Liquid from catalytic cracking

Products from catalytic cracking units are also more stable due to a lower olefin content in the liquid products. This reflects a higher hydrogen transfer activity, which leads to more saturated hydrocarbons than in thermally cracked products from delayed coking units, for example. 

Antdysis of Liquid Product from Catalytic Cracking of n-Octenes... 

Distillate firom the residue from catalytic cracking (blackish-brown liquid)... 

In a single stage, without liquid recycle, the conversion can be optimized between 60 and 90%. The very paraffinic residue is used to make lubricant oil bases of high viscosity index in the range of 150 N to 350 N the residue can also be used as feedstock to steam cracking plants providing ethylene and propylene yields equal to those from paraffinic naphthas, or as additional feedstock to catalytic cracking units. 

The Ce-Cg aromatic hydrocarbons—though present in crude oil—are generally so low in concentration that it is not technically or economically feasible to separate them. However, an aromatic-rich mixture can be obtained from catalytic reforming and cracking processes, which can be further extracted to obtain the required aromatics for petrochemical use. Liquefied petroleum gases (C3-C4) from natural gas and refinery gas streams can also be catalytically converted into a liquid hydrocarbon mixture rich in C6-C8 aromatics. 

It has been shown, however, that such catalysts may contain protons, either by design or because of the difficulty in removing all traces of moisture, and these protons have been shown to be superacidic with Hammett acidities up to —18. These protons will also play some role in the catalytic activity of these ionic liquids in practical situations. Ionic liquids in which superacidic protons have deliberately been generated by addition of small amounts of water, HCl or H2SO4 have been used to catalytically crack polyethene under relatively mild conditions. The main products are mixed C3-C5 alkanes, which would be a useful feedstock from waste polyethene recycling. In contrast to other cracking procedures no aromatics or alkenes are produced, although small amounts of polycyclic compounds are obtained. 

Figure 7.7b shows the essential features of a refinery catalytic cracker. Large molar mass hydrocarbon molecules are made to crack into smaller hydrocarbon molecules in the presence of a solid catalyst. The liquid hydrocarbon feed is atomized as it enters the catalytic cracking reactor and is mixed with the catalyst particles being carried by a flow of steam or light hydrocarbon gas. The mixture is carried up the riser and the reaction is essentially complete at the top of the riser. However, the reaction is accompanied by the deposition of carbon (coke) on the surface of the catalyst. The catalyst is separated from the gaseous products at the top of the reactor. The gaseous products leave the reactor... 

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... 

Addition of ZSM-5 in a catalytic cracking unit can permit a reduction in reformer severity. At a given pool octane requirement, the higher FGG octane contribution (Research/Motor) allows for lower reformer severity and, consequently, higher reformate yields. At EniGhem s Gela FGG unit fl2-14). when ZSM-5 was in the FGG, the reformate severity dropped from 95.0 RON clear to 90.0 RON clear while liquid yield increased by 4% vol. 

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