Discoloration of Congo Red by Rod-Plate Dielectric Barrier Discharge Processes at Atmospheric Pressure

A dielectric barrier discharge (DBD) reactor with a rod-plate electrode configuration was used for the oxidative decomposition of Congo red dye in an aqueous solution.Plasma was generated in the gas space above the water interface under atmospheric pressure.Discharge characteristics were analyzed by voltage-current waveforms.Effects of applied voltage,initial conductivity,and initial concentration were also analyzed.Congo red discoloration increased with increased applied voltage and decreased conductivity.The initial conductivity significantly influenced the Congo red discoloration.Under the same conditions,the highest discoloration rate was obtained at 25 mg/L.The presence of ferrous ions in the solutions had a substantial positive effect on Fenton dye degradation and flocculation.At an applied voltage of 20 kV,about 100％of dye was degraded after 4 min of Fe2+/DBD treatment.Results showed that adding a certain dosage of hydrogen peroxide to the wastewater could enhance the discoloration rate.Possible pathways of Congo red discoloration by DBD plasma were proposed based on GC/MS,FTIR,and UV-vis spectroscopy analyses.     

Destruction of Gaseous Styrene with a Low-Temperature Plasma Induced by a Tubular Multilayer Dielectric Barrier Discharge

The destruction of gaseous styrene was studied using a low-temperature plasma induced by tubular multilayer dielectric barrier discharge(DBD).The results indicate that the applied voltage,gas flow rate,inlet styrene concentration and reactor configuration play important roles in styrene removal efficiency(η_(styrene)) and energy yield(EY).Values of η_(styrene) and EY reached 96%and 15567 mg/kWh when the applied voltage,gas flow rate,inlet styrene concentration and layers of quartz tubes were set at 10.8 kV,5.0 m/s,229 mg/m~3 and 5 layers,respectively.A qualitative analysis of the byproducts and a detailed discussion of the reaction mechanism are also presented.The results could facilitate industrial applications of the new DBD reactor for waste gas treatment.     

Application of DBD and DBCD in SO2 Removal

The dielectric barrier corona discharge(DBCD) in a wire-cylinder configuration and the dielectric barrier discharge(DBD) in a coaxial cylinder configuration are studied. The discharge current in DBD has a higher pulse amplitude than in DBCD. The dissipated power and the gas-gap voltage are calculated by analyzing the measured Lissajous figure. With the increasing applied voltage, the energy utilization factor for SO2 removal increases in DBCD but decreases in DBD because of the difference in their electric field distribution. Experiments of SO2 removal show that in the absence of NH3 the energy utilization factor can reach 31 g/kWh in DBCD and 39 g/kWh in DBD.     

Research on quinoline degradation in drinking water by a large volume strong ionization dielectric barrier discharge reaction system

Quinoline is widely used in the production of drugs as a highly effective insecticide, and its derivatives can also be used to produce dyes. It has a teratogenic carcinogen to wildlife and humans once entering into the aquatic environment. In this study, the degradation mechanism of quinoline in drinking water by a strong ionization dielectric barrier discharge(DBD) lowtemperature plasma with large volume was explored. High concentration of hydroxyl radical(·OH)(0.74 mmol l-1) and ozone(O3)(58.2 mg l-1) produced by strongly ionized discharge DBD system were quantitatively analyzed based on the results of electron spin resonance and O3 measurements. The influencing reaction conditions of input voltages, initial p H value, ·OH inhibitors, initial concentration and inorganic ions on the removal efficiency of quinoline were systematically studied. The obtained results showed that the removal efficiency and TOC removal of quinoline achieved 94.8% and 32.2%, degradation kinetic constant was 0.050 min-1 at 3.8 k V and in a neutral p H(7.2). The proposed pathways of quinoline were suggested based on identified intermediates as hydroxy pyridine, fumaric acid, oxalic acid, and other small molecular acids by high-performance liquid chromatography/tandem mass spectrometry analysis. Moreover, the toxicity analysis on the intermediates demonstrated that its acute toxicity, bioaccumulation factor and mutagenicity were reduced. The overall findings provided theoretical and experimental basis for the application of a high capacity strong ionization DBD water treatment system in the removal of quinoline from drinking water.     

