O presente trabalho trata da manufatura direta de implantes de hidroxiapatita mediante a técnica de prototipagem rápida. A hidroxiapatita proveniente de estrutura óssea mineral bovina possui grande importância dentre os biomateriais devido a sua biocompatibilidade e grande similaridade com a estrutura óssea humana. A prototipagem rápida permite a obtenção de modelos com dimensões e formato miméticos ao do defeito ósseo do paciente e possibilita a obtenção de implantes com porosidade desejada e geometria complexas. Este trabalho tem como objetivo o estudo da obtenção de implantes por três diferentes técnicas de prototipagem rápida: usinagem a verde, 3DPrint e uma inovadora técnica de prototipagem rápida obtida pela polimerização da resina acrílica (fase líquida da barbotina) por luz ultravioleta presente em uma faixa da banda do espectro de luz emitido pelo laser azul (SLB). A diminuta pressão de conformação, típicas das técnicas de prototipagem rápida aditiva, exige pós altamente reativos para efetiva sinterização, dessa forma a hidroxiapatita obtida a partir do fêmur bovino foi calcinada e moída em moinhos de bolas e vibratório na busca de pós submicrométricos. A usinagem a verde de compactados foi considerada como padrão ouro da manufatura e foi aplicada para obtenção de corpos de prova cilíndricos, previamente conformados por prensagem isostática a 100 e 200 MPa e ensaiados por densificação, flexão, dureza e tenacidade à fratura. Introdução de partículas de alumina e whiskers de alumina foram ensaiados na busca de otimização das propriedades mecânicas. Para prototipagem rápida pelo método de SLB, misturas de hidroxiapatita e resina foram submetidas à emissão do laser azul com percurso direcionado em equipamento CNC, onde peças tridimensionais foram prototipadas e sinterizadas. A hidroxiapatita proveniente do osso bovino apresentou características de íons substitucionais de carbonato e após moagens em moinho de bolas seguido de vibratório foi obtida partículas de diâmetro médio equivalente de 0,35 µm que se mostraram reativas para promoção da sinterização. A sinterização a 1300 ºC-2h forneceu as melhores características cristalográfica e de propriedades mecânicas, resultando em corpos referências com hidroxiapatita sem decomposição em outros fosfatos de cálcio com 99,8 % da densidade, resistência mecânica à flexão de 100 MPa, dureza de 483 HV e tenacidade à fratura de 0,6 MPa.m1/2. A introdução de 1 vol% de alumina e whiskers de alumina elevaram a resistência mecânica do corpo para aproximadamente 140 MPa com tenacidade de 0,61 MPa.m1/2. Para a técnica 3DPrint aglomerados esféricos da composição cerâmica deve ter dimensões entre as malhas de 200 e 400 mesh (75 a 38 µm) e o binder deve ter resistividade superior à 290 kΩ, componentes reativos, emolientes, lubrificantes e estabilizantes. Na manufatura pela técnica SLB a incidência do laser com fluência de 170 mW.s/mm2 promoveu a cura da resina no diâmetro de 0,5 mm e profundidade próxima a 0,5 mm o que, permitiu a prototipagem de scaffolds com camadas de espessura de 0,5 mm resistente ao manuseio para remoção da barbotina não curada. / The study deals with the direct manufacturing of hydroxyapatite implants using rapid prototyping. Hydroxyapatite structure originated from bovine mineral bone has great importance among the biomaterials and biocompatibility due to its great similarity with the human bone structure. Rapid prototyping allows obtaining models with dimensions and shaping mimetics to the patient\'s bone defect and enables the achievement of implants with complex geometry and porosity desired. This study aims to obtain scaffolds for three rapid prototyping techniques: the green machining, 3DPrint and an innovative rapid prototyping technique, obtained by polymerization of acrylic resin (liquid phase of slurry) by ultraviolet light present in a range of the spectrum band a blue light emitted by the laser (SLB). The small conformation pressure, typical of additive rapid prototyping techniques requires highly reactive powders for effective sintering, and then hydroxyapatite obtained from bovine femur was calcined and milled in ball mill and vibratory mill for obtention of sub micrometrics