CN203707078U - Volatilized solvent auxiliary ionization low-voltage photo ionization mass spectrum device for ultrasonic atomization sample injection - Google Patents
Volatilized solvent auxiliary ionization low-voltage photo ionization mass spectrum device for ultrasonic atomization sample injection Download PDFInfo
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- CN203707078U CN203707078U CN201420051352.5U CN201420051352U CN203707078U CN 203707078 U CN203707078 U CN 203707078U CN 201420051352 U CN201420051352 U CN 201420051352U CN 203707078 U CN203707078 U CN 203707078U
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- mass spectrum
- ultrasonic atomizatio
- solvent flashing
- ionization
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- 239000002904 solvent Substances 0.000 title claims abstract description 41
- 238000001819 mass spectrum Methods 0.000 title claims abstract description 40
- 238000000889 atomisation Methods 0.000 title abstract description 6
- 238000002347 injection Methods 0.000 title abstract description 3
- 239000007924 injection Substances 0.000 title abstract description 3
- 238000005070 sampling Methods 0.000 claims abstract description 32
- 230000007246 mechanism Effects 0.000 claims abstract description 31
- 238000010438 heat treatment Methods 0.000 claims abstract description 28
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 239000012159 carrier gas Substances 0.000 claims description 19
- 239000007789 gas Substances 0.000 claims description 18
- 230000003287 optical effect Effects 0.000 claims description 15
- 239000000919 ceramic Substances 0.000 claims description 8
- 239000000498 cooling water Substances 0.000 claims description 8
- 238000007789 sealing Methods 0.000 claims description 8
- 230000008878 coupling Effects 0.000 claims description 7
- 238000010168 coupling process Methods 0.000 claims description 7
- 238000005859 coupling reaction Methods 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- 238000012546 transfer Methods 0.000 claims description 6
- 230000006641 stabilisation Effects 0.000 claims description 4
- 238000011105 stabilization Methods 0.000 claims description 4
- 235000014676 Phragmites communis Nutrition 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 235000013305 food Nutrition 0.000 abstract description 3
- 238000002309 gasification Methods 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 2
- 230000005540 biological transmission Effects 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 4
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical class C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 238000010183 spectrum analysis Methods 0.000 description 3
- 150000001793 charged compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229940035893 uracil Drugs 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 230000005596 ionic collisions Effects 0.000 description 1
- 238000000752 ionisation method Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
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- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
Abstract
The utility model relates to a volatilized solvent auxiliary ionization low-voltage photo ionization mass spectrum device for ultrasonic atomization sample injection. The device comprises a mass spectrum mechanism. The mass spectrum mechanism comprises a mass spectrum chamber and a photo ionization chamber which are connected adjacently. A back sampling cone is arranged on a wall at one side of the mass spectrum chamber. A mass spectrum chamber vacuum pump connector is arranged in a wall at the other side of the mass spectrum chamber. An ion transmission system and a mass analyzer are arranged in the mass spectrum chamber. The back sampling cone extends into the ionization chamber. A front sampling cone is arranged at one side of the ionization chamber, and the ionization chamber vacuum pump connector is arranged at the other side of the ionization chamber. A vacuum ultraviolet source is arranged at the top of the photo ionization chamber. The device also comprises an ultrasonic atomization mechanism, a heating gasification mechanism and a volatilized solvent introducing mechanism. The device achieves desolventing by utilization of ultrasonic atomization and heating gasification and carries out direct sampling of substances to be detected and difficult to volatilize. No pretreatment is needed, and therefore sensitive and rapid mass spectrum analysis is achieved. The device has wide application prospects in aspects of rapid mass spectrum analysis and the like of food, pesticides, environment and the like.
Description
Technical field
The utility model belongs to analytical technique of mass spectrum field, is specifically related to the quick mass spectrometer of difficult volatilization, complicated organic molecule and mixture.
