The electronic structure of some transition metal compounds, specifically, Ca-doped LaMnO3, fundamental Mn oxides (MnO, Mn2O3, Mn3O4, and MnO2), and Fe-doped ZnO is studied using a combination of soft X-ray spectroscopy and atomic multiplet calculations. X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES) are used as experimental tools to probe the unoccupied and occupied partial density of electronic states,respectively.<p> Ca-doped LaMnO3 perovskites have attracted great attention due to their colossal magnetoresistance and a wide range of magnetic and structural transitions. The magnetic and charge transport properties of these perovskites are directly related with Mn 3d-occupancy or Mn-valency and therefore, an investigation of the Mn-valence at Ca-doped LaMnO3 system is important. In this system, the Mn-valency is generally considered as a mixture of Mn3+ and Mn4+. But my research suggests the presence of Mn2+ at the surface of Ca-doped LaMnO3 samples. It is observed that increasing Ca-doping decreases Mn2+ concentration, and conversely, increases Mn3+ concentration. High temperature annealing at 1000 °C in air leads to the full reduction of surface Mn2+. Mechanisms for these observations are proposed in this study.<p> Mn oxides (MnO, Mn2O3, Mn3O4, and MnO2) are often used as reference standards for determining the Mn-valency in Mn-related complex systems and therefore a detailed understanding of their electronic structure is necessary. The Mn L2,3 XAS and O K XAS are measured for the four Mn oxides consisting of three common Mn oxidation states (Mn2+ in MnO, Mn3+ in Mn2O3, mixture of Mn2+ and Mn3+ in Mn3O4, and Mn4+ in MnO2). A significant energy shift with a systematic trend is observed in measured Mn L2,3 and O K absorption edges. These energy shifts are identified as a characteristic shift for different Mn oxidation states. Mn L2,3 Resonant Inelastic X-ray Scattering (RIXS) spectroscopy is demonstrated as a powerful tool in describing low energy excitations, e.g. d-d excitations and charge-transfer excited states in Mn oxides. For the first time, a RIXS study of Mn2O3,Mn3O4, and MnO2 is accomplished. Atomic multiplet calculations are used to successfully reproduce the energy positions and intensity variations of d-d excitation peaks observed in the experiment, and thus to describe the experimental RIXS spectra.<p> Finally, the local electronic structure of Fe implanted ZnO samples, a useful diluted magnetic semiconductor for spintronics, is investigated to shed light on the existing debate about the origin of ferromagnetism in these materials. Fe L2,3 XAS reveals that doped Fe ions are present in both Fe2+ and Fe3+ valence states. A combined theoretical and experimental study shows that doped ions are incorporated into Zn-sites of ZnO in tetrahedral symmetry. Fe L3- RIXS measurements demonstrate that a high Fe-ion dose of 8 × 107 cm-2 causes formation of FeO clusters, while low dose samples exhibit more free carriers.

Flying-wing aircraft are considered to have great advantages and potentials in aerodynamic performance and weight saving. However, they also have many challenges in design. One of the biggest challenges is the structural design of the inner wing (fuselage). Unlike the conventional fuselage of a tube configuration, the flying-wing aircraft inner wing cross section is limited to a noncircular shape, which is not structurally efficient to resist the internal pressure load. In order to solve this problem, a number of configurations have been proposed by other designers such as Multi Bubble Fuselage (MBF), Vaulted Ribbed Shell (VLRS), Flat Ribbed Shell (FRS), Vaulted Shell Honeycomb Core (VLHC), Flat Sandwich Shell Honeycomb Core (FLHC), Y Braced Box Fuselage and the modified fuselage designed with Y brace replaced by vaulted shell configurations. However all these configurations still inevitably have structural weight penalty compared with optimal tube fuselage layout. This current study intends to focus on finding an optimal configuration with minimum structural weight penalty for a flying-wing concept in a preliminary design stage. A new possible inner wing configuration, in terms of aerodynamic shape and structural layout, was proposed by the author, and it might be referred as ‘Wave-Section Configuration’. The methodologies of how to obtain a structurally efficient curvature of the shape, as well as how to conduct the initial sizing were incorporated. A theoretical analysis of load transmission indicated that the Wave-Section Configuration is feasible, and this was further proved as being practical by FE analysis. Moreover, initial FE analysis and comparison of the Wave-Section Configuration with two other typical configurations, Multi Bubble Fuselage and Conventional Wing, suggested that the Wave-Section Configuration is an optimal design in terms of weight saving. However, due to limitations of the author’s research area, influences on aerodynamic performances have not yet been taken into account.

