Method and apparatus for monitoring liquid for the presence of an additive

• US 7,919,325 B2
• Filed: 05/24/2004
• Issued: 04/05/2011
• Est. Priority Date: 05/24/2004
• Status: Active Grant

• Current Assignee: Authentix, Inc.
• Original Assignee: Authentix, Inc.
• Inventors: Al-Jafari, Mohammed Salem, Bergstrom, Edmund T., Goodall, David M., Dorland, Erwin, Eastwood, Ian M.
• Primary Examiner(s): Menon; Krishnan S
• Assistant Examiner(s): FRITCHMAN, REBECCA M
• Application Number:
  US10/852,336
• Publication Number:
  US 20050260764A1
• Time in Patent Office: 2,507 Days
• Field of Search: 436/56, 436/172
• US Class Current: 436/56
• CPC Class Codes: G01N 2021/6439 with indicators, stains, dyes, tags, labels, marks
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: Y10T 436/13 Tracers or tags

Abstract

The present invention relates to an apparatus and methods for the identification or authentication of liquid products by the addition of an anti-Stokes marker. The invention features an apparatus and method for the identification of a liquid, dynamic or static, that includes adding an anti-Stokes luminescent marker compound to the liquid followed by exposing the compound to a light source of a known wavelength or known wavelengths and then detecting one or more shorter wavelength emissions from the marker, where the identity of the liquid is confirmed by the emission wavelength or wavelengths that are detected and quantified. The irradiating source of light includes, but is not limited to, a laser and other conventional light sources.

Claims

1. A method for identifying a liquid comprising the steps of:

a) adding to the liquid a luminescent compound that absorbs electromagnetic radiation of a first wavelength and emits fluorescent light of a second wavelength which is shorter than the first wavelength, wherein the compound comprises atoms selected from the groups consisting of ytterbium and erbium;

ytterbium and thulium ytterbium and holmium; and

ytterbium and terbium,

b) exposing the compound to electromagnetic radiation of the first wavelength; and

,

c) detecting electromagnetic radiation of the second wavelength, thereby identifying the liquid.

2. The method of claim 1, wherein the compound is present in the liquid at a concentration of less than or equal to 10 parts per million.

3. The method of claim 2, wherein the compound is present in the liquid at a concentration of less than or equal to 1 part per million.

4. The method of claim 3, wherein the compound is present in the liquid at a concentration of less than or equal to 0.1 part per million.

5. The method of claim 1, wherein a laser is the source of the electromagnetic radiation of step b).

6. The method of claim 1, wherein in step c) the radiation of the second wavelength is quantified.

7. The method of claim 1, wherein the liquid is selected from the group consisting of a petroleum product, a perfume, water, a beverage, an agrochemical, a bulk liquid, and an additive for fuels or lubricants.

8. The method of claim 7 wherein the liquid is a petroleum product.

9. The method of claim 8 wherein the compound is used to differentiate a petroleum product in a pipeline.

10. The method of claim 1, wherein the wavelength of step b) is 300 nm to 1800 nm.

11. The method of claim 10, wherein the wavelength of step b) is 900 nm to 1100 nm.

12. The method of claim 11, wherein the wavelength of step b) is 960 nm to 985 nm.

13. The method of claim 10, wherein the wavelength of step b) is 1500 nm to 1600 nm.

14. The method of claim 1, wherein the emission of electromagnetic radiation of step c) is within the wavelength range of 300 nm to 1800 nm.

15. The method of claim 14, wherein the emission of electromagnetic radiation of step c) is within the wavelength range of 300 nm to 799 nm.

16. The method of claim 14, wherein the emission of electromagnetic radiation of step c) is within the wavelength range of 800 nm to 1050 nm.

17. The method of claim 1, wherein the liquid contains more than luminescent compound.

18. The method of claim 17, wherein each of the luminescent compounds in the liquid absorbs light of a wavelength or wavelength range that does not overlap that absorbed by any other luminescent compound in the liquid.

19. The method of claim 17 comprising the steps of:

a) adding two or more luminescent compounds to the liquid;

b) exposing the liquid to a first electromagnetic radiation of a first wavelength;

c) exposing the liquid to a second electromagnetic radiation of a second wavelength;

d) detecting a first emission of electromagnetic radiation from the liquid at a shorter wavelength than the wavelength of step b); and

,

e) detecting a second emission of electromagnetic radiation from the liquid at a shorter wavelength than the wavelength of step c), whereby the emissions of steps d) and e) identifies the liquid.

