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V Chornaya

Publications and source records attributed to V Chornaya.

5 recordsLinked to original sources

Temperature Dependence of Adsorption of Polymer Mixtures from Solutions.

Adsorption from binary (poly(butyl methacrylate)-CCl(4), poly-styrene-CCl(4)) and ternary (poly(butyl methacrylate)-polystyrene-CCl(4)) solutions has been studied at 10, 25, and 60 degrees C. It was found that with increasing temperature the values of adsorption grew due to worsening of the thermodynamic quality of the common solvent. Worsening of the quality of the solvent leads to a decrease in size of the macromolecular coils and to an increase in the critical concentrations of overlapping macromolecules in solution. As a result, the state of macromolecules in solution depends on temperature and determines adsorption values. From the temperature dependence of adsorption using the Clapeyron-Clausius equation, the differential enthalpy of adsorbate (polymer) DeltaH was calculated for each polymer, by adsorption both from binary solution and from the mixture. Determining DeltaH values from the temperature dependence of adsorption allows us to find this value simultaneously for each polymer in the polymer mixture. It was established that transition of a polymer from solution onto the surface leads to an increase in its enthalpy in the case of adsorption from both binary and ternary solutions. DeltaH increases with increasing coverage of the surface. By transition from solution onto the surface, the enthalpy of the adsorbed polymer increases; i.e., the polymer transits in an energetically less favorable state. This effect is more pronounced for adsorption from the mixture, which may be connected with the presence of the second polymer in the adsorption layer. Copyright 2000 Academic Press.

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Polydispersity Effect on the Adsorption of Polymer Mixtures.

The changes in molecular mass distribution (MMD) after adsorption from solution in concentration regions below and above the critical concentration of overlapping have been studied for various polymers and their mixtures. It was found that the formation of entanglements in both binary and ternary solutions affects the changes in MMD. For binary and ternary solutions above the critical concentration of overlapping, C*, the entanglements lead to diminishing selectivity of adsorption of high-molecular-weight fractions. Simultaneously, transition through C* diminishes adsorption of the fractions of higher surface activity. It may be assumed that the entanglements play the role of an additional energetic barrier which macromolecules must overcome to be adsorbed. The transition through the critical concentration of overlapping for the case of binary solutions diminishes the selectivity of adsorption of high molecular fractions. Adsorption of polar polymers from the ternary solutions both below and above C* leads to the appearance of the bimodality of MMD due to adsorption of surface-active fractions. Copyright 2000 Academic Press.

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Influence of Component Ratio on Adsorption of Polymer Mixtures under Phase Separation of Solutions.

The influence of the component ratio on polymer mixture adsorption in the two-phase condition is estimated. Transition toward the two-phase condition was attained by increasing the solution concentration up to phase separation. For solutions that have separated into two phases with increasing component concentration, the adsorption from each phase has been studied separately and the total adsorption from two phases has been calculated. The polystyrene-poly(butyl methacrylate)-CCl(4) system was investigated using fumed silica as adsorbent. Simultaneously, the fraction of segments of each type that were immobilized by the surface was determined from NMR spectra. In all cases, poly(butyl methacrylate) is characterized by preferential adsorption. The main features of adsorption are similar in both one-phase and two-phase states; however, the values for adsorption and fraction of immobilized segments are different in the case of adsorption from two separated phases because of the difference between the phases in the ratio of components and their concentration in each phase. The distinctions between adsorption from one-phase solutions before phase separation and from solutions modeling separated phases are connected with the redistribution of components between upper and lower phases. As a result, their ratio does not correspond to the initial ratio, and therefore the thermodynamic conditions of solutions, responsible for adsorption, are changed. Because of this, the shape of isotherms of adsorption and the adsorption values are determined by the different levels of aggregation in solutions with various ratios of components. Copyright 1999 Academic Press.

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Experimental Simulation of Polymer Mixture Adsorption from Two-Phase Solutions

The simulation of segregation of two polymers near an interface has been realized by studying adsorption from concentrated solutions of incompatible polymers at concentrations above that for coil overlapping and corresponding to one-phase and two-phase states. For solutions that have separated into two phases with increasing component concentration, the adsorption from each phase has been studied separately and the total adsorption from two phases has been calculated. The polystyrene-poly(butyl methacrylate)-CCl4 system was investigated using fumed silica as adsorbent. Simultaneously the fraction of segments of each type immobilized by the surface was determined from NMR spectra. In all cases, poly(butyl methacrylate) is characterized by preferential adsorption. The main features of adsorption are similar in both one-phase and two-phase states; however, the values of adsorption and fraction of immobilized segments are different for adsorption from two separated phases because of the difference in the ratio of components and their concentration in each phase. The total adsorption of poly(butyl methacrylate) from the two-phase state is higher than from the one-phase state. It is concluded that in two-phase systems adsorption proceeds simultaneously from both phases, leading to higher segregation of one of the components.

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Adsorption of Poly(butyl methacrylate) and Its Mixtures with Polystyrene from Solutions: Adsorption Kinetics and Structure of Adsorption Layers

Using IR spectroscopy of attenuated total inner reflectance (ATIR) the adsorption kinetics and structure of the adsorption layer of poly(butyl methacrylate) on the Ge surface from solutions in CCl4 of pure polymer and its mixtures with polystyrene have been investigated. It was shown that at the first stage of adsorption of poly(butyl methacrylate) from diluted solution, a layer of high connectivity of macromolecules with Ge surface is formed. The diffusion coefficient of macromolecules on this part of the kinetic curve corresponds to that for the glassy state. With increasing adsorption, the fraction of bonded segments diminishes and macromolecules in the adsorption layer become more mobile. On this part of the kinetic curve there is observed a sharp increase in both the diffusion coefficient of macromolecules and the adsorption rate. On transition from diluted to semidiluted solutions the mechanism of adsorption changes. The coefficient of diffusion of macromolecules coincides with that for reptation movement of macromolecules in the entanglement network. It was shown that introduction of polystyrene into solutions affects the adsorption value and structure of the adsorption layer. This effect is supposed to be connected to possible changes in combinatorial entropy of the system.

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