During high strain rate deformations of metals and metallic alloys, narrow regions of intense plastic deformations have been observed experimentally. The phenomenon is termed strain localization and is usually a precursor to catastrophic failure of a structure. Similar phenomenon has been observed in glassy polymers deformed both at slow and high strain rates. Whereas strain localization is attributed to material softening due to thermal heating in metallic alloys, it is believed to be due to the reorganization of the molecular structure in polymers. Here we numerically study the strain localization in Tungsten Heavy Alloys (WHAs), and glassy polymers. WHAs are heterogeneous materials and thus inhomogeneities in deformations occur simultaneously at several places. Thus strains may localize into narrow bands at one or more places depending upon the microstructure of the alloy. We analyze the strain localization phenomenon during explosion and implosion of WHA hollow cylinders. We have developed a procedure to generate three-dimensional microstructures from planar images so that the two have the same 2-point correlation function. The WHA considered here is comprised of W particulates in a Nickel-Iron (NiFe) matrix, and each constituent is modeled as a heat conducting, strain hardening, strain-rate hardening and thermally softening elastic-plastic material. Furthermore, the porosity is taken to evolve in each constituent and the degradation of material properties due to porosity is incorporated into the problem formulation. It is found that the strain localization initiation in WHA hollow cylinders does not significantly depend on microstructural details during either explosive or implosive loading. However, the number of disconnected regions of localized deformations is influenced by the microstructure. We have generalized constitutive equations for high strain rate deformations of two glassy polymers, namely, Polycarbonate (PC) and poly (methyl methacrylate) (PMMA). These have been validated by comparing computed results with test findings in uniaxial compression at different axial strain rates, and subsequently used to study strain localization in a plate with a through-the-thickness elliptic hole at the centroid and pulled axially at a nominal strain rate of 5,000 /s. For the problems studied, the intensely deformed narrow regions have very high shear strains in WHAs, but large axial strains in glassy polymers. / Ph. D.

Plane strain transient finite thermomechanical deformations of heat-conducting particulate composites comprised of circular tungsten particulates in nickel-iron matrix are analyzed using the finite element method to delineate the initiation and propagation of brittle/ductile failures by the nodal release technique. Each constituent and composites are modeled as strain hardening, strain-rate-hardening and thermally softening microporous materials. Values of material parameters of composites are derived by analyzing deformations of a representative volume element whose minimum dimensions are determined through numerical experiments. These values are found to be independent of sizes and random distributions of particulates, and are close to those obtained from either the rule of mixtures or micromechanics models. Brittle and ductile failures of composites are first studied by homogenizing their material properties; subsequently their ductile failure is analyzed by considering the microstructure. It is found that the continuously varying volume fraction of tungsten particulates strongly influences when and where adiabatic shear bands (ASB) initiate and their paths. Furthermore, an ASB initiates sooner in the composite than in either one of its constituents. We have studied the initiation and propagation of a brittle crack in a precracked plate deformed in plane strain tension, and a ductile crack in an infinitely long thin plate with a rather strong defect at its center and deformed in shear. The crack may propagate from the tungsten-rich region to nickel-iron-rich region or vice-a-versa. It is found that at the nominal strain-rate of 2000/s the brittle crack speed approaches Rayleigh's wave speed in the tungsten-plate, the nickel-iron-plate shatters after a small extension of the crack, and the composite plate does not shatter; the minimum nominal strain-rate for the nickel-iron-plate to shatter is 1130/s. The ductile crack speed from tungsten-rich to tungsten-poor regions is nearly one-tenth of that in the two homogeneous plates. The maximum speed of a ductile crack in tungsten and nickel-iron is found to be about 1.5 km/s. Meso and multiscale analyses have revealed that microstructural details strongly influence when and where ASBs initiate and their paths. ASB initiation criteria for particulate composites and their homogenized counterparts are different. / Ph. D.

