U.S. patent application number 09/727285 was filed with the patent office on 2001-11-08 for multipole ion guide for mass spectrometry.
Invention is credited to Gulcicek, Erol, Whitehouse, Craig M..
Application Number | 20010038069 09/727285 |
Document ID | / |
Family ID | 22750166 |
Filed Date | 2001-11-08 |
United States Patent
Application |
20010038069 |
Kind Code |
A1 |
Whitehouse, Craig M. ; et
al. |
November 8, 2001 |
Multipole ion guide for mass spectrometry
Abstract
A multipole ion guide which begins in one pumping stage and
extends continuously into one or more subsequent pumping stages has
been incorporated into an atmospheric pressure ion source mass
spectrometer system. Ions delivered into vacuum from an
Electrospray, Atmospheric Pressure Chemical Ionization or
Inductively Coupled Plasma ion source are guided and focused into a
mass analyzer with high efficiency using the multipole ion guide.
The background pressure over a portion of the multipole ion guide
length is high enough to cause kinetic energy cooling of ions
traversing the ion guide length due to ion collisions with neutral
background gas molecules. This ion kinetic energy cooling lowers
energy spread of ions traversing the multipole ion guide length.
The multipole ion guide DC offset potential can be used to adjust
the mean ion energy and the ion guide an and q values can be set to
reduce or expand the range of ion mass to charge which will be
transmitted through the ion guide. These features of multipole ion
guides and multiple pumping stage multipole ion guides are used to
improve performance and lower the cost of Atmospheric Pressure Ion
source mass spectrometer instruments.
Inventors: |
Whitehouse, Craig M.;
(Branford, CT) ; Gulcicek, Erol; (Cheshire,
CT) |
Correspondence
Address: |
Morris E. Cohen, Esq.
LEVISOHN, LERNER, BERGER & LANGSAM
Suite 2400
757 Third Avenue
New York
NY
10017
US
|
Family ID: |
22750166 |
Appl. No.: |
09/727285 |
Filed: |
November 30, 2000 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
09727285 |
Nov 30, 2000 |
|
|
|
09373337 |
Aug 12, 1999 |
|
|
|
6188066 |
|
|
|
|
09373337 |
Aug 12, 1999 |
|
|
|
08794970 |
Feb 5, 1997 |
|
|
|
5962851 |
|
|
|
|
08794970 |
Feb 5, 1997 |
|
|
|
08645826 |
May 14, 1996 |
|
|
|
5652427 |
|
|
|
|
08645826 |
May 14, 1996 |
|
|
|
08202505 |
Feb 28, 1994 |
|
|
|
Current U.S.
Class: |
250/288 |
Current CPC
Class: |
H01J 49/0481 20130101;
H01J 49/063 20130101; B01D 59/44 20130101 |
Class at
Publication: |
250/288 |
International
Class: |
H01J 049/00; B01D
059/44 |
Claims
we claim:
1. An apparatus used for analyzing chemical species comprising: a.
an ion source operated at or near atmospheric pressure which
produces ions from solution and delivers said ions into a first
vacuum pumping stage through an orifice; b. two or more vacuum
pumping stages with means for pumping away gas in each vacuum stage
whereby each successive vacuum pumping stage has a lower background
pressure than the previous pumping stage; c. a mass analyzer and
detector located in one or more of the vacuum pumping stages; d. a
multipole ion guide which begins in one vacuum pumping stage and
extends contiguously into one or more subsequent vacuum pumping
stages. Said multipole ion guide consisting of a multiple of
equally spaced parallel poles extending the length of said ion
guide. Said multipole ion guide is positioned in said vacuum
pumping stages to guide ions delivered from said ion source through
a portion of said vacuum stages;. e. a means for applying AC and DC
voltages to said poles of said multipole ion guide. f. a means for
controlling the AC frequency and said AC and DC voltages applied to
said poles of said multipole ion guide;
2. An apparatus according to claim 1 where said ion source is an
electrospray ion source.
3. An apparatus according to claim 1 where said ion source is an
Atmospheric Pressure Chemical Ionization source.
4. An apparatus according to claim 1 where said ion source is an
Inductively Coupled Plasma ion source.
5. An apparatus according to claim 1 where said multipole ion guide
is a hexapole.
6. An apparatus according to claim 1 where said multipole ion guide
is a quadrupole.
7. An apparatus according to claim 1 where said multipole ion guide
has more than six poles.
8. An apparatus according to claim 1 where said mass analyzer is a
quadrupole mass filter.
9. An apparatus according to claim 1 where said mass analyzer is a
magnetic sector mass spectrometer.
10. An apparatus according to claim 1 where said mass analyzer is a
Time-Of-Flight mass spectrometer.
11. An apparatus according to claim 11 where said mass analyzer is
orthogonal pulsing Time-Of-Flight mass spectrometer.
12. An apparatus according to claim 1 where said mass analyzer is a
hybrid ion trap Time-of Flight mass analyzer.
13. An apparatus according to claim 1 where said mass analyzer is
an ion trap mass spectrometer.
14. An apparatus according to claim 1 where said mass analyzer is a
Fourier Transform mass spectrometer.
15. An apparatus according to claim 1 which includes three of said
vacuum pumping stages.
16. An apparatus according to claim 1 which includes four of said
vacuum pumping stages.
17. An apparatus according to claim 1 which includes more than four
of said vacuum pumping stages.
18. An apparatus according to claim 1 where said ion guide extends
continuously from one vacuum pumping stage into the next of said
vacuum pumping stages.
19. An apparatus according to claim 15 where said multipole ion
guide begins in vacuum stage one and extends contiguously from said
vacuum pumping stage two.
20. An apparatus according to claim 15 where said multipole ion
guide begins in vacuum stage two and extends contiguously into said
vacuum pumping stage three.
21. An apparatus according to claim 1 where said ion guide extends
continuously from one of said of said vacuum pumping stages through
the next of said vacuum pumping stages and into the third of three
consecutive vacuum pumping stages.
22. An apparatus according to claim 18 where said multipole ion
guide begins in vacuum pumping stage one.
23. An apparatus according to claim 18 where said multipole ion
guide begins in vacuum pumping stage two.
24. An apparatus according to claim 1 where said ion guide extends
continuously from one vacuum pumping stage through more than three
additional vacuum pumping stages.
25. An apparatus according to claim 1 where said means for applying
AC and DC voltages to said poles of said multipole ion guide can be
set to select the energy of said ions entering said mass
analyzer.
26. A means according to claim 1 where said AC frequency and AC and
DC voltages applied to said poles of said multipole ion guide are
adjustable to maximize ion transmission efficiency through said
multipole ion guide.
27. A means according to claim 1 where said AC frequency is fixed
said AC voltage amplitude is adjusted and said DC voltages are
adjusted to said poles of said multipole ion guide to maximize ion
transmission efficiency through said multipole ion guide.
28. A means according to claim 1 where said means for controlling
said AC frequency and AC and DC voltages applied to said poles of
said multipole ion guide can be set to limit the range of
mass-to-charge of said ions which can be transmitted through said
multipole ion guide.
29. A means according to claim 28 where said AC frequency is fixed
and said AC voltage amplitude and said DC voltages are adjusted to
limit the range of mass-to-charge of ions which can be transmitted
through said multipole ion guide.
30. An apparatus according to claim 1 where said background
pressure in at least one of said vacuum pumping stages where said
multipole ion guide is located is high enough to cause cooling of
ion kinetic energy resulting in reduction of the ion energy spread
for said ions of a given mass to charge transmitted through said
multipole ion guide.
31. An apparatus according to claim 1 where the radial distance of
the inner surface of said pole of said multipole ion guide from the
centerline of said multipole ion guide is 1.5 millimeters or
less.
32. An apparatus according to claim 1 where said first vacuum stage
has a background pressure of less than 20 torr.
33. An apparatus according to claim 1 where said second vacuum
stage has a background pressure of less than 500 millitorr.
34. An apparatus according to claim 1 where said third vacuum stage
has a background pressure of less than 10 millitorr.
35. An apparatus used for analyzing chemical species comprising: a.
an ion source operated at or near atmospheric pressure which
produces ions from solution and delivers said ions into a first
vacuum pumping stage through an orifice; b. two or more vacuum
pumping stages with means for pumping away gas in each vacuum stage
whereby each successive vacuum pumping stage has a lower background
pressure than the previous pumping stage; c. a Time-Of-Flight mass
analyzer and detector with its ion pulsing region and
Time-Of-Flight tube located in one or more of said vacuum pumping
stages; d. a multipole ion guide which begins in one of the first
three of said vacuum pumping stages; Said multipole ion guide
consisting of a multiple of equally spaced parallel poles extending
the length of said ion guide. Said multipole ion guide is
positioned in said vacuum pumping stage or stages upstream of the
said Time-Of-Flight mass analyzer and transmits ions which are
delivered from said ion source through a portion of said vacuum
stages; e. a means for applying AC and DC voltages to the poles of
said multipole ion guide; f. a means for controlling the AC
frequency and said AC and DC voltages which are applied to said
poles of said multipole ion guide.
36. An apparatus according to claim 35 where said ion source is an
electrospray ion source.
37. An apparatus according to claim 35 where said ion source is an
Atmospheric Pressure Chemical Ionization source.
38. An apparatus according to claim 35 where said ion source is an
Inductively Coupled Plasma ion source.
39. An apparatus according to claim 35 where said multipole ion
guide is a hexapole.
40. An apparatus according to claim 35 where said multipole ion
guide is a quadrupole.
41. An apparatus according to claim 35 where said multipole ion
guide has more than six poles.
42. An apparatus according to claim 35 where said Time-Of-Flight
mass analyzer includes the means for orthogonal pulsing of said
ions from said pulsing region into said flight tube.
43. An apparatus according to claim 35 where said Time-Of-Flight
mass analyzer includes the means for in-line pulsing of said ions
from said pulsing region into said flight tube.
44. An apparatus according to claim 35 where said Time-OF-Flight
mass analyzer includes an ion trap for pulsing of said ions from
said pulsing region into said flight tube.
45. An apparatus according to claim 35 where said multipole ion
guide which is used to guide ions through a portion of said vacuum
pumping stage begins and ends in one of said vacuum pumping
stages.
46. An apparatus according to claim 45 where said ions are guided
through more than one vacuum pumping stage by individual multipole
ion guides each of which begins and ends within its respective
vacuum pumping stage.
47. A method according to claim 35 where said multipole ion guide
begins in one pumping stage and extends into one or more subsequent
pumping stages.
48. An apparatus according to claim 35 where said background
pressure in said vacuum pumping stages where said multipole ion
guide is located is high enough to cause cooling of ion kinetic
energy resulting in reduction of the ion energy spread for said
ions of a given mass to charge transmitted through said multipole
ion guide.
49. An apparatus according to claim 35 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to select the energy of said ions entering said
Time-Of-Flight mass analyzer.
50. An apparatus according to claim 35 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to reduce the range of mass to charge of said ions
which are transmitted through said multipole ion guide.
51. An apparatus according to claim 50 where said means to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be set to increase the duty
cycle of said Time-OF-Flight mass analyzer.
52. An apparatus according to claim 50 where said means to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be set to decrease the said
detector dead time.
53. An apparatus according to claim 35 where the radial distance of
the inner surface of said pole of said multipole ion guide from the
centerline of said multipole filter is 1.5 millimeters or less.
54. An apparatus according to claim 35 where the radial distance of
the inner surface of a pole of said multipole ion guide from the
centerline of said multipole filter is 1 millimeter or less.
55. An apparatus used for analyzing chemical species comprising: a.
an ion source operated at or near atmospheric pressure which
produces ions from solution and delivers said ions into a first
vacuum pumping stage through an orifice; b. two or more vacuum
pumping stages with means for pumping away gas in each vacuum stage
whereby each successive vacuum pumping stage has a lower background
pressure than the previous pumping stage; c. an Ion Trap mass
analyzer and detector located in one or more of the vacuum pumping
stages; d. a multipole ion guide which begins in one of the first
three of said vacuum pumping stages; Said multipole ion guide
consisting of a multiple of equally spaced parallel poles extending
the length of said ion guide. Said multipole ion guide is
positioned in said vacuum pumping stage or stages upstream of the
said Ion Trap mass analyzer and transmits ions which are delivered
from said ion source through a portion of said vacuum stages; e. a
means for applying AC and DC voltages to said poles of said
multipole ion guide; f. a means for controlling the AC frequency
and said AC and DC voltages applied to said poles of said multipole
ion guide;
56. An apparatus according to claim 55 where said ion source is an
electrospray ion source.
