Borated oxazolines as varnish inhibiting dispersants in lubricating oils

Claim 2

A lubricating oil composition comprising a major amount of lubricating oil and a minor but dispersing amount of a sludge dispersing and varnish inhibiting oil-soluble borated oxazoline material containing from about 0.1 to 2.0 wt. % boron, wherein said oxazoline material is formed by the reaction of (A) a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride, wherein said hydrocarbyl group is a polymer of C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 and 10,000; and (B) a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons and represented by the formula: ##STR14## wherein X is an alkyl, or hydroxy alkyl group, with at least one of the X substituents being a hydroxy alkyl group of the structure --(CH 2 ) n OH, said oxazoline material having one to two oxazoline rings.

Claim 3

The lubricating oil composition according to claim 1 wherein said borated oxazoline material is obtained from the reaction of one molar proportion of an alkenyl succinic anhydride or acid and from about 1.5 to about 2 molar proportions of said 2,2-disubstituted-2-amino-1-alkanol followed by condensation with a boron reactant selected from the group consisting of boron oxide hydrates, boron oxides, boron acids and esters of boron acids.

Claim 4

A composition comprising a major amount of an oil of lubricating viscosity and a minor but dispersing amount of an oil-soluble, borated derivative of the oxazoline reaction product of a substantially saturated aliphatic hydrocarbyl, substituted C 4 -C 10 mono-unsaturated dicarboxylic acid material, said hydrocarbyl group having a number average molecular weight ranging from about 700 to about 140,000 with from at least 1 to about 2 mole equivalent, per mole equivalent of said dicarboxylic acid material, of a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons, and which is represented by the formula: ##STR15## wherein X is an alkyl or hydroxyl alkyl group, with at least one of the X substituents being a hydroxyl alkyl group of the structure --(CH 2 ) n OH wherein n is 1 to 3, said reaction conditions being at a temperature of from about 140° C. to 240° C. for from 1/2 to 24 hours whereby at least one carboxylic acyl group is converted into an oxazoline ring, said reaction product being borated by condensation with a boron compound selected from the class consisting of boron oxide, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated ester derivative.

Claim 5

A composition comprising a major amount of an oil of lubricating viscosity and a minor but dispersing amount of an oil-soluble, borated derivative of the oxazoline reaction product of a substantially saturated aliphatic hydrocarbyl, substituted C 4 -C 10 mono-unsaturated dicarboxylic acid material, said hydrocarbyl group having a number average molecular weight ranging from about 700 to about 140,000 with from at least 1 to about 2 mole equivalent, per mole equivalent of said dicarboxylic acid material, of a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons, and which is represented by the formula: ##STR15## wherein X is an alkyl or hydroxyl alkyl group, with at least one of the X substituents being a hydroxyl alkyl group of the structure --(CH 2 ) n OH wherein n is 1 to 3, said reaction conditions being at a temperature of from about 140° C. to 240° C. for from 1/2 to 24 hours whereby at least one carboxylic acyl group is converted into an oxazoline ring, said reaction product being borated by condensation with a boron compound selected from the class consisting of boron oxide, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated ester derivative.

Claim 6

A composition according to claim 3, wherein said borated oxazoline reaction product is the mono-oxazoline product of an alkenyl succinic anhydride or acid which has been reacted with about one mole equivalent of tris-hydroxymethylaminomethane, said alkenyl substituent having a number average molecular weight within the range of about 1000 and about 20,000.

Claim 7

A composition according to claim 3 wherein said borated oxazoline reaction product is the bis-oxazoline product of hydrocarbon substituted succinic anhydride reacted with about two mole equivalent of tris-hydroxymethylaminomethane, said bis-oxazoline being condensed with boric acid at a temperature ranging from about 80° to 120° C.

Claim 8

A composition according to claim 1 wherein said borated oxazoline reaction product is the mono-oxazoline product of hydrocarbon substituted succinic anhydride which has been reacted with about one mole equivalent of tris-hydroxymethylaminomethane, said mono-oxazoline being further reacted with an amine which is an alkylene polyamine containing 2 to 12 nitrogen atoms, and wherein pairs of nitrogen atoms are joined by alkylene groups of 2 to 4 carbon atoms and subsequently condensed with boric acid at a temperature ranging from about 80° C. to 100° C.

