ABSTRACT The poly(aryl ether ketone) with spatial cardo structure is prepared from 4,4'-bis(phenoxy)benzophenone and 1-(4-bromobutyl)indoline-2,3-dione through a facile polyhydroxyalkylation reaction catalyzed by superacid. The number average molecular weight of the… Click to show full abstract
ABSTRACT The poly(aryl ether ketone) with spatial cardo structure is prepared from 4,4'-bis(phenoxy)benzophenone and 1-(4-bromobutyl)indoline-2,3-dione through a facile polyhydroxyalkylation reaction catalyzed by superacid. The number average molecular weight of the resultant polymer is achieved as high as 105.6 kg mmol−1. Three anion exchange membranes were prepared by reacting the polymer with trimethylamine, N-methyl-piperidine, and N,N,N',N',N''-pentaethylguanidine, respectively. Among the prepared membranes, N-methyl-piperidine based anion exchange membrane exhibited the highest OH− conductivity of 99.8 mS cm−1 at corresponding IEC of 1.54 meq g−1. In addition, the prepared membranes also exhibit excellent mechanical properties, in which the tensile strength and elongation at break can reach up to 50 MPa and 35%, respectively. Moreover, the anion exchange membranes exhibited good alkaline stability. When they were treated with 1 M KOH at 60°C for 600 h, their conductivity decreased by less than 5%.
               
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