Abstract: This disclosure relates to acidizing retarder compositions and methods of reducing the rate of carbonate dissolution in carbonate acidizing treatments of carbonate formations using the acidizing retarder compositions. The methods may include dissolving one or more retarder compounds in a solution comprising a strong acid to form acidizing retarder compositions, and introducing the acidizing retarder compositions to carbonate formations. The acidizing retarder compositions may include one or more retarder compounds and a strong acid. At least one of the one or more retarder compounds may be a poloxamer. A concentration of the strong acid in the acidizing retarder composition may be 5 weight percent or greater.

Abstract: Coated proppants include a proppant particle, a surface copolymer layer surrounding the proppant particle, and a resin layer surrounding the surface copolymer layer. The surface copolymer layer includes a copolymer of at least two monomers chosen from styrene, methyl methacrylate, ethylene, propylene, butylene, imides, urethanes, sulfones, carbonates, and acrylamides, where the copolymer is crosslinked by divinyl benzene. The resin layer includes a cured resin.

Abstract: A coated proppant having a proppant particle, an intermediate cross-linked terpolymer layer encapsulating the proppant particle, and an outer resin layer encapsulating the intermediate cross-linked terpolymer layer. The proppant particle is selected from sand, ceramic, glass, and combinations thereof. The intermediate cross-linked terpolymer layer includes styrene, methyl methacrylate, and divinyl benzene. The outer resin layer includes a cured epoxy resin formed from an epoxy resin and a curing agent.

Abstract: Hydraulic fracturing fluids include an aqueous fluid, an acrylamide-based polymers, and a hyperbranched crosslinker that crosslinks the acrylamide-based polymer to form a crosslinked gel. The hyperbranched crosslinker includes a hyperbranched polyethyleneimine polyoxiranylalkanol having a weight-average molecular weight from 10 kDa to 1500 kDa. The hyperbranched crosslinker may be a product of reacting a hyperbranched polyethyleneimine with an oxiranylalkanol to obtain the hyperbranched polyethyleneimine polyoxiranylalkanol. In examples, the oxiranylalkanol is glycidol. Methods for preparing the hydraulic fracturing fluids and methods for treating subterranean formations with the hydraulic fracturing fluids are disclosed.

Abstract: Coated proppants include a proppant particle, a surface copolymer layer surrounding the proppant particle, and a resin layer surrounding the surface copolymer layer. The surface copolymer layer includes a copolymer of at least two monomers chosen from styrene, methyl methacrylate, ethylene, propylene, butylene, imides, urethanes, sulfones, carbonates, and acrylamides, where the copolymer is crosslinked by divinyl benzene. The resin layer includes a cured resin.

Abstract: Methods of preparing a crosslinked hydraulic fracturing fluid include combining a hydraulic fracturing fluid comprising a polyacrylamide polymer with a plurality of coated proppants. The plurality of coated proppants include a proppant particle and a resin proppant coating on the proppant particle. The resin proppant coating includes resin and a zirconium oxide crosslinker. The resin includes at least one of phenol, furan, epoxy, urethane, phenol-formaldehyde, polyester, vinyl ester, and urea aldehyde. Methods further include allowing the zirconium oxide crosslinker within the resin proppant coating to crosslink the polyacrylamide polymer within the hydraulic fracturing fluid at a pH of at least 10, thereby forming the crosslinked hydraulic fracturing fluid.

Abstract: In accordance with one or more embodiments of the present disclosure, a low-density treatment fluid includes a base water-control system and at least one light-weight filler material. The base water-control system may include an inorganic material system comprising an aqueous colloidal silica and a water-soluble chemical activator for gelling the colloidal silica, or the base water-control system may include an organic material system comprising of polymeric material. The low-density treatment fluid may have a density of from 0.1 g/cm3 to 0.75 g/cm3. Also described are methods of recovering a target fluid from a subterranean cavity using such a low-density treatment fluid.

