2015
DOI: 10.1039/c4ra16203j
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Novel cross-linked anion exchange membrane based on hexaminium functionalized poly(vinylbenzyl chloride)

Abstract: A novel cross-linked poly(vinylbenzyl chloride) anion exchange membrane is prepared using β-hydrogen free ‘hexamine’ as an amination agent.

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Cited by 45 publications
(44 citation statements)
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“…The complete transformation of the CH2Cl groups to quaternary ammonium salts is shown by the FTIR spectra as bands representative of the CH2Cl group (1265 and 700 cm −1 ) are replaced by those representative of quaternary ammonium groups (1320-1465 and 1057 cm −1 ) (Figure 4) [31]. A large molar excess of DABCO was used to avoid the possibility of cross-linking between pVBC chains through the quaternization of both DABCO tertiary amine groups.…”
Section: Ionomer Synthesis and Performancementioning
confidence: 99%
“…The complete transformation of the CH2Cl groups to quaternary ammonium salts is shown by the FTIR spectra as bands representative of the CH2Cl group (1265 and 700 cm −1 ) are replaced by those representative of quaternary ammonium groups (1320-1465 and 1057 cm −1 ) (Figure 4) [31]. A large molar excess of DABCO was used to avoid the possibility of cross-linking between pVBC chains through the quaternization of both DABCO tertiary amine groups.…”
Section: Ionomer Synthesis and Performancementioning
confidence: 99%
“…whereas at the same temperature, P-25µm-0.5%CL and P-25µm-1%CL membranes exhibited proton conductivities values limited at 54.7 mS•cm -1 and 47.3 mS•cm -1 , respectively. These results could be explained by the effect of more a pronounced cross-linking which results in restrict chain mobility and thus lower PEM proton-conduction performance 7,[50][51] . Moreover, the cross-linker applied, i.e.…”
Section: Crosslinking Effectmentioning
confidence: 99%
“…16,17 For examples beyond other PBIs, [18][19][20] great alkaline stability was reported for blend membrane of poly(vinyl alcohol) (PVA) and poly(diallyldimethylammonium chloride) (PDDA) to survive in 8 M KOH up to 360 h with a hydroxide ion conductivity of 25 mS cm À1 in water at 25 C. 21,22 Benzyl halides in the polymer backbone or side chains when reacted with trimethylamine (TMA) or hexamethylenetetramine (HMTA) formed structures that contained no or less b-hydrogen atoms to the quaternary nitrogen. 23,24 In these cases, however, a different degradation mode became dominant where the hydroxide ion attacked at the a-carbon leading to deamination. In most cases, however, synthesis of polymers with no b-hydrogen atoms contained complex processes and therefore, a potential industrial scale-up would be costly.…”
Section: Introductionmentioning
confidence: 99%