Optochemical sensor
10876968 · 2020-12-29
Assignee
Inventors
- Daniel Aigner (Thalwil, CH)
- Robert Lettow (Zürich, CH)
- Toni Schneider (Winterthur, CH)
- Martin Winkler (Galgenen, CH)
- Stefanie Zuber (Zürich, CH)
Cpc classification
International classification
Abstract
An sensor (2) based on an optical-sensing technique measures gaseous or dissolved analytes in a measurement medium (4). The sensor has a sensor housing (6) and an optochemical sensor element (20, 220) arranged within the sensor housing. The optochemical sensor element (220) has a substrate (222), a sensing layer (224) and a barrier layer (230). The barrier layer is arranged to protect the optochemical sensor element from interfering substances (234) present in the measurement medium.
Claims
1. A sensor for measuring at least one of oxygen, carbon dioxide and ozone as an analyte, in a gaseous or dissolved form, in a measurement medium containing at least one interferent, comprising: a sensor housing; and an optochemical sensor element, arranged within the sensor housing to be in contact with the measurement medium during measurement operation, the optochemical sensor element comprising: a substrate, a sensing layer arranged on the substrate, the sensing layer comprising a luminescent indicator sensitive to the analyte; and a barrier layer, formed by applying a curable precursor on the sensing layer to prevent passage of the at least one interferent in the measurement medium, while allowing the passage of the analyte, the curable precursor comprising an organic part and at least one functional group suitable for curing; wherein the at least one interferent is selected from the group consisting of: volatile organic compounds, unsaturated organic compounds, aromatic compounds, sulfurous oxides, nitric oxides and gaseous or volatile compounds containing sulfur, nitrogen, chlorine and combinations thereof.
2. The sensor of claim 1, wherein the at least one functional group is selected from the group consisting of: trialkoxysilane, dialkoxysilane, and monoalkoxysilane.
3. The sensor of claim 1, further comprising: at least one light source; and at least one detection unit, arranged such that a light path from the at least one light source passes through the optochemical sensor element before striking the at least one detection unit.
4. The sensor of claim 1, wherein the sensing layer comprises an indicator immobilized in a polymer matrix.
5. The sensor of claim 1, wherein the selected gaseous or dissolved analyte is selected from the group consisting of: oxygen, carbon dioxide and ozone.
6. The sensor of claim 5, wherein the indicator is at least one oxygen sensitive indicator selected from the group consisting of: a polycyclic aromatic hydrocarbon, an oxygen sensitive transitional metal polypyridil complex, a metalloporphyrin complex and combinations or derivatives thereof.
7. The sensor of claim 6, wherein the oxygen-sensitive indicator is at least one of: pyrene, a derivative of pyrene, [Ru(bpy).sub.3].sup.2+, a metalloporphyrin complex comprising platinum and a metalloporphyrin complex comprising palladium.
8. The sensor of claim 5, wherein the indicator is at least one carbon dioxide sensitive indicator selected from the group consisting of: 8-hydroxypyrene-1,3,6-trisulfonic acid, a derivative of 1,4-diketo pyrrolo-[3,4-c]-pyrrole and combinations thereof.
9. The sensor of claim 8, wherein the carbon-dioxide sensitive is at least one of: 8-hydroxypyrene-1,3,6-trisulfonic acid or a 1,4-diketo pyrrolo-[3,4-c]-pyrrole derivative.
10. The sensor of claim 5, wherein the indicator is an ozone sensitive xanthene dye.
11. The sensor of claim 1, wherein the optochemical sensor element further comprises a temperature sensing layer having at least one temperature-sensitive indicator arranged to measure the temperature of the measurement medium.
12. The sensor of claim 11, wherein each of the at least one temperature sensitive indicators is selected from the group consisting of: rhodamine, rhodamine derivatives, temperature sensitive metal ligand complexes, lanthanide-doped bulk materials, and YAB doped with chromium ions.
13. The sensor of claim 12, wherein the at least one temperature sensitive indicator is [Ru(bpy).sub.3].sup.2+ or lanthanide-doped Al.sub.2O.sub.3.
14. The sensor of claim 1, further comprising at least one additional layer selected from the group consisting of: a reflection layer, an optical insulation layer, a protection layer, and combinations thereof.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) Other features and advantages disclosed herein will become more apparent from the following detailed description of exemplary embodiments when read in conjunction with the following figures. The figures show:
(2)
(3)
(4)
(5)
(6)
DETAILED DESCRIPTION
(7)
(8) The optochemical sensor comprises a light source 10, a detection unit 12 and optical elements 14 arranged within the sensor housing 6. Further, the optochemical sensor 2 can comprise more than one light source and/or more than one detector respectively within the sensor housing 6.
