Patent Grant
8563920
The present invention relates to a mass spectrometer. More precisely, it relates to an ion transport optical system for transporting an ion into the subsequent stage under a relatively high gas pressure.
A well-known mass-analyzing method for identifying a substance having a large molecular weight and for analyzing its structure is an MS/MS analysis (or tandem analysis).
In this MS/MS mass spectrometer, three-stage quadrupole electrodes 12, 13, and 15 each composed of four rod electrodes are provided, inside the analysis chamber 10 which is vacuum-evacuated, between an ion source 11 for ionizing a sample to be analyzed and a detector 16 for detecting an ion and providing a detection signal in accordance with the amount of ions. A voltage ±(U1+V1·cos ωt) is applied to the first-stage quadrupole electrodes 12, in which a direct current U1 and a radio-frequency voltage V1·cos ωt are synthesized. Due to the action of the electric field generated by this application, only a target ion having a specific mass-to-charge ratio m/z is selected as a precursor ion from among a variety of ions generated in the ion source 11 and passes through the first-stage quadrupole electrodes 12.
The second-stage quadrupole electrodes 13 are placed in the well-sealed collision cell 14, and Ar gas for example as a CID gas is introduced into the collision cell 14. The precursor ion sent into the second-stage quadrupole electrodes 13 from the first-stage quadrupole electrodes 12 collides with Ar gas inside the collision cell 14 and is dissociated by the collision-induced dissociation to produce a product ion. Since this dissociation has a variety of modes, two or more kinds of product ions with different mass-to-charge ratios are generally produced from one kind of precursor ion, and these product ions exit from the collision cell 14 and are introduced into the third-stage quadrupole electrodes 15. Since not every precursor ion is dissociated, some non-dissociated precursor ions may be directly sent into the third-stage quadrupole electrodes 15.
To the third-stage quadrupole electrodes 15, a voltage ±(U3+V3·cos ωt) is applied in which a direct current U3 and a radio-frequency voltage V3·cos ωt are synthesized. Due to the action of the electric field generated by this application, only a product ion having a specific mass-to-charge ratio is selected, passes through the third-stage quadrupole electrodes 15, and reaches the detector 16. The direct current voltage U3 and radio-frequency voltage V3·cos ωt which are applied to the third-stage quadrupole electrodes 15 are appropriately changed, so that the mass-to-charge ratio of an ion capable of passing the third-stage quadrupole electrodes 15 is scanned to obtain the mass spectrum of the product ions generated by the dissociation of the target ion.
In a general MS/MS mass spectrometer, the length of the collision cell 14 in the direction along the ion optical axis C which is the central axis of the ion stream is approximately 150 through 200 mm. The gas pressure in the collision cell 14 is a few mTorr and higher than that of the analysis chamber 10 surrounding the collision cell 14. When an ion proceeds in a radio-frequency electric field in the atmosphere of comparatively high gas pressure, the kinetic energy of the ion attenuates due to a collision with the gas, so that the ion decelerates. In an extreme case, a decelerated ion could stop in the radio-frequency electric field.
In the case where an MS/MS mass spectrometer as previously described is used as a detector of a chromatograph such as a liquid chromatograph for example, it is necessary to repeatedly perform an analysis at predetermined intervals of time. Hence, if the ion's time delay is significant due to the speed reduction, an ion which should normally pass through the third-stage quadrupole electrodes 15 might not be able to pass through it, which causes a degradation in the detection sensitivity. In addition, an ion remaining in the collision cell 14 may appear at a timing at which no ion should appear in reality, which causes a ghost peak. Moreover, since it takes time for an ion to reach the detector 16, the time interval of the repeated analysis is required to be previously determined in view of such a situation, which might cause an omission of analysis information in a multi-component analysis.
One conventional and general method for avoiding the previously described various problems is to form a direct current electric field having a potential gradient in the ion's passage direction in the collision cell 14, so that an ion should be accelerated by the action of the direct current electric field. In the mass spectrometer described in Patent Document 2, an electric field having a potential gradient in the direction of the ion optical axis is formed in order to accelerate an ion by the application of a direct current voltage to a radio-frequency ion guide in which each rod electrode has a different tilt to the ion optical axis, or by the application of a direct current voltage to each rod divided in the direction of the ion optical axis. In the mass spectrometer described in Patent Document 3, an ion that is allowed to pass through is accelerated by sequentially applying a pulse voltage to each aperture electrode of a radio-frequency ion guide in which approximately one hundred aperture plates are arranged in the direction of the ion optical axis.
However, if each rod electrode of a radio-frequency ion guide is obliquely disposed at different angles from each other or if an auxiliary electrode is used in order to form a direct current electric field having a potential gradient in the direction of the ion optical axis, a turbulence might occur in the radio frequency electric field appropriate for converging ions, which might deteriorate the ion passing properties. In addition, the configuration of Patent Document 3 has a complex structure, and simultaneously requires a complicated control since a pulse voltage for accelerating an ion should be appropriately controlled in accordance with each mass-to-charge ratio.
