Loss Circulation Material

Patent metadata

Field	Value
Publication number	US-2024294820-A1
Application number	US-202318114759-A
Country	US
Kind code	A1
Filing date	Feb 27, 2023
Priority date	Feb 27, 2023
Publication date	Sep 5, 2024
Grant date	—

Abstract

A method for mitigating loss circulation zones in a wellbore is provided. The method includes synthesizing a carbamate from an amine-curing agent, and the carbamate is mixed with an epoxy resin from the loss control composition. Chapter loss control composition is pumped into a wellbore with a loss circulation zone, wherein the loss control composition flows into the loss circulation zone. The carbamate of the loss control composition is allowed to decompose at wellbore temperatures, wherein the carbamate releases CO2 gas and the amine-curing agent. The CO2 gas foams the epoxy resin, expanding the epoxy resin to fill voids in the loss circulation zone, and the amine-curing agent cures the foamed epoxy resin, forming a loss control material that seals the loss circulation zone.

First claim

1 . A method for mitigating loss circulation zones in a wellbore, comprising:
synthesizing a carbamate from an amine-curing agent, wherein synthesizing the carbamate comprises reacting the amine-curing agent with carbon dioxide; mixing the carbamate with an epoxy resin to form a loss control composition; pumping the loss control composition into a wellbore with a loss circulation zone, wherein the loss control composition flows into the loss circulation zone; and allowing the carbamate of the loss control composition to decompose at wellbore temperatures, wherein:
the carbamate releases CO 2 gas and the amine-curing agent;
the CO 2 gas foams the epoxy resin, expanding the epoxy resin to fill voids in the loss circulation zone; and
the amine-curing agent cures the foamed epoxy resin, forming a loss control material that seals the loss circulation zone.

2 . (canceled)

3 . The method of claim 1 , comprising a reaction of the formula:

wherein R and R′ are each independently selected from hydrogen, aliphatic groups, or aryl groups, or any combination thereof.

4 . The method of claim 1 , wherein the amine curing agent comprises an amine, an aromatic amine, an aliphatic amine, a cyclo-aliphatic amine, polyamines, amides, polyamides, a polyethyleneimine, piperidine, triethylamine, benzyldimethylamine, N,N-dimethylaminopyridine,2-(N,N-dimethylaminomethyl)phenol, tris(dimethylaminomethyl)phenol, N-2-(aminoethyl)-3-aminopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, n-beta-(aminoethyl)-gamma-aminopropyl trimethoxysilane, n-beta-(aminoethyl)-gamma-aminopropyl trimethoxysilane, piperazine, derivatives of piperazine, (e.g., aminoethylpiperazine, pyrrole, imidazole, pyrazole, pyridine, pyrazine, pyrimidine, pyridazine, indolizine, isoindole, indole, indazole, purine, quinolizine, quinoline, isoquinoline, phthalazine, naphthyridine, quinoxaline, quinazoline, carbazole, carbazole, phenanthridine, acridine, phenanthroline, phenazine, imidazolidine, phenoxazine, cinnoline, pyrrolidine, pyrroline, imidazoline, piperidine, indoline, isoindoline, quinuclidine, morpholine, azocine, azepine, 1,3,5-triazine, thiazole, pteridine, dihydroquinoline, hexamethyleneimine, indazole, or 2-ethyl-4-methyl imidazole, or any combination thereof.

5 . The method of claim 1 , wherein the amine-curing agent comprises a polyethyleneimine.

6 . The method of claim 1 , wherein the epoxy resin comprises bisphenol A diglycidyl ether resin, butoxymethyl butyl glycidyl ether resin, bisphenol A-epichlorohydrin resin, or bisphenol F, or any combination thereof.

7 . The method of claim 1 , wherein the epoxy resin comprises bisphenol A diglycidyl ether resin.

8 . The method of claim 1 , wherein the loss control composition comprises a surfactant to enhance stability of the foam.

9 . The method of claim 8 , wherein the surfactant comprises a cationic surfactant, an anionic surfactant, or a zwitterionic surfactant, or any combination thereof.

10 . The method of claim 1 , comprising adjusting a concentration of the carbamate in the loss control composition to adjust a thickening time of the epoxy.

11 . The method of claim 10 , wherein the thickening time is between 0.5 hours and 24 hours.

12 . The method of claim 1 , comprising pumping drilling mud after the loss control composition to push the loss control composition into the loss circulation zone.

13 . The method of claim 1 , wherein the decomposition of the carbamate comprises a reaction of the formula:

wherein R and R′ are each independently selected from hydrogen, aliphatic groups, or aryl groups, or any combination thereof.

14 . The method of claim 1 , comprising selecting the epoxy resin based, at least in part, on well parameters, wherein the well parameters comprise well pressure, rock type, void type, or void size, or any combination thereof.

15 . (canceled)

16 . The method of claim 1 , comprising selecting the amine curing agent based, at least in part, on well parameters, wherein the well parameters comprise well pressure, rock type, void type, or void size, or any combination thereof.

17 . (canceled)

Assignees

• Saudi Arabian Oil Co

Inventors

• Wagle Vikrant
• Alyami Noktan Mohammed
• Al-Yami Abdullah Saleh Hussain
• Alanqari Khawlah

Classifications

• C08J2203/02

  CO2-releasing, e.g. NaHCO3 and citric acid · CPC title

• C08J2363/00

  Characterised by the use of epoxy resins; Derivatives of epoxy resins · CPC title

• C08J9/08

  developing carbon dioxide · CPC title

• C09K8/518 Primary

  Foams · CPC title

• C09K8/5086

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title