[0001] The present invention relates to mass spectrometers and methods of mass spectrometry.
[0002] Ion guides comprising rf-only multipole rod sets such as quadrupoles, hexapoles and
octopoles are well known.
[0003] Whitehouse and co-workers have disclosed in WO98/06481 and WO99/62101 an arrangement
wherein a multipole rod set ion guide extends between two vacuum chambers. However,
as will be appreciated by those skilled in the art, since each rod in a multipole
rod set has a typical diameter of around 5 mm, and a space must be provided between
opposed rods in order for there to be an ion guiding region, then the interchamber
aperture when using such an arrangement is correspondingly very large (i.e. > 15 mm
in diameter) with a corresponding cross sectional area > 150 mm
2. Such large interchamber apertures drastically reduce the effectiveness of the vacuum
pumps which are most effective when the interchamber orifice is as small as possible
(i.e. only a few millimetres in diameter).
[0004] It is therefore desired to provide an improved interchamber ion guide.
[0005] According to a first aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 1.
[0006] Conventional arrangements typically provide two discrete multipole ion guides in
adjacent vacuum chambers with a differential pumping aperture therebetween. Such an
arrangement suffers from a disruption to the rf field near the end of a multipole
rod set and other end effects. However, according to the preferred embodiment of the
present invention, the ions do not leave the ion guide as they pass from one vacuum
chamber to another. Accordingly, end effect problems are effectively eliminated thereby
resulting in improved ion transmission.
[0007] An ion guide comprised of electrodes having apertures may take two main different
forms. In a first form all the internal apertures of the electrodes are substantially
the same size. Such an arrangement is known as an "ion tunnel". However, a second
form referred to as an "ion funnel" is known wherein the electrodes have internal
apertures which become progressively smaller in size. Both forms are intended to fall
within the scope of the present invention. The apertured electrodes in either case
may comprise ring or annular electrodes. The inner circumference of the electrodes
is preferably substantially circular. However, the outer circumference of the electrodes
does not need to be circular and embodiments of the present invention are contemplated
wherein the outer profile of the electrodes takes on other shapes.
[0008] The preferred embodiment of the present invention uses an ion tunnel ion guide and
it has been found that an ion tunnel ion guide exhibits an approximately 25-75% improvement
in ion transmission efficiency compared with a conventional multipole, e.g. hexapole,
ion guide of comparable length. The reasons for this enhanced ion transmission efficiency
are not fully understood, but it is thought that the ion tunnel may have a greater
acceptance angle and a greater acceptance area than a comparable multipole rod set
ion guide.
[0009] Accordingly, one advantage of the preferred embodiment is an improvement in ion transmission
efficiency.
[0010] Although an ion tunnel ion guide is preferred, according to a less preferred embodiment,
the inter-vacuum chamber ion guide may comprise an ion funnel. In order to act as
an ion guide, a dc potential gradient is applied along the length of the ion funnel
in order to urge ions through the progressively smaller internal apertures of the
electrodes. The ion funnel is believed however to suffer from a narrow mass to charge
ratio bandpass transmission efficiency. Such problems are not found when using an
ion tunnel ion guide.
[0011] Various types of other ion optical devices are also known including multipole rod
sets, Einzel lenses, segmented multipoles, short (solid) quadrupole pre/post filter
lenses ("stubbies"), 3D quadrupole ion traps comprising a central doughnut shaped
electrode together with two concave end cap electrodes, and linear (2D) quadrupole
ion traps comprising a multipole rod set with entrance and exit ring electrodes. However,
such devices are not intended to fall within the scope of the present invention.
[0012] According to a particularly preferred feature of the present invention, one of the
electrodes forming the ion guide may form or constitute a differential pumping aperture
between two vacuum chambers. Such an arrangement is particularly advantageous since
it allows the interchamber orifice to be much smaller than that which would be provided
if a multipole rod set ion guide were used. A smaller interchamber orifice allows
the vacuum pumps pumping each vacuum chamber to operate more efficiently.
