Size and shape of the molecules in artificially branched polystyrene
- 1 May 1952
- journal article
- research article
- Published by Wiley in Journal of Polymer Science
- Vol. 8 (5), 477-494
- https://doi.org/10.1002/pol.1952.120080505
Abstract
A sample of copolymer of divinylbenzene and styrene has been prepared and fractionated. Using the techniques of light scattering and viscometry the relations between the molecular size, intrinsic viscosity, and weight‐average molecular weight have been determined. The results may be interpreted in terms of the already existing theory of branched polymers. The curve of logarithm of intrinsic viscosity plotted against logarithm of molecular weight shows clearly the effect of branching in the polymer chains, the intrinsic viscosities of the higher molecular weight fractions being low compared to those of pure polystyrene. The mean square radius of the molecules as determined by light scattering shows similar effects, though complications obscure the picture. Some of the other solution properties of the branched materials also are peculiar. The results show that the semiquantitative determination of branching is possible in this way.This publication has 8 references indexed in Scilit:
- Absolute Intensity of Light Scattering from Pure Liquids and SolutionsThe Journal of Chemical Physics, 1950
- Molecular configuration and thermodynamic parameters from intrinsic viscositiesJournal of Polymer Science, 1950
- Light Scattering Investigation of the Structure of PolystyreneThe Journal of Chemical Physics, 1950
- Solubility of Heterogeneous PolymersThe Journal of Chemical Physics, 1949
- Some Thermodynamic Properties of Polystyrene Solutions.The Journal of Physical Chemistry, 1949
- Synthesis of Multichain Polymers and Investigation of their Viscosities1Journal of the American Chemical Society, 1948
- Effects of Cross-Linking and Branching on the Molecular Constitution of Diene Polymers1Journal of the American Chemical Society, 1947
- Theory of Molecular Size Distribution and Gel Formation in Branched-Chain PolymersThe Journal of Chemical Physics, 1943