Method of in situ remediation of soils using a bioremediation composition including a time release material
A method of remediation of soil and groundwater containing hydrocarbons and halogenated compounds. The method includes introducing a remediation composition into the soil that includes: (a) a first bioremediation material including a first blend of organisms capable of degrading the hydrocarbons; (b) a second bioremediation material including a second blend of organisms differing from the first blend of organisms that is chosen for degrading the halogenated compounds; (c) an organic compound such as a complex carbohydrate (e.g., food grade starch); and (d) a third blend of organisms degrading the organic compound. The degrading of the organic compound breaks the complex carbohydrate into smaller molecules that are utilized by the microorganisms of at least one of the first and second bioremediation materials during the degrading of the hydrocarbons and the halogenated compounds. The first bioremediation composition typically includes activated carbon capable of adsorbing the hydrocarbons and the halogenated compounds.
1. A method of in situ remediation of contaminated media, comprising:
introducing into the contaminated media an aqueous suspension of a bioremediation composition,
wherein the bioremediation composition comprises:
a first bioremediation composition comprising a first blend of one or more organisms capable of degrading hydrocarbons;
a second bioremediation composition comprising a second blend of one or more organisms differing from the first blend of one or more organisms and being capable of degrading at least one halogenated compound;
an organic compound; and
a third blend of one or more organisms capable of degrading the organic compound, wherein the organic compound comprises at least one of starch and chitin.
2. The method of claim 1 , wherein degrading of the organic compound by the third blend of one or more organisms comprises, over a time period of at least 20 days, breaking the organic compound into a plurality of smaller molecules utilized by the second blend of one or more organisms of the second bioremediation composition during the degrading of the at least one halogenated compound.
3. The method of claim 1 , wherein the first bioremediation composition further comprises an adsorbent capable of adsorbing hydrocarbons and a compound that releases sulfate over a period of time and wherein the first blend of one or more organisms comprises a nutrient system for promoting growth of microorganisms capable of metabolizing the hydrocarbons.
4. The method of claim 3 , wherein the adsorbent comprises activated carbon and wherein the sulfate-containing compound comprises calcium sulfate.
5. The method of claim 4 , wherein the nutrient system includes a nitrogen source and a phosphorous source.
6. The method of claim 5 , wherein the nitrogen source comprises an ammonium salt and the phosphorous source comprises a monobasic alkali-metal phosphate.
7. The method of claim 5 , wherein the nitrogen source comprises ammonia and ammonium nitrate in a molar ratio of about 2.3 to 1.
8. A method of in situ remediation of contaminated media, comprising:
forming a bioremediation composition for remediation of soil, sludge, wastewater, or groundwater containing contaminants by mixing: (a) a first bioremediation material comprising at least one organism capable of degrading a first contaminant; (b) a second bioremediation material comprising at least one organism capable of degrading a second contaminant; and (c) a time release substrate combined with the first and second bioremediation materials;
forming an aqueous suspension of the bioremediation composition; and
introducing into the contaminated media the aqueous suspension of the bioremediation composition,
wherein the organic compound comprises at least one of starch and chitin,
wherein the time release substrate includes an organic compound and a third bioremediation material, mixed with the organic compound,
wherein the third bioremediation material comprises at least one organism capable of degrading the organic compound for use by the organisms of at least one of the first and second bioremediation materials during the degrading of the first and second contaminants, and
wherein the degrading of the organic compound by the organisms of the third bioremediation material is performed over a time period of at least 20 days.
9. The method of claim 8 , wherein the first contaminant includes a hydrocarbon and the second contaminant includes a halogenated compound.
10. The method of claim 8 , wherein degrading of the organic compound by the organisms of the third bioremediation material comprises breaking the organic compound into a plurality of smaller molecules utilized by the organisms of at least one of the first and second bioremediation materials during the degrading of the first and second contaminants.
11. The method of claim 8 , wherein the first remediation material comprises activated carbon capable of adsorbing the first and second contaminants.
12. The method of claim 11 , wherein the activated carbon has a surface area between about 800 and 2000 m 2 /g.
13. The method of claim 8 , wherein the first bioremediation material further comprises an adsorbent capable of adsorbing hydrocarbons and a compound that releases sulfate over a period of time and wherein the first bioremediation material comprises a nutrient system for promoting growth of microorganisms capable of metabolizing the adsorbed hydrocarbons.
14. The method of claim 13 , wherein the adsorbent comprises activated carbon and wherein the sulfate-containing compound comprises calcium sulfate.
15. The method of claim 13 , wherein the nutrient system includes a sulfide scavenging agent.
16. The method of claim 15 , wherein the sulfide scavenging agent comprises iron sulfate.
17. The method of claim 13 , wherein the nutrient system includes a nitrogen source and a phosphorous source.
18. The method of claim 17 , wherein the nitrogen source comprises an ammonium salt and the phosphorous source comprises a monobasic alkali-metal phosphate.
19. The method of claim 17 , wherein the nitrogen source comprises ammonia and ammonium nitrate in a molar ratio of about 2.3 to 1.
20. A method of in situ remediation of contaminated media, comprising:
preparing a bioremediation composition by mixing: (a) a first bioremediation composition comprising a first blend of one or more organisms capable of degrading hydrocarbons; (b) a second bioremediation composition comprising a second blend of one or more organisms differing from the first blend of one or more organisms and being capable of degrading at least one halogenated compound; (c) an organic compound; and (d) a third blend of one or more organisms capable of degrading the organic compound; and
introducing the bioremediation composition into the contaminated media,
wherein the degrading of the organic compound by the third blend of one or more organisms comprises, over a time period of at least 20 days, breaking the organic compound into a plurality of smaller molecules utilized by the second blend of one or more organisms of the second bioremediation composition during the degrading of the at least one halogenated compound, and
wherein the organic compound comprises at least one of starch and chitin.
21. The method of claim 20 , wherein the first bioremediation composition further comprises an adsorbent capable of adsorbing hydrocarbons and a compound that releases sulfate over a period of time, wherein the first blend of one or more organisms comprises a nutrient system for promoting growth of microorganisms capable of metabolizing the hydrocarbons, and wherein the adsorbent comprises activated carbon.
22. The method of claim 21 , wherein the nutrient system includes a nitrogen source and a phosphorous source.
23. The method of claim 22 , wherein the nitrogen source comprises an ammonium salt and the phosphorous source comprises a monobasic alkali-metal phosphate.
24. The method of claim 22 , wherein the nitrogen source comprises ammonia and ammonium nitrate in a molar ratio of about 2.3 to 1.