CN201387399Y - Preprocessor integrating extraction and filtering and being used for organic matter test - Google Patents
Preprocessor integrating extraction and filtering and being used for organic matter test Download PDFInfo
- Publication number
- CN201387399Y CN201387399Y CN200920107178U CN200920107178U CN201387399Y CN 201387399 Y CN201387399 Y CN 201387399Y CN 200920107178 U CN200920107178 U CN 200920107178U CN 200920107178 U CN200920107178 U CN 200920107178U CN 201387399 Y CN201387399 Y CN 201387399Y
- Authority
- CN
- China
- Prior art keywords
- container
- upper port
- preprocessor
- filtering
- extraction
- 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
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
The utility model relates to a preprocessor integrating extraction and filtering and being used for organic matter test. The preprocessor comprises a container, a filter membrane, bottle covers, an air inlet pipe and an air extraction pipe, wherein the filter membrane is vertically arranged in the container and divides the container into a first container and a second container; the bottle covers cover an upper port of the first container and an upper port of the second container simultaneously; the air inlet pipe is arranged on the bottle cover covering on the upper port of the first container; and the air extraction pipe is arranged on the bottle cover covering the upper port of the second container. The preprocessor integrates the extraction and filtering, only needs a small amount of samples, and has little usage of solvent, simple, fast and practical operation and little process loss when in preprocessing.
Description
Technical field
The utility model relates to a kind of treasury that is used for organism test and gets and filter front processor in one.
Background technology
Ultrasonic extraction (Ultrasound extraction) technology is a kind of new separation technology that development in recent years is got up, and compares with the abstraction technique of routine, and the ultrasonic extraction technology has characteristics such as quick, inexpensive, safe, efficient.At present, when sample pre-treatments was carried out in stratographic analysis, the ultrasonic extraction method was the simplest, pre-treating method the most fast.Conventional ultrasonic extraction method operation steps is, quantitatively take by weighing sample (being generally 1-2g), add an amount of solvent (being generally 15-20ml), put into ultrasound wave and carry out ultrasonic Extraction, behind ultrasonic the finishing, filter, mother liquor is transferred in the volumetric flask, and be settled to scale (being generally 25ml or 50ml) with solvent, only get at last and seldom measure solution (being no more than 1ml usually) and carry out instrumental analysis.The shortcoming of this operation is, on the one hand, the intermediate filtered step will be used a sets filtering device in addition, and during also comprise the solution transfer step, can cause sample loss unavoidably, thereby influence the accuracy of final test; On the other hand; this pre-treatment means need be settled in the volumetric flask; required quantity of solvent is relatively large; the not enough 1ml of quantity of solvent that finally is used for the machine test; and really in test, play a role have only several microlitres; excessive solution will not only cause cost waste as waste disposal, more increase the weight of the burden of environmental protection.
Summary of the invention
The utility model purpose is to provide a kind of treasury that is used for the organism test to get and filter front processor in one, with this processor when pre-treatment is carried out in organic stratographic analysis, only need small amount of sample, and solvent load is few, method of operating is simple, quick, practical, process loss is little.
The front processor in one is got and filtered to the treasury that is used for the organism test that the utility model provides, and it comprises:
One container 2;
The one vertical filtering membrane 3 that is positioned within the described container 2 and described container 2 is divided into first container 4 and second container 5;
Be covered on the bottle cap 1 of described first container, 4 upper port and second container, 5 upper port simultaneously;
Be located at the draft tube 7 on the bottle cap 1 that is covered on described first container, 4 upper port;
Be located at the exhaust tube 6 on the bottle cap 1 that is covered on described second container, 5 upper port.
Described container 2 is the container of glass material, and its volume is 2-8ml.
Described filtering membrane 3 is nylon-type, mixes the filtering membrane of fine class, polysulfones, fluorine material type or polypropylene class, and its aperture is 0.2-5um.
When organism is tested: quantitatively take by weighing small amount of sample (being generally 0.01g-0.1g) and put into first container 4, and quantitatively (being generally 1-5ml) pipettes suitable solvent in first container 4, the conventional bottle cap of suitable size is threaded onto the upper port (will screw) of described container 2, described container 2 is put into ultrasonic instrument carry out ultrasonic extraction; After ultrasonic extraction finishes, outward winding and remove conventional bottle cap; Upper port spiral cover upper bottle cover 1 in described container 2, slowly inflate by 7 pairs first containers 4 of air intake opening, or slowly bleed by 6 pairs second containers 5 of exhaust tube, solution (mixed liquor of sample and solvent) in first container 4 promptly enters in second container 5 from first container 4, when treating that first container, 4 interior solution all enter second container 5, stop to bleed; Can directly be transferred to the instrument test that carries out sample in the conventional Agilent sample introduction bottle with the solution in second container 5 this moment.
