Remediation of 3,4,3',4'-tetrachlorobiphenyl (PCB77) contaminated soil via a fluidized bed dielectric barrier discharge.

In this study, 3,4,3',4'-tetrachlorobiphenyl (PCB77) contaminated soil was remediated by a fluidization bed dielectric barrier discharge (DBD) reactor and a fixed bed DBD reactor. The fluidized bed reactor could attain superior removal efficiency of PCB77 under same experimental parameters. In-situ discharge mode was more conducive to the degradation of PCB77 than ex-situ discharge mode due to short-lived active species existing in in-situ discharge. The influence of experimental parameters in the fluidized bed DBD reactor on the degradation of PCB77 were discussed such as electric features, gas features, soil features and initial PCB77 concentration. PCB77 removal efficiency in air discharge could reach 88.5 % after 8 min under the alkaline condition. Optical emission spectroscopy (OES) and quench tests showed that reactive oxygen species (ROS) and reactive nitrogen species (RNS) were generated in the discharge system and they both played a vital role in the degradation of PCB77. Scanning electron microscopy (SEM) results demonstrated that discharge had little effect on the morphology of soil particles. Energy dispersive spectrometer (EDS), ion chromatography (IC), and total organic carbon (TOC) results showed that the DBD could effectively mineralize and dechlorinate PCB77. The possible degradation pathway of PCB77 was inferred at the end based on the degradation products determined by gas chromatography-mass spectrometry (GC-MS).

Atomically Dispersed Electron Traps in Cu Doped BiOBr Boosting CO2 Reduction to Methanol by Pure H2 O.

Overall photocatalytic conversion of CO2 and pure H2 O driven by solar irradiation into methanol provides a sustainable approach for extraterrestrial synthesis. However, few photocatalysts exhibit efficient production of CH3 OH. Here, BiOBr nanosheets supporting atomic Cu catalysts for CO2 reduction are reported. The investigation of charge dynamics demonstrates a strong built-in electric field established by isolated Cu sites as electron traps to facilitate charge transfer and stabilize charge carriers. As result, the catalysts exhibit a substantially high catalytic performance with methanol productivity of 627.66 µmol gcatal -1 h-1 and selectivity of ≈90% with an apparent quantum efficiency of 12.23%. Mechanism studies reveal that the high selectivity of methanol can be ascribed to energy-favorable hydrogenation of *CO intermediate giving rise to *CHO. The unfavorable adsorption on Cu1 @BiOBr prevents methanol from being oxidized by photogenerated holes. This work highlights the great potential of single-atom photocatalysts in chemical transformation and energy storage reactions.

Remediation of lindane contaminated soil by fluidization-like dielectric barrier discharge.

This study proposed the fluidization-like dielectric barrier discharge (DBD) plasma for the remediation of lindane contaminated soil and integrated physical and chemical reaction pathway. Soil particle distribution within the reactor was simulated with Euler-Euler and Gidaspow drag models, and a bipolar pulsed power supply was applied to energize the DBD reactor after full fluidized. The effect of soil particles movement on electric features was discussed in terms of voltage waveforms and Lissajous figures. Lindane degradation was found to be related to electrics parameters and soil properties. Soil samples before and after treatment were analyzed by XRD and SEM methods. A 95.98% lindane decomposition and 0.66 mgLindane/h average reaction rate were obtained with 3 wt% CaO injection by pulse power drove fluidization-like DBD after 32 min treatment. Ozone was proved to play a major role during lindane degrading by plasma. The reaction potential pathway of lindane decomposition contains 4 steps, including dehydrogen, dehydrochlorination, and dechlorination, respectively.

Solvent-free synthesis of FAU zeolite from coal fly ash.

FAU zeolite is successfully synthesized from coal fly ash (CFA) as the sole silicon and aluminum sources under solvent-free conditions. CO2 adsorption and ion-exchange tests show that the product possesses excellent CO2 adsorption capacity and even better Ca2+ and Mg2+ ion exchange capacity, which is particularly important for its wide application in industrial processes.

Decontamination of 2-Chloroethyl ethyl sulfide on the surface by atmospheric pressure plasma jet.

