Low Concentration Synthetic Polymer Fracturing Fluid with Ascorbic Acid

US2024368460A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2024368460-A1
Application numberUS-202318143840-A
CountryUS
Kind codeA1
Filing dateMay 5, 2023
Priority dateMay 5, 2023
Publication dateNov 7, 2024
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A fracturing fluid for fracturing subterranean formations comprising ascorbic acid. The fracturing fluid can use ascorbic acid to delay increases in viscosity until desired. The viscosity increase can then be maintained over a period of time to perform fracturing operations.

First claim

Opening claim text (preview).

1 . A method for well-stimulation through a wellbore in a rock formation, comprising the steps of: preparing a fracturing fluid system, the fracturing fluid system comprising: a proppant, water, a gelling agent, a stabilizer comprising ascorbic acid, a cross linking agent, and a pH adjuster; cross-linking the gelling agent with the cross-linking agent; delaying cross-linking of the gelling agent with the cross-linking agent using the ascorbic acid; adjusting a pH of the fracturing fluid system with the pH adjuster to about 5.5 to 6.5; pumping the fracturing fluid system to the rock formation, wherein the fracturing fluid system is capable of maintaining a viscosity above about 100 centipoise (cP) for at least 90 minutes; fracturing the rock formation at a temperature between about 100 to 149 degrees Celsius; and recovering the fluid components of the fracturing fluid system from the wellbore; wherein the ascorbic acid ranges from about 0.5 to 2 parts per thousand (ppt). 2 . The method of claim 1 , wherein the proppant is comprised of a granular material to prevent fractures from closing. 3 . The method of claim 1 , wherein the gelling agent is comprised of a synthetic polymer resistant to hydrolysis. 4 . The method of claim 3 , wherein the fracturing fluid system further comprises an inverting surfactant to invert an emulsion polymer for the hydration of the emulsion polymer in the water, wherein the synthetic polymer is the emulsion polymer. 5 . The method of claim 1 , wherein the gelling agent is comprised of a copolymer derived from acrylamide, 2-Acrylamido-2-methylpropane sulfonic acid (AMPS), and vinyl phosphonate. 6 . The method of claim 3 , further comprising: cross-linking the synthetic polymer with metal ions of the cross-linking agent so as to increase a viscosity of the fracturing fluid system. 7 . The method of claim 1 , wherein the cross-linking agent is a zirconium-based compound or a titanium-based compound. 8 . The method of claim 1 , wherein the fracturing fluid system further comprises a breaker to reduce the viscosity of the fracturing fluid system after the fracturing is complete. 9 . The method of claim 1 , further comprising: forming the ascorbic acid in the fracturing fluid system by loading an ascorbate salt and an acid into the fracturing fluid system. 10 . The method of claim 1 , further comprising: adding the cross-linking agent to the fracturing fluid system; and cross linking the gelling agent at a pre-set depth, after the step of delaying cross linking with the ascorbic acid. 11 . The method of claim 1 , further comprising: delaying cross linking for an amount of time by adjusting an amount of ascorbic acid in the fracturing fluid system. 12 . The method of claim 8 , further comprising: controlling timing and depth of release the breaker in order to break the fracturing fluid system. 13 . The method of claim 12 , wherein the breaker is encapsulated for controlling the timing and depth of release of the breaker into the fracturing fluid system. 14 . The method of claim 8 , wherein the breaker is comprised of an oxidizing breaker. 15 . The method of claim 14 , wherein the oxidizing breaker is sodium bromate, ammonium persulfate, or peroxide. 16 . The method of claim 1 , wherein the fracturing fluid system further comprises a buffer. 17 . The method of claim 16 , wherein the buffer is sodium bicarbonate or formic acid. 18 . The method of claim 1 , wherein the fracturing fluid system does not comprise sodium thiosulfate. 19 . The method of claim 14 wherein the oxidizing breaker is encapsulated ammonium persulfate. 20 . The method of claim 1 wherein the fracturing fluid system further comprises clay stabilizers, nonemulsifiers, surfactants aiding flowback, scale inhibitors, or biocides.

Assignees

Inventors

Classifications

  • containing organic compounds · CPC title

  • by forming crevices or fractures · CPC title

  • characterised by their form or by the form of their components, e.g. foams · CPC title

  • Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open · CPC title

  • C09K8/685Primary

    containing cross-linking agents · CPC title

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What does patent US2024368460A1 cover?
A fracturing fluid for fracturing subterranean formations comprising ascorbic acid. The fracturing fluid can use ascorbic acid to delay increases in viscosity until desired. The viscosity increase can then be maintained over a period of time to perform fracturing operations.
Who is the assignee on this patent?
Cnpc Usa Corp, Beijing Huamei Inc, China Nat Petroleum Corp
What technology area does this patent fall under?
Primary CPC classification C09K8/685. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Nov 07 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).