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Relevant bibliographies by topics / Voltammetry

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Academic literature on the topic 'Voltammetry'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2024

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Journal articles on the topic "Voltammetry"

1

Cemgil Sultan, Sinan, Esma Sezer, Yudum Tepeli, and Ulku Anik. "Centri-voltammetric dopamine detection." RSC Adv. 4, no. 59 (2014): 31489–92. http://dx.doi.org/10.1039/c4ra04887c.

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MENEK, Necati, Serpil ZEYREKLİ, and Yeliz KARAMAN. "Investigation of Electrochemical Behavior of Mordant Dye (C.I. 17135) at Glassy Carbon and Silver Electrodes." Chemia Naissensis 4, no. 1 (2021): 89–104. http://dx.doi.org/10.46793/chemn4.1.89m.

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In this study, the electrochemical behaviour of Mordant dye (C.I. 17135) was investigated in Britton-Robinson (BR) buffer (pH 2.0-12.0) media by using different voltammetric techniques: square wave voltammetry (SWV), cyclic voltammetry (CV), differential pulse voltammetry (DPV) and direct current voltammetry (DCV). The electrochemical behavior of the dye has been investigated by using a glassy carbon electrode (GCE) and silver electrode (SE). The brode peak of the azo dye occurred at SW and DP voltammograms, is due to its adsorption on the glassy carbon and silver electrode surfaces. Two reduction peaks were observed at pH < 9.5, and one reduction peak was observed at pH > 9.5 for SWV and DPV techniques at a glassy carbon electrode. From the voltammetric data electrochemical reaction mechanism of the azo dye has been suggested at glassy carbon and silver electrodes.

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Lu, Lin, Xianqiao Hu, and Zhiwei Zhu. "Joint Voltammetry Technology with a Multi-electrode Array for Four Basic Tastes." Current Analytical Chemistry 15, no. 1 (December 5, 2018): 75–83. http://dx.doi.org/10.2174/1573411014666180522100504.

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Background: Rapid and easy technology which can mimic the tongue for the simultaneous perception of several tastes based on sensory analysis and mathematical statistics is sorely needed. Methods: Joint voltammetry technology was developed to qualitatively and quantitatively analyze four basic tastes namely sweetness, saltiness, sourness and bitterness with the multi-electrode array. Four taste stimuli were corresponded to four tastes. Cyclic Voltammetry (CV), Differential Pulse Voltammetry (DPV) and Square Wave Voltammetry (SWV) were employed. The original voltammetric signals were transformed by Continuous Wavelet Transform (CWT) in order to reveal more feature information for sensing taste stimuli. Joint voltammetry was applied via the combination of voltammetry. The data of feature points from the transformed signal as the input were used for neural network model. Results: Layer-Recurrent neural network (LRNN) could effectively identify the types of stimuli. The accuracies of the training set and test set by joint voltammetry were both higher than that of regular voltammetry, confirming that Back Propagation neural network (BPNN) could quantitatively predict single taste stimulus of the mixture. Conclusion: Joint voltammetry technology had a strong ability to sense basic tastes as human tongue.

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Mirčeski, Valentin, Leon Stojanov, and Sławomira Skrzypek. "RECENT ADVANCES AND PROSPECTS OF SQUARE-WAVE VOLTAMMETRY." Contributions, Section of Natural, Mathematical and Biotechnical Sciences 39, no. 2 (December 28, 2018): 103. http://dx.doi.org/10.20903/csnmbs.masa.2018.39.2.123.

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This review concerns recent methodological advances of square-wave voltammetry as one of the most sophisticatedmembers of the pulse voltammetric techniques. Besides addressing recent theoretical works and representatives ofadvanced analytical studies, an emphasis is given to a few novel methodological concepts such as kinetic analysis atconstant scan rate, cyclic square-wave voltammetry, multisampling square-wave voltammetry, and electrochemical faradaicspectroscopy. For the purpose of improving analytical performances of the technique two new methods are proposedfor the first time.

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Shanmugam, Kumaran, Jiří Barek, and Jiří Zima. "Polarographic and Voltammetric Determination of Submicromolar Concentrations of Genotoxic 1,5-Dinitronaphthalene." Collection of Czechoslovak Chemical Communications 69, no. 11 (2004): 2021–35. http://dx.doi.org/10.1135/cccc20042021.

