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On the theory of the mechanochemical sorption-striction phenomenon in nanoporous bodies with dispersion forces. / Rusanov, A. I.; Kuni, F. M.

In: Russian Journal of General Chemistry, Vol. 77, No. 3, 01.03.2007, p. 371-392.

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Rusanov, A. I. ; Kuni, F. M. / On the theory of the mechanochemical sorption-striction phenomenon in nanoporous bodies with dispersion forces. In: Russian Journal of General Chemistry. 2007 ; Vol. 77, No. 3. pp. 371-392.

BibTeX

@article{1c157fabe972400e95ab5992f8d4f2a4,
title = "On the theory of the mechanochemical sorption-striction phenomenon in nanoporous bodies with dispersion forces",
abstract = "The soption-striction phenomenon is a change in the dimensions of a porous body in the course of sorption due to the strain caused by the action of molecular forces. The formulation of the theory of the phenomenon includes the following problems: the statistical-mechanical calculation of the pressure tensor in the pore interior as a function of the pore shape and size; the analysis of the role of surface tension in the mechanical equilibrium condition at the pore wall and producing strain at various mechanisms (physical or chemical) of sorption; the calculation of the body strain within the theory of elasticity. The calculation of the pressure tensor was performed for spherical, cylindrical, and flat (slit-like) pores using asymptotic relations for ordinary dispersion forces (in the context of the nano-scaled pore size) and dispersion forces with electromagnetic retardation (for micropores of larger dimensions), with the pair potential exponents -6 and -7, respectively. The results obtained consider both an initial contraction of a porous body in a vacuum and an additional contraction, if any, or the body expansion on the initial stage of the gas sorption. The exact calculation of strain is given for a cylindrical and spherical pore. The role of surface tension is shown to be reduced, first, to the initial contractive strain of a porous body in a vacuum and, second, to the body dilatation in the course of the gas sorption. A small additional contraction of a porous body on the initial stage of sorption (that, as is shown, cannot be caused by surface tension) is explained by the peculiarities of the sorbate pressure tensor in a pore. The effect is more pronounced the smaller the pore size and the lower the temperature, and is typical for nanoporous bodies. A general consideration based on the Irving-Kirkwood pressure tensor qualitatively confirms the regularities established for any kind of molecular interaction.",
author = "Rusanov, {A. I.} and Kuni, {F. M.}",
year = "2007",
month = mar,
day = "1",
doi = "10.1134/S1070363207030097",
language = "English",
volume = "77",
pages = "371--392",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "3",

}

RIS

TY - JOUR

T1 - On the theory of the mechanochemical sorption-striction phenomenon in nanoporous bodies with dispersion forces

AU - Rusanov, A. I.

AU - Kuni, F. M.

PY - 2007/3/1

Y1 - 2007/3/1

N2 - The soption-striction phenomenon is a change in the dimensions of a porous body in the course of sorption due to the strain caused by the action of molecular forces. The formulation of the theory of the phenomenon includes the following problems: the statistical-mechanical calculation of the pressure tensor in the pore interior as a function of the pore shape and size; the analysis of the role of surface tension in the mechanical equilibrium condition at the pore wall and producing strain at various mechanisms (physical or chemical) of sorption; the calculation of the body strain within the theory of elasticity. The calculation of the pressure tensor was performed for spherical, cylindrical, and flat (slit-like) pores using asymptotic relations for ordinary dispersion forces (in the context of the nano-scaled pore size) and dispersion forces with electromagnetic retardation (for micropores of larger dimensions), with the pair potential exponents -6 and -7, respectively. The results obtained consider both an initial contraction of a porous body in a vacuum and an additional contraction, if any, or the body expansion on the initial stage of the gas sorption. The exact calculation of strain is given for a cylindrical and spherical pore. The role of surface tension is shown to be reduced, first, to the initial contractive strain of a porous body in a vacuum and, second, to the body dilatation in the course of the gas sorption. A small additional contraction of a porous body on the initial stage of sorption (that, as is shown, cannot be caused by surface tension) is explained by the peculiarities of the sorbate pressure tensor in a pore. The effect is more pronounced the smaller the pore size and the lower the temperature, and is typical for nanoporous bodies. A general consideration based on the Irving-Kirkwood pressure tensor qualitatively confirms the regularities established for any kind of molecular interaction.

AB - The soption-striction phenomenon is a change in the dimensions of a porous body in the course of sorption due to the strain caused by the action of molecular forces. The formulation of the theory of the phenomenon includes the following problems: the statistical-mechanical calculation of the pressure tensor in the pore interior as a function of the pore shape and size; the analysis of the role of surface tension in the mechanical equilibrium condition at the pore wall and producing strain at various mechanisms (physical or chemical) of sorption; the calculation of the body strain within the theory of elasticity. The calculation of the pressure tensor was performed for spherical, cylindrical, and flat (slit-like) pores using asymptotic relations for ordinary dispersion forces (in the context of the nano-scaled pore size) and dispersion forces with electromagnetic retardation (for micropores of larger dimensions), with the pair potential exponents -6 and -7, respectively. The results obtained consider both an initial contraction of a porous body in a vacuum and an additional contraction, if any, or the body expansion on the initial stage of the gas sorption. The exact calculation of strain is given for a cylindrical and spherical pore. The role of surface tension is shown to be reduced, first, to the initial contractive strain of a porous body in a vacuum and, second, to the body dilatation in the course of the gas sorption. A small additional contraction of a porous body on the initial stage of sorption (that, as is shown, cannot be caused by surface tension) is explained by the peculiarities of the sorbate pressure tensor in a pore. The effect is more pronounced the smaller the pore size and the lower the temperature, and is typical for nanoporous bodies. A general consideration based on the Irving-Kirkwood pressure tensor qualitatively confirms the regularities established for any kind of molecular interaction.

UR - http://www.scopus.com/inward/record.url?scp=34247392386&partnerID=8YFLogxK

U2 - 10.1134/S1070363207030097

DO - 10.1134/S1070363207030097

M3 - Article

AN - SCOPUS:34247392386

VL - 77

SP - 371

EP - 392

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 3

ER -

ID: 51304949