Publications by authors named "Vladimir Yu Rudyak"

Emulsions have become a crucial product form in various industries in modern times. Expanding the class of substances used to stabilize emulsions can improve their stability or introduce new properties. Particularly, the use of stimuli-responsive microgels makes it possible to create "smart" emulsions whose stability can be controlled by changing any of the specified stimuli.

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In this work, we study the effect of covalent bonding on the behavior of non-equilibrium systems with the active force acting on particles along their velocity. Self-ordering of single particles does not occur in this model. However, starting from some critical polymerization degree, the ordered state is observed.

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Polymer microgel particles decorated with redox-active functional groups are a new and promising object for electrochemical applications. However, the process of charge exchange between an electrode and a microgel particle carrying numerous redox-active centers differs fundamentally from charge exchange involving only molecular species. A single act of contact between the microgel and the electrode surface may not be enough to fully discharge the microgel, and partial charge states are to be expected.

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Correction for 'Effect of network topology and crosslinker reactivity on microgel structure and ordering at liquid-liquid interface' by Rustam A. Gumerov , , 2022, , 3738-3747, https://doi.org/10.

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In this work, we investigated the behavior of cholesteric droplets with homeotropic boundary conditions experimentally and by computer simulations. Small droplets forming twisted radial structures were studied. We obtained two different paths of structural transformations under electric field in such droplets.

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Polymer microgels synthesized were studied at a liquid-liquid interface mesoscopic computer simulations and compared to microgels with ideal (diamond-like) structure. The effect of crosslinkers reactivity ratio on the single particle morphology at the interface and monolayer behavior was examined. It was demonstrated that single particles deform into an explicit core-corona morphology when adsorbed at the interface.

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Orientational structures of polymer-dispersed cholesteric liquid crystal under homeotropic anchoring and their transformations under the action of an electric field are studied. The switching of cholesteric droplets between different topological states are experimentally and theoretically demonstrated. Structures with λ+1/2-disclination are found and considered.

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Polymer stimuli-responsive microgels find their use in various applications. The knowledge of its internal structure is of importance for further improvement and expanding the scope. Interpenetrating network (IPN) microgels may possess a remarkable feature of strongly non-uniform inner architecture, even microphase separation, in conditions of a selective solvent.

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The electro-optical properties of polymer dispersed liquid crystal (PDLC) films are highly dependent on the features of the contained liquid crystal (LC) droplets. Cholesteric LC droplets with homeotropic boundaries can form several topologically different orientational structures, including ones with single and more point defects, layer-like, and axisymmetric twisted toroidal structures. These structures are very sensitive to an applied electric field.

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We report the results of an experimental and theoretical study of structure formation in mixtures of phenyl-C-butyric acid methyl ester (PCBM) with high boiling octane based solvent additives 1,8-octanedithiol (ODT), 1,8-dibromooctane, and 1,8-diiodooctane obtained by evaporation of a host-solvent (chlorobenzene). Experimental studies by DSC, SAXS and WAXS methods found evidence of crystallization of fullerenes in the presence of the high boiling additives in the mixtures. A molecular dynamics simulation of a PCBM/ODT mixture revealed the self-assembly of fullerenes into sponge-like network structures.

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In this paper, we have implemented the sequential template synthesis of interpenetrating network (IPN) microgels in computer simulations and studied the behavior of such particles. We explored the influence of the interaction between the components of primary and secondary networks on the polymerization process and determined the necessary conditions for IPN particle formation. The interconnection between the parameters of synthesis and topological properties of the resulting microgels was investigated.

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In this work we presented a novel computational model of precipitation polymerization allowing one to obtain core-shell microgels via a realistic cross-linking process based on the experimental procedure. We showed that the cross-linker-monomer reactivity ratios r are responsible for the microgel internal structure. Values of r lower than 1 correspond to the case when alternating sequences occur at the early reaction stages; this leads to the formation of microgels with pronounced core-shell structure.

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In this paper we propose a new method of coarse-grained computer simulations of the microgel formation in course of free radical precipitation polymerization. For the first time, we simulate the precipitation polymerization process from a dilute solution of initial components to a final microgel particle with coarse grained molecular dynamics, and compare it to the experimental data. We expect that our simulation studies of PNIPA-like microgels will be able to elucidate the subject of nucleation and growth kinetics and to describe in detail the network topology and structure.

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The dependency of orientational structures in cholesteric droplets with homeotropic surface anchoring on the helicity parameter has been studied by experiment and simulations. We have observed a sequence of structures, in which the director configurations and topological defects were identified by comparison of polarized microscopy pictures with simulated textures. A toron-like and low-symmetry intermediate layer-like structures have been revealed and studied in detail.

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We studied the static and dynamic mechanical properties of crosslinked polymer matrices using multiscale simulations and experiments. We continued to develop the multiscale methodology for generating atomistic polymer networks, and applied it to the case of phthalonitrile resin. The mechanical properties of the resulting networks were analyzed using atomistic molecular dynamics (MD) and dissipative particle dynamics (DPD).

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The formation of a thermoset polymer network is a complex process with great variability. In this study, we used dissipative particle dynamics and graph theory tools to investigate the curing process and network topology of a phthalonitrile thermoset to reveal the influence of initiator and plasticizer concentration on its properties. We also propose a novel way to characterize the network topology on the basis of two independent characteristics: simple cycle length (which is mainly affected by the initiator amount) and the number of simple cycles passing through a single covalent bond (which is determined primarily by plasticizer concentration).

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Polymer microgels with a dense outer shell offer outstanding features as universal carriers for different guest molecules. In this paper, microgels formed by an interpenetrating network comprised of collapsed and swollen subnetworks are investigated using dissipative particle dynamics (DPD) computer simulations, and it is found that such systems can form classical core-corona structures, shell-corona structures, and core-shell-corona structures, depending on the subchain length and molecular mass of the system. The core-corona structures consisting of a dense core and soft corona are formed at small microgel sizes when the subnetworks are able to effectively separate in space.

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Optical textures and appropriate orientational structures have been studied within droplets of chiral nematic dispersed in polymer assigning the homeotropic anchoring. The helix axis of the chiral structure inside droplets forms the bipolar configuration. The optical droplet textures were analysed in the unpolarised light, analyser switching-off scheme and in crossed polarisers.

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In this paper we show that Janus colloids, which are spherical particles with hybrid anchoring conditions, have preferable orientations in cholesteric media depending on the cholesteric wave vector. Simulations reveal that the tilt angle of a particle varies greatly with variation of the particle diameter to the cholesteric pitch ratio, which makes it possible to stabilize the appropriate particle orientation and to control it by variation of the cholesteric pitch.

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