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α,β— 蒎烯气相臭氧化速率常数的测定
引用本文:刘兆荣,胡娣.α,β— 蒎烯气相臭氧化速率常数的测定[J].光谱学与光谱分析,2001,21(5):585-587.
作者姓名:刘兆荣  胡娣
作者单位:刘兆荣(北京大学环境科学中心 北京 100871);胡娣(北京大学环境科学中心 北京 100871)
基金项目:国家自然科学基金重大项目(49899270)资助
摘    要:对α-蒎烯、β-蒎烯和O3的大气反应进行了初步实验室模拟,利用长光程傅里叶变换红外光谱技术结合相对速率法测得在1.0×105Pa,296±3K条件下,α-蒎烯、β-蒎烯和O3气相反应的速率常数分别为2.83×1017cm3@molecule-1@s-1和1.48×1017cm3@molecule-1@s.

关 键 词:α-蒎烯  β-蒎烯  速率常数  长光程傅里叶变换红外光谱  臭氧  氧化  测定
文章编号:1000-0593(2001)05-0585-03
修稿时间:2000年11月13

Determination of rate constants of gas-phase reactions of alpha-pinene and beta-pinene with ozone]
Z R Liu,D Hu.Determination of rate constants of gas-phase reactions of alpha-pinene and beta-pinene with ozone][J].Spectroscopy and Spectral Analysis,2001,21(5):585-587.
Authors:Z R Liu  D Hu
Institution:Environmental Science Center, Peking University, Beijing 100871, China.
Abstract:alpha-pinene and beta-pinene are the most dominating species among natural terpenes. Terpenes are mainly emitted from forest trees, flowers and grass. In the lower troposphere terpenes can react fast with OH radical, ozone, NO3 radical and ground state oxygen atom. These reactions may contribute to the occurring of aerosols, peroxides (hydrogen peroxide and organic peroxide), carbon cycle (mainly CO), acid rain (organic acids, NO3- and SO4(2-), ozone and active radicals such as OH radical. Reactions with ozone occur both in the daytime and in the night. The study in this field in China began in the late 1980. The main work focus on the source emission and the experimental simulation has just started. It is most of our group's work. In this paper preliminary experimental simulation of the gas-phase reactions of alpha-pinene and beta-pinene with ozone were carried out in the quartz chamber. The rate constants of these reactions were measured using long-path Fourier transform infra-red combined with relative rate constant method. And the rate constants for the gas-phase reactions of alpha-pinene, beta-pinene with ozone were determined as 2.83 x 10(17) cm3.molecule-1.s-1 and 1.48 x 10(17) cm3.molecule-1.s-1 at 1.0 x 10(5) Pa and 296 +/- 3 K. The results are quite similar to the data from Atkinson group. No cyclohexane was added to the reaction system during the measurement to restrain the formation of OH radical. The formation of OH radical could not be quantified, so that the effect of subsidiary reactions induced by OH radical has not been calculated. In the later simulation study and model this effect should be considered.
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