Relevant bibliographies by topics / Electrochemical measurement

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Electrochemical measurement'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 March 2023

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Journal articles on the topic "Electrochemical measurement"

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Hara, Takeshi, Yuta Kinoshita, Hiroki Yamamoto, and Masumi Ogishima. "Fabrication of a Fundamental Electrochemical Measurement System for an Electrochemical Sensor." Journal of the Institute of Industrial Applications Engineers 10, no. 4 (October 26, 2022): 72–76. http://dx.doi.org/10.12792/jiiae.10.72.

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Park, Su-Moon, Jung-Suk Yoo, Byoung-Yong Chang, and Eun-Shil Ahn. "Novel instrumentation in electrochemical impedance spectroscopy and a full description of an electrochemical system." Pure and Applied Chemistry 78, no. 5 (January 1, 2006): 1069–80. http://dx.doi.org/10.1351/pac200678051069.

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The evolution of impedance measurement methods into the current state of the art is reviewed briefly, and recent efforts to develop new instruments to make electrochemical impedance spectroscopy (EIS) measurements faster and more accurate are described. The most recent approach for impedance measurement uses a multichannel detection technique, which is analogous to a spectroscopic measurement such as in Fourier transform infrared spectroscopy. This method, which is capable of making impedance measurements in real time during an electrochemical experiment, allows us to come up with a new integrated equation that makes a full description of an electrochemical system possible.
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Anseth, Ronnie, Nils-Olav Skeie, and Magne Waskaas. "The effect of precipitation and deposition layer growth on impedance measurements." tm - Technisches Messen 86, no. 1 (January 28, 2019): 25–33. http://dx.doi.org/10.1515/teme-2018-0062.

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AbstractThe objective of the study was to examine how precipitation and deposition layer growth in an electrochemical cell impact impedance measurements. A measurement system, based on Electrochemical Impedance Spectroscopy (EIS), was used to observe the impedance of an electrochemical cell while precipitation was occurring. The measurement system was also used together with measurements of the solution concentration (in parts per million, ppm) to examine what impact deposition layer growth has on an electrochemical cell. Experimental results indicate a measurable change in the impedance magnitude as the ionic concentration is altered through precipitation. A change in both impedance magnitude and the interfacial capacitance was observed when a deposition layer was established within an electrochemical cell. Results show that impedance measurements are susceptible to changes in solution conductivity and to the presence of a deposition layer in an electrochemical cell. Impedance measurements may be used as an indicator for deposition layer growth, but changes in the solution concentration should be considered when creating a model.
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Periasamy, Vengadesh, Prince Nishchal Narayanaswamy Elumalai, Sara Talebi, Ramesh T. Subramaniam, Ramesh Kasi, Mitsumasa Iwamoto, and Georgepeter Gnana kumar. "Novel same-metal three electrode system for cyclic voltammetry studies." RSC Advances 13, no. 9 (2023): 5744–52. http://dx.doi.org/10.1039/d3ra00457k.

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Dražić, D. M., and J. P. Popić. "Electrochemistry of Active Chromium: Part 1—Anomalous Corrosion and Products of Chromium Dissolution in Deaerated Sulfuric Acid." Corrosion 60, no. 3 (March 1, 2004): 297–303. http://dx.doi.org/10.5006/1.3287734.

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Abstract Chromium corroding in deaerated aqueous solution of sulfuric acid (H2SO4; pH 1 to 3) produces Cr(II) and Cr(III) ions simultaneously in the ratio 7:1, as well as H2. The corrosion potentials of electrochemically activated chromium are determined by the electrochemical processes as expected according to the Wagner-Traud model. However, the real rates of chromium corrosion determined by collecting evolved hydrogen, spectrophotometric determination of the accumulated Cr ions in the solution, or by weight-loss measurements are higher than the electrochemical dissolution rate by up to 12 times for pH 1.0. The effect is smaller for higher pH. This was due to the simultaneous “anomalous” (or chemical) dissolution process of the direct chemical reaction of Cr with H2O molecules, as proposed some time ago by Kolotyrkin and coworkers. Since “anomalous” dissolution cannot be detected by electrochemical means, it has been pointed out that in the presence of “anomalous” dissolution processes during metal corrosion, electrochemical corrosion rate measurements should be taken only as approximate, while the level of approximation should be determined by some other direct corrosion rate measurement method.
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Ikeda, Hikaru, Satohiro Itagaki, Shigeki Nishii, Yojiro Yamamoto, Yasuhiro Sadanaga, and Hiroshi Shiigi. "Electrochemical measurement of microbial activity." Review of Polarography 68, no. 1 (May 19, 2022): 15–25. http://dx.doi.org/10.5189/revpolarography.68.15.

