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The purpose of this paper is to investigate, the effects of residual stress and microstructure on the corrosion behaviour of carburised 18CrNiMo7-6 steel in a 3.5% NaCl aqueous solution.

The electrochemical tests were conducted using an electrochemical workstation with a three-electrode system in a 3.5% NaCl aqueous solution, the residual stress of each working face was measured by a high-speed residual stress analyser, and microstructure of different carburised layers were observed scanning electron microscopy. Finally, the effect of carbon content, microstructure and residual stress on the corrosion behaviour of the steel was discussed.

The results showed that the residual compressive stress in the carburised layer initially increased and subsequently decreased with increasing depth of the carburised layer, reaching stability in the matrix layer. The electrochemical tests before and after stress reduction showed that the electrochemical impedance and the electrochemical potential increased with the reduction of residual compressive stress.

The residual compressive stress in the carburised layer initially increases and subsequently decreases with increasing carburised layer depth. The electrochemical impedance and the electrochemical potential increased with the reduction of residual compressive stress. The general relationship between electrochemical potential and residual stress was established.

This study aims to propose that the corrosion resistance of the neat epoxy coating can be further enhanced by incorporating reinforcing agents.

Chitosan, silica and their hybrid compound were used to study the subject of corrosion resistance of epoxy coating systems. This work used 3.5 Wt.% NaCl solution as the electrolyte, and electrochemical impedance spectroscopy (EIS) was used to investigate the electrochemical behaviour of the studied coating systems. Standard and accelerated states were used without and with scratch on the coating layer.

It was found that the impedance value of composite coating incorporated with the hybrid compound was significantly higher at 10¹⁰ Ω after 14 days of exposure in both testing states. The breakpoint frequency (f_b) determination also proves with large capacitive region at low-to-high frequency of impedance plots corresponding to the high corrosion resistance.

The hybrid compound consisting of chitosan as organic biopolymer and silica as inorganic material, respectively, served as a promising reinforcing agent for composite coating as a promising corrosion inhibitor. Different states of EIS measurement were used which are standard (without scratch) and accelerated (with scratch) states associated with the f_b values.

A new electrochemical analysis based on ß-cyclodextrin (ß-CD) was developed for penicillin V (Peni-V) using polyaniline as a conducting polymer.

The preparation of modified electrode involves the incorporation of β-CD with membrane of polyaniline. Polyaniline, incorporating β-CD, was prepared by electrochemical polymerization method in a medium of hypochloride. Cyclic voltammetry and electrochemical impedance have been used to characterize this sensor. The detection and the kinetic study of modified platinum electrode are evaluated.

Results clearly indicate that β-CDs interfere with the polymerization mechanism with an inhibition factor. The inclusion phenomenon of β-CDs has been studied and applied to detect Peni-V. The principle of this electrochemical sensor is based on the chemical properties of β-CD, which were studied using the cyclic voltammetric method and impedance spectroscopy. The electrochemical behavior of Peni-V at concentrations between 10^–8 and 10^–2 M was measured versus Ag/AgCl at pH 7.4 and 30°C in a phosphate alkaline buffer. Relationship of Peni-V concentration in logarithmic mathematical form with current in potentiometric method and with resistance in impedimetric method were obtained.

The present study showed that the Pt electrode modified with Polyaniline–β-CD was an excellent candidate for sensitive penicillin analysis. The proposed electroanalytical technique is rapid, simple and inexpensive.

This review provides an overview of recent advances in electrochemical sensors for analyte detection in saliva, highlighting their potential applications in diagnostics and health care. The purpose of this paper is to summarize the current state of the field, identify challenges and limitations and discuss future prospects for the development of saliva-based electrochemical sensors.

The paper reviews relevant literature and research articles to examine the latest developments in electrochemical sensing technologies for saliva analysis. It explores the use of various electrode materials, including carbon nanomaterial, metal nanoparticles and conducting polymers, as well as the integration of microfluidics, lab-on-a-chip (LOC) devices and wearable/implantable technologies. The design and fabrication methodologies used in these sensors are discussed, along with sample preparation techniques and biorecognition elements for enhancing sensor performance.

