Academic literature on the topic 'Variable-temperature powder X-ray diffraction'

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Journal articles on the topic "Variable-temperature powder X-ray diffraction"

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Tarling, S. E. "Laboratory high-temperature X-ray powder diffraction." Phase Transitions 39, no. 1-4 (1992): 199–213. http://dx.doi.org/10.1080/01411599208203482.

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Karjalainen, Milja, Sari Airaksinen, Jukka Rantanen, Jaakko Aaltonen, and Jouko Yliruusi. "Characterization of polymorphic solid-state changes using variable temperature X-ray powder diffraction." Journal of Pharmaceutical and Biomedical Analysis 39, no. 1-2 (2005): 27–32. http://dx.doi.org/10.1016/j.jpba.2005.02.036.

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Reddy, L. Sreenivas, Prashant M Bhatt, Rahul Banerjee, Ashwini Nangia, and Gert J Kruger. "Variable-Temperature Powder X-ray Diffraction of Aromatic Carboxylic Acid and Carboxamide Cocrystals." Chemistry – An Asian Journal 2, no. 4 (2007): 505–13. http://dx.doi.org/10.1002/asia.200600359.

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Chen, Xue, Ning Li, Yuan Li, and Ping Che. "Characterization on crystal structure of CH3NH3PbIxCl3−x perovskite by variable temperature powder X-ray diffraction." Materials Letters 235 (January 2019): 239–41. http://dx.doi.org/10.1016/j.matlet.2018.09.151.

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Kano, S., A. Yamazaki, R. Otsuka, et al. "Low-temperature X-ray powder diffraction of Bi2Sr2CaCu2Oxsuperconductor." Phase Transitions 41, no. 1-4 (1993): 249–53. http://dx.doi.org/10.1080/01411599308207787.

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Tayebifard, S. A., K. Ahmadi, R. Yazdani-Rad, and M. Doroudian. "New X-ray powder diffraction data for Mo2.85Al1.91Si4.81." Powder Diffraction 21, no. 3 (2006): 238–40. http://dx.doi.org/10.1154/1.2244544.

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X-ray powder diffraction data for Mo2.85Al1.91Si4.81 are reported. The new Mo2.85Al1.91Si4.81 compound was successfully prepared using the self-propagating high-temperature synthesis (SHS) technique. The starting atomic mixture of reactant powders was Mo+2(1−x)Si+2xAl with x=0.3. The final powder compound obtained by the SHS technique was determined to be Mo2.85Al1.91Si4.81 by ICP-AES. X-ray powder diffraction pattern of Mo2.85Al1.91Si4.81 was recorded using an X-ray powder diffractometer, Cu Kα radiation, and analyzed by automatic indexing programs. Mo2.85Al1.91Si4.81 was found to be hexagona
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Garin, Jorge L., and Rodolfo L. Mannheim. "X-ray powder diffraction pattern of Mo4.8Si3C0.6." Powder Diffraction 8, no. 1 (1993): 65–67. http://dx.doi.org/10.1017/s0885715600017784.

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The title compound was synthesized by high temperature reaction of the component elements. This phase, formerly classified in the group of Nowotny phases, crystallizes in the hexagonal system with space group P63/mcm. Crystal data and indexed X-ray powder diffraction data are reported.
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Nong, Liangqin, and Lingmin Zeng. "X-ray powder diffraction study on ErNi2Ge2." Powder Diffraction 14, no. 2 (1999): 145–46. http://dx.doi.org/10.1017/s0885715600010472.

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An X-ray diffraction pattern for ErNi2Ge2 at room temperature is reported. ErNi2Ge2 is tetragonal with lattice parameters a=4.0191(2) Å, c=9.7643(2) Å, space group I4/mmm, and Z=2. The lattice parameters derived from Rietveld analysis agree well with the results of a least-squares refinement.
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Burley, Jonathan C. "Structure and intermolecular interactions of glipizide from laboratory X-ray powder diffraction." Acta Crystallographica Section B Structural Science 61, no. 6 (2005): 710–16. http://dx.doi.org/10.1107/s0108768105025991.