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Polarographic and voltammetric behavior of 1,5-dinitronaphthalene was investigated using tast polarography and differential pulse polarography at a classic dropping mercury electrode and differential pulse voltammetry and adsorptive stripping voltammetry at a hanging mercury drop electrode. Optimum conditions have been found for the determination of tested substance in the concentration range 2-10 μmol l-1 in tast polarography, 0.2-1 μmol l-1 in differential pulse polarography at a classic dropping mercury electrode or differential pulse voltammetry at a hanging mercury drop electrode, and 0.02-0.1 μmol l-1 using adsorptive stripping voltammetry. A possible mechanism of the electrochemical reduction of 1,5-dinitronaphthalene at mercury electrodes is discussed.

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Karastogianni, Sophia, and Stella Girousi. "Electrochemical Behavior and Voltammetric Determination of a Manganese(II) Complex at a Carbon Paste Electrode." Analytical Chemistry Insights 11 (January 2016): ACI.S32150. http://dx.doi.org/10.4137/aci.s32150.

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Investigation of the electrochemical behavior using cyclic voltammetry and detection of [Mn2+(thiophenyl-2-carboxylic acid)2 (triethanolamine)] with adsorptive stripping differential pulse voltammetry. The electrochemical behavior of a manganese(II) complex [Mn2+(thiophenyl-2-carboxylic acid)2(triethanolamine)] (A) was investigated using cyclic and differential pulse voltammetry in an acetate buffer of pH 4.6 at a carbon paste electrode. Further, an oxidation-reduction mechanism was proposed. Meanwhile, an adsorptive stripping differential pulse voltammetric method was developed for the determination of manganese(II) complex.

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Elqudaby, Hoda M., Hassan A. M. Hendawy, Eglal R. Souaya, Gehad G. Mohamed, and Ghada M. G. Eldin. "Utility of Activated Glassy Carbon and Pencil Graphite Electrodes for Voltammetric Determination of Nalbuphine Hydrochloride in Pharmaceutical and Biological Fluids." International Journal of Electrochemistry 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/8621234.

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This work compares voltammetric response of nalbuphine hydrochloride (NP·HCl) at both activated glassy carbon and pencil graphite electrodes. The electrochemical oxidation of the drug was studied using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and square wave voltammetry (SWV) techniques. For analytical purpose a well-resolved irreversible diffusion controlled voltammetric peak was established in Britton-Robinson (B-R) buffer solution of pH 6.00 using pencil graphite electrode (PGE). Using activated glassy carbon electrode (GCE) a well-resolved irreversible diffusion controlled voltammetric peak was obtained at pH 7.00 using the same buffer solution. According to the linear relationship between the peak current and NP·HCl concentration, DPV and SWV methods were developed for their quantitative determination in pharmaceutical and human biological fluids. The linear response was obtained in the range from1.6×10-5to1.5×10-4 mol L−1using PGE and from12.5×10-6to13.75×10-5 mol L−1using a GC electrode, respectively. Precision and accuracy of the developed method were checked by recovery studies.

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Al-Owais, A. A., and I. S. El-Hallag. "Voltammetric Studies of Anthracen-9-ylmethylene-(3,4-dimethyl-isoxazol-5-yl)-amine Compound at Platinium Electrode." Journal of New Materials for Electrochemical Systems 18, no. 3 (September 9, 2015): 177–81. http://dx.doi.org/10.14447/jnmes.v18i3.366.

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The voltammetric behavior of anthracen-9-ylmethylene-(3,4-dimethyl-isoxazol-5-yl)-amine compound at Platinium electrode has been performed via convolutive cyclic voltammetry and digital simulation techniques using a conventional platinium electrode in 0.1 mol L-1 tetrabutylammonium perchlorate (TBAP) in acetonitrile solvent (CH3CN). The compound loss one electron forming radical cation followed by fast chemical step and the radical cation loss another two electrons producing trication which followed by chemical reaction (ECEC). Cyclic voltammetry and convolutive voltammetry were used for determination of the chemical and the electrochemical parameters of the electrode reaction pathway of the investigated compound. The Electrochemical parameters such as α, ks, Eo , D, and kc of the investigated isoxazol derivative were verified via digital simulation technique. Voltammetric studies of the investigated isoxazol derivative compound under consideration was presented and discussed.

