TY - JOUR
T1 - 磺化聚砜-聚多巴胺-ZrO2有机无机杂化复合质子交换膜的结构及性能
AU - Chen, Chuang
AU - Lin, Feng
AU - Cai, Rong
AU - Chen, Fang
AU - Ma, Xiaoyan
N1 - Publisher Copyright:
© 2019, Editorial Office of Acta Materiae Compositae Sinica. All right reserved.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - The main obstacle of wide commercialization of proton exchange membrane is to maintain the high conductivity and low swelling ratio of proton exchange membrane at higher temperature under fully hydrated state. In order to solve this issue, by using poly-dopamine (PDA) as an intermediate layer, ZrO2 was formed on the commercial sulfonated polysulfone (PSF) porous membrane matrix, a facial approach of preparing well performed composite proton exchange membrane was proposed. The influence of PDA deposition conditions and ZrO2 mineralization process on the surface morphology and element distribution of PSF-PDA-ZrO2 composite membrane were investigated. The PSF-PDA modified membrane with PDA deposition time of 5 h was selected for mineralization. It is found that the content of Zr element on the surface mineralized layer of PSF-PDA-ZrO2 composite membranes is significantly increased with increasing mineralization time. The water uptake, swelling ratio and proton conductivity of PSF-PDA-ZrO2 composite membrane were tested. The results show that the surface of ZrO2 mineralized layer significantly inhibits the swelling ratio of PSF-PDA-ZrO2 composite membranes at higher temperature compared with PSF porous membranes, and the swelling ratio of composite membranes gradually reduces with the increase of ZrO2 mineralization time. The proton conductivity of PSF-PDA-ZrO2 composite membranes with mineralization time for 1 h, 5 h, 12 h and 24 h is higher than that of the pure PSF porous membrane, and the conductivity of the PSF-PDA-ZrO2 composite membranes decreases gradually with the increase of mineralization time. The proton conductivity of PSF-PDA-ZrO2 composite membrane after PDA deposition for 5 h and mineralization for 1 h is up to 0.117 S•cm-1 at 90℃, which is 2.5 times of the PSF porous basement membrane.
AB - The main obstacle of wide commercialization of proton exchange membrane is to maintain the high conductivity and low swelling ratio of proton exchange membrane at higher temperature under fully hydrated state. In order to solve this issue, by using poly-dopamine (PDA) as an intermediate layer, ZrO2 was formed on the commercial sulfonated polysulfone (PSF) porous membrane matrix, a facial approach of preparing well performed composite proton exchange membrane was proposed. The influence of PDA deposition conditions and ZrO2 mineralization process on the surface morphology and element distribution of PSF-PDA-ZrO2 composite membrane were investigated. The PSF-PDA modified membrane with PDA deposition time of 5 h was selected for mineralization. It is found that the content of Zr element on the surface mineralized layer of PSF-PDA-ZrO2 composite membranes is significantly increased with increasing mineralization time. The water uptake, swelling ratio and proton conductivity of PSF-PDA-ZrO2 composite membrane were tested. The results show that the surface of ZrO2 mineralized layer significantly inhibits the swelling ratio of PSF-PDA-ZrO2 composite membranes at higher temperature compared with PSF porous membranes, and the swelling ratio of composite membranes gradually reduces with the increase of ZrO2 mineralization time. The proton conductivity of PSF-PDA-ZrO2 composite membranes with mineralization time for 1 h, 5 h, 12 h and 24 h is higher than that of the pure PSF porous membrane, and the conductivity of the PSF-PDA-ZrO2 composite membranes decreases gradually with the increase of mineralization time. The proton conductivity of PSF-PDA-ZrO2 composite membrane after PDA deposition for 5 h and mineralization for 1 h is up to 0.117 S•cm-1 at 90℃, which is 2.5 times of the PSF porous basement membrane.
KW - Biomimetic mineralization
KW - Composite membrane
KW - Poly-dopamine (PDA)
KW - Porous substrate
KW - Proton exchange membrane
UR - http://www.scopus.com/inward/record.url?scp=85075762460&partnerID=8YFLogxK
U2 - 10.13801/j.cnki.fhclxb.20190123.001
DO - 10.13801/j.cnki.fhclxb.20190123.001
M3 - 文章
AN - SCOPUS:85075762460
SN - 1000-3851
VL - 36
SP - 2522
EP - 2529
JO - Fuhe Cailiao Xuebao/Acta Materiae Compositae Sinica
JF - Fuhe Cailiao Xuebao/Acta Materiae Compositae Sinica
IS - 11
ER -