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The enthalpy of combustion of hexamethylenetetrammonium dodecahydro-closo-dodecaborate is determined via combustion in a KL-5 calorimeter and is found to be‒17660 kJ/mol. Its standard enthalpy of formation is calculated using the obtained experimental data (−538 kJ/mol).

The micromechanical properties (Young’s modulus, deformation, and adhesion) of the intercalated compound of graphite oxide with dodecahydro-closo-dodecaboric acid were studied by atomic force microscopy, transmission electron microscopy, and Raman spectroscopy and compared with the same characteristics of the starting graphite oxide. The significant difference in the micromechanical properties of the materials under study is dictated by differences in the topography and properties of their film surface, which, in turn, can be determined by their chemical composition. The introduction of dodecahydro-closo-dodecaboric acid in the interplanar space of graphite oxide affects the structuring of the latter. A considerable increase in the adhesion of the intercalated compound relative to that of oxide graphite is explained by high adhesive properties of the introduced acid, the Young’s modulus of graphite oxide being higher than that of the intercalated compound. This was attributed to the high hydrophilicity of dodecahydro-closo-dodecaboric acid and the difficulty of water removal from the interplanar space; water plasticizes the material, which becomes softer than graphite oxide. The difference in the structure of the coating of the intercalated compounds and the starting graphite oxide was found to be also reflected by their Raman spectra, namely, by the increased intensity of the D line with the preserved position of the G line, which points to the impurity nature of the intercalate and the unchanged hexagonal lattice of graphite.

It is shown that atomic force microscopy allows comparative estimates of the coefficient of thermal expansion of graphite oxide (GO). One possible explanation for its negative value is the formation of GO intercalated compounds, particularly with water.

The thermal behavior of chitosanium dodecahydro-closo-dodecaborate, (C6O4H9NH3)2B12H12, was studied by thermal analysis, X-ray diffraction, and IR and X-ray photoelectron spectroscopy. As this compound is heated at a rate above 10–20 K/min, it ignites at a temperature of about 300°C. As the compound is heated to 1000°C at a rate below 10 K/min in an inert atmosphere, it yields a mixture of carbon and amorphous boron and/or boron carbides. The presence of a small amount of boron oxide in the product is explained by the formation of a partially oxidized hydroborate anion at the early stages of (C6O4H9NH3)2B12H12 decomposition via the interaction between oxygen of the chitosanium cation and the B12H122− anion. Heating the initial compound in air at a rate below 10 K/min yields carbon and boron oxide as the main products. Molten boron oxide protects boron and/or boron carbides and boron nitride forming in small amounts in the particle bulk from oxidation.

The influence of light radiation with different wavelengths (546, 380, 365 nm) on the coatings of oxidized graphite and its intercalated compound with ammonium dodecahydro-(NH4)2B12H12 was studied. The transmission and absorption spectra of the coatings were measured before and after irradiation. It was shown that the optical density of the coatings increased because of carbon release (blackening), which was especially strong during UV irradiation. Under the same conditions (wavelength, power, time), the change in the optical density was much larger for the intercalated compound than for oxidized graphite. This can be explained by the presence of the B12H 12 2− anion in the former.

The effect of thermal gas dynamic destruction of polytetrafluoroethylene on its microscopic and supramolecular structure and dynamic properties is investigated by IR and 19F NMR spectroscopy. It is demonstrated that thermal gas dynamic dispersing changes the structure of polytetrafluoroethylene molecules. One of the possible mechanisms of PTFE depolymerization is the formation of oligomers with terminal –CF3 and –C=CF2 groups. This forms macromolecular packing with higher ordering and with dynamic characteristics other than those inherent in standard PTFE.