57. An apparatus according to claim 55 where said ion source is an
Atmospheric Pressure Chemical Ionization source.
58. An apparatus according to claim 55 where said ion source is an
Inductively Coupled Plasma ion source.
59. An apparatus according to claim 55 where said multipole ion
guide is a hexapole.
60. An apparatus according to claim 55 where said multipole ion
guide is a quadrupole.
61. An apparatus according to claim 55 where said multipole ion
guide has more than six poles.
62. An apparatus according to claim 55 where said background
pressure in said vacuum pumping stages where a portion of said
multipole ion guide is located is high enough to cause cooling of
ion kinetic energy resulting in reduction of the ion energy spread
for said ions of a given mass to charge transmitted through said
multipole ion guide.
63. An apparatus according to claim 55 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to select the energy of said ions entering said
Ion Trap mass analyzer.
64. An apparatus according to claim 55 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to reduce the range of mass to charge of said ions
which are transmitted through said multipole ion guide.
65. An apparatus according to claim 64 where said means to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be set to reduce the number of
ions which are not in the mass to charge window of analytical
interest, reducing effects due to space charging in said ion
trap.
66. A method for analyzing chemical species whereby: a. an ion
source operated at or near atmospheric pressure which produces ions
from solution and delivers said ions into a first vacuum pumping
stage through an orifice; b. vacuum pumping is applied to two or
more vacuum pumping stages such that each successive vacuum pumping
stage has a lower background pressure than the previous pumping
stage; c. a mass analyzer and detector located in one or more of
the vacuum pumping stages is used for mass analysis of said
chemical species. d. a multipole ion guide which begins within one
of the first two vacuum pumping stages and extends from one vacuum
pumping stage into one or more subsequent vacuum pumping stages is
used to transmit ions delivered from said ion source through a
portion of said vacuum stages. Said multipole ion guide consists of
a multiple of equally spaced parallel poles extending the length of
said ion guide. e. The method of controlling the AC frequency and
AC and DC voltages which are applied to the poles of said multipole
ion guide.
67. A method according to claim 66 where said ion source used is an
electrospray ion source.
68. A method according to claim 66 where said ion source used is an
Atmospheric Pressure Chemical Ionization source.
69. A method according to claim 66 where said ion source used is an
Inductively Coupled Plasma ion source.
70. A method according to claim 66 where said multipole ion guide
utilized is a hexapole.
71. A method according to claim 66 where said multipole ion guide
utilized is a quadrupole.
72. A method according to claim 66 where said multipole ion guide
utilized is has more than six poles.
73. A method according to claim 66 which utilizes a quadrupole mass
filter for mass analysis.
74. A method according to claim 66 which utilizes a magnetic sector
mass spectrometer for mass analysis.
75. A method according to claim 66 which utilizes a Time-Of-Flight
mass spectrometer for mass analysis.
76. A method according to claim 75 where orthogonal pulsing of ions
is used to pulse ions in said pulsing region into said flight
tube.
77. A method according to claim 75 where in-line pulsing of ions is
used to pulse ions in said pulsing region into said flight
tube.
78. A method according to claim 66 which utilizes an ion trap mass
spectrometer for mass analysis.
79. A method according to claim 66 which utilizes a Fourier
Transform Ion Cyclotron Resonance mass spectrometer for mass
analysis.
80. A method according to claim 66 which includes the utilization
of three of said vacuum pumping stages to remove gas entering
vacuum from said ion source.
81. A method according to claim 66 which includes the utilization
of four of said vacuum pumping stages to remove gas entering vacuum
from said ion source.
82. A method according to claim 66 which includes the utilization
of more than four of said vacuum pumping stages to remove gas
entering vacuum from said ion source.
83. A method according to claim 66 where ions are transmitted
through two of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously into the next of said vacuum pumping stages.
84. A method according to claim 83 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
85. A method according to claim 83 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
86. A method according to claim 66 where ions are transmitted
through three of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously through the next of said vacuum pumping stages and
extends contiguously into the third consecutive pumping stage.
87. A method according to claim 86 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
88. A method according to claim 86 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
89. A method according to claim 66 where ions are transmitted
through more than three of said vacuum pumping stages using said
ion guide which begins in one of said vacuum pumping stages and
extends contiguously through more th a n two additional vacuum
pumping stages.
90. A method according to claim 66 where AC and DC voltages applied
to said pole s o f said multipole ion guide are set to select the
energy of said ions entering said mass analyzer.
91. A method according to claim 66 where said AC and DC voltages
applied to said poles of said multipole ion guide are adjustable to
maximize ion transmission efficiency through said multipole ion
guide.
92. A method according to claim 91 where said AC frequency is fixed
said AC voltage amplitude is adjusted and said DC voltages are
adjusted to said poles of said multipole ion guide to maximize ion
transmission efficiency through said multipole ion guide.
93. A method according to claim 66 where said AC and DC voltages
applied to said poles of said multipole ion guide are adjustable to
limit mass-to-charge range of ions which are transmitted through
said multipole ion guide.
94. A method according to claim 93 where said AC frequency is fixed
said AC voltage amplitude is adjusted and said DC voltages are
adjusted to said poles of said multipole ion guide to allow a
limited mass-to-charge range of ions to pass through said multipole
ion guide.
95. A method according to claim 66 where said background pressure
in said vacuum pumping stages where said multipole ion guide is
located is maintained high enough to cause cooling of ion kinetic
energy resulting in reduction of the ion energy spread for said
ions of a given mass to charge transmitted through said multipole
ion guide.
96. A method for analyzing chemical species whereby: a. an ion
source operated at or near atmospheric pressure which produces ions
from solution and delivers said ions into a first vacuum pumping
stage through an orifice; b. vacuum pumping is applied to two or
more vacuum pumping stages such that each successive vacuum pumping
stage has a lower background pressure than the previous pumping
stage; c. a Time-Of-Flight mass analyzer and detector with its
primary ion beam pulsing region and Time-Of-Flight tube located in
one or more of the vacuum pumping stages is used for mass analysis
of said chemical species; d. a multipole ion guide which begins in
one of the first three of said vacuum pumping stages. Said
multipole ion guide consisting of a multiple of equally spaced
parallel poles extending the length of said ion guide. Said
multipole ion guide is positioned in said vacuum pumping stage or
stages upstream of the said Time-Of-Flight mass analyzer and
transmits ions which are delivered from said ion source through a
portion of said vacuum stages; e. The method of controlling the AC
frequency and AC and DC voltages which are applied to the poles of
said multipole ion guide;
97. A method according to claim 96 where said ion source used is an
electrospray ion source.
98. A method according to claim 96 where said ion source used is an
Atmospheric Pressure Chemical Ionization source.
99. A method according to claim 96 where said ion source used is an
Inductively Coupled Plasma ion source.
100. A method according to claim 96 where said multipole ion guide
utilized is a hexapole.
101. A method according to claim 96 where said multipole ion guide
utilized is a quadrupole.
102. A method according to claim 96 where said multipole ion guide
utilized is has more than six poles.
103. A method according to claim 96 which includes the utilization
of three of said vacuum pumping stages to remove gas entering
vacuum from said ion source.
104. A method according to claim 96 which includes the utilization
of four of said vacuum pumping stages to remove gas entering vacuum
from said ion source.
105. A method according to claim 96 which includes the utilization
of more than four of said vacuum pumping stages to remove gas
entering vacuum from said ion source.
106. A method according to claim 96 where orthogonal pulsing of
ions is used to pulse ions out of said pulsing region into said
flight tube.
107. A method according to claim 96 where in-line pulsing of ions
is used to pulse ions out of said pulsing region into said flight
tube.
108. A method according to claim 96 where an ion trap is used to
pulse ions out of said pulsing region into said flight tube.
109. A method according to claim 96 where said multipole ion guide
which is used to guide ions through a vacuum pumping stage begins
and ends in said vacuum pumping stage.
110. A method according to claim 109 where said ions are guided
through more than one vacuum pumping stages by individual multipole
ion guides each of which begins and ends within its respective
vacuum pumping stage.
111. A method according to claim 96 where said multipole ion guide
begins in one pumping stage and extends into one or more subsequent
pumping stages.
112. A method according to claim 111 where ions are transmitted
through two of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously into the next of said vacuum pumping stages.
113. A method according to claim 112 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
114. A method according to claim 112 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
115. A method according to claim 95 where ions are transmitted
through three of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously through the next of said vacuum pumping stages and
extends contiguously into the third consecutive pumping stage.
116. A method according to claim 115 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
117. A method according to claim 115 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
118. A method according to claim 95 where ions are transmitted
through more than three of said vacuum pumping stages using said
ion guide which begins in one of said vacuum pumping stages and
extends contiguously through more than two additional vacuum
pumping stages.
119. A method according to claim 95 where AC and DC voltages
applied to said poles of said multipole ion guide are set to select
the energy of said ions entering said mass analyzer.
120. A method according to claim 95 where said AC and DC voltages
applied to said poles of said multipole ion guide are adjustable to
maximize ion transmission efficiency through said multipole ion
guide.
121. A method according to claim 120 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide to maximize
ion transmission efficiency through said multipole ion guide.
122. A method according to claim 95 where said AC frequency and
said AC and DC voltages applied to said poles of said multipole ion
guide are adjustable to allow a limited mass-to-charge range of
ions to pass through said multipole ion guide.
123. A method according to claim 122 where said method to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be used to increase the duty
cycle of said Time-OF-Flight mass analyzer.
124. An apparatus according to claim 122 where said method to
reduce the range of mass to charge of said ions which are
transmitted through said multipole ion guide can be used to
decrease the said detector dead time.
125. A method according to claim 122 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide to allow a
limited mass-to-charge range of ions to pass through said multipole
ion guide.
126. A method according to claim 95 where said background pressure
in said vacuum pumping stages where said multipole ion guide is
located is maintained high enough to cause cooling of ion kinetic
energy resulting in reduction of the ion energy spread for said
ions of a given mass to charge transmitted through said multipole
ion guide.
127. A method according to claim 150 for transmitting said ions to
said mass analyzer with a small cross section ion beam diameter by
transmitting said ions through said multipole ion guide of small
size where the innermost surface of said pole of said multipole ion
guide from the centerline of said multipole in guide is 2.5
millimeters or less.
128. A method for analyzing chemical species whereby: a. an ion
source operated at or near atmospheric pressure which produces ions
from solution and delivers said ions into a first vacuum pumping
stage through an orifice; b. vacuum pumping is applied to one or
more vacuum pumping stages such that each successive vacuum pumping
stage has a lower background pressure than the previous pumping
stage; c. an ion trap mass analyzer and detector is used for mass
analysis of said chemical species; d. a multipole ion guide which
begins in one of the first three of said vacuum pumping stages.
Said multipole ion guide consisting of a multiple of equally spaced
parallel poles extending the length of said ion guide. Said
multipole ion guide is positioned in said vacuum pumping stage or
stages upstream of the said ion trap mass analyzer and transmits
ions which are delivered from said ion source through a portion of
said vacuum stages. e. The method of controlling the AC frequency
and AC and DC voltages which are applied to the poles of said
multipole ion guide.
129. A method according to claim 128 where said ion source used is
an electrospray ion source.
130. A method according to claim 128 where said ion source used is
an Atmospheric Pressure Chemical Ionization source.
131. A method according to claim 128 where said ion source used is
an Inductively Coupled Plasma ion source.
132. A method according to claim 128 where said multipole ion guide
utilized is a hexapole.
133. A method according to claim 128 where said multipole ion guide
utilized is a quadrupole.
134. A method according to claim 128 where said multipole ion guide
utilized is has more than six poles.
135. A method according to claim 128 which includes the utilization
of three of said vacuum pumping stages to remove gas entering
vacuum from said ion source.
136. A method according to claim 128 which includes the utilization
of four of said vacuum pumping stages to remove gas entering vacuum
from said ion source.
137. A method according to claim 128 where ions are transmitted
into the ion trap through an endplate aperture.
138. A method according to claim 128 where ions are transmitted
into the ion trap through a gap between the trap electrodes.
139. A method according to claim 128 where said multipole ion guide
which is used to guide ions through a vacuum pumping stage begins
and ends in said vacuum pumping stage.
140. A method according to claim 139 where said ions are guided
through more than one vacuum pumping stages by individual multipole
ion guides each of which begins and ends within its respective
vacuum pumping stage.
