Relevant bibliographies by topics / Reactiion kinetics

Contents

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

Academic literature on the topic 'Reactiion kinetics'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 July 2025

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Journal articles on the topic "Reactiion kinetics"

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Y., K. Gupta. "Some aspects of a chemical relationship. Kinetics and Analytical Chemistry in the service of each other." Journal of Indian Chemical Society Vol. 83, May 2006 (2006): 468–78. https://doi.org/10.5281/zenodo.5819365.

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Department of Chemistry. University of Rajasthan, Jaipur-302 004, India E-mail : ykgl924@yahoo.com <em>Manuscript received 5 October 2005, accepted 16 January 2006</em> Synopsis (A) Contribution of Kinetics to Analytical Chemistry (1) Trace metal-ion catalysis and its determination kinetically (2) General metal-ion catalysis and its kinetic determination (3) Volumetric methods (4) Fe<sup>II</sup> as a pre-reductor for the determination of H<sub>2</sub>0<sub> 2</sub> with Tl<sup>III</sup> (5) Nature of acid monitoring the reactivity and course of a metal-ion reaction (6) Modification of known m
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Chalyy, K. O., I. P. Kryvenko та M. D. Andriychuk. "KINETIC MODELLING OF BIOCHEMICAL REACTIONS USING MATHСAD ANALYTICAL TOOLKIT". Medical Science of Ukraine (MSU) 20, № 2 (2024): 68–78. http://dx.doi.org/10.32345/2664-4738.2.2024.09.

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Background. The study of the kinetics of biochemical reactions provides a better understanding of how biological processes occur in living organisms. Understanding the peculiarities of such reactions is important for the development of new technologies, in particular for the production of biologically active substances and for the synthesis of drugs. A powerful tool for solving problems in biochemical reaction kinetics is mathematical modelling, which can be carried out using computer mathematical systems, in particular the MATHCAD analytical toolkit. Aim: to substantiate the feasibility and e
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Zhong, Wei, and Zhou Tian. "The Chemical Kinetic Numerical Computation and Kinetic Model Parameters Estimating of Parallel Reactions with Different Reaction Orders." Advanced Materials Research 560-561 (August 2012): 1126–32. http://dx.doi.org/10.4028/www.scientific.net/amr.560-561.1126.

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Abstract. Parallel reaction is a common reaction of chemical kinetics, and there are two types of parallel reactions according to the reaction orders equivalence: parallel reactions with same reaction orders and parallel reactions with different reaction orders. For the reason that the reaction orders are different, the chemical kinetic numerical computation and kinetic model parameters estimating of parallel reactions with different reaction orders is more complicated than parallel reactions with same reaction orders. In this paper, the 4th order Runge-Kutta method was employed to solve the n
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Xiao, Hong, Han X. Xiao, Kurt C. Frisch, and Nelson Malwitz. "Kinetic studies of the reactions between isocyanates and carboxylic acids." High Performance Polymers 6, no. 3 (1994): 235–39. http://dx.doi.org/10.1088/0954-0083/6/3/006.

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Reaction kinetic studies between isocyanates and carboxylic acids were undertaken to evaluate the kinetic parameters. Various isocyanates (phenyl isocyanate, cyclohexyl isocyanate) and carboxylic acids (acetic acid, n-butyric acid, isobutyric acid, dimethylbutyric acid and benzoic acid) were used to study the kinetics of the reactions at different temperatures and in different solvents. It was found that these reactions followed the rate law of second-order reaction. From the Arrhenius plot, the activation energies of these reactions were computed.
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Liu, Yongchun, Chong Han, Jinzhu Ma, Xiaolei Bao, and Hong He. "Influence of relative humidity on heterogeneous kinetics of NO2 on kaolin and hematite." Physical Chemistry Chemical Physics 17, no. 29 (2015): 19424–31. http://dx.doi.org/10.1039/c5cp02223a.

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Rogozhnikov, D. A., and B. V. Kolmachikhin. "Polymetallic Ore Concentration Middlings Nitric Acid Leaching Kinetics." Solid State Phenomena 265 (September 2017): 1065–70. http://dx.doi.org/10.4028/www.scientific.net/ssp.265.1065.