[0013] The electrode forming the differential pumping aperture may either have an internal
aperture of different size (e.g. smaller) than the other electrodes forming the ion
guide or may have the same sized internal aperture. The electrode forming the differential
pumping aperture and/or the other electrodes may have an internal diameter selected
from the group comprising: (i) 0.5-1.5 mm; (ii) 1.5-2.5 mm; (iii) 2.5-3.5 mm; (iv)
3.5-4.5 mm; (v) 4.5-5.5 mm; (vi) 5.5-6.5 mm; (vii) 6.5-7.5 mm; (viii) 7.5-8.5 mm;
(ix) 8.5-9.5 mm; (x) 9.5-10.5 mm; (xi) ≤ 10.0 mm; (xii) ≤ 9.0 mm; (xiii) ≤ 8.0 mm;
(xiv) ≤ 7.0 mm; (xv) ≤ 6.0 mm; (xvi) ≤ 5.0 mm; (xvii) ≤ 4.0 mm; (xviii) ≤ 3.0 mm;
(xix) ≤ 2.0 mm; (xx) ≤ 1.0 mm; (xxi) 0-2 mm; (xxii) 2-4 mm; (xxiii) 4-6 mm; (xxiv)
6-8 mm; and (xxv) 8-10 mm.
[0014] The differential pumping aperture may have an area selected from the group comprising:
(i) ≤ 40 mm
2; (ii) ≤ 35 mm
2; (iii) ≤ 30 mm
2; (iv) ≤ 25 mm
2; (v) ≤ 20 mm
2; (vi) ≤ 15 mm
2; (vii) ≤ 10 mm
2; and (viii) ≤ 5 mm
2. The area of the differential pumping aperture may therefore be more than an order
of magnitude smaller than the area of the differential pumping aperture inherent with
using a multipole ion guide to extend between two vacuum regions.
[0015] The ion guide may comprise at least 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70,
80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190 or 200 electrodes. At least
90%, preferably 100% of the electrodes may be arranged and adapted to be maintained
at substantially the same dc reference potential upon which an AC voltage is superimposed.
[0016] According to the preferred embodiment, when the ion guide extends between two vacuum
chambers, the pressure in the upstream vacuum chamber may, preferably, be: (i) ≥ 0.5
mbar; (ii) ≥ 0.7 mbar; (iii) ≥ 1.0 mbar; (iv) ≥ 1.3 mbar; (v) ≥ 1.5 mbar; (vi) ≥ 2.0
mbar; (vii) ≥ 5.0 mbar; (viii) ≥ 10.0 mbar; (ix) 1-5 mbar; (x) 1-2 mbar; or (xi) 0.5-1.5
mbar. Preferably, the pressure is less than 30 mbar and further preferably less than
20 mbar. The pressure in the downstream vacuum chamber may, preferably, be: (i) 10
-3-10
-2 mbar; (ii) ≥ 2 x 10
-3 mbar; (iii) ≥ 5 x 10
-3 mbar; (iv) ≤ 10
-2 mbar; (v) 10
-3-5 x 10
-3 mbar; or (vi) 5 x 10
-3-10
-2 mbar.
[0017] At least a majority, preferably all, of the electrodes forming the ion guide may
have apertures having internal diameters or dimensions: (i) ≤ 5.0 mm; (ii) ≤ 4.5 mm;
(iii) ≤ 4.0 mm; (iv) ≤ 3.5 mm; (v) ≤ 3.0 mm; (vi) ≤ 2.5 mm; (vii) 3.0 ± 0.5 mm; (viii)
≤ 10.0 mm; (ix) ≤ 9.0 mm; (x) ≤ 8.0 mm; (xi) ≤ 7.0 mm; (xii) ≤ 6.0 mm; (xiii) 5.0
± 0.5 mm; or (xiv) 4-6 mm.
[0018] The length of the ion guide may be: (i) ≥ 100 mm; (ii) ≥ 120 mm; (iii) ≥ 150 mm;
(iv) 130 ± 10 mm; (v) 100-150 mm; (vi) ≤ 160 mm; (vii) ≤ 180 mm; (viii) ≤ 200 mm;
(ix) 130-150 mm; (x) 120-180 mm; (xi) 120-140 mm; (xii) 130 mm ± 5, 10, 15, 20, 25
or 30 mm; (xiii) 50-300 mm; (xiv) 150-300 mm; (xv) ≥ 50 mm; (xvi) 50-100 mm; (xvii)
60-90 mm; (xviii) ≥ 75 mm; (xix) 50-75 mm; (xx) 75-100 mm; (xxi) approx. 26 cm; (xxii)
24-28 cm; (xxiii) 20-30 cm; or (xxiv) > 30 cm.
