Polymer-Assisted Hydrothermal Synthesis of PbTiO3 Crystals

2012 ◽  
Vol 528 ◽  
pp. 176-179
Author(s):  
Yong Gang Wang ◽  
Lin Lin Yang ◽  
Xin Wang ◽  
Song Li ◽  
Yu Jiang Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Formation Mechanism ◽  
Powder Diffraction ◽  
Self Assembly ◽  
Hydrothermal Process ◽  
X Ray ◽  
Assembly Structure ◽  
Scanning Electron

Using polymer as a surfactant, we successfully synthesized of PbTiO3 crystals with a self-assembly structure by a hydrothermal process. The as-obtained powders were characterized by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The results show that the presence of PVP, PEG and PVA plays a key role on the formation of self-assembly structure and the corresponding formation mechanism was briefly discussed.

Synthesis of PZT Disks by a Hydrothermal Method

2012 ◽  
Vol 174-177 ◽  
pp. 592-595
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Method ◽  
Formation Mechanism ◽  
Powder Diffraction ◽  
Self Assembly ◽  
Hydrothermal Process ◽  
X Ray ◽  
Extended Length ◽  
Scanning Electron

The organization of nanostructures across extended length scales is a key challenge in the design of integrated materials with advanced functions. PbZr0.52Ti0.48O3multilayer disks which were constructed by oriented rectangle nanoparticles were easily prepared by a simple surfactant-free hydrothermal process. The as-prepared powders were characterized by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The results indicated that the as-prepared PZT disks were constructed by self-assembly of rectangle nanoparticles by a perfect manner. The formation mechanism of the products was discussed.

Effect of Precursor on the Hydrothermal Synthesis of K0.5Bi0.5TiO3 Crystals

2012 ◽  
Vol 184-185 ◽  
pp. 830-833
Author(s):  
Guo Hui Xu ◽  
Lin Lin Yang ◽  
Yang Hui Zu ◽  
Wei Guo Li ◽  
Yu Jiang Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Formation Mechanism ◽  
Powder Diffraction ◽  
Hydrothermal Process ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

K0.5Bi0.5TiO3 nanoparticles and quadrate nanoflakes were successfully prepared by a hydrothermal process. The as-synthesized powders were examined by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The results suggest that the precursor plays an important role on the formation of K0.5Bi0.5TiO3 crystals and the formation mechanism was also discussed.

Hydrothermal Synthesis of 3D Flower-Like Bismuth Trisulphide Microcrystallines

2013 ◽  
Vol 634-638 ◽  
pp. 2207-2210 ◽  
Author(s):  
Pin Jiang Li ◽  
Yan Ge Zhang ◽  
Bao Jun Huang ◽  
Chen Yu ◽  
Ling Zhuge ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Hydrothermal Process ◽  
X Ray Diffraction ◽  
Structure Directing Agent ◽  
X Ray ◽  
Laser Raman ◽  
One Step ◽  
Scanning Electron

3D flower-like bismuth trisulphide microcrystallines has been successfully prepared via one step hydrothermal process and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and laser Raman spectrometer techniques. The morphologies of the Bi2S3 microcrystallines were influenced by the surfactant Na2(EDTA), which acts as a structure directing agent.

Hydrothermal Synthesis of Zeolite a Using Non-Calcined Diatomite

2018 ◽  
Vol 930 ◽  
pp. 3-7 ◽  
Author(s):  
Alexandre Fontes Melo de Carvalho ◽  
Tiago Roberto da Costa ◽  
Gilvan Pereira de Figueredo ◽  
José Antônio Barros Leal Reis Alves ◽  
Rodrigo César Santiago ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Crystallite Size ◽  
Powder Diffraction ◽  
Average Crystallite Size ◽  
Zeolite A ◽  
X Ray ◽  
Prepared Sample ◽  
Scanning Electron

Optimization and reduction of zeolite A synthesis costs are the focus of several studies. Attention has been given to the use of residues and natural materials rich in Si and Al, such as diatomite. Diatomite needs to be calcined above 500°C to be used, which increases processing costs. This study aimed at evaluating the use of diatomite without calcination in preparing zeolite A. Alkaline hydrothermal synthesis melting and 24 h of crystallization were carried out. The materials were characterized by XRD (X-ray powder diffraction), XRF (X-ray fluorescence), BET (N2physisorption) and SEM (Scanning Electron Microscopy). XRD data and refinement show that the obtained material presents 99.84% crystallinity, average crystallite size of 54.92 nm, and a semi-quantitative percentage of 79% zeolite A. SiO2and Al2O3contents in the prepared sample proved the ratio SiO2/Al2O3= 2. The micrographies show cubic particles and agglomerated sodalite.

Preparation and Characterization of Magnesium Hydroxide by Hydrothermal Modification

2011 ◽  
Vol 332-334 ◽  
pp. 767-770
Author(s):  
Hai Quan Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Powder Diffraction ◽  
Magnesium Hydroxide ◽  
Hydrothermal Process ◽  
X Ray ◽  
Hydrothermal Modification ◽  
Bet Specific Surface Area ◽  
Scanning Electron

Magnesium hydroxide (Mg(OH)2) particles were synthesized and modified via a reaction-hydrothermal process in the present of NaOH. The resultant magnesium hydroxide was characterized by X-ray powder diffraction (XRD), field-emission scanning electron microscopy (SEM) and BET specific surface area. It was found that NaOH played a key role in the morphology and dispersion Mg(OH)2 particles.

