Simulation of structure formation in disperse systems

The main rules governing the redistribution of microparticles in disperse systems were revealed by computer simulation. These rules predetermine the character and properties of the structure being formed, which opens up the possibility to control the properties of disperse materials, including sorbents and catalysts based on high-dispersity solid phases.     

Mesoscopic structure formation in colloidal aggregation and gelation

Recent small-angle light scattering experiments have revealed that diffusively aggregating spherical particles develop structure on a mesoscopic length scale (∼ tens of particles). The mesoscopic structural length scale persists even when the aggregation proceeds to the formation of a space-spanning network (a gel). We review the technique of small-angle light scattering, survey the experimental evidence for mesoscopic structure formation, discuss attempts at understanding these experimental observations by computer simulation of irreversible and reversible diffusion-limited cluster aggregation (DLCA), and propose a coherent picture for the understanding of non-equilibrium aggregation in the context of phase transitions.     

Computer simulation of the structure formation and disruption processes in the solid-liquid disperse systems

Results of the computer simulation of solid-liquid disperse systems are reported. Main regularities of the formation and disruption of the internal structure of such systems are demonstrated under static and dynamic conditions (including the combination of shear and orthogonal vibrations). The effect of the character of the interaction of dispersed phase particles, as well as of a number of parameters concerning the type and intensity of external actions on the behavior of disperse systems is shown. The possibility of the regulation of the character of microstructure and rheological properties of disperse systems by the combination of shearing and orthogonal vibrations is illustrated.     

Elastification of shore and petroleum bitumen and compositions on their basis

The characteristics of new rubber sealant Elaston based on bitumen, the application of which allows one to replace sealants using expensive liquid rubbers, are given. A new modifier for paving and roofing bitumen is developed that increases the softening temperature of bitumen and decreases its brittleness temperature.     

Polymerization of vinyl monomers in petroleum bitumen and properties of the related composites

Kinetic features of the radical polymerization of styrene, methyl methacrylate, and n-butyl methacrylate in road petroleum bitumen are studied in relation to the initiator type. The prepared polymer-bitumen composites are characterized by better performance characteristics than bitumen.     

Dispersions of nanocrystalline cellulose in aqueous polymer solutions: structure formation of colloidal rods

The steady-state shear and linear viscoelastic deformations of semidilute suspensions of rod-shaped nanocrystalline cellulose (NCC) particles in 1.0% hydroxyethyl cellulose and carboxymethyl cellulose solutions were investigated. Addition of NCC at the onset of semidilute suspension concentration significantly altered the rheological and linear viscoelastic properties of semidilute polymer solutions. The low-shear viscosity values of polymers solutions were increased 20-490 times (depending on polymer molecular weight and functional groups) by the presence of NCC. NCC suspensions in polymer solutions exhibited yield stresses up to 7.12 Pa. Viscoelasticity measurements also showed that NCC suspended polymer solutions had higher linear elastic moduli than the loss moduli. All of those results revealed the gel formation of NCC particles and presence of internal structures. The formation of a weak gel structure was due to the nonadsorbing macromolecules which caused the depletion-induced interaction among NCC particles. A simple interaction energy model was used to show successfully the flocculation of NCC particles in the presence of nonadsorbing polymers. The model is based on the incorporation of the depletion interaction term between two parallel plates into the DLVO theory for cubic prismatic rod shaped NCC particles.     

Sample preparation procedure for the determination of polycyclic aromatic hydrocarbons in petroleum vacuum residue and bitumen

This paper describes a novel method of sample preparation for the determination of trace concentrations of polycyclic aromatic hydrocarbons (PAHs) in high-boiling petroleum products. Limits of quantitation of the investigated PAHs in materials of this type range from tens of nanograms per kilogram to <20 μg/kg. The studies revealed that in order to separate most of interferences from the analytes without a significant loss of PAHs, it is necessary to use size exclusion chromatography as the first step of sample preparation, followed by adsorption using normal-phase liquid chromatography. The use of orthogonal separation procedure described in the paper allows the isolation of only a group of unsubstituted and substituted aromatic hydrocarbons with a specific range of molar mass. The lower the required limit of quantitation of PAHs, the larger is the scale of preparative liquid chromatography in both steps of sample preparation needed. The use of internal standard allows quantitative results to be corrected for the degree of recovery of PAHs during the sample preparation step. Final determination can be carried out using HPLC-FLD, GC-MS, or HPLC-UV–VIS/DAD. The last technique provides a degree of identification through the acquired UV–VIS spectra.     