powders. The green machining was considered as the standard of mechanical properties and was used to obtain cylindrical specimens, previously shaped by isostatic pressing at 100 and 200 MPa, and tested by densification, bending, hardness and toughness fracture. Introduction of particles of alumina and alumina whiskers were tested in search engine optimization of the mechanical properties. For rapid prototyping by the method of SLB, mixtures of hydroxyapatite and resin were subjected to blue laser emission directed in CNC equipment where three-dimensional pieces were prototyped and sintered. Hydroxyapatite derived from bovine bone showed characteristics of substitutional carbonate ions and non-stoichiometry, after grinding in a ball mill followed by vibratory mill, particles obtained was equivalent average diameter of 0.35 micrometers that proved reactive to promote sintering. Sintering at 1300 °C-2h gave the best crystallographic characteristics and mechanical properties, resulting in references bodies with hydroxyapatite without decomposition of other calcium phosphates with 99.8 % of density, flexural strength of 100 MPa, hardness of 483 HV and fracture toughness of 0.6 MPa.m1/2. The introduction of 1 vol% alumina and alumina whiskers increased the mechanical strength of the body with approximately 140 MPa and toughness fracture of 0.61 MPa.m1/2. For technical 3DPrint spherical agglomerates of ceramic composition should have dimensions between 200 and 400 mesh (75-38 µm) and the binder should have resistivity higher than 290 kΩ and components reactive, emollients, lubricants and stabilizers. In the manufacturing technique SLB incidence of the laser with a fluency of 170 mW.s/mm2 promoted curing of the resin of 0.5 mm in diameter and depth about 0.5 mm, which enabled the prototyping of scaffolds with thick layers 0.5 mm resistant to handle for removal of slurry uncured.

L’objectif de cette étude est la réalisation de séparateurs de batterie haute performance par extrusion. Ces électrolytes polymères solides nécessitent d’être perméables au courant ionique mais aussi isolants électrique, tout en étant résistants mécaniquement. Une des possibilités étudiée pour le renfort mécanique est la dispersion de charges nanométriques (whiskers de cellulose) dans un polymère. Les whiskers de cellulose sont des bâtonnets cristallins d’une longueur entre 100 et 300nm et d’un diamètre entre 5 et 20 nm. Lorsque ces charges sont dispersées de façon homogène, elles forment un réseau percolant, améliorant de cette façon le renfort mécanique de la matrice pour de faibles concentrations. Le but est donc de réaliser cette dispersion dans un polymère fondu par extrusion, en comparaison avec le procédé bien établi d’évaporation de solvant. Les difficultés principales viennent de l’agglomération des whiskers de cellulose via des liaisons hydrogènes et du milieu très concentré dans lequel ces charges doivent être dispersées. Ainsi, la première partie de l’étude est de déterminer le processus de préparation des whiskers de cellulose, limitant l'agglomération et permettant d’obtenir une suspension stable. Ce système stable est nécessaire pour la formation d'un réseau par évaporation de solvant. Une fois le protocole optimisé, la deuxième partie de l’étude porte sur la dispersion de ces whiskers dans la matrice fondue au mélangeur interne et en extrusion. Les mélanges et films obtenus sont caractérisés par analyse en rhéologie dynamique, analyse thermique et analyse mécanique. Une dégradation de la matrice ainsi qu’une orientation des whiskers sont observées. Pour contourner ces contraintes, plusieurs alternatives sont utilisées. La première consiste à adsorber un copolymère sur les whiskers ; cette méthode augmente l’effet hydrodynamique mais aucun réseau n’est obtenu. La deuxième alternative est l’utilisation d’un polymère de faible masse molaire, permettant de diminuer la viscosité du mélange et par conséquent de limiter l’orientation des charges. Cette voie permet la formation d’un réseau percolant, tout en évitant la dégradation de la matrice dans l’extrudeuse. La troisième alternative utilise un copolymère de faible masse molaire synthétisé à partir d’un monomère porteur de