Yes / The effects of 0·5 wt-%Mo addition on the processing, microstructure, and strength of PM Fe–3·5Mn–0·7C steel are described. Water atomised and sponge irons, Astaloy 1·5Mo, milled ferromanganese, and graphite were the starting powders. During sintering in 75H2 /25N2 or pure hydrogen the dewpoint was controlled and monitored; in particular the effects of improving it from -35 to -60°C were investigated. Faster heating rates (20 K min-1), sufficient gas flowrates, milling the ferro alloy under nitrogen, a low dewpoint (<-60°C), and a getter powder can all contribute to the reduction or prevention of oxidation of the manganese, in particular formation of oxide networks in the sintered steels. For 600 MPa compaction pressure densities up to 7·1 g cm-3 were obtained; these were not significantly affected by sintering at temperatures up to 1180°C. The sintered microstructures were sensitively dependent on the cooling rate. Irrespective of the presence of Mo, slow furnace cooling at 4 K min-1 resulted in mainly pearlitic structures with some ferrite and coarse bainite, whereas fast cooling at 40 K min-1 produced martensite and some retained austenite, very fine pearlite, bainite, and some ferrite. Young's modulus, determined by tensile and ultrasonic tests, was in the range 110–155 GPa. Sintering with -60°C dewpoint resulted in tensile and transverse rupture strengths of 420 and 860 MPa for the Mn steel, rising to 530 and1130 MPa as a result of the Mo addition. This contrasts with strength decreases observed when processing included use of high oxygen containing ferromanganese and sintering with -35°C dewpoint.

Published Article / Until recently solid freeform fabrication (SFF) technology has been used mostly for production of prototype parts. However, as this technology matures, the initiative of utilising it for the manufacture of end-use products is establishing itself. As this tendency to use SFF for actual production runs increases, a demand is developing for sets of process-specific design for manufacture (DFM) guidelines that will assist designers who are designing parts for manufacture by a specific rapid manufacturing (RM) process. The purpose of this paper is to provideRMdesigners with such a series of processspecific design for manufacture guidelines.

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.

<p>Spark Plasma Sintering (SPS) is a promising rapid consolidation technique that allows a better understanding and manipulating of sintering kinetics and therefore makes it possible to obtain Si₃N₄-based ceramics with tailored microstructures, consisting of grains with either equiaxed or elongated morphology.</p><p> The presence of an extra liquid phase is necessary for forming tough interlocking microstructures in Yb/Y-stabilised α-sialon by HP. The liquid is introduced by a new method, namely by increasing the O/N ratio in the general formula RE_xSi_12-(3x+n)Al_3x+nO_nN_16-n while keeping the cation ratios of RE, Si and Al constant. </p><p>Monophasic α-sialon ceramics with tailored microstructures, consisting of either fine equiaxed or elongated grains, have been obtained by using SPS, whether or not such an extra liquid phase is involved. The three processes, namely densification, phase transformation and grain growth, which usually occur simultaneously during conventional HP consolidation of Si₃N₄-based ceramics, have been precisely followed and separately investigated in the SPS process.</p><p>The enhanced densification is attributed to the non-equilibrium nature of the liquid phase formed during heating. The dominating mechanism during densification is the enhanced grain boundary sliding accompanied by diffusion- and/or reaction-controlled processes. The rapid grain growth is ascribed to a <i>dynamic ripening</i> mechanism based on the formation of a liquid phase that is grossly out of equilibrium, which in turn generates an extra chemical driving force for mass transfer. Monophasic α-sialon ceramics with interlocking microstructures exhibit improved damage tolerance. Y/Yb- stabilised monophasic α-sialon ceramics containing approximately 3 vol% liquid with refined interlocking microstructures have excellent thermal-shock resistance, comparable to the best β-sialon ceramics with 20 vol% additional liquid phase prepared by HP. </p><p>The obtained sialon ceramics with fine-grained microstructure show formidably improved <i>superplasticity</i> in the presence of an electric field. The compressive strain rate reaches the order of 10^-2 s^-1 at temperatures above 1500oC, that is, two orders of magnitude higher than that has been realised so far by any other conventional approaches. The high deformation rate recorded in this work opens up possibilities for making ceramic components with complex shapes through super-plastic forming. </p>