In this Thesis the magnetic and structural properties of thin epitaxial Fe, Co, and Ni films are discussed. Some of the in-situ prepared samples were used to characterize the degree of circular polarization of the newly installed beamline D1011 at MAX-lab. By means of x-ray magnetic circular dichroism (XMCD) and utilizing the associated magneto optic sum rules, the orbital (ml) and spin (ms) moments are determined directly in mB/atom with elemental specificity. The extended x-ray absorption fine structure (EXAFS) measurements yield site specific information on the local crystallographic structure. These measurements were performed using the circular x-rays of several beamlines. The influence of the degree of spatial source coherence lspat of the x-rays was characterized by means of Fresnel diffractometry. A correlation between enhanced XAS white line intensities and higher values of lspat was established for 20 ML Fe, Co, and Ni films on Cu(100). The degree of circularly polarized x-rays (Pc) at beamline D1011 at MAX-lab was characterized by studying Fe films on Cu(100) by means of XMCD. The maximum value of Pc is experimentally determined to Pc =0.85. The Au/Co/Au trilayer system was studied as a function of Co thickness, temperature, and Au cap thickness. A 10 mono-layer (ML) Co film, with an Au cap of 20 Å, shows a spin reorientation transition (SRT) from an in-plane to an out-of-plane easy direction as the temperature is lowered from 300 K to 200 K. The magnetic properities of these Co films are very different to what is found for bulk samples due to, in particular, the broken symmetry at the interfaces. The thickness dependent spin reorientation transition in the Fe/Ag(100) system was characterized by means of XMCD and EXAFS measurements. 3 ML Fe films show an out-of-plane easy direction with an 125% enhanced orbital moment as compared to the 25 ML Fe in-plane film. Simulations of the Fe L-edge EXAFS indicate the bulk Fe bcc structure for film thicknesses of 6-25 ML Fe. For 3 ML Fe strong deviations from this bcc phase is observed. Ultrathin Co films deposited on flat and vicinal Cu(111) in the thickness region 1-25 ML were studied by means of XMCD and scanning tunneling microscopy (STM). The vicinal Cu(111) Co deposition leads to the formation of elongated islands preferentially oriented along the step edges. In connection to this particular Co growth mode we observe an increase of both the orbital and the spin moment on the vicinal Cu(111) of about 25% relative to what was observed for Co on flat Cu(111).

In this thesis the magnetic and structural properties of ultra-thin 3d transition metals films have been investigated, in particular Fe, Ni and Co films. X-ray Magnetic Circular Dichroism (XMCD) has provided element specific spin (ms ) and orbital (ml ) moments per atom by utilizing the magneto optic sum-rules. Element specific hysteresis curves have been measured by means of X-ray Resonant Magnetic Scattering (XRMS), and the local crystallographic structure has been investigated using Extended X-ray Absorption Fine Structure (EXAFS). By performing XMCD on Fe/Ag(100) we observe a spin reorientation from in-plane to out-of-plane as the Fe thickness is lowered. At temperatures below 300K it occurs around 5-7 mono layers (ML) of Fe. While reorienting the magnetization out-of-plane the orbital moment increases with 125% but only a minor increase (5%) of the spin moment is observed. Extended X-ray Absorption Fine Structure (EXAFS) measurements indicate that films 6 ML and thicker have a bulk-like bcc structure. For the thin out-of-plane films, the local crystallographic structure is more complicated. The spin reorientation of the Au/Co/Au tri-layer system has been studied as a function of temperature, Co layer and Au cap thickness. An unexpected behavior of the orbital moment upon spin reorientation is found in these systems. An ex-situ prepared sample shows a smooth spin reorientation from an in-plane to an out-of-plane easy magnetization direction as the temperature is lowered from 300K to 200K. In-situ prepared samples have also been investigated and a novel phase diagram has been identified. The Au/Co interface has been explored during the Au capping by means of photoemission measurements. In the bi- and tri-layer system of Fe and Ni we have been able to manipulate the spin reorientation by varying the Fe and Ni thickness. A novel non-collinear interlayer exchange interaction for 3d ferro magnets in direct contact has been discovered for a set of samples. This exchange interaction is found to be strongly dependant on the preparation conditions.

