MASS SPECTROMETER FOR DETECTING LEAKAGES VIA A TRACER GAS

Information

  • Patent Application
  • 20240183740
  • Publication Number
    20240183740
  • Date Filed
    March 14, 2022
    2 years ago
  • Date Published
    June 06, 2024
    8 months ago
Abstract
The present invention relates to a mass spectrometer (10) for detecting leakages via a tracer gas, said spectrometer (10) comprising:—an ionising means (3) intended to ionise said tracer gas;—at least one magnetic-field source (501) that generates a magnetic field (I) that is dependent on the electric current I supplied to said source (501) and that is intended to sort ionised elements;—a means (7) for detecting said tracer gas once ionised; characterized in that said spectrometer comprises a means (II) for adjusting the magnetic field, said adjusting means being configured to allow at least two separate adjustments, said adjustments having different sensitivities.
Description

The present invention relates to the field of mass spectrometers, and more particularly to detecting leakages by tracer-gas mass spectrometry.


As a reminder, a mass spectrometer is a device that uses the movement of the ions in electrical and/or magnetic fields, in order to classify them according to their mass/charge ratios. As illustrated in FIG. 1, a mass spectrometer 1 generally comprises an ionisation means 3, an analyser 5 and a detection means 7.


The ionisation means 3 is configured to ionise the chemical element or elements to be analysed. This ionisation also generates ions that will then be sorted and selected according to their mass/charge ratios.


This sorting can be obtained in various ways, but the concern is here, more particularly, with the analyses that proceed at least with a selection by dispersion of the ions by means of a magnetic field.


The ions thus sorted are next sent to the detection means 7, such as a detector that converts the stream of ions received into an electric current. Said electric current output from the detector subsequently undergoes a processing of the signal making it possible to obtain more precise measurements relating to the ions.


This type of mass spectrometer can in particular be used for detecting leakages or monitoring the gastightness of objects, for example by measuring and quantifying a tracer gas, such as helium or dihydrogen. However, other types of tracer gas can be used, such as dioxygen, carbon dioxide, etc.


However, the mass spectrometers used for detecting a leakage are intended to be used in industrial environments in which numerous environmental factors may disturb the measurements or settings, in particular variations in temperature, shocks, vibrations, movements, maintenance of the equipment, etc.


Moreover, a mass spectrometer for detecting leakages must also be as multipurpose as possible, in particular by operating with various tracer gases, for example to adapt to the tracer gases available and/or to the leakage levels sought.


The present invention thus makes it possible to remedy one or more of the problems mentioned above, by proposing a mass spectrometer for detecting leakages by tracer gas, said spectrometer comprising:

    • an ionisation means intended to ionise said tracer gas;
    • at least one magnetic field source generating a magnetic field {right arrow over (B)} dependent on the electric current I supplying said source intended for sorting the ionised elements;
    • a means for detecting said ionised tracer gas.


According to the invention, said spectrometer comprises a means for adjusting the magnetic field {right arrow over (B)} generated by said source, said adjustment means being configured to allow at least two distinct adjustments, said adjustments having different sensitivity.


According to a possible feature, said adjustment means comprises a pre-adjustment (or rough adjustment) and a fine adjustment.


According to another possible feature, one of the adjustments makes it possible to establish a nominal magnetic field {right arrow over (B0)}, while the other adjustment makes it possible to generate a variation in magnetic field Δ{right arrow over (B)} around the nominal value of the magnetic field {right arrow over (B0)}.


The electromagnetic field {right arrow over (B)} generated by the magnetic field source is therefore in this case the sum of the nominal magnetic field {right arrow over (B0)} and the magnetic field variation Δ{right arrow over (B)}.


According to another possible feature, said magnetic field source comprises an electromagnet.


It should be noted that the magnetic field source may also be a magnetic sector incorporating one or more electromagnets.


According to another possible feature, said adjustment means comprises at least two adjustment commands, a combinatorial circuit configured to combine the values of said at least two commands, and a circuit for controlling the current I circulating in said magnetic field source.


According to another possible feature, said at least two adjustment commands are electrical quantities, such as voltages.


According to another possible feature, the magnetic field {right arrow over (B)} depends on the values of the electrical quantities of said at least two adjustment commands.


According to another possible feature, the mass spectrometer comprises N adjustment commands and/or N magnetic field sources, where N is an integer greater than or equal to 3.


