Formations of Active Species and By-Products in Water by Pulsed High-Voltage Discharge

Formations of active species and by-products are different from bubbling different gases in a pulsed high-voltage discharge reactor. The identification of all the products and the formation rate determination of active species are quite important as the process is applied to wastewater disposal. Serials of measurements were conducted to do the identifications and determinations in this paper. Amounts of · OH all increased but that of H₂O₂ all decreased by bubbling gas. The · OH formation rate was 3.49 × 10⁻⁷, 3.56 × 10⁻⁷, 3.21 × 10⁻⁷ and 1.94 × 10⁻⁷ mol l⁻¹ s⁻¹ with bubbling nitrogen, argon, air and oxygen respectively, but it was 1.61 × 10⁻⁷ mol s⁻¹ l⁻¹ without bubbling. Without any bubbling, the H₂O₂ formation rate was up to 6.53 × 10⁻⁶ mol l⁻¹ s⁻¹, while it was 9.97 × 10⁻⁷, 1.663 × 10⁻⁷, 1.73 × 10⁻⁶ and 3.14 × 10⁻⁶ mol l⁻¹ s⁻¹ with bubbling nitrogen, argon, air and oxygen, respectively. NO₂⁻ and NO₃⁻ was detected in discharged water with bubbling nitrogenous gas. Their formation made the pH decreased.     

Oxidation of Elemental Mercury by Active Species Generated From a Surface Dielectric Barrier Discharge Plasma Reactor

A surface dielectric barrier discharge plasma reactor was employed to study Hg⁰ oxidation in coal-fired flue gas. The experimental results showed that 98 % of Hg⁰ oxidation efficiency and 13.7 μg kJ^?1 of energy yield were obtained under a specific energy density (SED) of 7.9 J L^?1. Increasing SED was beneficial for Hg⁰ oxidation due to higher production of active species. Higher initial concentration resulted in lower Hg⁰ oxidation efficiency, but higher amount of Hg⁰ oxidation. Water vapor inhibited Hg⁰ oxidation because the generation of O₃ was suppressed. The presence of NO remarkably restrained Hg⁰ oxidation, while SO₂ showed little effect on Hg⁰ oxidation. Roles of active species in Hg⁰ oxidation were examined under different gas atmospheres (O₂ and air), indicating that O₃ played an important role in Hg⁰ oxidation. Deposits on the internal surface of the reactor were analyzed by energy dispersive spectroscopy and the product was identified as HgO.     

Evaluation of Oxidative Species in Gaseous and Liquid Phase Generated by Mini-Gliding Arc Discharge

Plasma Chemistry and Plasma Processing - The gliding arc discharge plasma reactors are known as a source of non-equilibrium plasma at atmospheric pressure. In the present study, generation of...     

The Effects of Gas Composition on Active Species and Byproducts Formation in Gas–Water Gliding Arc Discharge

The effects of gas composition on hybrid gas–water gliding arc discharge plasma reactor have been studied. The voltage cycles are characterized by a moderate increase in the tension which is represented by a peak followed by an abrupt decrease and a current peak in the half period (10 ms). Emission spectrum measurements revealed that ^•OH hydroxyl radicals are present in the discharge with feeding any gas. The H₂O₂ concentrations reach 38.0, 15.0, 10.0, and 8.0 mg/l after 25 min plasma treatment with oxygen, argon, air, and nitrogen, respectively. O₃ was produced when oxygen and air are used, but not when nitrogen and argon. The O₃ concentration reached the highest value 1.0 mg/l after 25 min plasma treatment with oxygen feeding gas, but gradually decreased to 0.2 mg/l after that. With feeding nitrogenous gas, NO₂ ⁻ and NO₃ ⁻ byproducts were formed by the plasma chemical process.     