Abstract The purpose of this research is to investigate the influence of Manganese (Mn) on cast aluminum alloys where a substantial amount of Iron (Fe) is included. Ductility and tensile strength need to be improved in recycled aluminum alloys where greater amounts of Fe are found. Fe is a common impurity and is known to be detrimental to mechanical properties and in order to neutralize the effects of Fe; modifiers such as Mn are added. In this investigation, attempts will be carried out aiming to find the optimal amount of Mn. Other related topics that will be discussed are whether there exists a Mn/Fe ratio which clearly modifies the harmful iron- rich phases and improves the properties for a certain alloy or not. Also, will the heat treatment have a significant effect on mechanical properties? These are some of the questions that will be answered in this paper. It is hard to find research articles that focus only on the influence of Mn on the microstructure and mechanical properties of Al-Si cast alloys. Much of the work that is already published concerns only a specific alloy and casting method. In this work three different casting processes, sand-, die- and high pressure die-casting, will be simulated by using gradient solidification equipment. Furthermore, the influence of heat treatment on the mechanical properties will be examined. The results showed that the solidification rate had the biggest impact on the microstructure and mechanical properties of the alloys, where the fastest cooling rate gave the best results. The effect of Mn seems to influence the samples with coarser microstructures significantly where it had time to modify the Iron-rich needles, also called the β-phase. At higher cooling rates the impact of Mn was impeded. It has been observed that a high content of Mn (around 0.6%) needs to be added before the properties start to improve. UTS (Ultimate Tensile Strength) and YS (Yield Strength) are improved while ductility is lowered. Heat treatment did not seem to have any influence on the effects of Mn.

The electronic structure of some transition metal compounds, specifically, Ca-doped LaMnO3, fundamental Mn oxides (MnO, Mn2O3, Mn3O4, and MnO2), and Fe-doped ZnO is studied using a combination of soft X-ray spectroscopy and atomic multiplet calculations. X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES) are used as experimental tools to probe the unoccupied and occupied partial density of electronic states,respectively.<p> Ca-doped LaMnO3 perovskites have attracted great attention due to their colossal magnetoresistance and a wide range of magnetic and structural transitions. The magnetic and charge transport properties of these perovskites are directly related with Mn 3d-occupancy or Mn-valency and therefore, an investigation of the Mn-valence at Ca-doped LaMnO3 system is important. In this system, the Mn-valency is generally considered as a mixture of Mn3+ and Mn4+. But my research suggests the presence of Mn2+ at the surface of Ca-doped LaMnO3 samples. It is observed that increasing Ca-doping decreases Mn2+ concentration, and conversely, increases Mn3+ concentration. High temperature annealing at 1000 °C in air leads to the full reduction of surface Mn2+. Mechanisms for these observations are proposed in this study.<p> Mn oxides (MnO, Mn2O3, Mn3O4, and MnO2) are often used as reference standards for determining the Mn-valency in Mn-related complex systems and therefore a detailed understanding of their electronic structure is necessary. The Mn L2,3 XAS and O K XAS are measured for the four Mn oxides consisting of three common Mn oxidation states (Mn2+ in MnO, Mn3+ in Mn2O3, mixture of Mn2+ and Mn3+ in Mn3O4, and Mn4+ in MnO2). A significant energy shift with a systematic trend is observed in measured Mn L2,3 and O K absorption edges. These energy shifts are identified as a characteristic shift for different Mn oxidation states. Mn L2,3 Resonant Inelastic X-ray Scattering (RIXS) spectroscopy is demonstrated as a powerful tool in describing low energy excitations, e.g. d-d excitations and charge-transfer excited states in Mn oxides. For the first time, a RIXS study of Mn2O3,Mn3O4, and MnO2 is accomplished. Atomic multiplet calculations are used to successfully reproduce the energy positions and intensity variations of d-d excitation peaks observed in the experiment, and thus to describe the experimental RIXS spectra.<p> Finally, the local electronic structure of Fe implanted ZnO samples, a useful diluted magnetic semiconductor for spintronics, is investigated to shed light on the existing debate about the origin of ferromagnetism in these materials. Fe L2,3 XAS reveals that doped Fe ions are present in both Fe2+ and Fe3+ valence states. A combined theoretical and experimental study shows that doped ions are incorporated into Zn-sites of ZnO in tetrahedral symmetry. Fe L3- RIXS measurements demonstrate that a high Fe-ion dose of 8 × 107 cm-2 causes formation of FeO clusters, while low dose samples exhibit more free carriers.