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The crystal structure of glipizide, used as a major treatment of type-2 diabetes, has been determined ab initio using variable-temperature laboratory X-ray powder diffraction combined with a direct-space Monte Carlo/simulated annealing methodology. The strengths of the intermolecular interactions (van der Waals, π–π stacking, hydrogen bonding and steric interlock) were quantitatively estimated using the thermal expansion data, which were collected in the same set of experiments as those used to determine the structure.
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Schlicker, Lukas, Andrew Doran, Peter Schneppmüller, et al. "Transmission in situ and operando high temperature X-ray powder diffraction in variable gaseous environments." Review of Scientific Instruments 89, no. 3 (2018): 033904. http://dx.doi.org/10.1063/1.5001695.

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Dissertations / Theses on the topic "Variable-temperature powder X-ray diffraction"

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McDowell, John Christopher. "Preparation characterisation and stability of selected high critical temperature ceramic superconductors." Thesis, University of Ulster, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260854.

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Krogh, Andersen Anne. "Studies of Inorganic Layer and Framework Structures Using Time-, Temperature- and Pressure-Resolved Powder Diffraction Techniques." Doctoral thesis, Stockholm University, Department of Physical, Inorganic and Structural Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-23.

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<p>This thesis is concerned with <i>in-situ</i> time-, temperature- and pressure-resolved synchrotron X-ray powder diffraction investigations of a variety of inorganic compounds with twodimensional layer structures and three-dimensional framework structures. In particular, phase stability, reaction kinetics, thermal expansion and compressibility at non-ambient conditions has been studied for 1) Phosphates with composition <i>M</i><i>IV</i>(HPO<sub>4</sub>)<sub>2</sub>·<i>n</i>H<sub>2</sub>O (<i>M</i><i>IV</i> = Ti, Zr); 2) Pyrophosphates and pyrovanadates with composition<i> M</i><i>IV</i>X<su
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Oliver, David Elliot. "Phase-change materials for thermal energy storage." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/17910.

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There is a current requirement for technologies that store heat for both domestic and industrial applications. Phase-change materials (PCMs) represent an important class of materials that offer potential for heat storage. Heat-storage systems are required to undergo multiple melt/freeze cycles without any change in melting-crystallisation point and heat output. Salt hydrates are attractive candidates on account of their high energy densities, but there are issues associated with potential crystallisation of lower-hydrates, long-term stability, and reliable nucleation. An extensive review of th
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Mowat, John P. S. "Synthesis, characterisation and adsorption properties of metal-organic frameworks and the structural response to functionalisation and temperature." Thesis, University of St Andrews, 2012. http://hdl.handle.net/10023/3195.

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The synthesis of a scandium aluminium methylphosphonate ScAl₃(CH₃PO₃)₆ isostructural to the aluminium methylphosphonate AlMePO-α and with permanent microporosity is reported here for the first time. Structural characterisation of three lanthanide bisphosphonate structures (I,II,III) with the light lanthanides and N,N'-piperazine bis-(methylenephosphonic acid) and its 2-methyl and 2,5-dimethyl derivatives is described. The framework of structure type I shows considerable flexibility upon dehydration with a symmetry change from C2/c, a = 23.5864(2) Å, b = 12.1186(2) Å, c = 5.6613(2) Å, β = 93
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Ostach, Daniel Michael [Verfasser], and Andreas [Akademischer Betreuer] Schreyer. "High Temperature Oxidation Behavior of (Ti,Cr,Al)N Coatings Studied by in-situ Synchrotron Radiation X-ray Powder Diffraction / Daniel Michael Ostach ; Betreuer: Andreas Schreyer." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2018. http://d-nb.info/1153884445/34.