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Saito, Shunsuke, Satoshi Sunada, Mitsuaki Furui, Susumu Ikeno, and Seiji Saikawa. "Electrochemical Behavior of Mg-6mass%Al Alloy Corroded in Na2SO4 and NaCl Solutions." Advanced Materials Research 409 (November 2011): 368–72. http://dx.doi.org/10.4028/www.scientific.net/amr.409.368.

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The corrosion behavior of Mg-6mass%Al alloy with different microstructure conditions was studied by electrochemical method in Na2SO4 and NaCl solutions. A measurement of polarization curves was carried out in order to investigate the fundamental electrochemical characteristics. Electrochemical impedance spectroscopy was carried out to discuss the corrosion characteristics that were obtained from polarization curves. Electrochemical measurements were carried out with as-cast, as solution-treated and two kinds of aged specimens, respectively. For measurement of polarization curves, the apparent difference was exhibited in behavior showing the pitting corrosion by difference of solutions. In all specimens, the corrosion current density which occurred in four kinds of specimens was higher in the NaCl solution than in Na2SO4 solution.
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Kurihara, Kazue. "Surface forces measurement for materials science." Pure and Applied Chemistry 91, no. 4 (April 24, 2019): 707–16. http://dx.doi.org/10.1515/pac-2019-0101.

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Abstract This article reviews the surface forces measurement as a novel tool for materials science. The history of the measurement is briefly described in the Introduction. The general overview covers specific features of the surface forces measurement as a tool for studying the solid-liquid interface, confined liquids and soft matter. This measurement is a powerful way for understanding interaction forces, and for characterizing (sometime unknown) phenomena at solid-liquid interfaces and soft complex matters. The surface force apparatus (SFA) we developed for opaque samples can study not only opaque samples in various media, but also electrochemical processes under various electrochemical conditions. Electrochemical SFA enables us to determine the distribution of counterions between strongly bound ones in the Stern layer and those diffused in the Gouy-Chapman layer. The shear measurement is another active area of the SFA research. We introduced a resonance method, i.e. the resonance shear measurement (RSM), that is used to study the effective viscosity and lubricity of confined liquids in their thickness from μm to contact. Advantages of these measurements are discussed by describing examples of each measurement. These studies demonstrate how the forces measurement is used for characterizing solid-liquid interfaces, confined liquids and reveal unknown phenomena. The readers will be introduced to the broad applications of the forces measurement in the materials science field.
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Chapin, Ashley Augustiny, Jinjing Han, and Reza Ghodssi. "Adsorption Kinetic Model Predicts and Improves Reliability of Electrochemical Serotonin Detection." Methods and Protocols 6, no. 1 (January 9, 2023): 6. http://dx.doi.org/10.3390/mps6010006.