A specialty class of alloys known as tungsten heavy alloys (WHAs) possess extremely desirable qualities for adoption in nuclear fusion reactors. Their high temperature stability, improvement in fracture toughness over other brittle candidates, and promising performance in initial experimental trials have demonstrated their utility, and recent advancements have been made in understanding and applying these multiphase materials systems. To that end, Pacific Northwest National Laboratory in collaboration with Virginia Tech have sought to understand and tailor the structure and properties of these materials to optimize them for service in fusion reactor interiors; thereby improving the robustness, efficiency, and longevity of structural materials selected for service in an extremely hostile environment. In this analysis of material viability, a multiscale investigation of the connections between structure-property relationships in these multiphase composite microstructures has been undertaken, employing advanced characterization techniques to bridge the macro, micro, and nanoscales for the purpose of generating a framework for the understanding of the ductile phase toughening effect in these systems. This analysis has yielded evidence suggesting the effectiveness of WHA microstructures in the simultaneous expression of high strength and toughness owes to the intimately bonded nature of the boundary which exists between the dissimilar phases in these bi-phase microstructures. Analytical techniques have been employed to provide added dimensionality to traditional materials characterization techniques, providing the first three-dimensional microstructure reconstructions exhibiting the effects of thermomechanical processing on these dual-phase microstructures, and the first time-resolved approach to the observation of WHA deformation through in-situ uniaxial tension testing. The contributions of purposefully introduced microstructural anisotropy and its contribution to texturing and boundary conformations is discussed, and an emphasis has been placed on the study of the interface between the dissimilar phases and its role in the overall expression of ductile phase toughening. In short, this collective work utilizes multiscale and multidimensional characterization techniques in the in-depth analysis and discussion of WHA systems to connect their structure to the properties which make them excellent candidates for fusion reactor systems. / Doctor of Philosophy / In the ongoing effort to realize nuclear fusion for commercial energy generation, there are numerous hurdles which must be overcome. A primary issue in the creation of these reactors is the implementation of materials which interface with the superheated plasma in the reactor interior, called plasma facing materials and components (PFMCs). These PFMCs must be able to withstand environmental conditions which will melt, irradiate, embrittle, and fracture a majority of common structural materials. Therefore these materials must exhibit unparalleled robustness in the form of high thermal and irradiation resistance. One class of alloys which is currently being considered for this purpose is tungsten heavy alloys (WHAs). These materials have exhibited excellent viability in early-stage experimental trials, and have necessarily become the subject of extended examination as PFMC candidates. In a joint collaboration between Pacific Northwest National Laboratory and Virginia Tech, these materials have been subjected to rigorous experimental testing and analysis to determine what underlying physics are responsible for their excellent properties. Advanced analytical techniques have been applied to observe the connections which exist between the atomic structure of boundaries and have been connected to the expression of observable properties on the macroscale. This work has provided the first available data on the full three-dimensional approach to the study of WHAs as well as the first dynamic observation of how the materials deform, leading to the conclusion that the two-phase composite-like structure of these alloys owe their combination of strength and ductility to the strong bond which exists between the two phases. This information on how material structure influences properties can be used to improve alloy design and produce even more effective WHA materials going forward.

The objective of this project is to investigate hydrodeoxygenation (HDO), a crucial step in the treatment of bio-oil, on transition metal phosphide catalysts. The study focuses on reactions of simple oxygenated compounds present in bio-oil -- ethanol and 2-methyltetrahydrofuran (2-MTHF). The findings from this project provide fundamental knowledge towards the hydrodeoxygenation of more complex bio-oil compounds. Ultimately, the knowledge contributes to the design of optimum catalysts for upgrading bio-oil. A series of transition metal phosphides was prepared and tested; however, the focus was on Ni2P/SiO2. Characterization techniques such as X-ray diffraction (XRD), temperature-programmed reduction and desorption (TPR and TPD), X-ray photoelectron spectroscopy (XPS), and chemisorption were used. In situ Fourier transform infrared (FTIR) spectroscopy was employed to monitor the surface of Ni2P during various experiments such as: CO and pyridine adsorption and transient state of ethanol and 2-MTHF reactions. The use of these techniques allowed for a better understanding of the role of the catalyst during deoxygenation. / Ph. D.