Improving Hydrophobicity of Glass Surface Using Dielectric Barrier Discharge Treatment in Atmospheric Air

Non-thermal plasmas under atmospheric pressure are of great interest in industrial applications, especially in material surface treatment. In this paper, the treatment of a glass surface for improving hydrophobicity using the non-thermal plasma generated by dielectric barrier discharge （DBD） at atmospheric pressure in ambient air is conducted, and the surface properties of the glass before and after the DBD treatment are studied by using contact angle measurement, surface resistance measurement and wet flashover voltage tests. The effects of the applied voltage and time duration of DBD on the surface modification are studied, and the optimal conditions for the treatment are obtained. It is found that a layer of hydrophobic coating is formed on the glass surface after spraying a thin layer of silicone oil and undergoing the DBD treatment, and the improvement of hydrophobicity depends on DBD voltage and treating time. It seems that there exists an optimum treating time for a certain applied voltage of DBD during the surface treatment, The test results of thermal aging and chemical aging show that the hydrophobic layer has quite stable characteristics. The interaction mechanism between the DBD plasma and the glass surface is discussed. It is concluded that CHa and large molecule radicals can react with the radicals in the glass surface to replace OH, and the hydrophobicity of the glass surface is improved accordingly.     

OH and O radicals production in atmospheric pressure air/Ar/H2O gliding arc discharge plasma jet

Atmospheric pressure air/Ar/H_2O gliding arc discharge plasma is produced by a pulsed dc power supply. An optical emission spectroscopic(OES) diagnostic technique is used for the characterization of plasmas and for identifications of OH and O radicals along with other species in the plasmas. The OES diagnostic technique reveals the excitation Tx?≈?5550–9000 K, rotational Tr?≈?1350–2700 K and gas Tg?≈?850–1600 K temperatures, and electron density n?(1.1-1.9) ′101 4 cm~(-3) e under different experimental conditions. The production and destruction of OH and O radicals are investigated as functions of applied voltage and air flow rate. Relative intensities of OH and O radicals indicate that their production rates are increased with increasing Ar content in the gas mixture and applied voltage. nereveals that the higher densities of OH and O radicals are produced in the discharge due to more effective electron impact dissociation of H_2O and O_2 molecules caused by higher kinetic energies as gained by electrons from the enhanced electric field as well as by enhanced n e.The productions of OH and O are decreasing with increasing air flow rate due to removal of Joule heat from the discharge region but enhanced air flow rate significantly modifies discharge maintenance properties. Besides, Tgsignificantly reduces with the enhanced air flow rate. This investigation reveals that Ar plays a significant role in the production of OH and O radicals.     

Analysis of Energetic Species Caused by Contact Glow Discharge Electrolysis in Aqueous Solution

Contact glow discharge electrolysis is a non-Faradaic electrochemical process with an abnormal relationship between the current and voltage. Hydroxyl radicals, hydrogen radicals and hydrogen peroxide can be produced under the glow discharge, which are often used to degrade organic contaminants in aqueous solution. In this study, with 4-nitrophenol taken as an example of contaminants and tert-butanol as a scavenger of hydroxyl radicals, the role of energetic species in degrading organic compounds was examined in detail. Moreover, the effects of the applied voltage, solution conductivity and pH on the formation of three energetic species were also observed. The formation rate constants of the three energetic species were calculated based on the experimental data.     

Dielectric Barrier Discharge Plasma-Induced Photocatalysis and Ozonation for the Treatment of Wastewater

The physicochemical processes of dielectric barrier discharge （DBD） such as insitu formation of chemically active species and emission of ultraviolet （UV）/visible light were utilized for the treatment of a simulated wastewater formed with Acid Red 4 as the model organic contaminant. The chemically active species （mostly ozone） produced in the DBD reactor were well distributed in the wastewater using a porous gas diffuser, thereby increasing the gas-liquid contact area. For the purpose of making the best use of the light emission, a titanium oxide-based photocatalyst was incorporated in the wastewater treating system. The experimental parameters chosen were the voltage applied to the DBD reactor, the initial pH of the wastewater, and the concentration of hydrogen peroxide added to the wastewater. The results have clearly shown that the present system capable of degrading organic contaminants in two ways （photocatalysis and ozonation） may be a promising wastewater treatment technology.     

Destruction of H2S Gas with a Combined Plasma Photolysis（CPP） Reactor

A combined plasma photolysis(CPP) reactor that utilized the dielectric barrier discharge(DBD) plasma together with DBD-driven KrI excimer ultraviolet emission was applied to the decomposition of H 2 S gas.The effects of applied voltage,input current,gas flow velocity,original concentration as well as the ratio of Kr/I 2 mixture on H 2 S removal efficiency were investigated.Gas streams containing H 2 S were separately treated with single DBD and CPP reactor under the same conditions.In comparison to DBD,CPP could greatly enhance the H 2 S removal efficiency at the same applied voltage,inlet gas concentration and gas flow velocity.In addition,the reaction mechanism was also discussed in this paper.     

