Polymers as additives for fuels

Patent metadata

Field	Value
Publication number	US-10947467-B2
Application number	US-201716462759-A
Country	US
Kind code	B2
Filing date	Nov 29, 2017
Priority date	Dec 15, 2016
Publication date	Mar 16, 2021
Grant date	Mar 16, 2021

Abstract

A method for minimizing power loss, reducing a fuel consumption and/or for reducing and/or avoiding deposits in a fuel system in the direct injection diesel engines. The method contains adding a copolymer to a fuel composition, wherein the copolymer contains, in a copolymerized form: (A) an ethylenically unsaturated mono- or dicarboxylic acid or a derivative thereof, (B) an α-olefin having from 12 to 30 carbon atoms, (C) optionally an additional aliphatic or cycloaliphatic olefin which has at least 4 carbon atoms and is different from monomer (B) and (D) optionally an additional copolymerizable monomers other than monomers (A), (B) and (C), anhydride or carboxylic acid functionalities present in the copolymer are partly reacted with at least one compound (E) comprising an alcohol group and/or an amino group, and the anhydride functionalities present in the copolymer are hydrolysed and/or carboxylic ester functionalities present in the copolymer are partly hydrolyzed.

First claim

The invention claimed is:

1. A method for avoiding at least one deposit in a fuel system in a direct injection diesel engine, the method comprising:
adding a copolymer to a diesel fuel composition,
wherein the copolymer comprises, in a copolymerized form:
(A) maleic anhydride,
(B) an α-olefin having from 12 to 30 carbon atoms,
(C) optionally an additional aliphatic or cycloaliphatic olefin which has at least 4 carbon atoms and is different from monomer (B) and
(D) optionally an additional copolymerizable monomers other than monomers (A), (B) and (C), selected from the group consisting of
(Da) a vinyl ester,
(Db) a vinyl ether,
(Dc) a (meth)acrylic ester of an alcohol having at least 5 carbon atoms,
(Dd) an allyl alcohol or an ester thereof,
(De) a N-vinyl compound selected from the group consisting of a vinyl compound of a heterocycle containing at least one nitrogen atom, a N-vinylamide and a N-vinyllactam,
(Df) an ethylenically unsaturated aromatic,
(Dg) an α,β-ethylenically unsaturated nitrile,
(Dh) a (meth)acrylamide, and
(Di) an allylamine,
wherein anhydride functionalities present in the copolymer are partly reacted with at least one compound (E) comprising an alcohol group and/or an amino group, and the anhydride functionalities present in the copolymer are hydrolysed.

2. The method according to claim 1 , wherein the at least one compound (E) is selected from the group consisting of a monoalcohol, a diol, a polyol, a monoamine, a diamine, a polyamine and an amino alcohol.

3. The method according to claim 2 , wherein the at least one compound (E) is a monoalcohol,
the monoalcohol is a compound of formula (I):
R 1 —O—[—X i —] n —H  (I)

wherein
R 1 is a straight-chain or branched C 1 - to C 200 -alkyl or C 1 - to C 200 -alkenyl radical and
n is 0 or a positive integer from 1 to 50, and
each X i , where i=1 to n, is optionally independently selected from the group consisting of —CH 2 —CH 2 —O—, —CH 2 —CH(CH 3 )—O—, —CH(CH 3 )—CH 2 —O—, —CH 2 —C(CH 3 ) 2 —O—, —C(CH 3 ) 2 —CH 2 —O—, —CH 2 —CH(C 2 H 5 )—O—, —CH(C 2 H 5 )—CH 2 —O— and —CH(CH 3 )—CH(CH 3 )—O—.

4. The method according to claim 2 , wherein the at least one compound (E) is a monoamine and
the monoamine is a monoamine having 6 to 200 carbon atoms.

5. The method according to claim 4 , wherein the monoamine has formula (II):

wherein
R 2 is hydrogen or C 1-20 -alkyl and
R 3 is C 12-200 -alkyl which is optionally linear or branched.

6. The method according to claim 5 , wherein the monoamine is a polyisobuteneamine based on a polyisobutene having a weight average molecular weight of 550 to 2300 g/mol.

