Relevant bibliographies by topics / Solid-state sintering

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  2. Dissertations / Theses
  3. Books
  4. Book chapters
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Academic literature on the topic 'Solid-state sintering'

Author: Grafiati
Published: 4 June 2021
Last updated: 22 June 2024

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Journal articles on the topic "Solid-state sintering"

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Biswas, Koushik. "Solid State Sintering of SiC-Ceramics." Materials Science Forum 624 (June 2009): 71–89. http://dx.doi.org/10.4028/www.scientific.net/msf.624.71.

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The most interesting feature in silicon carbide is the structure-property relation where the formation of different types of microstructure due to different structural modifications (polytypism) and grain-boundary/interfacial phase chemistry dictate the final properties of the monoliths. Since synthesis of SiC in last century, several methods such as hot pressing with a sintering aid (B, C), pressureless sintering with a sintering aid (B, C, Al) and reaction bonded (Si-SiC) were used to fabricate dense SiC. A newer method of fast sintering (spark plasma sintering) using pulsed current is also employed to consolidate nano/submicron size SiC with or without additives. The solid state sintered SiC materials have fine-grained equiaxed microstructure (grain size 1 to 4 µm) with thin layer of intergranular phases (amorphous film), exhibit moderate high-temperature creep and oxidation resistance, fracture toughness (3 to 4 MPam1/2) and have highly flaw-sensitive strength at room temperature. The high temperature mechanical properties are highly influenced by the presence of free C, Al and B + C containing grain-boundary phases. Moreover, during prolong processing, abnormal grain growth occurs resulting in anisotropic -SiC phase formation. The Si-SiC materials are poor candidates for high-temperature applications due to the limit set by the melting point of silicon, and the limitations of hot pressing (HPSiC) as a densification technique are well known. SPSed SiC without sintering additive revealed inferior mechanical properties attributed to poor bonding between adjacent grains. In the present survey, an overview of the new developments in silicon carbide processing and properties will be presented together with the information on structure-properties correlationship. Information on the structure of the grain-boundary/secondary phases and interfaces until now was not comprehensively analyzed.
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Braginsky, Michael, Veena Tikare, and Eugene Olevsky. "Numerical simulation of solid state sintering." International Journal of Solids and Structures 42, no. 2 (January 2005): 621–36. http://dx.doi.org/10.1016/j.ijsolstr.2004.06.022.

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Ryan, Amy G., James K. Russell, and Michael J. Heap. "Rapid solid-state sintering in volcanic systems." American Mineralogist 103, no. 12 (December 1, 2018): 2028–31. http://dx.doi.org/10.2138/am-2018-6714.

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Hötzer, Johannes, Marco Seiz, Michael Kellner, Wolfgang Rheinheimer, and Britta Nestler. "Phase-field simulation of solid state sintering." Acta Materialia 164 (February 2019): 184–95. http://dx.doi.org/10.1016/j.actamat.2018.10.021.

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Gurwell, W. E. "Solid-State Sintering of Tungsten Heavy Alloys." Materials and Manufacturing Processes 9, no. 6 (November 1994): 1115–26. http://dx.doi.org/10.1080/10426919408934979.

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Maximenko, Andrey L., and Eugene A. Olevsky. "Effective diffusion coefficients in solid-state sintering." Acta Materialia 52, no. 10 (June 2004): 2953–63. http://dx.doi.org/10.1016/j.actamat.2004.02.042.

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Tikare, Veena, Michael Braginsky, and Eugene A. Olevsky. "Numerical Simulation of Solid-State Sintering: I, Sintering of Three Particles." Journal of the American Ceramic Society 86, no. 1 (January 2003): 49–53. http://dx.doi.org/10.1111/j.1151-2916.2003.tb03276.x.