Atmospheric pressure plasma jet (APPJ) were used to decontaminate the surface's 2-Chloroethyl ethyl sulfide (2-CEES), a kind of sulfur mustard (HD) simulant. The power of the APPJ device didn't exceed 7.77 W. Helium APPJ was easier to generate plasma jet than argon APPJ. The treated nude mouse skin surface's temperature slowly reached 30.4 °C and no obvious lesions in the dermis and skin appendages after 15 min treatment. Compared with argon APPJ, the helium APPJ produced more ·OH and the maximum concentration of ·OH was 3.748 × 10-9 mol/L. Attributed to the low density and more ·OH content, the helium APPJ had a better decontamination effect. With a maximum voltage of 7 kV and a helium flow rate of 4 L/min, 2-CEES (4.53 mg/cm2) can be completely decontaminated in 2.5 min, and no gaseous 2-CEES was detected. The detection of the 2-Hydroxyethyl ethyl sulfide proved the role of ·OH in the reaction system. During the reaction, 2-Chloroethyl ethyl sulfoxide and 2-Chloroethyl ethyl sulfone were also detected. The plasma jet could reduce the toxicity by destroying the parent molecule (2-CEES) in a short time, but it took more time to eliminate the intermediate products. No relevant intermediate products were detected in the gaseous, ensured the safety of personnel operating in open spaces.

Degradation of aniline in water with gaseous streamer corona plasma.

This paper demonstrated the effects and influencing factors in degrading aniline by gaseous streamer corona plasma along water surface under different discharging gas atmospheres. For aniline with an initial concentration of 100 mg l-1, the degradation was fastest when the reactor was not ventilated, and the degradation rate is 98.5% under 7.5 min treatment. While the degradation was slowest when Ar was ventilated, the degradation rate is 98.6% after treatment for 60 min. Some active particles were detected using a multi-channel fibre-optic spectrometer during the discharge, such as Ar, OH, N2, N 2 + and N. In particular, NO was detected during air discharge. The NO and N 2 + could produce NO 3 - ; then generated nitric acid would affect the pH value of the solution. The intermediate product by N2 discharge is nitrophenol, and nitrophenol would be converted to p-benzoquinone. The O2 discharge could produce an intermediate product of aminophenol. The intermediate products in Ar discharge were in small amounts and the final mineralization effect was the best.

Ultrastructural changes in hepatocellular carcinoma cells induced by exponential pulses of nanosecond duration delivered via a transmission line.

Clinical applications of high-intensity pulsed electric fields have proven useful in ablating solid tumors. However, novel ideas for the development of an effective tumor ablation device are urgently needed. Here, we studied cellular effects of the nanosecond exponential pulse, which is generated by a capacitor-discharging circuit and delivered via a transmission line. Pulses of peak voltage boosted by transmission line oscillation possess high capability to induce swelling and to cause loss of viability in cells. The appropriate parameter of the pulse was selected to investigate the ultrastructural changes in swollen cells, which present smoothened plasma membrane, loss of microvilli, and lowered cytoplasm electron density. We propose the equivalent force field hypothesis to understand the mechanism underlying cell swelling induced by pulsing. Wrinkles on the plasma membrane might indicate recovery from cell swelling, and this was verified by co-culture of pulsed PKH26-Cells with sham-treated PKH67-Cells. We concluded that the ultrastructural changes, such as irregular pores formed on the plasma membrane, were mainly induced by the effect of electric pulse applied on the charged molecules in the membrane.

Potential effect of non-thermal plasma for the inhibition of scar formation: a preliminary report.

Non-thermal plasma (NTP) is a promising biomedical tool for application to wound healing. However, there is limited scientific evidence that confirms its efficacy to inhibit scar formation. This study aims to investigate the role of non-thermal plasma in scar formation. Two full-thickness dorsal cutaneous wounds of rats were treated with either a non-thermal helium plasma jet or helium. It was determined that the non-thermal plasma jet accelerated the wound healing process from 5 days after surgery (day 5: 41.27% ± 2.351 vs 54.7% ± 5.314, p < 0.05; day 7: 56.05% ± 1.881 vs 75.28% ± 3.914, p < 0.01; day 14: 89.85% ± 2.991 vs 98.07% ± 0.839, p < 0.05). The width of the scars for the NTP group was narrower than those of control group (4.607 ± 0.416 mm vs 3.260 ± 0.333 mm, p < 0.05). In addition, a lower level of TGF-ß1, p-Smad2 and p-Smad3 were detected in the NTP treated wounds (p < 0.05, p < 0.01 and p < 0.01). As expected, α-SMA was also significantly decreased in the NTP treatment group (p < 0.01). Moreover, the expression of type I collagen and the proportion of type I to III collagen were lower in the NTP group (p < 0.05). The results of the study suggest that NTP may play a potential role in scar formation by inhibiting the TGF ß1 signal pathway and reducing the levels of α-SMA and type I collagen, and may have clinical utility in the future.

