Gotowe bibliografie tematyczne / Solid-state phase transformation

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Gotowa bibliografia na temat „Solid-state phase transformation”

Autor: Grafiati
Data publikacji: 6 września 2023

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Artykuły w czasopismach na temat "Solid-state phase transformation"

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Mittemeijer, Eric J., i Ferdinand Sommer. "Solid state phase transformation kinetics: a modular transformation model". Zeitschrift für Metallkunde 93, nr 5 (maj 2002): 352–61. http://dx.doi.org/10.3139/146.020352.

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刘, 慧敏. "“Iron-Carbon Phase Diagram” and “Solid-State Phase Transformation”". Open Journal of Nature Science 05, nr 03 (2017): 315–19. http://dx.doi.org/10.12677/ojns.2017.53043.

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Ma, Ya Zhu, i Feng Liu. "The Kinetic Description for Solid State Phase Transformation". Advanced Materials Research 123-125 (sierpień 2010): 591–94. http://dx.doi.org/10.4028/www.scientific.net/amr.123-125.591.

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The progress of solid-state phase transformation can be subdivided into three overlapping mechanisms: nucleation, growth, and impingement. On the basis of an analytical phase transformation model, the maximum in the transformation rate of an isothermal solid-state transformation has been evaluated. Then, the mode of nucleation, growth and impingement, and the separate activation energies for nucleation and growth can be determined. Finally, application in the crystallization kinetics of amorphous alloy was described.
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Yoo, Woo Sik, i Hiroyuki Matsunami. "Solid-State Phase Transformation in Cubic Silicon Carbide". Japanese Journal of Applied Physics 30, Part 1, No. 3 (15.03.1991): 545–53. http://dx.doi.org/10.1143/jjap.30.545.

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Jiang, Yi Hui, Bao Sun i Feng Liu. "Analytical Approach for Describing Solid-State Phase Transformation". Applied Mechanics and Materials 161 (marzec 2012): 42–46. http://dx.doi.org/10.4028/www.scientific.net/amm.161.42.

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A general analytical phase transformation model has been proposed and successfully applied to describe the crystallization of amorphous alloys. The “additivity rule” is proved to be compatible with the analytical model; the effects of anisotropic growth based on Monte Carlo (MC) simulations is reinterpreted using the analytical approach; and an improved temperature integral is also proved to be compatible with the analytical model. Kinetic analysis basing on the analytical model declares the transformation mechanism, e.g. nucleation, growth and impingement mode. On this basis, the kinetic behaviors of isothermal and non-isothermal crystallization of amorphous Zr50Al10Ni40are analyzed.
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Bin Anooz, S., R. Bertram i D. Klimm. "The solid state phase transformation of potassium sulfate". Solid State Communications 141, nr 9 (marzec 2007): 497–501. http://dx.doi.org/10.1016/j.ssc.2006.12.008.

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Mittemeijer, Eric Jan, i Ferdinand Sommer. "Solid state phase transformation kinetics: Evaluation of the modular transformation model". International Journal of Materials Research 102, nr 7 (lipiec 2011): 784–95. http://dx.doi.org/10.3139/146.110537.

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Kavokin, A. A., I. H. Kazmi i B. Munir. "Computational Model of Phase Transformations in Thermo-Chemical Cathodes Using Kinetic Approach". Key Engineering Materials 510-511 (maj 2012): 9–14. http://dx.doi.org/10.4028/www.scientific.net/kem.510-511.9.

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The paper presents the results of modeling of the processes of phases transformations occurring in cathode of plasmatron with zirconium insertion. Model describes temperature and liquid-solid phase transformation in cathode considering kinetics of transformation in accordance with a state diagram. The comparison between one-dimensional mathematical models was exploited for estimation of the kinetics coefficient. First model is based on well-known heat equation with Stefans condition on the free boundary between liquid and solid phases [. The standard analytical self-similar solution for two-phase case is applied. In the second model, for heat equation instead of Stefans conditions, differential equations of kinetics are used.
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Hamelin, Cory J., Ondrej Muránsky, Philip Bendeich, Ken Short i Lyndon Edwards. "Predicting Solid-State Phase Transformations during Welding of Ferritic Steels". Materials Science Forum 706-709 (styczeń 2012): 1403–8. http://dx.doi.org/10.4028/www.scientific.net/msf.706-709.1403.

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The current work presents the numerical analysis of solid-state transformation kinetics relating to conventional welding of ferritic steels, with the aim of predicting the constituent phases in both the fusion zone and the heat affected zone (HAZ) of the weldment. The analysis begins with predictions of isothermal transformation kinetics using thermodynamic principles, such that the chemical composition of the parent metal is the sole user-defined input. The data is then converted to anisothermal transformation kinetics using the Scheil-Avrami additive rule, including the effects of peak temperature and austenite grain growth. Subroutines developed for the Abaqus finite element package use the semi-empirical approach described to predict phase transformations in SA508 Gr.3 Cl.1 steel. To study the effect of the cooling rates and the ability of the current model to predict the final microstructure, two weld samples were subjected to autogenous beam TIG welds under a fast (TG5-F, 5.00 mm/s) and slow (TG5-S, 1.25 mm/s) torch speed. Model validation is carried out by direct comparison with microstructural observations and hardness measurements (via nanoindentation) of the fusion and heat affected zones in both welds. Excellent agreement between the measured and predicted hardness has been found for both weld samples. Additionally, it is shown that the correct identification of the partial austenisation region is a crucial input parameter.
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Miranda, Georgina, F. S. Silva i Delfim Soares. "Solid State Transformations and Equilibrium Crystal Structures of an Au-Cu Alloy with Shape Memory Effect". Materials Science Forum 730-732 (listopad 2012): 859–64. http://dx.doi.org/10.4028/www.scientific.net/msf.730-732.859.

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Au-50%Cu (at. %) alloy presents the shape memory effect (SME), which is dependent of the solid state transformation that happens during heating, after the introduction of an internal stress in the quenched state. The solid state phase transformation temperatures were determined by means of Differential Thermal Analysis (DTA), both in heating and cooling cycles. With the obtained DTA results, a sequence of high temperature X-ray diffraction (XRD) experiments were made, in order to confirm the presence of the solid state phase transformations and to determine their stable crystal structure and lattice parameters. These XRD results were compared with those obtained from the literature. The displacements of the lattice parameters were determined, for each equilibrium phase, for measurements at room temperature and at high temperature. The characteristics of the quenched samples were also studied in order to determine the phase transformations that are responsible for the shape memory effect in this alloy.
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Rozprawy doktorskie na temat "Solid-state phase transformation"

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Kempen, Antoine. "Solid state phase transformation kinetics". [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964251191.

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Kempen, Antonius Theodorus Wilhelmus. "Solid state phase transformation kinetics". Stuttgart : Max-Planck-Institut für Metallforschung, 2001. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB9795832.

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Miranda, Pérez Argelia Fabiola. "Solid state phase transformations in Advanced Steels". Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3422570.

