Early Debonding Detection of Rebar-Concrete Interface due to External Loading Utilizing AC Impedance Spectroscopy

A novel method for detecting early damage at the steel-concrete interface due to external loading based on AC impedance spectroscopy technology was proposed.Firstly,alkali pretreatment was introduced to ensure the accuracy and repeatability of the AC impedance test.Secondly,the AC impedance spectroscopy between the steel bar and concrete surface of different bonding positions was tested,and then the physical quantities reflecting the bonding damage condition were obtained by equivalent circuit fitting.Theoretical debonding position calculation and AC conductive structure analysis indicate that the change of interface resistance and interface capacitance can seize the development of bonding damage during the loading process.As the interface damage develops,obvious changes in interface resistance and interface capacitance are observed,and they cannot be recovered after unloading.

Degradation diagnosis of lithium-ion batteries using AC impedance technique in fixing the state of charge of an electrode

A sustainable society requires an increase in electrified vehicles(xEVs) with a low environmental impact. Among various types of xEVs, battery electric vehicles (BEVs) with lithium-ion batteries(LIBs) have received considerable research attention.

Hydration Process of Cement-Based Materials by AC Impedance Method

AC impedance is a new method to study the changes of pore structure and the hydration degree during the hydration and hardening process of cement paste by the change of the electrochemical parameters. Employing AC impedance method, we studied the hydration and hardening process of cement paste with fly ash and slag, and analyzed the influence of different hydration age, water-binder ratio and mineral admixture on the impedance parameters. Moreover, we compared the results with those by the conventional porosity testing method and X-ray diffraction method. The results showed that AC impedance could be taken as a new technology in cement and concrete research.

AC IMPEDANCE OF PHENYL ISO-THIOCYANATE ADSORBED ON PT ELECTRODE

The paper presents ac impedance behaviours of phenyl iso-thiocyanate adsorbed on Pt electrode.Nyquist plots are analysed and simulated,and parameters of relative equivalent circuits are obtained.

Impedance Characteristics of MgO-ZrO_2 Ceramics Doped with CeO_2

The ultrafine CexMg0.06Zr1-xO1.94 （ x = 0 16% ） powders were synthesized by a chemical co-precipitated method. The pressed compacts were sintered in air at 1300, 1400, 1500, 1600℃ for 3 h, respectively. The phase of the ceramics was characterized by the X-ray diffraction （XRD） method. The conductivity of the ceramics was measured by the AC complex impedance technique at 700- 1200 ℃. The ratio of the cubic phase in the ceramics improves with increasing CeO2 content, leading to a enlargement of the oxygen ionic migration channel. The contact resistance between conductive phase particles decreases with increasing CeO2 content, leading to a lower migration hindrance of the oxygen ionic. Consequently, the ionic conductivity of the ceramics improves with increas- ing CeO2 content. Additionally, an analysis for this phenomenon was also presented.

AC IMPEDANCE STUDY OF HYDROGEN STORAGE ELECTRODES

The impedance diagram of hdrogen storage electrodes(AH electrodes )displayed twosemicircles.Thelow frequency one is affected by cycle number and composition of MH electrodes.

Study of the electrochemical properties of a transition metallic ions modified electrode in acidic VOSO_4 solution

Graphite material was used as the electrode for an all-vanadium redox flow battery, and the electrode was modified by transition metallic ions to enhance its electrochemical behavior. An porous graphite composite electrode has high specific surface area and high current density. The electrode modified by transition metallic ions has improved catalysis behavior that can catalyze the V（Ⅱ）-V（Ⅴ） redox reaction showed by cyclic voltammograms. This article studied the impedance of the modified electrode by electrochemical impedance spectroscopy （EIS）, and approved that the electrode modified by Co^2＋ and Mn^2＋ has a lower charge transfer resistance than the non-modified electrode. The effect of average particle size distribution is at lower frequencies that the slope of Warburg impedance is reduced by large particle size distribution. The voltage efficiency of the Co^2＋ modified electrode test cell is 81.5%, which is higher than that of the non-modified electrode.

