Preferential oxidation of CO in H2 over highly loaded Au/ZrO2catalysts obtained by direct oxidation of bulk alloy

Literature Information

Publication Date 2004-11-30
DOI 10.1039/B413646B
Impact Factor 6.222
Authors

Marc Lomello-Tafin, Abdel Ait Chaou, Franck Morfin, Valérie Caps, Jean-Luc Rousset


View Original

Abstract

The intimate mixture of a skeletal gold structure with ZrO2 nanoparticles obtained simply by oxidation of Au0.5Zr0.5 alloy at room temperature turns out to be an efficient catalyst for the selective oxidation of CO in the presence of hydrogen.

Related Literature

Back cover

Cover

DOI: 10.1039/C7CP90042B

Nanoparticle–nanoparticle vs. nanoparticle–substrate hot spot contributions to the SERS signal: studying Raman labelled monomers, dimers and trimers

Kamila Moor, Kristina Gudun, Zarina Yelemessova, Rostislav Bukasov

2016-12-15 Paper

DOI: 10.1039/C6CP08254H

Fast and accurate MAS–DNP simulations of large spin ensembles

Shimon Vega

2017-01-05 Paper

DOI: 10.1039/C6CP07881H

Ionic liquids and deep eutectic solvents for lignocellulosic biomass fractionation

Dannie J. G. P. van Osch, Laura J. B. M. Kollau, Sari Asikainen, Marisa A. A. Rocha

2016-12-02 Perspective

DOI: 10.1039/C6CP07499E

Modeling the abnormally slow infiltration rate in mesoporous films

Claudio L. A. Berli, Magalí Mercuri, Martín G. Bellino

2016-12-12 Communication

DOI: 10.1039/C6CP06602J

Room-temperature ferromagnetism in the two-dimensional layered Cu2MoS4 nanosheets

Ke Zhang, Rashid Khan, Hongyan Guo, Irfan Ali, Xiuling Li, Yunxiang Lin, Haiping Chen, Wensheng Yan, Xiaojun Wu, Li Song

2016-12-12 Communication

DOI: 10.1039/C6CP07270D

Contents list

Front/Back Matter

DOI: 10.1039/C7CP90036H

Correlated/non-correlated ion dynamics of charge-neutral ion couples: the origin of ionicity in ionic liquids

G. W. Driver, Y. Huang, A. Laaksonen, T. Sparrman, Y.-L. Wang, P.-O. Westlund

2016-12-08 Paper

DOI: 10.1039/C6CP05801A

You might also like

Compound Q&A

What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?

When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...

79206-94-34-(2-Furylmethyl)thi...
Compound Q&A

What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?

When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...

71320-77-94-Chloro-N-[2-(4-mor...
Compound Q&A

How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?

Waste containing this compound (CAS: 62921-74-8) should be handled according to ...

62921-74-82-[2-(2-Methoxyethox...
Compound Q&A

How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?

Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...

40056-18-6(S)-Methyl 2-amino-3...
166882-70-85-({4-[(2S,4R)-4-Hyd...
Compound Q&A

Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?

There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...

7312-27-8(2E)-3-(3,4-Dichloro...
Compound Q&A

How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?

Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...

925437-84-9Ethyl 6-(2-nitrophen...
Compound Q&A

How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?

Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...

18453-07-12-(1,3-Thiazol-2-yl)...
Compound Q&A

How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?

Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...

103440-54-6Methyl 5-iodo-2-meth...
Compound Q&A

How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?

5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...

1427399-34-55-Chloro[1,2,4]triaz...

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.