This application is a U.S. national phase filing under 35 U.S.C. § 371 claiming the benefit of and priority to International Patent Application No. PCT/GB2018/052105, filed on Jul. 26, 2018, which claims priority from and the benefit of United Kingdom patent application No. 1712612.9, United Kingdom patent application No. 1712613.7, United Kingdom patent application No. 1712614.5, United Kingdom patent application No. 1712616.0, United Kingdom patent application No. 1712617.8, United Kingdom patent application No. 1712618.6 and United Kingdom patent application No. 1712619.4, each of which was filed on Aug. 6, 2017. The entire content of these applications is incorporated herein by reference.
The invention relates to the area of time of flight mass spectrometers, multi-turn and multi-reflecting time-of-flight mass spectrometers with pulsed ion sources and pulsed converters, and is particularly concerned with improved ion injection.
Time-of-flight mass spectrometers (TOF MS) are widely used for combination of sensitivity and speed, and lately with the introduction of ion mirrors and multi-reflecting schemes, for their high resolution and mass accuracy. Pulsed sources are used for intrinsically pulsed ionization methods, such as Matrix Assisted Laser Desorption and Ionization (MALDI), Secondary Ionization (SIMS), and pulsed EI. The first two ion sources become more and more popular for mass spectral surface imaging, where a relatively large surface area is analyzed simultaneously while using mapping properties of TOF MS.
Even more popular are TOF MS, where pulsed converters are used to form pulsed ion packets out of continuous ion beams produced by ion sources like Electron Impact (EI), Electrospray (ESI), Atmospheric pressure ionization (APPI), atmospheric Pressure Chemical Ionization (APCI), Inductively couple Plasma (ICP) and gaseous (MALDI). Most common pulsed converters are orthogonal accelerators (WO9103071) and radiofrequency ion traps with pulsed radial ejection, lately used for ion injection into Orbitraps®. Two aspects of prior art are relevant to the present invention: (a) all ion sources and converters for TOF MS employ pulsed accelerating fields; (b) a significant portion of ion sources and converters are spatially wide, so that bypassing of ion sources and converters by ion packets returned after one pass (reflection or turn) becomes an issue.
The resolution of TOF MS has been substantially improved in multi-pass TOFMS (MPTOF), by reflecting ions multiple times between ion mirrors in multi-reflecting TOF (MRTOF) mass analysers [e.g. as described in SU1725289, U.S. Pat. Nos. 6,107,625, 6,570,152, GB2403063, U.S. Pat. No. 6,717,132, incorporated herein by reference], or by turning ions multiple times in electrostatic sectors in multi-turn TOF (MTTOF) mass analysers [e.g. as described in U.S. Pat. Nos. 7,504,620, 7,755,036, and M. Toyoda, et. al, J. Mass Spectrom. 38 (2003) 1125, incorporated herein by reference].
MPTOF analyzers are arranged to fold ion trajectories for substantial extension of the ion flight path (e.g. 10-50 m or more) within commercially reasonably sized (0.5-1 m) instruments. The ion path folding in MRTOF analysers is arranged with ion packet reflection in the X-direction combined with slow ion drift in the drift Z-direction, thus producing zigzag ion trajectories. The ion path folding in MTTOF is arranged with ion circular, oval or figure-of-eight loops in the X-Y plane combined with slow drift in the drift Z-direction, thus producing spiral ion motion. The term “pass” generalizes ion mirror reflections and ion turns. The resolving power (also referred as resolution) of MP-TOF analysers grows at larger number of passes N by reducing the effect of the initial time spread of ion packets and of the detector time spread.
Most MPTOF analysers employ two dimensional (2D) electrostatic fields in the XY-plane between electrodes, substantially elongated in the drift Z-direction. The 2D-fields of ion mirrors or sectors are carefully engineered to provide for isochronous ion motion and for spatial ion packet confinement in the XY-plane. By nature, the electrostatic 2D-fields have zero component EZ=0 in the orthogonal drift Z-direction, i.e. they have no effect on the ion packets free propagation and its expansion in the drift Z-direction.
In earlier MPTOF schemes, the control over ion motion in the drift direction was arranged by the ion injecting mechanisms in ion sources or ion pulsed converters, defining the inclination angle of ion trajectory in the analyzer. In an attempt to increase MPTOF resolution by using denser folding of the ion trajectory, the injection angle α (to axis X) of ion packets shall be reduced, thus, requiring much lower energies of the injected continuous ion beam. Lower injection energies affect the ion beam admission into the OA and increase the ion packet angular divergence Δα. Ions start hitting rims of the accelerator and ion detector, and may produce trajectories that overlap, thus confusing spectra.
To address those problems, multiple complex solutions have been proposed to define the ion drift advance per reflection, to prevent or compensate the angular divergence of ion packets, and to withstand various distortions, such as stray fields and mechanical distortions of analyzer electrodes: e.g. U.S. Pat. No. 7,385,187 proposed periodic lens and edge deflectors for MRTOF analysers; U.S. Pat. No. 7,504,620 proposed laminated sectors for MTTOF analysers; WO2010008386 and then US2011168880 proposed quasi-planar ion mirrors having weak (but sufficient) spatial modulation of mirror fields; U.S. Pat. No. 7,982,184 proposed splitting mirror electrodes into multiple segments for arranging EZ field; U.S. Pat. No. 8,237,111 and GB2485825 proposed electrostatic traps with three-dimensional fields, though without sufficient isochronicity in all three dimensions and without non-distorted regions for ion injection; WO2011086430 proposed first order isochronous Z-edge reflections by tilting ion mirror edge combined with reflector fields; U.S. Pat. No. 9,136,101 proposed bent ion MRTOF ion mirrors with isochronicity recovered by trans-axial lens. Though prior art solutions do solve the problem of controlling Z-motion, they have several drawbacks, comprising: (i) technical complexity; (ii) additional time aberrations, affecting resolution; (iii) limited length of ion packets and limited duty cycle and charge capacity of pulsed converters; and (iv) fixed arrangement with low tolerance to manufacturing faults. Those drawbacks become particularly problematic when trying to construct a compact and low cost MPTOF instrument for higher resolutions.
From a first aspect the present invention provides a pulsed ion accelerator for a mass spectrometer comprising: a plurality of electrodes and at least one voltage supply arranged and configured to generate a wedge-shaped electric field region; wherein the ion accelerator is configured to apply a pulsed voltage to at least one of said electrodes for pulsing ions out of the ion accelerator, wherein the ions have a time front arranged in a first plane at the time the pulsed voltage is initiated, and wherein the ion accelerator is configured such that the pulsed ions pass through the wedge-shaped electric field region so as to cause the time front of the ions to be tilted at an angle to the first plane.
The above pulsed ion accelerator tilts the time front of the ions it pulses out. By introducing such a tilted time front, the pulsed ion accelerator is able to compensate for time front tilting that may occur at ion optical components of the mass spectrometer that are downstream of the pulsed ion accelerator. The embodiments are also able to introduce a relatively large time front tilt whilst altering the mean ion trajectory by only a relatively small angle.
For the avoidance of doubt, the time front of the ions may be considered to be a leading edge/area of ions in the ion packet having the same mass to charge ratio (and which may have the mean average energy).
The pulsed ion accelerator is an orthogonal accelerator.
The pulsed ion accelerator may be arranged to receive ions along a first axis and pulse the ions substantially orthogonally to the first axis.
The pulsed ion accelerator may comprise electrodes arranged and configured for generating said wedge-shaped electric field region therebetween such that equipotential field lines in the wedge-shaped electric field region are angled to each other so as to form the wedge-shape.
Therefore, the equipotential field lines may converge towards one another in a direction towards a first end of the wedge-shaped electric field region, and diverge away from one another in a direction towards a second opposite end of the wedge-shaped electric field region.
The first and second ends may be spaced apart in a direction substantially along said first axis along which ions are received.
Ions travelling through the wedge-shaped electric field region may be accelerated by the wedge-shaped electric field by an amount that increases as a function of distance towards the first end, since the equipotential field lines converge towards the first end. This may cause the time front of the ions to be tilted.
The pulsed ion accelerator may comprise one or more first electrode arranged in a first plane and one or more second electrode arranged in a second plane that is angled to the first plane so as to define the wedge-shaped electric field region between the one or more first electrode and one or more second electrode.
The pulsed ion accelerator may comprise one or more first electrode arranged in a first plane and a plurality of second electrodes arranged in a second plane, wherein the ion accelerator is configured to apply different voltages to different ones of the second electrodes so as to define the wedge-shaped electric field region between the one or more first electrode and the second electrodes.
This enables the time front tilt angle to easily be varied by varying the potentials applied to the second electrodes.
The first and second plane may be parallel.
The second electrodes may be connected by a resistive chain such that a voltage supply connected to the resistive chain applies different electrical potentials to the second electrodes.
The plurality of second electrodes may be arranged on a printed circuit board (PCB).
The one or more first electrodes may be a plurality of first electrodes, and the ion accelerator may be configured to apply different voltages to the first electrodes so as to define the wedge-shaped electric field region. This enables the time front tilt angle to be varied by varying the potentials applied to the first electrodes. The first electrodes may be connected by a resistive chain such that a voltage supply connected to the resistive chain applies different electrical potentials to the first electrodes. The first electrodes may be arranged on a printed circuit board (PCB).
PCB as used herein may refer to a component containing conductive tracks, pads and other features etched from, printed on, or deposited on one or more sheet layers of material laminated onto and/or between sheet layers of a non-conductive substrate.
In embodiments in which electrodes are arranged on a PCB, a resistive layer may be provide between the electrodes, so as to avoid the insulating material of the substrate from becoming electrically charged.
Embodiments are also contemplated in which at least some of the electrodes connected by the resistive chain are replaced by a resistive layer.
The pulsed ion accelerator may comprise electrodes spaced apart in a dimension for defining the wedge-shaped electric field region therebetween, and the ion accelerator may be configured to pulse ions in said dimension.
The electrodes for generating said wedge-shaped electric field region may be arranged so that equipotential field lines of the wedge-shaped electric field extend substantially in a first direction and the ion accelerator is configured to pulse the ions through the wedge-shaped electric field substantially transverse to the equipotential field lines.
The ion accelerator may be arranged and configured to receive ions travelling substantially in the first direction.
The ion accelerator may be arranged to receive ions at the wedge-shaped electric field region.
The ion accelerator may be arranged and configured to receive ions travelling in a first direction along a first axis that is substantially parallel to equipotential field lines of the wedge-shaped electric field.
The equipotential field lines of the wedge-shaped electric field may diverge, or converge, as a function of distance in the first direction.
Alternatively, the ion accelerator may be arranged to receive ions at an ion receiving region and then pulse the ions downstream into the wedge-shaped electric field region of the ion accelerator.
The pulsed ion accelerator may be configured to pulse said wedge-shaped electric field for pulsing ions out of the ion accelerator.