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In order to achieve progress in Advanced Steels development came more emphasis in solid state phase transformations are received. For achieving the desired mechanical and corrosion resistance properties in Duplex Stainless Steels (DSS), a precise knowledge of the precipitation kinetics of secondary phases, the morphology of the precipitates and effects of the alloying elements on different properties is needed. A complicated chemical composition and the production technology route make each grade of DSS a unique object for a study. Besides, when the market needs to reduce weight and increase product durability by utilizing Advance Strength Steels, a deeper understanding of their transformations is required. The aim of the present work was to study the main features of phase precipitation in diverse Duplex Stainless Steels grades, including Lean Duplex, Standard and Superduplex. Beside analyze the effects of metallurgical features on the properties of DSS and Advanced High Strength Dual Phase (DP) steels. One of the tasks was to study the effects plastic deformation after heat treatment in diverse duplex grades.
Con lo scopo di ottenere progressi industriali nello sviluppo di Advanced Steels, specie quando le necessità di mercato richiedono una riduzione di peso e un aumento della durabilità è fondamentale una più profonda comprensione delle loro trasformazioni di fase allo stato solido. Nel caso di acciai Inossidabili Duplex (DSS), per raggiungere le proprietà meccaniche desiderate e le proprietà di resistenza alla corrosione, è necessaria la precisa conoscenza della cinetica di precipitazione di fasi secondarie, la morfologia dei precipitati e gli effetti degli elementi alleganti su diverse proprietà. La complessa composizione chimica e la tecnologia di produzione rendono ciascuna tipologia di DSS come un caso di studio unico. L’obbiettivo del presente lavoro è stato quello di studiare le principali caratteristiche delle precipitazioni di fasi secondarie in diversi tipi di acciai inossidabili duplex, comprendendo i Lean Duplex, Standard e altamente legati duplex, ed inoltre di analizzare gli effetti delle caratteristiche metallurgiche sulle proprietà degli Acciai Duplex e Advanced High Strength Steels.
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Huan, C. H. A. "Phase transformation and nuclear resonance in acoustics". Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379905.

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Murphy, Gabriel L. "A Fundamental and Systematic Investigation into the Solid State Chemistry of Some Ternary Uranium Oxides". Thesis, The University of Sydney, 2018. http://hdl.handle.net/2123/20323.

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This Ph.D. dissertation explores the solid state chemistry of the AUO4 family of oxides (A = divalent or trivalent cation), addressing the role uranyl bonding and 5f electron chemistry play in influencing their physicochemical properties using high resolution measurement methods and ab initio calculations. The irreversible phase transformation that occurs between the rhombohedral and orthorhombic variants of SrUO4 is examined and demonstrated to be first order and reconstructive. The transformation is shown to involve a sequential reduction and oxidation process related to reducing the activation energy barrier that can be traced to the respective ability and inability for the rhombohedral and orthorhombic variants to host oxygen defects. The defect inventory in AUO4 rhombohedral structures is shown to be modulated by the size of the A site cation. When isostructural rhombohedral CaUO4, α-Sr0.4Ca0.6UO4 and SrUO4 obtain a critical amount of oxygen defects they can access novel reversible symmetry lowering and defect ordering transformations forming phases denoted δ. The transformations are purely thermodynamic where the origin is proposed to be related to decreasing entropy from defect ordering balanced by increasing electronic entropy with heating. AUO4 oxides that had been previously poorly described were examined at high resolution. This includes elucidation of NiUO4 polymorphs which provide the transformative “missing link" between the Pbcn and Ibmm orthorhombic variants. Consequently a structural hierarchy is developed for the family of AUO4 oxides that can be used for structure prediction for specific A and U cations. High pressure studies of SrUO4 found anomalous U-O bond lengthening to occur with increasing pressure related to electron delocalisation. This demonstrates the inapplicability of Badger’s rule to all uranyl bearing compounds. With the structural topology of rhombohedral SrUO4, this lengthening process produces bulk moduli comparable to diamond
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Yamada, Ryo. "Application of Steepest-Entropy-Ascent Quantum Thermodynamics to Solid-State Phenomena". Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/85866.