Regulation characteristics of oxide generation and formaldehyde removal by using volume DBD reactor

Discharge plasmas in air can be accompanied by ultraviolet(UV) radiation and electron impact,which can produce large numbers of reactive species such as hydroxyl radical(OH·),oxygen radical(O·),ozone(O3),and nitrogen oxides(NOx),etc.The composition and dosage of reactive species usually play an important role in the case of volatile organic compounds(VOCs) treatment with the discharge plasmas.In this paper,we propose a volume discharge setup used to purify formaldehyde in air,which is configured by a plate-to-plate dielectric barrier discharge(DBD) channel and excited by an AC high voltage source.The results show that the relative spectral-intensity from DBD cell without formaldehyde is stronger than the case with formaldehyde.The energy efficiency ratios(EERs) of both oxides yield and formaldehyde removal can be regulated by the gas flow velocity in DBD channel,and the most desirable processing effect is the gas flow velocity within the range from2.50 to 3.33 m s-1.Moreover,the EERs of both the generated dosages of oxides(O3 and NO2) and the amount of removed formaldehyde can also be regulated by both of the applied voltage and power density loaded on the DBD cell.Additionally,the EERs of both oxides generation and formaldehyde removal present as a function of normal distribution with increasing the applied power density,and the peak of the function is appeared in the range from 273.5 to 400.0 W l-1.This work clearly demonstrates the regulation characteristic of both the formaldehyde removal and oxides yield by using volume DBD,and it is helpful in the applications of VOCs removal by using discharge plasma.     

Enhanced removal of benzene in nonthermal plasma with ozonation,flow recycling,and flow recirculation

A double stage AC/DC sequential high voltage reactor has been developed to study the decomposition of benzene in the air stream at atmospheric pressure. The removal efficiency was measured as a function of ozonation, flow recycling, and flow recirculation. Ozonation in the inlet, and recycling of the exhaust stream increased the removal of benzene, also with increasing of specific input energy (J l⁻¹) the effect of inlet flow ozonation on benzene decomposition was enhanced. The highest removal efficiency was obtained up to >99% in recirculation six times, while CO₂ selectivity reached 99.9% and energy efficiency was 0.59 g kWh⁻¹. O₃ production/ decomposition > production of OH radicals > electronic and ionic collisions were indicated as the main mechanisms influencing benzene abatement in this research.     

Enhancing toluene removal in a plasma photocatalytic system through a black TiO_2 photocatalyst

An efficient toluene removal in air using a plasma photocatalytic system(PPS) not only needs favorable surface reactions over photocatalysts under the action of plasma,but also requires the photocatalysts to efficiently absorb light emitted from the discharge for driving the photocatalytic reactions. We report here that the PPS constructed by integrating a black titania(B-TiO_2)photocatalyst with a dielectric barrier discharge(DBD) can effectively remove toluene with above 70% CO_2 selectivity and remarkably reduced the concentration of secondary pollutants of ozone and nitrogen oxides at a specific energy input of 1500 J·l~(-1),while exhibiting good stability. Photocatalyst characterizations suggest that the B-TiO_2 provides a high concentration of oxygen vacancies for the surface oxidation of toluene in DBD,and efficiently absorbs ultraviolet–visible light emitted from the discharge to induce plasma photocatalytic oxidation of toluene. The presence of B-TiO_2 in the plasma region also results in a high discharge efficiency,facilitating the generation of large numbers of reactive species and thus the oxidation of toluene towards CO_2. The greatly enhanced performance of the PPS integrated with B-TiO_2 in toluene removal offers a promising approach to efficiently remove refractory volatile organic compounds from air at low temperatures.     

Application of dielectric barrier discharge (DBD) plasma packed with glass and ceramic pellets for SO2 removal at ambient temperature: optimization and modeling using response surface methodology

Air pollution is a major health problem in developing countries and has adverse effects on human health and the environment. Non-thermal plasma is an effective air pollution treatment technology. In this research, the performance of a dielectric barrier discharge (DBD) plasma reactor packed with glass and ceramic pellets was evaluated in the removal of SO₂ as a major air pollutant from air in ambient temperature. The response surface methodology was used to evaluate the effect of three key parameters (concentration of gas, gas flow rate, and voltage) as well as their simultaneous effects and interactions on the SO₂ removal process. Reduced cubic models were derived to predict the SO₂ removal efficiency (RE) and energy yield (EY). Analysis of variance results showed that the packed-bed reactors (PBRs) studied were more energy efficient and had a high SO₂ RE which was at least four times more than that of the non-packed reactor. Moreover, the results showed that the performance of ceramic pellets was better than that of glass pellets in PBRs. This may be due to the porous surface of ceramic pellets which allows the formation of microdischarges in the fine cavities of a porous surface when placed in a plasma discharge zone. The maximum SO₂ RE and EY were obtained at 94% and 0.81 g kWh⁻¹, respectively under the optimal conditions of a concentration of gas of 750 ppm, a gas flow rate of 2 l min⁻¹, and a voltage of 18 kV, which were achieved by the DBD plasma packed with ceramic pellets. Finally, the results of the model's predictions and the experiments showed good agreement.     

