METHOD AND APPARATUS FOR MEASURING OF THE CONCENTRATION OF A SUBSTANCE IN A FLUID MEDIUM

• US 20030025909A1
• Filed: 11/30/1999
• Published: 02/06/2003
• Est. Priority Date: 12/01/1998
• Status: Abandoned Application

• Current Assignee: Tetra Laval Holdings & Finance SA (Tetra Laval Holdings BV)
• Original Assignee: Tetra Laval Holdings & Finance SA (Tetra Laval Holdings BV)
• Inventors: HALLSTADIUS, HANS
• Application Number:
  US09/450,726
• Publication Number:
  US 20030025909A1
• Time in Patent Office: Days
• US Class Current: 356/436
• CPC Class Codes: A23L 3/003 Control or safety devices for sterilisation or pasteurisation systems
• CPC Class Codes: A23L 3/3409 in the form of gases, e.g. fumigation; Compositions or apparatus therefor
• CPC Class Codes: A23L 3/3445 in a controlled atmosphere comprising other gases in addition to CO2, N2, O2 or H2O
• CPC Class Codes: G01N 2021/3155 Measuring in two spectral ranges, e.g. UV and visible
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• CPC Class Codes: G01N 21/314 with comparison of measurements at specific and non-specific wavelengths dual wavelength spectrometry G01J3/427
• CPC Class Codes: G01N 21/33 using ultraviolet light G01N21/39 takes precedence

Abstract

The invention relates to a method for determining the concentration of a substance in a sample in the presence of an interfering material by means of light absorption, and an apparatus therefore. By measuring the light absorbance at two different wavelengths the disturbing influences of interfering materials such as dust particles, dirt and bubbles may be compensated for. By also measuring the intensity of the light emitted from the light source but which has not yet passed through the measurement sample, simultaneously with the measurements of the absorbance of the light transmitted through the sample, at each wavelength measured, the true concentration may be determined by improved accuracy. The invention further relates to a method for packaging of a food product into packages, at least comprising the steps of sterilising a packaging material or packages by a sterilising medium containing a sterilising substance, filling of the sterilised packages with a food product and sealing of the packages, further comprising determining the concentration of the sterilising substance in the sterilising medium. It also relates to a machine arrangement for such packaging and filling of food products.

Claims

1. A method for determining the concentration of a substance in a sample in the presence of an interfering material, comprising at least the steps of directing light from a light source through said sample, measuring the absorbance of said light at a first wavelength or range of wavelengths, at which light is absorbed by said substance and interfering material, and at a second wavelength or range of wavelengths, at which light is absorbed by said interfering material but substantially not by said substance, and deriving from said measurements the required determination of the concentration of said substance corrected for the presence of said interfering material, wherein to compensate for variations in the intensity of light emitted from said light source, measurements are made at each said wavelength(s) of the intensity of light from said light source which has not passed through said sample simultaneously with said measurements of absorbance, and the said determination of the concentration of said substance is corrected for errors resulting from said variations in emitted light intensity on the basis of said measurements of light intensity.

2. Method according to claim 1, wherein said light includes light from the UV spectrum as well as from the visible spectrum.

3. Method according to any one of claims 1 or 2, wherein said first wavelength(s) is selected from between about 220 nm and about 320 nm.

4. Method according to any one of claims 1-3, wherein said second wavelength(s) is selected from wavelengths about 385 nm and longer.

5. Method according to claim 1 for determining the concentration in a liquid or gas-phase medium (40), of a substance absorbing UV-light at one or more first wavelength(s) between about 220 and about 320 nm, in the presence of an interfering material, comprising the steps of

a) providing a light source (11) emitting light including said first wavelength(s) and at least one second wavelength or range of wavelengths of about 385 nm or longer;

b) directing light from the light source through a sample of a fluid medium (40), containing the substance to be measured as well as interfering material, along a monitoring path having the length (L);

c) measuring the intensity of the light transmitted (20) at said first wavelength and at said second wavelength respectively, through the sample medium (40);

d) directing light from the light source through a reference sample of the liquid or gas-phase medium (40′

), containing substantially less of the substance to be measured, along a monitoring path having the same length (L);

e) measuring the intensity of the light transmitted (20′

) at the first wavelength(s), and the second wavelength(s) respectively, through the reference sample (40′