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Kang, Suk-Joong L., Rajendra K. Bordia, and Eugene A. Olevsky. "Emerging challenges in solid-state sintering science and technology." Izvestiya Vuzov. Poroshkovaya Metallurgiya i Funktsional’nye Pokrytiya (Universitiesʹ Proceedings. Powder Metallurgy аnd Functional Coatings), no. 4 (December 15, 2018): 28–31. http://dx.doi.org/10.17073/1997-308x-2018-4-28-31.

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Major research challenges in the field of solid-state sintering are noted following the authors’ recent paper (J. Am. Ceram. Soc. 2017. Vol. 100. P. 2314–2352). They are highlighted in the areas of (i) modeling and simulation (mesoscale as well as macroscale), (ii) microstructural evolution with respect to interface structure, (iii) novel sintering techniques, and (iv) solutions for practical systems.
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Yasui, Kyuichi, and Koichi Hamamoto. "Comparison between cold sintering and dry pressing of CaCO3 at room temperature by numerical simulations." AIP Advances 12, no. 4 (April 1, 2022): 045304. http://dx.doi.org/10.1063/5.0087226.

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Numerical models of solid-state and liquid-phase sintering of CaCO3 at room temperature are developed for applied static pressures as high as 280 MPa. Under the applied static pressure of 280 MPa, solid-state sintering (dry pressing) also works at room temperature due to the significant increase in the magnitude of the strain rate caused by dislocation processes occurring within the grains. Under the applied static pressure as low as 10 MPa, solid-state sintering no longer works due to the drop in the magnitude of the strain rate caused by dislocation processes occurring within the grains. On the other hand, liquid-phase sintering (cold sintering) still works under 10 MPa at room temperature due to the significant contribution of densification due to rearrangement in the presence of liquid as well as that due to contact flattening by dissolution and precipitation.
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Savitskii, A. P., and Y. S. Kwon. "Solid state sintering of interacting two-component mixtures." Metal Powder Report 57, no. 6 (June 2002): 62. http://dx.doi.org/10.1016/s0026-0657(02)80310-1.

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Dissertations / Theses on the topic "Solid-state sintering"

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Ch'ng, Heok Ngee. "A numerical study of microstructural evolution during solid-state sintering." Thesis, University of Surrey, 2003. http://epubs.surrey.ac.uk/842990/.

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In this thesis, a new set of finite element formulations are developed for computer simulation of microstructural evolution which is controlled by solid-state diffusion and grain-boundary migration. The finite element formulations are based on the classical cubic spline interpolation and form a natural extension of the linear finite element scheme which was first developed by Pan, Cocks and Kucherenko (1997). The cubic spline elements are however much more efficient numerically than the previous linear elements and make it possible to undertake large scale computer simulations of microstructural evolution using ordinary personal computers. The newly developed finite element scheme is then used to study the sintering process of powder compacts. Two important issues are addressed in this thesis. First, the sintering kinetics of large pores is investigated in details. An established theory due to Kingery (1967) predicts that a pore will shrink only if its coordination number (number of grains surrounding the pore) is less than a critical value which depends on the dihedral angle of the powder material. However, there are increasing experimental evidences contradicting this theory. Very large pores were observed to shrink continuously in the sintering process. The numerical study presented in this thesis demonstrated that the critical coordination number theory is in fact not a general rule. The computer simulations show that a very large pore does shrink unless it is surrounded by identical grains, which is obviously not true in any real powder compact. Secondly, the finite element scheme is used to study the anisotropic shrinkage during the sintering process. The numerical study reveals the key factors which control anisotropic shrinkage and shows that models based on continuum mechanics are unable to capture the critical influence of these key factors.
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Lee, Jong-Heon. "Synthesis of TiC by shock-assisted solid-state reaction sintering." Diss., Georgia Institute of Technology, 1997. http://hdl.handle.net/1853/32830.

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Luo, Jian 1971. "Origin of solid-state activated sintering in BiO₂₃-doped ZnO." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/85326.

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Pouryazdi, Mohammad Reza Nasseri. "The sintering, microstructure and properties of permanent magnet materials." Thesis, University of Leeds, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305744.