The treasury that is used for the organism test of the present utility model is got and is filtered in the advantage of the front processor of one and is:
Front processor of the present utility model is that the front processor in one is got, filtered to a kind of treasury that is used for the organism test, with this processor when sample pre-treatments is carried out in stratographic analysis, only need small amount of sample, and solvent load is few, method of operating is simple, quick, practical, process loss is little.
Description of drawings
Fig. 1 gets, filters in the structural representation of the front processor of one for the treasury that is used for the organism test of the present utility model.
Wherein, bottle cap 1 container 2 filtering membranes 3
First container, 4 second containers, 5 exhaust tubes 6
Embodiment
Further describe the utility model below in conjunction with drawings and Examples.
Being illustrated in figure 1 as the treasury that is used for the organism test of the present utility model gets and filters in the structural representation of the front processor of one, as seen from the figure, the treasury that is used for the organism test that the utility model of the present utility model provides is got, is filtered the front processor in one, and it comprises:
One container 2;
The one vertical filtering membrane 3 that is positioned within the described container 2 and described container 2 is divided into first container 4 and second container 5;
Be covered on the bottle cap 1 of described first container, 4 upper port and second container, 5 upper port simultaneously;
Be located at the draft tube 7 on the bottle cap 1 that is covered on described first container, 4 upper port;
Be located at the exhaust tube 6 on the bottle cap 1 that is covered on described second container, 5 upper port.
When organism is tested: quantitatively take by weighing the 0.01g sample and put into first container 4, and the solvent that quantitatively pipettes 1ml is in first container 4, the conventional bottle cap of suitable size is threaded onto the upper port (will screw) of described container 2, described container 2 is put into ultrasonic instrument carry out ultrasonic extraction; After ultrasonic extraction finishes, outward winding and remove described conventional bottle cap; In the upper port spiral cover upper bottle cover 1 of described container 2, slowly to bleed by 6 pairs second containers 5 of exhaust tube, the solution (mixed liquor of sample and solvent) in first container 4 promptly enters in second container 5 from first container 4; When the solution for the treatment of first container 4 all enters second container 5, stop to bleed; Directly be transferred to the instrument test that carries out sample in the conventional Agilent sample introduction bottle with the solution in second container 5 this moment.
The container 2 of present embodiment is the container of glass material, and its volume is 2ml;
The filtering membrane 3 of present embodiment is nylon-type (aperture be 0.2um, 0.5um, 10um, 3um, 4um or 5um um all can)
Certainly, described filtering membrane 3 can also be for mixing the filtering membrane of fine class, polysulfones, fluorine material type or polypropylene class, all can in the 0.2-5um scope in its aperture.
Treasury of the present utility model gets, filter structural representation in the front processor of one with embodiment 1.
During experiment, quantitatively take by weighing the 0.1g sample and put into first container 4, the solvent that quantitatively pipettes 3ml is threaded onto the upper port (will screw) of described container 2 with the conventional bottle cap of suitable size in first container 4, described container 2 is put into ultrasound wave carry out ultrasonic extraction; Behind ultrasonic the finishing, outward winding and remove conventional bottle cap; In the upper port spiral cover upper bottle cover 1 of described container 2, slowly to inflate by air intake opening (7), solution (mixed liquor of sample and solvent) promptly enters in second container 5 from first container 4; When treating that first container, 4 interior solution all enter second container 5, stop inflation; Directly the solution in the container 5 is transferred in the conventional Agilent sample introduction bottle this moment and carries out instrument test.
In the present embodiment, container 2 is the container of glass material, and its volume is 8ml; Filtering membrane 3 is 0.45um for the aperture, and its material is the filtering membrane of nylon-type, mixed fine class, polysulfones, fluorine material type or polypropylene class.
