One-step upgrading of bio-based furfural to γ-valerolactone HfCl-mediated bifunctional catalysis.

RSC Adv

State Key Laboratory Breeding Base of Green Pesticide & Agricultural Bioengineering, Key Laboratory of Green Pesticide & Agricultural Bioengineering, Ministry of Education, State-Local Joint Laboratory for Comprehensive Utilization of Biomass, Center for R&D of Fine Chemicals, Guizhou University Guiyang Guizhou 550025 China

Published: October 2021

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043276PMC
http://dx.doi.org/10.1039/d1ra05637aDOI Listing

Publication Analysis

Top Keywords

one-step upgrading
4
upgrading bio-based
4
bio-based furfural
4
furfural γ-valerolactone
4
γ-valerolactone hfcl-mediated
4
hfcl-mediated bifunctional
4
bifunctional catalysis
4
catalysis γ-valerolactone
4
gvl
4
γ-valerolactone gvl
4

Similar Publications

Enzymatic Upgrading of Biomass-Derived Aldoses to Rare Deoxy Ketoses Catalyzed by Transketolase Variants.

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 PDF

Multifunctional HMoO-MoO/Carbon Composite Particles for Water Remediation.

ACS 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 PDF

Optimizing anaerobic digestion: Benefits of mild temperature transition from thermophilic to mesophilic conditions.

Environ 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.

Article Synopsis
  • * It finds that the sharp transition results in a significant decrease in methane production (88.8%) compared to the mild transition (38.9%), along with negative impacts on cell viability and microbial interactions.
  • * The mild transition promotes better microbial connections and stability, making it a more effective method for transforming thermophilic digesters into mesophilic ones for improved anaerobic digestion performance.
View Article and Find Full Text PDF

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 PDF
Article Synopsis
  • Covalent organic frameworks (COFs) are emerging as effective photocatalysts for producing hydrogen oxide (HO) from water through the oxygen reduction reaction (ORR), but understanding their mechanisms is essential for optimization.
  • The study highlights that protonation of functional groups like imine, amine, and triazine in COFs significantly enhances their activity for HO synthesis by improving light absorption and supplying protons directly involved in the reaction.
  • The research also reveals that protonation simplifies the ORR process from a complex mediating route to a more straightforward two-electron pathway, confirming that this strategy is beneficial for designing more efficient COFs for photocatalytic applications.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!