Relevant bibliographies by topics / Electrochemical analysis

Contents

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

Academic literature on the topic 'Electrochemical analysis'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 July 2024

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Journal articles on the topic "Electrochemical analysis"

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Wang, Qiong, Weiting Ye, Dongling Li, Jiangwei Zhu, Chenghang Liu, Cheng-Te Lin, Li Fu, and Zenglai Xu. "Analysis of Electrochemically Active Substances in Malvaceae Leaves via Electroanalytical Sensing Technology for Species Identification." Micromachines 14, no. 2 (January 18, 2023): 248. http://dx.doi.org/10.3390/mi14020248.

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Electrochemical analysis has become a new method for plant analysis in recent years. It can not only collect signals of electrochemically active substances in plant tissues, but can also be used to identify plant species. At the same time, the signals of electrochemically active substances in plant tissues can also be used to investigate plant phylogeny. In this work, we collected electrochemical finger patterns in Malvaceae leaves based on the established methodological strategy. After the second derivative treatment, the collected electrochemical fingerprints can show more obvious differences. Three different recognition models were used to attempt electrochemical fingerprinting. The results show that linear support vector classification can be used to identify species with high accuracy by combining the electrochemical fingerprint signals collected in the phosphoric acid buffer solution and acetic acid buffer solution. In addition, the fingerprint information collected by the electrochemical sensor is further used for phylogenetic investigation. The 18 species were divided into three clusters. Species of the same genus have been clustered together. Dendrogram obtained by electrochemical fingerprinting was used to compare previously reported results deduced from morphological and complete chloroplast genomes.
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Fan, Boyuan, Qiong Wang, Weihong Wu, Qinwei Zhou, Dongling Li, Zenglai Xu, Li Fu, Jiangwei Zhu, Hassan Karimi-Maleh, and Cheng-Te Lin. "Electrochemical Fingerprint Biosensor for Natural Indigo Dye Yielding Plants Analysis." Biosensors 11, no. 5 (May 14, 2021): 155. http://dx.doi.org/10.3390/bios11050155.

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Indigo is a plant dye that has been used as an important dye by various ancient civilizations throughout history. Today, due to environmental and health concerns, plant indigo is re-entering the market. Strobilanthes cusia (Nees) Kuntze is the most widely used species in China for indigo preparation. However, other species under Strobilanthes have a similar feature. In this work, 12 Strobilanthes spp. were analyzed using electrochemical fingerprinting technology. Depending on their electrochemically active molecules, they can be quickly identified by fingerprinting. In addition, the fingerprint obtained under different conditions can be used to produce scattered patter and heatmap. These patterns make plant identification more convenient. Since the electrochemically active components in plants reflect the differences at the gene level to some extent, the obtained electrochemical fingerprints are further used for the discussion of phylogenetics.
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Elmasly, Saadeldin E. T., Luca Guerrini, Joseph Cameron, Alexander L. Kanibolotsky, Neil J. Findlay, Karen Faulds, and Peter J. Skabara. "Synergistic electrodeposition of bilayer films and analysis by Raman spectroscopy." Beilstein Journal of Organic Chemistry 14 (August 21, 2018): 2186–89. http://dx.doi.org/10.3762/bjoc.14.191.

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A novel methodology towards fabrication of multilayer organic devices, employing electrochemical polymer growth to form PEDOT and PEDTT layers, is successfully demonstrated. Moreover, careful control of the electrochemical conditions allows the degree of doping to be effectively altered for one of the polymer layers. Raman spectroscopy confirmed the formation and doped states of the PEDOT/PEDTT bilayer. The electrochemical deposition of a bilayer containing a de-doped PEDTT layer on top of doped PEDOT is analogous to a solution-processed organic semiconductor layer deposited on top of a PEDOT:PSS layer without the acidic PSS polymer. However, the poor solubility of electrochemically deposited PEDTT (or other electropolymerised potential candidates) raises the possibility of depositing a subsequent layer via solution-processing.
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Zhang, Hong Bo, Yong Sheng Li, Ting Ting Ning, and Ying Ying Zhu. "Analysis of Electrochemical Mechanism of Electrolyte and Coal." Advanced Materials Research 962-965 (June 2014): 837–42. http://dx.doi.org/10.4028/www.scientific.net/amr.962-965.837.

