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国家自然科学基金(21190053)

作品数:10 被引量:57H指数:5
相关作者:陈建民赵希罗兰·詹森孔令东张拴勤更多>>
相关机构:复旦大学更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划国家教育部博士点基金更多>>
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10 条 记 录,以下是 1-10
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分子光谱技术在大气颗粒物非均相化学研究中的应用
对流层大气颗粒物参与的复杂非均相化学过程严重影响着区域空气质量和全球气候变化,多年来已成为国内外大气环境领域的研究热点。傅里叶变换红外光谱和拉曼光谱技术作为一种原位和在线研究方法已成为研究大气非均相化学的重要手段。基于傅...
陈忠明赵岳
关键词:拉曼光谱大气环境颗粒物
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氨和有机胺对羰基硫与α-Fe_2O_3非均相反应的影响(英文)被引量:1
2013年
利用原位漫反射傅里叶红外光谱(DRIFTS),考察了室温下羰基硫(COS)在经氨气和有机胺预吸附的α-Fe_2O_3上的非均相反应,并同时比较了氨气和不同有机胺(甲胺、三甲胺、三乙胺、苯胺、吡啶和吡咯)对反应活性的影响及其反应动力学.结果表明,经碱性物质预吸附后,COS可在α-Fe_2O_3表面发生氧化反应,主要产物为气态CO_2、表面HCO_3^-、表面CO_3^(2-)和表面SO_4^(2-),且α-Fe_2O_3表面预吸附的碱性物质大大提高了COS在α-Fe_2O_3上的反应能力,在碱性物质的影响中,甲胺对反应的促进能力最大,相比纯α-Fe_2O_3反应的反应活性提高了约4.5倍,然而苯胺和吡咯对COS的反应影响不是很明显.观察到的不同碱性物质对COS的转化能力依次为:甲胺>三甲胺>氨气>三乙胺>吡啶>吡咯>苯胺≈纯样品,受碱性物质的影响,COS的反应级数由一级转变为二级.此外,研究也发现碱性物质的覆盖度和表面吸附水对COS转化能力存在一定的影响.这些实验结果表明在碱性物质存在下,表面M―O-是COS在α-Fe_2O_3发生氧化反应的关键活性位点,对反应活性的贡献较大,并在此基础上探讨碱性条件下COS的反应转化机制.
张拴勤孔令东赵希罗兰·詹森陈建民
关键词:羰基硫氨气有机胺Α-FE2O3非均相反应
Airborne Submicron Particulate (PM_1) pollution in Shanghai: Chemical Compositions, Formation/Dissociation of Associated Semi-volatile Components and Influence on Visibility Impairment
<正>Water-soluble ions in submicron particle (PM 1 ) and associated precursor gases (NH 3 , HNO 3 , HCl) were o...
Yang ShiJianmin ChenDawei Hu
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Seasonal and Diurnal Variations of Particulate Organosulfates in Urban Shanghai, China
<正>Organosulfates (ROSO 3 H, OSs), normally recognized as sulfate esters and their derivatives, are formed fro...
Ye MaXinkai XuWeihua SongFuhai GengLin Wang
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Optical properties and chemical composition of PM_(2.5) in Shanghai in the spring of 2012被引量:4
2014年
The semi-diurnal mean aerosol mass concentration, chemical composition, and optical properties of PM2.s were investigated in Shanghai during the spring of 2012. Slight pollution was observed during the study period. The average PM2.s concentration was 64.11± 22.83μg/m3. The mean coefficients of extinction, scattering, and absorption at 532 nm were 125.9 ± 78.5, 91.1 ± 56.3, and 34.9 ±23.6 Mm-1, respectively. A relatively low mean single scattering alhedo at 532 nm (0.73 ±0.04) and low level of elemental carbon (EC, 2.67± 1.96 μg/m3) suggested that the light absorption was enhanced due to the internal mixing of the EC. Sulfate contributed the most to aerosol light scattering in Shanghai. The chemical composition of PM2.5 was dominated by particulate organic matter, sulfate, nitrate, ammonium, and EC. Anthropogenic sources made a significant contribution to the emission and loading of the particulate pollutants. A relatively good correlation between the aerosol chemical composition and the cloud condensation nuclei (CCN) activation indicated that aerosol chemistry is an important factor that influences the saturated hygroscopicity and growth of the aerosol.
