Radiation-chemical synthesis and properties of tetrafluoroethylene telomeres in fluorine-containing solvents

The kinetics of radiation telomerization of tetrafluoroethylene in a series of fluorine-containing solvents was studied. A comparative analysis of their reactivity was carried out. The structure and some properties of the telomeres were studied by IR spectroscopy, thermogravimetric and elemental analysis, and electron microscopy.     

An NMR, DSC, and IR spectroscopy study of the composite formed during low-temperature postradiation polymerization of C2F4 in the presence of a 3D graphene material

By solid-state magic angle-spinning nuclear magnetic resonance spectroscopy (NMR), differential scanning calorimetry (DSC), and IR spectroscopy, polytetrafluoroethylene (PTFE) samples obtained by low-temperature (T = ?196°C) postradiation polymerization of tetrafluoroethylene (C₂F₄) and C₂F₄ mixtures with a 3D graphene material formed by the microwave exfoliation of graphite oxide films (MEGO) have been investigated. It has been shown that the melting point of PTFE in the PTFE-MEGO composite is 332.5°C, which is 8.8°C above the melting point of pure PTFE obtained under the same conditions. According to the measured values of specific enthalpy of melting ΔH _m (51.5 and 45.4 J/g), the degrees crystallinity (x _c) of 0.63 and 0.55 have been calculated for the pure polymer and the composite, respectively. It has been also found that none of the PTFE-containing samples examined has terminal CF₃ groups typical of PTFE prepared by conventional suspension polymerization.     

Effect of Tetrafluoroethylene Concentration on Thermophysical Characteristics and Structure of Products of Its Radiation Telomerization in Flutec PP3

High Energy Chemistry - The influence of monomer concentration on the properties of radiation-synthesized tetrafluoroethylene telomers in perfluoro-1,3-dimethylcyclohexane has been studied by...     

Radiation-initiated synthesis of tetrafluoroethylene telomers in 1,2-dibromotetrafluoroethane at a constant pressure of the monomer in the reactor

The kinetics of radiation-initiated telomerization of tetrafluoroethylene in a 1,2-dibromotetrafluoroethane solution at a constant concentration (pressure) of the monomer in the reactor was studied. The properties, molecular structure, and morphology of the telomers were studied by IR spectroscopy, scanning electron microscopy, and elemental and thermal gravimetric analyses. The synthesized telomers show promise for the development of fluoropolymeric nanocomposites and protective hydrophobic and antifriction coatings.     

Hydrophobization of Porous Ceramic Materials Based on Quartz Fibers with Solutions of Tetrafluoroethylene Telomers

Russian Journal of Applied Chemistry - Hydrophobization of highly porous heat-shielding ceramic materials based on quartz fibers was studied. Radiation-synthesized tetrafluoroethylene telomers...     

Radiation synthesis of tetrafluoroethylene telomers in chlorosilanes and their use for modification of aluminoborosilicate glass fabric

The kinetics of radiation-initiated telomerization of tetrafluoroethylene in dichlorodimethylsilane and chlorotrimethylsilane have been studied, and the molecular structure and properties of the telomers have been revealed. It has been shown that the introduction of ~3.5 wt % product telomer into aluminoborosilicate glass fabric gives a fluorinated glass-reinforced polymer material with good hydrophobicity.     

Kinetics and mechanism of radiation telomerization of tetrafluoroethylene in hexafluoropropan-2-ol and trifluoroethanol

The kinetics of radiation telomerization of tetrafluoroethylene (TFE) in trifluoroethanol and hexafluoropropan-2-ol (HFIP) has been investigated by method of kinetic calorimetry. The nature of active centers initiating the process of telomerization of tetrafluoroethylene in hexafluoroisopropanol in the temperature range of 77—300 K was investigated by ESR spectroscopy. The molecular structure and properties of the obtained telomeres were studied by IR spectroscopy and TGA.     

Antioxidant Activity of Deferasirox and Its Metal Complexes in Model Systems of Oxidative Damage: Comparison with Deferiprone

Deferasirox is an orally active, lipophilic iron chelating drug used on thousands of patients worldwide for the treatment of transfusional iron overload. The essential transition metals iron and copper are the primary catalysts of reactive oxygen species and oxidative damage in biological systems. The redox effects of deferasirox and its metal complexes with iron, copper and other metals are of pharmacological, toxicological, biological and physiological importance. Several molecular model systems of oxidative damage caused by iron and copper catalysis including the oxidation of ascorbic acid, the peroxidation of linoleic acid micelles and the oxidation of dihydropyridine have been investigated in the presence of deferasirox using UV-visible and NMR spectroscopy. Deferasirox has shown antioxidant activity in all three model systems, causing substantial reduction in the rate of oxidation and oxidative damage. Deferasirox showed the greatest antioxidant activity in the oxidation of ascorbic acid with the participation of iron ions and reduced the reaction rate by about a 100 times. Overall, deferasirox appears to have lower affinity for copper in comparison to iron. Comparative studies of the antioxidant activity of deferasirox and the hydrophilic oral iron chelating drug deferiprone in the peroxidation of linoleic acid micelles showed lower efficiency of deferasirox in comparison to deferiprone.