US2921016A - Catalytic reforming of petroleum hydrocarbons - Google Patents

Catalytic reforming of petroleum hydrocarbons Download PDF

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Publication number
US2921016A
US2921016A US619511A US61951156A US2921016A US 2921016 A US2921016 A US 2921016A US 619511 A US619511 A US 619511A US 61951156 A US61951156 A US 61951156A US 2921016 A US2921016 A US 2921016A
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United States
Prior art keywords
octane number
platformate
hydrogen
catalytic reforming
petroleum hydrocarbons
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Expired - Lifetime
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US619511A
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English (en)
Inventor
Cuddington Kenneth Shephard
Mather John
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BP PLC
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BP PLC
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    • 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
    • C10G69/00Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
    • C10G69/02Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
    • C10G69/08Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only including at least one step of reforming naphtha

Definitions

  • This invention relates to the catalytic reforming of petroleum hydrocarbons in order to increase their suitability for use as motor fuels. More particularly the invention relates to improvements in the so-called Platforming process wherein hydrocarbons are contacted in the presence of hydrogen with a platinum-containing catalyst.
  • Platforming is capable of producing a considerable increase in the octane number of straight-run petroleum feedstocks in the motor gasoline boiling range, but it has recently been noted that the octane number of the Platformate falls off rapidly on exposure to light and air, and that this effect cannot be prevented by the use of oxidation inhibitors.
  • a similar loss of octane number is not shown by catalytically cracked or steam cracked n gasoline, so that the component or components causing the octane number loss appear to be formed by the reforming operation itself.
  • the extent of the loss in the octane number in respect of a typical Platformate is illustrated in the following Table 1, and compared with the loss for samples of catalytically cracked and steam cracked gasolines.
  • the preferred catalyst is a sulphur resistant hydrogenation catalyst particularly one or more of the sulphides of a group VI or group VIII metal, for example a mixture of nickel and tungsten sulphides.
  • a sample of debutanised Platformate having a research octane number of 87.1 was "ice exposed to air and light for 24 hours, after which time the research octane number had decreased to 81.5.
  • the Platformate After hydrogenation, the Platformate had a research octane number of 86.5 which after 96 hours exposure to ⁇ air and light had only decreased to 86.1.
  • the fraction of Platformate boiling between 100 and 138 C. is separated and subjected to mild hydrogenation as above described, the hydrogenated fraction being then blended back with the remaining portions of the Platformate.
  • the hydrogenation treatment in accordance with the invention may be carried out as an operation separate and distinct from the Platforming operation. If desired however, it may be carried out as part of a continuous process with the Platforming operation. In this case, the product from the Platforming operation is cooled and if necessary reduced in pressure before being passed to the hydrogenation reactor.
  • the products from a catalytic reformer 1 include liquid debutanised reformate and hydrogen-rich gas.
  • the former is fed via line 2 to a reformate splitter 3 where it is fractionated into three streams, the middle of which contains substantially all the components giving rise to the lightcatalysed octane number loss.
  • This stream is passed via line 4 to a hydrogenation plant 5 supplied through line 6 with the hydrogen-rich gas from the catalytic reformer 1. After hydrogenation, the stream is recombined with the splitter overheads and splitter bottoms which are fed via lines 7 and 8 respectively.
  • the dotted continuations of thesplitter overheads and the splitter bottoms lines (9 and 10 respectively) illustrate a possible variant of the process in which the splitter streams are not recombined.
  • the dotted line 11 by-passing the reformate splitter illustrates a further variant in which the total debutanised reformate is hydrogenated without previous splitting.
  • a process for reducing loss of octane number due to exposure to light and air of a platinum reformate obtained by contacting a straight-run petroleum feedstock boiling in the gasoline range with a reforming catalyst containing platinum which comprises contacting the platinum reformate in the presence of hydrogen with a hydrogenation catalyst at a temperature of 300 to 500 F. and at a pressure of 0 to 500 p.s.i.g.
  • a process for reducing loss of octane number due to exposure to light and air of a platinum reformate obtained by contacting a straight-run petroleum feedstock boiling in the gasoline range with a reforming catalyst containing platinum which comprises separating from the platinum reformate a fraction having a boiling range of approximately 100 to 138 C., contacting said fraction in the presence of hydrogen with a hydrogenation to 4000 s.c.f./b.
  • the catalyst comprises at least one sulphide of a metal selected from groups VI and VIII of the periodic table.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US619511A 1955-11-11 1956-10-31 Catalytic reforming of petroleum hydrocarbons Expired - Lifetime US2921016A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB32289/55A GB843177A (en) 1955-11-11 1955-11-11 Process for the hydrogenation of catalytic reformates

Publications (1)

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US2921016A true US2921016A (en) 1960-01-12

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US619511A Expired - Lifetime US2921016A (en) 1955-11-11 1956-10-31 Catalytic reforming of petroleum hydrocarbons

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US (1) US2921016A (enrdf_load_stackoverflow)
BE (1) BE552485A (enrdf_load_stackoverflow)
DE (1) DE1126551B (enrdf_load_stackoverflow)
FR (1) FR1187644A (enrdf_load_stackoverflow)
GB (1) GB843177A (enrdf_load_stackoverflow)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5658453A (en) * 1995-05-30 1997-08-19 Uop Integrated aromatization/trace-olefin-reduction scheme

