Laser-induced acoustic desorption/atmospheric pressure chemical ionization of compounds
The present disclosure provides a novel system and method for evaporating and ionizing compounds comprising an LIAD source and an ionization source that operates at atmospheric pressure. This system is readily adaptable for use with most commercially available mass spectrometers. Ionization sources include Atmospheric Pressure Chemical Ionization sources (APCI) and Atmospheric Pressure Photo Ionization (APPI) sources. The ionization sources are positioned such that the analyte desorbing from the surface of the LIAD is fed into the ion stream produced by the ionization source and ionized analyte and ionized fragments of the analyte are fed into the sample inlet of a mass spectrometer. These systems allow for the mass spectrometric analysis of non-polar compounds that lack readily ionizable functional groups, such as saturated and unsaturated hydrocarbons and compounds with medium to low polarity, as well as hydrocarbon mixtures, such as petroleum.
1. An apparatus for producing gaseous ions, comprising:
a laser-induced acoustic desorption probe, wherein the desorption probe includes a surface suitable for contact with an analyte; and
an ion source that operates at atmospheric pressure, wherein said ion source produces a stream of ions and wherein the surface of the desorption probe is positioned such that it can introduce an analyte on the surface of the desorption probe into the stream of ions produced by the ion source.
2. The apparatus according to claim 1 , wherein the apparatus is suitable for providing at least one ionized analyte or fragment thereof into the sample inlet of a mass spectrometer.
3. The apparatus according to claim 1 , wherein the ion source is an atmospheric pressure chemical ionization source.
4. The apparatus according to claim 1 , wherein the ion source is an atmospheric pressure photo ionization source.
5. The apparatus according to claim 2 , wherein the mass spectrometer is a quadrupole ion trap mass spectrometer.
6. The apparatus according to claim 2 , wherein the mass spectrometer is a Fourier-transform ion cyclotron resonance mass spectrometer.
7. The apparatus according to claim 2 , wherein the mass spectrometer is a quadrupole/time-of-flight mass spectrometer.
8. The apparatus according to claim 1 , wherein the desorption probe includes a neodymium doped yttrium aluminum garnet laser.
9. The apparatus according to claim 8 , wherein the neodymium doped yttrium aluminum garnet laser operates at a range of between about 450 to about 600 nm.
10. The apparatus according to claim 8 , wherein the neodymium doped yttrium aluminum garnet laser operates at a range of between about 950 to about 1200 nm.
11. The apparatus according to claim 1 , wherein the desorption probe includes a foil surface, the surface having a first side and a second side and where the laser is focus on the first side of the foil and a sample is applied to the second side of the foil and the laser can be pulsed so as to minimize the heating of the sample on the second side of the foil.
12. The apparatus according to claim 11 , wherein the laser is pulsed between about 150 to about 200 times per second.
13. The apparatus according to claim 3 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one gas produced from the group of gasses consisting of but not limited to: nitrogen, carbon dioxide, xenon and CS.
14. The apparatus according to claim 3 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one solvent produced from the group of solvents consisting of: methanol, methanol:water, benzene and carbon disulfide.
15. The apparatus according to claim 3 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one gas produced from the group of gasses consisting of: nitrogen, carbon dioxide, xenon and CS and at least one solvent produced from the group of solvents consisting of: methanol, methanol:water, benzene and carbon disulfide.
16. An apparatus for analyzing a compound, comprising:
a laser-induced acoustic desorption probe, wherein the desorption probe includes a surface suitable for contact with an analyte;
an ion source that operates at atmospheric pressure, wherein said ion source produces a stream of ions and wherein the surface of the desorption probe is positioned such that it can introduce an analyte on the surface of the desorption probe into the stream of ions produced by the ion source; and
a mass spectrometer having a sample inlet, wherein the laser induced acoustic desorption probe is positioned such that the desorption probe desorbs at least a portion of the analyte on the surface of the desorption probe into the ion stream and a least a portion of the analyte or an ionized species or fragment thereof is introduced into the sample inlet of the mass spectrometer.
17. The apparatus according to claim 15 , wherein the ion source is an atmospheric pressure chemical ionization source.
18. The apparatus according to claim 15 , wherein the ion source is an atmospheric pressure photo ionization source.
19. The apparatus according to claim 15 , wherein the mass spectrometer is a quadrupole ion trap mass spectrometer.
20. The apparatus according to claim 15 , wherein the mass spectrometer is a quadrupole ion trap mass spectrometer.
21. The apparatus according to claim 15 , wherein the mass spectrometer is a quadrupole/time-of-flight mass spectrometer.
22. The apparatus according to claim 15 , wherein the desorption probe includes a neodymium doped yttrium aluminum garnet laser.
23. The apparatus according to claim 21 , wherein the neodymium doped yttrium aluminum garnet laser operates at a range of between about 450 to about 600 nm.
24. The apparatus according to claim 21 , wherein the neodymium doped yttrium aluminum garnet laser operates at a range of between about 900 to about 1200 nm.
25. The apparatus according to claim 16 , wherein the desorption probe includes a foil surface, the surface having a first side and a second side and where the laser is focus on the first side of the foil and a sample is applied to the second side of the foil and the laser can be pulsed so as to minimize the heating of the sample on the second side of the foil.
26. The apparatus according to claim 24 , wherein the laser is pulsed between about 150 to about 200 times per second.
27. The apparatus according to claim 16 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one gas produced from the group of gasses consisting of: nitrogen, carbon dioxide, xenon and CS.
28. The apparatus according to claim 16 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one solvent produced from the group of solvents consisting of: methanol, methanol:water, benzene and carbon disulfide.
29. The apparatus according to claim 16 , wherein said atmospheric pressure ionization source produces a plasma that includes ionization products from at least one gas produced from the group of gasses consisting of: nitrogen, carbon dioxide, xenon and CS and at least one solvent produced from the group of solvents consisting of: methanol, methanol:water, benzene and carbon disulfide.
30. A method for analyzing a compound, comprising the steps of:
providing an apparatus, said apparatus including:
a laser-induced acoustic desorption probe, wherein the desorption probe includes a surface suitable for contact with an analyte;
an ion source that operates at atmospheric pressure, wherein said ion source produces a stream of ions; and
a mass spectrometer having a sample inlet, wherein the laser induced acoustic desorption probe is positioned such that the desorption probe desorbs at least a portion of the analyte on the surface of the desorption probe into the ion stream and a least a portion of the analyte or an ionized species or fragment thereof is introduced into the sample inlet of the mass spectrometer;
supplying at least one analyte; and
contacting the surface suitable for contact with an analyte with the analyte.
31. The method according to claim 29 , wherein the analyte is a polar compound.
32. The method according to claim 29 , wherein the analyte is a nonpolar compound.
33. The method according to claim 29 , wherein the nonpolar compound is present in petroleum.
34. The method according to claim 29 , wherein the nonpolar compound is a lipid.
35. The method according to claim 29 , wherein the nonpolar compound is selected from the group consisting of bathophenanthrolines, Coronenes, squalenes, cholestanes, androsterones, and the like.