Methods and Compositions to use Shape Changing Polymers in Subterranean Formations
US-2016312098-A1 · Oct 27, 2016 · US
US2016177167A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016177167-A1 |
| Application number | US-201314909956-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 4, 2013 |
| Priority date | Sep 4, 2013 |
| Publication date | Jun 23, 2016 |
| Grant date | — |
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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 at least one of the resin or the hardening agent comprises a molecule having at least one heavy atom; (B) introducing the treatment fluid into a well bore; and (C) allowing the treatment fluid to form a hardened mass 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 . (canceled) 6 . 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; a halogenated diglycidyl ether of polyhydroxyl phenol; and any combination thereof. 7 . The method according to claim 1 , wherein the hardening agent is selected from the group consisting of: aliphatic amines, aliphatic tertiary amines, aromatic amines, cycloaliphatic amines, heterocyclic amines, amido amines, polyamides, polyethyl amines, polyether amines, polyoxyalkylene amines, carboxylic anhydrides, 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. 8 . (canceled) 9 . (canceled) 10 . The method according to claim 1 , wherein the fluid composition additionally comprises a solvent selected from the group consisting of: polyethelenglycols, polyethyleneglycol ethers, limonene, propylene carbonate, isopariffinic fluids, and heavy aromatic fluids. 11 . (canceled) 12 . The method according to claim 1 , wherein the fluid composition additionally comprises a reactive diluent. 13 . (canceled) 14 . The method according to claim 1 , wherein the treatment fluid further comprises: an accelerator that comprises 2,4,6 tridimethylaminomethylphenol. 15 . (canceled) 16 . (canceled) 17 . The method according to claim 1 , wherein the hardening agent further comprises a silane coupling agent. 18 . (canceled) 19 . 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. 20 . 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. 21 . A method of treating a treatment zone of a well, the method comprising: (A) providing a treatment fluid comprising (i) a resin; (ii) a hardening agent for the resin; and (iii) a reactive diluent, wherein at least one of the resin, the hardening agent, or the reactive diluent comprises a molecule having at least one heavy atom; (B) introducing the treatment fluid into a well bore; and (C) allowing the treatment fluid to form a hardened mass the well bore. 22 . The method according to claim 21 , wherein the heavy atom is a halogen. 23 . The method according to claim 21 , wherein the resin is an epoxy resin. 24 . (canceled) 25 . (canceled) 26 . (canceled) 27 . (canceled) 28 . (canceled) 29 . (canceled) 30 . (canceled) 31 . (canceled) 32 . The method according to claim 21 , wherein the reactive diluent is selected from the group consisting of: alkyl glycidyl ethers and phenyl glycidyl ethers. 33 . (canceled) 34 . The method according to claim 21 , wherein the treatment fluid further comprises: an accelerator. 35 . (canceled) 36 . (canceled) 37 . The method according to claim 21 , wherein the hardening agent further comprises a silane coupling agent. 38 . (canceled) 39 . (canceled) 40 . The method according to claim 21 , further comprising selecting the molecule having at least one heavy atom to help control the density of the treatment fluid. 41 . (canceled) 42 . A fluid composition comprising: (A) a resin; and (B) a hardening agent for the resin; and (C) a reactive diluent; wherein at least one of the resin, the hardening agent, or the reactive diluent comprises a molecule having at least one heavy atom.
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