IP Library Granted Patent US 7,264,653
Granted Patent B2
US 7,264,653 · App. 10/918,191 · Granted Sep 4, 2007

Methods for inhibiting hydrate blockage in oil and gas pipelines using simple quaternary ammonium and phosphonium compounds

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Quick Facts
Patent No.
US 7,264,653
App. No.
10/918,191
Granted
Sep 4, 2007
Kind
B2
Abstract

A method and a quaternary ammonium or phosphonium composition used therein for inhibiting retarding, mitigating, reducing, controlling and/or delaying formation of hydrocarbon hydrates or agglomerates of hydrates. The method may be applied to prevent or reduce or mitigate plugging of conduits, pipes, transfer lines, valves, and other places or equipment where hydrocarbon hydrate solids may form under the conditions. At least one quaternary ammonium or phosphonium compound is added into the process stream, where the compound may be mixed with another compound selected from other amino alcohols, esters, quaternary ammonium, phosphonium or sulphonium salts, betaines, amine oxides, amides, simple amine salts, and combinations thereof.

Claims (67)

1. A method for inhibiting formation of gas hydrate plugs in conduits containing a mixture of hydrocarbons and water, the method comprising:

adding to the mixture an effective amount of at least one compound having the formula:

 where: R 1 is selected from hydrogen and normal or branched alkyls having from 1 to 3 carbon atoms;

R 2 is selected from normal or branched alkyls having from 1 to 4 carbon atoms;

R 3 is an organic moiew having 4 or 5 carbon atoms;

R 4 is an organic moiety having from 2 to 20 carbon atoms;

A is N; and

X 31 is an anion, wherein the at least one compound is the product of a reaction between butyl bromide having one of R 1 , R 2 , R 3 , and R 4 and an N,N-dimethyl-alkylamine having between 10 and 20 carbon atoms that provide the other three of R 1 , R 2 , R 3 , and R 4 .

2. The method of claim 1 , wherein R 2 has exactly 4 carbon atoms.

3. The method of claim 1 , wherein R 4 is selected from alkyl, alkenyl, aryl, arylalkyl, arylalkenyl, alkylaryl, alkenylaryl, glycol and combinations thereof.

4. The method of claim 1 , wherein R 4 includes one or more heteroatoms selected from oxygen, nitrogen, sulfur and combinations thereof.

5. The method of claim 1 , wherein the N,N-dimethyl-alkylamine is N,N-dimethyl-hexadecylamine.

6. The method of claim 1 , wherein the at least one compound is mixed with a solvent selected from water, simple alcohols, glycols, ethers, ketonic liquids, aromatic hydrocarbons, and combinations thereof.

7. The method of claim 1 , wherein the at least one compound is mixed with a solvent selected from water, methanol, ethanol, iso-propanol, n-butanol, iso-butanol, 2-ethyl hexanol, ethylene glycol, 1,2-propylene glycols, 1,3-propylene glycol, hexylene glycol, ethylene glycol mono butylether (butyl Cellosolve), ethylene glycol dibutyl ether, tetrahydrofuran, methylethylketone, methylisobutylketone, diisobutylketone, N-methylpyrrolidone, cyclohexanone, xylene, toluene, and combinations thereof.

8. The method of claim 1 , further comprising:

pumping the mixture through a conduit at greater than 10,000 psi.

9. A method for inhibiting formation of gas hydrate plugs in conduits containing a mixture of hydrocarbons and water, the method comprising:

adding to the mixture an effective amount of at least one compound having the formula:

 where: R 1 is selected from hydrogen and normal or branched alkyls having from 1 to 3 carbon atoms;

R 2 is selected from normal or branched alkyls having from 1 to 4 carbon atoms;

R 3 is an organic moiew having 4 or 5 carbon atoms;

R 4 is —[(CH 2 —CHR 5 —O)] n —H having from 2 to 20 carbon atoms, wherein R 5 is selected from a hydrogen, a methyl group, and

an ethyl group, and n ranges from 1 to 3;

A is N or P; and

X − is an anion.

10. The method of claim 9 , wherein the X— is selected from hydroxide, carboxylate, halide, sulfate, organic sulphonate, and combinations thereof.

11. The method of claim 9 , wherein the X − anion is a halide ion selected from bromide, chloride, and combinations thereof.

12. The method of claim 9 , wherein the R 1 and R 2 are different.

13. The method of claim 9 , wherein the at least one compound is the product of a reaction between an organic halide having one of R 1 , R 2 , R 3 , and R 4 and an amine or phosphene having the other three of R 1 , R 2 , R 3 , and R 4 .

14. The method of claim 9 , further comprising:

pumping the mixture through a conduit at greater than 10,000 psi.

15. The method of claim 9 , wherein R 1 and R 2 each have exactly one carbon atom.

16. The method of claim 9 , further comprising:

adding at least one amine salt to the mixture along with the at least one compound.

