IP Library Granted Patent US 8,921,478
Granted Patent B2
US 8,921,478 · App. 12/253,504 · Granted Dec 30, 2014

Method of controlling gas hydrates in fluid systems

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Quick Facts
Patent No.
US 8,921,478
App. No.
12/253,504
Granted
Dec 30, 2014
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 (16)

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 91.3 to about 85.5 mole percent of N-isopropyl methacrylamide monomer units and about 8.7 to about 14.5 mole percent of methacrylamidopropyltrimethylammonium chloride monomer units, wherein polymerization of said cationic copolymer is initiated by redox decomposition of a peroxide with a redox co-catalyst, and 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.

2. 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.

3. The method of claim 2 , wherein said hydroxyl-containing compound is selected from the group consisting of iso-propanol; 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.

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

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

6. The method of claim 5 , wherein the corrosion inhibitor is water soluble.

7. The method of claim 6 , 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.

8. The method of claim 6 , wherein the water soluble corrosion inhibitor is a quaternary amine-based corrosion inhibitor.

9. The method of claim 1 , wherein the redox co-catalyst is CuSO 4 .

10. The method of claim 1 , wherein the redox co-catalyst is Fe 2 (SO 4 ) 3 .

11. The method of claim 1 , wherein the inhibitor composition is derived from polymerization of about 9.32 mole percent of methacrylamidopropyltrimethylammonium chloride monomer units.

12. The method of claim 1 , wherein the inhibitor composition is derived from polymerization of about 9.45 mole percent of methacrylamidopropyltrimethylammonium chloride monomer units.

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

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

15. The method of claim 14 , 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.

16. The method of claim 14 , wherein the water soluble corrosion inhibitor is a quaternary amine-based corrosion inhibitor.

Assignments (12)
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: JPMORGAN CHASE BANK, N.A.
Reel/Frame 053250/0001 →
SECURITY INTEREST Recorded Jun 5, 2020
From: CHAMPIONX USA INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 052848/0368 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2017
From: NALCO COMPANY
To: ECOLAB USA INC.
Reel/Frame 042147/0420 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2017
From: NALCO COMPANY LLC; CALGON CORPORATION; CALGON LLC; ONDEO NALCO ENERGY SERVICES, L.P.
To: ECOLAB USA INC.
Reel/Frame 041836/0437 →
CHANGE OF NAME Recorded Feb 28, 2017
From: NALCO COMPANY
To: NALCO COMPANY LLC
Reel/Frame 041835/0903 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2017
From: BANK OF AMERICA, N.A.
To: NALCO COMPANY
Reel/Frame 041808/0713 →
RELEASE OF SECURITY INTEREST Recorded Jun 18, 2015
From: BANK OF AMERICA, N.A.
To: NALCO COMPANY
Reel/Frame 035976/0609 →
SECURITY AGREEMENT Recorded May 18, 2009
From: NALCO COMPANY; CALGON LLC; NALCO ONE SOURCE LLC; NALCO CROSSBOW WATER LLC
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 022703/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2008
From: CONRAD, PETER G.; ACOSTA, ERICK J.; MCNAMEE, KEVIN P.; BENNETT, BRIAN M.; S. LINDEMAN, OLGA E.; CARLISE, JOSEPH R.
To: NALCO COMPANY
Reel/Frame 021697/0593 →