End-to-End Vector Dynamics of Nonentangled Polymers in Lamellar Block Copolymer Melts: The Role of Junction Point Motion

被引:11
作者
Lund, Reidar [1 ]
Barroso-Bujans, Fabienne [2 ]
Zakaria Slimani, Mohammed [2 ]
Moreno, Angel J. [3 ,4 ]
Willner, Lutz [5 ,6 ]
Richter, Dieter [5 ,6 ]
Alegria, Angel [3 ,4 ,7 ]
Colmenero, Juan [2 ,3 ,4 ,7 ]
机构
[1] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
[2] Donostia Int Phys Ctr, San Sebastian 20018, Spain
[3] Univ Basque Country, CSIC, Ctr Fis Mat, San Sebastian 20018, Spain
[4] MPC, San Sebastian 20018, Spain
[5] Forschungszentrum Julich, JCNS, D-52425 Julich, Germany
[6] Forschungszentrum Julich, ICS, D-52425 Julich, Germany
[7] Univ Pais Vasco UPV EHU, Dept Fis Mat, San Sebastian 20080, Spain
关键词
DIBLOCK COPOLYMERS; SEGMENTAL DYNAMICS; MICROPHASE-SEPARATION; DIELECTRIC-RELAXATION; RHEOLOGY; HETEROGENEITY; SIMULATION; DIFFUSION; BEHAVIOR; PHASES;
D O I
10.1021/ma401162b
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
By using dielectric spectroscopy, we investigate the chain dynamics of nonentangled polyisoprene (PI) under soft confinement in lamellar domains of block copolymer melts with polydimethylsiloxane (PDMS). The data show a dramatic difference in the end-to-end vector dynamics of the PI blocks as compared not only with that of the corresponding homopolymer PI chains but also with respect to previous results for the same blocks under soft confinement in cylindrical domains. Two contributions to the dielectric normal mode relaxation are detected. The data are analyzed by means of a model including contributions from internal chain modes (accounting for the fastest component) and a slow component attributed to the junction point dynamics. The contribution of the internal chain modes is modeled according to the analysis of the Rouse modes obtained from simulations of a generic bead spring model for strongly segregated symmetric diblock copolymers. In this way it is shown that the internal chain modes of the blocks have time scales close to those expected from the homopolymer chain independently of the structural details. In contrast, the contribution attributed to the junction point dynamics depends critically on minor structural differences. We interpret these findings as a result of the presence of fast moving defects and/or grain boundaries in the lamellar structures formed by these relatively short, nonentangled diblock copolymers.
引用
收藏
页码:7477 / 7487
页数:11
相关论文
共 45 条
[1]   DIELECTRIC-RELAXATION IN DISORDERED POLY(ISOPRENE STYRENE) DIBLOCK COPOLYMERS NEAR THE MICROPHASE-SEPARATION TRANSITION [J].
ALIG, I ;
KREMER, F ;
FYTAS, G ;
ROOVERS, J .
MACROMOLECULES, 1992, 25 (20) :5277-5282
[2]  
Anastasiadis SH, 2000, CURR OPIN COLLOID IN, V5, P324
[3]   Influence of defect density on the rheology of ordered block copolymers [J].
Balsara, NP ;
Dai, HJ ;
Watanabe, H ;
Sato, T ;
Osaki, K .
MACROMOLECULES, 1996, 29 (10) :3507-3510
[4]  
Barroso-Bujans F., UNPUB
[5]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[6]   Molecular-dynamics simulation of a glassy polymer melt: Rouse model and cage effect [J].
Bennemann, C ;
Baschnagel, J ;
Paul, W ;
Binder, K .
COMPUTATIONAL AND THEORETICAL POLYMER SCIENCE, 1999, 9 (3-4) :217-226
[7]   Dielectric Behavior of Guest cis-Polyisoprene Confined in Spherical Microdomain of Triblock Copolymer. [J].
Chen, Quan ;
Matsumiya, Yumi ;
Iwamoto, Tatsuya ;
Nishida, Koji ;
Kanaya, Toshiji ;
Watanabe, Hiroshi ;
Takano, Atsushi ;
Matsuoka, Kohei ;
Matsushita, Yushu .
MACROMOLECULES, 2012, 45 (06) :2809-2819
[8]   Design of ABC triblock copolymers near the ODT with the random phase approximation [J].
Cochran, EW ;
Morse, DC ;
Bates, FS .
MACROMOLECULES, 2003, 36 (03) :782-792
[9]   DIFFUSION IN MICROSTRUCTURED BLOCK-COPOLYMERS - CHAIN LOCALIZATION AND ENTANGLEMENTS [J].
DALVI, MC ;
EASTMAN, CE ;
LODGE, TP .
PHYSICAL REVIEW LETTERS, 1993, 71 (16) :2591-2594
[10]  
Doi M., 1986, THEORY POLYM DYNAMIC