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1

Ina, Toshiaki. "Study on Cathodic Reaction Mechanism of All Solid State Electrochemical Devices." Kyoto University, 2012. http://hdl.handle.net/2433/157658.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(人間・環境学)<br>甲第16947号<br>人博第590号<br>新制||人||141(附属図書館)<br>23||人博||590(吉田南総合図書館)<br>29622<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 杉山 雅人, 教授 田部 勢津久, 准教授 藤原 直樹, 准教授 雨澤 浩史<br>学位規則第4条第1項該当
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2

Williams, Robert Earl Jr. "Simulation and Characterization of Cathode Reactions in Solid Oxide Fuel Cells." Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/16309.

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In this study, we have developed a dense La0.85Sr0.15MnO3-δ (LSM) Ce0.9Gd0.1O1.95 (GDC) composite electrode system for studying the surface modification of cathodes. The LSM and GDC grains in the composite were well defined and distinguished using energy dispersive x-ray (EDX) analysis. The specific three-phase boundary (TPB) length per unit electrode surface area was systematically controlled by adjusting the LSM to GDC volume ratio of the composite from 40% up to 70%. The TPB length for each tested sample was determined through stereological techniques and used to correlate the cell perfor
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3

Phillips, Janice Paige. "Rearrangements of Radical Anions Generated from Cyclopropyl Ketones." Diss., Virginia Tech, 1998. http://hdl.handle.net/10919/40178.

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Cyclopropyl-containing substrates have been frequently utilized as "probes" for the detection of SET pathways in organic and biorganic systems. These reactions are based on the cyclorpropylcarbinyl - homoallyl rearrangement, which is fast and essentially irreversible. The implicit assumption in such studies is that if a "radical" species is produced, it will undergo ring opening. We have found that there are two important factors to consider in the design of SET probes: 1) ring strain, the thermodynamic driving force for the rearrangement, and 2) resonance energy, which may
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4

Herle, Jan van Van herle Jan Van herle Jan Van herle Jan. "Oxygen reduction reaction mechanisms at solid fuel cell cathodes /." [S.l.] : [s.n.], 1993. http://library.epfl.ch/theses/?nr=1187.

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5

Rattakham, Krittin. "Mechanism of Cathodic Prevention of Carbon Steel in Concrete." Scholar Commons, 2017. http://scholarcommons.usf.edu/etd/6630.

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In this work, I aim to clarify the mechanism that allows steel to attain higher chloride threshold as it is cathodically polarized. Specifically, I seek to provide empirical information on whether an intrinsic (predominantly interfacial effects of polarization) or an extrinsic (predominantly concentration changes due to polarization) mechanism may be dominant in the beneficial effect of polarization. I carried out this experiment with 12 identical concrete specimens, each with a cast-in steel plate, constantly exposed them to high-chloride environment. The specimens were divided into 4 triplic
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6

Ishifune, Manabu. "Exploitation of New Synthetic Reactions by Means of Cathodic Reduction." Kyoto University, 1992. http://hdl.handle.net/2433/74620.

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7

Xiao, Yao. "Analysis for reaction mechanism of cathode materials for lithium-sulfur batteries." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263747.

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京都大学<br>新制・課程博士<br>博士(人間・環境学)<br>甲第23286号<br>人博第1001号<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 田部 勢津久, 教授 高木 紀明<br>学位規則第4条第1項該当<br>Doctor of Human and Environmental Studies<br>Kyoto University<br>DFAM
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8

Каракуркчі, Ганна Володимирівна. "Електрохімічне формування функціональних покриттів сплавами заліза з молібденом і вольфрамом". Thesis, НТУ "ХПІ", 2015. http://repository.kpi.kharkov.ua/handle/KhPI-Press/21865.

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Дисертація на здобуття наукового ступеня кандидата технічних наук за спеціальністю 05.17.03 – технічна електрохімія. – Національний технічний університет “Харківський політехнічний інститут”, Харків, 2015 р. Дисертацію присвячено розробці технології електрохімічного формування функціональних покриттів сплавами заліза з молібденом і вольфрамом із цитратних електролітів для одержання матеріалів з високою корозійною стійкістю, фізико-механічними та трибологічними характеристиками. На підставі аналізу кінетичних закономірностей встановлено механізм електрохімічного одержання сплавів Fe-Mo і Fe-Mo-
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9

Yan, Xuecheng. "Carbon-based Porous Materials for Electrochemical Reactions." Thesis, Griffith University, 2016. http://hdl.handle.net/10072/366852.

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The exploration of highly active and durable cathodic oxygen reduction reaction (ORR) catalysts with economical production cost is still the bottleneck to realize the large-scale commercialization of some emerging technologies, such as fuel cells and metal-air batteries. At present, the composite that contains expensive platinum (Pt) particles dispersed on a porous carbon support (e.g., activated carbon (AC)) is the most efficient ORR catalyst. In a common sense, the AC itself normally shows very low activity for the ORR, so the Pt particles are vital. Imagine that if we remove all of the Pt
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10

Сачанова, Юлія Іванівна. "Електрохімічне формування покривів сплавами і композитами Fe–Co–Mo(MoOₓ)". Thesis, Національний технічний університет "Харківський політехнічний інститут", 2020. http://repository.kpi.kharkov.ua/handle/KhPI-Press/43990.

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Дисертація на здобуття наукового ступеня кандидата технічних наук за спеціальністю 05.17.03 – Технічна електрохімія. – Національний технічний уні-верситет “Харківський політехнічний інститут”, Харків, 2019. Дисертаційну роботу присвячено розробці технології електроосадження функціональних покривів сплавами заліза з кобальтом і молібденом з комплек-сних цитратних електролітів. За результатами аналізу іонних рівноваг і кінетичних закономірностей встановлено, що молібден відновлюється у сплав з ферумом та кобальтом до металевого стану з гетероядерних комплексів через утворення проміжних сполук як
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11

Tuerxun, Feilure. "Elucidation of reaction mechanism at the anode/electrolyte interface and cathode material for rechargeable magnesium battery." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263749.

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京都大学<br>新制・課程博士<br>博士(人間・環境学)<br>甲第23288号<br>人博第1003号<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 高木 紀明, 教授 中村 敏浩<br>学位規則第4条第1項該当<br>Doctor of Human and Environmental Studies<br>Kyoto University<br>DFAM
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12

Komatsu, Hideyuki. "Elucidation of Reaction Mechanism for High Energy Cathode Materials in Lithium Ion Battery using Advanced Analysis Technologies." Kyoto University, 2019. http://hdl.handle.net/2433/242753.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(人間・環境学)<br>甲第21876号<br>人博第905号<br>新制||人||216(附属図書館)<br>2018||人博||905(吉田南総合図書館)<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授 内本 喜晴, 教授 田部 勢津久, 教授 吉田 鉄平<br>学位規則第4条第1項該当
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13

West, H. "Kinetics and mechanism of wood-isocyanate reactions." Thesis, Bangor University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.382248.

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14

Сачанова, Юлія Іванівна. "Електрохімічне формування покривів сплавами і композитами Fe–Co–Mo(MoOₓ)". Thesis, Національний технічний університет "Харківський політехнічний інститут", 2019. http://repository.kpi.kharkov.ua/handle/KhPI-Press/43993.

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Дисертація на здобуття наукового ступеня кандидата технічних наук за спеціальністю 05.17.03 – Технічна електрохімія. – Національний технічний університет «Харківський політехнічний інститут», Харків, 2019. Дисертаційну роботу присвячено розробці гальванохімічної технології покривів тернарними сплавами і композитами системи ферум-кобальт-молібден з підвищеним рівнем функціональних властивостей на підставі гіпотези про інкорпорацію оксидів тугоплавких компонентів як інтермедіатів електродних реакцій, до складу металевої матриці. Обґрунтовано компонентний склад електроліту та співвідношення конц
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15

Bondock, Samir. "Mechanism and synthetic use of Paternò-Büchi reactions spin mapping and photo aldol reactions /." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968091725.

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16

Besold, Daniel. "Kinetics and mechanism of model reactions in thermoresponsive nanoreactors." Doctoral thesis, Humboldt-Universität zu Berlin, 2021. http://dx.doi.org/10.18452/22367.

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Zwei Modellreaktionen wurden mit thermoresponsiven Nanoreaktoren untersucht. Die Reduktion von 4-Nitrophenol und von Kaliumhexacyanidoferrat(III) mit Natriumborhydrid. Die Nanoreaktoren bestehen aus einem Polystyrol Kern, umgeben von einer Hydrogel Schale aus Poly-(N-Isopropylacrylamid). Die Reaktionen werden auf der Oberfläche von Metall Nanopartikeln in der Hydrogel Schale katalysiert. In einer auf Gold- und Silberkatalysatoren fokussierten Literaturstudie zeigte sich, dass der geschwindigkeitsbestimmende Reaktionsschritt zwischen beiden Metallen variieren könnte. Kinetische Studien mit Sil
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17

Tanaka, Motomasa. "THE REGULATION MECHANISM OF CATALYTIC REACTIONS IN HEME-PEROXIDASE." Kyoto University, 1999. http://hdl.handle.net/2433/181790.

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18

Bethell, R. C. "The mechanism of some phosphoryl transfer reactions, including the mechanism and inhibition of glutamine synthetase." Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.382972.

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19

O'Brien, Harry. "Advances in iron-catalysed cross-coupling reactions : methodology and mechanism." Thesis, University of Bristol, 2018. http://hdl.handle.net/1983/84e24322-d526-4169-9ed4-e7a2fb2d710a.

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The replacement of noble metals with cheap, sustainable and non-toxic iron as catalysts for cross coupling reactions continues unabated. The significant advancement in methodology has been accompanied by elegant mechanistic studies; vital for further reaction development. Amongst this success, the development of reactions which work with milder coupling partners is paramount. Organoboron reagents are particularly useful, and accordingly there has been great progress in the development of iron-catalysed Suzuki cross-coupling reactions. However, the cross-coupling between an aryl halide and aryl
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20

Ridlehuber, Richard Walter. "The mechanism of reaction of alkyl halides with diphenylphosphides." Thesis, Georgia Institute of Technology, 1988. http://hdl.handle.net/1853/26812.

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21

Chung, Lung Wa. "Theoretical studies of organometallic reactions in water and the mechanism and stereochemistry of hydrosilylation and hydroacylation reactions /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202003%20CHUNG.

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22

Georgieva, Polina. "Quantum Chemical Modeling of Enzymatic Methyl Transfer Reactions." Doctoral thesis, Stockholm : Bioteknologi, Kungliga Tekniska högskolan, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-9695.

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23

Parera, Briansó Magda. "Transition metal-catalysed [2+2+2] cycloaddition reactions. Methodology and mechanism." Doctoral thesis, Universitat de Girona, 2014. http://hdl.handle.net/10803/145035.

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The transition-metal catalysed [2+2+2] cycloaddition reaction is a highly efficient synthetic tool that allows six-membered polysubstituted carbo- and heterocyclic derivatives to be obtained in an atom economy process. This doctoral thesis is based on methodological and mechanistic studies of the rhodium(I)-catalysed [2+2+2] cycloaddition reaction. In particular, the use of hemilabile S-stereogenic and P-stereogenic ligands for the rhodium-catalysed [2+2+2] cycloaddition is described. The activity of these new catalytic systems is evaluated in the cycloaddition of three alkynes and in the enan
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24

Patel, Jagvi Ramesh. "Kinetics and mechanism of hydrolysis and proton transfer reactions in solution." Thesis, King's College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271412.

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25

Besold, Daniel [Verfasser]. "Kinetics and mechanism of model reactions in thermoresponsive nanoreactors / Daniel Besold." Berlin : Humboldt-Universität zu Berlin, 2021. http://d-nb.info/1226757898/34.

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26

Kundu, Mainak. "Dynamics and Mechanism of Short-Range Electron Transfer Reactions in Flavoproteins." The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1557100528978923.

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27

Fu, Qiang [Verfasser], and H. [Akademischer Betreuer] Ehrenberg. "Reaction mechanism study of vanadium pentoxide as cathode material for beyond-Li energy storage via in operando techniques / Qiang Fu ; Betreuer: H. Ehrenberg." Karlsruhe : KIT-Bibliothek, 2019. http://d-nb.info/1189212447/34.

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28

Van, Zyl Johannes Jacobus. "The role of a direct knock-out mechanism in the inclusive (p, \03B1) reaction /." Link to the online version, 2008. http://hdl.handle.net/10019/797.

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29

Fernández, Alvarez Víctor Miguel. "A computational approach to the mechanism of light-driven reactions in solution." Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/402464.

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Aquesta tesi doctoral descriu l'aplicació, d'una combinació de mètodes DFT (Teoria del Funcional de la Densitat) i models cinètics, per elucidar el mecanisme de reaccions en solució iniciades per llum. Aquesta estratègia és usada per estudiar dos tipus de reaccions d'interès comercial. A la primera part, s'analitza el mecanisme de transformacions químiques activades directament per llum. En canvi, la segona part abasta reaccions en què l'activació lumínica passa a través d'un foto-catalitzador. En tots dos casos, els resultats i les propietats experimentals, com ara la selectivitat o el rendim
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30

Uchida, Takeshi. "Studies on the Regulation Mechanism of Ligand Binding Reactions in Heme Proteins." Kyoto University, 1998. http://hdl.handle.net/2433/77865.

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Couce, Ríos Almudena. "Mechanistic insights into metal-catalyzed hydroamination reactions." Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/403762.

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El tema de esta tesis es el estudio DFT del mecanismo de hidroaminaciones intermoleculares catalizadas por catalizadores de rodio y oro. Los compuestos que contienen nitrógeno son muy valiosos y tienen muchos usos que van desde productos farmacéuticos hasta productos químicos. La reacción de hidroaminación es la vía más económica para sintetizar aminas sustituidas. Los catalizadores metálicos que han sido desarrollados para la hidroaminación directa incluyen tanto lantánidos como metales de transición tempranos y tardíos. Los catalizadores más versátiles para la hidroaminación intermolecular
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Lau, Jason C. S. "Spin-selective chemical reactions in radical pair magnetoreception." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:695e3b49-c872-4403-8c70-153a3df8430b.

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Many animals on earth need to navigate in their own environments for breeding and foraging. The ability to determine a correct heading and the current location for a migratory bird is critical for its survival. Animals that are sensitive to the Earth’s magnetic field can use it to obtain their direction of travel. In 2000, a paper suggested that radical pair reaction could form the basis for magnetoreception in migratory birds and a flavoprotein, cryptochrome, was proposed as the candidate for the radical pair precursor. Recent in vivo experimental results strongly support the hypothesis that
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33

McKenna, Eugene Gerard. "The stereochemistry and mechanism of Wittig reactions of phosphonium and arsonium ylide anions." Thesis, Queen's University Belfast, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335560.

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Denha, Abdulahad Matti. "Rate and mechanism of some free radical reactions of importance in atmospheric photochemistry." Thesis, University of Leeds, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278274.

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35

Montoya, Arango Juan Felipe. "Photocatalytic reactions: Mechanistic and kinetic implications." Doctoral thesis, Universitat Autònoma de Barcelona, 2013. http://hdl.handle.net/10803/131320.

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La Fotocatálisis Heterogénea con Dióxido de Titanio (TiO2) ha sido ampliamente estudiada en los últimos 30 años. Como resultado de este esfuerzo de investigación se han obtenido grandes avances en la comprensión de los fenómenos fundamentales involucrados en el proceso y se ha logrado la aplicación exitosa de varios dispositivos con tecnología fotocatalítica en áreas como la remediación medioambiental, la producción de energía renovable, y el diseño de materiales con propiedades de “autolimpieza”. Sin embargo, la comunidad científica en el campo de la fotocatálisis reconoce que existen diversa
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Cho, Yong Kweon. "Kinetic and Chemical Mechanism of Pyrophosphate-Dependent Phosphofructokinase." Thesis, University of North Texas, 1988. https://digital.library.unt.edu/ark:/67531/metadc332128/.

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Data obtained from isotope exchange at equilibrium, exchange of inorganic phosphate against forward reaction flux, and positional isotope exchange of 18O from the (βγ-bridge position of pyrophosphate to a (β-nonbridge position all indicate that the pyrophosphate-dependent phosphofructokinase from Propionibacterium freudenreichii has a rapid equilibrium random kinetic mechanism. All exchange reactions are strongly inhibited at high concentrations of the fructose 6-phosphate/Pi and MgPPi/Pi substrate-product pairs and weakly inhibited at high concentrations of the MgPPi/fructose 1,6-bisphosphate
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Yan, Fan. "Mapping Students' Ideas About Chemical Reactions At Different Educational Levels." Diss., The University of Arizona, 2015. http://hdl.handle.net/10150/556950.

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Understanding chemical reactions is crucial in learning chemistry at all educational levels. Nevertheless, research in science education has revealed that many students struggle to understand chemical processes. Improving teaching and learning about chemical reactions demands that we develop a clearer understanding of student reasoning in this area and of how this reasoning evolves with training in the discipline. Thus, we have carried out a qualitative study using semi-structured interviews as the main data collection tool to explore students reasoning about reaction mechanism and causality.
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Dzierlenga, Anika L. "Mechanism and Functional Consequence of MRP2 Mislocalization in Nonalcoholic Steatohepatitis." Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/613592.

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Adverse drug reactions (ADRs) are a pervasive complication in the realm of pharmacotherapy. At the root of ADRs lies interindividual variability in drug response, which can range from allergic reactions, to genetic variability, to any factors that influence the pharmacokinetics of a drug. Nonalcoholic steatohepatitis (NASH) is the late-stage of non-alcoholic fatty liver disease (NAFLD), characterized by fat deposition, oxidative stress, inflammation, and fibrosis. Over the last several years, alterations in drug metabolizing enzymes and transporters have been broadly characterized through NAFL
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White, Colin L. "Mechanism & stereochemistry of some reactions of IV- & V- co-ordinated phosphorus compounds." Thesis, University of Leicester, 1985. http://hdl.handle.net/2381/33991.

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A series of cyclic phosphoranes and spirophosphoranes have been prepared and reacted with diethyl phosphorochlor- idite, the phosphorane acting as a nucleophile, and the subsequent products reacted further with methyl iodide and chloral. Reactions have also been carried out in which a nucleophilic attack on the phosphorane occurs, the nucleophile employed being the anion of thio-phenol. It was hoped these reactions might provide a new pathway to the type of phosphorus compound which have been involved for a number of years in the control of pestsoniiosects and that an insight into the stereoel
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Awan, I. A. "Kinetics and mechanism of the gas phase reactions of thermally and chemically activated methoxycyclopropanes." Thesis, University of Southampton, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355158.

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41

Ashtewi, Mahmud Ashtewi Saleh. "Electrochemical studies of the kinetics and mechanism of aqueous iron reactions in mine-water." Thesis, University of Newcastle upon Tyne, 2013. http://hdl.handle.net/10443/1918.

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This work has been conducted to investigate the chemical processes involved in the remediation of acidic mine drainages (AMD) using electroanalytical methods to study the chemistry of Fe(III) in pure laboratory solutions and samples obtained from Shilbottle Colliery (Northumberland, UK), which are heavily contaminated with soluble Fe leached from the spoil heap. One method for remediation is to raise the pH of the waters and precipitate Fe(III) in an artificial wetland; however microelectrode voltammetry shows significant soluble Fe(III) remains. The characterization of hydrolysed species of F
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42

Haegele, Joseph. "A mechanism based approach to evaluating adverse drug reactions in a medico-legal setting." Thesis, Boston University, 2012. https://hdl.handle.net/2144/12408.