Material erosion, melting, splashing, bubbling, and ejection during disruption events in future large tokamak reactors are of serious concern to component longevity. The majority of the heat flux during disruptions will be incident on the divertor, which will be made from tungsten in the future large tokamak ITER. Electrothermal plasma sources operating in the confined controlled arc discharge regime produce heat fluxes in the range expected for hard disruptions in future large tokamaks. The radiative heat flux produced inside of the capillary discharge channel is from the formed high density (10^23 - 10^27/m^3) plasma with heat fluxes of up to 125 GW/m^2 over a period of 100s of microseconds, making such sources excellent simulators for ablation studies of plasma-facing materials in tokamaks during hard disruptions. Experiments have been carried out with the PIPE device exposing tungsten to these high heat flux plasmas. SEM images have been taken of the tungsten surfaces, cross sections of tungsten surfaces, and ejected material. Melting and bubble/void formation has been observed on the tungsten surface. The tungsten surface shows evidence of melt-layer flow and the existence of voids and cracks in the exposed material. The ejected material does not show direct evidence of liquid material ejection which would lead to splashing. EDS analysis has been performed on the ejected material which demonstrates a lack of deposited solid tungsten particulates greater than micron size. / Master of Science

[ES] La presente tesis doctoral se sitúa en el marco de la actual transición energética, que plantea la sustitución progresiva de materias primas de origen fósil por fuentes renovables, tanto para la obtención de productos químicos como para la producción de combustibles. En este contexto de transición paulatina a las renovables, y teniendo en cuenta los últimos pronósticos, las fuentes fósiles (fundamentalmente gas natural) y derivados de la biomasa, jugarán un papel fundamental durante el cambio. Se ha llevado a cabo un estudio sobre el empleo de óxidos metálicos (basados en bronces de wolframio o en óxido de níquel), como catalizadores para: i) la transformación de derivados de biomasa: de glicerol a acroleína/ácido acrílico; y de compuestos oxigenados de cadena corta presentes en efluentes acuosos (procedentes de tratamientos de extracción de bio-aceites de pirolisis) a combustibles; y ii) la transformación de componentes del gas natural, concretamente la obtención de etileno a partir de etano, mediante deshidrogenación oxidativa (ODH). El trabajo se presenta desde una perspectiva de la química de materiales, haciendo hincapié en las propiedades fisicoquímicas de los distintos sistemas catalíticos, empleando técnicas de caracterización convencionales e in situ, además de reacciones modelo (transformación de metanol y etanol), con el objetivo de entender las funciones catalíticas presentes en cada caso. Tanto para la transformación de glicerol en fase gas, como para la valorización de mezclas acuosas de compuestos oxigenados de cadena corta, se han utilizado catalizadores basados en bronces de wolframio. Se ha tratado de poner de manifiesto la gran versatilidad composicional y estructural (con el consiguiente control de las propiedades funcionales), que presentan este tipo de materiales. En este sentido, las propiedades ácidas y redox de catalizadores W-V-O pueden ser moduladas, para una misma concentración de vanadio, mediante el control de la relación de fases cristalinas (hexagonal y monoclínica) del óxido de wolframio. Este efecto se ha estudiado empleando la transformación aeróbica de metanol como reacción "test", y tiene una gran influencia en la deshidratación oxidativa de glicerol a ácido acrílico. A su vez, mediante la sustitución isomórfica de wolframio por niobio (en el sistema WO3-Nb2O5) es posible controlar la relación de centros ácidos de tipo Brönsted y Lewis en la superficie de los materiales. Por un lado, los catalizadores con una alta relación Brönsted/Lewis se han mostrado más efectivos en la deshidratación de glicerol a acroleína, mientras que los catalizadores con altas concentraciones de centros de tipo Lewis presentan altos rendimientos a productos de condensación de compuestos oxigenados de cadena corta. Adicionalmente se han estudiado las diferencias entre catalizadores (bien óxidos mixtos W-V-O o W-Nb-O) preparados mediante un