20. The method of claim 19, wherein the first electromagnetic radiation of step d) is within the range of about 300 nm to 1800 nm and the second electromagnetic radiation of step e) is within the range of about 300 nm to 1800 nm, but not within the first electromagnetic radiation.

21. The method of claim 20, wherein the first electromagnetic radiation of step d) is within the range of about 300 nm to 799 nm and the second electromagnetic radiation of step e) is within the range of about 800 nm to 1050 nm.

22. The method of claim 19, wherein the first electromagnetic radiation of step b) is within the range of about 800 nm to 1800 nm and the second electromagnetic radiation of step c) is within the range of about 800 nm to 1800 nm but not within the first electromagnetic radiation.

23. The method of claim 22, wherein the electromagnetic radiation of step b) is within the range of about 900 nm to 1100 nm and the electromagnetic radiation of step c) is within the range of about 1500 nm to 1600 nm.

24. The method of claim 1, wherein the compound is phosphorescent.

25. The method of claim 1, wherein the compound is incorporated into a gel, a particle composite, a vitroceramic matrix, or a polymer.

26. The method of claim 1, wherein the compound is dissolved in the liquid.

27. The method of claim 1, wherein the compound is a particle suspended in the liquid.

28. The method of claim 27, wherein the compound has a particle size diameter of less than or equal to 100 μ

m.

29. The method of claim 28, wherein the particle size is less than or equal to 10 μ

m.

30. The method of claim 29, wherein the particle size is less than or equal to 1 μ

m.

31. The method of claim 30, wherein the particle size is less than or equal to 300 nm.

32. The method of claim 31, wherein the particle size is less than or equal to 100 nm.

33. The method of claim 32, wherein the particle size is less than or equal to 10 nm.

34. The method of claim 27, wherein the particle is mono-dispersed.

35. The method of claim 27, wherein the particle is poly-dispersed.

36. The method of claim 27, wherein the particle is colloidal.

37. The method of claim 1, wherein the luminescent compound is bound to a second compound to form a composition.

38. The method of claim 37, further comprising binding the composition to a complementary binding member specific for the composition before exposing the compound to the electromagnetic radiation.

39. The method of claim 38, wherein the complementary binding member comprises a protein.

40. The method of claim 39, wherein the protein is an antibody.

41. The method of claim 38, wherein the complementary binding member comprises a saccharide moiety.

42. The method of claim 38, wherein the complementary binding member comprises a polynucleotide.

43. The method of claim 37, wherein the second compound comprises a polynucleotide.

44. The method of claim 37, wherein the second compound increases the solubility of the luminescent compound in the liquid.

45. The method of claim 44, wherein the second compound comprises a C₁ to C₂₄ alkyl group and/or a C₆ to C₃₀ aryl group, each of which can be substituted with from 1 to 6 hydroxy, C₁ to C₆ ether, C₃ to C₂₄ polyether, thio, C₁ to C₆ thioether, amino, C₁ to C₆ alkylamino, C₂ to C₁₂ dialkylamino, nitro, carboxy, carboxy-C₁ to C₆-alkyl, sulfoxy, carboxamido, carbox-C₁ to C₆-alkylamido, C₁ to C₆ alkylamido, C₆ to C₁₈ arylamido, C₁ to C₆ alkarylamido, C₁ to C₆ alkylimido, C₁ to C₆ alkylhydrazido, or C₆ to C₁₈ arylhydrazido groups.

46. The method of claim 1, the liquid further comprising additives to increase the solubility of the compound in the liquid.

47. The method of claim 37, wherein the second compound enhances the dispersion of the luminescent compound in the liquid.

48. The method of claim 47, wherein the second compound comprises a C₁ to C₂₄ alkyl group and/or a C₆ to C₃₀ aryl group, each of which is optionally substituted with from 1 to 6 hydroxy, C₁ to C₆ ether, C₃ to C₂₄ polyether, thio, C₁ to C₆ thioether, amino, C₁ to C₆ alkylamino, C₂ to C₁₂ dialkylamino, nitro, carboxy, carboxy-C₁ to C₆-alkyl, sulfoxy, carboxamido, carbox-C₁ to C₆-alkylamido, C₁ to C₆ alkylamido, C₆ to C₁₈ arylamido, C₁ to C₆ alkarylamido, C₁ to C₆ alkylimido, C₁ to C₆ alkylhydrazido, or C₆ to C₁₈ arylhydrazido groups.

49. The method of claim 47, wherein the second compound is a surfactant.

50. The method of claim 1, wherein the compound is an organic dye.