Background technology
Mass-spectrometric technique is the important method of qualification molecular structure.Modern Mass Spectrometry instrument is mainly made up of vacuum system, sampling system, ion source, ion-optic system, mass analyzer, detector and data handling system.According to the difference of analysans structure, character, mass spectrum ionization mode is varied, and commercial mass spectrometer mainly contains five kinds of ion sources, electron impact ionization, chemi-ionization, electron spray ionisation, atmospheric pressure photoionization and substance assistant laser desorpted ionized; Vacuum ultraviolet ionized is that a kind of vacuum-ultraviolet light that utilizes wavelength to be less than 200nm makes the Ionized method of neutral molecule.He is a kind of soft ionization mode, does not almost have fragment ion to generate, and the polarity of molecule is not discriminated against, and has great advantage in the mass spectral analysis of complex mixture, more and more obtains people's attention.Now, on some commercialization mass spectrometers, be equipped with atmospheric pressure photoionization source, can be divided into Photomate and Photospray according to the difference of ionization source structure design, PhotoSpray is just equipped with for example, in the mass spectrometer that AB MDS SCIEX company produces,, but the atmospheric pressure photoionization source that Syagen technologies company promotes is but Photomate, they are all widely used.Direct injection analysis cannot be carried out to determinand in atmospheric pressure photoionization source, need to, with chromatograph joint used, determinand be carried out preliminary treatment and be separated; Secondly, atmosphere air molecule, solvent etc. can absorb a part of vacuum-ultraviolet light, not only affect the ionizing efficiency of determinand, also can shorten the useful life of uviol lamp; The 3rd, atmospheric pressure photoionization source need to apply high voltage in operating process; Finally, in atmospheric pressure photoionization, collision frequency increases, and molecular ion reaction is violent, still inapplicable for frangible especially determinand.
Utility model content
In order to solve the defect of above-mentioned existence, the utility model provides a kind of solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction from low-voltage optical from mass spectrometric apparatus.
The solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction comprises mass spectrum mechanism from low-voltage optical from mass spectrometric apparatus, described mass spectrum mechanism comprises mass spectrum chamber and the ionization chamber of adjacent connection, one sidewall of described mass spectrum chamber is provided with rear sampling cone, another sidewall is provided with mass spectrum chamber vacuum pump interface, is provided with ion transfer system and mass analyzer in mass spectrum chamber; Described rear sampling cone stretches in ionization chamber, and a side of described ionization chamber is provided with front sampling cone, and opposite side is provided with ionization chamber vacuum pump interface; Described ionization chamber is light-ionizated chamber, and top is provided with vacuum ultraviolet light source; Also comprise ultrasonic atomizatio mechanism, heating and gasifying mechanism and solvent flashing retraction mechanism; Described ultrasonic atomizatio mechanism comprises ultrasonic coupling chamber and ultrasonic atomizatio chamber, ultrasonic coupling chamber is divided into He Xia chamber, upper chamber by dividing plate, the lower indoor Vltrasonic device being formed by piezoelectric ceramic piece, vibrating reed, electronic controller that is provided with, the piezoelectric ceramic piece of Vltrasonic device is positioned at indoor bottom, the upper indoor coupled water that is equipped with; Described ultrasonic atomizatio chamber is upright tubulose, upper port is uncovered shape, lower port is by film seal, the port of export of carrier gas pipe is right-angle folding tubulose, stretch into ultrasonic atomizatio from a side pipe wall of ultrasonic atomizatio chamber indoor, the opposite side tube wall of ultrasonic atomizatio chamber is being communicated with one end of heating tube, and it is indoor that determinand solution is located at ultrasonic atomizatio; Described heating and gasifying mechanism comprises heating tube and condenser pipe, the outside of heating tube uniform heater strip, the other end of heating tube is being communicated with one end of condenser pipe, the other end of condenser pipe is outlet, and the front sampling cone of described outlet and ionization chamber is corresponding, and condenser pipe is vertical; Described solvent flashing retraction mechanism comprises the container that gas phase solvent flashing is housed, top is provided with gas outlet and carrier gas inlet, both are all more than solvent flashing liquid level, and the diameter of gas outlet and carrier gas inlet is all less than the diameter of container, described gas outlet correspondence is positioned at the mouth of pipe below of the outlet of condenser pipe.
The front sampling cone of ionization chamber and the rear sampling cone of mass spectrum chamber be all in same level position, and mutually vertical.
Described film is polyester material film, and film wrapped is in the lower end of ultrasonic atomizatio chamber, and is sealed by O-ring seals.
The temperature stabilization of described coupled water remains below 40 DEG C.
The tube wall of described condenser pipe is provided with the cooling water channel of up/down perforation, one end of cooling water channel is water inlet, the other end is delivery port, and water inlet and delivery port all extend condenser pipe outside, the outlet of described condenser pipe is being communicated with the arrival end of drainage tube, and the front sampling cone of the port of export of drainage tube and ionization chamber is in same plane; The bottom of the condenser pipe of vertical is being communicated with U-shaped water sealing (sealing water) pipe.
The carrier gas pipe of ultrasonic atomizatio outdoor is provided with flowmeter.
Described gas phase solvent flashing is acetone or toluene.
The light hole of vacuum ultraviolet light source is perpendicular to front sampling cone, and the vacuum degree of light-ionizated chamber is 1~1000Pa.