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Serotonin (5-HT) is a neurotransmitter involved in many biophysiological processes in the brain and in the gastrointestinal tract. Electrochemical methods are commonly used to quantify 5-HT, but their reliability may suffer due to the time-dependent nature of adsorption-limited 5-HT detection, as well as electrode fouling over repeated measurements. Mathematical characterization and modeling of adsorption-based electrochemical signal generation would improve reliability of 5-HT measurement. Here, a model was developed to track 5-HT electrode adsorption and resulting current output by combining Langmuir adsorption kinetic equations and adsorption-limited electrochemical equations. 5-HT adsorption binding parameters were experimentally determined at a carbon-nanotube coated Au electrode: KD = 7 × 10−7 M, kon = 130 M−1 s−1, koff = 9.1 × 10−5 s−1. A computational model of 5-HT adsorption was then constructed, which could effectively predict 5-HT fouling over 50 measurements (R2 = 0.9947), as well as predict electrode responses over varying concentrations and measurement times. The model aided in optimizing the measurement of 5-HT secreted from a model enterochromaffin cell line—RIN14B—minimizing measurement time. The presented model simplified and improved the characterization of 5-HT detection at the selected electrode. This could be applied to many other adsorption-limited electrochemical analytes and electrode types, contributing to the improvement of application-specific modeling and optimization processes.
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Othman, Ali. "2021 Colin Garfield Fink Postdoctoral Summer Fellowship – Summary Report Luciferase – Functionalized 3D Highly Porous Gold-based Electrochemical Biosensors." Electrochemical Society Interface 30, no. 4 (December 1, 2021): 36–37. http://dx.doi.org/10.1149/2.f08214if.

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Recent advances in electrochemical biosensors have focused on new materials and strategies to improve specificity, sensitivity, stability, and response time. Herein, we aim to develop an electrochemical biosensor device by modification of a screen-printed electrode (SPE) with highly porous Au nanostructures and a bioluminescence (BL)-producing enzyme (luciferase). This approach leverages the enhanced electrochemically active surface area and the mass transport effect and offers an alternative configuration for optical output from the enzyme. The BL presents an instantaneous measurement of enzyme activity and can be exploited to show that the enzyme is being electrochemically controlled (an ON-OFF switchable sensor).
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Dissertations / Theses on the topic "Electrochemical measurement"

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Sritongkam, Pornpimol. "Electrochemical measurement of polycyclic aromatic hydrocarbons." Thesis, Cranfield University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274039.

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Groeber, Elizabeth A. "Electrochemically generated transient gratings: The measurement of diffusion coefficients of electrochemical reaction products /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487946103567997.

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Goodwin, Stefan. "Fabrication and measurement of graphene electrochemical microelectrodes." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/fabrication-and-measurement-of-graphene-electrochemical-microelectrodes(68041aff-f4b6-4562-b807-dd547ef9c002).html.

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The electrochemical properties of graphene were investigated using a novel and clean method to fabricate device structures with mechanically exfoliated graphene samples. Graphene is known as being particularly sensitive to both contaminating fabrication methods and the substrate it is placed on, with these effects being detrimental to accurate research into the fundamental properties and sensing applications of graphene. This thesis presents micron scale graphene electrodes that have not been subject to polymer contamination or micro-lithography methods. The effect of utilising atomically flat hexagonal boron nitride as a substrate material was investigated, believed to be the first example of this for graphene electrochemical measurements. Cyclic voltammetry demonstrated the expected steady-state behaviour for microelectrodes in the hemispherical diffusion regime. The reduction of IrCl62- in weak KCl electrolytes was studied to investigate the electron transfer characteristics of the graphene devices and the reproducibility of the measurements. Average values of the standard rate constant, k0 and the transfer coefficient, alpha were found to be 3.04 ± 0.78 ×10-3 cms-1 and 0.272 ± 0.024 respectively. These values differ significantly from previous similar studies, with the effect of reduced charge doping from the substrate and the potential dependence of the density of electronic states thought to account for the differences. Despite the clean fabrication methods, a relatively large variation between separate devices was found, highlighting an inherent variation in the properties of graphene samples.
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Keay, Russell Warren. "Electrochemical sensors for measurement of water pollutants." Thesis, University of Newcastle Upon Tyne, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263016.

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Lowe, Alexander M. "Estimation of electrochemical noise impedance and corrosion rates from electrochemical noise measurements." Thesis, Curtin University, 2002. http://hdl.handle.net/20.500.11937/209.