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Vargas-Gonzalez, Lionel Ruben. "Microstructural optimization of solid-state sintered silicon carbide." Diss., Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/34691.

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In this work, the development of theoretically-dense, clean grain boundary, high hardness solid-state sintered silicon carbide (SiC) armor was pursued. Boron carbide and graphite (added as phenolic resin to ensure the carbon is finely dispersed throughout the microstructure) were used as sintering aids. SiC batches between 0.25-4.00 wt.% carbon were mixed and spray dried. Cylindrical pellets were pressed at 13.7 MPa, cold-isostatically pressed (CIP) at 344 MPa, sintered under varying sintering soaking temperatures and heating rates, and varying post hot-isostatic pressing (HIP) parameters. Carbon additive amounts between 2.0-2.5 wt.% (based on the resin source), a 0.36 wt.% B4C addition, and a 2050°C sintering soak yielded parts with high sintering densities (~95.5-96.5%) and a fine, equiaxed microstructure (d50 = 2.525 µm). A slow ramp rate (10°C/min) prevented any occurrence of abnormal grain growth. Post-HIPing at 1900°C removed the remaining closed porosity to yield a theoretically-dense part (3.175 g/cm3, according to rule of mixtures). These parts exhibited higher density and finer microstructure than a commercially-available sintered SiC from Saint-Gobain (Hexoloy Enhanced, 3.153 g/cm3 and d50 = 4.837 µm). Due to the optimized microstructure, Verco SiC parts exhibited the highest Vickers (2628.30 ± 44.13 kg/mm2) and Knoop (2098.50 ± 24.8 kg/mm2) hardness values of any SiC ceramic, and values equal to those of the "gold standard" hot-pressed boron carbide (PAD-B4C). While the fracture toughness of hot-pressed SiC materials (~4.5 MPa m1/2) are almost double that of Verco SiC (2.4 MPa m1/2), Verco SiC is a better performing ballistic product, implying that the higher hardness of the theoretically-dense, clean-grain boundary, fine-grained SiC is the defining mechanical property for optimization of ballistic behavior.
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Hossbach, Karl. "Investigation of the microwave effect." Thesis, Loughborough University, 2014. https://dspace.lboro.ac.uk/2134/16285.

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Over the past decades, microwave sintering has been investigated, and the effects of microwave sintering have been demonstrated, however there is still uncertainty as to what is causing the enhancements known as the microwave effect . For a better understanding of the microwave effect , the effect of microwaves on the pore size distribution during densification has been investigated for submicron-sized zinc oxide (ZnO), which was sintered with conventional heating and varying amounts of microwave power but always maintaining exactly the same time-temperature profile. Initially, the density of the sintered samples was measured and compared; this proved that the densification of the hybrid sintered samples was increased and that the higher the level of microwaves used, the more it enhanced the densification. After this, the porosity was investigated through the use of nitrogen adsorption analysis, mercury porosimetry and Field Emission Gun Scanning Electron Microscopy (FEGSEM). Initially, it was found that sintering with microwaves reduces pores faster than for conventional sintering as expected. However, the experiments also revealed that the mechanisms of the reduction in the porosity were not different for microwave sintering compared to conventional sintering. When the porosity was compared at equivalent densities, it was observed that there was no significant difference, either in terms of the amount of porosity or the microstructure development. Since the structural development was the same for both conventional and hybrid sintering, it was concluded that the cause for the enhancement of the densification was enhanced diffusion caused by an additional driving force induced by the microwave field. The investigation of the solid-state reaction between zinc oxide and alumina was designed to investigate whether the diffusion associated with reactions was also enhanced by the use of microwaves. Therefore, zinc oxide and alumina samples were reacted as diffusion couples using conventional and hybrid heating, the latter with varying amounts of microwave power. The analyses of the reaction layer using FEGSEM showed an increase in the reaction product layer thickness when hybrid heating was used, with a higher level of microwaves yielding more growth. These results supported the view that the enhanced reaction rates were caused by enhanced diffusion, again caused by an additional driving force induced by the microwave field. For both the densification and reaction cases, the most likely additional driving force is considered to be the ponderomotive effect.
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Kubanska, Agnieszka. "Toward the development of high energy lithium-ion solid state batteries." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4775.