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The purpose of this work is the kinetic evaluation of reactions occurring during nitric acid leaching of pollymetallic sulfide middlings, for the most complete translation of copper, zinc and sulfur in solution and concentration of precious metals in residue. Methodology is pollymetallic sulfide middlings nitric acid leaching kinetics were studied using mathematical methods such as the experimental data numerical differentiation. Relevance/value is the main sulfide minerals kinetic characteristics were obtained for the studied materials, including the rate of the process, order of reaction, th
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Komorsky-Lovrić, Š., and M. Lovrić. "Theory of staircase cyclic voltammetry of two electrode reactions coupled by a chemical reaction." Bulgarian Chemical Communications 51, no. 3 (2019): 348–57. http://dx.doi.org/10.34049/bcc.51.3.4983.

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Two reversible electrode reactions that are connected by either reversible or totally irreversible chemical reactions are theoretically analysed by staircase cyclic voltammetry. The dependence of peak potentials on the thermodynamic and kinetic parameters is calculated. If the mechanism is permanently in equilibrium, the stability constant of the reversible chemical reaction can be determined. Furthermore, the critical kinetic parameter is determined and its application to the measurement of the forward rate constant of the chemical reaction is demonstrated. Also, the influence of the kinetics
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Arpitha, M. K., K. M. Vidyashree, H. S. Sonakshi, and H. P. Jayadevappa. "A Comparative Kinetic Study of Uncatalyzed and Ce(IV) Catalyzed Cetrizine Dihydrochloride Oxidation in Aqueous Acid Medium by Chloramine-T." Asian Journal of Chemistry 36, no. 4 (2024): 955–62. http://dx.doi.org/10.14233/ajchem.2024.31305.

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A kinetic study of uncatalyzed and Ce(IV) catalyzed cetrizine dihydrochloride oxidation was carried out in aqueous acid medium using chloramine-T. Both uncatalyzed and catalyzed reactions follows first order kinetics with respect to [CAT] and fractional order kinetics with respect to [substrate]. The reaction follows first order dependence on [CeIV] catalyst. The uncatalyzed reaction shows inverse fractional order for [H+] and [Cl–] whereas catalyzed reaction follows fractional order. The effect of ionic strength is negligible in both cases. The dielectric constant has negative effect on uncat
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Lomova, Tatyana N., Mariya E. Klyueva, Elena Yu Tyulyaeva, and Nataliya G. Bichan. "Use of chemical kinetics for the description of metal porphyrin reactivity." Journal of Porphyrins and Phthalocyanines 16, no. 09 (2012): 1040–54. http://dx.doi.org/10.1142/s1088424612500769.

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The results of use of chemical kinetics receptions, approaches and methods for the study of porphyrins and their metal complexes reactivity are discussed on an example of oxidation, acid-basic, and catalytic reactions of rhodium, palladium, and rhenium complexes of porphyrin in liquid solutions. The peculiarity of the porphyrin reaction rates is analyzed in a brief context of general provisions of the chemical kinetics. The opportunity to use the quasistationarity principle at the definition of the kinetic equation of the reactions with participation of metal porphyrins is shown. The transitio
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Offurum, J. C., M. M. Chukwu, C. A. Mbadike, T. U. Nwaneri, and A. A. Nwakaudu. "JUSTIFICATION OF ORDER OF CORROSION INHIBITION KINETICS FOR ESTERS OF CASTOR AND RUBBER SEED OILS." JOURNAL OF THE NIGERIAN SOCIETY OF CHEMICAL ENGINEERS 37, no. 1 (2022): 88–93. http://dx.doi.org/10.51975/22370108.som.