Passivation Mechanism of 316L Stainless Steel in Oxidizing Acid Solution

The compositions and the chemical valence states of elements of 316L stainless steel passive film formed in the oxidizing acid solution were studied by X-ray Photoelectron Spectroscopic (XPS) analysis. The electrochemical polarization curve was measured. The passivation process in the oxidizing acid solution was studied by AC impedance technology. The results indicated that the stable compounds layer was formed on the surface of the sample and the adsorption was the main step in the nitrite solution during passivation process. The catalysis passivation mechanism was put forward according to the experimental results. During passivation process, the water molecule was adsorbed on the surface of the sample at first in the oxidizing acid solution. The oxidizer in the solution played a role as catalyst. The oxide and hydroxide, which could be changed each other and finally formed stable passive film, were generated from adsorbing intermediate under the catalytic action. The mathematical models for predicting the steady polarization curve and the AC impedance spectra at certain conditions have been obtained. The passivation mechanism of 316L stainless steel in the oxidizing acid solution can be interpreted by the catalysis passivation mechanism.

Structure and resistance of concentration polar layer on cation exchange membrane-solution interface

Membrane/solution interface consists of a neutral concentration polai layer(CPL) and a charge layer(CL) under external electrical field, and the neutral CPL can be neglected under high frequency AC electrical field. The relationship of CL thickness e with electrolyte concentration C and fixed ion exchange sites density σ in membrane surface layer can be expressed as e

Mixed Conduction in BaCe0.8Pr0.2O3-α Ceramic

BaCe0.8Pr0.2O3-α ceramic was synthesized by high temperature solid-state reaction. The structural characteristics and the phase purity of the crystal were determined using powder X-ray diffraction analysis. By using the methods of AC impedance spectroscopy, gas concentration cell and electrochemical pumping of hydrogen, the conductivity and ionic transport number of BaCe0.8Pr0.2O3-α were measured, and the electrical conduction behavior of the material was investigated in different gases in the temperature range of 500-900℃. The results indicate that the material was of a single perovskite-type orthorhombic phase. From 500℃ to 900 ℃, electronic-hole conduction was dominant in dry and wet oxygen, air or nitrogen, and the total conductivity of the material increased slightly with increasing oxygen partial pressure in the oxygen partial pressure range studied. Ionic conduction was dominant in wet hydrogen, and the total conductivity was about one or two orders of magnitude higher than that in hydrogen-free atmosphere （oxygen, air or nitrogen）

Anodic Layer of Pb-Ca-Sn-Ce Alloy for Maintenance-Free Lead/Acid Batteries

The anodic films of novel Pb-Ca-Sn-Ce alloy, traditional Pb-Ca-Sn and Pb-Sb alloys formed in sulfuric solution at anodic +0.9 V potential corrosion for 6 h were investigated by means of XPS, XRD methods and AC impedance measurement. The results show that the growth of Pb(Ⅱ) oxide on the new Pb-Ca-Sn-Ce alloy surface is inhibited. The AC impedance measurement shows that resistance of the corrosion layer of novel Pb-Ca-Sn-Ce alloy decreases. It is found that the novel Pb-Ca-Sn-Ce alloy can encourage the development of PbO2 in the scale, and enhance the conductivity of the anodic scale. Hence the deep recycling properties of the battery can be expected better.

The Phenomenon of Mutual Media in Polypyrrole with Electroactive Ions

The dependence of the differential capacitance of polypyrrole doped with several typical dopants on potential is presented, which shows that the differential capacitance varies with the potential, the doped polypyrroles with electroactive ions give the largest capacitance near their formal potentials, which is attributed to the mutual media for electron transfer between polypyrrole and electroactive dopants. The existence of two conducting phases was observed in the complex capacitance plots. The electroactive anions act as an intraconductingphase medium for electron transfer, the electroactive cations act as an interconductingphase medium for electron transfer. The mutual media between polypyrrole and redox dopants lead to the increase of the discharging time.

