WO2007129513A1 - 試料導入システム - Google Patents
試料導入システム Download PDFInfo
- Publication number
- WO2007129513A1 WO2007129513A1 PCT/JP2007/057160 JP2007057160W WO2007129513A1 WO 2007129513 A1 WO2007129513 A1 WO 2007129513A1 JP 2007057160 W JP2007057160 W JP 2007057160W WO 2007129513 A1 WO2007129513 A1 WO 2007129513A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gas
- sample
- flow rate
- flow path
- introduction
- Prior art date
Links
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
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/71—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light thermally excited
- G01N21/714—Sample nebulisers for flame burners or plasma burners
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/04—Preparation or injection of sample to be analysed
- G01N30/06—Preparation
- G01N30/14—Preparation by elimination of some components
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/26—Conditioning of the fluid carrier; Flow patterns
- G01N30/28—Control of physical parameters of the fluid carrier
- G01N30/32—Control of physical parameters of the fluid carrier of pressure or speed
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/26—Conditioning of the fluid carrier; Flow patterns
- G01N30/28—Control of physical parameters of the fluid carrier
- G01N30/32—Control of physical parameters of the fluid carrier of pressure or speed
- G01N2030/324—Control of physical parameters of the fluid carrier of pressure or speed speed, flow rate
Definitions
- the present invention relates to a sample introduction system for introducing an analysis sample into an analyzer.
- GC-MS method gas chromatography mass spectrometry
- ICP method inductively coupled plasma analysis method
- MIP method microwave plasma analysis method
- Analytical samples such as fine particles and specific gas components contained in the sample gas are being analyzed.
- high temperature plasma is generated using argon gas, nitrogen gas, helium gas, etc. as the plasma gas
- an analysis sample is introduced into the plasma, and signal changes from the plasma are detected. Analyzing.
- a pretreatment apparatus that performs pretreatment for removing unnecessary components from the sample gas is required.
- a sample gas containing a gaseous analysis sample it is necessary to remove impurities, moisture, and the like other than the analysis sample contained in the sample gas as unnecessary components.
- a solution in which an analytical sample is dissolved in a solvent is converted into droplets floating in the spray gas using a sprayer or the like, and the spray gas is used as a sample gas, solvent vapor or moisture contained in the sample gas is not required. It must be removed as a component.
- a gas displacement device As such a pretreatment device, a gas displacement device, a fine particle classification device, a dryer or the like is used.
- a solvent in which an analytical sample is melted is atomized by a sprayer to generate a sample gas, and the droplets are converted into solvent vapor by heating.
- the sample gas is separated from the analysis sample, and the sample gas is separated from the tubular sealing tube made of porous material. It is introduced into the filter and removed by diffusing the solvent vapor outside the sealed filter.
- the fine particle classifier described in Patent Document 2 when the fine particles, which are the analysis sample contained in the sample gas, are charged and classified, the gaseous contaminants in the sample gas are removed, and the fine particles are removed from the desired gas.
- Non-Patent Document 1 a sample gas is generated by dissolving the analytical sample and making the aqueous solution mist into a mist, and the moisture contained in the sample gas is converted to naphthion (DuPont registered trademark: It is removed through a non-porous membrane made of perfluoro-3, ri-dioxa- 4-methy ⁇ 7octene- sulfonic and tetrailuoroethylene).
- the flow rate of the gas containing the analysis sample introduced into the analyzer is changed according to the type of elements constituting the analysis sample, etc., so as to satisfy the optimal analysis conditions. For example, in high-sensitivity analysis using plasma, auto-tuning is performed to automatically switch the flow rate of gas introduced into the plasma together with the analysis sample in order to analyze a plurality of target elements contained in the analysis sample. Yes. In addition, in mass spectrometry using the ion action of plasma, the gas flow rate introduced into the plasma is automatically adjusted so that the analysis is not hindered by polyatomic ions having the same mass number as the target element. It is fluctuating.
- Patent Document 1 Japanese Patent Publication No. 7-500416
- Patent Document 2 Japanese Patent Laid-Open No. 2001-239181
- Non-special reference 1 Journal of Analytical Atomic pectrometry, January 1998, vol. 13 (13-18)
- the additional flow rate of the carrier gas to the processed sample gas flowing through the connection gas flow path between the pretreatment device and the analysis device is changed by the gas addition device, and the analysis sample is upstream of the gas addition device.
- the pressure fluctuation of the gas containing is regulated by the pressure regulator.
- a stable analysis result can be obtained.
- a stable plasma can be maintained without causing a change in plasma temperature or electron density, which can contribute to high sensitivity analysis.
- the pressure adjusting device has a seal gas flow path and a communication flow path, and the seal gas flow path communicates with an inlet connected to a supply source of the seal gas and in an atmosphere or an atmosphere of a constant pressure. And between the inlet and the outlet of the seal gas channel via the communication channel between the pretreatment device and the gas addition device in the connection gas channel.
- a means for setting the introduction flow rate of the untreated sample gas to the pretreatment device is provided, and the introduction flow rate of the untreated sample gas is preferably set to a constant value.
- the pretreatment device and the gas addition device in the connection gas channel communicate with each other in the atmosphere or an atmosphere at a constant pressure, and the introduction flow rate of the untreated sample gas to the pretreatment device becomes constant. . Therefore, when changing the additional flow rate of the carrier gas, it is possible to reliably prevent fluctuations in the gas pressure in the pretreatment device without changing the flow rate of the untreated sample gas introduced into the pretreatment device.
- the seal gas flowing in the seal gas channel can seal between the sample introduction system and the outside. That is, it is possible to regulate the gas pressure fluctuation in the pretreatment apparatus without using the movable member and to seal the surrounding environment.
- the sample introduction system of the present invention includes an introduction channel for introducing the untreated sample gas into the pretreatment device, and the pressure adjusting device has a seal gas channel and a communication channel,
- the seal gas flow path has an inlet connected to a supply source of the seal gas, and an outlet communicating with the atmosphere or an atmosphere at a constant pressure.
- the introduction channel is connected to the introduction channel through the communication channel, and the means for setting the introduction flow rate of the untreated sample gas to the pretreatment device is provided, and the introduction flow rate of the untreated sample gas is set to a constant value. Preferably it is done.
- the introduction channel communicates with the atmosphere or an atmosphere at a constant pressure, and the introduction flow rate of the untreated sample gas to the pretreatment apparatus becomes constant. Therefore, when changing the additional flow rate of the carrier gas, it is possible to reliably prevent gas pressure fluctuations in the pretreatment device without changing the flow rate of the untreated sample gas introduced into the pretreatment device.
- the seal gas flowing in the seal gas flow path can seal between the sample introduction system and the outside. In other words, it is possible to regulate gas pressure fluctuations in the pretreatment apparatus without using a movable member and to seal against the surrounding environment.
- the sample introduction system of the present invention includes an introduction flow path for introducing the untreated sample gas into the pretreatment apparatus, and the pressure adjusting device is an exhaust flow path branched from the introduction flow path.
- the exhaust flow path has an outlet communicating with the atmosphere or an atmosphere at a constant pressure, and means for setting the supply flow rate of the untreated sample gas to the introduction flow path, and the pretreatment device And means for setting the flow rate of the untreated sample gas introduced into the
- the introduction flow rate of the untreated sample gas is preferably set to a constant value, and the set value of the supply flow rate of the untreated sample gas is preferably larger than the set value of the introduction flow rate.
