Sintering Additives Effects on the Microstructure and Electrical Behavior of Yttrium Oxide Ceramic Composites

2021 ◽  
Vol 19 (6) ◽  
pp. 36-40
Author(s):  
Tarik T. Issa ◽  
Duha S. Ahmed ◽  
Sadeer M. Majeed
Keyword(s):  
Silicon Carbide ◽  
Yttrium Oxide ◽  
Sintered Density ◽  
Sintering Temperature ◽  
Ceramic Composites ◽  
Oxide Ceramic ◽  
Dry Milling ◽  
Electrical Behavior ◽  
Scanning Electron ◽  
Structure Test

Ceramics type Yttrium oxide with Silicon carbide. were selected to investigate its sintered density, microstructure and electrical properties, after adding V2O5, of 100 nm grain size. Different weight percentages ranging from (0.01, 0.02, 0.03 and 0.04) were used. Dry milling applied for twelve hours. The pelletized samples were sintered at atmospheric of static air and at sintering temperature 1400 ˚C, for three hours. The crustal structure test shoes the phase which is yttrium silicon carbide Scanning electron microscopy, scan sintered microstructure. Samples after sintering were electrically investigated by measuring its capacitance, dielectric constant and their results showed increasing after added V2O5 particles at the combination Yttrium oxide 80 Wt.% -Silicon carbide 20 Wt.% with 0.04 V2O5 Wt.%.

Sintering Additives Effects on the Microstructure and Electrical Behavior of Yttrium Oxide Ceramic Composites

2021 ◽  
Vol 19 (3) ◽  
pp. 62-68
Author(s):  
Tarik T. Issa ◽  
Samara J Mohammad
Keyword(s):  
Silicon Carbide ◽  
Yttrium Oxide ◽  
Sintered Density ◽  
Sintering Temperature ◽  
Ceramic Composites ◽  
Oxide Ceramic ◽  
Dry Milling ◽  
Electrical Behavior ◽  
Scanning Electron ◽  
Structure Test

Ceramics type Yttrium oxide with Silicon carbide. were selected to investigate its sintered density, microstructure and electrical properties, after adding V2O5, of 100 nm grain size. Different weight percentages ranging from (0.01,0.02,0.03 and 0.04) were used. Dry milling applied for twelve hours. The pelletized samples were sintered at atmospheric of static air and at sintering temperature 1400 ˚C, for three hours. The crustal structure test shoes the phase which is yttrium silicon carbide Scanning electron microscopy, scan sintered microstructure. Samples after sintering were electrically investigated by measuring its capacitance, dielectric constant and their results showed increasing after added V2O5 particles at the combination Yttrium oxide 80 Wt.% -Silicon carbide 20 Wt.% with 0.04 V2O5 Wt.%.

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

Two-Step Pressureless Sintering of Silicon Carbide-Based Materials

2014 ◽  
Vol 89 ◽  
pp. 70-75 ◽  
Author(s):  
Giuseppe Magnani ◽  
Giuliano Sico ◽  
Alida Brentari
Keyword(s):  
Silicon Carbide ◽  
Solid State ◽  
Grain Growth ◽  
Sintered Density ◽  
Sintering Temperature ◽  
Liquid Phase Sintering ◽  
Carbide Powder ◽  
Pressureless Sintering ◽  
Beneficial Effects ◽  
High Sintered Density

Pressureless sintering of silicon carbide powder requires addition of sintering aids and high sintering temperature (>2100°C) in order to achieve high sintered density (>95% T.D.). The high sintering temperature normally causes an exaggerated grain growth which can compromise the mechanical properties. Two-step sintering (TSS) can be used to overcome this problem. By this method, high sintered density is obtained avoiding the grain growth associated to the last step of the sintering. Two-step sintering was successfully applied to different commercial silicon carbide powders with different sintering mechanism: solid-state and liquid-phase sintering. In both cases the sintering temperature was set nearly 100 °C below the temperature conventionally required. Microstructures of samples obtained by TSS and conventional sintering (CS) processes were compared. TSS-SiC showed finer microstructure consisted of equiaxed grains with very similar density. The beneficial effects of the two-step sintering process were more evident in the solid state sintering. In this case sintered density higher than 98% was achieved with T<2000 °C.

