Method of measuring the ratio of isotopologue concentrations in the gas phase

• US 10,234,381 B2
• Filed: 12/28/2017
• Issued: 03/19/2019
• Est. Priority Date: 07/21/2017
• Status: Active Grant

• Current Assignee: Serguei Koulikov
• Original Assignee: Serguei Koulikov
• Inventors: Koulikov, Serguei
• Primary Examiner(s): Pham, Hoa Q
• Application Number:
  US15/857,607
• Publication Number:
  US 20190025201A1
• Time in Patent Office: 446 Days
• Field of Search: 356432-440, 25033913
• CPC Class Codes: G01J 3/42 Absorption spectrometry; Double beam spectrometry; Flicker spectrometry; Reflection spectrometry beam switching arrangements G01J3/08
• CPC Class Codes: G01N 2021/1704 in gases
• CPC Class Codes: G01N 2021/1748 Comparative step being essential in the method
• CPC Class Codes: G01N 2021/399 Diode laser
• CPC Class Codes: G01N 21/27 using photo-electric detection G01N21/31 takes precedence; circuits for computing concentration logarithmic circuits G06G7/24; photometric circuits in general G01J
• CPC Class Codes: G01N 21/31 Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry G01N21/72 takes precedence
• CPC Class Codes: G01N 21/3504 for analysing gases, e.g. multi-gas analysis
• CPC Class Codes: G01N 21/39 using tunable lasers
• CPC Class Codes: G01N 21/716 by measuring the radiation emitted by a test object treated by combustion gases for investigating the composition of gas mixtures
• CPC Class Codes: G01N 2201/0612 Laser diodes
• CPC Class Codes: G01N 33/15 Medicinal preparations ; Physical properties thereof, e.g. dissolubility

Abstract

Method of measuring a ratio of concentrations of two isotopologues of a chemical species in a first gas mixture using an optical absorption spectroscopy based gas analyzer; the method includes measuring the line intensity of a rotational-vibrational line of one isotopologue and the line intensity of another rotational-vibrational line of another isotopologue. The method also includes determining the ratio of two line intensities and comparing it with another ratio measured using another gas analyzer for a gas mixture with known concentration of isotopologues. The second ratio can be measured for the same pair of lines or for different pair of lines. The second ratio can be measured at the same gas temperature or at different gas temperature. The method includes determining a ratio of concentrations of two isotopologues based on two ratios of line intensities and two temperatures.

Claims

1. A method of measuring a ratio of concentrations of two isotopologues of a chemical species in a first gas mixture using a first optical absorption spectroscopy based gas analyzer, the method comprising the steps of:

i) measuring optical absorption spectra of the first gas mixture in a first spectral range containing a first rotational-vibrational line of a first rotational-vibrational band of a first isotopologue and in a second spectral range containing a second rotational-vibrational line of a second rotational-vibrational band of a second isotopologue at a first gas temperature;

ii) based on the measured spectra determining the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the first gas temperature;

iii) determining a first ratio of the line intensity of the first rotational-vibrational line and the line intensity of the second rotational-vibrational line at the first gas temperature;

iv) comparing the first ratio to a second ratio of the line intensity of a third rotational-vibrational line of a third rotational-vibrational band of the first isotopologue and the line intensity of a fourth rotational-vibrational line of a fourth rotational-vibrational band of the second isotopologue in a second gas mixture at a second gas temperature, the second gas mixture having a known ratio of concentrations of two said isotopologues, wherein the second ratio was determined using a second optical absorption spectroscopy based gas analyzer;

v) calculating the ratio of concentrations of the said isotopologues in the first gas mixture.

2. The method of claim 1, wherein the second ratio of the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue in the second gas mixture at a second gas temperature is calculated based on the ratio of the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue of the second gas mixture having the known ratio of concentrations of two said isotopologues at the standard temperature.

3. The method of claim 1, wherein the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue is the same as the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue is the same as the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue.

4. The method of claim 1, further comprising the steps of:

i) measuring an optical absorption spectrum in a fifth spectral range containing a fifth rotational-vibrational line of the first rotational-vibrational band of the first isotopologue;

ii) based on the measured spectrum determining the line intensity of the fifth rotational-vibrational line of the first rotational-vibrational band of the first isotopologue;

iii) determining the first gas temperature of the first gas mixture from the ratio of the line intensity of the first rotational-vibrational line and the line intensity of the fifth rotational-vibrational line.

5. A method of measuring a ratio of concentrations of two isotopologues of a chemical species in a first gas mixture using a first optical absorption spectroscopy based gas analyzer, the method comprising the steps of:

i) measuring an optical absorbance of the first gas mixture at a first wavelength in a first spectral range containing a first rotational-vibrational line of a first rotational-vibrational band of a first isotopologue and an optical absorbance of the first gas mixture at a second wavelength in a second spectral range containing a second rotational-vibrational line of a second rotational-vibrational band of a second isotopologue at a first gas temperature and at a first gas pressure;

ii) determining a first ratio of two said optical absorbances at the first gas temperature;

iii) comparing the first ratio to a second ratio of the optical absorbance at the first wavelength and the optical absorbance at the second wavelength of a second gas mixture at a second gas temperature and a second gas pressure, where the second gas mixture having a known ratio of concentrations of two said isotopologues, wherein the second ratio was determined using a second optical absorption spectroscopy based gas analyzer;

iv) calculating the ratio of concentrations of the said isotopologues in the first gas mixture.