- the outlet of the exhaust channel communicates with the atmosphere or an atmosphere at a constant pressure, and the flow rate of the untreated sample gas introduced into the pretreatment apparatus becomes constant. Therefore, the untreated sample gas introduced into the pretreatment apparatus It is possible to reliably prevent fluctuations in the gas pressure in the pretreatment device without changing the flow rate of the gas.
- the set value of the supply flow rate of the untreated sample gas to the introduction channel is larger than the set value of the introduction rate of the untreated sample gas to the pretreatment device, the untreated sample gas flowing through the exhaust channel By this, it is possible to seal between the sample introduction system and the outside. That is, it is possible to control gas pressure fluctuations in the pretreatment apparatus without using a movable member and to seal against the surrounding environment.
- the analysis sample is a solid fine particle
- the pretreatment device has a porous partition
- the pretreatment device diffuses at least a part of the gas component in the untreated sample gas due to a partial pressure difference in the porous partition. It is preferable that a gas replacement function of substituting with the replacement gas is provided, and that the processed sample gas is constituted by the replacement gas replaced with at least a part of the gas component in the untreated sample gas.
- the flow rate of the carrier gas is changed according to the change in the flow rate of the untreated sample gas.
- the gas flow rate introduced into the analyzer can be maintained at an optimum value for analysis. This optimizes the gas replacement efficiency in the pretreatment device and at the same time introduces it to the analyzer. It is possible to optimize the gas flow rate and to maintain a stable plasma especially in plasma analyzers.
- the sample introduction system of the present invention includes an introduction flow path for introducing the untreated sample gas to the pretreatment apparatus, and the pretreatment apparatus has a first pipe and a second pipe, and the first arrangement is provided.
- a pipe and the second pipe are separated by the porous partition wall, and the first pipe has a first inlet connected to the introduction flow path, a first outlet connected to the connection gas flow path, and the first A first gas flow path between the first inlet and the first outlet, and the second pipe is connected to a replacement gas supply source, and the second gas is replaced with the replacement gas.
- the pressure adjusting device has a branch channel that communicates the introduction channel with the second outlet in the vicinity of the first inlet, and the pressure regulation device is provided in the introduction channel.
- the pressure of the untreated sample gas is set to atmospheric pressure or constant pressure
- the introduction flow rate of the untreated sample gas is set to a constant value
- the set value of the total suction flow rate of the untreated sample gas and the exhaust gas is set. Is the supply flow of the replacement gas. Is larger than the set value, the gas discharge side of the gas suction means is preferably walking in the air communicates with the atmosphere of constant pressure.
- the pressure of the untreated sample gas supplied to the introduction flow path is set to atmospheric pressure or a constant pressure, and the set value of the total suction flow rate of the untreated sample gas and the exhaust gas is set to the replacement gas to the second pipe. It is made larger than the set value of the supply flow rate. Therefore, a part of the unprocessed sample gas supplied to the introduction channel is reliably sucked by the gas suction means through the branch channel. Since the gas discharge side of the gas suction means communicates with the atmosphere or an atmosphere of a constant pressure, the pressure of the untreated sample gas is reduced to the atmosphere near the first inlet in the introduction channel. Pressure or constant pressure.
- the pressure loss of the untreated sample gas is large due to the long introduction flow path, and even if the pressure loss is not constant due to the difference in length of the introduction flow path, the first inlet in the introduction flow path Gas pressure fluctuations in the vicinity of can be prevented, gas pressure fluctuations in the pretreatment device can be regulated, and the surrounding environment can be sealed.
- the analyzer is preferably a plasma analyzer having a tube for guiding the processed sample gas to which the carrier gas has been added to plasma.
- the internal pressure of the connecting gas flow path will fluctuate because the gas is throttled in the tube.
- fluctuations in the pressure of the gas in the connection gas flow path between the pretreatment device and the gas addition device are regulated by the pressure regulator, so that a seal or the like at the connection between the pretreatment device and the connection gas flow channel can be obtained. In this way, it is possible to prevent contaminants in the surrounding environment from entering the analyzer and leaking the processed sample gas to the outside.
- the gas addition device includes an aspirator that guides the processed sample gas to the connection gas flow path based on a pressure drop of a carrier gas introduced into the connection gas flow path.
- the carrier gas can be added without providing a power source in the connecting gas flow path.
- the untreated sample gas itself does not have the pressure necessary to introduce the untreated sample gas into the pretreatment device, a predetermined amount of untreated sample without providing a power source for the movable member. Gas can be introduced into the pretreatment device.
- FIG. 1 is an explanatory diagram of the overall configuration of the sample introduction system according to the first embodiment of the present invention.
- FIG. 2 is an explanatory diagram of a sprayer used in the sample introduction system according to the first embodiment of the present invention.
- FIG. 3 shows a gas addition device and a pressure adjustment device of the sample introduction system according to the first embodiment of the present invention.
- FIG. 4 is an explanatory diagram of the overall configuration of the sample introduction system according to the second embodiment of the present invention.
- FIG. 5 is a cross-sectional view for explaining the configuration of a gas addition device of a sample introduction system according to a second embodiment of the present invention.
- FIG. 6 is a cross-sectional view for explaining the configuration of the pressure adjusting device of the sample introduction system according to the second embodiment of the present invention.
- FIG. 7 is an explanatory diagram of the overall configuration of the sample introduction system according to the third embodiment of the present invention.
- FIG. 8 is a sectional view for explaining the configuration of a gas addition device and a pressure adjustment device of a sample introduction system according to a third embodiment of the present invention.
- FIG. 9 is an explanatory diagram of the overall configuration of the sample introduction system according to the fourth embodiment of the present invention.
- FIG. 10 is a partial sectional view of a pretreatment device according to a modification of the present invention.
- FIG. 11 is an explanatory diagram of the overall configuration of a sample introduction system according to a comparative example.
- Pretreatment device 2 ... Inner pipe, 2A ... Porous partition, 2a ... Inner inlet, 2b ... Inner outlet, 3 ... Outer pipe, 3a ... Outer inlet, 3b ... Outer outlet, 8, 43, 46 61 ...
- Flow controller 10 ... Introduction flow path, 20 ... Connecting gas flow path, 30 ... Analyzer, 30b ... Center tube, 40, 40A ... Gas addition device, 50, 50B, 50C ... Pressure adjustment device, 50a ... Branch channel, 50 '... Exhaust channel, 50 ⁇ Air outlet, 52a-sinore gas channel, 53a "-Communication channel, 60 ⁇ Vacuum pump, 101, 102 ... Self pipe G1 ... Untreated sample gas, G3 ... Replacement gas, G4 ... Processed sample gas, G7 ... Carrier gas, G8 ... Sino gas, P ... Plasma
- the sample introduction system A1 of the first embodiment shown in FIG. 1 is a pretreatment device 1 that performs pretreatment to remove unnecessary components such as moisture, impurities, and solvent vapor from an untreated sample gas G1 including an analysis sample. And an introduction flow path 10 for introducing the untreated sample gas G 1 from the supply source to the pretreatment apparatus 1.
- the analysis sample to be pretreated may be liquid or gaseous.
- the nebulizer 11 shown in FIG. 2 can be used as a supply source of the untreated sample gas G1.
- the nebulizer 11 uses a solution 12 in which an analysis sample is dissolved in a solvent in the form of droplets floating in the atomizing gas G2, and has a large particle size.
