The evolution of the chemical and pharmaceutical industry requires effective and less energy-intensive separation technologies. Engineering smart materials at a large scale with tunable properties for molecular separation is a challenging step to materialize this goal. Herein, we report thin film composite membranes prepared by the interfacial polymerization of porous organic cages (POCs) (RCC3 and tren cages). Ultrathin crosslinked polycage selective layers (thickness as low as 9.5 nm) are obtained with high permeance and strict molecular sieving for nanofiltration. A dual function is achieved by combining molecular separation and catalysis. This is demonstrated by impregnating the cages with highly catalytically active Pd nanoclusters ( ~ 0.7 nm). While the membrane promotes a precise molecular separation, its catalytic activity enables surface self-cleaning, by reacting with any potentially adsorbed dye and recovering the original performance. This strategy opens opportunities for the development of other smart membranes combining different functions and well-tailored abilities. 

/pdf/polycage-membranes-for-precise-molecular-separation-and-3tlhe4ks.pdf

Polycage membranes for precise molecular separation and catalysis

One of the most advanced, promising, and commercially viable research issues in the world of hydrogel dressing is gaining functionality to achieve improved therapeutic impact or even intelligent wound repair. In addition to the merits of ordinary hydrogel dressings, functional hydrogel dressings can adjust their chemical/physical properties to satisfy different wound types, carry out the corresponding reactions to actively create a healing environment conducive to wound repair, and can also control drug release to provide a long-lasting benefit. Although a lot of in-depth research has been conducted over the last few decades, very few studies have been properly summarized. In order to give researchers a basic blueprint for designing functional hydrogel dressings and to motivate them to develop ever-more intelligent wound dressings, we summarized the development of functional hydrogel dressings in recent years, as well as the current situation and future trends, in light of their preparation mechanisms and functional effects.

/pdf/advances-in-functional-hydrogel-wound-dressings-a-review-2honl4q2.pdf

Advances in Functional Hydrogel Wound Dressings: A Review

The thin-film composite (TFC) membranes fabricated by interfacial polymerization (IP) can be applied in the fields of nanofiltration (NF) and reverse osmosis (RO), which has the unparalleled advantages, such as high selectivity and permeability, small capital investment and low energy consumption, thus attracting great research interest in industry and academia field. The performance of TFC membranes is determined by their microstructure and physicochemical properties while IP monomer plays a decisive role regarding both. Over the past few decades, the researchers have paid intensive and sustained efforts to develop new IP monomers. This paper reviews these monomers and the corresponding membranes developed in recent years with the aim of establishing an intrinsic relationship between monomer structure and membrane properties. The excellent performances based on new monomers in enhancing the permeability, selectivity, anti-fouling and chemical stability of NF and RO membranes for liquid treatment are highlighted. Finally, various problems in the monomer development are summarized and the outlook for future development is also discussed. 

Effect of interfacial polymerization monomer design on the performance and structure of thin film composite nanofiltration and reverse osmosis membranes: A review

Solar‐driven synthesis of hydrogen peroxide (H2O2) through photocatalysis stands out as a promising avenue for sustainable energy generation, marked by environmental friendliness and industrial feasibility. However, the inherent limitations of carbon nitride (CN) in photocatalytic H2O2 production significantly impede their performance. Herein, a novel 0D/2D carbon dots‐modified CN nanosheet heterojunction (CDsMCN) is introduced, synthesized through a hydrothermal‐calcination tandem strategy induced by CDs derived from melamine. This innovative technique enhances the n→π* electronic transition in CDsMCN, accelerating the separation efficiency of electron‐hole pairs, boosting oxygen adsorption, and promoting a highly selective 2e− ORR. Comparative to pristine CN, CDs10MCN exhibited a remarkable tenfold increase in H2O2 production, reaching an impressive 1.48 mmol L−1. Furthermore, CDs10MCN demonstrates exceptional stability, maintaining its catalytic efficiency at the initial level over four consecutive cycles. The notable achievement of a molar selectivity of H2O2 ≈80% at an onset potential of 0.6 V (vs RHE) underscores its exceptional ability to produce the desired product selectively. Advanced in situ characterization together with DFT calculations revealed that the ultrathin CDs10MCN nanosheet heterojunction with enhanced n→π* electronic transition improves its optical properties, reduces bandgap, facilitates fast charge migration, and increases photocatalytic H2O2 performance, thereby serving as a promising candidate for advanced catalytic applications.

