聚苯胺粒子悬浮液的电流变特性

将聚苯胺作为分散粒子，电绝缘油 分散介质组成电流变流体，研究了电场强度，温度等因素与ＥＲＦ的静态屈服应力和电流密度的关系。结果表明：τｓ和ｉ随电场强度的变化皆成指数关系。     

稀土掺杂聚苯撑ER流体的研究

选用CeCl4和FeCl3等对自制的对苯撑进行掺杂,将制得的高介电聚苯撑粉末加入到硅油中得到电流变体流体,测量了在电场作用下粘度和漏电流密度,以及相关的物理常数。讨论了电场强度、粒子浓度与粘度和漏电流密度的关系,粘度变化的响应速度和恢复时间,并探讨了其相关机制。     

Electrorheological Response and Structure Growth of Colloidal Silica Suspensions

The electrorheological response and structure growth of colloidal silica suspension was studied with in situ measurements of the shear stress, electric conductivity, and dielectric permittivity of the suspension. The measurements were carried out under steady and sweep shears after the application of an electric field of alternative current (100 Hz) using silica particles with a diameter of 630 nm and a water content of 4.5 wt%. The measurements of the conductivity enabled the detection of structure growth formed by particle aggregation and clarified that the development of the particle aggregation enlarged the dielectric permittivity and the shear stress. Hysteretic behavior observed in the electrorheological response was explained by considering structure growth of the particle aggregation. The correlation equation for the shear stress and the dielectric permittivity obtained in our previous work (1) was found to be applicable to the present results. Copyright 2001 Academic Press.     

稀土掺杂TiO2颗粒的制备及其悬浮液的电流变特性

通过掺杂稀土元素,使TiO2电流变液的屈服强度提高到近5 kPa (3 kV/mm).用DSC-TG、 IR和XRD等手段对材料的Sol-gel制备过程和产物的晶体结构进行了分析.结果表明纯TiO2和掺杂稀土TiO2凝胶的分解分三阶段完成,并形成锐钛矿结构.掺杂浓度小于一定值时,稀土离子以置换Ti位固溶于TiO2晶格中并引起晶格膨胀.认为适当掺杂所导致的晶格常数变化改善了材料的介电性能,从而使TiO2的电流变性能优化.     

On the Theory of Condensation Phase Transitions in Magnetic and Electrorheological Suspensions

Particle condensation in nonconducting electro- and magnetorheological suspensions under the action of external electric (magnetic) field was theoretically studied. It was shown that the phase separation of the particle system of the gas-liquid type is preceded by the formation of fairly long chain aggregates. Phase transition occurs as a condensation of these chains as a result of their polar electric (magnetic) interaction. This fact denotes the essential difference between the phase separation in the considered suspensions of polarizable particles from the phase transitions in ferro- and Seignette-electric fluids, i.e., colloidal suspensions of monodomain particles with permanent intrinsic moments, as well as from the transitions in molecular systems, where the condensation occurs in the ensemble of individual particles (molecules).     

壳聚糖电流变体的导电特性

电流变体是由高介电颗粒分散在低介电油相中组成的悬浮液,在电场作用下,其表观粘度急剧增大甚至发生固化,这种转变过程速度快（达毫秒级）而且是可逆的［１］．由于这种独特的电场响应性,电流变体有广阔的工程应用前景．但电流变体在显示电流变效应的同时也表现出复杂...     

