CN2720448Y - Micro multifunctional sample-feeding device - Google Patents
Micro multifunctional sample-feeding device Download PDFInfo
- Publication number
- CN2720448Y CN2720448Y CN 200420084256 CN200420084256U CN2720448Y CN 2720448 Y CN2720448 Y CN 2720448Y CN 200420084256 CN200420084256 CN 200420084256 CN 200420084256 U CN200420084256 U CN 200420084256U CN 2720448 Y CN2720448 Y CN 2720448Y
- Authority
- CN
- China
- Prior art keywords
- reagent
- capillaries
- test solution
- segregator
- container
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Images
Landscapes
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
The utility model relates to a micro multifunctional sample-feeding device provided with double capillaries, and the lower ends of the double capillaries are respectively inserted into a container. The containers are respectively provided with a test solution and a reagent. The upper ends of the capillaries are built into capillaries and crookedly extend into the cavity of the gas-liquid segregator. The upper part of the segregator is provided with a gas outlet, the bottom part of the segregator is provided with a waste fluid outlet, and the outside of the lower part of the segregator is provided with an argon inlet. The double capillaries respectively suck the test solution and the reagent when using it. The strong reducer KBH4 is put into the reagent and contacts with the test solution to generate the chemical reaction and the covalent compound. The covalent compound is introduced into the flame and an electric heating quartz capsule can measure different kinds of microelements, which is easy, fast and practical.
Description
Technical field
The utility model relates to a kind of miniature multi-function sampling device, be that a cover double capillary is connected in NITRATE BY FLAME ATOMIC absorption (FAAS) sample introduction end, add the physicochemical property that entry or reagent change test solution by online, realize the purpose of detection, simultaneously can connect gas-liquid separator, T type quartz ampoule or quartzy stove carry out hydrogenation AAS or atomic fluorescence (AFS) is analyzed with being brought into by the carrier gas argon after the fluid separation applications of hydrogenation, belong to detect apparatus
Technical field.
Background technology
In the analytical test field, there are some problems in atom A AS and AFS.AAS can not measure the high-load composition, if artificial dilution for many times solution easily produces dilution error, therefore often needs with loaded down with trivial details chemical method.Occurred the automatic dilution device in recent years abroad, but its cost is higher and detection speed is slow, therefore presses in bigger concentration range and measure high content component with fast method.
Air acetylene flame AAS has handy and safe and cheap advantage, but the elements such as chromium, tin, arsenic, antimony, bismuth, mercury and Se of low content are difficult to measure, and it is very low to measure plumbous sensitivity.Therefore the sample of measuring low content is difficulty, adds the lanthanum (La) of 1mg/ml in addition in test solution for the mensuration length of calcium, magnesium, and mensuration potassium, sodium often add rubidium (Rb) or caesium (Cs) salt of 1mg/ml, but wherein 99% outwells and cause waste in company with waste liquid.
Summary of the invention
The purpose of this utility model is that a kind of miniature multi-function sampling device will be provided, it adopts double capillary to be connected in the sample introduction end of instrument or connects atomizer through after the gas-liquid separation, it can overcome above-mentioned shortcoming, and its structure miniization and can save analyzing and testing time and high purity reagent in a large number, reduce disturbing effect and enlarged the kind and the concentration range of tested element.
The structure of miniature multi-function sampling device is that insert in the container 11 and 12 lower end of double capillary 1,2, in the container 11 test solution is housed, and container 12 is equipped with KBH
4Reagent, upper end capillaceous is combined into kapillary 3 and crooked stretching in the inner chamber of gas-liquid separator 7, separation vessel 7 upper ends are crooked and to side stretching, extension formation gas vent 9, the outside, bottom has argon gas inlet port 8, separation vessel 7 lower end diameter to attenuate and forms a waste liquid delivery outlet 10.