Hydrothermal Synthesis and Characterization of PbTiO3 Microrods

2010 ◽  
Vol 148-149 ◽  
pp. 903-906
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Xiao Feng Wang ◽  
Yu Jiang Wang ◽  
Gao Rong Han
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Hydrothermal Method ◽  
Powder Diffraction ◽  
Energy Dispersive ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Scanning Electron

PbTiO3 microrods were successfully synthesized via a surfactants-free hydrothermal method. The powders were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and photoluminescent spectra techniques (PL). It was found that the precursor played a key role in the formation of PbTiO3 microrods.

Effect of TiC on coarsening and macrosegregation of Al–Bi alloys

2020 ◽  
Vol 111 (7) ◽  
pp. 607-615
Author(s):  
Congmin Li ◽  
Yanguo Yin ◽  
Ming Xu ◽  
Jianfeng Cheng ◽  
Lan Shen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Heterogeneous Nucleation ◽  
Self Assembly ◽  
Holding Time ◽  
Energy Dispersive ◽  
Melt Temperature ◽  
X Ray ◽  
Minority Phase ◽  
Scanning Electron

Abstract The microstructures of an Al-Bi immiscible alloy and the corresponding composites containing TiC (1 wt.% and 2 wt.%) were explored for melt temperatures of 800 °C, 850 °C, and 900°C. It was demonstrated that serious coarsening and macrosegregation of Bi-rich minority phase particles occurred, which was slightly alleviated by increasing the melt temperature from 800 °C to 900 °C. By adding TiC particles, the coarsening and macrosegregation of Bi-rich minority phase particles were significantly impeded. Scanning electron microscopy and energy-dispersive X-ray spectroscopy revealed that TiC particles were located inside and on the surface of Bi-rich minority phase particles, exhibiting heterogeneous nucleation and self-assembly behaviour. By properly increasing the holding time of the melt, finer and more uniform Bi-rich minority phase particles were obtained.

scholarly journals Improving the reactivity of phenylacetylene macrocycles toward topochemical polymerization by side chains modification

2014 ◽  
Vol 10 ◽  
pp. 1613-1619 ◽  
Author(s):  
Simon Rondeau-Gagné ◽  
Jules Roméo Néabo ◽  
Maxime Daigle ◽  
Katy Cantin ◽  
Jean-François Morin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Raman Spectroscopy ◽  
Self Assembly ◽  
Significant Enhancement ◽  
Side Chains ◽  
X Ray Diffraction ◽  
X Ray ◽  
Topochemical Polymerization ◽  
Scanning Electron

The synthesis and self-assembly of two new phenylacetylene macrocycle (PAM) organogelators were performed. Polar 2-hydroxyethoxy side chains were incorporated in the inner part of the macrocycles to modify the assembly mode in the gel state. With this modification, it was possible to increase the reactivity of the macrocycles in the xerogel state to form polydiacetylenes (PDAs), leading to a significant enhancement of the polymerization yields. The organogels and the PDAs were characterized using Raman spectroscopy, X-ray diffraction (XRD) and scanning electron microscopy (SEM).

SYNTHESIS, MORPHOLOGY AND STRUCTURAL PROPERTIES OF (GD,ND)SR2RUCU2O8 SAMPLES

2003 ◽  
Vol 17 (04n06) ◽  
pp. 899-904 ◽  
Author(s):  
A. VECCHIONE ◽  
M. GOMBOS ◽  
C. TEDESCO ◽  
A. IMMIRZI ◽  
L. MARCHESE ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Solid State ◽  
Powder Diffraction ◽  
Solid State Reaction ◽  
X Ray ◽  
Structure And Morphology ◽  
Polycrystalline Powder ◽  
Scanning Electron

NdSr 2 RuCu 2 O x material has been prepared as polycrystalline powder by solid state reaction. The compound has been investigated by synchrotron x-ray powder diffraction and scanning electron microscopy. The experimental results show that the average crystal structure is a disordered cubic perovskite with Nd and Sr cations occupying the same site and the same substitution is found for Cu and Ru atoms. A comparison between the crystal structure and morphology of this compound and the superconducting tetragonal GdSr 2 RuCu 2 O 8 is also discussed.

scholarly journals Preparation and Phase Relations in the CuSbSe2 – CuInSe2 System

2016 ◽  
Vol 1735 ◽  
Author(s):  
Barys V. Korzun ◽  
Valery R. Sobol ◽  
Marin Rusu ◽  
Ruben M. Savizky ◽  
Alena A. Fadzeyeva ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscopy ◽  
Mole Fraction ◽  
Powder Diffraction ◽  
Room Temperature ◽  
Phase Relations ◽  
X Ray ◽  
Ternary Compounds ◽  
Scanning Electron

ABSTRACTThe CuInSe2 and CuSbSe2 ternary compounds and alloys of the (CuSbSe2)1-x·(CuInSe2)x system with the mole fraction of CuInSe2 (x) equal to 0.05, 0.15, 0.25, 0.375, 0.50, 0.625, 0.75, 0.85, and 0.95 were prepared and the phase relations in this system were investigated by X-ray powder diffraction, optical microscopy, and scanning electron microscopy. It was shown that the alloys of the CuSbSe2-CuInSe2 system are biphasic at room temperature in the whole range of compositions, and the limits of solubility for CuSbSe2 in CuInSe2 and for CuInSe2 in CuSbSe2 do not exceed 0.001 mole fraction.

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