The paper describes some properties of new quaternized polysulfones obtained by quaternization of chloromethylated polysulfone with different tertiary amines - N,N-dimethylethylamine and N,N-dimethyloctylamine. Hydrophilic/hydrophobic properties, morphological aspects and compatibility with red blood cells and platelets are affected by the alkyl radicals and by history of the formed films. The results obtained are useful in biomedical applications, including evaluation of bacterial adhesion to the surfaces, or utilization of modified polysulfones as semipermeable membranes
New polyimides have been synthesized by the reaction of 3,3 0 ,4,4 0 -benzophenone tetracarboxylic dianhydride (BTDA) or/ and 5-[2,5-(dioxotetrahydrofuryl)]-3-methyl-3-cyclohexene-1,2-dicarboxylic anhydride (DOCDA) with 4,4 0 -methylene dianiline (DDM). Polycondensation reactions were carried out in N, N-dimethylformamide solution and the resulting polyimides gave flexible free-standing films. The introduction of alicyclic moieties in the polyimide backbone improved the solubility of the resulting polymers and facilitated their processing while maintaining a high thermal stability. The dielectric constant values (measured at 10 6 Hz at room temperature), were found in the range of 3.14-2.83 and decreased with increasing of the alicyclic units content.
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