Related Experiment Video
Updated: May 28, 2025

Utilization of Stop-flow Micro-tubing Reactors for the Development of Organic Transformations
Published on: January 4, 2018
Selective chemical looping combustion of acetylene in ethylene-rich streams
Matthew Jacob1, Huy Nguyen1, Rishi Raj1
1Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, USA.
Abstract:
The requirement for C2H2 concentrations below 2 parts per million (ppm) in gas streams for C2H4 polymerization necessitates its semihydrogenation to C2H4. We demonstrate selective chemical looping combustion of C2H2 in C2H4-rich streams by Bi2O3 as an alternative catalytic pathway to reduce C2H2 concentration below 2 ppm. Bi2O3 combusts C2H2 with a first-order rate constant that is 3000 times greater than the rate constant for C2H4 combustion. In successive redox cycles, the lattice O of Bi2O3 can be fully replenished without discernible changes in local Bi coordination or C2H2 combustion selectivity. Heterolytic activation of C-H bonds across Bi-O sites and the higher acidity of C2H2 results in lower barriers for C2H2 activation than C2H4, enabling selective catalytic hydrocarbon combustion leveraging differences in molecular deprotonation energies.
More Related Videos
06:34Operation of a 25 KWth Calcium Looping Pilot-plant with High Oxygen Concentrations in the Calciner
Published on: October 25, 2017
07:24Combustion Chemistry of Fuels: Quantitative Speciation Data Obtained from an Atmospheric High-temperature Flow Reactor with Coupled Molecular-beam Mass Spectrometer
Published on: February 19, 2018
Related Concept Videos
Structure and Physical Properties of Alkynes
In nature, compounds containing both carbon and hydrogen are known as "hydrocarbons". Aliphatic hydrocarbons are compounds whose molecules contain saturated single bonds (i.e., alkanes) or unsaturated double or triple bonds. Alkenes contain carbon–carbon double bonds and have a structural formula CnH2n. Unsaturated hydrocarbons containing carbon–carbon triple bonds are called "alkynes" and are structurally represented by the formula CnH2n-2.
The...
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Preparation of Alkynes: Alkylation Reaction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
Cycloaddition Reactions: MO Requirements for Photochemical Activation
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.
Combustion Energy: A Measure of Stability in Alkanes and Cycloalkanes
Alkanes undergo combustion in the presence of excess oxygen and high-temperature conditions to give carbon dioxide and water. A combustion reaction is the energy source in natural gas, liquified...