WO2004003524A1 - Vorrichtung zur photometrischen messung des gehalts einer chemischen substanz in einer messlösung - Google Patents
Vorrichtung zur photometrischen messung des gehalts einer chemischen substanz in einer messlösung Download PDFInfo
- Publication number
- WO2004003524A1 WO2004003524A1 PCT/EP2003/005768 EP0305768W WO2004003524A1 WO 2004003524 A1 WO2004003524 A1 WO 2004003524A1 EP 0305768 W EP0305768 W EP 0305768W WO 2004003524 A1 WO2004003524 A1 WO 2004003524A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- intensity
- measuring
- branch
- lamp
- control
- Prior art date
Links
- 239000000126 substance Substances 0.000 title claims abstract description 22
- 239000012491 analyte Substances 0.000 title abstract 4
- 230000005855 radiation Effects 0.000 claims abstract description 9
- 230000033228 biological regulation Effects 0.000 claims abstract description 3
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 3
- 238000011156 evaluation Methods 0.000 claims description 29
- 238000005259 measurement Methods 0.000 claims description 22
- 239000003990 capacitor Substances 0.000 claims description 8
- 238000005375 photometry Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 230000001105 regulatory effect Effects 0.000 claims description 5
- 229910052724 xenon Inorganic materials 0.000 claims description 3
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims description 3
- 230000007423 decrease Effects 0.000 claims 1
- 239000000284 extract Substances 0.000 abstract 1
- 229910002651 NO3 Inorganic materials 0.000 description 30
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 30
- 239000000243 solution Substances 0.000 description 20
- 239000000523 sample Substances 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000003550 marker Substances 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000011109 contamination Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000004364 calculation method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 229910052805 deuterium Inorganic materials 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/33—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using ultraviolet light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/314—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry with comparison of measurements at specific and non-specific wavelengths
Definitions
- the invention relates to a device for the photometric measurement of the content of a chemical substance in a measuring solution.
- the nitrate content in an aqueous solution or in a suspension is preferably determined by means of the device according to the invention.
- the invention is also ideally suited for the photometric measurement of organic substances dissolved in water.
- the invention can be used to detect any dissolved substance that can be detected using a photo-metric measurement method.
- STAMOSENS Known online systems for measuring nitrate or for measuring the content of organic substances are offered and sold by the applicant under the name STAMOSENS. The invention further develops the known prior art.
- the invention is based on the object of proposing a device which delivers highly reliable measured values.
- a device which has the following components: a lamp which emits electromagnetic radiation in a predetermined wavelength range; a first receiving unit in a measuring branch, which receives the radiation transmitted through the measuring solution at a first wavelength; a second receiving unit in a reference branch, which receives the radiation transmitted through the measurement solution at a second wavelength; a control / evaluation unit which, depending on the circumstances at the measuring location, either uses the intensity values determined via the measuring branch or the reference branch in order to regulate the intensity of the radiation emitted by the lamp in such a way that the measured values made available to a high degree are plausible.
- the invention also extends the measuring range.
- the measuring range can be compared to the known solutions double.
- the influence of disturbance variables, in particular of organic substances is significantly reduced.
- both receiving units are UV detectors.
- the UV detector positioned in the measuring branch preferably works at 214 nm - that is, in the vicinity of the absorption maximum of nitrate dissolved in water - while the UV detector arranged in the reference branch preferably works at 254 nm.
- the latter wavelength corresponds to the SAK measurement known from DIN 38404.
- control / evaluation unit controls the intensity of the lamp in such a way that at least one of the two intensity values measured in the measuring branch or in the reference branch lies within the permissible measuring range of the respective receiving unit.
- control / evaluation unit uses the intensity values determined in the reference branch to regulate the intensity of the lamp in the case of a high content of the substance in the measurement solution
- control / evaluation unit uses the intensity values determined in the measuring branch to regulate the intensity of the lamp. This configuration doubles the measuring range.
- the control / evaluation unit subsequently checks in a further method step whether at least one of the two intensity values - that is to say the intensity value measured in the reference branch or in the measuring branch - is at least as large as a predetermined maximum intensity value.
- the control / evaluation unit then checks whether the intensity value measured in the reference branch is greater than the predetermined maximum intensity value. In the event that the intensity value measured in the reference branch is greater than the predetermined maximum intensity value, the control / evaluation unit regulates the intensity of the lamp successively in predetermined steps until the intensity value measured in the reference branch is smaller than the predetermined maximum intensity value. In the event that neither the intensity value measured in the reference branch nor in the measuring branch is at least as large as the predetermined maximum intensity value, the control / evaluation unit increases the intensity of the lamp by a predetermined amount. The control / evaluation unit then checks whether the intensity value measured in the reference branch is greater than the predetermined maximum intensity value. In the event that the intensity value measured in the reference branch is greater than the predetermined maximum intensity value, the intensity of the lamp is successively reduced in predetermined steps until the intensity value measured in the reference branch is smaller than the predetermined maximum intensity value.
