Atmospheric chemistry of (Z)-CF2HCF=CHCl: Kinetics and products of reaction with Cl atoms and OH radicals

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL
Mads Peter Sulbaek Andersen, Josefine Ellerup Borcher, Ole John Nielsen
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Abstract

Long path length FTIR-smog chamber techniques were used to study the title reactions in 650 Torr of N2, oxygen, or air diluent at 296 ± 3 K. Values of k(Cl + (Z)-CF2HCF = CHCl)═(6.6 ± 0.7) × 10−11 and k(OH + (Z)-CF2HCF═CHCl)═(4.1 ± 0.7) × 10−12 cm3 molecule−1 s−1 were measured. The IR spectrum of (Z)-CF2HCF═CHCl is reported. The atmospheric lifetime of (Z)-CF2HCF═CHCl is determined by the reaction with OH and is approximately 2.8 days. Reaction of (Z)-CF2HCF═CHCl with Cl atoms gives HC(O)Cl and CF2HC(O)F as major primary products. Under environmental conditions, the OH radical initiated oxidation gives CF2HC(O)F and HC(O)Cl in yields of (98 ± 8)% and (100 ± 4)%, respectively. Accounting for non-uniform horizontal and vertical mixing leads to a 100-year time-horizon global warming potential value for (Z)-CF2HCF═CHCl of essentially zero.

Abstract Image

(Z)-CF2HCF=CHCl的大气化学:与Cl原子和OH自由基反应的动力学和产物
采用长径长的ftir -烟雾室技术,在650torr的N2、氧气或空气稀释剂条件下,在296±3k下研究了标题反应。测量了k(Cl + (Z)-CF2HCF = CHCl) =(6.6±0.7)× 10−11和k(OH + (Z)-CF2HCF = CHCl) =(4.1±0.7)× 10−12 cm3分子−1 s−1的值。报道了(Z)-CF2HCF = CHCl的红外光谱。(Z)-CF2HCF = CHCl的大气寿命由与OH的反应决定,大约是2.8天。(Z)-CF2HCF = CHCl与Cl原子反应得到HC(O)Cl和CF2HC(O)F作为主要的初级产物。在环境条件下,OH自由基引发氧化反应生成CF2HC(O)F和HC(O)Cl,产率分别为(98±8)%和(100±4)%。考虑到不均匀的水平和垂直混合导致100年时间范围内(Z)-CF2HCF = CHCl的全球变暖潜能值基本上为零。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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