System and method for determining aqueous nitrate concentration in solution containing dissolved organic carbon

Patent metadata

Field	Value
Publication number	US-12510470-B2
Application number	US-202218569282-A
Country	US
Kind code	B2
Filing date	Jun 8, 2022
Priority date	Jun 13, 2021
Publication date	Dec 30, 2025
Grant date	Dec 30, 2025

Abstract

A method for real-time determining a concentration level of nitrate in a water sample collected from soil at a given site, the water sample contains an unknown composition and unknown concentration of DOC, the method includes: (A) during an offline stage: (a.1) obtaining a testing sample from the soil; (a.2) determining first and second wavelengths correlated, respectively, to concentration levels of the DOC and nitrate in the testing sample; (a.3) creating a calibration equation for this site; and, (B) during real-time: (b.1) separately impinging on a real-time water sample from the soil light in said two wavelengths; (b.2) determining respective absorbances by the real-time sample in said two wavelengths; and (c) substituting the respective absorbances in the calibration equation to obtain the nitrate concentration in the real-time sample.

First claim

The invention claimed is:

1 . A method for determining a concentration of nitrate in a water sample collected from soil at a given site, said water sample also contains an unknown composition and unknown concentration of Dissolved Organic Carbon (DOC), the method comprising:
a. during an offline stage:
collecting a testing sample from the site;
analyzing the testing sample to determine a first wavelength in which a light absorbance by the testing sample is correlated to the concentration level of the DOC in the testing sample;
further analyzing the testing sample to determine a second wavelength in which a light absorbance by the testing sample is correlated to the concentration level of the nitrate in the testing sample;
based on the above two-step offline analysis, creating a multivariate polynomial calibration equation for use during a real-time stage analysis; and
b. during a real-time stage analysis:
collecting a real-time water sample from the site's soil;
impinging on the real-time sample light in said first wavelength, measuring the real-time sample's absorbance, and recording the measured absorbance as a first absorbance value;
impinging on the real-time sample light in said second wavelength, measuring the real-time sample's absorbance, and recording the measured absorbance as a second absorbance value; and
substituting in said calibration equation the first absorbance value and the second absorbance value, or values relative thereon, and calculating to determine the nitrate concentration in the real-time sample.

2 . The method of claim 1 , wherein said offline stage comprises a creation a calibration matrix of samples from the from the testing sample, and wherein said analyses steps are performed on the calibration matrix.

3 . The method of claim 2 , wherein said first wavelength and said second wavelength are determined by:
dividing the calibration matrix of samples to a plurality of sub-samples, and dividing the plurality of sub-samples to two groups; differently enriching in a controlled manner the sub-samples in said first group by nitrate; differently diluting in a controlled manner the sub-samples in said second group by DDW; dividing a wide light spectrum into a plurality of wavelengths to form a plurality of discrete wavelengths; in each discrete wavelength, impinging light on each sub-sample within said two groups, and recording respectively the absorbance by the sub-sample; and analyzing said respective absorbances to determine said first wavelength and said second wavelength.

4 . The method of claim 3 , wherein the creation of the calibration equation is based on applying a multivariate regression technique on the variety of recorded absorbances.

5 . The method of claim 1 , wherein at least one of said correlations is a linear or higher order correlation.

6 . The method of claim 1 , wherein the offline stage is performed separately for each site, to determine a calibration equation that is specific to each site.

7 . The method of claim 1 , for further determining the concertation of DOC in the sample.

8 . The method of claim 1 , wherein said correlations define spectrum regions, respectively, in which the extent of correlation R 2 is higher than 0.8.

9 . The method of claim 1 , wherein said correlations define spectrum regions, respectively, in which the extent of correlation R 2 is higher than 0.85, 0.9, 0.95, or 0.98 in either or both said concentration levels determinations.

10 . A system for determining in real-time a concentration of nitrate in a water sample collected from soil at a given site, said water sample also contains an unknown composition and unknown concentration of Dissolved Organic Carbon (DOC), the system comprising:
a first light source operating at a predetermined first wavelength in which light absorbance by the sample is correlated to a concentration level of DOC in the sample; a second light source operating at a second wavelength in which light absorbance by the sample is correlated to a concentration level of nitrate in the sample; at least partially transparent cell for containing said water sample, wherein each said light sources is directed to impinge light on said cell containing the sample; and an analysis unit receiving a first sample absorbance in said first wavelength, and a second sample absorbance in said second wavelength, and calculating the concentration of nitrate in the sample based on said two absorbances, and a predetermined calibration equation;
wherein said correlations define spectrum regions, respectively, in which the extent of correlation R 2 is higher than 0.8.

11 . The system of claim 10 , wherein at least one of said correlations is a linear or higher order correlation.

12 . The system of claim 10 , wherein at least one of said light sources are of LED or UV lamp.

13 . The system of claim 10 , wherein said predetermined calibration equation is specifically determined for each given site.

14 . The system of claim 10 , for further determining the concentration of the DOC in the water sample.

15 . The system of claim 10 , wherein said correlations define spectrum regions, respectively, in which the extent of correlation R 2 is higher than 0.8.

16 . The system of claim 10 , wherein said correlations define spectrum regions, respectively, in which the extent of correlation R 2 is higher than 0.85, 0.9, 0.95, or 0.98 in either or both said concentration levels determinations.

Assignees

• B G Negev Technologies And Applications Ltd At Ben Gurion Univ

Inventors

• Dahan Ofer
• Yeshno Elad
• Arnon Shlomi

Classifications

• G01N2201/127

  Calibration; base line adjustment; drift compensation · CPC title

• G01N33/18

  Water · CPC title

• G01N33/188

  Determining the state of nitrification · CPC title

• G01N21/33 Primary

  using ultraviolet light (G01N21/39 takes precedence) · CPC title

• G01N2201/129

  Using chemometrical methods · CPC title