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Les batteries au lithium tout solide présentent un grand intérêt pour le développement de systèmes de stockage de grande densité (volumique) d'énergie et sûrs notamment en raison de leur excellente stabilité thermique par rapport aux technologies lithium-ions à électrolyte liquide. Cependant, avec l'épaisseur de la batterie, de fortes limitations cinétiques sont observées, en raison i/ de la relativement faible mobilité des ions dans les matériaux inorganiques et ii/ de la présence de joints de grains généralement bloquants aux interfaces solide/solide. De plus au cours de la charge/décharge de la batterie, les matériaux actifs (réservoir de l'énergie) changent de volume ce qui induit des contraintes mécaniques interfaciales qui provoquent la formation de micro-fractures très dommageables à la cyclabilité de ces systèmes. Cette thèse concerne la réalisation et la caractérisation de batteries inorganiques monolithiques (avec les électrodes composites) en utilisant une méthode de frittage: Spark Plasma Sintering (SPS). La formulation des électrodes composites est fondamentale car ce sont de multi-matériaux qui doivent présenter de nombreuses fonctionnalités: 1) une grande densité d'énergie 2) une bonne percolation électronique (resp. ionique) enfin 3) une bonne tenue mécanique avec des interfaces électrodes/electrolyte stables afin d'assurer la durée de vie des cellules.Le principal objectif est de trouver des relations, pour des matériaux donnés, entre la texture des poudres initiales, la microstructure des céramiques obtenues par frittage SPS et les propriétés électriques (électronique et ionique) ainsi que les performances électrochimiques
All-solid batteries with inorganic solid electrolytes are attractive candidates in electrochemical energy storage since they offer high safety, reliability and energy density. Aiming to increase the surface capacity strong efforts have been made to increase the thickness of the electrode. However, the thicker electrode, the more stress is generated at the solid/solid interfaces because of the volume change of the active material during lithium insertion/desinsertion upon cycling, which leads to formation of micro-cracks between the components and finally a bad cycling life. The possible answer to this issue is to build in place of a dense phase pure electrode, a composite electrode which is a multifunctional material. This composite electrode should contain a lot of electrochemically active material, the reservoir of energy; together with electronic and ionic conductor additives, to ensure efficient and homogeneous transfer of electrons and ions in the electrode volume.The main scope of this thesis was to develop all-solid-state batteries prepared by SPS method for applications at elevated temperatures. These batteries consist of a two composite electrodes separated by the NASICON-type solid electrolyte Li1.5Al0.5Ge1.5(PO4)3. The main objective was to find relationships, for given materials, between the initial powder granulometry (grain size, size distribution, agglomeration), the microstructure of ceramics obtained by SPS sintering, and the electrochemical performances of the final batteries. By creating electrodes with novel materials and better composition, the trade-off of power density and energy density can be minimized
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Bu, Junfu. "Advanced BaZrO3-BaCeO3 Based Proton Conductors Used for Intermediate Temperature Solid Oxide Fuel Cells (ITSOFCs)." Doctoral thesis, KTH, Tillämpad processmetallurgi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-165073.

