What has brought on the effects of number-average molecular weight on the spinodals in polymer mixtures?

被引:6
作者
Yang, J [1 ]
Sun, ZY [1 ]
Jiang, W [1 ]
An, LJ [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
关键词
D O I
10.1021/jp020640j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
On the basis of the thermodynamics of Gibbs, the spinodal for the quasibinary system was derived in the framework of the Sanchez-Lacombe lattice fluid theory. All of the spinodals were calculated based on a model polydisperse polymer mixture, where each polymer contains three different molecular weight subcomponents. According to our calculations, the spinodal depends on both weight-average ((M) over bar (w)) and number-average ((M) over bar (n)) molecular weights, whereas that of the z-average molecular weight is invisible. Moreover, the extreme of the spinodal decreases when the polydispersity index (eta = (M) over bar (w)/(M) over bar (n)) of the polymer increases. The effect of polydispersity on the spinodal decreases when the molecular weight gets larger and can be negligible at a certain large molecular weight. It is well-known that the influence of polydispersity on the phase equilibrium (coexisting curve, cloud point curves) is much more pronounced than on the spinodal. The effect of M, on the spinodal is discussed as it results from the infuluence of composition temperatures, molecular weight, and the latter's distribution on free volume. An approximate expression, which is in the assumptions of v* v(1)* = v(2)* and 1/r --> 0 for both of the polymers, was also derived for simplification. It can be used in high molecular weight, although it failed to make visible the effect of number-average molecular weight on the spinodal.
引用
收藏
页码:11305 / 11314
页数:10
相关论文
共 28 条
[1]   Pressure dependence of the miscibility of poly(vinyl methyl ether) and polystyrene: Theoretical representation [J].
An, LJ ;
Horst, R ;
Wolf, BA .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (07) :2597-2602
[2]   STATISTICAL THERMODYNAMICS OF POLYDISPERSE POLYMER MIXTURES [J].
AN, LJ ;
KOU, XC ;
MA, RT ;
TANG, XY ;
JIANG, BZ .
POLYMER, 1993, 34 (14) :2989-2997
[3]   STATISTICAL THERMODYNAMICS IN THE FRAMEWORK OF THE LATTICE FLUID MODEL .2. BINARY MIXTURE OF POLYDISPERSE POLYMERS OF SPECIAL DISTRIBUTION [J].
AN, LJ ;
JIANG, BZ ;
JIANG, ZH ;
HU, YX ;
TANG, XY .
MACROMOLECULAR THEORY AND SIMULATIONS, 1994, 3 (04) :751-780
[4]   APPLICATION OF CONTINUOUS THERMODYNAMICS TO THE STABILITY OF POLYMER SYSTEMS .2. [J].
BEERBAUM, S ;
BERGMANN, J ;
KEHLEN, H ;
RATZSCH, MT .
JOURNAL OF MACROMOLECULAR SCIENCE-CHEMISTRY, 1987, A24 (12) :1445-1463
[5]   APPLICATION OF CONTINUOUS THERMODYNAMICS TO THE STABILITY OF POLYMER SYSTEMS .4. [J].
BERGMANN, J ;
TEICHERT, H ;
KEHLEN, H ;
RATZSCH, MT .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 1992, 29 (4-5) :371-379
[6]   Stability of polydisperse fluid mixtures [J].
Browarzik, D ;
Kehlen, H .
FLUID PHASE EQUILIBRIA, 1996, 123 (1-2) :17-28
[7]  
HAMADA F, 1980, MACROMOLECULES, V13, P729
[8]   CALCULATION OF PHASE-DIAGRAMS NOT REQUIRING THE DERIVATIVES OF THE GIBBS ENERGY DEMONSTRATED FOR A MIXTURE OF 2 HOMOPOLYMERS WITH THE CORRESPONDING COPOLYMER [J].
HORST, R .
MACROMOLECULAR THEORY AND SIMULATIONS, 1995, 4 (03) :449-458
[9]   Stability theory for polydisperse fluid mixtures [J].
Hu, Y ;
Prausnitz, JM .
FLUID PHASE EQUILIBRIA, 1997, 130 (1-2) :1-18
[10]   LATTICE-GAS TREATMENT OF SUPERCRITICAL PHASE-BEHAVIOR IN FLUID MIXTURES [J].
KLEINTJENS, LA ;
KONINGSVELD, R .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1980, 127 (11) :2352-2355