IP Library Granted Patent US 12692428
Granted Patent B2
US 12692428 · App. 19/412,927 · Granted Jul 28, 2026

Composition and methods for inhibiting corrosion of metal during acidizing a wellbore in a subterranean formation for fracking

Inventor: Roy W. Martin (Naples, FL)
C09K8/54C09K8/602C09K8/74E21B43/119E21B43/261E21B43/27C09K2208/32
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12692428
App. No.
19/412,927
Granted
Jul 28, 2026
Kind
B2
Abstract

An acid composition for acidizing a wellbore including at least one acid, an alkenylphenone, and a polycyclic diquaternary quinoxaline, and a method using the acid composition to reduce corrosion within a wellbore. The polycyclic diquaternary quinoxaline having the structure: where X − comprises a counter anion, R′ comprises an alkyl aryl group, and R 1 , R 2 , R 3 , R 4 and R 5 comprise hydrogen or a substitution group, the alkenylphenone the general structure: where R 1 is an unsubstituted or an inertly substituted aryl having 6 carbon atoms to 10 carbon atoms, and R 2 can be a substituted or unsubstituted C 1 -C 6 alkyl group.

Claims (38)

1 . An acid composition for acidizing a wellbore, the composition comprising:

at least one acid;

an effective amount of an alkenylphenone;

an effective amount of polycyclic diquaternary quinoxaline;

the polycyclic diquaternary quinoxaline having the general structure:

where X − comprises a counter anion,

R′ comprises an alkyl aryl group, and

R 1 , R 2 , R 3 , R 4 and R 5 comprise hydrogen or a substitution group;

the alkenylphenone having the general structure:

where R 1 is an unsubstituted or an inertly substituted aryl having 6 carbon atoms to 10 carbon atoms, and

R 2 can be a substituted or unsubstituted C 1 -C 6 alkyl group.

2 . The acid composition according to claim 1 , wherein the alkyl aryl group is selected from at least one of benzyl, benzoyl, vinylbenzyl and methyl naphthalene.

3 . The acid composition according to claim 1 , wherein R 1 , R 2 , R 3 , R 4 and R 5 comprise substitution groups selected from: halo, alkyl, aryl and alkyl aryl.

4 . The acid composition according to claim 1 , wherein the acid composition comprises from 0.5 parts by weight to 5.0 parts by weight of the polycyclic diquaternary quinoxaline for every 1.0 part by weight of the alkenylphenone.

5 . The acid composition according to claim 1 , wherein the acid composition comprises from 0.5 parts by weight to 2.0 parts by weight of the polycyclic diquaternary quinoxaline for every 1.0 part by weight of the alkenylphenone.

6 . The acid composition according to claim 1 , wherein the counter anion comprises at least one of a chloride, bromide and iodide.

7 . The acid composition according to claim 1 , further comprising an intensifier selected from at least one of an iodide donor, an aldehyde and formic acid.

8 . The acid composition according to claim 1 , wherein the polycyclic diquaternary quinoxaline comprises dibenzyl diquaternary quinoxaline having the general structure:

wherein X − comprises a counter anion.

9 . The acid composition according to claim 1 , further comprising at least one of a surfactant and hydrotrope.

10 . The acid composition according to claim 9 , wherein the surfactant comprises an ethoxylate alcohol have from 16-18 carbon atoms in an alkyl chain.

11 . The acid composition according to claim 1 , wherein the acid comprises 15 wt % HCl.

12 . The acid composition according to claim 1 , wherein the acid comprises a synthetic acid.

13 . The acid composition according to claim 1 , wherein the acid comprises a mineral acid selected from at least one of hydrochloric acid, hydrofluoric acid, sulfuric acid and nitric acid.

14 . The acid composition according to claim 1 , wherein the acid comprises an amount ranging from 5 to 28 wt %.

15 . The acid composition according to claim 1 , wherein the composition is diluted with water at a point-of-use to achieve a ratio of composition and water of 1:1 respectively.

16 . The acid composition according to claim 1 , wherein the composition is diluted with water at the point-of-use to achieve a ratio of composition and water of 1:2 respectively.

17 . An inhibited acid composition compatible with stainless steel tankers for transporting the inhibited acid composition, the composition comprising:

an acid;

an effective amount of alkenylphenone;

an effective amount of polycyclic diquaternary quinoxaline, and

wherein the inhibited acid composition is transported in stainless steel tankers,

wherein the alkenylphenone having the general structure:

where R 1 is an unsubstituted or an inertly substituted aryl having 6 carbon atoms to 10 carbon atoms and R 2 can be a substituted or unsubstituted C 1 -C 6 alkyl group;

the polycyclic diquaternary quinoxaline having the general structure:

wherein X − comprises a counter anion,

R′ comprises an alkyl aryl group, and

R 1 , R 2 , R 3 , R 4 and R 5 comprise hydrogen or a substitution group.