- the remaining droplets L are removed and supplied to the pretreatment apparatus 1 as pressurized untreated sample gas Gl.
- an atomizer 11 a known one can be used.
- the flow rate of the pressurized spray gas G2 supplied from a pressure vessel such as a gas cylinder is controlled by a mass flow controller (MFC), a flow rate controller 13 such as a flow rate control valve, and the flow rate controller. 13 is used as a means for setting the flow rate of the untreated sample gas G1 into the pretreatment device 1.
- MFC mass flow controller
- a flow rate controller 13 such as a flow rate control valve
- a pressure vessel filled with a pressurized gas containing a gaseous analysis sample is used as a supply source of the untreated sample gas G1, and the pressure vessel is connected to the pretreatment device 1 with a pipe constituting the introduction flow path 10.
- a flow controller may be installed in the pipe as a means for setting the flow rate for introducing the untreated sample gas G1 into the pretreatment device 1.
- the supply flow rate of the untreated sample gas G1 to the introduction flow path 10 is the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1, and the untreated sample gas G1 is untreated to the pretreatment device 1.
- the flow rate of sample gas G1 is set to a constant value.
- the analysis sample of the present embodiment is a solid fine particle. That is, the fine particles that are analysis samples contained in the untreated sample gas G1 are, for example, metals such as iron powder, metal compounds such as oxides and sulfides, and organic substances such as ceramics and polymer compounds.
- the pretreatment device 1 has a porous partition wall 2A, and replaces at least a part of gas components in the untreated sample gas G1 with the replacement gas G3 through diffusion due to a partial pressure difference in the porous partition wall 2A. Play. Thereby, unnecessary components such as solvent vapor contained in the untreated sample gas G1 can be removed.
- the pretreatment device 1 includes an inner pipe 2 that is a straight pipe having a circular cross section as a first pipe, and a second outer pipe 3 that is a straight pipe having a circular cross section that covers the inner pipe 2.
- Double pipe structure provided as piping. Both ends of the inner tube 2 protrude from the outer tube 3, and the vicinity of both ends of the outer tube 3 is gradually made smaller in diameter and joined to the outer periphery of the inner tube 2.
- the shapes of the inner and outer tubes 2 and 3 are not limited, and may be, for example, a curved tube instead of a straight tube.
- the inner pipe 2 has an inner inlet 2a formed at one end as a first inlet, an inner outlet 2b formed at the other end as a first outlet, and includes an inner inlet 2a and an inner outlet 2b.
- the inner gas flow path 2c is provided as the first gas flow path.
- the outer pipe 3 has an outer inlet 3a formed on the peripheral wall near one end as a second inlet for introducing the replacement gas G3, and an outer outlet 3b formed on the peripheral wall near the other end. It has two outlets, and has an outer gas passage 3c between the outer inlet 3a and the outer outlet 3b as a second gas passage.
- the outer inlet 3a is connected to a supply source of the replacement gas G3.
- a supply source for example, a pressure vessel filled with a pressurized replacement gas G3 is used, and as a means for setting the supply flow rate of the replacement gas G3 to the outer pipe 3 in a pipe connecting the pressure vessel to the outer inlet 3a.
- a flow controller 8 such as a mass flow controller (MFC) and a flow control valve is provided.
- MFC mass flow controller
- the inner inlet 2a, the inner outlet 2b, the outer inlet 3a, and the outer outlet 3b are defined by the flow direction of the untreated sample gas G1 in the inner gas flow path 2c and the flow direction of the replacement gas G3 in the outer gas flow path 3c. Are arranged in opposite directions.
- the inner pipe 2 as the first pipe and the outer pipe 3 as the second pipe are separated by the porous partition wall 2A. That is, the portion between both ends of the peripheral wall that covers the inner gas flow path 2c in the inner pipe 2 diffuses the untreated sample gas G1 outside the inner gas flow path 2c by diffusion due to the partial pressure difference between the untreated sample gas G1 and the replacement gas G3. And a porous partition wall 2A for moving the replacement gas G3 into the inner gas flow path 2c.
- Each pore diameter of the porous partition wall 2A is set so as to substantially prevent gas movement through the porous partition wall 2A due to the difference between the gas pressure in the inner gas channel 2c and the gas pressure in the outer gas channel 3c.
- each pore diameter is set to 0.001 ⁇ ⁇ or more, preferably 0.002 ⁇ m or more, more preferably 0 in order to prevent the displacement efficiency of the gases Gl and G3 from decreasing and the apparatus from becoming large. More than 02 / im.
- each pore diameter is set to 0.8 xm or less in order to prevent fine particles from passing through each pore or trapped in each pore, thereby reducing analysis accuracy or causing gas movement due to a gas pressure difference, and preferably 0 or less. .5 xm or less, more preferably 0.2 xm or less.
- the diameter of a small number of holes that does not affect the gas replacement function may be outside the range of 0.8 xm to 0.001 zm. 8 zm to 0.001 zm.
- the porosity of the porous partition wall 2A is not particularly limited, but the power of gas replacement efficiency and mechanical strength is preferably 40% to 80%.
- the material of the porous partition wall 2A is not particularly limited as long as it is a porous material that meets the above conditions, and glass such as quartz glass or ceramic is preferred, for example, shirasu porous glass. (SPG) can be used.
- SPG shirasu porous glass.
- the portions 2B and 2C in the vicinity of both ends of the inner tube 2 are smoothly joined to the porous partition wall 2A with the same inner and outer diameters.
- the entire peripheral wall covering the inner gas flow path 2c may be the porous partition wall 2A, and the portion covering at least part of the inner gas flow path 2c may be the porous partition wall 2A.
- the material of the inner tube 2 near both ends 2B, 2C and the outer tube 3 there are no particular restrictions on the material of the inner tube 2 near both ends 2B, 2C and the outer tube 3, and a plurality of different material forces may be used.
- metals such as ceramic, glass, and glass such as ceramic and quartz glass are preferred. It is desirable to do.
- an untreated sample gas G1 containing fine particles is introduced into the inner pipe 2 from the inner inlet 2a and flows in the inner gas flow path 2c surrounded by the porous partition wall 2A.
- G3 is allowed to flow from the outer inlet 3a into the outer tube 3 and flow in the direction opposite to the flow direction of the untreated sample gas G1 in the outer gas passage 3c around the porous partition wall 2A.
- the replacement gas G3 replaced with at least a part of the gas component of the untreated sample gas G1 constitutes the treated sample gas G4 flowing out from the inner outlet 2b together with the fine particles and a small amount of the untreated sample gas G1.
- the untreated sample gas G1 and the replacement gas G3 can be discharged from the outer outlet 3b as the exhaust gas G5.
- gas movement through the porous partition wall 2A due to the gas pressure difference between the inner gas channel 2c and the outer gas channel 3c that is, the gas pressure difference between the inside and outside of the inner gas channel 2c, is effectively performed by the porous partition wall 2A. Can be prevented.
- each pore diameter, porosity, thickness, tube diameter, length, shape of the porous partition wall 2A, inner diameter and shape of the outer tube 3, the flow rates of the untreated sample gas G1 and replacement gas G3, etc. are appropriately set. By doing so, the unnecessary components of the processed sample gas G4 flowing out from the inner outlet 2b can be reduced below the limit amount that does not adversely affect the analysis in the analyzer.
