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国家自然科学基金(40830101)

作品数:16 被引量:111H指数:4
相关作者:葛茂发王炜罡刘泽盖艳波王雷更多>>
相关机构:中国科学院更多>>
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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16 条 记 录,以下是 1-10
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Uptake kinetics of 3-buten-1-ol,4-penten-1-ol and 3-methy1-3-buten-1-ol into sulfuric acid solutions
Unsaturated alcohols are important components in complex mixtures of oxygenated volatile organic compounds,and...
XU ZhiFang~(1,2),LIU Ze~2,GE MaoFa~(2*) & WANG WeiGang~2 1 Key Laboratory of Engineering Geomechanics,Institute of Geology and Geophysics,Chinese Academy of Sciences,Beijing 100029,China
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二氧化氮与不同晶相氧化铝非均相反应过程的研究
利用原位漫反射傅里叶变换红外光谱(DRIFTS)研究了二氧化氮在不同晶相氧化铝(α-AlO和γ-AlO)表面的非均相反应过程,发现在两种氧化铝表面生成了不同产物。结合离子色谱检测,发现γ-AlO表面会有亚硝酸盐中间产物生...
吴玲燕佟胜睿葛茂发
关键词:二氧化氮氧化铝非均相反应DRIFTS
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An improved GC-ECD method for measuring atmospheric N_2O被引量:1
2013年
Gas chromatography equipped with an electron capture detector (GC-ECD) has been widely used for measuring atmospheric N2O,but nonlinear response and the influence of atmospheric CO2 have been recognized as defects for quantification.An original GCECD method using N 2 as carrier gas was improved by introducing a small flow rate of CO2 makeup gas into the ECD,which could well remedy the above defects.The N2O signal of the improved method was 4-fold higher than that of the original method and the relative standard deviation was reduced from 〉 1% to 0.31%.N2O concentrations with different CO2 concentrations (172.2×10-6-1722×10-6mol/mol) measured by the improved GC-ECD method were in line with the actual N2O concentrations.However,the N2O concentrations detected by the original method were largely biased with a variation range of-4.5%~7%.The N2O fluxes between an agricultural field and the atmosphere measured by the original method were greatly overestimated in comparison with those measured by the improved method.Good linear correlation (R2=0.9996) between the response of the improved ECD and N2O concentrations (93×10-9-1966×10-9mol/mol) indicated that atmospheric N2O could be accurately quantified via a single standard gas.Atmospheric N2O concentrations comparatively measured by the improved method and a high precision GC-ECD method were in good agreement.
Yuanyuan ZhangYujing MuShuangxi FangJunfeng Liu
Kinetic study of the reaction of chlorine atoms with 3-methyl-3-buten-1-ol被引量:4
2009年
The reaction of a typical unsaturated alcohol,3-methyl-3-buten-1-ol(MBO331),with Cl atoms,was investigated for the first time.The reaction was investigated using discharged flow-tube coupled with electron impact mass spectrometer.The experiments were performed over the temperature range of 248 K―298 K and at pressure of 1 torr in He as the bath gas.The obtained kinetic data were used to derive the Arrhenius expression:k1 =(3.47 ± 1.21) × 10-11 exp[(599 ± 69)/T] cm3 molecule-1 s-1.Finally,atmospheric lifetimes of the MBO331 with respect to OH radicals,NO3 radicals and Cl atoms have been calculated and the atmospheric implications are considered briefly.
WANG Lei GE MaoFa WANG WeiGang
关键词:不饱和醇丁烯-1氯原子OH自由基电子轰击质谱煤气灶
Uptake of isoprene, methacrylic acid and methyl methacrylate into aqueous solutions of sulfuric acid and hydrogen peroxide被引量:2
2012年
Multiphase acid-catalyzed oxidation by hydrogen peroxide has been suggested to be a potential route to secondary organic aerosol formation from isoprene and its gas-phase oxidation products, but the lack of kinetics data significantly limited the evaluation of this process in the atmosphere. Here we report the first measurement of the uptake of isoprene, methacrylic acid and methyl methacrylate into aqueous solutions of sulfuric acid and hydrogen peroxide. Isoprene cannot readily partition into the solution because of its high volatility and low solubility, which hinders its further liquid-phase oxidation. Both methacrylic acid and methyl methacrylate can enter the solutions and be oxidized by hydrogen peroxide, and steady-state uptake was observed with the acidity of solution above 30 wt.% and 70 wt.%, respectively. The steady-state uptake coefficient of methacrylic acid is much larger than that of methyl methacrylate for a solution with same acidity. These observations can be explained by the different reactivity of these two compounds caused by the different electron-withdrawing conjugation between carboxyl and ester groups. The atmospheric lifetimes were estimated based on the calculated steady-state uptake coefficients. These results demonstrate that the multiphase acid-catalyzed oxidation of methacrylic acid plays a role in secondary organic aerosol formation, but for isoprene and methyl methacrylate, this process is not important in the troposphere.
Ze LiuMaofa GeWeigang Wang
关键词:UPTAKE
Photoelectron spectroscopy of terpenoids and prediction of their rate constants in atmospheric oxidation reactions
2010年
The electronic structures of six mono-terpenoids and two of their oxygenated derivatives were studied by He I photoelectron spectroscopy(PES).The observed bands were interpreted on the basis of empirical arguments and theoretical calculations.The first vertical ionization potentials for β-pinene,α-terpinene,terpinolene,γ-terpinene,limonene,myrcene,citral,and terpinene-4-ol were determined to be 8.73,7.57,8.26,8.30,8.53,8.68,8.71,and 8.77 eV,respectively.Most of these values have not been determined by PES before.The correlations of the first vertical ionization potentials of these compounds to the natural logarithms of rate constants for their reactions with the radicals OH,NO3,and O3 were determined.The correlation coefficients for their reactions with OH,NO3,and O3 were 0.97,0.91,and 0.95,respectively.This method is a powerful technique for predicting the rate constants for the atmospheric oxidation reactions of terpenoids.
