The invention relates in general to mass analysis, and more particularly relates to a method of mass analysis in a two-dimensional substantially quadrupole field with added higher multipole harmonics.
The use of quadrupole electrode systems in mass spectrometers is known. For example, U.S. Pat. No. 2,939,952 (Paul et al.) (hereinafter “reference [1]”) describes a quadrupole electrode system in which four rods surround and extend parallel to a quadrupole axis. Opposite rods are coupled together and brought out to one of two common terminals. Most commonly, an electric potential V(t)=+(U−Vrf cos Ωt) is then applied between one of these terminals and ground and an electric potential V(t)=−(U−Vrf cos Ωt)is applied between the other terminal and ground. In these formulae, U is a DC voltage, pole to ground, Vrf is a zero to peak AC voltage, pole to ground, Ω is the angular frequency of the AC, and t is time. The AC component will normally be in the radio frequency (RF) range, typically about 1 MHz.
In constructing a linear quadrupole, the field may be distorted so that it is not an ideal quadrupole field. For example round rods are often used to approximate the ideal hyperbolic shaped rods required to produce a perfect quadrupole field. The calculation of the potential in a quadrupole system with round rods can be performed by the method of equivalent charges—see, for example, Douglas, D. J.; Glebova, T.; Konenkov, N.; Sudakov, M. Y. “Spatial Harmonics of the Field in a Quadrupole Mass Filter with Circular Electrodes”, Technical Physics, 1999, 44, 1215-1219 (hereinafter “reference [2]”). When presented as a series of harmonic amplitudes A0, A1, A2 . . . An, the potential in a linear quadrupole can be expressed as follows:
Field harmonics φN, which describe the variation of the potential in the X and Y directions, can be expressed as follows:
where Real [(f(x+iy)] is the real part of the complex function f(x+iy). For example:
In these definitions, the X direction corresponds to the direction toward an electrode in which the potential AN increases to become more positive when V(t) is positive.
As shown above, A0 φ0 is the constant potential component of the field (i.e. independent of X and Y), A1 φ1 is the dipole potential, A2 φ2 is the quadrupole component of the field, A3 φ3 is the hexapole component of the field, A4 φ4 is the octopole component of the field, and there are still higher order components of the field, although in a practical quadrupole the amplitudes of the higher order components are typically small compared to the amplitude of the quadrupole term.
In a quadrupole mass filter, ions are injected into the field along the axis of the quadrupole. In general, the field imparts complex trajectories to these ions, which trajectories can be described as either stable or unstable. For a trajectory to be stable, the amplitude of the ion motion in the planes normal to the axis of the quadrupole must remain less than the distance from the axis to the rods (r0). Ions with stable trajectories will travel along the axis of the quadrupole electrode system and may be transmitted from the quadrupole to another processing stage or to a detection device. Ions with unstable trajectories will collide with a rod of the quadrupole electrode system and will not be transmitted.
The motion of a particular ion is controlled by the Mathieu parameters a and q of the mass analyzer. For positive ions, these parameters are related to the characteristics of the potential applied from terminals to ground as follows:
where e is the charge on an ion, mion is the ion mass, Ω=2πf where f is the AC frequency, U is the DC voltage from pole to ground and Vrf is the zero to peak AC voltage from each pole to ground. If the potentials are applied with different voltages between pole pairs and ground, then in equation (7) U and V are ½ of the DC potential and the zero to peak AC potential respectively between the rod pairs. Combinations of a and q which give stable ion motion in both the X and Y directions are usually shown on a stability diagram.
With operation as a mass filter, the pressure in the quadrupole is kept relatively low in order to prevent loss of ions by scattering by the background gas. Typically the pressure is less than 5×10−4 torr and preferably less than 5×10−5 torr. More generally quadrupole mass filters are usually operated in the pressure range 1×10−6 torr to 5×10−4 torr. Lower pressures can be used, but the reduction in scattering losses below 1×10−6 torr are usually negligible.
