CN111239234A - Non-radioactive method for on-line monitoring of ammonia gas - Google Patents
Non-radioactive method for on-line monitoring of ammonia gas Download PDFInfo
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Abstract
The invention discloses a non-radioactive device and a non-radioactive method for quickly, accurately and continuously monitoring ammonia gas. The invention utilizes the nonradioactive ion mobility spectrometry of the photo-ionization assisted by the reagent molecules, selects butanone as the reagent molecules in the positive ion mode, and realizes the rapid, accurate and high-sensitivity online measurement of ammonia gas. The detection device comprises: floating gas, carrier gas, a reagent molecule generating device, an ion mobility spectrometry system, a pump and the like.
Description
Technical Field
The invention belongs to the technical field of ion mobility spectrometry. The method utilizes the non-radioactive vacuum ultraviolet lamp ion mobility spectrometry, adopts air-breathing sampling in a positive ion mode, and initiates a chemical reaction by optimizing and screening reagent molecules and paraxylene, thereby improving the sensitivity and selectivity of ammonia detection and realizing the rapid and accurate online monitoring of ammonia.
Technical Field
Ammonia gas is a colorless, strongly pungent inorganic gas, is very soluble in water, is a Lewis base, and exists in both human bodies and the environment.
Ammonia has a major role in the human body and is considered to be an important exhalation biomarker, the major sources of ammonia in humans include deamination of amino acids, where most of the amino acids are transaminated with α -ketoglutarate to glutamate by glutaminase, ammonia is also produced by the metabolism of purine and pyrimidine compounds, ammonia is also produced by the breakdown of amino acids in food by intestinal bacteria and monoamine oxidase breakdown.
In the environment, ammonia is the only high-concentration alkaline gas in the atmospheric environment, can react with sulfur dioxide, nitrogen oxide and volatile organic compounds VOCs and generate aerosol particles, thereby influencing the global radiation balance, being an important reason for the formation of secondary particles in the aerosol haze pollution process, and being capable of causing the eutrophication of rivers and lakes.
Therefore, the detection of ammonia gas has important significance in human disease diagnosis, atmospheric quality detection and the like.
The main instruments and methods currently used for detecting ammonia gas are Mass Spectrometry (MS), gas chromatography-mass spectrometry (GC-MS), spectroscopy, such as cavity ring-down spectroscopy (CRDS), acousto-optic spectroscopy (PAS), chemical sensors, and the like. The detection limit of mass spectrum and GC-MS can reach ppb to ppt magnitude, but the mass spectrum and GC-MS have large volume and high price and need professional operation. The detection limit of spectroscopy can be up to ppb level, but there is a large background interference. Chemical sensors are portable, simple, have low detection limits but generally have poor stability and short service life.
Ion mobility spectrometry is carried out at atmospheric pressureAn apparatus for effecting ion separation using differences in ion mobility. The ion mobility spectrometer is simple in structure, low in cost, easy to miniaturize, short in response time and very suitable for on-line monitoring, and the sensitivity of the ion mobility spectrometer is high. However, the currently used ionization sources are all radioactive63Ni, which limits its wide use.
Disclosure of Invention
The invention aims to provide a non-radioactive device and a non-radioactive method for rapid online monitoring of ammonia gas.
A non-radioactive device and a method for on-line monitoring of ammonia gas comprise: sample gas, carrier gas, a reagent molecule generating device, a pump, tail gas, a radio frequency vacuum ultraviolet lamp, a migration tube system and floating gas.
The adopted device comprises a migration spectrum taking a radio frequency vacuum ultraviolet lamp as an ionization source, a migration tube of the migration spectrum comprises a reaction zone, an ion gate and an ion migration zone, and a floating gas inlet is arranged on one side of the ion migration zone far away from the reaction zone; a gas main outlet is arranged on one side of the reaction zone far away from the ion migration zone, and a pump is arranged at the gas main outlet; a sample gas and carrier gas inlet is arranged on one side of the reaction area close to the ion gate, the sample gas and carrier gas inlet is connected with a sample gas source through a pipeline, the sample gas and carrier gas inlet is connected with a gas outlet of the reagent molecule generating device through a pipeline, and a gas inlet of the reagent molecule generating device is connected with the carrier gas source; the reagent molecule generating device is a closed container, an open container for containing reagent molecules is arranged in the closed container, and the upper part of the closed container is provided with a gas outlet and a gas inlet; the reagent molecule is butanone.
