Thermospray

Thermospray is a soft ionization source by which a solvent flow of liquid sample passes through a very thin heated column to become a spray of fine liquid droplets. As a form of atmospheric pressure ionization in mass spectrometry these droplets are then ionized via a low-current discharge electrode to create a solvent ion plasma. A repeller then directs these charged particles through the skimmer and acceleration region to introduce the aerosolized sample to a mass spectrometer. It is particularly useful in liquid chromatography-mass spectrometry (LC-MS).[1][2][3][4][5]

Diagram of thermospray ionization source

In more technical terms thermospray is the controlled partial vaporization of a liquid as it flows through a heated capillary tube. The nebulization is accomplished by pumping a liquid sample at moderately high pressure through an electrothermally heated capillary tube.[6] When sufficient power is coupled to the flowing sample stream, a partially vaporized mixture is produced consisting of some fraction of vaporized sample and some remaining liquid sample. Upon exiting the heated capillary, the rapidly expanding sample vapor converts the remaining liquid stream to an aerosol. The produced vapor acts as a nebulizing ‘gas’ and aids the breakup of the liquid stream into droplets,[4] in a process similar to pneumatic nebulization.[7] Thus, conceptually this can be thought of as a pneumatic process where the expanding solvent vapor is used as a nebulizer gas. The solution leaves the tube as a supersonic jet or spray of very small droplets in solvent vapor. Qualitatively, the aerosols appear dense with a moderately narrow particle size distribution.

History

The method of thermospray ionization was first introduced by a patent evidenced as early as 1983, and described in further detail by a patent published on March 8, 1988.[8] Inventors Marvin L. Vestal and Calvin R. Blakley proposed an ion vapor source for mass spectrometry of liquids under a US Grant from the Department of Health, Education, and Welfare. The proposed method detailed a coupling device between liquid chromatographic columns and various methods of detection for gaseous samples; like mass spectrometry, electron capture, atomic adsorption, etc. Four different representations of the thermospray vaporizer were presented in the 1988 patent - UA4730111A. Nonvolatile, ionic, and thermally labile solutes were investigated with the various control systems on the vaporizers to achieve partial vaporization.

Diagram of first representation of thermospray vaporizer
Diagram of second representation of thermospray vaporizer
Diagram of third representation of thermospray vaporizer
Diagram of fourth representation of thermospray vaporizer

First representation

A copper vaporizer block is electrically heated with two 100 watt cartridge heaters and a stainless steel capillary allow introduction of sample and consequent partial vaporization. The capillary and the vaporizer block are soldered together to ensure stable thermal contact. The resultant supersonic jet then passes through the ion source for introduction into the quadrupole mass spectrometer.

Second representation

The construction of the second representation is fundamentally the same as the first, however temperature and pressure sensors were implemented such that they could control the power to obtain both constant temperature and pressure for ideal operating conditions. This design is ideal for on-line LC-MS with chemical ionization and direct desorption.

Third representation

Given uncontrolled flow rate or varied solvent composition, another representation was designed such that a different heating source and control system would allow for partial vaporization. Two different heating methods were combined because one is capable of more rapid response time while the other is slower. This combination allows the third representation of vaporizer to handle fluctuations in flow rate coming of the LC column.

Fourth representation

The fourth version of the thermospray vaporizer heats the capillary tube only by direct DC/AC ohmic (Joule) heating. A thermocouple placed in thermal contact with the exit of the capillary is used to prevent the destructive thermal runaway caused by overheating. This representation was concluded to be the ideal design by the 1988 patent.

Mass spectrometry applications
Schematic of the thermospray probe and ion source used in EPA Method 8321B which utilized High Performance Liquid Chromatography-Thermospray-Mass Spectrometry (HPLC-TS-MS).[9]

As a direct sampling technique, thermospray is able to gently ionize various types of analytes such that the resulting spectrum shows few fragments of the molecular ion and accompanying buffer gas components. This lack of fragmentation typically hinders the acquisition of structural information,[10] however thermospray is still capable of quantitative results and is valued for its range of viable analytes.[11] When thermospray is coupled with High performance liquid chromatography mass spectrometry (TSP-HPLC-MS) the result is a highly sensitive method that is capable of lower detection limits than other HPLC-MS methods.[12]

Ionization processes

Thermospray ionization has three possible processes by which it can occur. The first involved direct desorption of analyte, where evaporation of the more volatile solvent allows the less volatile liquid sample ions to enter gas phase. The second type of ionization is an acid-base transfer such that solvent ions exchange a proton with ionic components of a buffer. This form of ionization is most commonly used with Reverse phase high performance liquid chromatography (RP-HPLC). The third process through which ionization can occur is termed plasmaspray ionization, where electron ionization is applied to the solvent flow under ambient conditions to produce a plasma source. This plasma source then chemically ionizes solvent reagent ions. (Also called filament-on operation)