- the amount of the untreated sample gas G1 that moves outside the inner gas flow path 2c and the amount of the replacement gas G3 that moves inside the inner gas flow path 2c are made substantially equal to each other.
- the path 2c most of the untreated sample gas G1 is replaced with the replacement gas G3, and the flow rate of the processed sample gas G4 flowing out from the inner outlet 2b can be prevented from fluctuating.
- the fine particles in the inner gas flow path 2c those whose diameter exceeds the pore diameter of the porous partition wall 2A are not transmitted through or trapped in each hole.
- the fine particles introduced together with the untreated sample gas G1 into the inner gas flow path 2c can be supplied to the analyzer together with the replacement gas G3 having substantially the same flow rate as that of the untreated sample gas G1 without deteriorating.
- the processed sample gas G4 pretreated by the pretreatment device 1 flows out from the inner outlet 2b to the connection gas channel 20, and is guided to the analyzer 30 via the connection gas channel 20.
- the analyzer 30 of this embodiment is a plasma analyzer.
- the analyzer 30 includes a plasma torch 30a for forming a plasma P using argon gas, nitrogen gas, helium gas, etc. as a plasma gas G6, and a center of the plasma torch 30a for guiding the processed sample gas G4 to the plasma P.
- a center tube 30b A known plasma analyzer can be used.
- the atomizing gas G2 and the replacement gas G3 preferably have the same composition as the plasma gas G6.
- connection gas flow path 20 As shown in FIG. 1 and FIG. 3, a gas addition device 40 and a pressure adjusting device 50 disposed downstream of the pretreatment device 1 and upstream of the gas addition device 40 are provided in the connection gas flow path 20. It is provided.
- the connection gas flow path 20 penetrates through the gas addition device 40 and the pressure adjustment device 50.
- the gas addition device 40 has a means for changing the additional flow rate of the carrier gas G7 by adding the carrier gas G7 to the processed sample gas G4 flowing toward the analysis device 30 in the connection gas flow path 20.
- the gas addition device 40 of the present embodiment has an aspirator that guides the processed sample gas G4 to the connection gas channel 20 based on the pressure head drop of the carrier gas G7 introduced into the connection gas channel 20. That is, the gas addition device 40 includes a first duct 41, a second duct 42 connected to the first duct 41, a mass flow controller (MFC) as a means for changing the additional flow rate of the carrier gas G7, and a flow rate. It has a flow controller 43 such as a control valve.
- MFC mass flow controller
- Both ducts 41 and 42 constitute a part of the connecting gas flow path 20.
- One end opening of the first duct 41 constitutes a gas outlet 20b of the connection gas flow path 20, and is connected to the inlet of the center tube 30b of the analyzer 30.
- a throttle part 41a and a diffuser 41b connected to the outlet of the throttle part 41a are formed in the first duct 41.
- the other end opening of the first duct 41 is connected to a carrier gas G7 supply source 44 via a flow rate controller 43.
- the inlet of the second duct 42 leads to the inner outlet 2b of the pretreatment device 1 via the first pipe 51 of the pressure adjusting device 50 described later, and the outlet of the second duct 42 is a carrier gas G7 in the vicinity of the outlet of the throttle 41a.
- the supply source 44 is a pressure vessel such as a gas cylinder, for example, and supplies the pressurized carrier gas G7 to the first duct 41.
- the processed sample gas G4 is sucked into the connection gas flow path 20 and the carrier gas G7 is processed based on the pressure head drop caused by the ejection of the carrier gas G7 introduced into the connection gas flow path 20 from the throttle 41a.
- the gas-equipped car device 40 constitutes an aspirator.
- This insulator a known one can be used.
- the additional flow rate of the carrier gas G7 is changed by the flow rate controller 43.
- the processed sample gas G4 to which the carrier gas G7 is added is guided to the plasma P through the center tube 30b of the analyzer 30.
- the carrier gas G7 preferably has the same composition as the plasma gas G6.
- the pressure adjusting device 50 regulates the pressure fluctuation of the gas including the analysis sample upstream of the gas adding device 40.
- the pressure adjusting device 50 according to the present embodiment regulates the gas pressure fluctuation between the pretreatment device 1 and the gas addition device 40 in the connection gas flow path 20. Therefore, the pressure adjusting device 50 of the present embodiment includes a first pipe 51 that constitutes the connection gas flow path 20, a second pipe 52 that constitutes the seal gas flow path 52a, and the first pipe 51 and the second pipe 52.
- the connecting pipe 53 is connected, and the inside of the connecting pipe 53 is a communication flow path 53a.
- One end opening of the first pipe 51 constitutes a gas inlet 20a of the connection gas flow path 20, and is connected to the inner outlet 2b of the pretreatment device 1.
- the other end opening of the first pipe 51 is connected to the inlet of the second duct 42 of the gas addition device 40.
- the inlet 52a 'of the seal gas channel 52a is connected to the supply source 54 of the seal gas G8 via a mass flow controller (MFC), a flow controller 55 such as a flow control valve, and the outlet 52a "of the seal gas channel 52a is Note that the outlet 52a ⁇ of the seal gas channel 52a may be connected to an atmosphere of a constant pressure between the inlet 52a and the outlet 52a ⁇ of the seal gas channel 52a. Is communicated between the pretreatment device 1 and the gas addition device 40 in the connection gas flow path 20 via the communication flow path 53a.
- MFC mass flow controller
- a flow controller 55 such as a flow control valve
- the gas pressure in the upstream connection gas channel 20 of the gas addition device 40 decreases due to suction of the treated sample gas G4 by the gas-attached gas device 40, the inlet gas 52a force is applied to the seal gas channel 52a. Part of the introduced seal gas G8 is led to the connecting gas flow path 20, and the pressure drop is cancelled. As a result, the inside of the connecting gas flow path 20 can be maintained at a substantially atmospheric pressure between the pretreatment device 1 and the gas-attached cage device 40. Therefore, when the additional flow rate of the carrier gas G7 is changed, the gas pressure in the pretreatment device 1 is regulated by regulating the pressure fluctuation of the gas in the connection gas flow path 20 between the pretreatment device 1 and the gas addition device 40. Can regulate fluctuations.
- the sealing gas G8 should have the same composition as the plasma gas G6.
- the flow rate of the seal gas G8 should be set to a sufficient flow rate that does not break the gas seal between the sample introduction system A1 and the outside.
- the additional flow rate of the carrier gas G7 to the processed sample gas G4 flowing through the connection gas flow path 20 is changed by the gas addition device 40, and the pressure fluctuation of the gas in the pretreatment region is adjusted by pressure. Regulated by device 50.
- the gas introduced into the analyzer 30 together with the analysis sample without changing the flow rate of the untreated sample gas G1 introduced into the pretreatment device 1 and without causing the gas pressure fluctuation in the pretreatment device 1.
- the flow rate of can be changed. Therefore, since it is not necessary to change the processing conditions of the pretreatment device 1, it can be adapted to the variety of analysis conditions.
- connection gas flow path 20 is communicated between the pretreatment apparatus 1 and the gas addition apparatus 40 through the seal gas flow path 52a to the atmosphere or an atmosphere at a constant pressure.
- the flow rate of untreated sample gas G1 is constant. Therefore, when changing the additional flow rate of the carrier gas G7, it is possible to reliably prevent the gas pressure fluctuation in the pretreatment device 1 without changing the flow rate of the untreated sample gas G1 introduced into the pretreatment device 1. .