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The present study centres on the justification of order of corrosion inhibition kinetics for esters of castor and rubber seed oils. Inhibition of mildsteel corrosion was studied in the presence of sulphuric acid medium. The study was justified by the regular misprediction of order of chemical reactions (especially corrosion reaction), due to varying individual perceptions in this regard. While many researchers assume that corrosion reaction kinetics is of first order in most cases, others resolve that it is of zero or even second order. Experimental (gravimetric) data from the mildsteel corros
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Dissertations / Theses on the topic "Reactiion kinetics"

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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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Rushworth, Philip John. "Quantitative asymmetric reaction kinetics." Thesis, University of Warwick, 2011. http://wrap.warwick.ac.uk/45827/.

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The comparison of catalysts for producing chiral materials is of vital importance in the improvement of reaction scope and efficacy. Here we describe a new method of analysing the kinetics of the stereodetermining steps in asymmetric reactions by performing ligand/catalyst competition experiments against an internal standard and measuring the enantiomeric excess obtained at a variety of ratios of ligand/catalyst to internal standard. From these enantiomeric excess measurements, we can establish the relative rate of reaction between the ligand/catalyst systems and the internal standard, allowin
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Melane, Pumeza. "Kinetics reactions of Ammonium Nitrate-Sodium Nitrite Reaction and Ammonium Nitrate Emulsion Explosives." Master's thesis, University of Cape Town, 2010. http://hdl.handle.net/11427/6333.

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The aim of this study was to understand and control the gasification rates in ammonium nitrate emulsion explosive using ammonium nitrate-sodium nitrite reaction. This reaction produces N2 gas which is the sensitizer in emulsion explosives. The NH4NO3-NaNO2 gassing reaction produces N2 gas and so the reaction could be followed by the pressure increase in a closed reaction vessel. The reaction is pH sensitive, so the role of pH was investigated in the pH range 2 to 5. Gasification reactions for unbuffered NH4NO3-NaNO2 reaction were found to be rapid below pH = 3 and maximum pressure was attained
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Iwamura, Hiroshi. "Mechanistic insights from kinetic analysis by reaction calorimetry into proline-catalyzed asymmetric reactions and autocatalytic reaction." 京都大学 (Kyoto University), 2006. http://hdl.handle.net/2433/136952.

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Vaidyaraman, Sundar. "Kinetics of the bosch reaction." Thesis, Georgia Institute of Technology, 1992. http://hdl.handle.net/1853/10277.

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Nelson, Dorothy Caroline. "Reaction kinetics of gasless pyrotechnics." Thesis, University of Leeds, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293701.

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Frömberg, Daniela. "Reaction Kinetics under Anomalous Diffusion." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2011. http://dx.doi.org/10.18452/16374.

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Die vorliegende Arbeit befasst sich mit der Verallgemeinerung von Reaktions-Diffusions-Systemen auf Subdiffusion. Die subdiffusive Dynamik auf mesoskopischer Skala wurde mittels Continuous-Time Random Walks mit breiten Wartezeitverteilungen modelliert. Die Reaktion findet auf mikroskopischer Skala, d.h. während der Wartezeiten, statt und unterliegt dem Massenwirkungsgesetz. Die resultierenden Integro-Differentialgleichungen weisen im Integralkern des Transportterms eine Abhängigkeit von der Reaktion auf. Im Falle der Degradation A->0 wurde ein allgemeiner Ausdruck für die Lösungen beliebiger D
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Rivera, Díaz del Castillo Pedro Eduardo José. "Kinetics of precipitation reactions." Thesis, University of Cambridge, 2002. https://www.repository.cam.ac.uk/handle/1810/221870.

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Saleh, Nail Asad. "Dynamical solvent effect in 1-(9-anthryl)-3-(4-dimethylaniline) propane charge transfer reactions /." free to MU campus, to others for purchase, 2002. http://wwwlib.umi.com/cr/mo/fullcit?p3060138.

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Tenney, Joel David. "The kinetics of the chlorine dioxide generation reaction." Thesis, Georgia Institute of Technology, 1988. http://hdl.handle.net/1853/10020.

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Books on the topic "Reactiion kinetics"

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Radhakrishnan, Krishnan. A critical analysis of the accuracy of several numerical techniques for combustion kinetric rate equations. National Aeronautics and Space Administration, Office of Management, Scientific and Technical Information Program, 1993.

