Related Experiment Video
Updated: Apr 16, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Effect of Cavity Microenvironment in Cobalt-Encapsulated Hollow Carbon Spheres on Selective Phenol Hydrogenation to
Luqingshan Xiao1, Shuo Ma1, Hao Li2,3
1National-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources Utilization, Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, 8 Guangrong Road, Tianjin 300130, China.
Abstract:
Cyclohexanol is not only an important intermediate in the chemical industry, but also a key component in the production of green energy. Catalyzed hydrogenation of phenol to produce cyclohexanol is a green and efficient method. This work employed the soft template method to prepare hollow carbon-coated cobalt nanoreactors with different physical microenvironments by varying the amount of HMT (Hexamethylenetetramine) added. The results show that the cavity size and curvature of the hollow carbon spheres reactor have a significant effect on the reaction. Comprehensive characterizations (TEM, XRD, XPS, H2-TPR, etc.) and experimental data indicate that the optimized Co@HCS-0.25-500 promotes the adsorption and hydrogenation of phenol through the synergistic effects of curvature-induced electronic metal-support interactions and enhanced reactant enrichment in the larger cavities. The optimized Co@HCS-0.25-500 achieved a phenol conversion of 56.4% and >99% cyclohexanol selectivity under conditions of 140 °C, 1 MPa H2, 1 h. Co@HCS-0.25-500 exhibited excellent stability in six consecutive cycles and demonstrated good general applicability in the hydrogenation of biomass-derived phenolic compounds.
More Related Videos
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Related Concept Videos
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.