TY - JOUR
T1 - Partially fluorinated arylene polyethers and their ternary blend membranes with PBI and H3PO4.
T2 - Part I. Synthesis and characterisation of polymers and binary blend membranes
AU - Kerres, J.
AU - Schonberger, F.
AU - Chromik, A
AU - Haering, T
AU - Li, Qingfeng
AU - Jensen, Jens Oluf
AU - Pan, Chao
AU - Noye, P
AU - Bjerrum, Niels
PY - 2008
Y1 - 2008
N2 - A partially fluorinated polyether ionomer from polycondensation of decafluorobiphenyl with 2,2-bis(4-hydroxyphenyl)-hexafluoropropane, followed by sulphonation with H2SO4 (60% SO3), has been prepared and optimised in terms of molecular weight and sulphonation degree. The partially fluorinated ionomer has been blended with poly(2,2'-mphenylene-5,5'-bibenzimidazole) (PBI), yielding base-acid blends with PBI in excess. The base-acid blend membranes have been characterised in terms of solubility in DMAc, water uptake and oxidative stability by immersion in aqueous 5 wt.-% H2O2 solutions and Fenton's Reagent, respectively. Ionomers with molecular masses of up to 140,000 Da (non-sulphonated) and 178,000 Da (sulphonated) with excellent thermal stabilities and high sulphonation degrees of up to 2.06 SO3H groups per repeat unit have been produced. Their base-excess blend membranes, where the ionomer blend component served as acidic ionomeric cross-linker, showed excellent oxidative stabilities which were better than that of pure PBI and comparable to the oxidative stability of Nafion (R) in Fenton's Reagent.
AB - A partially fluorinated polyether ionomer from polycondensation of decafluorobiphenyl with 2,2-bis(4-hydroxyphenyl)-hexafluoropropane, followed by sulphonation with H2SO4 (60% SO3), has been prepared and optimised in terms of molecular weight and sulphonation degree. The partially fluorinated ionomer has been blended with poly(2,2'-mphenylene-5,5'-bibenzimidazole) (PBI), yielding base-acid blends with PBI in excess. The base-acid blend membranes have been characterised in terms of solubility in DMAc, water uptake and oxidative stability by immersion in aqueous 5 wt.-% H2O2 solutions and Fenton's Reagent, respectively. Ionomers with molecular masses of up to 140,000 Da (non-sulphonated) and 178,000 Da (sulphonated) with excellent thermal stabilities and high sulphonation degrees of up to 2.06 SO3H groups per repeat unit have been produced. Their base-excess blend membranes, where the ionomer blend component served as acidic ionomeric cross-linker, showed excellent oxidative stabilities which were better than that of pure PBI and comparable to the oxidative stability of Nafion (R) in Fenton's Reagent.
KW - partially fluorinated polyether
KW - GPC
KW - PBI
KW - Fentons test
KW - oxidative stability
KW - sulfination
KW - base-acid blend membrane
U2 - 10.1002/fuce.200800011
DO - 10.1002/fuce.200800011
M3 - Journal article
SN - 1615-6846
VL - 8
SP - 175
EP - 187
JO - Fuel Cells
JF - Fuel Cells
IS - 3-4
ER -