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US3250819A Expired / Lapsed US ⏱️ 0.0 years remaining

Isomerization process for forming a cycloparaffin

Assignee: Phillips Petroleum Co
•
Filing: 1964-09-14
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Granted: 1966-05-10
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Expires: 1984-09-14
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Abstract

No abstract record available.

Inventors

  • 👤 John T Cabbage

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 15:24
CPC Classifications
C; C07; C07C; C07C13/00; C07C13/02; C07C13/16; C07C13/18; C07C5/00; C07C5/22; C07C5/27; C07C5/2702; C07C5/271; C07C5/2718; C07C5/2721; C07C5/29

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 166 words
A METHOD FOR PRODUCING A CYCLOPARAFFIN COMPRISING PROVIDING A HYDROCARBON FEED WHICH HAS FROM 50 TO 100 VOLUME PERCENT OF AROMATIC, ISOPARAFFIN, N-PARAFFIN AND ISOCYCLIC HYDROCARBON CONSTITUENTS EACH HAVING 6 CARBON ATOMS, CONTACTING SAID FEED WITH HYDROGEN IN THE PRESENCE OF A HYDROGENATION CATALYST TO CONVERT UNSATURATED CONSTITUENTS OF SATURATED CONSTITUENTS AND THEREBY PRODUCE A HYDROGENATED PRODUCT, HEATING THE HYDROGENATED PRODUCT AT AN ELEVATED TEMPERATURE IN THE PRESENCE OF A FIXED BED ISOMERIZATION CATALYST AND UNDER REACTION CONDITIONS WHICH FAVOR THE CONVERSION OF NORMAL PARAFFINS TO ISOPARAFFINS AND THEREBY PRODUCE A FIRST ISOMERIZATION PRODUCT RICH IN ISOPARAFFINS, FRACTIONATING SAID FIRST ISOMERIZATION PRODUCT TO REMOVE THEREFROM LOWER BOILING ISOPARAFFINS AND THEREBY PRODUCE AN ISOPARAFFIN LEAN PRODUCT, REACTING SAID ISOPARAFFIN LEAN PRODUCT IN THE PRESENCE OF AN ALUMINUM HALIDE-COMPLEX ISOMERIZATION CATALYST AND UNDER REACTION CONDITIONS WHICH FAVOR THE CONVERSION OF ISOCYCLIC CONSTITUENTS TO CYCLOPARAFFINS AND THEREBY PRODUCE A SECOND ISMERIZATION PRODUCT RICH IN CYCLOPARAFFINS, AND SEPARATING FROM SAID SECOND ISOMERIZATION PRODUCT CYCLOPARAFFINS AS A PRODUCT OF THE METHOD.
Claim 2
Independent Claim 166 words
A METHOD FOR PRODUCING A CYCLOPARAFFIN COMPRISING PROVIDING A HYDROCARBON FEED WHICH HAS FROM 50 TO 100 VOLUME PERCENT OF AROMATIC, ISOPARAFFIN, N-PARAFFIN AND ISOCYCLIC HYDROCARBON CONSTITUENTS EACH HAVING 6 CARBON ATOMS, CONTACTING SAID FEED WITH HYDROGEN IN THE PRESENCE OF A HYDROGENATION CATALYST TO CONVERT UNSATURATED CONSTITUENTS OF SATURATED CONSTITUENTS AND THEREBY PRODUCE A HYDROGENATED PRODUCT, HEATING THE HYDROGENATED PRODUCT AT AN ELEVATED TEMPERATURE IN THE PRESENCE OF A FIXED BED ISOMERIZATION CATALYST AND UNDER REACTION CONDITIONS WHICH FAVOR THE CONVERSION OF NORMAL PARAFFINS TO ISOPARAFFINS AND THEREBY PRODUCE A FIRST ISOMERIZATION PRODUCT RICH IN ISOPARAFFINS, FRACTIONATING SAID FIRST ISOMERIZATION PRODUCT TO REMOVE THEREFROM LOWER BOILING ISOPARAFFINS AND THEREBY PRODUCE AN ISOPARAFFIN LEAN PRODUCT, REACTING SAID ISOPARAFFIN LEAN PRODUCT IN THE PRESENCE OF AN ALUMINUM HALIDE-COMPLEX ISOMERIZATION CATALYST AND UNDER REACTION CONDITIONS WHICH FAVOR THE CONVERSION OF ISOCYCLIC CONSTITUENTS TO CYCLOPARAFFINS AND THEREBY PRODUCE A SECOND ISMERIZATION PRODUCT RICH IN CYCLOPARAFFINS, AND SEPARATING FROM SAID SECOND ISOMERIZATION PRODUCT CYCLOPARAFFINS AS A PRODUCT OF THE METHOD.

References Cited (Backward Citations)

US2953606A Cited
US2939896A Cited
US3078323A Cited
US3054832A Cited
US3009002A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1969-05-09 1969-11-08 1970-05-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1973-05-09 1973-11-08 1974-05-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1977-05-09 1977-11-08 1978-05-10 $7700.00 Window Closed / Lapsed

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