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用于直接观察悬浮液结构、动力学和流变学的粘性溶剂胶体系统。

Viscous solvent colloidal system for direct visualization of suspension structure, dynamics and rheology.

作者信息

Kogan Michael, Dibble Clare J, Rogers Reginald E, Solomon Michael J

机构信息

University of Michigan, 3410 G.G. Brown, 2300 Hayward St., Ann Arbor, MI 48109-2136, USA.

出版信息

J Colloid Interface Sci. 2008 Feb 15;318(2):252-63. doi: 10.1016/j.jcis.2007.10.064. Epub 2007 Nov 17.

Abstract

We introduce a model colloid system comprised of particles dispersed in a viscous solvent that can be applied to 3D direct visualization studies of suspension structure, dynamics and rheology. The colloids are poly(methyl methacrylate) (PMMA) spheres sterically stabilized by a copolymer of poly(diphenyl-dimethyl) (DPDM) siloxane that matches the refractive index of PMMA. The monodisperse particles, synthesized with mean diameter varying from 0.7 to 1.1 microm, are stably dispersed in a DPDM siloxane solvent, with viscosity varying from 2.2 to 4.3 Pa s at 20 degrees C. As opposed to other classes of PMMA colloids dispersed in organic solvents, this system displays minimal charge interactions. At room temperature, pair potential interactions (measured by extrapolation of pair correlation functions to infinite dilution) are well modeled by a generalized Lennard-Jones alpha-2alpha potential (alpha=10) with dimensionless interaction energy, epsilon/k(B)T=0.6. We use the DPDM-PMMA colloidal system in conjunction with confocal microscopy studies to measure: (i) the radial distribution function in 3D at dilute concentrations and (ii) the colloid self-diffusivity in 3D at dilute concentrations. Both measurements, neither previously reported in uncharged systems, are facilitated by the slow, viscous dynamics of the system. We also show that the viscosity and particle size of the system are such that the high-volume fraction shear thickening transition can be accessed at shear rates amenable to direct visualization.

摘要

我们引入了一种模型胶体系统,该系统由分散在粘性溶剂中的颗粒组成,可应用于悬浮结构、动力学和流变学的三维直接可视化研究。胶体是聚(甲基丙烯酸甲酯)(PMMA)球体,由与PMMA折射率匹配的聚(二苯基 - 二甲基)(DPDM)硅氧烷共聚物进行空间稳定化处理。合成的单分散颗粒平均直径在0.7至1.1微米之间,稳定地分散在DPDM硅氧烷溶剂中,在20摄氏度时粘度在2.2至4.3帕斯卡秒之间变化。与分散在有机溶剂中的其他类型的PMMA胶体不同,该系统显示出最小的电荷相互作用。在室温下,通过将对关联函数外推到无限稀释来测量的对势相互作用,可以用广义Lennard-Jonesα-2α势(α = 10)很好地建模,无量纲相互作用能ε/k(B)T = 0.6。我们将DPDM-PMMA胶体系统与共聚焦显微镜研究结合使用,以测量:(i)稀浓度下的三维径向分布函数,以及(ii)稀浓度下的三维胶体自扩散系数。这两种测量在以前的无电荷系统中均未报道过,该系统缓慢的粘性动力学有助于进行这些测量。我们还表明,该系统的粘度和粒径使得在适合直接可视化的剪切速率下可以观察到高体积分数的剪切增稠转变。

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