[0019] According to a preferred embodiment, the ion source is an atmospheric pressure ion
source such as an Electrospray ("ES") ion source or an Atmospheric Pressure Chemical
Ionisation ("APCI") ion source. According to an alternative embodiment, the ion source
may be a Matrix Assisted Laser Desorption Ionisation ("MALDI") ion source or an Inductively
Coupled Plasma ("ICP") ion source. The MALDI ion source may be either an atmospheric
source or a low vacuum source.
[0020] According to a preferred embodiment, the ion source is a continuous ion source.
[0021] The mass spectrometer preferably comprises either a time-of-flight mass analyser,
preferably an orthogonal time of flight mass analyser, a quadrupole mass analyser
or a quadrupole ion trap.
[0022] According to a second aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 21.
[0023] Preferably, an electrode of the ion guide forms a differential pumping aperture between
the input and intermediate vacuum chambers.
[0024] Preferably, the mass spectrometer comprises means for supplying an AC-voltage to
the electrodes. Preferably, an AC generator is provided which is connected to the
electrodes in such a way that at any instant during an AC cycle of the output of the
AC generator, adjacent ones of the electrodes forming the AC-only ion guide are supplied
respectively with approximately equal positive and negative potentials relative to
a reference potential.
[0025] In one embodiment the AC power supply may be an RF power supply. However, the present
invention is not intended to be limited to RF frequencies. Furthermore, "AC" is intended
to mean simply that the waveform alternates and hence embodiments of the present invention
are also contemplated wherein non-sinusoidal waveforms including square waves are
supplied to the ion guide.
[0026] According to a third aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 24.
[0027] Preferably, at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50 or 100 of the electrodes
are disposed in one or both vacuum chambers.
[0028] According to a fourth aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 29.
[0029] According to a fifth aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 30.
[0030] Preferably, a differential pumping aperture between the vacuum chambers is formed
by an electrode of the ion guide, the differential pumping aperture having an area
≤ 20 mm
2, preferably ≤ 15 mm
2, further preferably ≤ 10 mm
2.
[0031] According to a sixth aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 32.
[0032] According to a seventh aspect of the present invention, there is provided a mass
spectrometer as claimed in claim 33.
[0033] According to a eighth aspect of the present invention, there is provided a mass spectrometer
as claimed in claim 34.
[0034] According to this embodiment a substantially continuous ion tunnel ion guide may
be provided which extends through two, three, four or more vacuum chambers. Also,
instead of each vacuum chamber being separately pumped, a single split flow vacuum
pump may preferably be used to pump each chamber.
[0035] According to a ninth aspect of the present invention, there is provided a method
of mass spectrometry as claimed in claim 35.
[0036] According to a tenth aspect of the present invention, there is provided a method
of mass spectrometry as claimed in claim 36.
[0037] According to an eleventh aspect of the present invention, there is provided a mass
spectrometer as claimed in claim 37.
[0038] Various embodiments of the present invention will now be described, by way of example
only, and with reference to the accompanying drawings in which:
Fig. 1 shows an ion tunnel ion guide; and
Fig. 2 shows a preferred arrangement.
[0039] As shown in Fig. 1, an ion tunnel 15 comprises a plurality of electrodes 15a,15b
having apertures. Adjacent electrodes 15a,15b are connected to different phases of
an AC power supply which may in one embodiment be an RF power supply. For example,
the first, third, fifth etc. electrodes 15a may be connected to the 0° phase supply
16a, and the second, fourth, sixth etc. electrodes 15b may be connected to the 180°
phase supply 16b. Ions from an ion source pass through the ion tunnel 15 and are efficiently
transmitted by it. In contrast to an ion funnel arrangement, preferably all of the
electrodes 15a,15b are maintained at substantially the same dc reference potential
about which an AC voltage is superimposed. Unlike ion traps, blocking dc potentials
are not applied to either the entrance or exit of the ion tunnel 15.
