Effect of Different Sintering Temperature on the Performance of Mullite-Corundum Refractory Materials

2013 ◽  
Vol 750-752 ◽  
pp. 521-524
Author(s):  
Ping Li ◽  
Xing Yong Gu ◽  
Ting Luo ◽  
Yun Xia Chen
Keyword(s):  
Thermal Expansion ◽  
Thermal Stress ◽  
Stress Fracture ◽  
Bending Strength ◽  
Sintering Temperature ◽  
Coefficient Of Thermal Expansion ◽  
Refractory Materials ◽  
Corundum Refractory ◽  
X Ray Diffraction

Al (OH)3, Suzhou kaolin, AlF3 and V2O5 were premixed and pelleted to form the precursor for fabricating the mullite whisker, and then the precursor was added into the calcined bauxite and Suzhou kaolin mixture according to a certain mass percent. The mullite-corundum refractory materials with well-dispersed needle-like mullite formed in-situ were prepared. Through studying the effect of different sintering temperatures on the performances of the as-fabricated mullite-corundum refractory materials, it was concluded that the appropriate sintering temperature was 1450 °C. X-ray diffraction (XRD), scanning electron microscopy (SEM), water absorption, bending strength, coefficient of thermal expansion and the first thermal stress fracture factor were used to characterize and evaluate the materials. The results show that the sintering character and thermal expansion coefficient of the refractory materials increase with the rising sintering temperature. The bending strength of the refractory materials sintered at 1500 °C presented the maximum value and the first thermal stress fracture factor appeared the highest value at 1450 °C.

Fabrication and Properties of W-SiCP/Cu Composites by Hot Pressing Sintering

2016 ◽  
Vol 697 ◽  
pp. 207-210
Author(s):  
Lian Meng Zhang ◽  
Yao Liu ◽  
Cheng Cheng Zhang ◽  
Guo Qiang Luo ◽  
Huang Liu ◽  
...  
Keyword(s):  
Thermal Expansion ◽  
Low Temperature ◽  
Bending Strength ◽  
Coefficient Of Thermal Expansion ◽  
Hot Press ◽  
X Ray Diffraction ◽  
Ternary Composite ◽  
Hot Pressing Sintering ◽  
Hot Press Sintering ◽  
Structural Characterizations

Abstract. A new ternary composite of W-SiCP/Cu(40vol%) was designed and prepared by low-temperature hot-press sintering. The micro-structural characterizations were evaluated by X-ray diffraction (XRD) and scanning electron microstructure (SEM), coefficient of thermal expansion is measured. When sintered at 950°C-100MPa-2h, the relative density of the W-SiCP/Cu composites as a function of W content all exceeded 97%. Due to the plastic deformation of Cu, higher densification W-SiCP/Cu(40vol%) composites can be achieved at a relatively low temperature. The composites are characterized by the relatively low coefficient of thermal expansion, bending strength and hardness. The values of thermal expansion indicate that thermal expansion can be precisely controlled by adding SiC particles.

In Situ Synthesis of TiB2-TiC0.8-40vol%SiC by Hot Pressing

2013 ◽  
Vol 813 ◽  
pp. 179-187 ◽  
Author(s):  
Pei Qiu Sun ◽  
De Gui Zhu ◽  
Xiao Song Jiang ◽  
Hong Liang Sun ◽  
Song Chen
Keyword(s):  
Bending Strength ◽  
Sintering Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fine Grain ◽  
Pull Out ◽  
Sic Particles ◽  
Synergistic Mechanism ◽  
Multiphase Ceramics

TiB2-TiC0.8-40vol%SiC multiphase ceramics were prepared by in-situ hotpressing sintering. The phase composition and microstructures of the materials were characterized by optical mic- oscope, X-ray diffraction and scanning electron microscopy. The effects of sintering temperature on the phases, microstructures and mechanical properties of the ceramics were investigated. The results show that density, bending strength and fracture toughness of the ceramics are increased with the elevation of sintering temperature (1800-1950°C). High densified TiB2-TiC0.8-40vol%SiC multipha- se ceramics and optimized microstructure is obtained by sintering at 1900°C, in which the uniform distribution of lath-shape TiB2 and bulk TiC0.8 grains can be observed obviously. Nano-SiC particles distributed dispersively in the TiB2 and TiC0.8 grains and at boundaries. The Vickers hardness, fract- ure toughness, flexural strength and electrical conductivity of the TiB2-TiC0.8-40vol%SiC multipha- se ceramics sintered at 1900°C are 24.055GPa, 8.27±1.0MPa∙m1/2, 516.69MPa and 2.2×106S∙m-1, respectively. However, up to 1950°C, TiB2 and TiC0.8 grains gradually grew up, the bending stren- gth of multiphase ceramics was decreased greatly. In addition, TiB2, TiC0.8 and SiC particles were incorporated together to improve the particulate strength and toughness of composite material by the synergistic mechanism effects among the crystal phases in the multiphase ceramics, such as crack deflection, grain’s pull-out and fine-grain toughening.

scholarly journals Effect of Sintering Temperature on Microstructure and Mechanical Properties of Hot-Pressed Fe/FeAl2O4 Composite