17. The method of claim 16 , wherein the amine salt includes a cation moiety that is an amine selected from ammonia, dimethylamine, diethylamine, di-n-propylamine, trimethylamine, triethylamine, tri-n-propylamine, tri-iso-propylamine, ethanolamine, diethylethanolamine, triethanolamine, methyl ethanolamine, ethyl ethanolamine, propyl ethanolamine, methyl diethanolamine, ethyl diethanolamine, dimethyl ethanolamine, diethanolamine, dibutylethanolamine, dipropylethanolamine, dibutylpropanolamine, dipropylpropanolamine, morpholine, N-methylmorpholine, N-ethylmorpholine, N-propylmorpholine, dibutylethanolamine, N,N-dibutyl-cocoamidopropylamine, and combinations thereof.

18. The method of claim 16 , wherein the amine salt includes an anionic moiety that is an acid selected from carboxylic acids, sulfonic acids, and inorganic acids.

19. The method of claim 16 , wherein the amine salt includes an anionic moiety that is a carboxylic acid selected from formic acid, acetic acid, propionic acid, butyric acid, glycolic acid, malonic acid, succinic acid, acrylic acid, methacrylic acid, trifluoroacetic acid, methane sulfonic acid, and mixtures thereof.

20. The method of claim 16 , wherein the amine salt includes an anionic moiety that is an inorganic acid selected from nitric acid, hydrogen chloride, hydrogen bromide, and mixtures thereof.

21. The method of claim 9 , wherein the at least one compound includes at least one ammonium salt having an ammonium compound selected from trimethylhexadecylammonium, dimethylethylhexadecylammonium, dimethylbutyloctadecylammonium, dimethylbutylhexadecylammonium, dimethylbutyldodecylammonium, dimethylbutyltetradecylammonium, propyldibutylhexadecylammonium, dipropylbutylhexadecylammonium, and mixtures thereof.

22. The method of claim 9 , wherein the at least one compound includes at least one phosphonium salt having a phosphonium compound selected from trimethylhexadecylphosphonium, dimethylethylhexadecylphosphonium, dimethylbutyloctadecylphosphonium dimethylbutylhexadecylphosphonium, dimethylbutyldodecylphosphonium, dimethylbutyltetradecylphosphonium, propyldibutylhexadecylphosphonium, dipropylbutylhexadecylphosphonium, and mixtures thereof.

23. The method of claim 9 , further comprising:

pumping the mixture through a conduit at a pressure between 100 and 10,000 psi.

24. The method of claim 9 , wherein the at least one compound is mixed with a solvent selected from water, methanol, ethanol, iso-propanol, n-butanol, iso-butanol, 2-ethyl hexanol, ethylene glycol, 1,2-propylene glycols, 1,3-propylene glycol, hexylene glycol, ethylene glycol mono butylether (butyl Cellosolve), ethylene glycol dibutyl ether, tetrahydrofuran, methylethylketone, methylisobutylketone, diisobutylketone, N-methylpyrrolidone, cyclohexanone, xylene, toluene, and combinations thereof.

25. A method for inhibiting formation of gas hydrate plugs in conduits containing a mixture of hydrocarbons and water, the method comprising:

adding to the mixture an effective amount of at least one compound having the formula:

 where: R 1 is selected from hydrogen and normal or branched alkyls having from 1 to 3 carbon atoms;

R 2 is selected from normal or branched alkyls having from 1 to 4 carbon atoms;

R 3 is an organic moiety having 4 or 5 carbon atoms;

R 4 is an organic moiety having from 2 to 20 carbon atoms;

A is N or P; and

X − is an anion, wherein the at least one compound includes at least one dimethylbutylhexadecylammonium salt.

26. A method for inhibiting formation of gas hydrate plugs in conduits containing a mixture of hydrocarbons and water, the method comprising:

adding to the mixture an effective amount of at least one compound having the formula:

 where: R 1 is selected from hydrogen and normal or branched alkyls having from 1 to 3 carbon atoms;

R 2 is selected from normal or branched alkyls having from 1 to 4 carbon atoms;

R 3 is an organic moiety having 4 or 5 carbon atoms;

R 4 is an organic moiety having from 2 to 20 carbon atoms;

A is N or P; and

X − is an anion, wherein the at least one compound includes dimethylbutyloctadecylammonium bromide.

27. A method for inhibiting formation of gas hydrate plugs in conduits containing a mixture of hydrocarbons and water, the method comprising:

adding to the mixture an effective amount of at least one compound having the formula:

 where: R 1 is selected from hydrogen and normal or branched alkyls having from 1 to 3 carbon atoms;

R 2 is selected from normal or branched alkyls having from 1 to 4 carbon atoms

R 3 is an organic moiety having 4 or 5 carbon atoms;

R 4 is an organic moiety having from 2 to 20 carbon atoms;

A is N or P; and

X − is an anion, wherein the at least one compound includes at least one dimethylbutyldodecylammonium salt.

Assignments (5)
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 →