The multiplicity of the adjustment commands and/or of the magnetic field sources makes it possible to address a greater number of tracer gases and to facilitate the adjustments of said mass spectrometer according to the invention.


According to another possible feature, the combinatorial circuit comprises:

    • a plurality of resistors R1, R2, R3 and R4;
    • an operational amplifier AO1 associated with said resistors R1, R2, R3 and R4 to form a non-inverting summing circuit.


According to another possible feature, the control circuit comprises an operational amplifier AO2 associated with a grounding resistor RS and with a transistor T1, the assembly forming a circuit of the voltage to current converter type.


The present invention also relates to a system for detecting leakages via tracer gas, characterised in that it comprises a mass spectrometer as defined above.





The invention will be better understood, and other aims, details, features and advantages thereof will appear more clearly throughout the following description of a particular embodiment of the invention, given only for illustrative and non-limitative purposes, with reference to the appended drawings, wherein:



FIG. 1, referenced, is a highly schematic representation of a mass spectrometer and of the main functional parts thereof;



FIG. 2, referenced, is a highly schematic representation of an example of a circuit for monitoring the gastightness of an object by means of a tracer gas and of a mass spectrometer according to the invention;



FIG. 3, referenced, is an enlarged schematic representation of the mass spectrometer of FIG. 2;



FIG. 4, referenced, is a schematic representation of a means for adjusting a magnetic field source of the mass spectrometer of FIG. 2.






FIG. 2 is a highly schematic representation of an example of a leakage detection system 100 via tracer gas comprising a mass spectrometer 10 according to the invention. It should be noted that the mass spectrometer 10 comprises the same functional parts as the mass spectrometer 1 of FIG. 1, and thus the identical or similar elements will bear the same references and will not be detailed again.


Said system 100 thus comprises:

    • a test chamber 101 configured to accommodate an object the gas tightness of which is to be tested;
    • a leakage detection device 102 that is connected to the test chamber 101 and comprises the mass spectrometer 10, a main vacuum pump 107 and an auxiliary vacuum pump 109;
    • a gas source 103 connected to the object and configured to fill said object with a tracer gas, such as hydrogen or helium.


The main vacuum pump 107, such as a turbomolecular pump, has an inlet connected to the test chamber 101, but is also connected to the mass spectrometer 10. The auxiliary vacuum pump 109 is, for its part, connected to the outlet of the main vacuum pump 107.


Said system 100 also comprises a plurality of valves 111 and 113:

    • a first valve 111 disposed on the pipe connecting the gas source 103 to the object being tested, which for its part is disposed in the test chamber 101, said valve 111 making it possible to adjust the quantity of tracer gas injected into the object being tested;
    • a second valve 113 disposed on the pipe connecting the test chamber 101 to the main vacuum pump 107.


The main pump 107 generates a high vacuum by means of which the tracer gas, which is input into the test chamber 101 by a leakage of the object tested, is sucked. Subsequently, inside the main pump 107, the tracer gas then flows mainly in the direction of the auxiliary pump 109, but some of the tracer gas moves into the mass spectrometer 10 in order to be analysed therein.


10 The main vacuum pump 107 is for example a turbomolecular pump, a diffusion pump or any other type of molecular pump making it possible to achieve vacuum levels compatible with detecting leakages of the order of at least 10−3 mbar.L/sec.


As illustrated in FIG. 3, the mass spectrometer 10 thus comprises an ionisation means 3, comprising for example an ion source 301 with a cathode 301a and an anode 301b. The ion source 301 is surrounded by a screen in which an opening (or diaphragm) is formed, enabling a beam of ions F to emerge towards an analyser 5.


The analyser 5 is, for its part, configured to select the relevant ions, the sorting taking place in particular by means of a magnetic field {right arrow over (B)}. This is because the analyser 5 comprises in particular a magnetic-field source 501 configured to generate a magnetic field {right arrow over (B)} orthogonal to the plane of the path of the ions (i.e. orthogonal to the plane of FIG. 3, able to curve the path of the ions).


The magnetic-field source 501 is more particularly a source the magnetic field of which depends on the electric current that “supplies” said source.


Thus the magnetic-field source 501 is for example an electromagnet, i.e. a ferromagnetic material on which a winding is disposed, the magnetic field generated being dependent on the electric current circulating in said winding (in particular the direction of circulation and the intensity thereof).


