Synthesis and catalytic activity of sol-gel derived La–Ce–Ni perovskite mixed oxide on steam reforming of toluene

2012 ◽  
Vol 12 ◽  
pp. S80-S88 ◽  
Author(s):  
Kanit Soongprasit ◽  
Duangdao Aht-Ong ◽  
Viboon Sricharoenchaikul ◽  
Duangduen Atong
2013 ◽  
Vol 140-141 ◽  
pp. 652-662 ◽  
Author(s):  
Mitsuru Koike ◽  
Yuji Hisada ◽  
Lei Wang ◽  
Dalin Li ◽  
Hideo Watanabe ◽  
...  

2001 ◽  
Vol 68 (1-3) ◽  
pp. 53-61 ◽  
Author(s):  
Matina Thammachart ◽  
Vissanu Meeyoo ◽  
Thirasak Risksomboon ◽  
Somchai Osuwan

2017 ◽  
Vol 101 ◽  
pp. 138-141 ◽  
Author(s):  
Xiaoyong Zhao ◽  
Yaping Xue ◽  
Zhuoxin Lu ◽  
Ying Huang ◽  
Changqing Guo ◽  
...  

Author(s):  
Mohsen Nikoorazm ◽  
Maryam Khanmoradi ◽  
Masoumeh Sayadian

Introduction:: MCM-41 was synthesized using the sol-gel method. Then two new transition metal complexes of Nickel (II) and Vanadium (IV), were synthesized by immobilization of adenine (6-aminopurine) into MCM-41 mesoporous. The compounds have been characterized by XRD, TGA, SEM, AAS and FT-IR spectral studies. Using these catalysts provided an efficient and enantioselective procedure for oxidation of sulfides to sulfoxides and oxidative coupling of thiols to their corresponding disulfides using hydrogen peroxide at room temperature. Materials and Methods:: To a solution of sulfide or thiol (1 mmol) and H2O2 (5 mmol), a determined amount of the catalyst was added. The reaction mixture was stirred at room temperature for the specific time under solvent free conditions. The progress of the reaction was monitored by TLC using n-hexane: acetone (8:2). Afterwards, the catalyst was removed from the reaction mixture by centrifugation and, then, washed with dichloromethane in order to give the pure products. Results:: All the products were obtained in excellent yields and short reaction times indicating the high activity of the synthesized catalysts. Besides, the catalysts can be recovered and reused for several runs without significant loss in their catalytic activity. Conclusion:: These catalytic systems furnish the products very quickly with excellent yields and VO-6AP-MCM-41 shows high catalytic activity compared to Ni-6AP-MCM-41.


ACS Omega ◽  
2020 ◽  
Vol 5 (41) ◽  
pp. 26335-26346
Author(s):  
Min Lu ◽  
Zuhong Xiong ◽  
Kejing Fang ◽  
Jiqing Li ◽  
Xi Li ◽  
...  

2021 ◽  
Author(s):  
Kadriye Özlem Hamaloğlu ◽  
Rukiye Babacan Tosun ◽  
Serap Ulu ◽  
Hakan Kayi ◽  
Cengiz Kavaklı ◽  
...  

A synergistic catalyst in the form of monodisperse-porous CeO2 microspheres supported Pd nanoparticles (Pd NPs) was synthesized. CeO2 microspheres 4 μm in size were obtained by a newly developed “sol-gel...


2021 ◽  
Vol 219 ◽  
pp. 106871
Author(s):  
Shanmukapriya Jayaprakash ◽  
Nikita Dewangan ◽  
Ashok Jangam ◽  
Sibudjing Kawi

Energies ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1875
Author(s):  
Prashanth Reddy Buchireddy ◽  
Devin Peck ◽  
Mark Zappi ◽  
Ray Mark Bricka

Amongst the issues associated with the commercialization of biomass gasification, the presence of tars has been one of the most difficult aspects to address. Tars are an impurity generated from the gasifier and upon their condensation cause problems in downstream equipment including plugging, blockages, corrosion, and major catalyst deactivation. These problems lead to losses of efficiency as well as potential maintenance issues resulting from damaged processing units. Therefore, the removal of tars is necessary in order for the effective operation of a biomass gasification facility for the production of high-value fuel gas. The catalytic activity of montmorillonite and montmorillonite-supported nickel as tar removal catalysts will be investigated in this study. Ni-montmorillonite catalyst was prepared, characterized, and tested in a laboratory-scale reactor for its efficiency in reforming tars using naphthalene as a tar model compound. Efficacy of montmorillonite-supported nickel catalyst was tested as a function of nickel content, reaction temperature, steam-to-carbon ratio, and naphthalene loading. The results demonstrate that montmorillonite is catalytically active in removing naphthalene. Ni-montmorillonite had high activity towards naphthalene removal via steam reforming, with removal efficiencies greater than 99%. The activation energy was calculated for Ni-montmorillonite assuming first-order kinetics and was found to be 84.5 kJ/mole in accordance with the literature. Long-term activity tests were also conducted and showed that the catalyst was active with naphthalene removal efficiencies greater than 95% maintained over a 97-h test period. A little loss of activity was observed with a removal decrease from 97% to 95%. To investigate the decrease in catalytic activity, characterization of fresh and used catalyst samples was performed using thermogravimetric analysis, transmission electron microscopy, X-ray diffraction, and surface area analysis. The loss in activity was attributed to a decrease in catalyst surface area caused by nickel sintering and coke formation.


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