CN217820006U - A mixed structure for atmospheric peroxide automatic monitoring system - Google Patents
A mixed structure for atmospheric peroxide automatic monitoring system Download PDFInfo
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- CN217820006U CN217820006U CN202222035909.3U CN202222035909U CN217820006U CN 217820006 U CN217820006 U CN 217820006U CN 202222035909 U CN202222035909 U CN 202222035909U CN 217820006 U CN217820006 U CN 217820006U
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- mixing
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- buffer solution
- peroxide
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- 150000002978 peroxides Chemical class 0.000 title claims abstract description 41
- 238000012544 monitoring process Methods 0.000 title claims abstract description 23
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 22
- 238000005070 sampling Methods 0.000 claims abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
- 239000007853 buffer solution Substances 0.000 claims description 34
- 238000004458 analytical method Methods 0.000 claims description 17
- 239000012670 alkaline solution Substances 0.000 claims description 3
- 230000001737 promoting effect Effects 0.000 claims description 2
- 238000001514 detection method Methods 0.000 abstract description 13
- 239000007788 liquid Substances 0.000 abstract description 12
- 229910001873 dinitrogen Inorganic materials 0.000 abstract description 10
- 239000000203 mixture Substances 0.000 abstract description 8
- 238000003756 stirring Methods 0.000 abstract description 3
- -1 wherein Substances 0.000 abstract 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 10
- 239000003513 alkali Substances 0.000 description 5
- DDMKRZXDPHEQFG-UHFFFAOYSA-N 2-[3-[5-(carboxymethyl)-2-hydroxyphenyl]-4-hydroxyphenyl]acetic acid Chemical compound OC(=O)CC1=CC=C(O)C(C=2C(=CC=C(CC(O)=O)C=2)O)=C1 DDMKRZXDPHEQFG-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000001451 organic peroxides Chemical class 0.000 description 4
- 238000005086 pumping Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000001917 fluorescence detection Methods 0.000 description 3
- XQXPVVBIMDBYFF-UHFFFAOYSA-N 4-hydroxyphenylacetic acid Chemical compound OC(=O)CC1=CC=C(O)C=C1 XQXPVVBIMDBYFF-UHFFFAOYSA-N 0.000 description 2
- 102000016938 Catalase Human genes 0.000 description 2
- 108010053835 Catalase Proteins 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 108010001336 Horseradish Peroxidase Proteins 0.000 description 1
- 238000010420 art technique Methods 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000012482 calibration solution Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Abstract
The application provides a mixed structure for atmosphere peroxide automatic monitoring system for promote the mixture of fluorescence reagent, wherein, atmosphere peroxide automatic monitoring system includes a sampling device and an analytical equipment, is provided with a mixture tee bend S61 between the entrance point of analytical equipment' S second hybrid tube and tee bend S2, and tee bend S2 and nitrogen cylinder K61 are connected respectively through mixing tee bend S61 to the entrance point of second hybrid tube, and nitrogen gas in the nitrogen cylinder K61 is gone into through micropump P61 pump and is mixed tee bend S61. This application can be after fluorescence reagent pump goes into the system through increasing mixed structure, through micropump pump income nitrogen gas, forms the bubble through nitrogen gas, and the mixed liquid after adding fluorescence reagent stirs the mixture through the bubble, promotes fluorescence reagent's mixture. In addition, the mixing structure is added without increasing the length of a system pipeline to promote mixing, the original system structure is not required to be changed, the detection precision is improved, and the cost and the detection time are saved.
Description
Technical Field
The utility model relates to an atmospheric environment monitoring system especially relates to an automatic monitoring system of peroxide in atmosphere, in particular to a mixed structure for atmospheric peroxide automatic monitoring system.
Background
CN 105842216B, previously filed and published by the applicant, discloses an automatic monitoring system for atmospheric peroxide, which comprises a sampling device and an analysis device, wherein the sampling device comprises a horizontally arranged spiral pipe, a vertically arranged gas-liquid separator and an air pump, the inlet ends of the spiral pipe are respectively connected with atmosphere and a liquid collecting bottle, the outlet end of the spiral pipe is connected with the middle part of the gas-liquid separator, the upper end of the gas-liquid separator is connected with the air pump, and the lower end of the gas-liquid separator is connected with the analysis device through a first connecting pipeline. The prior art can realize automatic monitoring of the atmospheric peroxide and can obtain a more accurate content result of the atmospheric peroxide.
