23 results on '"Nobuyoshi Koga"'
Search Results
2. Thermal Decomposition of Maya Blue: Extraction of Indigo Thermal Decomposition Steps from a Multistep Heterogeneous Reaction Using a Kinetic Deconvolution Analysis
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Yui Yamamoto and Nobuyoshi Koga
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Maya blue ,indigo ,palygorskite ,sepiolite ,thermal decomposition ,kinetic deconvolution analysis ,Organic chemistry ,QD241-441 - Abstract
Examining the kinetics of solids’ thermal decomposition with multiple overlapping steps is of growing interest in many fields, including materials science and engineering. Despite the difficulty of describing the kinetics for complex reaction processes constrained by physico-geometrical features, the kinetic deconvolution analysis (KDA) based on a cumulative kinetic equation is one practical method of obtaining the fundamental information needed to interpret detailed kinetic features. This article reports the application of KDA to thermal decomposition of clay minerals and indigo−clay mineral hybrid compounds, known as Maya blue, from ancient Mayan civilization. Maya blue samples were prepared by heating solid mixtures of indigo and clay minerals (palygorskite and sepiolite), followed by purification. The multistep thermal decomposition processes of the clay minerals and Maya blue samples were analyzed kinetically in a stepwise manner through preliminary kinetic analyses based on a conventional isoconversional method and mathematical peak deconvolution to finally attain the KDA. By comparing the results of KDA for the thermal decomposition processes of the clay minerals and the Maya blue samples, information about the thermal decomposition steps of the indigo incorporated into the Maya blue samples was extracted. The thermal stability of Maya blue samples was interpreted through the kinetic characterization of the extracted indigo decomposition steps.
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- 2019
- Full Text
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3. Critical Appraisal of Kinetic Calculation Methods Applied to Overlapping Multistep Reactions
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Nikita V. Muravyev, Alla N. Pivkina, and Nobuyoshi Koga
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kinetic analysis ,overlapping reactions ,TG ,DSC ,kinetic deconvolution ,isoconversional analysis ,formal kinetic analysis ,Organic chemistry ,QD241-441 - Abstract
Thermal decomposition of solids often includes simultaneous occurrence of the overlapping processes with unequal contributions in a specific physical quantity variation during the overall reaction (e.g., the opposite effects of decomposition and evaporation on the caloric signal). Kinetic analysis for such reactions is not a straightforward, while the applicability of common kinetic calculation methods to the particular complex processes has to be justified. This study focused on the critical analysis of the available kinetic calculation methods applied to the mathematically simulated thermogravimetry (TG) and differential scanning calorimetry (DSC) data. Comparing the calculated kinetic parameters with true kinetic parameters (used to simulate the thermoanalytical curves), some caveats in the application of the Kissinger, isoconversional Friedman, Vyazovkin and Flynn−Wall−Ozawa methods, mathematical and kinetic deconvolution approaches and formal kinetic description were highlighted. The model-fitting approach using simultaneously TG and DSC data was found to be the most useful for the complex processes assumed in the study.
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- 2019
- Full Text
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4. Dissolution of Calcium Hydroxide in Water: A Guided Inquiry in University and High School Chemistry Laboratories
- Author
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Shun Iwasaki, Satoki Kodani, Yuto Zushi, Mito Hotta, Masami Hara, Tomoyuki Tatsuoka, and Nobuyoshi Koga
- Abstract
In this laboratory experiment, a guided inquiry exploring the physicochemical principles of the dissolution of Ca(OH)[subscript 2](s) in water is proposed for laboratory classes in university and high school. As part of students' inquiry, two experimental approaches are used. One is the change in solubility with temperature revealed by measuring the pH values of the suspended solution of Ca(OH)[subscript 2](s) at various temperatures, which is then extended to its thermodynamic relationship via examining the temperature dependence of the solubility constant. The other method is to determine the enthalpy of solution using the calorimetric measurements. Due to the poor solubility of Ca(OH)[subscript 2](s), for determining the enthalpy of the Ca(OH)[subscript 2](s) solution, development of an energy diagram composed of several paths of a reaction that involve the dissolution of Ca(OH)[subscript 2](s) as a component process and using Hess's law are essential. A combination of these experimental approaches yields a stepwise students' inquiry for revealing the source of the changes in Ca(OH)[subscript 2](s) solubility with temperature, which may be flexibly adapted as an appropriate program depending on the targeted students. The two experimental procedures are presented by critically examining the experimental results. Based on the results of educational practices, typical guided inquiry constructions suited for the university and high school chemistry courses are proposed.
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- 2023
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5. Thermally Induced Aragonite–Calcite Transformation in Freshwater Pearl: A Mutual Relation with the Thermal Dehydration of Included Water
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Nobuyoshi Koga and Taiga Tone
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Calcite ,Materials science ,General Chemical Engineering ,Aragonite ,Kinetics ,General Chemistry ,engineering.material ,Kinetic energy ,medicine.disease ,Isothermal process ,Article ,chemistry.chemical_compound ,Chemistry ,chemistry ,Chemical engineering ,Dehydration reaction ,Thermal ,engineering ,medicine ,Dehydration ,QD1-999 - Abstract
This study focuses on the relationship between the aragonite-calcite (A-C) transformation and the thermal dehydration of included water in the biomineralized aragonite construction using freshwater pearl. These thermally induced processes occur in the same temperature region. The thermal dehydration of included water was characterized through thermoanalytical investigations as an overlapping of three dehydration steps. Each dehydration step was separated through kinetic deconvolution analysis, and the kinetic parameters were determined. A single-step behavior of the A-C transformation was evidenced using high-temperature X-ray diffractometry and Fourier transform infrared spectrometry for the heat-treated samples. The kinetics of the A-C transformation was analyzed using the conversion curves under isothermal and linear nonisothermal conditions. The A-C transformation occurred in the corresponding temperature region of the thermal dehydration, ranging from the second half of the second dehydration step to the first half of the third dehydration step. Because the thermal dehydration process is constrained by the contracting geometry kinetics, the movement of the thermal dehydration reaction interface can be a trigger for the A-C transformation. In this scheme, the overall kinetics of the A-C transformation in the biomineralized aragonite construction is regulated by a contracting geometry.
- Published
- 2021
6. Universal Kinetics of the Thermal Decomposition of Synthetic Smithsonite over Different Atmospheric Conditions
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Loïc Favergeon, Masahiro Fukuda, Daichi Hara, Yasuhiro Sakai, Yuu Tanaka, Nobuyoshi Koga, Department of Science Education, Hiroshima University, Graduate School of Education, Laboratoire Georges Friedel (LGF-ENSMSE), École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Département Procédés de Mise en oeuvre des Milieux Granulaires (PMMG-ENSMSE), Centre Sciences des Processus Industriels et Naturels (SPIN-ENSMSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), and Hiroshima University, Graduate School of Education, Department Science Education
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Smithsonite ,Materials science ,smithsonite ,Kinetics ,Thermodynamics ,02 engineering and technology ,engineering.material ,[CHIM.INOR]Chemical Sciences/Inorganic chemistry ,Kinetic energy ,01 natural sciences ,physicogeometrical ,[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering ,Physical and Theoretical Chemistry ,thermal decomposition ,Reaction conditions ,Thermal decomposition ,ZnCO3 ,021001 nanoscience & nanotechnology ,010406 physical chemistry ,0104 chemical sciences ,Surfaces, Coatings and Films ,Electronic, Optical and Magnetic Materials ,[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry ,General Energy ,13. Climate action ,Scientific method ,engineering ,0210 nano-technology - Abstract
International audience; The thermal decomposition of smithsonite (ZnCO3) was studied to obtain a universal kinetic description of the process applicable to a range of reaction conditions. A synthesized ZnCO3 was subjected to thermoanalytical measurements under various heating and atmospheric conditions in a flow of dry N2gas, N2–CO2, or N2–H2O mixed gases. Systematic shifts of the reaction temperature to higher and lower temperatures by the effects of CO2 and H2O, respectively, were identified as specific characteristics of the system. With reference to the physico-geometrical kinetic behavior of the reactionin a flow of dry N2 gas, the retardation effect of CO2 was demonstrated in the scheme of the physicogeometrical consecutive surface reaction (SR) and phase boundary-controlled reaction (PBR). The individual kinetics of the SR and PBR were universally described over different CO2 pressures using an accommodation function (AF) obtained by considering the consecutive elementary steps of SR and PBR. The catalytic effect of water vapor was assumed to result from contributions of the water molecules on the consecutive elementary steps of SR and on the crystal growth of the solid product of the reaction (ZnO). An alternative AF derived considering the adsorption of water molecules on solid surfaces allowed us to obtain the universal kinetic description of the thermal decomposition over different water vapor pressures.
