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Title: Primitive models of chemical association. II. Polymerization into flexible chain molecules of prescribed length

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.473331· OSTI ID:463521
 [1]; ;  [1]
  1. Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794-3400 (United States)

The structural properties of the totally flexible sticky two-point (S2P) model for polymerization into chain molecules of fixed length are studied. The model is represented by an n-component mixture of hard spheres of the same size with species 2,{hor_ellipsis},n{minus}1 bearing two attractive sticky sites A and B, randomly distributed on the surface. The hard spheres of species 1 and n have only one site per particle, site B for species 1 and site A for species n. Due to the specific choice for the attractive interaction, which is present only between site B of the particles of species a and site A of the particles of species a+1, this version of the S2P model represents an associating fluid that polymerizes into freely jointed tangent hard-sphere chain molecules. The correlation functions of this model are studied at all degrees of association using a recently obtained general solution of the polymer Percus{endash}Yevick (PPY) approximation [Yu. Kalyuzhnyi and P. Cummings, J. Chem. Phys. {bold 103}, 3265 (1995)]. Comparison of the results of the present theory in the complete association limit with corresponding computer-simulation results and results of other theories is presented and discussed. The complete-association results constitute a quantitatively successful theory of the mean monomer{endash}monomer distribution functions for n{le}16 but for n=50 these functions are no longer quantitatively accurate. {copyright} {ital 1997 American Institute of Physics.}

OSTI ID:
463521
Journal Information:
Journal of Chemical Physics, Vol. 106, Issue 5; Other Information: PBD: Feb 1997
Country of Publication:
United States
Language:
English