IP Library Granted Patent US 11,049,707
Granted Patent B2
US 11,049,707 · App. 16/850,443 · Granted Jun 29, 2021

Apparatus and method for thermal assisted desorption ionization systems

Inventors: Jordan Krechmer (Melrose, MA); Brian D. Musselman (Melrose, MA)
Assignee: IONSENSE, INC.
H01J49/049G01N27/622G01N27/626G01N27/64H01J27/26H01J49/004H01J49/04H01J49/0431H01J49/10H01J49/126H01J49/14H01J49/24Y10T436/24
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,049,707
App. No.
16/850,443
Granted
Jun 29, 2021
Kind
B2
Abstract

The present invention is directed to a method and device to desorb an analyte using heat to allow desorption of the analyte molecules, where the desorbed analyte molecules are ionized with ambient temperature ionizing species. In various embodiments of the invention a current is passed through a mesh upon which the analyte molecules are present. The current heats the mesh and results in desorption of the analyte molecules which then interact with gas phase metastable neutral molecules or atoms to form analyte ions characteristic of the analyte molecules.

Claims (26)

1. A method of analyzing an analyte comprising:

contacting a plastic with an analyte;

introducing the plastic in proximity to a mesh positioned between a source and an entrance of a spectrometer;

heating the mesh with a supply;

directing a plurality of ionizing species formed by the source at the plastic, where analyte molecules desorbed from the plastic interact with the plurality of ionizing species to form one or more analyte ions which pass through the entrance of the spectrometer and are analyzed.

2. The method of analyzing an analyte of claim 1 , further comprising inserting a gas ion separator between the mesh and the entrance to improve efficiency of sampling.

3. The method of analyzing an analyte of claim 1 , where the one or more analyte ions are formed at approximately atmospheric pressure.

4. The method of analyzing an analyte of claim 1 , where the plurality of ionizing species are formed at approximately atmospheric pressure.

5. The method of analyzing an analyte of claim 1 , where the source is selected from the group consisting of a direct analysis real time (DART), Plasma Assisted Desorption/Ionization ( PADI ), Dielectric Barrier Discharge ionization source (DBDI or DCBI), Desorption Atmospheric Pressure Chemical Ionization (DAPCI), Desorption Sonic Spray Ionization (DeSSI), Desorption Atmospheric Pressure Photoionization (DAPPI), and Flowing Atmospheric-Pressure Afterglow (FAPA) and a desorption electrospray ionization (DESI), an atmospheric laser desorption ionization, a Corona discharge, an inductively coupled plasma (ICP) and a glow discharge source.

6. The method of analyzing an analyte of claim 1 , where the supply passes power to the mesh of between:

a lower limit of approximately 10.sup.-2 Watts; and

an upper limit of approximately 10.sup.3 Watts.

7. The method of analyzing an analyte of claim 1 , where a first potential is applied to the mesh.

8. The method of analyzing an analyte of claim 7 , where the first potential is approximately the same as a potential applied to the entrance of the spectrometer.

9. The method of analyzing an analyte of claim 1 , where the analyte is a solution.

10. The method of analyzing an analyte of claim 1 , further comprising where an auto sampler contacts the plastic with the analyte.

11. The method of analyzing an analyte of claim 1 , where the plastic is a sponge.

12. The method of analyzing an analyte of claim 1 , where the plastic is a foam.

13. A method of analyzing an analyte of ionizing an analyte comprising: contacting an analyte onto a plastic with an auto sampler; introducing the plastic in proximity to a mesh; heating the mesh with a supply; directing a plurality of ionizing species at the plastic, where analyte molecules desorbed from the plastic interact with the plurality of ionizing species to form one or more analyte ions.

14. The method of analyzing an analyte of claim 13 , where the plurality of ionizing species is generated by a method selected from the group consisting of a direct analysis real time (DART), Plasma Assisted Desorption/Ionization ( PADI ), Dielectric Barrier Discharge ionization source (DBDI or DCBI), Desorption Atmospheric Pressure Chemical Ionization (DAPCI), Desorption Sonic Spray Ionization (DeSSI), Desorption Atmospheric Pressure Photoionization (DAPPI), and Flowing Atmospheric-Pressure Afterglow (FAPA) and a desorption electrospray ionization (DESI), an atmospheric laser desorption ionization, a Corona discharge, an inductively coupled plasma (ICP) and a glow discharge source.

15. The method of analyzing an analyte of claim 13 , where the plurality of ionizing species is formed from a carrier gas.

16. The method of analyzing an analyte of claim 15 , where the carrier gas can be heated.

17. A method of ionizing an analyte comprising: contacting a plurality of analytes onto a plurality of formed plastic pieces with an auto sampler; introducing sequentially one or more of the plurality of formed plastic pieces in proximity to a mesh; heating the mesh with a supply; directing a plurality of ionizing species at the one or more of the plurality of formed plastic pieces, where analyte molecules desorbed from the one or more of the plurality formed plastic pieces interact with the plurality of ionizing species to form one or more analyte ions.

18. The method of ionizing an analyte of claim 17 , where the plurality of ionizing species are formed at approximately atmospheric pressure.

19. The method of ionizing an analyte of claim 17 , where one or more of the plurality of analytes comprise a solution containing the analyte.

20. The method of ionizing an analyte of claim 17 , where one or more of the plurality of formed plastic pieces comprise teflon.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Feb 1, 2023
From: IONSENSE INC
To: BRUKER SCIENTIFIC LLC
Reel/Frame 062609/0575 →
Continuity (11)
Continuation 16186413 · Nov 9, 2018
Continuation 15942162 · Mar 30, 2018
Continuation 15368490 · Dec 2, 2016
Continuation 14876677 · Oct 6, 2015
Continuation 14589687 · Jan 5, 2015
Continuation 14455611 · Aug 8, 2014
Continuation 13364322 · Feb 2, 2012
Provisional Application 61587218 · Jan 17, 2012
Provisional Application 61582204 · Dec 30, 2011
Provisional Application 61439866 · Feb 5, 2011
Related Publication 20200303175A1 · Sep 24, 2020
Cited By (1)
US 12,385,818