As well, when linear quadrupoles are operated as a mass filter the DC and AC voltages (U and V) are adjusted to place ions of one particular mass to charge ratio just within the tip of a stability region. Normally, ions are continuously introduced at the entrance end of the quadrupole and are continuously detected at the exit end. Ions are not normally confined within the quadrupole by stopping potentials at the entrance and exit. An exception to this is shown in the papers Ma'an H. Amad and R. S. Houk, “High Resolution Mass Spectrometry With a Multiple Pass Quadrupole Mass Analyzer”, Analytical Chemistry, 1998, Vol. 70, 4885-4889 (hereinafter “reference [3]”), and Ma'an H. Amad and R. S. Houk, “Mass Resolution of 11,000 to 22,000 With a Multiple Pass Quadrupole Mass Analyzer”, Journal of the American Society for Mass Spectrometry, 2000, Vol. 11, 407-415 (hereinafter “reference [4]”). These papers describe experiments where ions were reflected from electrodes at the entrance and exit of the quadrupole to give multiple passes through the quadrupole to improve the resolution. Nevertheless, the quadrupole was still operated at low pressure, although this pressure is not stated in these papers, and with the DC and AC voltages adjusted to place the ions of interest at the tip of the first stability region.
In accordance with an aspect of an embodiment of the invention, there is provided a method of processing ions in a quadrupole rod set, the method comprising
In various embodiments, the magnitude of Am is i) greater than 1% and is less than 20% of the magnitude of A2; and, ii) greater than 1% and is less than 10% of the magnitude of A2.
These and other features of the applicant's teachings are set forth herein.
The skilled person in the art will understand that the drawings, described below, are for illustration purposes only. The drawings are not intended to limit the scope of the applicant's teachings in anyway.
a-f illustrate the effect of changing q′ for a rod set with round rods and 8% hexapole (A1=0, A4≈0).
a shows the uppermost stability island calculated for the round rod set of
b shows the stability boundaries and island of stability for a quadrupole constructed with round rods with X rods of different diameter than the Y rods to make the octopole component substantially equal to zero.
Referring to
As described above, the motion of a particular ion is controlled by the Mathieu parameters a and q of the mass analyzer. These parameters are related to the characteristics of the potential applied from terminals 22 and 24 to ground as follows:
where e is the charge on an ion, mion is the ion mass, Ω=2πf where f is the AC frequency, U is the DC voltage from a pole to ground and Vrf is the zero to peak AC voltage from each pole to ground. Combinations of a and q which give stable ion motion in both the X and Y directions are shown on the stability diagram of
Ion motion in a direction u in a quadrupole field can be described by the equation
and t is time, C2n depend on the values of a and q, and A and B depend on the ion initial position and velocity (see, for example, R. E. March and R. J. Hughes, “Quadrupole Storage Mass Spectrometry”, John Wiley and Sons, Toronto, 1989, page 41 (hereinafter “reference [6]”). The value of β determines the frequencies of ion oscillation, and β is a function of the a and q values (see page 70 of reference [5]). From equation 8, the angular frequencies of ion motion in the X (ωx) and Y (ωy) directions in a two-dimensional quadrupole field are given by
where n=0, ±1, ±2, ±3 . . . , 0≦βx≦1, 0≦βy≦1, in the first stability region and βx and βy are determined by the Mathieu parameters a and q for motion in the X and Y directions respectively (equation 7).
As described in U.S. Pat. No. 6,897,438 (Soudakov et al.); U.S. Patent Publication No. 2005/0067564 (Douglas et al.); and U.S. Patent Publication No. 2004/0108456 (Sudakov et al.) two-dimensional quadrupole fields used in mass spectrometers can be improved at least for some applications by adding higher order harmonics such as hexapole or octopole harmonics to the field. As described in these references, the hexapole and octopole components added to these fields will typically substantially exceed any octopole or hexapole components resulting from manufacturing or construction errors, which are typically well under 0.1%. For example, a hexapole component A3 can typically be in the range of 1 to 6% of A2, and may be as high as 20% of A2 or even higher. Octopole components A4 of similar magnitude may also be added.
