Research output: Contribution to journal › Article › peer-review
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.Research output: Contribution to journal › Article › peer-review
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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