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- Bengtsson, Åsa, 1974-
(författare)
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Solubility and Surface Complexation Studies of Apatites
- 2007
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Apatites are a diverse class of phosphate minerals that are important in a great variety of natural and industrial processes. They are, for example, used as raw material in fertiliser production and in the remediation of metal-contaminated soils. Hydroxyapatite Ca5(PO4)3OH, (HAP) and fluorapatite Ca5(PO4)3F, (FAP) are similar to the biological apatite that is the main constituent of mammalian bone and teeth, and they are therefore promising materials for artificial bone and tooth implants. This thesis is a summary of four papers with focus on dissolution and surface complexation reactions of HAP and FAP in the absence and presence of both organic ligands and the natural and commonly occurring iron oxide goethite (α-FeOOH). The dissolution and surface complexation of HAP and FAP was investigated with a combination of different techniques. Potentiometric acid/base titrations and batch experiments were combined with X-ray Photoelectron Spectroscopy (XPS) and Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) Spectroscopy to generate dissolution and surface complexation models for both apatites. The results from these studies showed that both apatites form surface layers that are different from their bulk compositions when equilibrated in aqueous solutions. The modeling efforts predicted speciation of these surfaces as well as the concentration of the dissolution products in the solution. The interaction between organic ligands and the apatite surfaces was also investigated and the results from this study show that the organic ligands form outer-sphere complexes on the apatite surfaces over a large pH interval, and that this adsorption enhances the dissolution of apatites. The presence of goethite also enhances the dissolution of FAP as it acts as a sink for the phosphate released from FAP. Phase transformation in this system was detected using ATR-FTIR as the phosphate adsorbed to the goethite surface precipitates as FePO4 (s) after approximately 15 days of reaction time. This changes the speciation, and possibly also the bioavailability of phosphate in this two-mineral system.
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- Persson, Daniel H. E., 1974-
(författare)
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On the Mechanisms behind the Tribological Performance of Stellites
- 2005
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This thesis reveals the tribological mechanisms behind the intrinsic low friction potential of the Co-based family of alloys called Stellites. Although being an established and important group of materials, a satisfactory explanation to why they exhibit low-friction properties under severe sliding conditions has not previously been found in the literature. The main part of this thesis is dedicated to the clarification of the tribological performance of Stellites in highly loaded sliding contact. The results should assist the development of Co-free alternatives, suitable for replacing Stellites in nuclear applications. Owing to their beneficial properties they are today the most commonly used material in the sealing surfaces on gate valves in the primary circuits of boiling water reactors (BWR). The underlying reason for the replacement in the nuclear applications is an undesired contribution to the background radiation level, originating from the Co in the Stellite surfaces. The Stellites mainly consist of Cr-rich carbides in a solid solution dominated by Co. The commonly used Stellite 6 and Stellite 21 were chosen as primary test materials and applied by laser cladding, providing a metallically bonded clad layer with a fine dendritic microstructure. By combining information from a series of dedicated tribological tests and modern high-resolution analysis instruments (e.g. SEM, XRD and TEM) available at the Ångström Laboratory at Uppsala University, the following conclusions can be made regarding the tribological performance of Stellites under high load sliding. Mechanisms. The (tested) Stellites form a thick deformation hardened layer, topped with a superficial easily sheared layer of hcp basal planes aligned parallel to the worn surface. The easy-shear layer is continually regenerated, replacing worn off material. Technical benefits. The Stellites offer low-friction properties thanks to their easily sheared surface layers. The risk of severe galling is also avoided by restricting shear and adhesive transfer to very thin superficial layers. In closed sliding contacts, self-generated protective layers formed by re-deposition of wear fragments are also offered.
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