Characterization of Plasma Polymerized Hexamethyldisiloxane Films Prepared by Arc Discharge

Herein, we present a simple method for fabricating plasma polymerized hexamethyldisiloxane films (pp-HMDSO) possessing superhydrophobic characteristics via arc discharge. The pp-HMDSO films were deposited on a soda–lime–silica float glass using HMDSO monomer vapor as a precursor. A detailed surface characterization was performed using scanning electron microscopy and atomic force microscopy. The growth process of the pp-HMDSO films was investigated as a function of deposition time from 30 to 300 s. The non-wetting characteristics of the pp-HMDSO films were evaluated by means of contact angle (CA) measurements and correlated with the morphological characteristics, as obtained from microscopy measurements. The deposited films were found to be nano-structured and exhibited dual-scale roughness with the static CA values close to 170°. Fourier transform infrared spectroscopy analysis was carried out to investigate chemical and functional properties of these films. Methyl groups were identified spectroscopically to be present within the pp-HMDSO films and were proposed to result in the low surface energy of material. The synergy between the dual-scale roughness and low surface energy resulted in the superhydrophobic characteristics of the pp-HMDSO films. A possible mechanism for the pp-HMDSO film formation is proposed.     

Molecular Species Generated by Surface Dielectric Barrier Discharge Micro-plasma in Small Chambers Enclosing Atmospheric Air and Water Samples

In many applications of the atmospheric pressure plasmas, the plasma is generated in chambers that enclose samples to be treated. In the case of plasma treatments of water or water-containing materials, the humidity in gaseous medium rises during the treatment, and this affects considerably the plasma generation of reactive oxygen and nitrogen species (RONS). In this study, Fourier transform infrared absorption spectroscopy is used to investigate the kinetics of reactive species generated by surface dielectric barrier (SDBD) micro-plasma in a small volume of atmospheric air (0.5 L) enclosed in a discharge chamber. The investigations were made for dry air (in absence of liquid water) and for humid air in presence of liquid water. The SDBD plasma contributes to desorption of water from the inner wall of the discharge chamber and enhances evaporation of liquid water, which increases air humidity and decreases the generation rates of reactive species. Kinetics of RONS generated in small samples of liquid water in contact with discharge medium is investigated by ex situ UV absorption spectroscopy measurements of plasma treated water.

     

Degradation of Organic Contaminants in Water by Pulsed Corona Discharge

Degradation of organic contaminants in water by high-voltage pulse discharges was investigated. The effects of gas flow rate and liquid conductivity on the degradation of 4-chlorophenol were studied. With the increase of time, the liquid conductivity increases, which have an important effect on discharge. Meanwhile, with the increase of time, the concentration of H₂O₂ increases. Addition of 200 mg/L H₂O₂, the conversion of 4-chlorophenol was greatly enhanced. This may be due to the synergistic effect of high-voltage pulsed discharge and H₂O₂. Also, it was found that the influence of quantity of TiO₂or CuO on degradation of acetophenone is not apparent, maybe the presence of metal oxides hinders the formation of plasma channel due to increase of collusions between metal oxides and oxygen.     

Growth of Wall-controlled MWCNTs by Magnetic Field Assisted Arc Discharge Plasma

Carbon nanotubes have long attracted great scientific interest because of their simplicity, ease of synthesis and unique properties. The novel properties of nanostructured carbon nanotubes including its high surface area, stiffness, tensile strength, thermal and electrical properties which become suitable for the application in the fields of energy storage, hydrogen storage, electrochemical supercapacitor, field-emitting devices, transistors, nanoprobes and sensors, composite material, templates, etc. In this study, carbon nanotubes were synthesized through arc discharge plasma with two different configurations, transverse and axial field, applied across arc plasma synthesis process to enable a much rapid rate growing of tubular carbon multi-walled carbon nanotubes (MWCNTs). TEM, FESEM, RAMAN, FTIR and XRD were used to investigate the morphology and structural evolution of the MWCNT samples produced with different synthesis environment. Introduction of magnetic field during the MWCNTs synthesized through arc discharge plasma technique has also been found to enhance the carbon nanotube growth, increase the high aspect ratio and its chemical stability, and shows potential for regulating the number of walls formed.     