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Steepest-entropy-ascent quantum thermodynamics (SEAQT) is a mathematical and theoretical framework for intrinsic quantum thermodynamics (IQT), a unified theory of quantum mechanics and thermodynamics. In the theoretical framework, entropy is viewed as a measure of energy load sharing among available energy eigenlevels, and a unique relaxation path of a system from an initial non-equilibrium state to a stable equilibrium is determined from the greatest entropy generation viewpoint. The SEAQT modeling has seen a great development recently. However, the applications have mainly focused on gas phases, where a simple energy eigenstructure (a set of energy eigenlevels) can be constructed from appropriate quantum models by assuming that gas-particles behave independently. The focus of this research is to extend the applicability to solid phases, where interactions between constituent particles play a definitive role in their properties so that an energy eigenstructure becomes quite complicated and intractable from quantum models. To cope with the problem, a highly simplified energy eigenstructure (so-called ``pseudo-eigenstructure") of a condensed matter is constructed using a reduced-order method, where quantum models are replaced by typical solid-state models. The details of the approach are given and the method is applied to make kinetic predictions in various solid-state phenomena: the thermal expansion of silver, the magnetization of iron, and the continuous/discontinuous phase separation and ordering in binary alloys where a pseudo-eigenstructure is constructed using atomic/spin coupled oscillators or a mean-field approximation. In each application, the reliability of the approach is confirmed and the time-evolution processes are tracked from different initial states under varying conditions (including interactions with a heat reservoir and external magnetic field) using the SEAQT equation of motion derived for each specific application. Specifically, the SEAQT framework with a pseudo-eigenstructure successfully predicts: (i) lattice relaxations in any temperature range while accounting explicitly for anharmonic effects, (ii) low-temperature spin relaxations with fundamental descriptions of non-equilibrium temperature and magnetic field strength, and (iii) continuous and discontinuous mechanisms as well as concurrent ordering and phase separation mechanisms during the decomposition of solid-solutions.
Ph. D.
Many engineering materials have physical and chemical properties that change with time. The tendency of materials to change is quantified by the field of thermodynamics. The first and second laws of thermodynamics establish conditions under which a material has no tendency to change; these conditions are called equilibrium states. When a material is not in an equilibrium state, it is able to change spontaneously. Classical thermodynamics reliably identifies whether a material is susceptible to change, but it is incapable of predicting how change will take place or how fast it will occur. These are kinetic questions that fall outside the purview of thermodynamics. A relatively new theoretical treatment developed by Hatsopoulos, Gyftopoulos, Beretta and others over the past forty years extends classical thermodynamics into the kinetic realm. This framework, called steepest-entropy-ascent quantum thermodynamics (SEAQT), combines the tools of thermodynamics with quantum mechanics through a postulated equation of motion. Solving the equation of motion provides a kinetic description of the path a material will take as it changes from a non-equilibrium state to stable equilibrium. To date, the SEAQT framework has been applied primarily to systems of gases. In this dissertation, solid-state models are employed to extend the SEAQT approach to solid materials. The SEAQT framework is used to predict the thermal expansion of silver, the magnetization of iron, and the kinetics of atomic clustering and ordering in binary solid-solutions as a function of time or temperature. The model makes it possible to predict a unique kinetic path from any arbitrary, non-equilibrium, initial state to a stable equilibrium state. In each application, the approach is tested against experimental data. In addition to reproducing the qualitative kinetic trends in the cases considered, the SEAQT framework shows promise for modeling the behavior of materials far from equilibrium.
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Flores, Roxana Lili Roque. "Caracterização do estado sólido de ganciclovir". Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-16112017-173605/.

