对 Ns 脉冲大气压等离子体射流中 HO2 自由基的空间和时间分辨测量

Hamzeh Telfah, S. Raskar, I. V. Adamovich
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引用次数: 0

摘要

在一列 ns 放电脉冲驱动的准二维大气压 "帘式 "等离子体射流中,测量了氢过氧自由基的绝对数密度、空间分辨密度和时间分辨密度。HO2 的空间分布是在射流的较短维度上测量的。测量在两种不同的配置下进行:(a) H2O-O2-He 喷射撞击铜箔靶,(b) O2-He 喷射入射液态水表面。在第一种配置中,水蒸气加入到装有蒸馏去离子水的气泡器中的 O2-He 流中。测量使用的是之前开发的脉冲腔环向下光谱(CRDS)诊断仪,波长在 1.5 μm 附近。环向下空腔是在两个高反射率反射镜之间形成的,反射镜放置在用干燥空气吹扫的不锈钢 "臂 "的两端,等离子体射流放置在 "臂 "之间的空隙中。这项工作的目的是利用 HO2 的数量密度来评估使用先前开发的 "全局 "反应机制进行建模预测的准确性,并估算 ns 脉冲放电等离子体中过氧化氢的生成效率。只在第一种构型中检测到了 HO2,这很可能是由于等离子体中产生的惰性 He 原子和 O 原子的快速衰变阻止了蒸发/混合层中 H 原子(主要的 HO2 前体)的生成。对喷流中的水蒸气和等离子体中产生的 HO2 都进行了测量。结果表明,在 ns 脉冲放电爆发期间,HO2 迅速积累,随后在毫秒级的余辉中衰减。动力学模型对准稳态 HO2 数量密度以及放电关闭后的 HO2 衰减率预测过高。余辉中相对较慢的 HO2 衰减表明,它可能受到扩散以及自由基表面吸附和解吸的影响。本方法证明了二维帘幕等离子体射流在视线吸收光谱测量环境等离子体环境中存在的小浓度自由基和激发物种方面的实用性。
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Spatially- and time-resolved measurements of HO2 radicals in a Ns pulse atmospheric pressure plasma jet
The absolute, spatially-resolved, and time-resolved number density of the hydroperoxyl radical is measured in a quasi-two-dimensional, atmospheric pressure “curtain” plasma jet powered by a train of ns discharge pulses. The spatial distribution of HO2 is measured across the shorter dimension of the jet. The measurements are made in two different configurations, (a) H2O-O2-He jet impinging on a copper foil target, and (b) O2-He jet incident on the liquid water surface. In the first configuration, the water vapor is added to the O2-He flow in a bubbler filled with distilled, deionized water. The measurements are made using the previously developed pulsed Cavity Ring Down Spectroscopy (CRDS) diagnostic near 1.5 μm. The ring-down cavity is formed between two high-reflectivity mirrors placed at the ends of the stainless steel “arms” purged with dry air, with the plasma jet placed in the gap between the arms. The objectives of this work are to use the HO2 number density to assess the accuracy of the modeling predictions using a previously developed “global” reaction mechanism, and to estimate the efficiency of hydrogen peroxide generation in the ns pulse discharge plasma. HO2 was detected only in the first configuration, most likely due to the rapid decay of the metastable He atoms and O atoms generated in the plasma, which prevents the generation of H atoms (dominant HO2 precursors) in the evaporation/mixing layer. Both the water vapor in the jet and HO2 generated in the plasma have been measured. The results exhibit a rapid accumulation of HO2 during the ns pulse discharge burst, followed by the decay in the afterglow on a ms time scale. The kinetic model overpredicts the quasi-steady-state HO2 number density, as well as the HO2 decay rate after the discharge is turned off. The relatively slow HO2 decay in the afterglow suggests that it may be affected by diffusion, along with the surface adsorption and desorption of radicals. The present approach demonstrates the utility of a 2-D curtain plasma jet for the line-of-sight absorption spectroscopy measurements of radicals and excited species present in small concentrations in ambient plasma environments.
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