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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Mixed-matrix membranes based on 6FDA-ODA polyimide and silicalite-1 with homogeneous spatial distribution of particles
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Mixed-matrix membranes based on 6FDA-ODA polyimide and silicalite-1 with homogeneous spatial distribution of particles

机译:基于6FDA-ODA聚酰亚胺的混合基质膜和硅沸石-1颗粒的均匀空间分布

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We report an experimental procedure leading to defect-free mixed-matrix membranes with a homogeneous spatial distribution of filler particles, volume fractions of which are within the interval [0.10, 0.35]. A polyimide matrix was synthesized from 4,4'-(hexafluoroisopropylidene) diphtalic anhydride and 4,4'-oxydianiline in the solution with N,N-dimethylformamide. (3-aminopropyl) triethoxysilane was used as a linker to improve the phase contact between silicalite-1 particles and the polyimide matrix. We found that a homogeneous spatial distribution of particles in the resulting membrane was achieved if kinematic viscosity of a polyimide precursor solution was greater than 9.5 cm(2) s(-1). To do so, an initial mass fraction of the solids in the solution, a reaction temperature and a concentration of water in the solvent had to carefully be selected and controlled. Besides these conditions, we fine-tuned the process of imidization, particularly the rate of evaporation of N,N-dimethylformamide. We arrived at the conclusion that its effect on reproducibility of the entire process was minor rather than major. In addition, we characterised microstructures of the resulting membranes by imaging in a scanning electron microscope. In this context we examined two ways of preparation of membrane specimens and showed that back-scattered electron imaging of polished sections obtained using a metallographic technique clearly outperformed the often-used imaging of fractured surfaces. Finally, we evaluated the homogeneity of spatial distributions of particles by means of morphological descriptors, namely a position-dependent volume fraction of the silicalite-1 phase.
机译:我们报告了一种导致无缺陷的混合基质膜的实验程序,其具有均匀的填料颗粒的空间分布,其体积分数在间隔内[0.10,0.35]。用N,N-二甲基甲酰胺的溶液中的4,4' - (六氟异丙基)二苯甲酸酐和4,4'- oxydianiline合成聚酰亚胺基质。 (3-氨基丙基)三乙氧基硅烷用作接头以改善硅沸石-1颗粒和聚酰亚胺基质之间的相位接触。我们发现,如果聚酰亚胺前体溶液的运动粘度大于9.5cm(2)s(-1),则达到所得膜中颗粒的均匀空间分布。为此,必须仔细选择和控制溶液中固体的初始质量分数,溶剂中的反应温度和水浓度。除了这些条件外,我们微调了酰亚胺化的过程,特别是N,N-二甲基甲酰胺的蒸发速率。我们得出结论,其对整个过程的再现性的影响是较小的,而不是主要的。另外,我们通过在扫描电子显微镜中成像来表征所得膜的微观结构。在这种情况下,我们检查了两种制备膜样品的方式,并显示了使用金相技术获得的抛光部分的背散射电子成像显然优于裂缝表面的经常使用的成像。最后,我们通过形态描述符评估了颗粒的空间分布的均匀性,即硅沸石-1相的位置依赖性体积分数。

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