WANG XiaoPeng TONG ShengRui GE MaoFa WANG WeiGang WANG DianXun
关键词:反应速率常数萜类化合物光电子能谱垂直电离势异松油烯
Temperature dependent kinetics of the gas-phase reaction of OH radicals with EMS
2011年
Using an improved smog chamber system,the temperature dependence of OH radical reaction with EMS was investigated over the temperature range of 297-346 K at 1.01×105 Pa pressure of air. The Arrhenius expression of the reaction was obtained for the first time. The mechanism of the reaction was also investigated.
WANG KunGE MaoFaWANG WeiGang
关键词:环境管理体系温度相关气相反应OH自由基ARRHENIUS自由基反应
Nitrous oxide emissions from a maize field during two consecutive growing seasons in the North China Plain被引量:15
2012年
Nitrous oxide (N 2 O) emissions from a maize field in the North China Plain (Wangdu County,Hebei Province,China) were investigated using static chambers during two consecutive maize growing seasons in the 2008 and 2009.The N 2 O pulse emissions occurred with duration of about 10 days after basal and additional fertilizer applications in the both years.The average N 2 O fluxes from the CK (control plot,without crop,fertilization and irrigation),NP (chemical N fertilizer),SN (wheat straw returning plus chemical N fertilizer),OM- 1/2N (chicken manure plus half chemical N fertilizer) and OMN (chicken manure plus chemical N fertilizer) plots in 2008 were 8.51,72.1,76.6,101,107 ng N/(m 2 ·sec),respectively,and in 2009 were 33.7,30.0 and 35.0 ng N/(m 2 ·sec) from CK,NP and SN plots,respectively.The emission factors of the applied fertilizer as N 2 O-N (EFs) were 3.8% (2008) and 1.1% (2009) for the NP plot,3.2% (2008) and 1.2% (2009) for the SN plot,and 2.8% and 2.2% in 2008 for the OM-1/2N and OMN plots,respectively.Hydromorphic properties of the investigated soil (with gley) are in favor of denitrification.The large differences of the soil temperature and water-filled pore space (WFPS) between the two maize seasons were suspected to be responsible for the significant yearly variations.Compared with the treatments of NP and SN,chicken manure coupled with compound fertilizer application significantly reduced fertilizer loss rate as N 2 O-N.
Yuanyuan ZhangJunfeng LiuYujing MuZhu XuShuwei PeiXiaoxiu LunYing Zhang
关键词:MANURE
臭氧与二乙胺和三乙胺气相反应的速率常数(英文)被引量:2
2010年
利用自制的烟雾箱系统研究了臭氧与二乙胺和三乙胺的气相反应动力学.实验过程中保证二乙胺和三乙胺浓度远远大于臭氧浓度,使得实验在准一级条件下进行.加入环己烷以消除实验过程中可能产生的OH自由基对反应的影响.在(298±1)K和1.01×105Pa条件下,测得臭氧与二乙胺和三乙胺反应的绝对速率常数值分别为(1.33±0.15)×10-17和(8.20±1.01)×10-17cm3·molecule-1·s-1.与文献中已有的其它胺类的臭氧反应数据比较后发现,臭氧与胺的反应可以用亲电反应机制来解释.另外,通过对比发现,臭氧与三取代的烷基胺类的反应速率要远远大于其与二取代的烷基胺类的反应速率.这在一定程度上可有助于解释外场观测到的气溶胶相中二烷基胺盐较多的事实.利用测得的速率常数和大气中臭氧浓度,还估算了二乙胺和三乙胺与臭氧反应的大气寿命.结果显示,与臭氧的反应是二乙胺和三乙胺在大气中的一种重要的消除途径,尤其是在污染严重地区.
盖艳波葛茂发王炜罡
关键词:动力学臭氧二乙胺三乙胺速率常数
二次光化学氧化剂与气溶胶间的非均相过程被引量:17
2009年
光氧化剂和气溶胶颗粒物在大气环境中普遍存在,影响着大气氧化能力和气候,威胁着人类健康。而大气光氧化剂与气溶胶颗粒物间复杂的耦合相互作用能产生二次污染物,使得大气污染过程更为复杂,成为国际大气化学研究的前沿和热点课题。挥发性有机物(VOCs)和氮氧化物(NOx)等一次污染物在大气中经过复杂的光化学反应可形成以臭氧(O3)为主的二次光化学氧化剂,并以大气气溶胶为平台发生非均相反应,使大气污染更严重,引起人们普遍关注。二次光化学氧化剂和气溶胶颗粒物之间非均相过程的实验室研究是深入认识这两者间耦合相互作用的关键,实验室研究可以为分析和深入认识外场观测结果提供基础,还能为数值模式模拟研究提供基本参数。概括了大气二次光化学氧化剂的形成过程,总结了国际上近年来二次光化学氧化剂与大气气溶胶颗粒物非均相反应的实验室研究进展以及研究方法,最后提出了现有的一些主要科学问题,对未来这一重要领域的研究前景进行了展望。
葛茂发刘泽王炜罡
关键词:气溶胶
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