- the lamp is preferably a flash lamp, in particular a xenon or deuterium flash lamp.
- a first capacitor is preferably provided as the energy store for supplying the lamp with a predetermined energy, via which the regulating-Z evaluation unit regulates / controls the intensity of the lamp.
- a second capacitor is preferably connected to the first capacitor in order to increase the intensity of the lamp.
- a preferred embodiment of the device according to the invention provides that the control / evaluation unit provides a measured value for the content of the substance in the measuring solution, which results from the intensity values measured in the measuring branch and the reference branch.
- the control / evaluation unit subjects a determined measured value to a plausibility check by checking the intensity values determined in the measuring branch and in the reference branch for predetermined conditions; the control / evaluation unit then assigns an ascertained measured value to a disturbance variable found as a result of the plausibility check. The measured value and, if applicable, the interference variable found are shown on a display.
- a preferred embodiment of the device according to the invention proposes that the control / evaluation unit statistically determines a measured value on the basis of a large number of individual measured values. In this way, the known advantages can be achieved that short-term fluctuations have no influence on the measured value output and, if appropriate, the associated disturbance variable.
- Fig. 3b a flow chart for the part marked with B from Fig. 3 and
- 3c a flow chart for the part marked with C from FIG. 3b.
- the probe 11 according to the invention shows a schematic illustration of the probe 11 according to the invention.
- the probe 11 according to the invention is suitable for all substances whose content in an aqueous solution or in a suspension can be determined by a photometric measurement.
- the substances mentioned above are, for example, organic substances.
- the measuring principle of a nitrate probe 11 is based on the fact that nitrate has a pronounced absorption peak in the UV range. The amplitude of the absorption peak depends on the nitrate content of the measurement solution.
- the nitrate probe 11 is immersed in the aqueous solution or in the sludge.
- the measuring solution is then in the measuring channel or in the measuring cuvette 4.
- the measuring solution is irradiated with plane-parallel light via a broadband light source - for example a xenon or a deuterium flash lamp.
- the light emitted by the flash lamp 1 is preferably in a wavelength range of approximately 180-2000 nm.
- the alignment in parallel light takes place via the condenser 2; the deflection of the light from the condenser 2 to the measuring cuvette 4 arranged perpendicularly thereto takes place via the deflection mirror 3.
- the transmission light is split by the beam splitter 5 into two mutually perpendicular light branches, in the measuring branch and in the reference branch.
- the beam splitter 5 is preferably made of quartz glass.
- the advantage of using a beam splitter 5 is that punctual contamination can be compensated for and thus have no influence on the measuring accuracy of the nitrate probe 11.
- the measuring light in the measuring branch is detected by the receiver 6, the reference light in the reference branch strikes the receiver 7.
- the receiver 6 detects the measuring light at 214 nm, that is to say in the vicinity of the wavelength at which nitrate dissolved in water has its absorption maximum.
- the reference light is also measured in the UV range.
- the wavelength is preferably 254 nm, ie close to the wavelength of the measurement light.
- FIG. 2 shows a block diagram of a preferred embodiment of a system for online nitrate measurement.
- the system shown in FIG. 2 is ideally suited to match the intensity of the flashes emitted by the flash lamp 1 to the conditions prevailing at the measuring location.
- the system for online nitrate measurement consists of the nitrate probe 11 and the transmitter or the transmitter 10.
- the nitrate probe 11 comprises a flash lamp 1 with associated optics, the measuring channel (or the measuring cuvette 4), the receivers 6, 7 and the associated optics , the high-voltage power supply 16 and the control / evaluation unit 8.
- the intensity values measured by the receivers 6, 7 are forwarded to the control / evaluation unit 8.
- the intensity of the flash lamp 1 is regulated as a function of the conditions at the measuring location.
- a software algorithm is used for this.
- a preferred embodiment of the software algorithm is described in detail on the basis of the flow diagrams which can be seen in FIGS. 3, 3a, 3b and 3c.
- the intensity values detected in the reference branch and / or in the measuring branch are used in order to optimally match the intensity of the flashes emitted by the flash lamp 1 to the conditions prevailing at the measuring location.
- an optimized adaptation of the measuring system to the measuring task can be achieved; Even large disturbances can still be compensated for.
