TY - JOUR
T1 - Formation characteristics of calcium phosphate deposits on a metal surface by H2O2-electrolysis reaction under various conditions
AU - Kanamoto, Kazuaki
AU - Imamura, Koreyoshi
AU - Kataoka, Nobuhide
AU - Oshitani, Jun
AU - Imanaka, Hiroyuki
AU - Nakanishi, Kazuhiro
N1 - Funding Information:
This work was supported by the Industrial Technology Research Grant Program in 2003–2005 from the New Energy and Industrial Technology Development Organization (NEDO) of Japan and Core-To-Core Program of Japan Society for the Promotion of Science, “Advanced Powder Technology.”
PY - 2009/10/20
Y1 - 2009/10/20
N2 - The cathodic electrolysis of H2O2 (H2O2 + e- → OH- + {radical dot}OH) on a metal surface in the presence of calcium and phosphate ions results in the formation of calcium phosphate deposits on the metal surface. In this study, the deposits formed under various treatment conditions (pHs, concentrations and ratios of calcium/phosphate ions, and so on) were characterized by scanning electron spectroscopy (SEM), and X-ray diffractometry. The exclusive formation of hydroxyapatite, HAP, was observed under comparatively narrow conditions (pH 3-4, [Ca+]/[PO43-] = 25 mM/15 mM), which is clearly different from the reported conditions for the deposition of HAP on titanium substrates. HAP was deposited in the form of a layer, comprised of morphologically amorphous HAP flakes that were less than 20 nm thick. SEM and FTIR analyses of the deposit at different stages of H2O2-electrolysis revealed that a few dozen nanometer-sized spheres of amorphous calcium phosphate were formed in the first step and then fused with each other to form ribbon-like flakes of HAP or broken glass-like brushite, depending on the pH. The pH for HAP formation on a stainless steel surface was markedly lower than that used for titanium, and the observed process by which amorphous calcium phosphate is converted to HAP was markedly different from that for the electrochemical deposition (electrolysis of water) of HAP on a titanium substrate.
AB - The cathodic electrolysis of H2O2 (H2O2 + e- → OH- + {radical dot}OH) on a metal surface in the presence of calcium and phosphate ions results in the formation of calcium phosphate deposits on the metal surface. In this study, the deposits formed under various treatment conditions (pHs, concentrations and ratios of calcium/phosphate ions, and so on) were characterized by scanning electron spectroscopy (SEM), and X-ray diffractometry. The exclusive formation of hydroxyapatite, HAP, was observed under comparatively narrow conditions (pH 3-4, [Ca+]/[PO43-] = 25 mM/15 mM), which is clearly different from the reported conditions for the deposition of HAP on titanium substrates. HAP was deposited in the form of a layer, comprised of morphologically amorphous HAP flakes that were less than 20 nm thick. SEM and FTIR analyses of the deposit at different stages of H2O2-electrolysis revealed that a few dozen nanometer-sized spheres of amorphous calcium phosphate were formed in the first step and then fused with each other to form ribbon-like flakes of HAP or broken glass-like brushite, depending on the pH. The pH for HAP formation on a stainless steel surface was markedly lower than that used for titanium, and the observed process by which amorphous calcium phosphate is converted to HAP was markedly different from that for the electrochemical deposition (electrolysis of water) of HAP on a titanium substrate.
KW - Amorphous
KW - Calcium phosphate
KW - Cathodic electrolysis
KW - Hydrogen peroxide
KW - Hydroxyapatite
KW - Stainless steel
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U2 - 10.1016/j.colsurfa.2009.09.007
DO - 10.1016/j.colsurfa.2009.09.007
M3 - Article
AN - SCOPUS:70349783552
SN - 0927-7757
VL - 350
SP - 79
EP - 86
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
IS - 1-3
ER -