Sampling system for use with surface ionization spectroscopy

• US 8,026,477 B2
• Filed: 11/20/2008
• Issued: 09/27/2011
• Est. Priority Date: 03/03/2006
• Status: Active Grant

• Current Assignee: Bruker Scientific LLC (Bruker Corporation)
• Original Assignee: IonSense, Inc. (Bruker Corporation)
• Inventors: Musselman, Brian D.
• Primary Examiner(s): Wells; Nikita
• Application Number:
  US12/275,079
• Publication Number:
  US 20090090858A1
• Time in Patent Office: 1,041 Days
• Field of Search: 250/288, 250/281, 250/282, 250/287, 250/286, 250/423.R, 250/424
• US Class Current: 250/288
• CPC Class Codes: H01J 49/06 Electron- or ion-optical arrangements

Abstract

In various embodiments of the invention, a device permits more efficient collection and transmission of ions produced by the action of a carrier gas containing metastable neutral excited-state species into a mass spectrometer. In one embodiment of the invention, the device incorporates the source for ionization in combination with a jet separator to efficiently remove excess carrier gas while permitting ions to be more efficiently transferred into the vacuum chamber of the mass spectrometer. In an embodiment of the invention, improved collection of ions produced by the carrier gas containing metastable neutral excited-state species at greater distances from between the position of the analyte and the position of the mass spectrometer are enabled.

Claims

1. A spectroscopic device comprising:

(a) an external ion source, wherein the external ion source generates ions;

(b) a spectroscopic analyzer; and

(c) a gas ion separator, wherein the gas ion separator increases the number of ions generated by the external ion source introduced into the spectroscopic analyzer.

2. The spectroscopic device of claim 1, wherein the gas ion separator includes a vacuum pump.

3. The spectroscopic device of claim 1, wherein the gas ion separator pushes ions from the external ion source into the spectroscopic analyzer.

4. The spectroscopic device of claim 3, wherein the gas ion separator is made up of an inlet tube having a proximal end and a distal end and an outlet tube having a proximal end and a distal end;

wherein the distal end of the inlet tube is closest to and the proximal end is furthest from the spectroscopic analyzer.

5. The spectroscopic device of claim 1, wherein the gas ion separator pulls ions from the external ion source into the spectroscopic analyzer.

6. The spectroscopic device of claim 5, wherein the gas ion separator is made up of an inlet tube having a proximal end and a distal end and an outlet tube having a proximal end and a distal end;

wherein the proximal end of the inlet tube is closest to and the distal end is furthest from the spectroscopic analyzer.

7. The spectroscopic device of claim 1, wherein the gas ion separator pulls ions from the external ion source into a differential scanning mobility spectrometer.

8. The spectroscopic device of claim 7, wherein the gas ion separator is used to regulate the flow of ions and neutral gas molecules into the differential scanning mobility spectrometer.

9. The spectroscopic device of claim 1, wherein the external ion source and the spectroscopic analyzer are off axis to reduce the possibility of particulate matter disturbing the spectroscopic analysis.

10. The spectroscopic device of claim 1, wherein the external ion source temperature is used to reduce the possibility of particulate matter disturbing the spectroscopic analysis.

11. The spectroscopic device of claim 1, wherein the gas ion separator pulls ions from the external ion source into an ion mobility mass spectrometer.

16. The spectroscopic device of claim 1, wherein the gas ion separator is made up of an inlet tube having a proximal end and a distal end and an outlet tube, wherein the distal end of the inlet tube is closest to and the proximal end is furthest from the spectroscopic analyzer, wherein the gas ion separator pulls ions from the external ion source into the proximal end of the inlet tube.

17. The spectroscopic device of claim 1, wherein the gas ion separator is made up of an inlet tube having a proximal end and a distal end and an outlet tube, wherein the distal end of the inlet tube is closest to and the proximal end is furthest from the spectroscopic analyzer, wherein the gas ion separator pushes ions from the external ion source into the proximal end of the inlet tube.

18. The spectroscopic device of claim 1, wherein the gas ion separator is made up of an inlet tube and an outlet tube having a proximal end and a distal end, wherein the distal end of the outlet tube is closest to and the proximal end is furthest from the spectroscopic analyzer, wherein the gas ion separator pushes ions from the inlet tube into the proximal end of the outlet tube.

19. The spectroscopic device of claim 1, wherein the gas ion separator is made up of an inlet tube and an outlet tube having a proximal end and a distal end, wherein the distal end of the outlet tube is closest to and the proximal end is furthest from the spectroscopic analyzer, wherein the gas ion separator pulls ions from the inlet tube into the proximal end of the outlet tube.

20. The spectroscopic device of claim 1, wherein the gas ion separator is made up of an inlet tube and an outlet tube, wherein the gas ion separator one or both pulls ions into the inlet tube and pushes ions out of the outlet tube into the spectroscopic analyzer.

12. A method of detecting an analyte comprising:

(a) providing a device including a spectroscopic analyzer and a gas ion separator;

(b) generating an analyte ion, wherein the analyte ion is generated external to the spectroscopic analyzer; and

(c) pushing the analyte ion into the spectroscopic analyzer with the gas ion separator, wherein the gas ion separator increases the number of analyte ions generated that are sampled by the spectroscopic analyzer.

13. The method of claim 12, wherein the spectroscopic analyzer is selected from the group consisting of mass spectrometer, raman spectrometer, electromagnetic absorption spectrometer, electromagnetic emission spectrometer, surface detection spectrometer, differential scanning mobility spectrometer and ion mobility mass spectrometer.

14. A method of detecting an analyte comprising:

(a) providing a device including a spectroscopic analyzer and a gas ion separator;

(b) generating an analyte ion, wherein the analyte ion is generated external to the spectroscopic analyzer; and

(c) pulling the analyte ion into the spectroscopic analyzer with the gas ion separator, wherein the gas ion separator increases the number of analyte ions sampled by the spectroscopic analyzer.

15. The method of claim 14, wherein the spectroscopic analyzer is selected from the group consisting of mass spectrometer, raman spectrometer, electromagnetic absorption spectrometer, electromagnetic emission spectrometer, surface detection spectrometer, differential scanning mobility spectrometer and ion mobility mass spectrometer.