Relevant bibliographies by topics / Titration redox

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

Academic literature on the topic 'Titration redox'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Titration redox"

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FERNANDEZ-MAESTRE, Roberto. "THE IMPORTANCE OF TEACHING TITRATION CURVES IN ANALYTICAL CHEMISTRY." Periódico Tchê Química 17, no. 34 (March 20, 2020): 213–19. http://dx.doi.org/10.52571/ptq.v17.n34.2020.230_p34_pgs_213_219.pdf.

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Titration curves are an essential subject of an Analytical Chemistry course. The main objective of calculating titration curves is the selection of an indicator for such titrations. The calculation of titration errors is imperative because they establish if a given indicator can be used for a given titration. This study reviews the available literature on titration curves and calculating their errors. Its purpose is to draw attention to the importance of undergraduate chemistry students having competencies to determine the titration errors rather than skills to build titration curves as the ultimate purpose of these curves is to determine the failure committed when using a given indicator to assess their endpoints. It is shown that the pH and potential calculation at the equivalence point in acid-base and redox titrations, respectively, are not required to choose the titration indicator, one that yields an acceptable error according to the type of application needed. Methods to calculate these errors in the four main types of titrations are presented; those for complexometric and precipitation titrations are simpler than in the literature. Here, it is also demonstrated that calculating points immediately after and before the curve inflection are more critical for this selection in these two types of titrations. Also, it is deducted that complexometric and precipitation curves are not required to select indicators for these titrations. These demonstrations are essential because analytical chemistry teachers may disregard teaching important topics by spending time calculating unnecessary titration curves (complexometric and precipitation titrations) or additional points of titration curves (redox and acid-base titrations) when the calculation of titration errors of these reactions is more critical. Most analytical chemistry textbooks neglect this topic. Undergraduate chemistry programs should focus more on calculating titration errors than on the construction of titration curves.
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Meija, Juris, Anna Maria Michałowska-Kaczmarczyk, and Tadeusz Michałowski. "Redox titration challenge." Analytical and Bioanalytical Chemistry 409, no. 1 (December 31, 2016): 11–13. http://dx.doi.org/10.1007/s00216-016-0020-0.

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Michałowski, Tadeusz, Anna Maria Michałowska-Kaczmarczyk, and Juris Meija. "Solution to redox titration challenge." Analytical and Bioanalytical Chemistry 409, no. 17 (June 13, 2017): 4113–15. http://dx.doi.org/10.1007/s00216-017-0308-8.

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Ullmann, G. Matthias, and Elisa Bombarda. "pKa values and redox potentials of proteins. What do they mean?" Biological Chemistry 394, no. 5 (May 1, 2013): 611–19. http://dx.doi.org/10.1515/hsz-2012-0329.

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Abstract In this article, we review a microstate model that uses protonation and redox microstates in order to understand the complex pH and redox titration of proteins and other polyelectrolytes. From this model, it becomes obvious that it is impossible to assign pKa values or redox potentials to individual protonatable or redox-active sites in a protein in which many of such sites interact. Instead each site is associated with many microscopic equilibrium constants that may lead to irregular or even non-monotonic titration curves of some groups. The microstate model provides a closed theoretical framework to discuss such phenomena.
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Huang, Tzu-Yang, Matthew J. Crafton, Yuan Yue, Wei Tong, and Bryan D. McCloskey. "Deconvolution of intermixed redox processes in Ni-based cation-disordered Li-excess cathodes." Energy & Environmental Science 14, no. 3 (2021): 1553–62. http://dx.doi.org/10.1039/d0ee03526b.

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Michalowski, Tadeusz, and Andrzej Lesiak. "Acid-Base Titration Curves in Disproportionating Redox Systems." Journal of Chemical Education 71, no. 8 (August 1994): 632. http://dx.doi.org/10.1021/ed071p632.

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MOSS, DAVID A., and DEREK S. BENDALL. "Redox titration of the slow ΔA518 in chloroplasts." Biochemical Society Transactions 14, no. 1 (February 1, 1986): 57–58. http://dx.doi.org/10.1042/bst0140057a.

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Michałowska-Kaczmarczyk, Anna M., Maciej Rymanowski, Agustin G. Asuero, Marcin Toporek, and Tadeusz Michałowski. "Formulation of Titration Curves for Some Redox Systems." American Journal of Analytical Chemistry 05, no. 13 (2014): 861–78. http://dx.doi.org/10.4236/ajac.2014.513095.

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de Levie, Robert. "A simple expression for the redox titration curve." Journal of Electroanalytical Chemistry 323, no. 1-2 (January 1992): 347–55. http://dx.doi.org/10.1016/0022-0728(92)80022-v.

