Papers by Author: Hwan Kim

Abstract: Dissolving behavior of hydroxyapatite ceramics prepared from bovine teeth (BTHA) was investigated. The bovine teeth were soaked in 0.1 M of NaOH at 80°C for 1 h. After soaking, the teeth were calcined at 800°C for 1 h, and then they were attritor-milled for 24 h. BTHA powder consisted of mainly HA and small amount of MgO. The powders obtained were cold isostatically pressed and sintered at 1200°C with a dwell time of 1 h. Sintered density of BTHA was about 70%. After polishing the surface of sintered specimen, BTHA was immersed in buffered water at 37°C for 3 and 7 days. After immersion period, there is no evidence of dissolution for BTHA at the end of the immersion time. In addition, there is no change of peak intensity in XRD after immersion time. It was found that hydroxyapatite from bovine teeth was more stable than commercial HA in liquid environment.

Abstract: Hydroxyapatite derived from human teeth was sintered at 1200°C for 2 h. Dissolving behavior of the biologically derived HA (BHA) in distilled water was investigated and compared with an artificial hydroxyapatite (HA) made of synthetic HA powder. All disks were immersed in 40 ml of pH 7.4 distilled water (buffered using 0.05 M Tris.) for 7 and 14 days at 37°C. All detectable peaks in the HA are identical only to HA lattice planes, whereas BHA consisted of a mixture of HA and β-tricalcium phosphate (TCP). In the case of the HA specimen, the surface dissolution was initiated at grain boundaries followed by generated many separated grains and large defect like cavities. On the other hand, biologically derived HA showed that definite grains considered as β-TCP was predominantly dissolved and the grains were separated from the matrix leaving pores. In the mean time, the rest region, mainly consisting of HA, did not show any evidence of dissolution. It seems that BHA is more stable than the artificial HA in liquid environment.

Abstract: Homogeneous precipitated calcium carbonate(PCC) was synthesized by calcinations, hydration and carbonation of limestone which has been deposited in Danyang, Korea. In the reaction process, shapes(scalenohedral and cubic) and sizes(0.2~0.3μm and 2.0μm) of the powder were controlled by reaction temperature. Synthesized PCC was applied to hand-made paper as filler and coated paper. For the prepared papers, physical/optical properties(brightness, whiteness, opacity, roughness, gloss, tensile strength, internal tearing strength, stiffness, bursting strength) and printability(ink gloss, ink set-off, dry pick, wet pick) were characterized

Abstract: The purpose of this work is to influence of CaO concentrations of 5.0 wt.% and 10.0 wt.%, slurry feeding rate of 200~400
/min, rotating rate of drum of 5,000 and 10,000 rpm, inlet and outlet temperature on the synthesis of Ca(OH)2 powder, and the synthesis of precipitated calcium carbonate by carbonation process using Ca(OH)2 prepared by spray drying method. As the feeding rate of slurry was increased, the particle size of Ca(OH)2 was decreased. Regardless of rotating rate of drum, when the concentration of CaO was 5.0 wt.% and 10.0 wt.%, the morphology of Ca(OH)2 showed spherical shape of 10~30 μm and 20~60 μm, respectively. The specific surface area of synthesized Ca(OH)2 was 27~30 m2/g. When the initial reaction temperature was 11 °C and 30 °C, the shape and particle size of precipitated calcium carbonate synthesized in the carbonation process showed the rectangular shape of 0.1~0.4 μm and the spindle shape of 0.5~1.0 μm, respectively.