Microstructural Evaluation of Silicon Carbide Whisker Reinforced Alumina Fabricated with Carbon-Coated Whiskers

1991 ◽  
Vol 49 ◽  
pp. 920-921
Author(s):  
K. B. Alexander ◽  
P. F. Becher
Keyword(s):  
Silicon Carbide ◽  
High Resolution Electron Microscopy ◽  
Ceramic Composites ◽  
Interface Debonding ◽  
Resolution Electron ◽  
Microstructural Evaluation ◽  
Carbon Coated ◽  
Electron Energy Loss ◽  
Interfacial Films ◽  
Debonding Process

The presence of interfacial films at the whisker-matrix interface can significantly influence the fracture toughness of ceramic composites. The film may alter the interface debonding process though changes in either the interfacial fracture energy or the residual stress at the interface. In addition, the films may affect the whisker pullout process through the frictional sliding coefficients or the extent of mechanical interlocking of the interface due to the whisker surface topography.Composites containing ACMC silicon carbide whiskers (SiCw) which had been coated with 5-10 nm of carbon and Tokai whiskers coated with 2 nm of carbon have been examined. High resolution electron microscopy (HREM) images of the interface were obtained with a JEOL 4000EX electron microscope. The whisker geometry used for HREM imaging is described in Reference 2. High spatial resolution (< 2-nm-diameter probe) parallel-collection electron energy loss spectroscopy (PEELS) measurements were obtained with a Philips EM400T/FEG microscope equipped with a Gatan Model 666 spectrometer.

Effects of Sintering Conditions on Properties of a Warm Compacted Stainless Steel Powder

2012 ◽  
Vol 217-219 ◽  
pp. 483-486
Author(s):  
Mei Yuan Ke
Keyword(s):  
Tensile Strength ◽  
Stainless Steel ◽  
Sintered Density ◽  
Sintering Temperature ◽  
Steel Powder ◽  
Stainless Steel Powder ◽  
Sintering Atmosphere ◽  
Comprehensive Properties ◽  
Ammonia Atmosphere ◽  
Sintering Conditions

Effects of Sintering atmosphere and temperature on properties of warm compacted 410L stainless steel powder were studied. Sintered density, hardness, tensile strength and elongation were measured. Results showed that in order to achieve high comprehensive properties, the optimal sintering temperature was 1230°C for 410L stainless steel powder. At the same sintering temperature, density and hardness sintered in vacuum were much higher than that sintered in cracked ammonia while tensile strength sintered in cracked ammonia were much higher than that in vacuum. When sintered in vacuum at 1230°C, sintered density was 7.45 g•cm-3, hardness was 65 HRB, tensile strength was 410 MPa and elongation was 29.5%. When sintered in cracked ammonia atmosphere at 1230°C, sintered density was 7.26 g•cm-3, hardness was 97 HRB, tensile strength was 515 MPa and elongation was 3.8%.

scholarly journals Effects of Sintering Temperature on Densification, Microstructure and Mechanical Properties of Al-Based Alloy by High-Velocity Compaction

Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Xianjie Yuan ◽  
Xuanhui Qu ◽  
Haiqing Yin ◽  
Zaiqiang Feng ◽  
Mingqi Tang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
High Velocity ◽  
Sintered Density ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
High Velocity Compaction ◽  
Sintered Temperature

This present work investigates the effects of sintering temperature on densification, mechanical properties and microstructure of Al-based alloy pressed by high-velocity compaction. The green samples were heated under the flow of high pure (99.99 wt%) N2. The heating rate was 4 °C/min before 315 °C. For reducing the residual stress, the samples were isothermally held for one h. Then, the specimens were respectively heated at the rate of 10 °C/min to the temperature between 540 °C and 700 °C, held for one h, and then furnace-cooled to the room temperature. Results indicate that when the sintered temperature was 640 °C, both the sintered density and mechanical properties was optimum. Differential Scanning Calorimetry, X-ray diffraction of sintered samples, Scanning Electron Microscopy, Energy Dispersive Spectroscopy, and Transmission Electron Microscope were used to analyse the microstructure and phases.

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