Gel-polymer electrolytes based on polyurethane ionomers for lithium power sources.

Polyurethanes based on the aminoethers of ortho-phosphoric acid and polyisocyanates of an aliphatic nature were studied as a substrate for the preparation of new polymer electrolyte. The conductivity of polyurethane ionomer samples obtained using the optimal amount of aliphatic polyisocyanates and after keeping them in a 1 M LiBF4 solution in γ-butyrolactone reaches 0.62 mS cm-1. It has been established that the transport of positively charged ions through the polymer matrix is due to the formation of clusters of phosphate ions and their association into the conducting channels. The introduction of carboxylate ions into the conducting channels by modifying the aminoethers of ortho-phosphoric acid with phthalic anhydride leads to an increase in their size and rise in the mobility of cations. As a result, the conductivity of polyurethane gel electrolytes increased to 2.1 mS cm-1.

Polyurethane ionomers based on amino ethers of ortho-phosphoric acid.

The etherification of ortho-phosphoric acid with triethanolamine and polyoxypropylene glycol is studied. The reaction process is accompanied by the formation of hyperbranched amino ethers of ortho-phosphoric acid terminated by hydroxyl groups. A specific feature of the chemical structure of the compounds obtained is the existence of ion pairs in their structure separated in space. The reaction of the etherification of ortho-phosphoric acid with glycols becomes possible through the use of tertiary amines. The amino ethers of ortho-phosphoric acid are investigated as a polyol component for the synthesis of polyurethanes with high adhesion characteristics and strength properties. The experimental results presented allow us to relate polyurethanes obtained on the basis of ortho-phosphoric acid amino ethers to polymers of ionomeric nature.

Synthesis and characterization of amphiphilic branched silica derivatives associated with oligomeric medium.

Amphiphilic branched silica derivatives associated with oligomeric medium (ASiP) were obtained using tetraethoxysilane, polyoxyethylene glycol and low molecular weight polydimethylsiloxane. The creation of a silica core was based on tetraethoxysilane hydrolysis and condensation reactions by using water and a potassium diethylene glycolate as the catalyst. These reactions proceeded with the sequential participation of polyoxyethylene glycol and polydimethylsiloxane in parallel transetherification reactions. Microporous polymer film based on 2,4-toluene diisocyanate and block copolymers of propylene and ethylene oxides with terminal potassium-alcoholate groups were modified by ASiP. It has been shown that ASiP at the phase interface between thermodynamically incompatible macrochains performs the function of a link. It leads to a significant increase of intermolecular interactions and the supramolecular organization of the modified microporous polymers.

Water vapor permeable polyurethane films based on the hyperbranched aminoethers of boric acid.

The hyperbranched polymers have drawn intensive attention in the design of macromolecules and functional materials because of their unique physical and chemical properties resulting from the branched architecture and the high number of functional groups. In the present study, by means of light scattering, viscosimetry, thermomechanical analysis, tensile stress-strain, mechanical loss tangent and water vapor permeability measurements, we demonstrate the hierarchical macromolecular organization of organoboron polyurethanes synthesized using sterically hindered amino ethers (AEBA) of boric acid. It is shown that the water vapor permeability of polyurethanes obtained on the basis of sterically hindered aminoethers of boric acid is due to the peculiarities of the chemical structure of AEBA, which can exhibit an ionomeric nature and the presence of steric hindrances created in the hyperbranched structure of AEBA, which can lead to an increase in free volume in such polyurethanes.