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In order to study the electrochemical performance of coal in the HCL electrolyte system, researchers prepared the chemically modified carbon paste electrode, measured the volt-ampere curves and Tafel curves of the samples and analyzed the mechanism of the electrochemically catalysis of oxidation of coal. The studies indicate that what occurs to the coal sample in the process of electrolytic sulfur removing is a quasi-reversible diffusion controlled process. In the beginning of the sulfur removing, the rate of electrolytic corrosion is fast, in which oxidation on the anode denominates, and the cathode plays a role of reduction in the late period.
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Ueda, Tadaharu. "Recent Achievements in the Analysis of the Electrochemical Properties of Polyoxometalates." Review of Polarography 61, no. 1 (2015): 11–19. http://dx.doi.org/10.5189/revpolarography.61.11.

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Zhou, Xiao-Dong. "(Keynote) Theoretical Analysis of Electrochemical Stability in a Solid Oxide Cell." ECS Meeting Abstracts MA2022-01, no. 38 (July 7, 2022): 1670. http://dx.doi.org/10.1149/ma2022-01381670mtgabs.

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In this talk, I will describe a theoretical analysis and modeling of electrochemical stability in solid oxide cells, including solid oxide fuel cell, solid oxide electrolysis, and solid-state batteries. Focus will be on elucidating the origin for the electrochemically driven of phase change and the deposition of neutral species at the interfaces and inside a solid electrolyte.
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Slepushkin, V. V., Yu V. Rublinetskaya, and B. M. Stifatov. "Local electrochemical surface analysis." Journal of Analytical Chemistry 60, no. 2 (February 2005): 103–6. http://dx.doi.org/10.1007/pl00021912.

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Karadurmus, Leyla, Duru Kır, Sevinc Kurbanoglu, and Sibel A. Ozkan. "Electrochemical Analysis of Antipsychotics." Current Pharmaceutical Analysis 15, no. 5 (May 23, 2019): 413–28. http://dx.doi.org/10.2174/1573412914666180710114458.

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Introduction:Schizophrenia is seizures accompanied by severe psychotic symptoms, and a steady state of continuation in the form of periods of stagnation. Antipsychotics are now the basis of treatment for schizophrenia and there is no other molecule that is antipsychotic priority in treatment. Antipsychotics can be classified into two groups; dopamine receptor antagonists such as promazine, fluphenazine etc. and serotonin-dopamine antagonists including risperidone, olanzapine, ziprasidone, aripiprazole etc.Materials and Methods:Electrochemical methods have been used for the determination of antipsychotic agent just as used in the determination of many drug agents. Nearly all of the antipsychotics are electroactive and can be analyzed by electrochemical methods. Electroanalytical methods offer generally high sensitivity, are compatible with modern techniques, have low cost, low requirements, and compact design. Among the most commonly used types, there are cyclic voltammetry, differential pulse voltammetry, square wave voltammetry and linear sweep voltammetry.Conclusion:The aim of this review is to evaluate the main line and the advantages and uses of electroanalytical methods that employed for the determination of antipsychotic medication agents used in schizophrenia. Moreover, applications of the methods to pharmaceutical analysis of Antipsychotics upto- date is also summarized in a table.
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Bucher, Elizabeth S., and R. Mark Wightman. "Electrochemical Analysis of Neurotransmitters." Annual Review of Analytical Chemistry 8, no. 1 (July 22, 2015): 239–61. http://dx.doi.org/10.1146/annurev-anchem-071114-040426.

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Parsons, Roger. "Fundamentals of electrochemical analysis." Journal of Electroanalytical Chemistry 371, no. 1-2 (June 1994): 293. http://dx.doi.org/10.1016/0022-0728(94)03416-8.

