Levelset方法数值模拟单液滴传质中的Marangoni效应

用Levelset方法捕获界面建立了数值模拟变形单液滴萃取传质过程中Marangoni效应的控制方程。将浓度场和流场相耦合计算,数值模拟了变形单液滴传质中的Marangoni效应,描述了Marangoni效应的发生和发展过程,结果同Sternling ＆ Scriven的经典理论分析和前期数值模拟相吻合。     

异丁醇-水-硝基乙烷体系中的双因素自耦合界面不稳定现象

指导了发生在异丁醇、硝基乙烷和水三组分两相体系中的多因素复合界面不稳定现象，文中通过对一个滴加在异丁醇水溶液表面的硝基乙烷液滴的运动特征的分析，揭示了该现象的规律，在体系趋于热力学平衡的过程中，硝基乙烷液滴先表现出周期性的振荡运动，然后转变为螺旋线和圆周运动，提出了一个溶质迁移和相间溶解的双因素自耦合机理，认为该现象的根本起因是表面活性剂溶质相间迁移所导致的溶质Ｍａｒａｎｇｎｉ效应，但由于丁醇的相     

Marangoni效应与液膜振荡*

本文系统地总结了Marangoni效应的形成、发展及其与液膜振荡现象的关系,用Marangoni效应定量分析讨论了3种不同的液膜振荡体系,给出了有关数学公式,并与液膜振荡的化学本质学说作了对比。     

N2,O2水溶液光谱的分子动力学模拟

用分子动力学模拟方法研究了N2和O2水溶液的光谱性质．给出了能描述分子内部运动的溶质－溶剂相互作用势．对溶质和溶剂原子的速度自相关函数（VACF）作了计算．讨论了所得VACF的性质并计算了其谱密度．溶质分子振动谱出现的红移，与液态N2，O2的Raman实验结果相吻合．模拟得出的转动谱表明了溶剂分子对溶质转动运动的阻滞，模拟结果也表明VACF计算对溶液和液体光谱的研究十分有效．     

液滴在超疏水形状记忆微阵列表面上定向/非定向滚动的可逆调控

利用3D打印、 模板赋形和表面修饰的方法, 制备出具有竖直结构的超疏水形状记忆微阵列. 该微阵列的竖直状态和倾斜状态能够基于形状记忆效应进行可逆调控. 当微阵列的结构发生改变, 液滴在表面的滚动状态也随之发生变化. 液滴在竖直的微阵列上表现出非定向滚动特征, 即液滴向微阵列两侧运动的滚动角是一致的. 在倾斜的微阵列上, 液滴则表现出定向运动的功能, 即液滴沿着微阵列倾斜方向上的滚动角要小于逆着阵列倾斜方向的滚动角. 因此, 本文通过调控微阵列形态实现了对液滴定向/非定向滚动的可逆调控.     

甲酰胺,乙酰胺,尿素在两种极性非水溶液中的体积性质

以尿素、甲酰胺和乙酰胺为溶质，二甲基甲酰胺和二甲基亚砜为溶剂；或以二甲基甲酰胺、二甲基亚砜为溶质，以甲酰胺为溶剂，通过测定溶液在２９８．１５Ｋ下的密度数据，求得了溶质的表观磨尔体积以及与溶质－溶质相互作用相关的体积第二维里系数。利用定标粒子理论讨论了溶质分子的几何体积、溶质－溶剂相互作用对溶质偏摩尔体积的影响，结果表明，熔质的溶剂化与溶质－溶质相互作用的体积效应呈相反的变化趋势。     

质量、热量传递过程中的Marangoni效应*

由质量、热量传递引发,表面张力梯度驱动的Marangoni效应不但对化学工程、材料工程和热能工程等领域里的一系列过程具有重要的影响,而且具有非线性耗散系统理论研究的一个具有实际意义的课题。对Marangoni效应的实验及理论研究有助于增进对微观传热、传质机理的理解,它的合理利用也可以提高某些过程的效率。迄今为止,对Marangoni效应的认识还不能满足理论研究和工程应用的要求。按期在各相关领域内对Marangoni的研究十分活跃,本文回顾了这些研究成果。     