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Inam, Onur, Ersin Demir, and Bengi Uslu. "Voltammetric Pathways for the Analysis of Ophthalmic Drugs." Current Pharmaceutical Analysis 16, no. 4 (April 27, 2020): 367–91. http://dx.doi.org/10.2174/1573412915666190225163637.

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Background: This review investigates the ophthalmic drugs that have been studied with voltammetry in the web of science database in the last 10 years. Introduction: Ophthalmic drugs are used in the diagnosis, evaluation and treatment of various ophthalmological diseases and conditions. A significant literature has emerged in recent years that investigates determination of these active compounds via electroanalytical methods, particularly voltammetry. Low cost, rapid determination, high availability, efficient sensitivity and simple application make voltammetry one of the most used methods for determining various kinds of drugs including ophthalmic ones. Methods: In this particular review, we searched the literature via the web of science database for ophthalmic drugs which are investigated with voltammetric techniques using the keywords of voltammetry, electrochemistry, determination and electroanalytical methods. Results: We found 33 types of pharmaceuticals in nearly 140 articles. We grouped them clinically into seven major groups as antibiotics, antivirals, non-steroidal anti-inflammatory drugs, anti-glaucomatous drugs, steroidal drugs, local anesthetics and miscellaneous. Voltammetric techniques, electrodes, optimum pHs, peak potentials, limit of detection values, limit of quantification values, linearity ranges, sample type and interference effects were compared. Conclusion: Ophthalmic drugs are widely used in the clinic and it is important to determine trace amounts of these species analytically. Voltammetry is a preferred method for its ease of use, high sensitivity, low cost, and high availability for the determination of ophthalmic drugs as well as many other medical drugs. The low limits of detection values indicate that voltammetry is quite sufficient for determining ophthalmic drugs in many media such as human serum, urine and ophthalmic eye drops.

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CHENG, CHING-CHING, MING-SHING YOUNG, SHANG-WEN YOUNG, and CHANG-LIN CHUANG. "AN INTELLIGENT DIGITAL VOLTAMMETRIC SYSTEM WITH MULTIPLE FUNCTIONS EXECUTED THROUGH STAND-ALONE OPERATION OR PC-CONTROL." Biomedical Engineering: Applications, Basis and Communications 14, no. 05 (October 25, 2002): 218–36. http://dx.doi.org/10.4015/s1016237202000322.

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This study presents an intelligent voltammetric system consisting of a personal computer and a digital voltammeter with VXIbus architecture of system control board, voltammetric measurement board and electrode evaluation board. System is designed to provide superior, comprehensive, versatile and convenient storage, analysis and display of electrochemical and voltammetric waveforms. Voltammeter is capable of stand-alone operation or direct PC control through a Labview program and serial communication interface. Stand-alone offers several general voltammetric functions such as electrochemical treatment and evaluation of electrodes and experimental voltammetry. PC connection gives additional functions such as automatic scanning of oxidation potential, expanded storage and processing of experimental data, arbitrary voltammetric waveform parameters, etc. Standalone uses microcontroller and three-bus structure, with EEPROM storing waveform parameters, experimental data and machine code program downloaded from PC. Electrode evaluation board tests electrode quality by measuring electrode equivalent resistance and capacitance, requiring only one button to perform the entire procedure. Minimum potential unit is 1 mV, at which setting the voltage range is −2.05 to +2.05 V. At a minimum unit of 4.9 mV, the voltage range is −10 to +10V. Experimental results are presented using carbon fiber electrode to measure the dopamine concentration in PBS solution, showing minimum oxidation current can be measured to less than 10 pA, with a minimum detectable bulk concentration of less than 10 ppb. The combination of PC with stand-alone voltammeter offers high-speed, precision, automation, versatility and portability, while the VXIbus architecture allows easy expansion capability.

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Dissertations / Theses on the topic "Voltammetry"

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Rees, Neil V. "Innovations in voltammetry." Thesis, University of Oxford, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408686.

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Wildgoose, Gregory G. "Modified electrode voltammetry." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.432263.

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Adra, Mahmoud. "Voltammetry using microdevices." Thesis, University of Bath, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428375.

