Do you want to publish a course? Click here

Mesoscale solubilization and critical phenomena in binary and quasi binary solutions of hydrotropes

80   0   0.0 ( 0 )
 Added by Mikhail Anisimov
 Publication date 2015
  fields Physics
and research's language is English




Ask ChatGPT about the research

Hydrotropes are substances consisting of amphiphilic molecules that are too small to self assemble in equilibrium structures in aqueous solutions, but can form dynamic molecular clusters H bonded with water molecules. Some hydrotropes, such as low molecular weight alcohols and amines, can solubilize hydrophobic compounds in aqueous solutions at a mesoscopic scale, around 100 nm, with formation of long lived mesoscale droplets. In this work, we report on the studies of near critical and phase behavior of binary, 2,6-lutidine - H2O, and quasibinary, 2,6-lutidine - H2O - D2O, and tert-butanol - 2-butanol - H2O solutions in the presence of a solubilized hydrophobic impurity, cyclohexane. In additional to visual observation of fluid phase equilibria, two experimental techniques were used - light scattering and small - angle neutron scattering. It was found that the increase of the tert-butanol to 2-butanol ratio affects the liquid - liquid equilibria in the quasi-binary system at ambient pressure in the same way as the increase of pressure modifies the phase behavior of binary 2-butanol - H2O solutions. The correlation length of critical fluctuations near the liquid-liquid separation and the size of mesoscale droplets of solubilized cyclohexane were obtained by dynamic light scattering and by small - angle neutron scattering. It is shown that the effect of the presence of small amounts of cyclohexane on the near - critical phase behavior is twofold - the transition temperature changes towards increasing the two-phase domain, and long-lived mesoscopic inhomogeneities emerge in the macroscopically homogeneous domain. These homogeneities remain unchanged upon approach to the critical point of macroscopic phase separation and do not alter the universal nature of criticality. However, a larger amount of cyclohexane generates additional liquid-liquid phase separation at lower temperatures.



rate research

Read More

A systematics of grain boundary (GB) segregation transitions and critical phenomena has been derived to expand the classical GB segregation theory. This study uncovers when GB layering vs. prewetting transitions should occur and how they are related to one another. Moreover, a novel descriptor, normalized segregation strength, is introduced. It can represent several factors that control GB segregation, including strain and bond energies for both general and small-angle GBs, as well as misorientation for small-angle GBs, which had to be treated separately in prior models. In a strong segregation system with a large normalized segregation strength, first-order layering transitions occur at low temperatures and become continuous above GB roughing temperatures. With reducing normalized segregation strength, the layering transitions gradually merge and finally lump into prewetting transitions without quantized layer numbers, akin to Cahns critical-point wetting model. Furthermore, GB complexion diagrams with universal characters are constructed as the GB counterpart to the classical exemplar of Pelton-Thompson regular-solution binary bulk phase diagrams.
If a fluctuating medium is confined, the ensuing perturbation of its fluctuation spectrum generates Casimir-like effective forces acting on its confining surfaces. Near a continuous phase transition of such a medium the corresponding order parameter fluctuations occur on all length scales and therefore close to the critical point this effect acquires a universal character, i.e., to a large extent it is independent of the microscopic details of the actual system. Accordingly it can be calculated theoretically by studying suitable representative model systems. We report on the direct measurement of critical Casimir forces by total internal reflection microscopy (TIRM), with femto-Newton resolution. The corresponding potentials are determined for individual colloidal particles floating above a substrate under the action of the critical thermal noise in the solvent medium, constituted by a binary liquid mixture of water and 2,6-lutidine near its lower consolute point. Depending on the relative adsorption preferences of the colloid and substrate surfaces with respect to the two components of the binary liquid mixture, we observe that, upon approaching the critical point of the solvent, attractive or repulsive forces emerge and supersede those prevailing away from it. Based on the knowledge of the critical Casimir forces acting in film geometries within the Ising universality class and with equal or opposing boundary conditions, we provide the corresponding theoretical predictions for the sphere-planar wall geometry of the experiment. The experimental data for the effective potential can be interpreted consistently in terms of these predictions and a remarkable quantitative agreement is observed.
Self-assembly in natural and synthetic molecular systems can create complex aggregates or materials whose properties and functionality rises from their internal structure and molecular arrangement. The key microscopic features that control such assemblies remain poorly understood, nevertheless. Using classical density functional theory we demonstrate how the intrinsic length scales and their interplay in terms of interspecies molecular interactions can be used to tune soft matter self-assembly. We apply our strategy to two different soft binary mixtures to create guidelines for tuning intermolecular interactions that lead to transitions from fully miscible, liquid-like uniform state to formation of simple and core-shell aggregates, and mixed aggregate structures. Furthermore, we demonstrate how the interspecies interactions and system composition can be used to control concentration gradients of component species within these assemblies. The insight generated by this work contributes towards understanding and controlling soft multi-component self-assembly systems. Additionally, our results aid in understanding complex biological assemblies and their function and provide tools to engineer molecular interactions in order to control polymeric and protein-based materials, pharmaceutical formulations, and nanoparticle assemblies.
The velocity of dislocations is derived analytically to incorporate and predict the intriguing effects induced by the preferential solute segregation and Cottrell atmospheres in both two-dimensional and three-dimensional binary systems of various crystalline symmetries. The corresponding mesoscopic description of defect dynamics is constructed through the amplitude formulation of the phase-field crystal model which has been shown to accurately capture elasticity and plasticity in a wide variety of systems. Modifications of the Peach-Koehler force as a result of solute concentration variations and compositional stresses are presented, leading to interesting new predictions of defect motion due to effects of Cottrell atmospheres. These include the deflection of dislocation glide paths, the variation of climb speed and direction, and the change or prevention of defect annihilation, all of which play an important role in determining the fundamental behaviors of complex defect network and dynamics. The analytic results are verified by numerical simulations.
The dynamical behavior of the column that made up binary granular beads is investigated systematically by tracking the displacement of particles in the collapse process. An experimental setup is first devised to control the quasi-static collapse of a granular column, and then observe the trajectories of tracer particles by using an industrial camera controlled by the image acquisition program. It is found that there exist two zones in column: a sliding region in which particles are moving in a layered structure; a static region within which particles are stationary. According to this analytical result, a dynamical model is developed to predict the trajectory evolution of particles in the space-time. The calculating result for the trajectories of particles on the selected layers is well consistent with the experimental observation.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا