Chelation-directed interface engineering of in-place self-cleaning membranes

Author:

Yang Xiaobin1ORCID,Li Yangxue1,Wu Dan2,Yan Linlin3,Guan Jingzhu1,Wen Yajie1,Bai Yongping1,Mamba Bhekie B.4,Darling Seth B.567ORCID,Shao Lu1ORCID

Affiliation:

1. Ministry of Industry and Information Technology Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, State Key Laboratory of Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, People’s Republic of China

2. Longjiang Environmental Protection Group CO., LTD, Harbin 150050, People’s Republic of China

3. School of Marine Science and Technology, State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Weihai 264209, People’s Republic of China

4. Institute for Nanotechnology and Water Sustainability, College of Engineering, Science and Technology, University of South Africa, Roodepoort 1709, South Africa

5. Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL 60439

6. Advanced Materials for Energy-Water Systems Energy Frontier Research Center, Argonne National Laboratory, Lemont, IL 60439

7. Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637

Abstract

Water–energy sustainability will depend upon the rapid development of advanced pressure-driven separation membranes. Although energy-efficient, water-treatment membranes are constrained by ubiquitous fouling, which may be alleviated by engineering self-cleaning membrane interfaces. In this study, a metal-polyphenol network was designed to direct the armorization of catalytic nanofilms (ca. 18 nm) on inert polymeric membranes. The chelation-directed mineralized coating exhibits high polarity, superhydrophilicity, and ultralow adhesion to crude oil, enabling cyclable crude oil-in-water emulsion separation. The in-place flux recovery rate exceeded 99.9%, alleviating the need for traditional ex situ cleaning. The chelation-directed nanoarmored membrane exhibited 48-fold and 6.8-fold figures of merit for in-place self-cleaning regeneration compared to the control membrane and simple hydraulic cleaning, respectively. Precursor interaction mechanisms were identified by density functional theory calculations. Chelation-directed armorization offers promise for sustainable applications in catalysis, biomedicine, environmental remediation, and beyond.

Funder

National Natural Science Foundation of China

DOE | SC | Basic Energy Sciences

Natural Science Foundation of Heilongjiang Province for Distinguished Young Scholars

Heilongjiang Touyan Team

Publisher

Proceedings of the National Academy of Sciences

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