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Xiaobo, Sun, and Wang Jinping. "Application of Origin Software to Redox Titration Curve Plotting." University Chemistry 30, no. 4 (2015): 78–85. http://dx.doi.org/10.3866/pku.dxhx20150478.

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Dissertations / Theses on the topic "Titration redox"

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Relli-Dempsey, Vincent M. T. Relli-Dempsey. "A Thermometric Titration Study of Acetaminophen and Sodium Hypochlorite." Ohio Dominican University Honors Theses / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=oduhonors152621864170557.

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Bergdoll, Lucie. "Purification et caractérisation d'un super-complexe respiratoire." Thesis, Paris 6, 2014. http://www.theses.fr/2014PA066310/document.

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Les membranes impliquées dans les processus bioénergétiques arborent une très grande densité de protéines, paramètre déterminant pour leur organisation supra-moléculaire. Dans ce travail, nous avons utilisé la bactérie thermophile Geobacillus stearothermophilus comme modèle pour étudier la formation de super-complexes de protéines membranaires, en vue d'une étude structurale. Nous avons purifié et caractérisé un super-complexe comprenant une menaquinol: cytochrome c oxydoréductase (b6c), un cytochrome c550 et une cytochrome c oxydase caa3. En combinant des titrations par spectroscopie optique et résonance paramagnétique électronique, nous avons pu déterminer les potentiels d'oxydo-réduction de la plupart des cofacteurs et combler ainsi une lacune dans l'étude des chaînes de transfert d'électrons utilisant des quinones à bas potentiel redox, les ménaquinones. Nous avons ainsi montré que les potentiels redox des cofacteurs du cytochrome b6c terminés par celui des quinones. Ce travail va à l'encontre de données partielles antérieures publiées, mais est en parfait accord avec les modèles du Q-cycle de Peter Mitchell. Les résultats obtenus ont des répercussions sur les rendements bioénergétiques des différents maillons de la chaîne de transfert
Bioenergetic membranes present a high protein density - a crucial factor for their organizationinto super-complexes. This project uses the thermophilic bacteria Geobacillus stearothermophilusas a model to study the formation of membrane protein super-complexes with the aim of structuralstudies. We purified and characterized a super-complex between a menaquinone : cytochromec oxidoreductase (b6c), a cytochrome c550, and a cytochrome c oxidase caa3. Using both opticaland EPR spectroscopy methods, we performed the redox titrations of most of the redox cofactorsof the super-complex. Thus, these results enable a new understanding of menaquinone-usingelectron transport chains, showing that quinones’ redox potential determines the redox potentialof the cytochrome b6c’s cofactors. The conclusions differ from previous partial data, althoughthey fit perfectly with Peter Mitchell’s model of the Q-cycle. These unexpected redox potentialsimpact bioenergetic yields at different levels of the electron transfer chain
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Dragin, Fabienne Christelle. "Structure et propriétés électroniques de nanotubes de carbone en solution polyélectrolyte." Montpellier 2, 2008. http://www.theses.fr/2008MON20189.

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Lai-Thi, Thanh-Lan. "Propriétés physico-chimiques et structurales de deux hémoprotéines de cyanobactérie thermophile." Thesis, Paris 11, 2015. http://www.theses.fr/2015PA112187/document.

