scholarly journals Pengaruh Suhu Sintering Pada Pembuatan Strontium Titanat (SrTiO3) Terhadap Konstanta Dielektrik Menggunakan Metode Co-Precipitation

2017 ◽  
Vol 7 (1) ◽  
pp. 27
Author(s):  
Husnah Rofiko ◽  
Yofentina Iriani ◽  
Risa Suryana
Keyword(s):  
Strontium Titanate ◽  
Crystal Size ◽  
Sintering Temperature ◽  
Strontium Nitrate ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Titanium Tetrabutoxide ◽  
Co Precipitation ◽  
Scanning Electron

<p>Strontium Titanate (SrTiO<sub>3</sub>) with variation of sintering temperatures were prepared by co-precipitation methods. Sintering temperature were varied at 700<sup>o</sup>C, 800<sup>o</sup>C, and 900<sup>o</sup>C for 4 hours. SrTiO<sub>3</sub> samples were prepared by Strontium Nitrate and Titanium Tetrabutoxide. SrTiO<sub>3</sub> samples were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Resistance Capacitance Inductance (RCL) meter, and Sawyer Tower.  SEM images show that the sintering temperatures could affect the grain size of SrTiO<sub>3</sub>. In addition, crystal size of SrTiO<sub>3</sub> (110) affected by sintering temperature. The highest of dielectric constant is 137 on SrTiO<sub>3</sub> at sintering temperature of 900<sup>o</sup>C. Sawyer Tower curves confirmed that SrTiO3 has paraelectric property.</p><p>Keyword: Strontium Titanate, Co-precipitation, dielectrics constant, paraelectrics</p><p> </p>

scholarly journals Pembuatan Ba0,8Sr0,2TiO3 menggunakan Metode Co-precipitation dengan Variasi Suhu Sintering

2017 ◽  
Vol 7 (1) ◽  
pp. 51
Author(s):  
Isma Alvia Nita ◽  
Yofentina Iriani ◽  
Fahru Nurosyid
Keyword(s):  
Dielectric Constant ◽  
Crystal Size ◽  
Sintering Temperature ◽  
Microstructure Characterization ◽  
Temperature Measurements ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lcr Meter ◽  
Co Precipitation

<p>Ba<sub>0,8</sub>Sr<sub>0,2</sub>TiO<sub>3 </sub>was made by co-precipitation method with the sintering temperature of 600<sup>o</sup>C, 700<sup>o</sup>C, 800<sup>o</sup>C and 900<sup>o</sup>C for 4 hours. Sintering temperature was varied to investigate its effect on microstructure and dielectric constant of Ba<sub>0,8</sub>Sr<sub>0,2</sub>TiO<sub>3</sub>. microstructure characterization was performed by X-Ray Diffraction (XRD) instrument. Dielectric constant characterization was perform by LCR meter. The crystal size increased significantly with increasing sintering temperature. Measurements of dielectric constant were performed at range of frequency 0.01 to 100 KHz. Dielectric constant value is highest at the lowest frequency. Dielectric constant value size increased significantly with increasing sintering temperature.</p>

scholarly journals Morphology control of SrBi2Nb2O9 prepared by a modified chemical method

2019 ◽  
Vol 51 (4) ◽  
pp. 353-361
Author(s):  
Mohamed Afqir ◽  
Amina Tachafine ◽  
Didier Fasquelle ◽  
Mohamed Elaatmani ◽  
Jean-Claude Carru ◽  
...  
Keyword(s):  
Molten Salt ◽  
Reaction Medium ◽  
Precipitation Method ◽  
Molten Salt Synthesis ◽  
Synthesis Process ◽  
Strontium Nitrate ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Co Precipitation

