Method for treatment of underground reservoirs
AssigneeCleansorb Limited
InventorRalph Edmund Harris
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AssigneeCleansorb Limited
InventorRalph Edmund Harris
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A process is disclosed for treating an underground formation, which process comprises: (a) introducing into the underground formation a micellar dispersion comprising water, one or more organic acid precursors, one or more surfactants and, optionally, one or more salts, co-surfactants and/or organic liquids that are not organic acid precursors; and (b) allowing (i) the micellar dispersion to solubilize hydrocarbons, emulsions or water blocks present in the underground formation, and (ii) at least a portion of the organic acid precursor to hydrolyze in-situ to produce sufficient organic acid to substantively dissolve acid soluble material present in or adjacent to filter cakes or other damage in the underground formation.
A process for treating an underground formation, which process comprises:
Dependencies are inferred from the claim text.
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Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning: organic depositions, e.g. paraffins or asphaltenes
Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning: inorganic depositions, e.g. sulfates or carbonates
Compositions for forming crevices or fractures: eroding chemicals, e.g. acids
Earth boring, well treating, and oil field chemistry: controlled release agent
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This application is the U.S. national phase of International Application No. PCT/GB2008/002297 filed 3 Jul. 2008, which designated the U.S. and claims priority to UK Application No. GB 002297, filed 3 Jul. 2008, the entire contents of each of which are hereby incorporated by reference.
The present invention relates to the production of oil, gas or water from wells drilled into underground reservoirs. It is also applicable to injection wells.
During drilling, completion, workover and production operations there are numerous situations where the production or injection rate of an oil, gas or water well following these operations is limited or impaired due to the presence of formation damage. Types of damage include, but are not limited to, the presence of invert emulsion filter cakes, filter cakes from use of water-based muds, fluids filtrates or residues (including from hydraulic fracturing fluids, and gravel packing fluids) particulate materials such as fluid loss control agents and weighting agents, rock fines, biofilms, scales, emulsions, “water blocks” and hydrocarbon accumulations, including but not being limited to asphaltenes, waxes and paraffins.
In order to confirm the presence of micelles in the micellar dispersions of the present invention, a number of exemplary dispersions were made up in filtered artificial sea water (Sigma sea salts Sigma Aldrich product number S-9883) using 10% v/v ORCA 1 or ORCA 2 (proprietary blends of surfactants commercially available from Cleansorb Limited) in combination with 10% v/v ORCA A, ORCA B or ORCA C (proprietary blends of carboxylic acid esters commercially available from Cleansorb Limited). Particle size analysis of the dispersions was carried out at 25° C. using a Malvern Zetasizer Nano ZS by laser light scattering.
The average particle (micelle) size of the dispersions is shown in Table 1.
TABLE 1 Average particle size and polydispersity index in examples of micellar dispersions Composition Z average Polydispersity Sample (in artificial sea water) Particle size (nm) index A 10% v/v ORCA 2 plus 9.89 0.231 10% v/v ORCA A B 10% v/v ORCA 2 plus 11.49 0.241 10% v/v ORCA B C 10% v/v ORCA 2 plus 8.70 0.266 10% v/v ORCA C D 10% v/v ORCA 1 plus 10.12 0.265 10% v/v ORCA A E 10% v/v ORCA 1 plus 12.14 0.335 10% v/v ORCA B F 10% v/v ORCA 1 plus 23.87 0.214 10% v/v ORCA C