Relation of glass transition temperature to the hydrogen-bonding degree and energy in poly(N-vinyl pyrrolidone) blends with hydroxyl-containing plasticizers.: Part 1.: Effects of hydroxyl group number in plasticizer molecule

被引:58
作者
Feldstein, MM [1 ]
Shandryuk, GA [1 ]
Platé, NA [1 ]
机构
[1] Russian Acad Sci, AV Topchiev Petrochem Synth Inst, Moscow 117912, Russia
关键词
poly(N-vinyl pyrrolidone); glass transition temperature; hydrogen bonding degree and energy;
D O I
10.1016/S0032-3861(00)00445-6
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The well-known Fox equation has been modified to express the glass transition temperature, T-g, as an explicit function of the number of polymer-plasticizer hydrogen bonds in miscible poly(N-vinyl pyrrolidone) (PVP) blends with ethyl alcohol, water, short-chain poly(ethylene glycol) (PEG), and glycerol. The plasticization effect has been found to be dependent on the fraction of hydroxyl groups in the blend rather than on the plasticizer weight fractions. Negative deviations of the blend T-g from the relationship predicted with the original form of the Fox equation were shown to be in direct proportion to the number of hydroxyl groups in the plasticizer molecule. The following quantities can be evaluated based on the T-g-composition profiles: binding degree, fraction of plasticizer hydroxyl groups forming hydrogen bonds to PVP repeat units, the fraction of plasticizer molecules crosslinking the polymer units by hydrogen bonding through two or more hydroxyl groups in their molecule. The dynamics of PVP-PEG hydrogen bonding over the entire compositional range has been evaluated in terms of hydrogen-bonded network density. The stoichiometric composition of the PVP-PEG hydrogen-bonded complex, determined from the T-g-composition relationship, corresponds to the data obtained with independent methods. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:971 / 979
页数:9
相关论文
共 25 条
[1]   TEST OF THE ENTROPY BASIS OF THE VOGEL-TAMMANN-FULCHER EQUATION - DIELECTRIC-RELAXATION OF POLYALCOHOLS NEAR TG [J].
ANGELL, CA ;
SMITH, DL .
JOURNAL OF PHYSICAL CHEMISTRY, 1982, 86 (19) :3845-3852
[2]  
[Anonymous], POLYM SCI
[3]  
[Anonymous], 1999, POLYM SCI SER
[4]  
[Anonymous], DOKL AKAD NAUK SSSR
[5]   ANALYSIS OF THE GLASS-TRANSITION TEMPERATURE OF MISCIBLE POLYMER BLENDS [J].
AUBIN, M ;
PRUDHOMME, RE .
MACROMOLECULES, 1988, 21 (10) :2945-2949
[6]  
Bershtein V.A., 1994, DIFFERENTIAL SCANNIN
[7]   THE GLASS TEMPERATURE OF POLYMER BLENDS [J].
DIMARZIO, EA .
POLYMER, 1990, 31 (12) :2294-2298
[8]   Coherence of thermal transitions in poly(N-vinyl pyrrolidone)-poly(ethylene glycol) compatible blends 3.: Impact of sorbed water upon phase behaviour [J].
Feldstein, MM ;
Kuptsov, SA ;
Shandryuk, GA ;
Platé, NA ;
Chalykh, AE .
POLYMER, 2000, 41 (14) :5349-5359
[9]   Coherence of thermal transitions in poly(N-vinyl pyrrolidone)-poly(ethylene glycol) compatible blends 1.: Interrelations among the temperatures of melting, maximum cold crystallization rate and glass transition [J].
Feldstein, MM ;
Shandryuk, GA ;
Kuptsov, SA ;
Platé, NA .
POLYMER, 2000, 41 (14) :5327-5338
[10]   Coherence of thermal transitions in poly(N-vinyl pyrrolidone)-poly(ethylene glycol) compatible blends 2.: The temperature of maximum cold crystallization rate versus [J].
Feldstein, MM ;
Kuptsov, SA ;
Shandryuk, GA .
POLYMER, 2000, 41 (14) :5339-5348