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Nanoporous organic polymers (NPOPs) have emerged as versatile materials with robust thermal stability, large surface area (up to 2500 m g), and customizable porosity, making them ideal candidates for advanced hydrogen (H) storage applications. This review provides a comprehensive analysis of various NPOPs, including covalent organic frameworks (COFs), hypercrosslinked polymers (HCLPs), conjugated microporous polymers (CMPs), and porous aromatic frameworks (POAFs). Notably, these materials demonstrate superior H storage capacities, achieving up to 10 wt% at cryogenic temperatures, which is essential for applying H as a clean energy carrier.

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Polysaccharides-Directed Biomineralization of Enzymes in Hierarchical Zeolite Imidazolate Frameworks for Electrochemical Detection of Phenols.

ACS Appl Mater Interfaces

January 2025

Lab of Applied Biocatalysis, National Engineering Research Center of Wheat and Corn Further Processing, School of Food Science and Engineering, South China University of Technology, No. 381 Wushan Road, Guangzhou 510640, Guangdong China.

Biomineralization of enzymes inside rigid metal-organic frameworks (MOFs) is appealing due to its biocompatibility and simplicity. However, this strategy has hitherto been limited to microporous MOFs, leading to low apparent enzymatic activity. In this study, polysaccharide sodium alginate is introduced during the biomineralization of enzymes in zeolitic imidazolate frameworks (ZIFs) to competitively coordinate with metal ions, which endows the encapsulated enzyme with a 7-fold higher activity than that in microporous ZIFs.

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This work aimed to investigate the adsorption of organic compounds (4-nitroaniline and 4-chlorophenoxyacetic acid) on activated carbon in the presence of selected dyes (uranine and Acid Red 88) and surfactants (sodium dodecyl sulfate and hexadecyltrimethylammonium bromide). The adsorbent, i.e.

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Tailoring the Porous Structure of Carbon for Enhanced Oxidative Cleavage and Esterification of C(CO)-C Bonds.

ChemSusChem

December 2024

National & Local Joint Engineering Research Center on Biomass Resource Utilization, College of Environmental Science and Engineering, Nankai University, Tianjin, 300350, P. R. China.

The cleavage and functionalization of carbon-carbon bonds are crucial for the reconstruction and upgrading of organic matrices, particularly in the valorization of biomass, plastics, and fossil resources. However, the inherent kinetic inertness and thermodynamic stability of C-C σ bonds make this process challenging. Herein, we fabricated a glucose-derived defect-rich hierarchical porous carbon as a heterogeneous catalyst for the oxidative cleavage and esterification of C(CO)-C bonds.

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This study introduces the first metal organic framework using ammelide as the organic ligand, showcasing stability in boiling water and high sensitivity in detecting dichromate ions.

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