DIELECTRICS AND THERMODYNAMICS OF A MACROMOLECULES GROWTH

被引:31
作者
CASSETTARI, M
SALVETTI, G
TOMBARI, E
VERONSESI, S
JOHARI, GP
机构
[1] CNR, IST FIS ATOM & MOLEC, I-56127 PISA, ITALY
[2] MCMASTER UNIV, DEPT MAT SCI & ENGN, HAMILTON L8S 4L7, ON, CANADA
关键词
D O I
10.1016/0022-3093(94)90487-1
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The heat capacity, the exothermic heat (evolved) and the dielectric properties (in the range 10(4)-10(10) HZ) have been measured during the growth of a network macromolecule at a Bred temperature. From the latter, the dielectric relaxation spectra at different times of reaction have been obtained. The heat capacity of an initially monomeric liquid mixture first irreversibly increases as the macromolecule grows and then undergoes a step-decrease to a value which is mainly due to vibrational contributions. This mimics the behaviour of heat capacity of a liquid on its supercooling through the glass transition temperature. The number of covalent bonds, n, formed during the progress of reaction has been determined from the heat evolved. n in the macromolecule structure at its vitrification is less when the isothermal reaction temperature is low. From the dielectric measurements in the MHz frequency range, a dielectric relaxation process is observed, the characteristic time of which irreversibly increases as the reaction progresses. Measurements performed in the GHz frequency range reveal a second relaxation process, the rate of which changes little, while its strength decreases as the macromolecule grows. These findings have a remarkable resemblance to the evolution of relaxation properties observed on cooling a chemically and structurally stable liquid. The results are discussed and it is suggested that, for each macromolecular state characterized by its molecular weight, there is a corresponding state of its unreacted components at low temperatures with similar kinetic and thermodynamic properties.
引用
收藏
页码:554 / 561
页数:8
相关论文
共 21 条
[1]  
Bertolini D, 1990, REV SCI INSTRUM, V61, P450
[2]   ON THE EVOLUTION OF RELAXATION PROCESSES DURING THE FORMATION OF A MACROMOLECULE [J].
CASSETTARI, M ;
SALVETTI, G ;
TOMBARI, E ;
VERONESI, S ;
JOHARI, GP .
JOURNAL OF MOLECULAR LIQUIDS, 1993, 56 :141-152
[3]   SIMULTANEOUS MEASUREMENTS OF ENTHALPY AND HEAT-CAPACITY OF A THERMOSETTING POLYMER DURING THE CURING PROCESS [J].
CASSETTARI, M ;
PAPUCCI, F ;
SALVETTI, G ;
TOMBARI, E ;
VERONESI, S ;
JOHARI, GP .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1993, 64 (04) :1076-1080
[4]   CALORIMETRIC DETERMINATION OF VITRIFICATION TIME AND HEAT-CAPACITY OF A THERMOSETTING POLYMER [J].
CASSETTARI, M ;
SALVETTI, G ;
TOMBARI, E ;
VERONESI, S ;
JOHARI, GP .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1993, 31 (02) :199-205
[5]  
CASSETTARI M, 1994, IN PRESS PHYSICA A
[6]   MOLECULAR THEORY FOR THE RHEOLOGY OF GLASSES AND POLYMERS [J].
CAVAILLE, JY ;
PEREZ, J ;
JOHARI, GP .
PHYSICAL REVIEW B, 1989, 39 (04) :2411-2422
[7]   TIME DOMAIN REFLECTION METHODS FOR DIELECTRIC MEASUREMENTS TO GHZ [J].
COLE, RH ;
BERBERIAN, JG ;
MASHIMO, S ;
CHRYSSIKOS, G ;
BURNS, A ;
TOMBARI, E .
JOURNAL OF APPLIED PHYSICS, 1989, 66 (02) :793-802
[8]   DIELECTRIC-PROPERTIES OF A CURING EPOXY AMINE SYSTEM AT MICROWAVE-FREQUENCIES [J].
FINZEL, MC ;
HAWLEY, MC ;
JOW, J .
POLYMER ENGINEERING AND SCIENCE, 1991, 31 (16) :1240-1244
[9]   Constitution of three-dimensional polymers and the theory of gelation [J].
Flory, PJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1942, 46 (01) :132-140
[10]   Molecular size distribution in three dimensional polymers. I. Gelation [J].
Flory, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1941, 63 :3083-3090