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In this thesis, the focus is on studying BaZrO3-BaCeO3 based proton conductors due to that they represent very promising proton conductors to be used for Intermediate Temperature Solid Oxide Fuel Cells (ITSOFCs). Here, dense BaZr0.5Ce0.3Y0.2O3-δ (BZCY532) ceramics were selected as the major studied materials. These ceramics were prepared by different sintering methods and doping strategies. Based on achieved results, the thesis work can simply be divided into the following parts: 1) An improved synthesis method, which included a water-based milling procedure followed by a freeze-drying post-processing, was presented. A lowered calcination and sintering temperature for a Hf0.7Y0.3O2-δ (YSH) compound was achieved. The value of the relative density in this work was higher than previously reported data. It is also concluded that this improved method can be used for mass-production of ceramics. 2) As the solid-state reactive sintering (SSRS) represent a cost-effective sintering method, the sintering behaviors of proton conductors BaZrxCe0.8-xLn0.2O3-δ (x = 0.8, 0.5, 0.1; Ln = Y, Sm, Gd, Dy) during the SSRS process were investigated. According to the obtained results, it was found that the sintering temperature will decrease, when the Ce content increases from 0 (BZCLn802) to 0.3 (BZCLn532) and 0.7 (BZCLn172). Moreover, the radii of the dopant ions similar to the radii of Zr4+ or Ce4+ ions show a better sinterability. This means that it is possible to obtain dense ceramics at a lower temperature. Moreover, the conductivities of dense BZCLn532 ceramics were determined. The conductivity data indicate that dense BZCY532 ceramics are good candidates as either oxygen ion conductors or proton conductors used for ITSOFCs. 3) The effect of NiO on the sintering behaviors, morphologies and conductivities of BZCY532 based electrolytes were systematically investigated. According to the achieved results, it can be concluded that the dense BZCY532B ceramics (NiO was added during ball-milling before a powder mixture calcination) show an enhanced oxygen and proton conductivity. Also, that BZCY532A (NiO was added after a powder mixture calcination) and BZCY532N (No NiO was added in the whole preparation procedures) showed lower values. In addition, dense BZCY532B and BZCY532N ceramics showed only small electronic conductivities, when the testing temperature was lower than 800 ℃. However, the BZCY532A ceramics revealed an obvious electronic conduction, when they were tested in the range of 600 ℃ to 800 ℃. Therefore, it is preferable to add the NiO powder during the BZCY532 powder preparation, which can lower the sintering temperature and also increase the conductivity. 4) Dense BZCY532 ceramics were successfully prepared by using the Spark Plasma Sintering (SPS) method at a temperature of 1350 ℃ with a holding time of 5 min. It was found that a lower sintering temperature (< 1400 ℃) and a very fast cooling rate (> 200 ℃/min) are two key parameters to prepare dense BZCY532 ceramics. These results confirm that the SPS technique represents a feasible and cost-effective sintering method to prepare dense Ce-containing BaZrO3-BaCeO3 based proton conductors. 5) Finally, a preliminary study for preparation of Ce0.8Sm0.2O2-δ (SDC) and BZCY532 basedcomposite electrolytes was carried out. The novel SDC-BZCY532 based composite electrolytes were prepared by using the powder mixing and co-sintering method. The sintering behaviors, morphologies and ionic conductivities of the composite electrolytes were investigated. The obtained results show that the composite electrolyte with a composition of 60SDC-40BZCY532 has the highest conductivity. In contrast, the composite electrolyte with a composition of 40SDC-60BZCY532 shows the lowest conductivity. In summary, the results show that BaZrO3-BaCeO3 based proton-conducting ceramic materials represent very promising materials for future ITSOFCs electrolyte applications.

QC 20150423

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Srivastava, Deepanshu. "Effect of processing conditions and second-phase additives on thermoelectric properties of SrTiO3 based ceramics." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/effect-of-processing-conditions-and-secondphase-additives-on-thermoelectric-properties-of-srtio3-based-ceramics(ff3c590e-4fc5-4c5d-b47b-823369ae369d).html.

