Batch hydrothermal synthesis of nanocrystalline, thermostable hydroxyapatite at various pH and temperature levels

单斜晶系 纳米晶材料 热液循环 傅里叶变换红外光谱 微晶 材料科学 水热合成 核化学 扫描电子显微镜 灌木岩 矿物学 热重分析 粉末衍射 分析化学(期刊) 高压灭菌器 六角相 相(物质) 化学工程 结晶学 化学 无机化学 晶体结构 纳米技术 冶金 有机化学 复合材料 工程类
作者
Antonius Prihanto,S. Muryanto,Rifky Ismail,J. Jamari Funding aquisition,A.P. Bayuseno
出处
期刊:Inorganic Chemistry Communications [Elsevier BV]
卷期号:157: 111301-111301
标识
DOI:10.1016/j.inoche.2023.111301
摘要

This paper addresses the powder synthesis of nanocrystalline hydroxyapatite (HA) in a hydrothermal autoclave reactor using deionized water and the chemical reactants Ca(NO3)2 and (NH4)2HPO4 at varying pH values (7-11) and temperatures ranging from 50 to 130 OC. Analysis of the synthesized powder products included XRD (X-ray diffraction), FTIR (Fourier transform infrared spectroscopy), SEM/EDX (scanning electron microscopy), and TG/DTG (thermogravimetry). Hexagonal and monoclinic hydroxyapatite crystallized mostly after 24-h hydrothermal processing at different initial pH values and temperatures (50 to 130°C). When the temperature rose from 50 to 110 OC at a fixed pH of 10, the hexagonal phase became more prevalent while the monoclinic phase decreased proportionally. The monoclinic phase crystallite size reduced from 231.08 to 31.51 nm. Despite a constant temperature of 80 OC, pH levels ranging from 7 to 11 revealed substantial hexagonal and monoclinic hydroxyapatite with minimal monetite and brushite. FTIR spectroscopy confirmed the functional groups associated with hydroxyapatite spectra. The SEM method also revealed HA powder with spherules and anhedral agglomerates having Ca/P ratios (1.1-2.15). TG/DTG results confirmed that hydrothermal-derived HA nanosized powders are thermally stable microstructures for biomedical applications.
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