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Neutron and Light Scattering Studies of the Liquid-to-Glass and Glass-to-Glass Transitions in a Copolymer Micellar System

机译:中子和光散射研究在共聚物胶束系统中的液体 - 玻璃和玻璃转变的研究

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Recent mode coupling theory (MCT) calculations for a hard-sphere system with a short-range attraction show that one may observe a new type of structurally arrested state originating from clustering effect, called the "attractive glass", as a result of the attractive interaction. This is in addition to the well-known glass-forming mechanism due to the cage effect in the hard sphere system, called the repulsive glass. The calculations also indicate that, if the range of attraction is sufficiently short compared to the diameter of the hard sphere, within a certain interval of the volume fraction and the effective temperature, the two glass-forming mechanisms can compete with each other. For example, by varying, the effective temperature at appropriate volume fractions, one may observe respectively, the glass-to-liquid-to-glass re-entrance or the glass-to-glass transitions. Here we present experimental evidence for both transitions, obtained from small-angle neutron scattering (SANS) and photon correlation spectroscopy (PCS) measurements taken from dense L64 copolymer micellar solutions in heavy water. We show, by varying the temperature in the predicted volume fraction range triggers a sharp transition between the two types of glass. In particular, according to MCT, there is an end point (called A3 singularity) of this glass-to-glass transition line, beyond which the long-time dynamics of the two glasses become identical. Our findings confirm this theoretical prediction. Surprisingly, although the Debye-Waller factors (DWF), the long-time limit of the coherent intermediate scattering functions, of these two glasses obtained from PCS measurements indeed become identical at the predicted volume fraction, they exhibit distinctly different intermediate time relaxation. Furthermore, our SANS results on the local structure obtained from volume fractions beyond the end point are characterized by the the same features as the repulsive glass obtained before the end point. A complete phase diagram giving the boundaries of the structural arrest transitions for L64 micellar system is given.
机译:近期模式耦合理论(MCT)对于短距离吸引力的硬球系统的计算表明,人们可能会观察到源自聚类效应的新型结构滞留状态,称为“有吸引力的玻璃”,导致具有吸引力相互作用。这是由于硬球系统中的笼效应所称的众所周知的玻璃形成机制之外,称为排斥玻璃。计算还表明,如果与硬球的直径相比,如果吸引的范围足够短,则在体积分数和有效温度的一定间隔内,两个玻璃形成机构可以彼此竞争。例如,通过改变适当体积分数的有效温度,可以分别观察到玻璃 - 玻璃 - 玻璃再入口或玻璃到玻璃过渡。在这里,我们提出了从重度水中的小角度中子散射(SAN)和光子相关光谱(PCS)测量的两种过渡的实验证据。我们展示了预测体积分数中的温度,触发两种类型的玻璃之间的急剧过渡。特别地,根据MCT,存在该玻璃到玻璃过渡线的终点(称为A3奇点),超出了两个眼镜的长时间动态变得相同。我们的研究结果证实了这种理论预测。令人惊讶的是,尽管从PCS测量获得的这两个玻璃的Debye-Waller因子(DWF),相干中间散射功能的长时间限制确实在预测的体积分数中变得相同,但它们表现出明显不同的中间时间弛豫。此外,我们的SAN在超出终点之外的体积分数获得的局部结构的特征在于与在终点之前获得的排斥玻璃相同的特征。给出了给出了L64胶束系统结构停滞转变的边界的完整相图。

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