Electric birefringence in solutions of cellulose carbanilate as a function of molecular weight

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Electric birefringence in solutions of cellulose carbanilate as a function of molecular weight. / Tsvetkov, V. N.; Rjumtsev, E. I.; Andreeva, L. N.; Pogodina, N. V.; Lavrenko, P. N.; Kutsenko, L. I.

In: European Polymer Journal, Vol. 10, No. 7, 07.1974, p. 563-570.

Research output: Contribution to journal › Article › peer-review

Author

Tsvetkov, V. N. ; Rjumtsev, E. I. ; Andreeva, L. N. ; Pogodina, N. V. ; Lavrenko, P. N. ; Kutsenko, L. I. / Electric birefringence in solutions of cellulose carbanilate as a function of molecular weight. In: European Polymer Journal. 1974 ; Vol. 10, No. 7. pp. 563-570.

BibTeX

@article{73fba2cb172e4ad79e5441bb9769bae3,

title = "Electric birefringence in solutions of cellulose carbanilate as a function of molecular weight",

abstract = "Electro-optical, dynamo-optical and hydrodynamic properties of solutions of some fractions of cellulose carbanilate (CC) in dioxan have been investigated. In a variable electric field, strong dispersion of the Kerr effect is observed, indicating the dipole-orientational mechanism of electrical birefringence and its relaxation. A comparison of relaxation times of fractions with their molecular weights and intrinsic viscosities indicates that the mechanism responsible for the Kerr effect is the rotation of the molecule as a whole in an electric field (a kinetically rigid molecule). The dependence of relaxation time on molecular weight (M) shows that, with increase in M, the conformation of the CC molecule changes from a slightly curved rod to a rigid Gaussian coil. The same conclusion may be drawn from a study on the dependence of the equilibrium value of the Kerr constant on M. In the Gaussian range (high M), the Kerr effect depends on the longitudinal (with respect to the chain) component of the dipole moment formed by the CO bonds in the glucoside ring. At low M, the transverse components of the monomer dipoles begin to play an important part in birefringence.",

author = "Tsvetkov, {V. N.} and Rjumtsev, {E. I.} and Andreeva, {L. N.} and Pogodina, {N. V.} and Lavrenko, {P. N.} and Kutsenko, {L. I.}",

year = "1974",

month = jul,

doi = "10.1016/0014-3057(74)90163-3",

language = "English",

volume = "10",

pages = "563--570",

journal = "European Polymer Journal",

issn = "0014-3057",

publisher = "Elsevier",

number = "7",

}

RIS

TY - JOUR

T1 - Electric birefringence in solutions of cellulose carbanilate as a function of molecular weight

AU - Tsvetkov, V. N.

AU - Rjumtsev, E. I.

AU - Andreeva, L. N.

AU - Pogodina, N. V.

AU - Lavrenko, P. N.

AU - Kutsenko, L. I.

PY - 1974/7

Y1 - 1974/7

N2 - Electro-optical, dynamo-optical and hydrodynamic properties of solutions of some fractions of cellulose carbanilate (CC) in dioxan have been investigated. In a variable electric field, strong dispersion of the Kerr effect is observed, indicating the dipole-orientational mechanism of electrical birefringence and its relaxation. A comparison of relaxation times of fractions with their molecular weights and intrinsic viscosities indicates that the mechanism responsible for the Kerr effect is the rotation of the molecule as a whole in an electric field (a kinetically rigid molecule). The dependence of relaxation time on molecular weight (M) shows that, with increase in M, the conformation of the CC molecule changes from a slightly curved rod to a rigid Gaussian coil. The same conclusion may be drawn from a study on the dependence of the equilibrium value of the Kerr constant on M. In the Gaussian range (high M), the Kerr effect depends on the longitudinal (with respect to the chain) component of the dipole moment formed by the CO bonds in the glucoside ring. At low M, the transverse components of the monomer dipoles begin to play an important part in birefringence.

AB - Electro-optical, dynamo-optical and hydrodynamic properties of solutions of some fractions of cellulose carbanilate (CC) in dioxan have been investigated. In a variable electric field, strong dispersion of the Kerr effect is observed, indicating the dipole-orientational mechanism of electrical birefringence and its relaxation. A comparison of relaxation times of fractions with their molecular weights and intrinsic viscosities indicates that the mechanism responsible for the Kerr effect is the rotation of the molecule as a whole in an electric field (a kinetically rigid molecule). The dependence of relaxation time on molecular weight (M) shows that, with increase in M, the conformation of the CC molecule changes from a slightly curved rod to a rigid Gaussian coil. The same conclusion may be drawn from a study on the dependence of the equilibrium value of the Kerr constant on M. In the Gaussian range (high M), the Kerr effect depends on the longitudinal (with respect to the chain) component of the dipole moment formed by the CO bonds in the glucoside ring. At low M, the transverse components of the monomer dipoles begin to play an important part in birefringence.

UR - http://www.scopus.com/inward/record.url?scp=49549159048&partnerID=8YFLogxK

U2 - 10.1016/0014-3057(74)90163-3

DO - 10.1016/0014-3057(74)90163-3

M3 - Article

AN - SCOPUS:49549159048

VL - 10

SP - 563

EP - 570

JO - European Polymer Journal

JF - European Polymer Journal

SN - 0014-3057

IS - 7

ER -

ID: 94261128