U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Process for treating used industrial oil

Patent 4431524 Issued on February 14, 1984. Estimated Expiration Date: Icon_subject January 26, 2003. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3391076

3625881

3819508

3835035

Reclaiming used motor oil
Patent #: 3930988
Issued on: 01/06/1976
Inventor: Johnson

Method of rerefining oil by distillation and extraction
Patent #: 4021333
Issued on: 05/03/1977
Inventor: Habiby ,   et al.

Method of rerefining oil with recovery of useful organic additives
Patent #: 4028226
Issued on: 06/07/1977
Inventor: Forsberg

Process for preparing lubricating oil from used waste lubricating oil
Patent #: 4073719
Issued on: 02/14/1978
Inventor: Whisman ,   et al.

Method for reclaiming waste lubricating oils
Patent #: 4073720
Issued on: 02/14/1978
Inventor: Whisman ,   et al.

Reclaiming used lubricating oils with ammonium salts and polyhydroxy compounds
Patent #: 4287049
Issued on: 09/01/1981
Inventor: Tabler ,   et al.

More ...

Inventor

Application

No. 06/461034 filed on 01/26/1983

US Classes:

208/183, With acid or alkali208/180, With added organic material208/181, Plural treating agents (sequential or simultaneous)208/182, One is a solid contact material208/252With acid

Examiners

Primary: Gantz, Delbert E.
Assistant: McFarlane, Anthony

Attorney, Agent or Firm

International Class

C10M 175/00 (20060101)

Abstract

A process for rerefining used industrial oil comprising the steps of: (i) contacting said oil with an aqueous solution of the basic salt of an alkali metal to precipitate metal contaminants, polar compounds or particulates from said oil and to neutralize acid that may be present in said oil; (ii) separating bulk water and solid contaminants from said oil; (iii) separating fine particulates and remaining suspended water from said oil; (iv) vacuum drying said oil at a temperature in the range of about 250° F. to about 400° F. and a pressure in the range of about 2 to about 50 torr to remove dissolved water and light hydrocarbons from said oil; (v) contacting said oil with (A) from about 0.1 to about 3% by weight based on the weight of said oil of a polyfunctional mineral acid or the anhydride of said acid and (B) from about 0.1 to about 5% by weight based on the weight of said oil of a polyhydroxy compound, with the proviso that component (B) is in excess of component (A), until substantially all metallic contaminants in said oil have reacted with component (A) or (B) to form reaction products; (vi) separating the reaction products formed in step (v) and any unreacted components (A) or (B) from said oil; (vii) hydrotreating said oil in the presence of hydrogen and a hydrogenation catalyst at a temperature in the range of about 500° F. to about 800° F. to remove residual polar materials and unsaturated compounds; and (viii) stripping said oil to remove light hydrocarbons with boiling point below about 600° F.

Other References

  • Sullivan, R. F., "Distillate Fuels from Green River Oil Shale", SAE Technical Paper Series 820960
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