In the case where an atmospheric pressure ionization interface is used as in a liquid chromatograph mass spectrometer, a multi-stage differential evacuation system is used for maintaining a high vacuum atmosphere within an analysis chamber, which includes a mass separator and detector. In this case, the gas pressure inside the intermediate vacuum chamber in the subsequent stage of an ionization chamber is relatively high due do the atmosphere flowing from the ionization chamber, which causes the same problem as inside the collision cell as described earlier.
The present invention has been achieved to solve the aforementioned problems, and the main objective thereof is to provide a mass spectrometer capable of effectively preventing the delay or stagnation of ions with a relatively simple structure in a radio-frequency ion guide which is used under a relatively high gas pressure.
To solve the previously-described problem, the present invention provides a mass spectrometer having an ion guide for converging ions by a radio-frequency electric field under a gas pressure of a few mTorr or higher than that and simultaneously transporting the ions into a subsequent stage, wherein the ion guide forms a gradient of a magnitude or depth of a pseudopotential by the radio-frequency electric field along an ion's traveling direction, and an ion is accelerated in the traveling direction in accordance with the gradient.
In the mass spectrometer according to the present invention, the ion guide may be specifically disposed in the following portion for example: the inside of the collision cell into which a collision induced dissociation gas is provided for dissociating ions, or the inside of an intermediate vacuum chamber provided as the first stage of a plurality of intermediate vacuum chambers which comprise a multiple-stage differential evacuation system between an ionization chamber for ionizing a target component under an approximate atmospheric pressure and a mass analysis chamber in which a high vacuum atmosphere is maintained.
In such portions, due to a relatively high gas pressure, ions have more chances to collide with a gas and are particularly likely to decelerate. On the other hand, in the mass spectrometer according to the present invention, the magnitude or depth of the pseudopotential in the ion guide has a monotonic downward gradient along the ion's traveling direction, that is, a falling gradient in which the pseudopotential may maintain the same level at some portions but will never increase at any point. Due to this effect, an ion is given a kinetic energy toward the traveling direction. Accordingly, even if an ion collides with a gas and is thereby decelerated, it is accelerated once again. Therefore, it is possible to moderate the ion's delay in the ion guide, and also prevent an ion from stopping along the way.
The pseudopotential by a radio-frequency electric field is dependent on a parameter such as the radius of the inscribed circle of the ion guide, the number of poles of the ion guide, and the amplitude and frequency of the radio-frequency voltage applied to the ion guide. Hence, any of such parameters may be changed along the direction of the ion optical axis in order to form the pseudopotential's gradient as previously described.
As an embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of a plurality of linearly-extending rod electrodes surrounding an ion optical axis, and each rod electrode may be disposed at a tilt in such a manner that the distance from the ion optical axis increases toward the ion's traveling direction. That is, in this embodiment, the radius of the inscribed circle of the ion guide is increased along the direction of the ion optical axis.
With this configuration, the circuit of the electric system is kept from becoming complicated since it is not necessary to prepare a variety of radio-frequency voltages which have a different amplitude and frequency, for the voltage (i.e. a radio-frequency voltage or a voltage in which a radio-frequency voltage and direct current bias voltage are superimposed) applied to each rod electrode. In addition, all the rod electrodes are simply tilted in a rotationally-symmetrical manner with respect to the ion optical axis and as before, a linearly elongated cylinder (or tube) can be used as the rod electrode itself. Therefore, the structure of the electrode and the structure for holding the electrode are simple.
As another embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of rod electrodes surrounding the ion optical axis, and each rod electrode may have a tilted portion such that the radius of the inscribed circle of the rod electrodes increases toward the ion's traveling direction. In this embodiment, the tilted portion may be either a linear one or curved one.
Also in the case where the ion guide is composed of not a plurality of rod electrodes surrounding the ion optical axis but a plurality of plate electrodes arranged at predetermined intervals in the direction of the ion optical axis, the radius of the inscribed circle can be practically changed. That is, as another embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of a plurality of plate electrodes arranged in the direction of the ion optical axis, and each plate electrode may have a circular opening whose radius centering on the ion optical axis increases toward the ion's traveling direction.
As another embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of a plurality of virtual rod electrodes surrounding the ion optical axis, each virtual rod electrode may be composed of a plurality of short segmented rod electrodes separated in the direction of the ion optical axis, and the plurality of segmented rod electrodes belonging to the same virtual rod electrode may be disposed in such a manner that the distance from the ion optical axis increases toward the ion's traveling direction.
