Hydroxyapatite nanoparticles formed under a wet mechanochemical method.

Hydroxyapatite (HA) nanoparticles were synthesized using a wet mechanochemical method without a calcination process. Dicalcium phosphate dihydrate (CaHPO ·2H O) and calcium carbonate (CaCO ) were mixed and milled in a planary mill using ethanol or water as liquid media in the two different synthesized routes. Effects of rotation speed and milling time on the final products formed have been studied.

Improving shear bond strength between feldspathic porcelain and zirconia substructure with lithium disilicate glass-ceramic liner.

This study investigated the shear bond strength (SBS) between veneering porcelain and zirconia substructure using lithium disilicate glass-ceramic as a liner. The mineral phases and microstructures of lithium disilicate glass-ceramic at temperature range of 800-900°C were preliminarily investigated. SBSs of porcelain-veneered zirconia specimens with and without lithium disilicate glassceramic liner fired at the same temperature were determined.

Preparation and characterization of hydroxyapatite/poly(ethylene glutarate) biomaterials.

Hydroxyapatite/poly(ethylene glutarate) (HAp/PEG) biomaterial composites were prepared by ring-opening polymerization (ROP) of cyclic oligo(ethylene glutarate) (C-PEG) in porous HAp scaffolds. The HAp/C-PEG precomposites were prepared by immersing the porous HAp scaffolds in the mixture solution of C-PEG and dibutyl tinoxide catalyst overnight and polymerizing at 200 degrees C for 24, 48, and 72 h under vacuum. The successful ROP of C-PEG in the porous HAp scaffolds was corroborated by the signals of hydroxyl end-group of PEG shown in the (1)H NMR spectrum of the ROP-products extracted from the composites.