The pulsed ion accelerator may comprise an ion acceleration region downstream of the wedge-shaped electric field region for amplifying the time front tilt introduced by the wedge-shaped electric field.
The pulsed ion accelerator may comprise a voltage supply and electrodes configured to apply a static electric field in the ion acceleration region for accelerating the ions; and/or a voltage supply and electrodes configured to apply an electric field in the ion acceleration region having parallel equipotential field lines for accelerating the ions.
The pulsed ions may travel through the ion acceleration region substantially orthogonal to the parallel equipotential field lines.
The pulsed ion accelerator may comprise an ion deflector located downstream of the pulsed ion accelerator and configured to deflect the average ion trajectory of the ions, thereby tilting the angle of the time front of the ions received by the ion deflector. The wedge-shaped electric field region of the pulsed ion accelerator may be configured to tilt the time front of the ions passing therethrough so as to at least partially counteract the tilting of the time front by the ion deflector.
The angle of the time front may therefore be moved at least partially back towards the first plane (i.e. the angle the time front was at when the pulsed voltage was initiated) when the ions exit the ion deflector.
The initial mean ion energy of the ions prior to acceleration in the pulsed ion accelerator may be (significantly) smaller than the mean ion energy of the ions within said ion deflector.
It has been recognised that a conventional ion deflector inherently has a relatively high focusing effect on the ions, hence undesirably increasing the angular spread of the ion trajectories exiting the deflector, as compared to the angular spread of the ion trajectories entering the ion deflector. This may cause excessive spatial defocusing of the ions downstream of the focal point, resulting in ion losses and/or causing ions to travel significantly different path lengths through the spectrometer before they reach the detector. The mass resolution of the spectrometer may be adversely affected. Embodiments of the present invention provide an ion deflector configured to generate a quadrupolar field that controls the spatial focusing of the ions, e.g. so as to maintain substantially the same angular spread of the ions passing therethrough, or to allow only the desired amount of spatial focusing of the ions.
The pulsed ion accelerator may be one of: (i) a MALDI source; (ii) a SIMS source; (iii) a mapping or imaging ion source; (iv) an electron impact ion source; (v) a pulsed converter for converting a continuous or pseudo-continuous ion beam into ion pulses; (vi) an orthogonal accelerator; (vii) a pass-through orthogonal accelerator having an electrostatic ion guide; or (viii) a radio-frequency ion trap with pulsed ion ejection.
The present invention also provides a mass spectrometer comprising: a multi-pass time-of-flight mass analyser or electrostatic ion trap having the pulsed ion accelerator as described hereinabove, and electrodes arranged and configured so as to provide an ion drift region that is elongated in a drift direction (z-dimension) and to reflect or turn ions multiple times in an oscillating dimension (x-dimension) that is orthogonal to the drift direction.
The multi-pass time-of-flight mass analyser may be a multi-reflecting time of flight mass analyser having two ion mirrors that are elongated in the drift direction (z-dimension) and configured to reflect ions multiple times in the oscillation dimension (x-dimension), wherein the pulsed ion accelerator is arranged to receive ions and accelerate them into one of the ion mirrors. Alternatively, the multi-pass time-of-flight mass analyser may be a multi-turn time of flight mass analyser having at least two electric sectors configured to turn ions multiple times in the oscillation dimension (x-dimension), wherein the pulsed ion accelerator is arranged to receive ions and accelerate them into one of the sectors.
Where the mass analyser is a multi-reflecting time of flight mass analyser, the mirrors may be gridless mirrors.
Each mirror may be elongated in the drift direction and may be parallel to the drift dimension.
It is alternatively contemplated that the multi-pass time-of-flight mass analyser or electrostatic trap may have one or more ion mirror and one or more sector arranged such that ions are reflected multiple times by the one or more ion mirror and turned multiple times by the one or more sector, in the oscillation dimension.
The spectrometer may comprise an ion deflector located downstream of said pulsed ion accelerator, and that is configured to back-steer the average ion trajectory of the ions, in the drift direction, thereby tilting the angle of the time front of the ions received by the ion deflector.
The average ion trajectory of the ions travelling through the ion deflector may have a major velocity component in the oscillation dimension (x-dimension) and a minor velocity component in the drift direction. The ion deflector back-steers the average ion trajectory of the ions passing therethrough by reducing the velocity component of the ions in the drift direction. The ions may therefore continue to travel in the same drift direction upon entering and leaving the ion deflector, but with the ions leaving the ion deflector having a reduced velocity in the drift direction. This enables the ions to oscillate a relatively high number of times in the oscillation dimension, for a given length in the drift direction, thus providing a relatively high resolution.
The wedge-shaped electric field region of the pulsed ion accelerator may be configured to tilt the time front of the ions passing therethrough so as to at least partially counteract the tilting of the time front by the ion deflector.
The angle of the time front may therefore be moved at least partially back towards the first plane (i.e. the angle the time front was at when the pulsed voltage was initiated) when the ions exit the ion deflector.
The ion deflector may be configured to generate a quadrupolar field for controlling the spatial focusing of the ions in the drift direction.
It has been recognised that a conventional ion deflector inherently has a relatively high focusing effect on the ions, hence undesirably increasing the angular spread of the ion trajectories exiting the deflector, as compared to the angular spread of the ion trajectories entering the ion deflector. This may cause excessive spatial defocusing of the ions downstream of the focal point, resulting in ion losses and/or causing ions to undergo different numbers of oscillations in the spectrometer before they reach the detector. This may cause spectral overlap due to ions from different ion packets being detected at the same time. The mass resolution of the spectrometer may also be adversely affected. Such conventional ion deflectors are therefore particularly problematic in multi-pass time-of-flight mass analysers or multi-pass electrostatic ion traps, since a large angular spread of the ions will cause any given ion packet to diverge a relatively large amount over the relatively long flight path through the device. Embodiments of the present invention provide an ion deflector configured to generate a quadrupolar field that controls the spatial focusing of the ions in the drift direction, e.g. so as to maintain substantially the same angular spread of the ions passing therethrough, or to allow only the desired amount of spatial focusing of the ions in the z-direction.
The quadrupolar field for in the drift direction may generate the opposite ion focusing or defocusing effect in the dimension orthogonal to the drift direction and oscillation dimension. However, it has been recognised that the focal properties of MPTOF mass analyser (e.g. MRTOF mirrors) or electrostatic trap are sufficient to compensate for this.
The ion deflector may be configured to generate a substantially quadratic potential profile in the drift direction.
The ion deflector may back steer all ions passing therethrough by the same angle; and/or the ion deflector may control the spatial focusing of the ion packet in the drift direction such that the ion packet has substantially the same size in the drift dimension when it reaches an ion detector in the spectrometer as it did when it enters the ion deflector.
The ion deflector may control the spatial focusing of the ion packet in the drift direction such that the ion packet has a smaller size in the drift dimension when it reaches a detector in the spectrometer than it did when it entered the ion deflector.
At least one voltage supply may be provided that is configured to apply one or more first voltage to one or more electrode of the ion deflector for performing said back-steer and one or more second voltage to one or more electrode of the ion deflector for generating said quadrupolar field for said spatial focusing, wherein the one or more first voltage is decoupled from the one or more second voltage.
The ion deflector may comprise at least one plate electrode arranged substantially in the plane defined by the oscillation dimension and the dimension orthogonal to both the oscillation dimension and the drift direction (X-Y plane), wherein the plate electrode is configured back-steer the ions; and the ion deflector may comprise side plate electrodes arranged substantially orthogonal to the at least one plate electrode and that are maintained at a different potential to the plate electrode for controlling the spatial focusing of the ions in the drift direction.
The side plates may be Matsuda plates.
The at least one plate electrode may comprise two electrodes and a voltage supply for applying a potential difference between the electrodes so as to back-steer the average ion trajectory of the ions, in the drift direction.
The two electrodes may be a pair of opposing electrodes that are spaced apart in the drift direction.
However, it is contemplated that only the upstream electrode (in the drift direction) may be provided, so as to avoid ions hitting the downstream electrode.
The ion deflector may be configured to provide said quadrupolar field by comprising one or more of: (i) a trans-axial lens/wedge; (iii) a deflector with aspect ratio between deflecting plates and side walls of less than 2; (iv) a gate shaped deflector; or (v) a toroidal deflector such as a toroidal sector.
The ion deflector may be arranged such that it receives ions that have already been reflected or turned in the oscillation dimension by the multi-pass time-of-flight mass analyser or electrostatic ion trap; optionally after the ions have been reflected or turned only a single time in the oscillation dimension by the multi-pass time-of-flight mass analyzer or electrostatic ion trap.
The location of the deflector directly after the first ion mirror reflection allows yet denser ray folding
The pulsed ion accelerator and ion deflector may tilt the time front so that it is aligned with the ion receiving surface of the ion detector and/or to be parallel to the drift direction (z-dimension).
The mass analyser or electrostatic trap may be an isochronous and/or gridless mass analyser or an electrostatic trap.
The mass analyser or electrostatic trap may be configured to form an electrostatic field in a plane defined by the oscillation dimension and the dimension orthogonal to both the oscillation dimension and drift direction (i.e. the XY-plane).
This two-dimensional field may have a zero or negligible electric field component in the drift direction (in the ion passage region). This two-dimensional field may provide isochronous repetitive multi-pass ion motion along a mean ion trajectory within the XY plane.
The energy of the ions received at the pulsed ion accelerator and the average back steering angle of the ion deflector may be configured so as to direct ions to an ion detector after a pre-selected number of ion passes (i.e. reflections or turns).
The spectrometer may comprise an ion source. The ion source may generate an substantially continuous ion beam or ion packets.
The pulsed ion accelerator may be a gridless orthogonal accelerator.
The pulsed ion accelerator has a region for receiving ions (a storage gap) and may be configured to pulse ions orthogonally to the direction along which it receives ions. The pulsed ion accelerator may receive a substantially continuous ion beam or packets of ions, and may pulse out ion packets.
The drift direction may be linear (i.e. a dimension) or it may be curved, e.g. to form a cylindrical or elliptical drift region.
The mass analyser or ion trap may have a dimension in the drift direction of: ≤1 m; ≤0.9 m; ≤0.8 m; ≤0.7 m; ≤0.6 m; or ≤0.5 m. The mass analyser or trap may have the same or smaller size in the oscillation dimension and/or the dimension orthogonal to the drift direction and oscillation dimension.
The mass analyser or ion trap may provide an ion flight path length of: between 5 and 15 m; between 6 and 14 m; between 7 and 13 m; or between 8 and 12 m.
The mass analyser or ion trap may provide an ion flight path length of: ≤20 m; ≤15 m; ≤14 m; ≤13 m; ≤12 m; or ≤11 m. Additionally, or alternatively, the mass analyser or ion trap may provide an ion flight path length of: ≥5 m; ≥6 m; ≥7 m; ≥8 m; ≥9 m; or ≥10 m. Any ranges from the above two lists may be combined where not mutually exclusive.