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Limon, Petersen Juan Gualberto. "Weakly supported voltammetry." Thesis, University of Oxford, 2010. http://ora.ox.ac.uk/objects/uuid:c14f972c-8653-41c2-b2d1-b080e691e4dc.

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This thesis is concerned with dynamic electrochemical experiments with different concentrations of supporting electrolyte. Normally supporting electrolyte is added to a solution in order to avoid undesirable effects as migration and potential drop in solution. However, in the present thesis we focus on the study and understanding of such effects as the concentration of supporting electrolyte decreases. First a theoretical treatment is proposed, based on numerical simulation using the Nernst-Planck- Poisson system of equations. The theoretical treatment is compared with previous works as electroneutrality, the differences between both models are explained. The model is also compared with theoretical results to validate the theoretical treatment. Experimental results of chronoamperometry and cyclic voltammograms are compared with theoretical results obtaining remarkable agreement. Is noteworthy that to the best of the author’s knowledge this is the first time that experimental dynamic voltammetry under weakly supported conditions has been successfully modeled by a theoretical treatment. The electrochemical reaction of a non-charged electroactive species is presented for the system ferrocene/ferrocenium in acetonitrile in which the oxidized and reduced species are soluble in solution, the reaction is studied at different concentrations of supporting electrolyte. Comparison is presented between theoretical simulations and experimental results, for which potential drop in solution is studied. Then systems involving charged electroactive species are treated, in these cases the decrease of supporting electrolyte influence the mass transport of the electroactive species due to migration, comparison between different experimental systems as hexaammineruthenium (III)/(II), cobaltoceniun/cobaltocene and hexacyanoferrate (III)/(II) are presented in comparison with theoretical simulations. More complex mechanistic paths are also investigated, such as deposition and stripping, in which it is established that the level of support required to achieve ‘diffusion only’ voltammetry is on dependence of the concentration of amalgamated electroactive species prior to the stripping step. Comparison between theoretical simulation and experimental results of the deposition and stripping of thallium at a mercury hemisphere are presented, and found to be in good agreement for either chronoamperometry and cyclic voltammetry Simulations are also presented showing the necessary required amount of supporting electrolyte required to achieve ‘diffusion only’ cyclic voltammetry. This is obtained by comparison between diffusion only software and the simulation described in the present thesis. The required amount of supporting electrolyte is shown to depend on the concentration of the electroactive species and supporting electrolyte in the media, the electrode radius, the diffusion coefficient of species and the scan rate. Finally, the cyclic voltammetry in weakly supporting media is used to obtain mechanistic information, by using the migration of electroactive species to differentiate the mass transport of electroactive species to the electrode. The two single electron reductions of anthraquinone in acetonitrile is presented, and the comproportionation mechanistic path is observed in weakly supported media, diffusion only voltammetry is normally unable to present whether this mechanism path takes place, due to the similarity in diffusion coefficients of the electroactive species. In contrast in weakly support conditions the diffusion controlled comproportionation mechanistic path is observed experimentally and constraints for the rate constant are discussed.

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Bartlett, Thomas. "Nano-impact voltammetry." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:05ca3e7f-fea4-4d93-9f57-e86a2c397d1f.

