National Repository of Grey Literature 4 records found  Search took 0.01 seconds. 
Silicon substituted calcium phosphate based bioceramic scaffolds
Karkuszová, Karina ; Šťastná, Eva (referee) ; Novotná, Lenka (advisor)
The theoretical part of this bachelor thesis summarizes the current state of knowledge of bioceramic materials based on calcium, phosphorus and silicon. More specifically, it focuses on calcium phosphates, the demands placed on them, the porosity of 3D foams, and biological properties such as biodegradation and bioactivity. 3D bioceramic calcium phosphate foam doped with silicon appears to be a suitable material for use in biomedical applications. It is the silicon that plays a role in the development of healthy bone and the formation of new tissue. Silicon substitutions are important in the field of investigation because they improve the bioassay of phosphate calcium. In the experimental part, calcium phosphate powders were first prepared by the hydroxyapatite and silica fusion reaction. Selected powder contents were 0; 0.1; 1, 2.5, 5, 10 and 20 wt.% SiO2. The samples were sintered at 1100 °C, 1200 °C and 1300 °C. The second part consisted in the preparation of 3D foams by direct penetration with polyurethane and the subsequent characteristics of phase composition, solubility and bioactivity. Bioceramic foams had a highly porous structure. For 42 days, sample behavior in Tris-HCl and simulated body fluid (SBF) was monitored. The results of the experiment have shown that the samples are bioactive and silicon substitution increases phosphate calcium solubility. Therefore, these materials are potentially useful for biomedical applications
Fabrication of ceramic materials for piezoelectric applications
Karkuszová, Karina ; Spusta, Tomáš (referee) ; Částková, Klára (advisor)
The content of this thesis is about preparation and processing of lead-free piezoceramic materials with perovskite structure. Potassium sodium niobate (KNN) powder was prepared by solid state reaction (SSR) and liquid phase reaction (sol-gel reaction). The powders were formed by uniaxial and isostatic pressing and further sintered. The density, grain size and morphology were determined on the sintered samples. The powder, synthesised by SSR and sintered in a conventional furnace, was chosen as a standard. The maximum density achieved on samples after optimization of sintering cycle was 93 %TD. The sintering optimization involved a homogenization step at 950 °C, which promotes the correct development of the phase composition and microstructure, followed by sintering at 1120 °C. The same approach and sintering cycle were used for sintering the samples, prepared by sol-gel synthesis. The maximum density of the samples prepared by sol-gel reaction and sintered in a conventional way, was 92 %TD. For further comparison, both of the synthesised powders were sintered using SPS (spark plasma sintering), which increased their final density up to 97 %TD. The approximate value of the piezoelectric coefficient d33 (pC/N) has been measured on selected SSR samples with pure phase composition ((K0,5Na0,5)NbO3). The best measured value of d33 was around 100 pC/N.
Fabrication of ceramic materials for piezoelectric applications
Karkuszová, Karina ; Spusta, Tomáš (referee) ; Částková, Klára (advisor)
The content of this thesis is about preparation and processing of lead-free piezoceramic materials with perovskite structure. Potassium sodium niobate (KNN) powder was prepared by solid state reaction (SSR) and liquid phase reaction (sol-gel reaction). The powders were formed by uniaxial and isostatic pressing and further sintered. The density, grain size and morphology were determined on the sintered samples. The powder, synthesised by SSR and sintered in a conventional furnace, was chosen as a standard. The maximum density achieved on samples after optimization of sintering cycle was 93 %TD. The sintering optimization involved a homogenization step at 950 °C, which promotes the correct development of the phase composition and microstructure, followed by sintering at 1120 °C. The same approach and sintering cycle were used for sintering the samples, prepared by sol-gel synthesis. The maximum density of the samples prepared by sol-gel reaction and sintered in a conventional way, was 92 %TD. For further comparison, both of the synthesised powders were sintered using SPS (spark plasma sintering), which increased their final density up to 97 %TD. The approximate value of the piezoelectric coefficient d33 (pC/N) has been measured on selected SSR samples with pure phase composition ((K0,5Na0,5)NbO3). The best measured value of d33 was around 100 pC/N.
Silicon substituted calcium phosphate based bioceramic scaffolds
Karkuszová, Karina ; Šťastná, Eva (referee) ; Novotná, Lenka (advisor)
The theoretical part of this bachelor thesis summarizes the current state of knowledge of bioceramic materials based on calcium, phosphorus and silicon. More specifically, it focuses on calcium phosphates, the demands placed on them, the porosity of 3D foams, and biological properties such as biodegradation and bioactivity. 3D bioceramic calcium phosphate foam doped with silicon appears to be a suitable material for use in biomedical applications. It is the silicon that plays a role in the development of healthy bone and the formation of new tissue. Silicon substitutions are important in the field of investigation because they improve the bioassay of phosphate calcium. In the experimental part, calcium phosphate powders were first prepared by the hydroxyapatite and silica fusion reaction. Selected powder contents were 0; 0.1; 1, 2.5, 5, 10 and 20 wt.% SiO2. The samples were sintered at 1100 °C, 1200 °C and 1300 °C. The second part consisted in the preparation of 3D foams by direct penetration with polyurethane and the subsequent characteristics of phase composition, solubility and bioactivity. Bioceramic foams had a highly porous structure. For 42 days, sample behavior in Tris-HCl and simulated body fluid (SBF) was monitored. The results of the experiment have shown that the samples are bioactive and silicon substitution increases phosphate calcium solubility. Therefore, these materials are potentially useful for biomedical applications

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