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Pilling, Michael J. Reaction kinetics. Oxford University Press, 1995.

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Leib, Tiberiu M. Reaction kinetics. McGraw-Hill, 2008.

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W, Seakins Paul, ed. Reaction kinetics. Oxford University Press, 1995.

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Ancheyta, Jorge. Chemical Reaction Kinetics. John Wiley & Sons, Ltd, 2017. http://dx.doi.org/10.1002/9781119226666.

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Green, N. J. B. Unimolecular kinetics. Elsevier, 2003.

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G, Compton R., ed. Electrode kinetics: Reactions. Elsevier, 1987.

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Marin, Guy B., Gregory S. Yablonsky, and Denis Constales, eds. Kinetics of Chemical Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527808397.

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Vannice, M. Albert. Kinetics of Catalytic Reactions. Springer US, 2005. http://dx.doi.org/10.1007/b136380.

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Grunze, Michael, and Hans Jürgen Kreuzer, eds. Kinetics of Interface Reactions. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72675-0.

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Book chapters on the topic "Reactiion kinetics"

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Müller, Johannes, and Christina Kuttler. "Reaction Kinetics." In Lecture Notes on Mathematical Modelling in the Life Sciences. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27251-6_5.

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Evans, James W., and Lutgard C. De Jonghe. "Reaction Kinetics." In The Production and Processing of Inorganic Materials. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-48163-0_3.

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Stiesch, Gunnar, and Peter Eckert. "Reaction Kinetics." In Combustion Engines Development. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14094-5_5.

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Murray, J. D. "Reaction Kinetics." In Interdisciplinary Applied Mathematics. Springer New York, 1993. http://dx.doi.org/10.1007/978-0-387-22437-4_6.

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Murray, James D. "Reaction Kinetics." In Mathematical Biology. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-08539-4_5.

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Murray, James D. "Reaction Kinetics." In Mathematical Biology. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-662-08542-4_5.

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Shaw, D. J., and H. E. Avery. "Reaction Kinetics." In Work Out Physical Chemistry. Macmillan Education UK, 1989. http://dx.doi.org/10.1007/978-1-349-10006-4_4.

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Méndez, Vicenç, Sergei Fedotov, and Werner Horsthemke. "Reaction Kinetics." In Reaction–Transport Systems. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-11443-4_1.

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Cerro, R. L., B. G. Higgins, and S. Whitaker. "Reaction Kinetics." In Material Balances for Chemical Reacting Systems. CRC Press, 2022. http://dx.doi.org/10.1201/9781003283751-9.

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Dash, Sanjaya K., Pitam Chandra, and Abhijit Kar. "Reaction Kinetics." In Food Engineering. CRC Press, 2023. http://dx.doi.org/10.1201/9781003285076-5.

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Conference papers on the topic "Reactiion kinetics"

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Videm, Ketil. "The Anodic Behaviour of Iron and Steel in Synthetic Concrete Pore Water and in Cement Mortar." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99573.

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Abstract The kinetics of the anodic reaction has been studied in alkaline solutions and in cement mortar. Use of synthetic pore water has the advantage that environment is known and can be controlled. The anodic reactions can be studied without disturbance from the cathodic ones in deoxygenated water. Iron and steel exhibit passivation in alkaline media with a steady state passive current that is independent of potential after a days exposure. The properties of the passive film are changed by polarisation. This makes it difficult to explore the anodic kinetics. Due to the polarization induced
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Fuller, E. Loren, Otto C. Kopp, and April D. Underwood. "Corrosion Kinetics and Mechanisms for Nuclear Grade Graphites." In CORROSION 1993. NACE International, 1993. https://doi.org/10.5006/c1993-93602.

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ABSTRACT This report is an initial microgravimetric evaluation of the intrinsic reaction parameters for air reactions with H-451 graphite. The studies were made over a temperature range of 375 to 850 °C at atmospheric pressure and for water contents from zero to two (2) volume percent water vapor. Photographic results show the heterogeneous nature of the graphite and the consequential variation of reaction rate as the samples are etched and roughened in the corrosion processes. The reaction rate increases approximately two (2) fold to a near-constant value and subsequently approaches of zero a
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Vera, Jose, Kyle Hilgefort, Paul Evans, Wei Shi, and Ivan Mantilla. "Methodology to Evaluate the Performance of Liquid Scavenger Application Technologies in Gas Pipelines." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-19302.