doubles liaisons. La faible masse molaire permet de diminuer la cristallinité du séparateur et donc d’améliorer les performances ioniques à basse température. Les doubles liaisons permettent une réticulation assurant la tenue mécanique du film / The aim of this study is to produce high-performance battery separators through extrusion. These solid polymer electrolytes should be permeable to ionic current but electrically insulating, all the while maintaining sufficient mechanical resistance. To this end, the dispersion of nanometrics fillers (cellulose whiskers) in a polymer is studied. Cellulose whiskers are crystalline sticks, with a length between 100 and 300 nm and a diameter between 5 and 20 nm. It is well known that a homogeneous dispersion of these fillers allows a percolating network, improving the mechanical reinforcement of the matrix at low concentrations. The goal is to carry out this dispersion in molten polymer through extrusion, as opposed to the well-established solvent evaporation process. The main difficulties are the aggregation of cellulose whiskers which occurs through hydrogen bonding and the concentrated medium in which these fillers are dispersed. The first part of the study is to determine the optimum process to prepare cellulose whiskers in order to limit aggregation and thus obtain a stable aqueous suspension. This stable system is necessary to obtain a percolating network in the polymer matrix through solvent evaporation. Once the protocol optimised, the second part of the study focuses on the dispersion of these whiskers in the molten matrix using both the internal mixer and the extruder. Blends and films are characterized by dynamical rheology analysis, thermal analysis and mechanical analysis: a degradation of the matrix and an orientation of the whiskers are observed. To by-pass these issues, several alternatives are used. The first one involves the adsorption of a copolymer on the whiskers. This method increases the hydrodynamic effect; however no percolation network is obtained. The second alternative is to use a low molar mass polymer. This leads to a decreased polymer viscosity which limits the orientation of the fillers, allowing the percolating network to form and prevents polymer degradation. The third way uses a copolymer with a low mass molar, synthesized from a monomer which carries double bonds. The low molar mass allows the decrease of the separator crystallinity thus improving the ionic performances at low temperatures. The double bonds can crosslink under UV light, which enhances the mechanical strength of the film

No description available.

<p>A whisker is a common name of single crystalline inorganic fibre of small dimensions, typically 0.5-1 μm in diameter and 20-50 μm in length. Whiskers are mainly used as reinforcement of ceramics. This work describes the synthesis and characterisation of new whisker types. Ti0.33Ta0.33Nb0.33CxN1-x, TiB2, B4C, and LaxCe1-xB6 have been prepared by carbothermal vapour–liquid–solid (CTR-VLS) growth mechanisms in the temperature range 900-1800°C, in argon or nitrogen. Generally, carbon and different suitable oxides were used as whisker precursors. The oxides reacted via a carbothermal reduction process. A halogenide salt was added to form gaseous metal halogenides or oxohalogenides and small amount of a transition metal was added to catalyse the whisker growth. In this mechanism, the whisker constituents are dissolved into the catalyst, in liquid phase, which becomes supersaturated. Then a whisker could nucleate and grow out under continuous feed of constituents. </p><p>The syntheses of TiC, TiB2, and B4C were followed at ordinary synthesis conditions by means of mass spectrometry (MS), thermogravimetry (TG), differential thermal analysis (DTA) and quenching. The main reaction starting temperatures and reaction time for the different mixtures was revealed, and it was found that the temperature inside the crucible during the reactions was up to 100°C below the furnace set-point, due to endothermic nature of the reactions. Quench experiments showed that whiskers were formed already when reaching the temperature plateau, but the yield increased fast with the holding time and reached a maximum after about 20-30 minutes. Growth models for whisker formation have been proposed.