An Experimental Investigation of the Liquid Flow Induced by a Pulsed Electrical Discharge Plasma

In this work, particle image velocimetry has been used to visualize and quantify plasma-induced flow fields in liquid water. Experiments were performed in a rod-plane plasma reactor with a thin wire electrode suspended above the surface of the liquid in argon gas and a grounded plate immersed in the liquid. The velocity field has been quantified for two types of solutions: (1) aqueous NaCl solutions of varying solution conductivities and discharge frequencies and (2) aqueous NaCl solutions containing varying concentrations of the following four organic compounds: rhodamine B dye, caffeine, fluoxetine, and perfluorooctanoic acid. Results show that in neat water and aqueous caffeine solutions, the liquid is “pulled” along by the interaction of the gas molecules with the liquid molecules at the free surface and thus the direction of the liquid flow is in the direction of the gas phase flow (i.e., away from the discharge location). However, the flow was reversed (i.e., towards the discharge) for those solutions with strong surfactants such as perfluorooctanoic acid. The magnitude of the reversal depended on the initial concentration of the compound and for some compounds as time progressed the reversed flow pattern weakened and then reverted to a normal flow pattern. To determine the most likely cause of these flow reversals, a simple numerical model of the velocity field was developed to estimate relative contributions of various flow inducing mechanisms. The model indicates that in the presence of surfactants, Marangoni stresses are responsible for inducing the flow in the liquid.     

脉冲电弧放电电离甲醇溶液制备碳膜的研究

利用脉冲电弧放电电离甲醇溶液在常压下研究了含金刚石成分的碳膜的制备。用扫描电子显微镜(SEM)、傅里叶红外光谱(FT-IR)、激光Raman光谱和X射线衍射(XRD)研究了在确定的基片温度下甲醇浓度以及放电电压等沉积条件对薄膜的形貌和金刚石的合成的影响。研究结果表明：在放电电压低于2kV时，薄膜主要由无序石墨和无定形碳组成。提高放电电压有助于金刚石的合成，在高的放电电压下，降低甲醇溶液浓度有利于提高碳膜中金刚石成分的含量。     

The Roles of Various Plasma Active Species in Toluene Degradation by Non-thermal Plasma and Plasma Catalysis

Plasma Chemistry and Plasma Processing - Investigating the roles of plasma active species in plasma chemical reaction process can improve understanding of the mechanism of volatile organic...     

Determinations of Intermediate Neutral Species in Hydrocarbon Discharge Plasma

This work reports laser ionization combined with Time-Of-Flight (TOF) mass spectrometry investigation on intermediate species in the hydrocarbon plasma of atmospheric-pressure fast-flow pulsed dc-discharge. All neutral intermediate species including transient radicals from benzene/Ar discharge have been characterized by a molecular beam sampling combined with TOF mass spectrometry. This shows that with a hydrocarbon gas mixture of 0.3% C₆H₆ in Ar discharge the intermediate species consist of simple radicals (such as C₂, C₅H₅, C₇H₇) and polycyclic organic molecules (C₁₀H₈, C₁₃H₁₀, C₁₄H₁₀). Theoretical studies on total energies and ionization potentials of the intermediate species have been carried out using the hybrid density functional theory. Effect of the ionization potential on mass spectral intensity has been discussed. Based on the observed data, the possible major neutral reaction channels of the plasma chemistry have been discussed. The developed experimental method has implications in volatile organic compounds removing and impurities diagnosis in Tokamak edge-plasma.     

Pulsed Corona Discharge for Degradation of Methylene Blue in Water

A pulsed corona discharge in multiwire-plate geometry, generated above water was studied for the removal of organic compounds in liquids. The degradation of methylene blue (MB) and the formation of hydrogen peroxide (H₂O₂) were investigated. The MB solution was rapidly decolorized, evidencing the degradation of the dye after approximately 10 min plasma treatment. Nitrate, formate, sulphate and chlorine ions have been detected in the treated solution, explaining partly the change in the solution properties with plasma exposure, i.e. increase of electrical conductivity and decrease of pH. It was found that the concentration of H₂O₂ generated in water increased with plasma exposure time, reaching 200 mg/L after 30 min treatment. In the MB solution less hydrogen peroxide was detected, suggesting reactions with the dye and its degradation products. The addition of FeCl₂ catalyst had a slight favorable effect on methylene blue degradation due to Fenton’s reaction. It was observed that MB and H₂O₂ concentrations continue to decrease after the plasma treatment was stopped, suggesting that active species which accumulate in the solution may react post-plasma with methylene blue and its degradation products.     