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Oxide ceramics have been increasingly researched for high temperature thermoelectric (TE) applications. SrTiO3 based materials are promising candidates due to its chemical and thermal stability. In this study, oxide ceramics of composition (1-x)SrTiO3-(x)La1/3NbO3 (0 smaller or equal to x smaller or equal to 0.3) were prepared by single-step solid state sintering in Ar/5%H2 at 1700 K. The density of all the samples prepared was above 90%. All the samples were predominantly single-phase compositions crystallised with a cubic structure in Pm ̅3m space group. The impact of oxygen deficiency, A-site vacancies and mixed oxidation states of Ti3+/Nb4+ on electrical and thermal transport properties was assessed. Optimum TE properties were obtained for x=0.2 (Sr0.8La0.067Ti0.8Nb0.2O(3-delta) = L2), which has 13.4% A-site vacancies. The ZT values improved from 0.2 to 0.27 at 1000 K, with an increase in sintering time from 8 hours to 48 hours, due to increased carrier concentration. Complex interplay of oxygen vacancies and excess donor substitution on A/B-sites of L2 (substituting 5-10% Sr/Ti with La/Nb) exhibited 35% improvement in ZT values, whilst maintaining the A-site vacancies and core-shell structures within grains, which reduced the thermal conductivity by ~50% compared to undoped SrTiO3 samples, due to strong phonon scattering. A facile method to incorporate metallic inclusions (2.5 wt% Fe/Cu) at grain boundaries in L2 ceramics is demonstrated. The modified compositions displayed a maximum ZT of ~0.37 at 1000 K for L2 samples containing metallic inclusions due to increased carrier concentration (5.5 x 10^21 carriers/cm^3) and carrier mobility (2.4 cm^2/(V.s).The addition of graphene/Graphene Oxide (GO) flakes in L2 ceramics has been investigated to improve the electrical conductivity of L2 composites without significantly increasing the thermal conductivity. Spark plasma sintering (SPS) of the composite powders at 1473 K and 50 MPa produced dense samples (>95% relative density) with a homogeneous dispersion of graphene/GO flakes, for loadings smaller or equal to 1.0 wt%. The effect of interaction and distribution of graphene/GO flakes within the ceramics on TE properties is investigated. The composite samples demonstrate anisotropic ZT values, with 20% improvement in the direction normal to the orientation of graphene flakes. A novel sintering method has been proposed which has strong industrial potential. The L2 based composites were sintered in Air at 1700 K (ramp rate: ±300 K/min), whilst samples were covered uniformly. Strong reducing conditions and evolution of secondary phases in the microstructure helped achieve, the very low electrical resistivity of ~3.0 x 10^(-6) ohm.m at room temperature. Secondary phases, sub-micron voids in the grains and A-site vacancies reduced the lattice thermal conductivity (~2.0 W/m.K), comparable to the lowest lattice thermal conductivity achievable (~1.5 W/m.K) at 1000 K and obtain a maximum ZT of 0.4 at 1000 K for L210G-Air/C composites.
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Porfirio, Tatiane Cristina. "Influência do cálcio e do lítio na sinterização e na condutividade elétrica do óxido de cério contendo gadolínio." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/85/85134/tde-17062011-153902/.

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A introdução de cálcio e lítio como aditivos de sinterização na céria: 10% mol gadolínia foi investigada com o intuito de verificar sua influência na densificação e condutividade elétrica das cerâmicas sinterizadas. Pós contendo de 0 a 1,5% mol do metal foram preparados tanto por reação em estado sólido quanto pela co-precipitação dos oxalatos. As principais técnicas de caracterização utilizadas foram análise térmica, difração de raios X, microscopia eletrônica de varredura e medida da condutividade elétrica por espectroscopia de impedância. Os resultados obtidos mostraram que cerâmicas densas podem ser obtidas utilizando ambos os aditivos. O aumento no teor do aditivo resulta em aumento na densificação. A forma de adição, por reação em estado sólido ou por coprecipitação exerce influência na condutividade elétrica. A adição de cálcio promove maior crescimento dos grãos que o lítio. A condutividade elétrica das amostras contendo o segundo aditivo é inferior à da céria-gadolínia pura. Ambos os aditivos exercem influência na condutividade intergranular. Adição de cálcio resulta também em diminuição da condutividade intragranular. Os aditivos favorecem a exudação do gadolínio.
In this work, the use of calcium and lithium as sintering aid to gadolinia-doped ceria was systematically investigated. The main purpose was to verify the influence of these additives on the densification and electrical conductivity of sintered ceramics. Powder compositions containing up to 1.5 mol% (metal basis) of calcium or lithium were prepared by both solid state reaction and oxalate coprecipitation methods. The main characterization techniques were thermal analyses, X-ray diffraction, scanning electron microscopy and electrical conductivity by impedance spectroscopy. Both additives promoted densification of gadolinia-doped ceria. The densification increases with increasing the additive content. Different effects on microstructure and electrical conductivity result from the method of preparation, e.g., solid state reaction or coprecipitation. Calcium addition greatly enhances the grain growth compared to lithium addition. The electrical conductivity of specimens containing a second additive is lower than that of pure gadolinia-doped ceria. Both additives influence the intergranular conductivity and favor the exudation of gadolinium out of the solid solution.
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Books on the topic "Solid-state sintering"

