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Использование обратного преобразования Лапласа для определения поуровневых сечений диссоциации и обменов колебательной энергией. / Байков, Б. С.; Баялина, Д. К.; Кустова, Е. В.

In: ВЕСТНИК САНКТ-ПЕТЕРБУРГСКОГО УНИВЕРСИТЕТА. СЕРИЯ 1: МАТЕМАТИКА, МЕХАНИКА, АСТРОНОМИЯ, Vol. 3 (61), No. 4, 2016, p. 663-674.

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@article{46c31b2f73534ea393fa7875643a0499,
title = "Использование обратного преобразования Лапласа для определения поуровневых сечений диссоциации и обменов колебательной энергией",
abstract = "In the present work we study the cross sections of VV (vibration-vibration) and VT (vibration-translation) energy exchanges in nitrogen and oxygen as well as the vibrational state-specific cross sections of dissociation reaction in N2 molecules. For VV- and VT-transitions the original approximations of the rate coefficients have been modified to make it possible application of the inverse Laplace transformation in the analytical form. A satisfactory approximation of the state-to-state dissociation rate coefficient allowing for the application of the inverse Laplace transformation is also proposed. For all considered reactions, analytical expressions for the cross sections are obtained. The results are analyzed in the wide range of energies and vibrational levels. It is shown that cross sections of VV transitions increase almost linearly with the energy of colliding particles. VT-exchanges and dissociation reaction manifest threshold behaviour, and their cross sections are non-monotonic. Dissociation threshold is considerably shifted towards low energy region for high vibrational states. Using the hard sphere model for the dissociation cross section results in significant inaccuracy. The results of our work can be applied in non-equilibrium fluid dynamics while simulating rarefied gas flows using the direct Monte-Carlo methods. Refs 23. Figs 4. Tables 2.",
keywords = "неравновесная колебательно-химическая кинетика, сечения реакций, поуровневый коэффициент скорости диссоциации, коэффициенты скорости VV- и VT-обменов, non-equilibrium vibrational-chemical kinetics, reaction cross sections, state-to-state dissociation rate coefficient, rate coefficients of VV- and VT-exchanges",
author = "Байков, {Б. С.} and Баялина, {Д. К.} and Кустова, {Е. В.}",
note = "Байков Б. С., Баялина Д. К., Кустова Е. В. Использование обратного преобразования Лапласа для определения поуровневых сечений диссоциации и обменов колебательной энергией // Вестник Санкт-Петербургского университета. Серия 1. Математика. Механика. Астрономия. 2016. Т. 3 (61). Вып. 4. С. 663–674. DOI: 10.21638/11701/spbu01.2016.416",
year = "2016",
language = "русский",
volume = "3 (61)",
pages = "663--674",
journal = "ВЕСТНИК САНКТ-ПЕТЕРБУРГСКОГО УНИВЕРСИТЕТА. МАТЕМАТИКА. МЕХАНИКА. АСТРОНОМИЯ",
issn = "1025-3106",
publisher = "Издательство Санкт-Петербургского университета",
number = "4",

}

RIS

TY - JOUR

T1 - Использование обратного преобразования Лапласа для определения поуровневых сечений диссоциации и обменов колебательной энергией

AU - Байков, Б. С.

AU - Баялина, Д. К.

AU - Кустова, Е. В.

N1 - Байков Б. С., Баялина Д. К., Кустова Е. В. Использование обратного преобразования Лапласа для определения поуровневых сечений диссоциации и обменов колебательной энергией // Вестник Санкт-Петербургского университета. Серия 1. Математика. Механика. Астрономия. 2016. Т. 3 (61). Вып. 4. С. 663–674. DOI: 10.21638/11701/spbu01.2016.416

PY - 2016

Y1 - 2016

N2 - In the present work we study the cross sections of VV (vibration-vibration) and VT (vibration-translation) energy exchanges in nitrogen and oxygen as well as the vibrational state-specific cross sections of dissociation reaction in N2 molecules. For VV- and VT-transitions the original approximations of the rate coefficients have been modified to make it possible application of the inverse Laplace transformation in the analytical form. A satisfactory approximation of the state-to-state dissociation rate coefficient allowing for the application of the inverse Laplace transformation is also proposed. For all considered reactions, analytical expressions for the cross sections are obtained. The results are analyzed in the wide range of energies and vibrational levels. It is shown that cross sections of VV transitions increase almost linearly with the energy of colliding particles. VT-exchanges and dissociation reaction manifest threshold behaviour, and their cross sections are non-monotonic. Dissociation threshold is considerably shifted towards low energy region for high vibrational states. Using the hard sphere model for the dissociation cross section results in significant inaccuracy. The results of our work can be applied in non-equilibrium fluid dynamics while simulating rarefied gas flows using the direct Monte-Carlo methods. Refs 23. Figs 4. Tables 2.

AB - In the present work we study the cross sections of VV (vibration-vibration) and VT (vibration-translation) energy exchanges in nitrogen and oxygen as well as the vibrational state-specific cross sections of dissociation reaction in N2 molecules. For VV- and VT-transitions the original approximations of the rate coefficients have been modified to make it possible application of the inverse Laplace transformation in the analytical form. A satisfactory approximation of the state-to-state dissociation rate coefficient allowing for the application of the inverse Laplace transformation is also proposed. For all considered reactions, analytical expressions for the cross sections are obtained. The results are analyzed in the wide range of energies and vibrational levels. It is shown that cross sections of VV transitions increase almost linearly with the energy of colliding particles. VT-exchanges and dissociation reaction manifest threshold behaviour, and their cross sections are non-monotonic. Dissociation threshold is considerably shifted towards low energy region for high vibrational states. Using the hard sphere model for the dissociation cross section results in significant inaccuracy. The results of our work can be applied in non-equilibrium fluid dynamics while simulating rarefied gas flows using the direct Monte-Carlo methods. Refs 23. Figs 4. Tables 2.

KW - неравновесная колебательно-химическая кинетика

KW - сечения реакций

KW - поуровневый коэффициент скорости диссоциации

KW - коэффициенты скорости VV- и VT-обменов

KW - non-equilibrium vibrational-chemical kinetics

KW - reaction cross sections

KW - state-to-state dissociation rate coefficient

KW - rate coefficients of VV- and VT-exchanges

UR - http://vestnik.spbu.ru/html16/s01/s01v4/s01v4.html

M3 - статья

VL - 3 (61)

SP - 663

EP - 674

JO - ВЕСТНИК САНКТ-ПЕТЕРБУРГСКОГО УНИВЕРСИТЕТА. МАТЕМАТИКА. МЕХАНИКА. АСТРОНОМИЯ

JF - ВЕСТНИК САНКТ-ПЕТЕРБУРГСКОГО УНИВЕРСИТЕТА. МАТЕМАТИКА. МЕХАНИКА. АСТРОНОМИЯ

SN - 1025-3106

IS - 4

ER -

ID: 7595189