期刊
JOURNAL OF PHYSICAL CHEMISTRY A
卷 116, 期 19, 页码 4720-4725出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp302719j
关键词
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资金
- U.S. Department of Energy-Basic Energy Sciences [DE-FG02-88ER13857]
- U.S. Department of Energy (DOE) [DE-FG02-88ER13857] Funding Source: U.S. Department of Energy (DOE)
This work presents the first direct experimental study of the rate constant for the reaction of OH with iso-butanol (2-methyl-1-propanol) at temperatures from 907 to 1147 K at near-atmospheric pressures. OH time-histories were measured behind reflected shock waves using a narrow-linewidth laser absorption method during reactions of dilute mixtures of tert-butylhydroperoxide (as a fast source of OH) with iso-butanol in excess. The title reaction's overall rate constant (OH + iso-butanol ->(koverall) all products) minus the rate constant for the beta-radical-producing channel (OH + iso-butanol ->(k beta) 1-hydroxy-2-methyl-prop-2-yl radical + H2O) was determined from the pseudo-first-order rate of OH decay. A two-parameter Arrhenius fit of the experimentally determined rate constant in the current temperature range yields the expression (k(overall) - k(beta)) = 1.84 x 10(-10) exp(-2350/T[K]) cm(3) molecule(-1) s(-1). A recommendation for the overall rate constant, including k(beta),, is made, and comparisons of the results to rate constant recommendations from the literature are discussed.
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