TY - JOUR
T1 - Synthesis and properties of a polyimide containing pendant sulfophenoxypropoxy groups
AU - Miyatake, Kenji
AU - Yasuda, Tomohiro
AU - Hirai, Michiko
AU - Nanasawa, Masato
AU - Watanabe, Masahiro
PY - 2007/1/1
Y1 - 2007/1/1
N2 - The synthesis and properties of polyimide containing pendant sulfophenoxypropoxy groups was investigated. 3,3′- Dihydroxybenzidine (98%), Glacial acetic acid (99.7%), 1,3-dibromopropane (98.0%), potassium carbonate, (99.5%), anhydrous acetonitrile (99.5%), hydrochloric acid (35-37%)and benzoic acid (99.5%) was used. The proton conductivity and effect of aliphatic groups on hydraulic and oxidative stability, was analyzed. Diamine monomer containing pendant sulfophenoxypropoxy group was synthesized by reaction of 3,3′- dihydroxybenzidine with dibromopropane under basic conditions. Then, diamine monomer was polymerized with TCND in an m-cresol to obtain polyimide containing pendent acidic groups. It was observed that asymmetric stretching vibrations of the sulfonic acid group showed absorption for imide groups at 1349, 1674, and 1713 cm-1. Result shows that polymer was synthesized via acetylation, bromoalkoxylation, sulfophenoxylation, and acidification of diamine.
AB - The synthesis and properties of polyimide containing pendant sulfophenoxypropoxy groups was investigated. 3,3′- Dihydroxybenzidine (98%), Glacial acetic acid (99.7%), 1,3-dibromopropane (98.0%), potassium carbonate, (99.5%), anhydrous acetonitrile (99.5%), hydrochloric acid (35-37%)and benzoic acid (99.5%) was used. The proton conductivity and effect of aliphatic groups on hydraulic and oxidative stability, was analyzed. Diamine monomer containing pendant sulfophenoxypropoxy group was synthesized by reaction of 3,3′- dihydroxybenzidine with dibromopropane under basic conditions. Then, diamine monomer was polymerized with TCND in an m-cresol to obtain polyimide containing pendent acidic groups. It was observed that asymmetric stretching vibrations of the sulfonic acid group showed absorption for imide groups at 1349, 1674, and 1713 cm-1. Result shows that polymer was synthesized via acetylation, bromoalkoxylation, sulfophenoxylation, and acidification of diamine.
KW - Fuel cells
KW - Ionomers
KW - Membranes
KW - Polyimides
KW - Proton-conducting polymers
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U2 - 10.1002/pola.21816
DO - 10.1002/pola.21816
M3 - Article
AN - SCOPUS:33846523060
SN - 0887-624X
VL - 45
SP - 157
EP - 163
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 1
ER -