scholarly journals Inside Cover: Atomic-Scale Determination of Active Facets on the MoVTeNb Oxide M1 Phase and Their Intrinsic Catalytic Activity for Ethane Oxidative Dehydrogenation (Angew. Chem. Int. Ed. 31/2016)

2016 ◽  
Vol 55 (31) ◽  
pp. 8770-8770
Author(s):  
Daniel Melzer ◽  
Pinghong Xu ◽  
Daniela Hartmann ◽  
Yuanyuan Zhu ◽  
Nigel D. Browning ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Oxidative Dehydrogenation ◽  
Atomic Scale ◽  
M1 Phase ◽  
Ethane Oxidative Dehydrogenation

scholarly journals Innentitelbild: Atomic-Scale Determination of Active Facets on the MoVTeNb Oxide M1 Phase and Their Intrinsic Catalytic Activity for Ethane Oxidative Dehydrogenation (Angew. Chem. 31/2016)

2016 ◽  
Vol 128 (31) ◽  
pp. 8914-8914
Author(s):  
Daniel Melzer ◽  
Pinghong Xu ◽  
Daniela Hartmann ◽  
Yuanyuan Zhu ◽  
Nigel D. Browning ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Oxidative Dehydrogenation ◽  
Atomic Scale ◽  
M1 Phase ◽  
Ethane Oxidative Dehydrogenation

Atomic-Scale Determination of Active Facets on the MoVTeNb Oxide M1 Phase and Their Intrinsic Catalytic Activity for Ethane Oxidative Dehydrogenation

2016 ◽  
Vol 128 (31) ◽  
pp. 9019-9023 ◽  
Author(s):  
Daniel Melzer ◽  
Pinghong Xu ◽  
Daniela Hartmann ◽  
Yuanyuan Zhu ◽  
Nigel D. Browning ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Oxidative Dehydrogenation ◽  
Atomic Scale ◽  
M1 Phase ◽  
Ethane Oxidative Dehydrogenation

Atomic-Scale Determination of Active Facets on the MoVTeNb Oxide M1 Phase and Their Intrinsic Catalytic Activity for Ethane Oxidative Dehydrogenation

2016 ◽  
Vol 55 (31) ◽  
pp. 8873-8877 ◽  
Author(s):  
Daniel Melzer ◽  
Pinghong Xu ◽  
Daniela Hartmann ◽  
Yuanyuan Zhu ◽  
Nigel D. Browning ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Oxidative Dehydrogenation ◽  
Atomic Scale ◽  
M1 Phase ◽  
Ethane Oxidative Dehydrogenation

In Situ Environmental STEM Study of the MoVTe Oxide M1 Phase Catalysts for Ethane Oxidative Dehydrogenation

ACS Catalysis ◽  
2016 ◽  
Vol 6 (7) ◽  
pp. 4775-4781 ◽  
Author(s):  
Mimoun Aouine ◽  
Thierry Epicier ◽  
Jean-Marc M. Millet
Keyword(s):  
Oxidative Dehydrogenation ◽  
M1 Phase ◽  
Ethane Oxidative Dehydrogenation

scholarly journals On the Promoting Effects of Te and Nb in the Activity and Selectivity of M1 MoV-Oxides for Ethane Oxidative Dehydrogenation

2020 ◽  
Vol 63 (19-20) ◽  
pp. 1754-1764
Author(s):  
Daniel Melzer ◽  
Gerhard Mestl ◽  
Klaus Wanninger ◽  
Andreas Jentys ◽  
Maricruz Sanchez-Sanchez ◽  
...  
Keyword(s):  
Oxidative Dehydrogenation ◽  
Oxidation Mechanism ◽  
Oxide Catalysts ◽  
Ethane Oxidation ◽  
M1 Phase ◽  
Phase Type ◽  
Metal Composition ◽  
Ethane Oxidative Dehydrogenation

AbstractThe pathways of ethane oxidative dehydrogenation and total combustion have been elucidated for M1 phase type Mo–V oxide catalysts with different metal composition. The ethane oxidation mechanism is not affected by the presence of Te or Nb. Conversely, the selectivity is strongly affected by stoichiometry of M1 catalysts. This is attributed to the facile oxidation of ethene to COx upon formation of unselective VOx species in the absence of Te and Nb.

