scholarly journals Core/Shell Structure of TiO2-Coated MWCNTs for Thermal Protection for High-Temperature Processing of Metal Matrix Composites

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Laura Angélica Ardila Rodriguez ◽  
Dilermando Nagle Travessa
Keyword(s):  
Thermal Stability ◽  
Metal Matrix Composites ◽  
Shell Structure ◽  
Metal Matrix ◽  
Thermal Protection ◽  
Oxidation Stability ◽  
Core Shell ◽  
Matrix Composites ◽  
X Ray ◽  
Core Shell Structure

The production of metal matrix composites with elevated mechanical properties depends largely on the reinforcing phase properties. Due to the poor oxidation resistance of multiwalled carbon nanotubes (MWCNTs) as well as their high reactivity with molten metal, the processing conditions for the production of MWCNT-reinforced metal matrix composites may be an obstacle to their successful use as reinforcement. Coating MWCNTs with a ceramic material that acts as a thermal protection would be an alternative to improve oxidation stability. In this work, MWCNTs previously functionalized were coated with titanium dioxide (TiO2) layers of different thicknesses, producing a core-shell structure. Heat treatments at three different temperatures (500°C, 750°C, and 1000°C) were performed on coated nanotubes in order to form a stable metal oxide structure. The MWCNT/TiO2 hybrids produced were evaluated in terms of thermal stability. Thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy (RS), and X-ray photoelectron spectroscopy (XPS) were performed in order to investigate TiO2-coated MWCNT structure and thermal stability under oxidative atmosphere. It was found that the thermal stability of the TiO2-coated MWCNTs was dependent of the TiO2 layer morphology that in turn depends on the heat treatment temperature.

scholarly journals Lab and Pilot-Scale Synthesis of MxOm@SiC Core–Shell Nanoparticles

Materials ◽  
2020 ◽  
Vol 13 (3) ◽  
pp. 649 ◽  
Author(s):  
Àngela Ribes ◽  
Santiago Sánchez-Cabezas ◽  
Andy Hernández-Montoto ◽  
Luis A. Villaescusa ◽  
Elena Aznar ◽  
...  
Keyword(s):  
Metal Matrix Composites ◽  
Metal Matrix ◽  
Scale Up ◽  
Pilot Scale ◽  
Core Shell ◽  
Matrix Composites ◽  
Shell Nanoparticles ◽  
X Ray ◽  
Scanning Transmission ◽  
Core Shell Nanoparticles

The addition of light ceramic particles to bulk technological materials as reinforcement to improve their mechanical properties has attracted increasing interest in the last years. The metal matrix composites obtained using nanoparticles have been reported to exhibit an improvement of their properties due to the decrease in the size of the ceramic additives to the nanoscale. Additionally, important effects such as the dispersion of the nanoparticles, wettability, and low reactivity can be controlled by the modification of the nanoparticles’ surface. In this work, we present the preparation of core–shell MxOm@SiC nanoparticles with different shell compositions. The accurate and reproducible preparation is developed both at the lab and pilot scale. The synthesis of these core–shell nanoparticles and their scale-up production are fundamental steps for their industrial use as additives in metal matrix composites and alloys. Powder X-ray diffraction and energy dispersive X-ray (EDX) coupled with scanning transmission electron microscopy (STEM) are used to corroborate the formation of the core–shell systems, whereas line scan-EDX analysis allows measuring the average shell thickness.

Synthesis and Characterization on ATP/TiO2/PANI Core-Shell Nanocomposites

2011 ◽  
Vol 282-283 ◽  
pp. 354-358 ◽  
Author(s):  
Lu Lu Chen ◽  
Hong Yan Ding ◽  
Yue Zhang ◽  
Guang Hong Zhou
Keyword(s):  
Thermal Stability ◽  
Shell Structure ◽  
Oxidative Polymerization ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Analyzer ◽  
Degree Of Crystallization ◽  
Core Shell Structure ◽  
Thermal Stability Of

