Stable isotope fractionation of nitrous oxide during thermal decomposition and reduction processes

被引:3
作者
Ogawa, M
Yoshida, N
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Environm Chem & Engn, Midori Ku, Yokohama, Kanagawa 2268502, Japan
[2] Japan Sci & Technol Corp, Kawaguchi, Saitama, Japan
[3] Tokyo Inst Technol, Frontier Collaborat Res Ctr, Midori Ku, Yokohama, Kanagawa 227, Japan
关键词
stable nitrogen isotopes; intramolecular distribution of isotope; kinetic isotope effect; nitrous oxide; combustion;
D O I
10.1029/2004JD004652
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Kinetic isotope effects in nitrous oxide thermal decomposition and reduction reactions were investigated in flowing N2O/He and N2O/He/H-2 systems. The intramolecular distribution of stable isotopes, isotopomer, was measured and evaluated using an isotope ratio mass spectrometer equipped with a modified collector system. Thermal decomposition and reduction of nitrous oxide were carried out using a flow tube reactor made of quartz glass in the temperature range of 1173-1373 K. Both thermal decomposition and hydrogen reduction of nitrous oxide proceeded by first-order kinetics. Isotopomer ratios (delta(15)N(bulk), delta(15)N(alpha), delta(15)N(beta), and delta(18)O) of residual nitrous oxide were found to follow a Rayleigh model based on batch distillation. Residual nitrous oxide was depleted slightly in N-15 during thermal decomposition but slightly enriched in N-15 during hydrogen reduction. Regarding the nitrogen isotopomers, results showed that the central nitrogen atom, N-alpha, was enriched in N-15 during both destruction reactions of nitrous oxide. Although the N2O destruction reactions proceeded at high temperature, large isotopic fractionations of nitrogen isotopomers were observed. Enrichment factors for nitrous oxide as a result of thermal decomposition and reduction reactions were evaluated.
引用
收藏
页码:D193011 / 7
页数:7
相关论文
共 19 条
  • [11] Global air emission inventories for anthropogenic sources of NOx, NH3 and N2O in 1990
    Olivier, JGJ
    Bouwman, AF
    Van der Hoek, KW
    Berdowski, JJM
    [J]. ENVIRONMENTAL POLLUTION, 1998, 102 : 135 - 148
  • [12] Measurement of the isotopic fractionation of 15N14N16O, 14N15N16O and 14N14N18O in the UV photolysis of nitrous oxide
    Röckmann, T
    Brenninkmeijer, CAM
    Wollenhaupt, M
    Crowley, JN
    Crutzen, PJ
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2000, 27 (09) : 1399 - 1402
  • [13] MEASUREMENTS OF NITROUS-OXIDE EMISSIONS FROM PF FIRED POWER-STATIONS
    SLOAN, SA
    LAIRD, CK
    [J]. ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (05): : 1199 - 1206
  • [14] SMART JP, 1990, J I ENERGY, V63, P131
  • [15] NYLON PRODUCTION - AN UNKNOWN SOURCE OF ATMOSPHERIC NITROUS-OXIDE
    THIEMENS, MH
    TROGLER, WC
    [J]. SCIENCE, 1991, 251 (4996) : 932 - 934
  • [16] Determination of nitrogen isotopomers of nitrous oxide on a modified isotope ratio mass spectrometer
    Toyoda, S
    Yoshida, N
    [J]. ANALYTICAL CHEMISTRY, 1999, 71 (20) : 4711 - 4718
  • [17] Homogeneous formation of NO and N2O from the oxidation of HCN and NH3 at 600-1000°C
    Wargadalam, VJ
    Löffler, G
    Winter, F
    Hofbauer, H
    [J]. COMBUSTION AND FLAME, 2000, 120 (04) : 465 - 478
  • [18] Diurnal fluxes and the isotopomer ratios of N2O in a temperate grassland following urine amendment
    Yamulki, S
    Toyoda, S
    Yoshida, N
    Veldkamp, E
    Grant, B
    Bol, R
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2001, 15 (15) : 1263 - 1269
  • [19] Constraining the atmospheric N2O budget from intramolecular site preference in N2O isotopomers
    Yoshida, N
    Toyoda, S
    [J]. NATURE, 2000, 405 (6784) : 330 - 334