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This thesis introduces new concepts to the study of nanoparticles by nano-impact voltammetry. Utilising the special chemistries of metal halide and metal oxide nanoparticles, the use of the nano-impact technique is expanded beyond quantitative sizing towards the study of the in-situ synthesis and detection of nanoparticles, reversible agglomeration behaviour and the fabrication of nanoelectrode arrays. Nano-impact voltammetry is also demonstrated to be an informative tool for the tracking of chemical and photochemical conversion reactions of metal halide nanoparticles and for the mechanistic determination of metallic nanoparticle growth during synthesis. The use of forced convection to gain improvements in the detection limit achievable for the direct-impact of metallic nanoparticles is also reported. Initially, the work reported herein looks at the direct-impact voltammetry of previously unstudied nanomaterials; mercury(I) chloride, silver bromide and bismuth oxide. The first sizing of metal halide nanoparticles is reported as well as a method for synthesising particles through the electrolytic induced implosion of a nanoscale metal halide layer on a liquid electrode. The "upper-limit" of the nano-impact technique is also quantified through the use of silver bromide and silver nanoparticles with diameters approaching 100 nm successfully studied. Next, bismuth oxide nanoparticles are studied by the nano-impact method to probe the reversible agglomeration of particles. By reducing impacting bismuth oxide nanoparticles at the electrode, bismuth deposits are shown to result and can be imaged by scanning electron microscopy. Through the analysis of these deposits, in combination with nanoparticle tracking analysis, experimental evidence for the voltammetrically induced de-agglomeration of nanoparticles is proposed. In the subsequent chapter, nano-impact voltammetry is employed in the study of photochemical reactions. First, the photochemical reduction of silver bromide nanoparticles to silver nanoparticles is followed both by ultra-violet visible spectroscopy and nano-impacts, allowing mechanistic determination of the conversion process. Second, the nano-impact technique is used in combination with ultra-violet visible spectroscopy and transmission electron microscopy for the mechanistic determination of the photochemical Ostwald ripening of silver nanoprisms from silver nanoseeds. Finally, the inter-play between nano-impacts and electrode arrays is reported. Through the electrolysis of impacting silver bromide nanoparticles, it is shown that a functional silver nanoelectrode array can be formed. The formed nanoelectrode array is characterised by the electrocatalytic reduction of hydrogen peroxide. The lowest reported detection limit for silver nanoparticles is also reported, through the combination of a random array of microelectrodes and a specially developed, custom built, and characterised wall-jet flow cell.

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Nakagawa, Yasue. "Protein electrochemistry : applications of sonovoltammetry, microelectrode voltammetry and solid-state voltammetry." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325772.

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Owens, Dale Spencer. "Voltammetry in flowing streams." Diss., Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/27054.

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Helfrick, John C. "Cyclic square wave voltammetry." Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/30681.

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Fietkau, Nicole. "New directions in voltammetry." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442948.

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Davies, Trevor J. "Voltammetry at heterogeneous electrodes." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.427873.

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Books on the topic "Voltammetry"

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R, Smyth Malcolm, and Vos Johannes G, eds. Analytical voltammetry. Amsterdam: Elsevier, 1992.

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Mirceski, Valentin, Sebojka Komorsky-Lovric, and Milivoj Lovric. Square-Wave Voltammetry. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-73740-7.

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Eisenhardt, Ingo. Polarography and voltammetry: English/German = Polarographie und Voltammetrie : Deutsch/English. Weinheim: VCH, 1991.

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Justice, Joseph B. Voltammetry in the Neurosciences. New Jersey: Humana Press, 1987. http://dx.doi.org/10.1385/0896031039.

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Justice, Joseph B., ed. Voltammetry in the Neurosciences. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-59259-463-4.

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Christopher, Batchelor-McAuley, and Dickinson Edmund J. F, eds. Understanding voltammetry: Problems and solutions. London: Imperial College Press, 2012.

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7

Gorodyskiĭ, Aleksandr Vladimirovich. Volʹtamperometrii͡a︡: Kinetika stat͡s︡ionarnogo ėlektroliza. Kiev: Nauk. dumka, 1988.

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Kaplan, B. I͡A. Volʹtamperometrii͡a peremennogo toka. Moskva: "Khimii͡a", 1985.

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9

Mirčeski, Valentin. Square-wave voltammetry: Theory and application. Berlin: Springer, 2007.

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Mirceski, Valentin. Square-wave voltammetry: Theory and application. Germany [1990-onward]: Springer Verlag, 2007.

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Book chapters on the topic "Voltammetry"

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Pentel, Paul R., Mark G. LeSage, Mark G. LeSage, Paul R. Pentel, Lawrence H. Price, Tomasz Schneider, Maria-Inés López-Ibor, et al. "Voltammetry." In Encyclopedia of Psychopharmacology, 1366. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_7005.

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Olson, Mark P., and William R. LaCourse. "Voltammetry." In Ewing’s Analytical Instrumentation Handbook, Fourth Edition, 509–22. Fourth edition / [edited by] Nelu Grinberg, Sonia Rodriguez. | Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2019. http://dx.doi.org/10.1201/9781315118024-17.

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Borchert, Holger. "Cyclic Voltammetry." In Solar Cells Based on Colloidal Nanocrystals, 111–17. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04388-3_7.

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Lovrić, Milivoj. "Stripping Voltammetry." In Electroanalytical Methods, 201–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02915-8_10.

