Catalysis Hydrocracking

Catalysis. As of mid-1995, zeoHte-based catalysts are employed in catalytic cracking, hydrocracking, isomerization of paraffins and substituted aromatics, disproportionation and alkylation of aromatics, dewaxing of distillate fuels and lube basestocks, and in a process for converting methanol to hydrocarbons (54). 

During World War II German scientists developed a method of hydrogenating soHd fuels to remove the sulfur by using a cobalt catalyst (see Coal CONVERSION processes). Subsequently, various American oil refining companies used the process in the hydrocracking of cmde fuels (see CATALYSIS SuLFUR REMOVAL AND RECOVERY). Cobalt catalysts are also used in the Fisher-Tropsch method of synthesizing Hquid fuels (21—23) (see Fuels, synthetic). 

Fetzer, J. C., The Production of Large Polycyclic Aromatic Hydrocarbons During Catalytic Hydrocracking, in Catalysts in Petroleum Refining and Petrochemical Industries, 1996. Kuwait, Studies in Surface Science and Catalysis, Elsevier. 100 pp. 263-271. 

Since ITQ-4/SSZ-42/MCM-58 have been prepared as aluminosilicates with Si/Al ratios of 20 to °°, which possess Brpnsted sites, there is potential for acid catalysis. Some preliminary accounts of catalytic cracking, hydrocracking, dewaxing, alkylation, hydroisomerization, and reforming reactions have been reported (47, 62-64). 

A fairly large number of patents has been issued describing the application of aluminum-deficient Y zeolites in different areas of catalysis. Ultrastable Y zeolites have been used in the preparation of catalysts applied in hydrocarbon cracking, e.g. (94,95) hydrocracking, e.g. (96,97) hydrotreating, e.g. (98) and disproportionation, e.g. (99). 

Bifunctional catalysis is one of the most important routes to green (more economical and more environmentally friendly) processes. Indeed, the deactivation of bifunctional catalysts by coking is much slower than that of monofunctional catalysts and their selectivity generally higher (e.g., hydrocracking compared to... 

Rabo J.A. (ed.) (1979) Zeolite Chemistry and Catalysis, American Chemical Society, Washington, DC Ward J.W. and Qader, S.A. (eds) (1975) Hydrocracking and Hydrotreating, ACS Symposium Series, 20, American Chemical Society, Washington, DC,... 

Hydrocracking Science andTechnology, Julius Scherzer and A. J. Gruia Hydrotreating Technology for Pollution Control Catalysts, Catalysis, and Processes, edited by Mario L. Occelli and Russell Chianelli Catalysis of Organic Reactions, edited by Russell E. Malz, Jr. 

Fixed- or packed-bed reactors refer to two-phase systems in which the reacting fluid flows through a tube filled with stationary catalyst particles or pellets (Smith, 1981). As in the case of ion-exchange and adsorption processes, fixed bed is the most frequently used operation for catalysis (Froment and Bischoff, 1990 Schmidt, 2005). Some examples in the chemical industry are steam reforming, the synthesis of sulfuric acid, ammonia, and methanol, and petroleum refining processes such as catalytic reforming, isomerization, and hydrocracking (Froment and Bischoff, 1990). 

Hydrotreatment and Hydrocracking of Oil Fractions, Studies in Surface Science and Catalysis, Vol. 106, G. F. Froment, B. Delmon, and P. Grange, eds., Elsevier, Amsterdam, 1997. 

It is well known that the accessibility of the mesoporous materials would play an important role in catalysis, and catalytic activity depends on the free diffusion of the reactants, intermediates and products [5], Thus, a mesoporous molecular sieve with better mass transport pore would be a more suitable candidate for some industrial catalytic reactions of the largesized hydrocarbons in dehydrogenation, hydrocracking or hydrodesulfurization. 

In principle, all the kinetic concepts of intercalation introduced for layer-structured silicates hold for zeolites as well. Swelling, of course, is not found because of the rigidity of the three dimensional frame. The practical importance of zeolites as molecular sieves, cation exchangers, and catalysts (cracking and hydrocracking in petroleum industry) is enormous. Molecular shape-selective transport (large differences in diffusivities) and micro-environmental catalysis (in cages and channels)... 

The chain length of n-alkanes has a marked influence on reactivities for hydroisomerization, and especially for hydrocracking. To a very small extent a methane and ethane abstracting mechanism, probably hydrogenolysis as predicted in a basic work on bifunctional catalysis (14), is found to be superimposed when lower carbon number feeds (C, Cg, Cg) are used. n-Hexane is excluded from ideal hydrocracking. On the Pt/Ca-Y-zeolite catalyst it is cracked via a mechanism that is mainly hydrogeno-lytic. 

When metal centers act in conjunction with acid sites on the zeolite, bifunctional catalysis can occur (e.g., Pd/HY). This type of catalysis is used mainly for the hydrocracking and isomerization of long-chain n-alkanes. For example, the rates of formation of 2- and 5-methylnonane isomers obtained from n-decane isomerization over bifunctional zeolite catalysts depend on the size and structure of the zeolites used. This reaction has been developed as a test reaction to characterize zeolite structures (17-19). 

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