- a reproducible measurement can be achieved when used for a measuring branch and a reference branch.
- the measured values supplied by the probe 11 are statistically evaluated in the transmitter 10 and displayed to the operating personnel via a display 17. Furthermore, the operating personnel are provided with data that provide information about the reliability or the plausibility of the measured values.
- the transmitter 10 has an input unit 18.
- a transmitter / measuring transducer 10 which is preferably used in connection with the invention is offered and sold by the applicant under the name STAMOSENS CNM 750.
- the flow diagrams shown in FIGS. 3, 3a, 3b and 3c describe a preferred embodiment of the software algorithm via which the control / evaluation unit 8 controls the lamp intensity.
- the measuring range of the Nitrate probe 11 is limited by two limit measurement values dependent on the respective receivers 6, 7 and the circuit arrangement: If the intensity values exceed a maximum permissible intensity value I max , the receiver 6, 7 is overridden; If the measured intensity value is below a minimum intensity value 1 min , the measured value disappears in the noise.
- the lamp intensity is always regulated in such a way that an intensity value that is as constant as possible is detected in the reference branch; the intensity in the measuring branch then changes depending on the nitrate content of the measuring solution.
- the intensity value in the reference branch or the intensity value in the measuring branch is used depending on the conditions at the measuring location for regulating the intensity of the flash lamp 1.
- the intensity value in the reference branch is still relevant for the light control; however, if the nitrate content is low, the intensity value in the measuring branch is used for light control in the flash lamp 1.
- the program starts at point 100.
- the microprocessor 12 is initialized at 101.
- the initialization data are preferably written into a read-only memory assigned to the microprocessor. These data relate to the light control of the flash lamp 1 and the measurement sequence. In particular, the intensity ⁇ v of a flash of light from the flash lamp 1, the number N of flashes B required for the statistical calculation of a measured value, and the maximum intensity value 1 max and the minimum intensity value 1 min of the receivers 6, 7 are specified.
- the microprocessor 12 receives the information as to whether light control should take place or not. If the light control is not activated, a counter is set to 1 at program point 103.
- the program steps 104 to 110 are then run through N times.
- the flash lamp 1 emits a flash of light B with the intensity ⁇ v .
- the intensity of the flash of light is detected at point 105 by the receivers 6, 7 in the reference branch and in the measuring branch.
- a plausibility check is carried out at 106 (see also identification A in FIG. 3).
- the program items 114 to 117, which are successively run through in the plausibility check 106, are shown separately in FIG. 3a. Under point 114 it is checked whether the intensity measured in the measuring branch or in the reference branch is greater than the predetermined maximum intensity value l raax .
- the corresponding measured value under program points 107, 108 is provided with the marker "disturbance: light intensity”. In plain language, this means that the intensity ⁇ v of the flash of light from the flash lamp 1 - for whatever reason - is too high and that the corresponding measured value is therefore not plausible.
- the maximum intensity value l max is not exceeded in either the measuring branch or the reference branch, then a check is made at point 115 as to whether the intensity value in the measuring branch is greater than the predetermined minimum intensity value ⁇ mm and whether the intensity value in the reference branch is less than the predetermined minimum intensity value l ⁇ , If this condition is met, the corresponding measured value under program points 107, 108 is provided with the marker "disturbance: organic", which means that the content of organic substances in the measurement solution has exceeded a permissible level. This means that a sufficiently precise determination of the nitrate content in the aqueous solution or in the suspension is no longer possible - the plausibility of the measured value is questioned.
- a test for detecting a fourth disturbance variable: contamination is carried out under program point 117. For this purpose, it is checked whether the intensity value in the measuring branch and the intensity value in the reference branch are smaller than the predefined minimum intensity value l min . If this condition is met, the corresponding measured value under program points 107, 108 is provided with the marker "disturbance variable: contamination", which means that the contamination in the measurement solution makes a sensible nitrate measurement impossible. To generate a measured value, which is then ultimately displayed on the display unit 17, N measured values are used and statistically evaluated (point 111). If only a small number of the N measured values are shown as not plausible, the process variable, i.e.
- the nitrate content is calculated and displayed (point 112). If the number of non-plausible measured values is above a predetermined limit value, the measured value is also calculated (point 11), but it is output with the corresponding marker (point 113). It is then left to the operating personnel to take a suitable measure to counteract the disturbance variable.
- the disturbance variable light intensity
- the measure could consist in replacing the flash lamp 1.
- a far more effective compensation option is the activation of the lamp control according to the invention (program point 102).
- the activation can e.g. manually operated by a corresponding key on the input unit 18.
