Electrochemical degradation of pentachlorophenol on a palladium modified gas-diffusion electrode

2009 ◽  
Vol 59 (9) ◽  
pp. 1759-1767 ◽  
Author(s):  
H. Wang ◽  
J. L. Wang
Keyword(s):  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Hydrogen Reduction ◽  
Amorphous Structure ◽  
Gas Diffusion ◽  
Gas Diffusion Electrode ◽  
Hydrogen Gas ◽  
Electrochemical Degradation ◽  
X Ray

Pd/C catalyst was prepared by a hydrogen reduction method and used for making a Pd/C gas-diffusion electrode. It was fully characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV). In the catalyst, Pd particles with an average size of 4.0 nm were highly dispersed in the activated carbon with an amorphous structure; Pd content on the surface of the Pd/C catalyst reached 1.3 at% (atomic concentration). The Pd/C gas-diffusion electrode was then used as the cathode to investigate the electrochemical degradation of pentachlorophenol (PCP) in a diaphragm electrolysis device, feeding firstly with hydrogen gas then with air, compared with the carbon/polytetrafluoroethylene (C/PTFE) gas-diffusion cathode. The Pd/C gas-diffusion cathode can not only reductively dechlorinate PCP by feeding hydrogen gas, but also accelerate the two-electron reduction of O2 to hydrogen peroxide (H2O2) by feeding air. Therefore, both the removal efficiency and the dechlorination degree of PCP exceeded 80% after 100 min, and the average removal efficiency of PCP in terms of total organic carbon (TOC) was more than 75% after 200 min by using Pd/C gas-diffusion cathode, which was better than that of the C/PTFE gas-diffusion cathode. Phenol was identified as the dechorination product using high-performance liquid chromatography (HPLC).

Degradation of 4-chlorophenol by the anodic–cathodic cooperative effect with a Pd/MWNT gas-diffusion electrode

2012 ◽  
Vol 65 (11) ◽  
pp. 2010-2015 ◽  
Author(s):  
H. Wang ◽  
X. J. Wei ◽  
Z. Y. Bian
Keyword(s):  
High Performance ◽  
Amorphous Structure ◽  
Gas Diffusion ◽  
Gas Diffusion Electrode ◽  
X Ray Diffraction ◽  
Initial Ph ◽  
Multi Walled Carbon Nanotubes ◽  
Optimum Reaction ◽  
Average Size ◽  
Walled Carbon Nanotubes

Pd/multi-walled carbon nanotubes (MWNTs) catalyst used for the gas-diffusion electrode was prepared by ethylene glycol (EG) reduction and characterized by the X-ray diffraction (XRD) and scanning electron microscope (SEM). The results indicated that Pd particles with an average size of 8.0 nm were highly dispersed in the MWNTs with amorphous structure. In a diaphragm electrolysis system with a Ti/RuO2/IrO2 anode and the Pd/MWNT gas diffusion cathode, the degradation of 4-chlorophenol was performed by a combination of electrochemical reduction and oxidation. The combined process was in favor of improving 4-chlorophenol degradation efficiency. The optimum reaction conditions were as following: initial pH 7, aeration with hydrogen and air. Under the optimized electrolysis conditions the removal of 4-chlorophenol in the anodic and cathodic compartments were 98.5 and 90.5%, respectively. Additionally, based on the analysis of electrolysis intermediates using high performance liquid chromatography (HPLC) and ion chromatography (IC), the electrolysis degradation of 4-chlorophenol was proposed containing the intermediates, such as phenol, hydroquinone, benzoquinone, maleic acid, fumaric acid, succinic acid, malonic acid, oxalic acid, acetic acid and formic acid.

scholarly journals Electrochemical Reduction of CO2to Organic Acids by a Pd-MWNTs Gas-Diffusion Electrode in Aqueous Medium

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Guang Lu ◽  
Hui Wang ◽  
Zhaoyong Bian ◽  
Xin Liu
Keyword(s):  
Carbon Nanotubes ◽  
Organic Acids ◽  
Electrochemical Reduction ◽  
Photoelectron Spectroscopy ◽  
Gas Diffusion ◽  
Gas Diffusion Electrode ◽  
High Catalytic Activity ◽  
Present System ◽  
Multiwalled Carbon ◽  
X Ray

Pd-multiwalled carbon nanotubes (Pd-MWNTs) catalysts for the conversion of CO2to organic acids were prepared by the ethylene glycol reduction and fully characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV) technologies. The amorphous Pd particles with an average size of 5.7 nm were highly dispersed on the surface of carbon nanotubes. Functional groups of the MWNTs played a key role in the palladium deposition. The results indicated that Pd-MWNTs could transform CO2into organic acid with high catalytic activity and CO2could take part in the reduction reaction directly. Additionally, the electrochemical reduction of CO2was investigated by a diaphragm electrolysis device, using a Pd-MWNTs gas-diffusion electrode as a cathode and a Ti/RuO2net as an anode. The main products in present system were formic acid and acetic acid identified by ion chromatograph. The selectivity of the products could be achieved by reaction conditions changing. The optimum faraday efficiencies of formic and acetic acids formed on the Pd-MWNTs gas-diffusion electrode at 4 V electrode voltages under 1 atm CO2were 34.5% and 52.3%, respectively.

scholarly journals Novel Carbon Dots Derived from Glycyrrhizae Radix et Rhizoma and Their Anti-Gastric Ulcer Effect

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1512
Author(s):  
Yuhan Liu ◽  
Meiling Zhang ◽  
Jinjun Cheng ◽  
Yue Zhang ◽  
Hui Kong ◽  
...  
Keyword(s):  
Gastric Ulcer ◽  
Photoelectron Spectroscopy ◽  
Carbon Dots ◽  
High Performance ◽  
Raw264.7 Cells ◽  
Mice Model ◽  
X Ray ◽  
Glycyrrhizae Radix ◽  
Transmission Electron ◽  
High Resolution Tem

Glycyrrhizae Radix et Rhizoma (GRR) is one of the commonly used traditional Chinese medicines in clinical practice, which has been applied to treat digestive system diseases for hundreds of years. GRR is preferred for anti-gastric ulcer, however, the main active compounds are still unknown. In this study, GRR was used as precursor to synthesize carbon dots (CDs) by a environment-friendly one-step pyrolysis process. GRR-CDs were characterized by using transmission electron microscopy, high-resolution TEM, fourier transform infrared, ultraviolet-visible and fluorescence spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and high-performance liquid chromatography. In addition, cellular toxicity of GRR-CDs was studied by using CCK-8 in RAW264.7 cells, and the anti-gastric ulcer activity was evaluated and confirmed using mice model of acute alcoholic gastric ulcer. The experiment confirmed that GRR-CDs were the spherical structure with a large number of active groups on the surface and their particle size ranged from 2 to 10 nm. GRR-CDs had no toxicity to RAW264.7 cells at concentration of 19.5 to 5000 μg/mL and could reduce the oxidative damage of gastric mucosa and tissues caused by alcohol, as demonstrated by restoring expression of malondialdehyde, superoxide dismutase and nitric oxide in serum and tissue of mice. The results indicated the explicit anti-ulcer activity of GRR-CDs, which provided a new insights for the research on effective material basis of GRR.

scholarly journals Removal of hexavalent chromium from wastewater by Cu/Fe bimetallic nanoparticles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jien Ye ◽  
Yi Wang ◽  
Qiao Xu ◽  
Hanxin Wu ◽  
Jianhao Tong ◽  
...  
Keyword(s):  
Hexavalent Chromium ◽  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
Bimetallic Nanoparticles ◽  
Chemical Reduction ◽  
Particle Surface ◽  
Zerovalent Iron ◽  
Order Model ◽  
X Ray ◽  
Nanoscale Zerovalent Iron

