Crystal Structure of Sr-Substituted Hydroxyapatite Synthesized by Hydrothermal Method

1994 ◽  
Vol 113 (2) ◽  
pp. 373-378 ◽  
Author(s):  
Masanori Kikuchi ◽  
Atsushi Yamazaki ◽  
Ryohei Otsuka ◽  
Masaru Akao ◽  
Hideki Aoki
2012 ◽  
Vol 476-478 ◽  
pp. 1138-1141
Author(s):  
Zhi Qiang Wei ◽  
Qiang Wei ◽  
Li Gang Liu ◽  
Hua Yang ◽  
Xiao Juan Wu

Ag nanoparticles were successfully synthesized by hydrothermal method under the polyol system combined with traces of sodium chloride, Silver nitrate(AgNO3) and polyvinylpyrrolidone (PVP) acted as the silver source and dispersant respectively. The samples by this process were characterized via X-ray powder diffraction (XRD), Brunauer–Emmett–Teller (BET) adsorption equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED) to determine the chemical composition, particle size, crystal structure and morphology. The experiment results indicate that the crystal structure of the samples is face centered cubic (FCC) structure as same as the bulk materials, The specific surface area is 24 m2/g, the particle size distribution ranging from10 to 50 nm, with an average particle size about 26 nm obtained by TEM and confirmed by XRD and BET results.


2013 ◽  
Vol 631-632 ◽  
pp. 176-180 ◽  
Author(s):  
Ying Hao Xie ◽  
Zhan Chang Pan ◽  
Zhi Gang Wei ◽  
Wei Lin Feng ◽  
Jun Hui Zuo ◽  
...  

In this paper, nano TiO2 loaded on activated carbon fiber(ACF) was prepared by hydrothermal method as TiO2/ACF photocatalytic.The material crystal structure, the superficial appearance of catalyst, were analyzed and measured by XRD and SEM images.Moreover, it used for photocatalytic oxidation As(Ⅲ).The effect of pH on the oxidation of As(Ⅲ) was studied. The oxidation of As(Ⅲ) efficiency increasing markedly with pH, and the catalytic efficiency is much higher in the alkaline environment than in the acidic environment.


Minerals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 659
Author(s):  
Evgeny Nazarchuk ◽  
Dmitri Charkin ◽  
Oleg Siidra ◽  
Stepan Kalmykov

A new organically templated uranyl molybdate [C3H9NH+]4[(UO2)3(MoO4)5] was prepared by a hydrothermal method at 220 °C. The compound is monoclinic, Сс, a = 16.768(6), b = 20.553(8), c = 11.897(4) Å, β = 108.195(7), V = 3895(2) Å3, R1 = 0.05. The crystal structure is based upon [(UO2)3(MoO4)5]4− uranyl molybdate layers. The isopropylammonium cations are located in the interlayer. The layers in the structure of [C3H9NH+]4[(UO2)3(MoO4)5] are considered as modular architectures. Topological analysis of layers with UO2:TO4 ratio of 3:5 (TVI = S, Cr, Se, Mo) was performed. Modular description is employed to elucidate the relationships between different structural topologies of [(UO2)3(TO4)5]4− layers and inorganic uranyl-based nanotubules. The possible existence of uranyl molybdate nanotubules is discussed.


2019 ◽  
Vol 9 (3) ◽  
pp. 226-231 ◽  
Author(s):  
Solange Ivette Rivera Manrique ◽  
Felipe de Jesús Carrillo Romo ◽  
Antonieta García Murillo ◽  
Carlos Eduardo Rodríguez García ◽  
Jorge Roberto Oliva Uc

Introduction: Rare earth-doped Upconverting Nanoparticles (UCN's) can convert near-infrared photons into visible photons via multiphoton processes, which makes it a good material for generating white light. The production of luminescent materials for technology applications focuses on controlling powder characteristics such as chemical homogeneity and low impurity levels. Objective: In this research study, we synthesized Er3+ (1%) Tm3+ (1%) Yb3+ (at different percentages) by co-doping Y2O3 NPs, using the Controlled-Pressure Hydrothermal Method (CPHM), with nitrogen. The ratio used was chosen to conduct a detailed photolumniscence analysis. Methods: Samples of Y2O3: Er3+ (1%) Tm3+ (1%) Yb3+ (at 1.5%, 2%, and 2.5%) were prepared using the controlled-pressure hydrothermal method (CPHM). Each solution was transferred into a mini-clave drive Büchiglasuster with an inner Teflon vessel. In this case, the mini-clave was heated at 190°C for 3 h, and nitrogen was used to control the pressure. The initial pressure was 20 bars; it was increased during the process to 42 bars. The powders obtained were washed with distilled water using centrifugation at 4000 rpm for 15 min. The washed product was dried to 120°C, followed by subsequent heat treatment at 1000°C for 5 h. Results: The representative XRD patterns for the Y2O3: Er3+ (1%) Tm3+ (1%) and Yb3+ (at 1.5%, 2%, 2.5%) doped samples confirms the presence of a cubic Y2O3 crystal structure. Scanning Electron Microscope (SEM) images show that the morphology of these particles is spherical. Upconversion photoluminescence spectra of Y2O3:Er3+ (1% mol) Tm3+ (1% mol) Yb3+ (1.5% mol), Yb3+ (2.0% mol), and Yb3+ (2.5% mol), after 908-nm excitation. Blue, green, and red bands are centred at 440 nm, 469 nm, 618 nm, and 678 nm, respectively. Conclusion: The controlled-pressure hydrothermal method is a productive method for synthesizing rare earth-doped and codoped Y2O3; when Er3+, Yb3+, and Tm3+ ions are introduced into the host matrix, they do not cause any changes in the cubic structure nor influence the crystal structure. This method can used to synthesize any type of nanoparticle, because it involves low pressure (10-20 bars), low temperatures, and short time reactions.