método hidrotermal o mediante reflujo, así como el efecto de la utilización de un soporte mesoporoso (KIT-6), sobre sus propiedades catalíticas en la transformación aeróbica en fase gaseosa de etanol y glicerol. Finalmente, en lo que concierne a la transformación de componentes del gas natural, se han empleado materiales basados en óxido de níquel (soportado sobre distintos óxidos y/o promovido con distintos metales) como catalizadores para la ODH de etano. En este caso el estudio se ha centrado fundamentalmente en dilucidar los efectos de promotores y soportes en la naturaleza y propiedades fisicoquímicas del óxido de níquel, los cuales dan lugar a un cambio drástico en sus propiedades catalíticas. Así, se ha observado que modificando la reducibilidad y las características superficiales del óxido de níquel es posible transformar un catalizador muy poco selectivo en la ODH de etano (como es el NiO, con una selectividad a etileno del 30 %) en uno de los catalizadores más selectivos para llevar a cab / [CA] Aquesta tesi doctoral es situa dins del marc de l'actual transició energètica, la qual planteja la substitució progressiva de les primeres matèries d'origen fòssil per fonts renovables, tant per a l'obtenció de productes químics com per a la producció de combustibles. En aquest context de transició gradual a les renovables, i tenint en compte els últims pronòstics, les fonts fòssils (principalment el gas natural) i els derivats de la biomassa, exerciran un paper fonamental durant aquest canvi. S'ha dut a terme un estudi sobre la utilització d'òxids metàl·lics (basats en bronzes de wolframi o en òxid de níquel), com a catalitzadors per a: i) la transformació de derivats de la biomassa: de glicerol a acroleïna/àcid acrílic; i de compostos oxigenats de cadena curta presents en efluents aquosos (procedents de tractaments d'extracció de bio-olis de la piròlisi) a combustibles; i ii) la transformació de components del gas natural, concretament l'obtenció d'etilè a partir d'età, mitjançant la deshidrogenació oxidativa. El treball es presenta des del punt de vista de la química de materials, posant l'accent en les propietats fisicoquímiques dels diferents sistemes catalítics, utilitzant tècniques de caracterització convencionals i in situ, a més de reaccions model, amb l'objectiu d'entendre les funcions catalítiques presents en cadascun dels casos. Tant per a la transformació del glicerol en fase gasosa com per a la valorització de les mescles aquoses de compostos oxigenats de cadena curta, s'han utilitzat catalitzadors basats en bronze de wolframi. S'ha intentat posar de manifest la gran versatilitat de composicions i estructures (amb el conseqüent control de les propietats funcionals) que presenten aquest tipus de materials. En aquest sentit, les propietats àcides i redox dels catalitzadors de W - V - O poden ser modulades, per a una mateixa concentració de vanadi, mitjançant el control de la relació de fases cristal·lines (hexagonal i monoclínica) de l'òxid de wolframi. Aquest efecte s'ha estudiat utilitzant la transformació aeròbica de metanol com a reacció "test", i presenta una gran influència en la deshidratació oxidativa de glicerol a àcid acrílic. Al mateix temps, mitjançant la substitució isomòrfica de wolframi per niobi (en el sistema WO3 - Nb2O5), és possible controlar la relació de centres àcids de tipus Brönsted i Lewis en la superfície dels materials. Per una part, els catalitzadors que presenten una relació Brönsted / Lewis alta s'han mostrat més efectius en la deshidratació de glicerol a acroleïna, mentre que els catalitzadors amb unes altes concentracions de tipus Lewis presenten alts rendiments a productes de condensació de compostos oxigenats de cadena curta. Addicionalment, s'han estudiat les diferències entre catalitzadors (ja siguin òxids mixtos W-V-O o W-Nb-O) preparats mitjançant un mètode hidrotermal o mitjançant un mètode de reflux, així com l'efecte que presenta la utilització d'un suport mesoporós (KIT-6), sobre les seves propietats catalítiques en la reacció de transformació aeròbica en fase gasosa d'etanol i glicerol. Finalment, pel que fa referència a la transformació de components del gas natural, s'han utilitzat materials basats en òxid de níquel (suportat sobre diferents òxids i/o promoguts amb diferents metalls) i catalitzadors per a la deshidrogenació oxidativa d'età. En aquest cas, l'estudi s'ha focalitzat principalment