[0040] Fig. 2 shows a preferred embodiment of the present invention. An Electrospray ("ES")
ion source 1 or an Atmospheric Pressure Chemical Ionisation ("APCI") ion source 1
(which requires a corona pin 2) emits ions which enter a vacuum chamber 17 via a sample
cone 3. Vacuum chamber 17 is pumped by a rotary or mechanical pump 4. A portion of
the gas and ions pass through a differential pumping aperture 21 with the plate surrounding
the aperture being preferably maintained at 50-120V into a vacuum chamber 18 housing
an ion tunnel ion guide 15 which extends into another vacuum chamber 19. Vacuum chamber
18 is pumped by a rotary or mechanical pump 7. Ions are transmitted by the ion guide
15 through the vacuum chamber 18 and pass, without exiting the ion guide 15, through
another differential pumping aperture 8 formed by an electrode of the ion tunnel ion
guide 15 into vacuum chamber 19 which is pumped by a turbo-molecular pump 10. Ions
continue to be transmitted by the ion tunnel ion guide 15 through the vacuum chamber
19. The ions then leave the ion guide 15 and pass through differential pumping aperture
11 into an analyser vacuum chamber 20 which is pumped by a turbo-molecular pump 14.
Analyser vacuum chamber 20 houses a prefilter rod set 12, a quadrupole mass filter/analyser
13 and may include other elements such as a collision cell (not shown), another quadrupole
mass filter/analyser together with an ion detector (not shown) or a time of flight
analyser (not shown).
[0041] An AC-voltage is applied to the electrodes and the ion tunnel 15 is preferably maintained
at 0-2 V dc above the dc potential of the plate forming the differential pumping aperture
11 which is preferably at ground (0 V dc). According to other embodiments, the plate
forming the differential pumping aperture 11 may be maintained at other dc potentials.
[0042] The ion tunnel 15 is preferably about 26 cm long and in one embodiment comprises
approximately 170 ring electrodes. Upstream vacuum chamber 18 is preferably maintained
at a pressure ≥ 1 mbar, and downstream vacuum chamber 19 is preferably maintained
at a pressure of
10-3-10
-2 mbar. The ion guide 15 is preferably supplied with an AC-voltage at a frequency of
between 1-2 MHz. However, according to other embodiments, frequencies of 800kHz-3MHz
may be used. The electrodes forming the ion tunnel 15 preferably have circular apertures
which preferably have a diameter in the range of 3-5 mm.
[0043] Embodiments of the present invention are also contemplated wherein electrodes of
the ion tunnel in one vacuum chamber have a different peak AC voltage amplitude compared
with electrodes of the same ion tunnel which are disposed in another vacuum chamber.
For example, with reference to Fig. 2 the electrodes disposed in chamber 18 may be
coupled to the AC power supply 16a,16b via a capacitor but the electrodes disposed
in chamber 19 may be directly coupled to the AC power supply 16a,16b. Accordingly,
the electrodes disposed in chamber 19 may see a peak AC voltage of 500V, but the electrodes
disposed in chamber 18 may see a peak AC voltage of 300V. The electrode which forms
the differential pumping aperture 8 may be maintained at the AC voltage of either
the electrodes in chamber 18 or the electrodes in chamber 19, or alternatively the
electrode may be maintained at a voltage which is different from the other electrodes.
1. A mass spectrometer, comprising:
an ion source;
an input vacuum chamber;
an analyser vacuum chamber comprising an ion mass analyser; and
an intermediate vacuum chamber, said intermediate vacuum chamber being disposed between
said input vacuum chamber and said analyser vacuum chamber; and
an AC-only ion guide extending between said input vacuum chamber and said intermediate
vacuum chamber;
characterised in that:
said AC-only ion guide comprises a plurality of electrodes having internal apertures.
2. A mass spectrometer as claimed in claim 1, wherein at least a majority of said electrodes
have substantially similar sized internal apertures.
3. A mass spectrometer as claimed in claim 1, wherein at least a majority of said electrodes
have internal apertures which become progressively smaller.
4. A mass spectrometer as claimed in claim 1, 2 or 3, wherein an electrode of said ion
guide forms a differential pumping aperture between said input and said intermediate
vacuum chambers.
