TY - JOUR
T1 - Meta-PBI/methylated PBI-OO blend membranes for acid doped HT PEMFC
AU - Cho, Hyeongrae
AU - Hur, Eun
AU - Henkensmeier, Dirk
AU - Jeong, Gisu
AU - Cho, Eunae
AU - Kim, Hyoung Juhn
AU - Jang, Jong Hyun
AU - Lee, Kwan Young
AU - Hjuler, Hans Aage
AU - Li, Qingfeng
AU - Jensen, Jens Oluf
AU - Cleemann, Lars Nielausen
N1 - Funding Information:
This work was supported by the KORANET Joint Call on Green Technologies, KIST K-GRL, and the Danish Agency for Science, Technology and Innovation in the frame of the 4M project.
PY - 2014/9
Y1 - 2014/9
N2 - Methylation of polybenzimidazole leads to positively charged polymer backbones, and moveable anions. Ion exchange of methylated PBI-OO in phosphoric acid (PA) shows that the resulting polymers dissolve. meta-PBI, however, absorbs about 400 wt% PA while remaining a self supported membrane. We investigate the properties of blend membranes, employing meta-PBI for mechanical integrity and methylated PBI-OO for high PA uptake and resulting proton conductivity. While small additions of PBI-OO decrease the tensile strength of blend membranes (58 MPa for 10% PBI-OO), further addition leads to an increase, and 50% blend membranes show again a tensile strength of 74 MPa, just 3 MPa lower than pure meta-PBI membranes. Thermal stability of iodide exchanged blend membranes appears to be remarkably high, probably because cleaved iodomethane does not evaporate but methylates meta-PBI. PA concentration in doped membranes of 60-63% is reached by doping in 60% PA (blend; 6.3 PA/repeat unit) and 70% PA (meta-PBI; 4.6 PA/r.u.). This suggests that blends absorb PA more strongly. Both membranes show similar conductivity between rt and 140 °C, indicating that PA concentration describes these membranes better than PA/r.u. In the fuel cell, blend membranes show similar or better performance than meta-PBI. In the TGA, blends doped in 20% PA showed a stable plateau between 115 and 180 °C, while meta-PBI lost weight continuously.
AB - Methylation of polybenzimidazole leads to positively charged polymer backbones, and moveable anions. Ion exchange of methylated PBI-OO in phosphoric acid (PA) shows that the resulting polymers dissolve. meta-PBI, however, absorbs about 400 wt% PA while remaining a self supported membrane. We investigate the properties of blend membranes, employing meta-PBI for mechanical integrity and methylated PBI-OO for high PA uptake and resulting proton conductivity. While small additions of PBI-OO decrease the tensile strength of blend membranes (58 MPa for 10% PBI-OO), further addition leads to an increase, and 50% blend membranes show again a tensile strength of 74 MPa, just 3 MPa lower than pure meta-PBI membranes. Thermal stability of iodide exchanged blend membranes appears to be remarkably high, probably because cleaved iodomethane does not evaporate but methylates meta-PBI. PA concentration in doped membranes of 60-63% is reached by doping in 60% PA (blend; 6.3 PA/repeat unit) and 70% PA (meta-PBI; 4.6 PA/r.u.). This suggests that blends absorb PA more strongly. Both membranes show similar conductivity between rt and 140 °C, indicating that PA concentration describes these membranes better than PA/r.u. In the fuel cell, blend membranes show similar or better performance than meta-PBI. In the TGA, blends doped in 20% PA showed a stable plateau between 115 and 180 °C, while meta-PBI lost weight continuously.
KW - Blend membranes
KW - High temperature polymer electrolyte fuel cell
KW - Methylated PBI-OO
KW - Phosphoric acid doping
KW - Polybenzimidazole
KW - Polybenzimidazolium
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U2 - 10.1016/j.eurpolymj.2014.06.019
DO - 10.1016/j.eurpolymj.2014.06.019
M3 - Article
AN - SCOPUS:84904668390
SN - 0014-3057
VL - 58
SP - 135
EP - 143
JO - European Polymer Journal
JF - European Polymer Journal
ER -