Use of a borate-acid buffer in oil and gas operations
Provided herein are compositions comprising borate-acid buffers, as well as methods of using these compositions in oil and gas operations, including enhanced oil recovery (EOR) operations, fracturing operations, stimulation operations, etc.
1. A method for improving hydrocarbon recovery from a subterranean formation containing hydrocarbons therewithin, the method comprising:
injecting an aqueous composition comprising (i) a borate-acid buffer, (ii) a surfactant package; (iii) water; and (iv) optionally a water-soluble polymer into the subterranean formation through a wellbore in fluid communication with the subterranean formation;
wherein the borate-acid buffer exhibits a capacity to buffer at a pH of from 6.0 to 8.5;
wherein the borate-acid buffer is present in an effective amount to chelate divalent metal ions present in the water or in water present in the subterranean formation.
2. The method of claim 1 , wherein the wellbore is an injection wellbore; and
wherein injection of the aqueous composition into the subterranean formation through the wellbore increases a flow of hydrocarbons to a production wellbore in fluid communication with the subterranean formation.
3. The method of claim 1 , wherein the method for hydrocarbon recovery comprises an enhanced oil recovery (EOR) operation.
4. The method of claim 1 , further comprising:
adding a tracer to the aqueous composition prior to introducing or along with the aqueous composition or through the wellbore into the subterranean formation;
recovering the tracer from fluids produced from the subterranean formation through the wellbore, fluids recovered from a different wellbore in fluid communication with the subterranean formation, or any combination thereof; and
comparing the quantity of tracer recovered from the fluids produced to the quantity of tracer introduced.
5. The method of claim 1 , wherein the hydrocarbons further comprise CO 2 , H 2 S, or any combination thereof.
6. The method of claim 1 , wherein the borate-acid buffer is present in the aqueous composition in an amount of from 0.05% to 5% by weight, based on the total weight of the aqueous composition.
7. The method of claim 1 , wherein the borate-acid buffer exhibits a capacity to buffer at a pH of from 6.0 to 8.0.
8. The method of claim 1 , wherein the borate-acid buffer comprises a borate compound and a conjugate base of an acid.
9. The method of claim 8 , wherein the borate compound comprises sodium tetraborate, calcium tetraborate, sodium borate, sodium metaborate, or any combination thereof.
10. The method of claim 8 , wherein the conjugate base comprises acetate, citrate, tartrate, succinate, or any combination thereof.
11. The method of claim 8 , wherein the borate compound and the conjugate base of the organic acid are present at a weight ratio of from 1:1 to 5:1.
12. The method of claim 1 , wherein the borate-acid buffer comprises a boric acid and an alkali.
13. The method of claim 1 , wherein the aqueous composition comprises a surfactant package, and wherein the surfactant package comprises a primary surfactant and optionally one or more secondary surfactants.
14. The method of claim 13 , wherein the primary surfactant comprises an anionic surfactant, such as a sulfonate, a disulfonate, a sulfate, a disulfate, a sulfosuccinate, a disulfosuccinate, a carboxylate, a dicarboxylate, or any combination thereof.
15. The method of claim 14 , wherein the anionic surfactant comprises one of the following:
a branched or unbranched C6-C32:PO(0-65):EO(0-100)-carboxylate;
a C10-C30 internal olefin sulfonate;
a C8-C30 alkyl benzene sulfonate (ABS);
a sulfosuccinate surfactant;
a surfactant defined by the formula below
R 1 —R 2 —R 3
wherein
R 1 comprises a branched or unbranched, saturated or unsaturated, cyclic or non-cyclic, hydrophobic carbon chain having 6-32 carbon atoms and an oxygen atom linking R 1 and R 2 ;
R 2 comprises an alkoxylated chain comprising at least one oxide group selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide, and combinations thereof; and
R 3 comprises a branched or unbranched hydrocarbon chain comprising 2-12 carbon atoms and from 2 to 5 carboxylate groups; or
a surfactant defined by the formula below
wherein
R 4 is, individually for each occurrence, a branched or unbranched, saturated or unsaturated, cyclic or non-cyclic, hydrophobic carbon chain having 6-32 carbon atoms; and
M represents a counterion.
16. The method of claim 13 , wherein the primary surfactant comprises a non-ionic surfactant, such as a branched or unbranched C6-C32:PO(0-65):EO(0-100).
17. The method of claim 13 , wherein the primary surfactant has a concentration within the composition of from 0.05% to 5% by weight, based on the total weight of the aqueous composition.
18. The method of claim 1 , wherein the composition further comprises a polymer, a friction reducer, a gelling agent, a crosslinker, a breaker, a pH adjusting agent, a non-emulsifier agent, an iron control agent, a corrosion inhibitor, a scale inhibitor, a biocide, a clay stabilizing agent, a chelating agent, a proppant, a wettability alteration chemical, a co-solvent, or any combination thereof.
19. The method of claim 1 , wherein the borate-acid buffer is present in the aqueous composition in an amount of from 0.1% to 5% by weight, based on the total weight of the aqueous composition.
20. The method of claim 1 , wherein when present the water-soluble polymer comprises a synthetic polymer.
21. The method of claim 1 , wherein when present the water-soluble polymer comprises polyacrylamide or a copolymer thereof.
22. The method of claim 1 , wherein the surfactant package comprises a primary surfactant comprising a branched or unbranched C6-C32:PO(0-65):EO(0-100)-carboxylate, a dicarboxylate, or any combination thereof.
23. The method of claim 1 , wherein the divalent metal ions comprise Mg 2+ , Ca 2+ , or any combination thereof.