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Thesis (M.S.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.<br>The following thesis is an evaluation of the various mechanistic underpinnings of adverse drug reactions, including prescription drug-drug, drug-food, and dru gsupplement interactions, as well as "type B" advers
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ACHILLI, ELISABETTA. "Mechanism of electrocatalytic and photo-electrocatalytic reactions by in operando X-Ray absorption spectroscopy." Doctoral thesis, Università degli studi di Pavia, 2017. http://hdl.handle.net/11571/1215967.

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The purpose of my PhD research work is the investigation of the mechanism and the kinetics of electrocatalytic and photo-electrocatalytic reactions by means of in operando X-ray Absorption Spectroscopy. The attention has been focused on five electrochemical systems which can be divided into two groups on the basis of their catalytic properties. The first group essentially deals with the catalysis of the water splitting reaction: belonging to this group I firstly considered electrodes constituted of IrOx, which represents one of the major electrocatalysts in this field. Coupling IrOx electrocat
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Collins, Courtney Lloyd. "Examination of the mechanism by which lithium additives inhibit alkali-silica reaction gel expansion." Thesis, Georgia Institute of Technology, 2002. http://hdl.handle.net/1853/21295.

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Liao, Jing-Piin. "A Reinvestigation of the Kinetics and Mechanism of Ligand Exchange in Mu-(2,2,8,8-Tetramethyl-3, 7-Dithianonane)-Decacarbonylditungsten(0)." Thesis, University of North Texas, 1988. https://digital.library.unt.edu/ark:/67531/metadc500831/.

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This student is interested in reinvestigating the kinetics and mechanism of the bridged compound in l,2-dichloroethane with triisopropyl phosphite and in finding the reasons why the values of competition ratio k₋₂ /k₃ in this reaction are so large.
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Loiseau, Francis. "Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23794.

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Hydroamination stands as a desirable approach to nitrogen-containing molecules, which have important applications ranging from pharmaceuticals (fine chemicals) to paints, coatings, insecticides and agrochemicals (bulk chemicals). It features the use of alkene and alkyne starting materials, which are abundant and rarely used in the formation of C-N bonds. This work aims at building on the improved Cope-type reactivity developed in the Beauchemin group by expanding the reach of the reaction and understanding its mechanistic complexities. The first part of this thesis describes the development of
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Ribeiro, Joao Marcelo Lamim. "Kinetics and Reaction Mechanisms for Methylidyne Radical Reactions with Small Hydrocarbons." FIU Digital Commons, 2016. http://digitalcommons.fiu.edu/etd/3023.

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The chemical evolution with respect to time of complex macroscopic mixtures such as interstellar clouds and Titan’s atmosphere is governed via a mutual competition between thousands of simultaneous processes, including thousands of chemical reactions. Chemical kinetic modeling, which attempts to understand their macroscopic observables as well as their overall reaction mechanism through a detailed understanding of their microscopic reactions and processes, thus require thousands of rate coefficients and product distributions. At present, however, just a small fraction of these have been well-s
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Shi, Weiwei. "Kinetic and spectroscopic characterization of the reductive and oxidative half-reactions of trimethylamine dehydrogenase." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1085107954.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Title from first page of PDF file. Document formatted into pages; contains xvii, 215 p.; also includes graphics (some col.) Includes bibliographical references (p. 208-215). Available online via OhioLINK's ETD Center
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Inomata, Satoshi. "Spectroscopic measurement of halogenated vinoxy radicals and mechanism for the reactions of haloethylenes with atomic oxygen." 京都大学 (Kyoto University), 2003. http://hdl.handle.net/2433/149574.

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Liao, Rongzhen. "Quantum Chemical Cluster Modeling of Enzymatic Reactions." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-43026.

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The Quantum chemical cluster approach has been shown to be quite powerful and efficient in the modeling of enzyme active sites and reaction mechanisms. In this thesis, the reaction mechanisms of several enzymes have been investigated using the hybrid density functional B3LYP. The enzymes studied include four dinuclear zinc enzymes, namely dihydroorotase, N-acyl-homoserine lactone hydrolase, RNase Z, and human renal dipeptidase, two trinuclear zinc enzymes, namely phospholipase C and nuclease P1, two tungstoenzymes, namely formaldehyde ferredoxin oxidoreductase and acetylene hydratase, aspartat
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