Spectrophotometric determination of gas phase compositions

• US 6,794,649 B2
• Filed: 07/09/2001
• Issued: 09/21/2004
• Est. Priority Date: 07/09/2001
• Status: Expired due to Fees

• Current Assignee: Care Biopharma LLC
• Original Assignee: Pharmaceutical Systems, Inc.
• Inventors: Thrash, Robert J., Cullen, Thomas F., Fisher, Jimmy, Khorzad, Davoud
• Primary Examiner(s): Porta, David
• Assistant Examiner(s): Sung, Christine
• Application Number:
  US09/901,221
• Publication Number:
  US 20030006375A1
• Time in Patent Office: 1,170 Days
• Field of Search: 250/339.13, 250/339.12, 250/339.06, 250/339.01, 250/338.1, 250/336.1
• US Class Current: 250/339.13
• CPC Class Codes: G01N 21/3504 for analysing gases, e.g. multi-gas analysis

Abstract

Methods are disclosed for determining the monotonic functional relationship between (A) the integrated absorbance of spectral energy within a spectral region of interest of an analyte (i) that decomposes during the time experimental spectral data for determining the relationship are being obtained, or (ii) whose spectral data are pressure sensitive at pressures below a given pressure, or (iii) that decomposes during the time the spectral data are being obtained and whose spectral data are pressure sensitive and (B) the concentration of the analyte before decomposition commences. Methods are also disclosed for using the monotonic functional relationship to determine the concentration of the analyte in an unknown from the integrated absorbance of spectral energy within the spectral region of interest for the unknown. The methods are useful for determining the concentration of gaseous analytes, such as hydrogen peroxide, whose concentrations must be accurately and rapidly determined in processes such as sterilization processes at the time the processes are being conducted.

Claims

1. A method for determining the monotonic functional relationship between (A) the integrated absorbance of spectral energy within a spectral region of interest of an analyte that decomposes during the time experimental spectral data for determining the relationship are being obtained and whose spectral data are pressure sensitive below a total pressure P and (B) the concentration of the analyte before decomposition commences, the method comprising the steps:

(a) for a first known initial concentration of the analyte and while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P;

(i) determining the integrated absorbance of spectral energy within the spectral region of interest at a first time after the commencement of the obtention of spectral data, (ii) determining the integrated absorbance of spectral energy within the spectral region of interest at one or more times subsequent to the first time and different from each other if more than one subsequent time is used, and (iii) extrapolating from the integrated absorbance for the first time and the one or more subsequent times to the time at which the decomposition of the analyte commences to thereby establish at a time before the decomposition commences an estimated integrated absorbance of spectral energy within the spectral region of interest for the first known initial concentration;

(b) for each of one or more additional known initial concentrations of the analyte different from the first known concentration and different from each other if more than one additional initial concentration is used and while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P;

(i) determining the integrated absorbance of spectral energy within the spectral region of interest at a first time after the commencement of the obtention of spectral data, (ii) determining the integrated absorbance of spectral energy within the spectral region of interest at one or more times subsequent to the first time and different from each other if more than one subsequent time is used, and (iii) extrapolating from the integrated absorbance for the first time and the one or more subsequent times to the time at which the decomposition of the analyte commences to thereby establish at a time before the decomposition commences an estimated integrated absorbance of spectral energy within the spectral region of interest for each of the one or more additional known initial concentrations; and

(c) associating each of the known initial concentrations with its respective estimated integrated absorbance of spectral energy within the spectral region of interest to thereby determine for the analyte at a total pressure not less than pressure P the monotonic functional relationship between the concentration before the decomposition commences and the integrated absorbance of spectral energy within the spectral region of interest of the analyte.

2. The method of claim 1 further comprising determining pressure P prior to carrying out steps (a), (b), and (c).

3. The method of claim 1 further comprising maintaining the total pressure in each of steps (a) and (b) at a total pressure not less than pressure P by adding to the analyte as needed to raise the pressure a gas that is inert to the analyte.

4. The method of claim 3 wherein the gas that is inert to the analyte is dry air.

5. The method of claim 1 wherein the analyte is a sterilant.

6. The method of claim 1 wherein the analyte is a volatile inorganic or organic peroxidant.

7. The method of claim 6 wherein the analyte is hydrogen peroxide.

8. The method of claim 1 wherein the spectral region of interest is the infrared region.

9. The method of claim 8 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

10. A method for determining in an unknown the concentration of an analyte that decomposes and whose spectral data are pressure sensitive below a total pressure P, the method comprising the steps:

(d) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, carrying out the method of claim 1 to determine the monotonic functional relationship for the analyte, (e) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance for the unknown within the spectral region of interest, and (f) from the monotonic functional relationship determined in step (d) and the integrated absorbance determined in step (e), determining the concentration of the analyte in the unknown.