In addition, as another embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of a plurality of virtual rod electrodes surrounding the ion optical axis, each virtual rod electrode may be composed of a plurality of short segmented rod electrodes separated in the direction of the ion optical axis, and a radio-frequency voltage whose amplitude or frequency is different may be applied to the plurality of segmented rod electrodes belonging to the same virtual rod electrode. That is, with this configuration, the radio-frequency electric field's amplitude or frequency is changed in the ion's passage direction in order to form the gradient of the magnitude or depth of the pseudopotential.
Furthermore, as another embodiment of the mass spectrometer according to the present invention, the ion guide may be composed of a plurality of virtual rod electrodes surrounding the ion optical axis, each virtual rod electrode may be composed of a plurality of short segmented rod electrodes separated in the direction of the ion optical axis, and the plurality of segmented rod electrodes belonging to the same virtual rod electrode may have a different cross-sectional shape. With the change of the segmented rod electrodes' cross-sectional shape, the pseudopotential terms of the different number of poles are superimposed. Hence, the shape of the pseudopotential well changes in the ion's passage direction.
With the mass spectrometer according to the present invention, even in the case where an ion comes in contact with a collision induced dissociation gas inside the collision cell and the kinetic energy is decreased for example, the precursor ion and the product ions generated by a dissociation are assisted in their progress, which can prevent the ions' substantial delay inside the collision cell. Consequently, the amount of the target ions to be selected in the mass separator in the subsequent stage is increased, which improves the detection sensitivity. Simultaneously, the appearance of a ghost peak on the mass spectrum can also be prevented since an ion's stagnation inside the collision cell and intermediate vacuum chamber can be prevented.
a) is a front end elevational view of a radio-frequency ion guide according to another embodiment (the fifth embodiment), and
An MS/MS mass spectrometer which is an embodiment (the first embodiment) of the present invention will be described with reference to the figures.
In the MS/MS mass spectrometer of the present embodiment, as in the conventional configuration, a collision cell 14 is provided between the first-stage quadrupole electrodes 12 and the third-stage quadrupole electrodes 15 in order to generate a variety of product ions by dissociating a precursor ion. This collision cell 14 is an almost hermetically-closed structure except for an ion injection aperture 14a and ion exit aperture 14b: for example, a structure whose surrounding face is an approximately cylindrical form and both end faces are almost closed. Inside the collision cell, a radio-frequency ion guide 20 is provided in which eight cylindrically-shaped rod electrodes are placed in such a manner as to surround an ion optical axis C.
Under the control of a controller 30, a voltage of ±(U1+V1·cos ωt)+Vbias1 is applied to the first-stage quadrupole electrodes 12 from the RF (radio-frequency) +DC (direct current voltage for mass separation) +Bias (bias direct current voltage) voltage generator 31, in which a predetermined direct current bias voltage Vbias1 is further added to a voltage of ±(U1+V1·cos ωt) in which a direct current voltage U1 and a radio-frequency voltage V1·cos ωt are superimposed. A voltage of ±(U3+V3·cos ωt)+Vbias3 is applied to the third-stage quadrupole electrodes 15 from another RF+DC+Bias voltage generator 33, in which a predetermined direct current bias voltage Vbias3 is further added to a voltage of ±(U3+V3·cos ωt) in which a direct current voltage U3 and a radio-frequency voltage V3·cos ωt are superimposed. This is a conventional method.
A voltage of VBias+VRF in which a direct current bias voltage VBias and a radio-frequency voltage VRF (=V·cos Ωt) are superimposed or a voltage of VBias−VRF in which the same direct current bias voltage VBias and a radio-frequency voltage having a reversed polarity to the radio-frequency voltage VRF is applied to the eight rod electrodes which compose the ion guide 20. A detailed explanation will be made later.
In such a configuration, it is known that the pseudopotential Vp(R), which is formed in the space surrounded by the radio-frequency ion guide 20, at the position (the distance from the ion optical axis C in the radial direction) R is expressed by the following equation (1):
Vp(R)={q2n2/(4mΩ2)}·(V/r)2·(R/r)2(n−1) (1)
where, r is the radius of the inscribed circle of the ion guide, Ω is the frequency of the radio-frequency voltage, V is the amplitude of the radio-frequency voltage, n is the number of poles of the ion guide, m is the mass of the ion, and q is the electric charge. That is, it is understood that any one of the ion guide's inscribed circle's radius r, radio-frequency voltage's frequency Ω or amplitude V, and the number of poles of the ion guide n may be changed along the direction of the ion optical axis so that the pseudopotential Vp(R) should be changed along the ion optical axis. In the case where the magnitude or depth of the pseudopotential has a gradient, an ion having a charge is accelerated or decelerated in accordance with the gradient. Hence, if the gradient is appropriately formed, an ion can be accelerated while passing through the radio-frequency ion guide.
