# US 11,078,418 B2 · Corrosion inhibitors for fuels and lubricants

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- Number: US 11,078,418 B2
- Document ID: US11078418B2
- Status: Granted
- Kind: B2
- Application number: 16/313,751
- Filed: 2017-06-27
- Published: 2020-10-01
- Granted: 2021-08-03
- Earliest claimed: 2016-07-05
- Assignees: BASF SE
- Applicants: BASF SE
- Inventors: Jochen Mezger; Szilard Csihony
- Web page: https://patentgrep.com/patent/US11078418B2

## CPC

- C09K 15/06: containing oxygen
- C10M 129/42: polycarboxylic
- C08F 8/46: Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation
- C10L 1/1883: {polycarboxylic acid}
- C10L 1/195: obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L 1/198: obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds {homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid}
- C10L 10/04: for minimising corrosion or incrustation
- C10M 145/16: polycarboxylic
- C10L 2200/0423: Gasoline
- C10L 2250/04: Additive or component is a polymer
- C10L 2270/023: for gasoline engines
- C10M 2207/127: polycarboxylic
- C10M 2209/086: polycarboxylic, e.g. maleic acid
- C10N 2020/04: Molecular weight; Molecular weight distribution
- C10N 2030/12: Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
- C10N 2030/66: {Hydrolytic stability}
- C09K: MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C10M: LUBRICATING COMPOSITIONS (well drilling compositions C09K8/02); USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION (mould release, i.e. separating, agents for metals B22C3/00, for plastics or substances in a plastic state, in general B29C33/56, for glass C03B40/02; textile lubricating compositions D06M11/00, D06M13/00, D06M15/00; immersion oils for microscopy G02B21/33)
- C08F: MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C10L: FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10N: INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS

## Abstract

The present invention relates to novel uses of corrosion inhibitors in fuels and lubricants.

## Claims

### Claim 1

A process of reducing corrosion on a surface comprising iron, steel, copper, or a copper alloy, the process comprising:
contacting the surface with a corrosion inhibitor in the presence of sodium, potassium, magnesium, calcium, and/or zinc ions,
wherein the corrosion inhibitor comprises a reaction product of polyisobutene comprising free acid groups, the reaction product comprising, in reacted form: (A) a polyisobutene having a number-average molecular weight Mn in a range of from 200 to 10000 and (B) an α,β-unsaturated monomer that is a monocarboxylic acid, dicarboxylic acid, monoalkyl ester, dialkyl ester, or anhydride, in a stoichiometric ratio of more than one equivalent of the α,β-unsaturated monomer (B) per reactive double bond in the polyisobutene (A),
wherein the reaction product has a bismaleation level in a range of from at least 12% to 40%, and
wherein, when the monomer (B) comprises the monoalkyl ester and/or the dialkyl ester, at least 10% of the ester groups present in the reaction product are in hydrolyzed form, and/or
wherein, when the monomer (B) comprises the anhydride, at least 10% of the anhydride groups present in the reaction product are in hydrolyzed form.

### Claim 2 (depends on 1)

The process of claim 1, wherein the polyisobutene (A) has a number-average molecular weight Mn of 500 to 2500.

### Claim 3 (depends on 1)

The process of claim 1, wherein the monomer (B) is selected from the group consisting of acrylic acid, methacrylic acid, crotonic acid, ethylacrylic acid and derivatives thereof.

### Claim 4 (depends on 1)

The process of claim 1, wherein the monomer (B) is selected from the group consisting of maleic acid, fumaric acid, itaconic acid (2-methylenebutanedioic acid), citraconic acid (2-methylmaleic acid), glutaconic acid (pent-2-ene-1,5-dicarboxylic acid), 2,3-dimethylmaleic acid, 2-methyl-fumaric acid, 2,3-dimethylfumaric acid, methylenemalonic acid, tetrahydrophthalic acid, and derivatives thereof.

### Claim 5 (depends on 1)

The process of claim 1, wherein the monomer (B) is maleic anhydride.

### Claim 6 (depends on 1)

The process of claim 1, wherein the bismaleation level is at least 11%.

### Claim 7 (depends on 1)

The process of claim 1, wherein a proportion of unconverted polyisobutene in the reaction product is not more than 30% by weight.

### Claim 8 (depends on 1)

The process of claim 1, wherein the corrosion inhibitor is comprised in a gasoline fuel having a sodium content, a potassium content, or both, of at least 0.1 ppm by weight.

### Claim 9 (depends on 1)

The process of claim 1, wherein the corrosion inhibitor is comprised in a gasoline fuel having a magnesium content, a calcium content, or both, of at least 0.1 ppm by weight.

### Claim 10 (depends on 1)

The process of claim 1, wherein the corrosion inhibitor is comprised in a gasoline fuel having a zinc content of at least 0.1 ppm by weight.

### Claim 11 (depends on 1)

The process of claim 1, wherein the reducing of corrosion comprises preventing and reducing deposits in a fuel system.

### Claim 12 (depends on 1)

The process of claim 1, wherein the bismaleation level is at least 15%.

### Claim 13 (depends on 1)

The process of claim 1, wherein the bismaleation level is up to 35%.

### Claim 14 (depends on 1)

The process of claim 1, wherein the bismaleation level is up to 30%.

### Claim 15 (depends on 1)

The process of claim 1, wherein the polyisobutene (A) has a number-average molecular weight Mn of 700 to 2500.

### Claim 16 (depends on 1)

The process of claim 1, wherein the polyisobutene (A) has a number-average molecular weight Mn up to 1100.

### Claim 17 (depends on 1)

The process of claim 1, wherein the compound (B) comprises acrylic acid and/or methacrylic acid.

### Claim 18 (depends on 1)

The process of claim 1, wherein the compound (B) comprises crotonic acid and/or ethylacrylic acid.