Electrochemical sensors for salivary analyte detection have demonstrated excellent potential for noninvasive, rapid and cost-effective diagnostics. Recent advancements have resulted in improved sensor selectivity, stability, sensitivity and compatibility with complex saliva samples. Integration with microfluidics and LOC technologies has shown promise in enhancing sensor efficiency and accuracy. In addition, wearable and implantable sensors enable continuous, real-time monitoring of salivary analytes, opening new avenues for personalized health care and disease management.

This review presents an up-to-date overview of electrochemical sensors for analyte detection in saliva, offering insights into their design, fabrication and performance. It highlights the originality and value of integrating electrochemical sensing with microfluidics, wearable/implantable technologies and point-of-care testing platforms. The review also identifies challenges and limitations, such as interference from other saliva components and the need for improved stability and reproducibility. Future prospects include the development of novel microfluidic devices, advanced materials and user-friendly diagnostic devices to unlock the full potential of saliva-based electrochemical sensing in clinical practice.

Aims to evaluate the impedance of a rapidly‐evolving corrosion cell by developing an alternative method to the traditional frequency domain method, and to present a new method to analyze the coulostatically‐induced transient (CIT).

The coulostatic impulse signal was used to obtain the CIT. By transforming the CIT from the time domain into the frequency domain, the coulostatically induced impedance spectrum (CIS) can be obtained, which contributes to the evaluation of the impedance of the electrode and of its corrosion processes. The equations for the coulostatic response also can be obtained by using network analysis in the Laplace domain.

Obtaining the CIS of an electrode in the time domain can facilitate accurate evaluation of metal corrosion rate in a rapidly evolving system. Compared with the traditional method for deriving CIT equations, the proposed method based on network analysis is convenient for more complex circuit models to obtain the CIT equation.

It is difficult to obtain an impedance spectrum over a wide range of frequencies by the coulostatic measurement at one time, which perhaps limits its usefulness in systems with longer time constants.

The proposed method is advantageous compared with traditional analysis methods of CIT, because analysis of CIS can be conducted using commercial software and dispenses with the need for personal software to be developed, which greatly facilitates the interpretation of the coulostatic measurements involving multi‐time constants.

It is possible that the present work may pave the way for further work to investigate more complex corrosion systems by means of CIS.

This study aims to investigate the electrochemical corrosion performance of high velocity oxygen fuel (HVOF) sprayed WC–12Co coating in 3.5 Wt.% NaCl solution, which provided a guiding significance on the corrosion resistance of H13 hot work mould steel.

A WC–12Co coating was fabricated on H13 hot work mould steel using a HVOF, and the electrochemical corrosion behaviors of WC–12Co coating and substrate in 3.5 Wt.% NaCl solution was measured using open circuit potential (OCP), potentiodynamic polarization curve (PPC) and electrochemical impedance spectroscopy (EIS) tests.

The OCP and PPC of WC–12Co coating positively shift than those of substrate, its corrosion tendency and corrosion rate decrease to enhance its corrosion resistance. The curvature radius of capacitance curve on the WC–12Co coating is larger than that on the substrate, and the impedance and polarization resistance of WC–12Co coating increase faster than those of substrate, which reduces the corrosion process.

The electrochemical corrosion behaviors of WC–12Co coating and substrate in 3.5 Wt.% NaCl solution is first measured using OCP, PPC and EIS tests, which improve the electrochemical corrosion resistance of H13 hot work mould steel.

Coral aggregate seawater concrete (CASC) is a new type of lightweight aggregate concrete that is becoming widely used in reef engineering. To investigate the corrosion behavior of different kinds of rebar in CASC exposed to simulated seawater for 0-270 d, the electrochemical techniques, including linear polarization resistance (LPR) technique and the electrochemical impedance spectroscopy (EIS), were used in the present work.

The electrochemical techniques, including LPR technique and the EIS, were used in the present work.