The mass analyser or ion trap may be configured to reflect or turn the ions N times in the oscillation dimension, wherein N is: ≥5; ≥6; ≥7; ≥8; ≥9; ≥10; ≥11; ≥12; ≥13; ≥14; ≥15; ≥16; ≥17; ≥18; ≥19; or ≥20. The mass analyser or ion trap may be configured to reflect or turn the ions N times in the oscillation dimension, wherein N is: ≤20; ≤19; ≤18; ≤17; ≤16; ≤15; ≤14; ≤13; ≤12; or ≤11. Any ranges from the above two lists may be combined where not mutually exclusive.
The spectrometer may have a resolution of: ≥30,000; ≥40,000; ≥50,000; ≥60,000; ≥70,000; or ≥80,000.
The spectrometer may be configured such that the pulsed ion accelerator receives ions having a kinetic energy of: ≥20 eV; ≥30 eV; ≥40 eV; ≥50 eV; ≥60 eV; between 20 and 60 eV; or between 30 and 50 eV. Such ion energies may reduce angular spread of the ions and cause the ions to bypass the rims of the orthogonal accelerator.
The spectrometer may comprise an ion detector.
The detector may be an image current detector configured such that ions passing near to it induce an electrical current in it. For example, the spectrometer may be configured to oscillate ions in the oscillation dimension proximate to the detector, inducing a current in the detector, and the spectrometer may be configured to determine the mass to charge ratios of these ions from the frequencies of their oscillations (e.g. using Fourier transform technology). Such techniques may be used in the electrostatic ion trap embodiments.
Alternatively, the ion detector may be an impact ion detector that detects ions impacting on a detector surface. The detector surface may be parallel to the drift dimension.
The ion detector may be arranged between the ion mirrors or sectors, e.g. midway between (in the oscillation dimension) opposing ion mirrors or sectors.
The present invention also provides a method of mass spectrometry comprising: providing a pulsed ion accelerator or mass spectrometer as described herein; and applying a pulsed voltage to at least one of said electrodes so as to pulse ions out of the ion accelerator, wherein the ions have a time front arranged in a first plane at the time the pulsed voltage is initiated, and wherein the ions pass through the wedge-shaped electric field region so as to cause the time front of the ions to be tilted at an angle to the first plane.
Herein there are proposed several ion optical elements, believed to be novel at least for MRTOF field:
Further, the inventor has realized that applying a combination of compensated deflectors with amplifying wedge fields to MPTOF allows reaching: (a) spatial ion packet focusing Z|Z=0 onto detector; and (b) mutual compensation of multiple aberrations, including (i) first order time-front tilt T|Z, (ii) chromatic angular spread α|δ and, accounting analyzer properties, most of Y-related time-of-flight aberrations.
In application to orthogonal accelerators, there are achieved: (a) elevated energies of ion beams at the entrance of orthogonal accelerators for improved sensitivity and for reduced angular divergence Δα of ion packets; (b) dense folding of ion rays at small inclination angles for higher resolution of MPTOF.
The proposed schemes and some embodiments were tested and are presented here in ion optical simulations, which have verified the stated ion optical properties, including flexible tuning and compensation of misalignments; so as to confirm an ability of reaching a substantially improved combination of resolution and sensitivity within a compact MPTOF systems. As an example,
Embodiments provide an ion injection mechanism into an isochronous electrostatic mass spectrometer, comprising:
Preferably, said at least one deflector may comprise means for generating an additional quadrupolar field for independent control over ion ray's steering angle and focusing or defocusing.
Preferably, said mass spectrometer may comprise at least one field-free space and at least one ion mirror and/or at least one electric sector.
Preferably, said mass spectrometer may comprise one of the group: (i) a time-of-flight mass spectrometer; (ii) an open ion trap; and (iii) an ion trap.
Embodiments provide a method of ion injection into an electrostatic field of an isochronous mass spectrometer, comprising the following steps:
Preferably, the method may further comprise a step of adding a quadrupolar field to said deflecting field for independent control over ion ray's steering angle and focusing or defocusing.
Preferably, said field of isochronous mass spectrometer may comprise at least one field-free space and at least one ion reflecting field of ion mirror and/or at least one deflecting field of electric sector.
Preferably, said field of mass spectrometer may be arranged for one type of mass spectral analysis of the group: (i) a time-of-flight mass analysis; (ii) an analysis of ion oscillation frequencies within an ion electrostatic trap or an open ion trap.
Embodiments provide an isochronous electrostatic mass spectrometer comprising:
Preferably, for the purpose of controlling spatial defocusing or focusing of said at least one deflector, an additional quadrupolar field may be formed within said deflector by at least one electrode structure of the group: (i) Matsuda plates; (ii) gate shaped deflecting electrode; (iii) side shields of the deflector with the aspect ratio under 2; (iv) toroidal sector deflection electrodes; and (v) additional electrode curvature within a trans-axial wedge deflector.
Preferably, said accelerator may be part of one pulsed ion source of the group: (i) a MALDI source; (ii) a SIMS source; (iii) a mapping or imaging ion source; and (iv) an electron impact ion source.
Preferably, said accelerator may be part of one pulsed converter of the group: (i) an orthogonal accelerator; (ii) a pass-through orthogonal accelerator with an electrostatic ion guide; and (iii) a radio-frequency ion trap with radial pulsed ion ejection.
Embodiments provide a method of time-of-flight mass spectral analysis comprising the following steps:
Preferably, for the purpose of controlling spatial defocusing or focusing of said at least one deflector, an additional quadrupolar field may be formed within said deflector by at least one electrode structure of the group: (i) Matsuda plates; (ii) gate shaped deflecting electrode; (iii) side shields of the deflector with the aspect ratio under 2; (iv) toroidal sector deflection electrodes; and (v) additional electrode curvature within a trans-axial wedge deflector.
Preferably, said ion acceleration step may be part of one pulsed ion step of the group: (i) a MALDI ionization; (ii) a SIMS ionization; (iii) an ionization with mapping or imaging of analyzed surfaces; and (iv) an electron impact ionization.
Preferably, said accelerator step may be part of one pulsed conversion step of the group: (i) an orthogonal acceleration; (ii) a pass-through orthogonal acceleration assisted by ion beam guidance by an electrostatic field of an ion guide; and (iii) a radio-frequency ion trapping with radial pulsed ion ejection.
Various embodiments will now be described, by way of example only, and with reference to the accompanying drawings in which:
Referring to
In operation, ion source 11 generates continuous ion beam. Commonly, ion sources 11 comprise gas-filled radio-frequency (RF) ion guides (not shown) for gaseous dampening of ion beams. Lens 12 forms a substantially parallel continuous ion beam 13, entering OA 14 along the Z-direction. Electrical pulse in OA 14 ejects ion packets 15. Packets 15 travel in the MRTOF analyser at a small inclination angle α to the x-axis, which is controlled by the ion source bias UZ.
Referring to
In the Example 20, to fit 14 ion reflections (i.e. L=7 m ion flight path) the source bias is set to UZ=9V. Parallel ion rays with an initial ion packet length in the z-dimension of Z0=10 mm and no angular spread Δα=0 start hitting rims of OA 14 and of detector 17. In Example 21, the top ion mirror is tilted by λ=1 mrad, representing realistic overall effective angle of mirror tilt, considering built up faults of stack assemblies, standard accuracy of machining and moderate electrode bend by internal stress at machining. Every “hard” ion reflection in the top ion mirror then changes the inclination angle α by 2 mrad. The inclination angle α grows from α1=27 mrad to α2=41 mrad, gradually expanding central trajectory. To hit the detector after N=14 reflections, the source bias has to be reduced to UZ=6V. The angular divergence is amplified by mirror tilt and increase the ion packets width to ΔZ=18 mm, inducing ion losses on the rims. Obviously, slits in the drift space may be used to avoid trajectory overlaps and spectral confusion, however, at a cost of additional ionic losses.
In example 21, the inclination of ion mirror introduces yet another and much more serious problem. The time-front 15 of the ion packet becomes tilted by angle γ-14 mrad in front of the detector. The total ion packet spreading in the time-of-flight X-direction ΔX=ΔZ*γ=0.3 mm limits mass resolution to R<L/2ΔX=11,000 at L=7 m flight path, which is too low (for example compared to the desired R=80,000). To avoid the limitation, the electrode precision has to be brought to non-realistic level: λ<0.1 mrad, translated to better than 10 um accuracy and straightness of individual electrodes.
Summarizing problems of prior art MRTOF analysers, attempts of increasing flight path require much lower specific energies UZ of the continuous ion beam and cause larger angular divergences Δα of the ion packets, which induce ion losses on component rims and may produce spectral overlaps. Importantly, small mechanical imperfections strongly affect MRTOF resolution and require unreasonably high precision.
Referring to
ψ=D/2H*U/K; γ=−ψ=const (z) (Eq. 1)
Alternatively, compensated deflectors may be used that are trans-axial (TA) deflectors, e.g. formed by wedge electrodes such as those described herein in relation to the pulsed orthogonal accelerator. By “compensated”, it is meant that the angular dispersion of the ions caused by the ion deflection may be compensated for, e.g. by the quadrupolar field. Embodiments of the invention propose using a first order correction, produced by an additional curvature of TA-wedge. Controlled focusing/defocusing may also be generated by combination of the TA-wedge and TA-lens, arranged separately or combined into a single TA-device. For a narrower range of deflection angles, the compensated deflector may be arranged with a single potential while selecting the size of Matsuda plates or with a segment of toroidal sector.
Compensated deflectors perform well with MRTOF or MPTOF analysers. The quadrupolar field in the Z-direction generates an opposite focusing or defocusing field in the transverse Y-direction. Below simulations prove that the focal properties of MPTOF analyzers are sufficient to compensate for the Y-focusing of deflectors 30 without any significant TOF aberrations.
Again referring to
γ=0 and T|Z=0 at ψ1=ψ2*C1 (Eq. 2)
T|ZZ=0, if C1*C2=1 (Eq. 3)
Thus, using transformation of the Z-width of ion packets by compensated deflectors 37,37 allows adjusting the overall time front tilt angle after passing through a set of deflectors independent of the summary deflecting angle induced by this set.
Referring to
An exemplary orthogonal accelerator 40 comprises: a region of pulsed wedge field 45, arranged between a tilted push electrode 44 and ground plate 47 aligned with the Z-axis; and a flat DC accelerating field 48 formed by electrodes parallel to the Z-axis. Field 48 may have accelerating and decelerating regions for producing low time spread and spatial ion focusing of ion packets (e.g. in the XY-plane), however, all equi-potentials of field 48 may stay parallel to the Z-axis.
