Fracturing method using polyboronic compound
US-9534167-B2 · Jan 3, 2017 · US
US10066152B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10066152-B2 |
| Application number | US-201415312835-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 15, 2014 |
| Priority date | Aug 15, 2014 |
| Publication date | Sep 4, 2018 |
| Grant date | Sep 4, 2018 |
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Methods including preparing a treatment fluid comprising an aqueous base fluid, a gelling agent, and crosslinkable proppant particulates comprising proppant particulates having covalently grafted thereon a boronic acid functional group; crosslinking the crosslinkable proppant particulates with the gelling agent, thereby suspending the crosslinkable proppant particulates in the treatment fluid; introducing the treatment fluid into a subterranean formation having at least one fracture therein; and placing the crosslinkable proppant particulates into the at least one fracture to form a proppant pack therein.
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The invention claimed is: 1. A method comprising: forming crosslinkable proppant particulates by covalently grafting a boronic acid functional group to proppant particulates; preparing a treatment fluid by combining an aqueous base fluid, a gelling agent, and the formed crosslinkable proppant particulates; crosslinking the crosslinkable proppant particulates with the gelling agent, thereby suspending crosslinked proppant particulates in the treatment fluid; and introducing the treatment fluid with the suspended crosslinked proppant particulates into a subterranean formation having at least one fracture therein, thereby placing the suspended crosslinked proppant particulates into the at least one fracture to form a proppant pack therein. 2. The method of claim 1 , wherein the boronic acid functional group is from a compound selected from the group consisting of an alkyl boronic acid, an alkenyl boronic acid, an aryl boronic acid, a heteroaryl boronic acid, and any combination thereof. 3. The method of claim 1 , wherein the boronic acid functional group is a multifunctional polymer comprising at least one boronic acid monomer unit and at least one water-soluble monomer unit. 4. The method of claim 3 , wherein the at least one boronic acid monomer unit is selected from the group consisting of an aryl boronic acid, an alkyl boronic acid, an alkenyl boronic acid, an alkynyl boronic acid, and any combination thereof. 5. The method of claim 3 wherein the at least one water-soluble monomer unit is selected from the group consisting of an acrylamide, a 2-acrylamido-2-methyl propane sulfonic acid, a N,N-dimethylacrylamide, a vinyl pyrrolidone, a dimethylaminoethyl methacrylate, an acrylic acid, a dimethylaminopropylmethacrylamide, a vinyl amine, a vinyl acetate, a trimethylammoniumethyl methacrylate chloride, a methacrylamide, a hydroxyethyl acrylate, a vinyl sulfonic acid, a vinyl phosphonic acid, a vinylbenzene sulfonic acid, a methacrylic acid, a vinyl caprolactam, a N-vinylformamide, a diallyl amine, a N,N-diallylacetamide, a dimethyldiallyl ammonium halide, an itaconic acid, a styrene sulfonic acid, a methacrylamidoethyltrimethyl ammonium halide, a quaternary salt derivative of acrylamide, a quaternary salt derivative of acrylic acid, an alkyl acrylate, an alkyl methacrylate, an alkyl acrylamide, an alkyl methacrylamide, an alkyl dimethylammoniumethyl methacrylate halide, an alkyl dimethylammoniumpropyl methacrylamide halide, any derivative thereof, and any combination thereof. 6. The method of claim 1 , wherein the boronic acid functional group is a multifunctional polymer comprising the reaction product of at least one boronic acid monomer unit, at least one water-soluble monomer unit, and a solubilizing agent selected from the group consisting of a short chain polyol, a polysaccharide, an amino sugar, a sugar alcohol, a sugar acid, polyvinyl alcohol, tartaric acid, a catechol, a glycol, any derivative thereof, and any combination thereof. 7. The method of claim 1 , wherein the treatment fluid further comprises a solubilizing agent comprising at least two hydroxyl groups. 8. The method of claim 1 , wherein the treatment fluid further comprises a breaker selected from the group consisting of an enzyme, an oxidizer, a chelator, an acid, and any combination thereof. 