141. A method according to claim 128 where said multipole ion guide
begins in one pumping stage and extends into one or more subsequent
pumping stages.
142. A method according to claim 141 where ions are transmitted
through two of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously into the next of said vacuum pumping stages.
143. A method according to claim 142 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
144. A method according to claim 142 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
145. A method according to claim 128 where ions are transmitted
through three of said vacuum pumping stages using said ion guide
which begins in one of said vacuum pumping stages and extends
contiguously through the next of said vacuum pumping stages and
extends contiguously into the third consecutive pumping stage.
146. A method according to claim 145 where said ions enter said
multipole ion guide in the second vacuum pumping stage.
147. A method according to claim 145 where said ions enter said
multipole ion guide in the first vacuum pumping stage.
148. A method according to claim 128 where AC and DC voltages
applied to said poles of said multipole ion guide are set to select
the energy of said ions entering said ion trap mass
spectrometer.
149. A method according to claim 128 where said AC and DC voltages
applied to said poles of said multipole ion guide are adjustable to
maximize ion transmission efficiency through said multipole ion
guide.
150. A method according to claim 149 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide to maximize
ion transmission efficiency through said multipole ion guide.
151. A method according to claim 128 where said AC frequency and
said AC and DC voltages applied to said poles of said multipole ion
guide are adjustable to allow a limited mass-to-charge range of
ions to pass through said multipole ion guide.
152. A method according to claim 151 where said method to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be used to decrease the
effects due to space charging in the ion trap mass
spectrometer.
153. A method according to claim 151 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide limiting the
mass-to-charge range of ions passing through said multipole ion
guide.
154. A method according to claim 128 where said AC frequency and AC
and DC voltages are adjusted to reduce the range of mass to charge
of said ions which are transmitted through said multipole ion guide
to reduce the number of ions which are not in the mass to charge
window of analytical interest and reducing effects due to space
charging in said ion trap.
155. A method according to claim 128 where said background pressure
in said vacuum pumping stages where said multipole ion guide is
located is maintained high enough to cause cooling of ion kinetic
energy resulting in reduction of the ion energy spread for said
ions of a given mass to charge transmitted through said multipole
ion guide.
156. An apparatus used for analyzing chemical species comprising:
a. an ion source operated at or near atmospheric pressure which
produces ions from solution and delivers said ions into a first
vacuum pumping stage through an orifice; b. two or more vacuum
pumping stages with means for pumping away gas in each vacuum stage
whereby each successive vacuum pumping stage has a lower background
pressure than the previous pumping stage; c. an Fourier Transform
Ion Cyclotron Resonance (FT-ICR) mass analyzer and detector located
in one or more of the vacuum pumping stages; d. a multipole ion
guide which begins in one of the first three of said vacuum pumping
stages; Said multipole ion guide consisting of a multiple of
equally spaced parallel poles extending the length of said ion
guide. Said multipole ion guide is positioned in said vacuum
pumping stage or stages upstream of the said FT-ICR mass analyzer
and transmits ions which are delivered from said ion source through
a portion of said vacuum stages; e. a means for applying AC and DC
voltages to said poles of said multipole ion guide; f. a means for
controlling the AC frequency and said AC and DC voltages applied to
said poles of said multipole ion guide;
157. A method according to claim 160 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide to maximize
ion transmission efficiency through said multipole ion guide.
158. An apparatus according to claim 156 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to select the energy of said ions entering said
FT-ICR mass analyzer.
159. An apparatus according to claim 156 where said means for
applying AC and DC voltages to said poles of said multipole ion
guide can be set to reduce the range of mass to charge of said ions
which are transmitted through said multipole ion guide.
160. A method for analyzing chemical species whereby: a. an ion
source operated at or near atmospheric pressure which produces ions
from solution and delivers said ions into a first vacuum pumping
stage through an orifice; b. vacuum pumping is applied to one or
more vacuum pumping stages such that each successive vacuum pumping
stage has a lower background pressure than the previous pumping
stage; c. an FT-ICR mass analyzer and detector is used for mass
analysis of said chemical species; d. a multipole ion guide which
begins in one of the first three of said vacuum pumping stages.
Said multipole ion guide consisting of a multiple of equally spaced
parallel poles extending the length of said ion guide. Said
multipole ion guide is positioned in said vacuum pumping stage or
stages upstream of the said FT-ICR mass analyzer and transmits ions
which are delivered from said ion source through a portion of said
vacuum stages. e. The method of controlling the AC frequency and AC
and DC voltages which are applied to the poles of said multipole
ion guide.
161. A method according to claim 160 where said AC frequency is
fixed said AC voltage amplitude is adjusted and said DC voltages
are adjusted to said poles of said multipole ion guide to maximize
ion transmission efficiency through said multipole ion guide.
162. A method according to claim 160 where said AC frequency and
said AC and DC voltages applied to said poles of said multipole ion
guide are adjustable to allow a limited mass-to-charge range of
ions to pass through said multipole ion guide.
163. A method according to claim 160 where said method to reduce
the range of mass to charge of said ions which are transmitted
through said multipole ion guide can be used to decrease the
effects due to space charging in the FT-ICR mass spectrometer.
Description
FIELD OF INVENTION
[0001] This invention relates to the configuration and method of
using a multipole ion guide to transport and focus ions which enter
vacuum from an atmospheric pressure ion source, into a mass
analyzer. The multipole on guide which begins in one vacuum pumping
stage has been configured to extend contiguously through one or
more subsequent vacuum stages. Multipole ion guides are used to
efficiently transfer ions through one or more vacuum stages while
allowing the neutral background gas to be pumped away. The AC
frequency and AC and DC voltages which are applied to the poles of
a multipole ion guide can be set so that the multipole ion guide
will pass a selected range of ion mass to charge. The ion
transmission properties of multipole ion guides can be used to
enhance performance of specific mass analyzer types which are
interfaced to atmospheric pressure ion sources.
BACKGROUND OF THE INVENTION
[0002] Atmospheric pressure ion sources (API) have become
increasingly important as a means for generating ions used in mass
analysis. Electrospray or nebulization assisted Electrospray (ES),
Atmospheric Pressure Chemical Ionization (APCI) and Inductively
Coupled Plasma (ICP) ion sources produce ions from analyte species
in a region which is approximately at atmospheric pressure. The
ions must then be transported into vacuum for mass analysis. A
portion of the ions created in the API source are entrained in the
bath gas API source chamber and are swept into vacuum along with a
the bath or carrier gas through an orifice into vacuum. Mass
spectrometers (MS) generally operate in a vacuum maintained at
between 10.sup.-4 to 10.sup.-10 torr depending on the mass analyzer
type. The gas phase ions entering vacuum from an API source must be
separated from the background carrier gas and transported and
focused through a single or multiple staged vacuum system into the
mass analyzer. Variations in vacuum system and associated
electrostatic lens configurations have emerged in API/MS systems.
Where multiple pumping stages have been employed, the electrostatic
lens elements have been configured to serve as restricted orifices
between vacuum stages as well as providing ion acceleration and
focusing of ion into the mass analyzer. Performance tradeoffs may
occur where electrostatic lenses must also accommodate restricting
the neutral gas transmission from one pumping stage to the next.
For example, a skimmer placed between one pumping stage and the
next may restrict the neutral gas flow but may also restrict the
passage of ions as well due to its relatively small orifice. Two
types of Electrostatic elements have been used to transport and
focus ions in vacuum, particularly where ions are entering vacuum
from atmospheric pressure through a free jet expansion. The first
is a static voltage lens and the second is a dynamic field ion
guide. The most effective lens configurations used in API/MS
systems employ a judicious combination of both elements which have
static and dynamic fields applied.
[0003] The first electrostatic lens type has a fixed or static DC
voltage applied during the time an ion is traversing the lenses'
field. FIG. 1 is a diagrammatic representation of a four pumping
stage API/MS system with static voltage electrostatic lenses. Gas
emerging from the capillary exit 8 into vacuum expands as a
supersonic free jet and a portion of the gas passes through the
first 10 and second 14 skimmer. Skimmers between pumping stages
typically have small orifices to restrict the neutral gas flow into
each downstream vacuum stage. DC voltages are applied to the
capillary exit, skimmers and other electrostatic lenses 9, 14, 15,
16 and 17 with values set to maximize the ion transmission into the
mass spectrometer. Ions entrained in the expanding gas follow
trajectories that are driven by a combination of electrostatic and
gas dynamic forces. Strong influence from the gas dynamics can
extend up to and beyond the second skimmer 13 for the configuration
shown in Figure one. The efficiency of ion transmission through a
static voltage lens set can be reduced by scattering losses due to
collisions between ions and the background gas which occur along
the ion trajectory. Ions with different m/z may vary their
collisional cross sections and hence experience different numbers
of background collisions as they are transported through vacuum.
For a given electrostatic lens voltage setting the efficiency of
ion transport into the mass spectrometer may vary with m/z or the
collisional cross section. Changing the lens voltage values may
optimize transmission for a given ion species but the setting may
not be optimal for another ion species transmission. For example
static lens configurations used in API/MS applications may not
transmit lower molecular mass compounds as efficiently as higher
molecular mass compounds. The smaller ions may sustain higher
transmission losses due to collisional scattering from the
background gas than the higher molecular mass compounds. To
increase ion transmission efficiency through a static lens stack,
the electrostatic energy must be set sufficiently high so that ions
can be driven through the background gas. Static voltage lens
configurations also tend to focus ions of different energy at
different focal points. If the focal point is not located at the
mass spectrometer entrance transmission losses can occur. To
overcome the mass to charge transmission discrimination effects and
ion transport inefficiencies which occur when static voltage lenses
are used, multipole dynamic field ion guides have been employed to
transport ions through vacuum pumping stages in the vacuum region
of API/MS systems. The dynamic electrostatic fields within a
multipole ion guide dominate over the background gas scattering
collisions and effectively "trap" the ions while they traverse the
length of the multipole ion guide.
[0004] The use of multipole ion guides has been shown to be an
effective means of transporting ions through vacuum. Publications
by Olivers et. al. (Anal. Chem, Vol. 59, p. 1230-1232, 1987), Smith
et. al. (Anal. Chem. Vol. 60, p.436-441, 1988) and U.S. Pat. No.
4,963,736 (1990) have reported the use of a quadrupole ion guide
operated in the AC-only mode to transport ions from an API source
into a quadrupole mass analyzer. U.S. Pat. No. 4,963,736 describes
the use of a multipole ion guide in either vacuum pumping stage two
of a three stage system or in the first pumping stage of a two
stage vacuum system. This patent also reports that increasing the
background pressure up to 10 millitorr in the vacuum stage where
the ion guide was positioned resulted in an increase in ion
transmission efficiency and a decrease in ion energy spread of ions
transmitted. Ion signal intensity decreased for higher background
pressures in the reported quadrupole configuration. A commercially
available API/MS instrument manufactured by Sciex, a Canadian
company, incorporates a quadrupole ion guide operated in the
AC-only mode located before the quadruple mass filter in a single
stage vacuum system. Ions and neutral gas flowing into vacuum
through an orifice in the API source enter the quadrupole AC-only
ion guide. The ions are trapped from expanding in the radial
direction by the AC quadrupole fields and are transmitted along the
quadrupole ion guide rod length as the neutral gas is pumped away
through the rod spacing. Ions exiting the quadrupole ion guide are
focused into a quadrupole mass filter located in the same vacuum
chamber. Neutral gas is pumped away by a high capacity and
relatively expensive cyro pump. Multiple quadrupole ion guides have
been used to transport ions from API sources through multiple
vacuum pumping stages and into a Fourier-Transform Ion Cyclotron
Resonance mass analyzer. Beu et. al. (J. Am. Soc. Mass Spectrom
vol. 4. 546-556, 1993) have reported using three quadrupole ion
guides operated in the AC-only mode located in three consecutive
vacuum pumping stages of a five pumping stage Electrospray
Fourier-Transform Ion Cyclotron Resonance (FT-ICR) mass
spectrometer instrument. The multiple pumping stages are required
to achieve operating pressures in the mass analyzer of less than
2.times.10.sup.-9 torr. Orifices mounted in the partitions between
each vacuum pumping stage which restricted neutral gas conductance
from one pumping stage to the next were located between consecutive
quadrupole ion guides.