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- 2021
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7. Thermal Dehydration of Lithium Sulfate Monohydrate Revisited with Universal Kinetic Description over Different Temperatures and Atmospheric Water Vapor Pressures
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Yui Yamamoto, Loïc Favergeon, Nobuyoshi Koga, Graduate School of Education, Hiroshima University, Département Procédés de Transformations des Solides et Instrumentation (PTSI-ENSMSE), Centre Sciences des Processus Industriels et Naturels (SPIN-ENSMSE), École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Laboratoire Georges Friedel (LGF-ENSMSE), Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), and Hiroshima university
- Subjects
Lithium sulfate monohydrate ,Materials science ,Induction period ,Thermal dehydration ,Thermodynamics ,02 engineering and technology ,[CHIM.INOR]Chemical Sciences/Inorganic chemistry ,010402 general chemistry ,Kinetic energy ,01 natural sciences ,chemistry.chemical_compound ,Thermal ,medicine ,[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering ,Dehydration ,Physical and Theoretical Chemistry ,Atmospheric water ,Reaction step ,Accommodation function ,Lithium sulfate ,021001 nanoscience & nanotechnology ,medicine.disease ,0104 chemical sciences ,Surfaces, Coatings and Films ,Electronic, Optical and Magnetic Materials ,[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry ,Kinetics ,General Energy ,chemistry ,Kinetic equations ,Atmospheric water vapor ,0210 nano-technology - Abstract
International audience; This study aims to universally describe the kinetic features of the thermal dehydration of lithium sulfate monohydrate across different temperatures (T) and atmospheric water vapor pressures (p(H2O)) as a model reaction of the thermal dehydration of crystalline hydrates. The features of the physicogeometrical consecutive process, comprising the induction period (IP)–surface reaction (SR)–phase boundary-controlled reaction (PBR), and the effect of p(H2O) on kinetic behavior were revealed experimentally under various heating conditions. Then, the accommodation function (AF), accounting for the effect of p(H2O) on the kinetic behavior, was derived by considering the consecutive/concurrent elementary steps of SR and PBR at the atomic and molecular levels. The universal kinetic descriptions for the IP and subsequent mass-loss process were realized by introducing the AF into formal kinetic equations and using the isoconversional kinetic relationship. Furthermore, by combining the physicogeometrical consecutive IP–SR–PBR(n) model and the formulated AF, the universal kinetic descriptions for each physicogeometrical reaction step across different T and p(H2O) conditions were obtained, which reveal novel kinetic features of each reaction step and these variations as the reaction step advances. The significance of the revealed kinetic features is discussed through demonstrating the development of the novel kinetic approach.
