A novel CeO2 supported on carbon nanotubes coated with SiO2 catalyst for catalytic cracking of naphtha

2012 ◽  
Vol 417-418 ◽  
pp. 53-58 ◽  
Author(s):  
Kamyar Keyvanloo ◽  
Ali Mohamadalizadeh ◽  
Jafar Towfighi
2010 ◽  
Vol 149 (3-4) ◽  
pp. 352-357 ◽  
Author(s):  
Ismael González ◽  
Juan Carlos De Jesus ◽  
Caribay Urbina de Navarro ◽  
Miguel García

2009 ◽  
Vol 79-82 ◽  
pp. 585-588
Author(s):  
Li Zhen Gao ◽  
Wei Ke Zhang ◽  
Andrew Cornejo ◽  
Hui Tong Chua

The catalytic cracking of methane to produce COx free hydrogen and a spectrum of advanced carbon nano materials was studied. Over several genres of catalysts by cracking of undiluted methane we produced hydrogen and highly graphitic carbon nanotubes (single-, thin- and multi-walled), straight microfibers, nano onions over the solid oxides solution, perovskite structured mixed oxides and mesoporous supported catalysts. The influences of reaction temperature on the methane conversion over various catalysts were investigated. The yields of carbon materials were monitored during the cracking running and the results indicated that these series of catalysts are promising for the commercialization of carbon nanotubes, microfibers and microballs.


Author(s):  
J.K. Lampert ◽  
G.S. Koermer ◽  
J.M. Macaoy ◽  
J.M. Chabala ◽  
R. Levi-Setti

We have used high spatial resolution imaging secondary ion mass spectrometry (SIMS) to differentiate mineralogical phases and to investigate chemical segregations in fluidized catalytic cracking (FCC) catalyst particles. The oil industry relies on heterogeneous catalysis using these catalysts to convert heavy hydrocarbon fractions into high quality gasoline and fuel oil components. Catalyst performance is strongly influenced by catalyst microstructure and composition, with different chemical reactions occurring at specific types of sites within the particle. The zeolitic portions of the particle, where the majority of the oil conversion occurs, can be clearly distinguished from the surrounding silica-alumina matrix in analytical SIMS images.The University of Chicago scanning ion microprobe (SIM) employed in this study has been described previously. For these analyses, the instrument was operated with a 40 keV, 10 pA Ga+ primary ion probe focused to a 30 nm FWHM spot. Elemental SIMS maps were obtained from 10×10 μm2 areas in times not exceeding 524s.


Author(s):  
Clifford S. Rainey

The spatial distribution of V and Ni deposited within fluidized catalytic cracking (FCC) catalyst is studied because these metals contribute to catalyst deactivation. Y zeolite in FCC microspheres are high SiO2 aluminosilicates with molecular-sized channels that contain a mixture of lanthanoids. They must withstand high regeneration temperatures and retain acid sites needed for cracking of hydrocarbons, a process essential for efficient gasoline production. Zeolite in combination with V to form vanadates, or less diffusion in the channels due to coke formation, may deactivate catalyst. Other factors such as metal "skins", microsphere sintering, and attrition may also be involved. SEM of FCC fracture surfaces, AEM of Y zeolite, and electron microscopy of this work are developed to better understand and minimize catalyst deactivation.


Author(s):  
Jun Jiao

HREM studies of the carbonaceous material deposited on the cathode of a Huffman-Krätschmer arc reactor have shown a rich variety of multiple-walled nano-clusters of different shapes and forms. The preparation of the samples, as well as the variety of cluster shapes, including triangular, rhombohedral and pentagonal projections, are described elsewhere.The close registry imposed on the nanotubes, focuses attention on the cluster growth mechanism. The strict parallelism in the graphitic separation of the tube walls is maintained through changes of form and size, often leading to 180° turns, and accommodating neighboring clusters and defects. Iijima et. al. have proposed a growth scheme in terms of pentagonal and heptagonal defects and their combinations in a hexagonal graphitic matrix, the first bending the surface inward, and the second outward. We report here HREM observations that support Iijima’s suggestions, and add some new features that refine the interpretation of the growth mechanism. The structural elements of our observations are briefly summarized in the following four micrographs, taken in a Hitachi H-8100 TEM operating at an accelerating voltage of 200 kV and with a point-to-point resolution of 0.20 nm.


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