Dynamical study of the reaction of N+ ions with O2 neutrals

被引:0
|
作者
Swaraj, Dasarath [1 ]
Judy, Jerin [1 ]
Zappa, Fabio [1 ]
Viggiano, Albert A. [2 ]
Gerlich, Dieter [3 ]
Wester, Roland [1 ]
机构
[1] Univ Innsbruck, Inst Ionenphys & Angew Phys, Technikerstr 25, A-6020 Innsbruck, Austria
[2] Air Force Res Lab, Space Vehicles Directorate, Kirtland Afb, NM 87117 USA
[3] Tech Univ Chemnitz, Inst Phys, D-09107 Chemnitz, Germany
基金
欧洲研究理事会; 奥地利科学基金会;
关键词
ion-molecule reactions; reaction dynamics; crossed-beam scattering; velocity map imaging; product branching ratios; MOLECULE REACTION-RATE; BRANCHING RATIOS; TEMPERATURE-DEPENDENCE; RADIATIVE LIFETIME; METASTABLE STATE; O2; BEAM; O+;
D O I
10.1088/1402-4896/adaa32
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The ion-molecule reaction N+ + O2 has been investigated experimentally using crossed beam velocity map imaging in the collision energy range from 0.15 eV to 3.0 eV. From the differential scattering cross sections, information on the branching ratios, the electronic states and vibrational levels populated in the two product channels, O 2+ + N and NO+ + O, have been obtained. These data are compared with previous results obtained using a rotatable ion source setup developed many years ago at the University of Freiburg, Germany. Furthermore, a small fraction of NO+ products populate excited electronic states as observed in chemiluminescence measurements.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Rate constants for the reactions of N+ and N+2 with O2 as a function of temperature (300-@1800 K)
    Dotan, I.
    Hierl, P. M.
    Morris, R. A.
    Viggiano, A. A.
    International Journal of Mass Spectrometry and Ion Processes, 167/1 (1-3):
  • [32] Rate constants for the reactions of N+ and N2+ with O2 as a function of temperature (300-1800 K)
    Dotan, I
    Hierl, PM
    Morris, RA
    Viggiano, AA
    INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 1997, 167 : 223 - 230
  • [33] Kinetics of O2(1Σ) formation in the reaction O2(1Δ) + O2(1Δ) → O2(1Σ) + O2(3Σ)
    Zagidullin, M. V.
    Khvatov, N. A.
    Nyagashkin, A. Yu.
    QUANTUM ELECTRONICS, 2011, 41 (02) : 135 - 138
  • [34] FORMATION OF O2- IONS IN K(ND)-O2 COLLISIONS AT INTERMEDIATE N
    WALTER, CW
    ZOLLARS, BG
    JOHNSON, CB
    SMITH, KA
    DUNNING, FB
    PHYSICAL REVIEW A, 1986, 34 (05): : 4431 - 4432
  • [35] X-RAY PHOTOELECTRON STUDY OF THE REACTION OF O2, NO, N2O, AND D2O WITH GADOLINIUM
    SCHULZE, PD
    HARDEGREE, EL
    JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (13): : 5254 - 5256
  • [36] IONIZATION OF GASES BY FAST N+ AND N2+ IONS
    PIVOVAR, LI
    LEVCHENK.YZ
    GRIGOREV, AN
    KHAZAN, SM
    SOVIET PHYSICS JETP-USSR, 1969, 29 (03): : 399 - &
  • [37] ELECTRON TRANSFER TO MULTIPLY CHARGED IONS OF AR N2 N AND O2
    MCGOWAN, JW
    KERWIN, L
    CANADIAN JOURNAL OF PHYSICS, 1967, 45 (04) : 1451 - &
  • [38] COLLISIONAL EXCITATION OF NO BY H+, N+ AND O+ IONS
    ENOS, CS
    LEE, AR
    BRENTON, AG
    INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1992, 112 (01): : 111 - 120
  • [39] A STUDY OF THE SAFETY AND EFFICACY OF 51W89 IN SURGICAL PATIENTS N2O/O2/OPIOID, N2O/O2/ISOFLURANE, N2O/O2/ENFLURANE, AND N2O/O2/PROPOFOL ANESTHESIA
    OYOS, TI
    LILLEHAUG, SL
    HARLEY, PJ
    DOWNS, DD
    PATEL, SS
    GERGIS, SD
    SOKOLL, MD
    ANESTHESIOLOGY, 1994, 81 (3A) : A1117 - A1117
  • [40] KINETIC STUDY ON REACTION BETWEEN O2 AND HYDROXYLAMINE
    TOMAT, R
    RIGO, A
    SALMASO, R
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1975, 59 (03): : 255 - 260