Research output: Contribution to journal › Article › peer-review
Mass Spectrometric Study of Cations in a Non-Sooting Ethylene Flame. / Cherepanov, A. V.; Knyazkov, D. A.
In: Kinetics and Catalysis, Vol. 65, No. 4, 04.09.2024, p. 309-319.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Mass Spectrometric Study of Cations in a Non-Sooting Ethylene Flame
AU - Cherepanov, A. V.
AU - Knyazkov, D. A.
N1 - This study was supported by the Russian Science Foundation (project no. 23-23-00521, https://rscf.ru/project/23-23-00521/ ).
PY - 2024/9/4
Y1 - 2024/9/4
N2 - Understanding the kinetics and mechanism of formation of charged species in flames is of great importance for the development of ion-sensitive combustion control technologies. The development of predictive models involving ion-molecular reactions, however, is hampered by the lack of experimental data. The paper presents the results of our study of the spatial distribution of cations naturally occurring in a fuel-rich, non-sooting, laminar premixed ethylene/oxygen/argon flame using flame sampling molecular beam mass spectrometry. Particular attention is paid to the interpretation of the obtained mass spectra of cations, which are distorted by the influence of the sampling probe. The reliability of the proposed interpretation of the spectra is confirmed by consistency between the cationic and neutral flame structures. The study focused on cations with the general formula CxH (53 < m/z < 165), actively formed in the reaction zone of the fuel-rich flame. Two main mechanisms of their formation are discussed: proton transfer from HCO+ and H3O+ (key cations of flame) to neutral intermediates whose mass is 1 amu smaller and gradual increase in the mass of ions in the reactions of lighter CxH ions with neutral intermediates having high concentrations in the flame (acetylene, diacetylene, propylene, propyne, etc.).
AB - Understanding the kinetics and mechanism of formation of charged species in flames is of great importance for the development of ion-sensitive combustion control technologies. The development of predictive models involving ion-molecular reactions, however, is hampered by the lack of experimental data. The paper presents the results of our study of the spatial distribution of cations naturally occurring in a fuel-rich, non-sooting, laminar premixed ethylene/oxygen/argon flame using flame sampling molecular beam mass spectrometry. Particular attention is paid to the interpretation of the obtained mass spectra of cations, which are distorted by the influence of the sampling probe. The reliability of the proposed interpretation of the spectra is confirmed by consistency between the cationic and neutral flame structures. The study focused on cations with the general formula CxH (53 < m/z < 165), actively formed in the reaction zone of the fuel-rich flame. Two main mechanisms of their formation are discussed: proton transfer from HCO+ and H3O+ (key cations of flame) to neutral intermediates whose mass is 1 amu smaller and gradual increase in the mass of ions in the reactions of lighter CxH ions with neutral intermediates having high concentrations in the flame (acetylene, diacetylene, propylene, propyne, etc.).
KW - ethylene
KW - fuel-rich flame
KW - ion-molecular reactions
KW - ions in flames
KW - molecular beam mass spectrometry
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85203073444&origin=inward&txGid=5247b6080a4c0d31cd6d0ffc89f75d68
UR - https://www.mendeley.com/catalogue/eef4dee4-82a3-3a55-8250-926a57e9dbb0/
U2 - 10.1134/S0023158424601670
DO - 10.1134/S0023158424601670
M3 - Article
VL - 65
SP - 309
EP - 319
JO - Kinetics and Catalysis
JF - Kinetics and Catalysis
SN - 0023-1584
IS - 4
ER -
ID: 60828848