Microbial deactivation of explosive compositions

Patent metadata

Field	Value
Publication number	US-9814918-B2
Application number	US-201314376339-A
Country	US
Kind code	B2
Filing date	Jan 29, 2013
Priority date	Feb 2, 2012
Publication date	Nov 14, 2017
Grant date	Nov 14, 2017

Abstract

A method of deactivating an explosive composition being used in a blasting operation, which method comprises exposing the explosive composition to a micro-organism that is indigenous to the environment in which the explosive composition is being used and that is capable of producing an enzyme that degrades the explosive composition, wherein the explosive composition has associated with it a chemical inducing agent that promotes production of the enzyme by the micro-organism.

First claim

The claims defining the invention are as follows:

1. A method, comprising:
placing an explosive cartridge containing an explosive composition and a Michael acceptor into an environment of a blasting operation, the explosive cartridge being detonable when placed into the environment, the environment containing a microorganism indigenous to the environment, the microorganism capable of producing an enzyme that degrades the explosive composition, the Michael acceptor promoting production of the enzyme by the microorganism, placing the explosive cartridge into the environment exposing the Michael acceptor and the explosive composition to the microorganism; and
allowing the enzyme produced by the microorganism to degrade the explosive composition thereby deactivating the explosive composition and rendering the explosive cartridge non-detonable.

2. The method of claim 1 , wherein the microorganism is selected from the group consisting of Pseudomonas spp., Escherichia coli, Morganella morganii, Rhodococcus spp., Comamanos spp., Agrobacterium radiobacter, Enterobacter cloacae, Agrobacterium tumifaciens, Klebsiella pneumonia, and Gibberella moniliformis.

3. The method of claim 1 , wherein the enzyme that degrades the explosive composition is selected from the group consisting of Old Yellow Enzyme (OYE), a glycerol trinitrate (GTN) reductase, a nitroreductase, and an N-ethyl maleimide (NEM) reductase.

4. The method of claim 1 , wherein the Michael acceptor is selected from menadione (vitamin K precursor), dimethyl maleate, 3-hydroxycoumarin, o-coumaric acid, trans-4-phenyl-3-buten-2-one, N-ethylmaleimide, dimethyl fumarate, diethyl maleate, and tert-butyl-hydroquinone.

5. The method of claim 1 , wherein:
the environment contains water; and
the microorganism is transported into the explosive cartridge by the water present in the environment.

6. The method of claim 5 , wherein the explosive cartridge comprises at least one of an inlet or a water-degradable pathway to allow environmental water to flow into the cartridge and directly into contact with the explosive composition and the chemical inducing agent provided in the explosive composition.

7. The method of claim 5 , wherein the explosive composition comprises channels to allow the water present in the environment to travel through it and into contact with the chemical inducing agent.

8. The method of claim 5 , wherein the explosive cartridge comprises a water-permeable or water-degradable outer shell surrounding the explosive composition.

9. The method of claim 1 , wherein the Michael acceptor is included in or on one or more outer walls of the explosive cartridge.

10. The method of claim 9 , wherein the one or more outer walls are direct contact with the explosive composition and are water-permeable, water-degradable or water-soluble.

11. The method of claim 1 , wherein:
the explosive composition is provided in a first chamber of the explosive cartridge;
the environment contains water; and
the Michael acceptor is provided in a second chamber of the explosive cartridge separate from the first chamber such that the water present in the environment enters the second chamber thereby bringing the microorganism into contact with the Michael acceptor.

12. The method of claim 1 , wherein:
the explosive composition comprises a nutrient source to support growth of the microorganism and expression of the enzyme; and
the nutrient source is different from the Michael acceptor.

13. The method of claim 1 , wherein the microorganism is a denitrifying bacteria.

14. The method of claim 1 , wherein the enzyme produced by the microorganism is a glycerol trinitrate (GTN) reductase.

15. The method of claim 1 , further comprising placing the explosive cartridge into the environment via a borehole, the explosive cartridge being detonable when placed into the environment, the microorganism being indigenous to and present within soil associated with the environment.

16. The method of claim 1 , wherein the microorganism is selected from the group consisting of Pseudomonas spp., Escherichia coli, Morganella morganii, Comamanos spp., Enterobacter cloacae, Klebsiella pneumonia , and Gibberella moniliformis.

17. The method of claim 1 , wherein the microorganism is Escherichia coli , and the Michael acceptor is diethyl maleate (DEME).

18. The method of claim 1 wherein the microorganism is Klebsiella pneumonia and the Michael acceptor is dimethyl fumarate (DMFU).

19. The method of claim 1 , wherein the microorganism is Pseudomonas spp. and the Michael acceptor is menadione (MD).

Assignees

• Orica Int Pte Ltd

Inventors

• Brearley Clint
• Kotsonis Steven
• Liu Kaiyan
• Smylie Thomas
• Goodridge Richard

Classifications

• C06B21/0091

  Elimination of undesirable or temporary components of an intermediate or finished product, e.g. making porous or low density products, purifying, stabilising, drying; Deactivating; Reclaiming; (porous inert particles or chemicals compounded for these purposes C06B23/00) · CPC title

• C12N9/0036

  acting on NADH or NADPH (1.6) · CPC title

• C12N9/0004

  Oxidoreductases (1.) · CPC title

• C12N9/0044

  acting on other nitrogen compounds as donors (1.7) · CPC title

• C12N9/001

  acting on the CH-CH group of donors (1.3) · CPC title