首页> 外文期刊>The Journal of Chemical Physics >NUCLEAR MAGNETIC RESONANCE STUDIES OF DOMAIN GROWTH IN THE LATE STAGE OF PHASE SEPARATION OF A BINARY LIQUID MIXTURE
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NUCLEAR MAGNETIC RESONANCE STUDIES OF DOMAIN GROWTH IN THE LATE STAGE OF PHASE SEPARATION OF A BINARY LIQUID MIXTURE

机译:二元混合液相分离后期畴生长的核磁共振研究。

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The domain growth processes occurring during the gravity-dominated regime of the phase separation of a cyclohexane/aniline critical mixture, following a temperature quench in the unstable region below the temperature-composition coexistence curve, were investigated with high-resolution H-1 NMR. Diffusive exchange of cyclohexane molecules between a small volume fraction of immiscible droplets and the surrounding fluid with a different cyclohexane concentration leads to a domain-size dependent H-1 NMR cyclohexane chemical shift in the continuous phase. In this case, the equations of motion for the transverse magnetization density reduce to a first-order exchange between two immiscible phases with rate coefficients depending on the droplet size and the transport process across the liquid-liquid interface. Application of this model to the data yields a power law for the growing droplets, R(t) = At-phi, where R is a typical domain size, with the growth exponent phi=0.30+/-0.01 and the amplitude A congruent to 0.9X10(-6) ms(-phi). These values are in close ms agreement with previous visualization studies on the same binary mixture [F. Cau and S. Lacelle, Phys. Rev. E 47, 1429 (1993)]. The results also confirm the presence of a new domain growth regime involving Brownian coagulation and sedimentation in the very late stage of the phase separation processes of binary liquid mixtures. A strong linear composition dependence of the H-1 NMR cyclohexane chemical shift in one-phase cyclohexane/aniline mixtures was interpreted on the basis of solvent shift effects induced by intermolecular interactions and susceptibility effects. In each phase of the two-phase equilibrium mixture, inhomogeneous line broadening, arising from the magnetic susceptibility discontinuity at the interface between phases, is also investigated. (C) 1995 American Institute of Physics. [References: 59]
机译:用高分辨率的H-1 NMR研究了在重力主导的环己烷/苯胺临界混合物相分离过程中发生的畴生长过程,该过程在温度-组成共存曲线下方的不稳定区域进行温度淬灭后进行。环己烷分子的小体积部分与周围流体之间的扩散交换具有不同的环己烷浓度,导致连续相中与域大小相关的H-1 NMR环己烷化学位移。在这种情况下,横向磁化强度的运动方程式简化为两个不混溶相之间的一级交换,速率系数取决于液滴大小和液-液界面上的传输过程。将该模型应用于数据可得出生长液滴的幂定律,R(t)= At-phi,其中R是典型的畴尺寸,生长指数phi = 0.30 +/- 0.01,幅度A等于0.9X10(-6)ms(-phi)。这些值与先前对相同二元混合物的可视化研究非常吻合[F. Cau和S. Lacelle,物理学。 E 47,1429(1993)。结果还证实了在二元液体混合物相分离过程的最后阶段,存在涉及布朗凝聚和沉降的新的畴生长机制。基于分子间相互作用和磁化率效应引起的溶剂迁移效应,可以解释一相环己烷/苯胺混合物中H-1 NMR环己烷化学位移的强烈线性组成依赖性。在两相平衡混合物的每个相中,还研究了由于相之间界面处的磁化率不连续性引起的不均匀线展宽。 (C)1995年美国物理研究所。 [参考:59]

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