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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]

Au/SiO 2 -pDA-based nanocomposite ovalbumin-imprinted membranes with controllable biocompatibility/selectivity were first proposed and developed for the achievements of thermo-responsive recognition ability and reversible cell adhesion/detachment. Inspired by the biomimetic modification strategy of dopamine self-polymerization technique, molecularly imprinted nanocomposite membranes (MINCMs) with thermo-responsive rebinding and separation performance were synthesized and evaluated. Herein, the Au/SiO 2 -based multilevel structure had been successfully obtained onto the polydopamine (pDA) modified membrane surfaces. Afterward, the poly(N -isopropylacrylamide)-based biomolecule-imprinted sites were adequately constructed by developing a photoinitiated atom transfer radical polymerization (pATRP) imprinting strategy using the high-biocompatible ovalbumin (Ova, pI 4.6) as template molecule. Therefore, thermo-responsive 'specific recognition sites' toward Ova were then achieved on the as-prepared MINCMs after the well-designed imprinting process. When the external temperature was set at 37 °C, excellent ovalbumin rebinding capacity (33.26 mg/g), selectivity factor (3.06) and structural stability were obtained. Importantly, as to the controllable biocompatibility research of this work, the bare glass and Ova-bound-MINCMs (the MINCMs were bound with Ova) showed basically the same cell adhesion behaviors and viability, indicating the excellent biocompatibility of the Ova-bound-MINCMs. Additionally, efficient and rapid regulation of cell adhesion/detachment on ovalbumin-bound MINCMs could be still obtained even after 10 cycles of temperature-switch process, which indicated that the as-prepared MINCMs had strong ability to work under high intensity and long continuous operation. [ABSTRACT FROM AUTHOR]

PDA-induced molecularly imprinted nanocomposite membranes with three-dimensional MOFs-based imprinting structure, in which propranolol was template molecule, was constructed based on our newly-developed synergetic synthesis strategy of the sol-gel imprinting-initiated system. [Display omitted] Molecularly imprinted nanocomposite membranes with three-dimensional metal–organic frameworks (MOFs)-based structure (MINMs-TM) were successfully prepared by using propranolol as template molecule. Importantly, for the first time, polycarbonate track etch membranes had been used as the supporting surfaces to construct the polydopamine (PDA)-induced MOFs composite structure, in which the as-prepared PDA-modified surface would promote the crystallization and nucleation of ZIF-8-based composite layer. Based on the entire preparation processes of our design, the as-prepared PDA-induced ZIF-8-modified surfaces could be regarded as the imprinted-initiated units of sol–gel imprinting polymerization. Abundant recognition sits of propranolol were achieved in MINMs-TM, which showed characteristic properties of permeability and selectivity. Therefore, high adsorption capacity (41.31 mg/g) and fast adsorption equilibrium rate (within 30 min) had been successfully achieved. Meanwhile, excellent permselectivity rates (β) of MINMs-TM toward propranolol were also obtained as 5.04, 4.79 and 5.14, which MINMs-TM the successful synthesis of high-affinity and high-density propranolol-imprinted sites. Overall, for the practical selective separation and scalability, we had successfully MINMs-TM the preparation of MINMs-TM-based to selective rebinding and separation of propranolol from complex solution system and mimetic water sample, which had further confirmed the desired and potential applications of many environmental pollutants. [ABSTRACT FROM AUTHOR]