Preparation of TiB2/TiN Nanocomposites by SP

2013 ◽  
Vol 745-746 ◽  
pp. 551-554 ◽  
Author(s):  
Ming Hui Wang ◽  
Hua Jian Li ◽  
Wan Jiang
Keyword(s):  
X Ray Diffraction ◽  
Tem Analysis ◽  
X Ray ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Average Grain Size ◽  
High Resolution Tem ◽  
Spark Plasma ◽  
Xrd Techniques

TiB2/TiN nanocomposites were in-situ fabricated by spark plasma sintering (SPS) technique using Ti and BN powders as starting materials. The phase constituents and microstructures of the samples were analyzed by X-ray diffraction (XRD) techniques, scanning electron microscopy (SEM) and transmission electron microscope (TEM), respectively. The results showed that the average grain size of TiB2 and TiN was 1m and 300nm respectively. Furthermore, high resolution TEM analysis indicated that the as-prepared TiB2/TiN nanocomposites had very clean grain boundaries, and no amorphous phase or oxide layer was observed.

scholarly journals Microstructure and properties of nano-laminated Y3Si2C2 ceramics fabricated via in situ reaction by spark plasma sintering

2021 ◽  
Vol 10 (3) ◽  
pp. 578-586
Author(s):  
Lin-Kun Shi ◽  
Xiaobing Zhou ◽  
Jian-Qing Dai ◽  
Ke Chen ◽  
Zhengren Huang ◽  
...  
Keyword(s):  
Spark Plasma Sintering ◽  
Atomic Scale ◽  
Max Phase ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma ◽  
Diffraction Patterns

AbstractA nano-laminated Y3Si2C2 ceramic material was successfully synthesized via an in situ reaction between YH2 and SiC using spark plasma sintering technology. A MAX phase-like ternary layered structure of Y3Si2C2 was observed at the atomic-scale by high resolution transmission electron microscopy. The lattice parameters calculated from both X-ray diffraction and selected area electron diffraction patterns are in good agreement with the reported theoretical results. The nano-laminated fracture of kink boundaries, delamination, and slipping were observed at the tip of the Vickers indents. The elastic modulus and Vickers hardness of Y3Si2C2 ceramics (with 5.5 wt% Y2O3) sintered at 1500 °C were 156 and 6.4 GPa, respectively. The corresponding values of thermal and electrical conductivity were 13.7 W·m-1·K-1 and 6.3×105 S·m-1, respectively.

scholarly journals Microstructure and properties of nano-laminated Y3Si2C2 ceramics fabricated via in situ reaction by spark plasma sintering

2020 ◽  
Author(s):  
Lin-Kun Shi ◽  
Xiaobing Zhou ◽  
Jian-Qing Dai ◽  
Ke Chen ◽  
Zhengren Huang ◽  
...  
Keyword(s):  
Spark Plasma Sintering ◽  
Atomic Scale ◽  
Max Phase ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma ◽  
Diffraction Patterns

Abstract A new nano-laminated Y3Si2C2 ceramic material, for the first time, was successfully synthesized via in situ reaction between YH2 and SiC by spark plasma sintering. A MAX phase-like ternary layered structure of Y3Si2C2 was observed at the atomic-scale by high resolution transmission electron microscopy. The lattice parameters calculated from both X-ray diffraction and selected area electron diffraction patterns are in good agreement with the reported theoretical results. The nano-laminated fracture of kink boundaries, delamination, and slipping was observed at the tip of the Vickers indent. The values of elastic modulus and Vickers hardness of the Y3Si2C2 ceramics sintered at 1500 °C were 156 and 6.4 GPa, respectively. The corresponding values of thermal and electrical conductivity were 13.7 W m-1 k-1 and 6.3 × 105 S m-1, respectively.

scholarly journals Microstructure and Electrical Property of Ex-Situ and In-Situ Copper Titanium Carbide Nanocomposites

Metals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 735
Author(s):  
Nguyen Hoang Viet ◽  
Nguyen Thi Hoang Oanh
Keyword(s):  
Electrical Conductivity ◽  
Electron Microscope ◽  
Applied Pressure ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma

In this study, ex-situ Cu-TiC nanocomposites of 1, 3 and 5 vol. % TiC and in-situ Cu-TiH2-C nanocomposites (corresponding to 5 vol. % TiC) were prepared using ball milling and spark plasma sintering methods. Powder mixtures were milled for 4 h at 400 rpm. As-milled Cu-TiC composite powders were consolidated under an applied pressure of 70 MPa. The phase composition, and microstructure of the composite samples were characterized by X-ray diffraction, and scanning electron microscope and transmission electron microscope techniques, respectively. With the increasing TiC content from 1 to 5 vol. %, the hardness of the ex-situ composites when sintered at 600 °C changed between 161.4 and 178.5 HV and the electrical conductivity decreased from 52.1 to 47.6% IACS. In-situ Cu-TiH2-C nanocomposite sintered at 950 °C had higher hardness and electrical conductivity than ex-situ Cu-TiC composite due to having a homogenous distribution of nano reinforcement particles and dense structure.

