IP Library Granted Patent US 12,637,629
Granted Patent B2
US 12,637,629 · App. 18/437,923 · 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 12,637,629
App. No.
18/437,923
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 (26)

1 . A method for preparing a scavenging composition, the method comprising

combining a) an aldehyde and/or an aldehyde releaser, b) ethylamine, and c) an alcohol to form the scavenging composition,

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), 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 method according to 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 method according to claim 1 , wherein the aldehyde is formaldehyde, and water is also present in the scavenging composition.

4 . The method according to 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 method according to 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.

6 . The method according to claim 1 , wherein the scavenging composition further comprises water.

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

8 . The method according to 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.

9 . A method of forming a scavenging composition, the method comprising

combining ingredients 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).

10 . The method according to claim 9 , 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.

11 . The method according to claim 9 , 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 scavenging composition.

12 . The method according to claim 9 , 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.

13 . The method according to claim 9 , wherein the alcohol is a C 1 -C 6 alcohol, a C 1 -C 6 diol, or a C 1 -C 6 polyol.

14 . The method according to claim 9 , wherein the scavenging composition further comprises water.

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

16 . The method according to claim 9 , 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.

17 . The method according to claim 1 , wherein the ethylamine in the combining step is in an aqueous solution and the aldehyde and/or aldehyde releaser in the combining step is in an aqueous solution.

18 . The method according to claim 9 , wherein the ethylamine in the combining step is in an aqueous solution and the aldehyde and/or aldehyde releaser in the combining step is in an aqueous solution.

19 . The method according to 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).

20 . The method according to 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).

21 . The method according to claim 9 , 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).

22 . The method according to claim 9 , 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 20240228898A1 · Jul 11, 2024
References Cited (1)
US 6267938B1 · Warrender · 2001 [cited by examiner]