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首页> 外文期刊>Reactive & Functional Polymers >Design and fabrication of high performance membrane for carbon dioxide separation via blending poly(ethylene oxide-b-amid 6) with dense, glassy and highly CO_2-philic amidoximated polymers
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Design and fabrication of high performance membrane for carbon dioxide separation via blending poly(ethylene oxide-b-amid 6) with dense, glassy and highly CO_2-philic amidoximated polymers

机译:通过混合聚(环氧乙烷-B-酰胺6)具有致密,玻璃和高度CO_2-脒氧化聚合物的高性能膜对二氧化碳分离的高性能膜的设计和制造

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摘要

Blend membranes based on the poly(ethylene oxide-b-amid 6) (Pebax 1657) block copolymer and carbon dioxide (CO2)-philic glassy polymers including polyacrylonitrile (PAN), acrylonitrile/ vinylimidazole copolymer (P(ANco-VIm)) or corresponding amidoximated derivatives, i.e. P(AO-AN) and P(AO-AN-co-VIm), as additive were prepared using solution casting method. To increase CO2-philic groups, acrylonitrile- based polymers were amidoximated via reacting with hydroxyl ammonium chloride (NH2OH.HCl) reagent where amidoximation process was evaluated by FTIR and 1H NMR. Compatibility and morphology of components in the blend membranes and blend density were examined by ATR-IR and DSC, FE-SEM and densitometry tests, respectively. Shifting of the peaks in the ATR-IR spectra showed that the Pebax 1657 chains establish a hydrogen bonding with the homo- or copolymer chains. The crystallinity and melting temperature (Tm) of polyamide (PA) domains in the Pebax 1657 decreased by increasing the amount of acrylonitrile- based polymers and their amidoximated derivatives. Also, the glass transition temperature (Tg) of the polyethylene oxide (PEO) domains increased due to the glassy nature of the additives. FE-SEM results indicated that all membranes are dense and there is a good interaction between the Pebax and the additives. The dense structure and free volume reduction in the membranes were confirmed by increasing membrane density resulting from increase in the amount of acrylonitrilebased polymer and amidoximated derivatives. The permeability of CO2, nitrogen (N2) and methane (CH4) gases from pure and blend membranes was measured by constant pressure/ variable volume method at 3 bar and ambient temperature. By increasing the amount of acrylonitrile- based polymers, i.e. PAN and P(AN-co-VIm), up to 20 wt%, the permeability of CH4, N2 and CO2 increased and then decreased with further increasing of the additive content. In blend membranes containing amidoximated polymers, i.e. (P(AO-AN) and P(AO-AN-coVIm)), CO2 permeability and of CO2/N2 and CO2/CH4 selectivity showed an increased trend up to 60%wt additive due to increased number and type of nitrogen atoms in the membrane structure. Compared to the pure Pebax 1657, CO2 permeability and CO2/N2 and CO2/CH4 selectivity in blend membrane containing 40 wt% of P (AO-AN-co-VIm) copolymer increased by 193%, 497% and 495%, respectively.
机译:基于聚(氧化乙烷-B-酰胺6)(PEBAX 1657)嵌段共聚物和二氧化碳(CO 2) - 淫玻璃聚合物,包括聚丙烯腈(PAN),丙烯腈/乙烯基咪唑共聚物(P(ANCO-VIM))或使用溶液浇铸方法制备相应的酰胺氧化衍生物,即P(AO-AN)和P(AO-An-Co-Vim),作为添加剂。为了增加CO 2 - 腓基团,通过与羟基氯化铵(NH 2 OH -HCl)试剂反应,丙烯腈基聚合物酰胺化,其中通过FTIR和1H NMR评估酰胺氧化过程。通过ATR-IR和DSC,Fe-SEM和密度测定测试检查混合物膜中的组分和混合物密度的兼容性和形态。 ATR-IR光谱中的峰的变速表明,PEBAX 1657链与均外或共聚物链建立了氢键。通过增加丙烯腈基聚合物及其酰胺氧化衍生物的丙烯腈的聚合物的量,PEBAX 1657中聚酰胺(PA)结构域的结晶度和熔融温度(TM)降低。而且,由于添加剂的玻璃状性质,聚环氧乙烷(PEO)结构域的玻璃化转变温度(Tg)增加。 Fe-SEM结果表明,所有膜都是致密的,PEBAX与添加剂之间存在良好的相互作用。通过增加由于丙烯腈基于聚合物和酰胺氧化衍生物的增加而导致的膜密度增加膜密度来确认膜中的致密结构和自由体积。通过在3巴和环境温度下通过恒压/可变体积法测量来自纯和共混膜的CO 2,氮(N2)和甲烷(CH4)气体的渗透率。通过增加丙烯腈的聚合物的量,即PAN和P(AN-CO-VIM),高达20wt%,CH 4,N 2和CO 2的渗透性增加,然后随着添加剂含量的进一步增加而降低。在含有脒氧化聚合物的混合物膜中,即(P(AO-AN)和P(AO-AN-COVIM)),CO 2渗透率和CO 2 / N 2和CO 2 / CH 4选择性显示出增加的趋势增加了60%的增量增加膜结构中氮原子的数量和型型。与含有40wt%的P(AO-An-Co-Vim)共聚物的共混膜中的纯PEBAX 1657,CO 2渗透率和CO 2 / N 2和CO 2 / CH 4选择性分别增加了193%,497%和495%。

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