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La photosynthèse permet de convertir l’énergie solaire en énergie chimique. Ce processus met en jeu un grand nombre de protéines et complexes protéiques. Le premier complexe de la chaîne photosynthétique est le photosystème II où a lieu l’oxydation de l’eau. Le PSII est composé des protéines D1 et D2. Chez la cyanobactérie thermophile Thermosynechococcus elongatus, il y a trois gènes qui codent trois protéines D1 différentes. La première partie de la thèse décrit le développement d’outils protéomiques basés sur les gels d’électrophorèse 2D pour étudier le protéome des trois différents variants, qui expriment chacun une seule protéine pour D1. Peu de différences ont été trouvées. Toutefois, un seul des variants exprime Tll0287. La deuxième partie de la thèse décrit la caractérisation de Tll0287 avec différents techniques : spectroscopies d’absorption UV-visible ou de résonance Raman et spectro-électrochimie. Tll0287 a été identifié comme un cytochrome de type c, mais il présente beaucoup de caractéristiques inattendues. Les spectres d’absorption UV-visible et de résonance Raman de Tll0287 réduit montrent une dépendance vis-à-vis du pH. Deux formes d’hèmes sont présents dans chacun des états oxydé et réduit. Un changement du ligand cystéine a été observé quand l’hème est réduit. Les titrages redox présentent de multiples potentiels à pH 10 et pH 5. Tll0287 peut fixer une molécule de CO à pH 7,6. Ces caractéristiques suggèrent que Tll0287 pourrait être une protéine senseur. De plus, la structure cristallographique montre que Tll0287 n’a pas un repliement classique d’un cytochrome de type c mais celui d’une protéine senseur. Les mutants de délétion du gène tll0287 ont été construits et aideront à comprendre la fonction de ce nouveau cytochrome. La troisième partie décrit l’étude de PsbV2 : un autre cytochrome de type c. Afin d’obtenir en quantité suffisante la protéine pour permettre sa caractérisation, elle a été surexprimée dans un système homologue en utilisant le promoteur de l’enzyme de la rubisco. Le potentiel redox de PsbV2 a été déterminé, comme étant très bas, inférieur à -460 mV (vs SHE, pH 5). Le spectre d’absorption UV-visible de la forme réduite a été caractérisé. La structure cristallographique de PsbV2 a été résolue et a révélé une cystéine comme ligand axial et un repliement proche de celui de cytochromes connus de T.elongatus. Bien que Tll0287 et PsbV2 présentent une cystéine comme ligand axial, leurs structures et leurs propriétés physico-chimiques suggèrent que leurs fonctions sont bien différentes. Une contribution majeure de cette thèse est la caractérisation d’un nouveau senseur à hème de type c chez les cyanobactéries et le développement d’outils nécessaires pour son étude
Photosynthesis converts solar energy into chemical energy. This process involves a large number of proteins and protein complexes. The first protein complex in the photosynthetic chain is Photosystem II within the oxidation of water takes place. PSII is composed of the D1 and D2 proteins. In the thermophile cyanobacterium Thermosynechococcus elongatus, three genes encoded three different D1 proteins. The first part of this thesis describes the development of proteomics tools based on 2D gel-electrophoresis to study the proteome of three different variants, each expressing a single different D1 protein. Very few differences were found. However, only one expressed the protein Tll0287. The second part of the thesis describes the characterization of Tll0287. It was characterized using different techniques: electronic absorption and Raman resonance spectroscopies and spectro-electrochemistry. Tll0287 has been previously identified as a c-type cytochrome, but it presents some unexpected characteristics. The UV-visible absorption and Raman resonance spectra of reduced Tll0287 show a pH dependence. The reduced and oxidized states each had two different forms of the heme. A switch of ligands from a cysteine to histidine was observed in the reduced state. Redox titration showed multiple midpoints at pH 10 and 5. Tll0287 was shown to fix a CO molecule at pH 7.6. These physical properties suggested that Tll0287 could be a sensor. The crystallographic studies reveal that Tll0287 does not have a classical c-type cytochrome fold and is similar to other known sensor proteins, strengthening the hypothesis that it is a sensor. Deletion mutants were constructed that will help to better understand the function of this new cytochrome. The third part describes a study of the PsbV2, another c-type cytochrome. In order to obtain sufficient quantities to carry out characterization of this protein, it was overexpressed in a homologous system using the promotor of the rubisco enzyme. The redox midpoint potential of PsbV2 was found to be very low, below -460 mV (vs SHE, pH 5). The UV-visible absorption spectrum of the reduced form was determined. The crystallographic structure of PsbV2 was solved and reveals an axial cysteine ligand. Although both Tll0287 and PsbV2 share this feature, their different structures and physico-chemical properties suggest that their functions are unlikely to be similar. A major contribution of this thesis is the characterization of a new c-type cytochrome sensor in cyanobacteria and the development of proteomic tools required to study it
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HUNG, YU-HSUN, and 洪鈺勛. "Study of Spectral Analysis and Redox Titration Applied in Vanadium Redox Flow Battery State-of-Charge Monitoring." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/42h975.