en dilucidar els efectes de promotors i suports en la naturalesa i propietats fisicoquímiques de l'òxid de níquel, els quals impliquen un canvi dràstic en les seves propietats catalítiques. Així doncs, s'ha observat que modificant la reductibilitat i les característiques superficials de l'òxid de níquel és possible transformar un catalitzador molt poc selectiu en la deshidrogenació oxidativa de l'età (com és el cas del NiO, amb una selectivitat a l'etilè del 30%) en un dels cata / [EN] The present doctoral thesis is set within the scope of the current energy transition, which considers the progressive substitution of non-renewable fossil sources by renewable feedstocks for the production of chemicals and fuels. In this context of gradual transition, and according to recent energy outlooks, fossil sources (especially natural gas) and biomass feedstocks will play a key role during the shift. A study on the use of metal oxides (based on tungsten bronzes or nickel oxides) as catalysts for different reactions has been conducted. Particularly, they have been studied as catalytic materials for: i) the transformation of biomass-derived feedstocks: glycerol transformation into acrolein/acrylic acid, and the transformation of short-chain oxygenates present in aqueous effluents (derived from extraction processes of pyrolysis bio-oils) into fuels; and ii) the valorization of natural gas components, i.e. the transformation of ethane into ethylene by oxidative dehydrogenation. The work is presented from a materials chemistry perspective, emphasizing the physicochemical characteristics of the different catalytic systems by using conventional and in situ characterization techniques and model reactions (gas phase methanol and ethanol transformation); with the aim of understanding the specific catalytic functionalities present in each case. For both gas phase glycerol transformation and the valorization of short-chain oxygenates aqueous mixtures, catalyst based on tungsten oxide bronzes have been used. The compositional and structural versatility of this structural types (with the subsequent control of their functional properties) will be highlighted. In this sense, the acid-redox properties of W-V-O catalysts can be modulated by controlling the crystalline phase composition in the materials (i.e. hexagonal and monoclinic polymorphs of tungsten oxide) at a fixed V concentration. This effect has been studied by using the gas-phase aerobic transformation of methanol as a surface test reaction. The concentration of the hexagonal and monoclinic polymorphs in the catalysts has also an important influence in the gas-phase transformation of glycerol into acrylic acid. Also, it is possible to control the Brönsted/Lewis acid nature of the surface by the isomorphic substitution of Nb for W in WO3-Nb2O5 system. On the one hand, catalysts showing a higher proportion of Brönsted acid sites are more effective in the glycerol dehydration to acrolein. On the other hand, materials with a higher concentration of Lewis acid sites display high yields to condensation products in the aqueous phase valorization of short chain oxygenates. Additionally, the differences between W-V-O and W-Nb-O catalysts prepared by both reflux and hydrothermal methods have been studied. Also the effect of adding a mesoporous KIT-6 silica as support on the catalytic performance in the gas phase transformation of ethanol and glycerol will be underlined. Considering the transformation of natural gas components, nickel oxide-based materials were chosen (either supported on different oxides and/or promoted with different metals) to perform the oxidative dehydrogenation (ODH) of ethane. In this case the study has been focused on elucidating the effects of both promoters and supports on the nature and physicochemical features of nickel oxide, which lead to a drastic change in the catalytic behavior of these materials. This way, it has been observed that by the modification of the reducibility and the chemical nature of nickel oxide, it is possible to transform an apparently non-selective catalyst in the ODH of ethane (like NiO, showing a selectivity to ethylene of ca. 30 %) into one of the most selective catalysts reported in the literature (presenting a selectivity to ethylene of ca. 90 %). / También me gustaría agradecerle al Prof. Avelino Corma, investigador principal del proyecto SEV-2012-0267, a través del cual he podido realizar mi tesis doctoral enel Instituto de Tecnología Química (SVP-2014-068669). / Delgado Muñoz, D. (2019). Catalytic valorization of natural gas and biomass-derived feedstocks by metal oxides [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/122298