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Electrochemical noise refers to the spontaneous fluctuations in potential and current that can be observed on a corroding metal. The use of electrochemical noise for obtaining information on the corrosion process generates much interest in research fields. One important application is the measurement of corrosion rate. This can be achieved using the electrochemical noise of a pair of electrically coupled corroding metals to obtain an estimate of electrochemical impedance - an abstract quantity that reflects various aspects of the corrosion process.There are a number of problems associated with estimation of impedance information from the electrochemical noise data, particularly regarding data pre-treatment, accuracy and precision. In addition, the present methods are incomplete: current literature does not offer information regarding the phase of the impedance; and assumptions regarding symmetry of an electrode pair cannot be tested without additional measurements.The thesis addresses the above mentioned problems. Specifically,analysis of the impedance estimation process is given to determine how precision can be affected by various factors;a novel signal processing technique is described that is shown to yield a local optimum precision;the application of the proposed signal processing to time varying systems is demonstrated by use of a time varying, frequency dependent impedance estimate;a technique for recovering phase information, given certain conditions, is suggested so that Nyquist impedance diagrams can be constructed; anda technique for testing the symmetry of a coupled pair of corroding metals is described.An integral part of electrochemical noise analysis is the software used for numerical computation. The Matlab package from MathWorks inc. provides an extensible platform for electrochemical noise analysis. Matlab code is provided in Appendix A to implement much of the theory discussed in the thesis.Impedance analysis and many other electrochemical corrosion monitoring techniques are primarily used for uniform corrosion, where the corrosion patterns occur uniformly over the exposed surface. In order to map localised corrosion, where the corrosion is typically concentrated within a small area, a wire beam electrode can be used. A wire beam electrode is a surface that is divided into a matrix of mini-electrodes so that the corrosion rate at different points can be monitored. However, manual connection of each mini-electrode to the measurement device can prove cumbersome. The final chapter of this thesis describes the design and testing of specialised multiplexing hardware to automate the process.In general, the thesis shows that by careful conditioning of the electrochemical noise prior to analysis, many of the problems with the technique of impedance estimation from the electrochemical noise data can be overcome. It is shown that the electrochemical noise impedance estimation can be extended to encompass a time varying, frequency dependent quantity for studying dynamic systems; that phase information can be recovered from electrochemical noise for the purpose of constructing Nyquist impedance diagrams; and that asymmetric electrodes can be detected without requiring additional measurements.
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Bagley, Gillian. "The measurement and the analysis of electrochemical noise." Thesis, University of Manchester, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.488277.

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Newton, Hazel Victoria. "Porous platinised carbon electrodes for electrochemical glucose measurement." Thesis, University of Newcastle Upon Tyne, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384970.

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Lowe, Alexander M. "Estimation of electrochemical noise impedance and corrosion rates from electrochemical noise measurements." Curtin University of Technology, School of Electrical and Computer Engineering, 2002. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=12723.

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Electrochemical noise refers to the spontaneous fluctuations in potential and current that can be observed on a corroding metal. The use of electrochemical noise for obtaining information on the corrosion process generates much interest in research fields. One important application is the measurement of corrosion rate. This can be achieved using the electrochemical noise of a pair of electrically coupled corroding metals to obtain an estimate of electrochemical impedance - an abstract quantity that reflects various aspects of the corrosion process.There are a number of problems associated with estimation of impedance information from the electrochemical noise data, particularly regarding data pre-treatment, accuracy and precision. In addition, the present methods are incomplete: current literature does not offer information regarding the phase of the impedance; and assumptions regarding symmetry of an electrode pair cannot be tested without additional measurements.The thesis addresses the above mentioned problems. Specifically,analysis of the impedance estimation process is given to determine how precision can be affected by various factors;a novel signal processing technique is described that is shown to yield a local optimum precision;the application of the proposed signal processing to time varying systems is demonstrated by use of a time varying, frequency dependent impedance estimate;a technique for recovering phase information, given certain conditions, is suggested so that Nyquist impedance diagrams can be constructed; anda technique for testing the symmetry of a coupled pair of corroding metals is described.An integral part of electrochemical noise analysis is the software used for numerical computation. The Matlab package from MathWorks inc. provides an extensible platform for electrochemical noise analysis. Matlab code is provided in Appendix A to implement ++
much of the theory discussed in the thesis.Impedance analysis and many other electrochemical corrosion monitoring techniques are primarily used for uniform corrosion, where the corrosion patterns occur uniformly over the exposed surface. In order to map localised corrosion, where the corrosion is typically concentrated within a small area, a wire beam electrode can be used. A wire beam electrode is a surface that is divided into a matrix of mini-electrodes so that the corrosion rate at different points can be monitored. However, manual connection of each mini-electrode to the measurement device can prove cumbersome. The final chapter of this thesis describes the design and testing of specialised multiplexing hardware to automate the process.In general, the thesis shows that by careful conditioning of the electrochemical noise prior to analysis, many of the problems with the technique of impedance estimation from the electrochemical noise data can be overcome. It is shown that the electrochemical noise impedance estimation can be extended to encompass a time varying, frequency dependent quantity for studying dynamic systems; that phase information can be recovered from electrochemical noise for the purpose of constructing Nyquist impedance diagrams; and that asymmetric electrodes can be detected without requiring additional measurements.
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Labonté, Germain 1960. "Electrochemical potentials in flotation systems : measurement, interpretation and applications." Thesis, McGill University, 1987. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=63825.