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碩士
國立聯合大學
能源工程學系碩士班
104
Vanadium redox flow battery (VRFB) is currently the most mature technology of MW-level electricity storage. In order for VRFB to play a vital function as energy storage in the power grid containing renewable energy, the battery SOC (state-of-charge) must be in-situ and accurately estimated. At present, the open circuit voltage of the electrolyte (OCV) is used to estimate the SOC. From theoretical calculation result, the battery SOC cannot be estimated by measuring battery OCV along. This project develops two analytical methods to assess the electrolyte SOC and to evaluate their technical feasibility. They are absorption spectroscopy and redox electrode potential titration. Two electrolytes, electrolyte 3.5 is purchased from commercial vendor and electrolyte 4.0 is lab-prepared electrolyte are used for this purpose. With the electrolyte at different SOC, we found that there are several major absorption peaks in the UV-VIS absorption spectrum. Using these peaks can determine the type and concentration of vanadium ions. For electrolyte 4.0, electrolyte sampled from positive electrode at SOC = 10% and SOC = 50%, major absorption peak at wavelength of 420 nm and 615 nm were observed. At SOC = 90%, peak wavelength of 765 nm was observed. Electrolyte sampled from the negative electrode at SOC = 10% and SOC = 50%, major peak at wavelength of 770 nm was observed. At SOC = 90%, at wavelength of 420 to 610 nm were observed. For electrolyte 3.5, sampled from the positive electrode at SOC = 10% SOC = 50%, peak at wavelength of 765 nm was observed. At SOC = 90%, no peak can be detected. Sampled from the negative electrode, at SOC = 10% SOC = 50%, peak at the wavelength of 410 nm and 770 nm were observed. At SOC = 90%, peak at the wavelength of 610 nm was observed. The wave length of major peak are shift due to the interaction among vanadium ions in the electrolyte. In addition, experiments found that vanadium ions in the positive electrode and in the negative electrode are crossover each other. Mathematical models can simulated the UV-Vis spectra at different SOC. However, spectra results at different SOC need the redox potentiometric titration result to enhance its accuracy. Redox potential titration analysis is tested with electrolyte containing pure V2+, V3+, VO2+ ions. The test results verify that the potentiometric titration can detect concentrations and types of various vanadium ions. Then this method is tested with electrolyte 3.5 and electrolytic 4.0 sampled from positive electrode and negative electrode at SOC = 10%, 50%, 90%, respectively. Tested results shown that experimental measurement is consisted with theoretical predictions. The battery SOC can be analyzed using the potentiometric titration techniques. The titration result also indicated that there is a crossover phenomenon between positive and negative electrolyte during battery charge and discharge. This is similar to the observed results of UV-Vis spectroscopy. Due to sampling problem, titration of electrolyte 3.5 has no specific conclusions. V2+ ion end point potential range is 118-309 mV vs. AgCl/Ag. V3+ ion end point potential range is 645-703 mV. VO2+ ion end point potential range is 865-941 mV. In the metal bipolar plate experiment, the baking of metal bipolar plate coated with conductive adhesive is carried out in high-temperature furnace to avoid air bubbles formation. The charge/discharge performance of battery with various conductive adhesive metal bipolar plates is less that we expected. The single cell volumetric power density reach 22 W dm-3 and charge-discharge efficiency of 69%.
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Klingen, Astrid [Verfasser]. "Structure based theoretical characterisation of the redox dependent titration behaviour of cytochrome bc1 / vorgelegt von Astrid Klingen." 2007. http://d-nb.info/983252599/34.

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Dragin, Fabienne Christelle. "Structure et propriétés électroniques de nanotubes de carbone en solution polyélectrolyte." Thèse, 2009. http://hdl.handle.net/1866/6559.

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Henriques, João Manuel Almeida. "Application of QM and MM methodologies to cytochrome c3: charge parametrization of the heme group for classic force fields." Master's thesis, 2010. http://hdl.handle.net/10451/5783.

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Tese de mestrado, Bioquímica, Universidade de Lisboa, Faculdade de Ciências, 2010
In 2009, Machuqueiro and Baptista used Desulfovibrio vulgaris Hildenborough type I cytochrome c3 in the validation of their new implementation of the stochastic titration method, the constant-(pH,E) MD method. DvH-TpI-c3 is a small globular and monomeric tetraheme protein present in the periplasm of the sulfate reducing bacteria DvH. It is constituted by 107 residues plus four hemes covalently bound to cysteines in the polypeptide chain together with bis-histidinyl axial ligation. Therefore, it constitutes a tight densely packed structure where the heme reduction potentials are very close, making it a very demanding test case in terms of prediction. When tested, this method was shown to yield better results when a high dielectric constant, ", was assigned to the protein region. This dependence on " was never found in previous constant-pH MD simulations and poor heme charge parameterization may have been responsible for this effect. Hence, the main goal of this work was to refine the QM parameterization of the redox centers, i.e. obtain new and more accurate charge sets, incorporate them in the new 53A6 GROMOS force field, and finally run constant-(pH,E) MD simulations with a " of 2. Single and multi-conformational approaches were tested using the RESP scheme. Merz-Kollman and CHELPG methods were also used. All tested charge sets and respective charge parameterization methods were found to be valid, and there is not enough margin to unequivocally select one method as the absolute best. Still, the RESP fitting procedure is much more versatile than CHELPG and Merz-Kollman, making it a better suited tool for a generalized derivation of partial atomic charges. When applied to the constant-(pH,E) MD method, these new and more accurate charge sets, enabled us to improve Machuqueiro and Baptista's results. We were, however, unsuccessful in fully reproducing all experimental data. Theoretical and experimental results systematically disagreed when predicting the Ehalf values for hemes III and IV. The reason behind this incongruity is something we plan to investigate in future work.
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Books on the topic "Titration redox"

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Postma, James M., J. Leland Hollenberg, and Julian Roberts. Redox Titrations/The Oxidation Capacity: Separate from Chemistry in the Laboratory 5e. W. H. Freeman, 2000.

