Effect of Ni Coated SiC on Mechanical Properties of SiC/Fe Composites

2014 ◽  
Vol 602-603 ◽  
pp. 578-581
Author(s):  
Bin Bin Wang ◽  
Bing Bing Fan ◽  
Wen Li ◽  
Chen Yang Wang ◽  
Bing Sun ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Bending Strength ◽  
Chemical Deposition ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
Structure Morphology ◽  
Chemical Deposition Method ◽  
Shell Composite ◽  
Electronic Microscope

A facile onestep in situ chemical deposition method was introduced to synthesize Ni coated SiC composite powders, which used NiCl2·6H2O as nickel source and N2H4·H2O as reductant, respectively. SiC(Ni)/Fe composites were prepared by current-vacuum hot-pressed sintering at 850°C, 40MPa for 30min. Scanning electronic microscope (SEM) and X-ray diffraction (XRD) were used to characterize the structure, morphology and composition of the prepared Ni/SiC core/shell composite powders. It is found that the Ni coated SiC is favorable to improve the dispersion and compatibility of SiC(Ni)/ Fe composites. By a series of contrast experiments, it is shown that the sintering sample with 5wt% of SiC(Ni) has the best mechanical properties. The relative density, Vickers hardness and bending strength is 91.67%, 4.72GPa and 508MPa, respectively.

Study on Microstructure and Mechanical Properties of Ni/TiC Composites by Laser Induced Self-Propagating High-Temperature Synthesis

2011 ◽  
Vol 239-242 ◽  
pp. 1072-1075
Author(s):  
Yu Xin Li ◽  
Pei Kang Bai
Keyword(s):  
Mechanical Properties ◽  
High Temperature ◽  
Sintered Density ◽  
Bending Strength ◽  
Micro Hardness ◽  
X Ray Diffraction ◽  
Temperature Synthesis ◽  
X Ray ◽  
High Temperature Synthesis

Ni/TiC composites have been produced using laser induced self-propagating high-temperature synthesis. The chemical composition and microstructure were investigated by means of X-ray diffraction and scanning electron microscope. The sintered density and mechanical properties such as bending strength and micro-hardness were also measured. The results showed that the synthesized products were consisted of TiC and Ni phases, which indicated that the TiC was synthesized by the in-situ reaction. Moreover, the results revealed that the sintered density increased and the micro-hardness and bending strength of the synthesized products gradually decreased with the increasing of Ni contents.

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.

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.

Synthesis, Characterization and Properties of PANI/(La-Nd Doped BaFe12O19) Composites

2017 ◽  
Vol 727 ◽  
pp. 327-334
Author(s):  
Yan Wang ◽  
Jun Wang ◽  
Xiao Fei Zhang ◽  
Ya Qing Liu
Keyword(s):  
Sol Gel ◽  
Network Analyzer ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Structure Morphology ◽  
Xrd Patterns ◽  
Hexagonal Platelet ◽  
Peak Value ◽  
Properties Of Composites

La-Nd co-doped barium hexaferrites, Ba0.7(LamNdn)0.3Fe12O19 (D-BaM), were successfully prepared by sol-gel method. PANI / D-BaM composites were synthesized by in-situ polymerization in solution. The structure, morphology and properties of samples have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), four-probe conductivity tester and vector network analyzer. The XRD patterns showed that the crystal structure of all the samples exist as M-type phases. The SEM images revealed that the particles presented a hexagonal platelet-like morphology. The magnetic properties could be improved by substitutions of La and Nd ions. The saturation magnetization (Ms) and coercive force (Hc) increased with the change of La / Nd ratio to the maximum at La / Nd = 3:1. The doped particles have also been embedded in conductive PANI to prepare electromagnetic materials, and the conductivity kept on the order of 10-2. The microwave absorbing properties of composites at 30 MHz-6 GHz improved obviously, the peak value of reflection loss could reach-7.5 dB.

scholarly journals Sintering Behavior and Mechanical Properties of Mullite Fibers/Hydroxyapatite Ceramic

Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1859 ◽  
Author(s):  
Xueni Zhao ◽  
Qingyao Liu ◽  
Jianjun Yang ◽  
Weigang Zhang ◽  
Yao Wang
Keyword(s):  
Mechanical Properties ◽  
Hydrothermal Synthesis ◽  
Bending Strength ◽  
Fiber Content ◽  
Silicate Glasses ◽  
Sintering Behavior ◽  
Composite Powders ◽  
Hydroxyapatite Ceramic ◽  
Dense Microstructure ◽  
Mullite Fibers

The effect of fiber content and sintering temperature on sintering behavior and mechanical properties of mullite fibers/hydroxyapatite composites was studied. The composites were fabricated by hydrothermal synthesis and pressureless sintering. The amount of fibers was varied from 5 wt % to 15 wt % through hydrothermal synthesis, mullite fibers and hydroxyapatite composite powders were subsequently sintered at temperatures of 1150, 1250, and 1350 °C. The composites presented a more perturbed structure by increasing fiber content. Moreover, the composites experienced pore coalescence and exhibited a dense microstructure at elevated temperature. X-ray diffraction indicated that the composites underwent various chemical reactions and generated silicate glasses. The generation of silicate glasses increased the driving force of particle rearrangement and decreased the number of pores, which promoted densification of the composites. Densification typically leads to increased hardness and bending strength. The study proposes a densification mechanism and opens new insights into the sintering properties of these materials.

Preparation of Hydrophobic CaCO3-Wood Composite In Situ

2010 ◽  
Vol 113-116 ◽  
pp. 1712-1715
Author(s):  
Cheng Yu Wang ◽  
Chang Yu Liu ◽  
Jian Li
Keyword(s):  
Mechanical Properties ◽  
Organic Substrate ◽  
Dodecanoic Acid ◽  
Wood Composite ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Contact Angle Analysis ◽  
Double Diffusive

The preparation of hydrophobic CaCO3-wood composite through a double-diffusive method using dodecanoic acid as organic substrate is demonstrated. The product was characterized by the contact angle analysis, X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). The mechanical properties of the product were measured. The results show that the synthesized CaCO3 fills in the wood cell and covers the surface of wood. The CaCO3-wood composite is hydrophobic. The mechanical properties of wood composite have significantly increased.

Effect of Dehydration Methods on Mechanical Strength of Nanohydroxyapatite/Collagen Composites

2007 ◽  
Vol 330-332 ◽  
pp. 349-352
Author(s):  
Xiao Yan Lin ◽  
Xu Dong Li ◽  
Xing Dong Zhang
Keyword(s):  
Mechanical Properties ◽  
Binding Energy ◽  
Freeze Drying ◽  
Bending Strength ◽  
Bond Formation ◽  
In Situ Synthesis ◽  
Drying Methods ◽  
Key Factors ◽  
Air Drying

Hydroxyapatite/collagen composites were prepared in-situ synthesis. The composites were finally achieved by dehydration including air-drying and freeze-drying methods. FTIR, XPS and DSC were employed to investigate the composites dehydrated by two methods. The air-dried composites had better mechanical properties than those of the composites dried by freeze drying. Air-drying of the composite induced more bond formation and crosslink between collagen fibers and HA crystals compared with freeze-drying of the composite, as indicated by the shifting of amide A and I bands to the lower wavenumber and by the changes in the binding energy of O1s, Ca2p, and P2p, leading to the increase of the peak temperature of the composites. Collagen crosslink and bond formation in the air-dried composites were key factors to increase the bending strength of the composites. The results of this study confirm that in situ synthesis and air-dry method are effective ways to obtain nanoHA/COL composites with high mechanical properties.

