US3631084A

US3631084A - Silyl esters of terephthalic acid and isophthalic acid

Info

Publication number: US3631084A
Application number: US14895A
Authority: US
Inventors: Thomas V Liston
Original assignee: Chevron Research and Technology Co
Current assignee: Chevron USA Inc
Priority date: 1967-11-22
Filing date: 1970-02-13
Publication date: 1971-12-28
Anticipated expiration: 1988-12-28
Also published as: US3538000A

Abstract

SILYL ESTERS OF TEREPHTHALIC ACID AND ISOPHTHALIC ACID FIND USE AS CORROSION INHIBITORS IN COMBINATION WITH SLIGHTLY BASIC OR NEUTRAL ASHLESS LUBRICATING OIL DETERGENTS.

Description

United States Patent "ice 3,631,084 SILYL ESTERS 0F TEREPHTHALIC ACID AND ISOPHTHALIC ACID Thomas V. Liston, Kentfield, Califi, assignor to Chevron Research Company, San Francisco, Calif.

No Drawing. Original application Nov. 22, 1967, Ser. No. 684,922, now Patent No. 3,538,000, dated Nov. 3, 1970. Divided and this application Feb. 13, 1970, Ser.

Int. Cl. C07f 7/08 US. Cl. 260-4482 B 4 Claims ABSTRACT OF THE DISCLOSURE Silyl esters of terephthalic acid and isophthalic acid find use as corrosion inhibitors in combination with slightly basic or neutral ashless lubricating oil detergents.

CROSS REFERENCE TO RELATED APPLICATIONS This application is a divisional of copending application Ser. No. 684,922 filed Nov. 22, 1967 now US. Pat.

BACKGROUND OF THE INVENTION Field of the invention Corrosion inhibitors are included in modern-day lubricating oils. A large portion of the oxidation products formed in lubricating oils are acidic and corrosively attack such parts of the engine as pistons, piston rings, bearings, etc. Moreover, the water which accumulates can attack iron present in the engine causing corrosion or rustmg.

A particularly effective class of corrosion inhibitors, which are popularly used with ashless amine nitrogen containing detergents, are the aromatic dibasic acids. See for example US. Pat. No. 2,809,160 and British Pat. No. 809,198. While these dibasic aromatic acids are very effective as corrosion inhibitors, they are extremely insoluble in hydrocarbon media. Therefore, means for solubilizing the dibasic acids are necessary for their use as corrosion inhibitors.

With the ashless detergents, particularly the alkenyl succinimides of alkylene polyamines, the amines are able to interact with the dibasic acid and act to solubilize the dibasic acid. It is found, however, that when more than 1 amine nitrogen is reacted with an alkenyl succinic acid to form the irnide, the resulting dior polysuccinimide or succinamic acid is incapable of solubilizing sufficient aromatic dibasic acid to provide the desired concentration of the dibasic acid corrosion inhibitor.

Description of the prior art I The use of aromatic dibasic acids as corrosion inhibitors in lubricating oils is taught in US. Pat. No. 2,809,160 and British Pat. No. 809,198. The interaction of alkenyl succinimide ashless detergents and aromatic dibasic acids is taught in US. Pat. No. 3,287,271.

SUMMARY OF THE INVENTION Pursuant to this invention, silyl esters of aromatic dibasic acids are provided for use as corrosion inhibitors in lubricating oils, particularly in lubricating oils for internal combustion engines compounded with slightly basic or neutral amine nitrogen containing ashless detergents. The dibasic acids are other than ortho-substituted and may have an alkyl substituent of from 1 to 8 carbon atoms.

3,631,084 Patented Dec. 28, 1971 DESCRIPTION OF THE PREFERRED EMBODIMENTS The silyl esters which find use in this invention will for the most part have the following formula:

C OgSiAg wherein A is lower alkyl of from 1 to 3 carbon atoms, preferably methyl; R is lower alkyl of from 1 to 8 carbon atoms, more usually 1 to 4 carbon atoms, and n is an integer of from 0 to l. The carboxyl groups are separated by at least 3 annular carbon atoms. The preferred composition is the di(trimethyl silyl) ester of terephthalic acid.

Other dibasic acids which may be used are the silyl esters of isophthalic acid, tert.-butyl isophthalic acid, tert.- butyl terephthalic acid, methyl terephthalic acid, etc.

As already indicated, the silyl esters find particular use with amine nitrogen containing detergents which are incapable of solubilizing a sufficient amount of the nonesterified dibasic acid for use in a lubricating oil. Normally, in a lubricating oil composition, the detergent will be present in from 2 to 10 weight percent, more usually 2 to 8 weight percent. About 0.075 to 0.30 weight percent based on the total composition of the dibasic acid (includes ester derivative) will be used, usually about 0.10 to 0.2 weight percent of the dibasic acid will be used. Therefore, when less than about 0.05 weight percent of the total composition of the dibasic acid can be solubilized, the amount of dibasic acid must be augmented in order the maintain a satisfactory level of corrosion inhibition.

In lubricating oil concentrates, the detergent will be present in from about 10 to 40 Weight percent and concomitantly the total dibasic acid will be present in from 0.5 to about 1.2 weight percent of the total composition.

