Catalytic methane oxidation by a supramolecular conjugate based on a μ-nitrido-bridged iron porphyrinoid dimer

2019 ◽  
Vol 43 (29) ◽  
pp. 11477-11482 ◽  
Author(s):  
Yasuyuki Yamada ◽  
Kentaro Morita ◽  
Nozomi Mihara ◽  
Kazunobu Igawa ◽  
Katsuhiko Tomooka ◽  
...  

Catalytic CH4 oxidation using a μ-nitrido-bridged iron porphyrinoid dimer was successfully activated by supramolecular complexation.

ACS Catalysis ◽  
2013 ◽  
Vol 3 (4) ◽  
pp. 689-699 ◽  
Author(s):  
Ceri Hammond ◽  
Nikolaos Dimitratos ◽  
Robert L. Jenkins ◽  
Jose Antonio Lopez-Sanchez ◽  
Simon A. Kondrat ◽  
...  

2001 ◽  
Vol 676 ◽  
Author(s):  
Seung H. Oh ◽  
Michael L. Everett ◽  
Gar B. Hoflund ◽  
Johannes Seydel ◽  
Horst W. Hahn

ABSTRACTThe catalytic oxidation of methane was studied over palladium supported on nanocrystalline ceria. Three palladium weight loadings (1, 5, and 10 wt%) were tested after calcining at 500 °C, at 280 °C and after no calcination at all. For the 5 and 10 wt% loadings, the 280 °C-calcined and non-calcined catalysts exhibit enhanced activity after several heating and cooling cycles. Calcining these same catalysts at 500 °C results in a systematic decline in activity. For all pretreatments the 1 wt% Pd catalyst exhibits decreasing activity. For the 5 and 10 wt% Pd loadings, the non-calcined catalysts are more active than the 280 °C-calcined catalysts, which are more active than the 500 °C-calcined catalysts. For the 1 wt% Pd catalyst, the opposite is true. The catalyst activity improves as the Pd loading is increased.


2020 ◽  
Vol 10 (23) ◽  
pp. 7875-7882
Author(s):  
Junchen Du ◽  
Depeng Zhao ◽  
Chengxiong Wang ◽  
Yunkun Zhao ◽  
Hong Li ◽  
...  

Pd nanoparticles accompanied with distorted morphology result in considerable active sites and enhance the intrinsic activity for catalytic methane oxidation.


2021 ◽  
Author(s):  
Yasuyuki Yamada ◽  
Jyunichi Kura ◽  
Yuka Toyoda ◽  
Kentaro Tanaka

High catalytic methane oxidation activity of a μ-nitrido-bridged iron phthalocyanine dimer was achieved by introducing 16 electron-donating methyl groups onto the phthalocyanine rings.


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