In operation, a continuous ion beam 41 enters along the Z-axis at specific ion energy UZ, e.g. defined by voltage bias of an upstream RF ion guide. Preferably ion beam angular divergence, spatial expansion and beam initial position are controlled by some radial confinement means that may be selected, for example, from the group of: (i) a radiofrequency rectilinear multipolar ion guide; (ii) an electrostatic quadrupolar ion guide with ion beam compression in the X-direction; (iii) an electrostatic periodic lens; and (iv) proposed in a co-pending application, an electrostatic ion guide with quadupolar field being spatially alternated along the Z-axis. An electrical pulse may be applied periodically to the push plate 44, ejecting a portion of the beam 41 through an aperture in electrode 47, thus forming an ion packet with starting time-front 42, which crosses a starting equipotential 46 that is tilted at the angle λ0 to the x-axis. Ions start with zero mean energy in the X-direction K=0, at the exit of wedge field 45 ions gain specific energy K1 and at the exit of DC field 48 gains the energy K0. Assuming small angles λ0 of equipotential 46 (in further examples 0.5 deg), beam thickness of at least ΔX>1 mm and moderate ion packet length (examples use Z0=10 mm), the λ0 tilt of starting equipotential 46 produces negligible corrections onto energy spread of ions in the x-direction ΔK of ion packet 49.
By applying trivial mathematics a non-expected and previously unknown result was arrived at: in accelerator 40 with amplifying wedge accelerating field, the time front tilt angle relative to the z-axis (γ) and the ion steering angle ϕ introduced by the wedge field are controlled by the energy factor K0/K1 as:
γ=2λ*(K0/K1)0.5=2λ*u0/u1 (Eq. 4)
ϕ=2λ/3*(K1/K0)0.5=2λ/3*u1/u0 (Eq. 5)
i.e. γ/ϕ=3K0/K1>>1 (Eq. 6)
where K1 and K0 are mean ion kinetic energies at the exit of the wedge field 45 (index 1) and at the exit of flat field 48 (index 0) respectively, and u1 and u0 are the corresponding mean ion velocities.
Thus, novel accelerators with amplifying wedge field allow (i) operating with (e.g. continuous) ion beams introduced along the Z-axis, which allows convenient instrumental arrangements; (ii) tilting ion packets time front to a substantial angle γ, which may then be used for compensation of the time-front tilt in one or more ion deflector; (iii) controlling tilt angle electronically, either by adjusting the pulse potential or by minor steering of the (e.g. continuous) ion beam between various starting equipotential lines.
Again referring to
Ion injection into an MRTOF analysers may be improved by using higher energies of continuous ion beam for improving the ion beam admission into an orthogonal accelerator (OA) and for reducing angular divergence of ion packets in the MRTOF analyser. For higher MRTOF resolution, ion trajectories may be compact folded by using back steering of ion packets, achieved with a deflector. To compensate for the time front tilt produced by the deflector, it is proposed to use an amplifying wedge accelerating field such as that described above in the OA.
Referring to
The operation of embodiment 50 is illustrated by simulation example 51, showing time fronts 54 and 55 crossing ion rays. Continuous ion beam 41 at specific energy (e.g. UZ=57V) propagates along the Z-axis to cross starting (K=0) equipotential 46, which is tilted at the angle λ0 (e.g. λ0=0.5 deg) to the z-axis, with push plate 44 being tilted by 1 deg to the z-axis. Pulsed wedge field 45 accelerates ions to mean energy K1 (e.g. K1=800V), and flat field 48 to K0 (e.g. K0=8 kV), thus producing an amplifying factor K0/K1≅10. The amplifying wedge tilts the ion packets time front 54 at a large angle [e.g. γ=2λ0*(K0/K1)0.5≅6λ0], while having a small deflection effect on the trajectory of the ion ray relative to the x-axis (as compared to if a conventional non-wedged and untilted OA was used). For example, the OA may result in an angle α1=α0−ϕ=4.7 deg (where ϕ≅0.2 deg is the deflection angle caused by the wedged field). In other words, the ion rays are inclined almost at natural inclination angle α0=(UZ/UX)0.5=4.9 deg.
After the first ion mirror reflection, deflector 30 steers ion rays by angle ψ=−γ=−3.2 deg (in the x-z plane), thus reducing the inclination angle to the x-direction to α2=α1−ψ=1.5 deg, while aligning the ion packets time front 55 parallel with the Z-axis, i.e. γ=0. Much higher specific energies of the ion beam (e.g. UZ=57V as compared to 9V in the prior art) improves the ion admission into the OA and reduces the angular divergence Δα of ion packets, allowing denser folding of ion trajectories at smaller inclination angles, e.g. here at α2=α1−ψ=1.5 deg (as compared to the natural inclination angle α0=4.9 deg).
Table 1 below summarizes the equations for angles within the individual deflector 30 and wedge accelerator 40. Table 2 below presents conditions for compensation of the first order time-front tilt (T|Z=0) and of the chromatic spread of Z-velocity (α|K=0). It is of significant importance that both compensations are achieved simultaneously. This is a new finding by the inventor. The pair of wedge accelerator 40 and deflector 30 compensate multiple aberrations, including the first order time front tilt, the chromatic angular spread and, accounting focusing properties of gridless ion mirrors in example 51, the angular and spatial spreads of ion packets in the Y-direction.
Referring back to
Referring to
Example 60 illustrates spatial focusing of ion rays 61 for ion packets having an initial width in the z-dimension of Z0=10 mm, while not accounting angular spread of ion packets Δα=0 at ΔUZ=0 and not accounting relative energy spread of ion packets δ=ΔK/K=0 at ΔX=0. The chosen position of deflector 30 improves the ion packets bypassing of the deflector 30. The Matsuda plate voltage of the deflector 30 is electrically adjusted for geometrical focusing of ion packets onto the detector, which allows a denser folding of ion rays in MRTOF at α2=1.5 deg.
Example 62 illustrates angular divergence of ion rays 63 at ΔUZ=0.5V, while not accounting ion packets width Z0=0 and energy spread δ=0. Dual compensated deflector 30D (another novel component for MRTOF) helps spreading ion rays in-front of the detector 17 for bypassing the detector rims (here 5 mm).
Example 64 illustrates the (predicted by Table 4) simultaneous compensation of chromatic angular spread α|δ=0 and of the first order time-front tilt γ=0 at δ=0.05, ΔUZ=0, and Z0=0. Dark areas along the ion trajectories show lengths of ion packets due to the energy spread at equally spaced time intervals, and in particular time focusing after each reflection and at the detector.
Example 66 illustrates overall mass resolution RM=47,000 achieved in a compact 450×250 mm analyzer while accounting all realistic spreads of ion beam and ion packets, so as DET=1.5 ns time spread. The embodiment satisfies a goal of R>40,000 for resolving major isobars for μ=m/z<500 in GC-MS instruments.
Apparently, the injection mechanism 50 has a built-in and not yet fully appreciated virtue—an ability to compensate for mechanical imperfections of the MRTOF analyser by electrical tuning of the instrument, including adjustment of ion beam energies UZ, the pulse voltage on push plate 44, deflector 30 steering, or steering of continuous ion beam 41 to fit different equi-potentials 46.
Referring to
Referring to
Electrodes of sectors 82 and 83 are extended in the Z-direction to form two-dimensional fields in the XY-plane, i.e. they do not have laminating fields of the prior art. Sectors 82 and 83 have different radii and are arranged for isochronous cycled trajectory 81 (well seen in the view 86) with at least second order time per energy focusing, as described in WO (RMS).
As shown in view 87, continuous ion beam 41 propagates along the Z-axis at elevated specific energy UZ (expected from 20 to 50V). A compensated ion injection mechanism into MTTOF 80 is arranged with a wedge accelerator 40 and compensated deflector 30, similar to injection mechanism 50, described in
Embodiment 80 presents yet another novel ion optical solution a compensated reversing of ion trajectories in the drift Z-direction. The idea of time front compensation after reversing is similar to that shown in arrangement 35 of
Referring to
Deflectors 30 may be arranged anywhere downstream of the accelerator, which is illustrated by dashed ion rays between accelerator and deflector 30. However, to reduce the effect of ion packet angular divergence on compensation of time-front tilt, it is preferable to keep deflector 30 either immediately after the accelerator or after the first ion mirror reflection, or after the first electrostatic sector turn, or within the first full ion turn.
Example 90 presents an alternative spatial arrangement of the wedge accelerating field 45. An intermediate electrode 91 is tilted to produce the wedge at earlier stages of ion acceleration, though not immediately at ion starting point. Adjusting the potential of electrode 91 allows controlling the time front tilt angle γ electronically.
Example 92 presents an arrangement with an intermediate printed circuit board 93, having multiple electrode segments (in the x-direction) that are interconnected via a resistive chain for generating a wedge field structure similar to that in embodiment 90. The PCB embodiment 92 may provide a yet wider range of γ electronic tuning than 90.
Example 94 illustrates an application of the wedge accelerator to pulsed EI sources. Example 94 comprises an electron gun 95 and magnets B for controlling electron beam direction. Optionally, magnets may be tilted to align the electron beam with the tilted equipotential 46. Diverging electrodes within the EI source reduce the risk of electrode contamination by electron bombardment. Ions are produced by electron impact and are stored within the space charge field of the electron beam. Periodically electrical pulses are applied to tilted electrode 44. Example 94 provides compensated steering of ion rays past EI source, e.g. in order to bypass the accelerator and to adjust the inclination angle α of ion trajectories within an MRTOF or MTTOF analyser. The Matsuda plate potential in deflector 30 may be adjusted to control the ion packet spatial focusing.
Example 96 presents the application of the wedge accelerator to radio-frequency (RF) trap converters with radial ion ejection, known for their high (up to unity) duty cycle of pulsed conversion. The converter comprises side electrodes 97 at RF signal. The structure of electrodes 97 is better seen in the XY-plane. Ions are injected into the trap axially (in the x-direction) and are retained aligned with electrode 97 by the confining quadrupolar RF field of electrodes 97. In one (through) mode, the beam may propagate along equipotential 46 at small energy. In another (trapping) mode ions may be slowly dampened by gas at moderate mid-vacuum pressure (e.g. around 1 mTorr within several ms time). Ion packets are periodically ejected by energizing push plate 44. Tilting of push plate 44 controls the time-front tilt γ, which may be produced for compensating the downstream steering of time fronts by deflector 30. Example 96 provides compensated steering of ion rays past radial traps, e.g. in order to bypass the trap and to adjust the inclination angle α of ion trajectories within MRTOF or MTTOF analysers. The Matsuda plate potential in deflector 30 may be adjusted to control the ion packet spatial focusing. Note that to compensate T|ZZ aberrations at focusing in deflector 30 of substantially elongated ion packets, an additional compensating field curvature may be generated within accelerating field 45, either by curving electrode 97, or by curving of other trap electrodes, or by auxiliary fringing field, penetrating through or between trap electrodes.
