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5-Hydroxymethylfurfural (HMF) is a versatile carbohydrate-derived platform chemical that has been used for the synthesis of a number of commercially valuable compounds. In this study, several chromium (Cr)-doped, biomass-derived hydrochar catalysts were synthesized via the one-pot method using starch, eucalyptus wood, and bagasse as carbon sources. Then, the performance of these synthesized materials for the catalytic conversion of glucose into HMF was evaluated by, primarily, the yield of HMF. The synergistic interactions between the Cr salt and the different biomass components were investigated, along with their effects on the catalytic efficiency. The differences in the catalytic activity of the synthesized materials were analyzed through structural characterization, as well as assessments of the acid density and strength. Among the catalysts, CrBHC derived from bagasse presented the highest activity, achieving an HMF yield of 64.5% in an aqueous solvent system of dimethyl sulfoxide (DMSO) and saturated sodium chloride (NaCl) at 170 °C after 5 h. After four cycles, the HMF yield of CrBHC decreased to 38.7%. Characterization techniques such as N adsorption-desorption and Py-FTIR suggested that such a decline in the HMF yield is due to pore blockage and acid site coverage by humic by-products, as demonstrated by the fact that regeneration by calcination at 300 °C restored the HMF yield to 50.5%.
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http://dx.doi.org/10.3390/polym17101413 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
International Joint Research Center for Photoresponsive Molecules and Materials, School of Chemical and Material Engineering, Jiangnan University, Lihu Street 1800, Wuxi, 214122, P.R. China.
Electrocatalytic coupling of nitrate reduction (NORR) to ammonia with 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA) enables simultaneous wastewater remediation and biomass valorization. However, developing efficient bifunctional electrocatalysts for these multiproton-coupled electron transfer reactions remains challenging as conventional single-active-site catalysts inherently suffer from linear scaling relationships between intermediates and adsorption energies, particularly sluggish proton transfer. To address this, we engineered a triphasic N-doped CuO@CoO@Ni(OH) heterostructure with a gradient built-in electric field (BIEF), which synergistically enhances interfacial charge polarization and accelerates proton transport through dynamic coupling effects in both reactions: sufficient *H supply for NORR and fast Ni(OH)/NiOOH redox cycling during HMF oxidation (HMFOR), thus achieving unprecedented bifunctional performance: at - 0.
View Article and Find Full Text PDFSmall
September 2025
The Liaoning Province Key Laboratory of Paper and Pulp Engineering, The Key Laboratory of High Value Utilization of Botanical Resources of China, Light Industry College of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian, 116034, China.
2,5-Furandicarboxylic acid (FDCA), synthesized via selective oxidation of 5-hydroxymethylfurfural (HMF), is a structural analog to petroleum-derived terephthalic acid (PTA) and a key precursor for renewable polyesters like polyethylene furanoate (PEF). Recent advances in electrocatalytic HMF oxidation (HMFOR) enable efficient synthesis under mild conditions, aligning with renewable energy integration. In this work, catalysts with oxygen-rich vacancies by growing Ce, V bimetallic-dopsynthesizeded Ni(OH) nanosheets in situ on nickel foam for electrocatalytic HMF oxidation to FDCA are prepared.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P.R. China.
Accelerating proton deintercalation and transfer on the catalyst surface is crucial for the electrochemical oxidation of 5-hydroxymethylfurfural (HMF) into the high-value 2,5-furanodicarboxylic acid (FDCA). Herein, we have constructed a Ni(OH)─PO /Ni(PO) heterojunction catalyst that demonstrates exceptional selectivity (97.16%), yield (94.
View Article and Find Full Text PDFBioresour Technol
August 2025
State Key Laboratory of High-efficiency Coal Utilization and Green Chemical Engineering, College of Chemistry and Chemical Engineering, Ningxia University, Yinchuan 750021, People's Republic of China. Electronic address:
Anaerobic digestion of pretreated lignocellulosic hydrolysates valorizes biowaste into biomethane; however, the inherent inhibitory by-products severely suppress microbial metabolism. Electro-fermentation offers a promising strategy to simultaneously address the challenges of furfural detoxification and carbon recovery. Herein, we report the effect of externally applied voltages (0.
View Article and Find Full Text PDFMaterials (Basel)
August 2025
State Key Laboratory of Bio-Fibers and Eco-Textiles, Institute of Biochemical Engineering, College of Materials Science and Engineering, Qingdao University, Qingdao 266071, China.
Aiming to address the key challenges of poor enzyme stability, difficult recovery, and difficult synergistic optimization of catalytic efficiency in high-value conversion of biomass, this study utilizes mineralization self-assembly technology to combine laccase with FeO@SiO-PMIDA-Cu composite, constructing magnetic laccase nanoflower (MLac-NFs) materials with a porous structure and superparamagnetism. This synthetic material can efficiently catalyze the selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA). The characterization results indicated that MLac-NFs exhibit optimal catalytic activity (63.
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