SrBi2NbO9 compounds were prepared through three methods: oxalate co-precipitation, molten salt synthesis and polymerizable complex. The effect of the molecular precursor route has also been investigated. For oxalate co-precipitation method, a solution obtained from acid oxalate, niobium oxide, bismuth nitrate and strontium nitrate are precipitated by ammoniac solution. Then, the precipitated sample is calcined at 1100?C. A methanol-citric acid solution of solution of NbCl5, ethylene glycol, bismuth and strontium nitrates were used as precursors. A black powder ash was crystallized by heat-treating at 1100?C. Molten salt technique using oxides and carbonate as starting materials and NaCl and KCl to form a reaction medium. The formation temperature was at 1110?C. Multiple characterizations mainly X-ray diffraction, Fourier transformed infrared spectroscopy and scanning electron microscopy (SEM) measurements have provided to validate the structural feature. Careful, X-ray diffraction analysis showed the presence of two-layered Aurivillius structure. The crystallite size is discussed by Scherrer and Williamson-Hall approaches. SEM images of SrBi2NbO9 ceramics showed plate-like, polygonal and structureless morphologies obtained at different synthesis conditions. Whatever the synthesis process, there is no change on the band of infrared spectra.

scholarly journals The effect of CNT content and sintering temperature on some properties of CNT-reinforced MgAl composites

2017 ◽  
Vol 49 (4) ◽  
pp. 347-357
Author(s):  
Serkan Islak ◽  
Özkan Küçük ◽  
Özkan Eski ◽  
Cihan Özorak ◽  
Mehmet Akkaş
Keyword(s):  
Solid Solution ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Pressing Method ◽  
Density Measurements ◽  
X Ray ◽  
The Matrix ◽  
Hardness Increase ◽  
Scanning Electron

Magnesium and its alloys are considered as an important material for modern light structures at the present time and therefore they have a wide area of usage especially in electronics, aircraft, and automotive industries. Its popularity increases further as a result of its production as a composite material. In this study, carbon nanotube (CNT) reinforced MgAl matrix composite materials were produced by using the hot pressing method. While 0.25 wt%, 0.50 wt%, 0.75 wt%, and 1.00 wt% CNT were added, 450?C, 500?C, and 550?C was selected as sintering temperatures. The effect of sintering temperature and amount of CNT on some properties of the composites was examined. Microstructure and phase composition of the materials were examined by using optical microscopy (OM), scanning electron microscope (SEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). The hardness of the composites was measured in Brinell. Relative densities of the materials were determined in accordance with Archimedes? principle. A dense and slightly porous structure was obtained based on both SEM images and density measurements. XRD analyses showed that there were Mg, Mg17Al12, and MgO phases in the composites. The reason for the absence of Al in graphics was that Al formed the solid solution by being dissolved in Mg. Also, the C peak could not be determined for CNT. The hardness of the composites increased with the increasing sintering temperature and CNT addition. The highest hardness value was measured as 88.45 HB10 with the addition of 1.00 wt% CNT at 550?C. Free distribution of CNT in the matrix caused this hardness increase.

Effect of Sintering Temperature on Microstructure and Mechanical Properties of Al2O3-TiC-ZrO2 Ceramic Composites

2012 ◽  
Vol 476-478 ◽  
pp. 1031-1035
Author(s):  
Wei Min Liu ◽  
Xing Ai ◽  
Jun Zhao ◽  
Yong Hui Zhou
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Fracture Toughness ◽  
Flexural Strength ◽  
Relative Density ◽  
Sintering Temperature ◽  
Ceramic Composites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Al2O3-TiC-ZrO2ceramic composites (ATZ) were fabricated by hot-pressed sintering. The phases and microstructure of the composites were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The relative density and mechanical properties (flexural strength, fracture toughness and Vicker’s hardness) of the composites were tested. The results show that the microstructure of the composites was the gray core-white rim. With the increase of sintering temperature, the relative density and mechanical properties of the composites increased first and then decreased. The composite sintered at 1705°C has the highest synthetical properties, and its relative density, flexural strength, fracture toughness and Vickers hardness are 98.3%,970MPa,6.0 MPa•m1/2and 20.5GPa, respectively.

