2019
DOI: 10.1016/j.memsci.2018.11.079
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Friedel-Crafts alkylation route for preparation of pendent side chain imidazolium-functionalized polysulfone anion exchange membranes for fuel cells

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Cited by 34 publications
(24 citation statements)
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“…The first weight loss between 40 and 100 °C is associated with the retained water in the membranes. The second loss between 160 and 250 °C corresponds to the decomposition of the functional groups such as MIm [ 38 ], sulfonic groups in the case of the SPSU, and TMEDA used as a crosslinking agent. Around 400–450 °C, there was another weight loss associated with the degradation of the polymeric backbone [ 18 , 30 ].…”
Section: Resultsmentioning
confidence: 99%
“…The first weight loss between 40 and 100 °C is associated with the retained water in the membranes. The second loss between 160 and 250 °C corresponds to the decomposition of the functional groups such as MIm [ 38 ], sulfonic groups in the case of the SPSU, and TMEDA used as a crosslinking agent. Around 400–450 °C, there was another weight loss associated with the degradation of the polymeric backbone [ 18 , 30 ].…”
Section: Resultsmentioning
confidence: 99%
“…Tiantian Li et al synthesized PSU based anion exchange membrane via Friedel-Crafts alkylation method contains pendant imidazolium functionalized side chain to avoid conventional carcinogenic chloromethylation. It does not require any special functional groups on the polymeric materials, which is the main advantage compared with other mentioned chloromethylation-free routes in the literature [116]. Furthermore, the membranes synthesized in this methodology displayed excellent ionic conductivity and swelling ratio along with good mechanical, thermal, and alkaline stabilities.…”
Section: Alkaline Based Polysulfone and Its Composites For Amfcsmentioning
confidence: 87%
“…As for the conductivity, disclosures indicated that the conductivity of the PBI membranes was not only related to the ADL but also influenced by the number of proton acceptor sites [ 22 , 23 , 24 ]. Reports that focused on incorporating more proton acceptor sites, such as imidazole [ 21 , 25 , 26 ], pyridine rings [ 25 , 27 , 28 ], and nitro [ 29 ] into the monomer structure demonstrated a higher proton conductivity. For example, Han et al grafted Trifluoromethanesulfonylimide on PBI, and found that the higher proton concentration provided by TFSI with stronger acidity contributed much to proton conductivities [ 6 ].…”
Section: Introductionmentioning
confidence: 99%