[0005] Over the past few years as API/MS system design has evolved,
higher performance with lower system cost has been achieved by
using multiple vacuum stages to remove the background gas from the
ions which enter from atmospheric pressure into vacuum. The type of
mass analyzer to which an API source is interfaced places its
unique demands on the ion transport lens configurations and vacuum
requirements in the ion transport region between atmospheric
pressure and the mass analyzer. Each mass analyzer type has an
acceptable ion energy, ion energy spread and entrance angular
divergence which the upstream ion transport lens system must
satisfy when delivering ions to the entrance of a mass
spectrometer. For example, a quadrupole mass analyzer can accept
ions with axial translational energy generally below 40 electron
volts whereas a magnetic sector mass spectrometer requires ions
with thousands of volts of axial translational energy.
[0006] In the present invention, a multipole ion guide is
configured to increase the overall sensitivity of an API/MS system
while reducing instrument cost and complexity. In one embodiment of
the present invention, a multipole ion guide is used to transport
ions entering vacuum from an API source to non-dispersion type mass
analyzers. A range of ion mass to charge (m/z) can be efficiently
transmitted through a multipole ion guide provided the ion guide
operating stability region is set to pass those values of m/z. If
an ion with a given mass to charge ratio falls within the operating
stability region set for a multipole ion guide, the ion will be
effectively trapped from drifting to far in the off axis direction
but is free to move in the direction of ion guide axis. If the ion
m/z falls outside the stability region, it will not have a stable
trajectory and will be rejected from the ion guide before it
reaches the exit end. Collisions between an ion and the background
gas within the multipole assembly can also effect the ion
trajectory and the ion kinetic energy as it passes through the
multipole ion guide. The background gas, if present at high enough
pressure, may serve, through collisions, to damp the motion of ions
as they pass through the multipole ion guide, cooling their kinetic
and thermal energy. This aids in forming an ion beam which exits
the multipole ion guide with reduced energy spread for a given ion
species within the beam. The range of m/z which are transmitted
through a multipole ion guide for a given background pressure
environment can be varied by adjusting the AC frequency and AC
and/or a DC voltage which can be applied with alternate polarity to
each adjacent rod. The offset potential of the multipole lens, that
is the DC voltage applied uniformly to all the rods on which the AC
and alternate polarity DC rod potentials are floated and referenced
is one variable that can to be used to set the energy of ions
transmitted through the multipole ion guide. Multipole ion guides
can be configured to efficiently transport ions through a wide
range of vacuum pressures. The ability of a multipole ion guide to
deliver and ion beam with low energy spread and where the mean
energy and m/z range can be adjusted into a mass analyzer can be
used to improve the performance of an API/Time-Of-Flight, API/Ion
Trap and API/FT-ICR mass spectrometer systems.
[0007] Another embodiment of the invention is the incorporation of
a multiple vacuum pumping stage multipole ion guide into an API/MS
system. A multiple vacuum pumping stage multipole ion guide is a
multipole ion guide which begins in one pumping stage and extends
contiguously through one or more additional vacuum pumping stages
of a multiple pumping stage system. Multipole ion guides which are
located in only one vacuum pumping stage of a multiple pumping
stage system must deliver the ions exiting the ion guide into an
aperture with static voltage applied. If background pressure is
high enough to scatter the ions after the multipole ion guide exit
or the aperture to the next pumping stage has a smaller diameter
than the ion beam cross section, losses in ion transmission can
occur. If individual multipole ion guides are located progressively
in the first few pumping stages of an API/MS system, ion
transmission losses can occur when transferring ions between
pumping stages. If fewer pumping stages are used to reduce the ion
transmission losses between pumping stages, the total gas flow and
hence the total number of ions which can be delivered to vacuum may
be compromised. Over 95% ion transmission efficiency can be
achieved through multiple vacuum pumping stages using multipole ion
guides configured to extend contiguously through two or more vacuum
pumping stages. A multiple vacuum stage multipole ion guide must be
configured serve as an ion guide with an internal open area small
enough to minimize the neutral gas flow from one pumping stage to
the next. Xu at. el. (Nuclear Instr. and Methods in Physics
Research, Vol. 333, p. 274, 1993) have developed a hexapole lens
which extends through two vacuum pumping stages to transport ions
formed in a helium discharge source operated in a chamber
maintained at 75 to 150 torr of pressure through two vacuum pumping
stages into a faraday cup detector. The discharge ion source
delivered ions into a two stage vacuum system through an orifice in
the end wall of the source chamber. The background pressure in the
first vacuum pumping stage was 600 millitorr and the second vacuum
stage background pressure was 98 millitorr. Ion transmission
efficiencies through the hexapole ion guide beginning in vacuum
stage one and extending unbroken into vacuum stage two approached
90% for O.sub.2.sup.+. The helium discharge ion source background
pressure in this apparatus was 5 to 10 times below atmospheric
pressure and helium was used as the background gas. Different
configuration and performance criteria exist for multiple pumping
stage multipole ions guides incorporated into an API/MS system than
were required for the ion guide application described by Xu and
coworkers. Multipole ion guides incorporated into API/MS systems
must have the capability of efficiently transmitting ions of
various charge states over a wide range of mass to charge.
Nitrogen, not helium, is typically used as carrier gas in API
sources and the background pressures in API/MS multiple vacuum
stage systems are often widely different from the pressures
reported in the ion guide apparatus reported by Xu. An added
constraint imposed on API/MS systems which was not present in the
non API/MS application practiced by Wu et. al. is the ability to
fragment molecular ions by Collisional Induced Dissociation (CID)
in the gas expansion region in the first two vacuum stages.
Valuable structural information can be obtained from CID of
molecular ions produced in ES and APCI sources. CID conditions can
be set by adjusting relative potentials between static voltage
lenses and even the DC offset potentials of multipole ion guides
located in the first two vacuum pumping stages of a API source.
[0008] In the present invention, multiple pumping stage multipole
ion guides are configured to maximize performance of API/MS systems
while reducing system vacuum pump cost. Increasing signal
sensitivity while lowering vacuum pumping cost is achieved by
maximizing the ion transfer efficiency from the API source into the
mass analyzer while minimizing the amount of neutral gas
transferred. For the multiple pumping stage multipole ion guides
which begin in one vacuum pumping stage and extend through one or
more subsequent pumping stages, the rod diameter and rod spacing in
the multipole ion guide assembly were configured small enough to
minimize the transmission of neutral gas through the ion guide into
downstream pumping stages. Acceptable vacuum pressure per pumping
stage was be achieved with moderate capacity vacuum pumps. The ion
guide with a small inner diameter was configured to allow
sufficient conduction of neutral gas through the spaces between the
rods or poles so the neutral gas was pumped away efficiently in
each pumping stage. The small multipole ion guide inner diameter
produced an ion beam with a proportionally small cross section. The
smaller cross section ion beam focused into the mass analyzer
allowed the reduction of the mass analyzer entrance aperture
without compromising ion transmission efficiency. Efficient ion
transport, better control of ion energy and energy spread and a
small beam diameter is achieved by using a multiple vacuum pumping
stage multipole ion guide.
SUMMARY OF THE INVENTION
[0009] In accordance with the present invention, an Atmospheric
Pressure Ion source which includes Electrospray or nebulization
assisted Electrospray, Atmospheric Pressure Chemical Ionization and
Inductively Coupled Plasma ion sources interfaced to a mass
analyzer incorporates a multipole ion guide in the vacuum pumping
region between the API source and the mass analyzer.
[0010] In one embodiment of the invention, the API/MS system
includes multiple vacuum pumping stages and a multipole ion guide
which begins in one vacuum pumping stage and extends contiguously
through two or more vacuum pumping stages. The multipole ion guide
inner diameter is reduced to minimize the neutral gas conduction
between vacuum pumping stages while allowing the efficient
transport of ions through the multipole ion guide length. At least
one portion of a multiple vacuum stage multipole ion guide is
subject to background gas pressures which are high enough that the
ions traversing the ion guide length are subject to many collisions
with neutral background gas molecules. Ion transmission
efficiencies through such multipole ion guide assemblies can exceed
95% even with background pressures in a given vacuum pumping stage
of hundreds of millitorr. Collisions between the ions and the
background neutral was in the multipole ion guide cause cooling of
the ion kinetic energy, reducing the ion energy spread. The AC
field of the multipole ion guide traps ions within a radial cross
section and prevents scattering losses of the ions undergoing
collisions with the background gas as the ions traverse the ion
guide length. The energy of the ions exiting the multipole ion
guide relative to the mass analyzer entrance aperture potential can
be set by varying the multipole ion guide DC offset potential. With
sufficient ion kinetic energy cooling in the ion guide, ion energy
can be adjusted over a wide range with little change to the ion
energy spread for a given m/z. Ions with mean energies of a few
electron volts or lower can be transmitted into the mass analyzer
entrance aperture by using multiple vacuum pumping stage multipole
ion guides. Lower energy ions with a narrow energy spread
transmitted into quadrupole mass analyzers will result in higher
sensitivity for a given resolution than can be achieved with higher
energy ions. Increased sensitivity and resolution can be achieved
by using multiple vacuum pumping stage multipole ion guides with
reduced vacuum system costs for quadrupole, time-of-flight, ion
trap, FT-ICR and magnetic sector mass spectrometers.
[0011] When operating multipole ion guides in the AC only mode or
with AC and DC applied to the poles, the frequency and voltage
levels can be set so that a broad range of m/z ions will be
transmitted through the multipole ion guide. The AC frequency and
AC and DC voltages can also be set to restrict the range of m/z
values that will be transmitted through the multipole ion guide for
a given background pressure environment. Narrowing the range of m/z
values transmitted to the analyzer of a TOF mass spectrometer can
be used to increase the duty cycle and hence sensitivity of an
API/TOF mass spectrometer instrument. Limiting the range of m/z for
ions transmitted into an ion trap or the analyzer cell of an FT-ICR
mass spectrometer instrument can reduce the effects of space
charging in the trap or FT-ICR cell during mass analysis. This can
improve the mass measurement accuracy, resolution and dynamic range
of the mass analyzer.
DESCRIPTION OF THE DRAWINGS
[0012] FIG. 1 is a diagram of a four vacuum stage ES/MS quadrupole
instrument with a static lens configuration incorporated into
vacuum stages 1 through 3.
[0013] FIG. 2 is a diagram of a four vacuum stage ES/MS quadrupole
instrument with a multipole ion guide beginning in the second
vacuum pumping stage and extending contiguously into the third
pumping stage.
[0014] FIG. 3a shows the transmission efficiency of ions through a
two vacuum stage multipole ion guide for m/z 110 over a range of
values for q.sub.n.
[0015] FIG. 3b shows the transmission efficiency of ions through a
two vacuum stage multipole ion guide for m/z 872 over a range of
values for q.sub.n.
[0016] FIG. 3c shows the transmission efficiency of ions through a
two vacuum stage multipole ion guide for m/z 1743 over a range of
values for q.sub.n.
[0017] FIG. 4 is a mass spectrum of Glucagon with the two vacuum
pumping stage multipole ion guide q.sub.n value set to pass a wide
range of m/z values.
[0018] FIG. 5a is an Electrospray mass spectrum of Arginine where
the multipole ion guide q.sub.n value is set to pass a broad range
of m/z values.
[0019] FIG. 5b is a mass spectrum of Arginine where the multipole
ion guide q.sub.n value is set so that a low m/z cutoff ion
transmission occurs.
[0020] FIG. 6a is an Electrospray mass spectrum of Gramicidin S
where the multipole ion guide q.sub.n value is set to pass a broad
range of m/z values.
[0021] FIG. 6b is a mass spectrum of Gramicidin S where the
multipole ion guide q.sub.n value is set so that a low m/z cutoff
ion transmission occurs.
[0022] FIG. 7a is an Electrospray mass spectrum of a mixture of
Arginine, Leucine Enkephalin and Gramicidin S where the multipole
ion guide q.sub.n value is set to pass a broad range of m/z
values.
[0023] FIG. 7b is a mass spectrum of a mixture of Arginine, Leucine
Enkephalin and Gramicidin S where the multipole ion guide q.sub.n
value is set so that a high m/z cutoff ion transmission occurs.
[0024] FIG. 8a is a curve of ion signal for m/z 571 versus the
multipole ion guide exit lens potential for a multipole ion guide
DC offset potential set at 0.1 volts.
[0025] FIG. 8b is a curve of ion signal for m/z 571 versus the
multipole ion guide exit lens potential for a multipole ion guide
DC offset potential set at 15.3 volts.
[0026] FIG. 8c is a curve of ion signal for m/z 571 versus the
multipole ion guide exit lens potential for a multipole ion guide
DC offset potential set at 25.1 volts.
