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Preparation and characterization of polysulfones containing both hexafluoroisopropylidene and trimethylsilyl groups as gas separation membrane materials

机译:含六氟异亚丙基和三甲基甲硅烷基的聚砜作为气体分离膜材料的制备与表征

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摘要

Trimethylsilylated derivatives of hexafluoropolysulfone (6FPSf) and tetramethylhexafluoropolysulfone (TM6FPSf) were prepared by reaction of lithiated polymer intermediates with halotrimethylsilane electrophiles for a membrane gas separation study to compare improvements in gas permeabilities with those of unmodified polymers. Ortho sulfone substituted 6FPSf and TM6FPSf having pendant trimethylsilyl (TMS) groups were obtained by a two-step process involving first direct lithiation of 6FPSf and TM6FPSf solutions with n-butyllithium to afford ortho sulfone dilithiated intermediates, followed by reaction with a TMS electrophile. The corresponding ortho ether 6FPSf derivative was obtained by lithiation of dibrominated 6FPSf at the bromine sites, followed by reaction with a TMS electrophile. The degree of substitution (DS) of the TMS groups was 2.0 and was dependent on the molar ratio of n-butyllithium and electrophile quantity, electrophile reactivity, and reaction conditions. Detailed structural characterization and DS of the modified polymers were obtained by nuclear magnetic resonance spectroscopy. The glass transition temperatures and thermal stabilities were determined by differential scanning calorimetry and thermogravimetric analysis, respectively. Polymer chain d-spacing was investigated using wide-angle X-ray diffraction. Polymer free volume was calculated from the polymer density and specific van der Waals volume. The polymer gas permeability coefficients (P) were measured for He, CO2, O2, and N2. Both CO2 and O2 permeabilities of modified 6FPSf increased by 8-9-fold (P(CO2) = 110 barrers, P(O2) = 28 barrers) compared with those of the starting polymer 6FPSf (P(CO2) = 12 barrers, P(O2) = 3.4 barrers), which gives P and properties very close to the upper bound line.1 Almost no reduction in permselectivity () was observed for the CO2/N2 gas pair, while the O2/N2 gas pair showed moderate reduction.
机译:六氟聚砜(6FPSf)和四甲基六氟聚砜(TM6FPSf)的三甲基甲硅烷基化衍生物是通过将锂化的聚合物中间体与卤代三甲基硅烷亲电子试剂反应制备的,用于膜气体分离研究,以比较未改性聚合物的气体渗透性改进。具有两甲基三甲基甲硅烷基(TMS)侧基的邻砜取代的6FPSf和TM6FPSf是通过两步过程获得的,该过程包括首先用正丁基锂直接对6FPSf和TM6FPSf溶液进行直接锂化,得到邻砜二甲酸酯化的中间体,然后与TMS亲电子试剂反应。通过在溴位上将二溴化的6FPSf锂化,然后与TMS亲电试剂反应,可获得相应的邻醚6FPSf衍生物。 TMS基团的取代度(DS)为2.0,并且取决于正丁基锂的摩尔比和亲电子量,亲电子反应性和反应条件。通过核磁共振光谱法获得了改性聚合物的详细结构特征和DS。玻璃化转变温度和热稳定性分别通过差示扫描量热法和热重分析法确定。使用广角X射线衍射研究了聚合物链的d间距。由聚合物密度和比范德华体积计算无聚合物体积。测量了He,CO2,O2和N2的聚合物气体渗透系数(P)。与起始聚合物6FPSf(P(CO2)= 12 barrers,P)相比,改性6FPSf的CO2和O2渗透率均增加了8-9倍(P(CO2)= 110 barrers,P(O2)= 28 barrers)。 (O2)= 3.4 barrers),这使得P和特性非常接近上限线。1几乎没有观察到CO2 / N2气体对的渗透选择性()降低,而O2 / N2气体对显示出适度的降低。

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