IP Library Granted Patent US 12,084,364
Granted Patent B2
US 12,084,364 · App. 17/404,131 · Granted Sep 10, 2024

Modified sulfuric acid and uses thereof

Inventors: Clay Purdy (Medicine Hat, CA); Markus Weissenberger (Calgary, CA); Markus Pagels (Calgary, CA); Kyle G Wynnyk (Calgary, CA); Karl W Dawson (Calgary, CA)
Assignee: Chemical Evolution Ltd.
C02F1/722C02F2101/18C02F2103/10
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Quick Facts
Patent No.
US 12,084,364
App. No.
17/404,131
Granted
Sep 10, 2024
Kind
B2
Abstract

A modified aqueous acid composition comprising: sulfuric acid; a compound comprising an amine moiety and a sulfonic acid moiety; and a peroxide; wherein sulfuric acid, said compound comprising an amine moiety and a sulfonic acid moiety and said peroxide are present in a molar ratio of no less than 1:1:1. Also disclosed are methods of using such compositions for the decomposition of toxic chemicals such as cyanides.

Claims (15)

1. A method for the destruction of cyanide present in waste water, said method comprising:

providing said waste water;

exposing said waste water to a composition comprising:

sulfuric acid present in an amount ranging from 20 to 80 wt % of said composition;

a compound comprising an amine moiety and a sulfonic acid moiety selected from the group consisting of taurine and taurine derivatives; and

a peroxide;

for a period of time sufficient to degrade at least 80% of said cyanide present into non-cyanide containing compounds;

wherein said taurine derivatives are selected from the group consisting of: taurolidine; taurocholic acid; tauroselcholic acid; tauromustine; 5-taurinomethyluridine; 5-taurinomethyl-2-thiouridine; homotaurine (tramiprosate); acamprosate; taurates; and aminoalkylsulfonic acids where the alkyl is selected from the group consisting of C 1 -C 5 linear alkyl and C 1 -C 5 branched alkyl.

2. The method according to claim 1 , where said compound comprising an amine moiety and a sulfonic acid moiety is taurine.

3. The method according to claim 1 , where said sulfuric acid and said compound comprising an amine moiety and a sulfonic acid moiety are present in a molar ratio of no less than 3:1.

4. The method according to claim 1 , where the peroxide is hydrogen peroxide.

5. The method according to claim 1 , where said period of time is sufficient to degrade at least 90% of said cyanide present into non-cyanide containing compounds.

6. The method according to claim 1 , where said method is carried out under atmospheric pressure.

7. The method according to claim 1 , where said method is carried out under ambient temperature.

8. The method according to claim 1 , wherein the waste water is a result of heap leaching or vat leaching.

Assignments (2)
CHANGE OF NAME Recorded Apr 22, 2024
From: FLUID ENERGY GROUP LTD.
To: CHEMICAL EVOLUTION LTD.
Reel/Frame 067187/0147 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2023
From: PURDY, CLAY; WEISSENBERGER, MARKUS; PAGELS, MARKUS; WYNNYK, KYLE G.; DAWSON, KARL W.
To: FLUID ENERGY GROUP LTD.
Reel/Frame 063179/0742 →
Priority Claims (1)
CA CA 3110391 · Feb 25, 2021 · national
Continuity (1)
Related Publication 20220267178A1 · Aug 25, 2022
Cited By (3)
US 12,234,604 US 12,371,854 US 12,692,653