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Briers, Michael Geoffrey. "Electrochemical transducers for the continuous measurement of blood gases." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314888.

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Books on the topic "Electrochemical measurement"

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Kearns, JR, JR Scully, PR Roberge, DL Reichert, and JL Dawson, eds. Electrochemical Noise Measurement for Corrosion Applications. 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959: ASTM International, 1996. http://dx.doi.org/10.1520/stp1277-eb.

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1956-, Kearns Jeffery R., ASTM Committee G-1 on Corrosion of Metals., and International Symposium on Electrochemical Noise Measurement for Corrosion Applications (1st : 1994 : Montréal, Québec), eds. Electrochemical noise measurement for corrosion applications. West Conshohocken, PA: ASTM, 1996.

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1944-, Scribner L. L., Taylor S. R. 1953-, American Society for Testing and Materials. Committee G-1 on Corrosion of Metals., ASTM Committee G1.11 on Electrochemical Measurements in Testing., and Symposium on Ohmic Electrolyte Resistance Measurement and Compensation (1988 : Baltimore, Md.), eds. The Measurement and correction of electrolyte resistance in electrochemical tests. Philadelphia, PA: ASTM, 1990.

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Karrab, Salem Ali. Identification of localized corrosion using electrochemical noise measurement. Manchester: UMIST, 1998.

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Papavinasam, Sankara, Neal S. Berke, and Sean Brossia, eds. Advances in Electrochemical Techniques for Corrosion Monitoring and Measurement. 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959: ASTM International, 2009. http://dx.doi.org/10.1520/stp1506-eb.

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1962-, Papavinasam Sankara, Berke Neal Steven 1952-, and Brossia Sean, eds. Advances in electrochemical techniques for corrosion monitoring and measurement. West Conshohocken, PA: ASTM International, 2009.

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Papavinasam, Sankara. Advances in electrochemical techniques for corrosion monitoring and measurement. Edited by ASTM Committee G-1 on Corrosion of Metals. West Conshohocken, PA: ASTM International, 2009.

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Florian, Mansfeld, Huet F, Mattos O. R, and Electrochemical Society Corrosion Division, eds. New trends in electrochemical impedance spectroscopy (EIS) and electrochemical noise analysis (ENA): Proceedings of the international symposium. Pennington, NJ: The Electrochemical Society, Inc., 2001.

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Findlay, M. W. Construction and testing of electrochemical NOb2s PSDs. Research Triangle Park, NC: U.S. Environmental Protection Agency, Atmospheric Research and Exposure Assessment Laboratory, 1989.

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Taylor, R., and L. Scribner, eds. The Measurement and Correction of Electrolyte Resistance in Electrochemical Tests. 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959: ASTM International, 1990. http://dx.doi.org/10.1520/stp1056-eb.

