scholarly journals Improvement of stability and reduction of energy consumption for Ti-based MnOx electrode by Ce and carbon black co-incorporating in electrochemical degradation of ammonia nitrogen

2021 ◽  
Author(s):  
Jiao Zhao ◽  
Xuelu Xu ◽  
Zehui Liu ◽  
Xiaodan Bai ◽  
Yan Yang ◽  
...  
Keyword(s):  
Energy Consumption ◽  
Carbon Black ◽  
Organic Pollution ◽  
Ammonia Nitrogen ◽  
Charge Transfer Resistance ◽  
Electrochemical Process ◽  
Electrochemical Activity ◽  
Catalytic Layer ◽  
Cell Potential ◽  
Transfer Resistance

Abstract Ti-based electrode coated with MnOx catalytic layer has presented superior electrochemical activity for degradation of organic pollution in wastewater, however, the industrial application of Ti-based MnOx electrode is limited by the poor stability of electrode. In this study, the novel Ti-based MnOx electrodes co-incorporated with rare earth (Ce) and conductive carbon black (C) were prepared by spraying-calcination method. The Ti/Ce:MnOx-C electrode, with uniform and integrate surface and enhanced Mn(IV) content by C and Ce co-incorporating, could completely remove ammonia nitrogen (NH4+-N) with N2 as the main product. The cell potential and energy consumption of Ti/Ce:MnOx-C electrode during the electrochemical process was significantly reduced compared with Ti/MnOx electrode, which mainly originated from the enhanced electrochemical activity and reduced charge transfer resistance by Ce and C co-incorporating. The accelerated lifetime tests in sulfuric acid showed that the actual service lifetime of Ti/Ce:MnOx-C was ca. 25 times that of Ti/MnOx, which demonstrated the significantly promoted stability of MnOx-based electrode by Ce and C co-incorporating.

scholarly journals Impedimetric Determination of Kanamycin in Milk with Aptasensor Based on Carbon Black-Oligolactide Composite

Sensors ◽  
2020 ◽  
Vol 20 (17) ◽  
pp. 4738 ◽  
Author(s):  
Tatiana Kulikova ◽  
Vladimir Gorbatchuk ◽  
Ivan Stoikov ◽  
Alexey Rogov ◽  
Gennady Evtugyn ◽  
...  
Keyword(s):  
Carbon Black ◽  
Electrochemical Impedance ◽  
Limit Of Detection ◽  
3D Structure ◽  
Cationic Polyelectrolyte ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Chitosan Matrix ◽  
Negative Effect

The determination of antibiotics in food is important due to their negative effect on human health related to antimicrobial resistance problem, renal toxicity, and allergic effects. We propose an impedimetric aptasensor for the determination of kanamycin A (KANA), which was assembled on the glassy carbon electrode by the deposition of carbon black in a chitosan matrix followed by carbodiimide binding of aminated aptamer mixed with oligolactide derivative of thiacalix[4]arene in a cone configuration. The assembling was monitored by cyclic voltammetry, electrochemical impedance spectroscopy, and scanning electron microscopy. In the presence of the KANA, the charge transfer resistance of the inner interface surprisingly decreased with the analyte concentration within 0.7 and 50 nM (limit of detection 0.3 nM). This was attributed to the partial shielding of the negative charge of the aptamer and of its support, a highly porous 3D structure of the surface layer caused by a macrocyclic core of the carrier. The use of electrostatic assembling in the presence of cationic polyelectrolyte decreased tenfold the detectable concentration of KANA. The aptasensor was successfully tested in the determination of KANA in spiked milk and yogurt with recoveries within 95% and 115%.

