Formation of Nitrogen Oxides by Nanosecond Pulsed Plasma Discharges in Gas-Liquid Reactors

被引:60
|
作者
Wandell, Robert J. [1 ]
Wang, Huihui [1 ]
Bulusu, Radha K. M. [1 ]
Gallan, Rachel O. [1 ]
Locke, Bruce R. [1 ]
机构
[1] Florida State Univ, FAMU FSU Coll Engn, Dept Chem & Biomed Engn, Tallahassee, FL 32310 USA
基金
美国国家科学基金会;
关键词
Non-thermal plasma; Nitrogen fixation; Plasma activated water; Nanosecond discharge; Nitrogen oxides; GLIDING-ARC DISCHARGES; CORONA DISCHARGE; NO(X) REMOVAL; NO REMOVAL; FLUE-GAS; ELECTRON COLLISIONS; CHEMICAL-REACTIONS; ENERGY EFFICIENCY; CROSS-SECTIONS; WATER;
D O I
10.1007/s11090-019-09981-w
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A gas-liquid-film flow reactor with a nanosecond pulsed power supply was utilized to produce nitrogen oxides from Ar/N-2 mixtures (gas phase) and deionized water (liquid phase). Chemical analysis of the stable products found in both the gas and liquid phases was performed and chemical quenching was incorporated for the liquid phase samples in order to eliminate post plasma reactions. Significant amounts of NO and NO2 in the gas phase and NO2- and NO3- in the liquid phase were determined using FTIR spectroscopy and ion chromatography, respectively. The production rate of all nitrogen oxides produced increased significantly with N-2 concentration while H2O2 formation decreased slightly. The gas temperature of the plasma was approximately 525K and was unaffected by N-2 concentration while the electron density ranged from 1x10(17) cm(-3) in pure Ar to 5.5x10(17) cm(-3) in 28% N-2. The role of the OH in the reaction pathway was assessed by adding CO as a gas phase radical scavenger showing that OH is essential for conversion of the gas phase NO and NO2 into water soluble NO2- and NO3-. Conversely, atomic oxygen originating from water is likely responsible for NO and NO2 generation. Experiments with N-2/O-2/Ar mixtures and air showed a significant increase in NO2 production caused by the additional generation of reactive oxygen species. An overall energy yield for all nitrogen oxides produced in the most efficient case was 50eV/molecule.
引用
收藏
页码:643 / 666
页数:24
相关论文
共 50 条
  • [11] ROLE OF CAVITY FORMATION IN STIRRED GAS-LIQUID SOLID REACTORS
    WARMOESKERKEN, MMCG
    VANHOUWELINGEN, MC
    FRIJLINK, JJ
    SMITH, JM
    CHEMICAL ENGINEERING RESEARCH & DESIGN, 1984, 62 (03): : 197 - 200
  • [12] Microsecond pulse gas-liquid discharges in atmospheric nitrogen and oxygen: Discharge mode, stability, and plasma characteristics
    Wang, Sen
    Liu, Yawei
    Zhou, Renwu
    Liu, Feng
    Fang, Zhi
    Ostrikov, Kostya
    Cullen, Patrick J.
    PLASMA PROCESSES AND POLYMERS, 2021, 18 (02)
  • [13] Tutorial: electrical measurements in nanosecond pulsed plasma reactors
    Pavan, Colin A.
    Rao, Sankarsh R.
    Guerra-Garcia, Carmen
    JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2025, 58 (03)
  • [14] HYDROGEN PRODUCTION FROM WATER BY USING HYBRID GAS-LIQUID NANOSECOND PULSED DISCHARGE
    Ihara, T.
    Nagata, H.
    Yagyu, Y.
    Ohshima, T.
    Kawasaki, H.
    Suda, Y.
    2015 IEEE PULSED POWER CONFERENCE (PPC), 2015,
  • [15] Understanding ambient gas-liquid reactors
    Smith, JM
    Gao, ZM
    CHEMICAL PROCESSING, 2000, 63 (07): : 66 - 70
  • [16] MECHANICALLY AGITATED GAS-LIQUID REACTORS
    JOSHI, JB
    PANDIT, AB
    SHARMA, MM
    CHEMICAL ENGINEERING SCIENCE, 1982, 37 (06) : 813 - 844
  • [17] GRAPHICAL DESIGN OF GAS-LIQUID REACTORS
    VANKREVELEN, DW
    HOFTYZER, PJ
    CHEMICAL ENGINEERING SCIENCE, 1953, 2 (04) : 145 - 156
  • [18] Negative-polarity nanosecond-pulsed cryogenic plasma in liquid nitrogen
    Dobrynin, Danil
    Fridman, Alexander
    JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2024, 57 (44)
  • [19] Synthesis of Highly Energetic PolyNitrogen by Nanosecond-Pulsed Plasma in Liquid Nitrogen
    Dobrynin, Danil
    Song, Zhiheng
    Fridman, Alexander
    MATERIALS, 2021, 14 (15)
  • [20] Degradation of chemical warfare agent simulants using gas-liquid pulsed streamer discharges
    Sahni, Mayank
    Locke, Bruce R.
    JOURNAL OF HAZARDOUS MATERIALS, 2006, 137 (02) : 1025 - 1034