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Marken, Frank, Andreas Neudeck, and Alan M. Bond. "Cyclic Voltammetry." In Electroanalytical Methods, 57–106. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02915-8_4.

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Stojek, Zbigniew. "Pulse Voltammetry." In Electroanalytical Methods, 107–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02915-8_5.

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Lovrić, Milivoj. "Stripping Voltammetry." In Electroanalytical Methods, 191–210. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/978-3-662-04757-6_10.

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Marken, Frank, Andreas Neudeck, and Alan M. Bond. "Cyclic Voltammetry." In Electroanalytical Methods, 51–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/978-3-662-04757-6_4.

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Stojek, Zbigniew. "Pulse Voltammetry." In Electroanalytical Methods, 99–110. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/978-3-662-04757-6_5.

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Geiger, W. E. "Cyclic Voltammetry." In Inorganic Reactions and Methods, 110–16. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145302.ch46.

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Conference papers on the topic "Voltammetry"

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Anchidin-Norocel, Liliana, Gheorghe Gutt, and Sonia Amariei. "VOLTAMMETRIC BEHAVIOR AND DETERMINATION OF NICKEL IONS USING BIOPOLYMERS FOR RECEPTOR IMMOBILIZATION." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023v/6.2/s25.58.

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Voltammetry is an electrochemical technique widely used in quantitative analysis to determine nickel ions in food samples due to its excellent stability. Knowing the exact applied levels of metals such as nickel in different food samples is very important to prevent high nickel consumption, especially in people with allergies and nickel excess. Electrochemical analytical methods appear to be an alternative with many advantages, including high sensitivity, low detection limits on the g/L scale, ease of use, and simple sample preparation. This study describes the voltammetric behavior of nickel biosensors using biopolymers such as agar, chitosan, alginate, and carrageenan, to immobilize the receptors and investigates the analytical performance using three biopolymer concentrations. The analytical performance of screen-printed carbon electrodes (SPEs) immobilized with the biopolymer-biosensor combinations was analyzed by linear sweep voltammograms (LSVs). The voltammetric behavior favored the method using carrageenan in terms of linear sweep voltammetry (LSV) performance characteristics with sensitivities of 6.79 for 0.5%, and 6.87 for 1% (?A Mm-1 cm-2).

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Reich, Alton, Rodrigo Teixeira, Koy Cook, Waite Dykes, and Stelu Deaconu. "Initial Investigations Into the Development of Thin Film Voltammetric Sensors." In ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-26140.

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Voltammetry is an electrochemical sensing technique that has been in use for almost a century using macro-scale electrodes. This paper discusses initial investigations into the development of a prototype voltammetric sensing system that uses electrodes with nano-scale features to reduce the size of the electrodes and increase performance. Modeling, fabrication, and testing are discussed.

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HU, Hongsheng, Qunfeng NIU, Yinqing PAN, and Li WANG. "Voltammetric Electronic Tongue for Different Varieties of Rice Classification Based on Square Wave Voltammetry." In The 2015 International Conference on Mechanical Engineering and Control Systems (MECS2015). WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789814740616_0077.

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Kauffman, Robert E. "New, Rapid Techniques for Determining the Hydroperoxide Content, Oxidation Stability, and Thermal Stability of Jet Fuels." In ASME 1994 International Gas Turbine and Aeroengine Congress and Exposition. American Society of Mechanical Engineers, 1994. http://dx.doi.org/10.1115/94-gt-346.

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New, rapid analytical techniques based on cyclic voltammetry are being developed to determine the hydroperoxide contents and the thermal and thermaloxidation stabilities of different type jet fuels (straight run, hydrotreated, JP-4, and JP-5). The techniques are performed at room temperature, use less than 1 mL of fuel, and use common solvents containing different electrolytes or reactive compounds. The cyclic voltammetric techniques were used to quantify the natural antioxidants, easily oxidizable compounds, and hydroperoxides present in different type fuels. Mathematical relationships were then developed to evaluate the potential of the voltammetric results to predict the thermal and oxidative stabilities of the jet fuels determined by high temperature oxidation and thermal stability tests.

