Characterization of Alumina and Silica Sol-Gel Encapsulated Fe/Co/Ru Nanocatalysts in Microchannel Reactors for F-T Synthesis of Higher Alkanes

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.

2005 ◽  
Vol 44 (15) ◽  
pp. 5602-5607 ◽  
Author(s):  
Venkata S. Nagineni ◽  
Shihuai Zhao ◽  
Avinash Potluri ◽  
Yu Liang ◽  
Upali Siriwardane ◽  
...  

1987 ◽  
Vol 153 (Part_1_2) ◽  
pp. 27-36 ◽  
Author(s):  
H. Rosenberger ◽  
H. Bürger ◽  
H. Schütz ◽  
G. Scheler ◽  
G. Maenz

2012 ◽  
Vol 535-537 ◽  
pp. 178-185 ◽  
Author(s):  
Jie Zhu ◽  
Ming Shi Li ◽  
Mo Hong Lu

We reported the synthesis of a promising carbon nanofiber-titania-cordierite monolith composite (C/TiO2/monolith) and its application in citral hydrogenation. The composite was synthesized through two steps: TiO2 coating on the surface of the monolith with sol-gel method and the following carbon deposit by methane decomposition. C/TiO2/monolith was subsequently employed to prepare its supported palladium catalyst, Pd/C/TiO2/monolith and its catalytic performance was evaluated in selective hydrogenation of citral. Results revealed that 2.0 wt% tetrabutyl titanate sol in composite synthesis was the best in improving textural properties of C/TiO2/monolith. The optimal composite possessed a BET surface area of 39.4 m2/g and micropore area accounted for only 3.8% of its total BET surface area. It contained about 30 wt% of carbon, which was mainly composed of carbon nanofiber. Pd/C/TiO2/monolith exhibited the high citronellal selectivity (81%) at 90% citral conversion, which was attributed to the decrease of internal diffusion limitation due to its mesoporous structure.


2007 ◽  
Vol 280-283 ◽  
pp. 661-664 ◽  
Author(s):  
Jing Tao Ma ◽  
Xu Ping Lin ◽  
Bao Qing Zhang ◽  
Jiu Lin Wang

A sol-gel auto-ignited synthesis, which is a hybrid of sol-gel and auto-ignited techniques, was applied to preparation of homogeneous and stoichiometric BaCe0.8Y0.2O2.9 nanocrystalline ceramic powder as solid electrolyte used in solid oxide fuel cells at 1000°C. Optimal pH value for the mixed citrate-nitrate solutions was determined by calculation. The DTA-TG and XRD were used to investigate the thermal decomposition of the gel precursor. The structure and phase present of the nanocrystalline BaCe0.8Y0.2O2.9 powders were characterized by XRD, BET and SEM techniques.


2013 ◽  
Vol 856 ◽  
pp. 285-289
Author(s):  
M.S. Muhd Norhasri ◽  
M.S. Hamidah ◽  
A.G. Abd Halim ◽  
A. Mohd Fadzil

Nano kaolin is product from kaolin also known as white clay. Kaolin was established as supplementary cementitious materials in concrete. The inclusion of kaolin in concrete enhances strength and durability properties and prolongs concrete life span. In this research, nanokaolin will be develop by using sol gel technique by that involves high energy milling. The process of milling been influenced by time of milling, ball and jar type. Ceramic type Zirconia (Zi) is been used as jar and ball type in this process. Time of milling was set from four (4) hours and one (1) days. Sample will be analyse by using particle size analyser to see the particle size and surface area of kaolin. From the result shows the optimum milling period for nanokaolin is one day base on particle size compare to 4 hours. Furthermore, one day milling produces a massive increment of surface area compare to others. In conclusion, one day can be considered as the optimum cycle time in the production of nano kaolin.


2012 ◽  
Vol 620 ◽  
pp. 446-452 ◽  
Author(s):  
Izazi Azzahidah Amin ◽  
Mohd Ambar Yarmo ◽  
Nik Idris Nik Yusoff ◽  
Mohd Zahid Yusoff ◽  
Alifee Ayatillah

The synthesis of alkylpolyglucosides involves condensation of decanol with dextrose in the presence of mesoporous silica sol-gel as a catalyst. In this study, mesoporous silica was produced using sol-gel technique by converting tetraethyl orthosilicate (TEOS) into silica. The mesoporous silica was characterized using BET surface area measurement and X-ray Photoelectron Spectroscopy surface analysis. The specific BET surface area was 794m2/g. From the XPS analysis, the Si2p binding energy is 103.7 eV while the O1s binding energy is 532.8eV indicating the formation of Si-O-Si bond which attributed to SiO2. Mesoporous silica has been found efficient to be solid catalyst for synthesis alkylpolyglucosides and easy to be separated. The reaction was carried out 8 hours at 110°C-120°C under vacuum condition. The mass determination of alkylpoluglucosides has been achieved by ESI LC-MS/MS (ToF) positive-mode giving a mass peak at m/z = 343.21 corresponding to [M++ of alkylmonoglucoside peak at retention time 11.0 min.


1994 ◽  
Vol 346 ◽  
Author(s):  
Kyung Moon Choi ◽  
Kenneth J. Shea

ABSTRACTPoly(l,4-phenylene)-bridged and poly(1,6-hexylene)-bridged silsesquioxanes (PPS and HPS) were prepared by the sol-gel process. The surface areas and pore diameters of these porous xerogels were obtained by BET and BJH methods, respectively. These porous materials were used as a confinement matrix for the growth of small-sized semiconductor and transition metal clusters. Quantum-sized CdS particles in PPS (approximately 58+12 Â) and HPS (91+16 Â) matrices were prepared by first soaking the xerogel in a CdCl2 solution. Following a washing with water, a Na2S solution was then added. EDAX and electron diffraction techniques were used to identify the CdS particles. The particle sizes of CdS in PPS and HPS were determined by both UV measurements and from TEM images. Small-sized Cr clusters were prepared in dried xerogels by an internal doping method. Mixed Cr/CdS phases were also prepared by internal loading of a chromium metal precursor. Following deposition of CdS the xerogel was heated at 120 °C under high vacuum, resulting in formation of intimately mixed phases of Cr metal and CdS. Changes in morphology, in particular the surface area and pore size distribution were noted. A decrease in surface area and an increase in pore size were observed as a result of Cr metal deposition.


2006 ◽  
Vol 13 (3-4) ◽  
pp. 251-258 ◽  
Author(s):  
Chaochin Su ◽  
Kuei-Fen Lin ◽  
Ya-Hui Lin ◽  
Bor-Hou You

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