Self-assembled structure and relaxation dynamics of diblock copolymers made of polybutadiene and styrene/butadiene rubber

被引:3
作者
da Silva, C. A. [1 ,2 ]
Budde, H. [3 ]
Menzel, M. [4 ]
Wendler, U. [3 ]
Bartke, M. [3 ]
Weydert, M. [1 ]
Beiner, M. [2 ,4 ]
机构
[1] Goodyear Innovat Ctr Luxembourg, L-7750 Colmar Berg, Luxembourg
[2] Univ Halle Wittenberg, Nat Wissensch Fak 2, D-06099 Halle, Saale, Germany
[3] Fraunhofer PAZ, Value Pk A74, D-06258 Schkopau, Germany
[4] Fraunhofer IMWS, Walter Hulse Str 1, D-06120 Halle, Saale, Germany
关键词
FILLER-ELASTOMER INTERACTION; GLASS-FORMING LIQUIDS; TEMPERATURE-DEPENDENCE; MICROPHASE SEPARATION; LENGTH SCALE; MOLECULAR-WEIGHT; BLOCK-COPOLYMER; POLYMER-FILMS; TRANSITION; SCATTERING;
D O I
10.1039/c6ra06786g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structural features and relaxation dynamics of two series of crosslinked poly(butadiene-block-(styrenestat-butadiene)) diblock copolymers with systematically varied segregation strength and morphology are studied by atomic force microscopy (AFM) and dynamic shear measurements. Series I contains symmetric diblock copolymers with variable styrene content in the SBR block. In Series II the volume fraction of the SBR block Phi(SBR) is varied while keeping the styrene content in the SBR block almost constant. AFM results indicate that symmetric diblock copolymers of Series I with styrene contents >= 35 mol% in the SBR block are well microphase-separated in accordance with thermodynamic models using an effective interaction parameter chi(eff). The samples of Series II with volume fractions in the range 30 vol% <= Phi(SBR) <= 60 vol% show cylindrical and lamellar morphologies as expected based on thermodynamic equilibrium concepts. This shows that the diblock copolymer morphologies existing at the crosslinking temperature are fixed but not significantly altered by the vulcanization procedure. Depending on the segregation of PB and SBR blocks in the crosslinked state, there are three different relaxation scenarios: (i) two well separated dynamic glass transitions alpha(PB) and alpha(SBR) for strongly segregated samples consisting mainly of two pure phases, PB and SBR, (ii) significant relaxation modes located between the alpha relaxation processes of pure PB and SBR for weakly segregated systems with a lot of interfacial material and (iii) one single dynamic glass transition alpha at intermediate temperatures for practically miscible systems. These three situations are explained based on the chemical composition of subsystems having typical dimensions of about 1-3 nm consistent with the characteristic lengths xi(alpha) of the glass transition quantifying the dimensions of cooperative rearranging regions (CRRs).
引用
收藏
页码:50460 / 50470
页数:11
相关论文
共 49 条
[1]   ON TEMPERATURE DEPENDENCE OF COOPERATIVE RELAXATION PROPERTIES IN GLASS-FORMING LIQUIDS [J].
ADAM, G ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1965, 43 (01) :139-&
[2]   Effects of confinement on material behaviour at the nanometre size scale [J].
Alcoutlabi, M ;
McKenna, GB .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2005, 17 (15) :R461-R524
[3]   Length scale of cooperativity in the dynamic glass transition [J].
Arndt, M ;
Stannarius, R ;
Groothues, H ;
Hempel, E ;
Kremer, F .
PHYSICAL REVIEW LETTERS, 1997, 79 (11) :2077-2080
[4]   POLYMER-POLYMER PHASE-BEHAVIOR [J].
BATES, FS .
SCIENCE, 1991, 251 (4996) :898-905
[5]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[6]   Nanophase separation and hindered glass transition in side-chain polymers [J].
Beiner, M ;
Huth, H .
NATURE MATERIALS, 2003, 2 (09) :595-599
[7]   Direct experimental evidence of a growing length scale accompanying the glass transition [J].
Berthier, L ;
Biroli, G ;
Bouchaud, JP ;
Cipelletti, L ;
El Masri, D ;
L'Hôte, D ;
Ladieu, F ;
Pierno, M .
SCIENCE, 2005, 310 (5755) :1797-1800
[8]   Accelerated physical aging in PMMA/silica nanocomposites [J].
Boucher, Virginie M. ;
Cangialosi, Daniele ;
Alegria, Angel ;
Colmenero, Juan ;
Gonzalez-Irun, Juan ;
Liz-Marzan, Luis M. .
SOFT MATTER, 2010, 6 (14) :3306-3317
[9]   Route to calculate the length scale for the glass transition in polymers [J].
Cangialosi, D. ;
Alegria, A. ;
Colmenero, J. .
PHYSICAL REVIEW E, 2007, 76 (01)
[10]   Combining configurational entropy and self-concentration to describe the component dynamics in miscible polymer blends -: art. no. 144908 [J].
Cangialosi, D ;
Schwartz, GA ;
Alegría, A ;
Colmenero, J .
JOURNAL OF CHEMICAL PHYSICS, 2005, 123 (14)