Guanghan HuangTiantao ChengRenjian ZhangJun TaoChunpeng LengYunwei ZhangShuping ZhaDeqin ZhangXiang LiChunyang Xu
Observations of atmospheric pollutants at Lhasa during 2014-2015:Pollution status and the influence of meteorological factors被引量:10
2018年
Atmospheric pollutants including SO_2, NO_2, CO, O_3 and inhalable particulate matter(PM2.5 and PM10) were monitored continuously from March 2014 to February 2015 to investigate characteristics of air pollution at Lhasa, Tibetan Plateau. Species exhibited similar seasonal variations except O_3, with the peaks in winter but low valleys in summer. The maximum O_3 concentration was observed in spring, followed by summer, autumn, and winter. The positive correlation between O_3 and PM10 in spring indicated similar sources of them, and was assumed to be turbulent transport. Temperature was the dominant meteorological factor for most species in spring. High temperature accelerates O_3 photochemistry, and favors air disturbance which is conductive to dust resuspension in spring. Relative humidity(RH) and atmospheric pressure were the main meteorological factors in summer. RH showed negative correlations with species, while atmospheric pressure posed opposite situation. Wind speed(WS) was the dominant meteorological factor in autumn, the negative correlations between WS and species indicated diffusion by wind. Most species showed non-significant correlations with meteorological factors in winter, indicating the dependence of pollution on source emission rather than restriction by meteorology. Pollution weather character indicated that emissions were from biomass burning and dust suspension, and meteorological factors also played an important role. Air stream injection from the stratosphere was observed during O_3 pollution period. Air parcels from Southwest Asia were observed during air pollution period in winter. An enhancement in air pollutants such as O_3 would be expected in the future, more attention should be given to countermeasures for prevention of air pollution in the future.
Bu DuoLulu CuiZhenzhen WangRui LiLiwu ZhangHongbo FuJianmin ChenHuifang ZhangA.Qiong
Do vehicular emissions dominate the source of C6–C8 aromatics in the megacity Shanghai of eastern China?被引量:7
2015年
The characteristic ratios of volatile organic compounds(VOCs) to i-pentane, the indicator of vehicular emissions, were employed to apportion the vehicular and non-vehicular contributions to reactive species in urban Shanghai. Two kinds of tunnel experiments, one tunnel with more than 90% light duty gasoline vehicles and the other with more than 60% light duty diesel vehicles, were carried out to study the characteristic ratios of vehicle-related emissions from December 2009 to January 2010. Based on the experiments, the characteristic ratios of C6–C8aromatics to i-pentane of vehicular emissions were 0.53 ± 0.08(benzene), 0.70 ± 0.12(toluene),0.41 ± 0.09(m,p-xylenes), 0.16 ± 0.04(o-xylene), 0.023 ± 0.011(styrene), and 0.15 ± 0.02(ethylbenzene), respectively. The source apportionment results showed that around 23.3% of C6–C8 aromatics in urban Shanghai were from vehicular emissions, which meant that the non-vehicular emissions had more importance. These findings suggested that emission control of non-vehicular sources, i.e. industrial emissions, should also receive attention in addition to the control of vehicle-related emissions in Shanghai. The chemical removal of VOCs during the transport from emissions to the receptor site had a large impact on the apportionment results. Generally, the overestimation of vehicular contributions would occur when the VOC reaction rate constant with OH radicals(k OH) was larger than that of the vehicular indicator, while for species with smaller k OH than the vehicular indicator, the vehicular contribution would be underestimated by the method of characteristic ratios.
Hongli WangQian WangJianmin ChenChanghong ChenCheng HuangLiping QiaoShengrong LouJun Lu
在线小时分辨离子色谱技术在PM2.5研究中的应用
<正>本文总结了使用在线大气气体与气溶胶分析仪(MARGA)在我国PM2.5研究中的进展,着重阐述了该小时分辨离子色谱技术在PM2.5化学组成、灰霾形成机制、沙尘混合气溶胶的研究中的应用。通过2008年5月以来在上海、杭...
陈建民
关键词:大气颗粒物化学成分
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Individual particle analysis of aerosols collected at Lhasa City in the Tibetan Plateau被引量:5
2015年
To understand the composition and major sources of aerosol particles in Lhasa City on the Tibetan Plateau (TP), individual particles were collected from 2 February to 8 March, 2013 in Tibet University. The mean concentrations of both PM2.5 and PM10 during the sampling were 25.7 ± 21.7 and 57.2 ± 46.7 μg/m^3, respectively, much lower than those of other cities in East and South Asia, but higher than those in the remote region in TP like Nam Co, indicating minor urban pollution. Combining the observations with the meteorological parameters and back trajectory analysis, it was concluded that local sources controlled the pollution during the sampling. Transmission electron microscopy (TEM) combined with energydispersive X-ray spectra (EDS) was used to study 408 particles sampled on four days. Based on the EDS analysis, a total of 8 different particle categories were classified for all 408 particles, including Si-rich, Ca-rich, soot, K-rich, Fe-rich, Pb-rich, Al-rich and other particles. The dominant elements were Si, A1 and Ca, which were mainly attributed to mineral dust in the earth's crust such as feldspar and clay. Fe-, Pb-, K-, Al-rich particles and soot mainly originated from anthropogenic sources like firework combustion and biomass burning during the sampling. During the sampling, the pollution mainly came from mineral dust, while the celebration ceremony and religious ritual produced a large quantity of anthro- pogenic metal-bearing particles on 9 and 25 February 2013. Cement particles also had a minor influence. The data obtained in this study can be useful for developing pollution control strategies.
Bu DuoYunchen ZhangLingdong KongHongbo FuYunjie HuJianmin ChenLin LiA.Qiong
雾污染及其形成机制
2013年
雾污染是当前有害的天气现象之一。阐述了雾的发生与观测方法,并分析了当前雾研究的进展。重点介绍了雾污染的形成机制与雾过程中的污染物大气化学行为。最后分析了雾研究的难点及未来重要发展方向。
陈建民李想
关键词:气候变化大气化学
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