AbstractPassivation of nanoscale zerovalent iron hinders its efficiency in water treatment, and loading another catalytic metal has been found to improve the efficiency significantly. In this study, Cu/Fe bimetallic nanoparticles were prepared by liquid-phase chemical reduction for removal of hexavalent chromium (Cr(VI)) from wastewater. Synthesized bimetallic nanoparticles were characterized by transmission electron microscopy, Brunauer–Emmet–Teller isotherm, and X-ray diffraction. The results showed that Cu loading can significantly enhance the removal efficiency of Cr(VI) by 29.3% to 84.0%, and the optimal Cu loading rate was 3% (wt%). The removal efficiency decreased with increasing initial pH and Cr(VI) concentration. The removal of Cr(VI) was better fitted by pseudo-second-order model than pseudo-first-order model. Thermodynamic analysis revealed that the Cr(VI) removal was spontaneous and endothermic, and the increase of reaction temperature facilitated the process. X-ray photoelectron spectroscopy (XPS) analysis indicated that Cr(VI) was completely reduced to Cr(III) and precipitated on the particle surface as hydroxylated Cr(OH)3 and CrxFe1−x(OH)3 coprecipitation. Our work could be beneficial for the application of iron-based nanomaterials in remediation of wastewater.

Use of anti-solvent to enhance thermoelectric response of hybrid-halide perovskite thin films

2022 ◽  
Author(s):  
Shrikant SAINI ◽  
Izuki Matsumoto ◽  
Sakura Kishishita ◽  
Ajay Kumar Baranwal ◽  
Tomohide Yabuki ◽  
...  
Keyword(s):  
Thin Films ◽  
Electrical Conductivity ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Cost Effective ◽  
Performance Tuning ◽  
Charge Carrier Density ◽  
X Ray ◽  
Thermoelectric Energy Harvesting ◽  
Halide Perovskite

Abstract Hybrid halide perovskite has been recently focused on thermoelectric energy harvesting due to the cost-effective fabrication approach and ultra-low thermal conductivity. To achieve high performance, tuning of electrical conductivity is a key parameter that is influenced by grain boundary scattering and charge carrier density. The fabrication process allows tuning these parameters. We report the use of anti-solvent to enhance the thermoelectric performance of lead-free hybrid halide perovskite, CH3NH3SnI3, thin films. Thin films with anti-solvent show higher connectivity in grains and higher Sn+4 oxidation states which results in enhancing the value of electrical conductivity. Thin films were prepared by a cost-effective wet process. Structural and chemical characterizations were performed using x-ray diffraction, scanning electron microscope, and x-ray photoelectron spectroscopy. The value of electrical conductivity and the Seebeck coefficient were measured near room temperature. The high value of power factor (1.55 µW/m.K2 at 320 K) was achieved for thin films treated with anti-solvent.

Extraordinary Stability of Structural and Electronic Properties of Tin Oxide Nanoparticles Formed by Soft Chemistry

2010 ◽  
Vol 75 ◽  
pp. 36-42 ◽  
Author(s):  
Marina Rumyantseva ◽  
Irina Zhurbina ◽  
Elena Varechkina ◽  
Siranuysh Badalyan ◽  
Alexander Gaskov ◽  
...  
Keyword(s):  
Optical Properties ◽  
Photoelectron Spectroscopy ◽  
Tin Dioxide ◽  
Hydrogen Reduction ◽  
Nitrogen Adsorption ◽  
Ammonia Solution ◽  
Adsorption Method ◽  
X Ray ◽  
Wet Chemical Synthesis ◽  
Tin Chloride

