GB1379847A - Method of preparing a hydrorefining catalyst - Google Patents

Method of preparing a hydrorefining catalyst

Info

Publication number
GB1379847A
GB1379847A GB1381972A GB1381972A GB1379847A GB 1379847 A GB1379847 A GB 1379847A GB 1381972 A GB1381972 A GB 1381972A GB 1381972 A GB1381972 A GB 1381972A GB 1379847 A GB1379847 A GB 1379847A
Authority
GB
United Kingdom
Prior art keywords
per cent
hours
period
average pore
weight per
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
GB1381972A
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.)
Universal Oil Products Co
Original Assignee
Universal Oil Products 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 Universal Oil Products Co filed Critical Universal Oil Products Co
Publication of GB1379847A publication Critical patent/GB1379847A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08Heat treatment
    • B01J37/10Heat treatment in the presence of water, e.g. steam
    • 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
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals
    • B01J23/64Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/652Chromium, molybdenum or tungsten
    • 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
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • 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
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • B01J23/88Molybdenum
    • B01J23/883Molybdenum and nickel
    • 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
    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • C10G45/02Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
    • C10G45/04Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
    • C10G45/06Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
    • C10G45/08Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof in combination with chromium, molybdenum, or tungsten metals, or compounds thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/12Silica and alumina

Landscapes

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

Abstract

1379847 Hydrocarbon hydrorefining catalysts UNIVERSAL OIL PRODUCTS CO 24 March 1972 [25 March 1971] 13819/72 Heading B1E [Also in Division C5] Hydrocarbon hydrorefining catalyst comprising a Group VIB metal component and a Group VIII metal component is prepared by a method wherein refractory inorganic oxide carrier material is impregnated with an aqueous solution containing a soluble compound of a Group VIB metal and a soluble compound of a Group VIII metal and, after evaporating water therefrom, is calcined initially at a temperature of from 100 to 427‹C (212 to 800‹F) for a period of at least ¢ hour (for example at a temperature of from 260 to 427‹C (500 to 800‹F) for a period of from ¢ to 2 hours in an atmosphere containing less than 50 volume per cent steam, preferably substantially dry air) and thereafter at a temperature of from 427 to 621‹C (800 to 1150‹F) for a period of from 1 to 4 hours in an atmosphere containing at least 25, preferably from 60 to 80, volume per cent steam, the volume ratio of impregnating solution to carrier material being from 0.5:1 to 2:1, preferably from 0.6:1 to 1:1, for example about 0.7:1. Evaporation of water, which preferably is such as to provide material which exhibits a loss on ignition at 500‹C of less than 50, preferably from 35 to 45, weight per cent, may be effected for a period not greater than 4 hours. The refractory inorganic oxide carrier material may be alumina, silica, zirconia, boria, thoria or a combination thereof, for example silica-alumina having an Al 2 O 3 :SiO 2 molar ratio of at least 1:1, preferably an Al 2 O 3 :SiO 2 weight ratio of from 3:1 to 9:1; the carrier material preferably has a surface area of from 175 to 380m<SP>2</SP>/g, an average pore volume of from 0.5 to 0.9 ml/g and an average pore diameter of from 70 to 200 Angstroms. The metal of the Group VIB metal component may be selected from chromium, molybdenum and tungsten; the metal of the Group VIII metal component may be selected from iron, cobalt, nickel, ruthenium, rhodium. palladium, osmium, iridium and platinum; the Specification gives examples of suitable Group VIB metal compounds and Group VIII metal compounds for use in the preparation of the catalyst which may contain from 5 to 20 weight per cent molybdenum and from 0.1 to 10 weight per cent nickel. As exemplified, 1.6 mm spheres of silica-alumina containing 88 weight per cent Al 2 O 3 and 12 weight per cent SiO 2 and having a surface area of 285 m<SP>2</SP>/g, an average pore volume of 0.7 ml/g and an average bulk density of 0.44 g/ml are impregnated with a solution prepared by dissolving molybdic acid and nickel nitrate in aqueous ammonia and, after evaporating water therefrom over a period of 4 hours, are calcined initially at 343‹C (650‹F) for 1 hour in dry air and thereafter at 552‹C (1025‹F) for 2 hours in air containing 70 volume per cent steam to provide material haying a surface area of 150 m<SP>2</SP>/g, an average pore volume of 0.45 ml/g and an average pore diameter of 115 Angstroms, which material is used in the form of a plurality of beds separated by sand in a process for hydrorefining a residual crude oil.
GB1381972A 1971-03-25 1972-03-24 Method of preparing a hydrorefining catalyst Expired GB1379847A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12811471A 1971-03-25 1971-03-25

Publications (1)

Publication Number Publication Date
GB1379847A true GB1379847A (en) 1975-01-08

Family

ID=22433707

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1381972A Expired GB1379847A (en) 1971-03-25 1972-03-24 Method of preparing a hydrorefining catalyst

Country Status (14)

Country Link
JP (1) JPS5229717B1 (en)
AU (1) AU459131B2 (en)
BR (1) BR7201734D0 (en)
CA (1) CA986496A (en)
DE (1) DE2214207B2 (en)
ES (1) ES401056A1 (en)
FR (1) FR2130711B1 (en)
GB (1) GB1379847A (en)
IT (1) IT952359B (en)
NL (1) NL161371C (en)
PL (1) PL83329B1 (en)
SE (1) SE384802B (en)
YU (1) YU34627B (en)
ZA (1) ZA721900B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1386665A1 (en) * 2002-08-01 2004-02-04 Conoco Phillips Company Hydrothermal pretreatment for increasing average pore size in catalyst supports

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53149412U (en) * 1977-04-30 1978-11-24
FR2424577A1 (en) * 1978-02-24 1979-11-23 Scholtes Ets Eugen Convector heaters network temp. controller - has programmable clock monitoring changeover with master control circuit operating with individual heater controllers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1386665A1 (en) * 2002-08-01 2004-02-04 Conoco Phillips Company Hydrothermal pretreatment for increasing average pore size in catalyst supports
US6958309B2 (en) 2002-08-01 2005-10-25 Conocophillips Company Hydrothermal pretreatment for increasing average pore size in a catalyst support

Also Published As

Publication number Publication date
FR2130711B1 (en) 1977-08-05
BR7201734D0 (en) 1973-06-14
IT952359B (en) 1973-07-20
JPS5229717B1 (en) 1977-08-03
NL161371C (en) 1980-02-15
NL7203877A (en) 1972-09-27
ZA721900B (en) 1972-12-27
PL83329B1 (en) 1975-12-31
ES401056A1 (en) 1975-07-16
FR2130711A1 (en) 1972-11-03
YU34627B (en) 1979-12-31
NL161371B (en) 1979-09-17
AU4025872A (en) 1973-09-27
AU459131B2 (en) 1975-02-28
DE2214207A1 (en) 1972-10-12
SE384802B (en) 1976-05-24
CA986496A (en) 1976-03-30
YU74072A (en) 1979-07-10
DE2214207B2 (en) 1976-04-15

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee