Study on Glow Discharge in One-Dimensional Transverse Non-uniform Electric Field and Surface Processing of Aramid Fabric

Using a staggered contact electrode structure, the conditions for and mechanism of uniform discharge in one-dimensional transverse non-uniform electric field and with aramid fiber (AF) as a dielectric barrier material were explored for the first time in this study. An atmospheric pressure glow discharge (APGD) plasma was generated, and the large-area and continuous processing of AF was achieved. Through the electric field simulation as well as scanning electron microscope and X-ray photoelectron spectroscopy tests, it was found that the modification method of pressing the electrode closely to the AF could form the extremely strong electric field region of magnitude 1.444 × 10⁷ V/m under the premise of uniform discharge. The highly active plasma generated could not only effectively increase the surface roughness of the treated material, but also introduce nitrogen functional groups which can’t be introduced through traditional air plasma. As found through the contact angle measurement, the contact angle was greatly decreased (by 52.3%) after being treated with 12.05 W/cm³ of plasma for 10 s, indicating that APGD plasma can achieve a good modification effect and high modification efficiency at low discharge power density.     

Nickel Nanoparticles Formation from Solution Plasma Using Edge-Shielded Electrode

Because of the easy massproduction, synthesis of metallic nanoparticles from a solution plasma is an attractive method. However, a solution plasma produces a highly inhomogeneous electric field via transition to full-plasma, and the products are partially oxidized and agglomerated, with a wide size-distribution. Here, we show a simple method of suppressing oxidation of products. An electrode tip was shield by a glass tube and a voltage of up to 180 V was applied with the electrolyte of 0.1 M NaOH solution. Significantly, the edge-shield was quite effective for maintaining partially glow discharge. The results were (1) surface temperature of the electrode less than 100°C, (2) main phase of metallic nickel evaluated by XRD, and (3) nanoparticles of an average size of 220 nm. These results showed the potential for an application to the production of nanoparticles.     

甲醇溶液辉光放电等离子体电解

甲醇溶液辉光放电等离子体电解过程出现明显的非法拉第定律现象, 主要产物是氢气和甲醛, 还有少量一氧化碳、甲烷、乙烷、丙烷、1,3,5-三噁烷和水等, 产物和产量受放电极性和辅助电解质及放电电压等因素的影响. 在甲醇溶液电导率为11.40 mS·cm-1, 放电电压700 V 条件下, 阳极气体产量为55.90 mol/(mol electrons), 阴极气体产量为707.90 mol/(mol electrons), 阴极气体产量是阳极气体产量的12.66 倍, 气相产物中氢气含量在86%(molar fraction)以上. 在等离子体层中甲醇分解过程和其它类型的等离子体分解过程类似, 蒸汽鞘层中的加速电子是引发辉光放电过程非法拉第定律现象的决定因素. 阴极辉光放电过程中等离子体-溶液界面上的主要活性物种是中性粒子和电子,阳极辉光放电过程中等离子体鄄溶液界面上的主要活性物种是中性粒子和正离子. 辅助电解质对产物的影响主要是通过影响界面上发生的后续反应过程来表现.     

Microwave-Driven In-liquid Plasma in Chemical and Environmental Applications. III. Examination of Optimum Microwave Pulse Conditions for Prolongation of Electrode Lifetime,and Application to Dye-Contaminated Wastewater

Generating in-liquid plasma using continuous microwave radiation has proven problematic as the surface of the electrode undergoes significant deterioration because of the generated plasma. This article describes a method by which this problem can be resolved by the utilization of pulsed microwave radiation from a magnetron microwave generator and presents results in the search for optimal pulsed microwave irradiation conditions; these would avoid damage to the electrode and would afford reduced power consumption. Results show that continuous generation of in-liquid plasma that avoids electrode (antenna) damage requires strict and very limited pulsed oscillation conditions. Evaluation of this device was investigated by the discoloration of a rhodamine-B (RhB) dye-contaminated wastewater, for which it was shown that higher treatment efficiency can be obtained compared to more traditional methods such as the UV photolysis (UV), the UV-assisted photocatalytic TiO₂ method (UV/TiO₂), and the NaClO methodology (NaClO). The energy consumed during the 3 min needed to discolor 50 mL of a 0.10 mM aqueous RhB dye solution was 6.3?×?10^?3 kWh per mg of RhB; complete mineralization of the dye solution by the in-liquid plasma occurred within 15 min (loss of TOC).

