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烟雾箱模拟乙炔和NOx的大气光化学反应
引用本文:杜林,徐永福,葛茂发,贾龙,王庚辰,王殿勋.烟雾箱模拟乙炔和NOx的大气光化学反应[J].环境科学,2007,28(3):482-488.
作者姓名:杜林  徐永福  葛茂发  贾龙  王庚辰  王殿勋
作者单位:中国科学院化学研究所北京分子科学国家实验室,北京100080;中国科学院大气物理研究所大气边界层物理和大气化学国家重点实验室,北京100029;中国科学院化学研究所北京分子科学国家实验室,北京100080;北京师范大学大气环境研究中心,北京100875;中国科学院大气物理研究所中层大气遥感与探测开放实验室,北京100029;中国科学院化学研究所北京分子科学国家实验室,北京100080
基金项目:中国科学院知识创新工程项目(KJCX2-SW-H8)
摘    要:利用自制光化学烟雾箱进行了一系列表征实验并模拟了乙炔和氮氧化物NOx在室温(20±1)℃下的大气光化学反应.讨论了乙炔与NOx的协同作用对光化学反应产生O3的影响.实验得到了O3和NO2的壁损失分别为5.80×10-6 s-1和2.41×10-6 s-1,相对于模拟实验中的O3和NO2,该损失可以忽略.测得了单支40 W黑光灯的有效光强为0.64×10-3 s-1(以NO2的光解速率表示).经过净化空气的本底校正后,讨论了不同乙炔浓度、NOx浓度以及光照强度对体系产生O3的影响,计算了乙炔的增强反应活性值(incremental reactivity, IR),4组实验的IR最大值分别为1.76×10-2、2.68×10-2、2.04×10-2和2.84×10-2.并发现IR值与乙炔的初始浓度以及光照强度关系密切,与NOx初始浓度关系不大.

关 键 词:烟雾箱  乙炔  光化学反应  光化学烟雾
文章编号:0250-3301(2007)03-0482-07
收稿时间:2006/4/27 0:00:00
修稿时间:7/6/2006 12:00:00 AM

Smog Chamber Simulation of Atmospheric Photochemical Reactions of Acetylene and NOx
DU Lin,XU Yong-fu,GE Mao-f,JIA Long,WANG Geng-chen and WANG Dian-xun.Smog Chamber Simulation of Atmospheric Photochemical Reactions of Acetylene and NOx[J].Chinese Journal of Environmental Science,2007,28(3):482-488.
Authors:DU Lin  XU Yong-fu  GE Mao-f  JIA Long  WANG Geng-chen and WANG Dian-xun
Institution:1. Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China; 2. State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China; 3.Research Center for Atmospheric Environment, Beijing Normal University, Beijing 100875, China; 4. Division for Middle Atmosphere and Remote Sensing, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China
Abstract:A series of characteristic experiments were conducted in a self-made photochemical smog chamber, which was used to simulate atmospheric photochemical reactions of acetylene and NO(x) under room temperature of (20 +/- 1) degrees C. The effect of acetylene and NO(x) on ozone production by photochemical reactions was discussed. The wall decay of O3 and NO2 were determined, which were 5.80 x 10(-6) s(-1) and 2.41 x 10(-6) s(-1), respectively. Such decay should be omitted relative to O3 and NO2 in simulative experiments. The effective light intensity for a single black lamp of 40 W was determined to be 0.64 x 10(-3) s(-1), which was expressed by the photolysis rate of NO2. The effect of different light intensity, initial concentrations of acetylene and NO(x) on O3 production was discussed after correction of background O3 from purified air. The incremental reactivity (IR) of acetylene were calculated. For four different experiments, the maximum values of IR are 1.76 x 10(-2), 2.68 x 10(-2), 2.04 x 10(-2) and 2.84 x 10(-2), respectively. It is found that there are close relationships between IR and initial acetylene concentrations, and between IR and irradiation intensity, and that there is no significant relation between IR and initial NO(x) concentrations.
Keywords:smog chamber  acetylene  photochemical reaction  photochemical smog
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