Ordered Intermetallic Nanoparticles with High Catalytic Activity Prepared by an Electrochemically Induced Phase Transformation

2019 ◽  
Author(s):  
Du Sun ◽  
yunfei wang ◽  
Kenneth Livi ◽  
chuhong wang ◽  
ruichun luo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffusion Mechanism ◽  
Reduction Reaction ◽  
Atomic Scale ◽  
High Catalytic Activity ◽  
Ambient Conditions ◽  
Magnetic Devices ◽  
Disordered Alloys ◽  
Ordered Intermetallic ◽  
Intermetallic Nanoparticles

<div> <p>The synthesis of alloys with long range atomic scale ordering (ordered intermetallics) is an emerging field of nanochemistry. Ordered intermetallic nanoparticles are useful for a wide variety of applications such as catalysis, superconductors, and magnetic devices. However, the preparation of nanostructured ordered intermetallics is challenging in comparison to disordered alloys, hindering progress in materials development. We report a process for converting colloidally synthesized ordered intermetallic PdBi<sub>2</sub> to ordered intermetallic Pd<sub>3</sub>Bi nanoparticles under ambient conditions by an electrochemically induced phase transition. The low melting point of PdBi<sub>2</sub> corresponds to low vacancy formation energies which enables the facile removal of the Bi from the surface, while simultaneously enabling interdiffusion of the constituent atoms via a vacancy diffusion mechanism under ambient conditions. The resulting phase-converted ordered intermetallic Pd<sub>3</sub>Bi exhibits 11x and 3.5x higher mass activty and high methanol tolerance for the oxygen reduction reaction compared to Pt/C and Pd/C, respectively,which is the highest reported for a Pd-based catalyst, to the best of our knowledge. These results establish a key development in the synthesis of noble metal rich ordered intermetallic phases with high catalytic activity, and sets forth guidelines for the design of ordered intermetallic compounds under ambient conditions.</p> </div>

scholarly journals Role of CO2 During Oxidative Dehydrogenation of Propane Over Bulk and Activated-Carbon Supported Cerium and Vanadium Based Catalysts

2021 ◽  
Author(s):  
Petar Djinović ◽  
Janez Zavašnik ◽  
Janvit Teržan ◽  
Ivan Jerman
Keyword(s):  
Catalytic Activity ◽  
Activated Carbon ◽  
Oxidative Dehydrogenation ◽  
Active Phase ◽  
Lattice Oxygen ◽  
Chemisorbed Oxygen ◽  
Catalytically Active ◽  
Temperature Programmed ◽  
Propane Cracking

AbstractCeO2, V2O5 and CeVO4 were synthesised as bulk oxides, or deposited over activated carbon, characterized by XRD, HRTEM, CO2-TPO, C3H8-TPR, DRIFTS and Raman techniques and tested in propane oxidative dehydrogenation using CO2. Complete oxidation of propane to CO and CO2 is favoured by lattice oxygen of CeO2. The temperature programmed experiments show the ~ 4 nm AC supported CeO2 crystallites become more susceptible to reduction by propane, but less prone to re-oxidation with CO2 compared to bulk CeO2. Catalytic activity of CeVO4/AC catalysts requires a 1–2 nm amorphous CeVO4 layer. During reaction, the amorphous CeVO4 layer crystallises and several atomic layers of carbon cover the CeVO4 surface, resulting in deactivation. During reaction, V2O5 is irreversibly reduced to V2O3. The lattice oxygen in bulk V2O5 favours catalytic activity and propene selectivity. Bulk V2O3 promotes only propane cracking with no propene selectivity. In VOx/AC materials, vanadium carbide is the catalytically active phase. Propane dehydrogenation over VC proceeds via chemisorbed oxygen species originating from the dissociated CO2. Graphic Abstract

Comparison of structural and catalytic properties of monometallic Mo and V oxides and M1 phase mixed oxides for oxidative dehydrogenation

2020 ◽  
Author(s):  
Leelavathi Annamalai ◽  
Sopuruchukwu Ezenwa ◽  
Yanliu Dang ◽  
Haiyan Tan ◽  
Steven L. Suib ◽  
...  
Keyword(s):  
Oxidative Dehydrogenation ◽  
Mixed Oxides ◽  
Catalytic Properties ◽  
M1 Phase

Determination of surface composition of alloy nanoparticles and relationships with catalytic activity in Pd–Cu/SiO2 cogelled xerogel catalysts

2004 ◽  
Vol 270 (1-2) ◽  
pp. 201-208 ◽  
Author(s):  
Stéphanie Lambert ◽  
Benoı̂t Heinrichs ◽  
Alain Brasseur ◽  
André Rulmont ◽  
Jean-Paul Pirard
Keyword(s):  
Catalytic Activity ◽  
Surface Composition ◽  
Alloy Nanoparticles
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