scholarly journals Pengaruh Suhu Sintering Terhadap Sintesis Silicon Carbide (SiC) Berbahan Dasar Abu Sekam Padi dan Grafit Pensil 2B

2015 ◽  
Vol 5 (01) ◽  
pp. 31
Author(s):  
Resky Irfanita ◽  
Asnaeni Ansar ◽  
Ayu Hardianti Pratiwi ◽  
Jasruddin J ◽  
Subaer S
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silicon Carbide ◽  
Rice Husk Ash ◽  
Sintering Temperature ◽  
Solid State Reaction Method ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Scanning Electron

The objective of this study is to investigate the effect of sintering temperature on the synthesis of SiC produced from rice husk ash (RHA) and 2B graphite pencils. The SiC was synthesized by using solid state reaction method sintered at temperatures of 750°C, 1000°C and 1200°C for 26 hours, 11.5 hours and 11.5 hours, respectively. The quantity and crystallinity level of SiC phase were measured by means of Rigaku MiniFlexII X-Ray Diffraction (XRD). The microstructure of SiC was examined by using Tescan Vega3SB Scanning Electron Microscopy (SEM). The XRD results showed that the concentration (wt%) of SiC phase increases with the increasing of sintering temperature. SEM results showed that the crystallinity level of SiC crystal is improving as the sintering temperature increases

scholarly journals Structural and thermoelectric properties of the Pr2Zr2O7 compound

2019 ◽  
pp. 4-9
Author(s):  
Adolfo Quiroz-Rodríguez ◽  
Cesia Guarneros-Aguilar ◽  
Ricardo Agustin-Serrano
Keyword(s):  
Electron Microscopy ◽  
Thermal Conductivity ◽  
Thermoelectric Properties ◽  
Crystal Size ◽  
Ambient Pressure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Increasing Temperature ◽  
Thermal Stability Of ◽  
Scanning Electron

In this research, it is presented a detailed study of the structural and thermoelectric properties of the pyrochlore zirconium Pr2Zr2O7 compound prepared by solid-state reaction (SSR) in air at ambient pressure. The synthesized sample was characterized using powder X-ray diffraction. The thermal stability of the thermoelectric compound (TE) Pr2Zr2O7 was tested by thermogravimetric analysis (TGA) and differential thermal analysis (DTA). Scanning electron microscopy shows that the crystal size varies between 0.69 and 2.81μm. Electrical conductivity (\sigma) of the sample calcined at 1400 °C presented values increase irregularly with the increasing temperature from 0.001 to 0.018 S cm-1 as expected in a semiconductor material. The thermal conductivity is lower than 0.44 - 775 W m-1 K-1 which is quite anomalous in comparison with the thermal conductivity of other oxides.

Preparation and Microstructure of Pressureless Sintered Si2ON2-SiC Ceramic

2011 ◽  
Vol 335-336 ◽  
pp. 699-703
Author(s):  
Hui Hui Tan ◽  
Zhu Xing Tang ◽  
Xia Zhao ◽  
He Zhang
Keyword(s):  
Bulk Density ◽  
Sintering Temperature ◽  
Pressureless Sintering ◽  
Nitriding Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Effect Of Additives ◽  
Sic Ceramic ◽  
Sintering Method ◽  
Scanning Electron

This paper introduces Si2ON2-SiC ceramic fabricated by pressureless sintering method and studies the effect of additives, nitriding temperatures on bulk density, porosity, phase composition and microstructure. It is discovered that additives MgO, CeO2 can increase the densities of Si2ON2-SiC ceramic apparently, and MgO additive has a better effect than CeO2. Nitriding temperature also is an important factor. The bulk density of the specimen with MgO additive reaches maximum at 1.91 g/cm3 when sintered at 1450 °C, and the bulk density of specimen with CeO2 additive is 1.86 g/cm3 at the same condition while the bulk density of the specimen without additive is only 1.75 g/cSuperscript textm3. The X-ray diffraction and scanning electron microscopy of the specimens show that the amount of Si2ON2 increase with the sintering temperature increase. But when the temperature is higher than 1500 °C the Si2ON2 grains will decompose into Si3N4, and Si2ON2 will vanish at 1550 °C

