IP Library Granted Patent US 10,899,986
Granted Patent B2
US 10,899,986 · App. 16/324,203 · Granted Jan 26, 2021

Substituted Mannich base fuel additives, compositions, and methods

Inventors: Buford Brian Smith (Evansville, WI); Gamini Ananda Vedage (Bethlehem, PA)
Assignee: Evonik Operations GmbH
C10L1/236C07C209/48C07C253/30C08C19/22C08F132/06C10L1/143C10L1/238C10L10/04C10L10/06C10L1/1616C10L1/1985C10L2200/0423C10L2270/023
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Quick Facts
Patent No.
US 10,899,986
App. No.
16/324,203
Granted
Jan 26, 2021
Kind
B2
Abstract

Mannich base compositions include the reaction products of (1) an amine component including at least one multifunctional amine of structure (1): wherein each R is independently H or CH 2 CH 2 CH 2 NH 2 ; R 1 is H, CH 2 CH 2 CH 2 NH 2 , C1-C21 alkyl, or C2-C21 alkenyl; n is 2; and m is 1 or 2, with (2) an alkyl substituted hydroxyaromatic compound, and (3) and aldehyde. The Mannich base compositions are useful for fuel additives and other articles. Additive compositions, fuel additives, fuel compositions and methods for reducing deposit formations in a fuel system are also disclosed.

Claims (17)

1. A substituted Mannich base composition comprising a reaction product of (1) an amine component comprising at least one multifunctional amine of structure (I):

wherein each R is independently H or CH 2 CH 2 CH 2 NH 2 ; R 1 is H, CH 2 CH 2 CH 2 NH 2 , C 1 -C 21 alkyl, or C 2 -C 21 alkenyl; n is 2; and m is 1 or 2, and (2) an alkyl substituted hydroxyaromatic compound comprising an oligonieric or polymeric alkyl substituent being a polyisobutylene of 250-1500 molecular weight and (3) an aldehyde.

2. The composition of claim 1 , wherein the hydroxyaromatic is selected from the group consisting of phenol, o-cresol, and combinations thereof.

3. The composition of claim 1 , wherein in which the aldehyde component is an aliphatic or aromatic aldehyde of up to 18 carbons.

4. The composition of claim 3 , wherein the aldehyde is formaldehyde or paraformaldehyde.

5. The composition of claim 1 , wherein the amine component comprises a compound selected from the group consisting of N-3-aminopropyl diethylenetriamine; N-3-aminopropyl-[N′-3-[N-3-aminopropyl]aminopropyl]diethylenetriamine; N,N′-bis(3-aminopropyl)diethylenetriamine; N,N-bis(3-aminopropyl)diethylenetriamine; N,N,N′-tris(3-aminopropyl)diethylenetriamine; N,N′,N″-tris(3-aminopropyl)diethylenetriamine; N,N, N′,N′-tetrakis(3-aminopropyl)diethylenetriamine; N,N-bis(3-aminopropyl)-[N′-3-[N-3-aminopropyl]aminopropyl]-[N′-3-aminopropyl]diethylenetriamine; N-3-aminopropyl-[N′-3-[N-3-aminopropyl]aminopropyl]-[N′-3-aminopropyl]diethylenetriamine; and combinations thereof.

6. The composition of claim 1 , wherein the amine component comprises a compound wherein R1 is H or CH 2 CH 2 CH 2 NH 2 .

7. The composition of claim 1 , wherein the amine component comprises a mixture of amines of structure according to formula (I) in a parts-by-weight (pbw) ratio of 0 to 50 pbw amine having 4 nitrogen atoms, 40 to 95 pbw amine having 5 nitrogen atoms, and 0 to 50 pbw amine having at least 6 nitrogen atoms.

8. The composition of claim 1 , wherein the amine component comprises a mixture of amines of structure according to formula (I) in a parts-by-weight (pbw) ratio of 1 to 15 pbw amine having 4 nitrogen atoms, 50 to 90 pbw amine having 5 nitrogen atoms, and 5 to 35 pbw amine having at least 6 nitrogen atoms.

9. The composition of claim 1 , wherein the alkyl substituted hydroxyaromatic component, the aldehyde and amine component are reacted in a ratio of moles of alkyl substituted hydroxyaromatic component to aldehyde to multifunctional amine are from about 0.5-1:0.5-3.5:0.5-2.0.

10. The composition of claim 1 , further comprising at least one compound selected from the group consisting of alkyl substituted phenols, dimethylaminomethylphenol, bis(dimethylaminomethyl)phenol, and tris(dimethylaminomethyl)phenol.

11. The composition of claim 1 , wherein the composition comprises a reaction product of the amine component, the alkyl substituted hydroxyaromatic component, the aldehyde and at least one additional multifunctional amine having three or more active amine hydrogens or an amine having at least one primary and/or secondary amine as well as at least one tertiary amine.

12. The composition of claim 11 , wherein the at least one multifunctional amine is selected from the group consisting of an aliphatic amine, a cycloaliphatic amine, an aromatic amine, a poly(alkylene oxide) diamine or triamine, a Mannich base derivative of an aliphatic amine, a Mannich base derivative of a cycloaliphatic amine, a Mannich base derivative of an aromatic amine, an amine adduct derivative of an aliphatic amine with a glycidyl ether, an amine adduct derivative of a cycloaliphatic amine with a glycidyl ether, or an amine adduct derivative of an aromatic amine with a glycidyl ether, and the like, and combinations thereof.

13. The composition of claim 12 , wherein the at least one multifunctional amine is selected from the group consisting of ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, higher polyethyleneamines, aminoethylpiperazine, meta-xylylenediamine, the various isomers of diamine-cyclohexane, isophorone diamine, 3,3′-dimethyl-4,4′-diaminodicyclohexyl methane, 4,4′-diaminodicyclohexyl methane, 2,4′-diaminodicyclohexyl methane, the mixture of methylene bridged poly(cyclohexyl-aromatic)amines, 1,2-propylenediamine, 1,3-propylenediamine, 1,4-butanediamine, 1,5-pentanediamine, 1,3-pentanediamine, 1,6-hexanediamine, 3,3,5-trimethyl-1,6-hexane-diamine, 3,5,5-trimethyl-1,6-hexanediamine, 2-methyl-1,5-pentanediamine, bis-(3-amino-propyl)amine, N,N′-bis-(3-aminopropyl)-1,2-ethanediamine, N-(3-aminopropyl)-1,2-ethanediamine, 1,2-diaminocyclohexane, 1,3-diaminocyclohexane, 1,4-diamino-cyclohexane, the poly(alkylene oxide)diamines and triamines, aminopropylated ethylene glycols, aminopropylated propanediols, aminopropylated butanediols, aminopropylated hexanediols, aminopropylated polyethylene glycols, aminopropylated polypropylene glycols, aminopropylated polybutanediols, N,N-dimethyl-1,3-propanediamine, N-methyl piperazine, and combinations thereof.

14. A substituted Mannich base fuel additive comprising the composition of claim 1 .

15. A fuel composition comprising fuel and the substituted Mannich base fuel additive of claim 14 .

16. A method to reduce deposit formation in a fuel system of an internal combustion engine comprising operating the internal combustion system with a fuel according to claim 15 .

Assignments (2)
CHANGE OF NAME Recorded Nov 26, 2019
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051135/0315 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2019
From: SMITH, BUFORD BRIAN; VEDAGE, GAMINI ANANDA
To: EVONIK DEGUSSA GMBH
Reel/Frame 049874/0895 →
Cited By (4)
US 12,503,666 US 12,606,765 US 12,606,766 US 12,674,113