The material of the guide pipe adopted by the gas circuit is polytetrafluoroethylene so as to reduce ammonia adsorption.
The reagent molecule adopted by the ion mobility spectrometry is 2-butanone. The reagent molecule generating device comprises a constant temperature system, the temperature range is 30-60 ℃, and the temperature of the reagent molecule generating device is kept in a specific temperature range.
The flow rate range of the carrier gas is 50-100ml/min, the flow rate range of the floating gas is 500-750 ml/min and the flow rate range of the tail gas is 600-750 ml/min;
the temperature range of the migration tube is 100-150 ℃, and the electric field intensity range of the migration zone is 450-500V/cm.
The invention has the advantages that:
the instrument and the method developed by the invention are based on an ion mobility spectrometry technology with a simple structure, a vacuum ultraviolet lamp non-radioactive ionization source is adopted, butanone is taken as a reagent molecule, the ammonia gas can be rapidly and accurately monitored on line, the selectivity of ammonia gas detection is improved, and the instrument and the method are convenient for large-scale application.
Drawings
FIG. 1 is a schematic structural diagram of rapid online ammonia gas monitoring. Wherein: the device comprises a radio frequency vacuum ultraviolet lamp 1, a reaction zone 2, an ion gate 3, a migration zone 4, a migration tube system 5, a floating gas 6, a carrier gas 7, a reagent molecule generating device 8, a sample gas 9, a pump 10 and a tail gas 11.
FIG. 2 is the ion migration spectrum of ammonia gas when 2-butanone is used as reagent molecule
FIG. 3 working curves for ammonia gas
FIG. 4 is an outdoor atmosphere chart of continuously monitoring for one day
Detailed Description
The following examples illustrate the use of the invention without limiting the scope of application described.
The adopted device comprises a migration spectrum taking a radio frequency vacuum ultraviolet lamp as an ionization source, a migration tube of the migration spectrum comprises a reaction zone and an ion migration zone, and a floating gas inlet is arranged on one side of the ion migration zone far away from the reaction zone; a gas main outlet is arranged on one side of the reaction zone far away from the ion migration zone, and a vacuum pump is arranged at the gas main outlet; a sample gas and carrier gas inlet is arranged on one side of the reaction area close to the ion migration area, the sample gas and carrier gas inlet is connected with a sample gas source through a pipeline, the sample gas and carrier gas inlet is connected with a gas outlet of the reagent molecule generating device through a pipeline, and the gas inlet of the reagent molecule generating device is connected with the carrier gas source; the reagent molecule generating device is a closed container, an open container for containing reagent molecules is arranged in the closed container, and the upper part of the closed container is provided with a gas outlet and a gas inlet; the reagent molecule is butanone.
Example 1
Detecting ammonia gas by using a reagent molecule assisted photoionization positive ion mobility spectrometry, wherein the reagent molecule is butanone, the flow rate range of the carrier gas is 50-100ml/min, the flow rate range of the drift gas is 500-750 ml/min, and the flow rate range of the tail gas is 600-750 ml/min; the temperature range of the migration tube is 100-150 ℃, and the electric field intensity range of the migration zone is 450-500V/cm. The ion mobility spectrum of ammonia gas is shown in fig. 2, the product ion is a compound of butanone and ammonia gas, the reduced mobility of the compound is 1.87, the reduced mobility of the reagent ion is 1.66, and the two ions can be completely separated.
Example 2
Air and/or nitrogen containing a series of ammonia gases with known gradient concentrations are taken as standard gases, the standard gases enter a migration spectrum through a sample gas and a carrier gas inlet of the migration spectrum for detection, and a series of migration spectrograms of the standard gases with the gradient concentrations are obtained; plotting the signal intensity of a series of standard gases with gradient concentrations against the concentration to obtain a working curve of the ammonia gas, as shown in figure 3; the linear range is 25-455ppb, with a lower detection limit of 6 ppb.
Example 3
And introducing the sample gas to be detected into the mobility spectrum for detection, and substituting the signal intensity of the mobility spectrum of the sample gas to be detected into the working curve equation to obtain the concentration of ammonia gas in the sample gas. Fig. 3 is a graph showing the change in the concentration of ammonia in the outdoor atmosphere during the day.
