Preparation of magnetic, luminescent and mesoporous hydroxyapatite nanospindles with high specific surface area

被引:0
作者
Guo, Haifeng [1 ,2 ]
Zhou, Zhiqiang [1 ,3 ]
Ye, Feng [1 ]
Li, Guoping [2 ]
Zhang, Zhiheng [2 ]
机构
[1] Harbin Institute of Technology, Harbin,150001, China
[2] PetroChina Pipeline R and D Center, Langfang,065000, China
[3] Northeast Forestry University, Harbin,150040, China
来源
Xiyou Jinshu Cailiao Yu Gongcheng/Rare Metal Materials and Engineering | 2014年 / 43卷 / 11期
关键词
Transmission electron microscopy - X ray diffraction - Calcination - Gas adsorption - Scanning electron microscopy - Hematite - Luminescence - Samarium compounds - Drug delivery - Mesoporous materials;
D O I
暂无
中图分类号
学科分类号
摘要
Magnetic, luminescent and mesoporous nanospindles of Sm3+-Fe3+ co-doped hydroxyapatite (HAP) were prepared in the presence of monododecyl phosphate as templates. X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), vibration sample magnetometer (VMS), photoluminescence (PL) spectrum and nitrogen adsorption-desorption isotherm were used to characterize the products. The results show that the doped Sm3+ and Fe3+ existed in two forms: being solid-soluted in the HAP, or as oxides (amorphous Sm2O3 and γ-Fe2O3) nanoparticles embedded in the HAP. The doped HAP samples, both the as-dried and the calcined, display a good superparamagnetism. The calcination increases the magnetization from 13.45 emu/g to 19.51 emu/g. The calcined Sm3+-Fe3+ co-doped HAP has a spindle-like morphology with a length of 200~350 nm and a diameter of 50~100 nm, and possesses a large amount of mesopores with biomodal pore sizes of 3.64 and 9.01 nm. The biomodal mesoporous Sm3+-Fe3+ co-doped HAP nanospindles have a large pore volume of 0.3286 cm3/g and a high specific surface area of 153.52 m2/g. These make the mesoporous HAP nanospindles have a high drug payload ratio of 33.68wt% and a great application potential in drug delivery system. Copyright © 2014, Northwest Institute for Nonferrous Metal Research. Published by Elsevier BV. All rights reserved.
引用
收藏
页码:2647 / 2651
相关论文
empty
未找到相关数据