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O presente trabalho teve como objetivo o estudo do estado sólido do ganciclovir (GCV) e suas diferentes formas polimórficas. O GCV é um fármaco antiviral útil no tratamento de infecções por citomegalovírus (CMV). Embora seja um fármaco amplamente usado, poucos estudos têm sido realizados sobre seu estado sólido. Atualmente, o GCV é conhecido por apresentar quatro formas cristalinas, duas anidras (Forma I e II) e duas hidratas (III e IV). Neste trabalho, nós reportamos a solução da estrutura cristalográfica da Forma I do GCV, que foi encontrado durante o screening de cristalização do fármaco, em que nove ensaios de cristalização (GCV-1, GCV-A, GCV-B, GCV-C, GCV-D, GCV-E, GCV-F, GCV-G e GCV-H) foram realizados e os materiais resultantes foram caracterizados por Difratometria de raios X (DRX), análise térmica (DTA/TG) e Hot Stage Microscopy. De todas as cristalizações realizadas foram obtidas quatro formas sólidas, denominadas como Forma I (GCV-1, GCV-B e GCV-H), Forma III (GCV-C, GCV-D, GCV-F e GCV-G), Forma IV (GCV-A) e Forma V (GCV-E). Esta última está sendo descrita pela primeira vez na literatura e indica a presença de outra forma hidratada de GCV. As Formas I, III e IV corresponderam a forma anidra e as duas formas hidratadas do fármaco, respectivamente. Além disso, foi evidenciado por experimentos de conversão de slurry e análise térmica que o cristalizado de GCV-1 (Forma I) foi o mais estável entre os materiais obtidos, e este deu origem ao monocristal da Forma I de GCV, estrutura cristalina anidra do fármaco. Neste trabalho, pela primeira vez, a estrutura cristalina deste composto foi definida por cristalografia de raios X de monocristal. A análise estrutural mostrou que a Forma I do fármaco cristaliza no grupo espacial monoclínico P21/c e está composta por quatro moléculas de GCV na sua unidade assimétrica. Cada molécula está unida intermolecularmente por ligações de hidrogênio, que dão lugar à formação de cadeias infinitas e estas por sua vez se arranjam de maneira a formar uma estrutura tridimensional.
This presented work aims to study the solid state of ganciclovir (GCV) and its different polymorphic forms. GCV is an antiviral drug useful in the treatment of cytomegalovirus (CMV) infections. Although it is a widely-used drug, few studies have been conducted on its solid state. Currently, GCV is known to have four crystalline forms, two anhydrous (Form I and II) and two hydrates (III and IV). In this investigation, we report a successful preparation of GCV Form I and its crystallographic structure, which was found during the crystallization of the drug, in which nine crystallization tests (GCV-1, GCV-A, GCV-B, GCV- D, GCV-E, GCV-F, GCV-G and GCV-H) were performed and the resulting materials were characterized by X-ray diffractometry (XRD), thermal analysis (DTA/TG) and Hot Stage Microscopy. Of all the crystallizations performed, four solid forms were obtained, denoted as Form I (GCV-1, GCV-B and GCV- H), Form III (GCV-C, GCV-D, GCV-F and GCV-G), Form IV (GCV-A) and Form V (GCV-E). The latter is being described for the first time in the literature and indicates the presence of another hydrated form of GCV. Forms I, III and IV corresponded to the anhydrous form and the two hydrated forms of the drug, respectively. In addition, it was evident by both the slurry conversion and the thermal analysis methods that the GCV-1 crystallized (Form I) was indeed the most stable amongst the materials obtained. This gave rise to GCV Form I monocrystal, anhydrous crystalline structure of the drug. The compound was characterized by monocrystal X-ray crystallography. The structural analysis showed that Form I of the drug crystallized in the monoclinic system space group P21/c is composed of four molecules of GCV in its asymmetric unit. Each molecule is linked intermolecularly by hydrogen bonds, which give rise to the formation of infinite chains arranged in a way that form a three-dimensional structure.
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Schmidt, Marek Wojciech, i Marek Schmidt@rl ac uk. "Phase formation and structural transformation of strontium ferrite SrFeOx". The Australian National University. Research School of Physical Sciences and Engineering, 2001. http://thesis.anu.edu.au./public/adt-ANU20020708.190055.

