Methods and Compositions to use Shape Changing Polymers in Subterranean Formations
US-2016312098-A1 · Oct 27, 2016 · US
US9902891B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9902891-B2 |
| Application number | US-201314909956-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 4, 2013 |
| Priority date | Sep 4, 2013 |
| Publication date | Feb 27, 2018 |
| Grant date | Feb 27, 2018 |
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A fluid composition comprising: (A) a liquid hardenable resin component comprising a resin; and (B) a hardening agent component comprising a hardening agent for the resin; wherein at least one of the resin or the hardening agent comprises a molecule having at least one heavy atom. The substitution of one or more heavy atoms that have a higher atomic weight than the other atoms of the molecule, increases the molecular mass of the resin or hardening agent, and hence, the density of the fluid composition. A method of treating a treatment zone of a well, the method comprising: introducing the treatment fluid into a well bore; and allowing the treatment fluid to form a hardened mass the well bore.
Opening claim text (preview).
What is claimed is: 1. A method of treating a treatment zone of a well, the method comprising: (A) providing a treatment fluid comprising (i) a resin; and (ii) a hardening agent for the resin; wherein the resin comprises a molecule having four to six heavy atoms; (B) introducing the treatment fluid into a well bore; and (C) allowing the treatment fluid to form a hardened mass in the well bore. 2. The method according to claim 1 , wherein the heavy atom is a halogen. 3. The method according to claim 1 , wherein the resin is an epoxy resin. 4. The method according to claim 2 , wherein the epoxy resin comprises a diglycidyl ether. 5. The method according to claim 1 , wherein the resin is selected from the group consisting of: 3,3 ′, 5,5′ tetrabromobisphenol A diglycidyl ether; 3,3 ′, 5,5′ tetrachlorobisphenol A diglycidyl ether; 3,3 ′, 5,5′ tetraiodobisphenol A diglycidyl ether; 4,4′-hexafluoroisopropylidenediphenol diglycidyl ether; and any combination thereof. 6. The method according to claim 1 , wherein the hardening agent is selected from the group consisting of: an aliphatic amine, an aliphatic tertiary amine, an aromatic amine, a cycloaliphatic amine, a heterocyclic amine, an amido amine, a polyamide, a polyethyl amine, a polyether amine, a polyoxyalkylene amine, a carboxylic anhydride, triethylenetetraamine, ethylene diamine, N-cocoalkyltrimethylene, isophorone diamine, N-aminophenyl piperazine, imidazoline, 1,2-diaminocyclohexane, polytheramine, diethyltoluenediamine, 4,4′-diaminodiphenyl methane, methyltetrahydrophthalic anhydride, hexahydrophthalic anhydride, maleic anhydride, polyazelaic polyanhydride, and phthalic anhydride. 7. The method according to claim 1 , wherein the fluid composition additionally comprises a solvent selected from the group consisting of: polyethelenglycol, a polyethyleneglycol ether, d-limonene, propylene carbonate, an isopariffinic fluid, and a heavy aromatic fluid. 8. The method according to claim 1 , wherein the fluid composition additionally comprises a reactive diluent. 9. The method according to claim 1 , wherein the treatment fluid further comprises: an accelerator that comprises 2,4,6 tridimethylaminomethylphenol. 10. The method according to claim 1 , wherein the hardening agent further comprises a silane coupling agent. 11. The method according to claim 1 , wherein the introducing of the treatment fluid is into an annulus between a tubing string in the well bore and a subterranean formation; and wherein the allowing the treatment fluid to form a hardened mass the well bore is within the annulus. 12. The method according to claim 1 , further comprising selecting the molecule having at least one heavy atom to help control the density of the treatment fluid. 13. The method according to claim 1 , wherein the hardening agent component comprises: diethyltoluenediamine. 14. The method according to claim 8 , wherein the reactive diluent is selected from the group consisting of: an alkyl glycidyl ether and a phenyl glycidyl ether. 15. The method according to claim 1 , wherein the treatment fluid further comprises a solid particulate. 16. The method according to claim 1 , wherein the resin has a density of at least 10 ppg. 17. The method according to claim 1 , wherein the resin has a density of at least 12 ppg. 18. The method according to claim 1 , wherein the resin has a density of at least 14 ppg.
for cementing casings into boreholes · CPC title
Plastering the borehole wall; Injecting into the formation · CPC title
macromolecular compounds {(C09K8/512 takes precedence)} · CPC title
containing organic binders only · CPC title
Gravelling of wells · CPC title
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