La mise en œuvre des réacteurs nucléaires du futur nécessite des températures de fonctionnement élevées sous flux de neutrons. Parmi les candidats envisagés pour les matériaux de structure et de gainage du combustible, les composites à matrice céramique de type SiCf/SiCm présentent un potentiel élevé. Dans ce cadre, les travaux de thèse ont consisté à étudier un procédé alternatif et innovant pour la réalisation de fibres de carbure de silicium, mettant en jeu le frittage de poudres de taille nanométrique.Une étude sur le frittage sans contrainte du SiC a été réalisée. Celle-ci a permis de définir des systèmes d’ajouts appropriés pour la densification et de maîtriser la microstructure du matériau final à partir (i) de l’analyse de l’influence des paramètres opératoires et (ii) du contrôle de la transition de phase SiC β  SiC α grâce à l’introduction d’éléments extérieurs.Des fibres « crues » SiC/polymère ont ensuite été élaborées par deux procédés de mise en forme : par extrusion d’une solution concentrée en polymère et chargée en nanopoudres et par filage et coagulation d’une suspension aqueuse de poudres nanométriques contenant un polymère hydrosoluble. Le frittage de ces dernières conduit à des fibres céramiques présentant un diamètre de l’ordre de cinquante micromètres. / Silicon carbide ceramic matrix composites (SiCf/SiCm) are of interest for high temperature applications in aerospace or nuclear components for their relatively high thermal conductivity and low activation under neutron irradiation. While most of silicon carbide fibers are obtained through the pyrolysis of a polycarbosilane precursor, sintering of silicon carbide nanopowders seems to be a promising route to explore.For this reason, pressureless sintering of SiC has been studied. Following the identification of appropriate sintering aids for the densification, optimization of the microstructure has been achieved through (i) the analysis of the influence of operating parameters and (ii) the control of the SiC β  SiC α phase transition. Green fibers have been obtained by two different processes involving the extrusion of SiC powder dispersion in polymer solution or the coagulation of a water-soluble polymer containing ceramic particles. Sintering of these green fibers led to fibers of around fifty microns in diameter.

Os efeitos da atmosfera de sinterização e do tamanho inicial das partículas na sinterização da céria contendo 10% em mol de gadolínia (GdO1,5) foram sistematicamente estudados neste trabalho. Materiais de partida com três valores para a área de superfície específica foram utilizados, 210 m2/g, 36,2 m2/g e 7,4 m2/g. Diferentes cinéticas de sinterização foram verificadas. Quanto menor o tamanho inicial das partículas, menor é a temperatura para o início da sinterização e mais acelerada a densificação do material. Curvas mestres de sinterização foram construídas para cada um dos materiais analisados. Um programa computacional foi especialmente desenvolvido para este propósito. Diferenças significativas entre as energias de ativação para densificação foram verificadas. Para este trabalho foi determinado que, quanto menor o tamanho inicial de partícula, menores as energias de ativação. A evolução das distribuições de tamanhos de cristalitos foi investigada para os materiais de maior área superficial específica. Foi determinado que a eliminação e migração de poros (pore drag) é o mecanismo predominante para o crescimento de grãos durante o início da sinterização da céria gadolínia. Os efeitos da atmosfera de sinterização no desvio de estequiometria, na densificação, na evolução microestrutural e na condutividade elétrica da céria-gadolínia foram analisados. Atmosferas redutoras, oxidantes e inertes foram usadas para este propósito. Desvios na estequiometria da céria foram verificados no volume do material, sendo este dependente da área de superfície específica e da atmosfera utilizada. Quanto maior o potencial de redução da atmosfera utilizada, maior a concentração de Ce3+ no material. Com o aumento da concentração de Ce3+ um aumento no tamanho médio de grãos foi verificado. Uma diminuição na condutividade elétrica total, intra e intergranular foram determinadas para as amostras sinterizadas em atmosferas redutoras. / The effects of the sintering atmosphere and initial particle size on the sintering of ceria containing 10 mol% gadolinia (GdO1.5) were systematically investigated. The main physical parameter was the specific surface area of the initial powders. Nanometric powders with three different specific surface areas were utilized, 210 m2/g, 36,2 m2/g e 7,4 m2/g. The influence on the densification, and micro structural evolution were evaluated. The starting sintering temperature was verified to decrease with increasing on the specific surface area of raw powders. The densification was accelerated for the materials with smaller particle size. Sintering paths for crystallite growth were obtained. Master sintering curves for gadolinium-doped ceria were constructed for all initial powders. A computational program was developed for this purpose. The results for apparent activation energy showed noticeable dependence with specific surface area. In this work, the apparent activation energy for densification increased with the initial particle size of powders. The evolution of the particle size distributions on non isothermal sintering was investigated by WPPM method. It was verified that the grain growth controlling mechanism on gadoliniadoped ceria is the pore drag for initial stage and beginning of intermediate stage. The effects of the sintering atmosphere on the stoichiometry deviation of ceria, densification, microstructure evolution, and electrical conductivity were analyzed. Inert, oxidizing, and reducing atmospheres were utilized on this work. Deviations on ceria stoichiometry were verified on the bulk materials. The deviation verified was dependent of the specific surface area and sintering atmosphere. Higher reduction potential atmospheres increase Ce3+ bulk concentration after sintering. Accelerated grain growth and lower electrical conductivities were verified when reduction reactions are significantly present on sintering.

"De-lubrication is the first stage in a sintering operation, where the lubricants (higher weight hydrocarbons) are removed from the parts by controlled heating. Improper de-lubrication leads to defects such as blistering, sooting, micro-porosity etc in a sintered part. Most of these problems arise, as there exists a gap in the present understanding of de-lubrication. The primary motive of this work is to direct research towards the development of sensors and controls and thus, mitigate the various problems due to improper de-lubrication. Currently, there exists a myriad of lubricants being used during the process of compaction. They include metallic based lubricants, polymers and non-metallic lubricants. In this work, research was limited in understanding the de-lubrication of EBS (Ethylene Bisstearimide), as, it the most commonly used lubricant in the industry. It has replaced commonly used lubricant due to cleaner burnouts, absence of metallic residue and, cost effectiveness. The entire work is divided into three phases: • Phase 1: Ascertained the most important parameters that affect the kinetics of de-lubrication. • Phase 2: Investigated the type of gases released during the decomposition of EBS. • Phase 3: Recommended a control strategy. TGA (Thermo-gravimetric analysis) was used in the phase I, the results clearly show that the rate of heating is the most important parameter during de-lubrication. Identification of gases was performed using the FTIR (Fourier transform infrared spectroscopy) and DUV (Deep ultraviolet spectroscopy). This constituted the second phase of our experiments. The primary gases identified in Phase II were carbon dioxide and a hydrocarbon (hepta-decane). Finally, an empirical model for de-lubrication has been proposed in Phase III. The model was verified in an industrial furnace. It has been observed that there exists a very good correlation between the proposed empirical model and the experiments performed in Phase II of this study. This study lays down the following guidelines for the development of future sensors and controls: • The development of future sensors should focus in the detection of CO2 and hepta-decane. • Rate of heating determines how fast or slow the lubricant decomposes and finally escapes form the compacted part. • The empirical model may be used, as a means to determine the time a part should reside in a furnace for complete lubricant burnout at a given heating rate."

Laser Sintering (LS) is a powder based Additive Manufacturing (AM) technology capable of producing near-net shape objects from 3D data. The benefits of LS include almost unlimited design freedom and reduced material waste, however the number of commercially available materials are limited, with materials traditionally being optimised for the process using a trial and error method and material development being led by previous research into polyamide (PA). There is a desire for greater material choice in LS, particularly high performance polymers. The EOSINT P800 by AM systems manufacturer EOS GmbH is the first commercially available high temperature laser sintering (HT-LS) system capable of working high performance polymers; a PolyEtherKetone (PEK) known by the trade name HP3 PEK is the first material offered by EOS for use with the system. This research project undertakes to characterise the EOSINT P800 and HP3 PEK material with different thermal histories. Experimental work focusses on establishing material properties such as size and shape, crystallinity and decomposition. Characterisation of coalescence behaviour and comparison with theoretical models for viscous sintering is presented as a less experimentally intensive method of understanding how a material will behave during the LS process. A map of temperatures inside the powder bed in the EOSINT P800 is created for the first time and compared with output from on-board temperature sensors in the system, demonstrating the thermal distribution within the bed during building, and explaining differences between as-received and used powder. The results demonstrate that material and process characterisation methods are useful for understanding how and why a high temperature laser sintering material behaves the way it does. The behaviour of HP3 PEK observed during experimental work indicates that guidelines based on LS of PA are too restrictive as indicators of suitability for LS and newer systematic approaches are potentially better suited for qualification of HT-LS polymers. The novel method for mapping thermal distribution inside the LS system documented here shows the limitations of current hardware to effectively process high performance polymers. Overall, the finding of this research project is that understanding of material and process cannot be considered in isolation but combined have the potential to reduce the amount of trial and error required during qualification of new materials and increase the range and variety of polymers available for LS and HT-LS.

