Catalytic reaction rates in thermodynamically non-ideal systems

2000 ◽  
Vol 163 (1-2) ◽  
pp. 189-204 ◽  
Author(s):  
Rostam J. Madon ◽  
Enrique Iglesia
2009 ◽  
Vol 113 (11) ◽  
pp. 3579-3583 ◽  
Author(s):  
Malika Kumarasiri ◽  
Gregory A. Baker ◽  
Alexander V. Soudackov ◽  
Sharon Hammes-Schiffer

2001 ◽  
Vol 25 (9-10) ◽  
pp. 1185-1198 ◽  
Author(s):  
Sergio P. Bressa ◽  
Néstor J. Mariani ◽  
Néstor O. Ardiaca ◽  
Germán D. Mazza ◽  
Osvaldo M. Martı́nez ◽  
...  

Author(s):  
Xijia Lu ◽  
Ting Wang

In this paper, the coal-to-synthetic natural gas (SNG) technologies have been reviewed. Steam-oxygen gasification, hydrogasification, and catalytic steam gasification are the three major gasification processes used in coal-to-SNG production. So far, only the steam-oxygen gasification process is commercially proven by installing a catalytic methanation reactor downstream of the gasification process after syngas is produced, cleaned, and shifted to achieve an appropriate H2/CO ratio for methanation reaction. This process is expensive, less efficient, and time consuming. Ideally, it will be more effective and economic if methanation could be completed in an once-through entrained-flow gasifier. Technically, this idea is challenging because an effective gasification process is typically operated in a high-pressure and high-temperature condition, which is not favorable for methanation reaction, which is exothermic. To investigate this idea, a computational model is established and a sensitivity study of methanation reactions with and without catalysts are conducted in this study. In modeling the methanation process in a gasifier, correct information of the reaction rates is extremely important. Most of known methanation reaction rates are tightly linked to the catalysts used. Since the non-catalytic reaction rates for methanation are not known in a gasifer and the issues are compounded by the fact that inherent minerals in coal ashes can also affect the methanation kinetics, modeling of methanation in an entrained-flow gasifier becomes very challenging. Considering these issues, instead of trying to obtain the correct methnation reaction rate, this study attempts to use computational model as a convenient tool to investigate the sensitivity of methane production under a wide range methanation reaction rates with and without catalysts. From this sensitivity study, it can be learned that the concept of implementing direct methanation in a once-through entrained-flow gasifier may not be attractive due to competitions of other reactions in a high-temperature environment. The production of SNG is limited to about 18% (vol) with catalytic reaction with a pre-exponential factor A in the order of 107. A further increase of the value of A to 1011 doesn’t result in more production of SNG. This SNG production limit could be caused by the high-temperature and short residence time (3–4 seconds) in the entraind-flow gasifier.


2020 ◽  
Vol 56 (98) ◽  
pp. 15450-15453
Author(s):  
Inhak Song ◽  
Hwangho Lee ◽  
Se Won Jeon ◽  
Taejin Kim ◽  
Do Heui Kim

Reaction rates of Lewis-NH3 and Brønsted-NH3 species were measured to be equivalent in the selective catalytic reaction over V2O5/TiO2 catalyst.


1970 ◽  
Vol 74 (17) ◽  
pp. 3231-3236 ◽  
Author(s):  
Henry N. Blount ◽  
Nicholas Winograd ◽  
Theodore Kuwana

2004 ◽  
Vol 380 (1) ◽  
pp. 121-130 ◽  
Author(s):  
Jitka FRÉBORTOVÁ ◽  
Marco W. FRAAIJE ◽  
Petr GALUSZKA ◽  
Marek ŠEBELA ◽  
Pavel PEČ ◽  
...  

The catalytic reaction of cytokinin oxidase/dehydrogenase (EC 1.5.99.12) was studied in detail using the recombinant flavoenzyme from maize. Determination of the redox potential of the covalently linked flavin cofactor revealed a relatively high potential dictating the type of electron acceptor that can be used by the enzyme. Using 2,6-dichlorophenol indophenol, 2,3-dimethoxy-5-methyl-1,4-benzoquinone or 1,4-naphthoquinone as electron acceptor, turnover rates with N6-(2-isopentenyl)adenine of approx. 150 s−1 could be obtained. This suggests that the natural electron acceptor of the enzyme is quite probably a p-quinone or similar compound. By using the stopped-flow technique, it was found that the enzyme is rapidly reduced by N6-(2-isopentenyl)adenine (kred=950 s−1). Re-oxidation of the reduced enzyme by molecular oxygen is too slow to be of physiological relevance, confirming its classification as a dehydrogenase. Furthermore, it was established for the first time that the enzyme is capable of degrading aromatic cytokinins, although at low reaction rates. As a result, the enzyme displays a dual catalytic mode for oxidative degradation of cytokinins: a low-rate and low-substrate specificity reaction with oxygen as the electron acceptor, and high activity and strict specificity for isopentenyladenine and analogous cytokinins with some specific electron acceptors.


Biopolymers ◽  
1973 ◽  
Vol 12 (7) ◽  
pp. 1689-1704 ◽  
Author(s):  
Charles Delisi ◽  
Donald M. Crothers

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