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In situ-generated yttrium-based nanoparticle/polyethersulfone composite adsorptive membranes: Development, characterization, and membrane formation mechanism

机译:原位产生的基于钇的纳米粒子/聚醚砜复合吸附膜:显影,表征和膜形成机制

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In this study, a series of in situ-generated yttrium-based nanoparticle (NP)/polyethersulfone (PES) composite adsorptive membranes were prepared by the phase inversion method for the first time. The Y (NO3)(3)center dot 6H(2)O as precursor, uniformly dispersed at the molecular level in casting solution, reacted with OH- in a coagulation bath and ambient CO2 during the phase inversion process. The Y(CO3)(0.5)(OH)(2) NPs were formed in situ and distributed homogeneously in a PES matrix, which was confirmed by X-ray photoelectron spectroscopy (XPS) and Energy Dispersive X-Ray Spectroscopy (EDS) results. The compatibility of the nanocomposite membranes was improved by an in situ preparation method. With the increase in content of Y-based NPs in composite membranes, the surface hydrophilicity and water permeability first increased from M1 to M2, and then slightly decreased from M3 to M5, which was mainly related to membrane structure. From M1 to M5, the demixing way changed from instantaneous demixing to delayed demixing process as a result of thermodynamic enhancement and viscosity hindrance in the phase inversion process. A higher demixing rate led to a structure with large finger-like macro-voids, i.e., M1, whereas a lower demixing rate caused the suppression of finger-like macro-voids, i.e., M5. More importantly, the adsorption study indicated that the nanocomposite adsorptive membranes were stable in the treatment of fluoride-containing water, with no leakage of Y-based NPs from membrane matrix to solution. It is expected that the in situ preparation technique could be used to produce next-generation nanocomposite adsorptive membranes with improved comprehensive properties for application in water treatment. (C) 2018 Elsevier Inc. All rights reserved.
机译:在该研究中,通过第一次反相方法制备了一系列原位产生的基于钇基纳米粒子(NP)/聚醚砜(PES)复合吸附膜。 Y(NO3)(3)中心点6H(2)o作为前体,均匀地分散在浇铸溶液中的分子水平,在相常反转过程中与OH-在凝固浴和环境CO2中反应。 Y(CO 3)(0.5)(OH)(2)(2)(2)NPS原位形成并在PES基质中均匀分布,该PES基质通过X射线光电子能谱(XPS)和能量分散X射线光谱(EDS)结果证实。通过原位制备方法改善了纳米复合膜的相容性。随着复合膜中的Y基NP含量的增加,表面亲水性和水渗透率首先从M1至M2增加,然后从M3至M5略微降低,其主要与膜结构有关。从M1到M5,由于热力学增强和相位反转过程中的热力学增强和粘度障碍,脱模方式从瞬时解剖到延迟脱模过程。更高的解速速率导致具有大的指状宏观空隙的结构,即M1,较低的解剖率导致抑制指状宏空隙,即M5。更重要的是,吸附研究表明,纳米复合吸附膜在处理含氟水中是稳定的,没有Y基NPS从膜基质到溶液的泄漏。预期,原位制备技术可用于生产下一代纳米复合材料吸附膜,具有改进的综合性能,用于在水处理中的应用。 (c)2018 Elsevier Inc.保留所有权利。

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