IP Library Granted Patent US 10,059,872
Granted Patent B2
US 10,059,872 · App. 14/968,265 · Granted Aug 28, 2018

Corrosion inhibitor compositions for acidizing treatments

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Quick Facts
Patent No.
US 10,059,872
App. No.
14/968,265
Granted
Aug 28, 2018
Kind
B2
Abstract

A corrosion inhibitor composition and a method of inhibiting corrosion on a surface are disclosed. The corrosion inhibitor composition includes at least one nitrogen containing heteroaromatic compound and at least one haloalkynyl carbamate compound. The corrosion inhibitor composition may be utilized with acidizing treatments for wells, in particular for the production of oil, gas, and/or water.

Claims (41)

1. A composition for inhibiting corrosion, the composition comprising

at least one quaternized nitrogen containing heteroaromatic compound, and

at least one haloalkynyl carbamate compound,

wherein the weight ratio of the at least one nitrogen containing heteroaromatic compound to the at least one haloalkynyl carbamate compound is from 1:100 to 100:1, and

wherein the at least one nitrogen containing heteroaromatic compound is a pyridine.

2. The composition according to claim 1 , wherein the at least one nitrogen containing compound is substituted with a C 1-20 alkyl group.

3. The composition according to claim 1 , wherein the at least one nitrogen containing heteroaromatic compound comprises at least one nitrogen ring atom, wherein the at least one nitrogen ring atom has a substituent group selected from the group consisting of an alkyl group, an alkenyl group, an aryl group, an arylalkyl group, an alkaryl group, a heteroaryl group, a heteroarylalkyl group, and an alkylheteroaryl group.

4. The composition according to claim 3 , wherein the substituent group is an arylalkyl group comprising an aryl group containing from 5 to 9 carbon atoms and a C 1-5 alkyl group.

5. The composition according to claim 1 , wherein the at least one haloalkynyl carbamate compound has the following structure:

wherein

R8 is a hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an arylalkyl group, an alkaryl group, a heteroaryl group, a heteroarylalkyl group, an alkylheteroaryl group, a cycloalkyl group, an aminoalkyl group, or a hydroxyalkyl group;

R9 is an alkylene group,

X is a halide; and

n is from 1 to 3.

6. The composition according to claim 1 ; wherein the at least one haloalkynyl carbamate compound is 3-iodo-2-propynyl butyl carbamate.

7. The composition according to claim 1 , wherein the weight ratio of the at least one nitrogen containing heteroaromatic compound to the at least one haloalkynyl carbamate compound is from 1:50 to 50:1.

8. The composition according to claim 1 , wherein the composition further comprises an alkynol.

9. The composition according to claim 8 , wherein the alkynol is 2,5-dimethyl-3-hexyne-2,5-diol, a butynol, or a combination thereof.

10. The composition according to claim 1 , wherein the composition further comprises a weak base.

11. The composition according to claim 1 , wherein the composition further comprises a quaternary phosphonium halide.

12. The composition according to claim 1 , wherein the composition further comprises a biocide.

13. The composition according to claim 1 , wherein the composition further comprises at least one solvent.

14. The composition according to claim 13 , wherein the solvent comprises water, an organic solvent, or a combination thereof.

15. The composition according to claim 14 , wherein the organic solvent comprises methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, hexanol, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, diethylene glycol monomethyl ether, ethylene glycol monobutyl ether, butyl diglycol ether, or a combination thereof.

16. The composition according to claim 1 , wherein the at least one nitrogen containing heteroaromatic compound and the at least one haloalkynyl carbamate compound have a total active concentration of from about 5 wt. % to about 100 wt. %.

17. A method of inhibiting corrosion on a surface, the method comprising contacting the surface with the composition according to claim 1 .

18. The method according to claim 17 , wherein the surface is a steel surface.

19. The method according to claim 17 , the method further comprising mixing the composition with an aqueous acidic solution.

20. The method according to claim 19 , wherein the aqueous acidic solution comprises hydrochloric acid, hydrofluoric acid, acetic acid, citric acid, or a combination thereof.

21. The method according to claim 17 , the method further comprising introducing the composition into an oil well, a gas well, or a water well.

22. The composition according to claim 8 , wherein the alkynol comprises ethyl octynol.

23. The composition according to claim 8 , wherein the alkynol comprises propargyl alcohol.

24. The composition according to claim 1 , wherein the composition further comprises a surfactant.

25. The composition according to claim 24 , wherein the surfactant is a nonionic surfactant, an amphoteric surfactant, or a combination thereof, and wherein the surfactant has a hydrophilic/lipophilic balance of from about 5 to about 15.

26. The composition according to claim 24 wherein the surfactant is a polysorbate, a sorbitan, a sorbitan derivative, or a combination thereof.

27. A composition for inhibiting corrosion, the composition comprising

at least one quaternized nitrogen containing heteroaromatic compound, and

at least one haloalkynyl carbamate compound, and

wherein the weight ratio of the at least one nitrogen containing heteroaromatic compound to the at least one haloalkynyl carbamate compound is from 1:100 to 100:1,

wherein the at least one nitrogen containing heteroaromatic compound is a pyridine, and

wherein the at least one haloalkynyl carbamate compound is 3-iodo-2-propynyl butyl carbamate.

Assignments (4)
CHANGE OF NAME Recorded Feb 4, 2022
From: LONZA, LLC
To: ARXADA, LLC
Reel/Frame 058956/0087 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME PREVIOUSLY RECORDED AT REEL: 051975 FRAME: 0564. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 25, 2020
From: LONZA INC.
To: LONZA, LLC
Reel/Frame 053037/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2020
From: LONZA INC
To: LONZA LLC
Reel/Frame 051976/0564 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2016
From: JANAK, KEVIN E.; TANNENBAUM, SARAH
To: LONZA INC.
Reel/Frame 038116/0109 →