- the internal pressure of the connection gas flow path 20 between the pretreatment device 1 and the gas addition device 40 can be kept uniform and constant.
- the seal gas G8 flowing through the seal gas flow path 52a can gas seal between the sample introduction system A1 and the outside.
- the plasma analyzer 30 can maintain a stable plasma P without causing a temperature change or electron density change of the plasma P, and can contribute to a highly sensitive analysis.
- the gas can be replaced in the pretreatment device 1 regardless of the gas flow rate introduced into the analysis device 30, it is possible to keep the gas replacement efficiency constant while preventing the dissipation of fine particles as an analysis sample during the gas replacement. .
- the flow rate of the untreated sample gas G1 is changed so that the gas replacement efficiency does not change according to the type of analysis sample
- the flow rate of the carrier gas G7 is changed according to the change in the flow rate of the untreated sample gas G1.
- the gas flow rate introduced into the analyzer 30 can be maintained at an optimum value for analysis.
- the gas replacement efficiency in the pretreatment device 1 can be optimized, and at the same time, the gas flow rate introduced into the analyzer 30 can be optimized to maintain a stable plasma P.
- the gas is throttled in the center tube 30b. Therefore, if the pretreatment device 1 and the analysis device 30 are directly connected, the center tube 30b Connected gas due to change in gas flow rate to The internal pressure of the flow path 20 varies. However, in the present embodiment, the pretreatment device 1 and the analysis device 30 are connected via the gas addition device 40, and the gas addition device 40 changes the flow rate of the introduced gas into the center tube 30b.
- connection between the pretreatment device 1 and the connection gas flow channel 20 It is possible to prevent contaminants in the surrounding environment from entering the system and leaking the processed sample gas G4 to the outside through a seal in the unit. For example, if the inner diameter of the tip of the center tube 30b is:!
- the pretreatment device 1 and the analysis device 30 are directly connected, the pretreatment device Since the internal pressure of the inner pipe 2 of 1 is several hundred Pa, it is necessary to prevent the analysis sample from being dissipated out of the system through the porous partition wall 2A. For this purpose, it is necessary to control the gas pressure in the outer pipe 3 by strictly setting the supply conditions of the replacement gas G3, and therefore, it is not possible to easily cope with changes in the analysis conditions in the analyzer 30.
- the internal pressure fluctuation of the inner pipe 2 can be prevented by the pressure adjusting device 50, and thus such control of the gas pressure in the outer pipe 3 is unnecessary. This makes it easy to optimize analysis conditions by auto-tuning, which automatically switches the gas flow rate introduced into the plasma P according to the type of elements constituting the analysis sample.
- the carrier gas G7 can be attached to the connection gas flow path 20 without providing a movable member or power source.
- the untreated sample gas G1 itself does not have the pressure necessary to introduce the untreated sample gas into the pretreatment device 1, a predetermined amount of untreated material can be obtained without providing a power source.
- the sample gas G1 can be introduced into the pretreatment device 1.
- the performance of the aspirator is not particularly limited, but the flow rate of the processed sample gas G4 to be sucked is preferably equal to or higher than the flow rate of the carrier gas G7.
- the flow rate of the carrier gas G7 is 500 mlZmin
- the flow rate of the processed sample gas G4 to be sucked is 500 mlZmin or more.
- the material of the aspirator can be any problem, such as contaminating the system or selectively adsorbing specific components.
- quartz glass or Tygon Norton Performance Plastics Trademark: Polychlorinated Bull
- the pressure adjusting device 50 is arranged upstream of the pretreatment device 1, and introduced between the inlet 52a 'and the outlet 52a in the single gas channel 52a, not in the connecting gas channel 20. It communicates with the flow path 10 via the communication flow path 53a. Therefore, the inlet of the second duct 42 in the gas addition device 40 of the second embodiment is directly connected to the inner outlet 2b of the pretreatment device 1.
- One end opening of the first pipe 51 in the pressure adjusting device 50 constitutes a gas outlet 10a of the introduction channel 10 and is connected to the inner inlet 2a of the pretreatment device 1.
- the other end opening of the first pipe 51 is connected to a supply source of the untreated sample gas G1 through a pipe constituting the introduction flow path 10.
- the inlet 52a ′ and the outlet 52a ′′ in the seal gas channel 52a communicate with each other in the vicinity of the inner inlet 2a of the pretreatment device 1 in the introduction channel 10 via the communication channel 53a.
- FIG. 7 and 8 show a sample introduction system A3 according to a third embodiment of the present invention.
- the same parts as those in the first embodiment are denoted by the same reference numerals, and different points will be described.
- the pressure adjusting device 50B is arranged upstream of the pretreatment device 1, and prevents gas pressure fluctuations without using a seal gas. for that reason.
- the pressure regulator 50B of the third embodiment has an exhaust passage 5 (that is branched from the introduction passage 10.
- the exhaust flow In order to branch the passage 50 r from the introduction passage 10, the exhaust passage 5 (/ and the introduction passage 10 are It is composed.
- the pressurized untreated sample gas G1 which is supplied to the introduction flow path 10 in the same manner as in the first embodiment, is partially introduced into the pretreatment apparatus 1, and the remainder is discharged into the exhaust flow path 5 (the outlet 50 "
- the outlet 50 ⁇ of the exhaust passage 50 ' communicates with the atmosphere.
- the exhaust passage 5 (the outlet 50 ⁇ of the soot may be communicated with the atmosphere of a constant pressure.
- the inlet of the second duct 42 in the gas addition device 40A of the third embodiment is directly connected to the inner outlet 2b of the pretreatment device 1.
- the gas addition device 40A of the third embodiment includes a third duct 45 and a flow rate controller 46 in addition to the same configuration as the gas addition device 40 of the first embodiment.
- One end opening of the third duct 45 is connected to the inside of the first duct 41 downstream of the diffuser 41b, and the other end opening of the third duct 45 is connected to the supply source 47 of the carrier gas G7 ′ via the flow rate controller 46. Is done.
- the supply source 47 is a pressure vessel such as a gas cylinder, for example, and supplies the pressurized carrier gas to the first duct 41 via the third duct 45.
- the carrier gas preferably has the same composition as the plasma gas G6.
- the carrier gas G7 supplied from the supply source 44 via the flow rate controller 43 but also the flow rate controller 46 from the supply source 47 to the gas addition device 40A of the third embodiment. Is added to the processed sample gas G4.
- the means for changing the additional flow rate of the carrier gas by the gas adding device 40A in the third embodiment is constituted by a flow rate controller 46.
- the suction flow rate of the untreated sample gas G 1 by the aspirator that is configured by the gas addition device 40 A is the introduction flow rate of the untreated sample gas G 1 to the pretreatment device 1. Since the suction flow rate is determined according to the flow rate of the carrier gas G7 set by the flow rate controller 43, the flow rate controller 43 functions as a means for setting the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1. The introduction flow rate of the untreated sample gas G1 to the pretreatment device 1 is set to a constant value.
- the untreated sample gas G1 pressurized to the introduction channel 10 is supplied from the supply source in the same manner as the first embodiment, and the untreated sample gas to the introduction channel 10 is supplied.
- a means for setting the supply flow rate of G1 is provided.
- the flow rate controller 13 for setting the flow rate of the atomized gas G2 is a means for setting the supply flow rate of the untreated sample gas G1. Function as.