Study on the Properties of Doped La in BaBi4Ti4O15 Ceramic

2007 ◽  
Vol 26-28 ◽  
pp. 243-246
Author(s):  
Xing Hua Yang ◽  
Jin Liang Huang ◽  
Xiao Wang ◽  
Chun Wei Cui
Keyword(s):  
Crystal Structure ◽  
Grain Size ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Sintering Temperature ◽  
Solid Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lanthanum Content ◽  
Scanning Electron

BaBi4-xLaxTi4O15 (BBLT) ceramics were prepared by conventional solid phase sintering ceramics processing technology. The crystal structure and the microstructure were detected by X-ray diffraction (XRD) and scanning electron microscope (SEM). The XRD analyses show that La3+ ions doping did not change the crystal structure of BBT ceramics. The sintering temperature increased from 1120°C to 1150°C with increasing Lanthanum content from 0 to 0.5, but it widened the sintering temperature range from 20°C to 50°C and refined the grain size of the BBT ceramic. Additionally, polarization treatment was performed and finally piezoelectric property was measured. As a result, the piezoelectric constant d33 of the 0.1at.% doped BBLT ceramics reached its highest value about 22pc/N at polarizing electric field of 8kV/mm and polarizing temperature of 120°C for 30min.

Preparation of the System of BaO-MgO-Al2O3-TiO2 Acid-Resistant Fracturing Proppants

2011 ◽  
Vol 399-401 ◽  
pp. 855-859
Author(s):  
Ting Ting Wu ◽  
Bo Lin Wu
Keyword(s):  
Sintering Temperature ◽  
Raw Materials ◽  
Acid Resistance ◽  
Pressureless Sintering ◽  
Alumina Matrix ◽  
X Ray Diffraction ◽  
X Ray ◽  
Acid Solubility ◽  
Resistance Performance ◽  
Scanning Electron

In order to improve the acid resistance and reduce the apparent density of fracturing proppants, TiO2 powder added in the system of BaO-MgO-Al2O3 fracturing proppants were prepared by the technique of pressureless sintering. The properties of the samples were investigated by the measurements of acid solubility, X-ray diffraction and scanning electron microscopy. The results show that the acid solubility of alumina matrix fracturing proppants contenting TiO2 of the 4wt% and BaO/MgO with the ratio of 3:7 is 0.15%. It is an important development in acid resistance performance of fracturing proppants research on laboratory. TiO2 is added to the raw materials and then calcine them to ceramics, which can reduces the sintering temperature, promote the densification and improve acid-resistant property of fracturing proppants.

Synthesis of Magnetic Modified Organobentonite as Adsorbent for Degradation of Orange II

2013 ◽  
Vol 838-841 ◽  
pp. 2306-2309
Author(s):  
Guang Hua Wang ◽  
Kun Chen ◽  
Wen Bing Li ◽  
Dong Wan ◽  
Qin Hu ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Reaction Medium ◽  
Precipitation Method ◽  
Basal Spacing ◽  
Orange Ii ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Co Precipitation ◽  
Scanning Electron

Magnetic modified organobentonite (Fe3O4/CTAB–Bent) was synthesized by chemical co-precipitation method in which CTAB–Bent was firstly achieved via ion–exchange.The composite materials have been characterized by powder X–ray diffraction (XRD), Fourier transform infrared spectroscopy (FT–IR) and Scanning electron microscopy (SEM) . The results revealed that basal spacing of bentonite was increased through organic modification and the Fe3O4 particles synthesized which covering the surfaces of bentonite .Compared with natural bentonite, the adsorption capacity of Fe3O4/CTAB–Bent for Orange II was greatly enhanced and can be easily separated from the reaction medium by an external magnetic field after the treatment.

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