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Book chapters on the topic "Titration redox"

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Wörfel, P., M. Bitzer, U. Claus, H. Felber, M. Hübel, and B. Vollenweider. "Redox-Titration in nichtwässerigem Medium." In Laborpraxis, 117–21. Basel: Birkhäuser Basel, 1990. http://dx.doi.org/10.1007/978-3-0348-6162-5_8.

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Allemann. "Redox-Titration in nichtwässerigem Medium." In Analytische Methoden, 117–21. Basel: Birkhäuser Basel, 1988. http://dx.doi.org/10.1007/978-3-0348-5191-6_8.

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Bonomi, Francesco, and Stefania Iametti. "Redox Titration of Flavoproteins: An Overview." In Methods in Molecular Biology, 119–33. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1286-6_8.

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Burgot, Jean-Louis. "A Study of Some Redox Titration Curves." In Ionic Equilibria in Analytical Chemistry, 285–312. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-8382-4_17.

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Fritz, James S., and George H. Schenk. "Redox-Titrationen." In Quantitative Analytische Chemie, 334–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-61546-7_14.

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Wörfel, P., M. Bitzer, U. Claus, H. Felber, M. Hübel, and B. Vollenweider. "Redox-Titrationen in wässerigem Medium." In Laborpraxis, 99–115. Basel: Birkhäuser Basel, 1990. http://dx.doi.org/10.1007/978-3-0348-6162-5_7.

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Allemann. "Redox-Titrationen in wässerigem Medium." In Analytische Methoden, 99–115. Basel: Birkhäuser Basel, 1988. http://dx.doi.org/10.1007/978-3-0348-5191-6_7.

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Ritgen, Ulf. "Eine Kombination mit beachtlichem Potential: Redox-Titrationen." In Analytische Chemie I, 93–100. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-60495-3_7.

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Fritz, James S., and George H. Schenk. "Die Theorie der Redox-Reaktionen und -Titrationen." In Quantitative Analytische Chemie, 303–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-61546-7_13.

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Wagner, Clemens, and Dieter Walz. "Analysis of b-Cytochrome Titrations in Terms of Interacting Redox Couples." In Photosynthesis: from Light to Biosphere, 1759–62. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_414.

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Conference papers on the topic "Titration redox"

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Rizki, Rohazmy, Habib Hernando, Manihar Situmorang, and Simson Tarigan. "The Development of Innovative Learning Material with Project and Multimedia for Redox Titration." In Proceedings of the 7th Mathematics, Science, and Computer Science Education International Seminar, MSCEIS 2019, 12 October 2019, Bandung, West Java, Indonesia. EAI, 2020. http://dx.doi.org/10.4108/eai.12-10-2019.2296376.

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Alekseev, Pavel N., and Alexander L. Shimkevich. "On Voltage-Sensitive Managing the Redox-Potential of MSR Fuel Composition." In 16th International Conference on Nuclear Engineering. ASMEDC, 2008. http://dx.doi.org/10.1115/icone16-48176.

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The principles for optimal managing a composition of base solutions for the molten-salt reactor are formulated here for ensuring the given properties and exchange processes as a selective extracting of salt components. The correction of melt properties can be carried out by means of impurity additives parallel with the forced and controllable variation of reduction-oxidation (redox) potential of the non-stoichiometric salts. The accent is done on a possible application of the potentiometer for monitoring and managing of the properties of MSR fuel compositions. For this, one can use the precision methods of e.m.f and the coulomb-metric titration of sodium (lithium) in a galvanic cell upon the base of Na+(Li+)-β″-Al2O3 solid electrolyte with cation conductivity.
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Reports on the topic "Titration redox"

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Sopok, Samuel. Determination of Trivalent Chromium in Chromium Plating Solutions Using a Redox Titration and Indicator. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada252857.

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Sopok, Samuel. Determination of Chromic Acid in Chromium Plating Solutions Using a Redox Titration and Indicator. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada220641.

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