2021
DOI: 10.1016/j.ceramint.2021.07.215
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Effect of low temperature crystallization on 58S bioactive glass sintering and compressive strength

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Cited by 8 publications
(5 citation statements)
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“…This is followed by polycondensation reactions between the networks and resulted in gel formation. The gel is then aged to increase the amount of polycondensation processes and improve the chemical stability of the final products 26 . The gel is now known as xerogel after it has been dried to remove the solvent (water or ethanol).…”
Section: Discussionmentioning
confidence: 99%
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“…This is followed by polycondensation reactions between the networks and resulted in gel formation. The gel is then aged to increase the amount of polycondensation processes and improve the chemical stability of the final products 26 . The gel is now known as xerogel after it has been dried to remove the solvent (water or ethanol).…”
Section: Discussionmentioning
confidence: 99%
“…This can be explained by its high specific surface area, which will increase the contact surface area of BG, thereby increasing more nucleation sites for apatite creation and enhancing its biodegradation and bioactivity 29 . Factors that may influence the particle size of sol–gel biomaterials include the concentration of ammonia, the used of distilled water, as well as the types of alcohol and acid use as catalyzers that will influence the ultimate size of the particles synthesized 15,21,26,30 …”
Section: Discussionmentioning
confidence: 99%
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“…Indeed, the compression strength was increased due to high temperature sintering up to 29 MPa at 1200 °C for 12 h. However, the bioactive glass was crystallized, thereby reducing the bioactivity of the 58S bioactive glass. 37 Similarly, Sharifianjazi et al 38 developed magnesium (Mg)and strontium (Sr)-doped bioactive glass (60 SiO 2 , 4P 2 O 5 , 36x/y CaO; x ∼Mg, y ∼Sr) with improved elastic moduli of 90 GPa (in 58S BG with 10 wt % MgO) and 113 GPa (in 58S BG with 10 wt % SrO) due to the formation of strong Mg−O−Si and Sr−O−Si bonds. However, the BG powder was calcined at 800 °C, which led to the crystallization of BG, hence reducing its bioactivity, and the antibacterial aspects of these biocomposites are not discussed.…”
Section: Introductionmentioning
confidence: 99%
“…In another study, Dehaghani and Ahmadian improved the mechanical properties (compression strength) via sintering of Co–Cr–Mo/58S bioactive glass porous nanocomposites at high temperatures of 1100 –1250 °C. Indeed, the compression strength was increased due to high temperature sintering up to 29 MPa at 1200 °C for 12 h. However, the bioactive glass was crystallized, thereby reducing the bioactivity of the 58S bioactive glass . Similarly, Sharifianjazi et al developed magnesium (Mg)- and strontium (Sr)-doped bioactive glass (60 SiO 2 , 4P 2 O 5 , 36-x/y CaO; x ∼Mg, y ∼Sr) with improved elastic moduli of 90 GPa (in 58S BG with 10 wt % MgO) and 113 GPa (in 58S BG with 10 wt % SrO) due to the formation of strong Mg–O–Si and Sr–O–Si bonds.…”
Section: Introductionmentioning
confidence: 99%