MEASURING NITROGEN OXIDES AND OTHER GASES BY OZONE FORMATION

• US 20090137055A1
• Filed: 09/26/2006
• Published: 05/28/2009
• Est. Priority Date: 09/30/2005
• Status: Abandoned Application

• Current Assignee: John A. Bognar
• Original Assignee: John A. Bognar
• Inventors: Bognar, John A.
• Application Number:
  US12/067,976
• Publication Number:
  US 20090137055A1
• Time in Patent Office: Days
• US Class Current: 436/118
• CPC Class Codes: G01N 33/0037 NOx
• CPC Class Codes: Y02A 50/20 Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
• CPC Class Codes: Y10T 436/179228 Both nitrogen oxide and dioxide

Abstract

A photochemical sensing system enables the measurement of nitrogen oxides (nitrogen dioxide and nitric oxide) by photolyzing nitrogen dioxide to form oxygen atoms which combine with oxygen molecules to form ozone. Ozone reacts with nitric oxide to for nitrogen dioxide-decreasing ozone. Changes in ozone concentration are measured as a surrogate for the nitrogen dioxide and nitric oxide. Any species which photolyzes to yield oxygen atoms may be measured by this technique. Additional specificity for nitrogen oxides is conferred by allowing the nitric oxide to react with the ozone to recreate the nitrogen dioxide. By periodically photolyzing the nitrogen dioxide (to form ozone), and then allowing the resulting nitric oxide to react with the ozone (thereby reducing ozone), a pulsed signal is obtained whose amplitude is proportional to the total amount of nitrogen dioxide and nitric oxide present. Medical applications include measuring nitric oxide concentrations in expired air samples.

Claims

1. A system, comprising:

(a) a first radiation source operable to irradiate a gas sample to effect decomposition of a selected first sample component into a second component and oxygen atoms, the oxygen reacting with molecular oxygen in the gas sample to form ozone;

(b) the second component reacting with ozone to cause a decrease in ozone; and

(c) a first detector adapted to detect and/or measure ozone in the gas sample.

2. The system of claim 1, wherein the first detector measures at least one of an increase and decrease in ozone, wherein the selected first sample component is nitrogen dioxide, wherein the second component is nitric oxide, wherein, when the sample is irradiated by first radiation source with a first wavelength having sufficient energy to break nitrogen dioxide chemical bonds such that nitrogen dioxide is photolyzed to nitric oxide and oxygen atoms, which in turn recombine with molecular oxygen to form ozone and wherein nitric oxide decreases ozone by combining with ozone to form nitrogen dioxide and molecular oxygen.

3. The system of claim 2, wherein the gas sample is contacted with ozone before irradiation to convert substantially all nitric oxide in the sample into nitrogen dioxide.

4. The system of claim 1 wherein the first radiation source has a second wavelength which is absorbed by ozone and wherein the first radiation source emits both the radiation having the first and second wavelengths.

5. The system of claim 1, further comprising an optically transmissive window positioned between the gas sample and the radiation source, the window directing a portion of the radiation emitted by the radiation source to a second detector, and a neutral density filter positioned between the gas sample and the first detector to substantially attenuate radiation prior to contact of the radiation with the first detector.

6. The system of claim 1, further comprising a second radiation source, an optical filter, and beam splitter, the first and second radiation sources being positioned on opposing sides of the gas sample, wherein the first radiation source emits first radiation having at least a first wavelength with sufficient energy to break chemical bonds of nitrogen dioxide, wherein the second radiation source emits second radiation having at least a second wavelength to absorb ozone, wherein the first and second radiation are emitted over different periods of times, wherein the beam splitter is oriented so that a portion of the second radiation is directed to the first detector.