Impedance Spectroscopic Study on Room Temperature Ionic Liquid-Water Mixtures

AC impedance spectroscopy in pure room temperature ionic liquids （RTILs） and RTIL-water mixture was measured at the temperature of range from 30 ℃ down to -30 ℃. The cations of RTILs are N,N-diethyl-N-methyl-N-（2-methoxyethyl） ammonium （[DEME]）, 1-ethyl-3-methylimidazolium （[C2mim]） and l-butyl-3-methylimidazolium （[Camim]）, the anions are tetrafluoroborate （[BF4]） and bis（trifluoromethanesulfonyl）imide （[TFSI]）. In all pure RTILs, there are two kinds of local minima in real part of the AC impedance Zreal. By adding water to [DEME][BF4] （0 mol% 〈 x 〈 94 mol%） at room temperature, the local minimum value at higher frequency decreased remarkably at the fixed frequency with increasing water concentration. Above 94 mol% H20, a quite different profile of the AC impedance spectroscopy was obtained. In addition to Zreal. temperature dependence of an imaginary part of the impedance Zimag had an isosbestic point below 94 mol%. The isosbestic point disappeared above 94 mol%. The isosbestic point in Zing reveals an interaction between [DEME][BFa] and H2O.

An Experimental Study on Constant Current Load Test of Reinforced Concrete based on 3D Paraffin Isolation

Aiming at the complex corrosion degradation factors of reinforced concrete and clearing the deterioration mechanism in the constant stress state,a new type of constant current accelerated corrosion method in the saline soil environment was developed.The three-dimensional paraffin isolation specimens and the three-dimensional penetration specimens were taken as the research objects,and the Cl−content and AC impedance Bode diagram were measured.The macro morphology and micro analysis were also used to evaluate the corrosion degradation laws of the two groups of specimens.A constant current three-factor system accelerated model was established for the current acceleration factor,chloride ion,and sulfate ion acceleration factor.The experimental results show that,in the constant stress test of the saline soil environmental conditions,the paraffin isolation layer can effectively isolate corrosive chloride ions,which is a brand-new research method of single factor variable control in the constant stress test.According to the basic corrosion data,the law of constant current acceleration test is summarized and divided into five corrosion degradation stages,and each stage has significant changes in the accelerated corrosion efficiency.The corrosion degradation of a constant stress test is the combined effect of constant current,positive and negative penetration of chloride ions and sulfate ions.

Structures,dielectric properties and AC impedance characteristics of BiFeO_(3)–BaTiO_(3)high-temperature lead-free piezoceramics synthesized by the hydrothermal method

Among the lead-free piezoceramics,(1-x)BiFeO_(3)-xBaTiO_(3)(BF-BT)is considered a promising candidate for high-temperature piezoelectric materials owing to its high Curie temperature(TC>400℃)and good electromechanical properties.In this work,the hydrothermal synthesis method was used to prepare the precursor powders of BiFeO_(3)and BaTiO_(3),and then the mixed powder compacts with the chemical composition of 0.7BF–0.3BT were sintered under pressureless conditions.The influence of the hydrothermal reaction times(12–24 h)of BiFeO_(3)on the structures and electric properties of the sintered ceramics was instigated.First,all the samples synthesized with the tetragonal BaTiO_(3)and BiFeO_(3)powders were identified with relatively stable dielectric properties.As the hydrothermal reaction time to synthesize BiFeO_(3)increased,the dielectric properties as well as the temperature stability of the 0.7BiFeO_(3)–0.3BaTiO_(3)ceramics also improved.At the condition of a hydrothermal reaction time of 24 h,the sample obtained possesses both the lowest temperature coefficient of dielectric constant(Tkε=1.53×10^(-2)=℃between RT and 300℃)and the highest Curie temperature(TC?471℃at 100 kHz).Moreover,at high temperatures,it exhibits a higher AC impedance than others.The calculating result based on the resistive constant-phase-element model(R-CPE)circuit model showed that the grain boundary of the 0.7BF–0.3BT ceramics contributes more resistance to the conductivity at high temperatures.In summary,the hydrothermal reaction proved to be a useful way that achieves the preparation of single-phase 0.7BF–0.3BT ceramics with improved electrical properties.