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Dissertations / Theses on the topic "Electrochemical analysis"

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Sobocinski, Raymond Louis. "Electrochemical and Raman spectroscopic investigations of in situ and emersed silver-alcohol electrochemical interfaces." Diss., The University of Arizona, 1991. http://hdl.handle.net/10150/185476.

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The overall goal of this research is to characterize the potential-dependent structure and composition of the alcohol-Ag electrochemical interface. The approach involves the use of a variety of electrochemical and spectroscopic tools to arrive at a consistent model for a series of straight-chain alcohols (methanol, ethanol, 1-propanol, and 1-pentanol) at Ag electrodes. There are essentially four areas of investigation presented in this dissertation. The first portion of this work has been directed at the development of charge coupled device detection in Raman spectroscopy so that many of the interface investigations could be performed. The advantages and limitations of these detectors in Raman spectroscopy are addressed. The second area involves the characterization of in-situ alcohol-Ag electrochemical interfaces using Raman spectroscopy and associated surface selection rules for the evaluation of solvent orientation and bonding. Since the series of alcohols offers a systematic variation in solvent properties, these studies provide substantial insight regarding some of the chemical interactions which can dictate orientation. The development of emersed electrode technologies is also presented as a means to improve selectivity for surface molecular species over bulk molecular species. The utility of this approach is demonstrated for a variety of straight-chain alcohols at both rough and smooth Ag electrodes. Conditions for emersing the molecular interface, intact, under potential control are presented. Finally, double layer capacitance measurements are performed to offer additional insight regarding alcohol solvent structure and interfacial composition as a function of electrode potential. In addition, capacitance-potential plots are used along with the Hurwitz-Parsons analysis to determine absolute surface coverage of Br⁻ as a function of electrode potential. These results are correlated with the Raman spectroscopic results to obtain a consistent model for the structure and composition of the alcohol-Ag electrochemical interface.
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Song, Peng. "Microengineered electrochemical reactors." Thesis, University of Cambridge, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.709449.

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Alvarez, de Eulate Diaz de San Martin Eva Maria. "Electrochemical studies toward proteomic analysis." Thesis, Curtin University, 2014. http://hdl.handle.net/20.500.11937/702.

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This thesis provides the basis for a label-free bioanalytical platform using electrochemical analysis at liquid –liquid interfaces. The possibility to detect biomolecules such as proteins in a label-free manner via adsorption and ion-transfer was achieved. Several pre-treatment steps used in proteome analysis, such as protein pre-concentration and digestion, were studied. The results demonstrate the promise of this strategy for the detection and identification of proteins.
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Parrilla, Pons Marc. "New Electrochemical Sensors for Decentralized Analysis." Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/396297.