Fabrication and EIS Characterization of Titania Nanotube Arrays with Top Non-Tube Layer

2011 ◽  
Vol 689 ◽  
pp. 350-354 ◽  
Author(s):  
Xiang Li Li ◽  
Chun Hua Xu ◽  
Zhi Lei Wen ◽  
Wen Jie Zhang
Keyword(s):  
Electrochemical Impedance ◽  
Amorphous Structure ◽  
Charge Transfer Resistance ◽  
Electrochemical Process ◽  
Nanotube Arrays ◽  
X Ray Diffraction ◽  
Electronic Microscopy ◽  
Transfer Resistance ◽  
Titania Nanotube Arrays ◽  
Electrochemical Parameters

TiO2nanotube arrays were fabricated in the electrolyte containing 0.25wt% NH4F, 2.5vol% water and the ethylene glycol for various hours at room temperature by anodization of Ti foil in this paper. Some anodized specimens were annealed at 450°C for 3 hours. Electrochemical Impedance Spectroscopy (EIS) was employed to measure electrochemical parameters of anodized specimens. The morphology and crystalline structure of anodized products were characterized by Field Emission Scanning Electronic Microscopy (FESEM), X-ray Diffraction (XRD) and Transmission Electronic Microscopy (TEM). A non-tube layer appears on nanotube arrays with the increase in anodization time. Anodized TiO2nanotube arrays have an amorphous structure, which transfers to anatase structure after annealing at 450°C. A new equivalent circuit R(CR(R(QR)(CR))) was proposed to fit EIS data. The results show that the charge transfer resistance at the electrode/electrolyte interface controls the electrochemical process of TiO2nanotubes.

Preparation of novel Ti-based MnOx electrodes by spraying method for electrochemical oxidation of Acid Red B

2019 ◽  
Vol 80 (2) ◽  
pp. 365-376
Author(s):  
Xuelu Xu ◽  
Jiao Zhao ◽  
Subei Bai ◽  
Rongrong Mo ◽  
Yan Yang ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Photoelectron Spectroscopy ◽  
Manganese Oxides ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Cell Potential ◽  
Transfer Resistance ◽  
X Ray ◽  
Concentration Changes ◽  
Spraying Method

Abstract At different calcination conditions, titanium-based manganese oxides (MnOx) electrodes were fabricated by spraying method without adhesive. The MnOx/Ti electrodes were applied in electrochemical oxidation of wastewater treatment for the first time. The surface morphologies of electrodes were tested by scanning electron microscopy. The formation of different manganese oxidation states on electrodes was confirmed by X-ray diffraction and X-ray photoelectron spectroscopy. The electrochemical properties of the electrodes have been performed by means of cyclic voltammetry and electrochemical impedance spectroscopy. The characterizations revealed that the MnOx/Ti-350(20) electrode, prepared at calcination temperature of 350 °C for 20 min, exhibited fewer cracks on the electrode surface, larger electrochemically effective surface area and lower charge transfer resistance than electrodes prepared at other calcination conditions. Moreover, Acid Red B was used as target pollutant to test the electrode activity via monitoring the concentration changes by UV spectrophotometer. The results showed that the MnOx/Ti-350(20) electrode presented the best performance on decolorization of Acid Red B with the lowest cell potential during the process of electrochemical oxidation, and the chemical oxygen demand (COD) conversion was 50.7%. Furthermore, the changes of Acid Red B during the electrochemical oxidation process were proposed by the UV–vis spectra.

Improvement of Ti/RuO2–IrO2 Anode Lifetime and Electrocatalytical Properties by Using an Eco-Friendly Thermal Decomposition Method Using Polyvinyl Alcohol as Solvent

2019 ◽  
Author(s):  
Charlys Bezerra ◽  
Géssica Santos ◽  
Marilia Pupo ◽  
Maria Gomes ◽  
Ronaldo Silva ◽  
...  
Keyword(s):  
Thermal Decomposition ◽  
Polyvinyl Alcohol ◽  
High Efficiency ◽  
Electrochemical Impedance ◽  
Pechini Method ◽  
Low Cost ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Calcination Temperatures ◽  
Service Lifetime

