Enhanced catalytic activity of Ce1−xMxO2 (M = Ti, Zr, and Hf) solid solution with controlled morphologies

2010 ◽  
Vol 46 (19) ◽  
pp. 3286 ◽  
Author(s):  
Wei-Ta Chen ◽  
Kuei-Bo Chen ◽  
Ming-Fang Wang ◽  
Sheng-Feng Weng ◽  
Chi-Shen Lee ◽  
...  
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.


RSC Advances ◽  
2019 ◽  
Vol 9 (36) ◽  
pp. 21018-21024 ◽  
Author(s):  
Ning Wang ◽  
Zhangzhong Wang ◽  
Yajie Chu ◽  
Jialin Cheng ◽  
Hao Yu ◽  
...  

NPCS with an extreme fine microstructure displayed superior sono-Fenton-like catalytic activity compared to NPC.


RSC Advances ◽  
2019 ◽  
Vol 9 (66) ◽  
pp. 38882-38890 ◽  
Author(s):  
Md Samiul Islam Sarker ◽  
Takahiro Nakamura ◽  
Satoshi Kameoka ◽  
Yuichiro Hayasaka ◽  
Shu Yin ◽  
...  

Catalytic Rh-based alloy nanoparticles (NPs) with inhomogeneous solid-solution structures were prepared from homogeneous solid-solution alloy NPs.


2019 ◽  
Vol 7 (23) ◽  
pp. 14244-14252 ◽  
Author(s):  
Zeyi Wang ◽  
Xuelian Zhang ◽  
Zhuanghe Ren ◽  
Yong Liu ◽  
Jianjiang Hu ◽  
...  

In situ formed NbTi nanocrystals from a NbTiC solid-solution MXene offer highly stable catalytic activity for hydrogen storage in MgH2.


2017 ◽  
Vol 19 (44) ◽  
pp. 29998-30009 ◽  
Author(s):  
Shrabani Ghosh ◽  
Samrat Sarkar ◽  
Bikram Kumar Das ◽  
Dipayan Sen ◽  
Madhupriya Samanta ◽  
...  

Natural sunlight assisted catalytic activity of hydrothermally synthesized zinc blende ZnxCd1−xS solid solution with theoretical insights.


Author(s):  
Svetlana A. Naumova ◽  
Anastasia V. Obukhova ◽  
Ludmila I. Kuznetsova

The effect of the addition of La3+ cations on the structural properties of Pt/WOх/ZrO₂ catalysts and the characteristics of catalytic activity in the process of hydroisomerization of n-heptane and benzene mixture was studied. The phase composition of the catalysts is represented by a solid solution of lanthanum cations in nanocrystalline zirconia of tetragonal modification with localization of lanthanum in the surface layers predominantly. The positive effect of La3+ additives on the selectivity and yield of isomerized products was shown


Catalysts ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 646 ◽  
Author(s):  
Chaoqian Ai ◽  
Yaoyao Zhang ◽  
Pan Wang ◽  
Wei Wang

Cerium-zirconium (Ce-Zr) solid solutions have been extensively used in a wide variety of catalytic processes due to their unique catalytic features in conjunction with lower cost compared to noble metal-based systems. A series of Ce-Zr-based catalysts was prepared by the sol-gel method. The structure and morphology of these catalysts were characterized by X-ray diffraction, thermogravimetric-differential scanning calorimetry, scanning electron microscopy, energy dispersive spectroscopy, and X-ray photoelectron spectroscopy. Furthermore, investigation on catalytic performance was carried out by constructing a test platform, and the result indicated that the catalysts apparently decreased the soot ignition temperature. These catalysts exhibited higher catalytic activity for soot oxidation under narrow contact conditions. The results revealed that some soot particles could react with adsorbed oxygen, and other part of diesel soot reacted with lattice oxygen. The activity of these catalysts was attributed to synergistic effect arising from the combination of K/Co/Zr and Ce-Zr solid solution, which led to the decrease in the ignition temperature to 294 °C (data from the test platform). The catalyst still keeps good stability and catalytic activity after the cycle oxidation experiment. A reaction pathway was proposed to explain catalytic combustion process of soot, i.e., combination of K/Co/Zr with Ce-Zr solid solution reduced the binding energy of Ce-Zr solid solution, which was conducive to provide more active sites to release the active oxygen (O2−) or lattice oxygen (O2−).


2015 ◽  
Vol 137 (19) ◽  
pp. 6132-6135 ◽  
Author(s):  
Lina María Aguirre-Díaz ◽  
Felipe Gándara ◽  
Marta Iglesias ◽  
Natalia Snejko ◽  
Enrique Gutiérrez-Puebla ◽  
...  

1995 ◽  
Vol 10 (3) ◽  
pp. 545-552 ◽  
Author(s):  
H.C. Zeng ◽  
J. Lin ◽  
W.K. Teo ◽  
J.C. Wu ◽  
K.L. Tan

Monoclinic ZrO2 and its supported materials Co/Ni/ZrO2 (Co:Ni = 1:1) for catalytic decomposition of N2O have been studied with GC, FTIR, EDAX, XPS, and the evaluation of catalytic activity of the materials. It is found that monoclinic ZrO2 alone has the catalytic effect for N2O decomposition, although higher activities are found for Co/Ni/ZrO2 systems. XPS study shows that only Co exists in the surface region of ZrO2, which is attributed to the formation of NiO–ZrO2 solid solution resulting from an interdiffusion between Ni2+ and ZrO2 matrix. The gas decomposition on Co/Ni/ZrO2 can be described as first order with respect to partial pressure of N2O. Surface reactions on ZrO2 and Co/Ni/ZrO2 will also be addressed.


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