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Seyyidoglu, Semih. "High Temperature Chemistry Of Some Borophosphates, Phase Relations And Structural Studies." Master's thesis, METU, 2003. http://etd.lib.metu.edu.tr/upload/1045863/index.pdf.

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The solid state, hydrothermal and flux methods were used for the investigation of alkaline earth and transition metal borophosphate compounds. The products and the phase relations were investigated by XRD, IR, DTA, and EDX methods. The solid state reactions of several boron compounds with different phosphating agents have been studied in the temperature range of 400-1200 oC. Hydrothermal and flux techniques were performed at 150 oC and 1200 oC, respectively. On the other hand, an attempt has been made to prepare a novel borophosphate compound MIIMIV[BPO7] (where MIV= Zr4+, Si4+, and MII= Sr2+,
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FALCAO, RAILSON B. "Síntese por reação do TiFe nanoestruturado para o armazenamento de hidrogênio, a partir da moagem de alta energia de misturas de pós de TiH2 e Fe." reponame:Repositório Institucional do IPEN, 2016. http://repositorio.ipen.br:8080/xmlui/handle/123456789/27135.

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Submitted by Mery Piedad Zamudio Igami (mery@ipen.br) on 2017-03-10T16:23:34Z No. of bitstreams: 0<br>Made available in DSpace on 2017-03-10T16:23:34Z (GMT). No. of bitstreams: 0<br>Neste trabalho investigou-se a obtenção do composto TiFe a partir da moagem de alta energia de misturas de pós de TiH2 e Fe, seguida de aquecimento sob vácuo para a reação de síntese. No lugar do Ti, o TiH2 foi escolhido como precursor em razão de sua fragilidade, benéfica para a diminuição da aderência dos pós ao ferramental de moagem. Foram preparados dois lotes de misturas obedecendo-se a relação Ti:Fe de 50:50
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Ghorbani, Shaban Reza. "Structural and Electrical Transport Properties of Doped Nd-123 Superconductors." Doctoral thesis, KTH, Physics, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3461.

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<p>It is generally believed that one of the key parameterscontrolling the normal state and superconducting properties ofhigh temperature superconductors is the charge carrierconcentration<i>p</i>in the CuO<sub>2</sub>planes.By changing the non-isovalent dopingconcentration on the RE site as well as the oxygen content in(RE)Ba<sub>2</sub>Cu<sub>3</sub>O<sub>7−δ</sub>, an excellent tool is obtained tovary the hole concentration over a wide range from theunderdoped up to the overdoped regime.In the present thesis thefocus is on the doping effects on the structural and normalstate electrical prope
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Sheridan, Andrew Keith. "Kinetics and temperature- and pressure-induced polymorphic phase transformations in molecular crystals." Thesis, King's College London (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322597.

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Nilsson, Marita. "Hydrogen generation from dimethyl ether by autothermal reforming." Licentiate thesis, Stockholm : Kemi, Kungliga Tekniska högskolan, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4434.

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Books on the topic "Variable-temperature powder X-ray diffraction"

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Stoner, Troy A. Preparation of Extinction Free Gamma Ti-51at.%Al Alloy Powder and Characterization by X-ray Diffraction. Naval Postgraduate School, 1992.

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Book chapters on the topic "Variable-temperature powder X-ray diffraction"

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Vaucher, Sebastien, Rajmund Mokso, Kotaro Ishizaki, Manuela Stir, and Radu Nicula. "Dynamic High-Temperature Monitoring of Microwave Energy Absorption and Heating of Materials with Ultrafast Insitu Synchrotron X-ray Tomographic Microscopy and Powder Diffraction Techniques." In 2nd International Congress on 3D Materials Science. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118990278.ch17.

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Vaucher, Sebastien, Rajmund Mokso, Kotaro Ishizaki, Manuela Stir, and Radu Nicula. "Dynamic High-Temperature Monitoring of Microwave Energy Absorption and Heating of Materials with Ultrafast In Situ Synchrotron X-Ray Tomographic Microscopy and Powder Diffraction Techniques." In Proceedings of the 2nd International Congress on 3D Materials Science. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-48123-4_17.

