Morphological and isothermal diffusive probe analyses of low-molecular-weight diblock copolymers

被引:14
作者
Hong, SU
Laurer, JH
Zielinski, JM
Samseth, J
Smith, SD
Duda, JL [1 ]
Spontak, RJ
机构
[1] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[3] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[4] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
[5] Air Prod & Chem Inc, Allentown, PA 18195 USA
[6] Inst Energiteknikk, Dept Phys, N-2007 Kjeller, Norway
[7] Procter & Gamble Co, Corp Res Div, Cincinnati, OH 45239 USA
关键词
D O I
10.1021/ma971516e
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
While numerous scattering and theological studies have investigated the disordering mechanism of low-molecular-weight poly(styrene-b-isoprene) (SI) diblock copolymers, relatively few efforts have addressed the real-space morphologies and transport properties of such copolymers at conditions near the order-disorder transition (ODT). In this work, the morphological features of seven compositionally symmetric (50/50 w/w S/I) copolymers ranging in molecular weight from 5000 to 20000, as well as several of their blends, are examined by transmission electron microscopy and small-angle neutron scattering. These results are used to interpret toluene gravimetric sorption data collected at various temperatures. At temperatures above the styrenic glass transition temperature, microphase-ordered copolymer melts are found to exhibit Fickian diffusion. In the case of a copolymer with an experimentally accessible ODT, anomalous sorption (as evidenced by equilibrium overshoot in gravimetric mass-uptake curves) is observed at temperatures near, but below, the ODT. Within the disordered state, Fickian diffusion is regained, indicating that the onset of anomalous diffusion is related to a solvent-induced ODT under isothermal conditions.
引用
收藏
页码:2174 / 2184
页数:11
相关论文
共 69 条
[1]   OPTICAL CHARACTERIZATION OF ORDERING AND DISORDERING OF BLOCK COPOLYMER MICROSTRUCTURE [J].
AMUNDSON, K ;
HELFAND, E ;
PATEL, SS ;
QUAN, X ;
SMITH, SD .
MACROMOLECULES, 1992, 25 (07) :1935-1940
[2]  
ASHRAF A, 1994, POLYM PREPR, V35, P581
[3]   RHEOLOGICAL BEHAVIOR OF BINARY-MIXTURES OF POLYSTYRENE-BLOCK-POLYISOPRENE COPOLYMERS IN THE DISORDERED STATE [J].
BAEK, DM ;
HAN, CD .
POLYMER, 1995, 36 (25) :4833-4839
[4]   BIREFRINGENCE DETECTION OF THE ORDER-TO-DISORDER TRANSITION IN BLOCK COPOLYMER LIQUIDS [J].
BALSARA, NP ;
PERAHIA, D ;
SAFINYA, CR ;
TIRRELL, M ;
LODGE, TP .
MACROMOLECULES, 1992, 25 (15) :3896-3901
[5]   DIRECT MEASUREMENT OF CHAIN STRETCHING IN DIBLOCK COPOLYMERS AT THE MICROPHASE SEPARATION TRANSITION [J].
BARTELS, VT ;
STAMM, M ;
ABETZ, V ;
MORTENSEN, K .
EUROPHYSICS LETTERS, 1995, 31 (02) :81-86
[6]   POLYMER-POLYMER PHASE-BEHAVIOR [J].
BATES, FS .
SCIENCE, 1991, 251 (4996) :898-905
[7]   FLUCTUATION EFFECTS IN A SYMMETRIC DIBLOCK COPOLYMER NEAR THE ORDER-DISORDER TRANSITION [J].
BATES, FS ;
ROSEDALE, JH ;
FREDRICKSON, GH .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (10) :6255-6270
[8]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[9]  
BATES FS, 1994, FARADAY DISCUSS, P7
[10]  
Caneba G. T., 1983, Journal of Macromolecular Science - Physics, VB22, P693, DOI 10.1080/00222348308245750