Rate Constants for the Thermal Decomposition of Ethanol and Its Bimolecular Reactions with OH and D: Reflected Shock Tube and Theoretical Studies

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2010-09, Vol.114 (35), p.9425-9439
• Main Authors: Sivaramakrishnan, R, Su, M.-C, Michael, J. V, Klippenstein, S. J, Harding, L. B, Ruscic, B
• Format: Article
• Language: English
• Subjects: A: Kinetics, Spectroscopy
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp104759d

The thermal decomposition of ethanol and its reactions with OH and D have been studied with both shock tube experiments and ab initio transition state theory-based master equation calculations. Dissociation rate constants for ethanol have been measured at high T in reflected shock waves using OH optical absorption and high-sensitivity H-atom ARAS detection. The three dissociation processes that are dominant at high T are A C 2 H 5 OH → C 2 H 4 + H 2 O B → CH 3 + CH 2 OH C → C 2 H 5 + OH The rate coefficient for reaction was measured directly with high sensitivity at 308 nm using a multipass optical White cell. Meanwhile, H-atom ARAS measurements yield the overall rate coefficient and that for the sum of reactions and , since H-atoms are instantaneously formed from the decompositions of CH2OH and C2H5 into CH2O + H and C2H4 + H, respectively. By difference, rate constants for reaction 1 could be obtained. One potential complication is the scavenging of OH by unreacted ethanol in the OH experiments, and therefore, rate constants for D OH + C 2 H 5 OH → products were measured using tert-butyl hydroperoxide (tBH) as the thermal source for OH. The present experiments can be represented by the Arrhenius expression k = ( 2 .5 ± 0 .43 ) × 10 − 11 exp ( − 911 ± 191 K / T ) cm 3 molecule − 1 s − 1 over the T range 857−1297 K. For completeness, we have also measured the rate coefficient for the reaction of D atoms with ethanol E D + C 2 H 5 OH → products whose H analogue is another key reaction in the combustion of ethanol. Over the T range 1054−1359 K, the rate constants from the present experiments can be represented by the Arrhenius expression, k = ( 3 .98 ± 0 .76 ) × 10 − 10 exp ( − 4494 ± 235 K / T ) cm 3 molecule − 1 s − 1 The high-pressure rate coefficients for reactions and were studied with variable reaction coordinate transition state theory employing directly determined CASPT2/cc-pvdz interaction energies. Reactions , , and were studied with conventional transition state theory employing QCISD(T)/CBS energies. For the saddle point in reaction , additional high-level corrections are evaluated. The predicted reaction exo- and endothermicities are in good agreement with the current Active Thermochemical Tables values. The transition state theory predictions for the microcanonical rate coefficients in ethanol decomposition are incorporated in master equation calculations to yield predictions for the temperature and pressure dependences of reactions −. With mod