POLYMER IMMOBILIZATION MATRIX FOR CONTAINMENT OF HAZARDOUS MATERIALS AND METHODS OF USING THE SAME

Abstract

The present disclosure describes a unique, two-part, water-soluble polymer matrix material and a method of application that immobilizes a wide variety of loose powder or crystalline hazardous materials and renders them “safe” or at least “safer” for handling and transport. The polymer matrix material is a two-part polymer material comprising a liquid cross-linking polymer and a cross-linking agent, initiator, or biocide contained in a solution. The cross-linking agent functions to cross-link the polymer and cause it to harden in place.

Claims

1. A method of immobilizing a hazardous material comprising the steps of: identifying a hazardous material for immobilization; providing a polymer matrix material for immobilizing said hazardous material comprising a combination of: a first formulation of a crosslinking polymer, in concentrations less than 1% and as much as a fully saturated solution in solvent; and a second formulation of a cross-linking agent; applying the first formulation to the hazardous material to substantially cover the hazardous material; and applying the second formulation to the first formulation to cross-link and harden the hazardous material into an immobilized hazardous material.

2. The method of claim 1, further comprising the step of placing the immobilized hazardous material into a container for removal.

3. The method of claim 1, wherein the crosslinking polymer is selected from the group consisting of: Polyvinyl Alcohol (PVA), Starch, Cellulose, Protein and Gelatin, Agarose and chitosan, Chitosan, Guar Gum, Gellan gum, Glycol Chitosan, Hydroxamated alginates, Seleroglucan Poly (acrylic-co-vinylsulfonic) acid, Polyacrylamide, and polyacrylamide/guar gum graft copolymer.

4. The method of claim 2, wherein the crosslinking polymer is selected from the group consisting of: Polyvinyl Alcohol (PVA), Starch, Cellulose, Protein and Gelatin, Agarose and chitosan, Chitosan, Guar Gum, Gellan gum, Glycol Chitosan, Hydroxamated alginates, Seleroglucan Poly (acrylic-co-vinylsulfonic) acid, Polyacrylamide, and polyacrylamide/guar gum graft copolymer.

5. The method of claim 1, wherein the cross-linking agent is a multivalent metal ion salt or an organic material.

6. The method of claim 2, wherein the cross-linking agent is a multivalent metal ion salt or an organic material.

7. The method of claim 3, wherein the cross-linking agent is a multivalent metal ion salt or an organic material.

8. The method of claim 4, wherein the cross-linking agent is a multivalent metal ion salt or an organic material.

9. The method of claim 5, wherein said cross-linking agent is said multivalent metal ion salt, and wherein said multivalent metal ion salt includes one of AlCl.sub.3, CuCl.sub.2, CaCl.sub.2, FeCl.sub.3, and Zn(C.sub.2H.sub.3O.sub.2).

10. The method of claim 6, wherein said cross-linking agent is said multivalent metal ion salt, and wherein said multivalent metal ion salt includes one of AlCl.sub.3, CuCl.sub.2, CaCl.sub.2, FeCl.sub.3, and Zn(C.sub.2H.sub.3O.sub.2).

11. The method of claim 7, wherein said cross-linking agent is said multivalent metal ion salt, and wherein said multivalent metal ion salt includes one of AlCl.sub.3, CuCl.sub.2, CaCl.sub.2, FeCl.sub.3, and Zn(C.sub.2H.sub.3O.sub.2).

12. The method of claim 8, wherein said cross-linking agent is said multivalent metal ion salt, and wherein said multivalent metal ion salt includes one of AlCl.sub.3, CuCl.sub.2, CaCl.sub.2, FeCl.sub.3, and Zn(C.sub.2H.sub.3O.sub.2).

13. The polymer matrix material of claim 5, wherein said cross-linking agent is said organic material, and wherein said organic material includes one of glyoxal, glutaraldehyde, and epichlorohydrin.

14. The polymer matrix material of claim 6, wherein said cross-linking agent is said organic material, and wherein said organic material includes one of glyoxal, glutaraldehyde, and epichlorohydrin.

15. The polymer matrix material of claim 7, wherein said cross-linking agent is said organic material, and wherein said organic material includes one of glyoxal, glutaraldehyde, and epichlorohydrin.