Powders of tin dioxide (SnO2) have been prepared by two different modifications of wet chemical synthesis, i.e. (i) by conventional hydrolysis of tin chloride dissolved in aqueous ammonia solution and (ii) by precipitation from tin chloride dissolved in aqueous hydrazine monohydrate (N2H4*H2O) solution. The prepared gels were dried and then annealed at different temperatures varied from 300 to 700 oC in order to form nanocrystals. Structure and optical properties of the samples were investigated by using X-ray diffraction, transmission electron microscopy, thermoprogrammable hydrogen reduction, low temperature nitrogen adsorption method, photoluminescence, infra-red absorption, Raman spectroscopy, and X-ray photoelectron spectroscopy. The samples prepared by hydrazine-based method are characterized by surface area about 127-188 m2/g with high sintering resistance. The optical spectroscopy data revealed pure crystallinity and high defect concentration for the samples prepared by hydrazine-based method. The experimental results are discussed in view of different states of chemisorbed oxygen on SnO2 nanocrystal surfaces, which determine electronic and optical properties of the prepared samples.

scholarly journals Towards chemically neutral carbon cleaning processes: plasma cleaning of Ni, Rh and Al reflective optical coatings and thin Al filters for free-electron lasers and synchrotron beamline applications

2018 ◽  
Vol 25 (6) ◽  
pp. 1642-1649 ◽  
Author(s):  
Harol Moreno Fernández ◽  
Marco Zangrando ◽  
Guillaume Sauthier ◽  
Alejandro R. Goñi ◽  
Vincent Carlino ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Free Electron ◽  
Inductively Coupled Plasma ◽  
High Performance ◽  
Extreme Ultraviolet ◽  
Filter Material ◽  
Gas Mixture ◽  
Carbon Contamination ◽  
X Ray ◽  
Chemical Surface

The choice of a reflective optical coating or filter material has to be adapted to the intended field of application. This is mainly determined by the required photon energy range or by the required reflection angle. Among various materials, nickel and rhodium are common materials used as reflective coatings for (soft) X-ray mirrors. Similarly, aluminium is one of the most commonly used materials for extreme ultraviolet and soft X-ray transmission filters. However, both of these types of optics are subject to carbon contamination, which can be increasingly problematic for the operation of the high-performance free-electron laser and synchrotron beamlines. As an attempt to remove this type of contamination, an inductively coupled plasma source has been used in conjunction with N2/O2/H2 and N2/H2 feedstock gas plasmas. Results from the chemical surface analysis of the above materials before and after plasma treatment using X-ray photoelectron spectroscopy are reported. It is concluded that a favorable combination of an N2/H2 plasma feedstock gas mixture leads to the best chemical surface preservation of Ni, Rh and Al while removing the carbon contamination. However, this feedstock gas mixture does not remove C contamination as rapidly as, for example, an N2/O2/H2 plasma which induces the surface formation of NiO and NiOOH in Ni and RhOOH in Rh foils. As an applied case, the successful carbon removal from ultrathin Al filters previously used at the FERMI FEL1 using an N2/H2 plasma is demonstrated.

scholarly journals Fabrication of Strontium Bismuth Oxides as Novel Battery-Type Electrode Materials for High-Performance Supercapacitors

2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Yinghui Han ◽  
Le Li ◽  
Yunpeng Liu ◽  
Xue Li ◽  
Xiaohan Qi ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Electrode Materials ◽  
Specific Capacity ◽  
Structural Features ◽  
High Electron ◽  
Strontium Content ◽  
X Ray ◽  
Bismuth Oxides ◽  
Improved Performance

A simple and efficient process method for the preparation of strontium bismuth oxides (SBOs) via an impregnation-calcination method is presented. The synthesized active materials are characterized using X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. The electrochemical performance of the as-synthesized SBO samples is observed to decrease gradually as the strontium content is increased from 25% to 50%. The SBO sample with a Sr/Bi ratio of 1 : 3 shows the highest specific capacitance of 1228.7 F g−1 (specific capacity of 204.8 mAh g−1) at a current density of 1 A g−1 and a good cycling stability (75.1%) over 3000 charge-discharge cycles. The improved performance of the supercapacitors can be attributed to the unique structural features resulting from the addition of appropriate portions of Sr, which supports high electron conductivity and rapid ion/electron transport within the electrode and at the electrode/electrolyte interface. All the results show that the SBOs have considerable potential for use as high-performance battery-type electrodes in supercapacitors.

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