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Decomposition of Gaseous Sulfide Compounds in Air by Pulsed Corona Discharge

机译:脉冲电晕放电分解空气中的气态硫化物

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The effectiveness of applying a pulsed corona discharge to the destruction of olfactory pollution in air was investigated. This paper presents a comparative study of the decomposition of three representative sulfide compounds in diluted concentrations: hydrogen sulfide (H2S), dimethyl sulfide (DMS), and ethanethiol (C2H5SH), which could be completely removed when a sufficient but reasonable energy density was deposited in the gas. DMS showed the lowest energy cost (around 30 eV/molecules); C2H5SH and H2S had an EC of respectively 45 eV and 115 eV. The efficiency of the non-thermal plasma process increased with decreasing the initial concentration of sulfide compounds, while the energy yield remained almost unchanged. SO2 was the only identified byproduct of H2S decomposition, but the sulfur balance suggests the formation of undetected SO3. The byproducts analyzed during the degradation of DMS and C2H5SH enabled to propose a reaction mechanism, starting with radical attack and breaking of C–S bonds.
机译:研究了将脉冲电晕放电应用于破坏空气中的嗅觉污染的有效性。本文对三种代表性的硫化物在稀释浓度下的分解进行了比较研究:硫化氢(H2 S),二甲基硫醚(DMS)和乙硫醇(C2 H5 SH) ,如果在气体中沉积了足够但合理的能量密度,则可以将其完全去除。 DMS显示出最低的能源成本(约30 eV /分子); C2 H5 SH和H2 S的EC分别为45 eV和115 eV。非热等离子体工艺的效率随着硫化物化合物初始浓度的降低而增加,而能量产率几乎保持不变。 SO2 是H2 S分解的唯一鉴定出的副产物,但硫平衡表明未检测到SO3 的形成。 DMS和C2 H5 SH降解过程中分析的副产物能够提出一种反应机理,从自由基攻击和C–S键断裂开始。

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