2013 ◽  
Vol 1494 ◽  
pp. 291-296 ◽  
Author(s):  
T. Shiraishi ◽  
H. Einishi ◽  
M. Ishikawa ◽  
T. Hasegawa ◽  
M. Kurosawa ◽  
...  

ABSTRACTKNbO3 thick films were deposited on (100)c SrRuO3//(100)SrTiO3 substrates at 240 °C for 3 h by hydrothermal method. Film thickness increased linearly with increasing the deposition number of times and 130 μm thickness was achieved by the 6 time deposition. XRD analysis showed the growth of epitaxial orthorhombic films with the mixture orientation of (100), (010) and (001). Cross-sectional SEM observation showed that the 130 μm-thick film was dense and no obvious voids inside the film. In addition, the crystal structure change along film thickness direction was not detected from the cross-sectional Raman spectral observation.


2011 ◽  
Vol 356-360 ◽  
pp. 1253-1257
Author(s):  
Xiao Ming Gao ◽  
Yu Fei Wu ◽  
Jing Wang ◽  
Feng Fu ◽  
Li Ping Zhang ◽  
...  

An enhanced visible-light-driven catalyst BiVO4 doping with Cu was synthesized by hydrothermal method and characterized by XRD, UV-vis DRS, specific surface area. The characterization results indicated a better crystal structure of Cu-BiVO4. The photocatalytic properties were evaluated by degrading wastewater with phenol, taking pH of catalysts prepared, dosage of catalyst and air flow as the research factors. The results showed that Cu-BiVO4 has an effective photodegradation of phenol under the suitable conditions.


2011 ◽  
Vol 170 ◽  
pp. 29-32
Author(s):  
Shintaro Ogawa ◽  
Koji Okuta ◽  
Hirohiko Sato

We have discovered a novel compound Na0.12CrO2Ge0.18Ox•yH2O using a hydrothermal method. Its powder X-ray diffraction reveals a monoclinic unit cell with lattice parameters: a = 7.260 Å, b = 2.950 Å, c = 5.117 Å and β = 103.7°. A Rietveld analysis shows that this compound has a layered structure based on CrO2 sheets consisting of edge-shared CrO6 octahedra. Such a layered structure is commonly seen in many hexagonal Cr oxides such as NaCrO2. A heat treatment at 100 °C modifies the crystal structure without destruction of a layered structure based on Cr triangular-lattice, because H2O molecules among the CrO2 sheets are removed at high temperature. Magnetization measurements reveal a spin-glass behavior below Tg = 3 K.


2013 ◽  
Vol 798-799 ◽  
pp. 125-129
Author(s):  
Fu Yun Li ◽  
Jing Wang ◽  
Ying Yang Qin ◽  
Li Zhen Yang

The nano manganese oxides were prepared with the hydrothermal method by adding surface-active agent. The influence of the type and addition amount of surface-active agent on the preparation of nano manganese oxides was studied. The products were characterized with XRD. Experimental results show that MnOOH is obtained at 180°C with the addition of N,N,N-trimethyl-1-dodecanaminium bromide, and Mn3O4is obtained at 180 °C with OP Emulsifier or Tween-80 added. Different addition amount of surface-active agent would have diverse effects on the purity of products.


2020 ◽  
Vol 13 (3) ◽  
pp. 196-201 ◽  
Author(s):  
Fang Wei ◽  
Liu Ling ◽  
Xu Lan

Background: Nanocomposites loaded with metal oxides, such as CuO and ZnO, have excellent optical, electrical, mechanical and chemical properties, which result in their great potential applications in optoelectronic devices, sensors, photocatalysts and other fields. Especially, electrospun metal- oxide-loaded nanofibers have attracted much attention in many fields. However, the single-needle Electrospinning (ES) inhibits the industrial application of these electrospun nanofiber composites. Bubble-Electrospinning (BE) is an effective free surface ES for mass production of nanofiber membranes loaded with metal oxide. Few relevant patents to the topic have been reviewed and introduced. Methods: The BE was used to prepare mass production of Cu(Ac)2 /Zn(Ac)2/ PVDF/ PAN Composite Nanofiber Membranes (CNFMs). Then PVDF/PAN CNFMs containing CuO and ZnO nanocrystals were obtained by heat-treatment. Finally, CuO nanosheets and ZnO nanorods were successfully grown on the surface of PVDF/PAN CNFMs using hydrothermal method. In addition, the morphology and crystal structure of CNFMs were investigated by scanning electron microscopy (SEM) and X-Ray Powder Diffractometer (XRD). Results: The morphology and crystal structure of the samples were characterized by SEM and XRD. The results showed the heat treatment temperature of 150oC and the hydrothermal temperature of 150oC were the optimal process parameters for the fabrication of PVDF/PAN CNFMs loaded with CuO and ZnO nanocrystals, and a higher heat treatment temperature results in higher crystallinity of ZnO and CuO. Conclusion: CuO/ZnO/PVDF/PAN CNFMs were successfully prepared by a combination of BE, heattreatment and hydrothermal method. The ZnO/CuO beads obtained by heat treatment is the key point of growing ZnO/CuO nanocrystals, and the growth temperature has great effect on the morphology of ZnO/CuO nanocrystals.


Sign in / Sign up

Export Citation Format

Share Document