Synthesis of Nanostructured PZT Ceramics with Powder Obtained from Coprecipitate Method

2014 ◽  
Vol 798-799 ◽  
pp. 110-115
Author(s):  
Alexandre Costa Lanza ◽  
Daniel Thomazini ◽  
Maria Virgínia Gelfuso
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Grain Morphology ◽  
Microwave Oven ◽  
Spherical Particles ◽  
X Ray Diffraction ◽  
Pzt Ceramics ◽  
X Ray ◽  
Piezoelectric Devices ◽  
Scanning Electron

Ceramics of Pb1.02(Zr0.53Ti0.47)O3(PZT) comprise the majority of piezoelectric devices in use today. In general, these ceramics are obtained by solid-state reaction, which favors the formation of micrometric grains. Recent studies have shown that reducing the particle size from micro to nanoscale, it generates PZT ceramics with superior dielectric properties. In this way, this study aimed to obtain nanostructured PZT ceramics from the coprecipitate method, using precursor materials as oxides reagents. From the Differential Thermal Analysis (DTA) was observed that the formation of PZT through the proposed methodology is initiated at 550oC. However, the full phase crystallization was observed at 850oC confirmed by X-Ray Diffraction (XRD). Spherical particles near 200nm were observed using scanning electron microscopy (SEM). This powder was sintered in conventional and microwave oven. The ceramics obtained from both sintering methods showed substantial differences in microstructure such as presence of piroclore phase and grain morphology.

PENINGKATAN LAJU DISOLUSI ACYCLOVIR DENGAN METODE SISTEM DISPERSI PADAT MENGGUNAKAN POLOXAMER 188

2016 ◽  
Vol 5 (1) ◽  
pp. 6
Author(s):  
Budi Setiawan ◽  
Erizal Zaini ◽  
Salman Umar
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Differential Thermal Analysis ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
Poloxamer 188 ◽  
X Ray ◽  
Scanning Electron

Sebuah penelitian tentang sistem dispersi padat dari asiklovir dengan poloxamer 188 telah dilakukan formulasi dengan pencampuran secara fisika dengan rasio 1 : 1, 1 : 3, 1 : 5 dan dispersi padat 1 : 1, 1 : 3, 1 : 5 dan penggilingan 1:1 sebagai pembanding. Dispersi padat dibuat menggunakan metode pencairan (fusi), yang digabung dengan poloxamer 188 pada hotplate kemudian asiklovir dimasukkan ke dalam hasil poloxamer 188 lalu di kocok hingga membentuk masa homogen. Semua formula yang terbentuk termasuk asiklovir poloxamer 188 murni dianalisis karakterisasinya dengan Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), dan Fourier Transform Infrared (FTIR), kemudian pengambilan dilakukan  (penentuan kadar) mengunakan spektrofotometer UV pada panjang gelombang 257,08 nm dan uji laju disolusi dengan aquadest bebas CO2 menggunakan metode dayung. Hasil pengambilan  (penentuan kadar) menunjukkan bahwa semua formula memenuhi persyaratan farmakope Amerika edisi 30 dan farmakope Indonesia edisi 4 yaitu 95-110%. Sedangkan hasil uji laju disolusi untuk campuran fisik 1: 1, dan dispersi padat 1: 1, dan penggilingan 1: 1 menunjukkan peningkatan yang nyata dibandingkan asiklovir murni. Hal ini juga dapat dilihat dari hasil perhitungan statistik  menggunakan analisis varian satu arah  SPSS 17.

Electrochemical Synthesis and Photocatalytic Activity of Differently Shaped CuOx Particles

2017 ◽  
Vol 13 ◽  
pp. 330-333
Author(s):  
Anna Ulyankina ◽  
Igor Leontyev ◽  
Nina Smirnova
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Electrochemical Method ◽  
Spherical Particles ◽  
Photocatalytic Efficiency ◽  
X Ray Diffraction ◽  
X Ray ◽  
Polyhedral Particles ◽  
Copper Electrodes ◽  
Scanning Electron

CuOx powders with diff erently shaped particles were firstly prepared via an electrochemical method by oxidation and dispersion of copper electrodes in an electrolyte solution under pulse alternating current (PAC). By means of X-ray diffraction (XRD) and scanning electron microscopy (SEM) the current density is found to have an influence on the morphology and composition of CuOx particles. Photocatalytic efficiency of CuOx towards methyl orange (MO) degradation under visible light was investigated. The prepared polyhedral particles show the best photocatalytic activity of 81 % towards MO comparing to octahedral and spherical particles with 70 and 61 %, respectively.

