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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 309-311 (May 2006), p. 723-726 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Five kinds of gypsums, (1) CaSO4•2H2O (caldium sulfate dihydrate; CSD), (2) CaSO4•1/2H2O (calcium sulfate hemihydrate; CSH), (3) CaSO4 (calcium sulfate anhydrite; CSA), (4) CSH200 (CSH heat-treated at 200°C after self-hardening), and (5) CSH600 (CSH heat-treatedat 600°C after self-hardening) were used as candidates for coating materials on calcium metaphosphate (CMP) scaffod to control degradation rate of CMP and to extend degradation limit. The disks of CSD, CSH, CSA, CSH 200, and CSH600 were prepared by self-hardening after mixing with water, where CSH200 and CSH600 were heat-treated at 200°C and 600°C, respectively. In order to control fast resorption rate of gypsum, CMP-CSA composites were prepared with different CSA contents such as 0, 5, 10, 20, 30, 50, and 70 vol% and heat-treated at900°C for 4 hours. The degradation rates of various gypsums were evaluated in revised simulated body fluid (r-SBF) for 1, 3, 7, and 21 days, respectively. Degradation rate of each specimen was measured in terms of weight loss change with time and degraded surface morphology was examined by SEM. All kinds of gypsums were transformd into CSD after self-hardening with water. Most ofgypsums were degraded by 35~60 wt% at 7 days and by 70~99 wt% at 21 days of soaking in SBF. In the group of CMP-CSA composites, the degree of degradation of them was considerably retarded compared to that of five pure gypsums. The surface morphology showed elongated needle-like crystals during the degradation with time
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 330-332 (Feb. 2007), p. 207-210 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Bioresorbable calcium metaphosphate (CMP) nanofibers were produced by anelectrospinning technique. In order to produce the nanofibers, CMP sol was prepared by the mixing oftwo precursors, such as calcium nitrate tetrahydrate (Ca[NO3]⋅4H2O) and triethyl phosphate (TEP,[C2H5O]3PO), using methyl alcohol as a solvent. The Ca/P ratio of the mixture was set to be 0.50 toproduce stoichiometric CMP sol. At least 5 hrs of pre-hydrolysis of phosphorus precursor wererequired to obtain β-CMP phase. Viscous solutions for the electrospinning were made by the mixingof CMP sol and high-molecular weight polymeric solution at various ratios. The ratio of CMP sol andpolymer solution was controlled to obtain an appropriate viscosity for the electrospinning.As-electrospun CMP nanofibers were dried in a drying oven at 70°C for 24 hrs and then heat-treatedat various temperatures at a ramp of 1°C/min in air for 1hr. The as-electrospun and heat-treated CMPnanofibers were characterized using X-ray analysis, FT-IR, TG-DTA and SEM techniques. Theresults showed that the preparation of CMP sol, mixed solution properties, and heat-treatmentcondition of as-electrospun nanofibers significantly affect the spinability and surface morphology ofthe CMP nanofibers
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 342-343 (July 2007), p. 817-820 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: β-tricalcium phosphate (TCP) ceramic nanofibers via electrospinning route have been producedusing β-TCP sol, which was prepared by the mixing of calcium nitrate tetrahydrate and triethylphosphate as Ca sand P precursors, respectively. The as-prepared sol was tightly caped and aged ina drying oven at 90 °C for 16 hrs. The aged sol was evaporated in opened containers at 35 °C toreach a proper value of viscosity (100 cPs). Viscous solution was prepared by the mixing of β-TCPsol and high-molecular weight PVP to obtain appropriate viscosity for electrospinning. The mixedsolution of β-TCP and PVP with various ratios were vigorously mixed using hot plate/stirrer for 24hrs and then electrospun. The as-electrospun β-TCP nanofibers were dried in a drying oven at 60°Cfor 12 hrs and then heat-treated at 500, 600, 700 and 800 °C at 1°C/min heating rate in air. Surfacemorphology and phase identification of as-spun and heat-treated β-TCP nanofibers were studied.The results have shown that ratio between PVP and β-TCP sol and heat-treatment conditionssignificantly affected the crystalline phase and morphology of β-TCP nanofibers
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 330-332 (Feb. 2007), p. 7-10 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Biphasic calcium phosphate powders (BCP) of hydroxyapatite (HA) and tricalciumphosphate (β-TCP) with the various ratio of HA to β-TCP were prepared by utilizing mechanochemicalsynthesis. Calcium hydrogen-phosphate dihydrate (brushite, CaHPO4⋅2H2O) and calciumcarbonate (calcite, CaCO3) powders have been chosen as the starting materials. The original Ca/Pratio of CaHPO4⋅2H2O - CaCO3 batch was set to be 1.67. A mixture of starting materials was milledusing a planetary mill (ZrO2 jar and balls) with water for 3, 4, 5, 6 and 7 hrs. The XRD study ofcalcined powders was conducted for phase identification and for HA/β-TCP ratio as well. Thephases of the calcined powders were HA and β-TCP, and the HA/β-TCP ratio varied with themilling time. The mass fraction of HA and β-TCP phases was calculated from the XRD intensitiesof HA and β-TCP. The ratio of the mixture milled for 4 hrs and calcined at 900°C was85(HA):15(β-TCP) (BCP 85/15) and the content of β-TCP increased with the milling time. It isbelieved defective HA powder formed at relatively short period of milling time (less than 3 hrs Theresearch revealed that nanocrystalline BCP powders could be synthesized by an employment of amedium-high energy mechanical activation at room temperatures (~25°C) without any preliminarychemical processing
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Degradation characteristics of calcium metaphosphate (CMP) ceramics substituted by 5, 10, 15, 20 mol% of NaPO3 and KPO3, respectively, was evaluated in revised simulated body fluid (R-SBF) by measuring the weight change, flexural strength, crystalline phases, and surface morphology with immersion period. The weight loss of CMP substituted by KPO3 was significantly higher than that of CMP substituted by NaPO3. The weight loss in the KCa(PO3)3–CMP sampleswas due to the dissolution of KCa(PO3)3 phase. The flexural strength of NaCa(PO3)3–CMP samples increased, however, that of KCa(PO3)3–CMP samples decreased significantly due to the dissolution of KCa(PO3) phase with immersion period. The dissolution of KCa(PO3)3 phase formed a porestructure in KCa(PO3)3–CMP samples
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Surface morphology and degradation behavior of mechanically mixed and chemicallyprecipitated biphasic calcium phosphate (M-BCP and P-BCP) were compared. For the M-BCP powder, commercial HA and TCP powders were used. In order to prepare P-BCP powder, precipitation method was used. The particle size of P-BCP was smaller than that of M-BCP. The disk-type specimens of each powder were prepared for the morphology comparison and degradation test. The surface morphology of sintered samples was porous in M-BCP and dense in P-BCP. Thedegradation test was conducted in the revised simulated body fluid (R-SBF) for 1, 7, and 21 days. Surface morphology and degradation rate of two samples were different. The weight gain in both samples increased linearly with immersion period due to apatite-like layer formation. However, the weight gain in M-BCP was much higher than that in P-BCP. The weight gain was related to the surface morphology and degradation with immersion period
    Type of Medium: Electronic Resource
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