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首页> 外文期刊>Chemical Physics: A Journal Devoted to Experimental and Theoretical Research Involving Problems of Both a Chemical and Physical Nature >Gas-phase Boudouard disproportionation reaction between highly vibrationally excited CO molecules
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Gas-phase Boudouard disproportionation reaction between highly vibrationally excited CO molecules

机译:高度振动激发的CO分子之间的气相Boudouard歧化反应

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摘要

The gas-phase Boudouard disproportionation reaction between two highly vibrationally excited CO molecules in the ground electronic state has been studied in optically pumped CO. The gas temperature and the CO vibrational level populations in the reaction region, as well as the CO2 concentration in the reaction products have been measured using FTIR emission and absorption spectroscopy. The results demonstrate that CO2 formation in the optically pumped reactor is controlled by the high CO vibrational level populations, rather than by CO partial pressure or by flow temperature. The disproportionation reaction rate constant has been determined from the measured CO2 and CO concentrations using the perfectly stirred reactor (PSR) approximation. The reaction activation energy, 11.6 +/- 0.3 eV (close to the CO dissociation energy of 11.09 eV), was evaluated using the statistical transition state theory, by comparing the dependence of the measured CO2 concentration and of the calculated reaction rate constant on helium partial pressure. The disproportionation reaction rate constant measured at the present conditions is k(f) = (9 +/- 4) x 10(-18) cm(3)/s. The reaction rate constants obtained from the experimental measurements and from the transition state theory are in good agreement. (c) 2006 Elsevier B.V. All rights reserved.
机译:在光泵浦CO中研究了处于基态电子状态的两个高度振动激发的CO分子之间的气相Boudouard歧化反应。反应区中的气体温度和CO振动能级数以及反应中的CO2浓度产品已使用FTIR发射和吸收光谱法进行了测量。结果表明,光泵浦反应器中的CO2形成是由高CO振动能级总体控制的,而不是由CO分压或流动温度控制的。歧化反应速率常数已使用完全搅拌反应器(PSR)近似值从测得的CO2和CO浓度确定。通过统计跃迁状态理论,通过比较测得的CO2浓度和计算出的反应速率常数对氦气的依赖性,评估了反应活化能11.6 +/- 0.3 eV(接近11.09 eV的CO解离能)分压。在当前条件下测得的歧化反应速率常数为k(f)=(9 +/- 4)x 10(-18)cm(3)/ s。从实验测量和过渡态理论获得的反应速率常数非常吻合。 (c)2006 Elsevier B.V.保留所有权利。

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