Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98118
Title: Ab initio variational transition state theory and master equation study of the reaction (OH)3SiOCH2 + CH3 ⇌ (OH)3SiOC2H5
Authors: Nurkowski, Daniel
Klippenstein, Stephen J.
Georgievskii, Yuri
Verdicchio, Marco
Jasper, Ahren W.
Akroyd, Jethro
Mosbach, Sebastian
Kraft, Markus
Keywords: DRNTU::Science::Medicine::Biomedical engineering
Issue Date: 2015
Source: Nurkowski, D., Klippenstein, S. J., Georgievskii, Y., Verdicchio, M., Jasper, A. W., Akroyd, J., et al. (2015). Ab initio variational transition state theory and master equation study of the reaction (OH)3SiOCH2 + CH3 ⇌ (OH)3SiOC2H5. Zeitschrift fur physikalische chemie, 229(5), 691-708.
Series/Report no.: Zeitschrift fur physikalische chemie
Abstract: In this paper we use variable reaction coordinate variational transition state theory (VRC-TST) to calculate the reaction rate constants for the two reactions, R1: (OH)3SiOCH2 + CH3 ⇌ (OH)3SiOC2H5, and R2: CH2OH + CH3 ⇌ C2H5OH. The first reaction is an important channel during the thermal decomposition of tetraethoxysilane (TEOS), and its rate coefficient is the main focus of this work. The second reaction is analogous to the first and is used as a basis for comparison. The interaction energies are obtained on-the-fly at the CASPT2(2e,2o)/cc-pVDZ level of theory. A one-dimensional correction to the sampled energies was introduced to account for the energetic effects of geometry relaxation along the reaction path. The computed, high-pressure rate coefficients were calculated to be, R1: k1 = 2.406 × 10−10T−0.301 exp (− 271.4/T) cm3 molecule–1 s–1 and R2: k2 = 1.316 × 10−10T−0.189 exp (− 256.5/T) cm3 molecule–1 s–1. These rates differ from each other by only 10% – 30% over the temperature range 300–2000 K. A comparison of the computed rates with experimental data shows good agreement and an improvement over previous results. The pressure dependency of the reaction R1 is explored by solving a master equation using helium as a bath gas. The results obtained show that the reaction is only weakly pressure dependent over the temperature range 300–1700 K, with the predicted rate constant being within 50% of its high-pressure limit at atmospheric pressure.
URI: https://hdl.handle.net/10356/98118
http://hdl.handle.net/10220/25660
DOI: 10.1515/zpch-2014-0640
Rights: © 2015 De Gruyter. This paper was published in Zeitschrift fur Physikalische Chemie and is made available as an electronic reprint (preprint) with permission of De Gruyter. The paper can be found at the following official DOI: [http://dx.doi.org/10.1515/zpch-2014-0640]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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