The molecular dimensions of linear polyethylene published in the literature
were reevaluated in order to discuss the radii of gyration RG nd their dep
endence on molar mass, M. The relationships R-G = bM(G) and the exponents a
of this equation in comparison with the unperturbed dimensions of linear p
olyethylene obtained from viscometric measurements allowed the discussion o
f the reliability of the data and the reasons for deviations. The exponent
a determined by light scattering for linear polyethylene in good solvent, t
etraline, showed molecular dissolution, whereas in 1-chloronaphthalene and
trichlorobenzene, the exponent a is lower than expected for good solvents.
Microgels and aggregates of molecules affect the exponents. Radii of gyrati
on measured directly by light scattering at fractions of linear polyethylen
e in the theta solvent, diphenylmethane, indicate incomplete molecular diss
olution and the presence of branched structures. (C) 2001 Elsevier Science
Ltd. All rights reserved.