Quaternized nitrogen compounds and use thereof as additives in fuels and lubricants

Patent metadata

Field	Value
Publication number	US-10119085-B2
Application number	US-201815918201-A
Country	US
Kind code	B2
Filing date	Mar 12, 2018
Priority date	Jun 28, 2011
Publication date	Nov 6, 2018
Grant date	Nov 6, 2018

Abstract

The present invention relates to novel quaternized nitrogen compounds, to the preparation thereof and to the use thereof as a fuel and lubricant additive, more particularly as a detergent additive; to additive packages which comprise these compounds; and to fuels and lubricants thus additized. The present invention further relates to the use of these quaternized nitrogen compounds as a fuel additive for reducing or preventing deposits in the injection systems of direct-injection diesel engines, especially in common-rail injection systems, for reducing the fuel consumption of direct-injection diesel engines, especially of diesel engines with common-rail injection systems, and for minimizing power loss in direct-injection diesel engines, especially in diesel engines with common-rail injection systems.

First claim

The invention claimed is:

1. A fuel composition comprising, in a majority amount of a customary fuel, a proportion of at least one reaction product comprising a quaternized nitrogen compound, or a fraction thereof comprising a quaternized nitrogen compound, and being obtained from said reaction product by purification, said reaction product being obtainable by
a) reacting a hydrocarbyl-substituted polycarboxylic acid compound with a compound comprising at least one oxygen or nitrogen group capable of addition or condensation or otherwise reactive, with the polycarboxylic acid, and comprising at least one quaternizable amino group, to obtain a quaternizable hydrocarbyl-substituted polycarboxylic acid compound,
and
b) subsequent reaction thereof with a quaternizing agent which converts the at least one quaternizable amino group to a quaternary ammonium group, said quaternizing agent being the alkyl ester of a cycloaromatic or cycloaliphatic mono- or polycarboxylic acid, or of an aliphatic polycarboxylic acid;
or said reaction product being obtainable by
reacting a quaternizable hydrocarbyl-substituted polycarboxylic acid compound comprising at least one quaternizable amino group with a quaternizing agent which converts the at least one quaternizable amino group to a quaternary ammonium group, said quaternizing agent being the alkyl ester of a cycloaromatic or cycloaliphatic mono- or polycarboxylic acid, or of an aliphatic polycarboxylic acid,
wherein said compound comprising at least one oxygen or nitrogen group capable of addition or condensation or otherwise reactive, with the polycarboxylic acid, and comprising at least one quaternizable amino group is selected from the group consisting of aromatic or nonaromatic heterocycles having one primary and one tertiary amino group and aromatic or nonaromatic heterocycles having a tertiary amino group and a hydroxyalkyl group.

2. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having one primary and one tertiary amino group that is a N-heterocycle which is aminoalkylated on at least one ring nitrogen atom, wherein the N-heterocycle is selected from the group consisting of tetrahydrofuran, pyrrolidine, isoxazolidine, isothiazolidine, pyrazolidine, oxazolidine, thiazolidine, imidazolidine, pyrroline, piperidine, piperidinyl, 1,3-dioxane, tetrahydropyran, hexahydropyridazine, hexahydropyrimidine, piperazine, furan, thiane, pyrrole, pyrazole, oxazole, thiazole, imidazole and 1,3,4-triazole; isoxazole, isothiazole, thiadiazole, oxadiazole, pyridinyl, pyridazine, pyrimidine, pyrazinyl, 1,2,4-triazine, and 1,3,5-triazin-2-yl.

3. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having a tertiary amino group and a hydroxyalkyl group is a N-heterocycle which is aminoalkylated on at least one ring nitrogen atom, wherein the N-heterocycle is selected from the group consisting of tetrahydrofuran, pyrrolidine, isoxazolidine, isothiazolidine, pyrazolidine, oxazolidine, thiazolidine, imidazolidine, pyrroline, piperidine, piperidinyl, 1,3-dioxane, tetrahydropyran, hexahydropyridazine, hexahydropyrimidine, piperazine, furan, thiane, pyrrole, pyrazole, oxazole, thiazole, imidazole and 1,3,4-triazole; isoxazole, isothiazole, thiadiazole, oxadiazole, pyridinyl, pyridazine, pyrimidine, pyrazinyl, 1,2,4-triazine, and 1,3,5-triazin-2-yl.

4. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having one primary and one tertiary amino group is a N-heterocycles which is aminoalkylated on at least one ring nitrogen atom, wherein the N-heterocycle is selected from the group consisting of furan, thiane, pyrrole, pyrazole, oxazole, thiazole, imidazole and 1,3,4-triazole; isoxazole, isothiazole, thiadiazole, and oxadiazole.

5. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having a tertiary amino group and a hydroxyalkyl group is a N-heterocycle which is aminoalkylated on at least one ring nitrogen atom, wherein the N-heterocycle is selected from the group consisting of furan, thiane, pyrrole, pyrazole, oxazole, thiazole, imidazole and 1,3,4-triazole; isoxazole, isothiazole, thiadiazole, and oxadiazole.

6. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having one primary and one tertiary amino group is a N-heterocycle which is aminoalkylated on at least one ring nitrogen atom, wherein the N-heterocycle is selected from the group consisting of
1-(3-Aminopropyl)imidazole

4-(3-Aminopropyl)morpholine

1-(2-Aminoethylpiperidine)

2-(1-Piperazinyl)ethylamine (AEP)

N-Methylpiperazine

7. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having one primary and one tertiary amino group is
1-(3-Aminopropyl)imidazole

8. The fuel composition according to claim 1 , wherein said aromatic or nonaromatic heterocycles having a tertiary amino group and a hydroxyalkyl group is
1-(3-Hydroxypropyl)imidazole

9. The fuel composition according to claim 7 , wherein about 1.1 to about 2.0 equivalents of quaternizing agent are used per equivalent of quaternizable tertiary nitrogen atom.

10. The fuel composition according to claim 1 , wherein the hydrocarbyl-substituted polycarboxylic acid compound is a polyisobutenylsuccinic acid or an anhydride thereof, said acid having a bismaleation level of less than about 20%.

11. The fuel composition according to claim 1 , wherein the quaternizing agent is a compound of the general formula 1
R 1 OC(O)R 2   (1)

in which
R 1 is a lower alkyl radical and
R 2 is an optionally substituted monocyclic aryl or cycloalkyl radical, where the substituent is selected from OH, NH 2 , NO 2 , C(O)OR 3 , and R 1 OC(O)—, in which R 1 is as defined above and R 3 is H or R 1 .

12. The fuel composition according to claim 1 , wherein the quaternizing agent is a compound of the general formula 2
R 1 OC(O)-A-C(O)OR 1a   (2)

in which
R 1 and R 1a are each independently a lower alkyl radical and
A is hydrocarbylene, such as especially alkylene or alkenylene.

13. The fuel composition according to claim 1 , wherein the quaternizing agent is selected from alkyl salicylates, dialkyl phthalates and dialkyl oxalates.

14. The fuel composition according to claim 1 , selected from diesel fuels, biodiesel fuels, gasoline fuels and alkanol-containing gasoline fuels.

Assignees

• Basf Se

Inventors

• Roeger-Goepfert Cornelia
• Boehnke Harald
• Grabarse Wolfgang
• Koenig Hannah Maria
• Hansch Markus
• Voelkel Ludwig

Classifications

• C10N2070/00

  Specific manufacturing methods for lubricant compositions · CPC title

• C10N2030/04

  Detergent property or dispersant property · CPC title

• C10L10/06

  for facilitating soot removal · CPC title

• C10L2200/0259

  Nitrogen containing compounds · CPC title

• C10L2270/026

  for diesel engines, e.g. automobiles, stationary, marine · CPC title