γ-Valerolactone (GVL) is an attractive biomass-derived platform molecule that plays an important role in the production of biofuels and biopolymers. The synthesis of GVL from renewable biomass and its derivatives has great application prospects but also presents challenges due to the multiple conversion steps involved. Here, a HfCl-mediated acid-base bifunctional catalytic system was developed, which was demonstrated to be efficient for upgrading furfural (FF) to GVL in a single pot with unprecedented performance. The Lewis acidity of Hf and moderate basicity of HfO(OH)·HO, and strong Brønsted acidity of HCl generated from HfCl hydrolysis were found to play a synergistic role in the cascade reaction processes, mainly contributing to the pronounced catalytic activity. The effects of the key reaction parameters, such as the catalyst dosage, reaction time, and temperature, on GVL production were optimized by response surface methodology. It is worth mentioning that the recovered catalyst after thermal treatment could be directly used for the hydrogen transfer processes, like FF-to-furfuryl alcohol conversion. This catalytic strategy opens a new avenue for the selective conversion of biomass feedstocks involving multiple steps and complex processes.
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http://dx.doi.org/10.1039/d1ra05637a | DOI Listing |
ChemSusChem
December 2024
Université Clermont Auvergne, CNRS, Clermont Auvergne INP, Institut de Chimie de Clermont-Ferrand (ICCF), Clermont-Ferrand, F-63000, France.
A sustainable, convenient, scalable, one-step method for the two-carbon chain elongation of cheap and biomass-derived pentoses (l-arabinose, and 2-deoxy-d-ribose) and hexose l-rhamnose was developed to produce C deoxy ketoses (C-7 and C-8) using transketolase, an enzyme catalyzing the quasi-irreversible transfer of a ketol group from an α-keto acid to an aldehyde. Deoxygenated ketoses - commonly obtained by chemical synthesis - were afforded through a suitable combination of both nucleophile and electrophile substrates in the presence of rationally designed TK variants. Pyruvate as nucleophile with pentose l-arabinose (C-5) as electrophile gave 1-deoxy-L-gluco-heptulose (C-7), while ß-hydroxypyruvate (HPA) as nucleophile with acceptors 2-deoxy-d-ribose (C-5) and 6-deoxy-l-mannose (l-rhamnose) (C-6) led to formation of 4-deoxy-d-altro-heptulose (C-7) and 8-deoxy-l-glycero-l-galacto-octulose (C-8), respectively.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Advanced Ceramics Research Center, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Aichi, Japan.
Solving a scarcity of freshwater resources is an urgent global challenge by a safe and sustainable approach using renewable energy. We demonstrate the multifunctional catalyst of HMoO-MoO/carbon composite particles toward highly efficient water remediation. A one-step mechanochemical reaction successfully upgraded the composites from commercially available MoO-polypropylene (PP) powders without introducing hydrogen gas.
View Article and Find Full Text PDFEnviron Sci Ecotechnol
September 2024
Shanghai Key Lab for Urban Ecological Processes and Eco-Restoration, Shanghai Engineering Research Center of Biotransformation of Organic Solid Waste, School of Ecological and Environmental Sciences, East China Normal University, Shanghai, 200241, China.
Sci Rep
May 2024
Faculty of Chemistry, Silesian University of Technology, 44-100, Gliwice, Poland.
Transforming amines with low boiling points and high volatilities into protic salts is a versatile strategy to utilize low molecular weight compounds as precursors for N-doped carbon structures in a straightforward carbonization procedure. Herein, conventional mineral acids commonly used for the synthesis of protic salts were replaced by bio-derived phytic acid, which, combined with various amines and amino acids, yielded partially or fully bio-derived protic salts. The biomass-based salts showed higher char-forming ability than their mineral acid-based analogs (up to 55.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
School of Chemical Science and Engineering, Tongji University, Shanghai, 200092, P.R. China.
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