This prior art technique can achieve more accurate results, but there is still room for improvement.
Disclosure of Invention
The technical problem to be solved by the present invention is to provide a hybrid structure for an automatic monitoring system of atmospheric peroxide to reduce or avoid the aforementioned problems.
In order to solve the technical problem, the utility model provides a mixing structure for an atmospheric peroxide automatic monitoring system, which is used for promoting the mixing of a fluorescent reagent in the atmospheric peroxide automatic monitoring system, wherein the atmospheric peroxide automatic monitoring system comprises a sampling device and an analysis device, and the sampling device and the analysis device are connected through a first connecting pipeline; the analysis device comprises a first mixing pipe, a second mixing pipe and a third mixing pipe which are connected end to end in series; the inlet end of the first mixing pipe is respectively connected with the first connecting pipeline, the first buffer solution bottle and the second buffer solution bottle through a cross joint S1; the inlet end of the second mixing pipe is respectively connected with the outlet end of the first mixing pipe and the fluorescent reagent bottle through a tee S2, and the inlet end of the third mixing pipe is respectively connected with the outlet end of the second mixing pipe and the alkaline solution bottle through a tee S3; the outlet end of the third mixing pipe is connected with a sample collector, and the middle part of the sample collector is connected with a fluorescence detector through a pipeline; a mixing tee joint S61 is arranged between the inlet end of the second mixing pipe and the tee joint S2, the inlet end of the second mixing pipe is respectively connected with the tee joint S2 and a nitrogen cylinder K61 through the mixing tee joint S61, and nitrogen in the nitrogen cylinder K61 is pumped into the mixing tee joint S61 through a micro pump P61.
Preferably, the first buffer solution in the first buffer solution bottle is pumped into the cross joint S1 through a micro pump P4; the second buffer solution in the second buffer solution bottle is pumped into the cross-joint S1 by a micro-pump P5.
Preferably, the fluorescent reagent in the fluorescent reagent bottle is pumped into the tee S2 by the micro-pump P6.
Preferably, the alkali liquor in the alkali liquor bottle is pumped into the tee joint S3 through a micro pump P8.
This application can be after fluorescence reagent pump goes into the system through increasing mixed structure, through micropump pump income nitrogen gas, forms the bubble through nitrogen gas, and the mixed liquid after adding fluorescence reagent stirs the mixture through the bubble, promotes fluorescence reagent's mixture. Moreover, the mixing structure is added without increasing the length of a system pipeline to promote mixing, the original system structure is not required to be changed, the detection precision is improved, and the cost and the detection time are saved.
Drawings
The drawings are only intended to illustrate and explain the present invention and do not limit the scope of the invention.
Therein, fig. 1 shows a schematic view of a hybrid structure for an automatic atmospheric peroxide monitoring system according to a specific embodiment of the present application.
Detailed Description
In order to clearly understand the technical features, objects, and effects of the present invention, embodiments of the present invention will be described with reference to the accompanying drawings. Wherein like parts are given like reference numerals.
Fig. 1 shows a schematic diagram of a hybrid architecture for an automatic atmospheric peroxide monitoring system according to a specific embodiment of the present application. Similar to the prior art, the atmospheric peroxide automatic monitoring system of the present application is generally comprised of two parts, including a sampling device 100 and an analysis device 200. The sampling device 100 continuously collects the peroxides in the atmosphere and then continuously transmits the peroxides to the analysis device 200 through the first connecting pipeline 300, wherein the analysis device 200 analyzes the peroxides in the sample by adopting a fluorescence detection method to respectively obtain the concentration of the total peroxides and the concentration of the total organic peroxides in the sample, and the concentration of the hydrogen peroxide in the atmosphere can be obtained through conversion.
The analysis device 200 adopts a fluorescence detection method to analyze peroxide in a sample, and the principle is that the peroxide can convert non-fluorescent p-hydroxyphenylacetic acid into 2,2 '-dihydroxy-biphenyl-5,5' -diacetic acid with strong fluorescence under the action of horseradish peroxidase, the fluorescence intensity of a fluorescent substance is detected by a fluorescence detector to determine the concentration of the peroxide, and finally, the concentrations of total peroxide and organic peroxide can be calculated by utilizing a simulated regression equation of a calibration curve, and the concentration of hydrogen peroxide is obtained by calculation.
