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Сhemical interaction of cellulose with reactive groups of four-coordinate boron-nitrogen compounds is an intercrystalline process proceeding without destruction of cellulose crystalline structure; probably, the modifier molecules react with easier accessible hydroxyl groups of the amorphous cellulose regions. The formation of B-O-C ether bonds between OH groups of modifiers and more reactive hydroxyl groups of amorphous parts of cellulose results in redistribution of hydrogen bonds and, as a consequence, to rectification of cellulose macromolecules. Thus, when cellulose is treated with compositions based on four-coordinate boron-nitrogen compounds, crystalline structure of cellulose is not disrupted, hence this process can be called a "mild" modification. Such modification does not lead to accelerated aging of cellulose materials, rapid loss of strength and increases durability of wooden structures.

Abstract.Comparative thermal analysis in the presence of oxygen was carried out for samples of native pine wood and wood samples modified with aminophenylborates. Significant decrease in the amount of heat released during thermal decomposition of the modified samples was established, which is due to the increase of carbonaceous residues on the surface. Reduction of heat release during decomposition of the modified samples may be explained by the lower yield of combustible volatile products as well as by thin film of boron oxide, formed on the surface of the modified wood, that partially reflects heat flow. Produced upon the modifier decomposition water vapor and inert nitrogen oxides dilute gaseous mixture near the wood surface and isolate it from oxygen. This enhances fire-resistance of wood modified with mono-and diethanolamine(N→B)phenylborates. Hydroxyl group at the sixth carbon atom of the glucopyranose ring of cellulose participates in reactions of cellulose modification, which prevents formation of flammable levoglucosan and, consequently, improves the fire-resistance of the modified wood.