Os efeitos da atmosfera de sinterização e do tamanho inicial das partículas na sinterização da céria contendo 10% em mol de gadolínia (GdO1,5) foram sistematicamente estudados neste trabalho. Materiais de partida com três valores para a área de superfície específica foram utilizados, 210 m2/g, 36,2 m2/g e 7,4 m2/g. Diferentes cinéticas de sinterização foram verificadas. Quanto menor o tamanho inicial das partículas, menor é a temperatura para o início da sinterização e mais acelerada a densificação do material. Curvas mestres de sinterização foram construídas para cada um dos materiais analisados. Um programa computacional foi especialmente desenvolvido para este propósito. Diferenças significativas entre as energias de ativação para densificação foram verificadas. Para este trabalho foi determinado que, quanto menor o tamanho inicial de partícula, menores as energias de ativação. A evolução das distribuições de tamanhos de cristalitos foi investigada para os materiais de maior área superficial específica. Foi determinado que a eliminação e migração de poros (pore drag) é o mecanismo predominante para o crescimento de grãos durante o início da sinterização da céria gadolínia. Os efeitos da atmosfera de sinterização no desvio de estequiometria, na densificação, na evolução microestrutural e na condutividade elétrica da céria-gadolínia foram analisados. Atmosferas redutoras, oxidantes e inertes foram usadas para este propósito. Desvios na estequiometria da céria foram verificados no volume do material, sendo este dependente da área de superfície específica e da atmosfera utilizada. Quanto maior o potencial de redução da atmosfera utilizada, maior a concentração de Ce3+ no material. Com o aumento da concentração de Ce3+ um aumento no tamanho médio de grãos foi verificado. Uma diminuição na condutividade elétrica total, intra e intergranular foram determinadas para as amostras sinterizadas em atmosferas redutoras. / The effects of the sintering atmosphere and initial particle size on the sintering of ceria containing 10 mol% gadolinia (GdO1.5) were systematically investigated. The main physical parameter was the specific surface area of the initial powders. Nanometric powders with three different specific surface areas were utilized, 210 m2/g, 36,2 m2/g e 7,4 m2/g. The influence on the densification, and micro structural evolution were evaluated. The starting sintering temperature was verified to decrease with increasing on the specific surface area of raw powders. The densification was accelerated for the materials with smaller particle size. Sintering paths for crystallite growth were obtained. Master sintering curves for gadolinium-doped ceria were constructed for all initial powders. A computational program was developed for this purpose. The results for apparent activation energy showed noticeable dependence with specific surface area. In this work, the apparent activation energy for densification increased with the initial particle size of powders. The evolution of the particle size distributions on non isothermal sintering was investigated by WPPM method. It was verified that the grain growth controlling mechanism on gadoliniadoped ceria is the pore drag for initial stage and beginning of intermediate stage. The effects of the sintering atmosphere on the stoichiometry deviation of ceria, densification, microstructure evolution, and electrical conductivity were analyzed. Inert, oxidizing, and reducing atmospheres were utilized on this work. Deviations on ceria stoichiometry were verified on the bulk materials. The deviation verified was dependent of the specific surface area and sintering atmosphere. Higher reduction potential atmospheres increase Ce3+ bulk concentration after sintering. Accelerated grain growth and lower electrical conductivities were verified when reduction reactions are significantly present on sintering.

Spark Plasma Sintering (SPS) is a promising rapid consolidation technique that allows a better understanding and manipulating of sintering kinetics and therefore makes it possible to obtain Si3N4-based ceramics with tailored microstructures, consisting of grains with either equiaxed or elongated morphology. The presence of an extra liquid phase is necessary for forming tough interlocking microstructures in Yb/Y-stabilised α-sialon by HP. The liquid is introduced by a new method, namely by increasing the O/N ratio in the general formula RExSi12-(3x+n)Al3x+nOnN16-n while keeping the cation ratios of RE, Si and Al constant. Monophasic α-sialon ceramics with tailored microstructures, consisting of either fine equiaxed or elongated grains, have been obtained by using SPS, whether or not such an extra liquid phase is involved. The three processes, namely densification, phase transformation and grain growth, which usually occur simultaneously during conventional HP consolidation of Si3N4-based ceramics, have been precisely followed and separately investigated in the SPS process. The enhanced densification is attributed to the non-equilibrium nature of the liquid phase formed during heating. The dominating mechanism during densification is the enhanced grain boundary sliding accompanied by diffusion- and/or reaction-controlled processes. The rapid grain growth is ascribed to a dynamic ripening mechanism based on the formation of a liquid phase that is grossly out of equilibrium, which in turn generates an extra chemical driving force for mass transfer. Monophasic α-sialon ceramics with interlocking microstructures exhibit improved damage tolerance. Y/Yb- stabilised monophasic α-sialon ceramics containing approximately 3 vol% liquid with refined interlocking microstructures have excellent thermal-shock resistance, comparable to the best β-sialon ceramics with 20 vol% additional liquid phase prepared by HP. The obtained sialon ceramics with fine-grained microstructure show formidably improved superplasticity in the presence of an electric field. The compressive strain rate reaches the order of 10-2 s-1 at temperatures above 1500oC, that is, two orders of magnitude higher than that has been realised so far by any other conventional approaches. The high deformation rate recorded in this work opens up possibilities for making ceramic components with complex shapes through super-plastic forming.