Claims (3)
1, a kind of treasury that is used for the organism test is got, is filtered the front processor in one, it is characterized in that it comprises:
One container (2);
The one vertical filtering membrane (3) that is positioned within the described container (2) and described container (2) is divided into first container (4) and second container (5);
Be covered on the bottle cap (1) of described first container (4) upper port and second container (5) upper port simultaneously;
Be located at the draft tube (7) on the bottle cap (1) that is covered on described first container (4) upper port;
Be located at the exhaust tube (6) on the bottle cap (1) that is covered on described second container (5) upper port.
2, get, filter the front processor in one by the described treasury that is used for the organism test of claim 1, it is characterized in that described container (2) is the container of glass material, its volume is 2-8ml.
3, get, filter front processor by the described treasury that is used for the organism test of claim 1, it is characterized in that described filtering membrane (3) aperture is 0.25um-5um in one.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200920107178U CN201387399Y (en) | 2009-04-14 | 2009-04-14 | Preprocessor integrating extraction and filtering and being used for organic matter test |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200920107178U CN201387399Y (en) | 2009-04-14 | 2009-04-14 | Preprocessor integrating extraction and filtering and being used for organic matter test |
Publications (1)
Publication Number | Publication Date |
---|---|
CN201387399Y true CN201387399Y (en) | 2010-01-20 |
Family
ID=41579933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200920107178U Expired - Fee Related CN201387399Y (en) | 2009-04-14 | 2009-04-14 | Preprocessor integrating extraction and filtering and being used for organic matter test |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN201387399Y (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113687014A (en) * | 2021-08-04 | 2021-11-23 | 山东利特纳米技术有限公司 | Qualitative and quantitative analysis method for graphene oxide surface functional groups |
-
2009
- 2009-04-14 CN CN200920107178U patent/CN201387399Y/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113687014A (en) * | 2021-08-04 | 2021-11-23 | 山东利特纳米技术有限公司 | Qualitative and quantitative analysis method for graphene oxide surface functional groups |
CN113687014B (en) * | 2021-08-04 | 2024-09-17 | 山东利特纳米技术有限公司 | Qualitative and quantitative analysis method for graphene oxide surface functional groups |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111474132B (en) | Rapid detection method for content of micro-plastic in water body and application | |
CN101813582A (en) | Integrated pesticide residue detection pretreatment device and pretreatment method | |
CN101650349B (en) | Gas phase chromatograph-mass spectrum detection method for nonylphenol polyoxyethylene ether in leather, synthetic leather, paper and textile | |
CN102998411B (en) | A kind of detection method of ageratum dripping pill | |
CN103822999A (en) | Full-automatic QuEChERS preprocessing all-in-one machine and preprocessing method | |
CN103472025A (en) | Method for identifying quality of lignum pterocarri | |
CN201387399Y (en) | Preprocessor integrating extraction and filtering and being used for organic matter test | |
CN106582066A (en) | Cinnamate type ultraviolet sun-screening agent molecular engram solid-phase extraction column as well as preparation and application thereof | |
CN104155295A (en) | Method for quickly measuring hexavalent chromium in paper package material by solid-phase extraction purification and continuous flow analyzer | |
CN103293049A (en) | Serum separation method and serum separation device | |
CN201191248Y (en) | Novel counter-current type gas and liquid separator | |
CN201437087U (en) | Preprocessor integrated with extraction, filtration and on-computer test | |
CN205826387U (en) | A kind of pretreating device | |
CN104535548A (en) | Method for rapidly detecting sulfonamide antibacterial medicines in milk by using in-tube solid-phase micro-extraction technology | |
CN209024395U (en) | Portable sludge dewatering handles lab scale experimental box | |
CN201926625U (en) | Rapid detection case for detecting harmful substance in traditional Chinese medicine | |
CN207894765U (en) | A kind of oilfield sewage suspension content rapid determination device | |
CN104502481A (en) | Method for detecting vomitoxin and zearalenone in grains and feeds | |
CN109884199A (en) | Method for measuring content of flavonoid components in honey | |
CN103018235B (en) | Preparation method of separation-enrichment and color-developing measurement column for nickel | |
CN202387245U (en) | Preprocessor integrating extraction and filtration | |
CN103728399A (en) | Single-walled carbon nanohorn dispersion liquid-based dispersive micro solid phase extraction method | |
CN211978785U (en) | Novel extraction device for trace substances in hair, dry blood spots and dry urine spots | |
CN105004822B (en) | Novel nano chromatographic column for high-selectivity determination of Hg2+ and preparation method thereof | |
CN101419205B (en) | Method for measuring residual organic solvent in pectins |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20100120 Termination date: 20160414 |