[0027] FIG. 9 is a spectrum of a doubly charged Gramicidin S peak
scanned with the multipole ion guide offset potential set at 0.1
volt.
[0028] FIG. 10 is a diagram of a four vacuum stage ES/MS
Time-OF-Flight instrument with orthogonal pulsing including a
multipole ion guide beginning in the second vacuum pumping stage
and extending into the third vacuum pumping stage.
[0029] FIG. 11 is a diagram of a three vacuum stage ES/MS ion trap
instrument with a multipole ion guide beginning in the first vacuum
stage and extending through the second and into the third vacuum
pumping stages.
[0030] FIG. 12 is a cross section of a hexapole ion guide including
the electrically insulating mounting bracket.
[0031] FIG. 13 is a diagram of a three vacuum pumping stage API/MS
ion trap instrument with a single pumping stage multipole ion guide
located in the second vacuum stage.
[0032] FIG. 14 is a diagram of a four vacuum pumping stage
API/orthogonal pulsing TOF mass spectrometer instrument with single
vacuum stage multipole ion guides located in the second and third
vacuum stages.
DESCRIPTION OF THE INVENTION
[0033] Sample bearing liquid is introduced into atmospheric
pressure ionization sources including ES, APCI and ICP sources and
gas phase ions are produced from the analyte in solution. API/MS
systems are available which include from one to over five vacuum
pumping stages. An Electrospray ion source interfaced to a
quadrupole mass spectrometer is diagrammed in FIG. 1. The system
shown includes four vacuum pumping stages and a static voltage lens
configuration to transfer ions through the first three pumping
stages and focus them into the entrance of quadrupole mass
spectrometer 18. In the configuration shown, sample bearing liquid
is introduced through needle 1 and is Electrosprayed into the bath
gas in chamber 2. Liquid droplets evaporate in chamber 2 or as they
are swept into vacuum through capillary 3 and ions are released
from the evaporating droplets. The charged liquid droplets can be
dried by using a countercurrent drying gas 23 and/or a heated
capillary 3. A portion of the ions and charged droplets formed in
electrospray chamber 2 enter the capillary entrance 4 along with a
portion of the background bath gas and are swept into vacuum
through the capillary annulus 5. Alternatively the capillary
orifice into vacuum could be replaced by a nozzle with appropriate
orifice size. The bath or carrier gas and entrained ions are swept
through the capillary and enter the first vacuum stage 7 after
passing through the capillary exit 8. The pressure in vacuum stage
7 is generally maintained between 0.4 and 20 torr so the gas
exiting the capillary expands in a supersonic free jet. The ions
entrained in this free jet are accelerated by collisions with the
expanding background gas. The background gas used is usually
nitrogen but may be also be carbon dioxide, oxygen, helium or any
number of other gases which suit the analysis requirements and ion
source type. An electrostatic field is applied between the
capillary exit 8, the ring lens 9 and the first skimmer 10 to
electrostatically focus and accelerate ions through the skimmer 10
orifice 11 and on into the second vacuum stage 12. Vacuum stage 12
is typically operated at a pressure ranging from 5 to 200 millitorr
depending on pumping speeds and the size of skimmer orifice 11.
Electrostatic potentials are maintained between skimmers 10 and 13
and a portion of the ions passing through skimmer 10 are focused
through orifice 22 in skimmer 13 into the third vacuum pumping
stage 20. Pressure in pumping stage 20 is maintained typically
between 1.times.10.sup.-3 to below 8.times.10.sup.-5 torr.
Potentials are set on electrostatic lens elements 14, 15 and 16 to
focus ions through aperture 17 after which they pass into the
quadrupole mass filter 18 located in the fourth pumping stage
24.
[0034] The static voltage lens system shown in FIG. 1 transmits and
focuses ions through the vacuum stages and into the mass analyzer
while allowing the background gas to be pumped away. The ion energy
relative to the quadrupole mass filter offset voltage is
established by a combination of acceleration energy imparted by the
expanding carrier gas and the electrostatic potentials applied. The
capillary exit 8 potential relative to the ring electrode 9 and
skimmer electrode 10 can be set high enough to cause Collisional
Induced Dissociation (CID) which can affect the energy and energy
spread of the parent and fragment ions. Ion transmission losses can
occur in each pumping stage due to scattering from background
pressure and the inability to electrostatically focus ions through
the pumping stage skimmer orifices 11 and 22 and the quadrupole
entrance aperture 17. To achieve the desired pressures per pumping
stage while constraining the vacuum pumping speeds to fall below
800 L/sec to reduce the vacuum pump cost and size, skimmer orifice
11 in this configuration would typically have a diameter of 0.8 to
1.5 mm and skimmer orifice 22 may range from 0.8 to 3.0 mm. The
smaller the skimmer orifice size the fewer the number of ions that
can be transmitted through this static lens configuration. The
higher the energy spread for ions of a given m/z and the larger the
energy difference for ions with different m/z, the fewer the ions
that can be efficiently focused into the mass spectrometer and
effectively mass analyzed. Depending on vacuum pressures maintained
during operation, the static lens configuration shown may exhibit
different transmission efficiencies for different m/z values. Also,
with static voltage lens systems, ion transmission efficiency drops
off rapidly as the ion energy is reduced below 10 electron
volts.
[0035] To improve ion transmission performance yet retain the
advantages of multiple pumping stages to more cost effectively
remove neutral gas, a multipole ion guide has been used, replacing
some of the static voltage lenses. FIG. 2 illustrates a multipole
lens assembly 40 which begins in vacuum pumping stage 41 and
extends unbroken into vacuum pumping stage 42. Individual rods or
poles 45 in assembly 40 are held in place and electrically isolated
from the partition between vacuum pumping stage 41 and 42 by
insulator 43. A cross section of a hexapole ion guide is
illustrated in FIG. 12 with insulator 156 serving the dual purpose
of holding the six rods or poles 160 in position while minimizing
the effective aperture area inside the rods assembly diameter
through which neutral gas flows and ions are transmitted from one
pumping stage to the next. Multipole ion guide assembly 40 consists
of parallel electrodes 45 in FIG. 12 shown as round rods 160
equally spaced with a common radius from the centerline. An
octapole ion guide would have eight equally spaced rods and a
quadrupole would have four equally spaced rods or poles. When
multipole ion guide 40 is operated in the AC-only mode, every other
rod has the same AC frequency, voltage and phase and every adjacent
rod has the same AC frequency and voltage applied but a phase
difference of 180 degrees. So for a hexapole ion guide, three rods
or poles would be operated with the same AC frequency, voltage and
phase and the same AC frequency and voltage with a phase difference
of 180 degrees would be applied to the remaining three rods. A DC
offset voltage is applied to all rods 45 of the multipole ion guide
40 and plays a large role in establishing the ion energy. The
multipole ion guide DC offset potential is set to focus ions
passing through skimmer 47 orifice 48 into the multipole ion guide.
The kinetic energy of the ions entering multipole ion guide 40 has
contributions from the velocity imparted by the expanding gas
exiting capillary exit 50, the relative electrostatic DC potentials
applied to capillary exit 50, ring lens 51, skimmer 47 and the
multipole rod 40 DC offset potential as well as any AC voltage
component from fringing fields as ions enter multipole ion guide
40. Static voltage lens elements may be added at the exit end 52 of
the multipole ion guide to focus ions into the mass analyzer
entrance 47. Lens 53 is positioned at exit 52 of multipole ion
guide 40 to shield the exiting ions from the multipole AC voltage
fringing fields and to focus the ions into the mass analyzer
entrance aperture 47. The efficiency of ion transport through this
two pumping stage multipole ion guide 40 is over 95% for a wide
range of ion m/z values. Ion transmission efficiencies were
determined by measuring the total ion current which passed through
skimmer orifice 48 and by measuring the total ion current exiting
multipole ion guide 40 for the same electrospray ion source
operating conditions.
[0036] The performance characteristics of the two vacuum pumping
stage multipole ion guide 40 diagrammed in FIG. 2 will be used as
an example although many variations in multiple pumping stage
multipole ion guides are possible. A hexapole ion guide was
configured with rods beginning in vacuum pumping stage 41 and
extending contiguously into vacuum pumping stage 42 of a four stage
system as diagrammed in FIG. 2. For testing purposes, the
background pressures could be varied in the first and second
pumping stages 53 and 41. With multipole ion guide 40 operated in
the AC-only mode, the AC frequency and amplitude and the DC offset
potentials were varied to map out performance over a range of
background pressures.
[0037] A two vacuum stage hexapole ion guide was chosen over a
quadrupole or octapole because for this four vacuum stage API/MS
system because the hexapole configuration was the most favorable
compromise between trapping efficiency, vacuum pumping conduction
through the rod spacing and overlap of stability regions for a wide
range of m/z values and background pressures. Two non-dimensional
coefficients a.sub.n and q.sub.n are commonly used when mapping ion
trajectories in multipole ion guides or mass filters by solving the
Laplace equation of motion. The two coefficients are defined as: 1
a n = n 3 U 2 ( m z ) 2 r O 2 and q n = n 3 V 4 ( m z ) 2 r O 2
[0038] where n is the number of rod pairs (n=3 for a hexapole), U
is the DC potential applied to the rods, every other rod having
opposite polarity, m/z is the mass to charge ratio of the ion
traversing the multipole ion guide, co is the frequency applied, V
is the zero-to-peak AC potential applied to the rods, every other
rod being 180 degrees out of phase, and r.sub.0 is the radius from
the assembly centerline. When the multipole ion guide is operated
in the AC-only mode, U is set equal to zero so a.sub.n drops out of
the equation of motion. The DC rod offset potential applied equally
to all rods only effects the ion trajectories entering and leaving
the multipole ion guide 40. The offset potential should not effect
the stability of the ion trajectories once the ions pass into the
ion guide and are trapped within the rods other than to influence
their initial entrance trajectory. For the configuration shown in
FIG. 2, the background gas pressure inside the rod assembly varies
along the multipole ion guide length and will effect the ion
trajectories through the ion guide. To theoretically model the
effect of the background neutral gas collisions on the ion
trajectory through a multipole ion guide, the cross section of the
ions must be known. The collisional cross sections of ions
generated by API sources are not always known, however. In
particular, the cross section of multiply charged ions which can be
produced in the electrospray ion source are not always known.
Consequently, for a given multipole ion guide configuration, values
of a.sub.n and q.sub.n where efficient ion transmission through the
multipole lens can be achieved must be mapped for any given m/z and
background pressure combination encountered.
[0039] The rod AC voltages were ramped for different radio
frequency (RF) values using the multipole ion guide configuration
diagrammed in FIG. 2, to map the regions of stable q.sub.n for all
m/z falling within the range of the quadrupole mass spectrometer.
The background pressure gradient was held constant for each set of
ion transmission tests to establish the values of q.sub.n where
stable and efficient ion trajectories through the two vacuum stage
multipole ion guide 40 could be achieved. The number of ion to
neutral gas collisions that occur as an ion transverses the rod
length is a function of the background pressure as well as the rod
length. The longer the rods, the more collisions which occur for an
ion traversing the rods in a given background pressure. The
multipole ion guide assembly 40 was constructed with an effective
inner diameter smaller than 2.5 millimeters to minimize the neutral
gas conduction between vacuum stages 41 and 42. The rod length in
vacuum stage 41 was 2.9 cm and the rod length in stage 42 was 3.0
cm. For this multipole ion guide configuration and background
pressure gradient tested, the AC voltage applied was kept below the
point where electrical breakdown occurred between the rods. To
determine which values of q.sub.n allow a stable trajectory for an
ion with a given m/z and charge state, the multipole RF amplitude
was ramped for set frequencies ranging from 1 to 10 MHz.
