GB787575A - Improvements in or relating to process for the treatment of platinum catalyst - Google Patents

Improvements in or relating to process for the treatment of platinum catalyst

Info

Publication number
GB787575A
GB787575A GB7024/54A GB702454A GB787575A GB 787575 A GB787575 A GB 787575A GB 7024/54 A GB7024/54 A GB 7024/54A GB 702454 A GB702454 A GB 702454A GB 787575 A GB787575 A GB 787575A
Authority
GB
United Kingdom
Prior art keywords
oxygen
catalyst
gas
pipe
flue gas
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB7024/54A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB787575A publication Critical patent/GB787575A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/70Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with two hydrocarbon radicals attached in position 2 and elements other than carbon and hydrogen in position 6
    • C07D311/723,4-Dihydro derivatives having in position 2 at least one methyl radical and in position 6 one oxygen atom, e.g. tocopherols
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/90Regeneration or reactivation
    • B01J23/96Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the noble metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G35/00Reforming naphtha
    • C10G35/04Catalytic reforming
    • C10G35/10Catalytic reforming with moving catalysts
    • C10G35/14Catalytic reforming with moving catalysts according to the "fluidised-bed" technique
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

<PICT:0787575/IV (b)/1> Supported platinum catalyst which has become contaminated with carbonaceous deposits during the hydroforming at 900-1000 DEG F. of a naphthenic feedstock of boiling range 150-500 DEG F. is regenerated with an oxygencontaining gas at a temperature not exceeding 1100 DEG F. and then cooled by from 150-300 DEG F., the cooling taking place in the presence of an oxygen-containing gas having an oxygen partial pressure of at least one atmosphere. For pressures of 200-400 p.s.i.g., this oxygen partial pressure corresponds to 3.5 to 7 per cent by volume of oxygen or more. The catalyst support may be alumina (e.g. gamma alumina derived from boehmite), zirconia, magnesia, or magnesia-alumina. Hydroforming pressures may be 50-700 p.s.i.g. As shown in Fig. 1, hydrogen and vaporized feed pass through pipe 20 into a fluidized bed of catalyst in reactor 11, the product being withdrawn through pipe 21. Catalyst for regeneration is carried by flue gas through pipe 14 to regenerator 12; air, which may be mixed with flue gas or oxygen, is fed in at 50. Catalyst leaving the regenerator is treated in pipe 15 with gas introduced through pipe 54; this gas has an oxygen partial pressure of at least one atmosphere and a temperature of 1050-1100 DEG F. The catalyst is then cooled to 800-900 DEG F. in vessel 56 in the presence of a gas of similar oxygen partial pressure, oxygen is removed by stripping in vessel 18 with flue gas, nitrogen, or carbon dioxide, and the regenerated catalyst is mixed with the feed in pipe 20. The treatment in pipe 15, cooler 56, and stripper 18 may be carried out on only a portion of the catalyst, the remainder being returned directly to the reactor; alternatively, the treatment may be given only after several reaction and regeneration cycles. In fixed bed operation, Fig. 2 (not shown), two catalyst bed-are provided and are used alternately, regeneration being carried out by purging with flue gas at 600-1000 DEG F., adjusting the temperature of the gas to 700-800 DEG F. and then adding an oxygen-containing gas to the flue gas to burn off carbonaceous matter. The oxygen content of the flue gas is then increased to provide a partial pressure of at least one atmosphere and the temperature is increased to 1050-1100 DEG F. Cooling is effected by reducing the temperature of the gas to 800-900 DEG F. and then flue gas is used to purge oxygen from the bed. After passage of a hydrogen-containing gas, the bed is ready for re-use. In another embodiment, oxygen at 35-45 lbs. per square inch absolute is passed over the regenerated catalyst first at 1100 DEG F. and then at 800 DEG F.; nitrogen is used for purging the catalyst.ALSO:<PICT:0787575/III/1> Supported platinum catalyst which has become contaminated with carbonaceous deposits during the hydroforming at 900-1000 DEG F. of a naphthenic feedstock of boiling range 150-500 DEG F. is regenerated with an oxygen-containing gas at a temperature not exceeding 1100 DEG F. and then cooled by from 150-300 DEG F., the cooling taking place in the presence of an oxygen-containing gas having an oxygen partial pressure of at least one atmosphere. For pressures of 200-400 p.s.i.g., this oxygen partial pressure corresponds to 3.5 to 7 per cent by volume of oxygen or more. The catalyst support may be alumina (e.g. gamma alumina derived from boehmite), zirconia, magnesia, or magnesia - alumina. Hydroforming pressures may be 50-700 p.s.i.g. As shown in Fig. 1, hydrogen and vaporized feed pass through pipe 20 into a fluidized bed of catalyst in reactor 11, the product being withdrawn through pipe 21. Catalyst for regeneration is carried by flue gas through pipe 14 to regenerator 12; air, which may be mixed with flue gas or oxygen, is fed in at 50. Catalyst leaving the regenerator is treated in pipe 15 with gas introduced through pipe 54; this gas has an oxygen partial pressure of at least one atmosphere and a temperature of 1050-1100 DEG F. The catalyst is then cooled to 800-900 DEG F. in vessel 56 in the presence of a gas of similar oxygen partial pressure, oxygen is removed by stripping in vessel 18 with flue gas, nitrogen, or carbon dioxide, and the regenerated catalyst is mixed with the feed in pipe 20. The treatment in pipe 15, cooler 56 and stripper 18 may be carried out on only a portion of the catalyst, the remainder being returned directly to the reactor; alternatively, the treatment may be given only after several reaction and regeneration cycles. In fixed bed operation, Fig. 2 (not shown), two catalyst beds are provided and are used alternately, regeneration being carried out by purging with flue gas at 600-1000 DEG F., adjusting the temperature of the gas to 700-800 DEG F. and then adding an oxygen-containing gas to the flue gas to burn off carbonaceous matter. The oxygen content of the flue gas is then increased to provide a partial pressure of at least one atmosphere and the temperature is increased to 1050-1100 DEG F. Cooling is effected by reducing the temperature of the gas to 800-900 DEG F. and then flue gas is used to purge oxygen from the bed. After passage of a hydrogen-containing gas, the bed is ready for re-use. In another embodiment, oxygen at 35-45 lbs. per sq. inch absolute is passed over the regenerated catalyst first at 1100 DEG F. and then at 800 DEG F.; nitrogen is used for purging the catalyst.
GB7024/54A 1953-03-18 1954-03-10 Improvements in or relating to process for the treatment of platinum catalyst Expired GB787575A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US343198A US2856349A (en) 1953-03-18 1953-03-18 Two stage regeneration of platinum containing catalyst composite employed in hydroforming