6. The method of claim 5, wherein the first gas temperature and the second gas temperature are different by no more than 1 K and the first gas pressure and the second gas pressure are different by no more than 10 mBar.

7. The method of claim 5, wherein the first wavelength is at the maximum of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the second wavelength is at the maximum of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the second gas temperature and at the second gas pressure of the first gas mixture.

8. The method of claim 5, wherein the first wavelength is at a first local absorbance maximum closest to the maximum of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the second wavelength is at a second local absorbance maximum closest to the maximum of the second rotational-vibrational line from the second rotational-vibrational band of the second isotopologue at the second gas temperature and at the second gas pressure of the first gas mixture.

9. A method for defining a primary optical transfer standard of the ratio of concentrations of two gaseous isotopologues of a chemical species, the method comprising the steps of:

i) converting a first isotopic standard medium into a gas phase medium by producing a first gaseous isotopologue and a second gaseous isotopologue containing the type of atoms defined for the isotopic standard by first medium, unless the first medium is already in the gas phase;

ii) transferring gaseous isotopologues produced in the previous step into an optical absorption based gas analyzer, iii) stabilizing the gas temperature of the gas transferred into the said gas analyzer at a first temperature, iv) measuring rotational-vibrational absorption spectra of the said gas in a first spectral range containing a first rotational-vibrational line of a first rotational-vibrational band of the first isotopologue and in a second spectral range containing of a second rotational-vibrational line of a second rotational-vibrational band of the second isotopologue at the first gas temperature;

v) based on the said spectra determining the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the first gas temperature;

vi) defining a first ratio of the line intensity of the first rotational-vibrational line and the line intensity of the second rotational-vibrational line at the first gas temperature;

vii) defining the primary optical transfer standard of the ratio of concentrations of two gaseous isotopologues as the first ratio of the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the first gas temperature.

10. The method of claim 9, wherein the first temperature is the standard temperature of 273.15 K or the temperature of the triple point of water of 273.16 K.

11. The method of claim 9, further comprising the steps of:

i) measuring rotational-vibrational absorption spectra of the said gas in a third spectral range containing a third rotational-vibrational line of a third rotational-vibrational band of the first isotopologue and in a fourth spectral range containing a fourth rotational-vibrational line of a fourth rotational-vibrational band of the second isotopologue at the first gas temperature;

ii) based on the said spectra determining the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue at the first gas temperature;

iii) determining a second ratio of the line intensity of the third rotational-vibrational line and the line intensity of the fourth rotational-vibrational line at the first gas temperature;

iv) defining a secondary optical transfer standard of the ratio of concentrations of two gaseous isotopologues as the second ratio of the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue at the first gas temperature.

12. The method of claim 9, further comprising the steps of:

i) measuring rotational-vibrational absorption spectra of the said gas in a first spectral range containing the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and in a second spectral range containing the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at a second gas temperature;

ii) based on the said spectra determining the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the second gas temperature;

iii) determining a second ratio of the line intensity of the first rotational-vibrational line and the line intensity of the second rotational-vibrational line at the second gas temperature;

iv) defining a secondary optical transfer standard for the ratio of concentrations of two gaseous isotopologues as the second ratio of the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the second gas temperature.

13. The method of claim 9, further comprising the steps of:

i) measuring rotational-vibrational absorption spectra of the said gas in a third spectral range containing a third rotational-vibrational line of a third rotational-vibrational band of the first isotopologue and in a fourth spectral range containing a fourth rotational-vibrational line of a fourth rotational-vibrational band of the second isotopologue at a second gas temperature;

ii) based on the said spectra determining the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the second isotopologue at the second gas temperature;

iii) determining a second ratio of the line intensity of the third rotational-vibrational line and the line intensity of the fourth rotational-vibrational line at the second gas temperature;

iv) defining a secondary optical transfer standard for the ratio of concentrations of two gaseous isotopologues as the second ratio of the line intensity of the third rotational-vibrational line of the third rotational-vibrational band of the first isotopologue and the line intensity of the fourth rotational-vibrational line of the fourth rotational-vibrational band of the fourth isotopologue at the second gas temperature.

14. The method of claim 9, further comprising the steps of:

i) measuring rotational-vibrational absorption spectrum of the said gas in a third spectral range containing a third rotational-vibrational line of first rotational-vibrational band of the first isotopologue;

ii) based on the said spectrum determining the line intensity of the third rotational-vibrational line of the first rotational-vibrational band of the first;

iii) determining a second ratio of the line intensity of the first rotational-vibrational line of first rotational-vibrational band of the first isotopologue and the line intensity of the third rotational-vibrational line of first rotational-vibrational band of the first isotopologue;

iv) defining a secondary optical transfer standard of the ratio of concentrations of two gaseous isotopologues as the first ratio of the line intensity of the first rotational-vibrational line of the first rotational-vibrational band of the first isotopologue and the line intensity of the second rotational-vibrational line of the second rotational-vibrational band of the second isotopologue at the second ratio of the line intensity of the first rotational-vibrational line of first rotational-vibrational band of the first isotopologue and the line intensity of the third rotational-vibrational line of first rotational-vibrational band of the first isotopologue.