5. A mass spectrometer as claimed in claim 4, wherein the electrode forming said differential
pumping aperture has an internal diameter selected from the group comprising: (i)
0.5-1.5 mm; (ii) 1.5-2.5 mm; (iii) 2.5-3.5 mm; (iv) 3.5-4.5 mm; (v) 4.5-5.5 mm; (vi)
5.5-6.5 mm; (vii) 6.5-7.5 mm; (viii) 7.5-8.5 mm; (ix) 8.5-9.5 mm; (x) 9.5-10.5 mm;
(xi) ≤ 10.0 mm; (xii) ≤ 9.0 mm; (xiii) ≤ 8.0 mm; (xiv) ≤ 7.0 mm; (xv) ≤ 6.0 mm; (xvi)
≤ 5.0 mm; (xvii) ≤ 4.0 mm; (xviii) ≤ 3.0 mm; (xix) ≤ 2.0 mm; (xx) ≤ 1.0 mm; (xxi)
0-2 mm; (xxii) 2-4 mm; (xxiii) 4-6 mm; (xxiv) 6-8 mm; and (xxv) 8-10 mm.
6. A mass spectrometer as claimed in claim 4 or 5, wherein at least a majority, preferably
all, of the electrodes apart from the electrode forming said differential pumping
aperture have internal diameters selected from the group comprising: (i) 0.5-1.5 mm;
(ii) 1.5-2.5 mm; (iii) 2.5-3.5 mm; (iv) 3.5-4.5 mm; (v) 4.5-5.5 mm; (vi) 5.5-6.5 mm;
(vii) 6.5-7.5 mm; (viii) 7.5-8.5 mm; (ix) 8.5-9.5 mm; (x) 9.5-10.5 mm; (xi) ≤ 10.0
mm; (xii) ≤ 9.0 mm; (xiii) ≤ 8.0 mm; (xiv) ≤ 7.0 mm; (xv) ≤ 6.0 mm; (xvi) ≤ 5.0 mm;
(xvii) ≤ 4.0 mm; (xviii) ≤ 3.0 mm; (xix) ≤ 2.0 mm; (xx) ≤ 1.0 mm; (xxi) 0-2 mm; (xxii)
2-4 mm; (xxiii) 4-6 mm; (xxiv) 6-8 mm; and (xxv) 8-10 mm.
7. A mass spectrometer as claimed in claim 4, wherein the electrode forming said differential
pumping aperture has an internal aperture of different size to the other electrodes
forming said ion guide.
8. A mass spectrometer as claimed in claim 7, wherein the electrode forming said differential
pumping aperture has a smaller internal aperture than the other electrodes forming
said ion guide.
9. A mass spectrometer as claimed in claim 4, wherein the electrode forming said differential
pumping aperture has an internal aperture substantially the same size as the other
electrodes forming said ion guide.
10. A mass spectrometer as claimed in claim 4, wherein said differential pumping aperture
has an area selected from the group comprising: (i) ≤ 40 mm2; (ii) ≤ 35 mm2; (iii) ≤ 30 mm2; (iv) ≤ 25 mm2; (v) ≤ 20 mm2; (vi) ≤ 15 mm2; (vii) ≤ 10 mm2; and (viii) ≤ 5 mm2.
11. A mass spectrometer as claimed in any preceding claim, wherein said ion guide comprises
at least 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130,
140, 150, 160, 170, 180, 190 or 200 electrodes.
12. A mass spectrometer as claimed in any preceding claim, wherein the pressure in said
input vacuum chamber is selected from the group comprising: (i) ≥ 0.5 mbar; (ii) ≥
0.7 mbar; (iii) ≥ 1.0 mbar; (iv) ≥ 1.3 mbar; (v) ≥ 1.5 mbar; (vi) ≥ 2.0 mbar; (vii)
≥ 5.0 mbar; (viii) ≥ 10.0 mbar; (ix) 1-5 mbar; (x) 1-2 mbar; and (xi) 0.5-1.5 mbar.
