Sintering atmosphere and temperature effects on hydroxyapatite coated type 316L stainless steel

Abstract Electrophoretically deposited hydroxyapatite (HAP) coatings on type 316L SS was developed at the optimum coating parameters of 60 V and 3 min. Sintering of the coating enhances the metal–ceramic bond strength, but HAP structure is sensitive to temperature as it decomposes to other calcium phosphate phases. Sintering of HAP coatings in air at 900 °C for 1 h indicate the formation of a composite surface containing oxides of the alloy and decomposition products of HAP, mainly tricalcium phosphate. Open circuit potential–time measurements, potentiodynamic cyclic polarisation and electrochemical impedance experiments performed in Ringer’s solution indicate that the corrosion performance of HAP coatings were severely affected by the sintering atmosphere and temperature. Higher capacitance and low polarisation resistance values obtained from electrochemical impedance spectroscopic studies further indicate that the coatings are more prone to dissolution on comparison with the pristine type 316L SS. The sintering of the coatings in vacuum at 600, 800 and 900 °C for 1 h did not alter the phase purity of the coatings, and shifted the electrochemical parameters towards noble direction. Sintering of the coatings in vacuum lead to the formation of an adherent, stoichiometric HAP coating with enhanced corrosion resistance.

[1]  D. Mears Materials and orthopaedic surgery , 1979 .

[2]  A. Joshi,et al.  Chemistry of Grain Boundaries and Its Relation to Intergranular Corrosion of Austenitic Stainless Steel , 1972 .

[3]  I. Zhitomirsky Electrophoretic hydroxyapatite coatings and fibers , 2000 .

[4]  A. Matthews,et al.  Deposition of layered bioceramic hydroxyapatite/TiO2 coatings on titanium alloys using a hybrid technique of micro-arc oxidation and electrophoresis , 2000 .

[5]  P. Sarkar,et al.  Electrophoretic Deposition (EPD): Mechanisms, Kinetics, and Application to Ceramics , 1996 .

[6]  R. Pilliar,et al.  Evaluation of biodegradable ceramic. , 1977, Journal of biomedical materials research.

[7]  E. Lerner,et al.  Rapid precipitation of apatite from ethanol-water solution , 1989 .

[8]  J. Wit,et al.  Electrochemical impedance spectroscopy as a tool to obtain mechanistic information on the passive behaviour of aluminium , 1996 .

[9]  P Ducheyne,et al.  Calcium phosphate ceramic coatings on porous titanium: effect of structure and composition on electrophoretic deposition, vacuum sintering and in vitro dissolution. , 1990, Biomaterials.

[10]  K. Seah,et al.  A comparison between the corrosion characteristics of 316 stainless steel, solid titanium and porous titanium , 1993 .

[11]  Bi-Cheng Wang,et al.  Mechanical and histological evaluations of cobalt-chromium alloy and hydroxyapatite plasma-sprayed coatings in bone , 1996 .

[12]  A. Cigada,et al.  Post-deposition treatment effects on hydroxyapatite vacuum plasma spray coatings , 1994 .

[13]  R. L. Elkins,et al.  Casing Corrosion in West Texas-New Mexico★ , 1953 .

[14]  P. Brown,et al.  α-Tricalcium phosphate hydrolysis to hydroxyapatite at and near physiological temperature , 2000, Journal of materials science. Materials in medicine.

[15]  R. Heimann,et al.  Bioceramic coatings; state-of-the art and recent development trends , 1997 .

[16]  A. Ruys,et al.  Sintering effects on the strength of hydroxyapatite. , 1995, Biomaterials.

[17]  B. Kasemo,et al.  Surface properties and processes of the biomaterial-tissue interface☆ , 1994 .

[18]  Larry L. Hench,et al.  Bioceramics: From Concept to Clinic , 1991 .

[19]  A. Conde,et al.  Intergranular corrosion of 8090 Al–Li: Interpretation by electrochemical impedance spectroscopy , 2000 .

[20]  J. Galante,et al.  Release and excretion of metal in patients who have a total hip-replacement component made of titanium-base alloy. , 1991, The Journal of bone and joint surgery. American volume.

[21]  T. Kijima,et al.  Preparation and Thermal Properties of Dense Polycrystalline Oxyhydroxyapatite , 1979 .

[22]  S. Rajeswari,et al.  Compatibility of ferritic and duplex stainless steels as implant materials: in vitro corrosion performance , 1993, Journal of Materials Science.

[23]  D. Thierry,et al.  Localized Electrochemical Impedance Spectroscopy for Studying Pitting Corrosion on Stainless Steels , 1997 .

[24]  M V Swain,et al.  Interfacial bond strength of electrophoretically deposited hydroxyapatite coatings on metals , 1999, Journal of materials science. Materials in medicine.

[25]  P. Ducheyne,et al.  Plasma spraying induced changes of calcium phosphate ceramic characteristics and the effect onin vitro stability , 1992 .

[26]  T. Chaki,et al.  Sintering behaviour and mechanical properties of hydroxyapatite and dicalcium phosphate , 1993 .

[27]  H. Skinner,et al.  Thermal instability in synthetic hydroxyapatites , 1975 .

[28]  J. Oldfield Test techniques for pitting and crevice corrosion resistance of stainless steels and nickel-base alloys in chloride-containing environments , 1987 .

[29]  R. Newman,et al.  Effects of Sulfur Compounds on the Pitting Behavior of Type 304 Stainless Steel in Near-Neutral Chloride Solutions , 1982 .

[30]  J. B. Gnanamoorthy,et al.  Influence of thermal aging on the intergranular corrosion resistance of types 304LN and 316LN stainless steels , 1996 .

[31]  S. Rajeswari,et al.  Investigation of failures in stainless steel orthopaedic implant device , 1994 .

[32]  P. Ducheyne,et al.  Effect of hydroxyapatite impregnation on skeletal bonding of porous coated implants. , 1980, Journal of biomedical materials research.

[33]  S. Uchida,et al.  Synthesis of monodispersed hydroxyapatite using calcium polyphosphate gels as precursors , 1998 .