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US4474710A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of highly based magnesium sulfonate

Assignee: Ethyl Corp
•
Filing: 1982-03-22
•
Granted: 1984-10-02
•
Expires: 2002-03-22
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Abstract

Abstract Instead of total base number of about 30 for an alkaline earth metal sulfonate prepared by reacting up to 200 molar excess of alkaline earth metal compound at a temperature above 104° C. with an alkylbenzene sulfonic acid in the presence of from 0.5 to 10 weight parts of water per 1.0 weight part of alkaline earth metal compound under a pressure of from 2 to 10 atmospheres an oil-soluble magnesium-alkylbenzene sulfonate of total base number of 400 and higher is obtained by reacting at least on 8.5 to 1.0 molar ratios of magnesium oxide to ammonium alkylbenzene sulfonate at a temperature of from 100° C. to 130° C. under autogeneous pressure in the presence of at least 1.1 weight parts of water and 0.3 to 0.5 of methanol per weight part of magnesium oxide. After decompressing and removing water and methanol, the product high base number magnesium alkylbenzene sulfonate is obtained.

Inventors

  • 👤 Chang-Man Park
  • 👤 Eugene E. Richardson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 07:31
CPC Classifications
C; C07; C07C; C07C309/00

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 132 words
A method of preparing an oil soluble magnesium alkylbenzene sulfonate having a total base number of 400 and higher which comprises reacting an ammonium alkylbenzene sulfonate whose alkyl-substituent has a molecular weight of from 350 to 800 at a temperature of from 100° C. up to 130° C. with at least 8.5 gram mole of magnesium oxide per 1.0 gram mole of ammonium alkylbenzene sulfonate in the presence of from 1.1 to 1.5 weight parts of water and from 0.3 to 0.5 weight parts of methanol per 1.0 weight part of magnesium oxide in a closed reactor for from 10 to 20 minutes under the autogenetically produced gauge pressure and thereafter decompressing the resulting reaction mixture and removing methanol and water by distillative mean to a final temperature of about 120° C.
Claim 2
Independent Claim 132 words
A method of preparing an oil soluble magnesium alkylbenzene sulfonate having a total base number of 400 and higher which comprises reacting an ammonium alkylbenzene sulfonate whose alkyl-substituent has a molecular weight of from 350 to 800 at a temperature of from 100° C. up to 130° C. with at least 8.5 gram mole of magnesium oxide per 1.0 gram mole of ammonium alkylbenzene sulfonate in the presence of from 1.1 to 1.5 weight parts of water and from 0.3 to 0.5 weight parts of methanol per 1.0 weight part of magnesium oxide in a closed reactor for from 10 to 20 minutes under the autogenetically produced gauge pressure and thereafter decompressing the resulting reaction mixture and removing methanol and water by distillative mean to a final temperature of about 120° C.
Claim 3
Dependent Claim 21 words
The method of claim 1 wherein the alkylbenzene sulfonic acid portion of the ammonium sulfonate has a molecular weight of 550.

References Cited (Backward Citations)

US2467176A Cited
US2779784A Cited
GB958995A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-10-02 1988-04-02 1988-10-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-10-02 1992-04-02 1992-10-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-10-02 1996-04-02 1996-10-02 $7700.00 Window Closed / Lapsed

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