Energetic cocrystals for treatment of a subterranean formation

US2016177698A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016177698-A1
Application numberUS-201314910528-A
CountryUS
Kind codeA1
Filing dateAug 27, 2013
Priority dateAug 27, 2013
Publication dateJun 23, 2016
Grant date

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  1. Title

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Abstract

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The present invention relates to energetic cocrystals, and to methods for using the same for treatment of a subterranean formation. In various embodiments, the present invention provides a method of treating a subterranean formation, the method including obtaining or providing a composition including energetic cocrystals. Each energetic cocrystal independently includes an energetic compound and a secondary material. The method also includes placing the composition in a subterranean formation.

First claim

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1 - 104 . (canceled) 105 . A method of treating a subterranean formation, the method comprising: placing in the subterranean formation a composition comprising energetic cocrystals, each energetic cocrystal independently comprising an energetic compound; and a secondary material. 106 . The method of claim 105 , wherein placing the composition in the subterranean formation comprises placing the composition in at least one of a fracture, at least a part of an area surrounding a fracture, a flow pathway, an area surrounding a flow pathway, and an area desired to be fractured. 107 . The method of claim 106 , wherein the method further comprises hydraulic fracturing to generate the fracture or flow pathway. 108 . The method of claim 105 , wherein the method comprises a method of approximately measuring at least one dimension of a fracture or flow pathway in the subterranean formation. 109 . The method of claim 105 , further comprising detonating at least some of the cocrystals downhole. 110 . The method of claim 109 , comprising triggering the detonating. 111 . The method of claim 110 , wherein the triggering comprises exposing at least some of the cocrystals to at least one of a compression wave, a chemical activator, heat, pH change, pressure, friction, passage of time, and vibration. 112 . The method of claim 109 , wherein the detonating is sufficient to generate a compression wave downhole at least partially within a fracture or flow pathway, wherein the method further comprises using the compression wave to measure at least one characteristic of the fracture or the flow pathway. 113 . The method of claim 112 wherein the measured characteristic comprises at least one of length, height, width, volume, surface area, shape, degree of closure, and time of closure. 114 . The method of claim 112 , wherein using the compression wave to measure the characteristic comprises using a compression wave detector to approximately determine at least one dimension of an area surrounding the composition placed in the subterranean formation. 115 . The method of claim 114 wherein the compression wave detector is located at least one of downhole or above the surface. 116 . The method of claim 105 , wherein the composition further comprises a carrier fluid. 117 . The method of claim 105 , wherein the composition further comprises a viscosifier. 118 . The method of claim 105 , wherein the cocrystal comprises a crystalline structure comprising a unit cell comprising both the energetic compound and the at least one secondary material. 119 . The method of claim 105 , wherein the cocrystals are at least partially coated on a proppant. 120 . The method of claim 105 , wherein the energetic compound is at least one of acetone peroxide, ammonium azide, ammonium chlorate, ammonium dinitramide, ammonium nitrate, ammonium permanganate, 1,1′-azobis-1,2,3-triazole, barium azide, benzotrifuroxan (BTF), tricyclo[3.1.0.0 2,6 ]hex-3-ene or benzvalene, 1,2,4-butanetriol trinitrate; chlorine azide, copper(I) acetylide, copper(II) azide, cyanuric triazide, diacetyl peroxide, 2,6-diamino-3,5-dinitropyrazine-1-oxide (LLM-105), 6-diazo-2,4-dinitrocyclohexa-2,4-dien-1-one or diazodinitrophenol, diazomethane, diethylene glycol dinitrate, 4-dimethylaminophenylpentazole, 4,4′-dinitro-3,3′-diazenofuroxan (DDF), 2,4-dinitrotoluene, [(2R,3R)-1,3,4-trinitrooxybutan-2-yl] nitrate or erythritol tetranitrate, ethyl azide, ethylene glycol dinitrate, fluorine perchlorate, 1,1-diamino-2,2-dinitroethene (FOX-7 or DADNE), N,N′-bis-(1H-tetrazol-5-yl)-hydrazine (HMT), heptanitrocubane (HNC), 3,4,8,9,12,13-hexaoxa-1,6-diazabicyclo[4.4.4]tetradecane or hexamethylene triperoxide diamine (HMTD), hexanitrobenzene (HNB), 2,4,6-trinitro-N-(2,4,6-trinitrophenyl)aniline or hexanitrodiphenylamine (HND), hexanitroethane, 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (HNIW or CL-20), 1,3,5-trinitro-2-[2-(2,4,6-trinitrophenyl)ethenyl]benzene or hexanitrostilbene (HNS), 2,6-dioxo-1,3,4,5,7,8-hexanitrodecahydro-1H,5H-diimidazo[4,5-b:4′,5′-e] (HHTDD), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX), hydrazoic acid or hydrogen azide, lead 2,4,6-trinitrobenzene-1,3-diolate or lead styphnate, lead(II) azide, manganese heptoxide, (2R,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexol-1,2,3,4,5,6-hexanitrate or mannitol hexanitrate, methyl azide, methyl nitrate, methylammonium nitrate; 1-methyl-2-nitro-benzene or mononitrotoluene, nitrocellulose, nitrogen trichloride, nitrogen triiodide, nitroglycerin, nitroguanidine, nitromethane, nitrostarch, 5-nitro-1,2,4-triazol-3-one (NTO), nitrourea, octaazacubane, octanitrocubane (ONC), [3-nitrooxy-2,2-bis(nitrooxymethyl)propyl]nitrate or pentaerythritol tetranitrate (PETN), pentazenium, pentazole, picric acid, picryl chloride, polycarbonyl, polyvinyl nitrate, potassium picrate, propylene glycol dinitrate, 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), silicon tetraazide, silver acetylide, silver azide, silver nitride, sodium azide, 2,4,6-trinitrobenzene-1,3-diol or styphnic acid, 1,3-diamino-2,4,6-trinitrobenzene (DATB), 1,3,5-triamino-2,4,6-trinitrobenzene (TATB), tetraazidomethane, tetranitromethane, 1-(5-tetrazolyl)-3-guanyl tetrazene hydrate, N-methyl-N,2,4,6-tetranitroaniline or tetryl, 1,3,5-triazido-2,4,6-trinitrobenzene, 2,2′-(ethane-1,2-diylbis(oxy))bisethyl dinitrate] or tri ethylene glycol dinitrate, [2-methyl-3-nitrooxy-2-(nitrooxymethyl)propyl] nitrate or trimethylolethane trinitrate (TMETN or METN), 2,4,6-trinitroaniline, 2-methoxy-1,3,5-trinitrobenzene or trinitroanisole (TNA), 1,3,5-trinitrobenzene (TNB), 2,4,6-trinitrobenzenesulfonic acid, 1,3,3-trinitroazetidine (TNAZ), 1-methyl-amino-2,4,6-trinitrobenzene (MATNB), 2-methyl-1,3,5-trinitrobenzene or trinitrotoluene (TNT), 2,4,6-trinitro-1,3,5-triazine or trinitrotriazine, 2,4,6-tris(trinitromethyl)-1,3,5-triazine, urea nitrate, and 1,2,3,4,5-pentakis-nitrooxy-pentane or xylitol pentanitrate. 121 . The method of claim 105 , wherein the secondary material is a substantially non-energetic material or a substantially inert material, or an energetic material that is different than the energetic compound. 122 . The method of claim 105 , wherein the secondary material is at least one of acetone peroxide, ammonium azide, ammonium chlorate, ammonium dinitramide, ammonium nitrate, ammonium permanganate, 1,1′-azobis-1,2,3-triazole, barium azide, benzotrifuroxan (BTF), tricyclo[3.1.0.0 2,6 ]hex-3-ene or benzvalene, 1,2,4-butanetriol trinitrate, chlorine azide, copper(I) acetylide, copper(II) azide, cyanuric triazide, diacetyl peroxide, 2,6-diamino-3,5-dinitropyrazine-1-oxide (LLM-105), 6-diazo-2,4-dinitrocyclohexa-2,4-dien-1-one or diazodinitrophenol, diazomethane, diethylene glycol dinitrate, 4-dimethylaminophenylpentazole, 4,4′-dinitro-3,3′-diazenofuroxan (DDF), 2,4-dinitrotoluene, [(2R,3R)-1,3,4-trinitrooxybutan-2-yl] nitrate or erythritol tetranitrate, ethyl azide, ethylene glycol dinitrate, fluorine perchlorate, 1,1-diamino-2,2-dinitroethene (FOX-7 or DADNE), N,N′-bis-(1H-tetrazol-5-yl)-hydrazine (HBT), heptanitrocubane (HNC), 3,4,8,9,12,13-hexaoxa-1,6-diazabicyclo[4.4.4]tetradecane or hexamethylene triperoxide diamine (HMTD), hexanitrobenzene (HNB), 2,4,6-trinitro-N-(2,4,6-trinitrophenyl)aniline or hexanitrodiphenylamine (HND), hexanitroethane, 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (HNIW or CL-20), 1,3,5-trinitro-2-[2-(2,4,6-trinitrophenyl)ethenyl] benzene or hexanitrostilbene (HNS), 2,6-dioxo-1,3,4,5,7,8-hexanitrodecahydro-1H,5H-diimidazo[4,5-b:4′,5′-e] (HHTDD), octahydro-1,3,5,7-tetranitro-1

Assignees

Inventors

Classifications

  • by forming crevices or fractures · CPC title

  • E21B49/00Primary

    Testing the nature of borehole walls; Formation testing; Methods or apparatus for obtaining samples of soil or well fluids, specially adapted to earth drilling or wells · CPC title

  • Compositions for forming crevices or fractures · CPC title

  • the compound being a nitrated acyclic, alicyclic or heterocyclic amine · CPC title

  • C09K8/03Primary

    Specific additives for general use in well-drilling compositions · CPC title

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What does patent US2016177698A1 cover?
The present invention relates to energetic cocrystals, and to methods for using the same for treatment of a subterranean formation. In various embodiments, the present invention provides a method of treating a subterranean formation, the method including obtaining or providing a composition including energetic cocrystals. Each energetic cocrystal independently includes an energetic compound and…
Who is the assignee on this patent?
Halliburton Energy Services Inc
What technology area does this patent fall under?
Primary CPC classification E21B49/00. Mapped technology areas include Fixed Constructions.
When was this patent published?
Publication date Thu Jun 23 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).