超临界CO2-溶质二元系的密度及溶质的偏摩尔体积

在308．15和318．15K温度下，80－170bar压力范围内，测定了CO2-乙醇、CO2-丙酮和CO2-正庚烷混合物的密度，溶质的浓度范围是0－1．3mol·L－1．在此基础上，计算了溶质的偏摩尔体积，系统地研究了温度、压力和溶质浓度对二元混合物密度的影响，并从压力和溶质浓度对溶质偏摩尔体积影响的角度研究体系中的分子间相互作用．     

形状记忆磁性润滑表面的制备及对超顺磁液滴的滑动操控

将磁性粒子与形状记忆聚合物复合,通过设计渐变式构型构筑了梯度形状磁性材料,并与润滑涂层相结合,制备了一种磁性润滑表面.在磁性梯度的作用下,超顺磁液滴在表面上能够自发定向运动.借助于材料形状记忆效应对表面区域形态进行可逆调控,进一步展示了超顺磁液滴自发定向运动过程中的启停开关式控制,实现了将液滴定向自发运输与启停控制相结合.考察了磁性粒子含量对材料形状记忆性能的影响,以及区域形态调控尺寸与液滴滑动性能间的相互关系.机理分析进一步阐明磁场梯度提供的定向驱动力促使液滴定向自发输运,表面区域形态控制的可逆调控则可以在液滴运动过程中增加/消除黏滞阻力,基于两种因素的协同作用,可以实现对超顺磁液滴运动的智能操控.     

气相渗透法中的溶质吸附效应

在气相渗透仪上，用四个低分子量有机化合物和五个已知平均分子量的窄分布聚苯乙烯低聚体，对ＶＰＯ方法中的溶质吸附效应作了研究，提出了一种对吸附效应作改正的方法．所得结果表明，在扣除溶质吸附效应后，仪器常数Ｋ无分子量依赖性，提高了测定低分子量聚合物数均分子量的准确性．     

Interfacial forces and Marangoni flow on a nematic drop retracting in an isotropic fluid

Nematic-isotropic interfaces exhibit novel dynamics due to anchoring of the liquid crystal molecules on the interface. The objective of this study is to demonstrate the consequences of such dynamics in the flow field created by an elongated nematic drop retracting in an isotropic matrix. This is accomplished by two-dimensional flow simulations using a diffuse-interface model. By exploring the coupling among bulk liquid crystal orientation, surface anchoring and the flow field, we show that the anchoring energy plays a fundamental role in the interfacial dynamics of nematic liquids. In particular, it gives rise to a dynamic interfacial tension that depends on the bulk orientation. Tangential gradient of the interfacial tension drives a Marangoni flow near the nematic-isotropic interface. Besides, the anchoring energy produces an additional normal force on the interface that, together with the interfacial tension, determines the movement of the interface. Consequently, a nematic drop with planar anchoring retracts more slowly than a Newtonian drop, while one with homeotropic anchoring retracts faster than a Newtonian drop. The numerical results are consistent with prior theories for interfacial rheology and experimental observations.     

Measurement of the kinetic rate constants for the adsorption of superspreading trisiloxanes to an air/aqueous interface and the relevance of these measurements to the mechanism of superspreading