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Book chapters on the topic "Electrochemical measurement"

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Weppner, Werner. "Electrochemical Measurement Techniques." In NATO ASI Series, 197–225. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0509-5_7.

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Cerny, M., R. Drska, and M. Penhaker. "Automated Measurement of Electrochemical Sensors." In IFMBE Proceedings, 1521–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-29305-4_400.

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Ohtsuka, Toshiaki, Atsushi Nishikata, Masatoshi Sakairi, and Koji Fushimi. "Electrochemical Measurement of Wet Corrosion." In SpringerBriefs in Molecular Science, 17–39. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-6820-1_2.

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Ohtsuka, Toshiaki, Atsushi Nishikata, Masatoshi Sakairi, and Koji Fushimi. "Electrochemical Measurement of Atmospheric Corrosion." In SpringerBriefs in Molecular Science, 65–78. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-6820-1_4.

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Zia, Asif Iqbal, and Subhas Chandra Mukhopadhyay. "Human Endocrine System and Hormonal Measurement." In Electrochemical Sensing: Carcinogens in Beverages, 1–20. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-32655-9_1.

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Alahi, Md Eshrat E., and Subhas Chandra Mukhopadhyay. "Interdigitated Senor and Electrochemical Impedance Spectroscopy (EIS)." In Smart Sensors, Measurement and Instrumentation, 43–52. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-20095-4_3.

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Guth, U., J. Zosel, J. Riedel, T. N. Tran, M. Berthold, C. Vonau, U. Sasum, P. Shuk, M. Paramasivam, and V. Vashook. "New Developments in Electrode Materials for Electrochemical Sensors." In Smart Sensors, Measurement and Instrumentation, 181–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32180-1_11.

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D’Orazio, Paul. "Measurement of Complement Fixation with Ion Selective Membrane Electrodes." In Electrochemical Sensors in Immunological Analysis, 179–94. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-1974-8_13.

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Bennet, Kevin E., Charles D. Blaha, and Kendall H. Lee. "Chapter 19 Electrochemical Measurement of Neurochemical Concentrations." In Deep Brain Stimulation, 357–72. Pan Stanford Publishing Pte. Ltd. Penthouse Level, Suntec Tower 3 8 Temasek Boulevard Singapore 038988: Pan Stanford Publishing, 2016. http://dx.doi.org/10.1201/9781315364759-20.

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Shuk, P., and R. Jantz. "Aged Zirconia Electrochemical Oxygen Sensor Activation and Re-activation Using NEMCA." In Smart Sensors, Measurement and Instrumentation, 131–42. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-21671-3_6.

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Conference papers on the topic "Electrochemical measurement"

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Yu, L., E. Pun, and E. Meng. "A CONTACTLESS ELECTROCHEMICAL IMPEDANCE MEASUREMENT METHOD." In 2016 Solid-State, Actuators, and Microsystems Workshop. San Diego: Transducer Research Foundation, 2016. http://dx.doi.org/10.31438/trf.hh2016.35.

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Breniuc, Liviu, Cristian Gyozo Haba, Olga Plopa, and Laurentiu-Iulian Ungureanu. "Electrochemical RFID Sensor for Gas Concentration Measurement." In 2018 International Conference and Exposition on Electrical And Power Engineering (EPE). IEEE, 2018. http://dx.doi.org/10.1109/icepe.2018.8559841.

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Hebbar, Suraj, Vinay Kumar, M. S. Bhat, and Navakanta Bhat. "Handheld electrochemical workstation for serum albumin measurement." In 2016 IEEE Distributed Computing, VLSI, Electrical Circuits and Robotics (DISCOVER). IEEE, 2016. http://dx.doi.org/10.1109/discover.2016.7806232.

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Luo, Tao, Luyang Li, Vishal Ghorband, Yuanda Zhan, Hongjiang Song, and Jennifer Blain Christen. "A portable impedance-based electrochemical measurement device." In 2016 IEEE International Symposium on Circuits and Systems (ISCAS). IEEE, 2016. http://dx.doi.org/10.1109/iscas.2016.7539197.

