2017
DOI: 10.1016/j.jct.2016.11.031
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Ionic transport processes in polymer mixture solutions based on quaternized polysulfones

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Cited by 16 publications
(4 citation statements)
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“…Notably, with an increase in VBC content, both peaks at 915 cm –1 and 1640 cm –1 become more pronounced. Meanwhile, there is a gradual decline in intensity observed for the pyridine peak at 1590 cm –1 , further confirming successful quaternization . Additionally, upon heating, the presence of the −CH 2 – group resulted in an absorption band at 1460 cm –1 .…”
Section: Discussionmentioning
confidence: 69%
See 1 more Smart Citation
“…Notably, with an increase in VBC content, both peaks at 915 cm –1 and 1640 cm –1 become more pronounced. Meanwhile, there is a gradual decline in intensity observed for the pyridine peak at 1590 cm –1 , further confirming successful quaternization . Additionally, upon heating, the presence of the −CH 2 – group resulted in an absorption band at 1460 cm –1 .…”
Section: Discussionmentioning
confidence: 69%
“…Meanwhile, there is a gradual decline in intensity observed for the pyridine peak at 1590 cm −1 , further confirming successful quaternization. 28 Additionally, upon heating, the presence of the −CH 2 − group resulted in an absorption band at 1460 cm −1 . The intensity enhancement of this absorption band is indicative of methylene production through cross-linking reaction occurring at the C�C double bond.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Commercial aromatic polysulfone (PSF, UDEL-3500, Union Carbide Company, Texas), with number-average molecular weight M n = 39,000 g·mol −1 , was used in the synthesis of functionalized polysulfones [ 29 , 30 ]. Cationic polysulfone containing quaternary ammonium side groups (PSFQ, M n = 28,000 g·mol −1 , ionic chlorine content 5.44%; Table 2 ) was synthesized by reacting chloromethylated polysulfone (CMPSF) with a tertiary amine, namely N,N—dimethylbutylamine, according to the detailed procedure presented in previous studies [ 29 , 30 , 70 ].…”
Section: Methodsmentioning
confidence: 99%
“…Commercial aromatic polysulfone in powder form (UDEL-3500-PSF, Union Carbide Company, Houston, TX, USA) (Mn = 39,000 g/mol; Mw/Mn = 1.625) was used in the synthesis of functionalized polysulfones [10][11][12]. Thus, the cationic polysulfone containing quaternary ammonium side groups (PSFQ, Mn = 28,000 g/mol) was synthesized by the reaction of chloromethylated polysulfone (CMPSF with a content in chlorine of 7.42% and Mn = 29,000 g/mol) with a tertiary amine, N,Ndimethylbutylamine (DMBA) [12,26]. The quaternary polymer was isolated from the reaction medium by precipitation in diethylether, washed three times with diethylether, and dried for 48 h under vacuum, at room temperature.…”
Section: Methodsmentioning
confidence: 99%