Characterization of organic contaminants and assessment of remediation performance in subsurface formations

• US 5,905,036 A
• Filed: 09/26/1997
• Issued: 05/18/1999
• Est. Priority Date: 01/23/1995
• Status: Expired due to Fees

• Current Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Original Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Inventors: Pope, Gary A., Jackson, Richard E.
• Primary Examiner(s): Redding, David A.
• Application Number:
  US08/938,236
• Time in Patent Office: 599 Days
• Field of Search: 73/152.18, 73/152.23, 73/152.24, 73/152.41, 73/152.42, 166/250.01, 166/252.2, 166/252.6, 166/250.03, 166/250.16, 436/25, 436/27, 436/28, 436/30, 436/262, 588/260
• US Class Current: 435/262
• CPC Class Codes: B09C 1/00 Reclamation of contaminated soil
• CPC Class Codes: B09C 2101/00 In situ
• CPC Class Codes: E21B 47/11 using tracers; using radioactivity
• CPC Class Codes: E21B 49/08 Obtaining fluid samples or testing fluids, in boreholes or wells
• CPC Class Codes: G01N 33/24 Earth materials G01N33/42 takes precedence

Abstract

Characterization of organic contaminants in subsurface formation is performed by methods for detecting the presence of nonaqueous phase liquid in a subsurface formation, and for determining the composition and for determining the volume of nonaqueous phase liquids. Generally the methods comprise introducing one or more partitioning tracers and one or more non-partitioning tracers at one or more injection points located in the subsurface formation and measuring separation between the one or more partitioning tracers and the one or more non-partitioning tracers from one or more sampling points located in the subsurface formation to determine presence, composition and/or volume of nonaqueous phase liquid in the subsurface formation. In addition, the methods can be used to assess the performance of an attempted remediation.

Claims

1. A method for determining a three dimensional distribution of nonaqueous phase liquid located in a subsurface formation, comprising:

(A) introducing one or more non-partitioning tracers and one or more partitioning tracers into one or more injection points located in the subsurface formation;

(B) withdrawing the one or more non-partitioning tracers and one or more partitioning tracers from one or more sampling points located in the subsurface formation;

wherein the introducing occurs at two or more depths or the withdrawing occurs at two or more depths or wherein both the withdrawing and the introducing occur at two or more depths; and

(C) measuring separation between the one or more non-partitioning tracers and the one or more partitioning tracers from the one or more sampling points to determine the three dimensional distribution of the nonaqueous phase liquid in the subsurface formation.

2. The method of claim 1, wherein the tracers are introduced at two or more injection points located in the subsurface formation, the two or more injection points being at different depths.

3. The method of claim 1, wherein samples are taken at two or more sampling points located in the subsurface formation, the two or more sampling points being at different depths.

4. The method of claim 1, wherein the injection point and the sampling point are the same.

5. The method of claim 1, wherein the nonaqueous phase liquid comprises one or more components and further comprising determining the composition of the nonaqueous phase liquid by:

expressing each tracer partitioning coefficient as a function of activity coefficients for two or more of said components; and

calculating the respective mole fractions for each of said two or more components and volume of total nonaqueous phase liquid by simultaneously solving the following equation expressed in terms of each of said components and said volume of total nonamueous phase liquid;

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p = the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said nonpartitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of NAPL.

6. The method of claim 1, further comprising:

performing an attempted remediation to treat or remove nonaqueous phase liquid in the subsurface formation;

repeating steps (A) and (B) to assess performance of the attempted remediation.

7. The method of claim 1, further comprising determining the volume of total nonaqueous phase liquid in the subsurface formation.

8. The method of claim 1, wherein the nonaqueous phase liquid is more dense than water.

9. The method of claim 8, wherein the nonaqueous phase liquid is a chlorinated hydrocarbon, creosote or coal tar.

10. The method of claim 1, wherein the distribution of the nonaqueous phase liquid is irregular.

11. The method of claim 1, wherein the nonaqueous phase liquid is located in a substantially unconfined formation.

12. The method of claim 1, wherein one or more of the one or more partitioning tracers are reactive tracers.

13. The method of claim 12, wherein at least one of the reactive tracers is chemically reactive.

14. The method of claim 12, wherein at least one of the reactive tracers is biologically reactive.

15. The method of claim 1, wherein a thickening agent is introduced with the tracers.

16. The method of claim 1, wherein said nonaqueous phase liquid is a dense non-aqueous phase liquid.

17. The method of claim 7, wherein said volume of total nonaqueous phase liquid in said subsurface formation is determined using the following equation:

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p = the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said nonpartitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of NAPL.

18. The method of claim 1, wherein one or more of the partitioning tracers is a substance which hydrolyzes to form an alcohol and a carboxylic acid.

19. The method of claim 1, wherein one or more of the partitioning tracers is capable of being used as a fuel or nutrient for microorganisms.

20. The method of claim 1, wherein the presence or absence of nonaqueous phase liquid in said subsurface formation is unknown.