- Published
- 2020
- Full Text
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8. Impact of atmospheric water vapor on the thermal decomposition of calcium hydroxide: a universal kinetic approach to a physico-geometrical consecutive reaction in solid–gas systems under different partial pressures of product gas
- Author
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Nobuyoshi Koga, Loïc Favergeon, Satoki Kodani, Department of Science Education, Hiroshima University, Graduate School of Education, Laboratoire Georges Friedel (LGF-ENSMSE), Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Centre Sciences des Processus Industriels et Naturels (SPIN-ENSMSE), École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Département Procédés de Transformations des Solides et Instrumentation (PTSI-ENSMSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), and Hiroshima University - Graduate School of Education - Department of Science Education
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Reaction mechanism ,Materials science ,kinetic mechanism ,Reaction step ,Vapour pressure of water ,Thermal decomposition ,General Physics and Astronomy ,Thermodynamics ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Ca(OH)2 ,Arrhenius plot ,Isothermal process ,0104 chemical sciences ,Reaction rate ,accommodation function ,13. Climate action ,water vapor ,[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering ,Physical and Theoretical Chemistry ,0210 nano-technology ,Water vapor ,thermal decomposition - Abstract
International audience; Thermal decomposition of Ca(OH)2 under atmospheric water vapor exhibits special features, including an induction period (IP) and a subsequent sigmoidal mass-loss behavior under isothermal conditions. Atmospheric water vapor reduces the reaction rate at a specific temperature and causes a systematic shift of the mass-loss curve, which was recorded at a specific heating rate, to higher temperatures as the water vapor pressure, p(H2O), increases. The challenge in this study was to universally describe the kinetics of thermal decomposition under various p(H2O) conditions by introducing an accommodation function in the fundamental kinetic equation. The accommodation function in the multiplied form of two p(H2O) components with a variable exponent in each component was derived on the basis of the classical nucleation and interface reaction theories. The universal kinetic approach was realized by applying the accommodation function to formal kinetic analyses of the Arrhenius plot for the IP and the Friedman plot for the mass-loss process. Furthermore, the overall reaction process under isothermal conditions was analyzed kinetically on the basis of the physico-geometrical consecutive reaction model, which was composed of an IP, a surface reaction (SR), and a phase boundary-controlled reaction (PBR). Subsequently, the kinetic parameters for each physico-geometrical reaction step were determined by the modified Arrhenius plot with the accommodation function. The impact of the atmospheric water vapor on the kinetics of thermal decomposition was characterized in connection with physico-geometrical reaction mechanisms through the interpretation of the kinetic parameters and these variation behavior patterns as the overall reaction advanced.
- Published
- 2019
- Full Text
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9. Effects of Particle Size on the Kinetics of Physico-geometrical Consecutive Reactions in Solid-Gas Systems: Thermal Decomposition of Potassium Hydrogen Carbonate.
- Author
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Mito Hotta, Taiga Tone, and Nobuyoshi Koga
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- 2021
- Full Text
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10. Obituary Note: Prof. José Manuel Criado
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Jiri Malek, Nobuyoshi Koga, and Luis A. Pérez-Maqueda
- Subjects
media_common.quotation_subject ,Art ,Physical and Theoretical Chemistry ,Obituary ,Condensed Matter Physics ,Instrumentation ,Humanities ,media_common - Abstract
It is an obituary note., The late Prof. Jose Manuel Criado (1944.6.13–2018.2.27) It is with the profoundest regret that we must report the passing of Prof. José Manuel Criado on February 27, 2018 at the age of 73. We express our most sincere condolences to his family, colleagues and friends.
- Published
- 2018
11. Handbook of Thermal Analysis and Calorimetry : Recent Advances, Techniques and Applications
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Sergey Vyazovkin, Nobuyoshi Koga, Christoph Schick, Sergey Vyazovkin, Nobuyoshi Koga, and Christoph Schick
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- Calorimetry--Handbooks, manuals, etc
- Abstract
Handbook of Thermal Analysis and Calorimetry: Recent Advances, Techniques and Applications, Volume Six, Second Edition, presents the latest in a series that has been well received by the thermal analysis and calorimetry community. This volume covers recent advances in techniques and applications that complement the earlier volumes. There has been tremendous progress in the field in recent years, and this book puts together the most high-impact topics selected for their popularity by new editors Sergey Vyazovkin, Nobuyoshi Koga and Christoph Schick—all editors of Thermochimica Acta. Among the important new techniques covered are biomass conversion; sustainable polymers; polymer nanocompsoties; nonmetallic glasses; phase change materials; propellants and explosives; applications to pharmaceuticals; processes in ceramics, metals, and alloys; ionic liquids; fast-scanning calorimetry, and more. - Features 19 all-new chapters to bring readers up to date on the current status of the field - Provides a broad overview of recent progress in the most popular techniques and applications - Includes chapters authored by a recognized leader in each field and compiled by a new team of editors, each with at least 20 years of experience in the field of thermal analysis and calorimetry - Enables applications across a wide range of modern materials, including polymers, metals, alloys, ceramics, energetics and pharmaceutics - Overviews the current status of the field and summarizes recent progress in the most popular techniques and applications
- Published
- 2018
12. Stepwise Inquiry into Hard Water in a High School Chemistry Laboratory.
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Mami Kakisako, Kazuyuki Nishikawa, Masayoshi Nakano, Harada, Kana S., Tomoyuki Tatsuoka, and Nobuyoshi Koga
