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Proceedings Papers
ITSC 2009, Thermal Spray 2009: Proceedings from the International Thermal Spray Conference, 103-108, May 4–7, 2009,
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In this study, the deposition, microstructure, and resistivity of APS and HVOF sprayed Cr 2 O 3 -TiO 2 coatings is systematically investigated. Commercially available Cr 2 O 3 -rich feedstock powders are used along with five agglomerated and sintered experimental powders on the TiO 2 -rich side. Both processes are found to produce homogeneous, low-porosity coatings with phase compositions that can be changed by adjusting process parameters. Coating hardness and electrical resistivity are found to depend heavily on Cr 2 O 3 content.
Proceedings Papers
ITSC 2004, Thermal Spray 2004: Proceedings from the International Thermal Spray Conference, 934-945, May 10–12, 2004,
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Extensive research activities were conducted over the last few years on coatings made of titanium oxide, an established material for thermally sprayed coating solutions. Multiple existing and potential applications are closely connected with the existence of different titanium dioxide modifications and the formation of suboxides. This provides a basis for discussions on the Ti-O phase diagram as well as the properties and conditions of formation of relevant phases. Coating microstructures, phase compositions and mechanical properties are discussed as a result of interactions of different spray powders in different spray conditions of atmospheric and vacuum plasma spraying (APS and VPS), as well as of high-velocity oxyfuel (HVOF) spraying. The discussion on applications is focused on electrically conductive coatings, coatings with photocatalytic properties and coatings for wear applications.
Proceedings Papers
ITSC 2004, Thermal Spray 2004: Proceedings from the International Thermal Spray Conference, 946-952, May 10–12, 2004,
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Titanium dioxide (TiO 2 ) has emerged as an excellent photocatalyst material for environmental purification about two decades ago but only recently few works have focused on the photocatalytic properties of sprayed titanium oxide coatings. So far, the role of oxygen deficiency which can appear as a result of the spray process or by use of titanium suboxide powders on the photocatalytic activity has not been investigated. Also the possible influence of the shear plane structure of titanium suboxides (Magnéli phases) on the photocatalytic activity was not taken into consideration. In the present work, the photocatalytic properties of three powders and coatings sprayed from these powders by APS and VPS are investigated: (1) a commercial fused and crushed titanium oxide powder, (2) an agglomerated and sintered titanium suboxide powder consisting predominantly of Magnéli phases Ti 6 O 11 and Ti 5 O 9 , (3) an agglomerated and sintered powder consisting of Ti 2 Cr 2 O 7 and Ti 6 Cr 2 O 15 (Magnéli phases in the TiO 2 - Cr 2 O 3 phase diagram). The phase compositions of the powders and the coatings were investigated by X-ray diffraction. Neither for the spray powders nor for the coatings any ability to reduce the NOx concentration by the photocatalysis was found. From this it is concluded that both oxygen deficiency as well as Magnéli phase structure are not responsible for photocatalytic properties of materials in the Ti-O phase diagram.
Proceedings Papers
ITSC 2001, Thermal Spray 2001: Proceedings from the International Thermal Spray Conference, 497-502, May 28–30, 2001,
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The properties of thermal sprayed coatings depend mainly on the thermal and kinetic energy of the spray particles. Increase of thermal energy of sprayed particles can be realized using exothermic reactions between components in sprayed particles. Self propagating high temperature synthesis (SHS) is especially suitable to benefit from released energy in the spraying process. At present most commonly used spray material with exothermal reaction is Ni+Al. However, the highest amount of heat is produced in the reactions of aluminium and metal oxides. Of special interest are Cr 2 O 3 , NiO, CuO and V 2 O 5 because they obtain high reaction energies. Furthermore products of the reaction are of special, functional interest like NiAl as bonding agent or alumina as a wear resistant coating. To assure good contact between reacting substances (Al/Oxides) powders for plasma spraying were prepared by mechanical alloying. Calorimetric investigations of plasma sprayed coatings prove that during spraying Al reacts exothermically with oxides. Increase of oxide contents improves coating adhesion/ cohesion properties, hardness, and reduction of porosity. Results are discussed on the base of light microscopy, scanning electron microscopy (SEM) and X-ray structure analysis (XRD).
Proceedings Papers
ITSC2000, Thermal Spray 2000: Proceedings from the International Thermal Spray Conference, 333-339, May 8–11, 2000,
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Effects of spray parameters, such as spray distance, SD, and substrate temperature, Ts, and post heat treatment on the structure and properties of plasma-sprayed zircon coatings were investigated. Zircon was totally decomposed by plasma spray; the coatings were composed of tetragonal zirconia (t-ZrO2) and amorphous silica (a-SiO2), because of the rapid cooling of molten particle right after the impingement to the substrate. Porosity of the as-sprayed coatings was highly affected by both of substrate temperature and spray distance. In all range of the spray distance which had been tried in this study, higher substrate temperature resulted in lower porosity of the coatings; the coating with porosity of 2% was obtained at Ts = 1573K with SD = 95mm. Porosity also decreased with decrease of spray distance. By the heat treatment at 1473K, t-ZrO2 transformed to monoclinic zirconia (m-ZrO2) and a-SiO2 crystallized to cristobalite, respectively. Cracks in the coating disappeared, and open porosity decreased. This can be attributed to sintering of SiO2 and phase transformation of ZrO2. After the heat treatment at 1673K, the coating was composed of ZrSiO4 with dispersed fine m-ZrO2 particle. Open porosity of all the coatings increased up to 10% at this temperature. This is because of volume shrinkage during the formation of zircon.