</p><p>Alumina based composites reinforced by (2-5 vol.%) TiCnano and TiNnano and 25 vol.% of carbide, and boride phases (whiskers and particulates of TiC, TiN, TaC, NbC, (Ti,Ta)C, (Ti,Ta,Nb)C, SiC, TiB2 and B4C) have been prepared by a developed aqueous colloidal processing route followed by hot pressing for 90 min at 1700°C, 28 MPa or SPS sintering for 5 minutes at 1200-1600°C and 75 MPa. Vickers indentation measurements showed that the lowest possible sintering temperature is to prefer from mechanical properties point of view. In the TiNnano composites the fracture mode was typically intergranular, while it was transgranular in the SiCnano composites. The whisker and particulate composites have been compared in terms of e.g. microstructure and mechanical properties. Generally, additions of whiskers yielded higher fracture toughness compared to particulates. Composites of commercially available SiC whiskers showed best mechanical properties with a low spread but all the other whisker phases, especially TiB2, exhibited a great potential as reinforcement materials. </p>

The GABAergic system in adult sensory cortex is affected by sensory deprivation, but little is known about how this predominant inhibitory system is affected during ontogeny. The present study investigates developmental effects of whisker trimming on GABAa receptors in rat barrel cortex. Rats trimmed for 6 wk beginning at birth and adulthood showed similar decreases in [3H]muscimol binding in deprived relative to non-deprived barrels, suggesting absence of a critical period.

Tin electrodeposits produced from aqueous electrolytes are frequently used within the electronics industry due to their high solderability and corrosion protection. One limitation to using these deposits is their spontaneous formation of long conductive filament whiskers. These whiskers grow post-electrodeposition and increase the risk of unwanted electrical shorts within electronic devices. In this thesis, tin electrodeposits produced from a proprietary bright acid Tinmac electrolyte, currently used in industry, were studied. Electrodeposits were produced using a range of current densities with and without agitation and were characterised with respect to crystallographic orientation, topography and surface finish. Moreover, the intermetallic compound (IMC) growth produced at the copper substrate-tin coating interface was assessed over a period of time as its growth is considered to be a significant driving force behind whisker formation. In addition, a technique for the electrochemical anodic oxidation of tin electrodeposits on copper substrates was developed. This technique was used throughout this project for the study of IMC growth from tin electrodeposits as it was able to effectively remove the tin whilst leaving the IMCs and substrate unaffected. Ionic liquids exhibit promising electrochemical characteristics for electrodeposition but are still not widely utilised in industry. Their ability to deposit tin coatings has been studied in the present investigation. Trials concentrated on process optimisation to produce uniform electrodeposits by varying current density, SnCl2.2H2O concentration, and electrolyte composition. These deposits were then characterised and compared to tin coatings of similar thickness produced from Tinmac with respect to topography, surface finish, crystallographic orientation, IMC growth, and whisker propensity. Electrodeposits produced from the ionic liquid electrolyte exhibited a different crystallographic texture, topography, and IMC growth compared to those produced from Tinmac. Moreover, the deposit produced from the ionic liquid featured increased whisker growth compared to those produced from Tinmac, but in a wider context, far less growth than conventional tin electrodeposits in the literature. In addition, by exploiting other electrochemical characteristics of ionic liquids, such as their large potential window, future work may be able to produce novel tin or tin alloy electrodeposits which may further reduce the whisker propensity of deposits produced in this investigation.