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Abstract Liquid H2S scavengers are sometimes injected into pipelines transporting wet gas to reduce the H2S concentration below allowable values before reaching certain points of the system. Experimental protocols have been developed to qualify H2S scavengers based on their efficiency and kinetics. However, it has been recognized that the overall reaction kinetics can be affected by the injection method. A methodology was developed and implemented in a four-inch multiphase flow loop to evaluate the performance of scavenger application technologies in improving the reaction kinetics of liquid s
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Cline, Jason A., Kenji Takahashi, Timothy W. Marin, Charles D. Jonah, and David M. Bartels. "Kinetics of Electron Transfer Reactions in Hydrothermal and Supercritical Wate." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02362.

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Abstract The rates of several radiation-induced reactions are assessed via pulse radiolysis in order to extend a model for nuclear reactor coolant radiolysis to supercritical conditions. We find changes in radiolysis yields and significant deviations from Arrhenius behavior at 250 bar as the temperature approaches and exceeds the critical temperature of pure water. At 380°C we also observe a strong pressure dependence of the reaction rates of ions and hydrophobic species. Using a homogeneous chemistry model, we find by 350°C that the relatively mild changes in these reaction rates increase the
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Johnson, M. L., and M. B. Tomson. "Ferrous Carbonate Precipitation Kinetics and Its Impact CO2 Corrosion." In CORROSION 1991. NACE International, 1991. https://doi.org/10.5006/c1991-91268.

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Abstract Recent evidence indicates that ferrous carbonate (FeCO3, siderite) plays a critical role in forming corrosion resistant scale. The temperature dependent precipitation kinetics of ferrous carbonate were studied using a powerful new "temperature ramped" approach. The activation energy calculated using a second order precipitation model (123 kJ/mol) qualitatively indicates that precipitation was controlled by surface reaction rate over the temperature interval studied. At low temperatures (&amp;lt;60 C), precipitation is expected to progress more slowly than corrosion reactions. At eleva
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Cavanzo, E. A., S. F. Muñoz, A. Ordoñez, and H. Bottia. "Kinetics of Wet In-Situ Combustion: A Review of Kinetic Models." In SPE Heavy and Extra Heavy Oil Conference: Latin America. SPE, 2014. http://dx.doi.org/10.2118/171134-ms.

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Abstract In Situ Combustion is an enhanced oil recovery method which consists on injecting air to the reservoir, generating a series of oxidation reactions at different temperature ranges by chemical interaction between oil and oxygen, the high temperature oxidation reactions are highly exothermic; the oxygen reacts with a coke like material formed by thermal cracking, they are responsible of generating the heat necessary to sustain and propagate the combustion front, sweeping the heavy oil and upgrading it due to the high temperatures. Wet in situ combustion is variant of the process, in whic
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Nagy, Endre. "Mass Transport Through Biocatalytic Membrane Reactors." In ASME 2008 9th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2008. http://dx.doi.org/10.1115/esda2008-59403.

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A mathematical model and its solution were developed to calculate the mass transport through catalytic membrane layer by means of explicit, closed expressions even in the case of the nonlinear Michaelis-Menten reaction kinetics and/or of variable mass transport — diffusion coefficient, convective velocity — parameters. Some typical examples on the Thiele modulus, applying the Michaelis-Menten kinetics and its limiting cases, namely the first-order kinetic (KM≫cm) and zero-order kinetic (cm≫KM) are shown for the prediction of the concentration distribution and the mass transfer rates as a funct
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Giraldo, Jorge, Jaime Garci´a, Antonio Bula, Marco Sanjuan, and Adria´n A´vila. "Extended Arrhenius Kinetic Model for the Transesterification Reaction of Biodiesel From Palm Oil and Ethanol." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43512.

