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In this thesis, a synthesis concept has been developed, which uses nitrogen-rich liquid phases for sintering of Ca-α-sialon ceramics. First, keeping the Si/Al ratios constant, the effects of N/O ratio on the properties and microstructure were investigated through a liquid phase sintering process. Second, nitrogen-rich Ca-α-sialon ceramics, with nominal compositions: CaxSi12-2xAl2xN16, x < 2.0, was synthesized and characterized. Third, mechanical and thermal properties of nitrogen-rich Ca-α-sialons were investigated in terms of high temperature deformation resistance,reaction mechanism, phase stability and oxidation resistance, and further correlated to their phase assemblage and microstructure observation. It has been found that increasing the N/O and Ca/Al ratio simultaneously in the materials could result in development of a microstructure with well shaped, high-aspect-ratio Ca-α-sialon grains, and an improvement in both toughness and hardness. For the nitrogen-rich Ca-α-sialon, mono-phasic α-sialon ceramics were obtained for 0.51 ≤ x ≤ 1.32. The obtained Ca-α-sialon ceramics with elongated-grain microstructures show a combination of high hardness and high fracture toughness. Compared with the oxygen-rich Ca-α-sialons, the nitrogen-rich Ca-α-sialons exhibited approximately 150 oC higher deformation onset temperatures and decent properties even after the deformation. The α-sialon phase was first observed at 1400 oC, however the phase pure Ca-α-sialon ceramics couldn’t be obtained until 1800 oC. The nitrogen-rich Ca-α-sialons were thermal stable, no phase transformation observed in the temperatures range1400-1600 oC. In general, mixed α/β-sialon showed better oxidation resistance than pure α-sialon in the low temperature range (1250-1325 oC), while α-sialons with compositions located at α/β-sialon border-line showed significant weight gains over the entire temperature range (1250-1400 oC).

The aim with this study was to investigate the effects a change of manufacturing process would have on the mechanical properties of drill bits made of a WC/Co composite used for stone cutting. The method used today is sintering, where the material is heated in a conventional sintering oven. The other method was microwave sintering, where the material is heated by radiation in the microwave region. Also an investigation of the manufacturing cost were made. The main difference between the two heating methods is that the conventional way is a rather slow process and the microwave method is very fast. The material is also heated homogeniously in the method with mirowaves, aposed to the case with the conventional sintering where the material is heated from the outside in. This makes the material harder and more wear resistent. Another positive effect is that the pysical properties of the drill bits is easier to controll, because of the very small grain growth due to the short process time.The cost of manufacturing these drill bits by microwave sintering does not exceed the cost of the conventionall sintering.

The research in this thesis covers the design and implementation of a depleted uranium (DU) powder production system and the initial results of a DU-Zr-Mg alloy alpha phase sintering experiment where the Mg is a surrogate for Pu and Am. The powder production system utilized the uranium hydrogen interaction in order to break down larger pieces of uranium into fine powder. After several iterations, a successful reusable system was built. The nominal size of the powder product was on the order of 1 to 3 mm. The resulting uranium powder was pressed into pellets of various compositions (DU, DU-10Zr, DU-Mg, DU-10Zr-Mg) and heated to approximately 650?C, just below the alphabeta phase transition of uranium. The dimensions of the pellets were measured before and after heating and in situ dimension changes were measured using a linear variable differential transducer (LVDT). Post experiment measurement of the pellets proved to be an unreliable indicator of sintering do the cracking of the pellets during cool down. The cracking caused increases in the diameter and height of the samples. The cracks occurred in greater frequency along the edges of the pellets. All of the pellets, except the DU-10Zr-Mg pellet, were slightly conical in shape. This is believed to be an artifact of the powder pressing procedure. A greater density occurs on one end of the pellet during pressing and thus leads to gradient in the sinter rate of the pellet. The LVDT measurements proved to be extremely sensitive to outside vibration, making a subset of the data inappropriate for analysis. The pellets were also analyzed using electron microscopy. All pellets showed signs of sintering and an increase in density. The pellets will the greatest densification and lowest porosity were the DU-Mg and DU-10Zr-Mg. The DU-Mg pellet had a porosity of 14 +or- 2.%. The DU-10Zr-Mg porosity could not be conclusively determined due to lack of clearly visible pores in the image, however there were very few pores indicating a high degree of sintering. In the DU-10Zr-Mg alloy, large grains of DU were surrounded by Zr. This phenomena was not present in the DU-10Zr pellet where the Zr and DU stayed segregated. There was no indication of alloying between the Zr and DU in pellets.

