Papers by Author: Iis Sopyan

Abstract: Nanocrystalline hydroxyapatite (HA) powder was synthesized by a simple heating process involving simple chemical reaction. The characterization of the produced powder showed that the powder is nanosize with particle in the range of 30-70 mm in diameter and almost evenly spherical in shape. The powder also has a high surface area of 43.16 m2/g. Field Emission Scanning Electron Microscopy (FESEM) observation showed the crystallite and particle size become bigger with an increment of calcination temperature, indicating increasing of crystallinity.. FESEM observation showed the particle size become bigger with an increment of calcinations temperature. It is in agreement with the crystallite size analysis, obtained by Scherer’s formula and particle size analysis, measured by nanoSizer. X-ray Diffraction (XRD) and Fourier Transform Infra Red Spectroscopy (FTIR) analyses exhibited the same result, where HA phase was clearly observed at at various temperatures up to 600 ̊C. However, at temperature more than 600 ̊C, Tri calcium phosphate (TCP) phase appeared suppressing the HA phase, producing biphasic calcium phosphate.

Abstract: The effect of irradiation on the mechanical properties of Epoxidized Natural Rubber/Ethylene Vinyl Acetate/Carbon Nanotubes (ENR/EVA/CNTs) nanocomposites were investigated. CNTs at various amount (2, 3, 4 and 6 wt%) were incorporated into ENR50 by solvent casting method. The ENR/CNTs were then blended with EVA by mixing in a Brabender Plasticoder at 120°C. Next, the samples were irradiated by using electron beam with 3 MeV electron beam machine in a dose range of 50 to 200 kGy. The mechanical properties such as tensile strength (Ts), modulus at 100% elongation (M100), elongation at break (Eb) and hardness of reinforced ENR/EVA/CNTs nanocomposites were studied as a function of radiation dose. It was found that, the Ts and M100 has increased almost 2 times compared to the nanocomposites without irradiation up to 150 kGy dose of radiation, and a downward trend thereafter. Gel fraction further confirmed the powerful energy of electron beam radiation result in irradiation-induced crosslinking and further enhanced mechanical properties of the nanocomposites.

Abstract: The effect of irradiation on the mechanical properties of Epoxidized Natural Rubber/Ethylene Vinyl Acetate/Carbon Nanotubes (ENR/EVA/CNTs) nanocomposites were investigated. CNTs at various amount (2, 3, 4 and 6 wt%) were incorporated into ENR50 by solvent casting method. The ENR/CNTs were then blended with EVA by mixing in a Brabender Plasticoder at 120°C. Next, the samples were irradiated by using electron beam with 3 MeV electron beam machine in a dose range of 50 to 200 kGy. The mechanical properties such as tensile strength (Ts), modulus at 100% elongation (M100), elongation at break (Eb) and hardness of reinforced ENR/EVA/CNTs nanocomposites were studied as a function of radiation dose. It was found that, the Ts and M100 has increased almost 2 times compared to the nanocomposites without irradiation up to 150 kGy dose of radiation, and a downward trend thereafter. Gel fraction further confirmed the powerful energy of electron beam radiation result in irradiation-induced crosslinking and further enhanced mechanical properties of the nanocomposites.

Abstract: Porous tri-calcium phosphate which is to be applied as artificial bone was prepared via protein consolidation method and egg yolk is used to give binding effect as well as to create porosity. In this experiment, fractions of egg yolk is controlled from 50 wt%, 60 wt%, 70wt% and 80 wt% and the mixture of egg yolk and tri-calcium phosphate powder were dried at 60 °C before undergone uniaxial compaction method. Subsequently, pressure of 68.5 MPa is given to the mold to produce cylindrical shape samples with diameter to height ratio of 1:2. Samples were then sintered at 1100°C to achieve porous tri-calcium phosphate. This method produces porous tri-calcium phosphate with desired porosity of 20-54.5% and acceptable compressive strength between 0.7-0.07 MPa. Besides, microporosity of 0.4-1μm and macroporosity in the range of 100-800μm were successfully obtained from this method.

Abstract: In the present work, densification of synthesised hydroxyapatite (HA) bioceramic prepared via chemical precipitation method was investigated. HA samples was prepared by compaction at 200 MPa and sintered at temperatures ranging from 800°C to 1400°C. The results revealed that the HA phase was stable for up to sintering temperature of 1250°C. However, decomposition of HA was observed in samples sintered at 1300°C with the formation of tetra-calcium phosphate (TTCP) and CaO. Samples sintered above 1400°C were found to melt into glassy phases. The bulk density increases with increasing temperature and attained a maximum value of 3.14 gcm-3 at 1150°C whereas maximum hardness value of 6.64 GPa was measured in HA sintered at 1050°C. These results are discussed in terms of the role of grain size.