Nitrogen‐Rich Carbon Dot‐Mediated n→π* Electronic Transition in Carbon Nitride for Superior Photocatalytic Hydrogen Peroxide Production

Dye effluent is regarded as one of the most hazardous industrial effluents. Although loose nanofiltration (NF) membranes have been considered as an effective alternative technique for treating dye effluent, their development is still constrained by subpar permeance, separation efficiency and anti-fouling performance. In this work, a novel loose polyamide (PA) NF membrane was designed employing a conventional interfacial polymerization process using piperazine-2-carboxylic acid (PIP-COOH) and trimesoyl chloride as aqueous and organic phase monomers, respectively. The presence of unique electron-absorbing carboxyl groups on the PIP-COOH monomer not only provided abundant negative charge on the membrane surface, but also greatly reduced the reactivity, diffusion rate and solubility in n-hexane of the aqueous monomer, allowing for the formation of a more relaxed and smoother active layer. The balanced combination of pore size screening and Donnan effect achieved precise separations with high permeability. Moreover, the interaction of the carboxyl groups with the backbone structure increased the free volume of the PA layer and improved permeability significantly. The PIP-COOH/TMC membrane prepared under the optimal conditions exhibited high water permeance of 598.1 L·m−2·h−1·MPa−1, high reactive red rejection (99.3%) and low NaCl rejection (5.4%). Furthermore, the membrane possessed exceptional anti-fouling performance thanks to the ultra-smooth surface with crucial antifouling index flux recovery ratio as high as about 99%, which showed unexpected application possibilities. In conclusion, this study offers a potential novel membrane material for the development and application of loose NF membranes in the treatment of colored effluent. 

A novel loose nanofiltration membrane with high permeance and anti-fouling performance based on aqueous monomer piperazine-2-carboxylic acid for efficient dye/salt separation

Unspecific peroxygenases immobilized on Pd-loaded three-dimensional ordered macroporous (3DOM) titania photocatalyst for photo-enzyme integrated catalysis

Loose nanofiltration membrane constructed via interfacial polymerization using porous organic cage RCC3 for dye/salt separation

Shikonin (Shik), a natural pigment, has received growing interest in various biomedical fields due to its anti-inflammatory, antitumor, antimicrobial, and antioxidant ability. However, some inherent characteristics of Shik, such as its virulence, low bioavailability, and poor solubility, have limited its biomedical applicability. Here, we reported a facile synthetic method to produce the Shik-iron (III) nanoparticles (Shik-Fe NPs), which could overcome these limitations of Shik. The synthesized Shik-Fe NPs possessed a uniform size range of 110 ± 10 nm, negative surface charges, good water dispersity, and high safety. Iron distributed uniformly inside Shik-Fe NPs, and iron constituted 20% of total mass in PEGylated Shik-Fe NPs. When interacting with activated macrophages, Shik-Fe NPs significantly reduced the level of cellular inflammatory factors, for example, iNOS, IL-1β, and TNF-α. Furthermore, the Shik-Fe NPs demonstrated synergistic anti-inflammation and anti-bacterial properties in vivo, since they could release Fe3+ and Shik to eradicate bacteria (Staphylococcus aureus and P. aeruginosa were used as model microbes here) during wound infections and provide full recovery for scald wounds. Collectively, the study established a dual-functional Shik-derived nanoplatform, which could be useful for the treatment of various inflammation-involved diseases.

Nanosized Shikonin-Fe(III) Coordination Material for Synergistic Wound Treatment: An Initial Explorative Study.

Alpha-ketoglutaric acid (α-KG), as an essential intermediate in biosynthesis and drug synthesis, has a broad application prospect. However, the lower product concentration and impurities in the α-KG production make the downstream separation more complex and costly. In this study, α-KG was separated from biotransformation broth by salting-out extraction (SOE) combined with solar-driven distillation. First, the aqueous two-phase system (ATPS) consisting of acetone/(NH4)2SO4 was selected by comparison. The effects of acetone/(NH4)2SO4 concentration, temperature, α-KG concentration, and pH on the distribution behavior of α-KG in ATPS were investigated. Under the optimized conditions, higher extraction efficiency and purity of α-KG were obtained in the actual biotransformation broth. In addition, solar evaporation was used to achieve preconcentration of the organic phase and salt recovery, significantly reducing energy consumption. The method is environmentally friendly and easy to operate, providing a new idea for separating low concentration products in biosynthesis. 

Separation of α‐ketoglutaric acid by salting‐out extraction coupled with solar‐driven distillation

Abstract Nature has evolved highly efficient and complex systems to perform cascade reactions by the elegant combination of desired enzymes, offering a strategy for achieving efficient bioprocess intensification. Chemoenzymatic cascade reactions (CECRs) merge the complementary strengths of chemo-catalysis and bio-catalysis, such as the wide reactivity of chemo-catalysts and the exquisite selective properties of biocatalysts, representing an important step toward emulating nature to construct artificial systems for achieving bioprocess intensification. However, the incompatibilities between the two catalytic disciplines make CECRs highly challenging. In recent years, great advances have been made to develop strategies for constructing CECRs. In this regard, this chapter introduces the general concepts and representative strategies, including temporal compartmentalization, spatial compartmentalization and chemo-bio nanoreactors. Particularly, we focus on what platform methods and technologies can be used, and how to implement these strategies. The future challenges and strategies in this burgeoning research area are also discussed.

Integration of chemo- and bio-catalysis to intensify bioprocesses

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