IP Library Granted Patent US 8,372,336
Granted Patent B2
US 8,372,336 · App. 13/376,777 · Granted Feb 12, 2013

Polymeric corrosion inhibitors

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Quick Facts
Patent No.
US 8,372,336
App. No.
13/376,777
Granted
Feb 12, 2013
Kind
B2
Abstract

The present invention relates to the use of a product obtainable by the reaction of an alkoxylated fatty amine with a dicarboxyhc acid derivative, followed by partial or total quaternization of the reaction product obtained; or by reacting a product with a dicarboxylic acid derivative, followed by partial or total quaternization of the reaction product obtained. The product consists of >60% w/w of oligomers/polymers with at least two alkoxylated amine units and one or more diacid/acid anhydride unit or >50% w/w of oligomers/polymers with at least two alkoxylated amine units and two or more diacid/acid anhydride units; as a corrosion inhibitor for metal surfaces. The invention also relates to a method for protecting a metal surface from corrosion by contacting the metal surface with said corrosion inhibitor.

Claims (14)

1. A method for protecting a metal surface from corrosion by contacting the metal surface with a corrosion-inhibiting product obtainable by a reaction of an alkoxylated fatty amine having the formula

wherein R is a hydrocarbyl group having 8-24 carbon atoms; B is, independently, an alkyl group having 1-4 carbon atoms, a benzyl group, or the group (AO) n H, wherein each A, independently, is an alkylene group containing 2-4 carbon atoms; each n is, independently, at least 1 and the sum of all n is 2-30; each x, independently, is 2 or 3; and y is 0-3; or a partial or wholly quaternised derivative thereof; with a dicarboxylic acid derivative having the formula

wherein D is —OH, —Cl, or —OR3, wherein R3 is a C1-C4 alkyl group; R2 is selected from the group consisting of a direct bond, an alkylene radical of formula —(CH 2 ) z —, wherein z is an integer from 1 to 10, a substituted alkylene radical wherein said alkylene radical with formula —(CH 2 ) z — is substituted by 1 or 2 —OH groups, the group —CH═CH—, and the o-phenylene group; optionally said reaction between the amine and the dicarboxylic acid derivative is being followed by a further reaction step wherein part or all of the nitrogen atoms are quaternised; and wherein the reaction product consists for more than 60% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and one or more diacid/acid anhydride units and for more than 50% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and two or more diacid/acid anhydride units; as a corrosion inhibitor for metal surfaces.

2. The method according to claim 1 where the metal surfaces are part of pipelines, pumps, tanks and other equipment.

3. The method according to claim 2 where the corrosion inhibiting product is added to a flowing liquid at any point in a flow line upstream of the point or line that are intended to be protected.

4. The method according to claim 1 where in formula (I) y=0.

5. The method according to claim 1 where in formula (I) y=1, x is 3, and B is an alkyl group having 1-4 carbon atoms, or the benzyl group.

6. The method according to claim 1 where in formula (I) y=1, x is 3, and B is the group (AO) n H.

7. The method according to claim 1 where all nitrogen atoms of the corrosion inhibiting product are tertiary nitrogen atoms.

8. The method according to claim 1 where the dicarboxylic acid derivative has the formula (IIa) and D is OH.

9. The method according to claim 1 where the carboxylic acid derivative has the formula (IIb).

10. The method according to claim 1 where the carboxylic acid derivative is succinic acid or succinic anhydride.

11. The method according to claim 1 where the product is obtained by reaction of a compound of formula (I) with (IIa) or (IIb), and where the reactants are added in a molar ratio of 2:1 to 1:2, preferably 1.5:1 to 1:1.5, and most preferably 1.2:1 to 1:1.2.

12. The method according to claim 1 where the product consists of more than 75% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and one or more diacid/acid anhydride units and more than 65% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and two or more diacid/acid anhydride units, preferably the product contains for more than 90% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and one or more diacid/acid anhydride units and for more than 80% by weight of oligomers/polymers with two or more alkoxylated amine units, that are optionally quaternized, and two or more diacid/acid anhydride units.

Assignments (4)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
CHANGE OF ADDRESS Recorded May 15, 2017
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 042745/0406 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2012
From: HELLBERG, PER-ERIK; GOROCHOVCEVA, NATALIJA
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 027536/0494 →