As shown in fig. 1, the analysis device 200 includes a first mixing tube 21, a second mixing tube 22, and a third mixing tube 23 connected horizontally end-to-end in series. The inlet end of the first mixing tube 21 is respectively connected with the first connecting pipeline 300, the first buffer solution bottle 201 and the second buffer solution bottle 2011 through a four-way joint S1, the inlet end of the second mixing tube 22 is respectively connected with the outlet end of the first mixing tube 21 and the fluorescent reagent bottle 202 through a three-way joint S2, and the inlet end of the third mixing tube 23 is respectively connected with the outlet end of the second mixing tube 22 and the alkaline solution bottle 203 through a three-way joint S3; the outlet end of the third mixing pipe 23 is connected with a vertically arranged sample collector 24, and the middle part of the sample collector 24 is connected with a fluorescence detector 500 through a pipeline.
The upper end of the sample collector 24 is connected with the outlet end of the third mixing pipe 23, the lower end of the sample collector 24 is connected with an air pump P12, and the sample collector has the function of discharging redundant samples out of the analysis system, so that excessive liquid is prevented from being accumulated in the collecting pipe, and the peroxide cannot be monitored in real time and on line. A micro pump P10 is disposed in a pipeline connecting the middle of the sample collector 24 to the fluorescence detector 500 for pumping the liquid into the fluorescence detector 500.
The capture liquid sample dissolved with peroxide is pumped into the analysis apparatus 200 through the first connection pipe 300 by the micro pump P2, and is merged with the first buffer solution pumped out from the first buffer solution bottle 201 by the micro pump P4 at the cross S1, or merged with the second buffer solution pumped out from the second buffer solution bottle 2011 by the micro pump P5 at the cross S1 (the first buffer solution and the second buffer solution are not pumped in simultaneously), and then is sufficiently mixed in the first mixing pipe 21; thereafter, the sample flows out of the first mixing tube 21, joins the fluorescent reagent pumped out of the fluorescent reagent bottle 202 by the micro pump P6 at the three-way S2, and then undergoes a reaction in the second mixing tube 22; the reacted sample flows out of the second mixing tube 22, joins the alkali solution pumped out of the alkali solution bottle 203 by the micro pump P8 at the tee S3, and then is fully mixed in the third mixing tube 23.
The first buffer solution and the second buffer solution have the same functions of removing heavy metals in the solution to avoid interference, and simultaneously, the pH value is adjusted to be about 6.8 suitable for carrying out fluorescence reaction. The buffer solution in the second buffer solution bottle 2011 is different from the buffer solution in the first buffer solution bottle 201 in that catalase is further added to the buffer solution in the second buffer solution bottle 2011. The fluorescent reagent is used for generating the 2,2 '-dihydroxy-biphenyl-5,5' -diacetic acid which emits fluorescence, and the alkali liquor is used for finally adjusting the pH value of the detection solution to be 10.0-10.5 which is most suitable for fluorescence detection, so that the detection method has the highest sensitivity.
When pumping the second buffer solution by the micro-pump P5 is chosen, the hydrogen peroxide in the capture liquid sample with the peroxide dissolved therein can be decomposed by catalase, so that no hydrogen peroxide is present during the subsequent detection, and the last detected peroxide concentration in the analysis device 200 is completely the organic peroxide concentration in the atmosphere. Alternatively, the first buffer solution is pumped through the micro pump P4 and the total concentration of peroxide in the atmosphere is determined. Thus, finally by calculation, the concentration of hydrogen peroxide in the atmosphere can be obtained by subtracting the concentration of organic peroxide obtained by pumping the second buffer solution from the total peroxide concentration obtained by pumping the first buffer solution. According to the application, the first buffer solution and the second buffer solution can be pumped in by switching, and the detection of various peroxides in the atmosphere can be realized by using the same fluorescence detector 500, so that the system structure is simplified, and the cost is saved.
Through the above description of the automatic monitoring system for the peroxide in the atmosphere, the final detection result of the peroxide in the atmosphere is obtained by calculating the detection result of the fluorescence detector on the amount of the 2,2 '-dihydroxy-biphenyl-5,5' -diacetic acid which fluoresces. Thus, the inventors believe that the higher the accuracy of the amount of fluorescing 2,2 '-dihydroxy-biphenyl-5,5' -diacetic acid produced by the reaction, the higher the accuracy of the final peroxide detection.