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Dudina, Dina V. Sintering of powder materials. NSTU Publisher, 2022. http://dx.doi.org/10.17212/978-5-7782-4515-0.

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This study guide corresponds to “Sintering of powder materials” course of the Master degree program at Novosibirsk State Technical University 22.04.01 – Materials Science and Technology. The guide consists of six parts and contains a brief overview of historical aspects of sintering, powder fabrication and characterization methods, powder shaping and compaction processes, and the basics of solid state and liquid phase sintering. The guide also contains a description of advanced sintering methods and sintering processes found in additive manufacturing. Classical and novel materials obtainable by sintering are described. Current trends in the development of sintering science are discussed. Each part of the guide is followed by control questions. Problems with solutions are offered to help the student solve problems encountered in real research and industrial sintering practice. Problems for self-study are also provided, many of which were designed by the author based on her own research experience. Topics for self-study are provided and can be used for students’ presentations at seminars.
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Chaklader, A. C. D. Sintering 91: Proceedings of the 5th International Symposium on the Science and Technology of Sintering, Vancouver, Canada 1991 (Solid State Phenomena). Trans Tech Publications, 1992.

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Book chapters on the topic "Solid-state sintering"

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Naka, M., T. Saito, and I. Okamoto. "Solid State Bonding of SiC to Nb." In Sintering ’87, 1373–78. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1373-8_231.

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Kawai, S., M. Motoyama, and T. Ooi. "Solid State Reaction between Alumina and Iron." In Sintering ’87, 1379–84. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1373-8_232.

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Petzow, Gunter, and Hans Eckart Exner. "Particle Rearrangement in Solid State Sintering." In Sintering Key Papers, 639–55. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0741-6_40.

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Ruan, C. X., Wei Min Gao, R. F. Zhao, Yun Fa Chen, and Y. S. Xie. "Aided Sintering Behaviour of Nano Hydroxyapatite Particles." In Solid State Phenomena, 89–92. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-30-2.89.

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Tanaka, Satoshi. "Solid State Reactions and Sintering." In Materials Chemistry of Ceramics, 45–74. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9935-0_3.

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Boyun, Huang, and Xu Kuangdi. "Solid-State Sintering of Powder." In The ECPH Encyclopedia of Mining and Metallurgy, 1–2. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-19-0740-1_1480-1.

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Fukuzawa, Y., G. Elssner, and G. Petzow. "Characteristics of the Alumina-Niobium Solid State Bonding Interface." In Sintering ’87, 1391–96. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1373-8_234.

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Schatt, W., and E. Friedrich. "Solid-State Sintering as a High Temperature Deformation Process." In Sintering ’87, 267–72. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1373-8_45.

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Michalski, A., M. Rosiński, D. Siemiaszko, Jakub Jaroszewicz, and Krzysztof J. Kurzydłowski. "Pulse Plasma Sintering of Nano-Crystalline Cu Powder." In Solid State Phenomena, 239–44. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908451-22-1.239.

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Kiraura, Hiroshi. "Fabrication of Solid State Amorphized Metallic Powders by Mechanical Alloying." In Sintering ’87, 635–40. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1373-8_107.