Claim 9

A lubricant composition comprising a major proportion of a lubricant oil and from about 0.01 to 20% by weight of the oil-soluble borated oxazoline reaction product, of one mole equivalent alkenyl succinic acid or anhydride wherein said alkenyl substituent contains a chain of at least 50 carbons, with from at least 1 to about 2 mole equivalent tris-hydroxymethylaminomethane, further condensed by reaction with from 1 to 3 moles of a boron reactant selected from the group consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids.

Claim 10

A lubricant composition comprising a major proportion of a lubricant oil and from about 0.01 to 20% by weight of the oil-soluble borated oxazoline reaction product, of one mole equivalent alkenyl succinic acid or anhydride wherein said alkenyl substituent contains a chain of at least 50 carbons, with from at least 1 to about 2 mole equivalent tris-hydroxymethylaminomethane, further condensed by reaction with from 1 to 3 moles of a boron reactant selected from the group consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids.

Claim 11

A composition according to claim 7 wherein said oil-soluble derivative is the reaction product of 1 to 2 moles of boric acid with a molar proportion of a bis-oxazoline product resulting from the reaction of said alkenyl succinic anhydride with about two mole equivalent of said tris-hydroxymethylaminomethane.

Claim 12

A lubricating oil composition comprising: a major amount of lubricating oil and 0.01 to 20 wt. % of an oil-soluble, borated lactone oxazoline reaction product obtained from heating together a molar proportion of a hydrocarbon substituted lactone acid material and one molar proportion of a 2,2-disubstituted-2-amino-1-alkanol having 1 to 3 hydroxy groups and containing a total of 4 to 8 carbons at a temperature of from 100°-240° C. until cessation of water evolution indicating completion of the oxazoline reaction and thereafter condensing said product with a boron compound selected from the class consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated reaction product, wherein said lactone acid material is formed by converting one of the carboxy groups of a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride to a lactone, said hydrocarbyl substituent being a polymer of a C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 to 10,000.

Claim 13

A lubricating oil composition comprising: a major amount of lubricating oil and 0.01 to 20 wt. % of an oil-soluble, borated lactone oxazoline reaction product obtained from heating together a molar proportion of a hydrocarbon substituted lactone acid material and one molar proportion of a 2,2-disubstituted-2-amino-1-alkanol having 1 to 3 hydroxy groups and containing a total of 4 to 8 carbons at a temperature of from 100°-240° C. until cessation of water evolution indicating completion of the oxazoline reaction and thereafter condensing said product with a boron compound selected from the class consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated reaction product, wherein said lactone acid material is formed by converting one of the carboxy groups of a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride to a lactone, said hydrocarbyl substituent being a polymer of a C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 to 10,000.

Claim 14

A composition according to claim 9 wherein said amino-1-alkanol is tris-(hydroxymethyl) aminomethane and said boron compound is boric acid condensed at a temperature of from about 80° C. to 120° C.

Claim 15

A composition according to claim 1 wherein said borated oxazoline material has an infrared absorption at 6.03 microns which is greater than that at 5.87 microns.

Claim 16

An oil-soluble borated oxazoline material containing from about 0.1 to 2.0 wt. % boron, wherein said oxazoline material is formed by the reaction of (A) a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride, wherein said hydrocarbyl group is a polymer of C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 and 10,000; and (B) a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons and represented by the formula: ##STR16## wherein X is an alkyl, or hydroxy alkyl group, with at least one of the X substituents being a hydroxy alkyl group of the structure --(CH 2 ) n OH, said oxazoline material having one to two oxazoline rings.

Claim 17

An oil-soluble borated oxazoline material containing from about 0.1 to 2.0 wt. % boron, wherein said oxazoline material is formed by the reaction of (A) a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride, wherein said hydrocarbyl group is a polymer of C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 and 10,000; and (B) a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons and represented by the formula: ##STR16## wherein X is an alkyl, or hydroxy alkyl group, with at least one of the X substituents being a hydroxy alkyl group of the structure --(CH 2 ) n OH, said oxazoline material having one to two oxazoline rings.