21. A method for determining a three dimensional distribution of nonaqueous phase liquid located in a subsurface formation

(A) introducing one or more non-partitioning tracers and one or more partitioning tracers into one or more injection points located in the subsurface formation in which the presence or absence of nonaqueous phase liquid is unknown;

and

(B) withdrawing the one or more non-partitioning tracers and one or more partitioning tracers from one or more sampling points located in the subsurface formation;

wherein the introducing occurs at two or more depths or the withdrawing occurs at two or more depths or wherein both the withdrawing and the introducing occur at two or more depths; and

(C) measuring separation between the one or more non-partitioning tracers and the one or more partitioning tracers from the one or more sampling points to determine the three dimensional distribution of the nonaqueous phase liquid in the subsurface formation.

22. The method of claim 21, wherein the tracers are introduced at two or more injection points located in the subsurface formation, the two or more injection points being at different depths.

23. The method of claim 21, wherein samples are taken at two or more sampling points located in the subsurface formation, the two or more sampling points being at different depths.

24. The method of claim 21, wherein the injection point and the sampling point are the same.

25. The method of claim 21, wherein the nonaqueous phase liquid comprises one or more components, and further comprising determining the composition of the nonaqueous phase liquid by:

expressing each tracer partitioning coefficient as a function of activity coefficients for two or more of said components; and

calculating the respective mole fractions for each of said two or more components and volume of total nonaqueous phase liquid by simultaneously solving the following equation expressed in terms of each of said components and said volume of total nonaqueous phase liquid;

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p = the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said non partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of NAPL.

26. The method of claim 21, wherein the distribution of the nonaqueous phase liquid is irregular.

27. The method of claim 21, wherein the nonaqueous phase liquid is located in a substantially unconfined formation.

28. The method of claim 21, wherein one or more of the one or more partitioning tracers are reactive tracers.

29. The method of claim 28, wherein at least one of the reactive tracers is chemically reactive.

30. The method of claim 28, wherein at least one of the reactive tracers is biologically reactive.

31. The method of claim 21, wherein a thickening agent is introduced with the tracers.

32. The method of claim 21, further comprising determining a volume of the nonaqueous phase liquid in the subsurface formation.

33. The method of claim 32, wherein said volume of total nonaqueous phase liquid in said subsurface formation is determined using the following equation:

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p = the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said non partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of NAPL.

34. The method of claim 21, wherein one or more of the partitioning tracers is a substance which hydrolyzes to form an alcohol and a carboxylic acid.

35. The method of claim 21, wherein one or more of the partitioning tracers is capable of being used as a fuel or nutrient for microorganisms.

36. A method for determining a three dimensional distribution of dense nonaqueous phase liquid located in a subsurface formation

(A) introducing one or more non-partitioning tracers and one or more partitioning tracers into one or more injection points located in the subsurface formation in which the presence or absence of nonaqueous phase liquid is unknown;

and

(B) withdrawing the one or more non-partitioning tracers and one or more partitioning tracers from one or more sampling points located in the subsurface formation;

wherein the introducing occurs at two or more depths or the withdrawing occurs at two or more depths or wherein both the withdrawing and the introducing occur at two or more depths; and

(C) measuring separation between the one or more non-partitioning tracers and the one or more partitioning tracers from the one or more sampling points to determine the three dimensional distribution of the nonaqueous phase liquid in the subsurface formation.

37. The method of claim 36, further comprising determining a volume of dense nonaqueous phase liquid present in said subsurface formation.

38. The method of claim 37 wherein said volume of dense nonaqueous phase liquid in said surface formation is determined using the following equation:

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said nonpartitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of NAPL.

39. The method of claim 36, wherein the dense nonaqueous phase liquid is a chlorinated hydrocarbon, creosote or coal tar.

40. The method of claim 36, wherein the distribution of the dense nonaqueous phase liquid is irregular.

41. The method of claim 36, wherein the dense nonaqueous phase liquid is located in a substantially unconfined formation.

42. The method of claim 36, wherein one or more of the one or more partitioning tracers are reactive tracers.

43. The method of claim 42, wherein at least one of the reactive tracers is chemically reactive.

44. The method of claim 42, wherein at least one of the reactive tracers is biologically reactive.

45. The method of claim 36, wherein a thickening agent is introduced with the tracers.

46. The method of claim 36, wherein one or more of the partitioning tracers is a substance which hydrolyzes to form an alcohol and a carboxylic acid.

47. The method of claim 36, wherein one or more of the partitioning tracers is capable of being used as a fuel or nutrient for microorganisms.

48. The method of claim 36, wherein the dense nonaqueous phase liquid comprises one or more components, and further comprising determining the composition of the dense nonaqueous phase liquid by:

expressing each tracer partitioning coefficient as a function of activity coefficients for two or more of said components; and

calculating the respective mole fractions for each of said two or more components and volume of total dense nonaqueous phase liquid by simultaneously solving the following equation expressed in terms of each of said components and said volume of total dense nonaqueous phase liquid;

space="preserve" listing-type="equation">V.sub.N =(V.sub.p -V.sub.n)/K

where;

V_p = the first moment of one of said partitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

V_n = the first moment of one of said nonpartitioning tracers in terms of cumulative volume of detected tracer at the sampling point;

K is the partition coefficient of one of said partitioning tracers; and

V_N is the volume of dense nonaqueous phase liquid.