Example 98 presents the application of the wedge accelerator to surface ionization methods, such as MALDI, SIMS, FAB, or particle bombardment, defined by the nature of primary beam 99—either photons, or pulsed packets of primary ions, or neutral particles or glow discharge or heavy particles or charged droplets. Electrode 44 may be energized static or pulsed, depending on the overall arrangement of prior art ionization methods. It is assumed that the exposed surface is relatively wide, either for imaging purposes or for improved sensitivity, so that ion packet width does affect the time-of-flight resolution, if ion packets are steered without compensation. Arranging wedge accelerator field 45, for example by tilting the target 44, is used here for compensating the time front tilt steering or for the spatial focusing of ion packets, or as a part of the surface imaging ion optics. Benefits of example 98 may be immediately seen by experts such as: (a) steering of ion packets allows the ion source bypassing and denser folding of ion trajectory in MPTOF analysers; (b) focusing by deflector 30 improves sensitivity; (c) unintentional tilt of the target 44 or some uneven topology of the sample on the target may be compensated electronically; (d) ion steering off the source axis allows an orthogonal arrangement of the impinging primary beam 99A; (e) compensated edge and curvature of accelerating field may be used for improving stigmatic properties of the overall imaging ion optics. Some further benefits are likely to be found, since the scheme allows fine and electronically adjustable control over the spatial focusing and the time-of-flight aberrations of the surface ionizing sources.
Annotations
Coordinates and Times:
Potentials and Fields:
Angles:
Aberration Coefficients
indexes are defined within the text
Although the present invention has been describing with reference to preferred embodiments, it will be apparent to those skilled in the art that various modifications in form and detail may be made without departing from the scope of the present invention as set forth in the accompanying claims.
Number | Date | Country | Kind |
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1712612 | Aug 2017 | GB | national |
1712613 | Aug 2017 | GB | national |
1712614 | Aug 2017 | GB | national |
1712616 | Aug 2017 | GB | national |
1712617 | Aug 2017 | GB | national |
1712618 | Aug 2017 | GB | national |
1712619 | Aug 2017 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/GB2018/052105 | 7/26/2018 | WO |
Publishing Document | Publishing Date | Country | Kind |
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WO2019/030477 | 2/14/2019 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3898452 | Hertel | Aug 1975 | A |
4390784 | Browning et al. | Jun 1983 | A |
4691160 | Ino | Sep 1987 | A |
4731532 | Frey et al. | Mar 1988 | A |
4855595 | Blanchard | Aug 1989 | A |
4970390 | Szymczak | Nov 1990 | A |
5017780 | Kutscher et al. | May 1991 | A |
5107109 | Stafford, Jr. et al. | Apr 1992 | A |
5128543 | Reed et al. | Jul 1992 | A |
5202563 | Cotter et al. | Apr 1993 | A |
5331158 | Dowell | Jul 1994 | A |
5367162 | Holland et al. | Nov 1994 | A |
5396065 | Myerholtz et al. | Mar 1995 | A |
5435309 | Thomas et al. | Jul 1995 | A |
5464985 | Cornish et al. | Nov 1995 | A |
5619034 | Reed et al. | Apr 1997 | A |
5652427 | Whitehouse et al. | Jul 1997 | A |
5654544 | Dresch | Aug 1997 | A |
5689111 | Dresch et al. | Nov 1997 | A |
5696375 | Park et al. | Dec 1997 | A |
5719392 | Franzen | Feb 1998 | A |
5763878 | Franzen | Jun 1998 | A |
5777326 | Rockwood et al. | Jul 1998 | A |
5834771 | Yoon et al. | Nov 1998 | A |
5847385 | Dresch | Dec 1998 | A |
5869829 | Dresch | Feb 1999 | A |
5896829 | Rothenberg et al. | Apr 1999 | A |
5955730 | Kerley et al. | Sep 1999 | A |
5994695 | Young | Nov 1999 | A |
6002122 | Wolf | Dec 1999 | A |
6013913 | Hanson | Jan 2000 | A |
6020586 | Dresch et al. | Feb 2000 | A |
6080985 | Welkie et al. | Jun 2000 | A |
6107625 | Park | Aug 2000 | A |
6160256 | Ishihara | Dec 2000 | A |
6198096 | Le Cocq | Mar 2001 | B1 |
6229142 | Bateman et al. | May 2001 | B1 |
6271917 | Hagler | Aug 2001 | B1 |
6300626 | Brock et al. | Oct 2001 | B1 |
6316768 | Rockwood et al. | Nov 2001 | B1 |
6337482 | Francke | Jan 2002 | B1 |
6384410 | Kawato | May 2002 | B1 |
6393367 | Tang et al. | May 2002 | B1 |
6437325 | Reilly et al. | Aug 2002 | B1 |
6455845 | Li et al. | Sep 2002 | B1 |
6469295 | Park | Oct 2002 | B1 |
6489610 | Barofsky et al. | Dec 2002 | B1 |
6504148 | Hager | Jan 2003 | B1 |
6504150 | Verentchikov et al. | Jan 2003 | B1 |
6534764 | Verentchikov et al. | Mar 2003 | B1 |
6545268 | Verentchikov et al. | Apr 2003 | B1 |
6570152 | Hoyes | May 2003 | B1 |
6576895 | Park | Jun 2003 | B1 |
6580070 | Cornish et al. | Jun 2003 | B2 |
6591121 | Madarasz et al. | Jul 2003 | B1 |
6614020 | Cornish | Sep 2003 | B2 |
6627877 | Davis et al. | Sep 2003 | B1 |
6646252 | Gonin | Nov 2003 | B1 |
6647347 | Roushall et al. | Nov 2003 | B1 |
6664545 | Kimmel et al. | Dec 2003 | B2 |
6683299 | Fuhrer et al. | Jan 2004 | B2 |
6694284 | Nikoonahad et al. | Feb 2004 | B1 |
6717132 | Franzen | Apr 2004 | B2 |
6734968 | Wang et al. | May 2004 | B1 |
6737642 | Syage et al. | May 2004 | B2 |
6744040 | Park | Jun 2004 | B2 |
6744042 | Zajfman et al. | Jun 2004 | B2 |
6747271 | Gonin et al. | Jun 2004 | B2 |
6770870 | Vestal | Aug 2004 | B2 |
6782342 | LeGore et al. | Aug 2004 | B2 |
6787760 | Belov et al. | Sep 2004 | B2 |
6794643 | Russ, IV et al. | Sep 2004 | B2 |
6804003 | Wang et al. | Oct 2004 | B1 |
6815673 | Plomley et al. | Nov 2004 | B2 |
6833544 | Campbell et al. | Dec 2004 | B1 |
6836742 | Brekenfeld | Dec 2004 | B2 |
6841936 | Keller et al. | Jan 2005 | B2 |
6861645 | Franzen | Mar 2005 | B2 |
6864479 | Davis et al. | Mar 2005 | B1 |
6870156 | Rather | Mar 2005 | B2 |
6870157 | Zare | Mar 2005 | B1 |
6872938 | Makarov et al. | Mar 2005 | B2 |
6888130 | Gonin | May 2005 | B1 |
6900431 | Belov et al. | May 2005 | B2 |
6906320 | Sachs et al. | Jun 2005 | B2 |
6940066 | Makarov et al. | Sep 2005 | B2 |
6949736 | Ishihara | Sep 2005 | B2 |
7034292 | Whitehouse et al. | Apr 2006 | B1 |
7071464 | Reinhold | Jul 2006 | B2 |
7084393 | Fuhrer et al. | Aug 2006 | B2 |
7091479 | Hayek | Aug 2006 | B2 |
7126114 | Chernushevich | Oct 2006 | B2 |
7196324 | Verentchikov | Mar 2007 | B2 |
7217919 | Boyle et al. | May 2007 | B2 |
7221251 | Menegoli et al. | May 2007 | B2 |
7326925 | Verentchikov et al. | Feb 2008 | B2 |
7351958 | Vestal | Apr 2008 | B2 |
7365313 | Fuhrer et al. | Apr 2008 | B2 |
7385187 | Verentchikov et al. | Jun 2008 | B2 |
7388197 | McLean et al. | Jun 2008 | B2 |
7399957 | Parker et al. | Jul 2008 | B2 |
7423259 | Hidalgo et al. | Sep 2008 | B2 |
7498569 | Ding | Mar 2009 | B2 |
7501621 | Willis et al. | Mar 2009 | B2 |
7504620 | Sato et al. | Mar 2009 | B2 |
7521671 | Kirihara et al. | Apr 2009 | B2 |
7541576 | Belov et al. | Jun 2009 | B2 |
7582864 | Verentchikov | Sep 2009 | B2 |
7608817 | Flory | Oct 2009 | B2 |
7663100 | Vestal | Feb 2010 | B2 |
7675031 | Konicek et al. | Mar 2010 | B2 |
7709789 | Vestal et al. | May 2010 | B2 |
7728289 | Naya et al. | Jun 2010 | B2 |
7745780 | McLean et al. | Jun 2010 | B2 |
7755036 | Satoh | Jul 2010 | B2 |
7772547 | Verentchikov | Aug 2010 | B2 |
7800054 | Fuhrer et al. | Sep 2010 | B2 |
7825373 | Willis et al. | Nov 2010 | B2 |
7863557 | Brown | Jan 2011 | B2 |
7884319 | Willis et al. | Feb 2011 | B2 |
7932491 | Vestal | Apr 2011 | B2 |
7982184 | Sudakov | Jul 2011 | B2 |
7985950 | Makarov et al. | Jul 2011 | B2 |
7989759 | Holle | Aug 2011 | B2 |
7999223 | Makarov et al. | Aug 2011 | B2 |
8017907 | Willis et al. | Sep 2011 | B2 |
8017909 | Makarov et al. | Sep 2011 | B2 |
8063360 | Willis et al. | Nov 2011 | B2 |
8080782 | Hidalgo et al. | Dec 2011 | B2 |
8093554 | Makarov | Jan 2012 | B2 |
8237111 | Golikov et al. | Aug 2012 | B2 |
8354634 | Green et al. | Jan 2013 | B2 |
8373120 | Verentchikov | Feb 2013 | B2 |
8395115 | Makarov et al. | Mar 2013 | B2 |
8492710 | Fuhrer et al. | Jul 2013 | B2 |
8513594 | Makarov | Aug 2013 | B2 |
8633436 | Ugarov | Jan 2014 | B2 |
8637815 | Makarov et al. | Jan 2014 | B2 |
8642948 | Makarov et al. | Feb 2014 | B2 |
8642951 | Li | Feb 2014 | B2 |
8648294 | Prather et al. | Feb 2014 | B2 |
8653446 | Mordehai et al. | Feb 2014 | B1 |
