Linear low-density polyethylene/poly(ethylene-ran-butene) elastomer blends: Miscibility and crystallization behavior

被引:0
作者
Li, CX [1 ]
Zhao, J [1 ]
Zhao, DL [1 ]
Fan, QR [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, Ctr Mol Sci, State Key Lab Polymer Phys & Chem, Beijing 100080, Peoples R China
关键词
blends; crystallization; linear low-density polyethylene (LLDPE); phase separation; poly(ethylene-ran-butene);
D O I
暂无
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 phase and crystallization behavior of the blends consisting of LLDPE (0.7 mol% hexene copolymer) and PEB (26 mol% butene copolymer) have been investigated using optical microscopy (OM), differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXD). The blends exhibited an upper critical solution temperature of 162 degreesC. The solubility parameter analysis showed that the solubility parameter of LLDPE decreased more rapidly than that of PEB with temperature. However, due to the slow kinetics of phase separation, at lower crystallization temperatures. the crystallization and melting behavior of LLDPE mainly reflected the miscibility between LLDPE and PEB. Crystallization from the two-phase state could present two crystallization peaks. PEB didn't change the crystal cell unit and crystallinity of LLDPE, but changed its distribution of lamellar thickness or crystal perfection. ne dilute effect of PEB also changed the overall nature of the nucleation and growth process of LLDPE. The equilibrium melting temperature in this blend could be obtained by the Hoffman-Weeks method, and comparing with that of the pure LLDPE. it was reduced and kept relatively constant in the bi-phase state. The phase diagram made up of the LLPS boundary, equilibrium melting temperatures and melting temperatures observed may be better to indicate the phase and crystallization behavior of LLDPE/PEB blends.
引用
收藏
页码:323 / 331
页数:9
相关论文
共 35 条
[1]   Small angle neutron scattering investigations of melt miscibility and phase segregation in blends of linear and branched polyethylenes as a function of the branch content [J].
Alamo, RG ;
Graessley, WW ;
Krishnamoorti, R ;
Lohse, DJ ;
Londono, JD ;
Mandelkern, L ;
Stehling, FC ;
Wignall, GD .
MACROMOLECULES, 1997, 30 (03) :561-566
[2]  
ALAMO RG, 1994, MACROMOLECULES, V27, P2864
[3]   Thermal and morphological evaluation of very low density polyethylene/high density polyethylene blends [J].
Arnal, ML ;
Cañizales, E ;
Müller, AJ .
POLYMER ENGINEERING AND SCIENCE, 2002, 42 (10) :2048-2063
[4]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[5]   An X-ray diffraction and modelling study of short chain branch location within the structure of polyethylene [J].
Baker, AME ;
Windle, AH .
POLYMER, 2001, 42 (02) :681-698
[6]   Evidence for a partially ordered component in polyethylene from wide-angle X-ray diffraction [J].
Baker, AME ;
Windle, AH .
POLYMER, 2001, 42 (02) :667-680
[7]   THE MORPHOLOGY OF POLY(VINYLIDENE FLUORIDE) CRYSTALLIZED FROM BLENDS OF POLY(VINYLIDENE FLUORIDE) AND POLY(ETHYL ACRYLATE) [J].
BRIBER, RM ;
KHOURY, F .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1993, 31 (10) :1253-1272
[8]   THE PHASE-DIAGRAM AND MORPHOLOGY OF BLENDS OF POLY(VINYLIDENE FLUORIDE) AND POLY(ETHYL ACRYLATE) [J].
BRIBER, RM ;
KHOURY, F .
POLYMER, 1987, 28 (01) :38-46
[10]   Spherulite growth rates in binary polymer blends [J].
Di Lorenzo, ML .
PROGRESS IN POLYMER SCIENCE, 2003, 28 (04) :663-689