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Solution properties of poly(fluorostyrene‐co‐chlorostyrene) copolymers. I. Light scattering, differential refractometry and viscometry
Author(s) -
Segudovic Nikola,
Vukovic Radivoje,
Kuresevic Vjera,
Karasz Frank E.,
Macknight William J.
Publication year - 1993
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.4990310211
Subject(s) - virial coefficient , copolymer , intrinsic viscosity , refractometry , viscometer , polymer chemistry , solvent , polystyrene , molar mass , viscosity , materials science , light scattering , chloroform , chemistry , refractive index , scattering , polymer , thermodynamics , organic chemistry , optics , physics , composite material , optoelectronics
The weight‐average molecular weights (M̄ w ) of nominally random, unfractionated copolymers of ortho ‐ and para ‐fluorostyrene and ortho ‐ and para ‐chlorostyrene were determined by light scattering measurements in tetrahydro‐furan, toluene, carbon tetrachloride and chloroform. It was shown that there is no significant variation in measured M̄ w in the various solvents, a finding indicating that the copolymers are not compositionally heterogeneous. Intrinsic viscosity measurements in the same solvents established a consistent relationship between [ n ] and M̄ w despite the differences in copolymer compositions. It was not possible to establish a similar relationship between the second virial coefficient A 2 and M̄ w . It was concluded that measurements of the specific refractive index increment could be used for determining copolymer composition if the measurements were performed in thermodynamically poorer solvents. The results established for the Mark‐Houwink constant α, intrinsic viscosity, and A 2 values indicated that these solvated copolymer molecules are in a less expanded conformation than are polystyrene molecules of similar molecular weights in a given solvent.