New Instrument for Time-Resolved OH and HO2 Quantification in High-Pressure Laboratory Kinetics Studies

被引:1
|
作者
Sheps, Leonid [1 ]
Au, Kendrew [1 ]
机构
[1] Sandia Natl Labs, Combust Res Facil, Livermore, CA 94551 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2024年 / 128卷 / 19期
关键词
LOW-TEMPERATURE OXIDATION; GAS-PHASE REACTIONS; ATMOSPHERIC CHEMISTRY; FLUORESCENCE ASSAY; RADICALS; SPECTROSCOPY; CALIBRATION; EXPANSION; REACTOR;
D O I
10.1021/acs.jpca.4c00994
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have constructed a new time-resolved high-pressure fluorescence assay by gas expansion (HP-FAGE) apparatus, optimized for the detection of OH and HO2 radicals in complex gas-phase reactions. The new instrument fills a gap in the existing experimental toolkit for chemical kinetics by enabling the quantification of two key reactive species with microsecond time resolution from high-pressure sources, which was previously not attainable. The HP-FAGE is interfaced with a flow reactor, designed for pressures up to 100 bar and temperatures up to 1000 K, in which reactions are initiated by laser photolysis of radical precursors at repetition rates of 1-10 Hz. The HP-FAGE samples gas out of the reactor into a miniature FAGE chamber, where OH is detected by resonant laser-induced fluorescence using a time-delayed probe laser pulse. HO2 is converted to OH via reaction with NO and then detected by OH fluorescence. The novel FAGE design places the probe region very close to the gas expansion, minimizing the transport time of sampled molecules and resulting in time resolution better than 20 mu s for both OH and HO2. We calibrate the sensitivity of HP-FAGE, validate its performance with measurements of well-known reaction kinetics (OH + CH4, OH + OH, OH + HO2, and HO2 + HO2), and discuss prospects for its future use.
引用
收藏
页码:3916 / 3925
页数:10
相关论文
共 50 条
  • [41] High-pressure picosecond time-resolved fluorescence studies on the excited intramolecular charge-transfer kinetics of 4-(9-anthrylmethyl)-N,N-dimethylaniline in alcohol
    Hara, K
    Bulgarevich, DS
    Kajimoto, O
    BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1997, 101 (10): : 1443 - 1451
  • [42] A TIME-RESOLVED ASSAY OF DOPAMINE BETA-HYDROXYLASE ACTIVITY UTILIZING HIGH-PRESSURE LIQUID-CHROMATOGRAPHY
    FEILCHENFELD, NB
    RICHTER, HW
    WADDELL, WH
    ANALYTICAL BIOCHEMISTRY, 1982, 122 (01) : 124 - 128
  • [43] Study of the laser-induced decomposition of energetic materials at static high-pressure by time-resolved absorption spectroscopy
    Hebert, P.
    Saint-Amans, C.
    18TH APS-SCCM AND 24TH AIRAPT, PTS 1-19, 2014, 500
  • [44] HIGH-PRESSURE FLOW KINETICS - A STUDY OF THE OH + HCL REACTION FROM 2 TO 100 TORR
    KEYSER, LF
    JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (20): : 4750 - 4758
  • [45] High-pressure synthesis of REB5O8(OH)2 (RE= Ho, Er, Tm)
    Zoller, Michael
    Huppertz, Hubert
    ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 2021, 76 (01): : 71 - 77
  • [46] Development of an optical time-resolved measurement system under high-pressure and low-temperature with a piston-cylinder pressure cell
    Tsuchiya, Satoshi
    Kino, Yohei
    Nakagawa, Koichi
    Nakagawa, Daisuke
    Yamada, Jun-ichi
    Toda, Yasunori
    REVIEW OF SCIENTIFIC INSTRUMENTS, 2016, 87 (04):
  • [47] A new high-speed beam chopper for time-resolved X-ray studies
    McPherson, A
    Wang, J
    Lee, PL
    Mills, DM
    JOURNAL OF SYNCHROTRON RADIATION, 2000, 7 (01) : 1 - 4
  • [49] Protein dynamics and solvation from molecular simulations: Comparison to time-resolved and high-pressure X-ray crystallography
    Hummer, Gerhard
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233
  • [50] Deep learning-based denoising for fast time-resolved flame emission spectroscopy in high-pressure combustion environment
    Yoon, Taekeun
    Kim, Seon Woong
    Byun, Hosung
    Kim, Younsik
    Carter, Campbell D.
    Do, Hyungrok
    COMBUSTION AND FLAME, 2023, 248