Preparation and Characterization of SiC/MoSi2 Composites from Powder Resulting from a Mechanical-Assistant Combustion Synthesis Method

2010 ◽  
Vol 105-106 ◽  
pp. 70-74
Author(s):  
Jian Guang Xu ◽  
Hui Qiang Li ◽  
Hou An Zhang
Keyword(s):  
Mechanical Properties ◽  
Cyclic Oxidation ◽  
Room Temperature ◽  
Synthesis Method ◽  
Pressureless Sintering ◽  
Sintering Process ◽  
Oxidation Properties ◽  
Mosi2 Composite

SiC reinforced MoSi2 composites have been successfully prepared by pressureless sintering from mechanical-assistant combustion synthesized powders. The sintering temperatures and holding time were 1500°C~1650°C at a heating rate of 10K/min and 1 hour, respectively. The microstructure and mechanical properties of the as-sintered composites were investigated. SEM micrographs of SiC/MoSi2 composites showed that SiC particles were homogeneously distributed in MoSi2 matrix. The Vickers hardness, flexural strength and fracture toughness of the SiC/MoSi2 composites were up to 15.50GPa, 468.7MPa and 9.35MPa•m1/2, respectively. The morphologies of fractured surface of the composites revealed the mechanism to improve mechanical properties of MoSi2 matrix. At last, the cyclic oxidation behavior of the composites was discussed. The results of this work showed that in situ SiC/MoSi2 composite powder prepared by MASHS technique could be successfully sintered via pressureless sintering process and significant improvement of room temperature mechanical and anti-oxidation properties could be achieved.

Combustion Synthesis of Si3N4/MoSi2 Composite

2010 ◽  
Vol 92 ◽  
pp. 41-45
Author(s):  
Jian Guang Xu ◽  
Shi Bo Guo ◽  
Jian Hui Yan ◽  
Da Gong Zhang
Keyword(s):  
Mechanical Properties ◽  
Combustion Synthesis ◽  
Room Temperature ◽  
Composite Powder ◽  
Synthesis Method ◽  
Monolithic Material ◽  
Temperature Fracture ◽  
Mosi2 Composite ◽  
Fractured Surface

Si3N4 particle reinforced MoSi2 composite powder has been successfully synthesized combustion synthesis method. XRD and SEM results showed that the combustion product was mainly composed by MoSi2 and Si3N4. The as-prepared Si3N4/MoSi2 composite powder has been pressureless sintered at 1600°C for 1h. The microstructure and mechanical properties of the composite were investigated. Relative densities of the monolithic material and composite were 92.2% and 89.6%, respectively. The composite has higher Vicker’s hardness and flexural strength than monolithic MoSi2. Especially the room-temperature fracture toughness of the composite is from 4.21MPa•m1/2 for MoSi2 to 7.25MPa•m1/2 for composite, increased by 72.2%, respectively. The morphology of fractured surface of composite revealed the mechanism of improving mechanical properties of MoSi2 matrix. The results of this work showed that in situ Si3N4/MoSi2 composite powder prepared by combustion synthesis could be successfully pressureless sintered and significant improvement of mechanical properties could be achieved.

scholarly journals Improvement of mechanical properties of HfB2-based composites by incorporating in situ SiC reinforcement through pressureless sintering

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
S. Ghadami ◽  
E. Taheri-Nassaj ◽  
H. R. Baharvandi ◽  
F. Ghadami
Keyword(s):  
Mechanical Properties ◽  
Thermal Conductivity ◽  
Relative Density ◽  
Pressureless Sintering ◽  
Sintering Process ◽  
Vacuum Atmosphere ◽  
Sic Reinforcement ◽  
Microstructural Studies ◽  
Composite Samples

AbstractHfB2, Si, and activated carbon powders were selected to fabricate 0–30 vol% SiC reinforced HfB2-based composite. Pressureless sintering process was performed at 2050 °C for 4 h under a vacuum atmosphere. Microstructural studies revealed that in situ SiC reinforcement was formed and distributed in the composite according to the following reaction: Si + C = SiC. A maximum relative density of 98% was measured for the 20 vol% SiC containing HfB2 composite. Mechanical investigations showed that the hardness and the fracture toughness of these composites were increased and reached up to 21.2 GPa for HfB2-30 vol% SiC and 4.9 MPa.m1/2 for HfB2-20 vol% SiC, respectively. Results showed that alpha-SiC reinforcements were created jagged, irregular, and elongated in shape which were in situ formed between HfB2 grains and filled the porosities. Formation of alpha-SiC contributed to improving the relative density and mechanical properties of the composite samples. By increasing SiC content, an enhanced trend of thermal conductivity was observed as well as a reduced trend for electrical conductivity.