9. The method of claim 1 , wherein introducing the treatment fluid into the subterranean formation comprises introducing the treatment fluid through a tubular extending from a wellhead and into the subterranean formation, with a pump fluidly coupled to the tubular. 10. A method comprising: forming crosslinkable proppant particulates by covalently grafting at least one functional group to proppant particulates; preparing a treatment fluid by combining an aqueous base fluid, a gelling agent, a crosslinker, and the formed crosslinkable proppant particulates wherein the at least one functional group is selected from the group consisting of a hydroxyl group, cis-hydroxyl group, dihydroxyl group, a carboxylic acid group, a sulfate group, a sulfonate group, a phosphate group, a phosphonate group, an amino group, an amide group, a compound having at least one of the foregoing functional groups, and any combination thereof; crosslinking the crosslinkable proppant particulates with the crosslinker and crosslinking the crosslinker with the gelling agent, thereby suspending crosslinked proppant particulates in the treatment fluid; and introducing the treatment fluid with the suspended crosslinked proppant particulates into a subterranean formation having at least one fracture therein, thereby placing the suspended crosslinked proppant particulates into the at least one fracture to form a proppant pack therein. 11. The method of claim 10 , wherein the at least one functional group is the hydroxyl group, and wherein the hydroxyl group is from a compound selected from the group consisting of methanol, propanol, isopropanol, n-butanol, ethanol, and any combination thereof. 12. The method of claim 10 , wherein the at least one functional group is the carboxylic acid group, and wherein the carboxylic acid group is from a compound selected from the group consisting of methanoic acid, ethanoic acid, propanoic acid, 2-methylbutanoic acid, and any combination thereof. 13. The method of claim 10 , wherein the at least one functional group is the sulfate group, and wherein the sulfate group is from a compound selected from the group consisting of calcium hydrogen sulfate, copper(II) sulfate pentahydrate, barium hydrogen sulfate, magnesium sulfate heptahydrate, lead(II) hydrogen sulfate, zinc sulfate heptahydrate, lithium sulfate monohydrate, and any combination thereof. 14. The method of claim 10 , wherein the at least one functional group is the sulfonate group, and wherein the sulfonate group is from a compound selected from the group consisting of S-methyl methanethiosulfonate, 2,2,2-trifluoroethyl methane sulfonate, 2-chloroethyl methanesulfonate, ethyl methanesulfonate, trimethyl chlorosulfonate, 2,2,2-trifluoroethyl perfluorobutylsulfonate, phenyl methanesulfonate, phyenyl vinylsulfonate, 2-butynyl p-toluenesulfonate, 3-(4-methoxyphenoxy)-propyl methanesulfonate, S-phenol benzenethiosulfonate, phenyl-2-aminobenzenesulfonate, methyl dodecylbenzenesulfonate, and any combination thereof. 15. The method of claim 10 , wherein the at least one functional group is the phosphate group, and wherein the phosphate group is from a compound selected from the group consisting of magnesium ammonium phosphate hexahydrate, ammonium phosphate, magnesium dihydrogen phosphate, ammonium hydrogen phosphate, sodium dihydrogen phosphate, monopotassium phosphate, potassium hydrogen phosphate, and any combination thereof. 16. The method of claim 10 , wherein the at least one functional group is the phosphonate group, and wherein the phosphonate group is from a compound selected from the group consisting of dimethyl thiophosphonate, ethyl methylphosphonate, dimethyl vinylphosphonate, diethyl (trichloromethyl)phosphonate, diethyl (difluoromethyl)phosphonate, diethyl vinylphosphonate, tetramethyl-1,2-phylenediphosphonate, diethyl benzoylphosphonate, diethyl 3-bromobenzylphosphonate, diethyl 3-chlorobenzylphosphonate, tetraisopropyl methylenediphosphonate, dioctyl phenylphosphonate, and any combination thereof. 17. The method of claim 10 , wherein the at least one functional group is the amino group, and wherein the amino group is from a compound selected from the group consisting of a primary amine, a secondary amine, a tertiary amine, a cyclic amine, and any combination
containing boron · CPC title
reinforcing fractures by propping · CPC title
Gel breakers other than bacteria or enzymes · CPC title
Eroding chemicals, e.g. acids · CPC title
containing cross-linking agents · CPC title
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