IP Library Granted Patent US 12,637,628
Granted Patent B2
US 12,637,628 · App. 18/437,917 · Granted May 26, 2026

Compositions and methods for scavenging hydrogen sulfide

Inventors: James Begeal (Cypress, TX); Chris Williamson (Montgomery, TX); Ali Yousef (Tomball, TX); Dallas Watson (Guthrie, OK)
Assignee: Foremark Performance Chemicals
C10L3/103B01D53/1468B01D53/1493B01D2252/20478B01D2252/205B01D2252/502B01D2252/602C10L2290/545
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Quick Facts
Patent No.
US 12,637,628
App. No.
18/437,917
Granted
May 26, 2026
Kind
B2
Abstract

This invention provides compositions and methods that inhibit formation of alkenyl sulfide polymers and allow the hydrogen sulfide to be removed when scavenging hydrogen sulfide by reaction with aldehydes.

Claims (27)

1 . A scavenging composition formed from ingredients comprising

a) an aldehyde and/or an aldehyde releaser,

b) ethylamine, and

c) an alcohol,

wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to less than one molar equivalent in relation to the total amount of aldehyde provided by a), and wherein the scavenging composition does not comprise ethanolamine, and wherein the aldehyde releaser is not formed by a reaction of ethanolamine with an aldehyde.

2 . The scavenging composition as in claim 1 wherein the aldehyde is selected from the group consisting of formaldehyde, benzaldehyde, furfural, acrolein, glutaraldehyde, glyoxal and any combination of two or more of the foregoing, with the proviso that when the aldehyde is formaldehyde, water is also present in the composition.

3 . The scavenging composition as in claim 1 wherein the aldehyde is formaldehyde, and water is also present in the scavenging composition.

4 . The scavenging composition as in claim 1 wherein the aldehyde releaser is formed from i) an aldehyde and ii) a primary or secondary amine, an alkanolamine that is not ethanolamine, an alcohol or a combination of any two or more of the foregoing, optionally wherein the aldehyde releaser is formed from i) an aldehyde and ii) methylamine or ethanol.

5 . The scavenging composition as in claim 1 wherein the alcohol is a C 1 -C 6 alcohol, a C 1 -C 6 diol, or a C 1 -C 6 polyol; and wherein the C 1 -C 6 alcohol, C 1 -C 6 diol, or C 1 -C 6 polyol is optionally mixed with water.

6 . The scavenging composition according to claim 5 , wherein the C 1 -C 6 alcohol is selected from the group consisting of methanol, ethanol, and isopropyl alcohol.

7 . The scavenging composition as in claim 1 , wherein the scavenging composition comprises an amount of ethylamine that is less than one half mole of ethylamine per mole of aldehyde and optionally wherein the aldehyde is formaldehyde and the ingredients further comprise water.

8 . A scavenging composition consisting essentially of

a) an aldehyde and/or aldehyde releaser,

b) ethylamine, and

c) an alcohol;

wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to less than one molar equivalent in relation to the total amount of aldehyde provided by a).

9 . The scavenging composition of claim 8 , wherein the molar ratio of ethylamine to the total amount of aldehyde in the treatment solution is 0.2 to about 0.56 and optionally wherein the aldehyde is formaldehyde and the ingredients further comprise water.

10 . The scavenging composition of claim 8 , wherein the aldehyde is selected from the group consisting of formaldehyde, benzaldehyde, furfural, acrolein, glutaraldehyde, glyoxal and any combination of two or more of the foregoing, with the proviso that when the aldehyde is formaldehyde, water is also present in the composition.

11 . The scavenging composition of claim 8 , wherein the aldehyde releaser is formed from i) an aldehyde and ii) a primary or secondary amine, an alkanolamine that is not ethanolamine, an alcohol, or any combination of two or more of the foregoing, optionally wherein the aldehyde releaser is formed from i) an aldehyde and ii) methylamine or ethanol.

12 . The scavenging composition as in claim 8 , wherein the alcohol is a C 1 -C 6 alcohol, a C 1 -C 6 diol, or a C 1 -C 6 polyol; and wherein the C 1 -C 6 alcohol, C 1 -C 6 diol, or C 1 -C 6 polyol is optionally mixed with water.

13 . The scavenging composition according to claim 12 , wherein the alcohol is a C 1 -C 6 alcohol.

14 . The scavenging composition according to claim 13 , wherein the C 1 -C 6 alcohol is selected from the group consisting of methanol, ethanol, and isopropyl alcohol.

15 . The scavenging composition as in claim 8 , wherein the scavenging composition comprises an amount of ethylamine that is less than one half mole of ethylamine per mole of aldehyde and optionally wherein the aldehyde is formaldehyde and the ingredients further comprise water.

16 . The scavenging composition as in claim 1 , wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to 0.75 molar equivalent in relation to the total amount of aldehyde provided by a).

17 . The scavenging composition as in claim 1 , wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to 0.56 molar equivalent in relation to the total amount of aldehyde provided by a).

18 . The scavenging composition as in claim 8 , wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to 0.75 molar equivalent in relation to the total amount of aldehyde provided by a).

19 . The scavenging composition as in claim 8 , wherein the amount of ethylamine used to form the scavenging composition is in the range of 0.2 molar to 0.56 molar equivalent in relation to the total amount of aldehyde provided by a).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2026
From: NEXGEN OILFIELD CHEMICALS, LLC
To: FOREMARK PERFORMANCE CHEMICALS
Reel/Frame 074189/0724 →
SECURITY INTEREST Recorded Jul 1, 2024
From: FOREMARK PERFORMANCE CHEMICALS, INC.; NEXGEN OILFIELD CHEMICALS, LLC
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 067890/0287 →
Continuity (3)
Division 18143215 · May 4, 2023
Provisional Application 63338203 · May 4, 2022
Related Publication 20240228897A1 · Jul 11, 2024
References Cited (1)
US 6267938B1 · Warrender · 2001 [cited by examiner]