(9) During measurement operation of the optochemical sensor 2 based on the principle of luminescence, excitation light is emitted by the light source 10 and is directed by optical elements 14, such as filters, mirrors or lenses that are arranged within the sensor housing 6, towards the optochemical sensor element 20 such that the emitted light interacts with the optochemical sensor element 20. A light path 16 is indicated by arrows. The optochemical sensor element is arranged in the light path 16 between the light source 10 and detection unit 12. A photoluminescence response signal, in particular a fluorescence or phosphorescence response signal that is emitted after excitation interacts with the optochemical sensor element 20 and is detected by the detection unit 12. As previously described, in optochemical sensors based on photoluminescence a change in the luminescent signal caused by an analyte in the measurement medium is detected. The detection unit 12 comprises at least one detector, for example a photodiode. Depending on the number of analytes in the measurement medium to be measured, the detection unit can further comprise corresponding detectors for one or more of the parameters. The detection unit 12 further comprises optical filters 14 that are positioned in front of the detectors. These optical filters help in separating signals that are received from the optochemical sensor element 20. The optochemical sensor 2 further comprises optical fibers to direct the light to and/or emit the light from the optochemical sensor element.
(10) The response signal received by the detection unit 12 is amplified and processed by the control unit 8. The control unit is connected via a wired or wireless connection to the sensor head 18 and it can also function as a regulation unit. The control unit 8 can further be connected to a terminal 9 which in turn can be connected to a display, a process control system, a transmitter or a further processing unit and/or similar devices 11. The control unit 8 is arranged either as an external unit or entirely or in part inside the sensor housing 6. In this embodiment, the control unit 8 has either a wire-bound or wireless connection to the sensor head 18 of the optochemical sensor 2. The state of the art includes different variants of the control unit and the latter is therefore only symbolically illustrated. The optochemical sensor element 20 is releasably connected to the sensor housing 6 so that the optochemical sensor element 20 can be easily replaced.
(11)
(12) A barrier layer 230 is arranged on the sensing layer 224. The barrier layer 230 is arranged such that it provides protection to the optochemical sensor element 220 from one or more interferents 234 present in the measurement medium 204. In another embodiment, the barrier layer is formed and arranged on the substrate and is arranged to face the measurement medium. In this embodiment, the sensing layer is arranged on the substrate's side that is directed away from the measurement medium.
(13) The presence of one or more interferents in the measurement medium often interferes with detection measurements during photoluminescence quenching. Examples of possible interferents in a measurement medium include volatile organic compounds, unsaturated organic compounds, aromatic compounds, sulfurous oxides or other sulfur-containing gaseous or volatile compounds, nitric oxides or other nitrogen-containing gaseous or volatile compounds, and/or chlorine containing vapor or gaseous compounds. In particular, further examples of possible interferents are sulfur dioxide, carbon monoxide, methane, ethane, propane, butane, pentane, hexane, ethylene, acetylene, hydrogen, chlorine, methanol, benzol, ethylbenzol, toluole, o-xylene, m-xylene, p-xylene, propylene, hydrogen chloride and butadiene.
(14) The barrier layer 230 provides protection to the optochemical sensor element 220 by impeding the passage of one or more interferents from the measurement medium 204. At the same time the barrier layer 230 is permeable to the analyte to be measured, e.g. gaseous or dissolved oxygen, ozone or CO.sub.2.
(15) Examples of suitable indicators for the measurement of particularly oxygen are metal-organic complexes comprising polycyclic aromatic hydrocarbons such as pyrene and/or pyrene derivatives, oxygen sensitive transitional metal polypyridil complexes, in particular [Ru(bpy).sub.3].sup.2+ or metalloporphyrin complexes comprising in particular platinum or palladium. Additionally, there are numerous commercially available indicators that may be used in the measurement of oxygen.
(16) In a further exemplary embodiment, the optochemical sensor element is configured for measuring dissolved or gaseous carbon dioxide in the measurement medium. A suitable indicator for the measurement of dissolved or gaseous carbon dioxide is 8-hydroxypyrene-1,3,6-trisulfonic acid.
(17)
(18) The optochemical sensor element 320 is covered with at least one additional layer. Examples of such additional layers are a light reflection layer, an optical insulation layer, a protection layer etc. In a preferred embodiment the optochemical sensitive element is covered with three additional layers.