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Jung, Younsu, Hyejin Park, Jin-Ah Park, Jinsoo Noh, Yunchang Choi, Minhoon Jung, Kyunghwan Jung, et al. "Fully gravure printed wireless cyclic voltammetry tags." In 2014 Electronics System-Integration Technology Conference (ESTC). IEEE, 2014. http://dx.doi.org/10.1109/estc.2014.6962760.

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Hu, Z., P. R. Troyk, and S. F. Cogan. "Comprehensive Cyclic Voltammetry Characterization of AIROF Microelectrodes." In 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1615662.

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Tiwari, Kamalika, Bipan Tudu, Rajib Bandhopadhya, and Anutosh Chatterjee. "Discrimination of monofloral honey using cyclic voltammetry." In 2012 3rd National Conference on Emerging Trends and Applications in Computer Science (NCETACS). IEEE, 2012. http://dx.doi.org/10.1109/ncetacs.2012.6203312.

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Yanping Wang, Jing Cao, Yi Li, Xiaoyun Xia, and Xudong Xu. "Preparation and cyclic voltammetry behaviors of LaCoO3 nanocrystals." In 2010 International Conference on Mechanic Automation and Control Engineering (MACE). IEEE, 2010. http://dx.doi.org/10.1109/mace.2010.5535746.

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Clees, Tanja, Igor Nikitin, Lialia Nikitina, Sabine Pott, Ulrike Krewer, and Theresa Haisch. "Parameter Identification in Cyclic Voltammetry of Alkaline Methanol Oxidation." In 8th International Conference on Simulation and Modeling Methodologies, Technologies and Applications. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0006832002790288.

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Przenioslo, Lukasz, Michal Raczynski, Przemyslaw Makiewicz, Marcin Biegun, Daniel Matias, Andrzej Biedka, and Krzysztof Penkala. "Development of electrochemical measurement system using cyclic voltammetry method." In 2016 21st International Conference on Methods and Models in Automation and Robotics (MMAR). IEEE, 2016. http://dx.doi.org/10.1109/mmar.2016.7575319.

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Reports on the topic "Voltammetry"

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Hoyt, N., C. Pereira, J. Willit, and M. Williamson. Voltammetry Method Evaluation. Office of Scientific and Technical Information (OSTI), July 2016. http://dx.doi.org/10.2172/1326966.

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Ho, I.-Pin. Instrumentation for Multi-Electrode Voltammetry. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1140.

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Lakshmi Narayanan, Ranjitha. Anodic Stripping Voltammetry using EVAL-ADICUP 3029. Ames (Iowa): Iowa State University, January 2019. http://dx.doi.org/10.31274/cc-20240624-222.

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Rossiter, Walter J. Jr, Blaza Toman, Mary E. McKnight, Ijeoma Emenanjo, and Mana Baghai Anaraki. Ultrasonic extractionanodic stripping voltammetry for determining lead in dust:. Gaithersburg, MD: National Institute of Standards and Technology, 2004. http://dx.doi.org/10.6028/nist.ir.6998.

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Rossiter, Walter J. Jr, Blaza Toman, Mary E. McKnight, and Ijeoma Emenanjo. Ultrasonic extractionanodic stripping voltammetry for determining lead in dust:. Gaithersburg, MD: National Institute of Standards and Technology, 2004. http://dx.doi.org/10.6028/nist.ir.7109.

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Murray, R. W. Solid state voltammetry and sensors in solids and gases. Office of Scientific and Technical Information (OSTI), April 1992. http://dx.doi.org/10.2172/5830050.

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Murray, R. (Solid state voltammetry and sensors in solids and gases). Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5315509.

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Rossiter, Walter J. Jr, Mark G. Vangel, Mary E. McKnight, Andrew Signor, and W. Eric Byrd. Ultrasonic extractionanodic stripping voltammetry for determining lead in household paint:. Gaithersburg, MD: National Institute of Standards and Technology, 2001. http://dx.doi.org/10.6028/nist.ir.6571.

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Cahan, B. D., H. M. Villullas, and E. B. Yeager. The Effects of Trace Anions on the Voltammetry of Single Crystal Gold Surfaces. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada211886.

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Wei, X. L., and A. J. Epstein. Simulations of the In Situ Cyclic Voltammetry Dependent EPR Spectra and DC Conductivity. Fort Belvoir, VA: Defense Technical Information Center, September 1997. http://dx.doi.org/10.21236/ada330197.

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