Facile fabrication of amorphous Al/Fe based metal-organic framework as effective heterogeneous fenton catalyst for environmental remediation.

This study presents a facile preparation and durable amorphous Fe and Al-based MOF nanoplate (AlFe-BTC MOFs) catalyst with notable stability in Fenton reactions. Rigorous characterization using XRD, HR-TEM, and BET confirms the amorphous nature of the synthesized AlFe-BTC MOFs, revealing mesopores (3.4 nm diameter), a substantial surface area (232 m2/g), and a pore volume of 0.69 cc/g. XPS analysis delineates distinct Al2p and Fe2p binding energy values, signifying specific chemical bonding. FE-SEM elemental mapping elucidates the distinctive distribution of Fe and Al within the framework of AlFe-BTC MOFs. In catalytic activity testing, the amorphous AlFe-BTC MOFs exhibited outstanding performance, achieving complete degradation of Methylene blue (MB) dye and 78% TOC removal over 45 min of treatment under mild reaction conditions. The catalyst's durability was assessed, revealing about 75% TOC removal and complete dye decomposition over five successive recycles, with less than 1 mg/L of Fe and Al leaching. UV-Vis spectra revealed the destruction of MB dye over multiple recycling studies. Based on this finding, the amorphous AlFe-BTC MOF nanoplates emerge as a promising solution for efficient dye removal from industrial wastewater, underscoring their potential in advanced environmental remediation processes.

Stabilizing a zinc anode via a tunable covalent organic framework-based solid electrolyte interphase.

Zinc (Zn) is an excellent material for use as an anode for rechargeable batteries in water-based electrolytes. Nevertheless, the high activity of water leads to Zn corrosion and hydrogen evolution, along with the formation of dendrites on the Zn surface during repeated charge-discharge (CD) cycles. To protect the Zn anode and limit parasitic side reactions, an artificial solid electrolyte interphase (ASEI) protective layer is an effective strategy. Herein, an ASEI made of a covalent organic framework (COFs: HqTp and BpTp) was fabricated on the surface of a Zn anode via Schiff base reactions of aldehyde and amine linkers. It is seen that COFs can regulate the Zn-ion flux, resulting in dendritic-free Zn. COFs can also mitigate the formation of an irreversible passive layer and the hydrogen evolution reaction (HER). Zn plating/stripping tests using a symmetrical cell suggest that HqTpCOF@Zn shows superior stability and greater coulombic efficiency (CE) compared to bare Zn. The full cell having COFs@Zn also displays much improved cyclability. As a result, the COF proves to be a promising ASEI material to enhance the stability of the Zn anode in aqueous media.

Unraveling the inhibition mechanism of cyanidin-3-sophoroside on polyphenol oxidase and its effect on enzymatic browning of apples.

The hunt for anti-browning agents in the food and agricultural industries aims to minimize nutritional loss and prolong post harvest storage. In the present study, the effect of cyanidin-3-sophoroside (CS) from Garcinia mangostana rind, on polyphenol oxidase (PPO) activity was investigated. The non-competitive inhibition mode of CS was determined by Lineweaver Burk plot. CS forms a ground-state complex by quenching the intrinsic fluorescence of PPO. The static quenching was temperature-dependent with an activation energy of 4.654±0.1091kJmol-1 to withstand the disruption of amino acid residues of the enzyme binding site. The enzyme conformational change was validated by 3D fluorescence and CD spectrum. Docking (binding energy -8.124kcal/mol) and simulation studies confirmed the binding pattern and stability. CS decreased PPO activity and browning index of fresh cut apples and prolonged the shelf life. Thus, CS appears to be a promising anti-browning agent to control enzymatic browning.