     

Formation of charge states on the surface of a laminated polyimide-fluoropolymer film by glow- discharge treatment

The alteration of properties of both sides of the laminated polyimide-fluoropolymer film PMF-351 by treatment in a low-frequency glow discharge, depending on their position with respect to the electrode, was investigated. By the dynamic capacitance method, it was found that both positive and negative charges can be induced on both sides of the film modified in the cathode fall, depending on the arrangement of its polyimide and fluoropolymer sides with respect to the electrode. It was shown that the formation of a negative charge in PMF-351 is in all cases due to trapping of plasma electrons injected into the polymer surface layers.     

Contact Glow Discharge Electrolysis: A Novel Tool for Manifold Applications

Contact glow discharge electrolysis (CGDE)/plasma electrolysis (PE) which is associated with the formation of a light emitting plasma around an electrode in a high conductivity electrolyte solution at moderate voltages up to ~1 kV, has in recent years attracted considerable interest as a tool for generating a large quantity of heat and a high yield of solvent-split radicals. These potentialities of CGDE/PE have, in fact, been exploited by a large number of investigators for applications ranging over areas as varied as synthetic chemistry, waste water treatment, degradation of polymers, electrosurgical tools, surface engineering, nanoparticle fabrication, machining and micro-machining, hydrogen production with very encouraging results. The article reviews comprehensively these results.     

Plasma Induced Degradation of Azobenzene in Water

The degradation of azobenzene (AO) by a gaseous plasma is reported. The plasma was generated in a localized zone between an electrolytic solution and a tip of an anode in contact with the surface of solution by means of contact glow discharge electrolysis. There is an optimum pH for the degradation of AO. Iron (II) had a remarkable catalytic action on it. Furthermore, the degradation followed the first‐order kinetic law. Some of the intermediate products of the degradation process were detected by HPLC.     

Comparison of the Plasma Temperature and Electron Number Density of the Pulsed Electrolyte Cathode Atmospheric Pressure Discharge and the Direct Current Solution Cathode Glow Discharge

A novel-pulsed electrolyte cathode atmospheric pressure discharge (pulsed-ECAD) plasma source driven by an alternating current (AC) power supply coupled with a high-voltage diode was generated under normal atmospheric pressure between a metal electrode and a small-sized flowing liquid cathode. The spatial distributions of the excitation, vibrational, and rotational plasma temperatures of the pulsed-ECAD were investigated. The electron excitation temperature of H T_exc(H), vibrational temperature of N₂ T_vib(N₂), and rotational temperature of OH T_rot(OH) were from 4900?±?36 to 6800?±?108 K, from 4600?±?86 to 5800?±?100 K, and from 1050?±?20 to 1140?±?10 K, respectively. The temperature characteristics of the dc solution cathode glow discharge (dc-SCGD) were also studied for the comparison with the pulsed-ECAD. The effects of operating parameters, including the discharge voltage and discharge frequency, on the plasma temperatures were investigated. The electron number densities determined in the discharge system and dc-SCGD were 3.8–18.9?×?10¹⁴?cm^–3 and 2.6?×?10¹⁴ to 17.2?×?10¹⁴?cm^–3, respectively.     

Examination of the electrochemical reactivity of screen printed carbon electrode treated by radio-frequency argon plasma

The surface of screen printed carbon electrode (SPCE) with partially blocked surface was treated by argon plasma in order to improve their electrochemical performances. The argon plasma was generated by a radio-frequency electrical discharge at low pressure. Study of the electrode surface by scanning electronic microscopy (SEM) has revealed a significant change of the morphology of the SPCE surface after plasma pre-treatment. The electrochemical reactivity of the SPCEs was characterized using cyclic voltammetry. A drastic enhancement of the SPCEs electrochemical reactivity was highlighted after plasma pre-treatment. The effect of biasing the SPCE surface during the plasma treatment has been investigated and showed that depending on the nature of plasma treatment, the same electrode could show a radial or planar diffusion.     

Glow characterization in direct current plasma polymerization of trimethylsilane

Plasma polymerization of trimethylsilane (TMS) was carried out in a direct current (dc) glow discharge and was investigated by optical photography and plasma diagnostic techniques including optical emission spectroscopy and residual gas analysis. The nature of the glow formed in TMS discharge, which deposited plasma polymers, was significantly different from that of a simple gas such as Ar. In an Ar discharge, the dominant glow was the well known negative glow, which developed at a distinctive distance from the cathode, whereas the cathode surface remained in the dark space. In strong contrast to this situation, in TMS dc discharge the dominant or primary glow was the cathode glow, which appeared at the cathode surface. At a similar location where the Ar negative glow appeared, a very feeble glow as a secondary glow was also observed in TMS glow discharge. The deposition results and plasma diagnosis data evidently indicated that in TMS glow discharge, the cathode glow resulted from the low‐energy electron‐impact dissociation of TMS molecules that creates polymerizable species, but the negative glow was related to nonpolymerizable species such as hydrogen atoms and molecules. In this article, the cathode glow formed in glow discharges of organic compounds was designated as the dissociation glow according to its underlying plasma reactions. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1042–1052, 2004     

Surface Modification of Ultra-high Molecular Weight Polyethylene Membranes Using Underwater Plasma Polymerization

Ultra-high molecular weight polyethylene membranes were modified and subsequently polymer coated using the underwater plasma produced by glow discharge electrolysis. This plasma pretreatment generated various O-functional groups among them OH groups have dominated. This modified inner (pore) surface of membranes showed complete wetting and strong adhesion to a hydrogel copolymerized by glow discharge electrolysis also. The deposited hydrogel consists of plasma polymerized acrylic acid crosslinked by copolymerization with the bifunctional N,N′-methylenebis(acrylamide). Tuning the hydrogel hydrophilicity and bio-compatibility poly(ethylene glycol) was chemically inserted into the copolymer. Such saturated polymer could only be inserted on a non-classic way by (partial) fragmentation and recombination thus demonstrating the exotic properties of the underwater plasma. The modification of membrane was achieved by squeezing the reactive plasma solution into the pores by plasma-induced shock waves and supported by intense stirring. The deposited copolymer hydrogel has filled all pores also in the inner of membrane as shown by scanning electron microscopy of cross-sections. The copolymer shows the characteristic units of acrylic acid and ethylene glycol as demonstrated by infrared spectroscopy. A minimum loss in carboxylic groups of acrylic acid during the plasma polymerization process was confirmed by X-ray photoelectron spectroscopy. Additional cell adhesion tests on copolymer coated polyethylene using IEC-6 cells demonstrated the bio-compatibility of the plasma-deposited hydrogel.     

Atmospheric Pressure Glow Discharges Generated in Contact with Flowing Liquid Cathode: Production of Active Species and Application in Wastewater Purification Processes

Miniaturized atmospheric pressure glow discharges (APGDs) were generated in contact with small sized flowing liquid cathode systems. As anodes a solid pin electrode or a miniature flow Ar microjet were applied. Both discharge systems were operated in the open to air atmosphere. Hydrogen peroxide (H₂O₂) as well as ammonium (NH₄ ⁺), nitrate (NO₃ ^?), and nitrite (NO₂ ^?) ions were quantified in solutions treated by studied discharge systems. Additionally, an increase in the acidification of these solutions was noted in each case. Emission spectra of the near cathode zone of both systems were measured in order to elucidate mechanisms that lead to the formation of active species in gas and liquid phases of the discharge. Additionally, the concentration of active species in the liquid phase (H₂O₂, NH₄ ⁺, NO₃ ^? and NO₂ ^?) was monitored as a function of the solution uptake rate and the flow rate of Ar. The suitability of investigated discharge systems in the water treatment was tested on artificial wastewaters containing an organic dye (methyl red), hardly removable by classical methods non-ionic surfactants (light Triton x-45 and heavy Triton x-405) and very toxic Cr(VI) ions. Preliminary results presented here indicate that both investigated flow-through APGD systems may successfully be applied for the efficient and fast on-line continuous flow chemical degradation of toxic and hazardous organic and inorganic species in wastewater solutions.     

Studies on Optimal Gas Supply For a Maskless Etching System with Micro- Discharge Plasma Operated at Atmospheric Pressure

An optimal gas supply method for the micro discharge plasma generated along a quartz glass electrode, which was useful for the maskless fabrication of electrode grooves for surface electrodes on solar cells, was examined. We here constructed an electrode system with gas inlet and outlet holes. The gas supply directly to the plasma region contributed to reduce byproducts on the surface being etched, and then it was confirmed that the uniform etching was achieved in the case where the micro-discharge plasma locally produced at the etching area.     

