US2009307964A1PendingUtilityA1
Use of solubilizers for homogenizing additive concentrates
Est. expiryJun 12, 2028(~1.9 yrs left)· nominal 20-yr term from priority
C10L 1/1966C10L 1/221C10L 1/1852C10L 1/2425C10L 1/2383C10L 1/08C10L 1/2475C10L 1/143C10L 1/1963C10L 1/19C10L 1/1616C10L 1/1973C10L 1/2437C10L 10/00C10L 1/231C10L 1/224C10L 1/1824C10L 1/198C10L 1/1905C10L 1/1985C10L 10/14C10L 1/238
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Claims
Abstract
A cold-stabilized fuel oil composition comprising a major proportion by weight of a middle distillate fuel which boils in the range of 120-500° C. and minor proportions by weight of (A) at least one cold flow improver, (B) at least one detergent additive and (C) at least one cold solubilizer I which has at least one radical having at least 4 carbon atoms.
Claims
exact text as granted — not AI-modified1 . The use of at least one solubilizer of the general formula I
in which
R 1 denotes a hydrocarbylene radical having from 1 to 12 carbon atoms or a hydrocarbylene radical which has from 2 to 12 carbon atoms, is interrupted by one or more heteroatoms selected from the group of O, S and N, and may in each case bear one or more functional groups selected from the group of OH, OR 3 , NH 2 , NHR 4 , NR 4 R 5 , COOH, COOR 7 , CONHR 4 and CONR 4 R 5 , where amino groups may also be present in protonated form and carboxylic acid groups also in deprotonated form,
X is OH, OR 3 , NH 2 , NHR 4 or NR 4 R 5 , where, in the case that X together with the adjacent carbonyl group is a carboxylic acid radical, this radical is present in deprotonated form and the accompanying cation may be a hydrocarbyl-substituted ammonium cation selected from the group of [H 3 NR 8 ] + , [H 2 NR 8 R 9 ] + and [HNR 8 R 9 R 10 ] + ,
Y is O, S, NH or NR 6 , or, in the case that X is NH 2 or NHR 4 , is a chemical bond to X with formation of an imide structure,
where R 2 to R 10 are each independently hydrocarbyl radicals having from 1 to 30 carbon atoms,
with the proviso that at least one of the R 2 , R 3 , R 4 , R 5 , R 6 and R 7 radicals has at least 4 carbon atoms,
for homogenizing additive concentrates suitable for additizing fuel oil compositions which consist predominantly of a middle distillate fuel which boils in the range of 120-500° C. and/or a renewable fuel, said additive concentrates comprising
(A) at least one cold flow improver,
(B) at least one detergent additive and
(C) an inert organic solvent or a mixture of such solvents.
2 . The use of at least one solubilizer I according to claim 1 for homogenizing additive concentrates which additionally comprise
(D) at least one cetane number improver.
3 . The use of at least one solubilizer I according to claim 1 or 2 for homogenizing additive concentrates which comprise
(A) from 1 to 50% by weight of at least one cold flow improver, (B) from 0.5 to 40% by weight of at least one detergent additive, (C) from 0 to 80% by weight of at least one cetane number improver, and (D) from 1 to 60% by weight of an inert organic solvent or of a mixture of such solvents.
4 . The use of at least one solubilizer I according to claims 1 to 3 for homogenizing additive concentrates in an amount of from 1.05 to 15% by weight, based on the total amount of the additive concentrate.
5 . The use of at least one solubilizer I according to claims 1 to 4 for homogenizing additive concentrates comprising, as a cold flow improver, one or more representatives selected from
(Aa) copolymers of ethylene with at least one further ethylenically unsaturated monomer; (Ab) comb polymers; (Ac) polyoxyalkylenes; (Ad) polar nitrogen compounds; (Ae) sulfocarboxylic acids or sulfonic acids or derivatives thereof; and/or (Af) poly(meth)acrylic esters.
6 . The use of at least one solubilizer I according to claim 5 for homogenizing additive concentrates, comprising, as a cold flow improver, one or more representatives selected from
ethylene-vinyl acetate copolymers; ethylene-vinyl propionate copolymers; N,N-dialkylammonium salts of 2-N′,N′-dialkylamidobenzoates; the reaction products of 1 mol of ethylenediaminetetraacetic acid with 4 mol of a dialkylamine; the reaction products of 1 mol of nitrilotriacetic acid with 3 mol of a dialkylamine; the reaction products of 1 mol of phthalic anhydride with 2 mol of a dialkylamine; the reaction products of 1 mol of an alkenyl-spiro-bislactone with 2 mol of a dialkylamine; C 12 - to C 18 -alkyl fumarate-vinyl acetate or C 12 - to C 18 -alkyl fumarate-styrene comb polymers; and/or C 14 - to C 20 -alkyl itaconate comb polymers.
