Fuel, Journal Year: 2024, Volume and Issue: 384, P. 134045 - 134045
Published: Dec. 13, 2024
Language: Английский
Fuel, Journal Year: 2024, Volume and Issue: 384, P. 134045 - 134045
Published: Dec. 13, 2024
Language: Английский
Green Chemistry, Journal Year: 2024, Volume and Issue: 26(19), P. 9957 - 9992
Published: Jan. 1, 2024
This review highlights recent advancements in the selective conversion of biomass-derived furfural to high-value platform chemicals over various heterogeneous catalytic systems.
Language: Английский
Citations
16ChemCatChem, Journal Year: 2024, Volume and Issue: 16(14)
Published: April 1, 2024
Abstract Solvent effects add a new dimension for tuning the activity and selectivity of heterogeneous catalytic reactions, which is extensively employed in hydrogenation unsaturated compounds with multiple functional groups. In this concept, we briefly summarize recent developments on how solvent affect performance from following aspects: 1) polarity can influence interaction between reactant or intermediate; 2) composition mixed reactivity 3) effect varies metal identity support; 4) induce surface modification supported catalysts. This summarization will provide insights into rational development efficient selective system to realize precise synthesis desired chemicals.
Language: Английский
Citations
7Tetrahedron Green Chem, Journal Year: 2024, Volume and Issue: 3, P. 100037 - 100037
Published: Feb. 9, 2024
The transformation of biomass derived platform molecules is an interesting approach to produce valuable chemicals from biomass. In addition, process intensification by reducing the number steps for final production performing cascade-type catalytic reactions in one-pot mode largely desirable a biorefinery facility. this review possibilities valorization representative such as sugars, itaconic and levulinic acids furanic aldehydes through cascade processes using mono multifunctional heterogeneous catalysts are illustrated selected examples.
Language: Английский
Citations
5Fuel, Journal Year: 2024, Volume and Issue: 371, P. 131934 - 131934
Published: May 19, 2024
Language: Английский
Citations
5Applied Catalysis B Environment and Energy, Journal Year: 2023, Volume and Issue: 344, P. 123622 - 123622
Published: Dec. 19, 2023
Language: Английский
Citations
12Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 159752 - 159752
Published: Jan. 1, 2025
Language: Английский
Citations
0ACS Sustainable Chemistry & Engineering, Journal Year: 2025, Volume and Issue: unknown
Published: March 10, 2025
Language: Английский
Citations
0AIChE Journal, Journal Year: 2025, Volume and Issue: unknown
Published: March 15, 2025
Abstract Developing an efficient catalyst for converting furan alcohols to cyclopentenones fine chemical synthesis is crucial but challenging due the easy overhydrogenation side reactions tetrahydrofuran and cyclopentanones. This study demonstrates that cobalt disulfide (CoS 2 ) exhibits unprecedented yield of 80.1% during rearrangement–hydrodeoxygenation alcohol cyclopentenone. CoS acts not only as Lewis acid sites rearrangement step also adjustable H activation CC hydrogenation 4‐hydroxy‐2‐cyclopentenone intermediates, promoting Furthermore, it exhibits, first time, a similar route toward 3‐methyl cyclopentenone from 5‐methyl 2,5‐dihydroxymethyl furan. In addition, we further explored high‐value utilization high‐density fuels with densities 0.904–0.908 g/mL via self‐photosensitized [2 + 2] cycloaddition subsequent hydrodeoxygenation. presents green two way their fuels.
Language: Английский
Citations
0AIChE Journal, Journal Year: 2025, Volume and Issue: unknown
Published: April 8, 2025
Abstract Catalytic hydrogenative rearrangement of furanic aldehydes is crucial for producing biomass‐derived cyclopentanone fine chemicals. However, designing highly selective catalysts remains challenging due to the interplay among tandem hydrogenation, ring‐opening, aldol condensation, dehydration, and parallel ring‐hydrogenation. Here, we employ a single self‐assembly step by depositing phosphonic acids (PAs) on conventional Ni introduce tunable interfacial Brønsted acid sites (BAS), resulting in an unprecedented 3‐hydroxymethyl‐cyclopentanone yield 95.8% from hydroxymethylfurfural. Kinetic studies reveal one‐order‐of‐magnitude increase ring‐opening rates—the slow rearrangement—after PAs modification, accompanied drop apparent activation energy 154.1 105.4 kJ mol −1 . In contrast, ring‐hydrogenation side reaction almost unchanged. Theoretical calculations suggest that BAS synergize with adjacent lower C–O cleavage barrier providing protons attack hydroxymethyl oxygen atom, which key initiate ring‐opening.
Language: Английский
Citations
0Journal of Energy Chemistry, Journal Year: 2025, Volume and Issue: 108, P. 101 - 108
Published: April 18, 2025
Language: Английский
Citations
0