The field of tissue engineering aims to develop viable substitutes with the ability to repair and regenerate the functions of damaged tissue. Common practices to supplement bone regeneration in larger defects include bone graft biomaterials such as autografts, allografts, xenografts, and synthetic biomaterials. Autologous bone grafting is the current gold-standard procedure used to replace missing or damaged bone. However, these grafts have disadvantages such as donor site morbidity, limited availability, and the need for a secondary surgery. The focus of this study is to tissue engineer a lyophilized gelatin composite sponge composed of hydroxyapatite (HA), chitin whiskers (CW), and preparations rich in growth factors (PRGF) to provide sufficient structural support to the defect site while enhancing the body’s own reparative capacity, ultimately eliminating the need for autologous tissue harvesting or repeat operations. The present study investigates several in vitro evaluations on multiple compositions of modified gelatin sponge scaffolds for use in bone graft applications. Gelatin sponges were fabricated via freeze-drying, enhanced with PRGF, HA, and/or CW, and cross-linked with 50 mM 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC) either during or post gelation. Initial evaluation of all scaffold combinations indicated that scaffolds released contents up to 90 days, EDC cross-linking during gelation allowed for more protein release, and had the ability to swell. Since the incorporation of PRGF, HA, and CW increased cell infiltration, and production of cell-created mineral matrix over 90 days in culture, these scaffolds were further characterized. Freeze-dried gelatin sponges enhanced with PRGF, HA, and CW and cross-linked during gelation with EDC (PHCE) were mineralized (M) in 5x revised simulated body fluid (r-SBF) for 1 hour to create a bone-like mineral surface. Gelatin EDC scaffold controls (GE), GE-M, PHCE, and PHCE-M scaffolds were characterized for their ability to swell, mineralizing potential, surface morphology, growth factor incorporation and release, uniaxial compression properties, and cell attachment, proliferation, infiltration, and protein/cytokine secretion.. After mineralization, scanning electron microscopy showed sparse clusters of mineral deposition for GE-M scaffolds while PHCE-M scaffolds exhibited a more uniform mineral deposition. Both GE and PHCE scaffolds were porous structures that swelled up to 50% of their original volume upon hydration. Over 21 days incubation, PHCE-M scaffolds cumulatively released about 30% of their original protein content, significantly more than all other scaffolds. Multiplex Luminex assays confirmed the successful incorporation of PRGF growth factors within PRGF sponges. For acellular uniaxial compression testing, PHCE-M scaffolds reported lower Young’s modulus values (1.3 - 1.6 MPa) when compared to GE and GE-M scaffolds (1.6 – 3.2 MPa). These low modulus values were comparable to values of tissue found in early stages of bone healing. DAPI (4',6-diamidino-2-phenylindole) staining and imaging showed an increase in initial cell attachment and infiltration of PHCE and PHCE-M scaffolds on day 1. GE-M scaffolds also appeared to attach more cells than the GE control. MTS cell proliferation assay results indicated that on days 4 and 7, PHCE scaffolds increased cell proliferation (compared to GE controls). MTS also illustrated that the addition of a mineral coating increases and decreases cell proliferation on GE-M and PHCE-M scaffolds, respectively. Multiplexer analysis of MG-63 protein/cytokine secretion suggests that cells are responding in a bone regenerative fashion on all scaffolds, as evidence of osteocalcin secretion. Little to no secretion of osteopontin, IL-1β, and TNF-α demonstrates that scaffolds are not influencing cells to secrete factors associated with bone resorption. The compressive mechanical properties of cellularized scaffolds did not differ much from acellular scaffolds. The collective results indicated increased cellular attachment, infiltration, and bone regenerative protein/cytokine secretion by cells on GE-M scaffolds, which support the addition of a bone-like mineral surface on GE scaffolds. Cellularized PHCE and PHCE-M scaffolds report similar advantages as well as Young’s modulus values in the range of native tissues present in the early stages of bone healing. The results of this study propose that the developed PHCE and PHCE-M scaffolds exhibit good cellular responses and mechanical properties for use in early bone healing applications.

L'hydrolyse de microfibrilles de cellulose par l'acide sulfurique permet d'obtenir des suspensions stables de microcristaux aussi appelés "whiskers". Des whiskers de géométrie et de charge de surface différentes ont été préparés à partir de cellulose d'origines diverses (coton, Avicel, betterave et tunicier) et caractérisés par microscopie optique et électronique ainsi que par diffusion des rayons X aux petits et grands angles. L'influence de la géométrie des whiskers et de paramètres physico-chimiques sur leurs propriétés d'auto-organisation dans l'eau et dans des solvants organiques apolaires a ensuite été étudiée et les diagrammes de phases déterminés pour les deux types de systèmes. Des matériaux nanostructurés reproduisant les organisations hélicoïdales observées dans les organismes vivants ont été préparés à partir de whiskers de cellulose organisés en phase cholestérique, dispersés dans un solvant/monomère photopolymérisable.