16. The polymer matrix material of claim 8, wherein said cross-linking agent is said organic material, and wherein said organic material includes one of glyoxal, glutaraldehyde, and epichlorohydrin.

17. The method of claim 1, wherein the second formulation includes a biocide.

18. The method of claim 3, wherein the second formulation includes a biocide.

19. The method of claim 5, wherein the second formulation includes a biocide.

20. The method of claim 7, wherein the second formulation includes a biocide.

21. The method of claim 9, wherein the second formulation includes a biocide.

22. The method of claim 11, wherein the second formulation includes a biocide.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0010] While the specification concludes with claims particularly pointing out and distinctly claiming particular embodiments of the instant invention, various embodiments of the invention can be more readily understood and appreciated from the following descriptions of various embodiments of the invention when read in conjunction with the accompanying drawings in which:

[0011] FIGS. 1A and 1B illustrate one exemplary formulation for the instant two-part, water soluble polymer matrix materials;

[0012] FIGS. 2A-C illustrates exemplary form factors for the part one hydrogel materials;

[0013] FIGS. 3A-C illustrates an exemplary preparation of the part one hydrogel material from a concentrate material formulation;

[0014] FIGS. 4A-F illustrates an exemplary method of application of the part one hydrogel to a hazardous material and further application of the part two cross-linking agent to harden the material for removal;

[0015] FIG. 5 chemically illustrates an example of the cross-linking action when the cross-linking agent is applied to the part one polymer material;

[0016] FIG. 6 illustrates exemplary testing of the reduced sensitivity of an explosive material treated with the present immobilization material; and

[0017] FIGS. 7a and 7b illustrate an exemplary use of the formulation to encapsulate and immobilize a volatile material.

DETAILED DESCRIPTION OF THE EXEMPLARY EMBODIMENTS

[0018] Referring now to the drawings, exemplary embodiments of the invention are generally described and illustrated in the attached figures.

[0019] Referring to FIGS. 1-7, the present disclosure teaches a novel two-part, water soluble polymer matrix material and a method of application that immobilizes a wide variety of hazardous materials and renders them “safe” or at least “safer” for handling and transport.

[0020] Referring to FIGS. 1-7, the present disclosure teaches a novel two-part, water soluble polymer matrix material and a method of application that can immobilize a wide variety of hazardous materials and renders them “safe” or at least “safer” for handling and transport. The instant two-part material thereby renders otherwise unsafe materials transportable to aid in protecting the public, or other officials, by removing them from areas which the public would otherwise have access to.

[0021] Referring to FIGS. 1A and 1B, the polymer matrix material in general can be a two-part polymer material comprising a liquid or gel cross-linking polymer (hydrogel) 100 and a cross-linking agent or cross-linking initiator 200 contained in a sprayable solution in a spray container 250. The cross-linking agent 200, when combined with the polymer material 100, can function to immediately cross-link the polymer 100 and cause it to harden in place. Once hardened, the potentially offending material can thus be rendered “inert” such that it can be deemed less of a threat and no longer be inhaled, exploded, or otherwise endanger those in the area.

PART ONE (Hydrogel Polymer)

[0022] The first part of the instant two-part material can generally include various water-soluble polymers, such as polyvinyl alcohol, agar, gelatin, and sodium alginate. Such materials 100 were found to be suitable for use as Part One of the instant material. An exemplary, but not exhaustive, list of suitable polymers is set forth in Table 1 below. The polymer can preferably be in a ready-to-use liquid or gel form 110, shown in FIG. 3A, but can also be provided in a powder form 112 to be mixed with water or other appropriate solvent (ethanol/methanol) at the time of use. Alternatively, the polymer can be provided in a concentrate form in a syringe 120, to be mixed with water or other solvent 125 at the time of use, as shown in FIG. 2B. Examples of gel concentrate and ready-to-use materials are illustrated in FIG. 2C in a syringe 130.