The vacuum degree of mass spectrum chamber is less than 10
-2pa.
Angle between heating tube and condenser pipe is greater than 90, is less than 150.
Useful technique effect of the present utility model embodies in the following areas:
1. the utility model device can carry out Direct Analysis to not pretreated determinand, such as soil, food, crops etc.;
2. the ionization process of this device betides under low pressure condition, both can effectively ionize determinand, also can avoid uviol lamp surface contaminated.Fig. 2 is exactly is 130Pa in light-ionizated chamber vacuum, and temperature is in the time of 110 DEG C, and under positive ion mode condition, toluene is as solvent flashing, the mass spectrogram of the 1.16mg/ml uracil aqueous solution.When Fig. 3 is same vacuum and temperature, under negative ion mode condition, toluene is as solvent flashing, 0.04mg/ml1, and 4-naphthoquinones is dissolved in the mass spectrogram that the mixed solvent of methyl alcohol and water obtains;
3. this device also can carry out quantitative analysis for determinand, and Fig. 4 is that light-ionizated chamber vacuum is 130Pa, and when temperature is 110 DEG C, toluene is as solvent flashing, determinand 9, and 10-phenanthrenequione is dissolved in the mixed solvent of methyl alcohol and water, (M+H) of acquisition
+the linear relationship of peak area and concentration;
4. no matter the utility model device is in ion transfer or the process of ionization, and all, without high pressure and violent molecular ion collision, therefore it likely becomes a kind of ionization mode softer than atmospheric pressure photoionization.There is very large application potential at complex structure and frangible the analysis of Chinese herbal medicines field;
5. the utility model directly drops into undressed testing sample (as soil, sewage etc.) in ultrasonic atomizing device, after not volatile determinand dissolves in solvent, after ultrasonic atomizatio and the processing of heating and gasifying desolventizing, enter low-voltage optical from chamber, the vacuum ultraviolet light source of vertically being placed ionizes, thereby realize sensitive, mass spectral analysis fast, have broad application prospects at aspects such as the quick mass spectral analyses such as food, agricultural chemicals, environment.
Brief description of the drawings
Fig. 1 is the utility model structural representation.
Fig. 2 is the mass spectrogram of the uracil of positive ion mode acquisition.
Fig. 3 is the mass spectrogram of the 1,4-naphthoquinone of negative ion mode acquisition.
Fig. 4 is the linear relationship of 9,10-phenanthrenequione.
Sequence number in figure: carrier gas pipe 1, flowmeter 2, the port of export 3, determinand solution 4, ultrasonic atomizatio chamber 5, heater strip 6, heating tube 7, condenser pipe 8, drainage tube 9, front sampling cone 10, vacuum ultraviolet light source 11, light-ionizated chamber 12, ionization chamber vacuum pump interface 13, rear sampling cone 14, ion transfer system 15, mass spectrum chamber vacuum pump interface 16, mass spectrum chamber 17, mass analyzer 18, carrier gas inlet 19, solvent flashing retraction mechanism 20, U-shaped water sealing (sealing water) pipe 21, O-ring seals 22, piezoelectric ceramic piece 23, Vltrasonic device 24, ultrasonic coupling chamber 25, polyester film 26.
Embodiment
Below in conjunction with accompanying drawing, by embodiment, the utility model is described further.
Referring to Fig. 1, the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction comprises mass spectrum mechanism, ultrasonic atomizatio mechanism, heating and gasifying mechanism and solvent flashing retraction mechanism from low-voltage optical from mass spectrometric apparatus.
Described mass spectrum mechanism comprises mass spectrum chamber 17 and the light-ionizated chamber 12 of adjacent connection.Rear sampling cone 14 is installed on one sidewall of mass spectrum chamber 17, on another sidewall, offers mass spectrum chamber vacuum pump interface 16, ion transfer system 15 and mass analyzer 18 are installed in mass spectrum chamber 17; Rear sampling cone 14 stretches in light-ionizated chamber 12; The vacuum degree of mass spectrum chamber 17 is less than 10
-2pa.The top of light-ionizated chamber 12 is provided with vacuum ultraviolet light source 11, one sides front sampling cone 10 is installed, and opposite side is provided with ionization chamber vacuum pump interface 13.The front sampling cone 10 of light-ionizated chamber 12 and the rear sampling cone 14 of mass spectrum chamber 17 be all in same level position, and mutually vertical; The vacuum degree of light-ionizated chamber 12 is 130Pa, and temperature is controlled at 110 DEG C.
