IP Library Granted Patent US 8,851,174
Granted Patent B2
US 8,851,174 · App. 13/053,975 · Granted Oct 7, 2014

Foam resin sealant for zonal isolation and methods for making and using same

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Quick Facts
Patent No.
US 8,851,174
App. No.
13/053,975
Granted
Oct 7, 2014
Kind
B2
Abstract

Foamable epoxy-based zonal isolation sealing compositions include epoxy resin and a blowing agent and methods for isolating zones in borehole of oil and gas wells using the compositions, where the foam nature of the cured seals provide sufficient compressibility and resiliency to be used with expandable tubing without substantial loss in sealant integrity and in squeeze operations.

Claims (22)

1. A method for zone isolation comprising:

selecting a foamable epoxy-based composition comprising one epoxy resin or a plurality of epoxy resins, one hardening agent or a plurality of hardening agents, one blowing agent or a plurality of blowing agents based on a temperature of an annulus between a borehole and a tubing string, where the foamable epoxy-based composition comprises a foamable low temperature epoxy-based composition adapted to cure at a curing temperature between about 50° F. of to about 90° F., a foamable mid temperature epoxy-based composition between about 90° F. to about 150° F., or a foamable high temperature epoxy-based composition between about 150° F. to about 300° F. and where the low temperature, the mid temperature and the high temperature foamable epoxy-based compositions differ in amount of epoxy resins and amount and type of hardening agents,

pumping the epoxy-based composition into the annulus between the borehole and the tubing string, and

allowing the composition to cure and the blowing agent to decompose to form a foam zonal isolation structure having a Poisson ratio of less than or equal to about 0.5,

where the composition is compressible and where the structure continues to expand after setting allowing the structure to intrude into surface cavities and crevices of the borehole and into formations penetrated by the borehole, while adhering to the outer surface of the tubing string resulting in improved sealing and improved sealing integrity of the structure.

2. The method of claim 1 , further comprising:

prior to pumping, isolating a section of an annulus between the borehole and the tubing string so that the foam zonal isolation structure is located along a length of the tubing string.

3. The method of claim 1 , further comprising:

during or after curing, expanding a section of the tubing string, where the compressibility of the cured foam structure is sufficient to allow expansion of tubing without substantial loss in seal integrity or zonal isolation.

4. The method of claim 1 , wherein the zonal isolation structure is locate at a distal end of the borehole.

5. The method of claim 1 , wherein the zonal isolation structure cures to form a cured foam epoxy composition having sufficient compressibility and resilience properties to permit compression of the composition without substantial loss in seal integrity or zonal isolation.

6. The method of claim 1 , wherein the epoxy resins comprise: (a) glycidyl ethers epoxy resin prepared by the reaction of epichlorohydrin with a compound containing a hydroxyl group carried out under alkaline reaction conditions; (b) epoxy resins prepared by the reaction of epichlorohydrin with mononuclear di- and tri-hydroxy phenolic compounds; (c) epoxidized derivatives of natural oils with mixed long-chain saturated and unsaturated acids having between about 14 and 20 carbon atoms; (d) polyepoxides derived from esters of polycarboxylic acids with unsaturated alcohols; (e) polyepoxides derived from esters prepared from unsaturated alcohols and unsaturated carboxylic acids; (f) epoxidized butadiene based polymers; (g) epoxidized derivatives of dimers of dienes, and (h) mixtures or combinations thereof.

7. The method of claim 6 , wherein the epoxy resins have a molecular weight between about 50 and about 10,000.

8. The method of claim 1 , wherein the hardening agents for the high temperature foamable epoxy-based compositions comprise polyamine curing agents, alkoxylated polyamine curing agents, or mixtures and combinations thereof, wherein the hardening agents for the mid temperature and the low temperature foamable epoxy-based compositions comprise heterocylic amine curing agents.

9. The method of claim 8 , wherein the hardening agents for the high temperature foamable epoxy-based compositions comprise alkoxylated aliphatic polyamines, alkoxylated cycloaliphatic polyamines, alkoxylated aromatic polyamines, alkoxylated heterocyclic polyamines or mixtures and combinations thereof.

10. The method of claim 9 , wherein the hardening agents for the high temperature foamable epoxy-based compositions comprise alkoxylated N-alkyl- and N-alkylenyl-substituted 1,3-diaminopropanes or mixtures and combinations thereof.

11. The method of claim 9 , wherein the aromatic heterocyclic amine hardening agents for the mid temperature and the low temperature foamable epoxy-based compositions comprise pyrrolidine, alkyl pyrrolidines, oxazoline, alkyl oxazolines, triazoles, alkyl triazoles, pyrazolidine, alkyl pyrazolidine, piperidine, alkyl piperidines, piperazine, alkyl piperazines, imidazoline, imidazolidine, alkyl imidazolidines, azepane, alkyl azepane, azepine, alkyl azepines, morpholine, alkyl morpholines, diazapines, alkyl diazapines, or mixtures and combinations thereof.

12. The method of claim 11 , wherein the aromatic heterocyclic amine hardening agents for the mid temperature and the low temperature foamable epoxy-based compositions comprise alkyl pyridines and an ethoxylated N-tallow-1,3-diaminopropane, where the degree of ethoxylation is approximately 10 moles ethoxylate per mole of tallow diamine.

13. The method of claim 1 , the epoxy-based composition further comprises a solvent system, where the solvent system comprises aromatic solvents and heterocyclic aromatic solvents or mixtures and combinations thereof.

