Search PubMed⌕ Search

PubMed · 1662738

Hydroxylapatite prosthesis.

Also available from

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J J Grote. 1991. Hydroxylapatite prosthesis.. https://doi.org/10.1288/00005537-199009000-00019

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Solution deposition of hydroxyapatite on titanium pretreated with a sodium ion implantation.

Titanium surfaces were treated by exposing them to a beam of sodium ions. Sodium titanate was shown to be incorporated within the oxidic titanium surface. The ion-implanted surfaces were examined for their reactivity by immersion in a simulated body fluid, which showed the formation of surface-bound hydroxyapatite. The surface was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and optical and electron microscopy. The surface hydroxyl concentration was determined using the nuclear reaction (1)H((15)N, alpha gamma)(12)C. Surface-related parameters that may affect hydroxyapatite nucleation are discussed in terms of the electrical double layer.

Durapatite↗

Spark plasma sintering of hydroxyapatite powders.

Dense hydroxyapatite (HA) compacts have been successfully fabricated by a spark plasma sintering (SPS). The sintering behavior of HA powders at different temperatures ranging from 850 degrees C to 1100 degrees C was studied. Results showed that spark plasma sintering resulted in rapid densification to near theoretical density. The HA compact was homogeneously sintered at 950 degrees C in a short sintering duration of 5 min, while maintaining high quality and high relative density (>99.5%). The density, microhardness and Young's modulus of HA sintered compact initially increased with the sintering temperature, reached a maximum value at around 950-1000 degrees C, then decreased with further increase in the temperature due to the decomposition of HA into beta-tricalcium phosphates. Fracture toughness results showed no significant difference with increasing temperature due to the combined influences of density and grain size. Microstructure analysis showed no noticeable grain growth under different sintering temperatures due to the short time exposure at high temperatures.

Durapatite↗

Use of coupling agents to enhance the interfacial interactions in starch-EVOH/hydroxylapatite composites.

Different zirconate, titanate and silane coupling agents were selected in an effort to improve the mechanical properties of starch and ethylene-vinyl alcohol copolymer (EVOH) hydroxylapatite (HA) composites, through the enhancement of the filler particles-polymer matrix interactions and the promotion of the interfacial adhesion between these two phases. The mechanical performance was assessed by tensile tests and discussed on the basis of the respective interfacial morphology (evaluated by scanning electron microscopy). The main relevant parameters were found to be the surface properties and reactivity of the filler (non-sintered HA) and the chemical nature (pH and type of metallic centre) of the added coupling agent. Significant improvements in the stiffness were achieved (about 30% increase in the modulus) when using the acidic zirconate coupling agents. The acidic zirconate combined the capability of crosslinking the polymer matrix with the establishment of donor-acceptor interactions and hydrogen bonding between it and the ceramic particles, leading to very good interfacial adhesion. The optimization of these coupling processes associated with the introduction of higher amounts of filler, may be an effective way to produce composites with mechanical properties analogous to those of the human cortical bone.

Durapatite↗