Direct Synthesis of High Purity Silicon Wires by Electrorefining in Molten KF-NaF Eutectic

The electrochemical synthesis silicon wires by electrorefining metallurgical grade silicon in thermally dried and pre-electrolyzed molten KF-NaF eutectic were studied at temperatures 800-900 ℃ using cyclic voltammetry and ac impedance. One oxidation peak at -0.14 V could be attributed to the reaction of Si to Si4＋. A cathodic peak occurred at -0.56 V in the cyclic voltammogram and one response semicircle in the ac impedance spectrum was observed, supporting a one-step electrochemical reduction process of Si4＋-→Si. The electrochemical reaction of silicon was controlled by the diffusion process. The purity of electrorefined silicon wires was up to 99.999% by ICP-MS analysis.

Dielectric Properties of Self-assembled Monolayers of Dithiols

Dielectric properties of dithiol self-assemble monolayers （SAMs） under ac electric field were presented, Using a Hg-SAM/SAM-Ⅱg junction, the ac impedances of dithiol SAMs were measured using a sinusoidal perturbation of 30 mV （peak to-peak） with the frequency ranging from 1 Hz to 1 MHz at zero bias. The contributions from dithiol SAMs and solvent interlayers were separated due to their different behaviors at ac impedance. The peak position in the loss spectra （the plot; of tgδ vs. frequency） moves to low frequcney with the incrcase of chain length of dithiols. Using a correlation of peak position with the chain length, the active energies of 23-39 meV for dithiol SAMs of C6-C10 under an ac electric field were derived,

Electrical conductivity of MO(MO=FeO,NiO)-containing CaO-MgO-SiO_2-Al_2O_3 slag with low basicity

As a fundamental study on recovery of valuable metals from nonferrous metallurgical slags,electrical conductivity values of MO（MO=FeO,NiO）-containing CaO-MgO-SiO2-Al2O3 slag with a low basicity were measured at different temperatures using AC impedance spectroscopy.The result shows that the electrical conductivity increased from 1.4 S/m to 14.4 S/m with the increase of the temperature from 1 573 to 1 773 K and the content of MO which is less than 12% under the constant mass ratio of （CaO＋MgO） to （SiO2＋Al2O3） of 0.47.Moreover,the increase magnitude of the electrical conductivity was also promoted with the increase of the content of MO.The electrical conductivity of FeO-containing slags was close to that of NiO-containing slags when the content was less than 8%;however,it was obviously larger than that of NiO-containing slags when the content was 12%.The activation energy of the electrical conductivity decreased with the increase of MO content.

Effect of Cerium on Gas Evolution Behavior of Pb-Ca-Sn Alloy

The effect of Ce on the behavior of gas evolution on Pb-Ca-Sn alloy in 4.5 mol·L^-1 H2SO4 was investigated using cyclic voltammetry （CV）, cathodic polarization curves and AC impedance （EIS）. Cyclic voltammetry experiments show that the current of oxygen evolution on Pb-Ca-Sn-Ce electrode is lower than that of Pb-Ca-Sn electrode in the same anodic voltage. Moreover, the oxygen evolution potential on the former electrode is greater than that on the latter, and this means that Ce can increase the potential of oxygen evolution on Pb-Ca-Sn alloy. The AC impedance experiments show that Ce can also enhance the resistance of hydrogen evolution on Pb-Ca-Sn electrode, i.e., Ce can inhibit the hydrogen evolution on Pb-Ca-Sn electrode. The reason why Ce decreases the volume of hydrogen evolution on Pb-Ca-Sn alloy is that Ce increases the resistance of absorbing step of hydrogen evolution reaction. All the experimental results indicate that Pb-Ca-Sn-Ce alloy can rapidly decrease the oxygen and hydrogen evolution on Pb-Ca-Sn-Ce alloy. It is concluded that Pb-Ca-Sn-Ce alloy can promote the maintenance-free property of lead acid battery, and can serve as the candidate of the grid material for maintenance-free lead acid battery.