Analysis and Review of Chemical Reactions and Transport Processes in Pulsed Electrical Discharge Plasma Formed Directly in Liquid Water

Electrical discharges formed directly in liquid water include three general cases where (a) streamer-like plasma channels form in, but do not span, the electrode gap, (b) spark discharges produce transient plasma channels that span the electrode gap, and (c) arc discharges form plasma channels with relatively longer life times. Other factors including the input energy (from <1?J/pulse to >1?kJ/pulse) as well as solution properties and the rates of energy delivery affect the nature of the discharge channels. An understanding of the formation of chemical species, including the highly reactive hydroxyl radical and more stable molecular species such as hydrogen and hydrogen peroxide, in such plasma requires determination of temporal and spatial variations of temperature, pressure, plasma volume, and electrical characteristics including current, voltage (electric field), and plasma conductivity. In spark and arc discharges analysis of the physical processes has focused on hydrodynamic and thermal characterization, while only a limited amount of work has connected these physical processes to chemical reactions. On the other hand, the most successful model of the chemical reactions in streamer-like discharges relies on simple assumptions concerning the temperature and pressure in the plasma channels, while analysis of the physical processes is more limited. This paper reviews the literature on the mathematical modeling of electrical discharges in liquid water spanning the range from streamer-like to spark and arc discharges, and compares the properties and processes in these electrical discharges to those in electron beam radiolysis and ultrasound.     

Selective Synthesis of 2D Mesoporous CuO Agglomerates by Pulsed Spark Discharge in Water

Metal oxide nanomaterials, including copper oxide, have attracted great attention due to their unique physical and chemical properties that are dependent on particle size and morphology. In this study, we propose an alternative technique for the synthesis of 2D mesoporous CuO agglomerates that is both efficient and ecological. This technique is based on the use of pulsed spark discharges between copper electrodes immersed in deionized water. Detailed TEM analyses show that the synthesized CuO nanostructures are composed of elementary nanocrystals with sizes in the order of a few nanometers. Assessments of the effects of applied voltage (5 and 20 kV) and discharge pulse width (100 and 500 ns) demonstrate that the latter parameter influences the size and density of nanocrystals in a nanostructure. Moreover, voltage and pulse width may both be used to finely control the direct optical band gap energy of CuO nanostructures between 3.0 and 3.4 eV. The efficient and ecological technique developed in this study produces 2D mesoporous CuO agglomerates that can be readily used in other processes.

     

Degradation of 4-Chlorophenol using a Gas–Liquid Gliding Arc Discharge Plasma Reactor

The gas–liquid gliding arc discharge plasma is used directly to study degradation and dechlorination of 4-Chlorophenol (4-CP) in solution. The typical AC waveforms of discharge voltage and current revealed that the discharge behavior was not definitely periodic. The chemical oxygen demand (COD) abatement of 4-CP solution with stainless steel electrode is higher than that with aluminum or brass electrode; When air was used as carrier gas the COD abated from 1,679.2 to 190 mg/L (i.e., 88.68% abatement) after 76 min plasma treatment; Increasing gas–liquid mixing rate could also increase the degradation of 4-CP; adding appropriate amounts of Fe²⁺ or iron chips to the solution were found to be favorable for 4-CP degradation. The main intermediates of 4-CP degradation are p-benzoquinone, hydroquinone, 4-chlorocatechol, p-chloronitrobenzene, and ring cleavage products (acetic acid, glycol, propanone, and others). Furthermore, possible pathways of 4-CP degradation in solution are proposed.     