Super-spreading trisiloxane surfactants are a class of amphiphiles which consist of nonpolar trisiloxane headgroups ((CH3)3-Si-O)2-Si(CH3)(CH2)3-) and polar parts composed of between four and eight ethylene oxides (ethoxylates, -OCH2CH2-). Millimeter-sized aqueous drops of trisiloxane solutions at concentrations well above the critical aggregate concentration spread rapidly on very hydrophobic surfaces, completely wetting out at equilibrium. The wetting out can be understood as a consequence of the ability of the trisiloxanes at the advancing perimeter of the drop to adsorb at the air/aqueous and aqueous/hydrophobic solid interfaces and to reduce considerably the tensions of these interfaces, creating a positive spreading coefficient. The rapid spreading can be due to maintaining a positive spreading coefficient at the perimeter as the drop spreads. However, the air/aqueous and solid/aqueous interfaces at the perimeter are depleted of surfactant by interfacial expansion as the drop spreads. The spreading coefficient can remain positive if the rate of surfactant adsorption onto the solid and fluid surfaces from the spreading aqueous film at the perimeter exceeds the diluting effect due to the area expansion. This task is made more difficult by the fact that the reservoir of surfactant in the film is continually depleted by adsorption to the expanding interfaces. If the adsorption cannot keep pace with the area expansion at the perimeter, and the surface concentrations become reduced at the contact line, a negative spreading coefficient which retards the drop movement can develop. In this case, however, a Marangoni mechanism can account for the rapid spreading if the surface concentrations at the drop apex are assumed to remain high compared to the perimeter so that the drop is pulled out by the higher tension at the perimeter than at the apex. To maintain a high apex concentration, surfactant adsorption must exceed the rate of interfacial dilation at the apex due to the outward flow. This is conceivable because, unlike that at the contact line, the surfactant reservoir in the liquid at the drop center is not continually depleted by adsorption onto an expanding solid surface. In an effort to understand the rapid spreading, we measure the kinetic rate constants for adsorption of unaggregated trisiloxane surfactant from the sublayer to the air/aqueous surface. The kinetic rate of adsorption, computed assuming the bulk concentration of monomer to be uniform and undepleted, represents the fastest that surfactant monomer can adsorb onto the air/aqueous surface in the absence of direct adsorption of aggregates. The kinetic constants are obtained by measuring the dynamic tension relaxation as trisiloxanes adsorb onto a clean pendant bubble interface. We find that the rate of kinetic adsorption is only of the same order as the area expansion rates observed in superspreading, and therefore the unaggregated flux cannot maintain very high surface concentrations at the air/aqueous interface, either at the apex or at the perimeter. Hence in order to maintain either a positive spreading coefficient or a Marangoni gradient, the surfactant adsorptive flux needs to be augmented, and the direct adsorption of aggregates (which in the case of the trisiloxanes are bilayers and vesicles) is suggested as one possibility.     

Surface activity of lysozyme and dipalmitoyl phosphatidylcholine vesicles at compressed and supercritical fluid interfaces

The surface activities of lysozyme and dipalmitoyl phosphatidylcholine (DPPC) vesicles at aqueous/compressed fluid interfaces are examined via high-pressure interfacial tension measurements using the pendant drop technique. The density and interfacial tension in compressible fluid systems vary significantly with pressure, providing a versatile medium for elucidating interactions between biomolecules and fluid interfaces and a method to elicit pressure-dependent interfacial morphological responses. The effects of lysozyme concentration (0.0008, 0.01, and 1 mg/mL) and pressure (> or = 7 MPa) on the dynamic surface response in the presence of ethane, propane, N2, and CO2 at 298 K were examined. Interfacial lysozyme adsorption reduced the induction phase and quickly led to interfacial tensions consistent with protein conformational changes and monolayer saturation at the compressed fluid interfaces. Protein adsorption, as indicated by surface pressure, correlated with calculated Hamaker constants for the compressed gases, denoting the importance of dispersion interactions. For DPPC at aqueous/compressed or aqueous/supercritical CO2 interfaces (1.8-20.7 MPa, 308 K), 2-3-fold reductions in interfacial tension were observed relative to the pure binary fluid system. The resulting surface pressures infer pressure-dependent morphological changes within the DPPC monolayer.     

油酸-油酸钠水溶液/原油间的瞬时界面张力

羧酸盐表面活性剂以其价格低廉、资源丰富和较高的界面活性而受到重视[1]．我们将廉价的天然核酸盐复配体系用于提高采收率研究，取得良好效果问．据最近报道问，用瞬时界面张力（l）评价驱油体系更符合实际采油过程．本文应用试剂级油酸，试图从理论上探讨不同因素对混合体系瞬时界面张力的影响规律，为驱油体系配方的选择提供依据．1实验部分1．1试剂油酸（R17C00H），分析纯收京长城化学试剂厂产品）．水解聚丙烯酸胶（HPAM），平均分子量为1．7X10’，平均水解度为20％，（美国辉瑞公司产品）．1．2方法按设计量在电子分析天平（精…     

Mimic oil recovery with a SDBS–dodecane–silica gel system

The wettability of the solid powder of silica gel was determined via a modified Washburn equation expressed as contact angles. The interfacial tension (γ) between the dodecane and the dilute sodium dodecyl benzene sulfonate (SDBS) aqueous solution was obtained using the spinning drop (γ<10 mN m⁻¹) or drop volume methods (γ>10 mN m⁻¹). Contact angle changes for SDBS aqueous solutions on the surface of a silica gel powder were studied. The average aggregation number of SDBS micelles in aqueous solution was determined using the fluorescence quenching method. The relationship between the wettability of the powder surface, the critical micelle concentration (CMC) of SDBS and the mimic oil recovery of the resident oil on the powder surface has been explored. It has been found that good residual oil recovery was achieved by surface wettability changes at the interfacial tensions around 4–5 mN m⁻¹, which is far from the ‘ultra low’ condition (≤10⁻³ mN m⁻¹).     