[0040] An example a test series is given in FIGS. 3a, 3b and 3c
taken with following background pressures: pumping stage 53 was 2
torr, pumping stage 41, 150 millitorr, pumping stage 42,
4.times.10.sup.-4 torr and pumping stage 54 was 6.times.10.sup.-6
torr. For the data taken in FIG. 3a, the quadrupole mass filter was
scanned from m/z 109.6 to 110.6. The ion signal was measured at
each 1 MHz step of the RF frequency varying the RF amplitude to
find the maximum signal. At each RF frequency the RF amplitude was
ramped from minimum to maximum and then ramped back to its minimum
value. At point 61 in FIG. 3a the two vacuum stage multipole ion
guide is being operated in the AC-only mode with its RF frequency
set at 3 MHz and the RF amplitude set low. As the RF amplitude is
ramped to its maximum value at 62, the ion transmission efficiency
reaches its maximum at 63 for this frequency and m/z. From 62 the
amplitude is ramped down to its original low value at 64 where
little or no ion transmission is observed. The signal maximum
observed at 65 has the same RF amplitude as at 63 as expected since
the same value of q.sub.3 occurs at points 63 and 65. At an RF
frequency of 5 MHz, the RF amplitude is ramped from a minimum value
at 66 to a maximum at 67 returning to a minimum at 68. The
relatively flat top shape of the ion signal which occurs between 78
and 67 indicates that very efficient ion transmission at m/z 110 is
occurring over a range of RF amplitude or q.sub.3. FIG. 3b shows
the ion transmission efficiency for m/z 872 generated
simultaneously with the data shown in FIGS. 3a and 3c. The
quadrupole mass filter was scanned from m/z 871.7 to 872.7 while
applying the same values of RF frequency and amplitude as were run
for m/z 110 in FIG. 3a. The RF amplitude was set at 1 MHz with a
low amplitude at 69. As the RF amplitude was increased from a
minimum at 69 to a maximum at 71, the maximum ion transmission
occurred at 70. As expected, the maximum ion transmission occurs at
the same q.sub.3 value when ramping the RF amplitude from its
maximum value at 71 back to its minimum at 72. When the frequency
is increased to 3 MHz and the RF amplitude ramped from a minimum at
73 to a maximum at 74 back to a minimum at 75, efficient ion
transmission is achieved over a wide range of RF amplitude or
q.sub.3. FIG. 3c shows the ion transmission efficiency for m/z 1743
(scanned from 1742.5 to 1743.5) over the same RF frequency and
amplitude ranges as were used for m/z 110 shown in FIG. 3a. FIG. 3
illustrates that for a given background pressure gradient, varying
orders of magnitude over the multipole ion guide length, efficient
ion transmission through the ion guide operated in the AC-only mode
can be achieved for a broad range of m/z values. For example, if
the maximum efficiency in ion transmission were desired over the
entire range of m/z tested in FIG. 3 then the RF frequency would be
set at 4 MHz and run with an RF amplitude that could fall roughly
at the q.sub.3 value indicated at point 76. For this fixed value of
q.sub.3 and background pressures at which the transmission
efficiencies were measured, m/z values from less than 110 to over
1743 would be efficiently transmitted through the multipole ion
guide. FIG. 4 is a mass spectrum of Glucagon taken with the ion
guide q.sub.3 value set at the point indicated by 76 in FIG. 3. A
solution of 2 picomole/.mu.l of Glucagon in 1:1 methanol:water was
Electrosprayed using continuous infusion sample introduction in an
API/MS instrument as configured in FIG. 2 and the quadrupole mass
spectrometer was scanned from 20 to 1900 m/z. The (M+4H).sup.+4,
(M+3H).sup.+3 and (M+2H).sup.+2 Glucagon peaks are indicated by 80,
81 and 82 respectively. The use of a multiple pumping stage
multipole ion guide to transmit and focus ions exiting from a free
jet expansion into a mass analyzer allows flexibility in
configuring an API/MS instrument without compromising sensitivity.
Smaller multiple pumping stage API/MS instruments can be configured
with vacuum pumps chosen to minimize instrument cost without
compromising performance. Multiple pumping stage multipole ion
guides can be configured and operated to allow efficient ion
transmission and focusing over a a wide range of pressure
gradients. Multipole ion guides can be configured for use with a
number of mass analyzer types which may require different operating
pressure regimes. For example a quadrupole mass analyzer can
operate efficiently at a vacuum pressure of 2.times.10.sup.-5 torr
or below whereas a TOF analyzer requires background pressures in
the low 10.sup.-7 torr range or lower to avoid significant numbers
of collisions between ions and background gas during the ion flight
time. A multiple vacuum pumping stage API/MS instrument with a
single or a multiple pumping stage multipole ion guide can be
configured to maximize ion transmission and focusing yet minimize
pumping cost.
[0041] FIG. 3 illustrates that the a.sub.n and q.sub.n values can
be set so that a low or a high m/z cutoff in ion transmission
occurs. For example if the RF frequency were set at 3 MHz and the
RF amplitude operated anywhere from point 79 to 62 then ions with
m/z 110 or lower would not be transmitted through the multipole ion
guide to the mass analyzer. Similarly, if the RF frequency were
operated at 7 MHz with the RF amplitude set at the value indicated
by 77 then a high m/z cutoff in ion transmission through the ion
guide to the mass analyzer would occur. FIGS. 5a and 5b illustrate
operation of the multipole ion guide 40 with the q.sub.n value set
for passing a broad range of m/z and the q.sub.n value set at a
point where a low m/z transmission cutoff occurs. FIG. 5a is a mass
spectrum taken from electrospraying a solution of 2 picomole/.mu.l
of Arginine in 1:1 methanol:water using continuous infusion with
the multipole ion guide 40 q.sub.3 value set to transmit a wide
range of m/z values. The cation impurities of sodium 85 (m/z 23)
and potassium 86 (m/z 39) present in solution appear in the mass
spectrum as well as the protonated methanol monomer 87 (m/z 33) and
dimer 88 (m/z 65) and the sample Arginine protonated peak 90 at m/z
175. FIG. 5b shows a mass spectrum taken with the same solution
being Electrosprayed under identical spray conditions but with the
hexapole ion guide q.sub.3 value was set so that a low m/z cutoff
occurs. Ion transmission below 100 to 120 m/z has been effectively
cut off without reducing the ion transmission efficiency of
Arginine 91 or higher m/z values. Another example of this is
illustrated in FIGS. 6a and 6b where a 2 picomole/.mu.l sample of
Gramicidin S in 1:1 methanol:water was Electrosprayed with
continuous infusion using the API/MS configuration illustrated in
FIG. 2. In FIG. 6a the hexapole 40 q.sub.3 value is set to transmit
a wide m/z range and an impurity potassium peak 92 and the
protonated doubly charged Gramicidin S peak 93 (M+2H).sup.+2 are
observed in the mass spectrum. FIG. 6b is a mass spectrum of the
same Gramicidin S solution Electrosprayed using identical
conditions as in FIG. 6a but with the hexapole 40 q.sub.3 value is
set so that a low m/z cutoff occurs. The potassium ions are no
longer transmitted to the mass analyzer but the ion transmission
efficiency of the doubly charged Gramicidin S ions as shown by peak
94, is still retained. A q.sub.n value can also be selected to
cause a high m/z cutoff as illustrated in FIGS. 7a and 7b where a
mixture of Arginine, Leucine Enkephalin and Gramicidin S, 2
picomole/ul each in 1:1 methanol:water was Electrosprayed using the
API/MS configuration shown in FIG. 2. FIG. 7a is a mass spectrum
taken where the multipole ion guide 40 q.sub.3 value was set to
transmit a wide range of m/z values. The Arginine (M+H).sup.+ peak
95, Leucine Encephalon (M+H).sup.+ peak 96 and doubly charged
Gramicidin S (M+2H).sup.+2 peak 97 are present in the mass spectrum
as well as the lower m/z ion peaks 98. FIG. 3b is a mass spectrum
taken where the same solution is Electrosprayed using identical
spray conditions except that the ion guide 40 q.sub.3 value has
been set so that the lower m/z ions are transmitted as indicated by
peaks 99 but the higher m/z ions are not transmitted through the
multipole ion guide 40.
[0042] A valuable feature of multipole ion guides when operated in
higher background pressures is that ions traversing the length of
the ion guide experience a number of collisions with the background
gas resulting in the cooling of the ion kinetic energy. As the ions
enter the multipole ion guide and are transmitted through it, the
RF or combined RF-DC field effectively traps the ions from
dispersing in the radial direction due to collisions with the
background gas yet permits movement of ions in the axial direction
often driven by the gas dynamics. Ions which experience a number of
low energy collisions with the neutral gas within the multipole rod
assembly have their kinetic energy reduced resulting in a narrowing
of the ion energy spread for those ions which exit the multipole
rods. The number of collisions an ion experiences as it travels the
length of the ion guide is a function of the rod length and the
background pressure inside the rods. If the relative voltages of
the capillary exit lens 50, ring lens 51, skimmer 47 and the
multipole ion guide 40 DC offset potential remain the same then the
ions entering the multipole ion guide will have similar energy
spreads and will be transmitted to the exit of the multipole ion
guide with the same efficiency. With the relative upstream lens
potentials held constant with the ion guide DC offset potential,
the ion kinetic energy cooling due to collisions will remain
consistent as the multipole DC offset potential is adjusted.
Consequently, with a multipole ion guide operated in a higher
vacuum pressure region where ion collisional cooling occurs, the
narrow energy spread of the ions can be maintained independent of
changes in the mean ion energy when the ion guide DC offset
potential is adjusted.
[0043] To illustrate this point, the energy spread of a doubly
charged Gramicidin S (M+2H).sup.+2 on (m/z 571) was measured by
ramping the voltage of lens 53 in FIG. 2 while monitoring the mass
spectrometer ion signal. This technique will not give a precise
profile of ion energy because lens 53 is a focusing element as well
as having the ability to apply stopping potentials. However, even
though the focusing characteristics will change slightly as the
voltage of 53 is ramped, the boundaries of ion energy for a given
m/z can be attained. Using the multipole ion guide configuration of
FIG. 2 and maintaining background pressure in vacuum stage 53 at 2
torr, vacuum stage 41 at 150 millitorr, vacuum stage 42 at
4.times.10.sup.-4 torr and vacuum stage 54 at 6.times.10.sup.-6
torr, the mean ion energy was changed by adjusting the DC offset
potential of the hexapole relative to the quadrupole entrance
aperture 47 ground potential. FIGS. 8a, b and c show the ion signal
of the Gramicidin S protonated doubly charged peak (M+2H).sup.+2
for three different hexapole ion guide 40 DC offset potentials. In
FIG. 8a the hexapole ion guide 40 was operated in the AC only mode
with the DC offset potential set at 0.1 volt relative to the
quadrupole entrance aperture 47. FIG. 8a shows the ion signal level
100 at m/z 571.6 for three consecutive voltage ramps of lens 53
from 2 to 8.2 volts. Over ninety percent of the m/z 571.6 ions fall
within a one volt window of ion energy. FIG. 8b shows the ion
signal 101 at m/z 571.6 for three consecutive voltage ramps of lens
53 from 19 to 21.2 volts with the hexapole ion guide 40 DC offset
potential set at 15.3 volts. Ninety percent of the 571.6 m/z ions
detected have an energy that falls within a one volt window.
Similarly, FIG. 8c shows the ion signal 102 at m/z 571.6 for three
consecutive voltage ramps of lens 53 from 29 to 35 volts with the
hexapole ion guide 40 DC offset potential set at 25.1 volts. Once
again, over ninety percent of the m/z 571.6 ions exiting the
hexapole ion guide 40 are within a 1 volt energy window. The mean
ion energy ranges from roughly 3 to 5.2 volts higher than the DC
offset potential set on the hexapole ion guide 40 in FIGS. 8a, b
and c. Ion acceleration driven by the expanding gas in the free jet
occurring in vacuum stage 51 may account for 2.6 to 3 volts of this
added ion energy for Gramicidin S ions. It is not yet certain where
the one to two volts of energy over 3 volts is added as the
multipole ion guide DC offset potential is raised. The efficient
transport of ions with low energy spread combined with the ability
to control the average ion energy for a given m/z by adjusting the
multipole ion guide 40 DC offset potential, allows higher
sensitivity to be achieved at higher resolution for many mass
analyzer types.
