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Journal ArticleDOI

Unperturbed Dimension and Translational Friction Constant of Branched Polymers

Michio Kurata, +1 more
- 01 Nov 1964 - 
- Vol. 41, Iss: 9, pp 2934-2944
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TLDR
In this article, a theory of the conformational properties of random-flight branched molecules is developed for estimating the branching effect on the translational friction constant Ξb as well as on the mean-square statistical radius 〈S2〉b½.
Abstract
A theory of the conformational properties of random‐flight branched molecules is developed for estimating the branching effect on the translational friction constant Ξb as well as on the mean‐square statistical radius 〈S2〉b½. Calculations are made for three types of branching—star, normal (or linear), and random types, and for two types of distribution of the branch units—uniform and random types. It is found that the contraction of molecular dimensions produced by branching occurs to the highest degree in the star types of branching and to the lowest degree in the normal type of branching, and that the heterogeneity in the distance between the nearest pair of branch units generally diminishes the degree of the molecular contraction. The applicability of the Flory‐type equation, Ξb=η0Pb〈S2〉b½, to the branched molecules is discussed with the intention of searching the experimental method for determination of the number of branch units involved in the various types of branched molecules. Here η0 is the visc...

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Citations
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Book ChapterDOI

Static and dynamic light scattering from branched polymers and biopolymers

TL;DR: In this paper, the authors deal with branched macromolecules in dilute solution, where the individual molecules are observed, and the common technique for determining the shape of macromoles is static light scattering.
Book ChapterDOI

Preparation and properties of star-branched polymers

TL;DR: In this article, the effect of star-branching on T g of low molecular weight polymers is described. And the methods available for the preparation of starbranched polymers are described.
Book ChapterDOI

Conformational Properties of Branched Polymers: Theory and Simulations

TL;DR: In this article, a review of the application of numerical simulation techniques to relevant theoretical problems concerning branched polymer systems, taking also into account the related experimental data, is presented, where Monte Carlo, molecular dynamics and Brownian dynamics methods are employed to simulate the equilibrium and dynamic behavior, and also to reproduce hydrodynamic properties.
References
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Journal ArticleDOI

The Dimensions of Chain Molecules Containing Branches and Rings

TL;DR: In this paper, the mean square radii of various branched and ringed polymer molecules were derived under the usual assumptions regarding the statistics of chain configuration, and it was shown that the number of branches or rings can be determined from light scattering measurements.
Journal ArticleDOI

Theory of Molecular Size Distribution and Gel Formation in Branched Polymers II. General Cross Linking

TL;DR: In this paper, a statistical calculation of the gel point and of the molecular size distribution for cross-linked high polymers of arbitrary initial size distribution is made for crosslink polymers, which depends only on the weight-average polymerization degree of the initial polymer and the degree of cross linking.
Journal ArticleDOI

The general theory of irreversible processes in solutions of macromolecules

TL;DR: In this article, a general theory of irreversible processes in solutions of macromolecules, previously formulated by the author, is reviewed and applied to viscoelastic behavior, flow birefringence, and the Kerr effect, and to dielectric dispersion.
Journal ArticleDOI

The Behavior of Macromolecules in Inhomogeneous Flow

TL;DR: In this paper, the authors investigated the statistical behavior of the individual links of the solved molecules and found that the contribution of a single molecule to the viscosity coefficient as well as to the double refraction of the solution is proportional to the square of the degree of polymerization.