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Nous sensors electroquímics per a analisis decentralitzats és una tesis que emmarca diferents aspectes del desenvolupament de sensors potenciomètrics, des de la seva fabricació, el diseny adequat, i finalment, la seva aplicabilitat en escenaris reals. En el context actual, l'evolució de la tecnologia, especialment l'aparició a nivell global d'internet, i la disponibilitat d'aquesta a baix cost han permès la creació d'eines que ens permeten connectar el món físic i, en el cas d'aquesta tesis, el món químic a la xarxa. Aquesta connexió aporta un nou grau dins l'escala de valor per a la societat actual. Concretament, aquesta aportació tecnològica va adreçada a superar els nous reptes de l'actualitat, com poden ser la sostenibilitat del sistema sanitari a causa de l'embelliment de la societat, el control medioambiental, així com també mantenir la seguretat per a la societat del benestar del futur. Així doncs, aquesta tesis presenta solucions efectives per al desenvolupament d'eines de captació d'informació que serviràn per nudrir a la societat de major coneixement. Conseqüentment, produint nous negocis al voltant, de la fabricació, processament i creació de valor entorn a aquestes dades. La recerca i desenvolupament de sensors potenciomètrics integrats a la roba per detectar els nivells d'electròlits i sensors senzills de paper per a la determinació de biomolècules, com la glucosa, són alguns dels objectius aconseguits en aquesta tesis. A més a més, sensors integrats en globus permeten l'estudi de les seves propietats mecàniques i electroquímiques, així com també, aporten noves solucions a problemes reals. Totes aquestes aplicacions serveixen de portals de captació d'informació química cap a la integració dins la nova societat de la informació.
Nuevos sensores electroquímicos para analisis decentralizados es una tesis que enmarca diferentes aspectos del desarrollo de sensores potenciométricos, desde su fabricación, el diseño adecuado, i finalmente, su aplicabilidad en escenarios reales. En el contexto actual, la evolución de la tecnología, especialmente la aparición a nivel global de internet, y la disponibilidad de esta a bajo coste han permitido la creación de herramientas que nos permiten conectar el mundo físico y, en el caso de esta tesis, el mundo químico a la red. Esta conexión aporta un nuevo grado dentro la escala de valor para la sociedad actual. Concretamente, esta aportación tecnológica va dirigida a superar los nuevos retos de la actualidad, como pueden ser la sostenibilidad del sistema sanitario a causa del envejecimiento de la poblacion, el control medioambiental, así como también mantener la seguridad para la sociedad del bienestar del futuro. Entonces, esta tesis presenta soluciones efectivas para el desarrollo de herramientas de captación de información que servirán para nutrir a la sociedad de un mayor conocimiento. Por consiguiente, produciendo nuevos negocios alrededor, de la fabricación, procesado i creación de valor en los datos obtenidos. La investigación y desarrollo de sensores potenciométricos integrados en la ropa para detectar los niveles de electrolitos y sensores simples en papel para la determinación de biomoléculas, como la glucosa, son algunos de los objetivos conseguidos en esta tesis. Además, sensores integrados en globos permiten el estudio de sus propiedades mecánicas y electroquímicas, así como, aportando nuevas soluciones a problemas reales. Todas estas aplicaciones sirven de portales de captación de información química hacia la integración dentro de la nueva sociedad de la información.
ew Electrochemical Sensors for Decentralized Analysis is a thesis that wisely discuss the developments of potentiometric sensors, from the fabrication step, the use of a suitable design, to the applicability in real scenarios. Nowadays, the evolution of technology, specially the creation of the global internet network, and the low-cost availability of such technology have allowed the development of tools that connect the physical world and, addressed in this thesis, the chemical world into the network. This connection adds a new level in the value chain for the present society. Precisely, this technology approach is focus on circumvent new present challenges of society. For instance, sustainability of the healthcare system caused by the population aging, environmental monitoring, as well as, keep security and safety to the welfare of society of the future. Therefore, this thesis presents successful solutions for the development of tools to gather chemical information. This information will nurture society with high-value knowledge. Accordingly, new business development from, sensing products, data treatment and information management are going to be created. Research and development of potentiometric sensors integrated into garments for electrolyte detection and simple sensors built in paper for biomolecules determination, such as glucose, and liquid monitoring, such as sweat, are some of the accomplished objectives from this thesis. Furthermore, balloon-embedded sensors allow the study of the mechanical and electrochemical properties of the electrodes, as well as, contributing with new solutions to real problems. All the applications developed in this thesis are utilized as gateways for chemical information acquisition towards the integration into the new information society.
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Chu, Kevin Taylor. "Asymptotic analysis of extreme electrochemical transport." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/33669.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mathematics, 2005.
Includes bibliographical references (p. 237-244).
In the study of electrochemical transport processes, experimental exploration currently outpaces theoretical understanding of new phenomena. Classical electrochemical transport theory is not equipped to explain the behavior of electrochemical systems in the extreme operating conditions required by modern devices. In this thesis, we extend the classical theory to examine the response of two electrochemical systems that form the basis for novel electrochemical devices. We first examine the DC response of an electrochemical thin film, such as the separator in a micro-battery, driven by current applied through reactive electrodes. The model system consists of a binary electrolyte between parallel-plate electrodes, each possessing a compact Stern layer which mediates Faradaic reactions with Butler-Volmer kinetics. Our analysis differs from previous studies in two significant ways. First, we impose the full nonlinear, reactive boundary conditions appropriate for electrolytic/galvanic cells.
(cont.) Since surface effects become important for physically small systems, the use of reactive boundary conditions is critical in order to gain insight into the behavior of actual electrochemical thin films that are sandwiched between reactive electrodes, especially at high current densities. For instance, our analysis shows that reaction rate constants and the Stern-layer capacitance have a strong influence on the response of the thin film. Second, we analyze the system at high current densities (far beyond the classical diffusion-limited current) which may be important for high power-density applications. At high currents, we obtain previously unknown characterizations of two interesting features at the cathode end of the cell: (i) a nested boundary layer structure and (ii) an extended space charge region. Next, we study the response of a metal (i.e., polarizable) colloid sphere in an electrolyte solution over a range of applied electric fields.
(cont.) This problem, which underlies novel electrokinetically driven microfluidic devices, has traditionally been analyzed using circuit models which neglect bulk concentration variations that arise due to double layer charging. Our analysis, in contrast, is based on the Nernst-Planck equations which explicitly allow for bulk concentration gradients. A key feature of our analysis is the use of surface conservation laws to provide effective boundary conditions that couple the double layer charging dynamics, surface transport processes, and bulk transport processes. The formulation and derivation of these surface conservation laws via boundary layer analysis is one of the main contributions of this thesis. For steady applied fields, our analysis shows that bulk concentrations gradients become significant at high applied fields and affect both bulk and double layer transport processes. We also find that surface transport becomes important for strong applied fields as a result of enhanced absorption of ions by the double layer.
(cont.) Unlike existing theoretical studies which focus on weak applied fields (so that both of these effects remain weak), we explore the response of the system to strong applied fields where both bulk concentration gradients and surface transport contribute at leading order. For the unsteady problem at applied fields that are not too strong, we find that diffusion processes, which are necessary for the system to relax to steady-state, are suppressed at leading-order but appear as higher-order corrections. This result is derived in a novel way using time-dependent matched asymptotic analysis. Unfortunately, the dynamic response of the system to large applied fields seems to introduce several complications that make the analysis (both mathematical and numerical) quite challenging; the resolution of these challenges is left for future work. Both of these problems require the use of novel techniques of asymptotic analysis (e.g., multiple parameter asymptotic expansions, surface conservation laws, and time-dependent asymptotic matching) and advanced numerical methods (e.g., pseudospectral methods, Newton-Kantorovich method, and direct matrix calculation of Jacobians) which may be applicable elsewhere.
by Kevin Taylor Chu.
Ph.D.
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Ding, Wenwu Carleton University Dissertation Chemistry. "Electrochemical hydride generation for ultratrace analysis." Ottawa, 1995.

