CoFeO modified bentonite-based mixed matrix loose nanofiltration membranes for effective wastewater treatment.

Chemosphere

Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Bengaluru, 562112, Karnataka, India; School of Polymer Science and Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju, 61186, South Korea. Electronic address:

Published: February 2024

Mixed-matrix membranes (MMMs) with an ideal polymer/hydrophilic flux enhancer interface considerably recuperates the separation and purification performance of membrane. In this direction, a novel CoFeO functionalized natural clay-bentonite (CoFeO@BT) material as a compatible flux enhancer was synthesized for preparation of mixed matrix based in polyethersulfone (PES) matrix. Here, the influences of CoFeO@BT on the morphology and performance of the MMMs membranes were systematically investigated using various analytical techniques. Meanwhile, the water flux and sepration eficiency of the CoFeO@BT-PES membranes significantly enhanced due to the incorporation of CoFeO@BT that altered hydrophilicity, pore and surface characteristic features. The water flux as well as separation efficiency range up to 95%, 94.69%, 94.16% of Congo red (CR), Crystal violet (CV), and humic acid (HA) respectively. Meanwhile, the fouling parameters demonstrated that the CoFeO@BT-PES membranes exhibited better antifouling property in the long term experiment comparing with commercial polyamide membrane. CoFeO@BT material incorporated membranes showed less decline ratio and a better recovery ratio. The high rejection of dyes with a high permeation flux of the newly designed membranes indicated an amazing possibility for dye purification. In this study, a potential dye mechanism for composite membranes impacted by synthetic CoFeO@BT was also put forth. Within the context of application considerations for environmental protection, new materials stock in membranes show good potential for the separation of different organic contaminants.

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http://dx.doi.org/10.1016/j.chemosphere.2023.141051DOI Listing

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