8658984 | Makarov et al. | Feb 2014 | B2 |
8680481 | Giannakopulos et al. | Mar 2014 | B2 |
8723108 | Ugarov | May 2014 | B1 |
8735818 | Kovtoun et al. | May 2014 | B2 |
8772708 | Kinugawa et al. | Jul 2014 | B2 |
8785845 | Loboda | Jul 2014 | B2 |
8847155 | Vestal | Sep 2014 | B2 |
8853623 | Verenchikov | Oct 2014 | B2 |
8884220 | Hoyes et al. | Nov 2014 | B2 |
8921772 | Verenchikov | Dec 2014 | B2 |
8952325 | Giles et al. | Feb 2015 | B2 |
8957369 | Makarov | Feb 2015 | B2 |
8975592 | Kobayashi et al. | Mar 2015 | B2 |
9048080 | Verenchikov et al. | Jun 2015 | B2 |
9082597 | Willis et al. | Jul 2015 | B2 |
9082604 | Verenchikov | Jul 2015 | B2 |
9099287 | Giannakopulos | Aug 2015 | B2 |
9136101 | Grinfeld et al. | Sep 2015 | B2 |
9147563 | Makarov | Sep 2015 | B2 |
9196469 | Makarov | Nov 2015 | B2 |
9207206 | Makarov | Dec 2015 | B2 |
9214322 | Kholomeev et al. | Dec 2015 | B2 |
9214328 | Hoyes et al. | Dec 2015 | B2 |
9281175 | Haufler et al. | Mar 2016 | B2 |
9312119 | Verenchikov | Apr 2016 | B2 |
9324544 | Rather | Apr 2016 | B2 |
9373490 | Nishiguchi et al. | Jun 2016 | B1 |
9396922 | Verenchikov et al. | Jul 2016 | B2 |
9417211 | Verenchikov | Aug 2016 | B2 |
9425034 | Verentchikov et al. | Aug 2016 | B2 |
9472390 | Verenchikov et al. | Oct 2016 | B2 |
9514922 | Watanabe et al. | Dec 2016 | B2 |
9576778 | Wang | Feb 2017 | B2 |
9595431 | Verenchikov | Mar 2017 | B2 |
9673033 | Grinfeld et al. | Jun 2017 | B2 |
9679758 | Grinfeld et al. | Jun 2017 | B2 |
9683963 | Verenchikov | Jun 2017 | B2 |
9728384 | Verenchikov | Aug 2017 | B2 |
9779923 | Verenchikov | Oct 2017 | B2 |
9786484 | Willis et al. | Oct 2017 | B2 |
9786485 | Ding et al. | Oct 2017 | B2 |
9865441 | Damoc et al. | Jan 2018 | B2 |
9865445 | Verenchikov et al. | Jan 2018 | B2 |
9870903 | Richardson et al. | Jan 2018 | B2 |
9870906 | Quarmby et al. | Jan 2018 | B1 |
9881780 | Verenchikov et al. | Jan 2018 | B2 |
9899201 | Park | Feb 2018 | B1 |
9922812 | Makarov | Mar 2018 | B2 |
9941107 | Verenchikov | Apr 2018 | B2 |
9972483 | Makarov | May 2018 | B2 |
10006892 | Verenchikov | Jun 2018 | B2 |
10037873 | Wang et al. | Jul 2018 | B2 |
10141175 | Verentchikov et al. | Nov 2018 | B2 |
10141176 | Stewart et al. | Nov 2018 | B2 |
10163616 | Verenchikov et al. | Dec 2018 | B2 |
10186411 | Makarov | Jan 2019 | B2 |
10192723 | Verenchikov et al. | Jan 2019 | B2 |
10290480 | Crowell et al. | May 2019 | B2 |
10373815 | Crowell et al. | Aug 2019 | B2 |
10388503 | Brown et al. | Aug 2019 | B2 |
10593525 | Hock et al. | Mar 2020 | B2 |
10593533 | Hoyes et al. | Mar 2020 | B2 |
10622203 | Veryovkin et al. | Apr 2020 | B2 |
10629425 | Hoyes et al. | Apr 2020 | B2 |
10636646 | Hoyes et al. | Apr 2020 | B2 |
20010011703 | Franzen | Aug 2001 | A1 |
20010030284 | Dresch et al. | Oct 2001 | A1 |
20020030159 | Chernushevich et al. | Mar 2002 | A1 |
20020107660 | Nikoonahad et al. | Aug 2002 | A1 |
20020190199 | Li | Dec 2002 | A1 |
20030010907 | Hayek et al. | Jan 2003 | A1 |
20030111597 | Gonin et al. | Jun 2003 | A1 |
20030232445 | Fulghum | Dec 2003 | A1 |
20040026613 | Bateman et al. | Feb 2004 | A1 |
20040084613 | Bateman et al. | May 2004 | A1 |
20040108453 | Kobayashi et al. | Jun 2004 | A1 |
20040119012 | Vestal | Jun 2004 | A1 |
20040144918 | Zare et al. | Jul 2004 | A1 |
20040155187 | Axelsson | Aug 2004 | A1 |
20040159782 | Park | Aug 2004 | A1 |
20040183007 | Belov et al. | Sep 2004 | A1 |
20050006577 | Fuhrer et al. | Jan 2005 | A1 |
20050040326 | Enke | Feb 2005 | A1 |
20050103992 | Yamaguchi et al. | May 2005 | A1 |
20050133712 | Belov et al. | Jun 2005 | A1 |
20050151075 | Brown et al. | Jul 2005 | A1 |
20050194528 | Yamaguchi et al. | Sep 2005 | A1 |
20050242279 | Verentchikov | Nov 2005 | A1 |
20050258364 | Whitehouse et al. | Nov 2005 | A1 |
20060024720 | McLean et al. | Feb 2006 | A1 |
20060169882 | Pau et al. | Aug 2006 | A1 |
20060214100 | Verentchikov et al. | Sep 2006 | A1 |
20060289746 | Raznikov et al. | Dec 2006 | A1 |
20070023645 | Chernushevich | Feb 2007 | A1 |
20070029473 | Verentchikov | Feb 2007 | A1 |
20070176090 | Verentchikov | Aug 2007 | A1 |
20070187614 | Schneider et al. | Aug 2007 | A1 |
20070194223 | Sato et al. | Aug 2007 | A1 |
20080049402 | Han et al. | Feb 2008 | A1 |
20080121796 | Green et al. | May 2008 | A1 |
20080197276 | Nishiguchi et al. | Aug 2008 | A1 |
20080203288 | Makarov et al. | Aug 2008 | A1 |
20080290269 | Saito et al. | Nov 2008 | A1 |
20090090861 | Willis et al. | Apr 2009 | A1 |
20090114808 | Bateman et al. | May 2009 | A1 |
20090121130 | Satoh | May 2009 | A1 |
20090206250 | Wollnik | Aug 2009 | A1 |
20090250607 | Staats et al. | Oct 2009 | A1 |
20090272890 | Ogawa et al. | Nov 2009 | A1 |
20090294658 | Vestal | Dec 2009 | A1 |
20090314934 | Brown | Dec 2009 | A1 |
20100001180 | Bateman et al. | Jan 2010 | A1 |
20100044558 | Sudakov | Feb 2010 | A1 |
20100072363 | Giles et al. | Mar 2010 | A1 |
20100078551 | Loboda | Apr 2010 | A1 |
20100096543 | Kenny et al. | Apr 2010 | A1 |
20100108878 | Bateman et al. | May 2010 | A1 |
20100140469 | Nishiguchi | Jun 2010 | A1 |
20100193682 | Golikov et al. | Aug 2010 | A1 |
20100207023 | Loboda | Aug 2010 | A1 |
20100301202 | Vestal | Dec 2010 | A1 |
20110133073 | Sato et al. | Jun 2011 | A1 |
20110168880 | Ristroph et al. | Jul 2011 | A1 |
20110180702 | Flory et al. | Jul 2011 | A1 |
20110180705 | Yamaguchi | Jul 2011 | A1 |
20110186729 | Verentchikov et al. | Aug 2011 | A1 |
20120168618 | Vestal | Jul 2012 | A1 |
20120261570 | Shvartsburg et al. | Oct 2012 | A1 |
20120298853 | Kurulugama et al. | Nov 2012 | A1 |
20130048852 | Verenchikov | Feb 2013 | A1 |
20130056627 | Verenchikov | Mar 2013 | A1 |
20130068942 | Verenchikov | Mar 2013 | A1 |
20130161506 | Ugarov | Jun 2013 | A1 |
20130187044 | Ding et al. | Jul 2013 | A1 |
20130206978 | Verenchikov | Aug 2013 | A1 |
20130240725 | Makarov | Sep 2013 | A1 |
20130248702 | Makarov | Sep 2013 | A1 |
20130256524 | Brown | Oct 2013 | A1 |
20130313424 | Makarov et al. | Nov 2013 | A1 |
20130327935 | Wiedenbeck | Dec 2013 | A1 |
20140054454 | Hoyes et al. | Feb 2014 | A1 |
20140054456 | Kinugawa et al. | Feb 2014 | A1 |
20140084156 | Ristroph et al. | Mar 2014 | A1 |
20140117226 | Giannakopulos | May 2014 | A1 |
20140138538 | Hieftje et al. | May 2014 | A1 |
20140183354 | Moon et al. | Jul 2014 | A1 |
20140191123 | Wildgoose et al. | Jul 2014 | A1 |
20140239172 | Makarov | Aug 2014 | A1 |
20140246575 | Langridge | Sep 2014 | A1 |
20140291503 | Shchepunov et al. | Oct 2014 | A1 |
20140312221 | Verenchikov et al. | Oct 2014 | A1 |
20140361162 | Murray et al. | Dec 2014 | A1 |
20150028197 | Grinfeld et al. | Jan 2015 | A1 |
20150028198 | Grinfeld et al. | Jan 2015 | A1 |
20150034814 | Brown et al. | Feb 2015 | A1 |
20150048245 | Vestal et al. | Feb 2015 | A1 |
20150060656 | Ugarov | Mar 2015 | A1 |
20150122986 | Haase | May 2015 | A1 |
20150144779 | Verenchikov | May 2015 | A1 |
20150194296 | Verenchikov et al. | Jul 2015 | A1 |
20150228467 | Grinfeld et al. | Aug 2015 | A1 |
20150270115 | Furuhashi | Sep 2015 | A1 |
20150279650 | Verenchikov | Oct 2015 | A1 |
20150294849 | Makarov et al. | Oct 2015 | A1 |
20150318156 | Loyd et al. | Nov 2015 | A1 |
20150364309 | Welkie | Dec 2015 | A1 |
20150380206 | White et al. | Dec 2015 | A1 |
20150380233 | Verenchikov | Dec 2015 | A1 |
20160005587 | Verenchikov | Jan 2016 | A1 |
20160035558 | Verenchikov et al. | Feb 2016 | A1 |
20160079052 | Makarov | Mar 2016 | A1 |
20160225598 | Ristroph | Aug 2016 | A1 |
20160225602 | Ristroph et al. | Aug 2016 | A1 |
20160240363 | Verenchikov | Aug 2016 | A1 |
20170016863 | Verenchikov | Jan 2017 | A1 |
20170025265 | Verenchikov et al. | Jan 2017 | A1 |
20170032952 | Verenchikov | Feb 2017 | A1 |
20170084443 | Willis et al. | Mar 2017 | A1 |
20170098533 | Stewart et al. | Apr 2017 | A1 |
20170168031 | Verenchikov | Jun 2017 | A1 |
20170229297 | Green et al. | Aug 2017 | A1 |
20170338094 | Verenchikov et al. | Nov 2017 | A1 |
20180144921 | Hoyes et al. | May 2018 | A1 |
20180315589 | Oshiro | Nov 2018 | A1 |
20180330936 | Hoyes et al. | Nov 2018 | A1 |
20180366312 | Hamish et al. | Dec 2018 | A1 |
20180366313 | Hoyes et al. | Dec 2018 | A1 |
20190019664 | Furuhashi | Jan 2019 | A1 |
20190180998 | Stewart et al. | Jun 2019 | A1 |
20190206669 | Verenchikov et al. | Jul 2019 | A1 |
20190237318 | Brown | Aug 2019 | A1 |
20190360981 | Verenchikov | Nov 2019 | A1 |
