Disinfection of wastewater by a complete equipment based on a novel ultraviolet light source of microwave discharge electrodeless lamp: Characteristics of bacteria inactivation, reactivation and full-scale studies.

Ultraviolet (UV) light is widely used for wastewater disinfection. Traditional electrode-excited UV lamps, such as low-pressure mercy lamps (LPUV), encounter drawbacks like electrode aging and rapid light attenuation. A novel UV source of microwave discharge electrodeless lamp (MDEL) has aroused attention, yet its disinfection performance is unclear and still far from practical application. Here, we successfully developed a complete piece of equipment based on MDELs and achieved the application for disinfection in wastewater treatment plants (WWTPs). The light emitted by an MDEL (MWUV) shared a spectrum similar to that of LPUV, with the main emission wavelength at 254 nm. The inactivation rate of Gram-negative E. coli by MWUV reached 4.5 log at an intensity of 1.6 mW/cm2 and a dose of 20 mJ/cm2. For Gram-positive B. subtilis, an MWUV dose of 50 mJ/cm2 and a light intensity of 1.2 mW/cm2 reached an inactivation rate of 3.4 log. A higher MWUV intensity led to a better disinfection effect and a lower photoreactivation rate of E. coli. When inactivated by MWUV with an intensity of 1.2 mW/cm2 and a dose of 16 mJ/cm2, the maximum photoreactivation rate and reactivation rate constant Kmax of E. coli were 0.63 % and 0.11 % h-1 respectively. Compared with the photoreactivation, the dark repair of E. coli was insignificant. The full-scale application of the MDEL equipment was conducted in two WWTPs (10,000 m3/d and 15,000 m3/d). Generally 2-3 log inactivation rates of fecal coliforms in secondary effluent were achieved within 5-6 s contact time, and the disinfected effluent met the emission standard (1000 CFU/L). This study successfully applied MDEL for disinfection in WWTPs for the first time and demonstrated that MDEL has broad application prospects.

Synthesis of Pd/Carbon Hollow Spheres by the Microwave Discharge Method for Catalytic Debenzylation.

Pd/C catalysts have been widely applied in the debenzylation process due to their excellent ability of hydrogenolysis. However, they have been suffering from the problems of agglomeration and loss of active components, which lead to decreased and unstable activity. Thus, it is still a challenge to achieve Pd/C catalysts with high activity and stability. Herein, we propose a strategy for preparing Pd/C catalysts on porous carbon hollow spheres by a microwave discharge method. Due to the high-temperature property and reducibility of microwave discharge, Pd precursors can be rapidly reduced, resulting in well-dispersed Pd nanoparticles with a small size on the carbon carrier. Besides, the matched mesopores in the carbon hollow spheres can anchor Pd nanoparticles and effectively reduce the agglomeration and loss of Pd nanoparticles during the catalytic reaction. As a result, the as-prepared Pd/mesoporous carbon hollow spheres exhibit high and stable activity in the debenzylation reaction.

Synthesis of High-Loading Pt/C Electrocatalysts Using a Surfactant-Assisted Microwave Discharge Method for Oxygen Reduction Reactions.

High-loading Pt/C catalysts play an important role in the practical application of metal-air batteries and fuel cells because of their superior activity, high conductivity, and commercial availability. It is well known that high loadings always lead to the agglomeration of Pt nanoparticles, resulting in a loss of catalytic activity and stability; thus, it still remains a challenge to prepare high-loading Pt/C catalysts with high dispersion and small particle sizes. Here, we introduce a surfactant-assisted microwave discharge method to prepare high-loading (>40 wt %) Pt/C electrocatalysts with ultrafine particle sizes (∼3.19 nm) and good dispersion. Benefitting from the high-temperature property and reducibility of carbon-induced-arc, the surfactant and Pt precursors undergo rapid decomposition, reduction, and carbonization, generating the structure of Pt@C on carbon black. The carbon derived from the surfactant can not only inhibit the agglomeration of Pt nanoparticles but also prevent the Pt core from toxication, ensuring high activity and stability of the high-loading Pt/C catalyst. When evaluated in the oxygen reduction reaction, the as-prepared Pt/C catalyst demonstrates a comparable activity and better methanol resistance to commercial Pt/C.

Experimental Research on Microwave Ignition and Combustion Characteristics of ADN-Based Liquid Propellant.

