Direct N2O decomposition over ex-framework FeMFI catalysts. Role of extra-framework species

2002 ◽  
Vol 3 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Javier Pérez-Ramı́rez ◽  
Freek Kapteijn ◽  
Guido Mul ◽  
Jacob A Moulijn
2008 ◽  
Vol 137 (2-4) ◽  
pp. 423-428 ◽  
Author(s):  
Paweł Stelmachowski ◽  
Filip Zasada ◽  
Witold Piskorz ◽  
Andrzej Kotarba ◽  
Jean-Francois Paul ◽  
...  

2016 ◽  
Vol 180 ◽  
pp. 622-629 ◽  
Author(s):  
G. Grzybek ◽  
P. Stelmachowski ◽  
S. Gudyka ◽  
P. Indyka ◽  
Z. Sojka ◽  
...  

2006 ◽  
Vol 110 (22) ◽  
pp. 10691-10700 ◽  
Author(s):  
Dmitri A. Bulushev ◽  
Albert Renken ◽  
Lioubov Kiwi-Minsker

1993 ◽  
Vol 139 (2) ◽  
pp. 435-443 ◽  
Author(s):  
V.I. Sobolev ◽  
G.I. Panov ◽  
A.S. Kharitonov ◽  
V.N. Romannikov ◽  
A.M. Volodin ◽  
...  

2008 ◽  
Vol 07 (02) ◽  
pp. 263-276 ◽  
Author(s):  
WEN-KAI CHEN ◽  
BAO-ZHEN SUN ◽  
XIA WANG ◽  
CHUN-HAI LU

The role of a surface oxygen vacancy in the N 2 O dissociation over a Cu 2 O surface was studied using density functional theory — generalized gradient approximation periodic calculations. To perform this study, surface slab model — [Formula: see text] surface cell was used. The results indicated that N 2 O adsorption properties were associated with the surface oxygen vacancies. The presence of a surface oxygen vacancy, prepared by removing one O SUF atom from [Formula: see text] supercell, makes the N 2 O decomposition possible, which was believed to occur at a oxygen vacancy site. The N 2 O decomposition at the surface oxygen vacant site depends on whether the molecule is adsorbed with the O - or N -end on a vacancy. For the first case, the reaction proceeds spontaneously, which leads to an ejection of N 2 from the surface and the rest of the oxygen atoms occupying the vacancy. In the second case, even though there is an elongation of both N – N and N – O bonds, the dissociation is unfeasible due to very small adsorption energy and high activation energy. The role of the defective surface with surface oxygen vacancy is to provide electrons to the adsorbed molecule.


2009 ◽  
Vol 262 (1) ◽  
pp. 27-34 ◽  
Author(s):  
K. Jíša ◽  
J. Nováková ◽  
M. Schwarze ◽  
A. Vondrová ◽  
S. Sklenák ◽  
...  

2020 ◽  
Vol 09 ◽  
Author(s):  
B.M. Abu-Zied ◽  
S.A. Soliman ◽  
S.E. Abdellah

Background: The increased concerns about our environment protection urge more effort to develop new catalysts for the abetment of the greenhouse gases. N2O is known as a powerful greenhouse gas. The literature review revealed that various catalysts have been developed for the direct decomposition of N2O. Special attention was given to the cobalt-based spinel oxides. However, there are a lack of information about the performance of the cadmium promoted spinels for N2O abetment. Objective: This paper addresses the nitrous oxide direct decomposition over a novel series of Cd-Co catalysts. Method: These catalysts, with Cd/(Cd + Co) ratios 0.00-0.333, were prepared with the aid of the co-precipitation route, which is followed by calcination at 500 °C. Characterization of these catalysts was performed employing TGA-DTA, XRD, FTIR, N2 adsorption/desorption, and atomic absorption spectrophotometry. Results: Phase analysis revealed the absence of a solid-state interaction between CdO and Co3O4. However, it was found that increasing the Cd/(Cd + Co) ratio is associated with continuous enhancement of the N2O decomposition activity. The activity was correlated with the presence of catalyst’s redox couples. Moreover, the role of the Cd presence in improving the activity was discussed. Finally, the activity performance change accompanying the calcination temperature raise was, also, investigated. Conclusions: The presence of cadmium has a positive effect on the N2O decomposition performance of Co3O4. The activity increased continuously with Cd/(Cd + Co) ratio increase over the examined range 0.083–0.333. Structural, textural, and electronic roles of cadmium were proposed.


2009 ◽  
Vol 91 (1-2) ◽  
pp. 174-179 ◽  
Author(s):  
L.V. Pirutko ◽  
V.S. Chernyavsky ◽  
E.V. Starokon ◽  
A.A. Ivanov ◽  
A.S. Kharitonov ◽  
...  

2014 ◽  
Vol 35 (12) ◽  
pp. 1972-1981 ◽  
Author(s):  
Bo Zhang ◽  
Fudong Liu ◽  
Hong He ◽  
Li Xue
Keyword(s):  

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