14. The method of claim 13 , wherein the high temperature foamable epoxy-based compositions comprise from about 60 wt. % to about 85 wt. % of the epoxy resins, from about 1 wt. % to about 15 wt. % of the hardening agents, from about 39 wt. % to about 0 wt. % of the solvent system, and from about 5 wt. % to about 15 wt. % the blowing agents based on the weight of the other components, where the solvent system reduces the viscosity of the composition for ease of pumping, wherein the mid temperature foamable epoxy-based composition comprises from about 70 wt. % to about 50 wt. % of an epoxy resin or mixture of epoxy resins, from about 30 wt. % to about 50 wt. % of a curing agent or a mixture of curing agents, from about 5 wt. % to about 15 wt. % a blowing agent or mixture of blowing agents, and up to about 20 wt. % of a or solvent system and wherein the low-temperature zonal isolation composition comprises from about 75 wt. % to about 99 wt. % of an epoxy resin or a mixture of epoxy resins, from about 25 wt. % to about 1 wt. % of a curing agent or a mixture of curing agents, from about 5 wt. % to about 20 wt. % the blowing agents and up to about 20 wt. % of a solvent system.

15. The method of claim 14 , wherein the epoxy resins comprise glycidyl ethers epoxy resins, the high temperature hardening agents comprise alkoxylated polyamines, the mid temperature and low temperature hardening agents comprises heterocylic amines, the blowing agents comprise aryl hydrazides and the solvent system comprises an aromatic heterocyclic solvent or mixture of aromatic heterocyclic solvents.

16. The method of claim 14 , wherein the epoxy resin comprise a glycidyl ethers epoxy resin prepared by the reaction of epichlorohydrin with a compound containing a hydroxyl group carried out under alkaline reaction conditions, the high temperature hardening agent comprises an ethoxylated N-tallow-1,3-diaminopropane, where the degree of ethoxylation is approximately 10 moles ethoxylate per mole of tallow diamine, the mid temperature and low temperature hardening agents comprises heterocylic amines, the solvent system comprises a mixture of alkyl pyridines and the blowing agent comprises p-toluenesulfohydrazide, 4-methylbenzene p-toluenesulfohydrazide or mixtures thereof.

Assignments (10)
PATENT SECURITY INTEREST ASSIGNMENT AGREEMENT Recorded Apr 26, 2023
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 063470/0629 →
RELEASE OF SECURITY INTEREST Recorded Oct 1, 2021
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: WEATHERFORD TECHNOLOGY HOLDINGS, LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY, INC.; PRECISION ENERGY SERVICES, INC.; WEATHERFORD CANADA LTD; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; PRECISION ENERGY SERVICES ULC; WEATHERFORD U.K. LIMITED
Reel/Frame 057683/0423 →
SECURITY INTEREST Recorded Oct 1, 2021
From: WEATHERFORD TECHNOLOGY HOLDINGS, LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY, INC.; PRECISION ENERGY SERVICES, INC.; WEATHERFORD CANADA LTD.; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; WEATHERFORD U.K. LIMITED
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 057683/0706 →
RELEASE OF SECURITY INTEREST Recorded Aug 28, 2020
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: WEATHERFORD TECHNOLOGY HOLDINGS, LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY, INC.; PRECISION ENERGY SERVICES, INC.; WEATHERFORD CANADA LTD.; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; PRECISION ENERGY SERVICES ULC; WEATHERFORD U.K. LIMITED
Reel/Frame 053838/0323 →
SECURITY INTEREST Recorded Aug 28, 2020
From: WEATHERFORD TECHNOLOGY HOLDINGS, LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY, INC.; PRECISION ENERGY SERVICES, INC.; WEATHERFORD CANADA LTD.; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; PRECISION ENERGY SERVICES ULC; WEATHERFORD U.K. LIMITED
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 054288/0302 →
SECURITY INTEREST Recorded Dec 26, 2019
From: WEATHERFORD TECHNOLOGY HOLDINGS, LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY, INC.; PRECISION ENERGY SERVICES, INC.; WEATHERFORD CANADA LTD.; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; PRECISION ENERGY SERVICES ULC; WEATHERFORD U.K. LIMITED
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS ADMINISTRATIVE AGENT
Reel/Frame 051419/0140 →
SECURITY INTEREST Recorded Dec 18, 2019
From: WEATHERFORD TECHNOLOGY HOLDINGS LLC; WEATHERFORD NETHERLANDS B.V.; WEATHERFORD NORGE AS; HIGH PRESSURE INTEGRITY INC.; PRECISION ENERGY SERVICES INC.; WEATHERFORD CANADA LTD.; WEATHERFORD SWITZERLAND TRADING AND DEVELOPMENT GMBH; PRECISION ENERGY SERVICES ULC; WEATHERFORD U.K. LIMITED
To: WELLS FARGO BANK NATIONAL ASSOCIATION AS AGENT
Reel/Frame 051891/0089 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2015
From: LUBRIZOL OILFIELD SOLUTION, INC.
To: WEATHERFORD TECHNOLOGY HOLDINGS, LLC
Reel/Frame 037281/0505 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2015
From: CLEARWATER INTERNATIONAL, L.L.C.
To: LUBRIZOL OILFIELD SOLUTIONS, INC.
Reel/Frame 036822/0379 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2011
From: ZAMORA, FRANK; KAKADJIAN, SARKIS R.; GARZA, TINA
To: CLEARWATER INTERNATIONAL, LLC
Reel/Frame 026001/0001 →