IP Library Granted Patent US 9,550,935
Granted Patent B2
US 9,550,935 · App. 14/582,618 · Granted Jan 24, 2017

Method of controlling gas hydrates in fluid systems

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Quick Facts
Patent No.
US 9,550,935
App. No.
14/582,618
Granted
Jan 24, 2017
Kind
B2
Abstract

A method of inhibiting hydrates in a fluid comprising water and gas comprising adding to the fluid an effective hydrate-inhibiting amount of a composition comprising one or more copolymers of N-alkyl (alkyl)acrylamide monomers and one or more cationic monomers selected from acid and alkyl chloride quaternary salts of N,N-dialkylaminoalkyl (meth)acrylates and N,N-dialkylaminoalkyl (meth)acrylamides.

Claims (22)

1. A method of inhibiting hydrate formation in a fluid comprising water, gas and optionally liquid hydrocarbon comprising treating the fluid with an effective hydrate-inhibiting amount of an inhibitor composition comprising a cationic copolymer derived by polymerization of about 75 to about 99.9 mole percent of N-alkyl alkylacrylamide or N-alkyl acrylamide monomer units and about 0.1 to about 25 mole percent of alkylacrylamidoalkyltrialkylammonium chloride or acrylamidoalkyltrialkylammonium chloride monomer units.

2. The method of claim 1 , wherein polymerization of said cationic copolymer is initiated by redox decomposition of a peroxide with a redox co-catalyst.

3. The method of claim 2 , wherein the redox co-catalyst is CuSO 4 or Fe 2 (SO 4 ) 3 .

4. The method of claim 1 , wherein said cationic copolymer has a molecular weight distribution of about 60-100 percent in the range of 1,000 to 20,000 Daltons and 0-25 percent in the range from 20,000 to 6,000,000 Daltons.

5. The method of claim 1 , wherein said inhibitor composition further comprises a hydroxyl-containing compound selected from the group consisting of a low molecular weight alcohol, a low molecular weight glycol, a low molecular weight glycol ether, and combinations thereof.

6. The method of claim 5 , wherein said hydroxyl-containing compound is selected from the group consisting of isopropanol; 1,1,1-tris(hydroxymethyl) propane; triethylene glycol dimethyl ether; diethylene glycol dimethyl ether; 2-ethoxyethanol; diethylene glycol monomethyl ether; ethylene glycol monobutyl ether; diethylene glycol monoethyl ether; diethylene glycol monobutyl ether; and combinations thereof.

7. The method of claim 1 , wherein said cationic copolymer has an average molecular weight of about 1,000 to about 100,000 Dalton.

8. The method of claim 1 , further comprising treating the fluid with a corrosion-inhibiting amount of a corrosion inhibitor.

9. The method of claim 8 , wherein the corrosion inhibitor is water soluble.

10. The method of claim 9 , wherein the corrosion inhibitor is selected from the group consisting of a quaternary amine-based corrosion inhibitor, an imidazoline-based corrosion inhibitor, a phosphate ester-based corrosion inhibitor, and combinations thereof.

11. The method of claim 9 , wherein the water soluble corrosion inhibitor is a quaternary amine-based corrosion inhibitor.

12. The method of claim 1 , wherein the inhibitor composition further comprises a corrosion inhibitor.

13. The method of claim 12 , wherein the corrosion inhibitor is water soluble.

14. The method of claim 13 , wherein the corrosion inhibitor is selected from the group consisting of a quaternary amine-based corrosion inhibitor, an imidazoline-based corrosion inhibitor, a phosphate ester-based corrosion inhibitor, and combinations thereof.

15. The method of claim 13 , wherein the water soluble corrosion inhibitor is a quaternary amine-based corrosion inhibitor.

16. The method of claim 1 , wherein the N-alkyl acrylamide monomer is N-isopropyl acrylamide.

17. The method of claim 1 , wherein the N-alkyl (alkyl)acrylamide monomer is N-isopropyl methacrylamide.

18. The method of claim 1 , wherein the acrylamidoalkyltrialkylammonium chloride monomer is acrylamidopropyltrimethylammonium chloride.

19. The method of claim 1 , wherein the alkylacrylamidoalkyl-trialkylammonium chloride monomer is methacrylamidopropyltrimethylammonium chloride.

20. The method of claim 1 , wherein the N-alkyl (alkyl)acrylamide monomer is N-isopropyl methacrylamide and the alkylacrylamidoalkyltrialkylammonium chloride monomer is methacrylamidopropyltrimethylammonium chloride.

21. The method of claim 1 , wherein the cationic copolymer derived by polymerization of monomers consisting essentially of about 75 to about 99.9 mole percent of N-alkyl alkylacrylamide or N-alkyl acrylamide monomer units and about 0.1 to about 25 mole percent of alkylacrylamidoalkyltrialkylammonium chloride or acrylamidoalkyltrialkylammonium chloride monomer units.

22. The method of claim 1 , wherein the cationic copolymer derived by polymerization of monomers consisting of about 75 to about 99.9 mole percent of N-alkyl alkylacrylamide or N-alkyl acrylamide monomer units and about 0.1 to about 25 mole percent of alkylacrylamidoalkyltrialkylammonium chloride or acrylamidoalkyltrialkylammonium chloride monomer units.

Assignments (8)
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 →
CHANGE OF NAME Recorded Aug 22, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 043633/0992 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2017
From: NALCO COMPANY LLC
To: ECOLAB USA INC.
Reel/Frame 043357/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2016
From: CONRAD, PETER G.; ACOSTA, ERICK J.; MCNAMEE, KEVIN P.; BENNETT, BRIAN M.; LINDEMAN, OLGA E. S.; CARLISE, JOSEPH R.
To: NALCO COMPANY
Reel/Frame 037736/0306 →