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Non-stoichiometric strontium iron oxide is described by an abbreviated formula SrFeOx (2.5 ≤ x ≤ 3.0) exhibits a variety of interesting physical and chemical properties over a broad range of temperatures and in different gaseous environments. The oxide contains a mixture of iron in the trivalent and the rare tetravalent state. The material at elevated temperature is a mixed oxygen conductor and it, or its derivatives,can have practical applications in oxygen conducting devices such as pressure driven oxygen generators, partial oxidation reactors in electrodes for solid oxide fuel cells (SOFC). ¶ This thesis examines the behaviour of the material at ambient and elevated temperatures using a broad spectrum of solid state experimental techniques such as: x-ray and neutron powder diffraction,thermogravimetric and calorimetric methods,scanning electron microscopy and Mossbauer spectroscopy. Changes in the oxide were induced using conventional thermal treatment in various atmospheres as well as mechanical energy (ball milling). The first experimental chapter examines the formation of the ferrite from a mixture of reactants.It describes the chemical reactions and phase transitions that lead to the formation of the oxide. Ball milling of the reactants prior to annealing was found to eliminate transient phases from the reaction route and to increase the kinetics of the reaction at lower temperatures. Examination of the thermodynamics of iron oxide (hematite) used for the reactions led to a new route of synthesis of the ferrite frommagnetite and strontium carbonate.This chapter also explores the possibility of synthesis of the material at room temperature using ball milling. ¶ The ferrite strongly interacts with the gas phase so its behaviour was studied under different pressures of oxygen and in carbon dioxide.The changes in ferrite composition have an equilibrium character and depend on temperature and oxygen concentration in the atmosphere. Variations of the oxygen content x were described as a function of temperature and oxygen partial pressure, the results were used to plot an equilibrium composition diagram. The heat of oxidation was also measured as a function of temperature and oxygen partial pressure. ¶ Interaction of the ferrite with carbon dioxide below a critical temperature causes decomposition of the material to strontium carbonate and SrFe12O19 . The critical temperature depends on the partial pressure of CO2 and above the critical temperature the carbonate and SrFe12O19 are converted back into the ferrite.The resulting SrFe12O19 is very resistant towards carbonation and the thermal carbonation reaction does not lead to a complete decomposition of SrFeOx to hematite and strontium carbonate. ¶ The thermally induced oxidation and carbonation reactions cease at room temperature due to sluggish kinetics however,they can be carried out at ambient temperature using ball milling.The reaction routes for these processes are different from the thermal routes.The mechanical oxidation induces two or more concurrent reactions which lead to samples containing two or more phases. The mechanical carbonation on the other hand produces an unknown metastable iron carbonate and leads a complete decomposition of the ferrite to strontiumcarbonate and hematite. ¶ Thermally and mechanically oxidized samples were studied using Mossbauer spectroscopy. The author proposes a new interpretation of the Sr4Fe4O11 (x=2.75) and Sr8Fe8O23 (x=2.875)spectra.The interpretation is based on the chemistry of the compounds and provides a simpler explanation of the observed absorption lines.The Mossbauer results froma range of compositions revealed the roomtemperature phase behaviour of the ferrite also examined using x-ray diffraction. ¶ The high-temperature crystal structure of the ferrite was examined using neutron powder diffraction.The measurements were done at temperatures up to 1273K in argon and air atmospheres.The former atmosphere protects Sr2Fe2O5 (x=2.5) against oxidation and the measurements in air allowed variation of the composition of the oxide in the range 2.56 ≤ x ≤ 2.81. Sr2Fe2O5 is an antiferromagnet and undergoes phase transitions to the paramagnetic state at 692K and from the orthorhombic to the cubic structure around 1140K.The oxidized formof the ferrite also undergoes a transition to the high-temperature cubic form.The author proposes a new structural model for the cubic phase based on a unit cell with the Fm3c symmetry. The new model allows a description of the high-temperature cubic form of the ferrite as a solid solution of the composition end members.The results were used to draw a phase diagramfor the SrFeOx system. ¶ The last chapter summarizes the findings and suggests directions for further research.
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Bos, Cornelis. "Atomistic simulation of interface controlled solid state phase transformations". [S.l. : s.n.], 2005. http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-25279.

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Choudhry, Mohammad Arshad. "Crystallography of phase transformations and interphase boundaries in materials". Thesis, University of Surrey, 1985. http://epubs.surrey.ac.uk/847304/.