Fast formation of opal-like columnar colloidal crystals

We demonstrate that highly polydisperse colloidal gibbsite platelets easily form an opal-like columnar crystal with striking iridescent Bragg reflections. The formation process can be accelerated by orders of magnitude under a centrifugation force of 900 g without arresting the system in a disordered glassy phase. Using transmission electron microscopy and small-angle X-ray scattering techniques, we find that the forced sedimentation is accompanied by particle size fractionation, leading to inversion of the iridescent colors. The relatively easy self-organization of the polydisperse colloidal particles into opal-like crystals may be explained on the basis of the observed particle fractionation and possibly also on hexatic-like ordering.     

Stacking fault structure in shear-induced colloidal crystallization

We report measurements of the spatial distribution of stacking faults in colloidal crystals formed by means of an oscillatory shear field at a particle volume fraction of 52% in a system where the pair potential interactions are mildly repulsive. Stacking faults are directly visualized via confocal laser scanning microscopy. Consistent with previous scattering studies, shear orders the initially amorphous colloids into close-packed planes parallel to the shearing surface. Upon increasing the strain amplitude, the close-packed direction of the (111) crystal plane shifts from an orientation parallel to the vorticity direction to parallel the flow direction. The quality of the layer ordering, as characterized by the mean stacking parameter, decreases with strain amplitude. In addition, we directly observe the three-dimensional structure of stacking faults in sheared crystals. We observe and quantify spatial heterogeneity in the stacking fault arrangement in both the flow-vorticity plane and the gradient direction, particularly at high strain amplitudes (gamma> or =3). At these conditions, layer ordering persists in the flow-vorticity plane only over scales of approximately 5-10 particle diameters. This heterogeneity is one component of the random layer ordering deduced from previous scattering studies. In addition, in the gradient direction, the stacking registry shows that crystals with intermediate global mean stacking probability are comprised of short sequences of face-centered cubic and hexagonal close-packed layers with a stacking that includes a component that is nonrandom and alternating in character.     

Nonequilibrium structure of primary particles in colloidal bidispersion

The nonequilibrium aggregation structure of primary particles in colloidal bidispersions is investigated at high volume fractions by Brownian dynamics simulations. It is found that introducing limited different sized particles in the monodispersion can obviously affect the short-range structures of primary particles. In a bidispersion, fractal dimension of aggregates, only consisting of primary particles, increases with increasing the size difference in the long-range scale. The structure factor S(q) of aggregates, obtained from the particle correlation function g(r), suggests that fractal structure disappears when the primary particles become not “primary” in volume fraction.     

Model for cage formation in colloidal suspension of laponite

In this paper we investigate glass transition in aqueous suspension of synthetic hectorite clay, laponite. We believe that upon dispersing laponite clay in water, the system comprises of clusters (agglomerates) of laponite dispersed in the same. Subsequent osmotic swelling of these clusters leads to an increase in their volume fraction. We propose that this phenomenon is responsible for slowing down of the overall dynamics of the system. As clusters fill up the space, the system undergoes glass transition. Along with the mode coupling theory, the proposed mechanism rightly captures various characteristic features of the system in the ergodic regime as it approaches glass transition.     

Viscosity of liquid suspensions with fractal aggregates: Magnetic nanoparticles in petroleum colloidal structures

New physical model is presented resulting in a simple formula for the dependence of viscosity η of colloidal liquid solution on the shear rate G applicable to a wide variety of systems including complex natural liquids like petroleum. The principal point of the model is the fractal nature of colloid particle aggregates present in the liquid. Such aggregates are experimentally detected now in non-Newtonian liquids. The model is based on calculation of energy loss on colloidal particle aggregate of fractal structure localized in the flow of liquid with shear rate. We have performed the viscosity measurement experiments which confirmed successfully the developed physical model. Also, we demonstrate experimentally that petroleum colloidal particles and magnetic iron oxide nanoparticles can form composite fractal-like aggregates in natural petroleum materials. Our model can explain both the non-Newtonian properties of petroleum and sensitivity of petroleum viscosity to external magnetic fields.     