[Experimental study on silicone hand disinfection by a touchable non-thermal plasma].

In this study, silicone hand was disinfected by homemade touchable non-thermal plasma to simulate and evaluate its feasibility of application on human hand. Experimental results showed that there was no significant difference when Escherichia coli ( E. coli), Staphylococcus aureus ( S. au), Staphylococcus albus ( S. al), and Pseudomonas aeruginosa ( P. ae) were loaded on the silicone hand surface and treated with plasma. The efficiency of plasma disinfection was higher when the treatment time was prolonged or initial bacterial density was lower. When initial bacterial number was 1.0×10 6-1.0×10 7 CFU, the plasma disinfection process mainly occured in the first 5 s and more than 99% of bacteria could be disinfected. This study can provide guidelines for the development of a new plasma device for human hand disinfection.

A comparison study of toluene removal by two-stage DBD-catalyst systems loading with MnO(x), CeMnO(x), and CoMnO(x).

This paper studies the toluene removal by a two-stage dielectric barrier discharge (DBD)-catalyst system with three catalysts: MnO(x)/ZSM-5, CoMnO(x)/ZSM-5, and CeMnO(x)/ZSM-5. V-Q Lissajous method, Brunauer-Emmett-Teller (BET) surface area, X-ray diffraction (XRD), and X-ray photoelectron (XPS) are used to characterize the DBD and catalysts. The DBD processing partially oxidizes the toluene, and the removal efficiency has a linear relationship with ozone generation. Three DBD-catalyst systems are compared in terms of their toluene removal efficiency, Fourier transform infrared (FTIR) spectra, carbon balance, CO selectivity, CO2 selectivity, and ozone residual. The results show that the DBD-catalyst system with CoMnO(x)/ZSM-5 performs better than the other two systems. It has the highest removal efficiency of about 93.7%, and the corresponding energy yield is 4.22 g/kWh. The carbon balance and CO2 selectivity of CoMnO(x)/ZSM-5 is also better than the other two catalysts. The measurements of two important byproducts including aerosols and ozone are also presented.

Characteristics of back corona discharge in a honeycomb catalyst and its application for treatment of volatile organic compounds.

The main technical challenges for the treatment of volatile organic compounds (VOCs) with plasma-assisted catalysis in industrial applications are large volume plasma generation under atmospheric pressure, byproduct control, and aerosol collection. To solve these problems, a back corona discharge (BCD) configuration has been designed to evenly generate nonthermal plasma in a honeycomb catalyst. Voltage-current curves, discharge images, and emission spectra have been used to characterize the plasma. Grade particle collection results and flow field visualization in the discharge zones show not only that the particles can be collected efficiently, but also that the pressure drop of the catalyst layer is relatively low. A three-stage plasma-assisted catalysis system, comprising a dielectric barrier discharge (DBD) stage, BCD stage, and catalyst stage, was built to evaluate toluene treatment performance by BCD. The ozone analysis results indicate that BCD enhances the ozone decomposition by collecting aerosols and protecting the Ag-Mn-O catalyst downstream from aerosol contamination. The GC and FTIR results show that BCD contributes to toluene removal, especially when the specific energy input is low, and the total removal efficiency reaches almost 100%. Furthermore, this removal results in the emission of fewer byproducts.

Degradation of aqueous Rhodamine B by plasma generated along the water surface and its enhancement using nanocrystalline Fe-, Mn-, and Ce-doped TiO2 films.

The degradation of aqueous Rhodamine B (RhB) was examined using a dual-channel spark switch module designed to regulate the steepness of pulsed high voltage with microsecond rise time. Depending on the energy per pulse, a spark along the water surface (SPWS) or streamer along the water surface (STWS) was formed. STWS was found to have a better degradation effect and energy efficiency toward RhB than SPWS at the same power; however, addition of H2O2 amounts resulted in increased degradation, the effect being more pronounced using SPWS. The initial concentration of RhB also appeared to influence the rate constant of the degradation reaction. Furthermore, TiO2 films doped with Fe, Mn, and Ce were found to enhance the degradation performance of plasma. A possible reaction mechanism of plasma formation along the water surface was concluded by determination of the main inorganic products in the liquid and gas phases.