Microreactors for Syngas Conversion to Higher Alkanes:  Characterization of Sol−Gel-Encapsulated Nanoscale Fe−Co Catalysts in the Microchannels

2005 ◽  
Vol 44 (15) ◽  
pp. 5602-5607 ◽  
Author(s):  
Venkata S. Nagineni ◽  
Shihuai Zhao ◽  
Avinash Potluri ◽  
Yu Liang ◽  
Upali Siriwardane ◽  
...  
2004 ◽  
Vol 820 ◽  
Author(s):  
D. Kuila ◽  
V.S. Nagineni ◽  
S. Zhao ◽  
H. Indukuri ◽  
Y. Liang ◽  
...  

AbstractWe have been investigating conversion of syngas (CO: H2) to higher alkanes [Fischer-Tropsch (F-T) Process] in 5 μm and 25 μm channel microreactors coated with sol-gel encapsulated Fe/Co-nanocatalysts. These nano-metal-catalysts were incorporated into the sol-gel matrix by two methods: 1) metal nitrate solutions; 2) metal oxide nanoparticles. Characterization of these catalysts containing Co and Fe in alumina and silica sol-gel has been carried out by several techniques. The surface area measurements by BET method show an average specific surface area of 285 m2/g for alumina and 300 m2/g for silica sol-gel encapsulated catalysts. In order to optimize the sol-gel preparation and deposition in the microchannels, the elemental composition of sol-gel encapsulated catalyst was examined by EDX. The SEM and AFM images of the reactors before and after deposition of the catalysts have also been studied. Hydrogenation-reduction efficiency of the activated Fe-Co catalysts and the level of poisoning after the reaction were estimated using a vibrating sample magnetometer (VSM). The result suggests more efficient reduction in the case of the nano-particle metal oxides compared to that derived from metal nitrate solutions. In overall, 85% of the catalyst is poisoned after 25 hrs of catalytic reaction. The surface area and the syngas conversion results indicate that silica sol-gel matrix may be a better catalyst support. For alumina sol-gel support, higher conversion of syn-gas is observed with 25 μm microreactor channels. For silica sol-gel, syngas conversion as high as 73% has been achieved by adding Ru as a promoter to the Fe/Co catalyst mixture.


1992 ◽  
Vol 293 ◽  
Author(s):  
Herve Cheradame ◽  
F. Desbat ◽  
P. Mercier-Niddam ◽  
S. Boileau

AbstractIonically conducting materials containing PEO were prepared from telechelic di(methyl-diethoxy-silane) PEO, synthesized by the hydrosilylation of telechelic diallyl-PEO with methyldiethoxysilane. The network is obtained by the usual sol-gel chemistry. Then, it is filled with LiClO4 by diffusion of the salt and further drying. A comparison is made with the same kind of materials crosslinked using urethane chemistry. Diffusion studies show that the diffusion coefficient of solvent is similar for both types of materials, whilst the ionic conductivity is higher for the networks crosslinked with siloxane bonds. An experiment of diffusion of LiClO4 without solvent showed that this salt has a diffusion coefficient of the order of 2.10-8 cm2.sec-1 at 34°C. The conductivity calculated from this determination is compatible with the mechanism of lithium cation transport by the diffusion of salt molecules. Elasticity modulus measurements show that the salt aggregates are essentially located within the crosslinks at low concentration, but also in the PEO chains for salt concentrations higher than 1 mol/l.


2021 ◽  
Vol 395 (1) ◽  
pp. 2000197
Author(s):  
Michelina Catauro ◽  
Ignazio Blanco ◽  
Daniele Naviglio ◽  
Giovanni Dal Poggetto

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