Solvent-resistant Triazine-Piperazine Linked Porous Covalent Organic Polymer Thin-film Nanofiltration Membrane
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Biological and Environmental Sciences and Engineering (BESE) Division
Chemical Engineering Program
Physical Science and Engineering (PSE) Division
Online Publication Date2018-12-21
Print Publication Date2019-04
Permanent link to this recordhttp://hdl.handle.net/10754/630379
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AbstractWe present the fabrication of a novel porous covalent organic triazine-piperazine based membrane (CTP membrane) for solvent nanofiltration. The porous CTP skin layer grows on the top surface of polyacrylonitrile (PAN) support in presence of N, N-diisopropylethylamine (DIPEA) in the water/heptane interfacial reaction. The CTP skin layer membrane showed solvent-resistant property to a wide range of common solvents such as DMF, DMSO, and NMP; the stability of the composite membrane is limited by the PAN support. Chemical bonding and elemental analyses confirm the incorporation and linking of the triazine and piperazine components in the nanofilms skeleton. Electron microscopic image analysis demonstrates that the CTP skin layer nicely covers the PAN support and has porous and crumple morphology. The membrane exhibits excellent NF properties as demonstrated by the selective dye rejection and salt rejection experiment. The CTP membrane showed dye rejection (Reactive black-5; MW 992 gmol−1) and salt rejection (Na2SO4) 96.7%, and 91.3%, respectively. The membrane comprised a stable porous robust structure, large surface area, well-defined pore topology, and solvent durability coupled with the zeta potential. All of these cooperatively benefits to achieve superior performances in separation, reusability with high permeance, leading to state of the art performance in the NF application.
CitationDas SK, Manchanda P, Peinemann K-V (2019) Solvent-resistant triazine-piperazine linked porous covalent organic polymer thin-film nanofiltration membrane. Separation and Purification Technology 213: 348–358. Available: http://dx.doi.org/10.1016/j.seppur.2018.12.046.
SponsorsWe gratefully acknowledge the financial support from the King Abdullah University of Science and Technology (KAUST), Centre Competitive Research grant FCC/1/1972, and Baseline FundBAS/1/1332. The authors also acknowledge Abdul-Hamid Emwas for the NMR analysis.