20200083034 | Hoyes et al. | Mar 2020 | A1 |
20200090919 | Artaev et al. | Mar 2020 | A1 |
20200126781 | Kovtoun | Apr 2020 | A1 |
20200152440 | Hoyes et al. | May 2020 | A1 |
20200168447 | Verenchikov | May 2020 | A1 |
20200168448 | Verenchikov et al. | May 2020 | A1 |
20200243322 | Stewart et al. | Jul 2020 | A1 |
20200373142 | Verenchikov | Nov 2020 | A1 |
20200373143 | Verenchikov et al. | Nov 2020 | A1 |
20200373145 | Verenchikov et al. | Nov 2020 | A1 |
Number | Date | Country |
---|---|---|
2412657 | May 2003 | CA |
101171660 | Apr 2008 | CN |
101369510 | Feb 2009 | CN |
101523548 | Sep 2009 | CN |
102131563 | Jul 2011 | CN |
201946564 | Aug 2011 | CN |
102884608 | Jan 2013 | CN |
103270574 | Aug 2013 | CN |
104067116 | Sep 2014 | CN |
104508475 | Apr 2015 | CN |
105206500 | Dec 2015 | CN |
106463337 | Feb 2017 | CN |
107636795 | Jan 2018 | CN |
107833823 | Mar 2018 | CN |
107851549 | Mar 2018 | CN |
108292587 | Jul 2018 | CN |
4310106 | Oct 1994 | DE |
10116536 | Oct 2002 | DE |
102015121830 | Jun 2017 | DE |
102019129108 | Jun 2020 | DE |
112015001542 | Jul 2020 | DE |
0237259 | Sep 1987 | EP |
1137044 | Sep 2001 | EP |
1566828 | Aug 2005 | EP |
1901332 | Mar 2008 | EP |
2068346 | Jun 2009 | EP |
1665326 | Apr 2010 | EP |
1789987 | Sep 2010 | EP |
1522087 | Mar 2011 | EP |
2599104 | Jun 2013 | EP |
1743354 | Aug 2019 | EP |
3662501 | Jun 2020 | EP |
3662502 | Jun 2020 | EP |
3662503 | Jun 2020 | EP |
2080021 | Jan 1982 | GB |
2217907 | Nov 1989 | GB |
2274197 | Jul 1994 | GB |
2300296 | Oct 1996 | GB |
2390935 | Jan 2004 | GB |
2396742 | Jun 2004 | GB |
2403063 | Dec 2004 | GB |
2455977 | Jul 2009 | GB |
2476964 | Jul 2011 | GB |
2478300 | Sep 2011 | GB |
2484361 | Apr 2012 | GB |
2484429 | Apr 2012 | GB |
2485825 | May 2012 | GB |
2489094 | Sep 2012 | GB |
2490571 | Nov 2012 | GB |
2495127 | Apr 2013 | GB |
2495221 | Apr 2013 | GB |
2496991 | May 2013 | GB |
2496994 | May 2013 | GB |
2500743 | Oct 2013 | GB |
2501332 | Oct 2013 | GB |
2506362 | Apr 2014 | GB |
2528875 | Feb 2016 | GB |
2555609 | May 2018 | GB |
2556451 | May 2018 | GB |
2556830 | Jun 2018 | GB |
2562990 | Dec 2018 | GB |
2575157 | Jan 2020 | GB |
2575339 | Jan 2020 | GB |
2595530 | Dec 2021 | GB |
2610692 | Mar 2023 | GB |
S6229049 | Feb 1987 | JP |
2000036285 | Feb 2000 | JP |
2000048764 | Feb 2000 | JP |
2001297730 | Oct 2001 | JP |
2003031178 | Jan 2003 | JP |
2003502803 | Jan 2003 | JP |
3571546 | Sep 2004 | JP |
2005538346 | Dec 2005 | JP |
2006049273 | Feb 2006 | JP |
2007227042 | Sep 2007 | JP |
2010062152 | Mar 2010 | JP |
4649234 | Mar 2011 | JP |
2011119279 | Jun 2011 | JP |
4806214 | Nov 2011 | JP |
2013528892 | Jul 2013 | JP |
2013539590 | Oct 2013 | JP |
5555582 | Jul 2014 | JP |
2015506567 | Mar 2015 | JP |
2015521349 | Jul 2015 | JP |
2015185306 | Oct 2015 | JP |
2564443 | Oct 2015 | RU |
2015148627 | May 2017 | RU |
2660655 | Jul 2018 | RU |
198034 | Jun 1967 | SU |
1681340 | Sep 1991 | SU |
1725289 | Apr 1992 | SU |
9103071 | Mar 1991 | WO |
98001218 | Jan 1998 | WO |
98008244 | Feb 1998 | WO |
0077823 | Dec 2000 | WO |
2005001878 | Jan 2005 | WO |
2005043575 | May 2005 | WO |
2006049623 | May 2006 | WO |
2006102430 | Sep 2006 | WO |
2006103448 | Oct 2006 | WO |
2007044696 | Apr 2007 | WO |
2007104992 | Sep 2007 | WO |
2007136373 | Nov 2007 | WO |
2008046594 | Apr 2008 | WO |
2008087389 | Jul 2008 | WO |
2010008386 | Jan 2010 | WO |
2010034630 | Apr 2010 | WO |
2010138781 | Dec 2010 | WO |
2011086430 | Jul 2011 | WO |
2011107836 | Sep 2011 | WO |
2011135477 | Nov 2011 | WO |
2012010894 | Jan 2012 | WO |
2012023031 | Feb 2012 | WO |
2012024468 | Feb 2012 | WO |
2012024570 | Feb 2012 | WO |
2012116765 | Sep 2012 | WO |
2013045428 | Apr 2013 | WO |
2013063587 | May 2013 | WO |
2013067366 | May 2013 | WO |
2013093587 | Jun 2013 | WO |
2013098612 | Jul 2013 | WO |
2013110587 | Aug 2013 | WO |
2013110588 | Aug 2013 | WO |
2013124207 | Aug 2013 | WO |
2014021960 | Feb 2014 | WO |
2014074822 | May 2014 | WO |
2014110697 | Jul 2014 | WO |
2014142897 | Sep 2014 | WO |
2014152902 | Sep 2014 | WO |
2015142897 | Sep 2015 | WO |
2015152968 | Oct 2015 | WO |
2015153622 | Oct 2015 | WO |
2015153630 | Oct 2015 | WO |
2015153644 | Oct 2015 | WO |
2015175988 | Nov 2015 | WO |
2015189544 | Dec 2015 | WO |
2016064398 | Apr 2016 | WO |
2016174462 | Nov 2016 | WO |
2016178029 | Nov 2016 | WO |
2017042665 | Mar 2017 | WO |
2017087470 | May 2017 | WO |
2018073589 | Apr 2018 | WO |
2018109920 | Jun 2018 | WO |
2018124861 | Jul 2018 | WO |
2018183201 | Oct 2018 | WO |
2019030472 | Feb 2019 | WO |
2019030474 | Feb 2019 | WO |
2019030475 | Feb 2019 | WO |
2019030476 | Feb 2019 | WO |
2019030477 | Feb 2019 | WO |
2019058226 | Mar 2019 | WO |
2019162687 | Aug 2019 | WO |
2019202338 | Oct 2019 | WO |
2019229599 | Dec 2019 | WO |
2020002940 | Jan 2020 | WO |
2020021255 | Jan 2020 | WO |
2020121167 | Jun 2020 | WO |
2020121168 | Jun 2020 | WO |
2023285791 | Jan 2023 | WO |
Entry |
---|
Hoyes et al., “Electrostatic gimbal for correction of errors in Time of Flight mass spectrometers”, Waters, 2013 (Year: 2013). |
International Search Report and Written Opinion for International Application No. PCT/US2016/062174 dated Mar. 3, 2017, 8 pages. |
IPRP PCT/US2016/062174 issued May 22, 2018, 6 pages. |
Search Report for GB Application No. GB1520130.4 dated May 25, 2016. |
International Search Report and Written Opinion for International Application No. PCT/US2016/062203 dated Mar. 5, 2017, 8 pages. |
Search Report for GB Application No. GB1520134.6 dated May 26, 2016. |
IPRP PCT/US2016/062203, issued May 22, 2018, 6 pages. |
Search Report Under Section 17(5) for Application No. GB1507363.8 dated Nov. 9, 2015. |
International Search Report and Written Opinion of the International Search Authority for Application No. PCT/GB2016/051238 dated Jul. 12, 2016, 16 pages. |
IPRP for application PCT/GB2016/051238 dated Oct. 31, 2017, 13 pages. |
International Search Report and Written Opinion for International Application No. PCT/US2016/063076 dated Mar. 30, 2017, 9 pages. |
Search Report for GB Application No. 1520540.4 dated May 25, 2016. |
IPRP for application PCT/US2016/063076, dated May 29, 2018, 7 pages. |
IPRP PCT/GB17/51981 dated Jan. 8, 2019, 7 pages. |
International Search Report and Written Opinion for International Application No. PCT/GB2018/051206, dated Jul. 12, 2018, 9 pages. |
Author unknown, “Electrostatic lens,” Wikipedia, Mar. 31, 2017 (Mar. 31, 2017), XP055518392, Retrieved from the Intemet URL https://en.wikipedia.org/w/index.phptitle=Electrostaticlens oldid=773161674[retrieved on Oct. 24, 2018]. |
Hussein, O.A. et al., “Study the most favorable shapes of electrostatic quadrupole doublet lenses”, AIP Conference Proceedings, vol. 1815, Feb. 17, 2017 (Feb. 17, 2017), p. 110003. |
Guan S., et al., “Stacked-ring electrostatic ion guide”, Journal of the American Society for Mass Spectrometry, Elsevier Science Inc, 7(1):101-106 (1996). |
Scherer, S., et al., “A novel principle for an ion mirror design in time-of-flight mass spectrometry”, International Journal of Mass Spectrometry, Elsevier Science Publishers, Amsterdam, NL, vol. 251, No. 1, Mar. 15, 2006. |
International Search Report and Written Opinion for application No. PCT/GB2018/052104, dated Oct. 31, 2018, 14 pages. |
International Search Report and Written Opinion for application No. PCT/GB2018/052105, dated Oct. 15, 2018, 18 pages. |
International Search Report and Written Opinion for application PCT/GB2018/052100, dated Oct. 19, 2018, 19 pages. |
International Search Report and Written Opinion for application PCT/GB2018/052102, dated Oct. 25, 2018, 14 pages. |
International Search Report and Written Opinion for application No. PCT/GB2018/052099, dated Oct. 10, 2018, 16 pages. |
International Search Report and Written Opinion for application No. PCT/GB2018/052101, dated Oct. 19, 2018, 15 pages. |
Combined Search and Examination Report under Sections 17 and 18(3) for application GB1807605.9, dated Oct. 29, 2018, 5 pages. |
Combined Search and Examination Report under Sections 17 and 18(3) for application GB1807626.5, dated Oct. 29, 2018, 7 pages. |
Yavor, M.I., et al., “High performance gridless ion mirrors for multi-reflection time-of-flight and electrostatic trap mass analyzers”, International Journal of Mass Spectrometry, vol. 426, Mar. 2018, pp. 1-11. |