13. A mass spectrometer as claimed in any preceding claim, wherein the pressure in said
intermediate vacuum chamber is selected from the group comprising: (i) 10-3-10-2 mbar; (ii) ≥ 2 x 10-3 mbar; (iii) ≥ 5 x 10-3 mbar; (iv) ≤ 10-2 mbar; (v) 10-3-5 x 10-3 mbar; and (vi) 5 x 10-3-10-2 mbar.
14. A mass spectrometer as claimed in any preceding claim, wherein the length of said
ion guide is selected from the group comprising: (i) ≥ 100 mm; (ii) ≥ 120 mm; (iii)
≥ 150 mm; (iv) 130 ± 10 mm; (v) 100-150 mm; (vi) ≤ 160 mm; (vii) ≤ 180 mm; (viii)
≤ 200 mm; (ix) 130-150 mm; (x) 120-180 mm; (xi) 120-140 mm; (xii) 130 mm ± 5, 10,
15, 20, 25 or 30 mm; (xiii) 50-300 mm; (xiv) 150-300 mm; (xv) ≥ 50 mm; (xvi) 50-100
mm; (xvii) 60-90 mm; (xviii) ≥ 75 mm; (xix) 50-75 mm; (xx) 75-100 mm; (xxi) approx.
26 cm; (xxii) 24-28 cm; (xxiii) 20-30 cm; and (xxiv) > 30 cm.
15. A mass spectrometer as claimed in any preceding claim, wherein said ion source is
an atmospheric pressure ion source.
16. A mass spectrometer as claimed in claim 15, wherein said ion source is an Electrospray
("ES") ion source or an Atmospheric Pressure Chemical Ionisation ("APCI") ion source.
17. A mass spectrometer as claimed in any of claims 1-14, wherein said ion source is a
Matrix Assisted Laser Desorption Ionisation ("MALDI") ion source.
18. A mass spectrometer as claimed in claim 15, wherein said ion source is an Inductively
Coupled Plasma ("ICP") ion source.
19. A mass spectrometer as claimed in any preceding claim, wherein said mass analyser
is selected from the group comprising: (i) a time-of-flight mass analyser, preferably
an orthogonal time of flight mass analyser; (ii) a quadrupole mass analyser; and (iii)
a quadrupole ion trap.
20. A mass spectrometer as claimed in any preceding claim, wherein at least 90%, preferably
100% of said plurality of electrodes are arranged to be maintained at substantially
the same dc reference potential about which an AC voltage supplied to said electrodes
is superimposed.
21. A mass spectrometer, comprising:
an input vacuum chamber;
an analyser vacuum chamber comprising a mass analyser; and
an intermediate vacuum chamber, said intermediate vacuum chamber being arranged between
said input vacuum chamber and said analyser vacuum chamber;
characterised in that:
said mass spectrometer further comprises an ion guide comprising at least five electrodes
having apertures, said ion guide extending from said input vacuum chamber through
to said intermediate vacuum chamber.
22. A mass spectrometer as claimed in claim 21, wherein an electrode of said ion guide
forms a differential pumping aperture between said input vacuum chamber and said intermediate
vacuum chamber.
23. A mass spectrometer as claimed in claim 21 or 22, further comprising means for supplying
an AC-voltage to said electrodes.
24. A mass spectrometer, comprising:
an inter-vacuum chamber ion guide, said inter-vacuum chamber ion guide being > 5 cm
in length;
characterised in that:
said ion guide comprises a plurality of electrodes having apertures.
25. A mass spectrometer as claimed in claim 24, wherein said ion guide comprises at least
10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190
or 200 electrodes.
26. A mass spectrometer as claimed in claim 25, wherein at least 5, 10, 15, 20, 25, 30,
35, 40, 45, 50 or 100 of said electrodes are disposed in an input vacuum chamber.
27. A mass spectrometer as claimed in claim 26, wherein at least 5, 10, 15, 20, 25, 30,
35, 40, 45 or 50 or 100 of said electrodes are disposed in an intermediate vacuum
chamber, said intermediate vacuum chamber being arranged between said input vacuum
chamber and an analyser vacuum chamber comprising a mass analyser, said input and
intermediate vacuum chambers being separated by an inter-chamber differential pumping
aperture or orifice.
28. A mass spectrometer as claimed in claim 27, wherein an electrode of said ion guide
forms said inter-chamber aperture or orifice.