<p>The directive of the European parliament and of the council on the Restriction of the use of certain Hazardous Substances (RoHS) in Electrical and Electronic Equipment (EEE) took effect in the European Union on July 1, 2006. Japan, California, China and Korea are all closed markets for exporters of components containing lead from July 1, 2007. Taiwan and Australia are working with similar directives. The RoHS directive is the reason why this thesis about the implementation of lead-free soldering in highly reliable applications is necessary.</p><p>The European Lead Free soldering NETwork (ELFNET) status survey from 2005 shows that the majority of the companies are well informed, but 20% are still not active in lead-free soldering. The Swedish industry is for the most part prepared and 95% of the components are lead-free. The transition to lead-free soldering will have a major affect on logistics and administration, because the RoHS directive is 90% about administration and logistics problems. Only 10% is technical problems.</p><p>The higher melting point in lead-free soldering affects every stage of the lead-free manufacturing, from assembly to testing and repair.</p><p>The major concern for highly reliable applications are that there are not enough data to understand to what grade lead-free solders will perform differently from lead based solders. Five different types of reliability testing were studied in this thesis; vibration, mechanical shock, thermal shock, thermal cycling and combined environments. Whiskers, voids, brittle fractures and mixed assembly problems were also studied. Individual tests alone should not be used to make definite decisions on lead-free soldering reliability. The lower reliability for lead-free solders in some tests does not necessarily mean that lead-free solders not can be used in highly reliable applications like defence electronics.</p><p>The most important conclusions from this thesis are:</p><p>• Update or change the logistic system and mark/label according to available standards.</p><p>• Secure a good board layout.</p><p>• Secure a good process control.</p><p>• Alternative surface board should be used. Tin-silver-copper (SAC) is the most reliable solder and Electroless Nickel/Immersion Gold (ENIG) is the most reliable surface finish.</p><p>• Remember that the higher temperature affects every stage of the manufacturing.</p><p>• No increased problems with whiskers or risk of high voiding levels.</p><p>• Mixed assembly is a risk. Compatibility and contamination risks must be taken seriously.</p><p>• Which environment will the applications be in? If it is not a highly vibrating and thermal cycling environment, lead-free soldering should be safe to use.</p> / <p>Europaparlamentets och rådets direktiv om begränsning av användningen av vissa farliga ämnen i elektriska och elektroniska produkter började gälla i Europeiska unionen 1 juli, 2006. Japan, Kalifornien, Kina och Korea är alla stängda marknader för exportörer av komponenter som innehåller bly från och med 1 juli, 2007. Taiwan och Australien arbetar med liknande direktiv. RoHS-direktivet är anledningen till varför detta examensarbete om implementeringen av blyfri lödning i högtillförlitliga applikationer är nödvändigt.</p><p>En undersökning från 2005 av ELFNET visar att majoriteten av företagen är väl informerade, men 20% är fortfarande i aktiva med blyfri lödning. Den svenska industrin är till största delen väl förberedd och 95% av komponenterna är blyfria. Övergången till blyfri lödning kommer att ha stor effekt på logistik och administration, därför att 90% är administrations- och logistikproblem i RoHS-direktivet. Bara 10% är tekniska problem.</p><p>Den högre smälttemperaturen i blyfri lödning påverkar varje steg av den blyfria tillverkningen, från montering till testning och reparation.