Physics:Flowing-afterglow mass spectrometry

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The original flowing-afterglow instrument.jpg

Flowing-afterglow mass spectrometry (FA-MS), is an analytical chemistry technique for the sensitive detection of trace gases. Trace gas molecules are ionized by the production and flow of thermalized hydrated hydronium cluster ions in a plasma afterglow of helium or argon carrier gas along a flow tube following the introduction of a humid air sample.[1] These ions react in multiple collisions with water molecules, their isotopic compositions reach equilibrium and the relative magnitudes of their isotopomers are measured by mass spectrometry.

Brief History

Over the years many variations of the instrument have been made. In the beginning during the 1960s there was the study of flowing afterglow plasma. This study was done by Eldon Ferguson, Art Schmeltekopf and Fred Fehsenfeld at National Bureau of Standards in Boulder, Colorado.[2] Then in the 1970s it was flowing drift tube, flowing afterglow Langmuir probe (FALP), and variable temperature flowing afterglow Langmuir probe (VT-FLAP). With the addition of the drift tube the kinetics of a reaction could be studied in the gas phase.[3] With the flowing afterglow Langmuir probe the electron density within the reaction region of the drift tube can be studied.[3] With the VT-FLAP version of flowing afterglow the reactions temperature dependence could be studied.[3] Now in the 2000s the ambient version of flowing afterglow mass spectrometry is flowing atmospheric pressure afterglow mass spectrometry (FAPA-MS).The FAPA allows for simple or no sample preparations but the humidity of the instrument's environment may have an effect on a sample fragmentation pattern.[4][5] Since the cost of helium is steady rising some have started to use alternative methods with ambient flowing afterglow to conserve resources. Instead of using continuously flowing afterglow helium some use interrupted helium flow to conserve gas and Schlieren imaging to maximize the molecular ions produced and the instrument step-up.[6][7]

Application(s)

Trace gas analysis

One of the first papers reporting the use of the flowing afterglow studied ion-molecule reactions pertinent to the Martian atmosphere.[8] This flowing afterglow technique replaced the then standard stationary afterglow when the movable Langmuir probe was introduced.[3] The flowing afterglow has many attractive aspects: well-understood laminar behavior, viscous gas flow, a large density of carrier gas which allows the study of thermalized reactions, and the capability to make new reactant ions in situ. The ambipolar plasma is sampled using a nosecone and detected using conventional quadrupole or tandem mass spectrometry, depending on the application. One of the drawbacks of the flowing afterglow technique is the possibility of generating multiple reactant ions.[2] This problem is circumvented by implementing the selected ion flow tube (SIFT).[9]

The flowing afterglow technique can be used to identify and quantify the volatile organic compounds (VOCs) of a sample as long as the fundamental ion chemistry is known.[10] The commonly used ions are H3O+, O2+*, and NO+. All ions have drawbacks and advantages. Strategies that have been employed to identify the VOCs include using gas chromatography coupled with flowing afterglow and using a complement of reagent ions. Also in addition to being able to detect volatile organic compounds, the flowing afterglow technique has also been used to study chronic kidney disease. Studies have been done to create a spectrum of deuterium water and its isotopes to measure total body water, which can be used to determine the water body overload of a patient. That measurement will then be used to determine the stage of renal failure for a patient.[11][12]

See also

  • Charles H. DePuy (chemist)
  • Robert R. Squires

References

  1. ↑ Handbook of Stable Isotope Analytical Techniques. Elsevier. 2004. ISBN 0-444-51114-8. 
  2. ↑ 2.0 2.1 "Go with the Flow: Fifty Years of Innovation and Ion Chemistry Using the Flowing Afterglow". International Journal of Mass Spectrometry 377: 456–466. 2015. doi:10.1016/j.ijms.2014.07.021. Bibcode: 2015IJMSp.377..456B. 
  3. ↑ 3.0 3.1 3.2 3.3 "The SIFT and FALP Techniques; Applications to Ionic and Electronic Reactions Studies and Their Evolution to the SIFT-MS and FA-MS Analytical Methods". International Journal of Mass Spectrometry 377: 467–478. 
  4. ↑ "Critical Assessment of Ionization Patterns and Applications of Ambient Desorption/Ionization Mass Spectrometry Using FAPA–MS". Journal of Mass Spectrometry 51: 141–149. 2016. doi:10.1002/jms.3733. PMID 26889930. Bibcode: 2016JMSp...51..141B. 
  5. ↑ "Humidity Effects on Fragmentation in Plasma-Based Ambient Ionization Sources". Journal of the American Society for Mass Spectrometry 27: 135–143. 2016. doi:10.1007/s13361-015-1259-y. Bibcode: 2016JASMS..27..135N. 
  6. ↑ "Use of Interrupted Helium Flow in the Analysis of Vapor Samples with Flowing Atmospheric-Pressure Afterglow-Mass Spectrometry". Journal of the American Society for Mass Spectrometry 28: 263–269. 2017. doi:10.1007/s13361-016-1520-z. Bibcode: 2017JASMS..28..263S. 
  7. ↑ "Measurement and Visualization of Mass Transport for the Flowing Atmospheric Pressure Afterglow (FAPA) Ambient Mass-Spectrometry Source". Journal of the American Society for Mass Spectrometry 25: 800–808. 2014. doi:10.1007/s13361-014-0843-x. PMID 24658804. Bibcode: 2014JASMS..25..800P. 
  8. ↑ Norton, RB (1966). "Ion-neutral reactions in the Martian ionosphere". Planetary and Space Science 14 (10): 969–978. doi:10.1016/0032-0633(66)90133-4. Bibcode: 1966P&SS...14..969N. 
  9. ↑ "The Selected Ion Flow Tube (SIFT); A Technique for Studying Ion-Neutral Reactions". International Journal of Mass Spectrometry and Ion Physics 21: 349–359. 1976. doi:10.1016/0020-7381(76)80133-7. Bibcode: 1976IJMSI..21..349A. 
  10. ↑ "Organic mass spectrometry and control of fragmentation using a fast flow glow discharge ion source". Rapid Communications in Mass Spectrometry 20 (14): 2067–2073. 2006. doi:10.1002/rcm.2560. PMID 16767685. Bibcode: 2006RCMS...20.2067N. 
  11. ↑ "SIFT-MS and FA-MS Methods for Ambient Gas Phase Analysis: Developments and Applications in the UK". The Analyst 140: 2573–2591. 2015. doi:10.1039/C4AN02049A. Bibcode: 2015Ana...140.2573S. http://pubs.rsc.org/en/content/articlepdf/2015/an/c4an02049a. 
  12. ↑ "Comparative Measurements of Total Body Water in Healthy Volunteers by Online Breath Deuterium Measurement and Other Near-Subject Methods". American Journal of Clinical Nutrition 76: 1295–1301. 2002. doi:10.1093/ajcn/76.6.1295. PMID 12450896. 



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