<p>Electrochemical oxidation processes are promising solutions for wastewater treatment due to their high efficiency, easy control and versatility. Mixed metal oxides (MMO) anodes are particularly attractive due to their low cost and specific catalytic properties. Here, we propose an innovative thermal decomposition methodology using <a>polyvinyl alcohol (PVA)</a> as a solvent to prepare Ti/RuO<sub>2</sub>–IrO<sub>2</sub> anodes. Comparative anodes were prepared by conventional method employing a polymeric precursor solvent (Pechini method). The calcination temperatures studied were 300, 400 and 500 °C. The physical characterisation of all materials was performed by X-ray diffraction and scanning electron microscopy coupled with energy dispersive spectroscopy, while electrochemical characterisation was done by cyclic voltammetry, accelerated service lifetime and electrochemical impedance spectroscopy. Both RuO<sub>2</sub> and IrO<sub>2</sub> have rutile-type structures for all anodes. Rougher and more compact surfaces are formed for the anodes prepared using PVA. Amongst temperatures studied, 300 °C using PVA as solvent is the most suitable one to produce anodes with expressive increase in voltammetric charge (250%) and accelerated service lifetime (4.3 times longer) besides reducing charge-transfer resistance (8 times lower). Moreover, the electrocatalytic activity of the anodes synthesised with PVA toward the Reactive Blue 21 dye removal in chloride medium (100 % in 30 min) is higher than that prepared by Pechini method (60 min). Additionally, the removal total organic carbon point out improved mineralisation potential of PVA anodes. Finally, this study reports a novel methodology using PVA as solvent to synthesise Ti/RuO<sub>2</sub>–IrO<sub>2</sub> anodes with improved properties that can be further extended to synthesise other MMO compositions.</p>

scholarly journals Electrochemical Immunosensor for the Quantification of S100B at Clinically Relevant Levels Using a Cysteamine Modified Surface

Sensors ◽  
2021 ◽  
Vol 21 (6) ◽  
pp. 1929
Author(s):  
Alexander Rodríguez ◽  
Francisco Burgos-Flórez ◽  
José D. Posada ◽  
Eliana Cervera ◽  
Valtencir Zucolotto ◽  
...  
Keyword(s):  
Frequency Analysis ◽  
Surface Characterization ◽  
Electrochemical Impedance ◽  
Limit Of Detection ◽  
Neuronal Damage ◽  
Charge Transfer Resistance ◽  
Single Frequency ◽  
Response Analysis ◽  
Transfer Resistance ◽  
Therapeutic Decisions

Neuronal damage secondary to traumatic brain injury (TBI) is a rapidly evolving condition, which requires therapeutic decisions based on the timely identification of clinical deterioration. Changes in S100B biomarker levels are associated with TBI severity and patient outcome. The S100B quantification is often difficult since standard immunoassays are time-consuming, costly, and require extensive expertise. A zero-length cross-linking approach on a cysteamine self-assembled monolayer (SAM) was performed to immobilize anti-S100B monoclonal antibodies onto both planar (AuEs) and interdigitated (AuIDEs) gold electrodes via carbonyl-bond. Surface characterization was performed by atomic force microscopy (AFM) and specular-reflectance FTIR for each functionalization step. Biosensor response was studied using the change in charge-transfer resistance (Rct) from electrochemical impedance spectroscopy (EIS) in potassium ferrocyanide, with [S100B] ranging 10–1000 pg/mL. A single-frequency analysis for capacitances was also performed in AuIDEs. Full factorial designs were applied to assess biosensor sensitivity, specificity, and limit-of-detection (LOD). Higher Rct values were found with increased S100B concentration in both platforms. LODs were 18 pg/mL(AuES) and 6 pg/mL(AuIDEs). AuIDEs provide a simpler manufacturing protocol, with reduced fabrication time and possibly costs, simpler electrochemical response analysis, and could be used for single-frequency analysis for monitoring capacitance changes related to S100B levels.

scholarly journals Influence of HAP on the Morpho-Structural Properties and Corrosion Resistance of ZrO2-Based Composites for Biomedical Applications

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 202
Author(s):  
Réka Barabás ◽  
Carmen Ioana Fort ◽  
Graziella Liana Turdean ◽  
Liliana Bizo
Keyword(s):  
Electrochemical Impedance ◽  
Artificial Saliva ◽  
Synergetic Effect ◽  
Composite Layer ◽  
Charge Transfer Resistance ◽  
Processing Route ◽  
Dental Alloys ◽  
Metallic Electrode ◽  
Transfer Resistance ◽  
X Ray

