2.5)-bound trace elements Seasonal variations Source appointment Health risks Traffic-related source

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