Experimental Investigation of Laser Sintering of Conductive Adhesive for Functional Prototypes Produced by Embedding Stereolithography

2014 ◽  
Vol 1038 ◽  
pp. 75-81
Author(s):  
Bernd Niese ◽  
Philipp Amend ◽  
Uwe Urmoneit ◽  
Stephan Roth ◽  
Michael Schmidt
Keyword(s):  
Thermal Damage ◽  
Laser Sintering ◽  
Conductive Adhesive ◽  
Flexible Production ◽  
Sintering Process ◽  
Building Process ◽  
In Situ Generation ◽  
Functional Components

Embedding stereolithography (eSLA) is an additive, hybrid process, which provides a flexible production of 3D components and the ability to integrate electrical and optical conductive structures and functional components within parts. However, the embedding of conductive circuits in stereolithography (SLA) parts assumes usage of process technologies, which enables their direct integration of conductive circuits during the layer-wise building process. In this context, a promising method for in-situ generation of conductive circuits is dispensing of conductive adhesive on the current surface of the SLA part and its subsequent sintering. In this paper, the laser sintering (λ = 355 nm) of conductive adhesive mainly consisting of silver nanoparticles is investigated. The work intends to evaluate the curing behavior of the conductive adhesive, the beam-matter-interactions and the thermal damage of the SLA substrate. The investigations revealed a fast and flexible laser sintering process for the generation of conductive circuits with sufficient electrical conductivity and sufficient current capacity load. In this context, a characterization of the conductive structures is done by measuring their electrical resistance and their potential current capacity load.

Synthesis and Characterization of ZIF-8 Mixed Matrix Membranes

2014 ◽  
Vol 625 ◽  
pp. 661-664
Author(s):  
Chen Chuang Lok ◽  
Yin Fong Yeong
Keyword(s):  
Room Temperature ◽  
Synthesis Method ◽  
Mixed Matrix Membranes ◽  
Inorganic Filler ◽  
X Ray Diffraction ◽  
Mixed Matrix ◽  
Temperature Synthesis ◽  
X Ray ◽  
Matrix Membranes

In the present work, ZIF-8/6FDA-durene mixed matrix membranes (MMMs) were synthesized and characterized. ZIF-8 nanocrystals, which were used as the inorganic filler, were synthesized using rapid room-temperature synthesis method whereas 6FDA-durene polyimide was synthesized by polycondensation method followed by chemical imidization. Pure and 6FDA-durene membranes loaded with 5 wt%, 10 wt% and 15 wt% of ZIF-8 were fabricated. The structural properties and morphology of the resultant membranes were characterized by using X-ray Diffraction (XRD) and Field emission scanning electron microscope (FESEM) . The EDX images showed that ZIF-8 particles agglomerated in the polymer matrix. However, no phase separation was observed for all resultant MMMs.

Mechanical properties of NiAl-Mo composites produced by specially controlled directional solidification

2012 ◽  
Vol 1516 ◽  
pp. 255-260 ◽  
Author(s):  
G. Zhang ◽  
L. Hu ◽  
W. Hu ◽  
G. Gottstein ◽  
S. Bogner ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Fracture Toughness ◽  
Directional Solidification ◽  
Creep Resistance ◽  
Room Temperature ◽  
Growth Direction ◽  
Nominal Composition ◽  
Potential Candidate ◽  
In Situ Composites

ABSTRACTMo fiber reinforced NiAl in-situ composites with a nominal composition Ni-43.8Al-9.5Mo (at.%) were produced by specially controlled directional solidification (DS) using a laboratory-scale Bridgman furnace equipped with a liquid metal cooling (LMC) device. In these composites, single crystalline Mo fibers were precipitated out through eutectic reaction and aligned parallel to the growth direction of the ingot. Mechanical properties, i.e. the creep resistance at high temperatures (HT, between 900 °C and 1200 °C) and the fracture toughness at room temperature (RT) of in-situ NiAl-Mo composites, were characterized by tensile creep (along the growth direction) and flexure (four-point bending, vertical to the growth direction) tests, respectively. In the current study, a steady creep rate of 10-6s-1 at 1100 °C under an initial applied tensile stress of 150MPa was measured. The flexure tests sustained a fracture toughness of 14.5 MPa·m1/2at room temperature. Compared to binary NiAl and other NiAl alloys, these properties showed a remarkably improvement in creep resistance at HT and fracture toughness at RT that makes this composite a potential candidate material for structural application at the temperatures above 1000 °C. The mechanisms responsible for the improvement of the mechanical properties in NiAl-Mo in-situ composites were discussed based on the investigation results.

