Clarifying the impacts of surface hydroxyls on CO oxidation on CeO2(100) surfaces: a DFT+U study

2020 ◽  
Vol 22 (15) ◽  
pp. 7738-7746
Author(s):  
Hui Zhou ◽  
Dong Wang ◽  
Xue-Qing Gong

In heterogeneous catalysis, surface hydroxylation is well recognized as a common phenomenon under realistic reaction conditions.

2015 ◽  
Vol 93 (7) ◽  
pp. 696-701 ◽  
Author(s):  
Hui Li ◽  
Yuanbin She ◽  
Haiyan Fu ◽  
Meijuan Cao ◽  
Jing Wang ◽  
...  

The synergistic effect of cyclohexane and cyclohexanone promoted synthesis of adipic acid catalyzed by [MnIIIT(p-Cl)PP]Cl with cyclohexane and cyclohexanone as co-reactants. The results showed that the conversions of cyclohexane and cyclohexanone were significantly enhanced because of the cyclohexanone synergistic effect, and the higher selectivity to adipic acid was obtained with dioxygen as an oxidant. The studies indicated that the co-oxidation of cyclohexane and cyclohexanone was influenced by the initial molar ratio of cyclohexanone and cyclohexane, catalyst structure, catalyst concentrations, and reaction conditions. The preliminary mechanism of the co-oxidation reaction of cyclohexane and cyclohexanone using [MnIIIT(p-Cl)PP]Cl as the catalyst was proposed.


2018 ◽  
Vol 14 ◽  
pp. 1655-1659 ◽  
Author(s):  
Ugo Azzena ◽  
Massimo Carraro ◽  
Gloria Modugno ◽  
Luisa Pisano ◽  
Luigi Urtis

The application of heterogeneous catalysis and green solvents to the set up of widely employed reactions is a challenge in contemporary organic chemistry. We applied such an approach to the synthesis and further conversion of tetrahydropyranyl ethers, an important class of compounds widely employed in multistep syntheses. Several alcohols and phenols were almost quantitatively converted into the corresponding tetrahydropyranyl ethers in cyclopentyl methyl ether or 2-methyltetrahydrofuran employing NH4HSO4 supported on SiO2 as a recyclable acidic catalyst. Easy work up of the reaction mixtures and the versatility of the solvents allowed further conversion of the reaction products under one-pot reaction conditions.


2018 ◽  
Vol 5 (10) ◽  
pp. 2368-2381 ◽  
Author(s):  
Huixia Li ◽  
Liping Li ◽  
Shaofan Fang ◽  
Jianghao Wang ◽  
Shaoqing Chen ◽  
...  

A series of Pt/Ni1−xMgxO catalysts with a low Pt loading of 0.5 wt% are prepared by multistep co-precipitation and annealing processes followed by wet impregnation.


2020 ◽  
Vol 493 ◽  
pp. 111086
Author(s):  
E. Gonzalez-A ◽  
R. Rangel ◽  
A. Solís-Garcia ◽  
A.M. Venezia ◽  
T.A. Zepeda

2020 ◽  
Vol 10 (3) ◽  
pp. 625-629
Author(s):  
Behzad Tangeysh ◽  
Clarke Palmer ◽  
Horia Metiu ◽  
Michael J. Gordon ◽  
Eric W. McFarland

Suspensions of platinum nanoparticles (PtNPs) were formed in molten LiCl–LiBr–KBr via thermal decomposition of H2PtCl6, and subsequently evaluated for thermal stability and CO oxidation activity.


2019 ◽  
Vol 150 (3) ◽  
pp. 605-612 ◽  
Author(s):  
Y. Suchorski ◽  
I. Bespalov ◽  
J. Zeininger ◽  
M. Raab ◽  
M. Datler ◽  
...  

Abstract The catalytic CO oxidation reaction on stepped Rh surfaces in the 10−6 mbar pressure range was studied in situ on individual μm-sized high-Miller-index domains of a polycrystalline Rh foil and on nm-sized facets of a Rh tip, employing photoemission electron microscopy (PEEM) and field-ion/field-emission microscopy (FIM/FEM), respectively. Such approach permits a direct comparison of the reaction kinetics for crystallographically different regions under identical reaction conditions. The catalytic activity of the different Rh surfaces, particularly their tolerance towards poisoning by CO, was found to be strongly dependent on the density of steps and defects, as well as on the size (µm vs. nm) of the respective catalytically active surface. Graphic Abstract


Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 484 ◽  
Author(s):  
Jianfeng Zhou ◽  
Sebastian Matera ◽  
Sebastian Pfaff ◽  
Sara Blomberg ◽  
Edvin Lundgren ◽  
...  

A stagnation flow reactor has been designed and characterized for both experimental and modeling studies of single-crystal model catalysts in heterogeneous catalysis. Using CO oxidation over a Pd(100) single crystal as a showcase, we have employed planar laser-induced fluorescence (PLIF) to visualize the CO2 distribution over the catalyst under reaction conditions and subsequently used the 2D spatially resolved gas phase data to characterize the stagnation flow reactor. From a comparison of the experimental data and the stagnation flow model, it was found that characteristic stagnation flow can be achieved with the reactor. Furthermore, the combined stagnation flow/PLIF/modeling approach makes it possible to estimate the turnover frequency (TOF) of the catalytic surface from the measured CO2 concentration profiles above the surface and to predict the CO2, CO and O2 concentrations at the surface under reaction conditions.


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