Sampling system for use with surface ionization spectroscopy

• US 8,440,965 B2
• Filed: 12/28/2010
• Issued: 05/14/2013
• Est. Priority Date: 10/13/2006
• Status: Active Grant

• Current Assignee: Bruker Scientific LLC (Bruker Corporation)
• Original Assignee: IonSense, Inc. (Bruker Corporation)
• Inventors: Musselman, Brian
• Primary Examiner(s): Johnston, Phillip A
• Application Number:
  US12/979,729
• Publication Number:
  US 20110101216A1
• Time in Patent Office: 868 Days
• Field of Search: 250/285
• US Class Current: 250/285
• CPC Class Codes: H01J 49/04 Arrangements for introducing or extracting samples to be analysed, e.g. vacuum locks; Arrangements for external adjustment of electron- or ion-optical components
• CPC Class Codes: H01J 49/0404 Capillaries used for transferring samples or ions electrospray nozzles H01J49/167
• CPC Class Codes: H01J 49/16 using surface ionisation, e.g. field-, thermionic- or photo-emission

Abstract

The invention provides for efficient collection of analyte ions and neutral molecules from surfaces for their subsequent analysis with spectrometry. In an embodiment of the invention, a ‘multiple desorption ionization source’ includes a tube which can contain ions for subsequent sampling within a defined spatial resolution from desorption ionization at or near atmospheric pressures. In an embodiment, electrostatic fields are used to direct ions a plurality of tubes positioned in close proximity to the surface of the sample being analyzed. In an embodiment of the present invention, either narrow inside diameter capillary tubes or wide diameter tubes can be used in combination with a vacuum inlet to draw ions and neutrals into the spectrometer for analysis. In an embodiment of the invention, a dopant is introduced into a tube to analyze the sample. In an embodiment of the invention, a plurality of ionization sources is used to analyze the sample.

Claims

1. A device for analyzing an analyte comprising:

a plurality of ionization sources;

a plurality of flexible tubes, where each tube has a proximal end and a distal end, where the proximal end of the plurality of tubes is positioned at or near the analyte, where the distal end of the plurality of tubes combine into a single tube; and

a spectrometer, where the single tube connects with the spectrometer.

2. The device of claim 1, where one or more of the plurality of ionization sources are operated at atmospheric pressure.

3. The device of claim 1, where one or more of the plurality of ionization sources are desorption ionization sources.

4. The device of claim 1, where one or more of the plurality of ionization sources is operated with a positive polarity, where one or more of the plurality of ionization sources is operated with a negative polarity.

5. The device of claim 1, further comprising one or more dopants introduced into one or more of the plurality of tubes.

6. The device of claim 1, where one or more of the plurality of ionization sources are selected from the group consisting of a Direct Ionization in Real Time source, a desorption electrospray ionization (DESI) source, an atmospheric laser desorption ionization source, a Corona discharge source, an inductively coupled plasma (ICP) source and a glow discharge source.

7. The device of claim 1, where one or more of the plurality of ionization sources is operated with a first reagent gas, where one or more of the plurality of ionization sources is operated with a second reagent gas, where the first reagent gas is not the same as the second reagent gas.

8. The device of claim 1, where one or more of the plurality of ionization sources is operated at a first temperature and one or more of the plurality of ionization sources is operated at a second temperature, where there is a difference between the first temperature and the second temperature.

9. The device of claim 8, where the difference is between:

a lower limit of approximately 5°

C.; and

an upper limit of approximately 5×

10²°

C.

10. A method of analyzing an analyte comprising the steps of:

providing the device of claim 1;

orientating the plurality of ionization sources relative to the analyte to generate analyte ions;

orienting the plurality of tubes relative to one or both the analyte and the plurality of ionization sources to direct analyte ions into the proximal end of one or more of the plurality of tubes;

transferring the analyte ions through the single tube into the spectrometer; and

analyzing the analyte ions with the spectrometer.

11. The method of claim 10, where one or more of the plurality of ionization sources is selected from the group consisting of a Direct Ionization in Real Time source, a desorption electrospray ionization (DESI) source, an atmospheric laser desorption ionization source, a Corona discharge source, an inductively coupled plasma (ICP) source and a glow discharge source.

12. The method of claim 10, where one or more of the plurality of ionization sources is operated with a first reagent gas, where one or more of the plurality of ionization sources is operated with a second reagent gas, where the first reagent gas is not the same as the second reagent gas.

13. The method of claim 10, where one or more of the plurality of ionization sources is operated with a positive polarity, where one or more of the plurality of ionization sources is operated with a negative polarity.

14. The method of claim 10, where one or more dopants is introduced into one or more of the tubes.

15. The method of claim 10, where one or more of the plurality of ionization sources is operated at a first temperature and one or more of the plurality of ionization sources is operated at a second temperature, where there is a difference between the first temperature and the second temperature.

16. The method of claim 15, where the difference is between:

a lower limit of approximately 5°

C.; and

an upper limit of approximately 5×

10²°

C.

17. A system of analyzing an analyte comprising:

(a) a sample holder;

(b) a spectrometer;

(c) a plurality of ionization sources; and

(d) a plurality of flexible tubes positioned at or near the sample holder, where each tube has a proximal end and a distal end, where the proximal end of the plurality of tubes is positioned at or near the analyte, where the distal end of the plurality of tubes combine into a single tube which enters the spectrometer.

18. The system of claim 17, where one or more of the plurality of ionization sources is operated with a first method of ionization, where one or more of the plurality of ionization sources is operated with a second method of ionization.

19. A method of analyzing an analyte comprising the steps of:

providing the system of claim 17;

positioning the analyte on the sample holder;

orientating the plurality of ionization sources relative to the analyte to generate analyte ions;

orienting the plurality of tubes relative to one or both the analyte and the plurality of ionization sources to direct analyte ions into the proximal end of one or more of the plurality of tubes;

transferring the analyte ions through the single tube into the spectrometer; and

analyzing the analyte ions with the spectrometer.