</p><p>Den stora oron för högtillförlitliga applikationer är att det inte finns tillräckligt med data för att förstå i vilken grad som blyfria lod kommer att bete sig annorlunda jämfört med blybaserade lod. Fem olika typer av tillförlitlighetstester har undersökts i detta examensarbete; vibration, mekanisk chock, termisk chock, termisk cykling och kombinerade tester. Whiskers, voids, sprödbrott och blandad montering studerades också. Individuella tester ska inte användas för att ta några definitiva beslut om blyfri lödnings tillförlitlighet. Den lägre tillförlitligheten för blyfria lod i en del tester behöver nödvändigtvis inte betyda att blyfria lod inte kan användas i högtillförlitliga applikationer som försvarselektronik.</p><p>De viktigaste slutsatserna från detta examensarbete är:</p><p>• Uppdatera eller byt logistiskt system och märk enligt tillgängliga standarder.</p><p>• Säkerställ en bra kretskortsdesign.</p><p>• Säkerställ en bra processkontroll.</p><p>• Alternativa mönsterkort bör användas. SAC är det tillförlitligaste lodet och ENIG är den tillförlitligaste ytbehandlingen.</p><p>• Kom ihåg att den ökade temperaturen påverkar varje steg i tillverkningen.</p><p>• Inga ökade problem med whiskers eller stort antal voids.</p><p>• Blandmontage är riskfyllt. Kompatibilitet och risker med kontaminering måste tas på allvar.</p><p>• Vilken miljö kommer applikationen att befinna sig i? Är det inte en starkt vibrerande eller temperaturcyklisk miljö bör blyfri lödning vara säkert att använda.</p>

A whisker is a common name of single crystalline inorganic fibre of small dimensions, typically 0.5-1 μm in diameter and 20-50 μm in length. Whiskers are mainly used as reinforcement of ceramics. This work describes the synthesis and characterisation of new whisker types. Ti0.33Ta0.33Nb0.33CxN1-x, TiB2, B4C, and LaxCe1-xB6 have been prepared by carbothermal vapour–liquid–solid (CTR-VLS) growth mechanisms in the temperature range 900-1800°C, in argon or nitrogen. Generally, carbon and different suitable oxides were used as whisker precursors. The oxides reacted via a carbothermal reduction process. A halogenide salt was added to form gaseous metal halogenides or oxohalogenides and small amount of a transition metal was added to catalyse the whisker growth. In this mechanism, the whisker constituents are dissolved into the catalyst, in liquid phase, which becomes supersaturated. Then a whisker could nucleate and grow out under continuous feed of constituents. The syntheses of TiC, TiB2, and B4C were followed at ordinary synthesis conditions by means of mass spectrometry (MS), thermogravimetry (TG), differential thermal analysis (DTA) and quenching. The main reaction starting temperatures and reaction time for the different mixtures was revealed, and it was found that the temperature inside the crucible during the reactions was up to 100°C below the furnace set-point, due to endothermic nature of the reactions. Quench experiments showed that whiskers were formed already when reaching the temperature plateau, but the yield increased fast with the holding time and reached a maximum after about 20-30 minutes. Growth models for whisker formation have been proposed. Alumina based composites reinforced by (2-5 vol.%) TiCnano and TiNnano and 25 vol.% of carbide, and boride phases (whiskers and particulates of TiC, TiN, TaC, NbC, (Ti,Ta)C, (Ti,Ta,Nb)C, SiC, TiB2 and B4C) have been prepared by a developed aqueous colloidal processing route followed by hot pressing for 90 min at 1700°C, 28 MPa or SPS sintering for 5 minutes at 1200-1600°C and 75 MPa. Vickers indentation measurements showed that the lowest possible sintering temperature is to prefer from mechanical properties point of view. In the TiNnano composites the fracture mode was typically intergranular, while it was transgranular in the SiCnano composites. The whisker and particulate composites have been compared in terms of e.g. microstructure and mechanical properties. Generally, additions of whiskers yielded higher fracture toughness compared to particulates. Composites of commercially available SiC whiskers showed best mechanical properties with a low spread but all the other whisker phases, especially TiB2, exhibited a great potential as reinforcement materials.