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Haun, M. J., Y. H. Lee, H. A. McKinstry, and L. E. Cross. "High Temperature X-Ray Diffraction Study of Sol-Gel Derived Pb(ZrxTi1-x)03 Powders." In Advances in X-Ray Analysis. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1935-1_57.

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Kajitani, Masahiro, Motohide Matsuda, Akinori Hoshikawa, Takashi Kamiyama, Fujio Izumi, and Michihiro Miyake. "Investigation of the Oxide Ion Conduction Mechanism in LaGaO3-Based Electrolytes through High-Temperature Neutron Powder Diffraction." In Electroceramics in Japan X. Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-449-9.147.

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"High temperature X-ray diffraction investigation of an aluminium-siliconcorundum system." In Tenth European Powder Diffraction Conference. Oldenbourg Wissenschaftsverlag, 2007. http://dx.doi.org/10.1524/9783486992540-058.

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Skoko, Željko, and Stanko Popović. "Microstructure of Al-Cu, Al-Zn, Al-Ag-Zn, and Al-Zn-Mg Alloys." In Encyclopedia of Aluminum and Its Alloys. CRC Press, 2019. http://dx.doi.org/10.1201/9781351045636-140000172.

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The precipitation phenomena and their connection with the microstructure of several Al alloys (Al-Cu, Al-Zn, Al-Ag-Zn, Al-Zn-Mg) are described with respect to the concentration and applied thermal treatment. The alloys were rapidly quenched or slowly cooled from a temperature higher than the solid solution temperature to room temperature. Both quenched-aged and slowly cooled alloys were heated from room temperature to the solid solution state and cooled back to room temperature, and their microstructure and precipitation phenomena were followed in situ by X-ray powder diffraction, e.g., anisotropy of thermal expansion, phase transitions, thermal hysteresis in phase transitions, change of precipitate shape, partial or complete dissolution of precipitates in the matrix, and formation of solid solution. It has been shown that the microstructure strongly depends on the previous thermal history of the alloys.
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Krishnan, Kannan M. "X-Ray Diffraction." In Principles of Materials Characterization and Metrology. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780198830252.003.0007.

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X-rays diffraction is fundamental to understanding the structure and crystallography of biological, geological, or technological materials. X-rays scatter predominantly by the electrons in solids, and have an elastic (coherent, Thompson) and an inelastic (incoherent, Compton) component. The atomic scattering factor is largest (= Z) for forward scattering, and decreases with increasing scattering angle and decreasing wavelength. The amplitude of the diffracted wave is the structure factor, F <sub>hkl</sub>, and its square gives the intensity. In practice, intensities are modified by temperature (Debye-Waller), absorption, Lorentz-polarization, and the multiplicity of the lattice planes involved in diffraction. Diffraction patterns reflect the symmetry (point group) of the crystal; however, they are centrosymmetric (Friedel law) even if the crystal is not. Systematic absences of reflections in diffraction result from glide planes and screw axes. In polycrystalline materials, the diffracted beam is affected by the lattice strain or grain size (Scherrer equation). Diffraction conditions (Bragg Law) for a given lattice spacing can be satisfied by varying θ or λ — for study of single crystals θ is fixed and λ is varied (Laue), or λ is fixed and θ varied to study powders (Debye-Scherrer), polycrystalline materials (diffractometry), and thin films (reflectivity). X-ray diffraction is widely applied.
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Kurisu, Makio. "Study of High-Temperature Oxidation Behavior of Antimony and Bismuth Tellurides by Thermopiezic Analysis and Powder X-Ray Diffraction: A Case Study of Thermochemistry." In Functional Materials. Jenny Stanford Publishing, 2019. http://dx.doi.org/10.1201/9780429468131-3.