Search Report under Section 17(5) for application GB1707208.3, dated Oct. 12. 2017, 5 pages. |
Communication Relating to the Results of the Partial International Search for International Application No. PCT/GB2019/01118, dated Jul. 19, 2019, 25 pages. |
Doroshenko, V.M., and Cotter, R.J., “Ideal velocity focusing in a reflectron time-of-flight mass spectrometer”, American Society for Mass Spectrometry, 10(10):992-999 (1999). |
Kozlov, B. et al. “Enhanced Mass Accuracy in Multi-Reflecting TOF MS” www.waters.com/Posters, ASMS Conference (2017). |
Kozlov, B. et al. “Multiplexed Operation of an Orthogonal Multi-Reflecting TOF Instrument to Increase Duty Cycle by Two Orders” ASMS Conference, San Diego, CA, Jun. 6, 2018. |
Kozlov, B. et al. “High accuracy self-calibration method for high resolution mass spectra” ASMS Conference Abstract, 2019. |
Kozlov, B. et al. “Fast Ion Mobility Spectrometry and High Resolution TOF MS” ASMS Conference Poster (2014). |
Verenchicov, A. N. “Parallel MS-MS Analysis in a Time-Flight Tandem. Problem Statement, Method, and Instrumental Schemes” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2004). |
Yavor, M. I. “Planar Multireflection Time-Of-Flight Mass Analyzer with Unlimited Mass Range” Institute for Analytical nstrumentation RAS, Saint-Petersburg, (2004). |
Khasin, Y. I. et al., “Initial Experimental Studies of a Planar Multireflection Time-Of-Flight Mass Spectrometer” Institute tor Analytical Instrumentation RAS, Saint-Petersburg, (2004). |
Verenchicov, A. N. et al. “Stability of Ion Motion in Periodic Electrostatic Fields” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2004). |
Verenchicov, A. N. “The Concept of Multireflecting Mass Spectrometer for Continuous Ion Sources” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2006). |
Verenchicov, A. N., et al. “Accurate Mass Measurements for Interpreting Spectra of atmospheric Pressure Ionization” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2006). |
Kozlov, B. N. et al., “Experimental Studies of Space Charge Effects in Multireflecting Time-Of-Flight Mass Spectrometes” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2006). |
Kozlov, B. N. et al., “Multireflecting Time-Of-Flight Mass Spectrometer With an Ion Trap Source” Institute for Analytical nstrumentation RAS, Saint-Petersburg, (2006). |
Hasin, Y. I., et al.,“Planar Time-Of-Flight Multireflecting Mass Spectrometer with an Orthogonal Ion Injection Out of Continuous Ion Sources” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2006). |
Lutvinsky, Y. I., et al., “Estimation of Capacity of High Resolution Mass Spectra for Analysis of Complex Mixtures” Institute for Analytical Instrumentation RAS, Saint-Petersburg, (2006). |
International Search Report and Written Opinion for International appliication No. PCT/GB2020/050209, dated Apr. 28, 2020, 12 pages. |
Verenchicov., A. N. et al. “Multiplexing in Multi-Reflecting TOF MS” Journal of Applied Solution Chemistry and Modeling, 6:1-22 (2017). |
Supplementary Partial EP Search Report for EP Application No. 16869126.9, dated Jun. 13, 2019. |
Supplementary Partial EP Search Report for EP Application No. 16866997.6, dated Oct. 16, 2019. |
Wikipedia “Reflectron”, Oct. 9, 2015, Retrieved from the Internet URL https://en.wikipedia.org/wlindex.php?title=Reflectron&oldid=684843442 [retrieved on May 29, 2019]. |
Toyoda, M. et al., “Multi-turn time-of-flight mass spectrometers with electrostatic sectors,” Journal of Mass Spectrometry, 38:1125-1142(2003). |
IPRP for International application No. PCT/GB2018/051206, dated Nov. 5, 2019, 7 pages. |
International Search Report and Written Opinion for International Application No. PCT/EP2017/070508 dated Oct. 16, 2017, 17 pages. |
Search Report for United Kingdom Application No. GB1613988.3 dated Jan. 5, 2017, 4 pages. |
Wouters et al., “Optical Design of the TOFI (Time-of-Flight Isochronous) Spectrometer for Mass Measurements of Exotic Nuclei”, Nuclear Instruments and Methods in Physics Research, Section A, 240(1): 77-90, Oct. 1, 1985. |
Combined Search and Examination Report for United Kingdom Application No. GB1901411.7 dated Jul. 31, 2019. |
Examination Report for United Kingdom Application No. GB1618980.5 dated Jul. 25, 2019. |
Combined Search and Examination Report for GB 1906258.7, dated Oct. 25, 2019. |
Combined Search and Examination Report for GB1906253.8, dated Oct. 30, 2019. |
Search Report under Section 17(5) for GB1916445.8, dated Jun. 15, 2020. |
Extended European Search Report for EP Patent Application No. 16866997.6 dated Oct. 16, 2019. |
International Search Report and Written Opinion for International Application No. PCT/GB2019/051234 dated Jul. 29, 2019. |
International Search Report and Written Opinion for International Application No. PCT/GB2019/051839 dated Sep. 18, 2019. |
International Search Report and Written Opinion for International Application No. PCT/GB20180051320 dated Aug. 1, 2018. |
Stresau, D., et al., “Ion Counting Beyond 10ghz Using a New Detector and Conventional Electronics”, European Winter Conference on Plasma Spectrochemistry, Feb. 4-8, 2001, Lillehammer, Norway, Retrieved from the Internet URL htps://www.etp-ms.com/file-repository/21 [retrieved on Jul. 31, 2019]. |
Kaufmann, R., et al., “Sequencing of peptides in a time-of-flight mass spectrometer: evaluation of postsource decay Following matrix-assisted laser desorption ionisation (MALDI)”, International Journal of Mass Spectrometry and Ion Processes, Elsevier Scientific Publishing Co. Amsterdam, NL, 131:355-385, Feb. 24, 1994. |
International Search Report and Written Opinion for International Application No. PCT/GB2018/051320 dated Aug. 1, 2018, 10 pages. |
Shaulis, Barry, et al., “Signal linearity of an extended range pulse counting detector: Applications to accurate and precise U-Pb dating of zircon by laser ablation quadrupole ICP-MS”, G3: Geochemistry, Geophysics, Geosystems, 11(11):1-12, Nov. 20, 2010. |
Search Report for United Kingdom Application No. GB1708430.2 dated Nov. 28, 2017. |
Sakurai, T, et al., “A new multi-passage time-of-flight mass spectrometer at JAIST”, Nuclear Instruments and Methods in Physics Research A: Accelerators, Spectrometers, Detectors and Associated Equipment, 427(1-2):182-186 (1999). |
International Search Report and Written Opinion for International application No. PCT/GB2019/051235, dated Sep. 25, 2019, 22 pages. |
International Search Report and Written Opinion for International application No. PCT/GB2019/051416, dated Oct. 10, 2019, 22 pages. |
Search and Examination Report under Sections 17 and 18(3) for Application No. GB 1906258.7, dated Dec. 11, 2020, 7 pages. |
Carey, D.C., “Why a second-order magnetic optical achromat works”, Nucl. Instrum. Meth., 189(203):365-367 (1981). Abstract. |
Sakurai, T. et al., “Ion optics for time-of-flight mass spectrometers with multiple symmetry”, Int J Mass Spectrom Ion Proc 63(2-3):273-287 (1985). Abstract. |
Wollnik, H., and Casares, A., “An energy-isochronous multi-pass time-of-flight mass spectrometer consisting of two coaxial electrostatic mirrors”, Int J Mass Spectrom 227:217-222 (2003). Abstract. |
Author unknown, “Einzel Lens”, Wikipedia [online] Nov. 2020 [retrieved on Nov. 3, 2020]. Retrieved from Intemet URL: https://en.wikipedia.org/wiki/Einzel_lens, 2 pages. |
O'Halloran, G.J., et al., “Determination of Chemical Species Prevalent in a Plasma Jet”, Bendix Corp Report ASD-TDR-62-644, U.S. Air Force (1964). Abstract. |
Examination Report under Section 18(3) for Application No. GB1906258.7, dated May 5, 2021, 4 pages. |
Collision Frequency, https://en.wikipedia.org/wiki/Collision_frequency accessed Aug. 17, 2021. |
International Search Report and Written Opinion for International Application No. PCT/GB2020/050471, dated May 13, 2020, 9 pages. |
Search Report for GB Application No. GB2002768.6 dated Jul. 7, 2020. |
Search Report for GB Application No. GB 1903779.5, dated Sep. 20, 2019. |
Verentchikov, A., et al., “Stable ion beam transport through periodic electrostatic structures: linear and non-linear effects”, Physics Procedia, 1(1):87-97, Aug. 2008. |
Willis, P. et al., “Improving duty cycle in the Folded Flight Path high-resolution time-of-flight mass spectrometer”, International Journal of Mass Spectrometry, vol. 459, 116467, Nov. 1, 2020. |
Number | Date | Country | |
---|---|---|---|
20200373145 A1 | Nov 2020 | US |