As described in U.S. Patent Publication No. 2005/0067564, the contents of which are hereby incorporated by reference, a hexapole field can be provided to a two-dimensional substantially quadrupole field by providing suitably shaped electrodes or by constructing a quadrupole system in which the two-Y rods have been rotated in opposite directions to be closer to one of the X rods than to the other of the X rods. Similarly, as described in U.S. Pat. No. 6,897,438, the contents of which are hereby incorporated by reference, an octopole field can be provided by suitably shaped electrodes, or by constructing the quadrupole system to have a 90° asymmetry, by, for example, making the Y rods larger in diameter than the X rods.
It is also possible, as described in U.S. Patent Publication No. 2005/0067564 to simultaneously add both hexapole and octopole components by both rotating one pair of rods towards the other pair of rods, while simultaneously changing the diameter of one pair of rods relative to the other pair of rods. This can be done in two ways. The larger rods can be rotated toward one of the smaller rods, or the smaller rods can be rotated toward one of the larger rods.
Referring to
When round rods are used to add a hexapole or octopole harmonic to a two-dimensional substantially quadrupole field, the resolution, transmission and peak shape obtained in mass analysis may be degraded. Nonetheless, the addition of hexapole and octopole components to the field, and possibly other higher order multipoles, remains desirable for enhancing fragmentation and otherwise increasing MS/MS efficiency, as well as peak shape and ion excitation for MS/MS or for ion ejection. However, in some instruments, it is important that a linear quadrupole trap that is used for MS/MS also be capable of being operated as a mass filter. This can be made possible by adding an auxiliary quadrupole excitation to form islands of stability in the conventional stability diagram.
Islands of Stability
When an auxiliary quadrupole excitation waveform is applied to a quadrupole, ions that have oscillation frequencies that are resonant with the excitation are ejected from the quadrupole. Unstable regions corresponding to iso-β lines are formed in the stability diagram. The formation of such lines by auxiliary quadrupole excitation is described in Miseki, K. “Quadrupole Mass Spectrometer”, U.S. Pat. No. 5,227,629, Jul. 13, 1993 (hereinafter “reference [7]”), Devant, G.; Fercocq, P.; Lepetit, G.; Maulat, O. “Patent No. Fr. 2,620,568” (hereinafter “reference [8]”), Konenkov, N. V.; Cousins, L. M.; Baranov, V. I.; Sudakov, M. Yu. “Quadrupole Mass Filter Operation with Auxiliary Quadrupole Excitation: Theory and Experiment”, Int. J. Mass Spectrom. 2001, 208, 17-27 (hereinafter “reference [9]”), Baranov, V. I.; Konenkov, N. V.; Tanner, S. D.; “QMF Operation with Quadrupole Excitation”, in Plasma Source Mass Spectrometry in the New Millennium; Holland G; Tanner, S. D., Eds.; Royal Society of Chemistry: Cambridge, 2001; 63-72 (hereinafter “reference [10]”), and Konenkov, N. V.; Sudakov, M. Yu.; Douglas D. J. “Matrix Methods for the Calculation of Stability Diagrams in Quadrupole Mass Spectrometry”, J. Am. Soc. Mass Spectrom. 2002, 13, 597-613 (hereinafter “reference [11]”), and by modulation of the rf, dc or rf and dc voltages described in Konenkov, N. V.; Korolkov, A. N.; Machmudov, M. “Upper Stability Island of the Quadrupole Mass Filter with Amplitude Modulation of the Applied Voltage”, J. Am. Soc. Mass Spectrom. 2005, 16, 379-387 (hereinafter “reference [12]”). With quadrupole excitation at a frequency ωx=(N/M)Ω, where N and M are integers, bands of instability are formed on the stability diagram, and the diagram splits or changes into islands of stability (see, for example,
Mass Analysis with Cuadrupoles with Added Hexapole or Octopole Fields Using Islands of Stability
Computer simulations have been done to evaluate the performance of quadrupole mass filters with added hexapole fields when operated at the upper and lower tips of the uppermost stability island (that is, the island having the highest magnitude values of the Mathieu parameter a formed with quadrupole excitation. This has been done to compare mass filters that have (i) ideal quadrupole fields, (ii) quadrupole fields with an added hexapole field but no higher multipoles (A2 and A3 only), (iii) quadrupoles constructed with round rods with radii Rx≠Ry so that A4≈0 and operated so that the dipole term is zero, and (iv) quadrupoles constructed with round rods of equal diameter so that A4≠0 but operated so that the dipole amplitude A1=0. Simulations have also been done for quadrupoles that have added octopole fields, constructed with the Y rods greater in diameter than the X rods.