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Kosuge, Koji. "Non-Stoichiometric Compounds Derived From Point Defects." In Chemistry of Non-stoichiometric Compounds. Oxford University Press, 1994. http://dx.doi.org/10.1093/oso/9780198555551.003.0004.

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In this chapter, we discuss ‘classical’ non-stoichiometry derived from various kinds of point defects. To derive the phase rule, which is indispensable for the understanding of non-stoichiometry, the key points of thermodynamics are reviewed, and then the relationship between the phase rule, Gibbs’ free energy, and non-stoichiometry is discussed. The concentrations of point defects in thermal equilibrium for many types of defect structure are calculated by simple statistical thermodynamics. In Section 1.4 examples of non-stoichiometric compounds are shown referred to published papers. The technical term ‘non-stoichiometric compounds’ has been used for a long time, in contradiction to the term ‘stoichiometric compounds’. The existence of non-stoichiometric compounds, which have also been called Bertholides compounds, cannot be explained from the law of definite proportion in its simplest meaning. Proust insisted that only stoichiometric compounds (also named Daltonide compounds) existed, whereas Bertholet maintained the existence of not only stoichiometric compounds but also non-stoichiometric compounds. This is a very famous argument in the history of chemistry. In the early years of the twentieth century, Kurnakov investigated the physical and chemical properties of intermetallic compounds in detail and found that the maximum or minimum in melting point, electrical resistivity, and also in the ordering temperature of lattices does not necessarily appear at the stoichiometric composition. An important discovery of Dingman was that stoichiometric FeO1.00 is non-existent under ordinary conditions. (At present, we can synthesize stoichiometric FeO1.00 under high pressure.) Non-stoichiometry, which originates from various kinds of lattice defect, can be derived from the phase rule. As an introduction, let us consider a trial experiment to understand non-stoichiometry (this experiment is, in principle, analogous to the one described in Section 1.4.8). Figure 1.1 shows a reaction vessel equipped with a vacuum pump, pressure gauge for oxygen gas, pressure controller for oxygen gas, thermometer, and chemical balance. The temperature of the vessel is controlled by an outer-furnace and the vessel has a special window for in-situ X-ray diffraction. A quantity of metal powder is placed on the chemical balance, and then the vessel is evacuated at room temperature.
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Jemmali, Mosbah, and Lotfi Bessais. "Effect of M Substitution on Structural, Magnetic and Magnetocaloric Properties of R2Fe17-x Mx (R = Gd, Nd; M = Co, Cu) Solid Solutions." In Magnetic Skyrmions. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96299.

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The structure, magnetic and magnetocaloric properties of Nd2Fe17−xCox (x = 0; 1; 2; 3, 4) and Gd2Fe17-xCux (x = 0, 0.5, 1 and 1.5) solid solutions have been studied. For this purpose, these samples were prepared by arc melting and subsequent annealing at 1073 K for a 7 days. Structural analysis by Rietveld method on X-ray diffraction (XRD) have determined that these alloys crystallize in the rhombohedral Th2Zn17-type structure (Space group R¯3 m) and the substitution of iron by nickel and copper leads to a decrease in the unit cell volume. The Curie temperature (TC) of the prepared samples depends on the nickel and copper content. Based on the Arrott plot, these analyses show that Nd2Fe17-xCox exhibits a second-order ferromagnetic to paramagnetic phase transition around the Curie temperature. These curves were also used to determine the magnetic entropy change ∆SMax and the relative cooling power. For an applied field of 1.5 T, ∆SMax increase from 3.35 J/kg. K for x = 0 to 5.83 J/kg. K for x = 2. In addition the RCP increases monotonously. This is due to an important temperature range for the magnetic phase transition, contributing to a large ∆SMax shape. Gd2Fe17-xCux solid solution has a reduction of the ferromagnetic phase transition temperature from 475 K (for x = 0) to 460 K (for x = 1.5) is due to the substitution of the magnetic element (Fe) by non-magnetic atoms (Cu). The magnetocaloric effect was determined in the vicinity of the Curie temperature TC. By increasing the Cu content, an increase in the values of magnetic entropy (∆SMax) in a low applied field is observed.
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Conference papers on the topic "Variable-temperature powder X-ray diffraction"