11. The method of claim 10 wherein the analyte is a sterilant.

12. The method of claim 10 wherein the analyte is a volatile inorganic or organic peroxidant.

13. The method of claim 10 wherein the analyte is hydrogen peroxide.

14. The method of claim 10 wherein the spectral region of interest is the infrared region.

15. The method of claim 14 wherein the spectral region of interest is from about 1180 cm, to about 1331 cm⁻

1.

16. A method for determining in an unknown the concentration of an analyte that decomposes and whose spectral data are pressure sensitive below a total pressure P, a monotonic functional relationship between the concentration of the analyte and integrated absorbance at a total pressure not less than pressure P having been previously established using the method of claim 1, the method comprising the steps:

(a) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance for the unknown within the spectral region of interest and (b) from the monotonic functional relationship previously determined at a total pressure not less than pressure P using the method of claim 1, and the integrated absorbance determined in step (a), determining the concentration of the analyte in the unknown.

17. The method of claim 16 wherein the analyte is a sterilant.

18. The method of claim 16 wherein the analyte is a volatile inorganic or organic peroxidant.

19. The method of claim 16 wherein the analyte is hydrogen peroxide.

20. The method of claim 16 wherein the spectral region of interest is the infrared region.

21. The method of claim 20 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

22. A method for determining the monotonic functional relationship between (A) the integrated absorbance of spectral energy within a spectral region of interest of an analyte that is a peracid or a peroxide and that decomposes during the time experimental spectral data for determining the relationship are being obtained and (B) the concentration of the analyte before decomposition commences, the method comprising the steps:

(a) for a first known initial concentration of the analyte;

(i) determining the integrated absorbance of spectral energy within the spectral region of interest at a first time after the commencement of the obtention of spectral data, (ii) determining the integrated absorbance of spectral energy within the spectral region of interest at one or more times subsequent to the first time and different from each other if more than one subsequent time is used, and (iii) extrapolating from the integrated absorbance for the first time and the one or more subsequent times to the time at which the decomposition of the analyte commences to thereby establish at a time before the decomposition commences an estimated integrated absorbance of spectral energy within the spectral region of interest for the first known initial concentration;

(b) for each of one or more additional known initial concentrations of the analyte different from the first known concentration and different from each other if more than one additional initial concentration is used;

(i) determining the integrated absorbance of spectral energy within the spectral region of interest at a first time after the commencement of the obtention of spectral data, (ii) determining the integrated absorbance of spectral energy within the spectral region of interest at one or more times subsequent to the first time and different from each other if more than one subsequent time is used, and (iii) extrapolating from the integrated absorbance for the first time and the one or more subsequent times to the time at which the decomposition of the analyte commences to thereby establish at a time before the decomposition commences an estimated integrated absorbance of spectral energy within the spectral region of interest for each of the one or more additional known initial concentrations; and

(c) associating each of the known initial concentrations with its respective estimated integrated absorbance of spectral energy within the spectral region of interest to thereby determine for the analyte the monotonic functional relationship between the concentration before the decomposition commences and the integrated absorbance of spectral energy within the spectral region of interest of the analyte.

23. The method of claim 22 wherein the analyte is a sterilant.

24. The method of claim 22 wherein the analyte is a peroxide.

25. The method of claim 22 wherein the analyte is hydrogen peroxide.

26. The method of claim 22 wherein the spectral region of interest is the infrared region.

27. The method of claim 26 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

28. The method of claim 22 wherein the monotonic functional relationship is established for the analyte in the gas phase.

29. The method of claim 28 wherein the analyte is a sterilant.

30. The method of claim 28 wherein the analyte is a volatile peroxide.

31. The method of claim 28 wherein the analyte is hydrogen peroxide.

32. The method of claim 28 wherein the spectral region of interest is the infrared region.

33. The method of claim 32 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

34. A method for determining in an unknown the concentration of an analyte that is a peracid or a peroxide and that decomposes, the method comprising the steps:

(d) carrying out the method of claim 22 to determine the monotonic functional relationship for the analyte, (e) determining the integrated absorbance for the unknown within the spectral region of interest, and (f) from the monotonic functional relationship determined in step (d) and the integrated absorbance determined in step (e), determining the concentration of the analyte in the unknown.

35. The method of claim 34 wherein the analyte is a sterilant.

36. The method of claim 34 wherein the analyte is a peroxide.

37. The method of claim 34 wherein the analyte is hydrogen peroxide.

38. The method of claim 34 wherein the spectral region of interest is the infrared region.

39. The method of claim 38 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

40. The method of claim 34 wherein the monotonic functional relationship is established for the analyte in the gas phase.

41. The method of claim 40 wherein the analyte is a sterilant.

42. The method of claim 40 wherein the analyte is a volatile peroxide.

43. The method of claim 40 wherein the analyte is hydrogen peroxide.

44. The method of claim 40 wherein the spectral region of interest is the infrared region.

45. The method of claim 44 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

46. A method for determining in an unknown the concentration of an analyte that is a peracid or a peroxide and that decomposes, a monotonic functional relationship between the concentration of the analyte and integrated absorbance having been previously established using the method of claim 22, the method comprising the steps:

(a) determining the integrated absorbance for the unknown within the spectral region of interest and (b) from the monotonic functional relationship previously determined using the method of claim 22 and the integrated absorbance determined in step (a), determining the concentration of the analyte in the unknown.