Hofmeister effect on the interfacial dynamics of single polymer molecules

The Hofmeister effect on interfacial dynamics has been discovered for single charged polymer molecules (sodium polystyrene sulfonate) adsorbed on a hydrophobic surface from an aqueous solution. The presence of ions in the aqueous solution affects the surface diffusivity, and its amplitudes and the surface friction follow the Hofmeister series-the kosmotropic ions slowed down the surface diffusivity and the chaotropic ions speeded it up. The amplitude of the surface friction exhibits a good correlation with the surface tension increment, indicating the interfacial feature of the Hofmeister effect.     

Interfacial characteristics of food emulsifiers (proteins and lipids) at the air-water interface

Factors affecting the interfacial characteristics (structure, stability, interfacial rheology, molecular diffusion, and rate of film formation) of food emulsifiers (polar lipids and proteins) at the air-aqueous phase interface are reviewed. The effect of interfacial and aqueous phase (water, and aqueous solutions of ethanol, glycerol, sugars, electrolytes, and pH) compositions have been analyzed as variables. Many measurement methods—such as tensiometry (Wilhelmy plate and pendant drop methods), and Langmuir- and Wilhelmy-type film balances—have been used in the experiments. The effect of the interfacial, aqueous phase composition, and operational conditions (surface density, surface pressure, and temperature) of food emulsifiers (lipids and proteins) at the air-aqueous phase interface are discussed.     

Forces between two oil drops in aqueous solution measured by AFM

The surface and hydrodynamic forces between individual oil droplets in solution can provide insight into both emulsion stability and processes such as drop coalescence in liquid-liquid extraction. We present the first measurements of the interaction forces between alkane droplets in aqueous solution using atomic force microscopy. The radii of the droplets were well below the capillary lengths for the system, thus gravity effects are negligible, and interfacial tension and interaction forces governed the system behavior. The effects of modulating electrostatic double-layer interactions and interfacial tension through the presence of an anionic surfactant are demonstrated. Challenges in interpretation of the force data due to drop deformation are also discussed. A range of drop approach and retract speeds was used to determine the regime where hydrodynamic drainage effects had significant impact on the measurement.     

Determining the mechanical response of particle-laden fluid interfaces using surface pressure isotherms and bulk pressure measurements of droplets

The mechanical response of particle-laden fluid interfaces is determined by measuring the internal pressures of particle-coated drops as a function of the drop volume. The particle monolayers undergoing compression-expansion cycles exhibit three distinct states: fluid state, jammed state, and buckled state. The P-V curves are compared to the surface pressure isotherms Pi-A that are measured using a Langmuir trough and a Wilhelmy plate on a flat water-decane interface covered with the same particles. We find that in the fluid and jammed states, the water drop in decane can be described by the Young-Laplace equation. Therefore in these relatively low compression states, the bulk pressure measurements can be used to deduce the interfacial tension of the droplets and yield similar surface pressure isotherms to the ones measured with the Wilhelmy plate. In the buckled state, the internal pressure of the drop yields a zero value, which is consistent with the zero interfacial tension measured with the Wilhelmy plate. Moreover we find that the compressibility in the jammed state does not depend on the particle size.     

Synthesis and Applications of Alkylbenzene Sulfonate Gemini Surfactants

A series of anionic Gemini surfactants with the same structure except for the spacer and side chain length of the alkylbenzene sulfonate were synthesized based on dodecyl benzene and toluene. The structures of the compounds were confirmed by infrared and nuclear magnetic resonance spectroscopy, and elemental analyses. The effect of spacer and side chain length on the interfacial tension of Gemini surfactant solution was investigated by comparison of the critical micelle concentration (cmc) of the surfactants in aqueous solution using the drop volume method, and the surface tension at the cmc (γcmc). The Gemini surfactant with the best properties was used as emulsifier in emulsion polymerization of methyl methacrylate, and its foam stability was also determined.