USRE32239EExpiredUtility

Moving bed catalytic cracking process with platinum group metal or rhenium supported directly on the cracking catalyst

Priority: Sep 20, 1973Filed: May 24, 1985Granted: Sep 2, 1986
Est. expirySep 20, 1993(expired)· nominal 20-yr term from priority
C10G 11/16B01J 29/061C10G 11/05
4
PatentIndex Score
3
Cited by
9
References
5
Claims

Abstract

An improved moving bed continuous catalytic cracking process for cracking hydrocarbon feedstocks, such as gas oil, in the absence of added hydrogen, which includes the use of a minute amount of dispersed platinum supported directly on a cracking catalyst. The trace of platinum induces a substantial increase in the heat efficiency with which coke on catalyst is converted to CO 2 in the regenerator section with minimal or no detriment to the cracking reaction.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for increasing the reflexive heating of a catalyst in the regenerator section of a moving bed catalytic cracking apparatus with minimal or no detriment to cracking operation, said apparatus comprising a cracking section operating in the absence of added hydrogen, a regeneration section comprising two regeneration zones wherein .Iadd.coke is burned to form flue gases that contain CO, said .Iaddend.cracking apparatus containing a circulating inventory of inorganic porous acidic solid cracking catalyst comprising a zeolite component consisting essentially of crystalline aluminosilicate zeolite having a pore diameter of 6 to 15 angstroms, which method comprises circulating with said inventory a minute amount of at least one metal of the group consisting of platinum, palladium, iridium, osmium, rhodium, ruthenium,, and rhenium, said metal being dispersed on said cracking catalyst and supported directly thereon by adding said metal to an existing catalyst, said amount being effective to convert to CO 2  at least about 25% of the CO formed in one of said regeneration zones and substantially ineffective for converting to CO 2  the CO formed in the other said regeneration zone and insufficient to produce more dry gas in said cracking section than is provided by 0.2 wt % chromia. 
     
     
       2. The method of claim 1 wherein said metal is platinum. 
     
     
       3. The method of claim 1 wherein said amount of metal is effective to convert to CO 2  substantially all of the CO formed in one of said regeneration zones. 
     
     
       4. The method of claim 3 wherein said metal is platinum. 
     
     
       5. The method described in claim 1 wherein said cracking catalyst contains a measurable amount less than 0.1 wt. % of chromia and said metal is platinum.

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