Alkoxylated amines as fuel additives
View Patent ↗The present invention describes alkoxylated amines as fuel additives for reducing injector deposits in direct injection gasoline engines.
1. A fuel additive concentrate, comprising (A), (B1), (B2), and (B3):
(A) a compound of formula (I) or (II)
wherein
R is a divalent organic radical,
R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are independently H, C 1 - to C 7 -alkyl, C 5 - to C 7 -cycloalkyl, C 6 - to C 7 -aryl, or a —[—X i —] n —H radical, R 1 and R 2 optionally together with the nitrogen atom forming a five- to seven-membered ring,
x, y, and z are independently zero or a positive integer,
n and w are independently a positive integer, and
X i , i being in a range of from 1 to n, is independently —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/or —CH(CH 3 )—CH(CH 3 )—O—,
with the provisos that:
a sum total of x, y, and z is non-zero,
at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 is not H, and
at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 is —[—X i —] n —H;
(B1) a compound (B1a) which is a polyisobuteneamine obtained by hydroformylation and subsequent reductive amination of polyisobutene with a Mn in a range of from 300 to 5000,
(B2) a carrier oil comprising a polyolefin, (poly)ester, (poly)alkoxylate, polyether, aliphatic polyetheramine, alkylphenol-started polyether, alkylphenol-started polyetheramine, and/or carboxylic ester of long-chain alkanol; and
(B3) a corrosion inhibitor comprising a monocarboxylic acid having at least 12 carbon atoms, dicarboxylic acid having at least 12 carbon atoms, polycarboxylic acid having at least 12 carbon atoms, ammonium salt of an organic carboxylic acid, and/or heterocyclic aromatic.
2. The concentrate of claim 1 , wherein R is 1,2-ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,3-butylene, 1,4-butylene, 1,5-pentylene, 1,6-hexylene, 1,8-octylene, or 1,10-decylene.
3. The concentrate of claim 1 , wherein R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , if not —[—X i —] n —H, are independently H or an alkyl radical comprising 1 to 7 carbon atoms.
4. The concentrate of claim 3 , wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , if not —[—X i —] n —H, are independently methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, or tert-butyl.
5. The concentrate of claim 1 , comprising the compound of formula (I).
6. The concentrate of claim 5 , wherein x is 1 or 2 and R is 1,2-ethylene, 1,2-propylene, or 1,3-propylene.
7. The concentrate of claim 5 , wherein R 1 and R 2 are independently C 1 - to C 4 -alkyl and R 1 and R 4 are independently a —[—X i —] n —H.
8. The concentrate of claim 7 , wherein X i , for i being 1 to n, is independently —CH 2 —CH(CH 3 )—O— and/or —CH(CH 3 )—CH 2 —O—.
9. The concentrate of claim 1 , wherein the compound (A) is of formula (III)
wherein
R 1 , R 2 , and X i are as defined in claim 1 , and
p and q are independently a positive integer.
10. The concentrate of claim 9 , wherein, in the compound (A) of formula (III):
(IIIa) R is 1,2-ethylene and R 1 and R 2 are methyl;
(IIIb) R is 1,2-ethylene and R 1 and R 2 are ethyl;
(IIIc) R is 1,2-ethylene and R 1 and R 2 are n-butyl;
(IIId) R is 1,2-ethylene and R 1 and R 2 are collectively a 1,4-butylene chain;
(IIIe) R is 1,2-ethylene and R 1 and R 2 are collectively a 1,5-pentylene chain;
(IIIf) R is 1,2-ethylene and R 1 and R 2 are collectively a 3-oxa-1,5-pentylene chain;
(IIIg) R is 1,2-propylene and R 1 and R 2 are methyl;
(IIIh) R is 1,2-propylene and R 1 and R 2 are ethyl;
(IIIi) R is 1,2-propylene and R 1 and R 2 are n-butyl;
(IIIj) R is 1,2-propylene and R 1 and R 2 are collectively a 1,4-butylene chain;
(IIIk) R is 1,2-propylene and R 1 and R 2 are collectively a 1,5-pentylene chain;
(IIIl) R is 1,2-propylene and R 1 and R 2 are collectively a 3-oxa-1,5-pentylene chain;
(IIIm) R is 1,3-propylene and R 1 and R 2 are methyl;
(IIIn) R is 1,3-propylene and R 1 and R 2 are ethyl;
(IIIo) R is 1,3-propylene and R 1 and R 2 are n-butyl;
(IIIp) R is 1,3-propylene and R 1 and R 2 are collectively a 1,4-butylene chain;
(IIIq) R is 1,3-propylene and R 1 and R 2 are collectively a 1,5-pentylene chain; or
(IIIr) R is 1,3-propylene and R 1 and R 2 are collectively a 3-oxa-1,5-pentylene chain.