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D'Arcy, Karen Ann. "Electrochemical methods for speciation of inorganic arsenic." PDXScholar, 1986. https://pdxscholar.library.pdx.edu/open_access_etds/524.

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Arsenic is found in the environment in several oxidation states as well as in a variety of organoarsenic compounds. This situation puts additional demands on the analysis in that it is desirable to measure the amount of each species, not just all of the arsenic. The reason for this is that the different species have greatly different toxicities; of the major inorganic forms, As(III) is much more toxic than As(V). The goal of this research was to develop a convenient method for the analysis of mixtures of As(III) and As(V) at trace levels. Electroanalytical methods are inherently sensitive to oxidation states of elements and therefore are a natural choice for this problem. In fact, a method was developed some years ago for As(III) that used differential pulse polarography: the detection limit is 0.3 parts per billion (ppb). However, As(V) was not detected since in its usual form as an oxyanion it is electrochemically inactive. There are coordinate compounds formed with catechol, AsL(,n)(n = 1-3), that can be reduced at a mercury electrode, but the active species, AsL, is only a small fraction of the major species, AsL(,3), so the detection limit is only 500 ppb. Many details of the electrochemistry of this unusual compound were examined in this work. In order to improve detection limits, a method involving cathodic stripping was developed. It involves codeposition of copper with arsenic on a mercury electrode to effectively concentrate the analyte. Then the elemental arsenic is converted to arsine, AsH(,3), during a cathodic potential scan. The resulting current peak is proportional to As(III) in the absence of catechol and to the sum of As(III) and As(V) in the presence of catechol. It was observed that the current peak was considerably larger than expected and additional experiments revealed that there was evolution of hydrogen during the formation of arsine. This is rather unusual in electrochemical reactions and so some of the details of this catalyzed coreaction were examined. The result is a fortunate enhancement of detection limit so that As(v) at 40 ppb can be measured.
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Wengenack, Nancy L. "Design and testing of a computer-controlled square wave voltammetry instrument /." Online version of thesis, 1987. http://hdl.handle.net/1850/8853.