Based on this analysis, the inventors set a mixing tee S61 between the inlet end of the second mixing pipe 22 and the tee S2, the inlet end of the second mixing pipe 22 was connected to the tee S2 and a nitrogen gas cylinder K61 through the mixing tee S61, respectively, and nitrogen gas in the nitrogen gas cylinder K61 was pumped into the mixing tee S61 by a micro pump P61.
This application is after fluorescence reagent pump goes into the system, through micropump pump income nitrogen gas, forms the bubble through nitrogen gas, and the mixed liquid after adding fluorescence reagent stirs the mixture through the bubble, has promoted fluorescence reagent's mixture. After the mixed structure is added through the test of the calibration solution, the lower limit of the peroxide detected by the subsequent fluorescence detector can be improved by one order of magnitude. Moreover, the mixing structure is added without increasing the length of a system pipeline to promote mixing, the original system structure is not required to be changed, the detection precision is improved, and the cost and the detection time are saved.
It is to be understood by those skilled in the art that while the present invention has been described in terms of several embodiments, it is not intended that each embodiment cover a separate embodiment. The description is given for clearness of understanding only, and it is to be understood that all matters in the embodiments are to be interpreted as including all technical equivalents which are encompassed by the claims.
The above description is only exemplary of the present invention, and is not intended to limit the scope of the present invention. Any equivalent changes, modifications and combinations that may be made by those skilled in the art without departing from the spirit and principles of the invention should be considered within the scope of the invention.
Claims (4)
1. A mixing structure for an automatic atmospheric peroxide monitoring system is used for promoting the mixing of a fluorescent reagent in the automatic atmospheric peroxide monitoring system, wherein the automatic atmospheric peroxide monitoring system comprises a sampling device and an analysis device, and the sampling device and the analysis device are connected through a first connecting pipeline; the analysis device comprises a first mixing pipe, a second mixing pipe and a third mixing pipe which are connected end to end in series; the inlet end of the first mixing pipe is respectively connected with the first connecting pipeline, the first buffer solution bottle and the second buffer solution bottle through a cross joint S1; the inlet end of the second mixing pipe is respectively connected with the outlet end of the first mixing pipe and the fluorescent reagent bottle through a tee S2, and the inlet end of the third mixing pipe is respectively connected with the outlet end of the second mixing pipe and the alkaline solution bottle through a tee S3; the outlet end of the third mixing pipe is connected with a sample collector, and the middle part of the sample collector is connected with a fluorescence detector through a pipeline; the device is characterized in that a mixing tee joint S61 is arranged between the inlet end of the second mixing pipe and the tee joint S2, the inlet end of the second mixing pipe is respectively connected with the tee joint S2 and a nitrogen cylinder K61 through the mixing tee joint S61, and nitrogen in the nitrogen cylinder K61 is pumped into the mixing tee joint S61 through a micro pump P61.
2. The mixing structure for an atmospheric peroxide automatic monitoring system according to claim 1, wherein the first buffer solution in the first buffer solution bottle is pumped into the cross-joint S1 by a micro-pump P4; the second buffer solution in the second buffer solution bottle is pumped into the cross-joint S1 by a micro-pump P5.
3. The mixing structure for an automatic atmospheric peroxide monitoring system according to claim 1, wherein the fluorescent reagent in the fluorescent reagent bottle is pumped into the tee S2 by a micro pump P6.
4. The mixing structure for an automatic atmospheric peroxide monitoring system according to claim 1, wherein the lye in the lye bottle is pumped into the tee S3 by the micro pump P8.
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CN202222035909.3U CN217820006U (en) | 2022-08-03 | 2022-08-03 | A mixed structure for atmospheric peroxide automatic monitoring system |
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CN202222035909.3U CN217820006U (en) | 2022-08-03 | 2022-08-03 | A mixed structure for atmospheric peroxide automatic monitoring system |
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CN217820006U true CN217820006U (en) | 2022-11-15 |
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CN202222035909.3U Expired - Fee Related CN217820006U (en) | 2022-08-03 | 2022-08-03 | A mixed structure for atmospheric peroxide automatic monitoring system |
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- 2022-08-03 CN CN202222035909.3U patent/CN217820006U/en not_active Expired - Fee Related
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Granted publication date: 20221115 |
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