نتایج جستجو برای: au catalyst

تعداد نتایج: 121787  

2016
Gaowei Wu Gemma L. Brett Enhong Cao Achilleas Constantinou Peter Ellis Simon Kuhn Graham J. Hutchings Donald Bethell Asterios Gavriilidis

The stability of a bimetallic Au–Pd/TiO2 catalyst was examined in a packed bed microreactor for the oxidation of cinnamyl alcohol dissolved in toluene. The catalyst was prepared by co-impregnation with a Au–Pd weight ratio of 1 : 19. Experiments were performed at 80–120 °C, oxygen concentration 0–100% and total pressure 4 bara. Principal products observed were cinnamaldehyde, 3-phenyl-1-propano...

Journal: :Chemical communications 2012
Gao Li Chao Liu Yu Lei Rongchao Jin

The Au(25)(SR)(18)/CeO(2) nanocluster catalyst showed high activity in the homocoupling of aryl iodides (e.g. up to 99.8% yield with iodobenzene) and excellent recyclability.

Journal: :Chemical communications 2015
Guangchao Zheng Lakshminarayana Polavarapu Luis M Liz-Marzán Isabel Pastoriza-Santos Jorge Pérez-Juste

We report a robust and recyclable 'dip-catalyst' based on a gold nanoparticle (Au NP)-loaded filter paper composite, prepared by a simple dip-coating process using concentrated Au NP suspensions in toluene. While acting as catalysts, the composites display excellent surface enhanced Raman scattering (SERS) efficiency, allowing the real-time monitoring of chemical reactions.

Journal: :Chemical communications 2011
Teresa de Haro Cristina Nevado

A combination of IPrAuNTf(2) as catalyst in the presence of Selectfluor has been successfully used for the high yielding synthesis of α-fluoroenones via 1,3-acyloxy rearrangement of propargyl acetates followed by Csp(2)-F bond formation, likely involving a redox Au(I)/Au(III) catalytic cycle.

2011
Se Gyu Jang Anzar Khan Michael D. Dimitriou Bumjoon J. Kim Nathaniel A. Lynd Edward J. Kramer Craig J. Hawker

We report a facile strategy for the preparation of sub-5 nm gold/platinum (Au-Pt) nanoparticles which are thermally stabilized by a crosslinked polymer shell. Diblock copolymer (PS-b-PI-SH) ligands on the Au nanoparticles were used to crosslink the vinyl functionalities on PI via hydrosilylation with 1,1,3,3tetramethyldisiloxane in the presence of a platinum catalyst. The Pt catalyst was reduce...

2011
Nikolaos Dimitratos Laura Prati

The liquid phase oxidation of D-Sorbitol has been carried out in water using oxygen as the oxidant in the presence of gold based catalyst. Au/C, Pt/C and Pd/C monometallic systems were compared to bimetallic Au/Pd and Au/Pt on carbon. A strong synergistic effect was observed producing a significant increase of reaction rate. Moreover, the addition of gold to Pd or Pt catalyst produced a system ...

Journal: :The Journal of chemical physics 2013
Harald Oberhofer Karsten Reuter

We adapt the computational hydrogen electrode approach to explicitly account for photo-generated charges and use it to computationally screen for viable catalyst/co-catalyst combinations for photo-catalytic water splitting. The hole energy necessary to thermodynamically drive the reaction is employed as descriptor for the screening process. Using this protocol and hybrid-level density-functiona...

Journal: :Chemical communications 2015
Tesnim Chaieb Laurent Delannoy Sandra Casale Catherine Louis Cyril Thomas

This work provides the first experimental evidence of an H2 effect in C3H6-SCR over an Au/Al2O3 catalyst. This effect could only be observed when the number of Au catalytic sites was decreased. The N2 turnover rate estimated for the first time for the Au catalytic sites for H2-C3H6-SCR was found to be similar to that estimated for Ag ones supported on Al2O3.

2007
Laura Prati Alberto Villa Francesca Porta Dangsheng Su

The liquid phase oxidation of glycerol with oxygen has been studied using mono and bimetallic catalysts based on Au and Pd metals supported on activated carbon, in order to study the effect of the metal on the distribution of the products and on activity of catalysts. It was found that by using bimetallic catalysts (Au–Pd) a strong synergistic effect was shown. By using a preformed nucleating c...

Journal: :Chemical communications 2007
Veronica Aguilar-Guerrero Bruce C Gates

X-Ray absorption spectra show that a CeO(2)-supported CO oxidation catalyst prepared from Au(III)(CH(3))(2)(C(5)H(7)O(2)) initially incorporated Au(III) complexes that were catalytically active at 353 K; during operation in a flow reactor, the gold aggregated into clusters and the catalytic activity increased.

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