- the pressure vessel filled with the pressurized gas containing the analytical sample as the untreated sample gas Gl is used as a supply source, and the pressure vessel is connected to the introduction flow path 10 via a flow rate controller that functions as a supply flow rate setting means. Also good.
- the set value of the supply flow rate of the untreated sample gas G1 to the introduction flow path 10 is made larger than the set value of the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1, except that it is the same as in the first embodiment. Is done.
- the exhaust channel 5 (the outlet of the soot is communicated with the atmosphere or an atmosphere with a constant pressure, and the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1 is constant. Therefore, the gas pressure fluctuation in the pretreatment device 1 can be reliably prevented without changing the flow rate of the untreated sample gas G1 introduced into the pretreatment device 1. Also, the untreated sample into the introduction channel 10 can be prevented.
- the exhaust flow channel 5 (the untreated sample gas Gl flowing through Gas sealing can be provided between the sample introduction system A3 and the outside, that is, gas pressure fluctuations in the pretreatment device 1 without using a movable member can be regulated and the environment can be sealed.
- FIG. 9 shows a sample introduction system A4 according to the fourth embodiment of the present invention.
- the same parts as those in the first embodiment are denoted by the same reference numerals, and different points will be described.
- the pressure of the untreated sample gas G1 supplied to the introduction flow path 10 is set to atmospheric pressure or constant pressure, and the inlet of the introduction flow path 10 is a mass flow controller (MFC), flow control It communicates directly with the atmosphere of the untreated sample gas Gl without going through a flow controller such as a valve.
- MFC mass flow controller
- the inlet of the introduction channel 10 is communicated with the atmosphere or an atmosphere of a constant pressure, and the atmosphere or the atmosphere is the untreated sample gas G1.
- the pressure adjusting device 50C is disposed upstream of the pretreatment device 1, and prevents gas pressure fluctuations without using a seal gas.
- the pressure regulating device 50C of the fourth embodiment has a branch channel 50a that branches from the introduction channel 10 instead of the configuration of the pressure regulating device 50 in the first embodiment.
- One end of the pipe constituting the branch channel 50a is connected to the pipe constituting the introduction channel 10 in the vicinity of the inner inlet 2a of the pretreatment device 1, and the other end of the pipe constituting the branch channel 50a is the pretreatment device. Connected to 1 outer outlet 3b. to this Thus, the branch channel 50a connects the introduction channel 10 to the outer outlet 3b in the vicinity of the inner inlet 2a.
- a gas suction means for sucking a part of the untreated sample gas G1 supplied to the introduction channel 10 together with the exhaust gas G5 from the outer outlet 3b of the pretreatment device 1 through the branch channel 50a. It is.
- the gas suction means of this embodiment is constituted by a vacuum pump 60, and the gas suction side of the vacuum pump 60 is connected to a pipe constituting the branch channel 50a via a flow rate controller 61.
- the gas discharge side of the vacuum pump 60 is communicated with the atmosphere.
- the gas suction means is not limited to the vacuum pump 60.
- the gas suction means may be constituted by a blower or a fan. Further, the gas discharge side of the vacuum pump 60 may be communicated in an atmosphere having a constant pressure.
- the flow rate controller 61 constitutes a means for setting the total suction flow rate of the untreated sample gas G1 and the exhaust gas G5 by the vacuum pump 60.
- the total suction flow rate of the raw sample gas G1 and exhaust gas G5 by the vacuum pump 60 is larger than the set value of the supply flow rate of the replacement gas G3 to the outer pipe 3 set by the flow controller 8. .
- a gas addition device 40A similar to that of the third embodiment is provided instead of the gas addition device 40 of the first embodiment, and the flow rate controller 46 adds carrier gas by the gas addition device 40A. It functions as a means for changing the flow rate.
- the suction flow rate of the untreated sample gas G1 by the aspirator formed by the gas addition device 40A is the introduction flow rate of the untreated sample gas G1 into the pretreatment device 1. Since the suction flow rate is determined according to the flow rate of the carrier gas G7 set by the flow rate controller 43, the flow rate controller 43 functions as a means for setting the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1. .
- the introduction flow rate of the untreated sample gas G1 to the pretreatment device 1 is set to a constant value. Others are the same as in the first embodiment.
- the pressure of the untreated sample gas G1 supplied to the introduction flow path 10 is set to atmospheric pressure or constant pressure, and the total suction flow rate of the untreated sample gas G1 and the exhaust gas G5 is set.
- the constant value is set larger than the set value of the supply flow rate of the replacement gas G3 to the outer pipe 3. Therefore, a part of the untreated sample gas G1 supplied to the introduction flow path 10 is reliably sucked by the vacuum pump 60 via the branch flow path 50a. Since the gas discharge side of the vacuum pump 60 communicates with the atmosphere or an atmosphere with a constant pressure, the vicinity of the inner inlet 2a in the introduction channel 10 In the vicinity, the pressure of the untreated sample gas Gl can be made substantially atmospheric pressure or constant pressure. As a result, the pressure loss of the untreated sample gas G1 is large because the introduction flow path 10 is long. 10 prevents gas pressure fluctuations in the vicinity of the inner inlet 2a, restricts gas pressure fluctuations in the pretreatment device 1, and seals the surrounding environment.
- the present invention is not limited to the above embodiment.
- the pressure adjustment device may be constituted by a pressure adjustment valve.
- the processed sample gas is sucked by a gas suction means such as a pump, a blower, and a fan instead of an aspirator, and the connected gas flow downstream of the gas suction means
- a gas suction means such as a pump, a blower, and a fan instead of an aspirator
- the carrier gas discharged from the high pressure cylinder or pump is added to the processed sample gas via a mass flow controller (MFC) or flow controller such as a flow control valve.
- MFC mass flow controller
- the gas addition device 40A is replaced by an aspirator and the unprocessed sample gas G1 It may have a gas suction means such as a pump, a blower, or a fan for sucking air.
- the inner pipe 2 is the first pipe and the outer pipe 3 is the second pipe.
- the inner pipe 2 is the second pipe, and the outer pipe 3 Can be used as the first pipe.
- the inner inlet 2a is the second inlet
- the inner outlet 2b is the second outlet
- the inner gas passage 2c is the second gas passage
- the outer inlet 3a is the first inlet
- the outer outlet. 3b is the first outlet
- the outer gas channel 3c is the first gas channel.
- the inner inlet 2a is connected to the supply source of the replacement gas G3, the untreated sample gas G1 and the replacement gas G3 are discharged from the inner outlet 2b as the exhaust gas G5, and the introduction channel 10 is connected to the outer inlet 3a.
- the untreated sample gas G1 is introduced into the outer gas channel 3c, and the treated sample gas G4 is guided to the analyzer 30 through the connection gas channel 20 connected to the outer outlet 3b.
- the pretreatment device 1 of each of the above embodiments has a double-pipe structure in which the inner pipe 2 is the first pipe and the outer pipe 3 is the second pipe.
- the inner pipe 2 is the first pipe and the outer pipe 3 is the second pipe.
- both pipes 101, 102 have a porous partition wall 2A.
- a shared structure may be adopted.
- one of the pipes 101 and 102 is the first pipe, the other is the second pipe, and the pipes 101 and 102 are separated by the porous partition wall 2A.
- the analyzer is not limited to the plasma analyzer. For example, an analyzer that performs analysis by gas chromatography mass spectrometry may be used.
- the method for removing unnecessary components by the pretreatment device is not limited to the above embodiment.