The ashless detergents are those combining an alkylene polyamine having from 2 to 6 nitrogen atoms with at least 1.8 moles of an alkenyl succinic acid per mole of alkylene polyamine. The product of the reaction may be a succinamic acid, a disuccinamide, or succinimide, or combinations thereof. These compositions are prepared by heating from 1.8 to 3 moles of an alkenyl succinic anhydride, usually a polyisobutenyl alkenyl succinic anhydride, having a molecular weight in the range of about 500 to 2,000 with an alkylene polyamine, usually an ethylene polyamine or propylene polyamine having from 2 to 6 amine nitrogen atoms at a temperature in the range of C. to 200 C. for a time sufficient to cause reaction. Any Water formed during the reaction is driven ofl to drive the reaction to completion. These detergents are described in US. Pat. Nos. 3,219,666 and 3,172,892, the disclosures of which are incorporated herein by reference.

Of particular interest are the polyisobutenyl succin imides of triethylene tetramine and tetraethylene pentamine, wherein the polyisobutenyl groups are of from about 700 to 1,500 molecular weight and the mole ratio of polyisobutenyl succinic anhydride to alkylene poly amine is in the range of 1.8 to 2.2.

While the silyl esters may be compounded with the ashless detergent, without the addition of the parent dibasic acid, it is more economical to dissolve the maximum amount of dibasic acid in the oil which can be solubilized and then augment that amount with the silyl ester. Usually, the total concentration of parent dibasic acid and its silyl ester derivative will be at least 0.075, more usually at least 0.10 weight percent and generally not more than 0.3 weight percent, more usually not more than 0.15 weight percent. Preferably, a total of about 0.1 weight percent of the oil composition is preferred. The concentrate will be accordingly multiplied in relation to the detergent.

Usually, the parent dibasic acid will be present in from 0.01 to 0.05 weight percent, while the silyl ester will be present in at least 0.05, preferably 0.075 to 0.29 weight percent.

The lubricating oils which find use are hydrocarbonaceous oils of lubricating viscosity, particularly petroleum oils, which may be naphthenic base, parafiin base, asphaltic base and mixed base lubricating oils. Also, synthetic oils such as polymers of hydrocarbon olefins, alkyl aromatics, etc. may be employed.

The silyl esters of this invention may be prepared by any convenient means. Conveniently, a (trialkyl silyl) amine or di(trialkyl silyl)amine may be combined with the desired dicarboxylic acid and heated at elevated temperatures either neat or in an inert solvent. Reference to the method of preparation of silyl esters may be found in C. Eaborn, Organic Silicon Compounds, Academic Press, Inc., New York, NY. 1960, chapters 9 and 11.

The following example is offered by way of illustration and not by way of limitation.

EXAMPLE I Into a reaction flask was introduced 7 g. of terephthalic acid and 25 cc. of di(trimethyl silyl)amine and the mixture heated under nitrogen for 3 hours. After allowing the mixture to cool, long needle-like crystals formed. The mixture was filtered, the crystals dissolved in hexane, the hexane solution filtered and the hexane distilled 011. The residue weighed 11.2 g. An infrared spectrum of the product indicated that the desired di(trimethyl silyl) ester of terephthalic acid had been obtained.

Using a highly hindered polyisobutenyl succinimide of tetraethylene pentamine (approximately 2 succinimides per tetraethylene pentamine; the polyisobutenyl group being of about 1,000 molecular weight) the silyl ester of terephthalic acid was tested as a corrosion inhibitor in an L-38 strip test. Copper and lead strips are immersed in oil formulations using a 480 neutral oil at a temperature of 340 F. for hours and the weight loss determined at the end of this time. The following table l The strip is washed with dilute potassium cyanide solution (cone. wt. percent in 1120) to remove copper salts.

To further test the composition of this invention,

engine tests were performed. An L-38 test using a l-cylinder CLR engine was carried out for 40 hours at an engine speed of 3,150 r.p.m. The results are reported as the bearing weight loss in milligrams. The first compounded oil (A) prepared had 9.54 weight percent of the detergent described above and 0.022 weight percent of terephthalic acid, the maximum amount which could be solubilized. The second compounded oil (B) added to the first oil, the composition of Example I, in an amount to provide 0.16 weight percent of the lubricating oil composition, For (A) there was a bearing weight loss of 303 mg., while for (B), the loss was only 119 mg.

It is evident from the above results, that the silyl esters are effective corrosion inhibitors in lubricating oil in combination with an ashless amine-containing detergent. Moreover, because of the silyl ester solubility in the lubricating oil, a sufficient amount of the corrosion inhibitor can be maintained in the oil to provide adequate protection in an internal combustion engine.

As will be evident to those skilled in the art, various modifications on this invention can be made or followed, in the light of the foregoing disclosure and discussion, without departing from the spirit or scope of the disclosure or from the scope of the following claims.

What is claimed is:

1. A composition of the formula:

sa t

wherein A is lower alkyl of from 1 to 3 carbon atoms, R is lower alkyl from 1 to 8 carbon atoms, 11 is an integer of from 0 to 1 and the carboxyl groups are separated by at least 3 annular carbon atoms.

2. A composition according to claim 1 wherein A is methyl.

3. A composition according to claim 1 wherein the carboxyl groups are para.

4. A composition according to claim 1 wherein R is tert.-butyl and n is 1.

References Cited UNITED STATES PATENTS 2,707,191 4/1955 Martin et al. 260448.2 2,757,208 7/1956 Burkhard 260448.2

TOBIAS E. LEVOW, Primary Examiner P. F. SHAVER, Assistant Examiner U.S. Cl. X.R.