2019
DOI: 10.1016/j.reactfunctpolym.2019.06.003
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Crosslinked chitosan/poly(vinyl alcohol)-based polyelectrolytes for proton exchange membranes

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Cited by 33 publications
(17 citation statements)
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“…(iii) Unlike chitin, Chit is soluble in water under slightly acidic conditions due to the presence of ammine groups in diluted organic acids [5][6][7]. This allows gel formation in various configurations [8]. (iv) It has good film-forming properties due to the presence of intra-and inter-molecular hydrogen bonding [9].…”
Section: Why Chitosan?mentioning
confidence: 99%
See 1 more Smart Citation
“…(iii) Unlike chitin, Chit is soluble in water under slightly acidic conditions due to the presence of ammine groups in diluted organic acids [5][6][7]. This allows gel formation in various configurations [8]. (iv) It has good film-forming properties due to the presence of intra-and inter-molecular hydrogen bonding [9].…”
Section: Why Chitosan?mentioning
confidence: 99%
“…(v) The presence of polar functional groups in the structure, specifically hydroxyl (-OH), primary amine (-NH 2 ), and ether (C-O-C) groups, facilitates the chemical modifications of chitosan and the tailored synthesis of Chit-based materials for specific applications [10][11][12]. Owing to the very low proton conductivity of pristine chitosan (about 1.2 × 10 −2 S cm −1 at 25 • C [8]), chemical modification of the polymer has been intensively exploited in recent years to generate ion-exchange sites to improve proton/ionic conductivity of the composite material [13][14][15][16].…”
Section: Why Chitosan?mentioning
confidence: 99%
“…From a structural point of view, Chit is well known to behave as a semi-flexible rod (or stiff coil), with a calculated persistence length, l p , of ~ 16 nm down to 7 nm, as previously demonstrated [ 15 ]. These properties allow the development of easy procedures for gel formation [ 16 ] and chemical modification of Chit-based structures [ 17 , 18 , 19 ].…”
Section: An Overview Of Chitosan Properties and Methods Of Synthesmentioning
confidence: 99%
“…Thereby, the development of more affordable PEMs based on hydrocarbon structures of sulfonated aromatic polymers may involve incentive and cost‐effective opportunities in this field. Numerous examples of potential membrane materials functionalized with sulfonic groups have been proposed and can be found in the recent related bibliography such as poly(ether‐ether ketones), 4–7 poly(vinyl alcohol), 8–12 polyimides, 13–16 poly(benzimidazoles), 17–20 poly(phosphazenes) 21–23 or polystyrene‐block copolymers 24–27 …”
Section: Introductionmentioning
confidence: 99%