(19) Either of the additional layers may be comprised of the same base material, however, the two of the layers may be doped with different substances to provide optical protection and insulation to the optochemical sensor element and in turn to the optochemical sensor.
(20) As seen in
(21) An optical insulation layer 338, in this embodiment, is arranged on the reflection layer 336. In this case, the optical insulation layer 338 serves as a stray light protection layer and is for example a black silicone layer comprising carbon. The advantageous feature of including the stray light protection layer as the second layer is that it blocks stray light that could possibly enter from the measurement medium 304 and interfere with the measurement results. Further, a protection layer 340 can be arranged on the optical insulation layer 338, as shown in
(22)
(23) This additional sensing layer is a temperature sensing layer 450 for measuring temperature of the measurement medium 404. The temperature sensing layer 450 is arranged on the substrate 422 such that the temperature sensing layer 450 lies opposite to the sensing layer 424. The temperature sensing layer 450 comprises a temperature sensitive indicator 452 immobilized in a polymer matrix 454. The polymer matrix 454 is either same or different in composition of the polymer matrix 426 of the sensing layer 424.
(24) In a further embodiment (not shown in the figures), the temperature sensitive indicator and the analyte sensitive indicator are immobilized in the same polymer matrix. Therefore, a sensing layer comprising the temperature sensitive indicator and analyte sensitive indicator are arranged on a substrate such that the sensing layer faces towards the direction of the measurement medium.
(25) According to the present invention, the barrier layer 230 comprises a network with both organic and inorganic structural elements. It is formed from a solution of a curable precursor. Examples of suitable organic part include: carboxy ester, amide, imide, carbamate, thiocarbamate, amidine, imide acid ester, thioester, thioamide, dithio ester, carbonate, carbon diamide, guanidine, ether, acetal. Preferably, the organic part is composed such that the elements sulfur, nitrogen and oxygen together make up a ratio of 25-60% molecular weight, with respect to the total molecular weight of the organic part. More preferably, the organic part is composed such that the elements sulfur, nitrogen and oxygen together make up a ratio of 30-45% molecular weight, with respect to the total molecular weight of the organic part.
(26) The curable precursor was deposited in a layer form from a precursor solution. The curable precursor comprises at least one functional group suitable for curing that is linked to the organic part. The at least one functional group suitable for curing is selected from any of: trialkoxysilane, dialkoxyalkylsilane, or alkoxytrialkylsilane.
(27) The precursor molecule was prepared by a reaction between a diol and an iso-cyanato-silane in the presence of a catalyst under an inert atmosphere for a duration of about 30 minutes at 50 C.
(28) Exemplary diols suitable to be used to prepare the precursor can be selected from any of the following: ethylene glycol; proylene gylcol; all isomers of butane diol, butane diol, pentane diol, hexane diol, heptane diol, octane diol, nonane diol, or decane diol.
(29) Suitable isocyanatosilanes include for example: isocyanatosilanes, isocyanatomethyltriethoxysilane, isocyanatoethyltriethoxysilan, isocyanatopropyltriethoxysilane, isocyanatobutyltriethoxysilane, isocyanatomethyltrimethoxysilane, isocyanatoethyltrimethoxysilane, isocyanatopropyltrimethoxysilane, or isocyanatobutyltrimethoxysilane.
(30) Suitable catalysts include for example: tin organic compounds, preferably dibutyltin dilaurate, diethyltin dilaurate, diphenyltin dilaurate, dibutyltin dimyristate, diethyltin dimyristate, diphenyltin dimyristate, dibutyltin dipalmitate, diethyltin dipalmitate, diphenyltin dipalmitate, dibutyltin distearate, diethyltin distearate or diphenyltin distearate.
(31) The prepared precursor was dissolved in a common solvent, such as an organic solvent. Examples of organic solvents include: chloroform, toluene, methyl-tertbutyl ether, diisopropyl ether, tetahydrofurane, ethyl acetate and other esters of acetic acid, ethyl formiate and other esters of formic acid, ethyl propanoate and other esters of propanoic acid, ethyl butyrate and other esters of butyric acid, dimethylformamide and other formamides, dimethylacetamide and other acetamides; all isomers of trichloroethane, dichloroethane, chloroethane, xylenes, trimethylbenzene, ethylbenzene, benzene, hexanes, heptanes, octanes or pentanes.