表面活性剂对氧化锰悬浮体系流变学振荡行为的影响

对介孔氧化锰的溶胶-凝胶法合成和用表面活性剂（脂肪醇聚氧乙烯醚, AEO_9)的模板合成过程中所得的悬浮体系的流变性质进行了对比研究。结果表明： 上述体系均具有触变性,且无论是否预剪切,其表观粘度均随时间作周期性振荡; 同时上述体系的储能模量G'和损耗模量G"亦具有周期性的振荡行为。但表面活性剂 AEO_9的引入使体系的触变性大为减弱,屈服值明显降低,凝胶结构强度减弱。同 时还发现引入AEO_9的模板合成过程中,不仅体系的表观粘度及G'大幅度下降,且 G'与G"的振荡周期显著增大,振幅亦明显减小。这说明体系中两亲分子与无机物存 在较强的相互作用,作者还对这些现象进行了讨论。     

不同介电常数悬浮颗粒的电流变液固态结构

讨论了两种不同介电常数的固体颗粒不同配比时,对电流变液固态结构的影响.计算结果表明,颗粒的介电常数及配比变化时电流变液的固态结构没有变化,只影响其能量大小;而且发现在低介电常数颗粒的电流变液中加入少许高介电常数颗粒会引起体系能量的显著下降,从而增加了电流变液的稳定性和剪切应力.     

A Nonlinear Rupture Theory of Thin Liquid Films with Soluble Surfactant

The effects of soluble surfactant on the dynamic rupture of thin liquid films are investigated. A nonlinear coupling evolution equation is used to simulate the motion of thin liquid films on free surfaces. A generalized Frumkin model is adopted to simulate the adsorption/desorption kinetics of the soluble surfactant between the surface and the bulk phases. Numerical simulation results show that the liquid film system with soluble surfactant is more unstable than that with insoluble surfactant. Moreover, a generalized Frumkin model is substituted for the Langmuir model to predict the instability of liquid film with soluble surfactant. A numerical calculation using the generalized Frumkin model shows that the surfactant solubility increases as the values of parameters of absorption/desorption rate constant (J), activation energy desorption (nu(d)), and bulk diffusion constant (D(1)) increase, which consequently causes the film system to become unstable. The surfactant solubility decreases as the rate of equilibrium (lambda) and interaction among molecules (K) are increased, which therefore stabilizes the film system. On the other hand, an increase of relative surface concentration (the index of a power law), beta(n), will initially result in a decrease of corresponding shear drag force as beta and n increase from 0 to 0.3 and 0.85, respectively. This will enhance the Marangoni effect. However, a further increase of beta and n to greater than 0.3 and 0.85, respectively, will conversely result in an increase of the corresponding shear drag force. This will weaken the Marangoni effect and thus result in a reduction of interfacial stability. Copyright 2000 Academic Press.     

Dispersion Stability and Electrorheological Properties of Polyaniline Particle Suspensions Stabilized by Poly(vinyl methyl ether)

In the present article, a novel method of stabilization of a semi conductive polyaniline particle nonaqueous suspension of electrorheological (ER) materials was introduced. Using as the steric stabilizer poly(vinyl methyl ether) (PVME), a dispersion polymerization of aniline was performed and stable aqueous dispersions of the polyaniline were obtained. However, a stable colloidal suspension of polyaniline in silicone oil medium can be obtained only with a low concentration of PVME (0.75%), although the average size of the individual, redispersed particles in oil generally decreased with increasing concentration of PVME. At higher concentrations of PVME, formation of highly packed particle aggregates was investigated, as seen in the scanning electron microscopy images. The polyaniline suspension stabilized by 0.75% PVME content exhibited the best dispersing state and, therefore, showed the highest zero-field viscosity. Such a well-stabilized polyaniline suspension also showed the maximum ER property, namely the largest normalized yield stress in an electric field. Copyright 2001 Academic Press.     

Interaction of a Zwitterionic Surfactant with Synthetic Clays in Aqueous Suspensions: A Multinuclear Magnetic Resonance Study

(1)H and (13)C NMR signal assignment of laurylamidopropylbetain has been obtained from 2D COSY, HETCOR, and HMBC pulse sequences. (13)C and (14)N NMR relaxation data show interaction of the polar head of the surfactant with low-charged clays dispersed in aqueous solution. The sodium cation exchange rate between the solid surface and the bulk is strongly affected by the charge of the clay layer, as seen from (23)Na NMR data. Such an exchange is also observed with clay suspended in sodium dodecyl sulfate solutions. Copyright 2001 Academic Press.     

