Effect of Pressure on Catalyst Activity and Carbon Deposition During CO2 Reforming of Methane over Noble-Metal Catalysts

Author(s):  
Abolghasem Shamsi ◽  
Christopher D. Johnson
Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 159
Author(s):  
András Erdőhelyi

The conversion of CO2 and CH4, the main components of the greenhouse gases, into synthesis gas are in the focus of academic and industrial research. In this review, the activity and stability of different supported noble metal catalysts were compared in the CO2 + CH4 reaction on. It was found that the efficiency of the catalysts depends not only on the metal and on the support but on the particle size, the metal support interface, the carbon deposition and the reactivity of carbon also influences the activity and stability of the catalysts. The possibility of the activation and dissociation of CO2 and CH4 on clean and on supported noble metals were discussed separately. CO2 could dissociate on metal surfaces, this reaction could proceed via the formation of carbonate on the support, or on the metal–support interface but in the reaction the hydrogen assisted dissociation of CO2 was also suggested. The decrease in the activity of the catalysts was generally attributed to carbon deposition, which can be formed from CH4 while others suggest that the source of the surface carbon is CO2. Carbon can occur in different forms on the surface, which can be transformed into each other depending on the temperature and the time elapsed since their formation. Basically, two reaction mechanisms was proposed, according to the mono-functional mechanism the activation of both CO2 and CH4 occurs on the metal sites, but in the bi-functional mechanism the CO2 is activated on the support or on the metal–support interface and the CH4 on the metal.


1977 ◽  
Vol 32 (12) ◽  
pp. 1461-1466 ◽  
Author(s):  
Walter Strohmeier ◽  
Magdalena Pföhler ◽  
Hannelore Steigerwald

Unsaturated compounds are very rapidly hydrogenated with nickel-boride catalyst P-2-Ni without solvent under mild conditions (70-85 °C and 10 bar). Turnover numbers UZ up to 90,000 and space-time-yields of 7440 mmol product per 1 and 1 mgA Nickel in one hour with a mean catalyst activity ā = 124 were observed. This hydrogenation catalyst has a power, which is in the same magnitude of very active noble metal catalysts.


2021 ◽  
pp. 2150013
Author(s):  
Lei Wei ◽  
Xiaomeng Wang ◽  
Ya-Na Yu ◽  
Hongyan Liu ◽  
Yepei Li ◽  
...  

For practical application of sodium borohydride (NaBH[Formula: see text] hydrolysis to generate hydrogen, metallic catalysts with low cost but excellent activity are highly desired. However, it remains a big challenge to further improve the activity of non-noble metal catalysts. In this work, photocatalysis technology was successfully introduced to enhance the catalyst activity for NaBH4 hydrolysis. By means of conventional impregnation-reduction method, CoB nanocatalyst was evenly deposited on graphitic carbon nitride surface, resulting in a Schottky-type photocatalyst (CoB/CN). As expected, hydrogen generation rate was greatly boosted owing to light irradiation. According to the results of capture experiments, photoexcited electron from g-C3N4 could enrich the electron density of CoB surface, which leads to the improvement of catalyst activity. Additionally, the light irradiation facilitates the remarkable decrease of apparent activation energy. Compared with some reported noble metal catalysts, the CoB/CN presents higher activity, especially under light irradiation.


1981 ◽  
Vol 46 (11) ◽  
pp. 2657-2662
Author(s):  
Zdeněk Prokop ◽  
Karel Setínek

Some additional data about properties and applicability of a styrene-divinylbenzene polymer catalyst containing acidic and redox functional groups are reported. It is shown that the catalysts of this type can be prepared reproducibly and exhibit catalytic properties comparable to the properties of noble metal catalysts.


2017 ◽  
Vol 60 (3) ◽  
pp. 137-145 ◽  
Author(s):  
Fumihiro Watanabe ◽  
Ikuko Kaburaki ◽  
Naohiro Shimoda ◽  
Akira Igarashi ◽  
Shigeo Satokawa

ChemInform ◽  
2010 ◽  
Vol 24 (27) ◽  
pp. no-no
Author(s):  
F. KAPTEIJN ◽  
S. STEGENGA ◽  
N. J. J. DEKKER ◽  
J. W. BIJSTERBOSCH ◽  
J. A. MOULIJN

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