[0044] An API/MS system which incorporates a multipole ion guide
with a portion of its length operating in a vacuum pressure which
is high enough to cause collisional cooling as ions traverse the
rod length allows three significant performance features. The first
is that the ion guide operated in the presence of sufficient
background collisions can reduce the ion energy spread without
reducing ion transmission efficiency when run with the proper
values of a.sub.n and q.sub.n set. Second, the mean ion energy for
a given m/z can be adjusted by changing the DC offset potential of
the multipole ion guide without causing significant changes in ion
energy spread. Third, the ion energy can be adjusted by changing
the ion guide DC offset potential without reducing the ion
transmission efficiency through the multipole ion guide. An example
to illustrate these three features is given in FIG. 9 which shows a
mass spectrum 103 of a doubly charged protonated Gramicidin S
(M+2H).sup.+2 peak with partially resolved isotope peaks. The
spectrum was taken by electrospraying a 2 picomole/ul Gramicidin S
sample in a 1:1 methanol: water solution using an API quadrupole
mass spectrometer system as configured in FIG. 2. The DC offset
potential of hexapole 40 was set to 0.1 volts relative to the
ground potential quadrupole entrance aperture 47. With this low ion
guide DC offset voltage setting, higher resolution was achievable
at comparable sensitivities than could be attained with the
hexapole DC offset potential set at 15 volts. At lower ion
energies, transmission losses can occur between the multipole ion
guide exit 52 and the quadrupole mass filter 57 depending on the
focusing and transfer characteristics of static voltage lenses 53
and 47 in the presence of the multipole ion guide 40 and the
quadrupole mass filter 57 fringing fields. The performance
tradeoffs between ion energy, resolution and signal level for the
quadrupole mass filter 57 used, favored lower energy ions when
scanning with higher resolution settings. Using a static voltage
lens system as illustrated in FIG. 1 the resolution and
sensitivities shown in FIG. 9 could not be achieved. The use of a
multipole ion guide operated with the appropriate a.sub.n and
q.sub.n setting in a region where background pressures are high
enough to cause collisional cooling of ions as they traverse the
length of the ion guide improves API/MS system performance when
compared with static lens configurations having little or no ion
kinetic energy cooling.
[0045] The performance capabilities of a multipole ion guide
operated in a background pressure region where ion kinetic energy
cooling occurs can be used to improve the performance of different
mass spectrometer types. The advantages of improved ion
transmission efficiencies when using multiple vacuum pumping stage
multipole ion guides in conjunction with quadrupole mass analyzers
was illustrated with examples given above. The ability to set the
mean ion energy by adjusting the multipole DC offset potential
without changing the narrow energy spread per m/z value can be used
to improve the resolution and sensitivity of scanning and
non-dispersion mass analyzers including quadrupole, magnetic
sector, TOF, ion trap and FT-ICR mass spectrometers. Higher API/MS
system sensitivities and resolutions can be achieved and pumping
costs minimized when multipole ion guides which extend through two
or more vacuum pumping stages are used in the initial vacuum
pumping stages before the mass analyzer. The ability to operate a
multipole ion guide in a mode where a cutoff in ion transmission
for a given m/z range is set offers little operational advantage
when applied with scanning or dispersion mass analyzers such as
magnetic sector or quadrupole mass filters. These dispersion or
scanning mass analyzer types transmit ions only in a narrow range
of m/z at any given time to the detector. However, for mass
analyzers which are non dispersion such as TOF, ion traps and
FT-ICR which analyze packets of ions, the ability of the multipole
ion guides to limit the range of m/z values transmitted into the
mass analyzer can enhance system performance. FIG. 10 is a diagram
of a four vacuum pumping stage orthogonal pulsing API/MS system
with a reflectron Time-Of-Flight mass analyzer. For illustration
purposes, an electrospray ion source is shown as the API source
although this could alternatively be an APCI or an ICP source as
well. Sample bearing liquid is introduced through the electrospray
needle 110 and is Electrosprayed or nebulization assisted
Electrosprayed into chamber 111 as it exits the needle at 112. The
charged droplets produced, evaporate and desorb gas phase ions both
in chamber 111 and as they are swept into vacuum through the
annulus in capillary 113. A portion of the ions that enter the
first vacuum stage 133 through the capillary exit 114 are focused
through the orifice 136 in skimmer 116 with the help of lens 115
and the potential set on the capillary exit 114. Ions passing
through skimmer orifice 136 enter the multipole ion guide 118. The
ion guide 118 begins in vacuum pumping stage 117 and extends
unbroken into vacuum stage 119. If the multipole ion guide AC and
DC voltages are set to pass ions falling within a range of m/z then
ions within that range which enter the multipole ion guide will
exit at 121 and are focused with exit lens 120 through the TOF
analyzer entrance orifice 122. This primary ion beam 134 ion beam
passes between electrostatic lenses 123 and 124 located in the
fourth pumping stage 126. The relative voltages on lenses 123, 124
and 125 are pulsed so that a portion of the ion beam 134 falling in
between lenses 123 and 124 is ejected as a packet through grid lens
125 and accelerated down flight tube 127. The ions are steered by x
and y lens sets diagrammatically illustrated by 128 as they
continue their movement down flight tube 127. In the configuration
shown, the ion packet is reflected through a reflectron or ion
mirror 130 and detected at detector 131. As a pulsed ion packet
proceeds down flight tube 127, ions with different m/z separate in
space due to their velocity differences and arrive at the detector
at different times. The use of orthogonal pulsing in an API/TOF
system helps to reduce the ion energy spread of the initial ion
packet allowing higher resolution and sensitivity to be
achieved.
[0046] For a given primary ion beam current passing through the
mass analyzer aperture 122, the lower the ion energy, the more ions
that will be present in the pulsing region per pulse. This has a
direct impact on the ion signal response that can be achieved per
pulse. Also, the lower the primary ion beam electrostatic energy,
the less ion density versus m/z discrimination that will occur in
pulsing region 135. This discrimination occurs because the lower
m/z ions accelerated electrostatically will move faster than the
higher m/z ions and consequently will have less relative density
for a similar ion current per m/z in the pulsing region. A
distinction is made here between ions accelerated electrostatically
and those accelerated due to gas dynamics in the free jet. Although
some slippage occurs for higher molecular masses, ions accelerated
solely by the neutral gas expanding into vacuum in a free jet form
an ion beam that is closer to being mono-velocity rather than
mono-energetic. Electrostatic acceleration in the absence of
collisions with background gas will create an ion beam that is
closer to being mono-energetic. A mono-velocity beam entering
pulsing region 135 will reduce the differences in ion density
versus m/z for a given ion flux and hence allow generation of a
mass spectrum whose relative peak heights are more representative
of the relative m/z intensities in the original ion beam 134. The
translational energy of ions in the primary ion beam 134 will be
the sum of the energy imparted by the expanding gas and by
electrostatic acceleration. Multipole ion guide 118, a portion of
which is operated in a higher pressure vacuum region, can deliver
an ion beam having low translational energy through the mass
analyzer orifice 122 with minimal beam divergence. When static lens
systems are used, lowering of the ion beam energy generally results
in increased beam divergence. Beam divergence will not only reduce
the ion beam intensity entering aperture 122 but will also increase
the beam cross sectional area in pulsing region 135. Primary ion
beam divergence can result in reduced resolution in an orthogonal
pulsed TOF geometry. Use of the multipole ion guide 118 to aid in
delivering ions to the pulsing region can reduce the degree of ion
beam divergence for lower ion beam energies. The net result is
improved sensitivity and resolution.
[0047] The effective inner diameter of multipole ion guide 118 is
reduced to minimize the neutral gas conduction between vacuum
pumping stages 117 and 119 without compromising ion transmission
efficiency. The effective inner diameter for multipole ion guide
118 is typically 2.5 millimeters or less. The ion guide geometry
itself places an upper limit on the cross section of the ion beam
exiting at 121. By limiting the ion beam diameter exiting multipole
ion guide 118 to less than 2 mm, aperture 122 can be reduced to 2
mm with little or no loss ion transmission efficiency into pulsing
region 135. The smaller the aperture 122 size the less neutral gas
that will pass into vacuum pumping stage 126, reducing the vacuum
pumping speed requirements and lowering instrument cost. The
smaller the primary ion beam 134 which enters pulsing region 124,
the less spatial spreading which occurs before the ions are pulsed
out of region 135 and into flight tube 127. With orthogonal
pulsing, reducing the ion beam 134 width can reduce the pulsed ion
packet width or spatial and energy spread, potentially resulting in
increased TOF sensitivity and resolution performance.
[0048] A narrow ion energy spread is desirable in orthogonal
pulsing TOF because the orthogonal component of ion energy which is
the initial ion beam energy, translates into sideways movement of
ions as they traverse the flight tube. The lower the energy spread
in the initial ion beam the tighter the initial m/z ion packet
remains in the radial direction as it travels through flight tube
127 resulting in more ions focused onto the surface of detector
131. As shown in FIG. 8, operation of a multipole ion guide in a
vacuum pressure regime where ion kinetic energy cooling occurs
results in narrowing of the ion energy spread and the ability to
lower ion energy without reducing the ion transmission efficiency
or increasing the ion energy spread. The ability to lower ion
energy while maintaining a low ion energy spread can help to
improve the sensitivity and increase the duty cycle of a TOF mass
analyzer. Ions of a given m/z and energy will take time to refill
the gap between lenses 123 and 124 after a pulse has occurred. If
the length of the gap is roughly 2 cm then an ion at m/z 1000 with
20 volts of energy will take 10.2 .mu.sec to travel 2 cm and fill
the pulsing space. The same ion at 3 volts of energy will take 26.3
.mu.sec to travel 2 cm and fill the pulsing region. Those ions
which are not pulsed into the flight tube are lost as they impact
the walls of pulsing region 134 and are neutralized. If the ion
packets are pulsed at a rate of 10,000 times per second, that is
once every 100 .mu.sec, then pulsing a 3 volt primary ion beam 134
will improve the duty cycle and consequently the sensitivity by a
factor of 2.6 when compared with pulsing a primary ion beam 134
having 20 volts of translational energy. The ability of a multipole
ion guide to deliver ion beam 135 with a small cross section and a
mean energy of less than 5 volts, significantly improves
performance of an API/TOF system over that which can be achieved
using a static voltage lens system.
[0049] The ability of the multipole ion guide to selectively
transmit a range of m/z values while cutting off the transmission
of m/z outside that range can be used to increase the duty cycle
and detector sensitivity in an API/TOF system. The duty cycle can
be increased in TOF by reducing the range of ion m/z that enters
pulsing region 135. Recalling FIGS. 5, 6 and 7, the a.sub.n and
q.sub.n values of a multipole ion guide can be set so that the ion
guide behaves as a low pass or a high pass filter with m/z
transmission cutoff points. If a DC potential is applied to the
poles where each adjacent pole has opposite DC polarity, the
a.sub.n and q.sub.n values can be selected so that the multipole
ion guide will pass a narrower range of m/z. Quadrupoles are
commonly used in this mode as mass filters in vacuum pressure
regimes that are maintained below 2.times.10.sup.-5 torr where the
effects due to ion collisions with the background gas are
negligible. When +/- DC is imposed on the multipole rods with
considerable background pressure present, the transmission
characteristics of each type multipole ion guide or mass filter
assembly must tested and qualified. Ion transmission maps of
a.sub.n and q.sub.n may not be the same for multipole ion guides
with different numbers of poles and operated in different
background pressures. One variable which effects duty cycle in a
TOF instrument is the repetition rate at which ions are pulsed in
the flight tube, accelerated and detected. Assuming that the
pulsing region 135 can refill between pulses, that is the primary
ion beam 134 energy is set to satisfy this criteria, the pulsing
repetition rate will be limited by the fastest flight time of the
lowest m/z ion and the slowest flight time of the highest m/z ion
in consecutive ion packets traveling through flight tube 127 to the
detector. Any overlap of ions from one pulsed packet to the next
will increase the difficulty in interpreting the resulting mass
spectrum. If ions of lower or higher m/z were not of interest in a
given analysis, those ions could be preventing from entering the
pulsing region by selecting an appropriate a.sub.n and q.sub.n
value for the multipole rod 118 operation. By reducing the arrival
time spread of an ion packet as it travels down the flight tube,
the time in between pulses can be reduced resulting in an increase
in duty cycle.
[0050] Consider an example where an API/MS system as diagrammed in
FIG. 10 has an effective ion flight length of 2.5 meters and a
flight tube ion acceleration energy of 1500 electron volts (ev).
The larger the difference in arrival times at the TOF detector
between close ion m/z values, the higher the resolution which is
theoretically achievable. However, for continuous ion beam API
sources, increasing resolution by increasing the arrival time
spread of ion packets may reduce duty cycle. Relative flight times
in a 2.5 meter TOF tube with an ion accelerating energy of 1500 ev
would be as follows for different values of m/z:
1 m/z Flight time (.mu.sec) 1 4.6 19 20.3 100 46.5 500 103.9 1000
146.9 2000 207.8 3000 254.5 5000 328.6 10000 464.7
[0051] Subtracting the slowest from the most rapid flight time of
ions present in the pulsed packet will determine the minimum time
required in between consecutive pulses to avoid low m/z ions of the
trailing pulse catching up with high m/z ions of the leading pulse.
If m/z ions ranging from protonated water (m/z 19) to m/z 3000 are
present in the pulse ion packets, then a delay of 255 .mu.sec must
be maintained between consecutive pulses allowing approximately
3,921 pulses per second. A primary ion beam 134 with ions of m/z of
3000 and lower and with 3 volts of translational energy will fill
the 2 cm pulsing gap 135 length in less than 45 .mu.sec. The longer
the delay between pulsing of ions into the flight tube, the lower
the duty cycle resulting in lower sensitivity for a given primary
ion beam intensity. If the ions of interest for a given analysis
fell in a narrow m/z window, say below m/z 1000 then the multipole
ion guide a.sub.n and q.sub.n values could be set to pass only ions
below m/z 1000. The minimum time delay between pulses would be
reduced to 147 .mu.sec effectively increasing the duty cycle and
potentially sensitivity by a factor of 1.7. Conversely, if the mass
range of interest fell above m/z 500 and the m/z values present in
the primary ion beam were below 2000 m/z then the multipole ion
guide 118 operating a.sub.n and q.sub.n values could be set to
reject ions below 500 m/z. The ion packet pulse frequency could be
set to over 9500 pulses per second increasing duty for all m/z
values transmitted into pulsing region 135.
[0052] Layered Multichannel Plate (MCP) electron multipliers are
often used for detectors in TOF mass spectrometry. The individual
channel recovery time of an MCP channel after an ion hits and
causes an electron cascade can be as long as 1 millisecond. If an
ion hits the channel before it has recovered then little or no
electron cascade will occur and the ion will remain undetected.
Lower m/z ions which arrive at the detector first for a given
pulsed ion packet could deaden channels for heavier m/z ions which
follow. Also if the packet pulse rate exceeds 1000 hertz, that is
the time between pulses is shorter than the MCP channel recovery
time, this could result in reduction in signal intensity as ions
arriving at the detector yield reduced secondary electron cascade
intensity because ions from preceding pulses have deadened a number
of channels. If the ions of interest for a given analysis fall
within a limited m/z range, detector response can be increased for
ions of interest by preventing unwanted m/z values from reaching
the detector. The multipole ion guide 118 m/z transmission window
can be selected to minimize the number of unwanted m/z values from
entering the pulsing region 135, eliminating those m/z values from
reaching the detector. Selectively preventing ions from reaching
the detector has also been accomplished by deflecting a portion of
an ion packet as it traverses the TOF tube before it reaches the
detector. Ion lenses used for deflecting ions are diagrammatically
represented by 132 in FIG. 10. The use of multipole lens to limit
m/z values from entering the TOF pulsing region is a complimentary
technique to using deflectors in the flight tube. Deflecting
lenses, however, will not aid increasing duty cycle unless they are
employed very early in the ion flight path, a region where m/z
separation may be poor. A linear pulsed API/MS system as reported
by Boyle, Whitehouse and Fenn (Rapid Communications in Mass
Spectrom. Vol. 5, 400-405, 1991) would have a similar increase in
sensitivity and duty cycle by incorporation of a multipole ion
guide into the upstream vacuum stages as is achieved in orthogonal
pulsing TOF configurations.
[0053] When API sources are interfaced with ion traps and FT-ICR
mass analyzers, the use of multipole ion guides in the vacuum
transfer optics can be used to improve performance by increasing
ion transmission efficiency into the mass analyzer trapping region,
lower the ion energy spread and reducing space charge limits for
desired m/z ranges by selectively transmitting limited m/z ranges.
FIG. 11 diagrams a three vacuum pumping stage API/ion trap system
where a multipole ion guide begins in vacuum pumping stage 148 and
extends continuously through the three vacuum pumping stages. An
electrospray or nebulizer assisted electrospray ion source is shown
interfaced to ion trap mass spectrometer 154. Sample bearing liquid
is introduced into the electrospray needle entrance 140 and is
Electrosprayed or nebulizer assisted Electrosprayed as it emerges
from the electrospray needle tip 141. The charge liquid droplets
produced in the electrospray chamber 142 drift toward the capillary
entrance 144 against a flow of countercurrent drying gas 164. Ions
are produced from the evaporating charged droplets and are swept
into vacuum through capillary 145. This capillary may be heated by
capillary heater 146 which aids in heating the gas expanding
through the capillary into vacuum. Ions exiting the capillary at
147 are accelerated into the first vacuum pumping stage 148 by the
neutral gas free jet expansion. A large portion of ions exiting the
capillary enter the multipole ion guide 165 and are effectively
trapped and efficiently transported through its entire length. The
ions exit multipole ion guide 165 in the third vacuum stage 151 and
are focused into the ion trap 154 through the its endplate 155 by
lens 162. The pressure in vacuum stage 148 can range from 0.5 to 2
torr depending on the capillary 145 inner diameter and length, the
vacuum pump size chosen and the temperature at which the capillary
heater is run. The third pumping stage 151 is usually maintained at
a pressure below 5.times.10.sup.-5 torr to insure proper
functioning of the electron multiplier detector 152, however, the
internal trap pressure is often set higher than the background
pressure in stage 151 by the addition of helium directly into trap
154. The pressure in pumping stage 157 is generally maintained at a
pressure less than 150 millitorr.
[0054] The multipole ion guide 165 has rods or poles 150 which
begin in pumping stage 148, continue unbroken through pumping stage
157 and extend into pumping stage 151. Insulators and mounting
brackets 156 and 158 serve the dual purpose of supporting the
multipole rod assembly and partitioning the vacuum chambers to
minimize the flow of background gas into downstream pumping stages.
FIG. 12 illustrates a cross section of a hexapole assembly taken at
insulator 156. The six rods 160 are held in an equally spaced
position and equal radial distance from the centerline by
attachment to insulator 156. The insulator is configured to
minimize the effective cross sectional area of the internal opening
without distorting the electrostatic field produced by the hexapole
rods during operation inside multipole rod assembly cross section
area 161. Rod diameters as small as 0.5 mm have been constructed
with an inner rod spacing 166 of 2 mm to minimize neutral gas
conductance into downstream pumping stages and reduce the size and
cost of vacuum pumps required. Increasing the length of insulators
156 and 158 also helps to reduce the neutral gas conductance. The
smaller the ion guide assembly internal cross section area 161 with
proportionally small rod 160 diameters, the smaller the ion beam
cross section which exits the multipole ion guide. The smaller the
ion beam cross section which is transmitted through a multipole ion
guide 165 and exit lens 162, the smaller the effective aperture
size which is required in ion trap end plate 155.
[0055] The multipole ion guide 165 can efficiently transport ions
through gradient in background gas pressure. As was shown in FIGS.
8a, b and c, the ion energy spread is reduced due to ion
collisional cooling with the background gas. Higher trapping
efficiency can be achieved with ions entering ion trap 154 when the
ions have a narrow energy spread. Increased trapping efficiencies
result in higher signal sensitivity for a given ion current
entering trap 154. The ability to selectivity cutoff a range of m/z
transmission through multipole ion guide 165 can also be used to
increase sensitivity in ion trap mass spectrometers. Ion traps must
first trap ions and then conduct a mass analysis on a packet of
trapped ions. The trap can only hold a limited number of ions
before it suffers from space charge effects which can shift
measured m/z values and deteriorate resolution. For a given
analysis, the multipole ion guide a.sub.n and q.sub.n value can be
set to reduce the m/z range of ions which are transmitted to ion
trap 154 through exit lens 162 and ion trap endplate 155. This
extends the dynamic range signal response for the m/z values of
interest by reducing the effects of space charging from m/z values
which are not of interest for a given analysis. For example, the
contamination 85, 86 and solvent related peaks 87, 88 observed in
the spectrum of FIG. 5a would fill up the trap with charge and
reduce the signal intensity range over which the Arginine peak 90
could be observed in the ion trap because the lower m/z peaks would
be largely responsible for the space charge limits being reached in
the ion trap. If the multipole ion guide a.sub.n and q.sub.n value
were set for a low m/z cutoff as shown in the spectrum of FIG. 5b
then the Arginine peak 91 would be the primary source of ions
entering the trap and consequently the signal to noise observed
would have a higher dynamic range before the effects of space
charging would be observed. Increased dynamic range within a
spectrum is important for trace analysis and analysis where
accurate relative peak heights are needed to determine relative
concentrations in solution.
[0056] FT-ICR mass spectrometers also trap ions and conduct mass
analysis with packets of ions. Similar to ion traps, improvements
in performance with an API/FT-ICR MS instrument can be achieved by
using a multipole ion guide operated in vacuum pressure were ion
kinetic energy cooling occurs reducing the ion energy spread for a
given m/z. Effects due to space charge limits in the FT-ICR MS
trapping cell can be reduced in a similar manner as described for
ion traps above effectively increasing the dynamic range of the
FT-ICR MS for m/z values of interest in a given analysis. The
smaller effective inner diameter of these multipole ion guides
produces a small ion beam cross section allowing a reduction in the
aperture sizes leading to the FT-ICR mass analyzer without
significantly reducing ion transmission through the smaller
orifices.
[0057] Various configurations of hybrid API/mass spectrometers have
been reported whose performance would be enhanced by the
incorporation of a multipole ion guide in the vacuum ion transport
region. Chien, Michael and Ludman (Anal. Chem., vol. 65, 1916-1924,
1993) have used an ion trap to trap ions entering from an API
source and pulse them into a TOF mass spectrometer flight tube. A
multipole ion guide could be effectively employed in the upstream
vacuum stages to transmit ions from the higher pressure vacuum
regions into the ion trap of this API/ion trap/TOF instrument.
[0058] Each mass spectrometer type has its own ion energy, entrance
optics and vacuum requirements. The configuration of multipole ion
guides, particularly those that extend through two or more vacuum
pumping stages can be geometrically and operationally tailored to
the instrument in which they are incorporated. However, single
pumping stage multipole ion guides can be used effectively as well
with less constraint imposed on the geometry of the ion guide to
limit neutral gas conduction along its length. Two variations for
configuring multipole ion guides in API/MS TOF and ion trap systems
are shown in FIGS. 13 and 14. FIG. 13 is a diagram representation
of a 3 vacuum stage API/ion trap mass spectrometer system where a
multipole ion guide 170 is located in vacuum pumping stage 172.
Ions passing from pumping stage 171 through skimmer orifice 176 are
trapped from moving to far off axis in the radial direction and
transmitted through ion guide 170. The ions exiting ion guide 170
are focused by exit lens 175 into ion trap 177 through endplate
174. The ion trap endplate aperture 178, also serves as the orifice
into the third vacuum pumping stage 173. Ions can be injected into
an ion trap through different gaps or apertures in the ion trap
electrodes, however, this configuration is shown as one embodiment.
The vacuum pressure in vacuum stage 172 and the multipole ion guide
170 length can be configured to cause sufficient ion collisional
cooling with the background neutral gas resulting in a narrowing of
ion energy spread for a given m/z. Use of a single pumping stage
multipole ion guide may not allow the optimal tradeoffs in
performance increase and vacuum pumping cost reduction as is
possible with a continuous multiple pumping stage multipole ion
guide but some performance advantages can be realized when compared
to using a static voltage lens configuration.
[0059] Another variation with the use of multipole ion guides is
the incorporation of two or more ion guides in consecutive vacuum
pumping stages. This allows different a.sub.n and q.sub.n values to
be set per ion guide but increases system complexity and cost. FIG.
14 is a diagram of a four vacuum stage API/TOF mass spectrometer
system with single vacuum pumping stage multipole ion guides 180
and 181 located in pumping stages 184 and 185 respectively. Ions in
vacuum stage 183 pass through skimmer 190 and enter ion guide 180.
The ions which are transported through vacuum stage 184 by ion
guide 180 are focused through the aperture 194 by multipole 180
exit lens 187. The ions then enter the a second ion guide 181 in
vacuum stage 185 and are focused by lens 188 through aperture 189
as they exit the multipole ion guide 181. Ions passing though
aperture 189 into vacuum stage 186 are pulsed orthogonally with
lens set 191 into the TOF mass analyzer 192. The multipole ion
guides can be operated with independent values of a.sub.n and
q.sub.n may be set to optimize the TOF duty cycle and sensitivity.
Similar to the continuous multiple pumping stage multipole ion
guide configuration, the dual multipole ion guide configuration as
diagrammed in FIG. 14 can be used reduce the ion energy spread and
deliver low energy ions into the mass analyzer. However, with the
dual multipole ion guide configuration, losses in ion transmission
efficiency may occur in the region of static voltage lenses 187 and
195 between the two multipole assemblies 180 and 181.
* * * * *