There is great interest in the development of new polar dielectric ceramics and multiferroic materials with new and improved properties. A family of tetragonal tungsten bronze (TTB) relaxors of composition Ba₆M³⁺Nb₉O₃₀ (M³⁺ = Ga³⁺, Sc³⁺ and In³⁺, and also their solid solutions) were studied in an attempt to understand their dielectric properties to enable design of novel polar TTB materials. A combination of electrical measurements (dielectric and impedance spectroscopy) and powder diffraction (X-ray and neutron) studies as a function of temperature was employed for characterising the dynamic dipole response in these materials. The effect of B-site doping on fundamental dipolar relaxation parameters were investigated by independently fitting the dielectric permittivity to the Vogel-Fulcher (VF) model, and the dielectric loss to Universal Dielectric Response (UDR) and Arrhenius models. These studies showed an increase in the characteristic dipole freezing temperature (T[subscript(f)]) with increase B-cation radius. Crystallographic data indicated a corresponding maximum in tetragonal strain at T[subscript(f)], consistent with the slowing and eventual freezing of dipoles. In addition, the B1 crystallographic site was shown to be most active in terms of the dipolar response. A more in-depth analysis of the relaxor behaviour of these materials revealed that, with the stepwise increase in the ionic radius of the M³⁺ cation on the B-site within the Sc-In solid solution series, the Vogel-Fulcher curves (lnf vs. T[subscript(m)]) are displaced to higher temperatures, while the degree of relaxor behaviour (frequency dependence) increases. Unfortunately, additional features appear in the dielectric spectroscopy data, dramatically affecting the Vogel-Fulcher fitting parameters. A parametric study of the reproducibility of acquisition and analysis of dielectric data was therefore carried out. The applicability of the Vogel-Fulcher expression to fit dielectric permittivity data was investigated, from the simple unrestricted (“free”) fit to a wider range of imposed values for the VF relaxation parameters that fit with high accuracy the experimental data. The reproducibility of the dielectric data and the relaxation parameters obtained by VF fitting were shown to be highly sensitive to the thermal history of samples and also the conditions during dielectric data acquisition (i.e., heating/cooling rate). In contrast, UDR analysis of the dielectric loss data provided far more reproducible results, and to an extent was able to partially deconvolute the additional relaxation processes present in these materials. The exact nature of these additional relaxations is not yet fully understood. It was concluded application of the Vogel-Fulcher model should be undertaken with great care. The UDR model may represent a feasible alternative to the evaluation of fundamental relaxation parameters, and a step forward towards the understanding of the dielectric processes in tetragonal tungsten bronzes.

No description available.

Thesis (MScEng (Mechanical and Mechatronic Engineering))--University of Stellenbosch, 2011. / ENGLISH ABSTRACT: The purpose of this study is to investigate the machinability of commercially pure (CP) titanium, manufactured using the press-and-sinter PM process. To this end, CP titanium powder (-200 mesh) was compacted and sintered in vacuum (10-4 torr) for two hours at 1200°C. Small cylindrical samples were compacted at pressures varying from 350 to 600 MPa in order to determine the compressibility of the powder. Following these tests, four larger stepped-cylinder samples were compacted at pressures close to 400 MPa and sintered under similar conditions. These samples had sintered densities varying between 3.82 and 4.41 g/cm3. They were used to evaluate the machinability of the sintered titanium using face turning machining tests. The samples were machined dry, using uncoated carbide (WC-Co) cutting tool. Cutting speeds between 60-150 m/min were evaluated while keeping the feed rate and depth of cut constant at 0.15 mm/rev and 0.5 mm, respectively. The final machined surface finish and