It should be noted that said source 501 could also be a magnetic sector for example.


Thus, in the presence of a magnetic field {right arrow over (B)}, the beam of ions F is diverted. This is because a uniform magnetic field {right arrow over (B)} perpendicular to the plane of the path of the ions, because of the Lorentz force, will give said ions a curved path (the point of impact of the ion, and therefore the deviation thereof, making it possible to know the mass thereof from the charge).


The beam of ions F diverted by the magnetic field {right arrow over (B)} is then oriented towards one or more diaphragms after which a detection means 7 is disposed.


Said detection means 7 comprises for example one or more sensors 703 and/or 705 and an electronic circuit 701 connected to said sensors 703 and 705 to process the electrical signal coming from them.


It should be noted that the mass spectrometer 10 may also include the following elements (not shown), electrostatic lens or lenses for coupling, focusing, collecting, etc., accelerator plates, etc. These elements can be disposed at the ionisation source 3, the analyser 5 or the detection means 7, or between said means 3, 5 and 7.


Thus, when the magnetic field {right arrow over (B)} in the analyser 5 is adjusted so as to exactly address tracer gases having a determined mass M at the middle of at least one diaphragm 501a or 501b (serving as a selection slot), the other gases having the same electrical charge, but having masses different from M, will, in the analyser 4, turn on different radii. The gases with a mass lower than M will turn on a smaller radius, while the gases with a mass greater than M will turn on a larger radius than the one associated with the gas of mass M.


To allow adjustment of the magnetic field {right arrow over (B)}, the mass spectrometer 10 comprises a means 400 for adjusting the magnetic field generated by said source 501, for example by the electromagnet. This means is illustrated more particularly in FIG. 4.


As illustrated on this FIG. 4, said adjustment means 401 is connected to the coil of the electromagnet 501 and is configured to vary the intensity of the current I circulating in said coil.


The adjustment means 401 thus comprises two distinct adjustment commands 401 and 403, a circuit 405 for controlling the current of said electromagnet 501, and a combinatorial circuit 407 for said commands 401 and 403. Said combinatorial circuit 407 is configured to receive said commands 401 and 403 as an input and thus to generate as an output a function F dependent on the values of said commands 401 and 403.


The resulting function F is thus sent to the control circuit 405 so that there is adjustment of the current I according to the values of said commands 401 and 403.


Said commands 401 and 403 are for example digital to analogue converters that deliver, as an input of the combinatorial circuit 407, respectively voltages V1 and V2. It should be noted however that any electrical quantity could be adapted, by means of suitable arrangements.


Said combinatorial circuit 407, for its part, comprises in particular:

    • a plurality of resistors R1, R2, R3 and R4;
    • an operational amplifier AO1 associated with said resistors R1, R2, R3 and R4 to form a non-inverting summing circuit.


Thus, said combinatorial circuit 407 will have at its output a voltage V5 dependent on the input voltage values V1 and V2, and resistors R1, R2, R3 and R4, of the type:







F

(


V
1

,

V
2


)

=


V
S

=




R
4

+

R
3



R
3







R
2



V
1


+


R
1



V
2





R
1

+

R
2











    • By judiciously choosing the value of said resistors R1, R2, R3 and R4, for example by taking R1=R3=R4=R et R2=KR with k a constant greater than 1, and preferably very much greater than 1, the function F is simplified to give:










F

(


V
1

,

V
2


)

=


V
S

=

2


(


V
1

+


V
2

k


)







The two commands V1 and V2 will thus have a different weighting and will therefore influence the value of the output voltage V5 distinctly. It should be noted that the influence of the voltage V2 is K times less than the influence of the voltage V1 on the output voltage V5.


Said control circuit 405 for its part comprises an operational amplifier AO2 associated with a grounding resistor RS and with a transistor T1, the assembly forming a circuit of the voltage to current (or transconductance) converter type. The transistor T1 is for example a bipolar transistor (or of the MOSFET type) the base (or gate) of which is connected to the output of the operational amplifier AO2, the collector (or source) of which is connected to the electromagnet 501, and the emitter (or drain) of which is connected to the resistor RS.


The output voltage V5 coming from the combinatorial circuit 407 is sent to the inverting input of the operational amplifier AO2, while the non-inverting input is connected to the grounding resistor RS and to the emitter of the transistor T1 (more particularly connected to a node located between the emitter of the transistor T1 and the grounding resistor RS).