Abstract: The preparation device includes an upper main conveyor belt, and an aggregate box, a first silane emulsion container and a first paper mill sludge container sequentially arranged above the upper main conveyor belt in a conveying direction. A lower auxiliary conveyor belt is arranged below the upper main conveyor belt, and a second paper mill sludge container and a second silane emulsion container are sequentially arranged between the upper main conveyor belt and the lower auxiliary conveyor belt in a conveying direction of the lower auxiliary conveyor belt. A trolley is arranged at the conveying tail end of the lower auxiliary conveyor belt, a gravity sensing device is arranged below the trolley, a mixer is arranged beside the trolley, and a heater is arranged at the bottom of the mixer.

Abstract: Coated proppants include a proppant particle, a surface copolymer layer surrounding the proppant particle, and a resin layer surrounding the surface copolymer layer. The surface copolymer layer includes a copolymer of at least two monomers chosen from styrene, methyl methacrylate, ethylene, propylene, butylene, imides, urethanes, sulfones, carbonates, and acrylamides, where the copolymer is crosslinked by divinyl benzene. The resin layer includes a cured resin.

Abstract: This disclosure relates to acidizing retarder compositions and methods of reducing the rate of carbonate dissolution in carbonate acidizing treatments of carbonate formations using the acidizing retarder compositions. The methods may include dissolving one or more retarder compounds in a solution comprising a strong acid to form acidizing retarder compositions, and introducing the acidizing retarder compositions to carbonate formations. The acidizing retarder compositions may include one or more retarder compounds and a strong acid. At least one of the one or more retarder compounds may be a poloxamer. A concentration of the strong acid in the acidizing retarder composition may be 5 weight percent or greater.

Abstract: According to embodiments disclosed herein, a gel fluid composite may include a nanosilica gel and a plurality of quantum dot tracers. The nanosilica gel may be configured to seal one or more downhole fractures in a wellbore. The plurality of quantum dot tracers may be dispersed in the nanosilica gel. The plurality of quantum dot tracers may each include a semiconductor particle core housed in a silica shell.

Abstract: A silicon oxide Janus nanosheets relatively permeability modifier (RPM) for carbonate and sandstone formations. The silicon oxide Janus nanosheets RPM may be used to treat a water and hydrocarbon producing carbonate or sandstone formation to reduce water permeability in the formation and increase the production of hydrocarbons. The silicon oxide Janus nanosheets RPM for carbonate formations includes a first side having negatively charged functional groups and a second side having alkyl groups. The silicon oxide Janus nanosheets RPM for sandstone formations includes a first side having positively charged functional groups and a second side having alkyl groups. The negatively charged functional groups may include a negatively charged oxygen group groups and hydroxyl groups. The positively charged functional groups may include amino groups and an amine.

Abstract: According to embodiments disclosed herein, a gel fluid composite may include a nanosilica gel and a plurality of quantum dot tracers. The nanosilica gel may be configured to seal one or more downhole fractures in a wellbore. The plurality of quantum dot tracers may be dispersed in the nanosilica gel. The plurality of quantum dot tracers may each include a semiconductor particle core housed in a silica shell.

Abstract: According to embodiments disclosed herein, a method of monitoring a gel fluid composite may include directing the gel fluid composite into a wellbore extending into a subsurface where the wellbore has one or more downhole fractures so that the gel fluid composite enters the one or more downhole fractures, transforming the gel fluid composite from an aqueous phase to a gel phase, irradiating light onto the gel fluid composite so that the fluorescent compounds emit one or more photons, and detecting the one or more photons using a detection device. The gel fluid composite may include a nanosilica gel that includes silica nanoparticles and an activator, wherein the silica nanoparticles have a maximum cross-sectional dimension of from 3 nm to 100 nm, and one or more fluorescent compounds, wherein the one or more fluorescent compounds are dispersed in the nanosilica gel, bonded to the silica nanoparticles, or both.