7. The system of claim 1, further comprising a second radiation source, an optical filter, and a chopper, the first and second radiation sources being positioned on a common side of the gas sample, wherein the first radiation source emits first radiation having at least a first wavelength with sufficient energy to break chemical bonds of nitrogen dioxide, wherein the second radiation source emits second radiation having at least a second wavelength to absorb ozone, wherein the first and second radiation are emitted over different periods of times, wherein the chopper is oriented to block at least a portion of the first radiation from contacting the first detector.

8. The system of claim 1, wherein first radiation emitted by the first radiation source comprises non-ultraviolet radiation wavelengths, wherein a portion of the first radiation, after exiting the gas sample, is directed back through the gas sample to contribute further to decomposition of the first sample component,

9. The system of claim 1 which does not require recalibration, wherein the system further comprises a respiratory circuit to provide the gas sample, and wherein the first detector is one of a solid-state ozone sensor, a radiation sensor, and an electrochemical sensor.

10. A system adapted to measure one or more of nitric oxide and nitrogen dioxide in a sample using radiation-induced changes of ozone concentration.

11. The system of claim 10, wherein the sample is a gas sample and further comprising:

(a) a first radiation source with first wavelength operable to irradiate the sample to effect decomposition of nitrogen dioxide into nitric oxide and oxygen atoms, the oxygen reacting with molecular oxygen in the sample to form ozone;

(b) the nitric oxide reacting with ozone to decrease ozone; and

(c) a first detector adapted to detect and/or measure at least one of an increase and decrease in ozone, nitric oxide, and nitrogen dioxide in the sample.

12. The system of claim 11, wherein the first detector measures ozone and further comprising a controller adapted to correlate radiation changes in ozone concentration to concentrations of nitric oxide and/or nitrogen dioxide in the sample gas.

13. The system of claim 11, wherein the gas sample is a gas expired by a patient.

14. The system of claim 11, wherein the gas sample is contacted with ozone before irradiation to convert substantially all nitric oxide in the sample into nitrogen dioxide, wherein the radiation has a second wavelength absorbed by ozone and wherein a common radiation source emits radiation having the first and second wavelengths.

15. The system of claim 11, further comprising an optically transmissive window positioned between the gas sample and the radiation source, the window directing a portion of the radiation emitted by the radiation source to a second detector and a neutral density filter positioned between the gas sample and the first detector to attenuate substantially radiation prior to contact of the radiation with the first detector.

16. The system of claim 11, further comprising a second radiation source, an optical filter, and beam splitter, the first and second radiation sources being positioned on opposing sides of the gas sample, wherein the first radiation source emits first radiation having at least a first wavelength capable of breaking nitrogen dioxide chemical bonds, wherein the second radiation source emits second radiation having at least a second wavelength absorbed by ozone, wherein the first and second radiation are emitted over different periods of times, wherein the beam splitter is oriented so that a portion of the second radiation is directed to the first detector.

17. The system of claim 11, further comprising a second radiation source, an optical filter, and a chopper, the first and second radiation sources being positioned on a common side of the gas sample, wherein the first radiation source emits first radiation having at least a first wavelength capable of breaking nitrogen dioxide chemical bonds, wherein the second radiation source emits second radiation having at least a second wavelength absorbed by ozone, wherein the first and second radiation are emitted over different periods of times, wherein the chopper is oriented to block at least a portion of the first radiation from contacting the first detector.

18. The system of claim 11, further comprising a radiation source and detector, wherein first radiation emitted by the radiation source comprises non-ultraviolet radiation wavelengths, wherein a portion of the radiation, after exiting the sample, is directed back through the sample to contribute further to decomposition of the nitric dioxide, wherein the system does not require recalibration, wherein the sample is a gas sample, wherein the system further comprises a respiratory circuit to provide the gas sample, and wherein the detector is one of a solid-state ozone sensor, a radiation sensor, and an electrochemical sensor.