The sintering behavior of uranium and uranium-zirconium alloys in the alpha phase were characterized in this research. Metal uranium powder was produced from pieces of depleted uranium metal acquired from the Y-12 plant via hydriding/dehydriding process. The size distribution and morphology of the uranium powder produced by this method were determined by digital optical microscopy. Once the characteristics of the source uranium powder were known, uranium and uranium-zirconium pellets were pressed using a dual-action punch and die. The majority of these pellets were sintered isothermally, first in the alpha phase near 650°C, then in the gamma phase near 800°C. In addition, a few pellets were sintered using more exotic temperature profiles. Pellet shrinkage was continuously measured in situ during sintering. The isothermal shrinkage rates and sintering temperatures for each pellet were fit to a simple model for the initial phase of sintering of spherical powders. The material specific constants required by this model, including the activation energy of the process, were determined for both uranium and uranium-zirconium. Following sintering, pellets were sectioned, mounted, and polished for imaging by electron microscopy. Based on these results, the porosity and microstructure of the sintered pellets were analyzed. The porosity of the uranium-zirconium pellets was consistently lower than that of the pure uranium pellets. In addition, some formation of an alloyed phase of uranium and zirconium was observed. The research presented within this thesis is a continuation of a previous project; however, this research has produced many new results not previously seen. In addition, a number of issues left unresolved by the previous project have been addressed and solved. Most notably, the low original output of the hydride/dehydride powder production system has been increased by an order of magnitude, the actual characteristics of the powder have been measured and determined, shrinkage data was successfully converted into a sintering model, an alloyed phase of uranium and zirconium was produced, and pellet cracking due to delamination has been eliminated.

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<p>Cemented carbides based on tungsten carbide and cobalt arecommonly produced by a powder metallurgy route including liquidphase sintering. The pressed compact densifies to almost halfits volume during sintering due to pore elimination. Thesintering behaviour changes with material composition, such ascarbide grain size, binder fraction, carbon content andaddition of cubic carbides.</p><p>This thesis is devoted to the study of constitutivebehaviour, in particular densification, and the microstructuralevolution during cemented carbide sintering. Dimensionalchanges are monitored using dilatometry with and withoutapplied external load. The microstructural evolution isinvestigated with light optical microscopy and scanningelectron microscopy. Thermodynamic calculations are used asreference.</p><p>Constitutive relations are derived for uniaxial viscosity,viscous equivalent of Poisson’s ratio and sintering stressbased on relative density and temperature. The relations areextended to a model describing sintering shrinkage withexplicit dependencies on carbide grain size and binder content.The model is divided in three stages of which two pertain tothe solid state and the third to liquid phase sintering. Solidstate shrinkage is suppressed in a material with coarsecarbides and in the stage of liquid phase sintering grain sizestrongly influences the uniaxial viscosity. The binder contentaffects primarily the later densification.</p><p>The effects of carbon content and grain size distribution onshrinkage have been studied. High carbon content enhancesshrinkage rate, but the effect of grain size distribution israther small. The mean carbide grain size is insufficient todescribe densification for very broad distributions only.</p><p>Shrinkage occurs through rearrangement andsolution-reprecipitation. Rearrangement is studied through theevolution of the pore size distribution and simulatedgenerically using a discrete element method.</p><p><b>Keywords:</b>Cemented carbides, Sintering, Constitutiverelations, Microstructure, Densification, Modelling</p>

Thesis (M.S.)--Engineering, Georgia Institute of Technology, 2004. / McDowell, David, Committee Chair; Neu, Richard, Committee Member; Lee, Jim, Committee Member; Cochran, Joe, Committee Member. Includes bibliographical references (leaves 159-162).

Thesis (Ph. D.)--University of Missouri-Columbia, 2002. / Typescript. Vita. Includes bibliographical references. Also available on the Internet.