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Jagannathan, Sudhakar. "Process, structure and electrochemical." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29713.

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Thesis (Ph.D)--Polymer, Textile and Fiber Engineering, Georgia Institute of Technology, 2009.
Committee Chair: Kumar, Satish; Committee Member: Cook, Fred L.; Committee Member: Bottomley, Lawrence A.; Committee Member: Carter, William Brent; Committee Member: Yushin, Gleb. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Ismail, Iqbal M. I. "Electrochemical studies of polymer electrolytes." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242319.

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Books on the topic "Electrochemical analysis"

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1944-, Ngo T. T., ed. Electrochemical sensors in immunological analysis. New York: Plenum Press, 1987.

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Scully, JR, DC Silverman, and MW Kendig, eds. Electrochemical Impedance: Analysis and Interpretation. 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959: ASTM International, 1993. http://dx.doi.org/10.1520/stp1188-eb.

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Ngo, T. T., ed. Electrochemical Sensors in Immunological Analysis. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4899-1974-8.

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Fahidy, Thomas Z. Principles of electrochemical reactor analysis. Amsterdam: Elsevier, 1985.

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1958-, Scully John R., Silverman David C. 1947-, and Kendig Martin W, eds. Electrochemical impedance: Analysis and interpretation. Philadelphia: ASTM, 1993.

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Jong, Hans G. de. Electrochemical analysis of metal complexes. Wageningen, Netherlands?: Landbouwuniversiteit te Wageningen?, 1987.

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Fahidy, Thomas Z. Principles of electrochemical reactor analysis. Amsterdam: Elsevier, 1985.

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Li, Genxi, and Peng Miao. Electrochemical Analysis of Proteins and Cells. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34252-3.

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Xia, Fan, Hui Li, Shaoguang Li, and Xiaoding Lou, eds. Electrochemical Biosensors for Whole Blood Analysis. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-5644-9.

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Braĭnina, Kh Z. Inversionnye ėlektroanaliticheskie metody. Moskva: "Khimii͡a︡", 1988.

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Book chapters on the topic "Electrochemical analysis"

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Dornbusch, Michael. "Electrochemical Methods." In Corrosion Analysis, 38–110. Boca Raton, FL : CRC Press, Taylor & Francis Group, [2018] | "A science publishers book.": CRC Press, 2018. http://dx.doi.org/10.1201/9781315208480-2.

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Mitra, Somenath, Pradyot Patnaik, and Barbara B. Kebbekus. "Electrochemical Methods." In Environmental Chemical Analysis, 235–41. Second edition. | Boca Raton : CRC Press, [2018] | Previous edition by B.B. Kebbekus and S. Mitra.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429458200-8.

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Pa, P. S., and H. Hocheng. "Electrochemical Machining." In Advanced Analysis of Nontraditional Machining, 107–257. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-4054-3_3.

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LaCourse, William R. "Electrochemical Stripping Analysis." In Ewing’s Analytical Instrumentation Handbook, Fourth Edition, 523–38. Fourth edition / [edited by] Nelu Grinberg, Sonia Rodriguez. | Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2019. http://dx.doi.org/10.1201/9781315118024-18.

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O'Connell, P. "ANALYSIS | Electrochemical Analysis." In Encyclopedia of Dairy Sciences, 101–6. Elsevier, 2002. http://dx.doi.org/10.1016/b0-12-227235-8/00026-2.

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"Electrochemical Analysis." In Principles and Applications of Lithium Secondary Batteries, 231–61. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650408.ch7.