Claims (9)
1. A non-radioactive method capable of continuously monitoring ammonia gas on line is characterized in that:
the adopted device comprises an ion mobility spectrometry taking a radio frequency vacuum ultraviolet lamp as an ionization source, a migration tube of the mobility spectrometry comprises a reaction zone, an ion gate and an ion migration zone, and a drift gas inlet is arranged on one side of the ion migration zone far away from the reaction zone; a main gas outlet is arranged on one side of the reaction zone far away from the ion gate, and a pump is arranged at the main gas outlet; a sample gas and carrier gas inlet is arranged on one side of the reaction area close to the ion gate, the sample gas and carrier gas inlet is connected with a sample gas source through a pipeline, the sample gas and carrier gas inlet is connected with a gas outlet of the reagent molecule generating device through a pipeline, and a gas inlet of the reagent molecule generating device is connected with the carrier gas source; the reagent molecule generating device is a closed container, an open container for containing reagent molecules is arranged in the closed container, and the upper part of the closed container is provided with a gas outlet and a gas inlet;
the reagent molecule is p-butanone.
2. The method of claim 1, wherein:
the floating gas inlet is connected with a floating gas source; the air floating source is clean compressed air.
3. The method of claim 1, wherein:
and tail gas in the mobility spectrometry is discharged through a gas main outlet through a pump.
4. The method of claim 1, wherein: the gas inlet of the reagent molecule generating device is connected with a carrier gas source.
5. The method of claim 1, wherein: the guide pipe used by the gas pipeline is made of polytetrafluoroethylene.
6. The method of claim 1, wherein: the inner wall surface of the closed container of the reagent molecule generating device is provided with an electric heating device, namely, the wall surface of the closed container of the reagent molecule generating device is provided with an electric heating belt and/or an electric heating wire, the inner side wall of the reagent molecule generating device is provided with a thermocouple temperature measuring element, the thermocouple is in signal connection with a temperature controller through a lead, and the electric heating device is connected with an external circuit through the temperature controller.
7. The method according to any one of claims 1 to 6, wherein:
air and/or nitrogen containing a series of ammonia gases with known gradient concentrations are taken as standard gases, the standard gases enter a migration spectrum through a sample gas and a carrier gas inlet of the migration spectrum for detection, and a series of migration spectrograms of the standard gases with the gradient concentrations are obtained; plotting the signal intensity of a series of standard gases with gradient concentration against the concentration to obtain a working curve of the ammonia gas;
and introducing the sample gas to be detected into the mobility spectrum for detection, and substituting the signal intensity of the mobility spectrum of the sample gas to be detected into the working curve equation to obtain the concentration of ammonia gas in the sample gas.
8. The method of claim 7, wherein:
the ion mobility spectrometer comprises 4 working gas paths, namely a drift gas, a carrier gas, a sample gas and a tail gas, wherein the sample gas enters a sample gas inlet of a migration tube, the carrier gas enters a reagent molecule generating device at a certain flow velocity to generate a reagent molecule gas, and then the reagent molecule gas is connected with the sample gas and the carrier gas inlet;
the floating gas is clean air and enters the mobility spectrometer at a certain flow rate after passing through the mass flow meter; the tail gas is discharged from the pump through a tail gas port; and the difference value of the tail gas flow velocity, the floating gas flow velocity and the carrier gas flow velocity is the sample introduction amount of the sample.
9. A measuring method for rapidly monitoring ammonia gas on line according to claim 7 or 8, characterized in that:
the flow rate range of the carrier gas is 50-100ml/min, the flow rate range of the floating gas is 500-750 ml/min and the flow rate range of the tail gas is 600-750 ml/min;
the temperature range of the migration tube is 100-150 ℃, and the electric field intensity range of the migration area is 450-500V/cm;
the temperature range of the reagent molecule generating device is 30-60 ℃.