MECHANICAL PROPERTIES OF A POLYURETHANE/MONTMORILLONITE NANOCOMPOSITE FEATURING ORGANOMODIFICATION SYNTHESIZED VIA IN SITU POLYMERIZATION

2015 ◽  
Vol 88 (1) ◽  
pp. 138-146 ◽  
Author(s):  
Rouhollah Bagheri ◽  
Reza Darvishi
Keyword(s):  
Mechanical Properties ◽  
In Situ Polymerization ◽  
Xrd Analysis ◽  
Silicate Layer ◽  
X Ray Diffraction ◽  
X Ray ◽  
End Groups ◽  
Layer Sample ◽  
Silicate Layers

ABSTRACT In this study, polyurethane (PU)/organomodified montmorillonite (cloisite®30B) is synthesized via in situ polymerization by reaction of an ether-based prepolymer with the isocyanate end groups and adiamine chain extender (4, 4-methylene-bis(2-chloroaniline)) in the presence of different amounts of nanoparticles dispersed in the prepolymer matrix by an ultrasonic mixer for 1 h. The synthesized polymers are cast on a pretreated carbon steel sheet and cured at 120 °C in an oven. The PU and its composites have been characterized by using Fourier transform infrared spectroscopy, X-ray diffraction (XRD), and mechanical testing. The XRD analysis of the cured samples containing 1 to 3 wt% cloisite30B showed intercalation segments in the silicate layers and exfoliation for 0.5 wt% nanoparticles. The highest mechanical properties were obtained using the cured exfoliated silicate layer sample. A twofold increase in the ultimate tensile strength and a 2.3 times increase in the adhesion strength were found for 0.5 wt% organoclay/PU as compared with that of pure PU. In addition, the exfoliated structure sample exhibited a 16% reduction in abrasion compared with that of pure PU.

scholarly journals Si3N4-SiCpComposites Reinforced byIn SituCo-Catalyzed Generated Si3N4Nanofibers

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Juntong Huang ◽  
Zhaohui Huang ◽  
Shaowei Zhang ◽  
Minghao Fang ◽  
Yan’gai Liu
Keyword(s):  
Mechanical Properties ◽  
Bulk Density ◽  
Bending Strength ◽  
Sintering Temperature ◽  
Apparent Porosity ◽  
Network Connection ◽  
Opposite Trend ◽  
Low Sintering Temperature ◽  
Co Addition

Si3N4-SiCpcomposites reinforced byin situcatalytic formed nanofibers were prepared at a relatively low sintering temperature. The effects of catalyst Co on the phase compositions, microstructures, and physicochemical-mechanical properties of samples sintered at 1350°C–1450°C were investigated. The results showed that the catalyst Co enhanced the nitridation of Si. With the increase of Co addition (from 0 wt% to 2.0 wt.%), the apparent porosity of as-prepared refractories was initially decreased and subsequently increased, while the bulk density and the bending strength exhibited an opposite trend. TheSi3N4-SiCpcomposites sintered at 1400°C had the highest strength of 60.2 MPa when the Co content was 0.5 wt.%. The catalyst Co facilitated the sintering ofSi3N4-SiCpcomposites as well as the formation of Si3N4nanofibers which exhibited network connection and could improve their strength.

Fabrication and Mechanical Properties of SiC/Cu Composites with Zn Addition by Hot Pressing Sintering

2013 ◽  
Vol 745-746 ◽  
pp. 700-705
Author(s):  
Huang Liu ◽  
Guo Qiang Luo ◽  
Pin Gan Chen ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Mechanical Properties ◽  
Vickers Hardness ◽  
Hot Pressing ◽  
Bending Strength ◽  
Coefficient Of Thermal Expansion ◽  
High Volume ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zn Addition ◽  
Hot Pressing Sintering

SiC/Cu composites exhibit low density, low coefficient of thermal expansion and excellent mechanical properties. In this study, Zn of 2 wt. % was added as the sintering activator, and the high volume faction (60%) SiC/Cu composites was fabricated by hot pressing sintering technology. The phase composition and morphology of as-prepare samples were characterized by X-ray diffraction (XRD) system and scanning electron microscopy (SEM) equipped with an energy-dispersive spectroscopy (EDS) system. The as-prepared SiC/Cu composites were dense and uniform as well as void free. The results show that SiC/Cu composites can reach excellent mechanical properties of SiC/Cu composites. With the increase of sintering temperature, Vickers hardness and the bending strength of the samples increased obviously and the as-prepared SiC/Cu composites achieved a maximum Vickers hardness and bending strength respectively of 195MPa and 140MPa.

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