Water-soluble associative amphoteric polymer as a rheology modifier for subterranean treatments
US-2024199939-A1 · Jun 20, 2024 · US
US10934470B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10934470-B2 |
| Application number | US-201515769038-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 18, 2015 |
| Priority date | Dec 18, 2015 |
| Publication date | Mar 2, 2021 |
| Grant date | Mar 2, 2021 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
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 a low-dosage hydrate inhibitor additive into a fluid, wherein the low-dosage hydrate inhibitor additive comprises a quaternary or tertiary ammonium cation moiety, a lipophilic tail, and a sulfonate anion moiety; and exposing the low-dosage hydrate inhibitor additive to a temperature above about 200° F.
Opening claim text (preview).
What is claimed is: 1. A method comprising: introducing a low-dosage hydrate inhibitor additive into a fluid, wherein the low-dosage hydrate inhibitor additive 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 a C 1 to C 6 hydrocarbon chain, wherein R 4 is a C 1 to C 50 hydrocarbon chain, and wherein R 5 is an organic moiety; and exposing the low-dosage hydrate inhibitor additive to at least one temperature above about 200° F., wherein the low-dosage hydrate inhibitor additive does not substantially degrade for up to about 7 days after being substantially continually exposed to at least one temperature of above about 200° F. 2. The method of claim 1 wherein the organic moiety is selected from the group consisting of: an alkyl group, an alkenyl group, an aryl group, an arylalkyl group, an arylalkenyl group, an alkylaryl group, an alkenylaryl group, a heterocyclic group, a hydroxyl group, a carbonyl group, an amine group, 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 low-dosage hydrate inhibitor additive is introduced into a quaternary ammonium cation moiety or a tertiary ammonium cation moiety the fluid through a conduit or an injection point having at least one temperature above about 200° F. and the low-dosage hydrate inhibitor additive is exposed to at least one temperature above about 200° F. in the conduit or the injection point. 5. The method of claim 1 wherein the fluid has at least one temperature above about 200° F. and the low-dosage hydrate inhibitor additive is exposed to at least one temperature above about 200° F. in the fluid. 6. The method of claim 1 wherein the fluid resides within a location selected from the group consisting of: a conduit, a wellbore, a subterranean formation, and a vessel. 7. The method of claim 1 wherein the fluid comprises water and has a water cut of from about 1% to about 65%. 8. The method of claim 1 wherein the fluid comprises water and has a water cut of about 50% or greater. 9. The method of claim 1 wherein the low-dosage hydrate inhibitor additive is introduced in an amount such that the low-dosage hydrate inhibitor additive is present in the fluid in an amount from about 0.1% to about 10% volume based on the water cut of the fluid. 10. The method of claim 1 wherein the water is selected from the group consisting of: brine, deionized water, and any combination thereof. 11. A method comprising: introducing a low-dosage hydrate inhibitor additive into a wellhead of a wellbore penetrating at least a portion of a subterranean formation having at least one temperature above about 200° F., wherein the low-dosage hydrate inhibitor additive does not substantially degrade for up to about 7 days after being substantially continually exposed to at least one temperature of above about 200° F., wherein the low-dosage hydrate inhibitor additive 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 a C 1 to C 6 hydrocarbon chain, wherein R 4 is a C 1 to C 50 hydrocarbon chain, and wherein R 5 is an organic moiety; and allowing the low-dosage hydrate inhibitor additive to contact a fluid in the wellbore. 12. The method of claim 11 wherein the fluid comprises at least one component selected from the group consisting of: water, a gas, a liquid hydrocarbon, and any combination thereof. 13. The method of claim 11 wherein the fluid comprises water and has a water cut of about 50% or greater. 14. The method of claim 11 wherein wellbore has at least one temperature from about 250° F. to about 350° F. 15. A method comprising: introducing a low-dosage hydrate inhibitor additive into a conduit having at least one temperature above about 200° F. and containing a fluid, wherein the low-dosage hydrate inhibitor additive does not substantially degrade for up to about 7 days after being substantially continually exposed to at least one temperature of above about 200° F., wherein the low-dosage hydrate inhibitor additive 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 a C 1 to C 6 hydrocarbon chain, wherein R 4 is a C 1 to C 50 hydrocarbon chain, and wherein R 5 is an organic moiety. 16. The method of claim 15 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. The method of claim 15 wherein the conduit has at least one temperature from about 250° F. to about 350° F.
Hydrates inhibition by using well treatment fluids containing inhibitors of hydrate formers · CPC title
characterised by the use of specific surfactants · CPC title
Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning · CPC title
using chemical means for preventing or limiting {, e.g. eliminating,} the deposition of paraffins or like substances · CPC title
containing surfactants · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.