Fullerene-Metal Composites: Phase Transformations During Milling and Sintering

2011 ◽  
Vol 172-174 ◽  
pp. 727-732 ◽  
Author(s):  
Ileana Irais Santana ◽  
Francisco Carlos Robles Hernandez ◽  
Vicente Garibay-Febles ◽  
Hector A. Calderon
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Phase Transformations ◽  
Mechanical Milling ◽  
X Ray Diffraction ◽  
Metal Composites ◽  
X Ray ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma

Composites of Fe-C60and Al C60produced by mechanical milling and sinterized by Spark Plasma Sintering are investigated with special attention to the mechanical properties of the products. The processing involves phase transformations of the fullerenes that are interesting to follow and characterize. This involves formation of tetragonal/rhombohedral diamond and carbides during sintering and milling. Transmission Electron Microscopy (TEM) and Raman Spectroscopy techniques are also used to confirm preliminary results of X Ray Diffraction (XRD) related to the formation of nanostructures i.e., grain size of the crystals during mechanical milling and after sintering, spatial distribution of phases and the different phases that are developed during processing.

Synthesis of Physically Functionalized Carbon Nanotube Reinforced Al-Si Nanocomposite by Spark Plasma Sintering

2014 ◽  
Vol 783-786 ◽  
pp. 1542-1547
Author(s):  
Anway Maiti ◽  
Ram S. Maurya ◽  
Tapas Laha
Keyword(s):  
Carbon Nanotube ◽  
Spark Plasma Sintering ◽  
High Energy ◽  
X Ray Diffraction ◽  
Multiwalled Carbon ◽  
Tem Analysis ◽  
Activity Effect ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma

Multiwalled carbon nanotube (MWCNT) reinforced Al-Si (11 wt%) alloy based nanocomposites were synthesized by spark plasma sintering using high energy ball milled nanocrystalline Al-Si powders mixed with physically functionalized MWCNTs. Improvement in MWCNT dispersion and associated improvement in densification of the nanocomposites were confirmed. The microhardness and elastic modulus of the nanocomposites measured by nanoindentation exhibited appreciable improvement. Grain size measurement by X ray diffraction and transmission electron microscopy confirmed achievement of nanocrystalline grains in Al-Si powder after ball milling, as well as in the consolidated nanocomposites. TEM analysis was performed to reveal the dislocation activity, effect of presence of primary Si and distribution of MWCNTs in the nanocomposites.

Preparation and Properties of Spark Plasma Sintered AlN/BN Nano-Composites

2007 ◽  
Vol 352 ◽  
pp. 197-200
Author(s):  
Mei Juan Li ◽  
Lian Meng Zhang ◽  
Z.D. Wei ◽  
Qiang Shen ◽  
Dong Ming Zhang
Keyword(s):  
Thermal Conductivity ◽  
Chemical Process ◽  
Bending Strength ◽  
Nano Composites ◽  
X Ray Diffraction ◽  
Nitrogen Gas ◽  
X Ray ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma

Nano-sized turbostritic-BN (t-BN) was fabricated through chemical process using boric acid and urea in this work. By the same method, the AlN powders coated with nano-BN were prepared too. The results of X-ray diffraction (XRD) and transmission electron microscope (TEM) revealed that nano-sized t-BN was synthesized at about 600°C in nitrogen gas and it surrounded the surface of AlN particles. High-density AlN/BN nano-composites were fabricated spark plasma sintering (SPS). Microstructure and properties of AlN/BN nano-composites (5~30vol% BN) were investigated. The h-BN flake particles were homogenously dispersed at AlN grain boundaries and within grains in the AlN/BN composites. A little nano-BN additions significantly improved the bending strength of the nano-composites. However, the bending strength was decreased with the BN content increasing. The thermal conductivity of AlN/BN nano-composites was investigated too.

The Recognition of Amorphous Silica in Indurated Soil Profiles

Clay Minerals ◽  
1993 ◽  
Vol 28 (3) ◽  
pp. 461-474 ◽  
Author(s):  
Balbir Singh ◽  
R. J. Gilkes
Keyword(s):  
Amorphous Silica ◽  
Silica Content ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
The Matrix ◽  
Clay Matrix ◽  
Secondary Silica ◽  
Xrd Techniques

AbstractSilica-indurated subsurface horizons of an in situ lateritic profile in semi-arid western Australia were investigated using a range of electron-optical and X-ray diffraction (XRD) techniques. These indurated materials were compared with underlying non-indurated pallid zone material. The secondary silica content of the indurated horizons, as determined by electron microprobe analysis, varied from 8 to 33%. Quantitative digital images for secondary silica, generated by mathematical manipulation of digital Si and AI-Kα: images, showed that kaolinite pseudomorphs after mica contained the lowest amounts of secondary silica, with the highest amounts being present in the inter-pseudomorph clay matrix. Variations in the amount of silica in the matrix are considered to reflect variations in the initial porosity of the clay matrix. Such variations may arise from differences in the Al/Si ratio of parent minerals. Transmission electron microscopy (TEM) showed that amorphous silica adhered to the (001) face of kaolinite crystals. The secondary silica could not be detected by either standard or differential XRD procedures.