Microwave ignition has attracted much attention due to its advantages of reliable ignition, large ignition area and cold-start capability. In this paper, the experimental method is used to explore the ignition ability of the microwave device to ADN-based liquid propellant. Additionally, we discuss the influence of the inlet power and rate of propellant injected into the ignition system on the height of the combustion jet and the combustion temperature. In the experiment, a microwave-assisted ignition system was established based on a special microwave resonant cavity. The liquid propellant and working gas were sprayed into the resonator cavity through the hollow straight tube beneath the resonant cavity. The test results show that the device can ignite the propellant under the condition of 800 W input power, which proves the feasibility of the microwave ignition device for ADN-based liquid propellant. Microwave power has some influence on the flame spray height at the initial stage of combustion. The spray height at 2000 W is increased by 55.7% in comparison to 1000 W. In the stable combustion stage, the input power has a very significant increase in the average temperature of the flame, which is increased by 25%. The combustion is relatively better when the propellant flow rate is 30 mL/min, and the height of the flame spray increases by 25.2%. The increase in throughput did not have a significant impact on the flame temperature.

Development of a microwave-discharge light-emitting diode (MDLED): a novel UV source for the UV-driven microwave-assisted TiO2 photocatalytic treatment of contaminated wastewaters.

This brief article reports on the fabrication of a prototype novel semiconductor digital device, a microwave-discharge light-emitting diode (MDLED), consisting of an LED and a Schottky barrier diode encapsulated in a quartz ampoule. Coating the surface of this ampoule with TiO2 yielded a new photocatalytic TiO2 unit (MDLED-TiO2) for use in treating contaminated wastewaters. To the extent that this MDLED-TiO2 is driven only by microwave energy, there is no need for electric wires or electrical AC power. As much of the activity of TiO2 photocatalyst is enhanced and ultraviolet light emission is generated only by irradiating with microwaves, the MDLED-TiO2 affords a simple water treatment device as demonstrated in the present study. The digital device consisted of 14 pieces of MDLED-TiO2  units immersed into a model contaminated wastewater toward the decomposition of organic pollutants and sterilization of natural bacteria-contaminated wastewaters performed in an energy-saving manner simply by irradiating the wastewaters with microwaves.

Microwave Discharges in Liquid Hydrocarbons: Physical and Chemical Characterization.

Microwave discharges in dielectric liquids are a relatively new area of plasma physics and plasma application. This review cumulates results on microwave discharges in wide classes of liquid hydrocarbons (alkanes, cyclic and aromatic hydrocarbons). Methods of microwave plasma generation, composition of gas products and characteristics of solid carbonaceous products are described. Physical and chemical characteristics of discharge are analyzed on the basis of plasma diagnostics and 0D, 1D and 2D simulation.

Combination of microwave discharge electrodeless lamp and a TiO2/HZSM-5 composite for the photocatalytic degradation of dimethyl sulphide.

In this study, an integrated photocatalytic system consisting of a microwave discharge electrodeless lamp (MDEL) and TiO2/HZSM-5 was established to investigate the intensified degradation of dimethyl sulphide (DMS). The system targets optimisation of the reactive oxygen species (ROS) and photocatalytic degradation pathways without catalyst deactivation. TiO2/HZSM-5, containing highly dispersed TiO2 nanoparticles, was prepared through the sol-gel method. TiO2/HZSM-5 exhibits strong acidity and can adsorb DMS in multiple adsorption forms. Thus, the adsorption capacity of TiO2/HZSM-5 is 20 and 53 times higher than that of Aeroxide TiO2 (P25) in dry and highly humid air, respectively. UV-Vis analysis was performed to investigate the ROS in the gas phase. The results show that the concentrations of the ROS increased by 8% and 62.7% in dry and highly humid air, respectively. 1O2 and O (1D), as well as ·OH are the major ROS, accounting for 73.6% and 61.6% in dry and highly humid air, respectively. A total of 92.5% DMS was removed over 600 min in dry air. Microwaves have strong desorption effects on absorbed substances, promoting the degradation of DMS via ROS in the gas phase. Moreover, 1O2, O (1D), and ·OH can mineralise more DMS molecules into SO2 and SO3 through methanesulfonic acid. The highest mineralisation rate of 89.48% was obtained at 90% humidity over 600 min without catalyst deactivation. Therefore, this integrated system induced by microwave radiation can improve ROS production and prevent catalyst deactivation, providing an alternative to achieve higher photocatalytic performances in dry and highly humid air.

Degradation behaviors of naproxen by a hybrid TiO2 photocatalyst system with process components.