7. The method according to claim 4 ,
wherein the monoamine is a monoalkyl amine having 6 to 200 carbon atoms or a dialkylamine.

8. The method according to claim 2 , wherein the at least one compound (E) is a polyamine and
the polyamine is a polyethyleneamine.

9. The method according to claim 8 , wherein the polyamine is ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine and pentaethylenehexamine.

10. The method according to claim 2 , wherein the at least one compound (E) is a compound (E2) selected from the group consisting of 2-dimethylaminoethylamine, 3-dimethylaminopropylamine, and N′,N″,N″-trimethyldiethylenetriamine.

11. The method according to claim 1 , wherein at least one deposit in the injection system in the direct injection diesel engine is reduced and/or prevented.

12. The method according to claim 11 , wherein the at least one deposit is an internal diesel injector deposit.

13. The method according to claim 11 , wherein the at least one deposit is an internal diesel injector deposit caused by Na, Ca and/or K ions and/or at least one polymeric deposit.

14. The method according to claim 1 , wherein the direct injection diesel engine is a diesel engine with a common rail injection system.

15. The method according to claim 1 , wherein the copolymer is added to the diesel fuel in an amount effective for reducing formation of ionic and/or polymeric deposits in the injection system, in comparison to a method using the same amount of a comparative fuel that is the same as the diesel fuel but does not contain the copolymer.

16. A method, comprising:
injecting a diesel fuel into a direct injection diesel engine through a fuel system in fluid communication with the direct injection diesel engine, wherein the fuel system comprises an injection system having injection nozzles and a common rail, and
combusting the diesel fuel in the direct injection diesel engine;
wherein the diesel fuel comprises at least one copolymer in an amount effective for reducing the formation of internal ionic and/or polymeric deposits in the injection nozzles of the injection system in comparison to a method of injecting and combusting the same amount of a comparative fuel that is the same as the diesel fuel but does not contain the copolymer;
wherein the copolymer comprises, in a copolymerized form:
(A) maleic anhydride,
(B) an α-olefin having from 12 to 30 carbon atoms,
(C) optionally an additional aliphatic or cycloaliphatic olefin which has at least 4 carbon atoms and is different from monomer (B) and
(D) optionally an additional copolymerizable monomers other than monomers (A), (B) and (C), selected from the group consisting of
(Da) a vinyl ester,
(Db) a vinyl ether,
(Dc) a (meth)acrylic ester of an alcohol having at least 5 carbon atoms,
(Dd) an allyl alcohol or an ester thereof,
(De) a N-vinyl compound selected from the group consisting of a vinyl compound of a heterocycle containing at least one nitrogen atom, a N-vinylamide and a N-vinyllactam,
(Df) an ethylenically unsaturated aromatic,
(Dg) an α,β-ethylenically unsaturated nitrile,
(Dh) a (meth)acrylamide, and
(Di) an allylamine,
wherein the copolymer has one or more anhydride functionalities reacted with the compound (E) comprising an alcohol group and/or an amino group, and at least a portion of the anhydride functionalities are hydrolyzed.

17. The method according to claim 16 , wherein the internal ionic and/or polymeric deposits are metal soap deposits.

18. The method according to claim 17 , wherein the metal soap deposits comprise Na, Ca and/or K ions.

19. The method according to claim 1 , wherein the formation of the deposit is avoided inside an injection nozzle and the deposit is an internal metal soap deposit.

20. The method according to claim 16 , wherein the internal metal soap deposit comprise Na, Ca and/or K ions.

Assignees

• Basf Se

Inventors

• Peretolchin Maxim
• Garcia Castro Ivette
• Flores-Figueroa Aaron

Classifications

• C10L2300/20

  Mixture of two components · CPC title

• C10M149/06

  containing monomers having an unsaturated radical bound to an amido or imido group · CPC title

• C10M2209/086

  polycarboxylic, e.g. maleic acid · CPC title

• C10L1/2383

  Polyamines or polyimines, or derivatives thereof {(poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C) (C10L1/221 takes precedence)} · CPC title

• C10L1/2366

  homo- or copolymers derived from unsaturated compounds containing amine groups (C10L1/221 takes precedence) · CPC title