首页> 外文学位 >CONCENTRATION EFFECTS IN BULK COLLOIDS AND INTERFACIAL PHASES (ADSORPTION, CLUSTERING, MEMBRANES (POROUS), ZEOLITES, ADHESIVE POTENTIAL).
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CONCENTRATION EFFECTS IN BULK COLLOIDS AND INTERFACIAL PHASES (ADSORPTION, CLUSTERING, MEMBRANES (POROUS), ZEOLITES, ADHESIVE POTENTIAL).

机译:散装胶体和界面相的浓度效应(吸附,聚簇,膜(多孔),沸石,胶粘剂电位)。

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Three problems concerning the consequences of particle interactions in colloidal fluids and interfacial phases are undertaken: the aggregation of particles in bulk phases, the thermodynamics of particulate systems confined within narrow pores and cavities (such as those found in porous membranes), and the thermodynamics of a monolayer adsorbed onto a small surface.; Particle interaction effects on a structural, thermodynamic, or transport property can be adequately studied by developing an expansion for that property as a power series in particle concentration. Statistical mechanics is used to develop these concentration expansions and, in the study of monolayers, Scaled Particle Theory and Monte Carlo simulation are applied.; The clustering behavior of a system of particles which interact via the adhesive-sphere potential is examined, and the first non-trivial exact results for this model are obtained. Previous studies on the aggregation and percolation behavior of these particles are limited to the average cluster size, but this work provides detailed results for the suspension microstructure, such as the distribution of cluster sizes and shapes. In addition we find singularities in the structure of a fluid of adhesive particles, a characteristic previously unknown for the two- and three-dimensional models.; Particle adsorption in micropores is analyzed with the following theoretical model: an adhesive particle-wall interaction; hard-sphere like particle-particle interactions; and two micropore geometries, that of a slit and a cylindrical pore. Particle interactions in an adsorbed two-dimensional layer enhance the partitioning of solute particles between a microporous phase and a bulk phase, to a greater extent than the enhancement caused by interactions between particles residing in the micropore fluid.; The spreading pressure and chemical potential of a finite-sized, spherical monolayer of hard particles are obtained, and the results are applied to model adsorbate-adsorbate interactions inside zeolite molecular sieves.
机译:涉及胶体流体和界面相中颗粒相互作用后果的三个问题:本体相中颗粒的聚集,局限在狭窄的孔和腔中的颗粒系统的热力学(例如在多孔膜中发现的)以及热力学。单层吸附在小表面上。可以通过开发该性质的扩展作为粒子浓度的幂级数来充分研究粒子相互作用对结构,热力学或传输性质的影响。统计力学被用来发展这些浓度扩展,并且在单分子层的研究中,应用了比例粒子理论和蒙特卡洛模拟。检查了通过粘合剂球势相互作用的粒子系统的聚集行为,并获得了该模型的第一个重要的精确结果。以前有关这些颗粒的聚集和渗滤行为的研究仅限于平均团簇尺寸,但是这项工作为悬浮液的微观结构提供了详细的结果,例如团簇尺寸和形状的分布。另外,我们发现粘合剂颗粒的流体结构中存在奇异性,这是二维模型和三维模型以前未知的特征。用以下理论模型分析微孔中的颗粒吸附:粘合剂颗粒-壁相互作用;硬球状粒子间相互作用和两个微孔几何形状,分别是狭缝和圆柱孔。吸附的二维层中的颗粒相互作用增强了溶质颗粒在微孔相和本体相之间的分配,其程度大于由驻留在微孔流体中的颗粒之间的相互作用引起的增强。获得了有限尺寸的球形硬质颗粒单层的扩散压力和化学势,并将结果应用于沸石分子筛内部的吸附物-吸附物相互作用模型。

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