Viable analytes

Various compounds, including peptides, dinucleotides, prostaglandins, diquaternary ammonium salts, pesticides, drugs, dyes, and environmental pollutants can be analyzed using thermospray.[10]

Type Example Image
Peptides Beta-Peptide
Dinucleotides Nicotinamide adenine dinucleotide
Prostaglandins Prostaglandin
Diquarternary ammonium salts Quaternary ammonium cation
Pesticides Pesticide
Drugs Drug

Ibuprofen
DyesFluorescein
Environmental pollutantsDichlorodiphenyltrichloroethane

Recent studies

Recently thermospray was also utilized for the production of semiconductor nanocrystals,[13] analysis of bile acids,[14] identification of dyes,[15] and molecular weight determinations of proteins from multiply charged ions.[16]

See also

References
  1. Blakley, C. R.; Carmody, J. J.; Vestal, M. L. (1980). "Liquid chromatograph-mass spectrometer for analysis of nonvolatile samples". Analytical Chemistry. 52 (11): 1636–1641. doi:10.1021/ac50061a025. ISSN 0003-2700.
  2. Arpino, Patrick (1992). "Combined liquid chromatography mass spectrometry. Part III. Applications of thermospray". Mass Spectrometry Reviews. 11 (1): 3–40. doi:10.1002/mas.1280110103. ISSN 0277-7037.
  3. Gelpí E (1995). "Biomedical and biochemical applications of liquid chromatography-mass spectrometry". Journal of Chromatography A. 703 (1–2): 59–80. doi:10.1016/0021-9673(94)01287-O. PMID 7599744.
  4. Vestal, Marvin L. (1990). "[5] Liquid chromatography-mass spectrometry". Mass Spectrometry. Methods in Enzymology. 193. pp. 107–130. doi:10.1016/0076-6879(90)93413-F. ISBN 9780121820947. ISSN 0076-6879.
  5. Blakley, C. R.; Vestal, M. L. (1983). "Thermospray interface for liquid chromatography/mass spectrometry". Analytical Chemistry. 55 (4): 750–754. doi:10.1021/ac00255a036. ISSN 0003-2700.
  6. Koropchak, John A.; Veber, Marjan; Browner, Richard F. (1992). "Thermospray Sample Introduction to Atomic Spectrometry". Critical Reviews in Analytical Chemistry. 23 (3): 113–141. doi:10.1080/10408349208050851. ISSN 1040-8347.
  7. Boumans, P.W.J.M.; Barnett, Neil W. "Inductively coupled plasma emission spectroscopy, part 1: methodology, instrumentation and performance". Analytica Chimica.
  8. Ion vapor source for mass spectrometry of liquids, 1986-02-24, retrieved 2018-04-05
  9. EPA,ORD, US. "EPA Method 8321B (SW-846): Solvent-Extractable Nonvolatile Compounds by High Performance Liquid Chromatography-Thermospray-Mass Spectrometry (HPLC-TS-MS) or Ultraviolet (UV) Detection | US EPA". US EPA. Retrieved 2018-04-05.
  10. Dass, Chhabil (2007). Fundamentals of contemporary mass spectrometry. Hoboken, N.J.: Wiley-Interscience. ISBN 978-0471682295. OCLC 71189726.
  11. Arpino, Patrick (1990-11-01). "Combined liquid chromatography mass spectrometry. Part II. Techniques and mechanisms of thermospray". Mass Spectrometry Reviews. 9 (6): 631–669. doi:10.1002/mas.1280090603. ISSN 1098-2787.
  12. Voyksner, Robert D.; Haney, Carol A. (2002). "Optimization and application of thermospray high-performance liquid chromatography/mass spectrometry". Analytical Chemistry. 57 (6): 991–996. doi:10.1021/ac00283a007.
  13. Amirav, Lilac; Lifshitz, Efrat (2008). "Thermospray: A Method for Producing High Quality Semiconductor Nanocrystals". Journal of Physical Chemistry C. 112 (34): 13105–13113. doi:10.1021/jp801651g. ISSN 1932-7447.
  14. Setchell, K. D.; Vestal, C. H. (1989-09-01). "Thermospray ionization liquid chromatography-mass spectrometry: a new and highly specific technique for the analysis of bile acids". Journal of Lipid Research. 30 (9): 1459–1469. ISSN 0022-2275. PMID 2600546.
  15. Betowski, Leon D.; Ballard, John M. (2002). "Identification of dyes by thermospray ionization and mass spectrometry/mass spectrometry". Analytical Chemistry. 56 (13): 2604–2607. doi:10.1021/ac00277a078.
  16. Straub, Kenneth; Chan, Kelvin (1990-07-01). "Molecular weight determination of proteins from multiply charged ions using thermospray ionization mass spectrometry". Rapid Communications in Mass Spectrometry. 4 (7): 267–271. doi:10.1002/rcm.1290040710. ISSN 1097-0231.
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