- a dryer that removes moisture as unnecessary components, or fine particles that are analysis samples are charged and classified.
- a fine particle classifier that removes gaseous contaminants and floats the fine particles in an atmosphere of the desired gas species.
- the gas flow rate introduced into the center tube 30b of the analyzer 30 is changed, and the gas pressure and the center tube at the inner outlet 2b of the pretreatment device 1 are changed.
- the gas flow rate at 30b was measured.
- the flow rate of the untreated sample gas G1 was constant (300 ml / min), and the gas flow rate introduced into the center tube 30b of the analyzer 30 was changed by changing the flow rate of the carrier gas G7. .
- the inner diameter of the tip of the center tube 30b of the analyzer 30 was 1.5 mm.
- the gas pressures at the outer outlet 3b of the pretreatment device 1, the outlet 52a "of the seal gas passage 52a, and the outlet of the center tube 30b were each atmospheric pressure.
- the gas pressure at the inner outlet 2b of the pretreatment device 1 was measured in the same manner as in Example 1 except that the inner diameter of the tip of the center tube 30b was 1.8 mm.
- the sample introduction system B of the comparative example shown in Fig. 11 is used instead of the sample introduction system A1 of the first embodiment, and the pre-treatment is performed by changing the flow rate of the gas introduced into the center tube 30b of the analyzer 30. The gas pressure at the inner outlet 2b of the device 1 was measured.
- the sample introduction system B of the comparative example is an embodiment except that the pretreatment device 1 and the analysis device 30 are directly connected via the connection gas flow path 20 except for the gas addition device 40 and the pressure adjustment device 50.
- the sample introduction system Al has the same configuration, and the same parts as the sample introduction system A1 of the embodiment are denoted by the same reference numerals.
- the flow rate of the untreated sample gas G1 was changed in the same manner as the gas flow rate introduced into the center tube 30b of the analyzer 30 in Example 1.
- the inner diameter of the tip of the center tube 30b of the analyzer 30 was 1.5 mm.
- the gas pressures at the outer outlet 3b of the pretreatment device 1 and the outlet of the center tube 30b were each atmospheric pressure.
- the gas pressure at the inner outlet 2b of the pretreatment device 1 was measured in the same manner as in Comparative Example 1 except that the inner diameter of the tip of the center tube 30b was 1.8 mm.
- Table 1 below shows the measurement results in each example, and Table 2 shows the measurement results in each comparative example.
Landscapes
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Plasma & Fusion (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Sampling And Sample Adjustment (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007513566A JP4462575B2 (ja) | 2006-05-09 | 2007-03-30 | 試料導入システム |
US12/227,075 US8020458B2 (en) | 2006-05-09 | 2007-03-30 | Sample introducing system |
EP07740596A EP2017598A4 (en) | 2006-05-09 | 2007-03-30 | SAMPLE INTRODUCTION SYSTEM |
TW096113345A TW200806968A (en) | 2006-05-09 | 2007-04-16 | Sample introduction system |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006-130626 | 2006-05-09 | ||
JP2006130626 | 2006-05-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007129513A1 true WO2007129513A1 (ja) | 2007-11-15 |
Family
ID=38667623
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/057160 WO2007129513A1 (ja) | 2006-05-09 | 2007-03-30 | 試料導入システム |
Country Status (7)
Country | Link |
---|---|
US (1) | US8020458B2 (ja) |
EP (1) | EP2017598A4 (ja) |
JP (1) | JP4462575B2 (ja) |
KR (1) | KR20090014156A (ja) |
CN (1) | CN101432613A (ja) |
TW (1) | TW200806968A (ja) |
WO (1) | WO2007129513A1 (ja) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2312291A1 (en) * | 2008-08-12 | 2011-04-20 | Sumitomo Seika Chemicals CO. LTD. | Analytical method and analytical system |
WO2011125610A1 (ja) * | 2010-03-31 | 2011-10-13 | 日本たばこ産業株式会社 | エアロゾル粒子サンプリング装置 |
JP2012189582A (ja) * | 2011-02-24 | 2012-10-04 | Sumitomo Seika Chem Co Ltd | 気体中金属元素の測定方法、測定用演算式決定方法および測定システム |
JP2013205241A (ja) * | 2012-03-28 | 2013-10-07 | Keisuke Utani | 測定対象気体の測定方法及び測定システム |
JP2014222178A (ja) * | 2013-05-13 | 2014-11-27 | 新日鐵住金株式会社 | 脱溶媒試料導入装置および脱溶媒試料導入方法 |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5352331B2 (ja) * | 2009-04-15 | 2013-11-27 | ダイトエレクトロン株式会社 | ウェーハの面取り加工方法 |
CN102589934A (zh) * | 2011-11-01 | 2012-07-18 | 江苏江山制药有限公司 | 一种气流输送系统氧浓度测量采样流量补偿装置 |
JP1530328S (ja) * | 2015-02-17 | 2015-08-03 | ||
JP6366657B2 (ja) * | 2015-11-20 | 2018-08-01 | 株式会社日立ハイテクサイエンス | 発生ガス分析装置及び発生ガス分析方法 |
US10485219B1 (en) * | 2016-10-19 | 2019-11-26 | The United States Of America As Represented By The Secretary Of The Army | Canine scent detection training device and method |
TWI654415B (zh) * | 2017-08-25 | 2019-03-21 | 大陸商賽默飛世爾(上海)儀器有限公司 | 流體取樣裝置 |
KR102403636B1 (ko) * | 2020-01-15 | 2022-05-30 | 주식회사 베이스 | 실시간 중금속 분석 시스템 |
US11417508B2 (en) * | 2020-01-16 | 2022-08-16 | Ut-Battelle, Llc | Porous membrane enabled mass spectrometry characterization of microfluidic devices |
CN112117180B (zh) * | 2020-09-24 | 2022-03-01 | 中国核动力研究设计院 | 一种高凝固温度气态组分取样装置及取样方法 |
CN114383933B (zh) * | 2022-01-06 | 2023-06-13 | 西安交通大学 | 一种高温气体流动换热安全压力容器 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5245267Y2 (ja) * | 1972-12-16 | 1977-10-14 | ||
WO1990009585A1 (de) | 1989-02-16 | 1990-08-23 | Siemens Aktiengesellschaft | Verfahren und einrichtung zu regelung des trägergasdrucks bei der ventilosen trennsäulenschaltung in der gaschromatographie |
JPH052846Y2 (ja) * | 1985-02-22 | 1993-01-25 | ||
JPH05172750A (ja) * | 1991-10-22 | 1993-07-09 | Yokogawa Electric Corp | 微粒子導入装置 |
JPH07500416A (ja) | 1991-09-25 | 1995-01-12 | セタク テクノロジーズ インコーポレイテッド | 試料導入装置 |
US5400665A (en) | 1991-09-25 | 1995-03-28 | Cetac Technologies Incorporated | Sample introduction system for inductively coupled plasma and other gas-phase, or particle, detectors utilizing an enclosed filter solvent removal system, and method of use |