Degradation of Acid Orange 7 by Gliding Arc Discharge Plasma in Combination with Advanced Fenton Catalysis

A new plasma–catalysis process of gliding arc discharge (GAD) plasma with zero–valent iron (ZVI) was examined. Because GAD plasma creates an acidic environment, solid iron releases ferrous ions which act as a catalyst for the decomposition of the hydrogen peroxide. A comparative study of the catalytic effects between Fe²⁺ and Fe⁰ in GAD plasma was investigated. The decolorization reactions of Acid Orange 7 (AO7) followed pseudo–first–order kinetics. And the rate constants for the process of GAD with ZVI was increased by 30% and by 19%, respectively, compared with the process of GAD alone and the process of GAD with ferrous. The investigations of solution pH and hydrogen peroxide both demonstrated that the GAD plasma induced conditions are much suitable for advanced Fenton reactions. The corrosion of ZVI in GAD plasma can give continuous ferrous ions to sustain Fenton reaction. Also, ZVI was demonstrated to have favorable reusable feature.     

A Comparison of PE Surfaces Modified by Plasma Generated Neutral Nitrogen Species and Nitrogen Ions

The surface modification of polyethylene (PE) by neutral nitrogen species (ground and excited state N₂ as well as atomic N; modified nitrogen plasma treatment) has been compared to the effect of nitrogen ion bombardment using X-ray Photoelectron Spectroscopy (XPS) and contact angle measurements. XPS results indicate that a greater nitrogen concentration was grafted during the modified nitrogen plasma treatment of PE, an effect that was attributed to surface sputtering during ion beam modification. The distribution of nitrogen-containing functionalities was strongly dependent upon the treatment strategy; the modified nitrogen plasma treatment lead predominantly to imine groups being formed at the PE surface, while amine groups were the dominant species produced during ion beam modification. The presence of electron irradiation during the modified nitrogen plasma treatment of PE did not modify the rate of nitrogen incorporation or change the nature of N-containing functional groups produced but did lead to a systematic decrease in contact angle.     

空心阴极N2等离子体放电光源实现普通PS版感光

本文利用直流空心阴极放电方式产生了一种新型氮气等离子体蓝紫光源,实现了针对传统的预涂感光版(PS版)的感光,当N₂气压70 Pa、放电电压580 V、电流1.8 A时,产生的蓝紫光功率密度为0.46 mW/cm².本文进一步从曝光前后颜色密度值变化、感光材料红外分析方面,对PS版的曝光效果做了详细的测量.     

Concentrations of Active Species in the Flowing Afterglow of a Nitrogen Microwave Plasma

Measurements of nitrogen atom density, by means of NO chemical titration, along with an evaluation of the densities of some excited species N ₂ (B, v=11), N ₂ (B, v=2), N ₂ (C, v=0), and N ₂ ⁺ (B,v=0), by means of a spectroscopic study of some bands of dinitrogen, are achieved along the flowing afterglow of a dinitrogen microwave plasma (2450 MHz) for several pressures. The concentrations obtained are in the following range: [N]10 ⁺¹⁵ , [N ₂ (B, 2)]10 ⁺⁹ –10 ⁺¹⁰ , [N ₂ (B, 11)]10 ⁺⁸ –10 ⁺⁹ , [N ₂ (C, 0)]10 ⁺⁶ –10 ⁺⁷ , [N ₂ ⁺ (B,0)]10 ⁺⁶ -10 ⁺⁸ (cm^-3). From a kinetic study of the formation and decay of excited and charged species, an estimation of N ₂ (A, v), N ₂ (X, v, and N ₂ ⁺ (X) densities can be derived: [N ₂ (A, v)]10 ⁺¹² , [N ₂ (X, v6)]10 ⁺¹⁵ –10 ⁺¹⁶ , [N ₂ (X, v12)]10 ⁺¹⁴ –10 ⁺¹⁵ , [N ₂ ⁺ (X)]10 ⁺¹⁰ (cm ^-3 ).