稀土掺杂PMMA包裹硅铝氧烷凝胶的ER效应

以二氧化硅微粒制备电流变液是研究者使用较多的一种方法[1] ,但由于二氧化硅的密度相对于分散相硅油来说太大 ,所以制成的电流变液稳定性较差。而用导电高分子微粒制成的电流变液则有在高电场时漏电流密度较大的问题[2 ] 。有研究者用直接聚合法在二氧化硅纳米微粒外包裹一层有机共聚物 ,生成一种微囊复合颗粒 ,可以使其相对密度减小 ,提高了电流变液的稳定性[3] 。我们以廉价水玻璃为原料制取硅铝氧烷溶胶 ,在其表面包裹聚甲基丙烯酸甲酯 (ＰＭＭＡ)后 ,得到ＰＭＭＡ包裹的硅铝氧烷凝胶具有相当的稳定性和易极化性 ,易形成较稳定的悬浮液 …     

A Surfactant Concentration Model for the Systematic Determination of the Critical Micellar Concentration and the Transition Width

The critical micellar concentration (cmc) is a fundamental property of surfactant solutions. Many proposed methods for the definition and determination of the cmc from property-concentration plots yield values, which depend on the studied property, on the specific technique used for its analysis and in many cases on the subjective choice of the chosen type of plot and concentration interval. In this focus review, we revise the application of a surfactant concentration model we proposed earlier that defines the cmc directly based on the surfactant concentration. Known equations for the concentration-dependence of different surfactant properties can then be combined with this concentration model and fitted to experimental data. This modular concept makes it possible to determine the cmc and the transition width in a systematic and unambiguous way. We revise its use in the literature in different contexts: the determination of the cmc of surfactants and their mixtures from different properties (electrical conductivity, NMR chemical shift, self-diffusion, surface tension, UV-Vis absorption, fluorescence intensity and fluorescence correlation). We also revise the dependence of the width of the transition region on composition, detailed studies of the properties of fluorescent probes and the aggregation of non-surfactant systems, namely amyloid peptides.     

Electrophoretic Deposition: A Quantitative Model for Particle Deposition and Binder Formation from Alcohol-Based Suspensions

We investigated electrophoretic deposition from a suspension containing positively charged particles, isopropanol, water, and Mg(NO(3))(2), with the aim of describing the deposition rates of the particles and Mg(OH)(2), which is formed due to chemical reactions at the electrode, in terms of quantitative models. LaB(6) particles were used as a model system. The particle layer is consolidated by simultaneous precipitation of Mg(OH)(2) which acts as a binder to hold the particles together. The Mg(OH)(2) content was determined solely by the amount of charge passed through the cell. Quantitative precipitation of all OH(-) formed at the electrode was observed, except at very low current. The occurrence of a minimum current was ascribed to a threshold for Mg(OH)(2) deposition. The same minimum current was observed for particle deposition. In combination with results using NaNO(3), where no adherent layer was formed, this illustrates that Mg(OH)(2) binder is necessary for consolidation. Once the minimum current was exceeded, it was found that all particles that migrate to the electrode under the influence of the electric field contribute to the formation of the layer, i.e., the "sticking coefficient" for the particles equals 1.0. The applicability of the particle and Mg(OH)(2) deposition models was tested by variation of the Mg(NO(3))(2) concentration, pH, and water content. Copyright 2000 Academic Press.     

Viscous Elasticity of Suspensions in a Structural Model

Moscow University Chemistry Bulletin - An oscillating shear flow of suspensions is considered as a case of a periodically varying shear flow similar to a stationary shear flow. In the structural...     