Claim 18

The oxazoline material according to claim 12 wherein said oxazoline material is obtained from the reaction of one molar proportion of an alkenyl succinic anhydride or acid and from about 1.5 to about 2 molar proportions of said 2,2-disubstituted-2-amino-1-alkanol, followed by condensation with a a boron reactant selected from the group consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids.

Claim 19

A borated oxazoline material which is a borated derivative of the oxazoline reaction product of a substantially saturated aliphatic hydrocarbyl, substituted C 4 -C 10 mono-unsaturated dicarboxylic acid material, said hydrocarbyl group having a number average molecular weight ranging from about 700 to about 140,000 with from at least 1 to about 2 mole equivalent, per mole equivalent of said dicarboxylic acid material, of a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons, and which is represented by the formula: ##STR17## wherein X is an alkyl or hydroxyl alkyl group, with at least one of the X substituents being a hydroxyl alkyl group of the structure --(CH 2 ) n OH wherein n is 1 to 3, said reaction conditions being at a temperature of from about 140° C. to 240° C. for from 1/2 to 24 hours whereby at least one carboxylic acyl group is converted into an oxazoline ring, said oxazoline reaction product being borated by condensation with a boron compound selected from the class consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated ester derivative.

Claim 20

A borated oxazoline material which is a borated derivative of the oxazoline reaction product of a substantially saturated aliphatic hydrocarbyl, substituted C 4 -C 10 mono-unsaturated dicarboxylic acid material, said hydrocarbyl group having a number average molecular weight ranging from about 700 to about 140,000 with from at least 1 to about 2 mole equivalent, per mole equivalent of said dicarboxylic acid material, of a 2,2-disubstituted-2-amino-1-alkanol having 2 to 3 hydroxy groups and containing a total of 4 to 8 carbons, and which is represented by the formula: ##STR17## wherein X is an alkyl or hydroxyl alkyl group, with at least one of the X substituents being a hydroxyl alkyl group of the structure --(CH 2 ) n OH wherein n is 1 to 3, said reaction conditions being at a temperature of from about 140° C. to 240° C. for from 1/2 to 24 hours whereby at least one carboxylic acyl group is converted into an oxazoline ring, said oxazoline reaction product being borated by condensation with a boron compound selected from the class consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated ester derivative.

Claim 21

The oxazoline material of claim 14 wherein said material is the bis-oxazoline product of hydrocarbon substituted succinic anhydride reacted with about two mole-equivalent of tris-hydroxymethyl-aminomethane, said bis-oxazoline being condensed with boric acid at a temperature ranging from about 80° to 120° C. and having infrared absorption at 6.03 microns which significantly exceeds the infrared absorption at 5.87 microns.

Claim 22

The oxazoline material of claim 12 wherein said material is obtained from heating together a molar proportion of a hydrocarbon substituted lactone acid material and one molar proportion of a 2,2-disubstituted-2-amino-1-alkanol having 1 to 3 hydroxy groups and containing a total of 4 to 8 carbons at a temperature of from 100°-240° C. until cessation of water evolution indicating completion of the oxazoline reaction and thereafter condensing said product with a boron compound selected from the class consisting of boron oxides, boron oxide hydrates, boron acids and esters of boron acids in an amount to provide from about 0.1 to 2.0 wt. % boron based on the total weight of said borated reaction product, wherein said lactone acid material is formed by converting one of the carboxy groups of a hydrocarbyl substituted C 4 to C 10 dicarboxylic acid or anhydride to a lactone, said hydrocarbyl substituent being a polymer of a C 2 to C 5 monoolefin, said polymer having a molecular weight of about 900 to 10,000.

Claim 23

A process of making an oil-soluble borated oxazoline material according to claim 12 comprising the step of condensing said oxazoline material with said boron compound at a temperature of above about 60° C. for at least a time sufficient that the reaction product does not show infrared absorption at 3.0 and 9.6 microns with the restriction that when boric acid or oxide is employed, the temperature employed is from 60° C. to 100° C.