IP Library Granted Patent US 10,920,131
Granted Patent B2
US 10,920,131 · App. 15/754,428 · Granted Feb 16, 2021

Weighted acid compositions comprising amino acids

Inventors: Robert Lawrence Blackbourn (Houston, TX); Jonathan Joseph Brege (Spring, TX); Paul Richard Weider (Houston, TX); Allen Dale Gabrysch (Paige, TX); Andrew James Murphy (Amsterdam, NL); Lorna Beatriz Ortiz-Soto (Houston, TX); Ryan Matthew Van Zanten (Houston, TX)
Assignee: SHELL OIL COMAPNY
C09K8/74
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Quick Facts
Patent No.
US 10,920,131
App. No.
15/754,428
Granted
Feb 16, 2021
Kind
B2
Abstract

A weighted acid composition comprising an acid, a brine, and an amino acid and associated methods.

Claims (21)

1. A method comprising:

providing a weighted acid solution comprising an acid precursor, a brine, and an amino acid comprising glycine; and

placing the weighted acid solution into a subterranean formation.

2. The method of claim 1 , wherein the concentration of the acid precursor in the weighted acid solution is an amount in the range of from 0.2 mol/L to 8 mol/L.

3. The method of claim 1 , wherein the brine comprises at least one of calcium chloride, zinc chloride, zinc bromide, calcium bromide, sodium chloride, and sodium bromide.

4. The method of claim 1 , wherein the concentration of the brine in the weighted acid solution is an amount in the range of from 2 mol/L to 8 mol/L.

5. The method of claim 1 , wherein the concentration of the amino acid in the weighted acid solution is an amount in the range of from 0.05 mol/L to 16 mol/L.

6. The method of claim 1 , wherein the weighted acid solution has a molar ratio of amino acid to the acid precursor in the range of from 0.25:1 to 2:1.

7. The method of claim 1 , further comprising allowing the weighted acid solution to generate a protonated amino acid.

8. The method of claim 1 , wherein the acid precursor is selected from the group consisting of a hydrolysable carboxylic acid ester, a polylactic acid, a polyglycolic acid, and an ethylene glycol diformate.

9. The method of claim 1 , wherein the acid precursor is a thermally activated strong acid precursor.

10. The method of claim 9 , wherein the thermally activated strong acid precursor is selected from the group consisting of a sulfone adduct of butadiene, a sulfone adduct of piperylene, a sulfone adduct of isoprene, a sulfite ester, ethylene sulfite, dimethyl sulfite, 1,2-propylene sulfite, 1,3-propylene sulfite, a sulfone adduct of paraformaldehyde, a sulfone adduct of polyoxymethylene, a sulfone adduct of metaldehyde, a sulfone adduct of trioxane, a sulfone adduct of formaldehyde, a sulfone adduct of acetaldehyde, a sulfone adduct of propionaldehyde, a sulfone adduct of n-butyraldehyde, a sulfone adduct of i-butyraldehyde, a sulfone adduct of glycolaldehyde, a sulfone adduct of glyceraldehyde, a sulfone adduct of glyoxal, a sulfone adduct of benzaldehyde, a sulfone adduct of cyclohexanone, a sulfone adduct of acetone, a sulfone adduct of chloroacetone, a sulfone adduct of methyl ethyl ketone, a sulfone adduct of mesityl oxide, and a sulfone adduct of methyl i-butyl ketone.

11. A method comprising:

providing a weighted acid solution comprising an acid precursor, a brine, and an amino acid; and

placing the weighted acid solution into a subterranean formation;

allowing the weighted acid solution to generate a protonated amino acid.

12. The method of claim 11 , wherein said allowing the weighted acid solution to generate a protonated amino acid comprises comprise allowing the acid precursor to generate an acid and reacting said acid with the amino acid.

13. A method comprising:

providing a weighted acid solution comprising an acid precursor, a brine, and an amino acid; and

placing the weighted acid solution into a subterranean formation;

wherein the acid precursor is a thermally activated strong acid precursor selected from the group consisting of a sulfone adduct of butadiene, a sulfone adduct of piperylene, a sulfone adduct of isoprene, a sulfite ester, ethylene sulfite, dimethyl sulfite, 1,2-propylene sulfite, 1,3-propylene sulfite, a sulfone adduct of paraformaldehyde, a sulfone adduct of polyoxymethylene, a sulfone adduct of metaldehyde, a sulfone adduct of trioxane, a sulfone adduct of formaldehyde, a sulfone adduct of acetaldehyde, a sulfone adduct of propionaldehyde, a sulfone adduct of n-butyraldehyde, a sulfone adduct of i-butyraldehyde, a sulfone adduct of glycolaldehyde, a sulfone adduct of glyceraldehyde, a sulfone adduct of glyoxal, a sulfone adduct of benzaldehyde, a sulfone adduct of cyclohexanone, a sulfone adduct of acetone, a sulfone adduct of chloroacetone, a sulfone adduct of methyl ethyl ketone, a sulfone adduct of mesityl oxide, and a sulfone adduct of methyl i-butyl ketone.

Assignments (1)
CHANGE OF NAME Recorded Mar 7, 2022
From: SHELL OIL COMPANY
To: SHELL USA, INC.
Reel/Frame 059694/0819 →
Continuity (2)
Provisional Application 62212305 · Aug 31, 2015
Related Publication 20180282613A1 · Oct 4, 2018