Reactivity in the chromium oxide-calcium fluoride system: An empirical approach

1999 ◽  
Vol 14 (6) ◽  
pp. 2518-2523
Author(s):  
Frans Vos ◽  
Luc Delaey ◽  
Marc De Bonte ◽  
Ludo Froyen
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Calcium Fluoride ◽  
Reaction Mechanisms ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
Reaction Behavior ◽  
X Ray ◽  
Scanning Electron

The reaction mechanisms observed when sintering loose Cr2O3–CaF2 powder mixtures were analyzed, and the influence of the sintering parameters on the reaction behavior is presented. Using x-ray diffraction (XRD), energy-dispersive spectroscopy (EDS), and differential thermal analysis (DTA) measurements, CaCrO4 was shown to be the reaction product when sintering in air. The reaction occurs in two steps: CaF2 transforms to CaO at the Cr2O3–CaF2 interface, followed by a CaO–Cr2O3 interaction, which creates the reaction product. Scanning electron microscopy (SEM) and x-ray fluorescence (XRF) analysis showed an increasing loss of CaF2 with increasing sintering temperature and heating rate, while an opposite evolution of the amount of reaction product was observed.

Immobilization of ASH by Microwave Melting

1992 ◽  
Vol 269 ◽  
Author(s):  
Kazuki Morita ◽  
Vinh Q. Nguyen ◽  
Ron Nakaoka ◽  
John D. Mackenzie
Keyword(s):  
Electron Microscopy ◽  
Lithium Carbonate ◽  
Microwave Oven ◽  
Toxicity Characteristic Leaching Procedure ◽  
Leaching Rate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Leaching Procedure ◽  
Pb Immobilization ◽  
Scanning Electron

ABSTRACTNon-radioactive ash was immobilized via microwave melting. The ash composed mainly of silica (SiO2), titania (TiO2), calcia (CaO), alumina (Al2O3), and carbon (C). The ash was melted with various additives, such as magnetite (Fe3O4), lithium carbonate (Li2CO3), sodium carbonate (Na2CO3), and boron oxide (B2O3) by using a 2.45 GHz, 750 W microwave oven. Samples with different ash and additive concentrations were melted when subjected to microwave radiation. Ease of melting was dependent on the carbon and magnetite concentrations. Melted samples were characterized by X-ray diffraction and scanning electron microscopy (SEM), and subjected to the Toxicity Characteristic Leaching Procedure in regard to lead (Pb) immobilization. Melted samples with more than 30 wt% additives has an undetectable leaching rate of less than 0.1 ppm of lead for TCLP test, which was found to be due to the reduction and evaporation of the lead during melting. More than 80 % of the lead was lost through evaporation leaving less than 0.1 wt% Pb in the melted glass.

Synthesis, Characterization and Magnetism of Nanosized Copper Ferrite

2008 ◽  
Vol 368-372 ◽  
pp. 604-606 ◽  
Author(s):  
Wei Zhong Lv ◽  
Zhong Kuang Luo ◽  
Bo Liu ◽  
Xiang Zhong Ren ◽  
Hong Hua Cai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Copper Ferrite ◽  
Sonochemical Method ◽  
Thermal Gravimetric ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

Copper ferrite powders were successfully synthesized by sonochemical method. The resultant powders were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR, differential thermal analysis-thermal gravimetric (DTA-TG), differential scanning calorimetry (DSC) and VSM. The particle saturation magnetization (Ms) is 66 emu/g and an intrinsic coercive force (iHc) is 2100 Oe when the precursor calcined at 950 °C for 15 h.

Darstellung und Charakterisierung des Silber(I,II,III)-oxidclathrates Ag7O8HCO3 / Synthesis and Characterization of the Silver(I,II,III) Oxide Clathrate Ag7O8HCO3

2000 ◽  
Vol 55 (9) ◽  
pp. 882-886 ◽  
Author(s):  
Martin Jansen ◽  
Sascha Vensky
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Magnetic Susceptibility ◽  
Solid State Nmr ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The silver(I,II,III) oxide clathrate Ag7O8HCO3 was synthesized by anodic oxidation of silver(I) in a suspension of Ag2CO3 in an aqueous AgF solution. The title compound was characterized by single crystal X-ray diffraction (cubic, Fm3̄m, a = 9.8085(3) Å, Z = 4), scanning electron microscopy, thermal analysis, IR spectroscopy, 1H-solid state-NMR and measurement of the magnetic susceptibility

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