The output voltage V's coming from the operational amplifier AO2 thus adjusts the value of the current I circulating through the transistor T1, but also through the electromagnet 501. The current I depends on the voltages V1 and V2 of the commands 401 and 403 in accordance with the following formula:






I
=


2

R
S




(


V
1

+


V
2

k


)






The magnetic field {right arrow over (B)} is thus dependent (more particularly proportional for an electromagnet) on the intensity of the current I circulating in the coil of the electromagnet 501, and consequently the field {right arrow over (B)} is here dependent on the commands 401 and 403.


It can also be defined that the current I circulating in the electromagnet 501 in the following manner:






I=I
0
+ΔI


where I0 is a nominal current, dependent on the voltage V1, which generates a nominal magnetic field {right arrow over (B0)}, and where ΔI is a small variation in current around the nominal current I0, dependent on V2, which generates a variation Δ{right arrow over (B)} in the magnetic field around the value of the nominal magnetic field {right arrow over (B0)}.


Thus, one of the adjustment commands 401 makes it possible to establish a nominal magnetic field {right arrow over (B0)}, while the other adjustment command makes it possible to generate a variation in magnetic field Δ{right arrow over (B)} around the value of the nominal magnetic field {right arrow over (B0)}.


It can also be defined that said adjustment means 400 comprises an adjustment command 401 equivalent to a preadjustment (or rough adjustment), while the adjustment command 403 is a fine adjustment.

Claims
  • 1. Mass spectrometer (10) for detecting leakages via a tracer gas, said spectrometer (10) comprising: an ionisation means (3) intended to ionise said tracer gas;at least one magnetic field source (501) generating a magnetic field {right arrow over (B)} dependent on the electric current I supplying said source (501) intended for sorting the ionised elements;a means (7) for detecting said ionised tracer gas;characterised in that said spectrometer comprises a means (400) for adjusting the magnetic field {right arrow over (B)} generated by said source (501), said adjustment means (400) being configured to allow at least two distinct adjustments, said adjustments having different sensitivities.
  • 2. Mass spectrometer according to the preceding claim, characterised in that said adjustment means comprises a pre-adjustment and a fine adjustment.
  • 3. Mass spectrometer according to any one of the preceding claims, characterised in that one of the adjustments makes it possible to establish a nominal magnetic field {right arrow over (B0)}, while the other adjustment makes it possible to generate a variation in magnetic field Δ{right arrow over (B)} around the value of the nominal magnetic field {right arrow over (B0)}.
  • 4. Mass spectrometer according to any one of the preceding claims, characterised in that said magnetic-field source (501) comprises an electromagnet.
  • 5. Mass spectrometer according to any one of the preceding claims, characterised in that said adjustment means comprises at least two adjustment commands (401 and 403), a combinatorial circuit (407) configured to combine the values of said at least two commands (401 and 403), and a circuit (405) for controlling the current I circulating in said magnetic field source (501).
  • 6. Mass spectrometer according to the preceding claim, characterised in that said at least two adjustment commands are electrical quantities V1 et V2, such as voltages.
  • 7. Mass spectrometer according to the preceding claim, characterised in that the magnetic field {right arrow over (B)} depends on the values of the electrical quantities V1 and V2 of said at least two adjustment commands.
  • 8. Mass spectrometer according to claim 5, characterised in that the combinatorial circuit (407) comprises: a plurality of resistors R1, R2, R3 and R4;an operational amplifier AO1 associated with said resistors R1, R2, R3 and R4 to form a non-inverting summing circuit.
  • 9. Mass spectrometer according to claim 5, characterised in that the control circuit (405) comprises an operational amplifier AO2 associated with a grounding resistor (RS) and with a transistor (T1), the assembly forming a circuit of the voltage to current converter type.
  • 10. Mass spectrometer according to any one of the preceding claims, characterised in that it comprises N adjustment commands and/or N magnetic field sources, where N is an integer greater than or equal to 3.
  • 11. System for detecting leakages via tracer gas, characterised in that it comprises a mass spectrometer (10) according to any one of the preceding claims.
Priority Claims (1)
Number Date Country Kind
2102968 Mar 2021 FR national
PCT Information
Filing Document Filing Date Country Kind
PCT/EP2022/056452 3/14/2022 WO