Abstract: The sinterability of magnesium oxide (MgO) doped hydroxyapatite (HA) ranging from 1 to 10 wt% when sintered at 1150°C was investigated in terms of phase stability, bulk density, Young’s modulus, Vickers hardness and fracture toughness. The addition of up to 1 wt% MgO as sintering additive was found to be beneficial in promoting the densification of HA. Further addition of MgO in the HA matrix would deteriorate its densification properties. Similar results were observed for its stiffness and Vickers hardness. Nevertheless, the fracture toughness of HA was greatly enhanced by the incorporation of 5 wt% MgO. An increased toughness of up to 35% was obtained for the MgO-doped HA when compared to the undoped HA. This improvement is associated to the smaller grain size of the doped sample as compared to the undoped HA.

Abstract: The aim of this work is to study the phase stability and sinterability of bismuth oxide (Bi2O3) doped HA ranging from 0.05 wt% to 1 wt%. The green samples were sintered in air at temperature ranging from 1000oC to 1400oC. In this experiment, the results from XRD analysis revealed that the stability of HA phase was disrupted when addition of 0.3, 0.5 and 1.0 wt% Bi2O3 were used and when samples sintered above 1100oC, 1000oC and 950oC, respectively. In general, HA containing 0.5 wt% of Bi2O3 and when sintered at 1000oC was found to be beneficial in enhancing densification, Young’s modulus, Vickers hardness and fracture toughness. Throughout the sintering regime, the highest value of relative bulk density of 98.7% was obtained for 0.5 wt% Bi2O3-doped HA when sintered at 1000oC. A maximum Young’s modulus of 119.2 GPa was observed for 0.1 wt% Bi2O3-doped HA when sintered at 1150oC. Additionally, 0.5 wt% Bi2O3-doped HA was able to achieve highest hardness of 6.04 GPa and fracture toughness of 1.21 MPam1/2 at sintering temperature of 1000oC. Furthermore, the Young’s modulus of HA was found to vary linearly with bulk density.

Abstract: The effects of adding a small amount of nano silica in hydroxyapatite (HA) on the sinterability and mechanical properties of hydroxyapatite were studied. The starting HA powder was synthesized using a novel wet chemical precipitation method. Different amount of silica powder was mechanically mixed with the synthesized HA. The green samples were subsequently cold isostatically pressed at 200 MPa. Sintering in air was accomplished by firing the green samples at temperatures ranging from 1050°C to 1250°C. Sintered samples were analyzed to determine phase composition and mechanical properties. The XRD analysis revealed that with increasing the amount of silica in the HA powder, decomposition of HA to TCP occurred at sintering temperature higher than 1050°C. The bulk density of all silica-doped samples decreased through the temperature range studied. In agreement with the bulk density trend, the increasing silica additives in HA depleted the Young’s modulus and Vickers hardness of the HA body. The study revealed that the addition of silica have an adverse effect on the sintered properties of hydroxyapatite bioceramics.

Abstract: The sinterability of hydroxyapatite (HA) powder synthesized through a novel wet chemical method (HAp) and a wet mechanochemical method (HAwm) was investigated over a temperature range of 1000oC to 1400oC in terms of phase stability, bulk density, hardness and fracture toughness. The results indicated that the sinterability of HAp powder were significantly better than HAwm powder. Moreover, the XRD traces of HAwm sintered samples showed signs of decomposition into TTCP when sintered at 1300oC and above. Densification of ~98% of theoretical density was attained by HAp compacts at 1100oC while the HAwm compacts exhibited only ~96% of theoretical density even at 1350oC with no significant increase of density at 1400oC. The Vickers hardness of HAp showed increasing trend for temperature range of 1000oC to 1100oC with the compacts attaining HV of ~7 GPa at 1100oC. Subsequently, the hardness decreased with increasing sintering temperature though the value does not dropped below ~5 GPa. Similarly, HAwm compacts showed an increasing trend from 1000oC to 1300oC with the largest HV attained was ~4.57 GPa. Further increased in sintering temperature resulted in the decreased of Vicker’s hardness. Moreover, the HAp samples reached a maximum fracture toughness of ~0.9 MPam1/2 at 1050oC while the HAwm attained maximum KIc of only ~0.7 MPam1/2 at 1300oC.

Abstract: It is known that polystyrene must be chemically modified to make its surface amenable to covalent cross-linking with protein. The aim of this study was to set up a UV/Ozone system and investigate the effects of UV/Ozone treatment on polystyrene surface. Microsize polystyrene beads with an average size of 150 μm in diameter were treated with and without distilled water at the same treatment time, ozone flow-rate and UV intensity. The treated beads were analyzed by ATR-FTIR, SEM, EDX and hydrophilicity measurement. The results show that the hydrophilicity of the surface of polystyrene beads was increased after the UV/ozone treatment and the introduction of carbonyl, carboxyl and hydroxyl groups on the polystyrene beads surface was also confirmed. It was demonstrated that the UV/Ozone system was effective for treatment of polystyrene bead and the best result was obtained without distilled water.