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Dual-imprinted GO/TiO 2 -loaded nanocomposite membranes based on polydopamine-based and sol–gel imprinting methods were prepared for selective separation of tetracycline. [Display omitted] Molecularly imprinted membranes (MIMs) with sufficient and even-distributed recognition sites that can break the permeability-selectivity trade-off phenomenon are desirable in chemical field of selective separation. Herein graphene oxide (GO)/TiO 2 -loaded nanocomposite fibrous membranes were prepared by developing two kinds of tetracycline (TC)-imprinted systems in the same MIMs-based material. Thereinto, polydopamine-based and sol–gel-based imprinting processes were applied to the synthesis of GO/TiO 2 -loaded dual-imprinted mixed matrix membranes (GT-DIMs). The as-prepared GT-DIMs encompassed innovative GO/TiO 2 -based nanocomposite fibrous channels and two kinds of TC-imprinted systems, and critical comparisons regarding the fluxes, rebinding capacities and permselectivity were provided and studied. Importantly, dual-imprinted system of GT-DIMs could not only allow for largely enhanced rebinding result (70.63 mg/g) and fast adsorption equilibrium rate within 30 min, but also facilitate the high permselectivity of TC in complex separation systems and lab-simulated wastewater samples. The permselectivity factors were all around 5.0, which strongly demonstrated the efficiently selective recognition and separation performance of GT-DIMs. Overall, based on testing results of practical separation and scalability, excellent structural stability and separation continuity had been successfully obtained for selective separation applications of pollutants. [ABSTRACT FROM AUTHOR]

A MXene-based SA-imprinted membrane using cooperative dual-imprinting strategy has been rationally developed to obtain high-selectivity double-layer-based SA-imprinted sites for selective recognition and separation of SA. [Display omitted] Ti 3 C 2 T x (MXene) has attracted extensive attention from scholars at home and abroad due to its rich surface termination functional groups and two-dimensional multilayer structure. In this work, MXene was introduced to the membrane by vacuum-assisted filtration processes, and the formed interlayer channel facilitated the construction of recognition sites and molecular transmission. In this paper, PDA@MXene@PDA@SiO 2 -PVDF dual-imprinted mixed matrix membrane (PMS-DIMs) were developed by the cooperative dual-imprinting strategy, which was used for the adsorption of shikimic acid (SA). Firstly, SiO 2 -PVDF nanofiber basement membrane were prepared by electrospinning method and the first Polydopamine (PDA)-based imprinted layer was constructed on the membrane. PDA not only realized the imprinting process, PDA modification was used to give MXene nanosheets better antioxidant properties and to confer the SiO 2 -PVDF nanofiber membrane the interface stability. After that, the second-imprinted sites were constructed on the stacked MXene nanosheets surface as well as between the layers. The SA dual-imprinted sites significantly increased the efficiency of the selective adsorption efficiency, when the template molecule passed through the membrane, the cooperative dual-imprinting strategy enabled multiplex recognition and adsorption of template molecules. As a consequence, which greatly improving the rebinding ability(262.17 g m−2), and mselectivity factors (β Catechol/SA , β P-HB/SA , β P-NP/SA were 2.34, 4.50 and 5.68). High stability proved the potentials of the PMS-DIMs for practical application. Precise SA-recognition sites were constructed on the PMS-DIMs, PMS-DIMs not only exhibit excellent selective rebinding properties but also have high permeability. [ABSTRACT FROM AUTHOR]