Wikipedia

Chemi-ionization

Not to be confused with chemical ionization.

Chemi-ionization is the formation of an ion through the reaction of a gas phase atom or molecule with another atom or molecule when the collision energy is below the energy required to ionize the reagents.[1][2] The reaction may involve a reagent in an excited state[3] or may result in the formation of a new chemical bond.[1][4] Chemi-ionization can proceed through the Penning, associative, dissociative or rearrangement ionization reactions. Includes reactions that produce a free electron or a pair of ions (positive and negative).[5]

This process is helpful in mass spectrometry because it creates unique bands that can be used to identify molecules.[6] This process is extremely common in nature as it is considered the primary initial reaction in flames.[citation needed]

Definitions edit

In the literature, the term "chemi-ionization" is used inconsistently.[7] Berry broadly defined chemi-ionization as "processes that lead to the formation of free charges, electrons and ions under the conditions of chemical reactions". Fontijn defined chemi-ionization more narrowly as reactions "in which the number of elementary charge carriers is increased as a direct result of the formation of new chemical bonds". Fontijn explicitly specified that the number of charge carriers increases, but Berry's definition includes the Penning ionization.[8]

The IUPAC defined chemi-ionization in the context of mass spectrometry as "ionization of an atom or molecule by interaction with another internally excited atom or molecule". The IUPAC definition includes only reactions that involve an atom or a molecule in an excited state. Also, IUPAC mentioned that chemi-ionization includes reactions in which chemical bonds are not changed.[3]

Energy requirements edit

A certain amount of energy, which may be large enough, is required to remove an electron from an atom or a molecule in its ground state.[9][10] In chemi-ionization processes, the energy consumed by the ionization must be stored in atoms or molecules in a form of potencial energy or can be obtained from an accompanying exothermic chemical change (for example, from a formation of a new chemical bond). In atoms or molecules, the energy can be stored in the form of an excited state. In molecules, it can alternatively be stored in the form of vibrational excitation.[9] In exothermic chemical reactions, the released energy can be acquired by the molecule in the form of internal vibrational excitation and then cause ionization if the released energy is large enough.[11]

Reactions edit

Reactions involving a reagent in an excited state edit

Chemi-ionization can be represented by

 

where G is the excited state species (indicated by the super-scripted asterisk), and M is the species that is ionized by the loss of an electron to form the radical cation (indicated by the super-scripted "plus-dot").

Astrophysical implications edit

Chemi-ionization has been postulated to occur in the hydrogen rich atmospheres surrounding stars. This type of reaction would lead to many more excited hydrogen atoms than some models account for. This affects our ability to determine the proper optical qualities of solar atmospheres with modeling.[12]

In flames edit

The most common example of chemi-ionization occurs in hydrocarbon flame. The reaction can be represented as

  [13]

This reaction is present in any hydrocarbon flame and can account for deviation in the amount of expected ions from thermodynamic equilibrium.[14]

History edit

The term chemi-ionization was coined by Hartwell F. Calcote in 1948 in the Third Symposium on Combustion and Flame, and Explosion Phenomena.[15] The Symposium performed much of the early investigation into this phenomenon in the 1950s. The majority of the research on this topic was performed in the 1960s and '70s. It is currently seen in many different ionization techniques used for mass spectrometry.[16][17]