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"Electrochemical Analyzers." In Analysis and Analyzers, 290–302. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315370323-22.

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"Electrochemical Detection Methods." In Flow Injection Analysis, 107–61. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812813725_0003.

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"Electrochemical Stripping Analysis." In Analytical Instrumentation Handbook, 571–86. CRC Press, 2004. http://dx.doi.org/10.1201/9780849390395-21.

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Lacourse, William. "Electrochemical Stripping Analysis." In Analytical Instrumentation Handbook, Second Edition, 545–59. CRC Press, 2004. http://dx.doi.org/10.1201/9780849390395.ch18.

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Conference papers on the topic "Electrochemical analysis"

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Schmid, Robert, and Christophe Pillot. "Introduction to energy storage with market analysis and outlook." In REVIEW ON ELECTROCHEMICAL STORAGE MATERIALS AND TECHNOLOGY: Proceedings of the 1st International Freiberg Conference on Electrochemical Storage Materials. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4878476.

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HANSEN, WILFORD N., GALEN J. HANSEN, and DAVID GLENN. "ANALYSIS OF SOME ELECTROCHEMICAL CALORIMETRY DATA." In Proceedings of the 10th International Conference on Cold Fusion. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701510_0024.

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Ondruch, V., J. Krejci, and D. Krejcova. "Simple Electrochemical Analysis of Enzyme Kinetics." In 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1615490.

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Bardt, Hubertus. "Raw materials in the field of electrochemical energy storage – A risk analysis." In ELECTROCHEMICAL STORAGE MATERIALS: SUPPLY, PROCESSING, RECYCLING AND MODELLING: Proceedings of the 2nd International Freiberg Conference on Electrochemical Storage Materials. Author(s), 2016. http://dx.doi.org/10.1063/1.4961894.

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Filsø, Mette Ø., Espen Eikeland, and Bo B. Iversen. "Procrystal analysis as a tool for the visualization of ion migration pathways." In ELECTROCHEMICAL STORAGE MATERIALS: SUPPLY, PROCESSING, RECYCLING AND MODELLING: Proceedings of the 2nd International Freiberg Conference on Electrochemical Storage Materials. Author(s), 2016. http://dx.doi.org/10.1063/1.4961902.

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Azahidi, A., R. Rusdi, N. A. Mohd Mokhtar, and K. Elong. "Fe doped in LiCo0.6Ni0.4O2 and their electrochemical behaviour." In INTERNATIONAL CONFERENCE “FUNCTIONAL ANALYSIS IN INTERDISCIPLINARY APPLICATIONS” (FAIA2017). Author(s), 2017. http://dx.doi.org/10.1063/1.4999871.

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Anderson, Mark R., Dennis H. Evans, and Mary J. Wirth. "Indirect Determination of a Local pH Change by Surface Enhanced Raman Spectroscopy." In Laser Applications to Chemical Analysis. Washington, D.C.: Optica Publishing Group, 1987. http://dx.doi.org/10.1364/laca.1987.pdp5.

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Surface enhanced Raman scattering (SERS) is, potentially, a very powerful technique for in situ surface analysis, particularly in an electrochemical environment. Unfortunately, few studies to date have taken advantage of the technique for the purpose of analysis. The present study, however, utilizes SERS to probe analyte molecules in the electrochemical double layer in order to obtain information about the behavior of the double layer as the electrode potential is altered.
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Selvaraj, Gowri, Cecilia Devi Wilfred, and Neo Kian Eang. "Recrystallized quinolinium ionic liquids for electrochemical analysis." In 4TH INTERNATIONAL CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCES (ICFAS2016). Author(s), 2016. http://dx.doi.org/10.1063/1.4968082.

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Lai, Qingzhi, Sidharth Jangra, Hyoung Jun Ahn, Geumbee Kim, Won Tae Joe, and Xinfan Lin. "Analytical Sensitivity Analysis for Battery Electrochemical Parameters." In 2019 American Control Conference (ACC). IEEE, 2019. http://dx.doi.org/10.23919/acc.2019.8814950.