- Published
- 2016
- Full Text
- View/download PDF
13. Reactivity of Household Oxygen Bleaches: A Stepwise Laboratory Exercise in High School Chemistry Course.
- Author
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Masayoshi Nakano, Haruka Ogasawara, Takeshi Wada, and Nobuyoshi Koga
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- 2016
- Full Text
- View/download PDF
14. Model Experiment of Thermal Runaway Reactions Using the Aluminum-Hydrochloric Acid Reaction.
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Suguru Kitabayashi, Masayoshi Nakano, Kazuyuki Nishikawa, and Nobuyoshi Koga
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- 2016
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15. Identifying Liquid-Gas System Misconceptions and Addressing Them Using a Laboratory Exercise on Pressure-Temperature Diagrams of a Mixed Gas Involving Liquid-Vapor Equilibrium.
- Author
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Masahiro Yoshikawa and Nobuyoshi Koga
- Subjects
- *
GAS-liquid interfaces , *VAPOR-liquid equilibrium , *PRESSURE measurement , *TEMPERATURE , *UNDERGRADUATES , *CHEMISTRY education in universities & colleges , *CHARTS, diagrams, etc. - Abstract
This study focuses on students' understandings of a liquid-gas system with liquid-vapor equilibrium in a closed system using a pressure-temperature (P-T) diagram. By administrating three assessment questions concerning the P-T diagrams of liquid-gas systems to students at the beginning of undergraduate general chemistry course, lack of understanding of the fundamental concepts concerning liquid-vapor equilibria, the ideal gas law, and boiling points was identified. A learning program for liquid-gas systems was then designed for students at the undergraduate general chemistry level to address this issue. It consists of a laboratory experiment and postlaboratory exercise and is intended to provide integrated student understanding. During the learning program, students actively used the related concepts to explain the physical chemistry of a liquid-gas system and integrated the concepts to explain practical systems in their daily lives using a P-T diagram. An outline of the learning program is reported on the basis of our educational practice. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
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16. Exothermic Behavior of Thermal Decomposition of SodiumPercarbonate: Kinetic Deconvolution of Successive Endothermic andExothermic Processes.
- Author
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Masayoshi Nakano, Takeshi Wada, and Nobuyoshi Koga
- Published
- 2015
- Full Text
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17. Multistep Kinetic Behavior of the Thermal Decompositionof Granular Sodium Percarbonate: Hindrance Effect of the Outer SurfaceLayer.
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Takeshi Wada, Masayoshi Nakano, and Nobuyoshi Koga
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- 2015
- Full Text
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18. Using a Laboratory Inquiry with High School Students To Determine the Reaction Stoichiometry of Neutralization by a Thermochemical Approach.
- Author
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Tomoyuki Tatsuoka, Kana Shigedomi, and Nobuyoshi Koga
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- 2015
- Full Text
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19. Physico-Geometrical Kinetics of Solid-State Reactions in an Undergraduate Thermal Analysis Laboratory.
- Author
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Nobuyoshi Koga, Yuri Goshi, Masahiro Yoshikawa, and Tomoyuki Tatsuoka
- Subjects
- *
THERMAL analysis , *CHEMICAL decomposition , *THERMOGRAVIMETRY , *CHEMICAL reactions , *CURRICULUM research - Abstract
An undergraduate kinetic experiment of the thermal decomposition of solids by microscopic observation and thermal analysis was developed by investigating a suitable reaction, applicable techniques of thermal analysis and microscopic observation, and a reliable kinetic calculation method. The thermal decomposition of sodium hydrogen carbonate is selected as the suitable reaction for the student experiments, because its physico-geometrical reaction mechanism is approximately described by the two-dimensional phase boundary controlled model, and its reaction kinetics are less sensitive to the measurement conditions of thermal analyses. On the basis of simple microscopic observations of this reaction, development of the physico-geometrical reaction model and derivation of the kinetic model function are imposed on students. The kinetic analysis is also performed using the kinetic rate data recorded by a single thermogravimetric run under modulated temperature conditions. This reduces the time spent in the laboratory and enables the application of a two-step kinetic calculation that provides reliable kinetic results. From the results, students can interpret the kinetics, which are closely related to the physico-geometrical characteristics of the reaction. A one-day undergraduate course in a thermal analysis laboratory is proposed from research and trials conducted in our university. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
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20. Chemical Composition of Sodium Percarbonate: An Inquiry-Based Laboratory Exercise.
