2013
DOI: 10.1016/j.memsci.2013.02.053
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SPPEK/TPA composite membrane as a separator of vanadium redox flow battery

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Cited by 80 publications
(35 citation statements)
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“…This can be due to the degradation of sulfonic acid groups in VO 2 þ solution. In testing the stability after 30 days of soaking, the weight losses of SPPEK-P-70, SPPEK-P-80 and SPPEK-P-90 membranes are lower than that of SPPEK-TPA membranes (3.87%) at the same conditions [30], and also lower than that of sulfonated poly(ether ether ketone)/polyacrylonitrile acid blend membrane (4.0%) after soaking for two weeks [31]. Even after 60 days of soaking, the weight losses of SPPEK-P-70 and SPPEK-P-80 are still lower than 4.0%.…”
Section: The Stability Of Sppek-p Membranesmentioning
confidence: 94%
“…This can be due to the degradation of sulfonic acid groups in VO 2 þ solution. In testing the stability after 30 days of soaking, the weight losses of SPPEK-P-70, SPPEK-P-80 and SPPEK-P-90 membranes are lower than that of SPPEK-TPA membranes (3.87%) at the same conditions [30], and also lower than that of sulfonated poly(ether ether ketone)/polyacrylonitrile acid blend membrane (4.0%) after soaking for two weeks [31]. Even after 60 days of soaking, the weight losses of SPPEK-P-70 and SPPEK-P-80 are still lower than 4.0%.…”
Section: The Stability Of Sppek-p Membranesmentioning
confidence: 94%
“…1), a new peak at 4.64 ppm was assigned to the methylene protons in the chloromethyl groups [34]. As mentioned in the experimental part, degree of substitution (DS) of chloromethylated poly(phenyl sulfone) was calculated from 1 H NMR spectroscopy by taking the integral ratio of eCH 2 Cl (H(2)) at 4.64 ppm to the poly(phenyl sulfone) backbone protons at 7.90 ppm (H (11,12,13,14)) which were intact during the chloromethylation reaction, and the calculation equation was shown as following:…”
Section: Membrane Synthesis and Propertiesmentioning
confidence: 99%
“…where A 2 was the integration value of H(2), A 11,12,13,14 was the integration value of H (11,12,13,14), respectively.…”
Section: Membrane Synthesis and Propertiesmentioning
confidence: 99%
“…Consequently, development of more stable non-fluorinated proton conductive membranes is an ongoing effort undertaken by many researchers. Commonly-used strategies to improve the stability of non-fluorinated proton conductive membranes are as the following: On one hand, organic-inorganic composite membranes such as sulfonated poly (ether ether ketone)/graphene oxide (SPEEK/GO) [13], sulfonated poly(phthalazinone ether ketone)/tungstophosphoric acid (SPPEK/TPA) [14], sulfonated poly(arylene ether sulfone)/laponite-SO 3 H (SPEAS/SLa) [15] and sulfonated polyimide/s-MoS 2 (SPI/s-MoS 2 ) membranes [16] were prepared by adding inorganic fillers or segments into non-fluorinated polymers; On another hand, the monomers used to synthesize non-fluorinated polymers were designed and optimized, in order that the stability of nonfluorinated polymers themselves can be improved. Our earlier work [17] verified the feasibility of the latter strategy, which spurs us to do more relative work about preparation of non-fluorinated polymer membranes made of more stable monomers.…”
Section: Introductionmentioning
confidence: 99%