scholarly journals The control of catalytic performance of rutile-type Sn/V/Nb/Sb mixed oxides, catalysts for propane ammoxidation to acrylonitrile

2008 ◽  
Vol 138 (1-2) ◽  
pp. 97-103 ◽  
Author(s):  
Elena Arcozzi ◽  
Nicola Ballarini ◽  
Fabrizio Cavani ◽  
Massimo Cimini ◽  
Carlo Lucarelli ◽  
...  
2020 ◽  
Vol 15 (2) ◽  
pp. 490-500
Author(s):  
Neha Neha ◽  
Ram Prasad ◽  
Satya Vir Singh

A series of nickel-cobalt bimetal oxides in varying molar ratios and its single metal oxides were synthesized by reactive calcination of coprecipitated basic-carbonates. Several characterization techniques, such as: Bruneuer Emmett Teller (BET), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infra Red (FTIR), and Hydrogen Temperature Programmed Reduction (H2-TPR), were performed over the oxides. Activities of oxides were evaluated in methane total oxidation in the presence or the absence of CO. The best catalytic performance was observed over NiCo catalyst with a Ni/Co molar ratio of 1:1, and the complete conversion of CO-CH4 mixture was achieved at 390 °C. Moreover, the presence of carbon monoxide improves CH4 total oxidation over nickel-cobalt mixed oxides. Structural analysis reveals that the insertion of nickel into the spinel lattice of cobalt oxide causes the structural disorder, which probably caused the increase of the amount of octahedrally coordinated divalent nickel cations that are responsible for catalytic activity. Stability of the best-performed catalyst has been tested in the two conditions, showing remarkable long-term stability and thermal stability, however, showed deactivation after thermally ageing at 700 °C. Copyright © 2020 BCREC Group. All rights reserved 


1992 ◽  
Vol 31 (1) ◽  
pp. 107-119 ◽  
Author(s):  
Roberto Catani ◽  
Gabriele Centi ◽  
Ferruccio Trifiro ◽  
Robert K. Grasselli

RSC Advances ◽  
2017 ◽  
Vol 7 (39) ◽  
pp. 24177-24187 ◽  
Author(s):  
Haidi Xu ◽  
Mengmeng Sun ◽  
Shuang Liu ◽  
Yuanshan Li ◽  
Jianli Wang ◽  
...  

The calcined temperature of the carrier obviously affected SCR activity of catalysts, WO3/Ce0.68Zr0.32O2-500 showed the best low-temperature NH3-SCR activity due to its more Lewis acid sites and stronger redox property.


2005 ◽  
Vol 83 (6-7) ◽  
pp. 574-580 ◽  
Author(s):  
Prem Pal ◽  
Juliette Quartararo ◽  
Sharifah B Abd Hamid ◽  
Eric G Derouane ◽  
Jacques C Védrine ◽  
...  

71Ga, 27Al, and 29Si MAS NMR and DRIFT spectroscopies were used to characterize the state of gallium in Ga/H-ZSM5 catalysts tested for their ability to catalyse the ammoxidation of propane. Ga species were observed in two different possible environments: octahedrally coordinated gallium in small Ga2O3 particles at the external surface of the zeolite crystals, octahedrally coordinated gallium in GaO(OH) or related species, and tetrahedrally coordinated gallium in cationic-exchange positions inside the zeolite. Redox (H2–O2) cycles promote the migration of gallium from the GaO(OH) or Ga2O3 species at the external surface of the zeolite crystals to cationic-exchange sites within the zeolite channels. The redox treatment definitely had a beneficial effect on its catalytic performance for the ammoxidation of propane, which is known to occur via a bifunctional mechanism. The main product was acetonitrile at high Ga and Al contents while acrylonitrile was also observed as a side product at high Ga and low Al contents.Key words: ZSM5, MFI, in situ studies, MAS NMR, DRIFT, propane activation, ammoxidation.


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.


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