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CN113588767A (en) * | 2021-08-03 | 2021-11-02 | 大连工业大学 | Biogenic amine detection method based on time-resolved dynamic thermal desorption ion mobility spectrometry |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101413919A (en) * | 2007-08-01 | 2009-04-22 | 中国科学院大连化学物理研究所 | Method for recognizing and analyzing sample and ion transfer spectrometer |
CN102033100A (en) * | 2009-09-25 | 2011-04-27 | 同方威视技术股份有限公司 | Detecting system of ion migration spectrometer (IMS) using doping agent and detecting method thereof |
US20120138783A1 (en) * | 2009-11-20 | 2012-06-07 | Nuctech Company Limited | Ion mobility spectrometer and method for improving the detection sensitivity thereof |
CN204204795U (en) * | 2014-11-27 | 2015-03-11 | 中国科学院大连化学物理研究所 | A kind of radio frequency electrical of vacuum UV lamp is from excitation apparatus |
CN105628783A (en) * | 2014-10-28 | 2016-06-01 | 中国科学院大连化学物理研究所 | Application of reagent molecules in ion mobility spectrometry detection of explosive peroxide HMTD |
CN106226384A (en) * | 2016-09-22 | 2016-12-14 | 大连工业大学 | A kind of trimethylamine detection method based on Ion mobility spectrometry |
CN106501346A (en) * | 2016-09-22 | 2017-03-15 | 大连工业大学 | A kind of method of trimethylamine in quick detection aquatic products |
CN106841365A (en) * | 2015-12-07 | 2017-06-13 | 中国科学院大连化学物理研究所 | A kind of online high speed detection method of ammonia |
CN108007999A (en) * | 2016-10-28 | 2018-05-08 | 中国科学院大连化学物理研究所 | A kind of ionic migration spectrum detection method of Etomidate in Etomidate Injection |
CN108072689A (en) * | 2016-11-17 | 2018-05-25 | 中国科学院大连化学物理研究所 | A kind of quantitative analysis method for ion mobility spectrometry |
CN108088892A (en) * | 2016-11-21 | 2018-05-29 | 中国科学院大连化学物理研究所 | A kind of SF6On-line rapid measurement device and method |
-
2018
- 2018-11-29 CN CN201811443928.1A patent/CN111239234B/en active Active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101413919A (en) * | 2007-08-01 | 2009-04-22 | 中国科学院大连化学物理研究所 | Method for recognizing and analyzing sample and ion transfer spectrometer |
CN102033100A (en) * | 2009-09-25 | 2011-04-27 | 同方威视技术股份有限公司 | Detecting system of ion migration spectrometer (IMS) using doping agent and detecting method thereof |
US20120138783A1 (en) * | 2009-11-20 | 2012-06-07 | Nuctech Company Limited | Ion mobility spectrometer and method for improving the detection sensitivity thereof |
CN105628783A (en) * | 2014-10-28 | 2016-06-01 | 中国科学院大连化学物理研究所 | Application of reagent molecules in ion mobility spectrometry detection of explosive peroxide HMTD |
CN204204795U (en) * | 2014-11-27 | 2015-03-11 | 中国科学院大连化学物理研究所 | A kind of radio frequency electrical of vacuum UV lamp is from excitation apparatus |
CN106841365A (en) * | 2015-12-07 | 2017-06-13 | 中国科学院大连化学物理研究所 | A kind of online high speed detection method of ammonia |
CN106226384A (en) * | 2016-09-22 | 2016-12-14 | 大连工业大学 | A kind of trimethylamine detection method based on Ion mobility spectrometry |
CN106501346A (en) * | 2016-09-22 | 2017-03-15 | 大连工业大学 | A kind of method of trimethylamine in quick detection aquatic products |
CN108007999A (en) * | 2016-10-28 | 2018-05-08 | 中国科学院大连化学物理研究所 | A kind of ionic migration spectrum detection method of Etomidate in Etomidate Injection |
CN108072689A (en) * | 2016-11-17 | 2018-05-25 | 中国科学院大连化学物理研究所 | A kind of quantitative analysis method for ion mobility spectrometry |
CN108088892A (en) * | 2016-11-21 | 2018-05-29 | 中国科学院大连化学物理研究所 | A kind of SF6On-line rapid measurement device and method |
Non-Patent Citations (2)
Title |
---|
GARY A.EICEMAN: "《离子迁移谱》", 31 July 2010, 国防工业出版社 * |
蒋丹丹: "《离子迁移谱定量检测复杂基质中新型炸药六亚甲基三过氧化二胺》", 《分析化学研究报告》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113588767A (en) * | 2021-08-03 | 2021-11-02 | 大连工业大学 | Biogenic amine detection method based on time-resolved dynamic thermal desorption ion mobility spectrometry |
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