US5477048A (en) | 1992-09-10 | 1995-12-19 | Seiko Instruments Inc. | Inductively coupled plasma mass spectrometer |
US6021678A (en) * | 1998-05-27 | 2000-02-08 | Kennecott Utah Copper Corporation | Apparatus for transporting emissions from a stack |
JP2001239181A (ja) | 2000-02-29 | 2001-09-04 | Natl Inst Of Industrial Health Ministry Of Labour | 微粒子分級装置及びその方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5245267A (en) | 1975-10-07 | 1977-04-09 | Nec Home Electronics Ltd | Process for production of semiconductor device |
JP2606490B2 (ja) | 1991-06-25 | 1997-05-07 | 日本ビクター株式会社 | 可動体の位置制御装置 |
WO2005114691A2 (en) * | 2004-05-21 | 2005-12-01 | Whitehouse Craig M | Charged droplet sprayers |
-
2007
- 2007-03-30 US US12/227,075 patent/US8020458B2/en not_active Expired - Fee Related
- 2007-03-30 CN CNA2007800155918A patent/CN101432613A/zh active Pending
- 2007-03-30 JP JP2007513566A patent/JP4462575B2/ja active Active
- 2007-03-30 WO PCT/JP2007/057160 patent/WO2007129513A1/ja active Application Filing
- 2007-03-30 KR KR1020087027123A patent/KR20090014156A/ko not_active Application Discontinuation
- 2007-03-30 EP EP07740596A patent/EP2017598A4/en not_active Withdrawn
- 2007-04-16 TW TW096113345A patent/TW200806968A/zh unknown
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5245267Y2 (ja) * | 1972-12-16 | 1977-10-14 | ||
JPH052846Y2 (ja) * | 1985-02-22 | 1993-01-25 | ||
WO1990009585A1 (de) | 1989-02-16 | 1990-08-23 | Siemens Aktiengesellschaft | Verfahren und einrichtung zu regelung des trägergasdrucks bei der ventilosen trennsäulenschaltung in der gaschromatographie |
JPH07500416A (ja) | 1991-09-25 | 1995-01-12 | セタク テクノロジーズ インコーポレイテッド | 試料導入装置 |
US5400665A (en) | 1991-09-25 | 1995-03-28 | Cetac Technologies Incorporated | Sample introduction system for inductively coupled plasma and other gas-phase, or particle, detectors utilizing an enclosed filter solvent removal system, and method of use |
JPH05172750A (ja) * | 1991-10-22 | 1993-07-09 | Yokogawa Electric Corp | 微粒子導入装置 |
US5477048A (en) | 1992-09-10 | 1995-12-19 | Seiko Instruments Inc. | Inductively coupled plasma mass spectrometer |
US6021678A (en) * | 1998-05-27 | 2000-02-08 | Kennecott Utah Copper Corporation | Apparatus for transporting emissions from a stack |
JP2001239181A (ja) | 2000-02-29 | 2001-09-04 | Natl Inst Of Industrial Health Ministry Of Labour | 微粒子分級装置及びその方法 |
Non-Patent Citations (3)
Title |
---|
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, vol. 13, January 1998 (1998-01-01), pages 13 - 18 |
NISHIGUCHI K. ET AL.: "Kitai Shiryo Chokusetsu Donyu Sochi no Shisaku to Seino Hyoka", THE JAPAN SOCIETY FOR ANALYTICAL CHEMISTRY DAI 53 NENKAI KOEN YOSHISHU, 18 August 2004 (2004-08-18), pages 9, ABSTR. NO. A1027, XP003016982 * |
See also references of EP2017598A4 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2312291A1 (en) * | 2008-08-12 | 2011-04-20 | Sumitomo Seika Chemicals CO. LTD. | Analytical method and analytical system |
EP2312291A4 (en) * | 2008-08-12 | 2012-11-07 | Sumitomo Seika Chemicals | ANALYTICAL METHOD AND ANALYTICAL SYSTEM |
JP5459867B2 (ja) * | 2008-08-12 | 2014-04-02 | 住友精化株式会社 | 分析方法および分析システム |
WO2011125610A1 (ja) * | 2010-03-31 | 2011-10-13 | 日本たばこ産業株式会社 | エアロゾル粒子サンプリング装置 |
JP5640078B2 (ja) * | 2010-03-31 | 2014-12-10 | 日本たばこ産業株式会社 | エアロゾル粒子サンプリング装置 |
JP2012189582A (ja) * | 2011-02-24 | 2012-10-04 | Sumitomo Seika Chem Co Ltd | 気体中金属元素の測定方法、測定用演算式決定方法および測定システム |
JP2013205241A (ja) * | 2012-03-28 | 2013-10-07 | Keisuke Utani | 測定対象気体の測定方法及び測定システム |
JP2014222178A (ja) * | 2013-05-13 | 2014-11-27 | 新日鐵住金株式会社 | 脱溶媒試料導入装置および脱溶媒試料導入方法 |
Also Published As
Publication number | Publication date |
---|---|
US8020458B2 (en) | 2011-09-20 |
KR20090014156A (ko) | 2009-02-06 |
JPWO2007129513A1 (ja) | 2009-09-17 |
CN101432613A (zh) | 2009-05-13 |
TW200806968A (en) | 2008-02-01 |
US20090173171A1 (en) | 2009-07-09 |
EP2017598A1 (en) | 2009-01-21 |
JP4462575B2 (ja) | 2010-05-12 |
EP2017598A4 (en) | 2011-04-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007129513A1 (ja) | 試料導入システム | |
JP5459867B2 (ja) | 分析方法および分析システム | |
EP3088889B1 (en) | Flow reduction system for isotope ratio measurements | |
US10338044B2 (en) | Method and apparatus for reducing gas consumption in continuous flow analytical instruments | |
KR970011799A (ko) | 배출가스계측장치 | |
FR2897157B1 (fr) | Systeme a regulation d'humidite pour instrument thermogravimetrique,et procede pour reguler une atmosphere dans une chambre d'un instrument thermogravimetrique | |
JP2019526037A (ja) | 空気中の粒子の質量濃度を計測するためのセンサシステム | |
RU2008143115A (ru) | Изо-кинетический зонд для анализа загрязнения газов, генерируемых авиационным двигателем | |
US10446377B2 (en) | Control of gas flow | |
CN101583409B (zh) | 将含微粒的气流分离成微粒部分和无微粒气流部分的设备 | |
JP2008538002A (ja) | ガス供給源を備えたプラズマ分光システム | |
JPH01223347A (ja) | 液体試験装置 | |
CN1112619C (zh) | 用于调节具有显著不同的摩尔质量的气体流量的装置 | |
JPH0444696B2 (ja) | ||
CN108896704A (zh) | 一种气体在线稀释采样及标气发生装置和方法 | |
KR102583117B1 (ko) | 분석 기기에 입자 함유 샘플을 도입하기 위한 시스템 및 사용 방법 | |
JP2001351569A (ja) | ガス測定用オンラインモニター装置 | |
JP4315348B2 (ja) | ガス置換方法およびガス置換装置並びに分析システム | |
JP4491607B2 (ja) | 全量導入型ネブライザー対応シースガス導入型スプレーチャンバー | |
JP2010122160A (ja) | 水銀分析装置およびその方法 | |
JP2007101281A (ja) | Tvoc測定装置 | |
JP2008275372A (ja) | プラズマ分析装置及びプラズマ分析方法 | |
US20230298877A1 (en) | Membrane-based purge gas and sample transfer for laser ablation sample processing | |
JP2006066312A (ja) | Icp分析用試料導入装置及び方法 | |
KR102403636B1 (ko) | 실시간 중금속 분석 시스템 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2007513566 Country of ref document: JP Kind code of ref document: A |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07740596 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 200780015591.8 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007740596 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087027123 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12227075 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |