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Articles de revues sur le sujet "Reaction Mechanism - Theoretical Study"
Wang, Zhi-Xiang, Ming-Bao Huang. et Ruo-Zhuang Liu. « Theoretical study on the insertion reaction of CH(X2Π) with CH4 ». Canadian Journal of Chemistry 75, no 7 (1 juillet 1997) : 996–1001. http://dx.doi.org/10.1139/v97-119.
Texte intégralChen, Shi-Lu, Wei-Hai Fang et Fahmi Himo. « Theoretical Study of the Phosphotriesterase Reaction Mechanism ». Journal of Physical Chemistry B 111, no 6 (février 2007) : 1253–55. http://dx.doi.org/10.1021/jp068500n.
Texte intégralHimo, Fahmi, Jing-Dong Guo, Agnes Rinaldo-Matthis et Pär Nordlund. « Reaction Mechanism of Deoxyribonucleotidase : A Theoretical Study ». Journal of Physical Chemistry B 109, no 42 (octobre 2005) : 20004–8. http://dx.doi.org/10.1021/jp0546150.
Texte intégralSuhail, Mohammad, Sofi Danish Mukhtar, Imran Ali, Ariba Ansari et Saiyam Arora. « Theoretical DFT study of Cannizzaro reaction mechanism : A mini perspective ». European Journal of Chemistry 11, no 2 (30 juin 2020) : 139–44. http://dx.doi.org/10.5155/eurjchem.11.2.139-144.1975.
Texte intégralAmano, Tatsuo, Noriaki Ochi, Hirofumi Sato et Shigeyoshi Sakaki. « Oxidation Reaction by Xanthine Oxidase. Theoretical Study of Reaction Mechanism ». Journal of the American Chemical Society 129, no 26 (juillet 2007) : 8131–38. http://dx.doi.org/10.1021/ja068584d.
Texte intégralYU, LINGJUAN, DACHENG FENG, MAOXIA HE, RUI LI et ZHENGTING CAI. « THEORETICAL STUDY ON HYDROLYSIS MECHANISM OF β-PHOSPHOLACTAMS ». Journal of Theoretical and Computational Chemistry 05, spec01 (janvier 2006) : 421–31. http://dx.doi.org/10.1142/s0219633606002362.
Texte intégralWu, Nan-Nan, Shun-li OuYang et Liang Li. « Theoretical Study of C2H5 + NCO Reaction : Mechanism and Kinetics ». Journal of Chemistry 2018 (2018) : 1–8. http://dx.doi.org/10.1155/2018/3036791.
Texte intégralIshikawa, Ryo, Yasuko Y. Maruo, Keiji Kobayashi et Hiroyuki Teramae. « Theoretical Study on Reaction Mechanism ofLutidine Derivative Formation ». Journal of Computer Chemistry, Japan 14, no 2 (2015) : 30–35. http://dx.doi.org/10.2477/jccj.2015-0006.
Texte intégralLi, Yan, Hui-ling Liu, Xu-ri Huang, Dequan Wang, Chia-chung Sun et Au-chin Tang. « Reaction Mechanism of HCN++ C2H4 : A Theoretical Study ». Journal of Physical Chemistry A 112, no 47 (27 novembre 2008) : 12252–62. http://dx.doi.org/10.1021/jp805285p.
Texte intégralTan, Wei, Tian-jing He, Fan-chen Liu et Dong-ming Chen. « Theoretical Study on Mechanism of C5H7 +O2 Reaction ». Chinese Journal of Chemical Physics 20, no 3 (juin 2007) : 249–57. http://dx.doi.org/10.1088/1674-0068/20/03/249-257.
Texte intégralThèses sur le sujet "Reaction Mechanism - Theoretical Study"
Markovi, Z., JP Engelbrecht et S. Markovi. « Theoretical Study of the Kolbe-Schmitt Reaction Mechanism ». A Journal of Chemical Sciences, 2002. http://encore.tut.ac.za/iii/cpro/DigitalItemViewPage.external?sp=1002008.
