Catalytic cracking vapor-phase reactions

Thermal polymerization is not as effective as catalytic polymerization but has the advantage that it can be used to polymerize saturated materials that caimot be induced to react by catalysts. The process consists of the vapor-phase cracking of, for example, propane and butane, followed by prolonged periods at high temperature (510—595°C) for the reactions to proceed to near completion. Olefins can also be conveniendy polymerized by means of an acid catalyst. Thus, the treated olefin-rich feed stream is contacted with a catalyst, such as sulfuric acid, copper pyrophosphate, or phosphoric acid, at 150—220°C and 1035—8275 kPa (150—1200 psi), depending on feedstock and product requirement. 

The catalytic reactions occur in the vapor phase. Cracking reactions begin as soon as the feed is vaporized. The expanding volume of the vapors that are generated are the main driving force to carry the catalyst up the riser. 

C. D. Prater, J. Wei, V. W. Weekman, Jr., and B. Gross, A Reaction Engineering Case History Coke Burning in Thermofor Catalytic Cracking Regenerators Costei D. Denson, Stripping Operations in Polymer Processing Robert C. Reid, Rapid Phase Transitions from Liquid to Vapor John H. Seinfeld, Atmospheric Diffusion Theory... 

The new Brownsville, Tex., plant for the manufacture of synthetic liquid fuels from natural gas makes use of this reaction to increase the octane number of its product by as much as 20 units. Synthetic naphtha produced over iron catalyst is highly olefinic and contains substantial amounts of straight-chain isomers with terminal double bonds (8). The shifting of these double bonds toward the center of the molecule may be accomplished by vapor-phase treatment employing synthetic cracking catalyst in the fluid state, under mild catalytic cracking conditions. Oxygenated compounds also present are converted under the isomerization conditions to hydrocarbons and water. 

Tphe rate-limiting processes in catalytic reaction over zeolites remain A largely undefined, mainly because of the lack of information on counterdiffusion rates at reaction conditions. Thomas and Barmby (7), Chen et al. (2, 3), and Nace (4) speculate on possible diffusional limitations in catalytic cracking over zeolites, and Katzer (5) has shown that intracrystalline diffusional limitations do not exist in liquid-phase benzene alkylation with propene. Tan and Fuller (6) propose internal mass transfer limitations and rapid fouling in benzene alkylation with cyclohexene over Y zeolite, based on the occurrence of a maximum in the reaction rate at about 100 min in flow reaction studies. Venuto et al (7, 8, 9) report similar rate maxima for vapor- and liquid-phase alkylation of benzene and dehydro-... 

Catalytic cracking is the cracking of heavy hydrocarbons using catalyst. The polyolefins such as PP and PE are recycled through this method. In the laboratory scale setup, these reactions are carried out in a flow reactor. There are two modes of catalytic treatment, liquid phase contact and vapor phase contact. In first case, the catalyst is in contact with molten polymers and here the catalyst reacts mainly with oligomers. In vapor phase contact, the catalyst is in contact with thermally degraded polymer [27]. 

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