Microstructural Transformation of Titanium-Boron Carbide (B4C) Powder Mixture during Spark Plasma Sintering

2015 ◽  
Vol 764-765 ◽  
pp. 51-55
Author(s):  
V.S. Balaji ◽  
S. Kumaran
Keyword(s):  
Boron Carbide ◽  
Microstructural Evolution ◽  
Powder Mixture ◽  
Optical Microscope ◽  
X Ray Diffraction ◽  
X Ray ◽  
Plasma Sintering ◽  
Spark Plasma ◽  
Energy Dispersive Spectroscope

Present study investigates the microstructural evolution and in-situ formation of Ti/(TiB+TiC) composite. The sintered compacts are having near theoretical density. The relative density of Ti/(TiB+TiC) composites decreases with increasing TiB and TiC content.The phase evolutions of TiB and TiC according to the in-situ reactions are analyzed by X-Ray diffraction technique (XRD). Optical microscope (OM) and Energy dispersive spectroscope (EDS) observations of the Ti/(TiB+TiC) composites shows the presence of TiC and TiB reinforcements as equiaxed and needle like structures respectively.

scholarly journals Ordered Domains and Microwave Properties of Sub-micron Structured Ba(Zn1/3Ta2/3)O3 Ceramics Obtained by Spark Plasma Sintering

Materials ◽  
2019 ◽  
Vol 12 (4) ◽  
pp. 638
Author(s):  
Fei Liu ◽  
Shaojun Liu ◽  
Xuejiao Cui ◽  
Lijin Cheng ◽  
Hao Li ◽  
...  
Keyword(s):  
Spark Plasma Sintering ◽  
Annealing Temperature ◽  
Microwave Dielectric Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Dielectric ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma ◽  
Dielectric Ceramics

The degree of Zn2+ and Ta5+ ions ordering could play an important role in the dielectric loss in Ba(Zn1/3Ta2/3)O3 (BZT) ceramics. However, the influence of the grain size of Ba(B′1/3B″2/3)O3 ceramics with nano or sub-micron grains on the ordering domains structure is still not clear. In the present paper, highly dense (~98%) BZT microwave dielectric ceramics with homogeneous sub-micron structure (~330 nm) were prepared through spark plasma sintering (SPS). High resolution transmission electron microscopy combined with X-ray diffraction (XRD)clearly showed that the B-site ordering structure of sintered BZT samples by SPS becomes the B-site long-range 1:2 ordering as annealing proceeds. In contrast, the short-range 1:2 ordering in non-annealed counterparts was also present, which was not detectable by XRD. The size of B-site ordering domains enlarged with annealing temperature. The sub-micron structure of sintered BZT ceramics by SPS remained stable at up to 1400 C; however, the size of B-site 1:2 ordering domain was more than five times larger, which led to a significant increase of the quality factor (Q·f) to 37,700 GHz from 15,000 GHz.

scholarly journals Synthesis of Uniformly Sized Bi0.5Sb1.5Te3.0 Nanoparticles via Mechanochemical Process and Wet-Milling for Reduced Thermal Conductivity

Materials ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 536
Author(s):  
Bo-In Park ◽  
Miri Shin ◽  
Jaeho Park ◽  
Jae-Seung Lee ◽  
Seung Yong Lee ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Milling Process ◽  
Wet Milling ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Mechanochemical Process ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma

In this study, Bi0.5Sb1.5Te3.0 (BST) nanoparticles (NPs) with high crystallinities were synthesized via a mechanochemical process (MCP). X-ray diffraction (XRD), and Raman and X-ray photoelectron spectroscopy (XPS) spectra of the BST NPs showed that the Bi, Sb, and Te powders successfully formed BiSbTe phase and transmission electron microscopy (TEM) images, verifying the high crystallinity and smaller size, albeit agglomerated. The as-synthesized BST NPs with agglomerated clusters were ground into smaller sizes of approximately 41.8 nm with uniform distribution through a simple wet-milling process during 7 days. The thermal conduction behaviors of bulk alloys fabricated by spark plasma sintering (SPS) of the BST NPs were studied by comparing those of samples fabricated from as-synthesized BST NPs and a BST ingot. The thermal conductivities (κ) of the BST nanocomposites were significantly reduced by introducing BST NPs with smaller grain sizes and finer distributions in the temperature range from 300 to 500 K. The BST nanocomposites fabricated from wet-milled BST NPs offered ultralow κ values of 0.84 W m−1 K−1 at approximately 398 K.

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