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The main purposes of this study were; (i) to apply the theory of martensite crystallography to martensitic transformations in low-symmetry materials, (ii) to investigate, using the computer simulation method, the microscopic structure of complex interphase boundaries which are not yet fully understood in terms of the martensitic mechanism. Although the unique symmetry of a twin boundary makes it a rather exceptional kind of interface, it is clearly a particularly appropriate starting point especially due to the role which twinning plays in martensitic transformations. The accuracy of twinning modes is vital for their use as lattice-invariant shears in theories of martensite crystallography. Potential twinning modes for zirconia were determined using the analysis due to Bilby and Crocker (1965) and the associated atomic shuffling was also considered. Twinning orientation relationships involving a screw axis and a glide plane have been established. The theory of martensite crystallography (Acton et al. 1970) was then applied to the tetragonal to monoclinic martensitic transformation in zirconia. The predictions for the habit plane, shape strain and the direction of the shape deformation were obtained and compared with available experimental observations. The application of the theory was also extended to the face-centred cubic to monocline martensitic transformation in plutonium alloys. The predictions of the crystallographic features for this transformation are reported. The computer simulation method was applied to investigate the relaxed atomic structure and energies of the complex interphase boundaries. The (100)b//(100)f and the (011)b /(111)f interphase boundaries were investigated using interatomic potential. Special consideration was given to the misfit dislocations at the interface which can accomplish the lattice-invariant shear of the phenomenological theories of martensite crystallography. A new equilibrium interatomic potential for iron was developed to study the relaxed structure of the (225)f b. c. c. /f. c. c. interphase boundary. These results are also compared with experimental information. Finally the general results of the thesis are discussed and main conclusions summarized.
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Książki na temat "Solid-state phase transformation"

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Alain, Hazotte, red. Solid state transformation and heat treatment. Weinheim: Wiley-VCH, 2005.

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C, Domb, i Lebowitz J. L. 1930-, red. Phase transitions and critical phenomena. London: Academic, 1991.

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C, Domb, i Lebowitz J. L. 1930-, red. Phase transitions and critical phenomena. London: Academic, 1992.

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J, Čermák, i Stloukal I, red. Solid phase transformations. Stafa-Zurich: Trans Tech, 2008.

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J, Čermák, i Stloukal I, red. Solid phase transformations II. Stafa-Zurich, Switzerland: Trans Tech Publications, 2009.

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W, Lorimer G., i Institute of Metals. Metal Science Committee., red. Phase transformations '87. London: Institute of Metals, 1988.

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France) International Conference on Solid-Solid Phase Transformations in Inorganic Materials (2010 Avignon. Solid-solid phase transformations in inorganic materials. Durnten-Zuerich: Trans Tech Publications, 2011.

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Conference, on Solid State Amorphizing Transformations (1987 Los Alamos N. M. ). Solid state amorphizing transformations: Proceedings of the Conference on Solid State Amorphizing Transformations, Los Alamos, NM, August 10-13, 1987. Lausanne: Elsevier Sequoia, 1988.

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Walker, J. R. Phase transitions in crystalline solids I: Automorphisms and extensions of crystallographic and icosahedral point groups. Chalk River, Ont: Chalk River Laboratories, 1993.

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International Conference on Solid [to] Solid Phase Transformations (2005 Phoenix, Az.). Proceedings of an International Conference on Solid [to] Solid Phase Transformations in Inorganic Materials 2005: Held at the Pointe Hilton Resort at Squaw Peak, Phoenix, Arizona, USA, May 29-June 3, 2005. Redaktorzy Howe James M. 1955-, Minerals, Metals and Materials Society. i ASM International. Warrendale, Pa: TMS, 2005.

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Części książek na temat "Solid-state phase transformation"

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Perez, Nestor. "Solid-State Phase Change". W Phase Transformation in Metals, 397–459. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49168-0_9.

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Lekston, Zdzisław, i Tomasz Goryczka. "Phase Transformation in Ti-Ni-Ta Shape Memory Alloy". W Solid State Phenomena, 147–50. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-40-x.147.

