Institutional Repository of Institute of Process Engineering, CAS (IPE-IR)
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Catalytic template assisted interfacial polymerization for high-performance acid-resistant membrane preparation
Highly permeable acid-resistant nanofiltration (NF) membranes are of critical significance for the efficient treatment of acidic streams. Enhancing permeability while maintaining the high solute rejection of acid-resistant NF membranes remains a great challenge due to the low reactivity of monomers. In this work, a novel catalytic template assisted interfacial polymerization (IP) strategy of 3-aminobenzenesulfonamide (ABSA) and trimesoyl chloride (TMC) was provided to prepare a poly(amide-sulfonamide) membrane. Aminopyridine doped graphene quantum dots rich in acylation catalytic sites and ZIF-8 nanoparticles are co-loaded on a substrate as template. Benefiting from the enhanced phase integrity and self-inhibition effect of the template assisted IP process, the resulting ultra-thin acid-resistant membrane exhibits an excellent water permeance (20.4 Lm(-2)h(-1)bar(-1)) with a high Na2SO4 rejection of 90.5%, which outperforms almost all the reported acid-resistant NF membranes. Our work paves a versatile way for synthesis of special separation membranes
Bioelectrocatalysis for CO2 reduction: recent advances and challenges to develop a sustainable system for CO2 utilization
Activation and turning CO2 into value added products is a promising orientation to address environmental issues caused by CO2 emission. Currently, electrocatalysis has a potent well-established role for CO2 reduction with fast electron transfer rate; but it is challenged by the poor selectivity and low faradic efficiency. On the other side, biocatalysis, including enzymes and microbes, has been also employed for CO2 conversion to target Cn products with remarkably high selectivity; however, low solubility of CO2 in the liquid reaction phase seriously affects the catalytic efficiency. Therefore, a new synergistic role in bioelectrocatalysis for CO2 reduction is emerging thanks to its outstanding selectivity, high faradic efficiency, and desirable valuable Cn products under mild condition that are surveyed in this review. Herein, we comprehensively discuss the results already obtained for the inte-gration craft of enzymatic-electrocatalysis and microbial-electrocatalysis technologies. In addition, the intrinsic nature of the combination is highly dependent on the electron transfer. Thus, both direct electron transfer and mediated electron transfer routes are modeled and concluded. We also explore the biocompatibility and syn-ergistic effects of electrode materials, which emerge in combination with tuned enzymes and microbes to improve catalytic performance. The system by integrating solar energy driven photo-electrochemical technics with bio-catalysis is further discussed. We finally highlight the significant findings and perspectives that have provided strong foundations for the remarkable development of green and sustainable bioelectrocatalysis for CO2 reduction, and that offer a blueprint for Cn valuable products originate from CO2 under efficient and mild conditions