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Tanaka, Masahiko. "A New Furnace For High-Temperature Synchrotron X-ray Powder Diffraction Experiments — Electron Density Analysis By Powder X-ray Diffraction At 1300°C." In SYNCHROTRON RADIATION INSTRUMENTATION: Eighth International Conference on Synchrotron Radiation Instrumentation. AIP, 2004. http://dx.doi.org/10.1063/1.1757979.

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Wang, Yang, and Dayong Lu. "STUDY ON ORAL ULCER POWDER USING TEMPERATURE-DEPENDENT X-RAY DIFFRACTION TECHNIQUE." In International Conference on New Materials and Intelligent Manufacturing (ICNMIM). Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.104.106.

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Trnka, Hjalte, Jukka Rantanen, and Holger Grohganz. "Investigation of Solid State Changes in Freeze-dried Biomacromolecular Samples: Process Simulation by Variable Temperature X-ray Powder Diffraction." In The 1st Electronic Conference on Pharmaceutical Sciences. MDPI, 2011. http://dx.doi.org/10.3390/ecps2011-00526.

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Younesi, Mousa, Mehdi Javidi, Mohammad Ebrahim Bahrololoom, and Hamidreza Fooladfar. "Effect of Heat Treating Temperature on Chemical and Physical Properties of Natural Hydroxyapatite Produced From Bovine Bone." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-12574.

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This study focused on chemical and physical properties of Hydroxyapatite powder was prepared by burning bone and heat treating the obtained bone ash at different temperatures (600, 700, 800, and 1100 °C) in an air furnace. The black ash was converted to a white powder after heat treatment. Results of X-ray diffraction analysis and Fourier transform infra-red spectroscopy that were done on heat treated powders in different temperatures indicated that the white powder was hydroxyapatite and did not contain any organic components of the bone. Furthermore, results of X-ray diffraction analysis wer
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Bacci, T., U. Bardi, F. Borgioli, et al. "Reactive Plasma Spray for the Deposition of Ti/TiN Coatings: A Comparative Compositional Study by X-Ray Diffraction (XRD) and X-Ray Photoelectron Spectroscopy (XPS)." In ITSC 2000, edited by Christopher C. Berndt. ASM International, 2000. http://dx.doi.org/10.31399/asm.cp.itsc2000p0289.

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Abstract This paper compares two methods for determining the composition of Ti/TiN coatings deposited by reactive plasma spraying. The coatings were obtained by spraying titanium powder in a low-pressure N2/Ar atmosphere. The resulting film has a variable nitrogen content in the form of titanium nitrides, depending on gas partial pressure, total pressure, sample-source distance, and other parameters. The composition of the film was determined using X-ray diffraction and X-ray photoelectron spectroscopy. The two techniques provide similar results and either can be used for the compositional cha
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Allen, Kyle M., James F. Klausner, Eric N. Coker, Nick AuYeung, and Rishi Mishra. "Synthesis and Analysis of Cobalt Ferrite in YSZ for Use as Reactive Material in Solar Thermochemical Water and Carbon Dioxide Splitting." In ASME 2013 7th International Conference on Energy Sustainability collocated with the ASME 2013 Heat Transfer Summer Conference and the ASME 2013 11th International Conference on Fuel Cell Science, Engineering and Technology. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/es2013-18254.

