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The accurate protein-protein separation is important but technically challenging. Achieving such a precise separation using membrane requires the selective channels with appropriate pore geometry structure and high anti-fouling property. In this study, polyethersulfone-b-poly(sulfobetaine methyl methacrylate) (PES-b-PSBMA) was synthesized and engineered onto polysulfone (PSF) ultrafiltration (UF) membrane to fabricate zwitterionic nanospheres engineered co-polymer (ZN-e-CoP) composite membrane via dynamic self-assembly micelle deposition. On the one hand, self-assembly zwitterionic nanospheres were used as blocks to construct hydrophilic layers with size-dependent sieving channels, endowing ZN-e-CoP composite membranes with enhanced permselectivity and protein-protein separation abilities, meanwhile zwitterionic groups from nanospheres reinforced the structure stability of nanospheres/nanospheres and nanospheres/membrane via multiple intermolecular interactions. On the other hand, zwitterionic nanospheres can induce to produce the hydration layer enveloping themselves by binding water molecules, where hydration layer acts as a protective barrier on the membrane surface, impeding the protein adhesion. Hence, ZN-e-CoP_1a composite membrane exhibited superior separation properties with Lysozyme/Bovine Serum Albumin (BSA) separation factor of 18.1 and 95.4 % rejection against BSA, 10.1 and 2.3 times, respectively, higher these of pristine PSF membrane (1.8 and 42.1 %), without obviously sacrificing water flux. Simultaneously, hydration layer enables the ZN-e-CoP_1a membrane with enhanced anti-fouling performance and durability during the long-term operations. The proposed approach opens new pathways to fabricate excellent anti-fouling membranes for precise protein-protein separation., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Under the environmental sustainability concept, landfill leachate concentrate can be up-cycled as a useful resource. Practical strategy for effective management of landfill leachate concentrate is to recover the existing humate as fertilizer purpose for plant growth. Herein, we designed an electro-neutral nanofiltration membrane to separate the humate and inorganic salts for achieving a sufficient humate recovery from leachate concentrate. The electro-neutral nanofiltration membrane yielded a high retention of humate (96.54 %) with an extremely low salt rejection (3.47 %), tremendously outperforming the state-of-the-art nanofiltration membranes and exhibiting superior promise in fractionation of humate and inorganic salts. With implementation of the pressure-driven concentration process, the electro-neutral nanofiltration membrane enriched the humate from 1756 to 51,466 mg∙L -1 at a fold of 32.6, enabling 90.0 % humate recovery and 96.4 % desalination efficiency from landfill leachate concentrate. Furthermore, the recovered humate not only exerted no phytotoxicity, but also significantly promoted the metabolism of red bean plants, serving as an effective green fertilizer. The study provides a conceptual and technical platform using high-performance electro-neutral nanofiltration membranes to extract the humate as a promising nutrient for fertilizer application, in view of sustainable landfill leachate concentrate treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

In this work, a recyclable self-floating A-GUN-coated (Ag/AgCl@g-C 3 N 4 @UIO-66(NH 2 )-coated) foam was fabricated for effective inactivation of Microcystis aeruginosa (M. aeruginosa) under visible light. The floating photocatalyst was able to inactivate 98% of M. aeruginosa within 180 min under the visible-light irrigation, and the floating photocatalyst exhibited a stable performance in various conditions. Moreover, the inactivation efficiency can still maintain nearly 92% after five times recycle experiments, showing excellent photocatalytic stability. Furthermore, effects of A-GUN/SMF floating catalyst on the physiological properties, cellular organics, and algal functional groups of M. aeruginosa were studied. The floating photocatalyst can not only make full use of excellent photocatalytic activities of A-GUN nanocomposite, but also promote contact between catalyst and algae, and realize the effective recovery of the photocatalyst. Finally, possible photocatalytic inactivation mechanisms of algae were obtained, which provides references for removing cyanobacteria blooms in real water bodies., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Effective extraction of useful resources from high-salinity textile wastewater is a critical pathway for sustainable wastewater management. In this study, an integrated loose nanofiltration-electrodialysis process was explored for simultaneous recovery of dyes, NaCl and pure water from high-salinity textile wastewater, thus closing the material loop and minimizing waste emission. Specifically, a loose nanofiltration membrane (molecular weight cutoff of ~800 Da) was proposed to fractionate the dye and NaCl in the high-salinity textile wastewater. Through a nanofiltration-diafiltration unit, including a pre-concentration stage and a constant-volume diafiltration stage, the dye could be recovered from the high-salinity textile wastewater, being enriched at a factor of ~9.0, i.e., from 2.01 to 17.9 g·L -1 with 98.4% purity. Assisted with the subsequent implementation of electrodialysis, the NaCl concentrate and pure water were effectively reclaimed from the salt-containing permeate coming from the loose nanofiltration-diafiltration. Simultaneously, the produced pure water was further recycled to the nanofiltration-diafiltration unit. This study shows the potential of the integration of loose nanofiltation-diafiltration with electrodialysis for sufficient resource extraction from high-salinity textile wastewater., (Copyright © 2021 Elsevier B.V. All rights reserved.)