Abstract: Coated proppants include a proppant particle, a surface copolymer layer surrounding the proppant particle, and a resin layer surrounding the surface copolymer layer. The surface copolymer layer includes a copolymer of at least two monomers chosen from styrene, methyl methacrylate, ethylene, propylene, butylene, imides, urethanes, sulfones, carbonates, and acrylamides, where the copolymer is crosslinked by divinyl benzene. The resin layer includes a cured resin.

Abstract: A chemical gel system having a polymer and a silicon oxide Janus nanosheets crosslinker for treating thief zones in carbonate formations. The polymer and silicon oxide Janus nanosheets crosslinker may form a crosslinked polymer gel to reduce or prevent water production via thief zones during hydrocarbon production. The silicon oxide Janus nanosheets crosslinker includes a first side having negatively charged functional groups and a second side having amines. The negatively charged functional groups may include negatively charged oxygen groups and hydroxyl groups. Methods of reducing water production in a thief zone using the silicon oxide Janus nanosheets crosslinker and methods of manufacturing the silicon oxide Janus nanosheets crosslinker are also provided.

Abstract: A chemical gel system having a polymer and a graphene oxide Janus nanosheets crosslinker for treating thief zones in carbonate formations. The polymer and graphene oxide Janus nanosheets crosslinker may form a crosslinked polymer gel to reduce or prevent water production via thief zones during hydrocarbon production. The graphene oxide Janus nanosheets crosslinker includes a first side having negatively charged functional groups and a second side having amines. The negatively charged functional groups may include carboxyl groups, negatively charged oxygen groups, and hydroxyl groups. Methods of reducing water production in a thief zone using the graphene oxide Janus nanosheets crosslinker and methods of manufacturing the graphene oxide Janus nanosheets crosslinker are also provided.

Abstract: A method for producing a coated proppant having an intermediate cross-linked terpolymer layer includes mixing a monomers solution including a first monomer, a second monomer that is different from the first monomer, a cross-linking agent, and an initiator. The proppant particle is combined with the monomers solution, and the monomer solution on the surface of the at least one proppant particle is polymerized to form at least one proppant particle having the intermediate cross-linked terpolymer layer on a surface of the at least one proppant particle. A resin solution including an epoxy resin, a curing agent, and graphene is mixed, and combined with the at least one proppant particle having the intermediate cross-linked terpolymer layer on a surface of the at least one proppant particle. The resin solution is cured to form the coated proppant comprising an intermediate cross-linked terpolymer layer.

Abstract: A graphene oxide Janus nanosheets relative permeability modifier (RPM) for carbonate formations. The graphene oxide Janus nanosheets RPM may be used to treat a water and hydrocarbon producing carbonate formation to reduce water permeability in the formation and increase the production of hydrocarbons. The graphene oxide Janus nanosheet RPM includes a first side having negatively charged functional groups and a second side having alkyl groups. The alkyl groups may include C8 to C30 alkyls. The negatively charged functional groups may include carboxyl groups, epoxy groups, and hydroxyl groups. Methods of reducing water permeability of a carbonate formation using the graphene oxide Janus nanosheets RPM and methods of manufacturing the graphene oxide Janus nanosheets RPM are also provided.

Abstract: Coated particles include a particulate substrate, a surface copolymer layer surrounding the particulate substrate, and a resin layer surrounding the surface copolymer layer. The surface copolymer layer includes a copolymer of at least two monomers chosen from styrene, methyl methacrylate, ethylene, propylene, butylene, imides, urethanes, sulfones, carbonates, and acrylamides. The resin layer includes a cured resin. Methods of preparing the coated particles include preparing a first mixture including at least one polymerizable material, an initiator, and optionally a solvent; contacting the first mixture to a particulate substrate to form a polymerization mixture; heating the polymerization mixture to cure the polymerizable material and form a polymer-coated particulate; preparing a second mixture including the polymer-coated substrate, an uncured resin, and a solvent; and adding a curing agent to the second mixture to cure the uncured resin and form the coated particle.