11. The concentrate of claim 1 , wherein a sum total of p and q is in a range of from 2 to 50.
12. The concentrate of claim 1 , comprising the compound of formula (I), wherein:
(Ia) R is 1,2-ethylene, w is 1, R 1 to R 3 are methyl, and R 4 is —[—X i —] n —H;
(Ib) R is 1,2-ethylene, w is 1, R 1 and R 2 are methyl, and R 3 and R 4 are independently —[—X i —] n —H;
(Ic) R is 1,2-propylene, w is 1, R 1 and R 2 are methyl, and R 3 and R 4 are independently —[—X i —] n —H;
(Id) R is 1,3-propylene, w is 1, R 1 and R 2 are methyl, and R 3 and R 4 are independently —[—X i —] n —H;
(Ie) R is 1,3-propylene, w is 1, R 1 and R 2 are ethyl, and R 3 and R 4 are independently —[—X i —] n —H;
(If) R is 1,3-propylene, w is 1, R 1 and R 2 are n-butyl, and R 3 and R 4 are independently —[—X i —] n —H; or
(Ig) R is 1,2-ethylene, w is 1, R 1 to R 4 are —[—X i —] n —H.
13. The concentrate of claim 1 , comprising the compound of formula (II), wherein:
(IIa) R is 1,2-ethylene, x and y are 1, z is 0, and R 1 to R 4 and R 6 are independently —[—X i —] n —H;
(IIb) R is 1,2-propylene, x and y are 1, z is 0, and R 1 to R 4 and R 6 are independently —[—X i —] n —H; or
(IIc) R is 1,3-propylene, x and y are 1, z is 0, and R 1 to R 4 are independently —[—X i —] n —H, and R 6 is C 1 - to C 2 -alkyl.
14. The concentrate of claim 1 , wherein, in at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , X in X i is —CH 2 —C(CH 3 ) 2 —O— and/or —C(CH 3 ) 2 —CH 2 —O—.
15. The concentrate of claim 1 , wherein, in at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , X in X is —CH 2 —CH(C 2 H)—O— and/or —CH(C 2 H 5 )—CH 2 —O— or —CH(CH 3 )—CH(CH 3 )—O—.
16. A fuel composition, comprising (A), (B1), (B2), (B3), (C), and optionally (D):
(A) a compound of formula (I) or (II)
wherein
R is a divalent organic radical,
R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are independently H, C 1 - to C 7 -alkyl, C 5 - to C 7 -cycloalkyl, C 6 - to C 7 -aryl or a —[—X i —] n —H radical, R 1 and R 2 optionally together with the nitrogen atom forming a five- to seven-membered ring,
x, y, and z are independently zero or a positive integer,
n and w are independently a positive integer, and
X i , i being in a range of from 1 to n, is independently —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/or —CH(CH 3 )—CH(CH 3 )—O—,
with the provisos that:
a sum total of x, y, and z is non-zero,
at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 is not H, and
at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 is —[—X i —] n —H;
(B1) a compound having detergent action;
(B2) a carrier oil comprising a polyolefin, (poly)ester, (poly)alkoxylate, polyether, aliphatic polyetheramine, alkylphenol-started polyether, alkylphenol-started polyetheramine, and/or carboxylic ester of long-chain alkanol;
(B3) a corrosion inhibitor comprising a monocarboxylic acid having at least 12 carbon atoms, dicarboxylic acid having at least 12 carbon atoms, polycarboxylic acid having at least 12 carbon atoms, ammonium salt of an organic carboxylic acid, and/or heterocyclic aromatic;
(C) a gasoline fuel; and
(D) optionally, an alcohol.
17. The composition of claim 16 , wherein, in at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , X in X i is —CH 2 —CH(CH 3 )—O— and/or —C(CH 3 ) 2 —CH 2 —O—.
18. The composition of claim 16 , wherein, in at least one of R 1 , R 2 , R 3 , R 4 , R, and R 6 , X in X i is —CH 2 —C(CH 3 ) 2 —O— and/or —C(CH 3 ) 2 —CH 2 —O—.
19. The composition of claim 16 , wherein, in at least one of R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 , X in X i is —CH 2 —CH(C 2 H)—O— and/or —CH(C 2 H 5 )—CH 2 —O— or —CH(CH 3 )—CH(CH 3 )—O—.
20. The composition of claim 16 , wherein, when admixed with 55 ppm by weight, improves the FR value relative to a fuel formulation comprising (iso-C 13 H 27 O(CH 2 CHEtO) 21 —(CH 2 CHEt)-NH 2 ) in place of the compound (A).