Improved sensitivity on detection of Cu and Cr in liquids using glow discharge technology assisted with LIBS

Laser-induced breakdown spectroscopy-assisted glow discharge (LIBS-GD) for analysis of elements in liquid was proposed, and it was applied to detect heavy metals in highly sensitive mixed solutions of Cu and Cr. During the experiments of GD and LIBS-GD, the experimental parameters have been optimized and the optimal voltage is 450 V, laser energy is 60 mJ, and the delay time is 4000 ns. Furthermore, the calibration curves of Cu and Cr under GD and LIBS-GD experiments have been established, and the limits of detection (LODs) of Cu and Cr were obtained with the method of GD and LIBS-GD, respectively. The LOD of Cu decreased from 3.37 (GD) to 0.16 mg l⁻¹ (LIBS-GD), and Cr decreased from 3.15 to 0.34 mg l⁻¹. The results prove that the capability of elemental detection under LIBS-GD has improved compared with the GD method. Therefore, LIBS-GD is expected to be developed into a highly sensitive method for sewage detection.     

DBD coupled with MnOx/γ-Al2O3 catalysts for the degradation of chlorobenzene

This paper investigates the degradation of chlorobenzene by dielectric barrier discharge(DBD)coupled with MnOx/γ-Al2O3 catalysts.MnOx/γ-Al2O3 catalysts were prepared using the impregnation method and were characterized in detail by N2 adsorption/desorption,x-ray diffraction and x-ray photoelectron spectroscopy.Compared with the single DBD reactor,the coupled reactor has a better performance on the removal rate of chlorobenzene,the selectivity of COx,and the inhibition of ozone production,especially at low discharge voltages.The degradation rate of chlorobenzene and selectivity of COx can reach 96.3%and 53.0%,respectively,at the specific energy density of 1350 J l-1.Moreover,the ozone concentration produced by the discharge is significantly reduced because the MnOx/Al2O3 catalysts contribute to the decomposition of ozone to form oxygen atoms for the oxidation of chlorobenzene.In addition,based on analysis of the byproducts,the decomposition mechanism of chlorobenzene in the coupled reactor is also discussed.     

1,2,4-trichlorobenzene decomposition using non-thermal plasma technology

Non-thermal plasma(NTP)is regarded as a potential application for environmental pollution control due to its ability to remove pollutants.As a major precursor of dioxins,the influence of the parameters of 1,2,4-trichlorobenzene(TCB)decomposition using NTP technology was investigated through a series of experiments,including voltage,frequency,water content,initial concentration,flow rate,and oxygen content.The experimental results show that the energy injected into the NTP system has a positive correlation to voltage and frequency.Oxygen has the greatest influence on TCB decomposition.The optimal reaction condition was at 15 kV,1000 Hz,an initial concentration of 20 mg m^?3,a flow rate of 2 l min^?1,H2O at 4%,and O2 at 0%.Under this condition,the TCB removal efficiency could reach 92%.According to the generated product backstepping,the hydroxyl radical(·OH)plays an important role in TCB decomposition due to its strong oxidation,which participates in the dechlorination and oxidation reactions as free radicals,and the possible decomposition pathway of TCB by NTP is inferred from the identified byproducts.It is of great significance to investigate the influence of the parameters of TCB decomposition using NTP technology in order to provide references for industrial application.     

Study on purification technology of polyacrylamide wastewater by non-thermal plasma

In this work, non-thermal plasma has been applied to treat polyacrylamide (PAM) wastewater. We have investigated the influence of the rule of PAM wastewater initial pH, solution concentration and discharge time, discharge voltage on chemical oxygen demand (COD) degradation rate. At the same time, the effect of pH and discharge time on the viscosity removal rate of PAM solution was also studied. Then, the effect of pH on the viscosity removal rate of 1.0 gl ⁻¹ PAM solution was studied separately. Through orthogonal test, the factors affecting the COD degradation rate of PAM wastewater were determined as follows: discharge time>discharge voltage>solution concentration>wastewater initial pH. The COD highest removal rate of PAM wastewater reached 85.74%, when the optimal conditions are as follows: discharge voltage 40 kV, discharge time 5 h, solution concentration 1.0 gl ⁻¹, pH 1.5. This research provides some basic data and new theoretical basis for PAM wastewater purification.     

