IP Library Granted Patent US 10,393,319
Granted Patent B2
US 10,393,319 · App. 15/441,656 · Granted Aug 27, 2019

Kinetic hydrate inhibitors for controlling gas hydrate formation in wet gas systems

Inventors: Regan Andrew Jones (Sugar Land, TX); Jeremy Wayne Bartels (Sugar Land, TX); Jeremy Moloney (Katy, TX)
Assignee: Ecolab USA Inc.
F17D3/12C09K8/03C10L3/107F17D1/005F17D1/04F17D1/08C10L2230/14C10L2250/04C10L2290/141
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Quick Facts
Patent No.
US 10,393,319
App. No.
15/441,656
Granted
Aug 27, 2019
Kind
B2
Abstract

The present invention generally relates to methods and hydrate inhibitor compositions for inhibiting the formation of hydrates in a fluid comprising gas and water. More specifically, the method comprises contacting a hydrate inhibitor composition to a fluid. The hydrate inhibitor composition comprises a nonpolar solvent; a polar solvent; and a polymer, an oligomer, a dendrimer, or an acid or salt thereof.

Claims (20)

1. A method for inhibiting hydrate formation in a fluid comprising water and a gas, the method comprising contacting the fluid with an effective amount of a hydrate inhibitor composition comprising from about 20 to about 55 wt. % of a nonpolar solvent; from about 1 to about 15 wt. % of a polar solvent; and from about 0.1 to about 50 wt. % of a polymer, an oligomer, a dendrimer, or an acid or salt thereof.

2. The method of claim 1 , wherein the polymer, oligomer, or dendrimer is a kinetic hydrate inhibiting polymer, oligomer, or dendrimer.

3. The method of claim 2 , wherein the fluid is substantially free of a liquid hydrocarbon before contacting the hydrate inhibitor composition.

4. The method of claim 2 , wherein the polymer or oligomer comprises repeat units derived from a first monomer, a second monomer, or a combination thereof; the first monomer comprising an acrylamide monomer, acrylate monomer, N-vinyl amide monomer, N-vinyl caprolactam monomer, N-vinyl amine monomer, anhydride monomer, dicarboxylic acid monomer, diester monomer, diol monomer, amine monomer, diamine monomer, dihydroxy acid monomer, dihydroxy ester monomer, hydroxy ester monomer, hydroxy acid monomer, or a combination thereof; and the second monomer comprising methacrylamidopropyltrimethylammonium chloride (MAPTAC), 2-(dimethylamino)ethyl methacrylamide, 3-(acryloylamino)propyl]trimethyl ammonium chloride (APTAC), 2-acryloyloxyethyltrim ethyl ammonium chloride (AETAC), 2-methacryloyloxyethyltrimethyl ammonium chloride (METAC), diallyldimethyl ammonium chloride (DADMAC), acryloyloxyethyldimethylbenzyl ammonium chloride (AEDBAC), or methacryloyloxyethyldimethylbenzyl ammonium chloride (MEDBAC), or a combination thereof.

5. The method of claim 2 , wherein the polymer or oligomer is a copolymer or cooligomer comprising repeat units derived from N-isopropyl methacrylamide, methacrylamidopropyltrimethylammonium chloride, 2-(dimethylamino)ethyl methacrylamide, or a combination thereof.

6. The method of claim 5 , wherein the polymer or oligomer is a copolymer or cooligomer comprising repeat units derived from isopropyl methacrylamide and methacrylamidopropyltrimethylammonium chloride.

7. The method of claim 2 , wherein the weight average molecular weight of the polymer is from about 500 Daltons to about 25,000 Daltons.

8. The method of claim 2 , wherein the nonpolar solvent comprises an aromatic hydrocarbon solvent, an aliphatic hydrocarbon solvent, a cycloaliphatic hydrocarbon solvent, or a combination thereof, and the polar solvent comprises an alcohol having a molecular weight less than 300 Daltons.