- Author
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Takeshi Wada and Nobuyoshi Koga
- Subjects
- *
SODIUM compounds , *CHEMICALS , *BLEACHING materials , *SODIUM carbonate , *HYDROGEN peroxide , *INQUIRY-based learning , *CHEMISTRY education , *SECONDARY education - Abstract
An inquiry-based laboratory exercise is described to determine the chemical composition of sodium percarbonate (SPC), which is a major component of domestic oxygen bleach. The students' knowledge of the chemical properties and reactions of sodium carbonate (SC) and hydrogen peroxide (HPO) is used to determine the chemical composition of SPC because SPC is the adduct of SC and HPO. If the hypothetical composition is assumed to be xNa2CO3⋅yH2O2, the composition can be determined by selecting one experimental method from the range of methods available. Synthetic SPC crystals or commercially available granular SPC can be used as the sample in the experiment. Because many choices involving different experimental methods are available, various learning programs can be designed to match the objectives and students' knowledge stage. This inquiry-based laboratory exercise is suitable for a high school chemistry course or a college introductory chemistry course and requires three hours. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
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21. Thermal dehydration of crystalline hydrates.
- Author
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Haruhiko Tanaka and Nobuyoshi Koga
- Subjects
- *
SOLID state chemistry , *CHEMICAL kinetics , *SCIENTIFIC experimentation - Abstract
Presents microscopic studies and introductory experiments to the kinetics of solid-state reactions. Theory of solid-state reactions; Kinetics of solid-state decompositions; Rate equations; Kinetics of nucleation and nuclear growth; Nucleus dimensions; Kinetics of established reaction; Microscopic studies of crystal dehydrations.
- Published
- 1995
- Full Text
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22. A Simple Oxygen Detector Using Zinc-Air Battery.
- Author
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Yoong Kin Hooi, Masayoshi Nakano, and Nobuyoshi Koga
- Published
- 2014
- Full Text
- View/download PDF
23. Kinetics and mechanisms of solid-gas reactions
- Author
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Michèle Pijolat, Loïc Favergeon, École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT), Université de Lyon, Centre National de la Recherche Scientifique (CNRS), Laboratoire Georges Friedel (LGF-ENSMSE), Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT), Centre Sciences des Processus Industriels et Naturels (SPIN-ENSMSE), Département Procédés de Transformations des Solides et Instrumentation (PTSI-ENSMSE), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-École des Mines de Saint-Étienne (Mines Saint-Étienne MSE), Sergey Vyazovkin, Nobuyoshi Koga, and Christoph Schick
- Subjects
Materials science ,Series (mathematics) ,growth ,nucleation ,Nucleation ,Thermodynamics ,mechanism ,elementary step ,02 engineering and technology ,Function (mathematics) ,Rate equation ,kinetic model ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Rate-determining step ,Kinetic energy ,01 natural sciences ,Chemical reaction ,0104 chemical sciences ,rate-determining step ,rate equation ,[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering ,0210 nano-technology ,Unified field theory - Abstract
eBook ISBN: 9780444640635; International audience; The kinetic modeling of chemical reactions in gas-solid systems necessitates a mathematical expression of the rate as a function of variables. For a long time the rate equations used for transformations of powders were different from those describing the oxidation of a metal or an alloy. Both approaches and a unified theory that intends to cover any type of reacting solids with the production/reaction of gases are discussed. Owing to kinetic assumptions of pseudo-steady-state and rate-determining step approximations, a general equation of the rate may be established. The kinetic rate is then a product of two functions, one depending on the thermodynamic variables and the other depending on the geometrical variables and time. According to the various possibilities of geometry, growth direction, rate-determining step localization, nucleation, and/or growth processes, about 40 kinetic models may be obtained for the variations of the kinetic rate with time. The mechanism decomposition in elementary steps is shown to get the calculation of the function, which governs the effect of the thermodynamic variables on the kinetic rate. A series of experimental tests (most of them based on the jump method) are shown to validate the kinetic assumptions and the geometrical modeling.
- Published
- 2018
- Full Text
- View/download PDF
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