Creation of Polymerizable Species in Plasma Polymerization

Plasma polymerization of trimethylsilane (TMS) was carried out and investigated in a direct current (dc) glow discharge. The formation of TMS plasma glow was carefully examined with optical photography as compared with an Ar dc glow discharge. It was found that there exists a significant difference in the nature of glow and how the glow is created in TMS glow discharge, which polymerizes or causes deposition, and that of monatomic gas such as Ar, which does not polymerize or deposit. In dc Ar discharge, the negative glow, which is the most luminous zone in the discharge, develops in a distinctive distance away from the cathode surface, and the cathode remains in the dark space. In a strong contrast to this situation, in TMS dc discharge, the primary glow that is termed as cathode-glow in this paper appears at cathode surface, while a much weaker negative glow as a secondary glow was observed at the similar location to where the Ar negative glow appears. The deposition results of plasma polymers and gas phase composition data of TMS in a closed reactor acquired by ellipsometry and residual gas analyzer (RGA) measurements clearly indicated that the cathode-glow in TMS glow discharge is mainly associated with chemically reactive species that would polymerize or form deposition, but the negative glow is related to species from simple gases that would not polymerize or deposit. Based on the glow location with respect to the cathode, it was deduced that the cathode-glow is due to photon emitting species created by molecular dissociation of the monomer that is caused by low energy electrons emanating from the cathode surface. The negative glow is due to the ionization and the formation of excited neutrals of fragmented atoms caused by high-energy electrons. Polymerizable species that would cause deposition of material (plasma polymers) are created mainly by the fragmentation of monomer molecules by low energy electrons, but not by electron-impact ionization of the monomer.     

Keggin型磷钼杂多蓝的制备新方法——射频氢等离子体固相还原法

将射频等离子体技术应用于杂多蓝的制备中, 成功地制备出四电子还原的磷钼杂多蓝, 并对所制备的杂多蓝进行了结构表征及性质研究, 探讨了磷钼杂多酸在射频氢等离子体中的还原行为.     

活性炭和H2O2存在下辉光放电等离子体降解邻苯二胺

活性炭和H2O2存在下辉光放电等离子体降解邻苯二胺;辉光放电等离子体;降解;邻苯二胺;废水处理     

Activation of natural aluminosilicates in the argon glow-discharge positive column

The plasma surface activation of natural aluminosilicates in the positive column of a glow discharge was proposed in order to improve their sorption properties toward serum albumin in alkaline media. The mechanism of surface modification of aluminosilicates in argon was considered using kaolin as an example. The concomitant effect of a specific change in the electric conductivity of samples with different types of layers after plasma treatment was revealed.     

Physicochemical and Engineering Problems in Studies on Plasma–Solution Systems

The example of an atmospheric-pressure glow discharge with an electrolytic cathode was used to show a significant role of the processes of transfer of solution components to the plasma zone, which were induced by ion bombardment of the surface of the solution. These processes not only determine the chemical composition of the plasma zone but also initiate redox reactions in the gas phase. In turn, the gas discharge alters the properties of the solution, in particular, its acidity, interfering with liquid-phase chemical reactions.     

Non-thermal Plasma as a Priming Tool to Improve the Yield of Pea in Outdoor Conditions

Seed priming is a pre-treatment of seeds leading to the improvement of their germination, the plant growth, and the product yield. In this study we investigated the possibility of the use of non-thermal plasma operating in atmospheric pressure air for seed priming with the objective to improve the yield of pea seeds. Two priming ways were used: an indirect way by using plasma activated water (PAW) generated by the transient spark discharge with water electrospray or the glow discharge batch treatment and a direct exposure of seeds to the pulsed corona discharge. After treatment, the seeds were planted in the outdoor field for about 14 weeks until harvest. The direct plasma treatment resulted in two key results: the strong effectiveness of the pulsed corona plasma improving the yield, and the long-term effect of the plasma seed treatment. The results of the indirect treatment showed that the pea plants from the seeds primed using PAW gained some improved growth parameters, especially the number of seeds per pod and the total number of seeds per plant. The scanning electron microscopy analysis showed that PAW and direct treatment induced some morphology changes at the surface of the pea seeds. This study documents a long-term effect of non-thermal plasma seed priming and contributes to the plasma agriculture applications by suggesting the implementation of non-thermal plasma direct or indirect treatments into the field.

     

Characteristics of Light Emission and Radicals Formed by Contact Glow Discharge Electrolysis of an Aqueous Solution

In this work, light emissions and radicals formed by plasma of contact glow discharge electrolysis were investigated. The plasma was generated by glow discharges at the tip of a Pt anode in contact with a sulfuric acid solution. Emissions of H atoms and OH radicals were observed when the applied voltage was above 430 V. When the applied voltage increased to 450 V, emissions of O atoms were additionally detected. The emission intensities of these radicals and atoms increased with the increasing applied voltage. When the applied voltage exceeded 460 V, thermal radiation from the Pt anode was apparent in the visible and near infrared region. Electron temperature of the plasma increased with the applied voltage from 1.0 × 10⁴ to 1.5 × 10⁴ K by comparison of the intensities of H_α and H_β lines. The mean electron density was estimated to be 7.4 × 10¹⁷ cm⁻³ by the method of Stark broadening.