FR2161524A5 - Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation - Google Patents

Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation

Info

Publication number
FR2161524A5
FR2161524A5 FR7142601A FR7142601A FR2161524A5 FR 2161524 A5 FR2161524 A5 FR 2161524A5 FR 7142601 A FR7142601 A FR 7142601A FR 7142601 A FR7142601 A FR 7142601A FR 2161524 A5 FR2161524 A5 FR 2161524A5
Authority
FR
France
Prior art keywords
tetrahydro
naphtalene
reacted
naphthalene
catalyst
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
FR7142601A
Other languages
French (fr)
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.)
IFP Energies Nouvelles IFPEN
Original Assignee
IFP Energies Nouvelles IFPEN
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 IFP Energies Nouvelles IFPEN filed Critical IFP Energies Nouvelles IFPEN
Priority to FR7142601A priority Critical patent/FR2161524A5/en
Application granted granted Critical
Publication of FR2161524A5 publication Critical patent/FR2161524A5/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/02Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
    • C07C5/10Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of aromatic six-membered rings
    • C07C5/11Partial hydrogenation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Naphthalene is hydrogenated in liq. phase to tetrahydro naphthalene with H2 gas (at 100-200 degrees C and 0.1-100 bars) with sol. catalyst contg. (a) gp. VIII metal (Fe, Co, Ni) salt (acetylacetonate) (b) AlR1R2R3 where R1R2R3 are H or 1-20C hydrocarbon, (c) tetrahydro naphthalene. (a) is a salt of 1-20C carboxylic acid sol in (c). (b) is triethyl aluminium. Concn of metal in (a) is 0.001-0.1 wt.%. Vol. ratio of catalyst soln to charge is 1:500-1:10. The catalyst improves activity and selectivity in (de)hydrogenation, isomerisation reactions.
FR7142601A 1971-11-26 1971-11-26 Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation Expired FR2161524A5 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR7142601A FR2161524A5 (en) 1971-11-26 1971-11-26 Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7142601A FR2161524A5 (en) 1971-11-26 1971-11-26 Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation

Publications (1)

Publication Number Publication Date
FR2161524A5 true FR2161524A5 (en) 1973-07-06

Family

ID=9086531

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7142601A Expired FR2161524A5 (en) 1971-11-26 1971-11-26 Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation

Country Status (1)

Country Link
FR (1) FR2161524A5 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352772A2 (en) * 1988-07-27 1990-01-31 Nippon Oil Co., Ltd. Method for preparing resin having light color
CN1074400C (en) * 1998-12-10 2001-11-07 中国石化辽阳石油化纤公司 Preparation of C5 alkane

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0352772A2 (en) * 1988-07-27 1990-01-31 Nippon Oil Co., Ltd. Method for preparing resin having light color
EP0352772A3 (en) * 1988-07-27 1991-07-03 Nippon Oil Co., Ltd. Method for preparing resin having light color
CN1074400C (en) * 1998-12-10 2001-11-07 中国石化辽阳石油化纤公司 Preparation of C5 alkane

Similar Documents

Publication Publication Date Title
GB1306087A (en)
GB1293247A (en) Hydrocarbon conversion process and catalyst therefor
GB1475309A (en) Process for the production of maleic anhydride
IE34193L (en) Hydrocarbon conversion catalyst.
GB1508868A (en) Catalytic oxidation process
FR2161524A5 (en) Ziegler catalyst - reacted in presence of tetrahydro naphtalene for naphthalene hydrogenation
GB1399078A (en) Process for the prepatation of cycloalkanones and or cycloalkanols
GB1506773A (en) Method for preparing hydrocarbon conversion catalyst
GB1174747A (en) Preparation of Unsaturated Acyl Halides
GB1471588A (en) Desulphurisation catalyst and process
GB1440147A (en) Catalyst for hydrocarbon conversion
GB1399116A (en) Preparation and use of hydrocarbon conversion catalysts comprising silica-alumina
GB1463320A (en) Method of conversion of hydrocarbons
GB1462097A (en) Catalysts for hydrocarbon isomerisation and reforming their preparation and use
GB1429884A (en) Process for the activation of catalysts
GB1400970A (en) Production of alpha-olefins by displacement from aluminium trialkyl growth products
GB1535158A (en) Catalytically isomerizing 1-butene
GB1343469A (en) Process for preparing unsaturated compounds
GB644665A (en) A process for the production of oxygen-containing organic compounds
GB1159245A (en) Process for the Preparation of Pyromellitic Acid and its Mono- and Dianhydrides
GB1240731A (en) Process for the manufacture of aliphatic diamines
FR2061718A1 (en) Catalytic naphtha hydroforming process
GB1421160A (en) Production of dealkylated aromatic hydrocarbons and hydrogen
GB1184022A (en) Process for the Preparation of Cyclo-Alkyl Aromatics
GB1267719A (en) Isomerization of olefins

Legal Events

Date Code Title Description
ST Notification of lapse