Described ultrasonic atomizatio mechanism comprises ultrasonic coupling chamber 25 and ultrasonic atomizatio chamber 5, ultrasonic coupling chamber 25 is divided into He Xia chamber, upper chamber by dividing plate, lower indoor location is by the Vltrasonic device 24 being made up of piezoelectric ceramic piece 23, vibrating reed, electronic controller, the piezoelectric ceramic piece 23 of Vltrasonic device 24 is positioned at indoor bottom, the upper indoor coupled water that is equipped with, the temperature stabilization of coupled water remains below 40 DEG C.Ultrasonic atomizatio chamber 5 is upright tubulose, and upper port is uncovered shape, when work, need use plug seal, and lower port is sealed by polyester film 26, and polyester film 26 is wrapped in the lower end of ultrasonic atomizatio chamber 5, and is sealed by O-ring seals 22.The port of export 3 of carrier gas pipe 1 is right-angle folding tubulose, stretch into ultrasonic atomizatio from a side pipe wall of ultrasonic atomizatio chamber 5 indoor, the arrival end of carrier gas pipe 1 is being communicated with carrier gas passage, and flowmeter 2 is installed on carrier gas pipe 1, adjust flux meter after atomization, is controlled at 300ml/min by carrier gas flux; The opposite side tube wall of ultrasonic atomizatio chamber 5 is being communicated with one end of heating tube 7, and determinand solution 4 is placed in ultrasonic atomizatio chamber 5.
Described heating and gasifying mechanism comprises heating tube 7 and condenser pipe 8, and the angle between heating tube 7 and condenser pipe 8 is 105.The outside of heating tube 7 uniform heater strip 6, the other end of heating tube 7 is being communicated with one end of condenser pipe 8, the other end of condenser pipe 8 is outlet, the outlet of condenser pipe 8 is being communicated with the arrival end of drainage tube 9, condenser pipe 8 is vertical; The front sampling cone 10 of the port of export of drainage tube 9 and light-ionizated chamber 12 is in same plane; The bottom of the condenser pipe 8 of vertical is being communicated with U-shaped water sealing (sealing water) pipe 21; The front sampling cone 10 of the outlet of condenser pipe 8 and light-ionizated chamber 12 is corresponding; The tube wall of described condenser pipe 8 is provided with the cooling water channel of up/down perforation, and one end of cooling water channel is water inlet, and the other end is delivery port, and water inlet and delivery port all extend condenser pipe outside.
Described solvent flashing retraction mechanism 20 comprises the container that gas phase solvent flashing is housed, top is provided with gas outlet and carrier gas inlet 19, both are all more than solvent flashing liquid level, and the diameter of gas outlet and carrier gas inlet 19 is all less than the diameter of container, described gas outlet correspondence is positioned at the mouth of pipe below of the outlet of condenser pipe 8.Gas phase solvent flashing is toluene (or acetone).
Operation principle of the present utility model is described as follows:
Testing sample, before mass spectral analysis, is first dissolved in organic solvent or water and forms determinand solution 4, then heating tube 7 is heated to 10min, makes the temperature stabilization of heating tube 7 inwalls 200 DEG C of left and right; Determinand solution 4 is added to ultrasonic atomizatio chamber 5, open Vltrasonic device 24, the piezoelectric ceramic piece 23 of Vltrasonic device 24 is started working, hyperacoustic frequency, at 1.53-1.87MHz, is opened the water inlet of cooling water channel on condenser pipe 8 simultaneously, makes cooling water implement cooling to condenser pipe 8, in the time that the drop of atomization generation is full of ultrasonic atomizatio chamber 5, open gas flowmeter 2, carrier gas pipe 1 is inputted nitrogen, and the ultrafine drop that the nitrogen of input is atomized into determinand solution 4 is brought heating tube 7 and condenser pipe 8 into; In solvent flashing retraction mechanism 20, gas phase solvent flashing toluene is taken out of gas outlet from the nitrogen of carrier gas inlet 19 stable inputs, under the effect of the pressure reduction producing at atmospheric pressure and light-ionizated chamber 12, toluene enters light-ionizated chamber 12 together with molecule and solvent flashing in the determinand solution 4 of gasification etc., by vacuum ultraviolet light source 11 at 130Pa, under 110 DEG C of conditions, ionize, the ion generating is under the acting in conjunction of front sampling cone 10, rear sampling cone 14 and ion transfer system 15 electric fields, enter mass spectrum chamber 17, finally by mass analyzer 18 determination and analysis.