Decomposition of a gas mixture of four n-alkanes using a DBD reactor

This study investigates the decomposition of a gas mixture of four n-alkanes (n-heptane, n-octane, n-nonane, and n-decane) using a dielectric barrier discharge reactor. We show that the conversion of n-alkanes increased from 7.2% (C₇H₁₆), 9.7% (C₈H₁₈), 8.4% (C₉H₂₀), and 10.5% (C₁₀H₂₂) to 23.8% (C₇H₁₆), 25.0% (C₈H₁₈), 27.9% (C₉H₂₀), and 32.1% (C₁₀H₂₂) when the energy density increased from 84 J l⁻¹ to 324 J l⁻¹. The conversion of n-alkanes when using the gas mixture is close to that found when using a single n-alkane. The influences of reaction temperature and O₂ concentration are also investigated, and the activation energies for the decomposition of each alkane are given.     

Evaluation on a double-chamber gas-liquid phase discharge reactor for benzene degradation

A double-chamber gas-liquid phase DBD reactor (GLDR), consisting of a gas-phase discharge chamber and a gas-liquid discharge chamber in series, was designed to enhance the degradation of benzene and the emission of NOx. The performance of the GLDR on discharge characteristics, reactive species production and benzene degradation was compared to that of the single-chamber gas phase DBD reactor (GPDR). The effects of discharge gap, applied voltage, initial benzene concentration, gas flow rate and solution conductivity on the degradation and energy yield of benzene in the GLDR were investigated. The GLDR presents a higher discharge power, higher benzene degradation and higher energy yield than that of the GPDR. NO₂ emission was remarkably inhibited in the GLDR, possibly due to the dissolution of NO₂ in water. The benzene degradation efficiency increased with the applied voltage, but decreased with the initial concentration, gas flow rate, and gas discharge gap, while the solution conductivity presented less influence on benzene degradation. The benzene degradation efficiency and the energy yield reached 61.11% and 1.45 g kWh^–1 at 4 mm total gas discharge gap, 15 kV applied voltage, 200 ppm benzene concentration, 0.2 L min⁻¹ gas flow rate and 721 μS cm⁻¹ water conductivity. The intermediates and byproducts during benzene degradation were detected by FT-IR, GC-MS and LC-MS primarily, and phenols, CO_x, and other aromatic substitutes, O₃, NO_x, etc, were determined as the main intermediates. According to these detected byproducts, a possible benzene degradation mechanism was proposed.     

Plasma-assisted ammonia synthesis in a packed-bed dielectric barrier discharge reactor: roles of dielectric constant and thermal conductivity of packing materials

In this article, plasma-assisted NH₃ synthesis directly from N₂ and H₂ over packing materials with different dielectric constants (BaTiO₃, TiO₂ and SiO₂) and thermal conductivities (BeO, AlN and Al₂O₃) at room temperature and atmospheric pressure is reported. The higher dielectric constant and thermal conductivity of packing material are found to be the key parameters in enhancing the NH₃ synthesis performance. The NH₃ concentration of 1344 ppm is achieved in the presence of BaTiO₃, which is 106% higher than that of SiO₂, at the specific input energy (SIE) of 5.4 kJ·l⁻¹. The presence of materials with higher dielectric constant, i.e. BaTiO3 and TiO₂ in this work, would contribute to the increase of electron energy and energy injected to plasma, which is conductive to the generation of chemically active species by electron-impact reactions. Therefore, the employment of packing materials with higher dielectric constant has proved to be beneficial for NH₃ synthesis. Compared to that of Al₂O₃, the presence of BeO and AlN yields 31.0% and 16.9% improvement in NH₃ concentration, respectively, at the SIE of 5.4 kJ·l⁻¹. The results of IR imaging show that the addition of BeO decreases the surface temperature of the packed region by 20.5% to 70.3°C and results in an extension of entropy increment compared to that of Al₂O₃, at the SIE of 5.4 kJ·l⁻¹. The results indicate that the presence of materials with higher thermal conductivity is beneficial for NH₃ synthesis, which has been confirmed by the lower surface temperature and higher entropy increment of the packed region. In addition, when SIE is higher than the optimal value, further increasing SIE would lead to the decrease of energy efficiency, which would be related to the exacerbation in reverse reaction of NH₃ formation reactions.