Based on the time-varying law of linear polarization curves, self-corrosion potential (E_corr), polarization resistance (R_p), corrosion current density (I_corr), corrosion rate (i), and the characteristics of EIS diagrams for different types of rebar in CASC, it can be found that the anti-corrosion property of them can be ranked as epoxy resin coated steel > 2205 duplex stainless steel (2205S) > 316 L stainless steel (316 L) > organic coated steel > ordinary steel. Additionally, the linear regression equation between R_p and charge transfer resistance (R_ct) was established. Finally, the EIS corrosion standard of rebar was established from the LPR corrosion standard, which provides a direct standard for the EIS technique to determine the condition of rebar in CASC.

The linear regression equation between polarization resistance and charge transfer resistance was established. And the EIS corrosion standard of rebar was established from the LPR corrosion standard, which provides a direct standard for the EIS technique to determine the condition of rebar in CASC.

The purpose of this paper is to develop a real-time methodology to detect damages in coating and metallic structure in buried pipelines by using DC bias added to AC signal under field operation conditions, including cathodic protection.

Impedance measurements were performed on buried pipeline for different field conditions, to develop a methodology to detect and locate damages by impedance distribution along the metallic structure.

Field condition measurements were conducted as a pilot test on a buried steel pipeline segment with a diameter of 16 inches and length of 20 km. The frequency-based technology shows some differences but overall good behavior between impedance magnitudes vs localization of the interface changes at the soil-coating-steel interface at different frequencies using DC bias added to AC signal under field operation conditions, including cathodic protection.

The methodology is not applicable to highly resistive soil or high degradation coatings.

In this work, we depict a methodology that describes real time monitoring technology for buried metallic structures using AC signal. This monitoring is capable to detect and locate real time damage occurrences on the pipe surface (coating break). Field measurements include different conditions, such as temperature, soil resistivity and soil physical structure and chemical composition.

In consideration of the satisfied application in the field of the methodology, it is believed that it can be used for the monitoring of damages in pipes in areas with high consequences and hence pipe integrity can be increased.

This real-time methodology is based on the impedance distribution signal and the differential changes along the pipeline under operating conditions. The results showed good agreement with the proposed methodology, which is able to discriminate some situations inherent of field conditions by using different impedance measurements performed along ±10 km of buried steel pipeline and assuming the reference location as the cathodic protection set up.

Electrochemical impedance spectroscopy has become a very important tool in the analysis of an equivalent circuit of an electrochemical cell. Recently a new model was proposed by Taylor and Gileadi for the better understanding of the Warburg process. The model describes an equivalent circuit consisting of capacitance in series with resistance to replace the conventional Warburg impedance in the Randels equivalent circuit. Discusses the above model highlighting the defects in their assumption. Attempts to find a better understanding of the Warburg impedance and discusses various possibilities.

The purpose of this paper is to focus on diversification between electrical parameters determined on the basis of instantaneous impedance measurements within the activation and reactivation scan of dissolution of sensitized AISI 304 stainless steel during a proceeding intergranular corrosion process.

The investigations were carried out by means of dynamic electrochemical impedance spectroscopy (DEIS). DEIS measurements were conducted “on‐line” while the samples were polarized in agreement with a measurement procedure presented in the ASTM G108‐94 standard, in order to guarantee conditions equivalent with the DL‐EPR tests performed on AISI 304 stainless steel.

Performed researches revealed the advantages of the DEIS technique over standard double‐loop electrochemical potentiokinetic reactivation (DL‐EPR) tests in the field of intergranular corrosion investigations. Application of the DEIS technique made it possible to trace instantaneous changes in the examined system's impedance versus potential during the intergranular corrosion process. The form of recorded DEIS spectra and obtained distribution of measurement frequencies within the reactivation potential range were equivalent to those obtained for pure iron dissolution in sulfuric acid medium. As a result, instantaneous changes of electrical double layer capacitance and charge transfer resistance as a function of potential have been obtained in the range of activation and reactivation scans.

The paper provides information regarding diversification between the electrical double layer capacitance and the charge transfer resistance determined for sensitized AISI 304 stainless steel with respect to polarization conditions during the standard DL‐EPR test, which were obtained in order to evaluate the susceptibility to intergranular corrosion.