9. The method of claim 8 , wherein the nonpolar solvent comprises heavy aromatic naphtha, toluene, a xylene, a hexane, a diesel, kerosene, a heptane, an octane, iso-octane, or a combination thereof, and the polar solvent comprises 2-ethyl hexanol, n-butanol, t-butanol, pentanol, hexanol, octanol, decanol, dodecanol, tetradecanol, hexadecanol, octadecanol, or a combination thereof.

10. The method of claim 9 , wherein the nonpolar solvent comprises heavy aromatic naphtha, and the polar solvent comprises 2-ethyl hexanol.

11. The method of claim 2 , wherein the hydrate inhibitor composition comprising from about 30 wt. % to about 45 wt. % of heavy aromatic naphtha; from about 4 to about 15 wt. % of 2-ethyl hexanol; and from about 15 to about 20 wt. % of the kinetic hydrate inhibiting polymer.

12. The method of claim 11 , wherein the polymer has a weight average molecular weight of from about 500 Daltons to about 25,000 Daltons.

13. The method of claim 2 , wherein the effective amount of a hydrate inhibitor composition is from about 0.1 volume % to about 10 volume % based on the total volume of produced water in the fluid comprising gas and water.

14. The method of claim 2 , wherein the hydrate inhibitor composition comprising from about 20 wt. % to about 45 wt. % of the nonpolar solvent; from about 2 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

15. The method of claim 4 , wherein the hydrate inhibitor composition comprising from about 20 wt. % to about 45 wt. % of the nonpolar solvent; from about 2 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

16. The method of claim 5 , wherein the hydrate inhibitor composition comprising from about 20 wt. % to about 45 wt. % of the nonpolar solvent; from about 2 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

17. The method of claim 6 , wherein the hydrate inhibitor composition comprising from about 20 wt. % to about 45 wt. % of the nonpolar solvent; from about 2 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

18. The method of claim 4 , wherein the hydrate inhibitor composition comprising from about 30 wt. % to about 45 wt. % of heavy aromatic naphtha; from about 4 to about 15 wt. % of 2-ethyl hexanol; and from about 15 to about 20 wt. % of the kinetic hydrate inhibiting polymer.

19. The method of claim 2 , wherein the hydrate inhibitor composition comprising from about 30 wt. % to about 45 wt. % of the nonpolar solvent; from about 4 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

20. The method of claim 2 , wherein the hydrate inhibitor composition comprising from about 30 wt. % to about 45 wt. % of the nonpolar solvent; from about 4 to about 15 wt. % of the polar solvent; and from about 15 to about 50 wt. % of the kinetic hydrate inhibiting polymer.

Assignments (6)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 17, 2025
From: JPMORGAN CHASE BANK, N.A.
To: CHAMPIONX LLC; APERGY ESP SYSTEMS, LLC; APERGY BMCS ACQUISITION CORP; HARBISON-FISCHER, INC.; NORRIS RODS, INC.,; NORRIS RODS, INC.,; NORRISEAL-WELLMARK, INC.; PCS FERGUSON, INC.; QUARTZDYNE, INC.; US SYNTHETIC CORPORATION
Reel/Frame 072004/0019 →
RELEASE OF SECURITY INTEREST Recorded Jun 7, 2022
From: BANK OF AMERICA, N.A.
To: CHAMPIONX USA INC.
Reel/Frame 060304/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2020
From: ECOLAB USA INC.
To: CHAMPIONX USA INC.
Reel/Frame 053849/0537 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 052848/0368 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053250/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2017
From: JONES, REGAN ANDREW; BARTELS, JEREMY WAYNE; MOLONEY, JEREMY
To: ECOLAB USA INC.
Reel/Frame 041399/0702 →
Continuity (2)
Provisional Application 62300552 · Feb 26, 2016
Related Publication 20170248276A1 · Aug 31, 2017
Cited By (1)
US 12,590,179