In the configuration of the first embodiment, as illustrated in
For the eight rod electrodes 21 through 28, four alternate electrodes in the circumferential direction centering on the ion optical axis C are considered to be a single group. A voltage of VBias+VRF is applied to the four rod electrodes 21, 23, 25, and 27, which belong to one group, from an RF+Bias voltage generator 32, and a voltage of VBias−VRF is applied to the four rod electrodes 22, 24, 26, and 28, which belong to the other group, from the same RF+Bias voltage generator 32. The application of the radio-frequency voltage VRF forms a radio-frequency electric field in the space surrounded by the eight rod electrodes 21 through 28. Since each of the rod electrodes 21 through 28 is placed at a tilt as previously described, the gradient of the depth of the pseudopotential is formed in the ion's traveling direction.
In the collision cell 14, a radio-frequency electric field is formed by the radio-frequency ion guide 20 as previously described, and ions are captured by the action of this radio-frequency electric field. A precursor ion collides with a CID gas, and due to the collision energy, the bond of the precursor ion is cut to be dissociated. Since there are generally many types of dissociation, the product ions generated from one species by a dissociation is not always limited to one species. Although a portion of the kinetic energy that a precursor ion originally has possessed is lost due to a collision with the CID gas, a kinetic energy is given by the gradient of the depth of the pseudopotential formed in the internal space of the radio-frequency ion guide 20 as previously described. Consequently, a precursor ion and product ion which have lost some kinetic energy due to a collision with the CID gas are accelerated once again, smoothly progress toward the ion exit aperture 14b without stagnating in the collision cell 14, and are expelled from the collision cell 14 via the ion exit aperture 14b.
As just described, with the MS/MS mass spectrometer according to the present invention, it is possible to prevent the delay and stagnation of ions in the collision cell 14 by using the gradient of the magnitude or depth of the pseudopotential formed in the radio-frequency ion guide 20. Consequently, the product ions originating from the precursor ion to be targeted are introduced into the third-stage quadrupole electrodes 15 without a significant delay and then mass separated. Accordingly, many product ions can be sent into the detector 16, which ensures a high detection sensitivity. In addition, since ions do not stagnate in the collision cell 14, the generation of a ghost peak in a mass spectrum can also be prevented.
The inventors of the present invention have experimentally confirmed the previously described effect of the pseudopotential. The experiment will now be explained. In this experiment, the speed of the expelled ions has been measured for the following three configurations as experimental objects: the configuration of the present embodiment as illustrated in
Next, the radio-frequency ion guides in other embodiments having the same effect as the radio-frequency ion guide 20 adopted in the MS/MS mass spectrometer according to the first embodiment will be described with reference to
The radio-frequency ion guide 40 illustrated in
The radio-frequency ion guide 50 illustrated in
The radio-frequency ion guide 60 illustrated in
The ion guide 70 illustrated in
In the case where the segmented rod electrodes have different cross-sectional shapes, to be more precise, where some have a cross-sectional shape other than a circle, pseudopotential terms of poles other than the n poles are superimposed in the equation (1), which changes the pseudopotential's shape. Accordingly, a substantial gradient is formed in the magnitude or depth of the pseudopotential, which brings about the same effect as the first embodiment.
In the radio-frequency ion guide 80 illustrated in
In the radio-frequency ion guide 90 illustrated in
In the aforementioned examples, the radio-frequency ion guide which is characteristic of the present invention is provided in the collision cell. In the same manner, the radio-frequency ion guide may be provided in the portion where ions need to be converged under a relatively high gas pressure and transported to the subsequent stage.
In particular, an LC/MS or other apparatuses often adopt a multiple-stage differential evacuation system in which a plurality of intermediate vacuum chambers are disposed between the atmospheric pressure ionization interface such as an electrospray ionization interface and the analysis chamber containing a mass separator and detector in a high vacuum atmosphere. In this case, inside the intermediate vacuum chamber that immediately follows the atmospheric pressure ionization interface, the gas pressure is relatively high due to the air flowing in from the atmospheric pressure ionization interface, and an ion is likely to be decelerated due to the effect of the air. Therefore, the provision of the radio-frequency ion guide as previously described in such an intermediate vacuum chamber to increase the ion's passage efficiency increases the ion's detection sensitivity.
It should be noted that every embodiment described thus far is merely an embodiment of the present invention, and that any modification, addition or correction appropriately made within the spirit of the present invention will be included in the scope of the claims of the present application.
This is a Continuation Application of application Ser. No. 12/440,324, filed Mar. 6, 2009, which is a National Stage entry of PCT/JP2007/001438 filed Dec. 20, 2007, the disclosure of which is hereby incorporated by reference in its entirety.
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| Number | Date | Country | |
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| Number | Date | Country | |
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| Parent | 12440324 | US | |
| Child | 13159974 | US |
