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Atmospheric Vinyl Alcohol to Acetaldehyde Tautomerization Revisited

机译:再谈大气乙烯醇制乙醛互变异构

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摘要

The atmospheric oxidation of vinyl alcohol (VA) produced by photoisomerization of acetaldehyde (AA) is thought to be a source of formic acid (FA). Nevertheless, a recent theoretical study predicted a high rate coefficient k1(298 K) of ≈10**–14 cm3 molecule–1 s–1 for the FA-catalyzed tautomerization reaction 1 of VA back into AA, which suggests that FA buffers its own production from VA. However, the unusually high frequency factor implied by that study prompted us to reinvestigate reaction 1. On the basis of a high-level ab initio potential energy profile, we first established that transition state theory is applicable, and derived a k1(298 K) of only ≈2 × 10**–20 cm3 molecule–1 s–1, concluding that the reaction is negligible. Instead, we propose and rationalize another important VA sink: its uptake by aqueous aerosol and cloud droplets followed by fast liquid-phase tautomerization to AA; global modeling puts the average lifetime by this sink at a few hours, similar to oxidation by OH.
机译:通过乙醛(AA)的光异构化产生的乙烯醇(VA)的大气氧化被认为是甲酸(FA)的来源。尽管如此,最近的一项理论研究预测,FA催化的VA互变异构反应1回到AA的速率系数k1(298 K)约为10 ** – 14 cm3分子–1 s–1,这表明FA可以缓冲其由VA自己生产。但是,该研究暗示的异常高频率因素促使我们重新研究反应1。基于高水平的从头算势能图,我们首先确定了过渡态理论是适用的,并得出了k1(298 K)仅≈2×10 ** – 20 cm3分子–1 s-1,认为该反应可忽略不计。相反,我们提出并合理化了另一个重要的VA吸收剂:水溶液中的气溶胶和云滴吸收VA,然后将液相快速互变异构化为AA。全局建模使该水槽的平均寿命为几个小时,类似于OH的氧化。

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