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Modeling and understanding reaction kinetics is essential for processes and equipment design. This paper presents a kinetic analysis of the transesterification reaction of palm oil extracted in the Colombian north coast with ethanol to produce biodiesel. The analysis is based in actual lab scale production and it considers a set of three reactions in a batch reactor with dynamic behavior. It was found that the kinetics does not adjust to the common Arrhenius equation model, therefore an extended Arrhenius equation model was proposed. This extended model captures temperature effects better than
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Le Cong, Tanh, and Philippe Dagaut. "Effect of Water Vapor on the Kinetics of Combustion of Hydrogen and Natural Gas: Experimental and Detailed Modeling Study." In ASME Turbo Expo 2008: Power for Land, Sea, and Air. ASMEDC, 2008. http://dx.doi.org/10.1115/gt2008-50272.

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The dilution of fuels by exhausts gases (mainly CO, CO2 and H2O) affects the kinetics of combustion. This dilution is used in gas turbines and flameless combustor. It helps reducing pollutant emissions, particularly NOx. Therefore, it is useful to study the effect of such compounds on the kinetics of oxidation of fuels such as natural gas and hydrogen. The oxidation of hydrogen and that of methane were studied experimentally in a fused silica jet-stirred reactor (JSR) over the temperature range 800–1500 K, from fuel-lean to fuel-rich conditions. The experiments were repeated in presence of 10%
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Ou, Juan, Yuchao Yan, Ruomiao Yang, Zhentao Liu, and Jinlong Liu. "Enhancement of the Ammonia Kinetic Mechanism for Nitrogen-Based Pollutant Chemistry." In ASME 2024 ICE Forward Conference. American Society of Mechanical Engineers, 2024. https://doi.org/10.1115/icef2024-140869.

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Abstract Ammonia is a promising carbon-neutral fuel for internal combustion engines. However, its widespread application requires accurate ammonia kinetic models for numerical simulations used in engine development. Current development of ammonia kinetics mainly focuses on predicting fundamental combustion parameters such as ignition delay and laminar flame speed. Yet, significant discrepancies remain among different kinetics in predicting nitrogen-based pollutants (such as NOx and N2O). To improve the immature ammonia kinetics, especially for nitrogen-based pollutant chemistry, this study app
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Reports on the topic "Reactiion kinetics"

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Chulalaksananukul, Warawut. Synthesis and amyl acetate by lipases from various microorgamisms. Chulalongkorn University, 1997. https://doi.org/10.58837/chula.res.1997.15.

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The main objective of this study is to synthesize biofragrance "amyl acetate" naturally extractable from the flowers of the Thai plant called "Nom Maew" (Rauwenhoffia siamenesis Scheff.) by a biotechnological method. Lipases from various microorganisms namely Aspergillus niger, Candida cylindracea, Pseudomonas species and Mucor miehei were applied to catalyze the synthetic reaction between amyl alcohol and octyl acetate through the process of "transesterification". The reaction mixture was incubated in organic solvent, hexane, at 40 ํC, with continous stirring by magnetic stirrer. The products
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Redner, Sidney. Kinetics of Heterogeneous Reaction Processes. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada324886.

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Johnsen, Rainer, B. K. Chatterjee, and R. Tosh. Kinetics of Organophosphate Reactions. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada225269.

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Guo, Yili. Spectroscopy and reaction kinetics of HCO. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6416970.

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Redner, Sidney. Kinetics of Diffusion-Controlled Reactions. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada212161.

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Clutter, J. K. Kinetics Based Reaction Modeling for Heterogeneous Explosives. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada474367.

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Greenwood, N. N. Kinetics of Boron Hydride Interconversion Reactions. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada196824.

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Garlick, Stephanie M. Mechanisms and Kinetics of Catalytic Reactions. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada229912.

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9

Balooch, M., L. N. Dinh, and D. F. Calef. The Reaction Kinetics of LiD with Water Vapor. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/15005289.

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Failor, R. A. Kinetics of the gas phase tritium oxidation reaction. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6090146.

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