NO reduction by hydrocarbons in an oxidizing atmosphere over transition metal-zirconium mixed oxides

1994 ◽  
Vol 25 (1-2) ◽  
pp. 37-48 ◽  
Author(s):  
Kathleen A. Bethke ◽  
David Alt ◽  
Mayfair C. Kung
2012 ◽  
Vol 113-114 ◽  
pp. 255-260 ◽  
Author(s):  
Jihène Jemal ◽  
Hassib Tounsi ◽  
Kamel Chaari ◽  
Carolina Petitto ◽  
Gérard Delahay ◽  
...  

2017 ◽  
Vol 53 (5) ◽  
pp. 967-970 ◽  
Author(s):  
Xiuyun Wang ◽  
Zhixin Lan ◽  
Yi Liu ◽  
Yongjin Luo ◽  
Jianjun Chen ◽  
...  

The 1D nanowire or hollow tubular structure of various transition metal oxides can be tuned by controlling heating rates.


Author(s):  
Ali Bahadur ◽  
Waseem Hussain ◽  
Shahid Iqbal ◽  
Farman Ullah ◽  
Muhammad Shoaib ◽  
...  

Transition metal mixed oxides have drawn extensive interest as oxygen evolution electrocatalysts alternatives to noble metals-based material but generally involve prolonged synthesis routes and limited electrocatalytic activity and stability. Herein...


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 613
Author(s):  
Hussein Mahdi S. Al-Aani ◽  
Mihaela M. Trandafir ◽  
Ioana Fechete ◽  
Lucia N. Leonat ◽  
Mihaela Badea ◽  
...  

To improve the catalytic performance of an active layered double hydroxide (LDH)-derived CuCeMgAlO mixed oxide catalyst in the total oxidation of methane, it was promoted with different transition-metal cations. Thus, two series of multicationic mixed oxides were prepared by the thermal decomposition at 750 °C of their corresponding LDH precursors synthesized by coprecipitation at constant pH of 10 under ambient atmosphere. The first series of catalysts consisted of four M(3)CuCeMgAlO mixed oxides containing 3 at.% M (M = Mn, Fe, Co, Ni), 15 at.% Cu, 10 at.% Ce (at.% with respect to cations), and with Mg/Al atomic ratio fixed to 3. The second series consisted of four Co(x)CuCeMgAlO mixed oxides with x = 1, 3, 6, and 9 at.% Co, while keeping constant the Cu and Ce contents and the Mg/Al atomic ratio. All the mixed oxides were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) coupled with X-ray energy dispersion analysis (EDX), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption at −196 °C, temperature-programmed reduction under hydrogen (H2-TPR), and diffuse reflectance UV-VIS spectroscopy (DR UV-VIS), while thermogravimetric and differential thermal analyses (TG-DTG-DTA) together with XRD were used for the LDH precursors. The catalysts were evaluated in the total oxidation of methane, a test reaction for volatile organic compounds (VOC) abatement. Their catalytic performance was explained in correlation with their physicochemical properties and was compared with that of a reference Pd/Al2O3 catalyst. Among the mixed oxides studied, Co(3)CuCeMgAlO was found to be the most active catalyst, with a temperature corresponding to 50% methane conversion (T50) of 438 °C, which was only 19 °C higher than that of a reference Pd/Al2O3 catalyst. On the other hand, this T50 value was ca. 25 °C lower than that observed for the unpromoted CuCeMgAlO system, accounting for the improved performance of the Co-promoted catalyst, which also showed a good stability on stream.


Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 505 ◽  
Author(s):  
Xiaoli Wang ◽  
Gongde Wu ◽  
Tongfa Jin ◽  
Jie Xu ◽  
Shihao Song

A series of transition metal oxides or mixed oxides supported nano-Au catalysts were prepared for the selective oxidation of glycerol to glyceric acid using 3% H2O2. It was found that the composition and structure of supports significantly influenced the catalytic performance of catalysts. The mesoporous trimetal mixed oxide (CuNiAlO) supported nano-Au catalysts were more active in comparison with the others. In the present catalytic system, the highest glycerol conversion was 90.5%, while the selectivity of glyceric acid could reach 72%. Moreover, the catalytic performance remained after 11 times of reaction.


1998 ◽  
Vol 18 (1-2) ◽  
pp. 163-170 ◽  
Author(s):  
Ken-ichi Shimizu ◽  
Hajime Maeshima ◽  
Atsushi Satsuma ◽  
Tadashi Hattori

1985 ◽  
Vol 95 (1) ◽  
pp. 155-158 ◽  
Author(s):  
D. Mehandjiev ◽  
E. Zhecheva ◽  
S. Angelov

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