Hydrate inhibitors and methods of use
Compositions and methods of using of such compositions to, for example, inhibit of the formation of gas hydrate agglomerates are provided. In one embodiment, the methods comprise: introducing hydrate inhibitor composition comprising a compound into a fluid, wherein the compound comprises a hydrophobic cation moiety, one or more lipophilic tails, and a linking moiety.
1. A method comprising:
introducing a hydrate inhibitor composition into a fluid, wherein the hydrate inhibitor composition comprises at least one compound having the structural formula:
wherein each of R 1 and R 2 is independently a C 1 to C 6 hydrocarbon chain,
wherein R 3 is selected from the group consisting of hydrogen and any C 1 to C 6 hydrocarbon chain,
wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain,
wherein R 5 is a C 1 to C 50 hydrocarbon chain,
wherein X − is a counter anion, and
wherein each of a and b is independently an integer from 1 to 10.
2. The method of claim 1 wherein X − is selected from the group consisting of: a carboxylate, a halide, a sulfate, an organic sulfonate, a hydroxide, and any combination thereof.
3. The method of claim 1 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof.
4. The method of claim 1 wherein the hydrate inhibitor composition is introduced into the fluid through a conduit or an injection point in fluid communication with a wellbore in which the fluid resides.
5. The method of claim 1 wherein the hydrate inhibitor composition is introduced into a wellbore penetrating at least a portion of a subterranean formation through which the fluid is flowing.
6. The method of claim 1 wherein the hydrate inhibitor composition is introduced into a conduit through which the fluid is flowing.
7. The method of claim 1 wherein the fluid comprises water and has a water cut of about 55% or more.
8. The method of claim 1 wherein the fluid comprises water and the hydrate inhibitor composition is introduced into the fluid in an amount such that the compound is present in the fluid in an amount from about 0.1% to about 10% by volume based on a water cut of the fluid.
9. The method of claim 1 wherein each of R 4 and R 5 is a C 1 to C 50 hydrocarbon chain resulting from a reaction between an acrylate or a methacrylate and an amine, the amine being selected from the group consisting of:
a synthetic primary or secondary amine selected from the group consisting of: butylamine, hexylamine, octylamine, dodecylamine, N-methyldodecylamine, N-methyloctylamine, didodecylamine, and any combination thereof;
a primary or secondary fatty amine derived from one or more fatty acids selected from the group consisting of: corn oil, canola oil, coconut oil, safflower oil, sesame oil, palm oil, cottonseed oil, soybean oil, olive oil, sunflower oil, hemp oil, wheat germ oil, palm kernel oil, vegetable oil, caprylic acid, capric acid, lauric acid, myristic acid, myristoleic acid, palmitic acid, palmitoleic acid, stearic acid, sapienic acid, elaidic acid, vaccenic acid, linoleic acid, arachidic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoic acid, behenic acid, lignoceric acid, cerotic acid, oleic acids (cis- and trans-), and any combination thereof; and
any combination thereof.
10. The method of claim 1 wherein the compound is a reaction product of a reaction between (i) an alkylating agent and (ii) a second intermediate resulting from a reaction between a dialkylaminoalkylamine and a first intermediate, the first intermediate resulting from a reaction between an acrylate or a methacrylate and an amine.
11. A method comprising:
introducing a hydrate inhibitor composition into a wellbore penetrating at least a portion of a subterranean formation, wherein the hydrate inhibitor composition comprises at least one compound having the structural formula:
wherein each of R 1 and R 2 is independently a C 1 to C 6 hydrocarbon chain,
wherein R 3 is selected from the group consisting of hydrogen and any C 1 to C 6 hydrocarbon chain,
wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain,
wherein R 5 is a C 1 to C 50 hydrocarbon chain,
wherein X − is a counter anion, and
wherein each of a and b is independently an integer from 1 to 10.
12. The method of claim 11 wherein the hydrate inhibitor composition is introduced into the wellbore through a conduit or an injection point in fluid communication with the wellbore.
13. The method of claim 11 wherein X − is selected from the group consisting of: a carboxylate, a halide, a sulfate, an organic sulfonate, a hydroxide, and any combination thereof.
14. The method of claim 11 further comprising allowing the hydrate inhibitor composition to contact a fluid residing in the wellbore.
15. The method of claim 14 wherein the fluid comprises water and has a water cut of about 55% or more.
16. The method of claim 14 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof.
17. A hydrate inhibitor composition comprising a compound having the structural formula:
wherein each of R 1 and R 2 is independently a C 1 to C 6 hydrocarbon chain,
wherein R 3 is selected from the group consisting of hydrogen and any C 1 to C 6 hydrocarbon chain,
wherein R 4 is selected from the group consisting of hydrogen and any C 1 to C 50 hydrocarbon chain,
wherein R 5 is a C 1 to C 50 hydrocarbon chain,
wherein X − is a counter anion, and
wherein each of a and b is independently an integer from 1 to 10.
18. The hydrate inhibitor composition of claim 17 wherein X − is selected from the group consisting of: a carboxylate, a halide, a sulfate, an organic sulfonate, a hydroxide, and any combination thereof.
19. The hydrate inhibitor composition of claim 17 wherein each of R 4 and R 5 is a C 1 to C 50 hydrocarbon chain resulting from a reaction between an acrylate or a methacrylate and an amine, the amine being selected from the group consisting of:
a synthetic primary or secondary amine selected from the group consisting of: butylamine, hexylamine, octylamine, dodecylamine, N-methyldodecylamine, N-methyloctylamine, didodecylamine, and any combination thereof;
a primary or secondary fatty amine derived from one or more fatty acids selected from the group consisting of: corn oil, canola oil, coconut oil, safflower oil, sesame oil, palm oil, cottonseed oil, soybean oil, olive oil, sunflower oil, hemp oil, wheat germ oil, palm kernel oil, vegetable oil, caprylic acid, capric acid, lauric acid, myristic acid, myristoleic acid, palmitic acid, palmitoleic acid, stearic acid, sapienic acid, elaidic acid, vaccenic acid, linoleic acid, arachidic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoic acid, behenic acid, lignoceric acid, cerotic acid, oleic acids (cis- and trans-), and any combination thereof; and
any combination thereof.
20. The hydrate inhibitor composition of claim 17 further comprising a solvent selected from the group consisting of: an alcohol, methanol, isopropyl alcohol, glycol, ethylene glycol, an organic solvent, toluene, xylene, monobutyl ether, hexane, cyclohexane, and any combination thereof.