Publications (1)

Publication Number Publication Date
GB787575A true GB787575A (en) 1957-12-11

Family

ID=23345094

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7024/54A Expired GB787575A (en) 1953-03-18 1954-03-10 Improvements in or relating to process for the treatment of platinum catalyst

Country Status (5)

Country Link
US (1) US2856349A (en)
BE (1) BE527396A (en)
ES (1) ES214265A1 (en)
FR (1) FR1096790A (en)
GB (1) GB787575A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2939897A (en) * 1958-08-15 1960-06-07 Pure Oil Co Process and catalyst for the isomerization of light paraffin
US3270790A (en) * 1964-03-09 1966-09-06 Plastronics Inc Detachable tube to bag connector means and method of making same
CA1100474A (en) * 1976-12-13 1981-05-05 Robert J. Houston Catalyst reduction method
FR2603044B1 (en) * 1986-08-25 1988-11-04 Inst Francais Du Petrole PROCESS FOR REGENERATING A HYDROCONVERSION HYDROCONVERSION CATALYST

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2368507A (en) * 1940-12-31 1945-01-30 Standard Oil Dev Co Regeneration of catalysts
US2701230A (en) * 1949-07-01 1955-02-01 Standard Oil Dev Co Hydroforming process and apparatus
US2664404A (en) * 1949-08-18 1953-12-29 Standard Oil Dev Co Regeneration of selective hydrogenation catalyst
US2641582A (en) * 1950-10-03 1953-06-09 Universal Oil Prod Co Regeneration of a platinumcontaining catalyst
US2662861A (en) * 1951-08-15 1953-12-15 Kellogg M W Co Platinum and palladium catalysts

Also Published As

Publication number Publication date
US2856349A (en) 1958-10-14
BE527396A (en) 1900-01-01
FR1096790A (en) 1955-06-24
ES214265A1 (en) 1954-07-01

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