Synthesis of Micro and Nano-Sized Hydroxyapatite Fibers Through the Microwave Assisted Hydrothermal Method

被引:13
作者
Alanis-Gomez, J. R. [1 ]
Rivera-Munoz, E. M. [2 ]
Cervantes-Medina, J. S. [2 ]
Almanza-Reyes, H. [3 ]
Nava-Mendoza, R. [1 ]
Cortes-Romero, C. [4 ]
Velazquez-Castillo, R. [1 ]
机构
[1] Univ Autonoma Queretaro, Fac Ingn, Div Invest & Posgrad, Cerro Campanas S-N, Queretaro 76010, Qro, Mexico
[2] Univ Nacl Autonoma Mexico, Ctr Fis Aplicada & Tecnol Avanzada, AP 1-1010, Queretaro 76000, Qro, Mexico
[3] Univ Autonoma Baja California Tijuana, Fac Med & Psicol, Calzada Univ 14418,Parque Ind Int, Tijuana 22390, Baja California, Mexico
[4] Univ Autonoma Queretaro, Fac Quim, Cerro Campanas S-N, Queretaro 76010, Qro, Mexico
关键词
Nanofibers; Hydroxyapatite; Biomaterials; TEMPERATURE; MORPHOLOGY; ETHANOL; PHASE;
D O I
10.1166/jnn.2016.12829
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of hydroxyapatite (HAp) fibers was performed using a microwave assisted hydrothermal methodology. The actual reaction mixture was placed in a Teflon tube inside a microwave oven at 170 degrees C and 80 bar. Polycrystalline hydroxyapatite nanofibers were obtained under these operating conditions. The control on heating and cooling rates inside the reactor was critical as well as the use glutamic acid to guide the crystal growth. According to the results, the nanofibers showed a preferential crystalline orientation in the [300] but they grew in the [001] with high crystallinity and good purity. These nanofibers were closed packed inside hexagonal microfibers with a singular arrangement. Additionally, structural studies were done using X-ray diffraction by powders along with the chemical composition supported by infrared spectroscopy (FTIR) analyses. The morphology and microstructure characterization as well as crystalline features of the HAp nanocrystals were done through Scanning Electron Microscopy and High Resolution Electron Microscopy.
引用
收藏
页码:7557 / 7566
页数:10
相关论文
共 33 条
[1]   Dielectric and piezoelectric properties of hydroxyapatite-BaTiO3 composites [J].
Bowen, C. R. ;
Gittings, J. ;
Turner, I. G. ;
Baxter, F. ;
Chaudhuri, J. B. .
APPLIED PHYSICS LETTERS, 2006, 89 (13)
[2]  
Bowen CR, 2009, ADV SCI TECH, V54, P1
[3]   Synthesis of Hydroxyapatite Nanostructures Using Microwave Heating [J].
Cabrera, J. L. ;
Velazquez-Castillo, R. ;
Rivera-Munoz, E. M. .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2011, 11 (06) :5555-5561
[4]  
Campa J., 2007, BIOMATERIALES FUNDAM
[5]   Microwave-assisted solid-state synthesis of hydroxyapatite nanorods at room temperature [J].
Cao, JM ;
Feng, J ;
Deng, SG ;
Chang, X ;
Wang, J ;
Liu, JS ;
Lu, P ;
Lu, HX ;
Zheng, MB ;
Zhang, F ;
Tao, J .
JOURNAL OF MATERIALS SCIENCE, 2005, 40 (23) :6311-6313
[6]  
Chengfeng L., 2011, ADV POWDER TECHNOL, V22, P537
[7]  
Chetty A., 2012, HYDROXYAPATITE SYNTH, P133
[8]   Hydrothermal synthesis of hydroxyapatite [J].
Earl, J. S. ;
Wood, D. J. ;
Milne, S. J. .
EMAG-NANO 2005: IMAGING, ANALYSIS AND FABRICATION ON THE NANOSCALE, 2006, 26 :268-+
[9]  
Goudarzi A, 2007, P 10 INT C EUR CER S, P964
[10]   Effect of calcining temperature on particle size of hydroxyapatite synthesized by solid-state reaction at room temperature [J].
Guo, Xiaojun ;
Yan, Hudong ;
Zhao, Shengguo ;
Zhang, Li ;
Li, Yutian ;
Liang, Xiaohu .
ADVANCED POWDER TECHNOLOGY, 2013, 24 (06) :1034-1038