The advantage of miniature multi-function sampling device is that this device is microminiaturized, and reaction compartment is minimum and transport path short, has multiple function in FAAS, and velocity of separation is fast in HGAAS or HGAFS, and detectability reaches 10
-10, and the consumption of argon gas can reduce 90% when test, and KBH
4The strong reductant consumption also reduces 2/3 to 90%, basically there is not memory effect, disturb allowance to increase 5~200 times, can reduce more than 1/2 analysis time, the double capillary of this device is exactly a generator, its size have only penholder 1/2 and quality has only several grams, can directly introduce flame, fast measuring As, sb, Bi, Hg, Se, Sn and Pb, its sensitivity can improve 1~2 order of magnitude, can be used for measuring As, sp, Bi, Hg, Sn and Pb in ore deposit rock, metal and the alloy cell, also can be used among the AFS, detectability reaches 10
-10~10
-11
Description of drawings
Fig. 1. double capillary combination synoptic diagram
Fig. 2. miniature multi-function sampling device synoptic diagram
By Fig. 1, insert in the container 11 and 12 lower end of double capillary 1,2, in the container 11 test solution is housed, container 12 is equipped with water or reagent, the upper end of double capillary 1,2 is combined into kapillary 3 and is contained in the porch of atomizer 4, air inlet port 5 is arranged at the top of atomizer 4, and upper right quarter has impact bead 6, and it is by the bracing frame support.
By Fig. 2, insert in the container 11 and 12 lower end of double capillary 1,2, in the container 11 test solution is housed, and container 12 is equipped with KBH
4Reagent, upper end capillaceous is combined into kapillary 3 and crooked stretching in the inner chamber of gas-liquid separator 7, separation vessel 7 upper ends are crooked and to side stretching, extension formation gas vent 9, the outside, bottom has argon gas inlet port 8, separation vessel 7 lower end diameter to attenuate and forms a waste liquid delivery outlet 12.
Embodiment
In the structure of Fig. 1, the caliber difference of double capillary 1,2, simultaneously can suck two kinds of liquid, instantaneous mixing mutually in entering atomizer 4, at this moment many reagent that should add in the test solution can online adding in the several seconds of measuring, not only saved the time, the analyzing and testing function is increased, because the difference of caliber, its soakage is also different, therefore extension rate is also different, if cooperate a small amount of claim sample and suitable pre-dilution, just can measure 60% copper, if mix automatic constant positioner, just can guarantee enough transfusion precision, also not have dilution error.If adding inhibitor in test solution disturbs or chemical interference effect to suppress ionization, at this moment only in the several seconds, just suck the reagent of minute quantity, measure the amount of reagent of a sample at ordinary times, can measure the sample more than 100 this moment, save reagent more than 99%, it is too low for example to have solved the sensitivity of measuring chromium when measuring chromium, three problems of the narrow and chemical interference of the range of linearity.
In Fig. 2, test solution flows in the inner chamber of separation vessel 7 through kapillary 3, by the inflow entrance 8 inflow argon gas (Ar) in the outside, its underpart, because online suction strong reductant KBH
4, when it contacts with the test solution that contains As, sb, Bi, Hg, Se, Sn and Pb, strong chemical reaction takes place and generate the covalency compound, be introduced in flame or the electrothermal quartz tube, can measure trace elements such as As, sb, Bi, Hg, Se, Sn and Pb.Gas all flows out from delivery outlet 9, and waste liquid all flows out from the waste liquid flow export 10 of bottom, and this device can enlarge the range of application of atomic absorption (AAS) effectively in sum.
Claims (1)
1. a miniature multi-function sampling device is characterized in that the lower end of double capillary (1,2) is inserted in the container (11) and (12), and container is equipped with test solution in (11), and container (12) is equipped with KBH
4Reagent, upper end capillaceous is combined into kapillary (3) and bending is stretched in the inner chamber of gas-liquid separator (7), separation vessel (7) upper end is crooked and stretch to a side and to form gas vent (9), the outside, bottom has argon gas inlet port (8), separation vessel (7) lower end diameter to attenuate and forms a waste liquid delivery outlet (10).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200420084256 CN2720448Y (en) | 2004-07-27 | 2004-07-27 | Micro multifunctional sample-feeding device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200420084256 CN2720448Y (en) | 2004-07-27 | 2004-07-27 | Micro multifunctional sample-feeding device |
Publications (1)
Publication Number | Publication Date |
---|---|
CN2720448Y true CN2720448Y (en) | 2005-08-24 |
Family
ID=35009407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 200420084256 Expired - Fee Related CN2720448Y (en) | 2004-07-27 | 2004-07-27 | Micro multifunctional sample-feeding device |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN2720448Y (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105115949A (en) * | 2005-12-21 | 2015-12-02 | 梅索斯卡莱科技公司 | Assay apparatuses, methods and reagents |
CN109709054A (en) * | 2019-01-21 | 2019-05-03 | 广西科技大学鹿山学院 | Flame atomic absorption spectrophotometer aeration sample introduction regulating device |
US11300571B2 (en) | 2005-12-21 | 2022-04-12 | Meso Scale Technologies, Llc. | Assay apparatuses, methods and reagents |
-
2004
- 2004-07-27 CN CN 200420084256 patent/CN2720448Y/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105115949A (en) * | 2005-12-21 | 2015-12-02 | 梅索斯卡莱科技公司 | Assay apparatuses, methods and reagents |
CN105115949B (en) * | 2005-12-21 | 2018-06-22 | 梅索斯卡莱科技公司 | Analytical equipment, method and reagent |
US11300571B2 (en) | 2005-12-21 | 2022-04-12 | Meso Scale Technologies, Llc. | Assay apparatuses, methods and reagents |
US11892455B2 (en) | 2005-12-21 | 2024-02-06 | Meso Scale Technologies, Llc. | Assay apparatuses, methods and reagents |
CN109709054A (en) * | 2019-01-21 | 2019-05-03 | 广西科技大学鹿山学院 | Flame atomic absorption spectrophotometer aeration sample introduction regulating device |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102445442B (en) | Intelligent general type mercury measuring device and detection method thereof | |
Mitani et al. | Automated headspace single-drop microextraction via a lab-in-syringe platform for mercury electrothermal atomic absorption spectrometric determination after in situ vapor generation | |
CN106404765B (en) | The preparation method of silver-colored gold-covered nano stick colorimetric probe and its method for detecting copper ion | |
CN106290334B (en) | The chemistry in detecting of cobalt and manganese content in cobalt manganese raw material | |
Fang et al. | Developments and trends in flow injection atomic absorption spectrometry | |
CN106770730B (en) | Method for measuring methyl mercury and ethyl mercury | |
CN102707005A (en) | Method for synchronously analyzing ferric iron and ferrous iron in water sample online | |
Puanngam et al. | Automated on-line preconcentration of trace aqueous mercury with gold trap focusing for cold vapor atomic absorption spectrometry | |
JP2022506106A (en) | Atomic fluorescence spectroscopic analysis method and equipment using water as carrier fluid | |
CN105738431B (en) | It is non-evaporating to evaporate micro easy release cyanogen and total cyanogen device and method in non-color developing detection aqueous solution | |
CN2720448Y (en) | Micro multifunctional sample-feeding device | |
Gong | Synthesis of polyacrylaminoimidazole chelating fiber and properties of concentration and separation of trace Au, Hg and Pd from samples | |
CN106644994A (en) | Method for detecting inorganic mercury and organic mercury in water by solid-phase extraction-mercury analyzer | |
CN109870420A (en) | The quantitative detecting method of two kinds of valence state thallium ions in a kind of acid waste water | |
Sun et al. | Copper isotope fractionation during magma differentiation: evidence from lavas on the East Pacific Rise at 10 30′ N | |
CN107037176B (en) | The method and apparatus of sulfide content in a kind of detection methane gas | |
Ferreira et al. | Preconcentration and determination of copper and zinc in natural water samples by ICP-AES after complexation and sorption on Amberlite XAD-2 | |
CN201229325Y (en) | Mini extraction separation device for trace material | |
CN107037115B (en) | ICP-MS hydride sampling system and hydride detection method thereof | |
CN105021692A (en) | Method for simultaneously determining multiple inorganic elements in cigarette liquid of electronic cigarette | |
CN107860728B (en) | Flow injection non-connection eight-way valve adsorption pre-enrichment elution method | |
CN211348093U (en) | Trace element measuring device in dangerous waste | |
CN106644665A (en) | Gas-liquid separation device | |
Huizhi et al. | Catalytic spectrophotometric determination of trace selenium in microemulsion after separation and enrichment by SDG | |
CN209640300U (en) | A kind of high-precision liquid chromatograph |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
DD01 | Delivery of document by public notice |
Addressee: Gong Zhixiang Document name: Notification to Pay the Fees |
|
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20050824 Termination date: 20100727 |