IP Library Granted Patent US 10,408,792
Granted Patent B2
US 10,408,792 · App. 16/268,214 · Granted Sep 10, 2019

Mass spectrometer with tandem ion mobility analyzers

Inventors: Thomas Betz (Hamburg, DE); Melvin Andrew Park (Billerica, MA); Mark Ridgeway (Stow, MA)
G01N27/622H01J49/004
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Quick Facts
Patent No.
US 10,408,792
App. No.
16/268,214
Granted
Sep 10, 2019
Kind
B2
Abstract

The invention proposes a mass spectrometer comprising two ion mobility analyzers in tandem arrangement, of which at least one is a trapped ion mobility spectrometer (TIMS), and an ion gate which is located between the two ion mobility analyzers, and use thereof wherein ions are selectively transferred between the two ion mobility analyzers by adjusting the transmission of the ion gate while ions are separated in time according to ion mobility in the first ion mobility analyzer.

Claims (20)

1. A method for analyzing ions in a mass spectrometer comprising an ion source, first and second trapped ion mobility spectrometry (TIMS) analyzers, a mass filter located between the first and second TIMS analyzers and a mass analyzer located downstream of the second TIMS analyzer, the method comprising the steps of:

transferring ions from the ion source to the first TIMS analyzer;

driving the ions transferred to the first TIMS analyzer by a first gas flow against a first counter-acting electric DC field barrier such that the ions are trapped and spatially separated according to their mobilities at different positions along a ramp of the first electric field barrier at which a friction force of the first gas flow equals the counter-acting force of the first electric DC field barrier;

temporally separating ions according to mobility in the first TIMS analyzer by adjusting a height of the first electric DC field barrier or the velocity of the first gas flow;

separating undesirable ion mobility species from ion mobility species of interest by varying the transmitted mass range of the mass filter while the ions are separated in the first TIMS analyzer;

transferring the filtered ions to the second TIMS analyzer;

driving the ions transferred to the second TIMS analyzer by a second gas flow against a second counter-acting electric DC field barrier such that the ions are trapped and spatially separated according to their mobilities at different positions along a ramp of the second electric DC field barrier at which a friction force of the second gas flow equals the counter-acting force of the second electric DC field barrier; and

separating the transferred ions according to mobility in the second TIMS analyzer by adjusting a height of the second electric DC field barrier or the velocity of the gas flow.

2. The method according to claim 1 , wherein the mass filter is operated at a gas pressure above 10 Pascal.

3. The method according to claim 1 , wherein the mass filter is operated at a gas pressure of one of or both TIMS analyzers.

4. The method according to claim 1 , wherein the undesirable ion mobility species are singly charged.

5. The method according to claim 1 , wherein the undesirable ion mobility species are chemical background.

6. The method according to claim 1 , wherein the ions which are separated in the second TIMS analyzer are further analyzed by acquiring mass spectra or fragment mass spectra.

7. A mass spectrometer comprising an ion source, first and second trapped ion mobility spectrometry analyzers (TIMS), a mass filter located between the two ion mobility analyzers and a mass analyzer,

wherein the first and second TIMS analyzers each comprise a gas flow and a counter-acting electric DC field barrier configured to spatially separate ions according to their mobilities at different positions along a ramp of the electric field barrier at which a friction force of the first gas flow equals the counter-acting force of the electric DC field barrier and to temporally separate ions according to mobility by adjusting a height of the electric DC field barrier or a velocity of the gas flow, and

wherein the mass filter is configured to vary the transmitted mass range during operation of the first TIMS analyzer.

8. The mass spectrometer according to claim 7 , wherein the mass filter is one of a low-pass filter, a high-pass filter and a band-pass filter.

9. The mass spectrometer according to claim 8 , wherein the mass filter is operated at a gas pressure above 10 Pascal.

10. The mass spectrometer according to claim 8 , wherein the mass filter is a Loeb-Eiber mass filter.

11. The mass spectrometer according to claim 7 , further comprising a fragmentation cell between the second TIMS analyzer and the mass analyzer.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 18, 2021
From: BRUKER DALTONIK GMBH
To: BRUKER DALTONICS GMBH & CO. KG
Reel/Frame 057209/0070 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2019
From: BETZ, THOMAS; PARK, MELVIN ANDREW; RIDGEWAY, MARK
To: BRUKER DALTONIK GMBH
Reel/Frame 048243/0667 →
Continuity (2)
Continuation 15603600 · May 24, 2017
Related Publication 20190170689A1 · Jun 6, 2019
Cited By (6)
US 12,228,546 US 12,300,479 US 12,422,402 US 12,531,221 US 12,620,567 US 12,712,170