(32) Further, a wetting agent, such as modified polydimethylsiloxane (BYK-306 procured from BYK), was added to the solution followed by the addition of a curing catalyst. Examples of curing catalysts include: any protic acid or Lewis-acid and any compound releasing such an acid/Lewis-acid at elevated temperature. Preferably, curing catalysts can be selected from any one of the following: hydrochloric acid, sulfuric acid, nitric acid, aluminum acetylacetonate, acetic acid, formic acid, propanoic acid or butyric acid.
(33) The resulting precursor solution was then applied as a coat to the substrate of the optochemical sensor element, wherein the substrate was provided with a sensing layer. The methods used for coating are from any of the following methods: knife coating, screen printing, spray coating, dip coating, other forms of printing, micro-dispensing. Thereafter, the optochemical sensor element was left to dry in air in order to dry the applied the solution to result in a barrier layer. Examples of further curing methods include but are not limited to: thermal curing, UV curing or microwave curing.
(34) The following method elaborates the steps of applying a barrier layer on an optochemical sensor element of an optochemical sensor for the determination of dissolved or gaseous oxygen in a measurement medium.
EXAMPLE 1
(35) A mixture of 11.1 g of distilled 1,6-hexandiole and 46.503 mL of isocyanatopropyl-triethoxysilane (ICTES) was stirred under argon for 30 minutes at 50 C. After 30 minutes the oil bath was removed and 31 mg of dibutyltin-dilaurate was added. After a subsequent increase and decrease of the temperature of the reaction mixture, the reaction mixture was further heated with the oil bath to 50 C. The reaction was terminated after approximately 60 minutes when the reaction mixture solidified to a waxlike product. Thereafter, the waxlike product was stored under argon.
(36) A wetting agent, such as a solution of modified polydimethylsiloxane (BYK-306 procured from BYK), the waxlike product, and a catalyst for curing were added to an organic solvent. Preferably, the organic solvent chosen was such that it has a boiling point in the range of 30-200 C., in particular in the range of 60-150 C. at atmospheric pressure. Further, any protic acid or Lewis-acid and any compound releasing such an acid/Lewis-acid at elevated temperature can be used in principle as a catalyst for curing. Preferably, 30.5 L of wetting agent, 1.666 g of the waxlike product, and 35 mg of catalyst were added to in the order mentioned to 3 mL of the organic solvent, therefore resulting in a precursor solution. Between the consecutive additions of each component, the mixture was stirred for 10-15 min to result in a clear precursor solution. Examples of catalysts that can be used for the step of curing include but are not limited to hydrochloric acid, sulfuric acid, nitric acid, aluminum acetylacetonate, acetic acid, formic acid, propanoic acid or butyric acid.
(37) A substrate with a sensing layer was provided. The sensing layer comprised an oxygen sensitive indicator that was immobilized in a polymer matrix. The indicator suited for the measurement of oxygen was chosen from any of the following: metal-organic complexes comprising a polycyclic aromatic hydrocarbon, such as pyrene and/or its derivatives, oxygen sensitive transitional metal polypyridil complex, in particular [Ru(bpy).sub.3].sup.2+, or a metalloporphyrin complex comprising in particular platinum or palladium.
(38) The resulting precursor solution was coated on the substrate by any of the following coating methods: knife coating, spray coating, dip coating, micro-dispensing or other known forms of printing. Preferably, spin coating was the method chosen to apply the precursor solution to the substrate.
(39) The substrate coated with the precursor solution was then introduced in an oven that was pre-heated to 150 C. The substrate was allowed to age in the oven for 5 hours at the end of which the optochemical sensor element with a scratch-resistant, glassy appearing barrier layer was obtained. Further, protection layers were applied on the barrier layer to yield the entire optochemical sensor element. A reflection layer serving as a light reflection layer was applied on barrier layer. An optical insulation layer serving as an optical insulation layer was applied on the reflection layer. A protection layer composed of a PTFE membrane or a foil was applied on the optical insulation layer.
(40) In a further embodiment, a temperature sensing layer was applied on the surface of the substrate facing away from the measurement medium.
(41) The resulting optochemical sensor element was incorporated in an optochemical sensor and the sensor was exposed to experimental conditions. The experiments involved exposing an optochemical sensor with and without a barrier layer to a medium comprising different gases that serve as interferents. The error in measurements for the exposure of the sensor to these gases was studied over a total exposure time and corresponding experimental results were noted.
(42)
(43) It is to be understood that the present invention is not limited to the methods described above, but encompasses any and all methods within the scope of the following claims.