);

f) thus producing first detector output signals (15;

15′

) for indication of the difference in light intensity from sample and reference sample respectively at said first wavelength(s) and second detector output signals (22;

22′

), for the corresponding indication of the difference in light intensity at said second wavelength(s);

g) determining the concentration of the UV-absorbing substance from the relative values of the output signals (15, 15′

) by means of the Beer-Lambert equation,

h) correcting the value of the concentration determined in g), by means of the second detector output signals (22, 22′

), thus eliminating the influence from impurities in the sample (40), wherein

i) the intensities of the light from said light source which has not passed through said sample medium (40) or reference sample medium (40′

) respectively, at the first and second wavelength(s) respectively, are detected simultaneously with the measurements in c) and e), and

j) the said determination of the concentration in h) is corrected for errors resulting from variations in the intensity of the light emitted from the light source, on the basis of the measurements in i).

6. Method according to any one of the preceding claims, wherein the light absorbing substance is selected from the group consisting of ozone and hydrogen peroxide.

7. Method according to any one of the preceding claims, wherein the fluid medium (40) is an aqueous medium.

8. Method according to any one of the preceding claims, wherein the fluid medium (40) is based on air and/or aqueous vapour.

9. Method according to any one of claims 1-8, wherein the light absorbing substance is hydrogen peroxide in an aqueous medium, the first wavelength is about 313 nm, and the second wavelength is selected from about 436 or 546 nm.

10. Method according to any one of claims 1-8, wherein the light absorbing substance is hydrogen peroxide in a gas-phase medium, the first wavelength is about 254 nm and the length of the monitoring path (L) through the sample medium (40) is from 10 to 250 mm.

11. Method according to any one of claims 1-8, wherein the light absorbing substance is ozone, the first wavelength is about 254 nm and the length of the monitoring path (L) through the sample medium (40) is from 0,5 to 5 mm.

12. Method according to any one of the preceding claims, wherein the sterilising medium is a liquid medium and the amount of gas bubbles is reduced by separating gas bubbles from the liquid before determining the concentration.

15. Apparatus according to claim 12, wherein the light source (11) is a low pressure mercury lamp.

13. Apparatus (10) for determining the concentration of a substance in a sample (40) in the presence of an interfering material, comprising at least a light source (11) and means for directing light from the light source through said sample,

means (14) for measuring the absorbance of said light transmitted through the sample at a first wavelength or range of wavelengths, at which light is absorbed by said substance and interfering material, and (19) at a second wavelength or range of wavelengths, at which light is absorbed by said interfering material but substantially not by said substance, and means (36) for determining the concentration of said substance, on the basis of said measurements of light absorbance,

which apparatus, in order to compensate for variations in the intensity of light emitted from said light source, further comprises

means (26, 33) for measuring the intensity of light from said light source which has not passed through said sample at each said wavelength simultaneously with said measurements of absorbance, and

means (36′

) for correcting said determined concentration for errors resulting from said variations in intensity of light emitted from the light source, on the basis of said measurements of light intensity.

14. Apparatus according to claim 13, wherein the light source (11) emits light including a first wavelength or range of wavelength(s) selected from between about 220 nm and about 320 nm, as well as a second wavelength or range of wavelength(s) of about 385 nm or longer.

20. Apparatus according to any one of claims 13-19, which further includes a device 90 for reducing the amount of gas bubbles in a sterilising liquid medium.

16. Apparatus (10) for determining the concentration of a substance absorbing UV-light at one or more first wavelength(s) of between about 220 and about 320 nm, in a fluid medium (40) containing the substance to be measured, in the presence of an interfering material, comprising at least

a) a light source (11) emitting light including said first wavelength(s) and at least

one second wavelength or range of wavelength(s) of about 385 nm or longer,

b) a monitoring path having the length (L) traversing the medium (40),

c) means for directing the light through said medium (40) over said monitoring path,

d) at least one first detector (14) being adapted to measure the intensity of the UV-light transmitted over the monitoring path at the first wavelength(s), the first detector(s) providing a first, first detector output signal (15) representing the intensity of the light, at said first wavelength(s), transmitted through a sample of the liquid or gas-phase medium (40) containing the substance to be measured as well as interfering material, and a second, first detector output signal (15′