- the individual program steps are shown in FIGS. 3b and 3c.
- the microprocessor 12 is again initialized.
- a measuring cycle is started.
- the program steps 120 to 131 are subsequently run through N times in a loop.
- the flash lamp 1 emits a flash of light B with the intensity ⁇ v .
- the intensity of the flash of light is detected by the receivers 6, 7 in the reference branch and in the measuring branch (point 121).
- the intensity value in the reference branch or whether the intensity value in the measuring branch is greater than or equal to a predetermined maximum intensity value l maxl .
- the default value l maxl is preferably smaller than the default value l max when the light control is switched off.
- point 123 checks whether the intensity value in the reference branch is greater than I maxl . If this condition is also met, the intensity of the flash lamp is reduced by a predetermined amount X. A flash is emitted at 125 and the corresponding intensity value is determined in the reference branch. The loop 124, 125, 126 is run through until the condition specified under point 123 is fulfilled; the run is carried out a maximum of M times.
- the measured value may be output stating a disturbance variable (points 128 to 134).
- a second capacitor 15 is connected to the capacitor 14 via a relay under point 143.
- the intensity of the light flashes of the flash lamp 1 is thus increased, in particular in this case the intensity of the light flashes is doubled.
- the program points already described in FIG. 3b are then run through, that is, if necessary, the intensity of the flash lamp 1 is successively regulated downwards until the intensity value in the reference branch is below the predetermined maximum intensity value I maxl .
- sufficiently reliable measured values can always be determined if at least the intensity value in the reference branch or the intensity value in the measuring branch lies in the working range of the probe. If the nitrate content in the measurement solution is high, the light is controlled using the intensity values measured in the reference branch; If the nitrate content in the measuring solution is low, the intensity values determined in the measuring branch are relevant for the light control. On in this way it is possible to double the working range of the nitrate probe according to the invention compared to the known solutions.
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/517,779 US7339178B2 (en) | 2002-06-28 | 2003-06-03 | Device for the photometric measurement of the content of a chemical substance in an analyte |
EP03735520A EP1518105A1 (de) | 2002-06-28 | 2003-06-03 | Vorrichtung zur photometrischen messung des gehalts einer chemischen substanz in einer messlösung |
AU2003238195A AU2003238195A1 (en) | 2002-06-28 | 2003-06-03 | Device for the photometric determination of the content of a chemical substance in an analyte |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10228929.8 | 2002-06-28 | ||
DE10228929A DE10228929A1 (de) | 2002-06-28 | 2002-06-28 | Anordnung zur Messung des Nitratgehaltes in Flüssigkeiten |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004003524A1 true WO2004003524A1 (de) | 2004-01-08 |
Family
ID=29723520
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2003/005768 WO2004003524A1 (de) | 2002-06-28 | 2003-06-03 | Vorrichtung zur photometrischen messung des gehalts einer chemischen substanz in einer messlösung |
Country Status (6)
Country | Link |
---|---|
US (1) | US7339178B2 (de) |
EP (1) | EP1518105A1 (de) |
CN (1) | CN100473973C (de) |
AU (1) | AU2003238195A1 (de) |
DE (1) | DE10228929A1 (de) |
WO (1) | WO2004003524A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9568458B2 (en) | 2014-08-21 | 2017-02-14 | Sharp Kabushiki Kaisha | Optical sensor for fluid analysis |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004050045B3 (de) * | 2004-10-14 | 2006-04-13 | Robert Bosch Gmbh | Verfahren zur Signalauswertung bei einem Kohlendioxidsensor |
US7927883B2 (en) * | 2007-11-09 | 2011-04-19 | The Regents Of The University Of California | In-situ soil nitrate ion concentration sensor |
CN102262065B (zh) * | 2011-04-27 | 2013-03-20 | 河北先河环保科技股份有限公司 | 一种在线测定水中硝酸盐氮的仪器 |
