A Theory on the Relationship between Viscosity and Molecular Weight in Bulk Polymers
スポンサーリンク
概要
- 論文の詳細を見る
A statistical mechanical theory of steady viscosity in bulk polymers is presented.In slowly relaxing phenomena such as steady viscosity, the inter-chain relaxation is predominant and the segmental conformation of each polymer molecule attains to a state of dynamic equilibrium. It is assumed tbat the intermolecular force between two molecules consists of two parts: the force derived from potential and the friction due to entanglements between them. The general expression of viscosity is derived from the fundamental equation for the velocity distribution function of a polymer molecule, using Born-Green's method. The molecular weight dependence of viscosity η is roughly estimated by taking into account the inner structure and conformation of polymer molecules. The result is η=C_1N+0_2N^3, where N is the number of segments constituting a polymer molecule, C_1 and C_2 are constants, and C_1≫0_2. This prediction agrees semi-quantitatively with experiment.
- 社団法人日本物理学会の論文
- 1964-01-05
著者
-
Chikahisa Yoshiaki
Department Of Physics Faculity Of Science Tokyo Metropolitan University
-
Chikahisa Y.
Department of Physics, Faculity of Science, Tokyo Metropolitan University
関連論文
- Non-Newtonian Intrinsic Viscosity of Coiled Chain Polymers. : II.. Molecular Expansions and Solvent Effect
- A Theory on the Relationship between Viscosity and Molecular Weight in Bulk Polymers