the tool wear experienced during the face turning machining tests were monitored in order to evaluate PM titanium’s machining performance. This study showed that it is possible to use the press-and-sinter PM process with CP titanium powder, with a particle size of less than 75 μm (-200 mesh), to manufacture sintered titanium. However, particle shape influences the compressibility of the powder and pressing parts of larger volume, such as the machining test sample shape, is challenging when using such small particle size powder. Processing conditions, such as compaction pressure, sintering temperature and sintering time, influence the sintered density. Results from the machinability tests show that tool wear increases with a decrease in the porosity of the sintered titanium. A more porous sintered material has both lower strength and thermal conductivity. As these factors have opposing effects on the machinability of materials, it is concluded that the strength of the sintered titanium has a stronger influence on its machinability than the thermal conductivity. The cutting tool wear was uniform but showed indications of crater wear. The machined surface of the denser parts had minimal defects compared to less dense parts. Chip shape is long for the dense parts, and spiral for the less dense parts. The chips formed were all segmented, which is typical for titanium. The machinability of the sintered CP titanium was compared to that of wrought titanium alloys. As expected, it was found that the machinability of the sintered titanium was poor in comparison. / AFRIKAANSE OPSOMMING: Die doel van hierdie studie is om die masjineerbaarheid van kommersieel suiwer (KS) titaan, wat deur die pers-en-sinter poeiermetallurgie (PM) metode vervaardig word, te ondersoek. Om hierdie doel te bereik, is KS titaan poeier (-200 ogiesdraad) gekompakteer en gesinter in ‘n vakuum (10-4 torr) teen 1200°C vir 2 ure. Klein silindriese monsters is tussen drukke van 350en 600 MPa gekompakteer om die samedrukbaarheid van die poeier te bepaal. Na aanleiding van hierdie toetse, is vier groter trapvormige-silinder monsters by drukke naby aan 400MPa gekompakteer en onder soortgelyke omstandighede gesinter. Hierdie monsters het gesinterde digthede tussen 3.82 en 4.41 g/cm3 gehad. Hulle is gebruik om die masjineerbaarheid van die gesinterde titaan te ondersoek deur middel van vlak-draai masjineringstoetse. Die monsters is sonder smeermiddel gemasjineer met onbedekte karbied (WC-Co) snygereedskap. Snysnelhede tussen 60 – 150 m/min is geëvalueer terwyl die voertempo en diepte van die snit konstant by 0.15 mm/rev en 0.5 mm, onderskeidelik, gehou is. Die finale gemasjineerde oppervlak afwerking en gereedskapsslytasie tydens die vlak-draai masjinering toets is van die faktore wat gemonitor is sodat PM titaan se optrede tydens masjinering geëvalueer kan word. Hierdie studie wys dat diepers-en-sinter metode wel met KS titaan poeier, met ‘n partikel grootte van minder as 75 μm (-200 maas), gebruik kan word om gesinterde titaan te vervaardig. Die partikelgrootte beïnvloed wel die samedrukbaarheid van die poeier. Die samedrukking van parte met groter volume, soos bv die masjinerings toetsmonster, is uitdagend wanneer klein partikelgrootte poeier gebruik word. Proses omstandighede, soos kompaksie druk, sinteringstemperatuur en sinteringstyd, beïnvloed die gesinterde digtheid. Resultate van die masjineerbaarheidstoetse wys dat beitelslytasie toeneem met ‘n afname in porositeit van die gesinterede titaan. ‘n Meer poreus gesinterde materiaal het beide laer sterkte en termiese geleidingsvermoë. Aangesien hierdie faktore teenoorgestelde uitwerkings op masjineerbaarheid het, word dit dan afgelei dat die sterkte van gesinterde titaan ‘n groter invloed het op sy masjineerbaarheid as die termiese geleidingsvermoë. Die beitel se slytasie is hoofsaahlik, maar het tekens van kraterslytasie getoon. Die gemasjineerde oppervlak van die meer digte onderdele of toetsmonters het min gebreke gehad in vergelyking met die minder digte dele. Die vorm van die spaanders is lank vir digte parte, en spiraalvormig vir minder digte toetsmonsters. Die spaanders wat gevorm het, was almal gesegmenteerd, wat tipies is vir titaan. Die masjineerbaarheid van die gesinterde KS titaan is met dié van gesmede titaanallooie vergelyk. Soos verwag is, is gevind dat die masjineerbaarheid van die gesinterde titaan in vergelyking swak is.