Definitions of Variables
Calculation Methods
In general, as described above a two dimensional time-dependent electric potential can be expanded in multipoles as
where AN is the dimensionless amplitude of the multipole φN(x,y) and φ(t) is a time dependent voltage applied to the electrodes, as described in Smythe, W. R. “Static and Dynamic Electricity”, McGraw-Hill Book Company, New York, 1939 (hereinafter “reference [13]”). For a quadrupole mass filter, φ(t)=U−Vrf cos Ωt. Without loss of generality, for N≧1, φN(x,y) can be calculated from
where Re[(ƒ(ζ)] means the real part of the complex function ƒ(ζ), ζ=x+iy, and i2=−1. For rod sets with round rods, amplitudes of multipoles given by eq 2 were calculated with the method of effective charges, as described in reference [2].
Ion Source Model
Collisional cooling of ions in an RF quadrupole (or other multipole) has become a common method of coupling atmospheric pressure ion sources such as electrospray ionization (ESI) to mass analyzers, as described in Douglas, D. J.; French, J. B. “Collisional Focusing Effects in Radio Frequency Quadrupoles”, J. Am. Soc. Mass Spectrom. 1992, 3, 398-40. and Douglas, D. J.; Frank, A. J.; Mao, D. “Linear Ion Traps in Mass Spectrometry”, Mass Spec. Rev. 2005, 24, 1-29 (hereinafter “reference [14a] and [14b] respectively”). Collisions with background gas thermalize ions and concentrate ions near the quadrupole axis. We use an approximate model of a thermalized distribution of ions as the source for calculations of peak shapes and stability diagrams. At the input of the quadrupole, the ion spatial distribution can be approximated as a Gaussian distribution with the probability density function f(x,y)
where σx determines the spatial spread.
Modeling initial ion coordinates X and Y with a random distribution given by eq 16 is based on the central limit theorem as described in Venttsel E. S. “Probability Theory”. Mir Publishers, Moscow. 1982. p. 303 (hereinafter “reference [15]”) for uniformly distributed values xi and yi on the interval [−r0, r0] or dimensionless variables on the interval [−1, 1]. The distribution of eq 16 can be generated from
where m is the number of random numbers xi and yi generated by a computer. In our calculations m=100. The standard deviations σx and σy determine the radial size of the ion beam.
The initial ion velocities in the x and y directions, vx and vy respectively, are taken from a thermal distribution given by
is ion velocity dispersion, k is Boltzmann's constant, T is the ion temperature, m is the ion mass. Transverse velocities in the interval [−3σv, 3σv] were used for every initial position. The dimensionless variables
are used in the ion motion equations. Then
The dimensionless velocity dispersion σu is
where R is the gas constant, and M is the ion mass in Daltons. For typical conditions: M=390 Da, r0=5×10−3 m, f=1.0×106 Hz, and T=300K, eq 19 gives σu=σv/πr0f=0.0072. The ion velocity dispersion σv decreases with M as M−1/2. This helps to improve the transmission of a quadrupole mass filter at higher mass.
The ion source model is characterized by the two parameters σx and σv. The influence of the radial size of the ion beam on transmission for different values σv is shown in
Peak Shape and Stability Region Calculations
Ion motion in quadrupole mass filters is described by the two Mathieu parameters a and q given by
where e is the charge on an ion, U is the DC applied from an electrode to ground and Vrf is the zero to peak RF voltage applied from an electrode to ground. For given applied voltages U and Vrf, ions of different mass to charge ratios lie on a scan line of slope
The presence of high order spatial harmonics in a quadrupole field leads to changes in the stability diagram as described in Ding, C.; Konenkov, N. V.; Douglas, D. J. “Quadrupole Mass Filters with Octopole Fields”, Rapid Commun. Mass Spectrom. 2003, 17, 2495-2502 (hereinafter “reference [16]”). The detailed mathematical theory of the calculation of the stability boundaries for Mathieu and Hill equations is given in McLachlan, N. W. “Theory and Applications of Mathieu Functions” Oxford University Press, UK, 1947 (hereinafter “reference [17]”) and for mass spectrometry applications is reviewed in reference [11]. However these methods cannot be used when the X and Y motions are coupled by higher spatial harmonics. Instead, the stability boundaries can be found by direct simulations of the ion motion. With higher multipoles in the potential, ion motion is determined by
(see Douglas, D. J.; Konenkov, N. V. “Influence of the 6th and 10th Spatial Harmonics on the Peak Shape of a Quadrupole Mass Filter with Round Rods”. Rapid Commun. Mass Spectrom. 2002, 16, 1425-1431 (hereinafter “reference [18]”)).
