US2012234544A1PendingUtilityA1
Degradable gels in zonal isolation applications
Est. expiryJun 28, 2027(~1 yrs left)· nominal 20-yr term from priority
C09K 8/68C09K 8/58C09K 2208/26
53
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Claims
Abstract
A method of treating a formation that includes emplacing an oxidizing breaker fluid into a region of the formation occupied by a gel; and allowing sufficient time for the oxidizing breaker fluid to degrade the gel is disclosed.
Claims
exact text as granted — not AI-modified1 . A method of treating a formation, comprising:
emplacing an oxidizing breaker fluid into a region of the formation occupied by a gel; and allowing sufficient time for the oxidizing breaker fluid to degrade the gel, wherein the gel comprises at least one of a lignin, a lignosulfonate, a tannin, a tannic acid, a modified lignin, a modified lignosulfonate, a modified tannin, a modified tannic acid, and combinations thereof or biopolymers, starches, carboxy methyl cellulose, polyacrylates, polyacrylamides, polyamines, polyetheramines, poly vinyl amines, polyethylene imines, and combinations thereof crosslinked with a crosslinking agent.
2 . The method of claim 1 , wherein the oxidizing breaker fluid comprises at least one of a hypochlorite and a peroxide.
3 . The method of claim 2 , wherein the oxidizing breaker fluid comprises at least one of lithium and sodium hypochlorite.
4 . (canceled)
5 . (canceled)
6 . The method of claim 5 , wherein the crosslinking agent comprises at least one of ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, butylene glycol diglycidyl ether, trimethylolpropane triglycidyl ether, sorbitol polyglycidyl ether, diglycidyl ether of neopentyl glycol, epoxidized 1,6-hexanediol, aziridine derivatives, carbodiimides, blocked isocyanates, epoxy functionalized polyalkalene glycols, an oxidized starch, a polymeric dialdehyde, an aldehyde adduct, a tetra methoxy propane, a hydrolyzed acetal, and combinations thereof.
7 . (canceled)
8 . The method of claim 1 , further comprising:
emplacing gel components to form the gel.
9 . The method of claim 1 , further comprising:
emplacing gel components to form a second gel.
10 . The method of claim 1 , wherein the gel possesses a break through pressure of greater than 1000 psi.
11 . A method of treating a formation, comprising:
emplacing a gelling fluid comprising an internal oxidizer into the formation; allowing the gelling fluid to gel in a region of the formation; and activating the internal oxidizer to break the formed gel, wherein the gel comprises at least one of a lignin, a lignosulfonate, a tannin, a tannic acid, a modified lignin, a modified lignosulfonate, a modified tannin, a modified tannic acid, and combinations thereof or biopolymers, starches, carboxy methyl cellulose, polyacrylates, polyacrylamides, polyamines, polyetheramines, poly vinyl amines, polyethylene imines, and combinations thereof crosslinked with a crosslinking agent.
12 . The method of claim 11 , wherein the internal oxidant is encapsulated.
13 . The method of claim 11 , wherein the internal oxidant comprises at least one of calcium or magnesium peroxide.
14 . (canceled)
15 . (canceled)
16 . The method of claim 15 , wherein the crosslinking agent comprises at least one of ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, butylene glycol diglycidyl ether, trimethylolpropane triglycidyl ether, sorbitol polyglycidyl ether, diglycidyl ether of neopentyl glycol, epoxidized 1,6-hexanediol, aziridine derivatives, carbodiimides, blocked isocyanates, epoxy functionalized polyalkalene glycols, an oxidized starch, a polymeric dialdehyde, an aldehyde adduct, a tetra methoxy propane, a hydrolyzed acetal, and combinations thereof.
17 . (canceled)
18 . The method of claim 11 , wherein the gel possesses a break through pressure of greater than 1000 psi.Cited by (0)
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