Related Experiment Video
Updated: Aug 22, 2025

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
Published on: February 19, 2018
Anisole hydrodeoxygenation over Ni-Co bimetallic catalyst: a combination of experimental, kinetic and DFT study
Adarsh Kumar1, Meenu Jindal2,3, Shivam Rawat2,3
1Bioproducts, Sciences, and Engineering Laboratory, Department of Biological Systems Engineering, Washington State University Richland WA 99354 USA bin.yang@wsu.edu.
Abstract:
Catalytic hydrodeoxygenation (HDO) of anisole was performed with a series of Ni and Co containing catalysts with different weight ratios on activated carbon (AC) for cyclohexanol production. The catalytic activities of various catalysts revealed that Ni5Co5-AC was the best catalytic system. Structural analysis obtained from XRD, TPR, XPS, and TEM evidently demonstrates that Ni5Co5-AC sample consists of a distorted metal alloy spinel structure and optimum particle size, enhancing its catalytic performance. Kinetics were investigated to identify cyclohexanol production rate, activation energy, and reaction pathway. Structural, experimental, kinetics and density functional simulations suggested that high amount of distorted metallic alloy in Ni5Co5-AC, presence of water, high adsorption efficiency of anisole, and low adsorption tendency of cyclohexanol on metallic alloy surface were the critical factors for HDO of anisole to cyclohexanol.
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
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Related Concept Videos
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...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.