Characterization of Hot-Pressed Silicon Nitride Ceramics with Alkoxide-Derived Oxide Mixtures As the Sintering Aid

1992 ◽  
Vol 287 ◽  
Author(s):  
Y. Sato ◽  
C. Sakurai ◽  
M. Ueki ◽  
K. Sugita
Keyword(s):  
Mechanical Properties ◽  
Room Temperature ◽  
Weight Ratio ◽  
Sintering Aids ◽  
Sintering Aid ◽  
Oxide Powders ◽  
Nitride Ceramics ◽  
Final Weight ◽  
Alkoxide Method

ABSTRACTA homogeneous mixture of Y2O3, CeO2 and MgO with a final weight ratio of 3:1: 2 was prepared by the alkoxide method. The powder mixture was then added into Si3N4 powder in amounts ranging from 4 to 12 wt%, andconsolidated by hot-pressing. Microstructure and mechanical properties of the sintered bodies were determined and compared to those of materials prepared by the conventional route of mixing the oxide powders as sintering aids individually in essentially same composition. The β-fraction (modification ratio) in same composition was higher in thesintered bodies made through the alkoxide method than those made through the conventional one. The room temperature flexural strength was maximized with 6wt% addition of the alkoxide derived oxide, whereas, 12wt% addition of the total oxide was required to maximize the strength by conventional processing.

scholarly journals Microstructural and Mechanical Characterization of Al-0.80Mg-0.85Si-0.3Zr Alloy

2017 ◽  
Vol 17 (4) ◽  
pp. 73-78 ◽  
Author(s):  
F. Kahrıman ◽  
M. Zeren
Keyword(s):  
Mechanical Properties ◽  
Automotive Industry ◽  
Room Temperature ◽  
Tensile Tests ◽  
Direct Chill ◽  
Peak Hardness ◽  
Casting Method ◽  
Industry Standard ◽  
Three Stages

Abstract In this study, Al-0.80Mg-0.85Si alloy was modified with the addition of 0.3 wt.-% zirconium and the variation of microstructural features and mechanical properties were investigated. In order to produce the billets, vertical direct chill casting method was used and billets were homogenized at 580 °C for 6 h. Homogenized billets were subjected to aging practice following three stages: (i) solution annealing at 550 °C for 3 h, (ii) quenching in water, (iii) aging at 180 °C between 0 and 20 h. The hardness measurements were performed for the alloys following the aging process. It was observed that peak hardness value of Al-0.80Mg-0.85Si alloy increased with the addition of zirconium. This finding was very useful to obtain aging parameters for the extruded hollow profiles which are commonly used in automotive industry. Standard tensile tests were applied to aged profiles at room temperature and the results showed that modified alloy had higher mechanical properties compared to the non-modified alloy.

scholarly journals Characterization of Ti/SnO2 Interface by X-ray Photoelectron Spectroscopy

Nanomaterials ◽  
2022 ◽  
Vol 12 (2) ◽  
pp. 202
Author(s):  
Miranda Martinez ◽  
Anil R. Chourasia
Keyword(s):  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Chemical Interaction ◽  
Photoelectron Spectra ◽  
X Ray ◽  
Increasing Trend ◽  
Substrate Temperatures ◽  
Beam Technique

The Ti/SnO2 interface has been investigated in situ via the technique of x-ray photoelectron spectroscopy. Thin films (in the range from 0.3 to 1.1 nm) of titanium were deposited on SnO2 substrates via the e-beam technique. The deposition was carried out at two different substrate temperatures, namely room temperature and 200 °C. The photoelectron spectra of tin and titanium in the samples were found to exhibit significant differences upon comparison with the corresponding elemental and the oxide spectra. These changes result from chemical interaction between SnO2 and the titanium overlayer at the interface. The SnO2 was observed to be reduced to elemental tin while the titanium overlayer was observed to become oxidized. Complete reduction of SnO2 to elemental tin did not occur even for the lowest thickness of the titanium overlayer. The interfaces in both the types of the samples were observed to consist of elemental Sn, SnO2, elemental titanium, TiO2, and Ti-suboxide. The relative percentages of the constituents at the interface have been estimated by curve fitting the spectral data with the corresponding elemental and the oxide spectra. In the 200 °C samples, thermal diffusion of the titanium overlayer was observed. This resulted in the complete oxidation of the titanium overlayer to TiO2 upto a thickness of 0.9 nm of the overlayer. Elemental titanium resulting from the unreacted overlayer was observed to be more in the room temperature samples. The room temperature samples showed variation around 20% for the Ti-suboxide while an increasing trend was observed in the 200 °C samples.

scholarly journals Synthesis of "in situ" reinforced silicon nitride composites

2004 ◽  
Vol 69 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Aleksandra Vuckovic ◽  
Snezana Boskovic ◽  
Ljiljana Zivkovic
Keyword(s):  
Mechanical Properties ◽  
Fracture Toughness ◽  
Silicon Nitride ◽  
Pressureless Sintering ◽  
Sintering Additives ◽  
Sintering Time

The objective of this work was to investigate the effect of two different sintering additives (CeO2 and Y2O3 + Al2O3), sintering time and amount of ?-Si3N4 seeds on the densification, mechanical properties and microstructure of self-reinforced Si3N4 based composites obtained by pressureless sintering. Preparation of ?-Si3N4 seeds, also obtained by a pressureless sintering procedure, is described. Samples without seeds were prepared for comparison. The results imply that self-reinforced silicon nitride based composites with densities close to the theoretical values and with fracture toughness of 9.3MPa m1/2 can be obtained using a presureless sintering procedure.

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