We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized ...We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized by FT-IR,H-NMR,C-NMR, TGA, XRD and SEM. Their COadsorption capacities were measured under different pressures and temperatures by constant-volume technique. It was observed that quaternary ammonium PILs of P[VBTHEA]Cl have higher adsorption capacity for COthan those imidazolium PILs, following P[VBTHEA]Cl > P[VEIm]PF> P[VEIm]BF> P[VEIm]Br, which may be ascribed to higher positive charge density on ammonium cation than that on imidazolium cation and thus stronger interaction with CO, consistent with the results from dual-mode adsorption model that ammonium PILs have much higher CObulk absorption than imidazolium PILs. COadsorption capacity of P[VBTHEA]Cl is 9.02 mg/g under 295 K and 1 bar, which is comparable to that of some other PILs, and is much higher than that of the corresponding ILs monomer. These PILs have good adsorption selectivity for COover Nand regeneration efficiency.展开更多
This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional sma...This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional small-molecule probe of acid fuchsin with HBPILs. The obtained HBPIL vesicle displayed ultraviolet absorption at 544 nm, and was used as a novel SO2 derivative sensor with high sensitivity and visualization. Due to the functional ion pairs enriching on the surface, the SO32 detection limit of the HBPILs vesicles was as low as 0.138 gmol/L, which was about 1.5 orders of magnitude lower than that of acid fuchsin.展开更多
Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-...Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-NMR） and gel permeation chromatography （GPC）. The resulting copolymer was used to prepare poly（vinylidene fluoride） （PVDF） blend membranes via a phase inversion method. The effects of the copolymer on the polymorphism, surface wettability and zeta potential （0 of the blend membranes were investigated by ATR-FTIR, contact angle instrument and zeta potential analyzer. Scanning electron microscopy （SEM and SEM-EDS） was also applied to investigate the morphology and the surface element changes of the fabricated membranes. The results indicated that P（MMA-co-BVIm-Br） copolymer existed on the surface of the membrane which made the blend membrane have a positive surface during the experimental pH range. The copolymer was also in favor of the formation of βcrystal phase in PVDF membranes. The contact angle experiment indicated that P（MMA-co-BVIm-Br） copolymer could switch the wettability of the blend membranes from hydrophilic to hydrophobic by exchanging Br- anion with PF6-. Compared with pure PVDF membranes, the water flux and water recovery flux of the blend membranes were enhanced obviously. The results from the flux recovery ratio （FR） and total fouling ratio （Rt） all suggested that the blend membranes had good anti-fouling properties.展开更多
基金financially supported by State Key Laboratory of Organic-Inorganic Composites(oic-201601012)the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP#0080
文摘We synthesized one quaternary ammonium polymeric ionic liquids（PILs）P[VBTHEA]Cl and three imidazolium PILs of P[VEIm]Br, P[VEIm]BF, P[VEIm]PFby free-radical polymerization in solution. These PILs were characterized by FT-IR,H-NMR,C-NMR, TGA, XRD and SEM. Their COadsorption capacities were measured under different pressures and temperatures by constant-volume technique. It was observed that quaternary ammonium PILs of P[VBTHEA]Cl have higher adsorption capacity for COthan those imidazolium PILs, following P[VBTHEA]Cl > P[VEIm]PF> P[VEIm]BF> P[VEIm]Br, which may be ascribed to higher positive charge density on ammonium cation than that on imidazolium cation and thus stronger interaction with CO, consistent with the results from dual-mode adsorption model that ammonium PILs have much higher CObulk absorption than imidazolium PILs. COadsorption capacity of P[VBTHEA]Cl is 9.02 mg/g under 295 K and 1 bar, which is comparable to that of some other PILs, and is much higher than that of the corresponding ILs monomer. These PILs have good adsorption selectivity for COover Nand regeneration efficiency.
基金supported by the National Basic Research Program(No.2013CB834506)the National Science Fund for Distinguished Young Scholars(No.21225420)+1 种基金the National Natural Science Foundation of China(Nos.91127047,21474062 and 21404070)Program of Shanghai Subject Chief Scientist(No.15XD1502400)
文摘This work reports a SO2 derivative-detecting and colorful hyperbranched polymeric ionic liquid （HBPIL） vesicle through aqueous self-assembly. By a simple anion-exchange, we achieved the combination of functional small-molecule probe of acid fuchsin with HBPILs. The obtained HBPIL vesicle displayed ultraviolet absorption at 544 nm, and was used as a novel SO2 derivative sensor with high sensitivity and visualization. Due to the functional ion pairs enriching on the surface, the SO32 detection limit of the HBPILs vesicles was as low as 0.138 gmol/L, which was about 1.5 orders of magnitude lower than that of acid fuchsin.
基金financially supported by the National Natural Science Foundation of China(Nos.51103130 and 21004051)Qianjiang Talents Project of Technology Office in Zhejiang Province(No.2013R10070)
文摘Polymerizable ionic liquid copolymer P（MMA-co-BVIm-Br） was synthesized by radical polymerization technique, and characterized by Fourier transform infrared spectrometry （FTIR）, 1H Nuclear magnetic resonance （1H-NMR） and gel permeation chromatography （GPC）. The resulting copolymer was used to prepare poly（vinylidene fluoride） （PVDF） blend membranes via a phase inversion method. The effects of the copolymer on the polymorphism, surface wettability and zeta potential （0 of the blend membranes were investigated by ATR-FTIR, contact angle instrument and zeta potential analyzer. Scanning electron microscopy （SEM and SEM-EDS） was also applied to investigate the morphology and the surface element changes of the fabricated membranes. The results indicated that P（MMA-co-BVIm-Br） copolymer existed on the surface of the membrane which made the blend membrane have a positive surface during the experimental pH range. The copolymer was also in favor of the formation of βcrystal phase in PVDF membranes. The contact angle experiment indicated that P（MMA-co-BVIm-Br） copolymer could switch the wettability of the blend membranes from hydrophilic to hydrophobic by exchanging Br- anion with PF6-. Compared with pure PVDF membranes, the water flux and water recovery flux of the blend membranes were enhanced obviously. The results from the flux recovery ratio （FR） and total fouling ratio （Rt） all suggested that the blend membranes had good anti-fouling properties.
