H3 PO4 /HF Siliceous formation treating composition and method

Claim 2

A composition for treatment of siliceous formations, comprising an aqueous solution having a phosphoric acid concentration in the range of from about 10 to about 30% by weight, to which is added at least one flourine donor compound in an amount to provide a generated hydrofluoric acid concentration in the range of from about 1 to about 7% by weight.

Claim 3

A composition according to claim 1, wherein the fluorine donor is selected from the group consisting of ammonium fluoride and ammonium bifluoride.

Claim 4

A composition according to claim 2, wherein the fluorine donor is ammonium bifluoride.

Claim 5

A composition according to claim 1, 2 or 3, wherein the phosphoric acid concentration is about 10% by weight and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 1 to about 2% by weight.

Claim 6

A composition according to claim 1, 2 or 3, wherein the phosphoric acid concentration is about 20% by weight and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight.

Claim 7

A composition according to claim 1, 2 or 3, wherein the phosphoric acid concentration is about 30% by weight and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 3 to about 7% by weight.

Claim 8

A composition according to claim 1, 2 or 3, wherein the aqueous solution is an aqueous solution having from about 10 to about 30 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phsophonic acid or a phosphonate.

Claim 9

A composition according to claim 1, 2 or 3, wherein the aqueous solution is an aqueous solution having from about 10 to about 30 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight.

Claim 10

A composition according to claim 1, 2 or 3, wherein the aqueous solution is an aqueous solution having a phosphoric acid concentration of about 20% by weight, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 11

A composition according to claim 1, 2 or 3, wherein the aqueous solution is an aqueous solution having a phosphoric acid concentration of about 20% by weight, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight.

Claim 12

A composition according to claim 1, 2 or 3, wherein the aqueous solution is an aqueous solution having about 20 weight % phosphoric acid, about 1.1 weight % of a highly polar surface active agent which is a citric acid-monomethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and wherein the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of about 3% by weight.

Claim 15

A method according to claim 12, wherein in the composition the added fluorine donor is selected from the group consisting of ammonium fluoride and ammonium bifluoride.

Claim 16

A method according to claim 13, wherein in the composition the added fluorine donor is ammonium bifluoride.

Claim 17

A method according to claim 12, 13 or 14, wherein in the composition the phosphoric acid concentration is about 10% by weight and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 1 to about 2% by weight.

Claim 18

A method according to claim 12, 13 or 14, wherein in the composition the phosphoric acid concentration is about 20% by weight and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight.

Claim 19

A method according to claim 12, 13 or 14, wherein in the composition the phosphoric acid concentration is about 30% by weight and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 3 to about 7% by weight.

Claim 20

A method according to claim 12, 13 or 14, wherein in the composition the aqueous solution is an aqueous solution having from about 10 to about 30 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 21

A method according to claim 12, 13 or 14, wherein in the composition the aqueous solution is an aqueous solution having from about 10 to about 30 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from 2 to about 5% by weight.

Claim 22

A method according to claim 12, 13 or 14, wherein in the composition the aqueous solution is an aqueous solution having a phosphoric acid concentration of about 20% by weight, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 23

A method according to claim 12, 13 or 14, wherein in the composition the aqueous solution is an aqueous solution having a phosphoric acid concentration of about 20% by weight, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight.

Claim 24

A method according to claim 12, 13 or 14, wherein in the composition the aqueous solution is an aqueous solution having about 20 weight % phosphoric acid, about 1.1 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and the fluorine donor is added in an amount to provide a generated hydrofluoric acid concentration in the range of about 3% by weight.

Claim 25

A method according to claim 12, 13 or 14, including the additional step of preflushing the formation with fluorine-free acid or salt solution.

Claim 26

A method according to claim 12, 13 or 14, including the additional step of afterflushing the formation with fluorine-free acid or salt solution.

Claim 27

A method according to claim 12, 13 or 14, including the additional steps of preflushing and afterflushing the formation with fluorine-free acid or salt solution.

Claim 28

A method according to claim 14, wherein in the composition the aqueous solution is an aqueous solution having a phosphoric acid concentration of about 20% by weight, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate, and the ammonium bifluoride is added in an amount to provide a generated hydrofluoric acid concentration in the range of from about 2 to about 5% by weight and including at least one additional step selected from the group consisting of preflushing and afterflushing the formation with fluorine-free acid or salt solution.

Claim 29

A method according to claim 26, wherein in the composition the ammonium bifluoride is added in an amount to provide a generated hydrofluoric acid concentration to about 3% by weight.

Claim 30

A method according to claim 26 or 27, wherein the additional step comprises preflushing the formation with at least one acid solution selected from the group consisting of a hydrochloric acid solution, and a solution being an acidic aqueous solution comprising from about 5 to about 36 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 31

A method according to claim 26 or 27, wherein the additional step comprises afterflushing the formation with at least one acid solution selected from the group consisting of a hydrochloric acid solution, and a solution being an acidic aqueous solution comprising from about 5 to about 36 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 32

A method according to claim 26 or 27, including the additional steps of both preflushing and afterflushing the formation with at least one acid solution selected from the group consisting of a hydrochloric acid solution, and a being an acidic aqueous solution comprising from about 5 to about 36 weight % phosphoric acid, from about 0.6 to about 5 weight % of a highly polar surface active agent which is a citric acid-monoethanolamine elimination reaction product characterized by a visible absorption spectrum which displays an increasing extinction coefficient from the red to the near U.V. with some structure, an absorption maximum at 475 nm, a plateau from 460 nm to 465 nm, an absorption maximum at 450 nm and extinction coefficients as follows: ε.sub.475 =0.325 l/gm.cm ε.sub.462 =0.379 l/gm.cm ε.sub.450 =0.509 l/gm.cm, an effective amount of a ferrous metal corrosion inhibitor, and an amount of a crystal modifying agent sufficient to control crystal growth, minimize crystal agglomeration and minimize crystal adhesion to the formation, said crystal modifying agent being selected from the group consisting of polyacrylate polymers and blends of such polymers with phosphonic acid or a phosphonate.

Claim 33

A method according to claim 26 or 27, wherein the additional step comprises preflushing the formation with a fluorine-free clay stabilizing salt solution.

Claim 34

A method according to claim 26 or 27, wherein the additional step comprises preflushing the formation with a fluorine-free salt solution to displace connate water containing cations which can form insoluble precipitates in association with anionic products of the reaction between the hydrofluoric acid and the formation.