XAFS and LIBD investigation of the formation and structure of colloidal Pu(IV) hydrolysis products

Pu(IV) oxyhydroxide colloid growth is investigated with XAFS and LIBD. From combined results a model of colloid formation is proposed, which leads to a face-centered cubic Pu sublattice having cation defects, as observed with EXAFS, and a linear dependency of log [Pu(IV)] on -log [H+] with slope -2, in accord with LIBD. The solubility for Pu(IV) measured with LIBD is close to the lower limit of the solubility curve from previously reported data.     

Features of the structure formation of polymer composites modified by a liquid lubricant

Structure formation processes in polytetrafluoroethylene under the action of liquid lubricant components and zeolite particles are considered. Based on the results of single crystal X-ray diffraction, electron and atomic force microscopic, chromato mass spectroscopic studies, the formation mechanisms of polymer composites, which were obtained by liquid phase filling with motor oils, are proposed.     

Copolymerization of styrene with vinyl acetate in a construction petroleum bitumen medium and properties of obtained composite materials

The regularities of the copolymerization of styrene (Sr) with vinyl acetate (VA) in a construction petroleum bitumen (CPB) medium are studied. It is established that, in the bitumen medium, the superiority of styrene in terms of reactivity when compared to vinyl acetate is not expressed as critically as in the case of in-bulk copolymerization. Polymer-bitumen composite materials with improved operating performance as compared to bitumen were obtained by copolymerization.     

Rheological aspects of colloidal gels in thermoresponsive microgel suspensions: formation,structure, and linear and nonlinear viscoelasticity

This review focuses on the rheological aspects of colloidal gels that are a three-dimensional sparse network made of aggregated attractive particles formed in the aqueous suspensions of microgels composed of thermoresponsive polymers. Heating changes the dominant interparticle interactions from repulsive to attractive because of the hydrophilic-to-hydrophobic transition. Under appropriate conditions, the hydrophobic microgel suspensions form colloidal gels behave as a yield fluid. The elastic and yielding features of the colloidal gels are considerably different from those of the repulsive glass which is formed by the dense packing of the hydrophilic microgels at low temperatures. The thermoresponsive microgel suspensions undergoing colloidal gelation have attracted much attention from not only the academic interests but also the potentials as a functional suspension because they show interesting and marked changes in viscoelasticity when subjected to temperature variation. We discuss the criteria and dynamics of colloidal gelation, the structure, and linear and nonlinear viscoelasticity of the colloid gels with an emphasis on the results of the experimental studies.     

String formation and demixing in monolayers of dipolar colloidal mixtures

Employing hypernetted chain (HNC) integral equations and a stability analysis we investigate the structure and phase behavior of bidisperse mixtures of dipolar hard spheres with different size ratios s=σ(S)/σ(L) confined to a plane. The dipole moments of the particles are perfectly ordered along an in-plane direction, yielding anisotropic interactions favoring chain formation. Exploring a range of size ratios and compositions, our study predicts a complex interplay between aggregation phenomena, on the one hand, and volume phase transitions, on the other hand. In dilute, strongly asymmetric systems (s = 0.5), our HNC analysis indicates chain formation of the large particles, while the small particles act as a weakly correlated background. According to our fluctuation analysis, this aggregation behavior results in combined condensation-demixing transitions, with a trend towards pure demixing when the concentration of the large particles, c(L), becomes small. In dense systems, the most interesting results are found for intermediate size ratios, s ~ 0.7-0.8. Here we find signatures of a concentration-driven transition from pure chains of large particles (large c(L)) to mixed chains with alternating order of large and small particles (small c(L)). The two regimes are separated by a characteristic "jump" in the HNC non-solution line.     

Assessing the structure of recycled polyethylene-modified bitumen using the calorimetry method

Journal of Thermal Analysis and Calorimetry - The thermo-physical properties enhancement of nanolubricants can improve the heat transfer performance in refrigeration system. In this study,...