X-ray diffraction studies of mixed oxide catalysts

1968 ◽  
Vol 11 (3) ◽  
pp. 266-269 ◽  
Author(s):  
R LEVY
Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 878 ◽  
Author(s):  
Abdallah Zedan ◽  
Amina AlJaber

In this study, xCuO-CeO2 mixed oxide catalysts (Cu weight ratio x = 1.5, 3, 4.5, 6 and 15 wt.%) were prepared using solution combustion synthesis (SCS) and their catalytic activities towards the methane (CH4) oxidation reaction were studied. The combustion synthesis of the pure CeO2 and the CuO-CeO2 solid solution catalysts was performed using copper and/or cerium nitrate salt as an oxidizer and citric acid as a fuel. A variety of standard techniques, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), thermo-gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were employed to reveal the microstructural, crystal, thermal and electronic properties that may affect the performance of CH4 oxidation. The CuO subphase was detected in the prepared solid solution and confirmed with XRD and Raman spectroscopy, as indicated by the XRD peaks at diffraction angles of 35.3° and 38.5° and the Ag Raman mode at 289 cm−1, which are characteristics of tenorite CuO. A profound influence of Cu content was evident, not only affecting the structural and electronic properties of the catalysts, but also the performance of catalysts in the CH4 oxidation. The presence of Cu in the CeO2 lattice obviously promoted its catalytic activity for CH4 catalytic oxidation. Among the prepared catalysts, the 6% CuO-CeO2 catalyst demonstrated the highest performance, with T50 = 502 °C and T80 = 556 °C, an activity that is associated with the availability of a fine porous structure and the enhanced surface area of this catalyst. The results demonstrate that nanocrystalline copper-ceria mixed oxide catalysts could serve as an inexpensive and active material for CH4 combustion.


ChemInform ◽  
2005 ◽  
Vol 36 (27) ◽  
Author(s):  
Guido Schimanke ◽  
Manfred Martin ◽  
Jan Kunert ◽  
Herbert Vogel

1996 ◽  
Vol 61 (8) ◽  
pp. 1131-1140 ◽  
Author(s):  
Abd El-Aziz Ahmed Said

Vanadium oxide catalysts doped or mixed with 1-50 mole % Fe3+ ions were prepared. The structure of the original samples and those calcined from 200 up to 500 °C were characterized by TG, DTA, IR and X-ray diffraction. The SBET values and texture of the solid catalysts were investigated. The catalytic dehydration-dehydrogenation of isopropanol was carried out at 200 °C using a flow system. The results obtained showed an observable decrease in the activity of V2O5 on the addition of Fe3+ ions. Moreover, Fe2V4O13 is the more active and selective catalyst than FeVO4 spinels. The results were correlated with the active sites created on the catalyst surface.


ACS Catalysis ◽  
2021 ◽  
pp. 10294-10307
Author(s):  
Satoshi Ishikawa ◽  
Yudai Yamada ◽  
Naoki Kashio ◽  
Nagisa Noda ◽  
Kosuke Shimoda ◽  
...  

2014 ◽  
Vol 469 ◽  
pp. 165-172 ◽  
Author(s):  
K. Jagadeeswaraiah ◽  
Ch. Ramesh Kumar ◽  
P.S. Sai Prasad ◽  
S. Loridant ◽  
N. Lingaiah

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