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US2948743A Expired / Lapsed US ⏱️ 0.0 years remaining

Oxo-aluminum acylates, alkoxides and phenoxides

Assignee: J W Ayers & Co
•
Filing: 1955-09-08
•
Granted: 1960-08-09
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Expires: 1975-09-08
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Abstract

No abstract record available.

Inventors

  • 👤 Rinse Jacobus

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 20:49
CPC Classifications
C; C07; C07F; C07F5/00; C07F5/06; C07F5/069; B; B01; B01J; B01J19/00; B01J19/06; C10; C10L; C10L7/00; C10L7/02

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 176 words
A PROCESS FOR THE PRODUCTION OF OXO-ALUMINUM CARBOXYLATES WHICH COMPRISES REACTING AN ALIPHATIC MONOCARBOXYLIC ACID FREE OF ANY FUNCTIONAL GROUPS WHICH WOULD INTERFERE WITH THE REACTION HEREIN SPECIFIED WITH AN ALUMINUM R-OXIDE IN THE MOL PROPORTION OF SUBSTANTIALLY 1:1 DURING HEATING OF THE REACTION MIXTURE AT A TEMPERATURE OF AT LEAST 150*C. WHEREBY R-HYDROXIDE IS LIBERATED, CONTINUING THE HEATING UNTIL ONE MOL PORPORTION OF THE R-HYDROXIDE HAS DISTILLED OFF, ADDING AN ADDITIONAL MOL PROPORTION OF THE MONOCARBOXYLIC ACID TO THE REACTION MASS, HEATING THE REACTION MASS AT A TEMPERATUE OF AT LEAST 150*C. UNTIL AN ADDITIONAL MOL PROPORTION OR RHYDROXIDE IS LIBERATED BY THE REACTION AND DISTILLED OFF, HEATING THE RESULTING REACTION MASS TO A HIGHER TEMPERATURE OF AT LEAST 200 AT WHICH ESTER IS LIBERATED AND CONTINUING THE HEATING UNTIL A TOTAL OF SUBSTANTIALLY ONE MOL PROPORTION OF ESTER HAS BEEN LIBERATED BY THE REACTION, SAID R RADICALS BEING SELECTED FROM THE GROUP CONSISTING OF HYDROCARBON RADICALS OF ALCOHOLS AND PHENOLS OF A VOLATILITY PERMITTING VAPORIZATION OF THE R-HYDROXIDE FORMED IN THE STEPS HEREINBEFORE SPECIFIED.
Claim 2
Dependent Claim 176 words
A PROCESS FOR THE PRODUCTION OF OXO-ALUMINUM CARBOXYLATES WHICH COMPRISES REACTING AN ALIPHATIC MONOCARBOXYLIC ACID FREE OF ANY FUNCTIONAL GROUPS WHICH WOULD INTERFERE WITH THE REACTION HEREIN SPECIFIED WITH AN ALUMINUM R-OXIDE IN THE MOL PROPORTION OF SUBSTANTIALLY 1:1 DURING HEATING OF THE REACTION MIXTURE AT A TEMPERATURE OF AT LEAST 150*C. WHEREBY R-HYDROXIDE IS LIBERATED, CONTINUING THE HEATING UNTIL ONE MOL PORPORTION OF THE R-HYDROXIDE HAS DISTILLED OFF, ADDING AN ADDITIONAL MOL PROPORTION OF THE MONOCARBOXYLIC ACID TO THE REACTION MASS, HEATING THE REACTION MASS AT A TEMPERATUE OF AT LEAST 150*C. UNTIL AN ADDITIONAL MOL PROPORTION OR RHYDROXIDE IS LIBERATED BY THE REACTION AND DISTILLED OFF, HEATING THE RESULTING REACTION MASS TO A HIGHER TEMPERATURE OF AT LEAST 200 AT WHICH ESTER IS LIBERATED AND CONTINUING THE HEATING UNTIL A TOTAL OF SUBSTANTIALLY ONE MOL PROPORTION OF ESTER HAS BEEN LIBERATED BY THE REACTION, SAID R RADICALS BEING SELECTED FROM THE GROUP CONSISTING OF HYDROCARBON RADICALS OF ALCOHOLS AND PHENOLS OF A VOLATILITY PERMITTING VAPORIZATION OF THE R-HYDROXIDE FORMED IN THE STEPS HEREINBEFORE SPECIFIED.

References Cited (Backward Citations)

US2618536A Cited
US2744074A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1963-08-09 1964-02-08 1964-08-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1967-08-09 1968-02-08 1968-08-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1971-08-09 1972-02-08 1972-08-09 $7700.00 Window Closed / Lapsed

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