Equations 20 and 21 were solved by the Runge-Kutta-Nystrom-Dormand-Prince (RK-N-DP) method, as described in Hairer, E.; Norsett, S. P.; Wanner, G. “Solving Ordinary Differential Equations”. Springer-Verlag, Berlin, N.Y. 1987 (hereinafter “reference [19]”) and multipoles up to N=10 were included. For the calculation of peak shapes, the values of a and q were systematically changed on a scan line with a fixed ratio λ. With the ion source model described above N ion trajectories were calculated for fixed rf phases ξ0=0, π/20, 2*π/20, 3*π/20, . . . , 19*π/20. If a given ion trajectory is not stable (x or y≧r0) in the time interval 0<ξ<nπ, the program starts calculating a new trajectory. Here n is the number of rf cycles which the ions spend in the quadrupole field. From the number of transmitted ions, Nt, at a given point (a,q) the transmission is T=Nt/N. For the calculation of stability boundaries, a was fixed and q was systematically varied. The true boundaries correspond to the number of cycles that ions spend in the field, n, n→∞. For a practical calculation we choose n=150 and the 1% level of transmission. The value of a was fixed and q was scanned to produce a curve of transmission vs. q. For both peak shape and stability boundary calculations, the number of ion trajectories, N, was 6000 or more at each point of a transmission curve.
In all calculations the ions spend 150 rf cycles in the field. For rods with added hexapoles, the positive dc was applied to the X rods and the negative dc to the Y rods (a>0, λ>0). For rods with added octopoles, simulations were done for the positive dc applied to the X rods and the negative dc to the Y rods (a>0, λ>0). Simulations were then done with the polarity of the dc reversed (negative dc on the X rods and positive dc on the Y rods, a<0, λ<0).
A2 Only and A2+A3 Only
Round Rods, Rx>Ry, A1=0 A4≈0.
The Dipole Term A1
When a hexapole is added to a linear quadrupole field by rotating the Y rods towards the X rod, a significant dipole term, A1 is added. The dipole term in the potential has the form
This term arises because the field is no longer symmetric about the y axis 119. The dipole term can be removed by applying different voltages to the two x rods, either with a larger voltage applied to the x rod in the positive x direction or a smaller voltage applied to the x rod in the negative x direction, or a combination of these changes (see U.S. Patent Publication No. 2005/0067564 (Douglas et al.).
The dipole term arises because the centre of the field is no longer at the point x=0, y=0 of
Expanding the terms gives
Consider the coefficient of {circumflex over (x)} when y=0. This will be zero if
The last term is much smaller than the first two, so to a good approximation the coefficient of the dipole is zero if
More exactly eq 25 is a quadratic in x0 which can be solved to give
It is the solution with the minus sign that is realistic. Table 1 below shows the approximate and exact values of x0 calculated from eq 27 and eq 28 respectively for three rotation angles which give nominal hexapole fields of 4, 8, and 12%.
Because A1<0, x0<0. e.g. {circumflex over (x)}=x−0.0315r0. When {circumflex over (x)}=0, x=+0.0315r0. When x=0, {circumflex over (x)}=−0.0315r0. The centre of the field is shifted in the direction of the positive x axis. This calculation is still approximate because it does not include the higher multipoles. However it is likely adequate for practical purposes. Thus, the effects of the dipole can be minimized by injecting the ions centered at the point where {circumflex over (x)}=0.
