Repurposing trityl-substituted triphenylamine-based polyimides for gas separation membranes by blending with a fluorinated polyimide

IF 4.5 3区 工程技术 Q1 CHEMISTRY, APPLIED Reactive & Functional Polymers Pub Date : 2024-10-30 DOI:10.1016/j.reactfunctpolym.2024.106081
Adriana-Petronela Chiriac , Catalin-Paul Constantin , Mihai Asandulesa , Violeta Melinte , Andrzej Jankowski , Mariana-Dana Damaceanu
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Abstract

In the attempt to develop gas separation membranes by reusing polymers with no film-forming ability but with great potential for this purpose, blending has been approached as a simple, time- and cost-effective strategy. Herein, blends of trityl-substituted triphenylamine (TTA)-based polyimides and a fluorinated polyimide (6F-PI) were involved to prepare dense membranes by drop-casting technique. The two blend components involved in variable amounts led to different film morphologies with a strong impact on most blends' properties and gas separation performance. According to optical microscopy, SEM, AFM, and FTIR investigations, the blend series containing hexafluoroisopropylidene (6F) groups in both polyimide components proved to be fully miscible at the molecular levels. When a single 6F-based component was integrated into the blend, the polymers proved to be compatible, but only partially miscible, with a two-phase structure, in which 6F-PI wrapped around the TTA-PI growth fibrillar domains. However, all blends displayed a single glass transition and FTIR bands which do not sum the ones of the polymer components, as well as a high thermal stability, close to that of 6F-PI. Regardless of their miscibility level, all blends behaved as classical polyimide films, with good mechanical properties and chemical resistance to corrosive media like acid vapors or basic solutions. The blend composition and diimide structure of TTA-PI little affected the dielectric behavior, unlike the gas separation performance that strongly depended on these characteristics. The higher amount of 6F groups in the miscible blends endowed the membranes with superior permeability and selectivity, allowing in some cases to surpass the trade-off rule. Generally, the gas permeability decreased with the increase of TTA-PI content, with some exceptions. The low intermolecular interfacial interactions promoted by TTA-PI were found to be beneficial in preserving a good selectivity of gas molecules with a small kinetic diameter (He, CO2) though their permeability is lost. The gas permeability changes as a function of the blend composition and structure were mostly due to changes in the solubility coefficient and less from gas diffusion capability, at least for CO2 and N2.

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通过与含氟聚酰亚胺混合,将三苯甲基取代的三苯胺基聚酰亚胺重新用于气体分离膜
在试图通过重复使用不具备成膜能力但具有巨大潜力的聚合物来开发气体分离膜的过程中,混合是一种简单、省时且具有成本效益的策略。在这里,三苯甲基取代三苯胺(TTA)基聚酰亚胺和氟化聚酰亚胺(6F-PI)的混合物被用来通过滴铸技术制备致密膜。两种混合物成分的不同用量导致了不同的薄膜形态,对大多数混合物的性能和气体分离性能产生了很大影响。根据光学显微镜、扫描电子显微镜、原子力显微镜和傅立叶变换红外光谱研究,在两种聚酰亚胺成分中都含有六氟异丙亚基(6F)基团的混合物系列在分子水平上被证明是完全混溶的。当在共混物中加入单一的 6F 组分时,聚合物被证明是兼容的,但只是部分混溶,具有两相结构,其中 6F-PI 包裹在 TTA-PI 生长的纤维畴中。不过,所有混合物都显示出单一的玻璃化转变,傅立叶变换红外光谱带与聚合物成分的光谱带不同,而且热稳定性很高,接近 6F-PI 的热稳定性。无论其混溶程度如何,所有共混物都表现为传统的聚酰亚胺薄膜,具有良好的机械性能和对酸蒸汽或碱性溶液等腐蚀性介质的耐化学性。TTA-PI 的共混物成分和二亚胺结构对介电性能的影响很小,而气体分离性能则与这些特性密切相关。混溶混合物中 6F 基团的含量越高,膜的渗透性和选择性就越好,在某些情况下甚至超越了权衡规则。一般来说,气体渗透性随着 TTA-PI 含量的增加而降低,但也有一些例外。研究发现,TTA-PI 所促进的低分子间界面相互作用有利于保持对动力学直径较小的气体分子(He、CO2)的良好选择性,尽管它们的渗透性会降低。气体渗透性随混合物成分和结构而变化的主要原因是溶解度系数的变化,而不是气体扩散能力的变化,至少对 CO2 和 N2 而言是如此。
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来源期刊
Reactive & Functional Polymers
Reactive & Functional Polymers 工程技术-高分子科学
CiteScore
8.90
自引率
5.90%
发文量
259
审稿时长
27 days
期刊介绍: Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers. Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.
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