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Leping, Zhang, Hu Shanshan, Wang Baoshuai, Mei Neng, Li Ruoqian, and Xiao Xia. "Electrochemical corrosion in electric energy meters." In 2019 14th IEEE International Conference on Electronic Measurement & Instruments (ICEMI). IEEE, 2019. http://dx.doi.org/10.1109/icemi46757.2019.9101771.

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Olarte, Oscar, Kurt Barbe, Wendy Van Moer, and Yves Van Ingelgem. "Glucose characterization based on electrochemical impedance spectroscopy." In 2014 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2014. http://dx.doi.org/10.1109/i2mtc.2014.6860860.

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Alahi, M. E. E., Li Xie, Asif I. Zia, Subhas Mukhopadhyay, and Lucy Burkitt. "Practical nitrate sensor based on electrochemical impedance measurement." In 2016 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2016. http://dx.doi.org/10.1109/i2mtc.2016.7520554.

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Pavel, Steffan, Hubalek Jaromir, Ficek Richard, and Radimir Vrba. "Electrochemical measurement System Based on Thick-Film Sensors." In 2006 International Symposium on Communications and Information Technologies. IEEE, 2006. http://dx.doi.org/10.1109/iscit.2006.340031.

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Hossain, Md Kamal, and S. M. Rakiul Islam. "Battery Impedance Measurement Using Electrochemical Impedance Spectroscopy Board." In 2017 2nd International Conference on Electrical & Electronic Engineering (ICEEE). IEEE, 2017. http://dx.doi.org/10.1109/ceee.2017.8412902.

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Murphy, Aidan, Kathy Hanley, Niamh Creedon, Alan O'Riordan, and Ivan O'Connell. "Advanced data acquisition for emerging nano-electrochemical sensors." In 2018 IEEE International Instrumentation and Measurement Technology Conference (I2MTC ). IEEE, 2018. http://dx.doi.org/10.1109/i2mtc.2018.8409766.

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Reports on the topic "Electrochemical measurement"

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Vargo, G. F. Test procedure for measurement of performance vs temperature of Whittaker electrochemical cell. Office of Scientific and Technical Information (OSTI), January 1997. http://dx.doi.org/10.2172/325412.

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Vargo, G. F. ,. Fluor Daniel Hanford. Test report for measurement of performance vs temperature of Whittaker Electrochemical Cell. Office of Scientific and Technical Information (OSTI), February 1997. http://dx.doi.org/10.2172/330707.

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Olsen, Khris B., and Joseph Wang. Detection and Measurement of Explosives in Groundwater Using In Situ Electrochemical Sensors. Fort Belvoir, VA: Defense Technical Information Center, May 2002. http://dx.doi.org/10.21236/ada409108.

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Hu, Hongqiang, Yanhao Dong, Ju Li, Claire Xiong, and Mike Hurley. (M4CT-18IN0707093) Investigating Electrochemical Impedance Spectroscopic (EIS) Measurement of Surrogate Oxide at High Temperatures. Office of Scientific and Technical Information (OSTI), March 2018. http://dx.doi.org/10.2172/1468637.

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Delwiche, Michael, Boaz Zion, Robert BonDurant, Judith Rishpon, Ephraim Maltz, and Miriam Rosenberg. Biosensors for On-Line Measurement of Reproductive Hormones and Milk Proteins to Improve Dairy Herd Management. United States Department of Agriculture, February 2001. http://dx.doi.org/10.32747/2001.7573998.bard.