Texte intégralInagaki, Taichi. « Theoretical Study on Mechanism and Dynamics of Hydrogen Transfer Reaction ». 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/189341.
Texte intégralPérez, Gallegos Ayax. « Theoretical study on the mechanism of the reaction catalyzed by protein kinase ». Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/386487.
Texte intégralDespite extensive experimental and computational studies about the structure and function of kinases, exact details regarding the complex structural changes and the mechanistic details of individual stages involved in the catalyzed phosphoryl-transfer reaction remain uncertain. In principle, computational studies can provide detailed information and insights to complement experimental studies, but this goal can only be attained when the appropriate computational approaches are employed and the theoretical model used is a good mimic of the biological system. In this Thesis, the QM/MM approach at the DFT/MM level of theory was used to describe the different reaction mechanisms on the potential energy hypersurface of the global phosphoryl-transfer reaction catalyzed by the Protein Kinase A (PKA). Remarkably, besides making use of more complete solvated models of the biomolecular system and higher levels of theory than the ones employed in previous works, several techniques and algorithms within the computational chemistry suite ChemShell were used to improve the accuracy of the reaction path calculations and stationary points optimizations. In particular, more flexible reaction coordinates, the location of the stationary points with the hybrid delocalized internal coordinates, and the microiterative method to locate transition structures allowed us to apply a consistent and reliable multiscale methodology to examine minutely both the associative (involving a concomitant phosphoryl-transfer and protonation of transferred phosphate) and dissociative (involving two steps: phosphoryl-transfer and back protonation of the phosphorylated substrate) mechanisms of the phosphoryl-transfer reaction catalyzed by PKA. Special attention was paid in the specific roles of the invariant residues Asp166, Lys168, and Thr201, the conserved Gly-rich loop, the metal ions, and the conformation and protonation state of the substrate residue side chain and transferred phosphate along the chemical reaction. The results in this Thesis demonstrate that the catalytic reaction catalyzed by PKA is not substrate-dependent and that the dissociative mechanism is clearly more favorable than the associative one. Nevertheless, the presented calculations also show the plausibility of the associative reaction pathway when the dissociative counterpart is impeded as it is in the D166A mutant. This reopens the debate about the plausibility of the associative reaction pathway that in view of the last theoretical works in the field seemed to be overcame. Moreover, the reaction paths for the back protonation of the phosphorylated substrate by Asp166 have been located, so demonstrating that Asp166 behaves as a general acid/base catalyst along the dissociative mechanism. In addition, QM/MM potential energy profiles determined in this Thesis also demonstrate, for the first time, that the catalyzed phosphoryl-transfer is plausible with alkali earth metal ions other than Mg2+ ions, what confirms recent experimental results where the physiological role of Ca2+ in kinase activity has been proposed. For both the associative and the dissociative mechanisms, the precise location and orientation of the triad Asp166-Lys168-Thr201 and the hydrogen bond network these residues establish within the active site are shown to be essential for catalysis, particularly in the stabilization of the transition state structures involved. Lastly, the results in this Thesis provide a complete sequence of the geometrical evolution of the structure of the ternary complex along the catalytic reaction. This permits an accurate comparison with new X-ray crystallographic structures that have been suggested as experimental snapshots of the catalyzed-phosphorylation process In particular, the good agreement between the theoretically determined structures and the crystallographic studies validate the atomic view of the reaction presented in this Thesis, thus revealing conformational, coordination, and hydrogen bond changes that occur during the chemical step and its relation with the enzyme dynamics.
Moagi, Kgotso Herbet. « Reaction Mechanism of 2-monosubstituted Quinoxalines with Organolithium Compounds : a Theoretical Study ». Diss., University of Pretoria, 2020. http://hdl.handle.net/2263/75182.
Texte intégralDissertation (MSc)--University of Pretoria, 2020.
National Research Foundation (NRF)
Chemistry
MSc
Unrestricted
Nowroozi-Isfahani, Taraneh. « Theoretical study on the mechanism of removing nitrogen oxides using isocyanic acid ». [Johnson City, Tenn. : East Tennessee State University], 2001. http://etd-submit.etsu.edu/etd/theses/available/etd-0528101-112444/unrestricted/nowroozi0621.pdf.
Texte intégralJiménez, Halla José Óscar Carlos. « Theoretical study of catalytic reactions of carbenes : haptotropic rearrangements and the Dötz reaction ». Doctoral thesis, Universitat de Girona, 2009. http://hdl.handle.net/10803/7942.
Texte intégralZhang, Tianhou. « Theoretical Studies of Fuel Cell Reaction Mechanisms : Water and Oxygen on Platinum Electrodes ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1215456813.
Texte intégralTussupbayev, Samat. « Theoretical study of reactivity and dynamics of hybride-bridged diruthenium complexes and silylium ». Doctoral thesis, Universitat de Girona, 2009. http://hdl.handle.net/10803/8052.
Texte intégralEn la segunda parte, se estudió el comportamiento fluxional de dos complejos μ-silileno y de un catión sililio. Con esto, se estableció la ruta más favorable en donde se realiza el intercambio de los ligandos hidruro y de los grupos metilo en los complejos μ-silileno. Finalmente, se encontró que hay dos posibles rutas relativas al cambio en la posición del puente Si-H-Si en el cation sililio poliagóstico, asociadas con la rotación interna de los grupos sililo.
The thesis presents a computational study of hydride bridged systems. The chemistry of diruthenium tetrahydride-bridged complex was studied in the first part. It includes the next reactions: the hydride exchange with dihydrogen; the C-H bond activation in ethylene to yield bis(vinyl) ethylene complex; the C-C coupling between coordinated ethy¬lene and two vinyl ligands to yield ruthenacyclopentadiene complex. The detailed mechanism of these reactions has been determined. The importance of flexibility of hydride ligands and cooperation between two metal centers has been demonstrated.
The fluxional behavior of two μ-silylene complexes and a silylium cation was studied in the second part. The pathway responsible for the site-exchange of hydride ligands and methyl groups in the μ-silylene complexes has been established. Two possible mecha¬nisms of the shift of Si-H-Si bridge position in the polyagostic silylium cation, associated with internal rota¬tion of si¬lyl groups have been found.
Fernández, Villanueva Estefanía. « Theoretical Study of the Geometrical, Electronic and Catalytic properties of Metal Clusters and Nanoparticles ». Doctoral thesis, Universitat Politècnica de València, 2020. http://hdl.handle.net/10251/135277.
Texte intégral[CAT] Atès que són de grandària subnanomètrica, els clusters metàl·lics estan regits pel confinament quàntic, el qual els fa més "moleculars" i menys "metàl·lics". En conseqüència, manifesten propietats que són diferents a les de partícules més grans del mateix element, i que sovint són avantatjoses per a la catàlisi de reaccions específiques. A més a més, la seua menor grandària fa que siguen més econòmics, amb una major superfície exposada. Així, els clusters són una opció molt interesant en catàlisi, i el seu estudi, síntesi i aplicació ha cres-cut contínuament des del seu descobriment als anys 90. Aquesta tesi s'ha centrat principalment en el coure, del qual es presenta, en primer lloc, un estudi fonamental sobre la dissociació de l'oxígen per clusters de diferents grandàries. Després, s'explora computacionalment la catàlisi de les oxidacions de CO i de propè, confirmant que els clusters de Cu5 (o inferior) són prometedors per a reaccions d'oxidació. Les dues reaccions utilitzades són bons exemples de l'aplicació potencial en indústria, siga per reduir emissions de CO o per produir epòxid de propè, que és un intermedi important en la producció de plàstics i adhesius, entre altres. A més, també es va estudiar la influència de dos suports en els clusters de coure i la seua capacitat d'oxidació: N-grafè com a un sistema més inert i cèria com a un que pot participar activament en reaccions d'oxidació. Finalment, s'inclouen altres dos estudis més específics, sobre la capacitat dels clusters de Pt3 y Pd3 per catalitzar reaccions d'acoblament C-C com la reacció de Heck, important per a la síntesi de productes de la química fina, i sobre la reacció CO + NO als clusters de Pt, motivat pel seu ús potencial com a catalitzadors per a la conversió d'eixes espècies en els menys perjudicials CO2 i N2 als motors de combustió interna.
[EN] Due to their subnanometric size, metal clusters belong to the regime affected by quantum confinement, which makes them more "molecular" and less "metallic". As a result, they exhibit properties that differ with respect to those of larger particles of the same element, and which are often advantageous in the catalysis of specific reactions. Besides, their smaller size makes them more economic and with a higher surface exposed. All of this renders metal clusters very interesting options for catalysis, and their study, synthesis and application has steadily increased since their discovery in the 90s. In this work we have largely focused on copper, of which a fundamental study on the oxygen dissociation by clusters of different sizes is first presented. Then, the catalysis of the CO and propene oxidation reactions is theoretically explored, confirming that Cu5 (or smaller) clusters are promising systems for oxidation reactions. The two reactions used are good examples of the potential application in industry, either to reduce CO emissions or to produce propene epoxide, an important intermediate in the production of plastics and adhesives, among others. In addition, the influence of two supports in the copper clusters and their oxidation capability is explored: on N-graphene as a more inert system and on ceria as one that can actively participate in oxidation reactions. Finally, two other more specific studies are included, regarding the capability of Pt3 and Pd3 clusters to undergo C-C coupling reactions such as the Heck reaction, important for the synthesis of many products of fine chemistry, and regarding the CO + NO reaction on Pt clusters, motivated by their potential use as catalysts for the conversion of those species in less harmful CO2 and N2 in internal combustion engines.
En primer lugar me gustaría agradecer al Ministerio de Economía y Competitividad de España (MINECO) por la financiación de esta tesis mediante el programa Severo Ochoa (SVP-2013-068146), incluyendo los costes adicionales de mi estancia de investigación (EEBB-I-17-12057).
Fernández Villanueva, E. (2019). Theoretical Study of the Geometrical, Electronic and Catalytic properties of Metal Clusters and Nanoparticles [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/135277
TESIS
Acuña-Parés, Ferran. « Theoretical study of water oxidation and reduction mechanisms by aminopyridine first row transition metal catalysts ». Doctoral thesis, Universitat de Girona, 2016. http://hdl.handle.net/10803/398411.
Texte intégralUn dels grans reptes actuals consisteix en el desenvolupament de fonts d'energia renovables. Una alternativa eficaç als combustibles fòssils consisteix en la conversió de l'energia solar en combustibles químics. L’hidrogen molecular provinent de l’aigua és considerat el portador d’energia més prometador. En la fotosíntesi natural l’energia solar és emmagatzemada en els enllaços químics dels carbohidrats obtinguts a partir d’aigua i CO2. L’etapa clau del procés és la foto-oxidació de l'aigua en O2, que aporta els protons i electrons necessaris per produir H2. El coneixement detallat del mecanisme de reacció resulta essencial per millorar el rendiment catalític i assegurar la compatibilitat dels catalitzadors d’oxidació de l’aigua i reducció de protons. En aquesta tesi, les etapes fonamentals del mecanisme de les reaccions d’oxidació de l’aigua o la reducció de protons catalitzades per un grup de complexos metàl·lics i les característiques estructurals dels catalitzadors que beneficien ambdues reaccions són estudiades utilitzant eines computacionals
Livres sur le sujet "Reaction Mechanism - Theoretical Study"
G, Compton R., et Hamnett A, dir. New techniques for the study of electrodes and their reactions. Amsterdam : Elsevier, 1989.
Trouver le texte intégralP, Kundu Krishna, Acosta Waldo A, United States. National Aeronautics and Space Administration. et United States. Army Aviation Systems Command., dir. Jet-A reaction mechanism study for combustion application. [Washington, DC] : National Aeronautics and Space Administration, 1991.
Trouver le texte intégralP, Kundu Krishna, Acosta Waldo A, United States. National Aeronautics and Space Administration. et United States. Army Aviation Systems Command., dir. Jet-A reaction mechanism study for combustion application. [Washington, DC] : National Aeronautics and Space Administration, 1991.
Trouver le texte intégralMichael, Mortimer, Taylor Peter, Royal Society of Chemistry (Great Britain) et Open University, dir. Chemical kinetics and mechanism. Cambridge : Royal Society of Chemistry, 2002.
Trouver le texte intégralCrowley, John N. A study of reaction mechanism by matrix isolation/FTIR spectroscopy. Norwich : University of East Anglia, 1987.
Trouver le texte intégralUnited States. National Aeronautics and Space Administration. Scientific and Technical Information Division., dir. An analytical study of the hydrogen-air reaction mechanism with application to scramjet combustion. [Washington, D.C.] : National Aeronautics and Space Administration, Scientific and Technical Information Division, 1988.
Trouver le texte intégralUnited States. National Aeronautics and Space Administration. Scientific and Technical Information Division., dir. An analytical study of the hydrogen-air reaction mechanism with application to scramjet combustion. [Washington, D.C.] : National Aeronautics and Space Administration, Scientific and Technical Information Division, 1988.
Trouver le texte intégralPolischuk, Nikolay, et Dmitriy Kohman. The legal mechanism for the implementation of amnesty in the Russian Federation and the social consequences of its application. ru : INFRA-M Academic Publishing LLC., 2023. http://dx.doi.org/10.12737/1863097.
Texte intégralScialpi, Angela, et Alessio Mengoni, dir. La PCR e le sue varianti. Florence : Firenze University Press, 2008. http://dx.doi.org/10.36253/978-88-6453-159-5.
Texte intégralKaragodin, Valeriy, et Nikolay Karepanov. Features of investigation of fraud committed by Bank employees in the field of lending. ru : INFRA-M Academic Publishing LLC., 2020. http://dx.doi.org/10.12737/1064906.
Texte intégralChapitres de livres sur le sujet "Reaction Mechanism - Theoretical Study"
García Melchor, Max. « The Negishi Reaction Mechanism ». Dans A Theoretical Study of Pd-Catalyzed C-C Cross-Coupling Reactions, 59–88. Cham : Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_4.
Texte intégralGarcía Melchor, Max. « The Cu-Free Sonogashira Reaction Mechanism ». Dans A Theoretical Study of Pd-Catalyzed C-C Cross-Coupling Reactions, 89–111. Cham : Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_5.
Texte intégralGarcía Melchor, Max. « An Asymmetric Suzuki-Miyaura Reaction Mechanism ». Dans A Theoretical Study of Pd-Catalyzed C-C Cross-Coupling Reactions, 113–33. Cham : Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_6.
Texte intégralMonge-Palacios, Manuel, Cipriano Rangel, Joaquin Espinosa-García, Hong Fu et Minghui Yang. « Isotope effects on the dynamics properties and reaction mechanism in the Cl(2P) + NH3 reaction : a QCT and QM study ». Dans Highlights in Theoretical Chemistry, 69–78. Berlin, Heidelberg : Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-41272-1_9.
Texte intégralKabanda, Mwadham M., et Kgalaletso P. Otukile. « A Theoretical Study of the Preferred Reaction Mechanism Between Chloroacetic Acid and Thiourea ». Dans Advances in Quantum Systems in Chemistry, Physics, and Biology, 119–42. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-34941-7_7.
Texte intégralAlagona, Giuliano, et Caterina Ghio. « Theoretical Calculations on an Enzyme Catalyzed Reaction Mechanism ». Dans The Enzyme Catalysis Process, 345–55. Boston, MA : Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-1607-8_23.
Texte intégralLi, Jie, Tianshuang Li, Hongliang Zhang, Jingkun Wang, Kena Sun et Jin Xiao. « DFT Study on COS Oxidation Reaction Mechanism ». Dans Light Metals 2019, 879–84. Cham : Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-05864-7_107.
Texte intégralCambeiro, Xacobe C., et Miquel A. Pericàs. « The Mechanism of the Pauson-Khand Reaction : Hypothesis, Experimental Facts, and Theoretical Investigations ». Dans The Pauson-Khand Reaction, 23–48. Chichester, UK : John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119941934.ch2.
Texte intégralFreindorf, Marek, Thomas Sexton, Elfi Kraka et Dieter Cremer. « The mechanism of the cycloaddition reaction of 1,3-dipole molecules with acetylene : an investigation with the unified reaction valley approach ». Dans Highlights in Theoretical Chemistry, 173–90. Berlin, Heidelberg : Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-662-47051-0_16.
Texte intégralVergote, Thomas, Thomas Gathy, Fady Nahra, Olivier Riant, Daniel Peeters et Tom Leyssens. « Mechanism of ketone hydrosilylation using NHC–Cu(I) catalysts : a computational study ». Dans Highlights in Theoretical Chemistry, 135–47. Berlin, Heidelberg : Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-41315-5_12.
Texte intégralActes de conférences sur le sujet "Reaction Mechanism - Theoretical Study"
Ormachea, Carla, Mauro Cainelli, María Kneeteman et Pedro Mancini. « Reaction Mechanism of Polar Diels-Alder Reactions Between 3-Nitrofuran and different Dienes. A Theoretical Study ». Dans The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-e014.
Texte intégralFleisher, Mendel, E. Lukevics, L. Leite, D. Jansone, K. Edolfa, I. Liepina et V. Stonkus. « Theoretical study of the ketonization reaction mechanism of acetic acid over SiO2 ». Dans The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00148.
Texte intégralYusuf, Muhammad. « Theoretical Study on the Reaction Mechanism of Acetalization of 3-Chlorobenzaldehyde Catalyzed by Halogen Acid ». Dans Proceedings of The 5th Annual International Seminar on Trends in Science and Science Education, AISTSSE 2018, 18-19 October 2018, Medan, Indonesia. EAI, 2019. http://dx.doi.org/10.4108/eai.18-10-2018.2287347.
Texte intégralMaia, Thalita Vaneska Moreira, Denilma Maurício Cardoso da Silva, Andréa Claudia Oliveira Silva et Régis Casimiro Leal. « Theoretical study of the reaction mechanism of triiodide ion (I3–) from iodine (I2) and iodide anion (I–) ». Dans VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020155.
Texte intégralSemenikhin, A. S., A. S. Savchenkova, I. V. Chechet, S. G. Matveev, M. Frenklach et A. M. Mebel. « BRIDGING NUCLEATION REACTIONS BETWEEN ACENAPHTHYLENE AND NAPHTHALENE : A THEORETICAL STUDY ». Dans 9TH INTERNATIONAL SYMPOSIUM ON NONEQUILIBRIUM PROCESSES, PLASMA, COMBUSTION, AND ATMOSPHERIC PHENOMENA. TORUS PRESS, 2020. http://dx.doi.org/10.30826/nepcap9a-09.
Texte intégralShi, Shaoping, Daniel Lee, Sandra McSurdy, Michael McMillian, Steven Richardson et William Rogers. « Theoretical Investigation of Autoignition of Combustible Gas Mixtures in Rapid Compression Machines ». Dans ASME 2002 Internal Combustion Engine Division Fall Technical Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/icef2002-489.
Texte intégralBhopatkar, Neelesh S., Heng Ban et Thomas K. Gale. « Prediction of Mercury Speciation in Coal-Combustion Systems ». Dans ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-15502.
Texte intégralWang, Songtao, Xiaoqing Qiang, Weichun Lin, Guotai Feng et Zhongqi Wang. « A Study of Parameter Selection Principle and Internal Flow Mechanism in a Multi-Stage Low-Reaction Axial Flow Compressor ». Dans ASME Turbo Expo 2008 : Power for Land, Sea, and Air. ASMEDC, 2008. http://dx.doi.org/10.1115/gt2008-50554.
Texte intégralWen, Zhengcheng, Jiangrong Xu, Zhihua Wang et Kefa Cen. « Theoretical Study on the Mechanism and Kinetic of the Reactions between Elemental Mercury and Oxidizing Radicals ». Dans 2011 Asia-Pacific Power and Energy Engineering Conference (APPEEC). IEEE, 2011. http://dx.doi.org/10.1109/appeec.2011.5747700.
Texte intégralWU, ZHIJIAN, FUQIANG BAN et RUSSELL J. BOYD. « THEORETICAL STUDY ON THE REACTION MECHANISMS OF THE IMIDE FORMATION IN AN N-(O-CARBOXYBENZOYL)-L-AMINO ACID ». Dans Proceedings of the International Symposium on Solid State Chemistry in China. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776846_0077.
Texte intégralRapports d'organisations sur le sujet "Reaction Mechanism - Theoretical Study"
Rice, Betsy M., William Mattson, John Grosh et S. F. Trevino. A Molecular Dynamics Study of Detonation. 2. The Reaction Mechanism. Fort Belvoir, VA : Defense Technical Information Center, mars 1996. http://dx.doi.org/10.21236/ada305237.
Texte intégralPope, David P. Combined Theoretical and Experimental Study of a New Mechanism of Yielding with Application to the Brittle-Ductile Transition. Fort Belvoir, VA : Defense Technical Information Center, juin 2001. http://dx.doi.org/10.21236/ada403571.
Texte intégralBanin, Amos, Joseph Stucki et Joel Kostka. Redox Processes in Soils Irrigated with Reclaimed Sewage Effluents : Field Cycles and Basic Mechanism. United States Department of Agriculture, juillet 2004. http://dx.doi.org/10.32747/2004.7695870.bard.
Texte intégralTITOVA, E. HISTORIOGRAPHIC REVIEW ON THE TOPIC OF THE STUDY OF MIGRATION PROCESSES IN THE RUSSIAN FAR EAST AT THE BEGINNING OF THE XXI CENTURY. Science and Innovation Center Publishing House, 2021. http://dx.doi.org/10.12731/2077-1770-2021-13-4-2-34-53.
Texte intégralChapman et Toema. PR-266-07209-R01 Phase 2 - Assessment of the Robustness and Transportability of the Gas Turbine Model. Chantilly, Virginia : Pipeline Research Council International, Inc. (PRCI), décembre 2010. http://dx.doi.org/10.55274/r0010719.
Texte intégralAsenath-Smith, Emily, Emma Ambrogi, Eftihia Barnes et Jonathon Brame. CuO enhances the photocatalytic activity of Fe₂O₃ through synergistic reactive oxygen species interactions. Engineer Research and Development Center (U.S.), septembre 2021. http://dx.doi.org/10.21079/11681/42131.
Texte intégralKharadzhian, Natalia, Larysa Savchenko, Karyna Safian, Yuliia Kulinka et Oksana Mykolaivna Kopylova. Future Professional Education Specialists’ Mastering of Project Methodology of Creating Pedagogical Situations in the Service Sector. [б. в.], août 2020. http://dx.doi.org/10.31812/123456789/4142.
Texte intégralKalman, Joseph, et Maryam Haddad. Wastewater-derived Ammonia for a Green Transportation Fuel. Mineta Transportation Institute, juillet 2022. http://dx.doi.org/10.31979/mti.2021.2041.
Texte intégralKalman, Joseph, et Maryam Haddad. Wastewater-derived Ammonia for a Green Transportation Fuel. Mineta Transportation Institute, juillet 2022. http://dx.doi.org/10.31979/mti.2022.2041.
Texte intégralFinkelstain, Israel, Steven Buccola et Ziv Bar-Shira. Pooling and Pricing Schemes for Marketing Agricultural Products. United States Department of Agriculture, août 1993. http://dx.doi.org/10.32747/1993.7568099.bard.
Texte intégral