Low temperature consolidation of hydroxyapatite-reduced graphene oxide nano-structured powders

In this study, hydroxyapatite-reduced graphene oxide (HA-rGO) powders were first synthesized in situ using a hydrothermal method. These powders were then consolidated using a cold sintering method. The solvent used in this method was water + dimethylformamide + brushite which was added to the powder...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Materials advances 2020-08, Vol.1 (5), p.1337-1346
Hauptverfasser: Nosrati, Hassan, Sarraf-Mamoory, Rasoul, Zolfaghari Emameh, Reza, Le, Dang Quang Svend, Canillas Perez, Maria, Bünger, Cody Eric
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:In this study, hydroxyapatite-reduced graphene oxide (HA-rGO) powders were first synthesized in situ using a hydrothermal method. These powders were then consolidated using a cold sintering method. The solvent used in this method was water + dimethylformamide + brushite which was added to the powders at different ratios. The sintered samples were then evaluated using X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, high-resolution transmission electron microscopy, and Vickers microindentation. The results of this study showed that the best conditions for the sintering of rGO-HA nanopowders were a temperature of 200 °C, a holding time of >30 min, and a pressure of 500 MPa. The best mechanical properties were achieved when the solvent content was considered to be 20 wt%. Crack deflection and graphene bridging were among the mechanisms that increased the fracture toughness of these nanocomposites. By adding 1.5% rGO, the fracture toughness of this nanocomposite (using the cold sintering method) was approximately equivalent to that of spark plasma sintered HA. In this study, hydroxyapatite-reduced graphene oxide (HA-rGO) powders were first synthesized in situ using a hydrothermal method.
ISSN:2633-5409
2633-5409
DOI:10.1039/d0ma00212g