Mass spectrometry device
View Patent ↗With regard to an object of the invention, in a tandem type mass spectrometry system including three stages of a QMS, sensitivity of a daughter ion decreases due to loss resulting from destabilization of the daughter ion or a decrease in daughter ion generation rate, and an improvement insensitivity of the daughter ion is a significant issue. To solve the above-mentioned problem, the invention provides a mass spectrometry system having means of decreasing a q value of a parent ion and not decreasing a fundamental vibration frequency of the parent ion. According to the means of the invention, the invention may have effects that a mass number range of a daughter ion that may be stably transmitted is expanded, the number of vibrations of a parent ion is substantially the same as that in a first stage of the QMS, and generation efficiency of the daughter ion does not decrease and can be maintained.
1. A mass spectrometry device, comprising:
a mass spectrometer unit which includes at least four rod-like electrodes, applies a direct current voltage U and a high frequency voltage V cos Ωt to the rod-like electrodes to generate a multi-pole field greater than or equal to a quadrupole field of a high frequency between the rod-like electrodes, and mass-selects/separates an ion species having a specific mass-to-charge ratio m/z; and
a detector which detects an ion passing through the mass spectrometer unit,
wherein at least two or more stages of the mass spectrometer unit are coaxially provided in series, and
the voltages applied to the rod-like electrodes are controlled and a half value r 0 of a distance between the rod-like electrodes of the mass spectrometer unit is changed in a first stage of the mass spectrometer unit and a second stage of the mass spectrometer unit such that a fundamental vibration frequency of a certain ion species is substantially the same between the first stage and the second stage.
2. The mass spectrometry device according to claim 1 , wherein at least three stages of the mass spectrometer unit are included, an ion species having a certain mass-to-charge ratio is passed in a first stage of the mass spectrometer unit, a dissociated ion is generated by collision induced dissociation with respect to a certain ion passing through the first stage in a second stage of the mass spectrometer unit, and the dissociated ion is mass-analyzed in a third stage of the mass spectrometer unit.
3. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes are controlled and the distance between the rod-like electrodes of the mass spectrometer unit is changed in the first stage of the mass spectrometer unit and the second stage of the mass spectrometer unit such that a value of V/(r 0 2 Ω) is substantially the same between the first stage and the second stage.
4. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes of the mass spectrometer unit are controlled in the first stage of the mass spectrometer unit and the second stage of the mass spectrometer unit such that a value of a ratio V/Ω) of an amplitude value V of the high frequency voltage to an angular vibration frequency Ω of the high frequency voltage is substantially the same between the first stage and the second stage.
5. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes are controlled and the distance between the rod-like electrode of the mass spectrometer unit is changed such that a value of V/(r 0 2 Ω 2 ) in the second stage of the mass spectrometer unit is smaller than a value of V/(r 0 2 Ω 2 ) in the first stage of the mass spectrometer unit by γ times with respect to the high frequency voltage V cos Ωt applied to the rod-like electrodes and the half value r 0 of the distance between the rod-like electrodes.
6. The mass spectrometry device according to claim 5 , wherein an optimum γ value from which an optimum analysis result is obtained is automatically derived by assigning the γ value within a certain range.
7. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes are controlled and a distance between the rod-like electrode of the mass spectrometer unit is changed such that a value of V/(r 0 2 Ω 2 ) in the second stage of the mass spectrometer unit is larger than a value of V/(r 0 2 Ω 2 ) in the first stage of the mass spectrometer unit by γ times with respect to the high frequency voltage V cos Ωt applied to the rod-like electrodes and the half value r 0 of the distance between the rod-like electrodes.
8. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes of the mass spectrometer unit are controlled such that a value Ω in the second stage of the mass spectrometer unit is larger than a value Ω in the first stage of the mass spectrometer unit by γ times with respect to the high frequency voltage V cos Ωt applied to the rod-like electrodes.
9. The mass spectrometry device according to claim 1 , wherein the voltages applied to the rod-like electrodes of the mass spectrometer unit are controlled such that a value Ω in the second stage of the mass spectrometer unit is smaller than a value Ω in the first stage of the mass spectrometer unit by γ times with respect to the high frequency voltage V cos Ωt applied to the rod-like electrodes.
10. A mass spectrometry device, comprising:
a mass spectrometer unit which includes at least four rod-like electrodes, applies a direct current voltage U and a high frequency voltage V cos Ωt to the rod-like electrodes to generate a multi-pole field greater than or equal to a quadrupole field of a high frequency between the rod-like electrodes, and mass-selects/separates an ion species having a specific mass-to-charge ratio m/z; and
a detector which detects an ion passing through the mass spectrometer unit,
wherein at least two or more stages of the mass spectrometer unit are coaxially provided in series, and
a stability parameter of a first stage of the mass spectrometer unit is set to be γ times (γ>1) a stability parameter of a second stage of the mass spectrometer unit, and an angular vibration frequency Ω 1 of the first stage of the mass spectrometer unit and an angular vibration frequency Ω 2 of the second stage of the mass spectrometer unit are set to satisfy a following relation:
Ω 2 =Ω 1 ·γ′, 1<γ′≤γ,
(stability parameter)=4eZV/Ω 2 mr 0 2 , where r 0 denotes a half value of a distance between rod-like electrodes facing each other, e denotes an elementary charge, V denotes an amplitude of a high frequency voltage, and Ω denotes an angular vibration frequency.
11. The mass spectrometry device according to claim 10 , wherein the stability parameter is set by changing the distance between the rod-like electrodes.
12. The mass spectrometry device according to claim 10 , wherein the stability parameter is set by controlling voltages applied to the rod-like electrodes.