DocumentCode
164064
Title
Selecting super hydrophilic phosphate masses coatings electrodeposited on titanium for medical applications
Author
Romonti, D. Covaciu ; Anghel, G. ; Voicu, G.
Author_Institution
Fac. of Appl. Chem. & Mater. Sci., Univ. Politeh. of Bucharest, Bucharest, Romania
fYear
2014
fDate
13-15 Oct. 2014
Firstpage
113
Lastpage
116
Abstract
In order to elaborate a very strong hydrophilic phosphate masses coating on titanium, an electrodeposition method was performed after polishing, etching and ultrasonication of samples. Electrodeposition took place in three electrodes cell at different working parameters (time and temperature). After electrodeposition all samples were calcinated for 1 hour at 4000C, in order to increase the crystalinitty and the purity. The coating characterization has included FT-IR SEM, XRD, AFM, and contact angle determinations and has indicated a rough coating with plaques crystals and small needles of HAP, good ratio Ca/P, and superhydrophilic character. The high surface energy denotes good bioadhesion.
Keywords
Fourier transform spectra; X-ray diffraction; atomic force microscopy; calcination; contact angle; electrochemical electrodes; electrodeposition; etching; hydrophilicity; infrared spectra; polishing; scanning electron microscopy; surface energy; titanium; AFM; FTIR spectra; SEM; Ti; XRD; bioadhesion; calcination; contact angle; crystalinitty; electrode cell; electrodeposition method; etching; medical application; plaques crystal; polishing; super hydrophilic phosphate masses coating; surface energy; temperature 400 degC; time 4 hour; ultrasonication; Coatings; Materials; Scanning electron microscopy; Surface treatment; Titanium; X-ray scattering; AFM; SEM; XRD; contact angle; electrochemical deposition; hydroxyapatite; titanium;
fLanguage
English
Publisher
ieee
Conference_Titel
Semiconductor Conference (CAS), 2014 International
Conference_Location
Sinaia
ISSN
1545-827X
Print_ISBN
978-1-4799-3916-9
Type
conf
DOI
10.1109/SMICND.2014.6966408
Filename
6966408
Link To Document