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Author(s):  
Jin Liu ◽  
Xinbo Zhu ◽  
Xueli Hu ◽  
Xin Tu

Abstract In this article, plasma-assisted NH3 syntheses 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 are 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 the 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 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 the 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.


Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1476
Author(s):  
Richard Cimerman ◽  
Mária Cíbiková ◽  
Leonid Satrapinskyy ◽  
Karol Hensel

Plasma catalysis has been utilized in many environmental applications for removal of various hydrocarbons including tars. The aim of this work was to study the tars removal process by atmospheric pressure DBD non-thermal plasma generated in combination with packing materials of various composition and catalytic activity (TiO2, Pt/γAl2O3, BaTiO3, γAl2O3, ZrO2, glass beads), dielectric constant (5–4000), shape (spherical and cylindrical pellets and beads), size (3–5 mm in diameter, 3–8 mm in length), and specific surface area (37–150 m2/g). Naphthalene was chosen as a model tar compound. The experiments were performed at a temperature of 100 °C and a naphthalene initial concentration of approx. 3000 ppm, i.e., under conditions that are usually less favorable to achieve high removal efficiencies. For a given specific input energy of 320 J/L, naphthalene removal efficiency followed a sequence: TiO2 > Pt/γAl2O3 > ZrO2 > γAl2O3 > glass beads > BaTiO3 > plasma only. The efficiency increased with the increasing specific surface area of a given packing material, while its shape and size were also found to be important. By-products of naphthalene decomposition were analyzed by means of FTIR spectrometry and surface of packing materials by SEM analysis.


2020 ◽  
Vol 12 (21) ◽  
pp. 9240
Author(s):  
Steffen Helbich ◽  
Daniel Dobslaw ◽  
Andreas Schulz ◽  
Karl-Heinrich Engesser

A combined system of a biotrickling filter and a non-thermal plasma (NTP) in a downstream airflow was operated for 1220 days for treatment of emissions of styrene and secondary emissions of germs formed in the biological process. The biotrickling filter was operated at variable inlet concentrations, empty bed residence times (EBRT), type and dosage of fertilizers, irrigation densities, and starvation periods, while dielectric barrier discharge and corona discharge were operated at different specific input energy levels to achieve optimal conditions. Under these conditions, efficiencies in the removal of volatile organic compounds (VOCs), germs and styrene of 96–98%, 1–4 log units and 24.7–50.1 g C m−3 h−1 were achieved, respectively. Fluid simulations of the NTP and a germ emission-based clocking of the discharge reveal further energy saving potentials of more than 90%. The aim of an energy-efficient elimination of VOCs through a biotrickling filter and of secondary germ emissions by a NTP stage in a downstream airflow for potential re-use of purified waste gas as process gas for industrial application was successfully accomplished.


Author(s):  
Prince Junior Asilevi ◽  
Chengwu Yi ◽  
Jue Li ◽  
Huijuan Wang ◽  
Muhammad Imran Nawaz

Atmospheric volatile organic compounds (VOCs) from industry and automobiles are posing a serious threat to the environment and human health, and hence efficient control methods are indispensable. This paper presents a laboratory-scale study on the decomposition mechanism for benzene using strong ionization dielectric barrier discharge (DBD) at atmospheric pressure. The specific input energy (SIE), current density, and concentration were studied. The results show that the removal efficiency of benzene increased from 12% to 69% with the increase of SIE from 0.5 to 3.8 kJ/L. The decline in current density by 66.48% and 43.7% for an initial benzene concentration of 300 ppm, was due to increased oxygen content (from 2.4% to 20.9%) and relative humidity (from 18.9% to 90%), respectively, thus electron concentration and consequentially enhancing the removal efficiency over 93%. Further, the beta parameter of the VOC decomposition law decreased from 3.1 kJ/L at 300 ppm to 1.6 kJ/L at 100 ppm. This shows that •O and •OH radicals are key species for the decomposition of benzene and electron dissociation reactions principally control the process. The highest ozone concentration was detected at 5.5 mg/L when no benzene is present, while the main NOx species (NO and NO2) increased with increasing SIE. The Maxwell–Boltzmann electron energy distribution function was solved using the strong ionization discharge reactor (~10 eV), showing that approximately 84.8 % of high-energy electrons possess enough energy to cause the benzene ring cleavage and free radical production. Finally, GCMS and FTIR test results suggested that the byproducts mainly consisted of phenol and substitutions of phenol. The study results show that the strong ionization DBD reactor efficiently removes benzene from polluted air.


Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 853 ◽  
Author(s):  
Van Toan Nguyen ◽  
Duc Ba Nguyen ◽  
Iljeong Heo ◽  
Young Sun Mok

The challenge that needs to be overcome regarding the removal of nitrogen oxides (NOx) and soot from exhaust gases is the low activity of the selective catalytic reduction of NOx at temperatures fluctuating from 150 to 350 °C. The primary goal of this work was to enhance the conversion of NOx and soot simulant by employing a Ag/α-Al2O3 catalyst coupled with dielectric barrier discharge plasma. The results demonstrated that the use of a plasma-catalyst process at low operating temperatures increased the removal of both NOx and naphthalene (soot simulant). Moreover, the soot simulant functioned as a reducing agent for NOx removal, but with low NOx conversion. The high efficiency of NOx removal required the addition of hydrocarbon fuel. In summary, the combined use of the catalyst and plasma (specific input energy, SIE ≥ 60 J/L) solved the poor removal of NOx and soot at low operating temperatures or during temperature fluctuations in the range of 150–350 °C. Specifically, highly efficient naphthalene removal was achieved with low-temperature adsorption on the catalyst followed by the complete decomposition by the plasma-catalyst at 350 °C and SIE of 90 J/L.


Catalysts ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 303 ◽  
Author(s):  
Zixian Jia ◽  
Xianjie Wang ◽  
Emeric Foucher ◽  
Frederic Thevenet ◽  
Antoine Rousseau

In the context of coupling nonthermal plasmas with catalytic materials, CeO2 is used as adsorbent for toluene and combined with plasma for toluene oxidation. Two configurations are addressed for the regeneration of toluene saturated CeO2: (i) in plasma-catalysis (IPC); and (ii) post plasma-catalysis (PPC). As an advanced oxidation technique, the performances of toluene mineralization by the plasma-catalytic systems are evaluated and compared through the formation of CO2. First, the adsorption of 100 ppm of toluene onto CeO2 is characterized in detail. Total, reversible and irreversible adsorbed fractions are quantified. Specific attention is paid to the influence of relative humidity (RH): (i) on the adsorption of toluene on CeO2; and (ii) on the formation of ozone in IPC and PPC reactors. Then, the mineralization yield and the mineralization efficiency of adsorbed toluene are defined and investigated as a function of the specific input energy (SIE). Under these conditions, IPC and PPC reactors are compared. Interestingly, the highest mineralization yield and efficiency are achieved using the in-situ configuration operated with the lowest SIE, that is, lean conditions of ozone. Based on these results, the specific impact of RH on the IPC treatment of toluene adsorbed on CeO2 is addressed. Taking into account the impact of RH on toluene adsorption and ozone production, it is evidenced that the mineralization of toluene adsorbed on CeO2 is directly controlled by the amount of ozone produced by the discharge and decomposed on the surface of the coupling material. Results highlight the key role of ozone in the mineralization process and the possible detrimental effect of moisture.


2018 ◽  
Vol 29 (9) ◽  
pp. 1986-1994 ◽  
Author(s):  
Ke Zhang ◽  
Shi-Tang Cui ◽  
Yi-Chao Chen ◽  
Zhi-Ping Tang

In this article, a new hydraulic shape memory alloy shock absorber is introduced. The shape memory alloy bars are used as the kernel components for energy dissipation and restoration in the stress mode of pure tension, and their initial deformation is enlarged by a hydraulic system with two pistons of different sizes. This particular arrangement yields high shape memory alloy material utilization and large displacement–length ratio simultaneously. A prototype device was fabricated and tested. The specific input energy (input energy/mass of shape memory alloy) and energy dissipation ratio (dissipated energy/input energy) in the experiments were about 2 J/g and 30%, respectively, at the full stroke. Based on this hydraulic shape memory alloy shock absorber, a combined device including viscous damping was theoretically investigated. According to the calculation results, the maximum specific input energy and energy dissipation ratio can increase by onefold from the initial model without viscous damping. Based on the works and results of this study, the three guidelines in the designing of shape memory alloy–based shock absorbers have been brought up: (1) keep the shape memory alloy parts in the pure tension state to increase the material utilization, (2) introduce deformation or displacement enlargement structures to amplify the work stroke, and (3) combine with other energy dissipation mechanisms.


2015 ◽  
Vol 17 (1) ◽  
pp. 32-40 ◽  
Author(s):  
Kamaladdin Abedi ◽  
Farshid Ghorbani-Shahna ◽  
Abdolrahman Bahrami ◽  
Babak Jaleh ◽  
Rasoul Yarahmadi

Abstract In this study, the catalytic effect of TiO2-ZnO/GAC coupled with non-thermal plasma was investigated on the byproducts distribution of decomposition of chlorinated VOCs in gas streams. The effect of specific input energy, and initial gas composition was examined in a corona discharge reactor energized by a high frequency pulsed power supply. Detected by-products for catalytic NTP at 750 J L-1 included CO, CO2, Cl2, trichloroacetaldehyde, as well as trichlorobenzaldehyde with chloroform feeding, while they were dominated by CO, CO2, and lower abundance of trichlorobenzaldehyde and Cl2 with chlorobenzene introduction. Some of the by-products such as O3, NO, NO2, and COCl2 disappeared totally over TiO2-ZnO/GAC. Furthermore, the amount of heavy products such as trichlorobenzaldehyde decreased significantly in favor of small molecules such as CO, CO2, and Cl2 with the hybrid process. The selectivity towards COx soared up to 77% over the catalyst at 750 J L-1 and 100 ppm of chlorobenzene.


2014 ◽  
Vol 3 (2) ◽  
pp. 220 ◽  
Author(s):  
R. Subash ◽  
CM Meenakshi ◽  
K. Samuel Jayakaran ◽  
C. Venkateswaran ◽  
R. Sasidharan

In this Paper, Pedal operated hacksaw machine which can be used for industrial applications and Household needs in which no specific input energy or power is needed. This project consists of a sprocket arrangement, the crank and slider mechanism, the chain drive. In the mechanism, chain drive is directly connected to the hacksaw for the processing of cutting the wooden blocks. The objective of the paper is using the conventional mechanical process which plays a vital role. The main aim is to reduce the human effort for machining various materials such as wooden blocks, steel, PVC etc. Keywords: Sprocket Arrangement, Crank and Slider Mechanism.


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