Crystallization in oriented semicrystalline diblock copolymers

被引:206
作者
Hamley, IW
Fairclough, JPA
Terrill, NJ
Ryan, AJ
Lipic, PM
Bates, FS
TownsAndrews, E
机构
[1] UMIST,MANCHESTER MAT SCI CTR,MANCHESTER M1 7HS,LANCS,ENGLAND
[2] UNIV LEEDS,SCH CHEM,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[3] UNIV MINNESOTA,DEPT CHEM ENGN & MAT SCI,MINNEAPOLIS,MN 55455
[4] CLRC,DARESBURY LAB,WARRINGTON WA4 4AD,CHESHIRE,ENGLAND
关键词
D O I
10.1021/ma960343a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Crystallization in oriented diblock copolymers containing poly(ethylene) (PE) has been investigated using simultaneous small-angle and wide-angle X-ray scattering (SAXS/WAXS). The orientation of the crystallized PE stems was deduced from the orientation of peaks in the WAXS pattern with respect to those in the SAXS to be parallel to the lamellar interface for symmetric diblocks containing PE and either a rubbery or glassy amorphous black. For a symmetric diblock with a poly(vinylcyclohexane) block that is glassy at room temperature we observe diffuse scattering parallel to the meridian in the SAXS pattern that is consistent with lateral correlations between PE crystallites within the layers of semicrystalline PE. In contrast, in all the samples containing an amorphous component, PE crystallization occurred with no lateral positional correlations of crystallites. Crystallization in asymmetric diblocks with compositions f(PE) = 0.35 and 0.46 was also investigated. It was found that a lamellar structure is the stable solid structure and that this melts epitaxially to a hexagonal-packed cylinder structure in the f(PE) = 0.35 sample. For the f(PE) = 0.46 sample that forms a perforated layer phase in the melt, chain-folded PE stems were found to be parallel to the lamellar interface, as for the symmetric diblocks.
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页码:8835 / 8843
页数:9
相关论文
共 23 条
[1]   SYNTHESIS AND CHARACTERIZATION OF A MODEL SATURATED-HYDROCARBON DIBLOCK COPOLYMER [J].
BATES, FS ;
ROSEDALE, JH ;
BAIR, HE ;
RUSSELL, TP .
MACROMOLECULES, 1989, 22 (06) :2557-2564
[2]   FLUCTUATIONS, CONFORMATIONAL ASYMMETRY AND BLOCK-COPOLYMER PHASE-BEHAVIOR [J].
BATES, FS ;
SCHULZ, MF ;
KHANDPUR, AK ;
FORSTER, S ;
ROSEDALE, JH ;
ALMDAL, K ;
MORTENSEN, K .
FARADAY DISCUSSIONS, 1994, 98 :7-18
[3]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[4]   W16.1 - A NEW FIXED WAVELENGTH DIFFRACTION STATION AT THE SRS DARESBURY [J].
BLISS, N ;
BORDAS, J ;
FELL, BD ;
HARRIS, NW ;
HELSBY, WI ;
MANT, GR ;
SMITH, W ;
TOWNSANDREWS, E .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1995, 66 (02) :1311-1313
[5]  
BRANDRUP J, 1989, POLYM HDB
[6]   CRYSTALLINITY OF UNIFORM OLIGO(OXYETHYLENE) MONO-N-ALKYL ETHERS STUDIED BY X-RAY-DIFFRACTION AND DIFFERENTIAL SCANNING CALORIMETRY [J].
CRAVEN, JR ;
HAO, Z ;
BOOTH, C .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1991, 87 (08) :1183-1186
[7]   CHAIN FOLDING IN EBEE SEMICRYSTALLINE DIBLOCK COPOLYMERS [J].
DOUZINAS, KC ;
COHEN, RE .
MACROMOLECULES, 1992, 25 (19) :5030-5035
[8]   CRYSTAL-GROWTH MODELS AND ISING MODELS - DISORDER POINTS [J].
ENTING, IG .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1977, 10 (09) :1379-1388
[9]   KINETICS OF POLYMER CRYSTALLIZATION .1. DISCRETE AND CONTINUUM MODELS [J].
GATES, DJ ;
WESTCOTT, M .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 1988, 416 (1851) :443-461
[10]   HETEROGENEOUS CATALYTIC-HYDROGENATION OF POLY(STYRENE) - THERMODYNAMICS OF POLY(VINYLCYCLOHEXANE) CONTAINING DIBLOCK COPOLYMERS [J].
GEHLSEN, MD ;
BATES, FS .
MACROMOLECULES, 1993, 26 (16) :4122-4127