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首页> 外文期刊>RSC Advances >Self-assembled structure and relaxation dynamics of diblock copolymers made of polybutadiene and styrene/butadiene rubber
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Self-assembled structure and relaxation dynamics of diblock copolymers made of polybutadiene and styrene/butadiene rubber

机译:由聚丁二烯和苯乙烯/丁二烯橡胶制成的二嵌段共聚物的自组装结构和弛豫动力学

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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).
机译:通过原子力显微镜(AFM)和动态剪切测量,研究了两系列交联的聚(丁二烯 - 嵌段 - (丁二烯 - 丁二烯))二嵌段共聚物的二串交联聚(丁二烯 - 嵌段 - (苯乙烯 - 丁二烯))二嵌段共聚物的二嵌段共聚物。系列I含有在SBR块中具有可变苯乙烯含量的对称二嵌段共聚物。在II系列中,改变SBR块PHI(SBR)的体积分数,同时保持SBR块中的苯乙烯含量几乎恒定。 AFM结果表明,根据使用有效相互作用参数Chi(EFF),SBR嵌段中具有苯乙烯含量的串联I的对称二嵌段共聚物= 35mol%是微妙的分离。基于热力学平衡概念的预期,II系列II系列II系列的样品,其体积级分在30体积%<= PHI(SBR)<= 60 Vol%的情况下显示出圆柱形和层状形态。这表明在交联温度下存在的二嵌段共聚物形态是固定的,但不能显着改变硫化过程。根据交联状态的Pb和SBR块的分离,有三种不同的弛豫情景:(i)两个良好分离的动态玻璃转换α(Pb)和α(SBR),用于主要由两个纯相组成的强偏析样品, Pb和SBR,(ii)位于纯Pb和SBR的α松弛方法之间的显着弛豫模式,用于具有大量界面材料的弱分离系统和(iii)在实际上混溶系统的中间温度下的单一动态玻璃转换α。基于具有约1-3nm的典型尺寸的子系统的化学成分来解释这三种情况,该尺寸与玻璃化转变的特征长度xi(alpha)量化的玻璃化转换量量化的玻璃化转换,该尺寸是定量配合重排区域(CRR)的尺寸。

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  • 来源
    《RSC Advances》 |2016年第56期|共11页
  • 作者单位

    Goodyear Innovat Ctr Luxembourg L-7750 Colmar Berg Luxembourg;

    Fraunhofer PAZ Value Pk A74 D-06258 Schkopau Germany;

    Fraunhofer IMWS Walter Hulse Str 1 D-06120 Halle Saale Germany;

    Fraunhofer PAZ Value Pk A74 D-06258 Schkopau Germany;

    Fraunhofer PAZ Value Pk A74 D-06258 Schkopau Germany;

    Goodyear Innovat Ctr Luxembourg L-7750 Colmar Berg Luxembourg;

    Univ Halle Wittenberg Nat Wissensch Fak 2 D-06099 Halle Saale Germany;

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  • 正文语种 eng
  • 中图分类 化学;
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