Method of manipulating hydrophilicity and hydrophobicity of conventional dye molecules for tracer applications
US-2023183488-A1 · Jun 15, 2023 · US
US12037893B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12037893-B2 |
| Application number | US-202217815393-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 27, 2022 |
| Priority date | Jul 27, 2022 |
| Publication date | Jul 16, 2024 |
| Grant date | Jul 16, 2024 |
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A method includes introducing a fluoro-based small molecule tracer into a stimulation fluid, injecting the stimulation fluid into a target zone of a subterranean formation, and maintaining the fluoro-based small molecule tracer inside the target zone of the subterranean formation for an amount of time. While being maintained inside the target zone, the fluoro-based small molecule tracer comes into contact with water at a downhole temperature resulting in hydrolysis of the fluoro-based small molecule tracer to produce a fluorinated tracer and a nonfluorinated group. Then, produced fluid that includes the fluorinated tracer is recovered, a concentration of the fluorinated tracer in the hydrocarbons is determined, and the concentration of the fluorinated tracer is correlated to a productivity of the target zone of the subterranean formation.
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What is claimed: 1. A method comprising; introducing a fluoro-based molecule-tracer into a stimulation fluid; injecting the stimulation fluid comprising the fluoro-based molecule tracer into a target zone of a subterranean formation; maintaining the fluoro-based molecule tracer inside the target zone of the subterranean formation for an amount of time, during which the fluoro-based molecule tracer comes into contact with water at a downhole temperature, wherein the water at the downhole temperature hydrolyzes bonds of the fluoro-based molecule tracer to produce a fluorinated tracer and a nonfluorinated group; recovering produced fluid from the subterranean formation, wherein the produced fluid comprises the fluorinated tracer; determining a concentration of the fluorinated tracer in the produced fluid; and correlating the concentration of the fluorinated tracer to a productivity of the target zone of the subterranean formation. 2. The method of claim 1 , wherein the produced fluid comprises gaseous hydrocarbons. 3. The method of claim 2 , wherein the fluorinated tracer is a low boiling fluoro alcohol having a boiling point of 90° C. or less. 4. The method of claim 3 , wherein the low boiling fluoro alcohol is selected from the group consisting of trifluoromethanol, trifluoroethanol, hexafluoro-2-propanol, nanofluoro-tert-butyl alcohol, 1,1,1,3,3,3-hexafluoro-2-methyl-2-propanol, 1,1,1-trifluoro-2-propanol, and combinations thereof. 5. The method of claim 1 , wherein the produced fluid comprises a crude oil and a water phase, wherein the water phase comprises the fluorinated tracer and the crude oil comprises the nonfluorinated group and any unhydrolyzed fluoro based molecular tracer. 6. The method of claim 5 , wherein the fluorinated tracer is a high boiling fluoro alcohol having a boiling point above 90° C. 7. The method of claim 6 , wherein the high boiling fluoro alcohol is selected from the group consisting of 2,2-difluoroethanol, 2-fluoroethanol, 2,2,3,3-tetrafluoro-1-propanol, pentafluorophenol, fluoroalcohols having an alkyl chain length ranging from C4-C12, pentafluorophenol, 5-fluoro-1H-benzo[d][1,2,3]triazole-6-carboxylic acid, 4-fluoro-phenylcarbamoyl)-3H-imidazole-4-carboxylic acid, 5-fluoro-1H-benzo[d]imidazole-2-carboxylic acid, 2,2,3,3-tetrafluoro-1,4-butanediol, 2,2,3,3,4,4,5,5-octafluoro-1,6-hexanediol, and combinations thereof. 8. The method of claim 1 , wherein the stimulation fluid is fracturing fluid. 9. The method of claim 1 , further comprising; during a second stimulation stage, injecting a second fluoro-based molecule tracer into a second target zone of the subterranean formation; maintaining the second fluoro-based molecule tracer inside the second target zone of the subterranean formation for an amount of time, during which the second fluoro-based molecule tracer comes into contact with water at a downhole temperature, wherein the water at the downhole temperature hydrolyzes bonds of the second fluoro-based molecule tracer to produce a second fluorinated tracer and a second nonfluorinated group; recovering produced fluid from the subterranean formation, wherein the produced fluid comprises the fluorinated tracer and the second fluorinated tracer; determining a concentration of the second fluorinated tracer; and correlating the concentration of the second fluorinated tracer to a productivity of the target zone and the second target zone of the subterranean formation.
by forming crevices or fractures · CPC title
Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent (E21B43/241 takes precedence) · CPC title
by use of eroding chemicals, e.g. acids · CPC title
reinforcing fractures by propping · CPC title
using tracers; using radioactivity · CPC title
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