A novel plasmonic Ag/AgCl@LaFeO 3 (ALFO) photocatalyst was successfully synthesized by a simple in-situ synthesis method with enhanced photocatalytic activity under visible light for harmful algal blooms (HABs) control. The structure, morphology, chemical states, optical and electrochemical properties of the photocatalyst were systematically investigated using a series of characterization methods. Compared with pure LaFeO 3 and Ag/AgCl, ALFO-20% owned a higher light absorption capacity and lower electron-hole recombined rate. Therefore, ALFO-20% had higher photocatalytic activity with a near 100% removal rate of chlorophyll a within 150 min, whose kinetic constant was 15.36 and 9.61 times faster than those of LaFeO 3 and Ag/AgCl. In addition, the changes of zeta potential, cell membrane permeability, cell morphology, organic matter, total soluble protein, photosynthetic system and antioxidant enzyme system in Microcystis aeruginosa (M. aeruginosa) were studied to explore the mechanism of M. aeruginosa photocatalytic inactivation. The results showed that ALFO-20% could change the permeability and morphology of the algae cell membrane, as well as destroy the photosynthesis system and antioxidant system of M. aeruginosa. What's more, ALFO could further degrade the organic matters flowed out after algae rupture and die, reducing the secondary pollution and avoiding the recurrence of HABs. Finally, the species of reactive oxygen species (ROS) (mainly •O 2 - and •OH) produced by ALFO were determined through quenching experiments, and a possible photocatalytic mechanism was proposed. Overall, ALFO can efficiently remove the harmful algae under the visible light, providing a promising method for controlling HABs., (Copyright © 2021 Elsevier B.V. All rights reserved.)

In this work, a novel Ag/AgCl@g-C 3 N 4 @UIO-66(NH 2 ) heterojunction was constructed for photocatalytic inactivation of Microcystis aeruginosa (M. aeruginosa) under visible light. The photocatalyst was synthesized by a facile method and characterized by XRD, SEM, TEM, BET, XPS, FT-IR, UV-vis DRS, PL and EIS. The nanocomposite can not only provide lots of active sites, but also improve capacities to utilize visible-light energy and effectively transfer charge carriers, thus enhancing removal efficiencies of cyanobacteria (99.9% chlorophyll a was degraded within 180 min). Various factors in photodegradation of chlorophyll a were studied. Besides, changes on cellular morphologies, membrane permeability, physiological activities of M. aeruginosa during photocatalysis were investigated. Moreover, the cycle test indicated that Ag/AgCl@g-C 3 N 4 @UIO-66(NH 2 ) exhibits excellent reusability and photocatalytic stability. Finally, a possible mechanism of M. aeruginosa inactivation was proposed. In a word, Ag/AgCl@g-C 3 N 4 @UIO-66(NH 2 ) can efficiently inactivate cyanobacteria under visible light, thus providing useful references for further removal of harmful algae in real water bodies., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Developing a highly efficient, cost-effective, easily scalable and sustainable cathode for oxygen reduction reaction (ORR) is a crucial challenge in terms of future "green" energy conversion technologies, e.g., microbial fuel cells (MFCs). In this study, a natural and widely available lotus leaf with intrinsically hierarchical structure was employed to serve as the single precursor to prepare the catalyst applied as the MFC cathode. The hierarchically particle-coated bio‑carbon was self-constructed from the lotus leaf, which yielded a large specific surface area, highly porous structure and superhydrophobicity via facile pyrolysis coupling hydrothermal activation by ZnCl 2 /(NH 4 ) 2 SO 4 . Electrochemical evaluation demonstrated that these natural leaf-derived carbons have an efficient ORR activity. Specifically, the HC-900 catalyst with hydrothermal activation achieved an onset potential of -0.015 V vs. Ag/AgCl, which was comparable to the commercial Pt/C catalyst (-0.010 V vs. Ag/AgCl) and was more efficient than the DC-900 catalyst through direct pyrolysis. Furthermore, the HC-900 catalyst achieved an outstanding ORR activity via a one-step and four-electron pathway, exhibiting a potential alternative to Pt/C as electrocatalyst in ORR, due to its better long-term durability and methanol resistance. Additionally, the HC-900 catalyst was applied as an effective electrocatalytic cathode in an MFC system with a maximum power density of 511.5 ± 25.6 mW⋅m -2 , exhibiting a superior energy harvesting capacity to the Pt/C cathode., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Alkaline glyphosate neutralization liquors containing a high salinity pose a severe environmental pollution problem by the pesticide industry. However, there is a high potential for glyphosate recovery due to the high concentration of glyphosate in the neutralization liquors. In the study, a three-compartment bipolar membrane electrodialysis (BMED) process was applied on pilot scale for the recovery of glyphosate and the production of base/acid with high concentration in view of zero discharge of wastewater. The experimental results demonstrate that BMED can remove 99.0% of NaCl from the feed solution and transform this fraction into HCl and NaOH with high concentration and purity. This is recycled for the hydrolysis reaction of the intermediate product generated by the means of the Mannich reaction of paraformaldehyde, glycine and dimethylphosphite catalyzed by triethylamine in the presence of HCl and reclamation of the triethylamine catalyst during the production process of glyphosate. The recovery of glyphosate in the feed solution was over 96%, which is acceptable for industrial production. The current efficiency for producing NaOH with a concentration of 2.0 mol L(-1) is above 67% and the corresponding energy consumption is 2.97 kWh kg(-1) at a current density of 60 mA cm(-2). The current efficiency increases and energy consumption decreases as the current density decreases, to 87.13% and 2.37 kWh kg(-1), respectively, at a current density of 30 mA cm(-2). Thus, BMED has a high potential for desalination of glyphosate neutralization liquor and glyphosate recovery, aiming at zero discharge and resource recycling in industrial application., (Copyright © 2013 Elsevier B.V. All rights reserved.)