Method of selecting an optimum formation stabilization treatment for subterranean formations is described. The methods include obtaining formation material, adding a test fluid to the formation material to form a first mixture, adding the test fluid to the formation material to form a second mixture, agitating the first and second mixtures, measuring capillary suction time of the first mixture, and measuring turbidity of the second mixture.

Certain metal surfaces are often unable to be effectively contacted with fluids containing hydrofluoric acid due to significant corrosion issues. Titanium and titanium alloy surfaces represent but one example. Corrosion inhibitor compositions comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof can be used to suppress metal corrosion, including that taking place on titanium and titanium alloy surfaces. Methods for suppressing corrosion of a metal surface can comprise: contacting a metal surface with a corrosive environment, the corrosive environment comprising hydrofluoric acid; introducing a corrosion inhibitor composition to the corrosive environment, the corrosion inhibitor composition comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof; contacting the metal surface with the corrosion inhibitor composition; and allowing the corrosion inhibitor composition to suppress corrosion of the metal surface being contacted by the corrosive environment.

Certain metal surfaces are often unable to be effectively contacted with fluids containing hydrofluoric acid due to significant corrosion issues. Titanium and titanium alloy surfaces represent but one example. Corrosion inhibitor compositions comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof can be used to suppress metal corrosion, including that taking place on titanium and titanium alloy surfaces. Methods for suppressing corrosion of a metal surface can comprise: contacting a metal surface with a corrosive environment, the corrosive environment comprising hydrofluoric acid; introducing a corrosion inhibitor composition to the corrosive environment, the corrosion inhibitor composition comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof; contacting the metal surface with the corrosion inhibitor composition; and allowing the corrosion inhibitor composition to suppress corrosion of the metal surface being contacted by the corrosive environment.

Certain metal surfaces are often unable to be effectively contacted with fluids containing hydrofluoric acid due to significant corrosion issues. Titanium and titanium alloy surfaces represent but one example. Corrosion inhibitor compositions comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof can be used to suppress metal corrosion, including that taking place on titanium and titanium alloy surfaces. Methods for suppressing corrosion of a metal surface can comprise: contacting a metal surface with a corrosive environment, the corrosive environment comprising hydrofluoric acid; introducing a corrosion inhibitor composition to the corrosive environment, the corrosion inhibitor composition comprising an N-(phosphonoalkyl)iminodiacetic acid or any salt thereof; contacting the metal surface with the corrosion inhibitor composition; and allowing the corrosion inhibitor composition to suppress corrosion of the metal surface being contacted by the corrosive environment.

The invention provides resin, hardener, and organosilicon compositions for use as coatings on proppant particles in a method of treating subterranean formations.

The invention provides resin, hardener, and organosilicon compositions for use as coatings on proppant particles in a method of treating subterranean formations.

A fines-fixing agent that has improved compatibility with organic complexed borate fracturing fluids is disclosed. Existing fines fixing agents have a high concentration of unreacted caustic that results in a product pH of approximately 12. This high pH affects the crosslinker and the overall fracturing fluid system stability, promoting precipitation of the organic crosslinker. These effects can be mitigated by neutralizing the fines fixing agents with an acid such as hydrochloric or acetic acid to a pH of 6 or lower.

A fines-fixing agent that has improved compatibility with organic complexed borate fracturing fluids is disclosed. Existing fines fixing agents have a high concentration of unreacted caustic that results in a product pH of approximately 12. This high pH affects the crosslinker and the overall fracturing fluid system stability, promoting precipitation of the organic crosslinker. These effects can be mitigated by neutralizing the fines fixing agents with an acid such as hydrochloric or acetic acid to a pH of 6 or lower.

A well treatment composition for use in a hydrocarbon-bearing reservoir comprising a reversible aminal gel composition is disclosed. The reversible aminal gel composition includes a liquid precursor composition. The liquid precursor composition is operable to remain in a liquid state at about room temperature. The liquid precursor composition comprises an organic amine composition; an aldehyde composition; a polar aprotic organic solvent; and a metal salt composition with valence 3, 4, or 5. The liquid precursor composition transitions from the liquid state to a gel state responsive to an increase in temperature in the hydrocarbon-bearing reservoir. The gel state is stable in the hydrocarbon-bearing reservoir at a temperature similar to a temperature of the hydrocarbon-bearing reservoir, and the gel state is operable to return to the liquid state responsive to a change in the hydrocarbon-bearing reservoir selected from the group consisting of: a decrease in pH in the hydrocarbon-bearing reservoir and an addition of excess metal salt composition in the hydrocarbon-bearing reservoir.

A well treatment composition for use in a hydrocarbon-bearing reservoir comprising a reversible aminal gel composition is disclosed. The reversible aminal gel composition includes a liquid precursor composition. The liquid precursor composition is operable to remain in a liquid state at about room temperature. The liquid precursor composition comprises an organic amine composition; an aldehyde composition; a polar aprotic organic solvent; and a metal salt composition with valence 3, 4, or 5. The liquid precursor composition transitions from the liquid state to a gel state responsive to an increase in temperature in the hydrocarbon-bearing reservoir. The gel state is stable in the hydrocarbon-bearing reservoir at a temperature similar to a temperature of the hydrocarbon-bearing reservoir, and the gel state is operable to return to the liquid state responsive to a change in the hydrocarbon-bearing reservoir selected from the group consisting of: a decrease in pH in the hydrocarbon-bearing reservoir and an addition of excess metal salt composition in the hydrocarbon-bearing reservoir.