A hybrid system combining microwave and a microwave discharge electrodeless lamp (MDEL) was proposed to overcome the limitations of conventional TiO2 photocatalysts. The degradation efficiency and mechanism of naproxen were determined using a series of single processes, including conventional TiO2 photocatalyst reactors and a hybrid system that fuses them. Although the degradation efficiency tended to increase after changing the experimental condition of a single process, the optimal conditions existed for these experimental conditions. On the other hand, remarkable synergy was observed in the fused process, whose efficiency was significantly higher than that of the unit process. In particular, the optimal degradation ability was obtained by adding hydrogen peroxide together with microwave irradiation. The seven intermediates in the proposed photocatalytic degradation pathway were generated by the demethylation and hydroxylation by hydroxyl radicals. These results are expected to provide new data on the design of high efficiency photocatalytic systems at low cost.

Mineralization of cefoperazone in acid medium by the microwave discharge electrodeless lamp irradiated photoelectro-Fenton using a RuO2/Ti or boron-doped diamond anode.

The mineralization of 125 mL of 50-300 mg L-1 cefoperazone (CFPZ) has been comparatively studied by electrochemical advanced oxidation processes (EAOPs) like anodic oxidation (AO), electro-Fenton (EF) and photoelectro-Fenton (PEF) with a RuO2/Ti or boron-doped diamond (BDD) anode and an activated carbon fiber (ACF) cathode. A microwave discharge electrodeless lamp (MDEL) was used as the UV source in PEF process. CFPZ decays always followed pseudo-first-order kinetics and their constant rates increased in the order: AO < EF < MDEL-PEF, regardless of anode types. Higher mineralization was achieved in all methods using BDD instead of RuO2/Ti, while the most potent BDD-MDEL-PEF gave 88% mineralization under its optimum conditions of 0.36 A, pH 3.0 and 1.0 mmol L-1 Fe2+. The synergistic mechanisms were explored by quantifying the electrogenerated H2O2 and formed •OH, in which 2.27 and 2.58 mmol L-1 H2O2 were accumulated in AO-H2O2 with RuO2/Ti or BDD anode, respectively, while 92.0 and 263.5 µmol L-1 •OH were generated in EF with RuO2/Ti or BDD anode, respectively. The oxidation power of EAOPs with different anodes was also compared by measuring the evolutions of NO3- and NH4+ as well as four generated carboxylic acids including oxalic, oxamic, formic and fumaric acids.

Microwave Discharge Electrodeless Lamps (MDELs). Part XI. Photolytic, Chemical Oxidation, and Photocatalytic Treatment of Aqueous Urea Solution with a Novel MDEL Photoreactor.

Decomposition of urea in aqueous solution was carried out using a microwave discharge electrodeless lamp (MDEL) consisting of two photoreactors with a triple tube structure that generate vacuum-UV/UV light and reactive oxygen species (ROS) using microwaves (MW) as an energy source. The rate of decomposition of urea was highest under acidic conditions (pH 4) compared with those at pH 7 and 10. When used in combination with dispersed TiO2, a photocatalyst, high decomposition efficiency was achieved with less power consumption. Moreover, decomposition efficiency more than two times higher than that of ozone oxidation and sodium hypochlorite oxidation could be realized.

Efficient mineralization of antibiotic ciprofloxacin in acid aqueous medium by a novel photoelectro-Fenton process using a microwave discharge electrodeless lamp irradiation.

In this study, a novel photoelectro-Fenton (PEF) process using microwave discharge electrodeless lamp (MDEL) as a UV irradiation source was developed for the removal of antibiotic ciprofloxacin (CIP) in water. Comparative degradation of 200mgL-1 CIP was studied by direct MDEL photolysis, anodic oxidation (AO), AO in presence of electrogenerated H2O2 (AO-H2O2), AO-H2O2 under MDEL irradiation (MDEL-AO-H2O2), electro-Fenton (EF) and MDEL-PEF processes. Higher oxidation power was found in the sequence: MDEL photolysis < AO < AO-H2O2< MDEL-AO-H2O2< EF < MDEL-PEF. Effects of current density, pH, initial Fe2+ concentration and initial CIP concentration on TOC removal in MDEL-PEF process were examined, and the optimal conditions were ascertained. The releases of three inorganic ions (F-, NH4+ and NO3-) and two carboxylic acids (oxalic and formic acids) were qualified. Seven aromatic intermediates mainly generated from hydroxylation, dealkylation and defluorination of CIP were detected by UPLC-QTOF-MS/MS technology. Therefore, plausible degradation sequences for CIP degradation in MDEL-PEF process including all detected products were proposed.