US9188512B2 (en) * | 2011-05-20 | 2015-11-17 | Woods Hole Oceanographic Institution | Aquatic sample analysis system |
DE102012112541A1 (de) | 2012-12-18 | 2014-06-18 | Zentrum für Biomedizinische Technologie Donau-Universität Krems | Vorrichtung zur optischen Überwachung eines Parameters einer Flüssigkeitsprobe |
AT513774B1 (de) * | 2012-12-18 | 2014-11-15 | Zentrum Für Biomedizinische Technologie Der Donau Universität Krems | Vorrichtung und Verfahren zur optischen Überwachung eines Parameters einer Flüssigkeitsprobe |
CA3016601C (en) * | 2016-03-07 | 2021-09-14 | Ysi, Inc. | Optical nitrate sensor for multiparameter water quality measurement |
EP3427021B1 (de) * | 2016-03-09 | 2023-11-22 | YSI Incorporated | Optische nitratsensorkompensationsalgorithmen zur multiparameterüberwachung der wasserqualität |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3403253A (en) * | 1965-11-29 | 1968-09-24 | Navy Usa | Humidiometer having feedback means to control the energization of the tube |
US4447150A (en) * | 1981-02-27 | 1984-05-08 | Bentley Laboratories | Apparatus and method for measuring blood oxygen saturation |
DE3324606A1 (de) * | 1983-07-08 | 1985-01-17 | Dr. Bruno Lange Gmbh, 1000 Berlin | Vorrichtung zum messen und bestimmen des nitratgehaltes von fluessigkeiten |
US4627284A (en) * | 1985-07-22 | 1986-12-09 | Spectral Sciences, Inc. | Ultraviolet absorption hygrometer |
DE19902396A1 (de) * | 1999-01-22 | 2000-08-17 | Staiger Mohilo & Co Gmbh | Verfahren zum Messen des Nitratgehalts von Flüssigkeiten und Anordnung zur Durchführung des Verfahrens |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61172031A (ja) * | 1986-01-09 | 1986-08-02 | Agency Of Ind Science & Technol | 硝酸態窒素と亜硝酸態窒素の合量を測定する方法 |
DE3726524A1 (de) * | 1987-08-10 | 1989-02-23 | Fresenius Ag | Haemoglobindetektor |
US4873470A (en) * | 1988-05-27 | 1989-10-10 | Ncr Corporation | Programmable ultraviolet lamp control system |
US5745243A (en) * | 1996-11-15 | 1998-04-28 | Optical Solutions, Inc. | Photometer apparatus |
DE19835335C1 (de) * | 1998-08-05 | 1999-11-25 | Draeger Sicherheitstech Gmbh | Infrarotoptischer Gassensor |
DE19840570A1 (de) * | 1998-09-05 | 2000-03-16 | M & R Mes Und Regelungstechnik | Verfahren zur Signalverarbeitung eines Gasanalysators mit Interferenzfiltern und elektronischen Strahlungsdetektoren |
-
2002
- 2002-06-28 DE DE10228929A patent/DE10228929A1/de not_active Withdrawn
-
2003
- 2003-06-03 AU AU2003238195A patent/AU2003238195A1/en not_active Abandoned
- 2003-06-03 WO PCT/EP2003/005768 patent/WO2004003524A1/de not_active Application Discontinuation
- 2003-06-03 US US10/517,779 patent/US7339178B2/en not_active Expired - Fee Related
- 2003-06-03 EP EP03735520A patent/EP1518105A1/de not_active Withdrawn
- 2003-06-03 CN CNB038180812A patent/CN100473973C/zh not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3403253A (en) * | 1965-11-29 | 1968-09-24 | Navy Usa | Humidiometer having feedback means to control the energization of the tube |
US4447150A (en) * | 1981-02-27 | 1984-05-08 | Bentley Laboratories | Apparatus and method for measuring blood oxygen saturation |
DE3324606A1 (de) * | 1983-07-08 | 1985-01-17 | Dr. Bruno Lange Gmbh, 1000 Berlin | Vorrichtung zum messen und bestimmen des nitratgehaltes von fluessigkeiten |
US4627284A (en) * | 1985-07-22 | 1986-12-09 | Spectral Sciences, Inc. | Ultraviolet absorption hygrometer |
DE19902396A1 (de) * | 1999-01-22 | 2000-08-17 | Staiger Mohilo & Co Gmbh | Verfahren zum Messen des Nitratgehalts von Flüssigkeiten und Anordnung zur Durchführung des Verfahrens |
Non-Patent Citations (1)
Title |
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See also references of EP1518105A1 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9568458B2 (en) | 2014-08-21 | 2017-02-14 | Sharp Kabushiki Kaisha | Optical sensor for fluid analysis |
US10139386B2 (en) | 2014-08-21 | 2018-11-27 | Sharp Kabushiki Kaisha | Optical sensor for fluid analysis |
Also Published As
Publication number | Publication date |
---|---|
AU2003238195A1 (en) | 2004-01-19 |
CN100473973C (zh) | 2009-04-01 |
US20060091319A1 (en) | 2006-05-04 |
EP1518105A1 (de) | 2005-03-30 |
CN1672035A (zh) | 2005-09-21 |
DE10228929A1 (de) | 2004-01-15 |
US7339178B2 (en) | 2008-03-04 |
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