Thesis (PhD (Chemistry and Polymer Science))--Stellenbosch University, 2008. / Novel gold(I) trithiophosphite complexes were synthesised by utilising the ligands P(SR)3 (R = Me, Ph) and 1,2-bis(1,3,2-dithiaphospholan-2-ylthio)ethane (2L). Reaction with (tht)AuCl or (tht)AuC6F5 readily yielded the corresponding complexes (RS)3PAuX and 2L(AuX)2 (X = Cl, C6F5) as well as {Au[P(SMe)3]2}CF3SO3. Structural characterisation by X-ray diffraction revealed linear complexes in part associating by Au…Au and/or Au…S contacts, two polymorphs of one compound associating by either Au…S interactions or p-stacking was also obtained. (MeS)3PAuCl and (MeO)3PAuCl were found to be isostructural in the solid state. The complex chloro[tris(4-methylthiazol-2-yl)phosphane]gold, A, was used to probe the electronic influence tris(azol-2-yl)phosphanes exert upon gold(I) by substituting the chloride with various thiolates. In contrast to Ph3PAuCl, only NCS– and PhC(O)S– afforded stable compounds which could be attributed to a weaker donating capability of the tris- (azolyl)phosphane ligand class. The compounds A and chloro[tris(thiazol-2-yl)phosphane]- gold, B, were shown to crystallise in 4 new polymorphs and solvates bringing the total to an exceptional seven. Among the solid-state structures of A the rare instance of a polymorph and a thf solvate not exhibiting aurophilic interactions as opposed to the original structure were observed. Complex B was shown to crystallise in polymorphs where dimers are associated either by Au…Au or Au…Cl interactions but otherwise exhibit similar arrangements of the ligand, this set of polymorphs is unprecedented amongst gold complexes. An NMR experiment proved that tris(thiazolyl)phosphane complexes are subject to hydrolysis under alkaline conditions. A trimeric gold(I) heterometallacycle, obtained by reacting (tht)AuCl with 4,4-dimethyl-2-(2- thienyl)oxazoline deprotonated at C-5 of the thiophene ring, was structurally characterised. Intramolecular Au…S interactions were found to be present which precluded interaction of the gold atoms with other metal centres such as Me3CNCAuCl or AgNO3. A second solvate obtained additionally exhibits Au…Au interactions. The scope of uncommon bis-imine coordination to AuI was expanded by utilising 1,2-bis(1-imidazolylmethyl)-2,4,6-trimethylbenzene (2L) to synthesise the [Au2(μ-2L)2]2+ cation. The triflate salt forms the first porous crystal structure of gold and the co-crystallised solvent could be partially removed by evacuation at elevated temperatures. Utilising a ditopic phosphite ligand instead of the commonly used ditopic phosphane ligands, a new cationic species of the type [Au2(μ-2L)3]2+ was characterised in the solid state for the first time. Finally, employing 2-phenylthiazole and 1-(thiazol-2-yl)piperidine which can be deprotonated at C-5 of the thiazole ring, Fischer-type pentacarbonyltungsten carbeniate complexes were prepared and structurally characterised. Starting from these complexes, the analogous Fischertype methoxycarbene as well as carbyne complexes could be obtained by alkylation and formal oxide abstraction, respectively. The latter products readily formed dinuclear adducts with AuCl. A Fischer-type methoxycarbene could be transferred to AuI affording the first such gold(I) complex exhibiting Au…Au interactions in the solid state as well as a rare agostic Au…H interaction which was examined by low-temperature 1H NMR measurements. Transfer of the carbeniate ligand derived from 1-(thiazol-2-yl)piperidine to Ph3PAu+ afforded an aurated thiazole product (by an unprecedented loss of CO) which may be represented as a pseudoabnormal azolylidene complex owing to W(CO)5-coordination at a distant nitrogen. The carbeniate originating from 2-phenylthiazole, on the other hand, afforded, by rare W(CO)5- trapping and without CO-loss, a pseudo Fischer-type carbene complex. Carbene transfer to gold was complemented by the first transfers of rNHC ligands from chromium and tungsten to gold(I) affording a novel class of complexes, all of which were structurally characterised. This work bridges the unnatural divide created between Fischer and N-heterocyclic carbene complexes.