TY - JOUR
T1 - Synthesis of morphologically controlled hydroxyapatite from fish bone by urea-assisted hydrothermal treatment and its Sr2+ sorption capacity
AU - Goto, Tomoyo
AU - Sasaki, Keiko
N1 - Funding Information:
Financial support was provided to K. Sasaki by the Funding Program for Next Generation World-Leading Researchers (“NEXT program” GR078 ) and “ Progress 100 ” (World Premier International Researcher Invitation Program of Kyushu University), provided from the operating expense grants of the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan. Chemically produced calcium orthophosphates (HAP-100, HAP-200, and β-TCP) were supplied courtesy of Taihei Chemical Industrial Co. Ltd., Japan. Elemental analyses (carbon, hydrogen, and nitrogen) were carried out at the elementary analysis centre in Kyushu University. TEM images and SAED patterns were collected at the Research Laboratory for High Voltage Electron Microscopy (HVEM) in Kyushu University. XAFS experiments were performed at Kyushu University Beamline (SAGA-LS/BL06) under proposal No. 2013IIK024.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Needle- and sponge-shaped hydroxyapatite (HAp) particles were synthesized from calcined tuna fish bone (Tn1000) and commercially available HAp reagent (ChemHAP) by a urea-assisted hydrothermal treatment using 0.1-1.0 M urea solution at 160 °C for 3 h. The Sr2+ sorption capacity of the synthesized HAp was also investigated using 0-50 mM Sr2+ solution at 25 °C for 72 h to evaluate its performance as a sorbent for environmental remediation. Sponge-shaped HAp was formed under hydrothermal conditions with a urea concentration of 1.0 M. With decreasing urea concentration, the morphology of HAp changed from sponge-shaped to needle-shaped crystals, regardless of the starting material. Some calcium carbonate and/or β-tricalcium phosphate impurities were formed from Tn1000 at 0.1-0.5 M urea concentration. The Sr2+ sorption mechanism of the synthesized HAp was estimated using Ca ion-exchange reaction and precipitation of SrCO3. The sponge-shaped HAp crystals, which had high specific surface area and CO32- content, exhibited a large ion-exchange capacity with Sr2+. In contrast, the ion-exchange ratio of needle-shaped HAp dramatically decreased with increasing initial Sr concentration. No clear difference in Sr2+ sorption behaviour caused by the choice of HAp synthesis starting material was observed. These results indicate that the Sr sorption mechanism of HAp is influenced by not only its composition but also its crystal morphology.
AB - Needle- and sponge-shaped hydroxyapatite (HAp) particles were synthesized from calcined tuna fish bone (Tn1000) and commercially available HAp reagent (ChemHAP) by a urea-assisted hydrothermal treatment using 0.1-1.0 M urea solution at 160 °C for 3 h. The Sr2+ sorption capacity of the synthesized HAp was also investigated using 0-50 mM Sr2+ solution at 25 °C for 72 h to evaluate its performance as a sorbent for environmental remediation. Sponge-shaped HAp was formed under hydrothermal conditions with a urea concentration of 1.0 M. With decreasing urea concentration, the morphology of HAp changed from sponge-shaped to needle-shaped crystals, regardless of the starting material. Some calcium carbonate and/or β-tricalcium phosphate impurities were formed from Tn1000 at 0.1-0.5 M urea concentration. The Sr2+ sorption mechanism of the synthesized HAp was estimated using Ca ion-exchange reaction and precipitation of SrCO3. The sponge-shaped HAp crystals, which had high specific surface area and CO32- content, exhibited a large ion-exchange capacity with Sr2+. In contrast, the ion-exchange ratio of needle-shaped HAp dramatically decreased with increasing initial Sr concentration. No clear difference in Sr2+ sorption behaviour caused by the choice of HAp synthesis starting material was observed. These results indicate that the Sr sorption mechanism of HAp is influenced by not only its composition but also its crystal morphology.
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U2 - 10.1016/j.powtec.2016.01.041
DO - 10.1016/j.powtec.2016.01.041
M3 - Article
AN - SCOPUS:84958260656
SN - 0032-5910
VL - 292
SP - 314
EP - 322
JO - Powder Technology
JF - Powder Technology
ER -