When a hexapole is added to a linear quadrupole field by rotating two Y rods toward an X rod, the next highest term in the multipole expansion A1, A2 and A3 is the octopole term (see U.S. Patent Publication No. 2005/0067564 (Douglas et al)). This term can be minimized by constructing the rod sets with different diameters for the X and Y rods. For a given rotation angle, the diameter of the x rods can be increased to make A4≈0. These diameters are shown in Table 2. With conventional mass analysis with applied RF and DC, when A4 is minimized the peak shape improves. For the data in Table 2, Ry=1.1487r0.
The resolution is controlled by the scan parameter λ, but also by the value of q′. For a given transmission level, there is an optimum q′. Six figures show the effects of changing q′ for a rod set with round rods and 8% hexapole (A1=0, A4≈0). These are summarized in Table 3.
a-16f and Table 3 show that the optimum value of q′ for these operating conditions is q′=0.025, because this produces the highest resolution with 15% transmission.
Round Rods with Rx=Ry=1.1487r0, A4≠0
The above calculations for round rod sets are for the electrode geometries that make A4≈0. i.e. larger diameter X rods than Y rods. When equal diameter round rods are used, mass analysis at the lower tip of the upper stability island produces good peak shape and resolution.
a shows the uppermost island of stability calculated for this round rod set. The upper and lower tips are labeled U and L. All the multipoles up to N=10, in a co-ordinate system that makes A1=0, are included in the calculation. This figure also shows that a scan line with λ=0.17 crosses this region.
Added Octopole Field
A positive octopole field (A4>0) can be added to a linear quadrupole by making the Y rods greater in diameter than the X rods. If positive dc is applied to the X or smaller rods a>0. If negative dc is applied to the X or smaller rods, then a<0. With a>0, when quadrupole excitation is applied to make islands in the first stability region, an island can be formed at the upper tip of the stability region near a=+0.23. This island has two tips, one with a larger value of the |a| and another with a lesser |a|. Similarly, when a<0 an island is formed at the tip of the stability diagram near a=−0.23. This island has two tips, one with a larger value of the |a| and another with a lesser |a|.
A rod set with A4=0.026 was modeled. This rod set has round rods with Rx=r0, Ry/Rx=1.304 and is in a case with radius 4r0, giving the multipoles in Table 4.
With a quadrupole with an added octopole field constructed with Y rods greater in diameter than the X rods, when the polarity of the dc is reversed so that the negative dc is applied to the X rods and the positive dc is applied to the Y rods, the performance in conventional mass analysis is greatly degraded. The transmission drops and the resolution is poor as described in U.S. Pat. No. 6,897,438, May 24, 2005 and as described in reference [16]. This has been ascribed to changes in the stability diagram. The stability boundaries move out, become diffuse and are no longer even approximately straight lines. Nevertheless, mass analysis is still possible if the island of stability is used. With the negative dc applied to the X rods, the ion motion is described by a<0, λ<0 and the portion of the stability diagram with a<0 should be considered. Thus the upper stability tip of the island with a>0 becomes the lower tip of the stability island. To avoid confusion we will refer to the tips with greater |a| and lesser |a|.
Other variations and modifications of the invention are possible. All such modifications or variations are believed to be within the sphere and scope of the invention as defined by the claims appended hereto.
This application claims priority to U.S. Provisional Application No. 60/771,258 filed Feb. 7, 2006. The contents of the aforementioned application are hereby incorporated by reference.
Number | Name | Date | Kind |
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2939952 | Paul et al. | Jun 1960 | A |
5177359 | Hiroki et al. | Jan 1993 | A |
5227629 | Miseki | Jul 1993 | A |
6897438 | Soudakov et al. | May 2005 | B2 |
7045797 | Sudakov et al. | May 2006 | B2 |
7141789 | Douglas et al. | Nov 2006 | B2 |
20040108456 | Sudakov et al. | Jun 2004 | A1 |
20050067564 | Douglas et al. | Mar 2005 | A1 |
20050263696 | Wells | Dec 2005 | A1 |
Number | Date | Country |
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2620568 | Mar 1989 | FR |
WO2004013891 | Feb 2004 | WO |
Number | Date | Country | |
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20070295900 A1 | Dec 2007 | US |
Number | Date | Country | |
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60771258 | Feb 2006 | US |