Conducting attapulgite/titania/polyaniline/ (ATP/TiO2/PANI) core-shell nanocomposites (CSNs) were synthesized via oxidative polymerization of aniline after the surface modification of the ATP carried with TiO2nanoparticles. The structure and morphology of the ATP/TiO2/PANI CSNs were characterized by X-ray diffraction, scanning electron microscopy, and fourier transform infrared. The thermal stability of the ATP/TiO2/PANI CSNs was also investigated by thermal analyzer. The results show that the ATP/TiO2/PANI CSNs display “capsule like” core-shell structure, of which ranging in diameter of about 80 nm and length of about 250 nm. In addition, the ATP/TiO2/PANI CSNs present a higher degree of crystallization and better thermal stability. We believe that the excellent core-shell structure and better thermal stability should be prone to improve their other properties and enlarge their application.

scholarly journals In Situ Synthesis of Core-Shell-Structured SiCp Reinforcements in Aluminium Matrix Composites by Powder Metallurgy

Metals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1201
Author(s):  
Xinghua Ji ◽  
Cheng Zhang ◽  
Shufeng Li
Keyword(s):  
Particle Size ◽  
Powder Metallurgy ◽  
Shell Structure ◽  
Ex Situ ◽  
Aluminium Matrix ◽  
Core Shell ◽  
Matrix Composites ◽  
Aluminium Matrix Composites ◽  
Core Shell Structure

SiCp reinforced aluminium matrix composites (AMCs), which are widely used in the aerospace, automotive, and electronic packaging fields along with others, are usually prepared by ex situ techniques. However, interfacial contamination and poor wettability of the ex situ techniques make further improvement in their comprehensive performance difficult. In this paper, SiCp reinforced AMCs with theoretical volume fractions of 15, 20, and 30% are prepared by powder metallurgy and in situ reaction via an Al-Si-C system. Moreover, a combined method of external addition and an in situ method is used to investigate the synergistic effect of ex situ and in situ SiCp on AMCs. SiC particles can be formed by an indirect reaction: 4Al + 3C → Al4C3 and Al4C3 + 3Si → 3SiC + 4Al. This reaction is mainly through the diffusion of Si, in which Si diffuses around Al4C3 and then reacts with Al4C3 to form SiCp. The in situ SiC particles have a smooth boundary, and the particle size is approximately 1–3 μm. A core-shell structure having good bonding with an aluminium matrix was generated, which consists of an ex situ SiC core and an in situ SiC shell with a thickness of 1–5 μm. The yield strength and ultimate tensile strength of in situ SiCp reinforced AMCs can be significantly increased with a constant ductility by adding 5% ex situ SiCp for Al-28Si-7C. The graphite particle size has a significant effect on the properties of the alloy. A criterion to determine whether Al4C3 is a complete reaction is achieved, and the forming mechanism of the core-shell structure is analysed.

scholarly journals Well-Dispersed Nanoscale Zero-Valent Iron Supported in Macroporous Silica Foams: Synthesis, Characterization, and Performance in Cr(VI) Removal

2017 ◽  
Vol 2017 ◽  
pp. 1-13 ◽  
Author(s):  
Chaoxia Zhao ◽  
Jie Yang ◽  
Yihan Wang ◽  
Bo Jiang
Keyword(s):  
Removal Efficiency ◽  
Shell Structure ◽  
Zero Valent Iron ◽  
Core Shell ◽  
Ambient Atmosphere ◽  
Order Kinetic ◽  
Macroporous Silica ◽  
X Ray ◽  
Nanoscale Zero Valent Iron ◽  
Core Shell Structure