See also edit

References edit

  1. ^ a b Jozef Paulovic; Laura Gagliardi; John M Dyke; Kimihiko Hirao (1 April 2005). "A theoretical study of the gas-phase chemi-ionization reaction between uranium and oxygen atoms". The Journal of Chemical Physics. 122 (14): 144317. doi:10.1063/1.1879832. ISSN 0021-9606. PMID 15847532. Wikidata Q51494633.
  2. ^ Andre Venter; Marcela Nefliu; R. Graham Cooks (April 2008). "Ambient desorption ionization mass spectrometry". Trends in Analytical Chemistry. 27 (4): 284–290. doi:10.1016/J.TRAC.2008.01.010. ISSN 0165-9936. Wikidata Q29541795.
  3. ^ a b Kermit K. Murray; Robert K. Boyd; Marcos N. Eberlin; G. John Langley; Liang Li; Yasuhide Naito (6 June 2013). "Definitions of terms relating to mass spectrometry (IUPAC Recommendations 2013)". Pure and Applied Chemistry. 85 (7): 1515–1609. doi:10.1351/PAC-REC-06-04-06. ISSN 0033-4545. Wikidata Q55872037.
  4. ^ Klucharev, A. N. (1993), "Chemi-ionization processes", Physics-Uspekhi, 36 (6): 486, Bibcode:1993PhyU...36..486K, doi:10.1070/PU1993v036n06ABEH002162
  5. ^ P. Pradel; J. J. Laucagne (1983). "Chemi-ionization reactions involving metastable helium atoms at high energy". Journal de physique. 44 (11): 1263–1271. doi:10.1051/JPHYS:0198300440110126300. ISSN 0302-0738. Wikidata Q125499439.
  6. ^ Dyke, John M.; Shaw, Andrew M.; Wright, Timothy G. (1994). "Study of Chemiionization Reactions in the O + 2-Butyne Reaction Mixture". The Journal of Physical Chemistry. 98 (25): 6327–6331. doi:10.1021/j100076a016. ISSN 0022-3654.
  7. ^ R. Feltgen; H. Ferkel; R. K. B. Helbing; A. Lindinger; D. Pikorz; H. Vehmeyer (22 October 1999). "The chemi-ionization of He*(21,3S)+Xe, Kr, Xe for collision energies from 0.003 to 6 eV". The Journal of Chemical Physics. 111 (16): 7298–7315. doi:10.1063/1.480103. ISSN 0021-9606. S2CID 93944181. Wikidata Q125693344.
  8. ^ John M. Dyke; Andrew M. Shaw; Timothy G. Wright (September 1995). "Study of Chemiionization Reactions in the O + C2H2 Reaction Mixture: Evidence for Involvement of the CH(X2.PI.) and CH(a4.SIGMA.-) States". The journal of physical chemistry. 99 (39): 14207–14216. doi:10.1021/J100039A005. ISSN 0022-3654. Wikidata Q57948440.
  9. ^ a b V. Aquilanti; G. G. Volpi (1992). "Molecular beam studies of the dynamics of elementary chemical processes". In S. Carrà; N. Rahman (eds.). From Molecular Dynamics to Combustion Chemistry: Proceedings of the Conference. World Scientific. pp. 67−81. doi:10.1142/9789814536790. ISBN 978-981-4536-79-0. Wikidata Q125491026.
  10. ^ The Editors of Encyclopaedia Britannica, Ionization energy at the Encyclopædia Britannica
  11. ^ Colin F. Poole; Salwa K. Poole (1991). "Chapter 3. Instrumental Aspects of Gas Chromatography". Chromatography Today. Elsevier. p. 262. ISBN 9780444596192. Wikidata Q125738588.
  12. ^ Mihajlov, Anatolij A.; Ignjatović, Ljubinko M.; Srećković, Vladimir A.; Dimitrijević, Milan S. (2011). "CHEMI-IONIZATION IN SOLAR PHOTOSPHERE: INFLUENCE ON THE HYDROGEN ATOM EXCITED STATES POPULATION". The Astrophysical Journal Supplement Series. 193 (1): 2. arXiv:1105.2134. Bibcode:2011ApJS..193....2M. doi:10.1088/0067-0049/193/1/2. ISSN 0067-0049.
  13. ^ Vinckier, C.; Gardner, Michael P.; Bayes, Kyle D. (1977). "A study of chemi-ionization in the reaction of oxygen atoms with acetylene". The Journal of Physical Chemistry. 81 (23): 2137–2143. doi:10.1021/j100538a001. ISSN 0022-3654.
  14. ^ Fontijn, A.; Miller, W.J.; Hogan, J.M. (1965). "Chemi-ionization and chemiluminescence in the reaction of atomic oxygen with C2H2, C2D2, and C2H4". Symposium (International) on Combustion. 10 (1): 545–560. doi:10.1016/S0082-0784(65)80201-6. ISSN 0082-0784.
  15. ^ Calcote, Hartwell F. (1948). "Electrical properties of flames". Symposium on Combustion and Flame, and Explosion Phenomena. 3 (1): 245–253. doi:10.1016/S1062-2896(49)80033-X. hdl:2027/uva.x030313059. ISSN 1062-2896.
  16. ^ Chen, Lee Chuin; Yu, Zhan; Hiraoka, Kenzo (2010). "Vapor phase detection of hydrogen peroxide with ambient sampling chemi/chemical ionization mass spectrometry". Analytical Methods. 2 (7): 897. doi:10.1039/c0ay00170h. ISSN 1759-9660.
  17. ^ Mason, Rod S.; Williams, Dylan R.; Mortimer, Ifor P.; Mitchell, David J.; Newman, Karla (2004). "Ion formation at the boundary between a fast flow glow discharge ion source and a quadrupole mass spectrometer". Journal of Analytical Atomic Spectrometry. 19 (9): 1177. doi:10.1039/b400563p. ISSN 0267-9477.
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