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Conference papers on the topic "Solid-state sintering"

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Singh, Rajan, P. K. Patro, Ajit R. Kulkarni, and C. S. Harendranath. "Estimation of the activation energy of sintering in KNN ceramics using master sintering theory." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872708.

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Yin, Danlei, Jun Wang, Zhili Dong, and Dingyuan Tang. "Powder Synthesis and Sintering of Lasing Grade Yb:Lu2O3 Ceramics." In Advanced Solid State Lasers. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/assl.2019.jm5a.13.

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Joshi, Zalak, Davit Dhruv, Sanjay Kansara, Megha Vagadia, Nishant Barot, P. K. Mehta, P. S. Solanki, D. G. Kuberkar, and N. A. Shah. "Dielectric behavior of nanostructured Y0.95Ca0.05MnO3: Role of sintering temperature." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872939.

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M., Nirmal Prashanth, Rajesh Paulraj, and Ramasamy Perumalsamy. "Sintering effect on tin oxide electrode for supercapacitor applications." In DAE SOLID STATE PHYSICS SYMPOSIUM 2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4980296.

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Patil, B. B., A. D. Pawar, P. S. Patil, S. V. Godase, J. S. Ghodake, and T. J. Shinde. "Ni-Cu-Zn nanoferrite prepared at lower sintering temperature." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0017414.

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Jha, Vikash Kumar, H. S. Mund, Saroj Dhaka, Jaya Verma, M. Roy, and V. Singh. "Effect of sintering temperature on dielectric properties of MgFe2O4." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0024716.

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Hoff, Linda, Walter S. Scheld, Christian Vedder, and Jochen Stollenwerk. "Laser sintering of ceramic-based solid-state battery materials." In Laser-based Micro- and Nanoprocessing XVI, edited by Rainer Kling and Akira Watanabe. SPIE, 2022. http://dx.doi.org/10.1117/12.2607752.

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Janrao, Prashant, and V. L. Mathe. "Effect of sintering on structural and dielectric properties of PLZT ferroelectrics." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4873111.

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Obulesu, K. Rama, and K. C. James Raju. "Effect of conventional and microwave sintering on ceramic BiFeO[sub 3]." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4791494.

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Hostaša, Jan, Mariastefania De Vido, Andreana Piancastelli, Danielle Clarke, Gary Quinn, Valentina Biasini, Laura Esposito, and Paul D. Mason. "Transparent Ceramic Yb:YAG Gain Medium for High-Energy Lasers: Process Optimisation Through the Use of Sintering Aids." In Advanced Solid State Lasers. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/assl.2022.jm4a.15.

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Abstract:
Ceramic Yb:YAG is a suitable gain medium candidate for high-energy lasers. The use of a combination of TEOS and MgO sintering aids led to uniform microstructure independently on the increase of thickness. Samples were thoroughly characterised.
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Reports on the topic "Solid-state sintering"

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Gurwell, W. E. Solid-state sintering of tungsten heavy alloys. Office of Scientific and Technical Information (OSTI), October 1994. http://dx.doi.org/10.2172/28381.

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Ramos, E., J. Ye, and A. Browar. Reactive laser sintering for solid state electrolytes. Office of Scientific and Technical Information (OSTI), September 2022. http://dx.doi.org/10.2172/1885658.

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Mangels, J., and B. Mikijelj. Solid state sintering of silicon nitride ARL-CR-114. Final report. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/28361.

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Santomauro, A., E. Ramos, and J. Ye. Rapid Laser Reactive Sintering of Garnet Li6.4La3Zr1.4Ta0.6O12 and Li6.1La3Zr2Al0.3O12 and Solid-State Electrolytes. Office of Scientific and Technical Information (OSTI), September 2023. http://dx.doi.org/10.2172/2205719.

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Munir, Z. A. An investigation of the mechanisms of solid state powder reaction in the combustion synthesis and sintering of high temperature materials. Office of Scientific and Technical Information (OSTI), August 1989. http://dx.doi.org/10.2172/7258522.

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