Critical Review of Atmospheric Chemistry of Alkoxy Radicals

2017 ◽  
pp. 185-269 ◽  
Author(s):  
Theodore S. Dibble ◽  
Jiajue Chai
2004 ◽  
Vol 82 (6) ◽  
pp. 854-866 ◽  
Author(s):  
Lily Zu ◽  
Jinjun Liu ◽  
Sandhya Gopalakrishnan ◽  
Terry A Miller

Laser-induced fluorescence excitation spectra of five vibronic bands of 1-hexoxy and three bands of 1-heptoxy have been recorded in a jet-cooled environment. Experimental values of rotational constants for both the [Formula: see text] and [Formula: see text] states and components of the spin-rotational tensor for the [Formula: see text] state were obtained by an analysis of the partially resolved rotational structure of the vibronic bands. Comparing these experimental results with quantum chemistry calculations, and using corresponding assignments of smaller alkoxy radicals as a guide, permitted unambiguous conformational assignments for the bands. The extension of similar assignments to larger alkoxy radicals is also discussed. Key words: electronic spectroscopy, organic radicals, combustion, atmospheric chemistry.


2020 ◽  
Author(s):  
Mikael Ehn ◽  
Zhandong Wang ◽  
Matti Rissanen ◽  
Olga Garmash ◽  
Lauriane Quéléver ◽  
...  

<p>Autoxidation is a process whereby organic compounds become oxidized by molecular oxygen (O<sub>2</sub>). It is ubiquitous in various reaction systems, contributing to the spoilage of food and wine, ignition in internal combustion engines, and formation of atmospheric secondary organic aerosol (SOA) from volatile emissions. Autoxidation thus greatly influences both engine operation and efficiency, and, via SOA, climate and air quality. Recent progress in atmospheric chemistry has identified double bonds and oxygen-containing moieties as structural facilitators for efficient autoxidation, and subsequent OA formation. Lacking either of these functionalities, alkanes, the primary molecular class in fuels for combustion engines and an important class of urban trace gases, have been expected to have low susceptibility to undergo autoxidation. In this work, we show that alkanes can indeed undergo efficient autoxidation both under combustion-relevant and atmospheric temperatures, consequently producing more highly oxygenated species than previously expected. By bridging methodologies and knowledge from both combustion and atmospheric chemistry, we mapped the autoxidation potential of a range of alkane structures under various conditions, from the combustion domain to the atmospheric domain. We identified the importance of isomerization steps driven by both peroxy and alkoxy radicals, and show that isomerization and production of low-volatile condensable vapors is efficient even under highly polluted ([NO]>10ppb) conditions. Our findings, currently under review, provide insights into the underlying chemical mechanisms causing highly variable SOA yields from alkanes, which were observed in previous atmospheric studies. The results of this inter-disciplinary effort provide crucial new information on oxidation processes in both combustion engines and the atmosphere, with direct implications for engine efficiency and urban air quality.</p>


RSC Advances ◽  
2016 ◽  
Vol 6 (68) ◽  
pp. 63954-63964 ◽  
Author(s):  
Feng-Yang Bai ◽  
You-Jun Liu ◽  
Xu Wang ◽  
Yan-Qiu Sun ◽  
Xiu-Mei Pan

The atmospheric and kinetic properties of CF3(CX2)2CH2OH (X = H, F) with chlorine atoms were studied by density functional and canonical variational transition state theories in conjunction with the small-curvature tunneling correction.


2016 ◽  
Vol 40 (7) ◽  
pp. 6148-6155 ◽  
Author(s):  
Bhupesh Kumar Mishra ◽  
Makroni Lily ◽  
Ramesh Chandra Deka ◽  
Asit K. Chandra

The calculated rate constants for C4F9OCH3 + OH/Cl reactions are found to be 1.94 × 10−14 and 1.74 × 10−12 cm3 molecule−1 s−1, respectively, at 298 K. The atmospheric lifetime and global warming potential for HFE-7100 are computed to be 2.12 years and 155.3, respectively.


Author(s):  
Jack G. Calvert ◽  
John J. Orlando ◽  
William R. Stockwell ◽  
Timothy J. Wallington

The atmospheric chemistry of alkoxy radicals determines the first-generation oxidation products of organic compounds in the atmosphere. There are three competing fates for alkoxy radicals: reaction with molecular oxygen (O2), isomerization, and decomposition (Atkinson and Arey, 2003b; Devolder, 2003; Orlando et al., 2003b; Calvert et al., 2008). Reaction with O2 preserves the carbon chain of the parent alkane and results in the production of a carbonyl compound and HO2. Unimolecular decomposition usually results in the formation of an alkyl radical and a carbonyl compound with a shortening of the carbon chain. Unimolecular isomerization usually leads to multifunctional oxidation products (e.g., 1,4-hydroxycarbonyls and 1,4-hydroxynitrates) and a preservation of the carbon chain. These potentially competing pathways are illustrated in Figure VI-A-1 for the 2-pentoxy radical: Absolute rate coefficients for these processes have been obtained for only a few of the smaller alkoxy radicals. For example, rate coefficients have been firmly established only over a range of temperatures for reaction of a subset of the C1–C6 alkoxy radicals with O2; dissociation rate coefficients have only been directly measured for ethoxy, 2-propoxy, 2-butoxy, and tert-butoxy radicals (Balla et al., 1985; Blitz et al., 1999; Caralp et al., 1999; Devolder et al., 1999; Fittschen et al., 1999, 2000; Falgayrac et al., 2004); and no direct measurement of isomerization rates have been reported to date. A large portion of the database describing the atmospheric behavior of alkoxy radicals has been built up primarily from two sources: (1) environmental chamber experiments, where end-product distributions observed under atmospheric conditions have been used to infer relative rates of competing alkoxy radical reactions (e.g., Carter et al., 1976; Cox et al., 1981; Niki et al., 1981a; Eberhard et al., 1995; Aschmann et al., 1997; Orlando et al., 2000a; Cassanelli et al., 2006); and (2) from theoretical methodologies that lend themselves well to the study of unimolecular processes (e.g., Somnitz and Zellner, 2000a, 2000b, 2000c; Mereau et al., 2000a, 2000b; Fittschen et al., 2000; Lin and Ho, 2002; Mereau et al., 2003; Davis and Francisco, 2011). An overview of these three classes of competing alkoxy radical reactions (reaction with O2, unimolecular decomposition, and isomerization) is given in this section.


1997 ◽  
Vol 101 (29) ◽  
pp. 5302-5308 ◽  
Author(s):  
Timothy J. Wallington ◽  
Michael D. Hurley ◽  
James C. Ball ◽  
Ann M. Straccia ◽  
Jesper Platz ◽  
...  

ChemInform ◽  
2004 ◽  
Vol 35 (12) ◽  
Author(s):  
John J. Orlando ◽  
Geoffrey S. Tyndall ◽  
Timothy J. Wallington

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