TABLE-US-00001 Polymer Crosslinker Poly Vinyl Alcohol Sodium Borate, Boric Acid, and Glyoxal Starch Glyoxal Cellulose Glyoxal Protein and Gelatin Glyoxal Agarose and chitosan Oxidized dextrin Chitosan Glutaraldehyde Guar Gum Epichlorohydrin Gellan gum Endogen Polyamine spermidine Glycol Chitosan Oxidized Alginate Hydroxamated alginates +2 and +3 Metal Cations Seleroglucan Borax Poly (acrylic-co-vinylsulfonic) acid Ethylene glyco dimethacrylate Polyacrylamide N,N′-methlynebisacrylamide Polyacrylamide/guar gum graft copolymer Glutaraldehyde

[0023] In one example, FIG. 3A illustrates one exemplary method of mixing a concentrated hydrogel polymer 120 into a water 125 for use in the field. In a preferred exemplary composition, a solution of water, sodium alginate, and an organic solvent can be combined. The percent of sodium alginate can vary depending on the form factor and in one use case can account for 1% to 20% percent of the total solution. Appropriate organic solvents can include, but are not limited to, methanol, ethanol, and isopropanol. The percent of organic solvent used can be between 1% to 50% percent with 5% to 20% being preferred of the total solution. Once combined, the concentrated hydrogel polymer 120 and solvent 125, can be shaken for two minutes, or until mixed.

Part Two (Cross-Linking Agent)

[0024] Referring back to FIG. 1, an exemplary cross-linking solution 200 can include a metal salt with a cation of +2 or +3 charge. Appropriate examples of metal salts include, but are not limited to, calcium, zinc, iron, aluminum, copper, nickel, and magnesium salts with salts of calcium, zinc, and iron being preferred. The percent of salt in Part Two can vary between 10% to 50% of the total solution, with 15% being a preferred example. Other cross-linking agents can be used for different hydrogels, examples of suitable cross-linking agent are included in TABLE 1 above. The cross-linking agent 200 can preferably be deployed in a solvent as a sprayable material, in a spray bottle 250, for quick and easy application over a wide surface area.

[0025] In another exemplary embodiment, a biocide can be added to the cross-linking solution to retard the growth of any biological materials within the Part One composition. Biocides include but are not limited to calcium hypochlorite and sodium hypochlorite.

[0026] FIGS. 4A-F illustrate an exemplary embodiment of the chemical interaction and cross-linking of the polymer chains when the cross-linking agent is applied. In general, a hazardous material 300 can be found or identified by a member of the public or an official, as shown in FIG. 4A. An officer, agent or other first responder, can then determine that it is necessary to immobilize the aforementioned hazardous material 300 to protect themselves during removal or the public at large. As shown in FIG. 4B, the user can apply the Part One composition 330 to the target material until full coverage of the area of is achieved such that the hazardous material 300 is isolated, as shown in FIG. 4C. Once the hazardous material is isolated 300a, the user or first responder can then apply the Part Two composition 350 as shown in FIG. 4D, by the use of a spray bottle for example. After application of the Part Two composition 350, the Part One 330 and Part Two 350 compositions can be crosslinked 400 to harden the material, as shown in FIG. 5. After the cross-linking occurs, the now cross-linked polymer matrix 400 is hardened, as shown in FIG. 4E, and the encapsulated material 300b can be picked up and removed. In some embodiments, the process can be completed in a time frame of less than one minute. In some instances, the encapsulated and hardened hazardous material 300b can be placed in a sample container 360 for further testing in a lab like setting, as shown in FIG. 4F.

[0027] Advantageously, the solidified (encapsulated) explosive 300b can, as shown in FIG. 6, exhibit increased safety threshold margins. For example, the resultant hazardous material can have increased thresholds for initiation by electrical discharge (ESD), friction, and impact as compared to an explosive material (TATP) by itself. Testing of the instant two-part matrix material shows an insensitivity to impact initiation at maximum height of instrument, a 15 times improvement in electrostatic discharge initiation, and a 150 times improvement in friction initiation.

[0028] Turning to FIGS. 7A-7B, the polymer and initiation as described hereinabove can also be used to encapsulate volatile materials 500 which emit questionable and potentially dangerous fumes 502 into the surrounding air (FIG. 7A). Once the volatile materials 500 are encapsulated with the cross-linked matrix 400, the volatile material 500 may have a dramatically lower mobility and thus increase the ability to safely handle the material. 500 (FIG. 7).

[0029] While there is shown and described herein certain specific structures embodying various embodiments of the invention, it will be manifest to those skilled in the art that various modifications and rearrangements of the parts may be made without departing from the spirit and scope of the underlying inventive concept and that the same is not limited to the particular forms herein shown and described except insofar as indicated by the scope of the appended claims.