RESUMO
New crosslinked (polydimethylsiloxane-ethylene-propylene oxide)-polyisocyanurate multiblock copolymers (MBCs) were synthesized, and their supramolecular structure and sorption characteristics were studied. It was found that the interaction of PPEG and D4 leads to polyaddition of D4 initiated by potassium-alcoholate groups. The use of the amphiphilic silica derivatives associated in an oligomeric medium (ASiPs) leads to structuring of the MBC due to the transetherification reaction of the terminal silanol groups of the MBC with ASiPs. It was established that the supramolecular structure of an MBC is built according to the "core-shell" structure. The obtained polymers were tested as sorbents for the development of new methods for the concentration and determination of inorganic compounds. The efficiency of sorption of reagents increased with an increase in the "thickness" of the polydimethylsiloxane component of the "shell" and with a decrease in the size of the polyisocyanurate "core". The use of the obtained polymers as adsorbents of organic reagents is promising for increasing the efficiency of field methods of chemical testing and inorganic analysis, including the determination of the elemental composition and the detection of traces of contamination.
RESUMO
Amphiphilic poly(dimethylsiloxane-ethylene-propylene oxide)-polyisocyanurate cross-linked block copolymers based on triblock copolymers of propylene and ethylene oxides with terminal potassium-alcoholate groups (PPEG), octamethylcyclotetrasiloxane (D4) and 2,4-toluene diisocyanate (TDI) were synthesized and investigated. In the first stage of the polymerization process, a multiblock copolymer (MBC) was previously synthesized by polyaddition of D4 to PPEG. The usage of the amphiphilic branched silica derivatives associated with oligomeric medium (ASiP) leads to the structuring of block copolymers via the transetherification reaction of the terminal silanol groups of MBC with ASiP. The molar ratio of PPEG, D4, and TDI, where the polymer chains are packed in the "core-shell" supramolecular structure with microphase separation of the polyoxyethylene, polyoxypropylene and polydimethylsiloxane segments as the shell, was established. Polyisocyanurates build the "core" of the described macromolecular structure. The obtained polymers were studied as membrane materials for the separation of gas mixtures CO2/CH4 and CO2/N2. It was found that obtained polymers are promising as highly selective and productive membrane materials for the separation of gas mixtures containing CO2, CH4 and N2.