19. A method, comprising:

(a) irradiating a sample to convert a selected first sample component into a second component and oxygen atoms, the oxygen reacting with molecular oxygen in the sample to form ozone;

(b) the second component reacting with ozone to cause a decrease in ozone; and

(c) measuring at least one of a concentration and a change in concentration of ozone, nitric monoxide, and nitric dioxide after step (b).

20. The method of claim 19, wherein the sample is a gas, wherein first sample component is nitrogen dioxide, wherein the second component is nitric oxide, wherein:

(a) during irradiation of the sample, the first sample component is photolyzed to the second component and oxygen atoms, wherein oxygen atoms combine with molecular oxygen to form ozone, wherein ozone combines with second component to form first component causing a decrease in ozone;

(b) wherein, in the measuring step, at least one of a concentration and change in concentration of ozone is measured by ultraviolet absorption of ozone in a detector; and

(c) based on the measurement of step (b), determining at least one of concentration of and a change in concentration of the first sample component and/or second component.

21. The method of claim 19, further comprising:

(a) receiving the sample;

(b) contacting the sample with a gas comprising ozone and molecular oxygen to form a mixture of the sample and gas, introducing a portion of the mixture into a cell, wherein, in the irradiating step and while the mixture is in the cell, the mixture is irradiated with an intermittent radiation sufficient to photolyze nitrogen dioxide, wherein the photolytic reaction forms nitric oxide and oxygen atoms, the oxygen atoms then reacting with ambient molecular oxygen to form ozone, and then ozone combines with nitric oxide to form nitrogen dioxide causing a decrease in ozone; and

(c) wherein the determination is made by measuring absorption of ozone by ultraviolet light in a detector.

22. The method of claim 20, wherein a first portion of the radiation is directed to a first detector and a second portion is directed to the cell, and further comprising:

after the second portion of the radiation has passed through the cell, attenuating the second portion of the radiation; and

contacting the attenuated second portion with a second detector.

23. The method of claim 21, wherein the irradiating step is performed by a first radiation source and wherein the determining step comprises the sub-steps:

a second radiation source irradiating the mixture with second radiation, a portion of the second radiation being absorbed by ozone in the mixture;

after the second radiation exits the cell, directing a first portion of the second radiation to a detector and a second portion of the second radiation away from the detector;

passing the first portion of the second radiation to a detector; and

, wherein the first and second radiation are emitted over different periods of times.

24. The method of claim 21, wherein the irradiating step is performed by a first radiation source and wherein the determining step comprises the sub-steps:

a second radiation source irradiating the mixture with second radiation;

and wherein the first and second radiation are emitted over different periods of times.

25. The method of claim 21, wherein the sample gas is obtained from a biological system capable of providing said sample gas and wherein said biological system is blood.

26. The method of claim 21, wherein the sample gas is obtained from a biological system capable of providing said sample gas and wherein said biological system is skin.

27. The method of claim 21, wherein the sample gas is obtained from a biological system capable of providing said sample gas and wherein said biological system is the lung, such that measurement of NO concentration in exhaled breath samples during anaphylaxis is used as a biomarker of anaphylaxis to support diagnosis of anaphylaxis and to monitor treatment of anaphylaxis.

28. The method of claim 21, wherein at least one of an increase and decrease in ozone concentration is measured, wherein, in the irradiating step, a portion of the radiation, after passing through the sample, is redirected back through the sample to contribute further to photolysis of the first sample component, and wherein a common radiation source provides radiation having a first wavelength to photolyze the first sample component and to measure the ozone.

29. A method to determine NO in a breath sample from a human, said method comprising:

(a) exhaling breath sample through a respiratory circuit into a NO analyzer;

b) said analyzer capable of measuring photochemically modulated changes of ozone concentration in said sample;

c) said changes of ozone concentration converted into concentration of NO in said air ample.

30. The method of claim 29 wherein the breath sample is comprised of inspired air filtered through a NO filter.

31. The method of claim 29 wherein the expired breath sample courses through a nitrogen dioxide filter prior to entering said analyzer.