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The original objectives of this research project were to: (1) develop immunoassays, photometric sensors, and electrochemical sensors for real-time measurement of progesterone and estradiol in milk, (2) develop biosensors for measurement of caseins in milk, and (3) integrate and adapt these sensor technologies to create an automated electronic sensing system for operation in dairy parlors during milking. The overall direction of research was not changed, although the work was expanded to include other milk components such as urea and lactose. A second generation biosensor for on-line measurement of bovine progesterone was designed and tested. Anti-progesterone antibody was coated on small disks of nitrocellulose membrane, which were inserted in the reaction chamber prior to testing, and a real-time assay was developed. The biosensor was designed using micropumps and valves under computer control, and assayed fluid volumes on the order of 1 ml. An automated sampler was designed to draw a test volume of milk from the long milk tube using a 4-way pinch valve. The system could execute a measurement cycle in about 10 min. Progesterone could be measured at concentrations low enough to distinguish luteal-phase from follicular-phase cows. The potential of the sensor to detect actual ovulatory events was compared with standard methods of estrus detection, including human observation and an activity monitor. The biosensor correctly identified all ovulatory events during its testperiod, but the variability at low progesterone concentrations triggered some false positives. Direct on-line measurement and intelligent interpretation of reproductive hormone profiles offers the potential for substantial improvement in reproductive management. A simple potentiometric method for measurement of milk protein was developed and tested. The method was based on the fact that proteins bind iodine. When proteins are added to a solution of the redox couple iodine/iodide (I-I2), the concentration of free iodine is changed and, as a consequence, the potential between two electrodes immersed in the solution is changed. The method worked well with analytical casein solutions and accurately measured concentrations of analytical caseins added to fresh milk. When tested with actual milk samples, the correlation between the sensor readings and the reference lab results (of both total proteins and casein content) was inferior to that of analytical casein. A number of different technologies were explored for the analysis of milk urea, and a manometric technique was selected for the final design. In the new sensor, urea in the sample was hydrolyzed to ammonium and carbonate by the enzyme urease, and subsequent shaking of the sample with citric acid in a sealed cell allowed urea to be estimated as a change in partial pressure of carbon dioxide. The pressure change in the cell was measured with a miniature piezoresistive pressure sensor, and effects of background dissolved gases and vapor pressures were corrected for by repeating the measurement of pressure developed in the sample without the addition of urease. Results were accurate in the physiological range of milk, the assay was faster than the typical milking period, and no toxic reagents were required. A sampling device was designed and built to passively draw milk from the long milk tube in the parlor. An electrochemical sensor for lactose was developed starting with a three-cascaded-enzyme sensor, evolving into two enzymes and CO2[Fe (CN)6] as a mediator, and then into a microflow injection system using poly-osmium modified screen-printed electrodes. The sensor was designed to serve multiple milking positions, using a manifold valve, a sampling valve, and two pumps. Disposable screen-printed electrodes with enzymatic membranes were used. The sensor was optimized for electrode coating components, flow rate, pH, and sample size, and the results correlated well (r2= 0.967) with known lactose concentrations.
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Steven A. Attanasio, David S. Morton, and Mark A. Ando. Measurement and Calculation of Electrochemical Potentials in Hydrogenated High Temperature Water, including an Evaluation of the Yttria-Stabilized Zirconia/Iron-Iron Oxide (Fe/Fe3O4) Probe as Reference Electrode. Office of Scientific and Technical Information (OSTI), October 2001. http://dx.doi.org/10.2172/821313.

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Hayden, Carl C., and Roger L. Farrow. Molecular-scale measurements of electric fields at electrochemical interfaces. Office of Scientific and Technical Information (OSTI), January 2011. http://dx.doi.org/10.2172/1010418.

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Stansbury, E. E. A round robin evaluation of the corrosiveness of wet residential insulation by electrochemical measurements. Office of Scientific and Technical Information (OSTI), October 1991. http://dx.doi.org/10.2172/6232230.

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Baumann, E. W., and G. R. Jr Caskey. Reactor Materials Program electrochemical potential measurements by ORNL with unirradiated and irradiated stainless steel specimens. Office of Scientific and Technical Information (OSTI), July 1993. http://dx.doi.org/10.2172/10185742.

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WALL, FREDERICK D., MICHAEL A. MARTINEZ, CORBETT C. BATTAILE, and NANCY A. MISSERT. Quantifying Atmospheric Corrosion Processes Using Small Length-Scale Electrochemical Measurements and 3-D Electric Field Modeling. Office of Scientific and Technical Information (OSTI), November 2001. http://dx.doi.org/10.2172/789582.

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