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国家自然科学基金(21077025)

作品数:3 被引量:3H指数:1
相关作者:赵希罗兰·詹森孔令东陈建民张拴勤更多>>
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更多>>
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Hygroscopicity of ambient submicron particles in urban Hangzhou,China被引量:2
2011年
In this study,hygroscopicity of size-segregated ambient submicron particles in urban Hangzhou was studied from 28th December 2009 to 18th January 2010,using a hygroscopicity-tandem differential mobility analyzer(H-TDMA).The submicron particles in Hangzhou showed a minor hygroscopic growth at 73%relative humidity(RH),and then grew significantly between 77%and 82%RH.Monomodal distribution accounted for 90%for 30 nm particles,17%for 50 nm particles,and less than 7%for particles larger than 50 nm at 82%RH.Deconvolution of the bimodal distribution indicated a less hygroscopic group and a more hygroscopic group,with the fraction of the more hygroscopic group increasing with the initial dry particle size and then remaining almost constant for accumulation mode particles.Our results imply that submicron particles in urban Hangzhou were almost entirely externally mixed,and the hygroscopic properties of ambient particles in urban Hangzhou were mainly a function of their size and chemical composition.
Jiachen ZHANGLin WANGJianmin CHENShengmao FENGJiandong SHENLi JIAO
关键词:HYGROSCOPICITY
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
Effect of relative humidity and the presence of aerosol particles on the α-pinene ozonolysis
2018年
The α-pinene ozonolysis under the different environmental conditions were observed in a smog chamber. The second-order rate constant (k) was determined to be (7.25 ± 0.06) x 10^-17 cm^3/(molecule.sec) under 20% of relative humidity (RH) and room temperature. RH showed a marked influence on the α-pinene ozonolysis. The value of k increased with KH increase, which was 1.6 times faster at RH = 80% than that at RH = 20%. Additionally, the value of k apparently changed in the presence of the aerosol particles. The diesel soot increased the k value. The fly ash prohibited the reaction, however, H2SO4-treated fly ash promoted the reaction. The information of products gained using FT-IR and SPAMS showed that pinonic acid, 10-hydroxy-pinonic acid and pinic acid could be generated during the α- pinene ozonolysis. Water molecules could take part in the formation of the products, and play a vital role in the degradation of α-pinene. The atmospheric residence time calculation showed that the ozonolysis in the atmosphere is an important way of the α-pinene consumption as compared to that reacted with OH during daytime. The results suggested that the degradation of α-pinene via the ozonization in the atmosphere may be affected greatly by RH, as well as the presence of aerosol particles. The ozonolysis reaction may be an important way of the a-pinene consumption during daytime.
Guoqiang ZhangHongbo FuJianmin Chen
关键词:Α-PINENEOZONOLYSIS
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