Claims (10)
1. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction is from low-voltage optical from mass spectrometric apparatus, comprise mass spectrum mechanism, described mass spectrum mechanism comprises mass spectrum chamber and the ionization chamber of adjacent connection, one sidewall of described mass spectrum chamber is provided with rear sampling cone, another sidewall is provided with mass spectrum chamber vacuum pump interface, is provided with ion transfer system and mass analyzer in mass spectrum chamber; Described rear sampling cone stretches in ionization chamber, and a side of described ionization chamber is provided with front sampling cone, and opposite side is provided with ionization chamber vacuum pump interface; It is characterized in that: described ionization chamber is light-ionizated chamber, and top is provided with vacuum ultraviolet light source; Also comprise ultrasonic atomizatio mechanism, heating and gasifying mechanism and solvent flashing retraction mechanism; Described ultrasonic atomizatio mechanism comprises ultrasonic coupling chamber and ultrasonic atomizatio chamber, ultrasonic coupling chamber is divided into He Xia chamber, upper chamber by dividing plate, the lower indoor Vltrasonic device being formed by piezoelectric ceramic piece, vibrating reed, electronic controller that is provided with, the piezoelectric ceramic piece of Vltrasonic device is positioned at indoor bottom, the upper indoor coupled water that is equipped with; Described ultrasonic atomizatio chamber is upright tubulose, upper port is uncovered shape, lower port is by film seal, the port of export of carrier gas pipe is right-angle folding tubulose, stretch into ultrasonic atomizatio from a side pipe wall of ultrasonic atomizatio chamber indoor, the opposite side tube wall of ultrasonic atomizatio chamber is being communicated with one end of heating tube, and it is indoor that determinand solution is located at ultrasonic atomizatio; Described heating and gasifying mechanism comprises heating tube and condenser pipe, the outside of heating tube uniform heater strip, the other end of heating tube is being communicated with one end of condenser pipe, the other end of condenser pipe is outlet, and the front sampling cone of described outlet and ionization chamber is corresponding, and condenser pipe is vertical; Described solvent flashing retraction mechanism comprises the container that gas phase solvent flashing is housed, top is provided with gas outlet and carrier gas inlet, both are all more than solvent flashing liquid level, and the diameter of gas outlet and carrier gas inlet is all less than the diameter of container, described gas outlet correspondence is positioned at the mouth of pipe below of the outlet of condenser pipe.
2. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the front sampling cone of ionization chamber and the rear sampling cone of mass spectrum chamber be all in same level position, and mutually vertical.
3. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: described film is polyester material film, and film wrapped is in the lower end of ultrasonic atomizatio chamber, and is sealed by O-ring seals.
4. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the temperature stabilization of described coupled water remains below 40 DEG C.
5. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1 is from low-voltage optical from mass spectrometric apparatus, it is characterized in that: the tube wall of described condenser pipe is provided with the cooling water channel of up/down perforation, one end of cooling water channel is water inlet, the other end is delivery port, and water inlet and delivery port all extend condenser pipe outside, the outlet of condenser pipe is being communicated with the arrival end of drainage tube, and the front sampling cone of the port of export of drainage tube and ionization chamber is in same plane; The bottom of the condenser pipe of vertical is being communicated with U-shaped water sealing (sealing water) pipe.
6. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the carrier gas pipe of ultrasonic atomizatio outdoor is provided with flowmeter.
7. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: described gas phase solvent flashing is acetone or toluene.
8. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the light hole of vacuum ultraviolet light source is perpendicular to front sampling cone, and the vacuum degree of light-ionizated chamber is 1~1000Pa.
9. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the vacuum degree of mass spectrum chamber is less than 10
-2pa.
10. the solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction according to claim 1, from low-voltage optical from mass spectrometric apparatus, is characterized in that: the angle between heating tube and condenser pipe is greater than 90, is less than 150.
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CN201420051352.5U CN203707078U (en) | 2014-01-27 | 2014-01-27 | Volatilized solvent auxiliary ionization low-voltage photo ionization mass spectrum device for ultrasonic atomization sample injection |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103762150A (en) * | 2014-01-27 | 2014-04-30 | 中国科学技术大学 | Ultrasonic atomization sample introduction volatile solvent assisting ionization low-pressure photo ionization mass spectrum device |
-
2014
- 2014-01-27 CN CN201420051352.5U patent/CN203707078U/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103762150A (en) * | 2014-01-27 | 2014-04-30 | 中国科学技术大学 | Ultrasonic atomization sample introduction volatile solvent assisting ionization low-pressure photo ionization mass spectrum device |
CN103762150B (en) * | 2014-01-27 | 2016-03-30 | 中国科学技术大学 | The solvent flashing auxiliary electrical of ultrasonic atomizatio sample introduction is from low-voltage optical from mass spectrometric apparatus |
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C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CX01 | Expiry of patent term |
Granted publication date: 20140709 |
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CX01 | Expiry of patent term |