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This paper aims to create a hard modification layer of WC/Co/Fe on the surface of SKD11 work steel by using a new closed-type method of surface electrical discharge coating with the self-made tool electrode and CNC electrical discharge machine. The tool electrode is the composition of a semi-sintered powder compacted electrode and a cooper rod. The sintered powder compacted electrode making process is first to mix the WC/Co and Fe powders uniformly at 8:1, 4:1, 2:1 and 1:1 in weight ratio. Continually, it will form the cylinder of 8mm in diameter and 18mm in length approximately by compacting in different pressure (50~200 MPa) and sintering temperature (300~900 ¢J). The EDM condition is 1~12A discharge current, 25~500£gs pulse time, and 50% duty factor. The electrical discharge machining is proceeding in kerosene with tool electrode as cathode and workpiece as anode. The result is as following. It can be concluded that the best condition to fabricate the sintered powder compacted electrode is 1:1 in weight ratio between WC/Co and Fe powders; with 200Mpa compacting pressure and sintering temperature at 900¢J, which results in lowest electrical resistivity. Under such condition, the area covered ratio can reach 100% at best EDM condition, which is pulse time £non = 50 £gs, rest time £noff = 50 £gs, 8A in current and 1.5 min in machining time. The surface hardness of workpiece increases with machining time. The surface hardness dramatically increases to Hv1500 as machining time over 1.5 min. The hardness of modification layer equals to the WC/Co particle itself which brings to the best wear ability. Moreover, the hardness of under surface in between 48 £gm is much higher than it of the SKD11 work steel. The hardness in between 30 £gm can reach up to Hv1200 in particular. The hardness of surface modification layer increases linearly with machining time. However, the limit of surface modification layer is about 30 £gm, and the needed time is below 5 min.

No description available.

Iron-based degradative solidification/stabilization (Fe(II)-DS/S) is a treatment method that could be economically applied to smaller DNAPL-contaminated sites and to those sites with impermeable soils. Reductive dechlorination is achieved by compounds that are formed by reaction of ferrous iron with components of Portland cement or with defined chemicals (FeCl3 + Ca(OH)2). These dechlorinating agents can effectively degrade chlorinated hydrocarbons (PCE, TCE, and 1,1,1-TCA) that are dissolved in aqueous solution. This research investigated the application of Fe(II)-DS/S to remove chlorinated hydrocarbons that are present as DNAPLs in source zones and to compared the reactivity of ferrous iron in different mixtures, including the conventional mixture with cement (Fe(II)+C) and an iron-solid mixture (ISM) that was synthesized without the addition of cement. The modified first-order model, which the rate was proportional to the concentration of target in the aqueous phase and it was also nearly constant when DNAPL was present, was developed to describe dechlorination kinetics. The modified second-order model assumed that the rate was proportional to the product of the concentration of target in the aqueous phase and the concentration of reductive capacity of the solid reductant. The modified first-order model was used to describe degradation of target compounds with ISM, and the modified second-order model was used to describe removals for TCE and 1,1,1-TCA with Fe(II)+C. Results of experiments on PCE dechlorination with ISM indicated that the increase of Fe(II) in ISM increased rate constants and decreased the solubility of targets. The half-life was increased with increasing total PCE concentration. The product analysis implied that degradation of PCE with ISM was via a combination of the hydrogenolysis and β-elimination pathways. A comparison of the types of targets and reductants indicated that Fe(II)+C had better reactivity for chlorinated ethenes (PCE and TCE) than ISM. However, ISM could dechlorinate a chlorinated ethane (1,1,1-TCA) as rapidly as Fe(II)+10%C. The ratio of [RC]o/[Fe(II)]o implied that Fe(II) in Fe(II)+C was more involved in reducing chlorinated ethenes than was Fe(II) in ISM. Dechlorination of a DNAPL mixture followed the same order of reactivity as with individual DNAPLs with both reductants.