7 . The use of at least one solubilizer I according to claims 1 to 6 for homogenizing additive concentrates, comprising, as detergent additive (B), one or more amphiphilic substances which have at least one hydrophobic hydrocarbon radical having a number-average molecular weight (Mn) of from 85 to 20 000 and at least one polar moiety which is selected from
(Ba) mono- or polyamino groups having up to 6 nitrogen atoms, at least one nitrogen atom having basic properties; (Bb) nitro groups, if appropriate in combination with hydroxyl groups; (Bc) hydroxyl groups in combination with mono- or polyamino groups, at least one nitrogen atom having basic properties; (Bd) carboxyl groups or their alkali metal or alkaline earth metal salts; (Be) sulfonic acid groups or their alkali metal or alkaline earth metal salts; (Bf) polyoxy-C 2 -C 4 -alkylene moieties which are terminated by hydroxyl groups, mono- or polyamino groups, at least one nitrogen atom having basic properties, or by carbamate groups; (Bg) carboxylic ester groups; (Bh) moieties which derive from succinic anhydride and have hydroxyl and/or amino and/or amido and/or imido groups; and/or (Bi) moieties obtained by Mannich reaction of substituted phenols with aldehydes and mono- or polyamines.
8 . The use of at least one solubilizer I according to claim 7 for homogenizing additive concentrates, comprising, as detergent additive (B), one or more derivatives which derive from polyisobutenylsuccinic anhydride and have amino and/or amido and/or imido groups.
9 . The use of at least one solubilizer I according to claims 1 to 8 for homogenizing additive concentrates in which the inert organic solvents (C) are selected from hydrocarbons, alcohols, carboxylic esters or mixtures thereof.
10 . The use of at least one solubilizer I according to claims 2 to 9 for homogenizing additive concentrates in which the at least one cetane number improver (D) is selected from organic nitrates.
11 . The use of at least one solubilizer I according to claims 1 to 10 for homogenizing additive concentrates where at least one of the R 2 , R 3 , R 4 , R 5 , R 6 or R 7 radicals in said solubilizer has at least 10 carbon atoms.
12 . The use of at least one solubilizer I according to claims 1 to 10 for homogenizing additive concentrates, where X in said solubilizer is OH.
13 . The use of at least one solubilizer I according to claims 1 to 12 for homogenizing additive concentrates, said solubilizer deriving from maleic acid or phthalic acid.
14 . The use of at least one solubilizer I according to claims 1 to 13 for homogenizing additive concentrates, said solubilizer being a monoamide of maleic acid or of phthalic acid, in which at least one of the R 2 or R 6 radicals has at least 10 carbon atoms.
15 . An additive concentrate suitable for additizing fuel oil compositions which consist predominantly of a middle distillate fuel which boils in the range of 120-500° C. and/or a renewable fuel, said additive concentrate comprising at least one solubilizer of the general formula I
in which
R 1 denotes a hydrocarbylene radical having from 1 to 12 carbon atoms or a hydrocarbylene radical which has from 2 to 12 carbon atoms, is interrupted by one or more heteroatoms selected from the group of O, S and N, and may in each case bear one or more functional groups selected from the group of OH, OR 3 , NH 2 , NHR 4 , NR 4 R 5 , COOH, COOR 7 , CONHR 4 and CONR 4 R 5 , where amino groups may also be present in protonated form and carboxylic acid groups also in deprotonated form,
X is OH, OR 3 , NH 2 , NHR 4 or NR 4 R 5 , where, in the case that X together with the adjacent carbonyl group is a carboxylic acid radical, this radical is present in deprotonated form and the accompanying cation may be a hydrocarbyl-substituted ammonium cation selected from the group of [H 3 NR 8 ] + , [H 2 NR 8 R 9 ] + and [HNR 8 R 9 R 10 ] + ,
Y is O, S, NH or NR 6 , or, in the case that X is NH 2 or NHR 4 , is a chemical bond to X with formation of an imide structure,
where R 2 to R 10 are each independently hydrocarbyl radicals having from 1 to 30 carbon atoms,
with the proviso that at least one of the R 2 , R 3 , R 4 , R 5 , R 6 and R 7 radicals has at least 4 carbon atoms,
in an amount of from 1.05 to 15% by weight, based on the total amount of the additive concentrate, and
(A) at least one cold flow improver,
(B) at least one detergent additive and
(C) an inert organic solvent or a mixture of such solvents.Join the waitlist — get patent alerts
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