) representing the intensity of the light at said first wavelength(s), transmitted through a reference sample of the liquid or gas-phase medium (40′

), containing none, or substantially less, of the substance to be measured,

e) at least one second detector (19) being adapted to measure the intensity of the light transmitted over the monitoring path at the second wavelength(s), the second detector(s) providing a first, second detector output signal (22) representing the intensity of the light at said second wavelength(s), transmitted through a sample of the fluid medium (40) containing the substance to be measured as well as interfering material, and a second, second detector output signal (22′

) representing the intensity of the light at said second wavelength(s), transmitted through a reference sample of the liquid or gas-phase medium (40′

), containing none, or substantially less, of the substance to be measured, and

f) computing means (36) for deriving the determined concentration of the UV-absorbing substance from the relative values of the output signals by applying the Beer-Lambert equation, which apparatus, in order to compensate for variations in the intensity of light emitted from said light source, further comprises

g) at least one third detector (26) being designed to measure the intensity of the UV-light before being transmitted through the sample, at the first wavelength(s), simultaneously with the measurements by the first detector(s),

h) at least one fourth detector (33) being designed to measure the intensity of the light before being transmitted through the sample, at the second wavelength(s), simultaneously with the measurements by the second detector(s), and

i) computing means (36′

) for correcting said determined concentration for errors resulting from said variations in intensity of light emitted from the light source.

17. Apparatus according claim 16, for determining the concentration of ozone, wherein the length (L) of the monitoring path is from 0,5 to 5 mm and the first and third detectors (14, 26) are adapted to measure UV-light of 254 nm.

18. Apparatus according to claim 16, for determining the concentration of hydrogen peroxide in a gas-phase medium (40), wherein the length (L) of the monitoring path is from 10 to 250 mm and the first and third detectors (14, 26) are adapted to measure UV-light of 254 nm.

19. Apparatus according to claim 16, for determining the concentration of hydrogen peroxide in an aqueous medium (40), wherein the length (L) of the monitoring path is from 0,5 to 5 mm and the first and third UV-detectors (14, 26) are adapted to measure UV-light of 313 nm.

21. Method for packaging of a food product into packages, at least comprising the steps of sterilising a packaging material or packages by a sterilising medium containing a sterilising substance, filling of the sterilised packages with a food product and sealing of the packages, further comprising the method for determining the concentration of the sterilising substance in a sample of the sterilising medium, comprising at least the steps of

directing light from a light source through said sample,

measuring the absorbance of said light at a first wavelength or range of wavelengths, at which light is absorbed by said sterilising substance, and at a second wavelength or range of wavelengths, at which light is absorbed by said interfering material but substantially not by said sterilising substance, and

deriving from said measurements the required determination of the concentration of said sterilising substance corrected for the presence of said interfering material in the sterilising medium,

wherein to compensate for variations in the intensity of light emitted from said light source,

measurements are made at each said wavelength(s) of the intensity of light from said light source which has not passed through said sample of sterilising medium, simultaneously with said measurements of absorbance,

and the said determination of the concentration of said substance is corrected for errors resulting from said variations in emitted light intensity on the basis of said measurements of light intensity.

22. Arrangement (50;

70;

80) for packaging of a food product into packages, at least comprising means for sterilisation of a packaging material or a formed package by a sterilising substance in a sterilising medium (60), means for filling the packages with a food product (62) and means for sealing the packages (63a;

63b), further comprising an apparatus (10) for determining the concentration of the sterilising substance in the presence of an interfering material in the sterilising medium (40;

61), which apparatus comprises at least

a light source (11) and means for directing light from the light source through a sample of said sterilising medium (40),

means (14) for measuring the absorbance of said light at a first wavelength or range of wavelengths, at which light is absorbed by said sterilising substance, and (19) at a second wavelength or range of wavelengths, at which light is absorbed by said interfering material but substantially not by said sterilising substance and means (36) for determining the concentration of said substance on the basis of said measurements of light absorbance,

which apparatus, in order to compensate for variations in the intensity of light emitted from said light source, further comprises

means (26, 33) for measuring the intensity of light from said light source which has not passed through said sample, at each said wavelength simultaneously with said measurements of absorbance, and

means (36′

) for correcting said determined concentration for errors resulting from said variations in intensity of light emitted from the light source, on the basis of said measurements of light intensity.