The roles of carbide and hydride in oxide-supported palladium nanoparticles for alkyne hydrogenation

Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of the palladium carbide-like phase by alkyne is responsible for the constantly high selectivity up to almost 100% conversion. When the reaction became non-selective...

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Published inJournal of catalysis Vol. 283; no. 1; pp. 45 - 54
Main Authors Tew, Min Wei, Janousch, Markus, Huthwelker, Thomas, van Bokhoven, Jeroen A.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 06.10.2011
Elsevier
Elsevier BV
Subjects
Online AccessGet full text
ISSN0021-9517
1090-2694
DOI10.1016/j.jcat.2011.06.025

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Abstract Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of the palladium carbide-like phase by alkyne is responsible for the constantly high selectivity up to almost 100% conversion. When the reaction became non-selective, the carbide-like structure remained: Full hydrogenation can also occur in the absence of hydride. [Display omitted] ► A palladium carbide-like phase forms when the palladium NPs are exposed to alkyne. ► Partial and full hydrogenation occur over a palladium carbide-like phase. ► Full hydrogenation can also occur in the absence of hydride. ► Poisoning of the carbide-like phase by alkyne led to constantly high selectivity. ► Larger palladium particles are more selective to partial-hydrogenation of 1-pentyne. Particle size affects the activity and selectivity to partial hydrogenation of 1-pentyne over oxide-supported palladium nanoparticles. Larger particles are intrinsically more selective because of the weaker bond strength of 1-pentene. In situ X-ray absorption near edge structure (XANES) at the Pd L 3 edge revealed the formation of a carbide-like phase as soon as the catalyst is exposed to alkyne, irrespective of particle size. The newly formed phase prevented hydride formation. Surface poisoning of the palladium carbide by alkyne is responsible for the constantly high selectivity, up to almost complete conversion. At almost 100% conversion, all catalysts show low selectivity. The lack of significant pentyne adsorption on the surface causes pentene to undergo consecutive reactions, such as isomerization and complete hydrogenation. The structure of the catalyst was that of carbide-like phase and did not change. Palladium hydride did not form under any of the conditions. Exposure of a carbided catalyst to pure hydrogen leads to partial reversal of the structure. Hydride is not essential for complete hydrogenation to occur.
AbstractList Particle size affects the activity and selectivity to partial hydrogenation of 1-pentyne over oxide-supported palladium nanoparticles. Larger particles are intrinsically more selective because of the weaker bond strength of 1-pentene. In situ X-ray absorption near edge structure (XANES) at the Pd L₃ edge revealed the formation of a carbide-like phase as soon as the catalyst is exposed to alkyne, irrespective of particle size. The newly formed phase prevented hydride formation. Surface poisoning of the palladium carbide by alkyne is responsible for the constantly high selectivity, up to almost complete conversion. At almost 100% conversion, all catalysts show low selectivity. The lack of significant pentyne adsorption on the surface causes pentene to undergo consecutive reactions, such as isomerization and complete hydrogenation. The structure of the catalyst was that of carbide-like phase and did not change. Palladium hydride did not form under any of the conditions. Exposure of a carbided catalyst to pure hydrogen leads to partial reversal of the structure. Hydride is not essential for complete hydrogenation to occur.
Graphical abstract Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of the palladium carbide-like phase by alkyne is responsible for the constantly high selectivity up to almost 100% conversion. When the reaction became non-selective, the carbide-like structure remained: Full hydrogenation can also occur in the absence of hydride. Display Omitted Highlights A palladium carbide-like phase forms when the palladium NPs are exposed to alkyne. Partial and full hydrogenation occur over a palladium carbide-like phase. Full hydrogenation can also occur in the absence of hydride. Poisoning of the carbide-like phase by alkyne led to constantly high selectivity. Larger palladium particles are more selective to partial-hydrogenation of 1-pentyne. Particle size affects the activity and selectivity to partial hydrogenation of 1-pentyne over oxide-supported palladium nanoparticles. Larger particles are intrinsically more selective because of the weaker bond strength of 1-pentene. In situ X-ray absorption near edge structure (XANES) at the Pd L3 edge revealed the formation of a carbide-like phase as soon as the catalyst is exposed to alkyne, irrespective of particle size. The newly formed phase prevented hydride formation. Surface poisoning of the palladium carbide by alkyne is responsible for the constantly high selectivity, up to almost complete conversion. At almost 100% conversion, all catalysts show low selectivity. The lack of significant pentyne adsorption on the surface causes pentene to undergo consecutive reactions, such as isomerization and complete hydrogenation. The structure of the catalyst was that of carbide-like phase and did not change. Palladium hydride did not form under any of the conditions. Exposure of a carbided catalyst to pure hydrogen leads to partial reversal of the structure. Hydride is not essential for complete hydrogenation to occur. [PUBLICATION ABSTRACT]
Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of the palladium carbide-like phase by alkyne is responsible for the constantly high selectivity up to almost 100% conversion. When the reaction became non-selective, the carbide-like structure remained: Full hydrogenation can also occur in the absence of hydride. [Display omitted] ► A palladium carbide-like phase forms when the palladium NPs are exposed to alkyne. ► Partial and full hydrogenation occur over a palladium carbide-like phase. ► Full hydrogenation can also occur in the absence of hydride. ► Poisoning of the carbide-like phase by alkyne led to constantly high selectivity. ► Larger palladium particles are more selective to partial-hydrogenation of 1-pentyne. Particle size affects the activity and selectivity to partial hydrogenation of 1-pentyne over oxide-supported palladium nanoparticles. Larger particles are intrinsically more selective because of the weaker bond strength of 1-pentene. In situ X-ray absorption near edge structure (XANES) at the Pd L 3 edge revealed the formation of a carbide-like phase as soon as the catalyst is exposed to alkyne, irrespective of particle size. The newly formed phase prevented hydride formation. Surface poisoning of the palladium carbide by alkyne is responsible for the constantly high selectivity, up to almost complete conversion. At almost 100% conversion, all catalysts show low selectivity. The lack of significant pentyne adsorption on the surface causes pentene to undergo consecutive reactions, such as isomerization and complete hydrogenation. The structure of the catalyst was that of carbide-like phase and did not change. Palladium hydride did not form under any of the conditions. Exposure of a carbided catalyst to pure hydrogen leads to partial reversal of the structure. Hydride is not essential for complete hydrogenation to occur.
Author Tew, Min Wei
Huthwelker, Thomas
Janousch, Markus
van Bokhoven, Jeroen A.
Author_xml – sequence: 1
  givenname: Min Wei
  surname: Tew
  fullname: Tew, Min Wei
  organization: ETH Zurich, Institute for Chemical and Bioengineering, 8093 Zurich, Switzerland
– sequence: 2
  givenname: Markus
  surname: Janousch
  fullname: Janousch, Markus
  organization: Paul Scherrer Institute, 5232 Villigen, Switzerland
– sequence: 3
  givenname: Thomas
  surname: Huthwelker
  fullname: Huthwelker, Thomas
  organization: Paul Scherrer Institute, 5232 Villigen, Switzerland
– sequence: 4
  givenname: Jeroen A.
  surname: van Bokhoven
  fullname: van Bokhoven, Jeroen A.
  email: j.a.vanbokhoven@chem.ethz.ch
  organization: ETH Zurich, Institute for Chemical and Bioengineering, 8093 Zurich, Switzerland
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Issue 1
Keywords Selective partial hydrogenation
1-Pentyne
Oxide-supported palladium nanoparticles
Palladium carbide
Effect of particle size
Palladium hydrides
Pd L 3 edge in situ X-ray absorption near edge structure
Particle size
XANES spectrometry
Acetylenic compound
Support
edge in situ X-ray absorption near
Hydrogen
Nanoparticle
In situ
Oxides
Hydrogenation
Particle
Structure
Platinoid
Hydrocarbon
Catalyst selectivity
Pd L
Isomerization
Transition metal
Palladium
Conversion
Heterogeneous catalysis
Pentene
Adsorption
Catalyst
Palladium hydride
edge structure
X ray absorption
Alkyne
Language English
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Snippet Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of the palladium...
Particle size affects the activity and selectivity to partial hydrogenation of 1-pentyne over oxide-supported palladium nanoparticles. Larger particles are...
Graphical abstract Selective and non-selective hydrogenation of 1-pentyne occurs over carbided oxide-supported palladium nanoparticles. Surface poisoning of...
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StartPage 45
SubjectTerms 1-Pentyne
absorption
adsorption
alkynes
Catalysis
catalysts
Chemistry
Colloidal state and disperse state
Effect of particle size
Exact sciences and technology
General and physical chemistry
hydrides
hydrogen
Hydrogenation
isomerization
Nanoparticles
Oxidation
Oxide-supported palladium nanoparticles
palladium
Palladium carbide
Palladium hydrides
particle size
Pd L 3 edge in situ X-ray absorption near edge structure
Physical and chemical studies. Granulometry. Electrokinetic phenomena
poisoning
Selective partial hydrogenation
Surface physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
X-radiation
Title The roles of carbide and hydride in oxide-supported palladium nanoparticles for alkyne hydrogenation
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