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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Darr, J. A.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (14/14 displayed)
- 2012Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesiscitations
- 2010Measure of microhardness, fracture toughness and flexural strength of N-vinylcaprolactam (NVC)-containing glass-ionomer dental cementscitations
- 2009Effects of N-vinylpyrrolidone (NVP) containing polyelectrolytes on surface properties of conventional glass-ionomer cements (GIC)citations
- 2009Synthesis of a proline-modified acrylic acid copolymer in supercritical CO2 for glass-ionomer dental cement applicationscitations
- 2008Effects of incorporation of hydroxyapatite and fluoroapatite nanobioceramics into conventional glass ionomer cements (GIC)citations
- 2008Synthesis and characterisation of magnesium substituted calcium phosphate bioceramic nanoparticles made via continuous hydrothermal flow synthesiscitations
- 2008Modification of conventional glass-ionomer cements with N-vinylpyrrolidone containing polyacids, nano-hydroxy and fluoroapatite to improve mechanical propertiescitations
- 2008Synthesis of N-vinylpyrrolidone modified acrylic acid copolymer in supercritical fluids and its application in dental glass-ionomer cementscitations
- 2007Preparation and characterisation of controlled porosity alginate hydrogels made via a simultaneous micelle templating and internal gelation processcitations
- 2007Formation of porous natural-synthetic polymer composites using emulsion templating and supercritical fluid assisted impregnationcitations
- 2007Synthesis and characterization of grafted nanohydroxyapatites using functionalized surface agentscitations
- 2006Recent developments in processing and surface modification of hydroxyapatitecitations
- 2005Surface modification of bioceramics by grafting of tailored allyl phosphonic acidcitations
- 2003Synthesis and characterization of nano-biomaterials with potential osteological applicationscitations
Places of action
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article
Synthesis and characterisation of magnesium substituted calcium phosphate bioceramic nanoparticles made via continuous hydrothermal flow synthesis
Abstract
Continuous hydrothermal flow synthesis (CHFS) technology has been used as an efficient and direct route to produce a range of largely crystalline magnesium substituted calcium phosphate bioceramics. Initially, magnesium substituted hydroxyapatite, Mg-HA, according to the formula [Ca 10-xMgx(PO4)6(OH)2] was prepared in the CHFS system for x = 0.2 [where x:(10 - x) is the Mg:Ca ratio used in the reagents]. Biphasic mixtures of Mg-HA and Mg-whitlockite were obtained corresponding to x values in the range x = 0.4-1.6. The direct synthesis of phase pure crystalline Mg-whitlockite [based on the formula (Ca3-yMgy(HPO4)z(PO 4)2-2z/3] was also achieved using the CHFS system for the range y = 0.7-1.6 (this corresponds to the range x = 1.6-5.3). With increasing substitution of magnesium for calcium, the material became ever more amorphous and the BET surface area generally increased. All the as-precipitated powders (without any additional heat treatments) were analyzed using techniques including X-ray powder diffraction, Raman spectroscopy and Fourier transform infra-red spectroscopy. Transmission electron microscopy (TEM) images revealed that in the case of y = 1.2, the Mg-whitlockite material comprised of ca. 28 nm sized spheres. The use of the CHFS system in this context facilitated rapid production of combinations of particle properties (crystallinity, size, shape) that were hitherto unobtainable in a single step process. © The Royal Society of Chemistry 2008.