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 422
Author(s):  
Kuai Zhang ◽  
Yungang Li ◽  
Hongyan Yan ◽  
Chuang Wang ◽  
Hui Li ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Bending Strength ◽  
Sintering Temperature ◽  
Raw Materials ◽  
Hot Press ◽  
Microstructure And Mechanical Properties ◽  
Powder Particles ◽  
Hot Press Sintering ◽  
Sintering Method

An Fe/FeAl2O4 composite was prepared with Fe-Fe2O3-Al2O3 powder by a hot press sintering method. The mass ratio was 6:1:2, sintering pressure was 30 MPa, and holding time was 120 min. The raw materials for the powder particles were respectively 1 µm (Fe), 0.5 µm (Fe2O3), and 1 µm (Al2O3) in diameter. The effect of sintering temperature on the microstructure and mechanical properties of Fe/FeAl2O4 composite was studied. The results showed that Fe/FeAl2O4 composite was formed by in situ reaction at 1300 °C–1500 °C. With the increased sintering temperature, the microstructure and mechanical properties of the Fe/FeAl2O4 composite showed a change law that initially became better and then became worse. The best microstructure and optimal mechanical properties were obtained at 1400 °C. At this temperature, the grain size of Fe and FeAl2O4 phases in Fe/FeAl2O4 composite was uniform, the relative density was 96.7%, and the Vickers hardness and bending strength were 1.88 GPa and 280.0 MPa, respectively. The wettability between Fe and FeAl2O4 was enhanced with increased sintering temperature. And then the densification process was accelerated. Finally, the microstructure and mechanical properties of the Fe/FeAl2O4 composite were improved.

scholarly journals Thermal expansion of La-based BMG studied by in situ high-energy X-ray diffraction

2010 ◽  
Vol 504 ◽  
pp. S155-S158 ◽  
Author(s):  
J. Bednarcik ◽  
C. Curfs ◽  
M. Sikorski ◽  
H. Franz ◽  
J.Z. Jiang
Keyword(s):  
Thermal Expansion ◽  
High Energy ◽  
X Ray Diffraction ◽  
X Ray

In Situ Preparation and Mechanical Properties of (ZrB2+ZrC)/Zr3[Al(Si)]4C6 Composites

2014 ◽  
Vol 602-603 ◽  
pp. 438-442
Author(s):  
Lei Yu ◽  
Jian Yang ◽  
Tai Qiu
Keyword(s):  
Mechanical Properties ◽  
Fracture Toughness ◽  
Bending Strength ◽  
Coefficient Of Thermal Expansion ◽  
Raw Materials ◽  
Linear Increase ◽  
Fine Grain ◽  
Fine Grain Strengthening ◽  
Uniform Microstructure

Fully dense (ZrB2+ZrC)/Zr3[Al (Si)]4C6 composites with ZrB2 content varying from 0 to 15 vol.% and fixed ZrC content of 10 vol.% were successfully prepared by in situ hot-pressing in Ar atmosphere using ZrH2, Al, Si, C and B4C as raw materials. With the increase of ZrB2 content, both the bending strength and fracture toughness of the composites increase and then decrease. The synergistic action of ZrB2 and ZrC as reinforcements shows significant strengthening and toughing effect to the Zr3[Al (Si)]4C6 matrix. The composite with 10 vol.% ZrB2 shows the optimal mechanical properties: 516 MPa for bending strength and 6.52 MPa·m1/2 for fracture toughness. With the increase of ZrB2 content, the Vickers hardness of the composites shows a near-linear increase from 15.3 GPa to 16.7 GPa. The strengthening and toughening effect can be ascribed to the unique mechanical properties of ZrB2 and ZrC reinforcements, the differences in coefficient of thermal expansion and modulus between them and Zr3[Al (Si)]4C6 matrix, fine grain strengthening and uniform microstructure derived by the in situ synthesis reaction.

Thermally boosted upconversion and downshifting luminescence in Sc2(MoO4)3:Yb/Er with two-dimensional negative thermal expansion

2021 ◽  
Author(s):  
Jinsheng Liao ◽  
Minghua Wang ◽  
Fulin Lin ◽  
Zhuo Han ◽  
Datao Tu ◽  
...  
Keyword(s):  
Thermal Expansion ◽  
Near Infrared ◽  
Negative Thermal Expansion ◽  
Thermal Quenching ◽  
Relative Sensitivity ◽  
Strong Temperature Dependence ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Higher Temperature

Abstract Lanthanide (Ln3+)-doped phosphors generally suffer from thermal quenching, in which their photoluminescence (PL) intensities decrease at the higher temperature. Herein, we report a class of unique two-dimensional negative-thermal-expansion phosphor of Sc2(MoO4)3:Yb/Er. By virtue of the reduced distances between sensitizers and emitters as well as confined energy migration with increasing the temperature, a 45-fold enhancement of green upconversion (UC) luminescence and a 450-fold enhancement of near-infrared downshifting (DS) luminescence of Er3+ are achieved from 25 to 500 ˚C. The thermally boosted UC and DS luminescence mechanism is systematically investigated through in situ temperature-dependent Raman spectroscopy, synchrotron X-ray diffraction and PL dynamics. Moreover, the luminescence lifetime of 4I11/2 of Er3+ in Sc2(MoO4)3:Yb/Er displays a strong temperature dependence, enabling ratiometric thermometry with the highest relative sensitivity of 13.4%/K at 298 K. These findings may gain a vital insight into the design of negative-thermal-expansion Ln3+-doped phosphors for versatile applications.

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