Publications by authors named "Galina Bondarenko"

Hybrid nanocomposites based on poly(3,6-dianiline-2,5-dichloro-1,4-benzoquinone) (PDACB) in salt form and graphene oxide (GO) have been obtained for the first time, and the significant influence of the preparation method on the composition and structure of nanocomposites and their functional properties has been demonstrated. Nanocomposites were prepared in three ways: via ultrasonic mixing of PDACB and GO; via in situ oxidative polymerization of 3,6-dianiline-2,5-dichloro-1,4-benzoquinone (DACB) in the presence of GO; and by heating a suspension of previously prepared PDACB and GO in DMF with the removal of the solvent. The results of the study of the composition, chemical structure, morphology, thermal stability and electrical properties of nanocomposites obtained via various methods are presented.

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Morphological transformations in emulsions of cellulose and polyacrylonitrile (PAN) ternary copolymers containing acrylonitrile, methyl acrylate, and methylsulfonate comonomers in -methylmorpholine--oxide were studied over the entire range of concentrations depending on temperature and intensity of the deformation action. Based on the morphological and rheological features of the system, the temperature-concentration range of spinnability of mixed solutions was determined, and composite fibers were spun. The fibers are characterized by a heterogeneous fibrillar texture.

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Membrane gas-liquid contactors have great potential to meet the challenges of amine CO capture. In this case, the most effective approach is the use of composite membranes. However, to obtain these, it is necessary to take into account the chemical and morphological resistance of membrane supports to long-term exposure to amine absorbents and their oxidative degradation products.

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Hybrid composites based on electroactive polymers of diphenylamine-2-carboxylic acid (PDPAC) and highly porous carbon with a hierarchical pore structure were prepared for the first time. Activated IR-pyrolyzed polyacrylonitrile (IR-PAN-a), characterized by a highly developed surface, was chosen as a highly porous N-doped carbon component of the hybrid materials. IR-PAN-a was prepared using pyrolysis of polyacrylonitrile (PAN) in the presence of potassium hydroxide under IR radiation.

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Article Synopsis
  • The study focuses on aqueous solutions of monoethanolamine (MEA), a chemical used to capture CO2 from gases, using both experimental and theoretical vibrational spectroscopy methods.
  • It investigates how MEA interacts with water to form various molecular associations that influence CO2 retention, examining both the structural and energy characteristics of these interactions.
  • The research also looks into how high temperatures and different concentrations of MEA affect these associations, identifying specific infrared spectral bands linked to effective CO2 adsorption and delayed desorption.
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The application of gas-liquid membrane contactors for ethane-ethylene separation seems to offer a good alternative to conventional energy-intensive processes. This work aims to develop new hydrophobic composite membranes with active ethylene carriers and to demonstrate their potential for ethylene/ethane separation in gas-liquid membrane contactors. For the first time, hybrid membrane materials based on polyoctylmethylsiloxane (POMS) and silver tetrafluoroborate, with a Si:Ag ratio of 10:0.

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The work is focused on the study of the influence of the cellulose type and processing parameters on the structure, morphology, and permeability of cellulose films. The free volume of the cellulose films was evaluated by the sorption of n-decane, which is a non-solvent for cellulose. The structural features of the membranes and their morphology were studied using X-ray diffraction, IR spectroscopy, SEM, and AFM methods.

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Commercial metathesis polynorbornene is used for the fabrication of high-damping coatings and bulk materials that dissipate vibration and impact energies. Functionalization of this non-polar polymer can improve its adhesive, gas barrier, and other properties, thereby potentially expanding its application area. With this aim, the post-modification of polynorbornene was carried out by inserting ethylene-vinyl acetate-vinyl alcohol blocks into its backbone via the cross-metathesis of polynorbornene with poly(5-acetoxy-1-octenylene) and subsequent deacetylation and hydrogenation of the obtained multiblock copolymers.

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Embedding quantum dots (QDs) into an organic matrix of controllable order requires the identification of their structural characteristics. This analysis is necessary for the creation of anisotropic composites that are sensitive to external stimuli. We have studied the QD structures formed during the single-step synthesis of CdSe/ZnS QDs and their transformations after the initial ligand's substitution for another ligand.

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The work is devoted to the chemical modification of a polymer that is promising for the creation of gas separation membranes, aimed at increasing the selectivity with respect to CO. The introduction of ionic liquids into the structure of poly(1-trimethylsilyl-1-propyne) is realized by a two-step process: bromination of the initial polymer with -bromosuccinimide and subsequent addition of tertiary amine (-butylimidazole) to it. Depending on the process conditions, the method allows polymers with different contents of the ionic liquid to be obtained.

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Hybrid nanocomposites based on electroactive polydiphenylamine-2-carboxylic acid (PDPAC) and single-walled carbon nanotubes (SWCNTs) were obtained for the first time. Polymer-carbon nanomaterials were synthesized via in situ oxidative polymerization of diphenylamine-2-carboxylic acid (DPAC) in the presence of SWCNTs by two different ways. Hybrid SWCNT/PDPAC nanocomposites were prepared both in an acidic medium and in the heterophase system in an alkaline medium.

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New microporous homopolymers were readily prepared from norbornadiene-2,5, its dimer and trimer by addition (vinyl) polymerization of the corresponding monomers with 60⁻98% yields. As a catalyst Pd--heterocyclic carbene complex or Ni(II) 2-ethylhexanoate activated with Na⁺[B(3,5-(CF₃)₂C₆H₃)₄] or methylaluminoxane was used. The synthesized polynorbornenes are cross-linked and insoluble.

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Crystals of mononuclear tris[bis(2,6-diisopropylphenyl) phosphato-κO]pentakis(methanol-κO)lanthanide methanol monosolvates of lanthanum, [La(CHOP)(CHOH)]·CHOH, (1), cerium, [Ce(CHOP)(CHOH)]·CHOH, (2), and neodymium, [Nd(CHOP)(CHOH)]·CHOH, (3), have been obtained by reactions between LnCl(HO) (n = 6 or 7) and lithium bis(2,6-diisopropylphenyl) phosphate in a 1:3 molar ratio in methanol media. Compounds (1)-(3) crystallize in the monoclinic P2/c space group and have isomorphous crystal structures. All three bis(2,6-diisopropylphenyl) phosphate ligands display a κO-monodentate coordination mode.

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We report on the structure, uniaxial orientation, and photoluminescent properties of CdS nanorods that form stable nanocomposites with smectic C hydrogen-bonded polymers from the family of poly(4-(n-acryloyloxyalkoxy)benzoic acids. TEM analysis of microtomed films of nanocomposites reveals that CdS nanorods form small domains that are homogeneously distributed in the LC polymer matrix. They undergo long-range orientation with the formation of one-dimensional aggregates of rods when the composite films are uniaxially deformed.

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Raman spectra of 1-butanol have been obtained at a constant pressure of 500 bar up to 350 degrees C and along isotherms 250, 300, and 350 degrees C up to 600 bar. The purpose of the experiment was to compare responses of Raman and IR absorption spectroscopy to the forming of O-H..

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