TY - JOUR
T1 - Synthesis and Characterization of Eggshell-derived Hydroxyapatite for Dental Implant Applications
AU - Odusote, Jamiu
AU - Adeleke, Adekunle
AU - Ikubanni, Peter
AU - Omoniyi, Peter
AU - Jen, Tien Chien
AU - Odedele, G.
AU - Okolie, Jude
AU - Akinlabi, Esther
PY - 2023/10/6
Y1 - 2023/10/6
N2 - Hydroxyapatite (HAp) production from eggshells for dental implant purposes involved a novel approach utilizing a wet chemical precipitation technique. The eggshells, finely ground to a size below 250 μm, underwent calcination at a high temperature of 900°C for 2 hours. This thermal treatment facilitated the conversion of calcium carbonate into calcium oxide (CaO) while eliminating any organic components in the eggshell. To initiate the synthesis of HAp, a solution comprising 0.6 M phosphoric acid was added to the CaO dispersed in water. The resulting mixture was allowed to undergo aging at different time intervals ranging from 0 to 24 hours, promoting the formation of HAp. Subsequently, the HAp particles were oven-dried at 100°C for 2 hours to remove residual moisture. Finally, the dried particles were sintered at 1200°C in a muffle furnace to achieve the desired properties for dental implant applications. XRD peaks at 25, 33, 40, and 50° confirm the synthesized material as HAp. Vibrational modes of phosphate (PO43-), hydroxyl (OH-), and carbonate (CO32-) groups indicate carbonated HAp. Synthesized HAp holds potential for biomedical applications.
AB - Hydroxyapatite (HAp) production from eggshells for dental implant purposes involved a novel approach utilizing a wet chemical precipitation technique. The eggshells, finely ground to a size below 250 μm, underwent calcination at a high temperature of 900°C for 2 hours. This thermal treatment facilitated the conversion of calcium carbonate into calcium oxide (CaO) while eliminating any organic components in the eggshell. To initiate the synthesis of HAp, a solution comprising 0.6 M phosphoric acid was added to the CaO dispersed in water. The resulting mixture was allowed to undergo aging at different time intervals ranging from 0 to 24 hours, promoting the formation of HAp. Subsequently, the HAp particles were oven-dried at 100°C for 2 hours to remove residual moisture. Finally, the dried particles were sintered at 1200°C in a muffle furnace to achieve the desired properties for dental implant applications. XRD peaks at 25, 33, 40, and 50° confirm the synthesized material as HAp. Vibrational modes of phosphate (PO43-), hydroxyl (OH-), and carbonate (CO32-) groups indicate carbonated HAp. Synthesized HAp holds potential for biomedical applications.
UR - http://www.scopus.com/inward/record.url?scp=85175477746&partnerID=8YFLogxK
U2 - 10.1051/e3sconf/202343001299
DO - 10.1051/e3sconf/202343001299
M3 - Conference article
AN - SCOPUS:85175477746
SN - 2555-0403
VL - 430
JO - E3S Web of Conferences
JF - E3S Web of Conferences
M1 - 01299
T2 - 15th International Conference on Materials Processing and Characterization, ICMPC 2023
Y2 - 5 September 2023 through 8 September 2023
ER -