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US3959239A Expired / Lapsed US ⏱️ 0.0 years remaining

Use of nickel cyclooctadiene as a hydrogenation catalyst

Assignee: Mobil Oil AS
•
Filing: 1975-05-05
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Granted: 1976-05-25
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Expires: 1995-05-05
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Abstract

Abstract A process for the hydrogenation of hydrocarbon materials having olefinic unsaturation and/or olefinic-aromatic unsaturation, and particularly wherein hydrogenation is carried out at relatively low catalyst levels and mild reaction conditions whereby olefinic bonds are reduced and, when components of the reaction mixture contain aromatic unsaturation, to effect selective hydrogenation of olefinic bonds, without substantial, if any, hydrogenation of aromatic unsaturation; said process comprising contacting such hydrocarbon materials under hydrogenation reaction conditions of temperature and pressure in the presence of bis(1,5-cyclooctadiene) nickel as the hydrogenation catalyst.

Inventors

  • 👤 Stephen A. Butter
  • 👤 James G. Murray

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 22:24
CPC Classifications
C; C08; C08C; C08C19/00; C08C19/02; C07; C07C; C07C5/00; C07C5/02; C07C5/03; C08F; C08F8/00; C08F8/04; C07C2531/00; C07C2531/16; C07C2531/22

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 67 words
A process for hydrogenating hydrocarbon materials having olefinic unsaturation and/or olefinic-aromatic unsaturation whereby olefinic bonds are reduced and when components of the reaction mixture contain aromatic unsaturation selective hydrogenation of olefinic bonds is effected without substantial, if any, hydrogenation of aromatic unsaturation; said process comprising contacting such hydrocarbon materials under hydrogenation reaction conditions of temperature and pressure in the presence of bis (1,5-cyclooctadiene) nickel as hydrogenation catalyst.
Claim 2
Dependent Claim 67 words
A process for hydrogenating hydrocarbon materials having olefinic unsaturation and/or olefinic-aromatic unsaturation whereby olefinic bonds are reduced and when components of the reaction mixture contain aromatic unsaturation selective hydrogenation of olefinic bonds is effected without substantial, if any, hydrogenation of aromatic unsaturation; said process comprising contacting such hydrocarbon materials under hydrogenation reaction conditions of temperature and pressure in the presence of bis (1,5-cyclooctadiene) nickel as hydrogenation catalyst.
Claim 3
Dependent Claim 17 words
The process of claim 1 wherein the hydrocarbon material is a copolymer derived from styrene and butadiene.
Claim 4
Dependent Claim 25 words
The process of claim 2 wherein that portion of the copolymer attributable to butadiene is reduced while that portion attributable to styrene is substantially unhydrogenated.
Claim 5
Dependent Claim 14 words
The process of claim 1 wherein the hydrocarbon material has alpha- or internal-olefinic unsaturation.
Claim 6
Dependent Claim 27 words
The process of claim 1 wherein the reaction temperature is from about 50° to about 65°C and the pressure is from about atmospheric to about 500 psig.
Claim 7
Dependent Claim 20 words
The process of claim 5 wherein the reaction temperature is from about 55°-60°C and the pressure is about 400 psig.
Claim 8
Dependent Claim 17 words
The process of claim 1 wherein the nickel catalyst is stabilized by minor amounts of triphenyl phosphine.
Claim 9
Dependent Claim 22 words
The process of claim 7 wherein the nickel catalyst is stabilized by from about 0.1:1-0.1:0.5 mole of phosphine per mole of catalyst.

References Cited (Backward Citations)

US3130237A Cited
US3432518A Cited
US3525729A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-05-25 1979-11-24 1980-05-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-05-25 1983-11-24 1984-05-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-05-25 1987-11-24 1988-05-25 $7700.00 Window Closed / Lapsed

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