A New Method for Study of Magnetic Suspensions

A procedure for determining the magnetization of a ferrofluid from the shift of ¹H NMR signal of the solvent by rotating a sample having the shape of an oblate ellipsoid is suggested. The possibility of using the NMR spectroscopy for evaluating the size of magnetite particles and for examining the distribution of the local magnetization of the ferrofluid in a magnetic field is analyzed. The NMR method is compared with the classical Gouy technique.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 4, 2005, pp. 556–558.Original Russian Text Copyright © 2005 by Zhernovoi, Naumov.     

An Insoluble Surfactant Model for a Vertical Draining Free Film

A mathematical model is constructed to study the evolution of a vertically oriented thin liquid film draining under gravity when there is an insoluble surfactant with finite surface viscosity on its free surface. Lubrication theory for this free film results in three coupled nonlinear partial differential equations describing the free surface shape, the surface velocity, and the surfactant transport at leading order. We will show that in the limit of large surface viscosity, the evolution of the free surface is that obtained for the tangentially immobile case. For mobile films with small surface viscosity, transition from a mobile to an essentially immobile film is observed for large Marangoni effects. It is verified that increasing surface viscosity and the Marangoni effect retard drainage, thereby enhancing film stability. The theoretical results are compared with experiment; the purpose of both is to act as a model problem to evaluate the effectiveness of surfactants for potential use in foam-fabrication processes. Copyright 2000 Academic Press.     

A Theoretical Model of Pulmonary Surfactant Multilayer Collapse under Oscillating Area Conditions

Monolayers of adsorbed pulmonary surfactant collapse under compression and respread to the interface when the area expands. These mechanisms contribute to the large area hysteresis seen experimentally in a pulsating bubble surfactometer. This paper presents an analytical model which adds monolayer collapse and respreading to the more standard transport processes (diffusion, adsorption, and desorption). The model is robust and can mimic a large range of responses, from that of an insoluble monolayer to the large area hysteresis indicative of collapse and respreading. Our model suggests that multilayer dynamics are necessary to mimic the ultralow surface tensions of pulmonary surfactant. Copyright 2000 Academic Press.     

Swelling of Water/Nonionic Surfactant Lamellar Liquid Crystals: A Model

A model is presented to provide quantitative measures to estimate the trends of the change in the penetration of the added component into the polar part of the amphiphile layer in lamellar liquid crystals of water and ethoxylated surfactants with added water (or polar solvents). The total thickness of the bi‐layer is treated as composed of an aqueous layer, of a layer of the polar groups from the surfactant and of the hydrocarbon chains of the latter. A fraction α of the added water is assumed penetrating the polar group layer leading to its expansion. The evaluation is built on the fact that experimental determinations of the interlayer spacing in the overwhelming majority of cases show a first order linear dependence on the ratio of added water. In the model this linearity is obtained by variation of the degree of penetration of water. The model indicated a reduction in the degree of penetration with added water, which is a rational trend. The model demonstrates the earlier interpretation of a structure, whose interlayer spacing is invariant with water contents as nonswelling; for example, in which all added water penetrates the amhiphile layer, is not appropriate. The model demonstrates the constancy of the interlayer spacing to be a consequence of a balance between the expansion of the amphiphile layer and the increase of a “free water” layer.     

表面活性剂对苯胺电聚合的影响

利用胶束在电极一有面的定向及增溶作用研究了表面活性剂对苯胺电聚合的影响，结果表明：在阴离子表面活性剂十二烷基硫酸钠（ＳＤＳ）胶束体系中，胶束介质能催化苯胺的电聚合反应，使其氧化电位负移，减少膜的降解，提高膜的稳定性，同时，也使得聚合速率增大，在０．１ｍｏｌ／Ｌ的ＳＤＳ的胶束溶液中，其聚合效率提高到不含ＳＤＳ的纯体系的２５倍，在含有１０＾－４ｍｏｌ／ＬＳＤＳ的硫酸溶液中，聚苯胺（ＰＡＮ）的成核生长为