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Ma, Junliang, Zhidong Wang, and Shuming Zhang. "Benefit Assessment Analysis of Electrochemical Energy Storage." In 2023 IEEE International Conference on Power Science and Technology (ICPST). IEEE, 2023. http://dx.doi.org/10.1109/icpst56889.2023.10164815.

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Reports on the topic "Electrochemical analysis"

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Canaday, J. D., A. K. Kuriakose, A. Ahmad, and T. A. Wheat. An electrochemical analysis of solid electrolyte/electrode systems. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/307075.

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Lafreniere, Philip. Application of Principal Component Analysis to Electrochemical Reprocessing PM and NMAC. Office of Scientific and Technical Information (OSTI), September 2023. http://dx.doi.org/10.2172/2005795.

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Hughes, Sydney, Marc Turner, Mark Woods, Sue Carr, Douglas Kauffman, and Gregory Hackett. Sensitivity Analysis Tool for Electrochemical Conversion of CO2 To CO: User Guide. Office of Scientific and Technical Information (OSTI), December 2023. http://dx.doi.org/10.2172/2234013.

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Hu, Hongqiang, Dong Ding, Lane Knighton, Daniel Wendt, and Richard Boardman. Techno-Economic Analysis on an Electrochemical Non-oxidative Deprotonation Process for Ethylene Production from Ethane. Office of Scientific and Technical Information (OSTI), December 2019. http://dx.doi.org/10.2172/1643942.

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Sarkar, Abhishek. Multiphysics analysis of electrochemical and electromagnetic system addressing lithium-ion battery and permanent magnet motor. Office of Scientific and Technical Information (OSTI), July 2019. http://dx.doi.org/10.2172/1593376.

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Reynolds, Jonathan. A System Engineering Approach in the Analysis of Electrochemical and Structural Properties of Ionic Liquids. Office of Scientific and Technical Information (OSTI), March 2022. http://dx.doi.org/10.2172/1853911.

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Moore, D. G., and N. R. Sorensen. Nondestructive inspection assessment of eddy current and electrochemical analysis to separate inconel and stainless steel alloys. Office of Scientific and Technical Information (OSTI), February 1998. http://dx.doi.org/10.2172/572689.

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Latanision, R. M. Deterministic analysis of processes at corroding metal surfaces and the study of electrochemical noise in these systems. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/5132868.

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Latanision, R. Deterministic analysis of processes at corroding metal surfaces and the study of electrochemical noise in these systems. Office of Scientific and Technical Information (OSTI), December 1990. http://dx.doi.org/10.2172/6074547.

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Glasscott, Matthew, Johanna Jernberg, Erik Alberts, and Lee Moores. Toward the electrochemical detection of 2,4-dinitroanisole (DNAN) and pentaerythritol tetranitrate (PETN). Engineer Research and Development Center (U.S.), March 2022. http://dx.doi.org/10.21079/11681/43826.

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Analytical methods to rapidly detect explosive compounds with high precision are paramount for applications ranging from national security to environmental remediation. This report demonstrates two proof-of-concept electroanalytical methods for the quantification of 2,4-dinitroanisol (DNAN) and pentaerythritol tetranitrate (PETN). For the first time, DNAN reduction was analyzed and compared at a bare graphitic carbon electrode, a polyaniline-modified (PANI) electrode, and a molecularly imprinted polymer (MIP) electrode utilizing PANI to explore the effect of surface-area and preconcentration affinity on the analytical response. Since some explosive compounds such as PETN are not appreciably soluble in water (<10 μg/L), necessitating a different solvent system to permit direct detection via electrochemical reduction. A 1,2-dichloroethane system was explored as a possibility by generating a liquid-liquid extraction-based sensor exploiting the immiscibility of 1,2-dichloroethane and water. The reduction process was explored using a scan rate analysis to extract a diffusion coefficient of 6.67 x 10⁻⁶ cm/s, in agreement with literature values for similarly structured nitrate esters. Once further refined, these techniques may be extended to other explosives and combined with portable electrochemical hardware to bring real-time chemical information to soldiers and citizens alike.
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