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2345575A (en) * 1940-12-09 1944-04-04 Standard Oil Co Process of preparing gasoline of low gum-forming tendency
US2425506A (en) * 1945-07-13 1947-08-12 Standard Oil Dev Co Production of premium aviation fuel components
US2534025A (en) * 1941-05-05 1950-12-12 Anglo Iranian Oil Co Ltd Production of aviation or motor fuels
US2731506A (en) * 1953-01-28 1956-01-17 Exxon Research Engineering Co Production of hydrocarbon solvents of low acid wash color
US2740751A (en) * 1952-02-23 1956-04-03 Universal Oil Prod Co Reforming of both straight run and cracked gasolines to provide high octane fuels

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE508926A (enrdf_load_stackoverflow) *
US1981305A (en) * 1929-08-10 1934-11-20 Union Oil Co Process and apparatus for the catalytic treatment of petroleum
DE734151C (de) * 1933-07-15 1943-04-12 Ig Farbenindustrie Ag Verfahren zur Herstellung nicht verharzender Motortreibstoffe
DE685595C (de) * 1934-01-19 1939-12-20 I G Farbnenindustrie Akt Ges Verfahren zur Raffination von Benzinen
US2063113A (en) * 1934-08-22 1936-12-08 Universal Oil Prod Co Treatment of hydrocarbon oils
FR833971A (fr) * 1936-12-28 1938-11-08 Int Hydrogenation Patents Co Procédé pour améliorer l'indice d'octane des essences
US2249461A (en) * 1937-08-17 1941-07-15 Standard Oil Co Manufacture of antiknock gasoline
US2220699A (en) * 1937-09-29 1940-11-05 Universal Oil Prod Co Production of high antiknock gasoline
FR850011A (fr) * 1939-02-08 1939-12-06 Procédé et appareil pour l'obtention d'hydrocarbures
FR862421A (fr) * 1939-12-19 1941-03-12 Phillips Petroleum Co Perfectionnements au traitement des hydrocarbures
DE881643C (de) * 1941-01-15 1953-07-02 Basf Ag Verfahren zur Herstellung klopffester Motorbetriebsstoffe
DE894104C (de) * 1941-04-27 1953-10-22 Basf Ag Verfahren zur Herstellung klopffester Treibstoffe durch Druckhydrierung hochsiedender Kohlenwasserstoffoele
DE875801C (de) * 1943-04-04 1953-05-07 Basf Ag Verfahren zur Herstellung eines Hochleistungskraftstoffes aus Schwerbenzinen oder Mitteloelen
US2498559A (en) * 1945-10-15 1950-02-21 Kellogg M W Co Desulfurization and conversion of a naphtha
US2512570A (en) * 1948-07-20 1950-06-20 Shell Dev Desulfurization of hydrocarbon oils
DE864721C (de) * 1951-04-19 1953-01-26 Basf Ag Verfahren zur Herstellung klopffester Treibstoffe
DE865337C (de) * 1951-05-27 1953-02-02 Basf Ag Verfahren zur Herstellung klopffester Treibstoffe
GB711670A (en) * 1951-06-13 1954-07-07 Bataafsche Petroleum Process for improving hydrocarbons boiling in the gasoline range
US2695866A (en) * 1951-12-27 1954-11-30 Kellogg M W Co Desulfurizing and reforming naphthas
NL92559C (enrdf_load_stackoverflow) * 1952-10-07
DE933648C (de) * 1953-06-27 1955-09-29 Basf Ag Verfahren zur Herstellung von feststoff- und asphaltfreiem und schwefelarmem Schweroel
US2763358A (en) * 1953-08-19 1956-09-18 Exxon Research Engineering Co Integrated process for the production of high quality motor fuels and heating oils
FR1109475A (fr) * 1953-08-31 1956-01-30 Standard Oil Dev Co Perfectionnements relatifs à l'hydroformation
DE945587C (de) * 1954-01-16 1956-07-12 Basf Ag Verfahren zur Entschwefelung von Rohoelen

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2345575A (en) * 1940-12-09 1944-04-04 Standard Oil Co Process of preparing gasoline of low gum-forming tendency
US2534025A (en) * 1941-05-05 1950-12-12 Anglo Iranian Oil Co Ltd Production of aviation or motor fuels
US2425506A (en) * 1945-07-13 1947-08-12 Standard Oil Dev Co Production of premium aviation fuel components
US2740751A (en) * 1952-02-23 1956-04-03 Universal Oil Prod Co Reforming of both straight run and cracked gasolines to provide high octane fuels
US2731506A (en) * 1953-01-28 1956-01-17 Exxon Research Engineering Co Production of hydrocarbon solvents of low acid wash color

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5658453A (en) * 1995-05-30 1997-08-19 Uop Integrated aromatization/trace-olefin-reduction scheme

Also Published As

Publication number Publication date
BE552485A (enrdf_load_stackoverflow)
GB843177A (en) 1960-08-04
DE1126551B (de) 1962-03-29
FR1187644A (fr) 1959-09-14

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