In the present work, ZrO2-based composites were prepared by adding different amounts of antibacterial magnesium oxide and bioactive and biocompatible hydroxyapatite (HAP) to the inert zirconia. The composites were synthesized by the conventional ceramic processing route and morpho-structurally analyzed by X-ray powder diffraction (XRPD) and scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS). Two metallic dental alloys (i.e., Ni–Cr and Co–Cr) coated with a chitosan (Chit) membrane containing the prepared composites were exposed to aerated artificial saliva solutions of different pHs (i.e., 4.3, 5, 6) and the corrosion resistances were investigated by electrochemical impedance spectroscopy technique. The obtained results using the two investigated metallic dental alloys shown quasi-similar anticorrosive properties, having quasi-similar charge transfer resistance, when coated with different ZrO2-based composites. This behavior could be explained by the synergetic effect between the diffusion process through the Chit-composite layer and the roughness of the metallic electrode surface.

scholarly journals Corrosion behaviors of 316 stainless steel and Inconel 625 alloy in chloride molten salts for solar energy storage

2020 ◽  
Vol 39 (1) ◽  
pp. 340-350
Author(s):  
Mingjing Wang ◽  
Song Zeng ◽  
Huihui Zhang ◽  
Ming Zhu ◽  
Chengxin Lei ◽  
...  
Keyword(s):  
Stainless Steel ◽  
Molten Salt ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Inconel 625 ◽  
Transfer Resistance ◽  
316 Stainless Steel ◽  
Corrosion Rates ◽  
Inconel 625 Alloy ◽  
Corrosion Behaviors

AbstractCorrosion behaviors of 316 stainless steel (316 ss) and Inconel 625 alloy in molten NaCl–KCl–ZnCl2 at 700°C and 900°C were investigated by immersion tests and electrochemical methods, including potentiodynamic polarization and electrochemical impedance spectroscopy. X-ray diffraction and scanning electron microscopy/energy dispersive spectroscopy were used to analyze the phases and microstructures of the corrosion products. Inconel 625 alloy and 316 ss exhibited high corrosion rates in molten chlorides, and the corrosion rates of these two alloys accelerated when the temperature increased from 700°C to 900°C. The results of the electrochemical tests showed that both alloys exhibited active corrosion in chloride molten salt, and the current density of 316 ss in chloride molten salt at 700°C was 2.756 mA/cm−2, which is about three times the value for Inconel 625 alloy; and the values of the charge transfer resistance (Rt) for Inconel 625 were larger than those for 316 ss. The corrosion of these two alloys is owing to the preferred oxidation of Cr in chloride molten salt, and the corrosion layer was mainly ZnCr2O4 which was loose and porous and showed poor adherence to metal.

scholarly journals Combined Experimental and Theoretical Insights into the Corrosion Inhibition Activity on Carbon Steel Iron of Phosphonic Acids

Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 135
Author(s):  
Aurelia Visa ◽  
Nicoleta Plesu ◽  
Bianca Maranescu ◽  
Gheorghe Ilia ◽  
Ana Borota ◽  
...  
Keyword(s):  
Carbon Steel ◽  
Corrosion Inhibition ◽  
Density Functional ◽  
Energy Gap ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Phosphonic Acids ◽  
Transfer Resistance ◽  
Potential Map ◽  
Chlorine Ions

The inhibition effect of N,N′-phosphonomethylglycine (PMG) and vinyl phosphonic acid (VPA) on the 3% NaCl acidic solution corrosion of carbon steel iron was studied at different immersion times by potentiodynamic polarization, electrochemical impedance spectroscopy, attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, and computational methods. It is found from the polarization studies that PMG and VPA behave as mixed-type inhibitors in NaCl. Values of charge transfer resistance (Rct) and double layer capacitance (Cdl) in the absence and presence of inhibitors are determined. The PMG and VPA inhibitors were capable of inhibiting the corrosion process up to ≈91% and ≈85%, respectively. In the presence of PMG, the synergic effect of chlorine ions was observed. Density functional theory (DFT) was engaged to establish the adsorption site of PMG, VPA, and their deprotonated states. For studied compounds, the resulted values of ELUMO, EHOMO, energy gap (∆E), dipole moment (μ), electronic hardness (η), global softness (σ), electrophilic index (ω), and the electronic potential map are in concordance with the experimental data results regarding their corrosion inhibition behavior and adsorption on the metal surface.

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