THE GLASS-TRANSITION OF ORGANIC LIQUIDS CONFINED TO SMALL PORES

被引:409
作者
JACKSON, CL
MCKENNA, GB
机构
[1] Polymer Division, The National Institute of Standards and Technology, Gaithersburg
关键词
D O I
10.1016/0022-3093(91)90305-P
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 glass-transition temperatures, T(g), of organic liquids confined to small pores were studied by differential scanning calorimetry (DSC). The T(g) was measured as a function of pore size in controlled pore glasses (CPG) having pore diameters in the range of 40-730 angstrom. The surface of the glass was treated with hexamethyldisilazane to promote wetting by the organic liquids studied (o-terphenyl and benzyl alcohol). Glasses formed in the pores had a lower T(g) than in the bulk and the reduction in T(g) increased as the pore size decreased. For example, the depression of the glass transition temperature, DELTA-T(g), of benzyl alcohol in 40 angstrom and 85 angstrom pores was 7.2 K and 3.1 K, respectively. The magnitude of DELTA-T(g) also depends on the material; e.g. for o-terphenyl in the 85 angstrom pores, DELTA-T(g) was 8.8 K versus 3.1 K for benzyl alcohol. In general, it was noted that DELTA-T(g) was considerably less than for the depression of the crystalline melting point, DELTA-T(m), studied in related work. For example, for benzyl alcohol in the 85 angstrom pores, DELTA-T(m) was approximately 25 K and DELTA-T(g) was approximately 3 K.
引用
收藏
页码:221 / 224
页数:4
相关论文
共 21 条
[1]   GLASS-FORMING MICROEMULSIONS [J].
ANGELL, CA ;
KADIYALA, RK ;
MACFARLANE, DR .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (20) :4593-4596
[2]   GLASS IN A STRETCHED STATE FORMED BY NEGATIVE-PRESSURE VITRIFICATION - TRAPPING IN AND RELAXING OUT [J].
ANGELL, CA ;
ZHENG, Q .
PHYSICAL REVIEW B, 1989, 39 (12) :8784-8787
[3]   PRESSURE-DEPENDENCE OF THE GLASS-TRANSITION TEMPERATURE IN MOLECULAR LIQUIDS AND PLASTIC CRYSTALS [J].
ATAKE, T ;
ANGELL, CA .
JOURNAL OF PHYSICAL CHEMISTRY, 1979, 83 (25) :3218-3223
[4]  
AWSCHALOM DD, 1987, PHYS REV B, V35, P6774
[5]  
BRAUN G, 1963, PHYS CHEM GLASSES-B, V4, P152
[6]   STUDIES OF CRAZE FIBRIL DEFORMATION DURING FATIGUE IN POLYSTYRENE [J].
BROWN, HR ;
KRAMER, EJ ;
BUBECK, RA .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1987, 25 (08) :1765-1778
[7]   HEAT-CAPACITY AND THERMODYNAMIC PROPERTIES OF ORTHO-TERPHENYL CRYSTAL, GLASS, AND LIQUID [J].
CHANG, SS ;
BESTUL, AB .
JOURNAL OF CHEMICAL PHYSICS, 1972, 56 (01) :503-+
[8]   DIFFUSION-MODEL FOR VOLUME RECOVERY IN GLASSES [J].
CURRO, JG ;
LAGASSE, RR ;
SIMHA, R .
MACROMOLECULES, 1982, 15 (06) :1621-1626
[9]   CHAIN STIFFNESS AND THE LATTICE THEORY OF POLYMER PHASES [J].
DIMARZIO, EA ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1958, 28 (05) :807-813
[10]  
DIMARZIO EA, COMMUNICATION