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This paper reports the synthesis, characterization and evaluation of different weight loadings of cobalt ferrite (CoFe2O4) in 8 mol% yttria-stabilized zirconia (8YSZ) via the co-precipitation method. Prepared powders were calcined at 1350 °C for 36 hours and 1450 °C for 4 hours in air. These powders were then formed into a porous structure using sacrificial pore formation via oxidation of co-mixed graphite powder. These formed structures obtained were then characterized using thermogravimetric analysis (TGA), X-ray diffraction (XRD), high temperature X-ray diffraction (HT-XRD), scanning electr
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Huang, Jianbing, Zongqiang Mao, Bin Zhu, Lizhai Yang, Ranran Peng, and Ruifeng Gao. "Direct Preparation of Ce0.8Sm0.2O1.9 Powders Oxidized With H2O2 for Low Temperature SOFCs Application." In ASME 2005 3rd International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2005. http://dx.doi.org/10.1115/fuelcell2005-74027.

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A novel method was developed to prepare fine doped ceria (DCO) powders directly. Ceria doped with 20 mol. % of samarium (Ce0.8Sm0.2O1.9, SDC) was prepared by in-situ oxidization of hydroxide precipitates with H2O2 in the solutions. The resultant powder desiccated at 85°C overnight was characterized by X-ray diffraction (XRD), thermogravimetry /differential thermal analysis (TG/DTA), and transmission electron microscopy (TEM). The XRD pattern showed that the as-dried SDC powder is single phase with a cubic fluorite structure like that of pure CeO2. An anode-supported SOFC was also fabricated ba
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Yarmolenko, Sergey, Kristofer Gordon, Brandon Hancock, Vladislav Kharton та Jag Sankar. "Characterization of (La0.9Sr0.1)0.95Cr0.85Mg0.10Ni0.05O3−δ Ceramics for Perovskite Related Membrane Reactor". У ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43845.

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(La0.9Sr0.1)0.95Cr0.85Mg0.10Ni0.05O3 (LSCMN) ceramics sintered at temperatures 1100–1700°C in air were characterized using powder x-ray diffraction, field emission scanning electron microscopy coupled with energy dispersive x-ray spectroscopy, transmission electron microscopy, differential scanning calorimetry, and inductively-coupled plasma spectroscopic analysis. Pervoskite ceramics with the highest density (porosity between 2–5%) were sintered at 1650°C for 24 hours. Secondary phases at a level of 3–5% porousity have been detected in the LSCMN initial powder received and sintered samples. L
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Saladi, Sekar, Jyoti V. Menghani, and Satya Prakash. "High Temperature Oxidation Behaviour of Detonation-Gun-Sprayed Cr3C2-NiCr-CeO2 Coatings on Inconel-718 at 900°C." In ASME Turbo Expo 2014: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/gt2014-26447.

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The high temperature oxidation behavior of detonation-gun sprayed Cr3C2-NiCr coatings with and without 0.4 wt. % CeO2 additive on Ni-based superalloy inconel-718 is comparatively discussed in the present study. Oxidation studies were carried out at 900°C for 100 cycles in air under cyclic heating and cooling conditions on bare and coated superalloys. The thermo-gravimetric technique was used to establish kinetics of oxidation. X-ray diffraction, SEM/EDAX and X-ray mapping techniques were used to analyze the oxidation products of bare and coated samples. The results indicate that Cr3C2-NiCr-CeO
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Froning, Marc J., and Purush Sahoo. "Influence of Powder Manufacturing Process on TBC Lifetime." In ASME 1995 International Gas Turbine and Aeroengine Congress and Exposition. American Society of Mechanical Engineers, 1995. http://dx.doi.org/10.1115/95-gt-364.

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Abstract:
Thermal barrier coatings (TBC) have been used extensively in aircraft engines to protect the gas turbines’ hot section from mechanical and enviromental degradation as well as to improve thermodynamic efficiency. Because TBC’s enhance operating temperature and service life, they are expected to play and increasingly important role in protecting both flight and land based industrial turbine engines. This investigation examines the functionality of air plasma sprayed two-layer TBC systems with a MCrAlY bond coat and a yttria partially stabilized zirconia (YSZ) top coat. Qualitative X-ray diffract
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