29. A mass spectrometer comprising:
an ion source selected from the group comprising: (i) an Electrospray ("ES") ion source;
(ii) an Atmospheric Pressure Chemical Ionisation ("APCI") ion source; (iii) a Matrix
Assisted Laser Desorption Ionisation ("MALDI") ion source; and (iv) an Inductively
Coupled Plasma ("ICP") ion source;
an input vacuum chamber;
an intermediate vacuum chamber separated from the input vacuum chamber by a differential
pumping aperture; and
a mass analyser, preferably a time of flight or a quadrupole mass analyser disposed
in an analyser vacuum chamber; and
an ion guide spanning said input and intermediate vacuum chambers;
characterised in that:
said ion guide comprises ≥ 10 electrodes having apertures with a said electrode forming
said differential pumping aperture.
30. A mass spectrometer comprising:
an AC-only ion guide comprising a plurality of electrodes having apertures spanning
two vacuum chambers, each said vacuum chamber comprising a vacuum pump for pumping
gas from said vacuum chamber so as to produce a partial vacuum in said vacuum chamber.
31. A mass spectrometer as claimed in claim 30, wherein a differential pumping aperture
between said vacuum chambers is formed by an electrode of said ion guide, said differential
pumping aperture having an area ≤ 20 mm2, preferably ≤ 15 mm2, further preferably ≤ 10 mm2.
32. A mass spectrometer comprising:
an input vacuum chamber, said input vacuum chamber including a port connected to a
vacuum pump;
an intermediate vacuum chamber, said intermediate vacuum chamber including a port
connected to another vacuum pump; and
an interchamber orifice or aperture separating said vacuum chambers;
characterised in that:
said interchamber orifice is formed by an electrode of an ion guide comprised of a
plurality of electrodes having apertures.
33. A mass spectrometer, comprising:
an ion source;
an input vacuum chamber;
an intermediate vacuum chamber; and
an AC-only ion guide disposed in said input vacuum chamber and extending beyond said
input vacuum chamber into said intermediate vacuum chamber;
characterised in that:
said ion guide comprises a plurality of electrodes each having substantially similar
internal apertures and wherein at least one electrode of said ion guide forms a differential
pumping aperture between said vacuum chambers.
34. A mass spectrometer comprising:
at least two, preferably at least three or four, vacuum chambers, said vacuum chambers
preferably connected to a split flow turbo vacuum pump; and
a substantially continuous ion guide extending between said vacuum chambers, said
ion guide comprising a plurality of electrodes having apertures.
35. A method of mass spectrometry, comprising:
guiding ions from a vacuum chamber to another vacuum chamber by passing said ions
through an ion guide extending between the two vacuum chambers, said ion guide comprising
a plurality of electrodes having apertures.
36. A method of mass spectrometry, comprising:
generating a beam of ions from an ion source;
passing said ions into an ion guide comprised of a plurality of electrodes having
apertures, said ion guide extending between two vacuum chambers;
guiding the ions along the ion guide so that they pass from a vacuum chamber into
another vacuum chamber without leaving said ion guide; and then
mass analysing at least some of said ions.
37. A mass spectrometer comprising a substantially continuous ion guide, preferably comprising
a plurality of electrodes having apertures, extending through three or more vacuum
chambers.
38. A mass spectrometer as claimed in any of claims 1-20, further comprising an AC power
supply for supplying an AC voltage to said electrodes.
39. A mass spectrometer as claimed in claim 38, wherein electrodes in said input vacuum
chamber are arranged to be supplied with an AC voltage having an amplitude and electrodes
in said intermediate vacuum chamber are arranged to be supplied with an AC voltage
having another different amplitude.
40. A mass spectrometer as claimed in claim 39, wherein the amplitude of the AC voltage
supplied to the electrodes in said input vacuum chamber is smaller than the amplitude
of the AC voltage supplied to the electrodes in the intermediate vacuum chamber, preferably
at least 100 V smaller.
41. A mass spectrometer as claimed in claim 39 or 40, wherein the amplitude of the AC
voltage supplied to the electrodes in said input vacuum chamber is in the range 200-400
V and/or the amplitude of the AC voltage supplied to the electrodes in said intermediate
vacuum chamber is in the range 400-600 V.