47. The method of claim 46 wherein the analyte is a sterilant.

48. The method of claim 46 wherein the analyte is a peroxide.

49. The method of claim 46 wherein the analyte is hydrogen peroxide.

50. The method of claim 46 wherein the spectral region of interest is the infrared region.

51. The method of claim 50 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

52. The method of claim 46 wherein the monotonic functional relationship was established for the analyte in the gas phase.

53. The method of claim 52 wherein the analyte is a sterilant.

54. The method of claim 52 wherein the analyte is a volatile peroxide.

55. The method of claim 52 wherein the analyte is hydrogen peroxide.

56. The method of claim 52 wherein the spectral region of interest is the infrared region.

57. The method of claim 56 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

58. A method for determining the monotonic functional relationship between (A) the integrated absorbance of spectral energy within a spectral region of interest of an analyte in the gas phase whose spectral data are pressure sensitive below total pressure P and (B) the concentration of the analyte, the method comprising the steps:

(a) for a first known initial concentration of the analyte and while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance of spectral energy within the spectral region of interest for the first known initial concentration;

(b) for each of one or more additional known initial concentrations of the analyte different from the first known concentration and different from each other if more than one additional initial concentration is used and while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance of spectral energy within the spectral region of interest for each of the one or more additional known initial concentrations; and

(c) associating each of the known initial concentrations with its respective integrated absorbance of spectral energy within the spectral region of interest to thereby determine for the analyte at a total pressure not less than pressure P the monotonic functional relationship between the concentration and the integrated absorbance of spectral energy within the spectral region of interest of the analyte.

59. The method of claim 58 further comprising determining pressure P prior to carrying out steps (a), (b), and (c).

60. The method of claim 58 further comprising maintaining the total pressure in each of steps (a) and (b) at a total pressure not less than pressure P by adding to the analyte as needed to raise the pressure a gas that is inert to the analyte.

61. The method of claim 60 wherein the gas that is inert to the analyte is dry air.

62. The method of claim 58 wherein the analyte is a sterilant.

63. The method of claim 58 wherein the analyte is an inorganic or organic peroxidant.

64. The method of claim 58 wherein the analyte is hydrogen peroxide.

65. The method of claim 58 wherein the spectral region of interest is the infrared region.

66. The method of claim 65 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

67. A method for determining in a gas phase unknown the concentration of an analyte whose spectral data are pressure sensitive below a total pressure P, the method comprising the steps:

(d) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, carrying out the method of claim 58 to determine the monotonic functional relationship for the analyte, (e) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance for the unknown within the spectral region of interest, and (f) from the monotonic functional relationship determined in step (d) and the integrated absorbance determined in step (e), determining the concentration of the analyte in the unknown.

68. The method of claim 67 further comprising maintaining the total pressure in each of steps (d) and (e) at a total pressure not less than pressure P by adding to the analyte as needed to raise the pressure a gas that is inert to the analyte.

69. The method of claim 68 wherein the gas that is inert to the analyte is dry air.

70. The method of claim 67 wherein the analyte is a sterilant.

71. The method of claim 67 wherein the analyte is an inorganic or organic peroxidant.

72. The method of claim 67 wherein the analyte is hydrogen peroxide.

73. The method of claim 67 wherein the spectral region of interest is the infrared region.

74. The method of claim 73 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.

75. A method for determining in an unknown the concentration of an analyte whose spectral data are pressure sensitive below a total pressure P, a monotonic functional relationship between the concentration of the analyte and integrated absorbance having been previously established using the method of claim 58, the method comprising the steps:

(a) while intentionally maintaining the total pressure at a pressure not less than pressure P because of the spectral data being pressure sensitive below pressure P, determining the integrated absorbance for the unknown within the spectral region of interest and (b) from the monotonic functional relationship previously determined using the method of claim 58 and the integrated absorbance determined in step (a), determining the concentration of the analyte in the unknown.

76. The method of claim 75 further comprising maintaining the total pressure in step (a) at a total pressure not less than pressure P by adding to the analyte as needed to raise the pressure a gas that is inert to the analyte.

77. The method of claim 76 wherein the gas that is inert to the analyte is dry air.

78. The method of claim 75 wherein the analyte is a sterilant.

79. The method of claim 75 wherein the analyte is an inorganic or organic peroxidant.

80. The method of claim 75 wherein the analyte is hydrogen peroxide.

81. The method of claim 75 wherein the spectral region of interest is the infrared region.

82. The method of claim 81 wherein the spectral region of interest is from about 1180 cm⁻

1 to about 1331 cm<sup>−

1</sup>.