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Burch, Damian, Gogi Singh, Gerbrand Ceder i Martin Z. Bazant. "Phase-Transformation Wave Dynamics in LiFePO4 ". W Solid State Phenomena, 95–100. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/3-908451-56-6.95.

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Lee, Sang Hwan, Jong Min Choi, Yeol Rae Cho i Kyung Jong Lee. "The Effects of Si and Deformation on the Phase Transformation in Dual Phase Steels". W Solid State Phenomena, 1617–20. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-31-0.1617.

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Date, Hidefumi, i Masaaki Naka. "Evaluation of Compound Layer Formed by Impact Welding Using Phase Transformation Technique". W Solid State Phenomena, 283–88. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-33-7.283.

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Jianu, A., H. R. Sinning, I. S. Golovin i E. Burkel. "Solid-Solid Phase Transformation of Amorphous Titanium Based Alloys". W Solid State Transformation and Heat Treatment, 144–51. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527604839.ch18.

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Kim, Sang Woo, i Shin Young Kim. "Effect of Phase Transformation and Fine Particle Dispersion on Densification of High Purity Nanocrystalline γ-Phase Dispersed α-Alumina". W Solid State Phenomena, 831–34. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-31-0.831.

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Lee, Seok Jae, i Young Kook Lee. "A Computational Model for Phase Transformation-Temperature-Distortion Coupling of AISI 5120 Steel". W Solid State Phenomena, 387–92. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908451-25-6.387.

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Pielaszek, J., J. R. Dygas, F. Krok, D. Lisovytskiy, Monika Kopeć i M. Marzantowicz. "X-Ray Diffraction and Electric Measurements of Phase Transformation in Li-Mn Spinels". W Solid State Phenomena, 63–68. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-40-x.63.

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Guillon, I., C. Servant i O. Lyon. "Phase Transformations in a Co-Cu-Ni Alloy". W Solid State Transformation and Heat Treatment, 34–41. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527604839.ch5.

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Streszczenia konferencji na temat "Solid-state phase transformation"

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Ghosh, Partha S., A. Arya i G. K. Dey. "HCP to omega martensitic phase transformation pathway in pure Zr". W SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4790904.

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Sahoo, B. D., K. D. Joshi i Satish C. Gupta. "High pressure phase transformation in uranium carbide: A first principle study". W SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4790919.

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Sahoo, B. D., K. D. Joshi i Satish C. Gupta. "High pressure phase transformation in yttrium sulfide(YS): A first principle study". W SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872486.

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Rawat, Sunil, i Nilanjan Mitra. "Twinning assisted α to ω phase transformation in titanium single crystal". W DAE SOLID STATE PHYSICS SYMPOSIUM 2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4980197.

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Behera, Mukta, N. C. Mishra i R. Naik. "Influence of thermal annealing on phase transformation in Bi10As40Se50 thin films". W DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112841.

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Gond, Ritambhara, Sai Pranav, Shashwat Singh i Prabeer Barpanda. "Phase transformation and functional behavior of Na2MP2O7 (M = Mn, Co) pyrophosphates". W DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112862.

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Dwibedi, Debasmita, Shashwat Singh, Sai Pranav i Prabeer Barpanda. "Phase transformation in Na-Fe-S-O quaternary sulfate cathode materials". W DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5113405.

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Cao, W. D. "Solidification and Solid State Phase Transformation of Allvac 718Plus Alloy". W Superalloys. TMS, 2005. http://dx.doi.org/10.7449/2005/superalloys_2005_165_177.

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Tomida, Kazuyuki, Koji Kita i Akira Toriumi. "Origin of Structural Phase Transformation of SiO2-doped HfO2". W 2007 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2007. http://dx.doi.org/10.7567/ssdm.2007.f-9-3.

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Ramakrishna, K., Manjunatha Pattabi, Alka B. Garg, R. Mittal i R. Mukhopadhyay. "Effect of Thermal Cycling at Different Rates on Phase Transformation Behavior of NiTi Shape Memory Alloy". W SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605779.

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