Well-dispersed nanoscale zero-valent iron (NZVI) supported inside the pores of macroporous silica foams (MOSF) composites (Mx-NZVI) has been prepared as the Cr(VI) adsorbent by simply impregnating the MOSF matrix with ferric chloride, followed by the chemical reduction with NaHB4 in aqueous solution at ambient atmosphere. Through the support of MOSF, the reactivity and stability of NZVI are greatly improved. Transmission electron microscopy (TEM) results show that NZVI particles are spatially well-dispersed with a typical core-shell structure and supported inside MOSF matrix. The N2 adsorption-desorption isotherms demonstrate that the Mx-NZVI composites can maintain the macroporous structure of MOSF and exhibit a considerable high surface area (503 m2·g−1). X-ray photoelectron spectroscopy (XPS) and powder X-ray diffraction (XRD) measurements confirm the core-shell structure of iron nanoparticles composed of a metallic Fe0 core and an Fe(II)/Fe(III) species shell. Batch experiments reveal that the removal efficiency of Cr(VI) can reach 100% when the solution contains 15.0 mg·L−1 of Cr(VI) at room temperature. In addition, the solution pH and the composites dosage can affect the removal efficiency of Cr(VI). The Langmuir isotherm is applicable to describe the removal process. The kinetic studies demonstrate that the removal of Cr(VI) is consistent with pseudo-second-order kinetic model.

X-ray welding of metal-matrix composites

1997 ◽  
Vol 68 (6) ◽  
pp. 2550-2553 ◽  
Author(s):  
Richard A. Rosenberg ◽  
Qing Ma ◽  
William Farrell ◽  
Mark Keefe ◽  
Derrick C. Mancini
Keyword(s):  
Metal Matrix Composites ◽  
Metal Matrix ◽  
Matrix Composites ◽  
X Ray

Preparation of Amorphous Calcium Phosphate/Triclcium Silicate Composite Powders

2009 ◽  
Vol 79-82 ◽  
pp. 1643-1646 ◽  
Author(s):  
Qing Lin ◽  
Yan Bao Li ◽  
Xiang Hui Lan ◽  
Chun Hua Lu ◽  
Zhong Zi Xu
Keyword(s):  
Calcium Phosphate ◽  
Shell Structure ◽  
Amorphous Calcium Phosphate ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
X Ray ◽  
Core Shell Structure

The amorphous calcium phosphate (ACP)/tricalcium silicate (Ca3SiO5, C3S) composite powders were synthesized in this paper. The exothermal behavior of C3S determined by isothermal conduction calorimetry indicated that the ACP could be synthesis by chemical precipitation method during the induction period (stage II) of C3S. The composite powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results indicated that nanosized ACP particles deposited on the surface of C3S particles to form core-shell structure at pH=10.5, and the nCa/nP of ACP could be controlled between 1.0 and 1.5. The core-shell structure is stable after sintered at 500 oC for 3 h to remove the β-cyclodextrin (β-CD). As compared with the irregular C3S particles (1~5 μm), the composite powders particles are spherical with a diameter of 40~150 μm. Therefore, to obtain the smaller size of composite powders, it is expected to avoid the aggregate of C3S particles in the aqueous solution by addition of dispersant. As compared with C3S, the composite powders may contribute better injectability, strength and biocompatibility.

Characterization of Metal Matrix Composites by Synchrotron Refraction Computed Topography

2010 ◽  
Vol 638-642 ◽  
pp. 967-972
Author(s):  
Bernd R. Müller ◽  
Axel Lange ◽  
M. Harwardt ◽  
M.P. Hentschel
Keyword(s):  
Computed Tomography ◽  
Metal Matrix Composites ◽  
Metal Matrix ◽  
High Performance ◽  
Three Dimensional ◽  
Matrix Composites ◽  
X Rays ◽  
X Ray ◽  
Surface And Interface ◽  
Federal Institute

X-ray computed tomography is an important tool for evaluating the three dimensional microstructure of modern materials non-destructively. To resolve material structures in the micrometre range and below high brilliance synchrotron radiation has to be taken. But materials of low absorption or mixed phases show a weak absorption contrast at there interfaces. A Contrast enhancement can be achieved by exploiting the refraction of X-rays at interfaces. This technique was developed and applied at the NDT department of the Federal Institute for Materials Research and Testing (BAM) during the last decade. It meets the actual demand for improved non-destructive characterisation of high performance composites, ceramics and other low density materials and components. The technique is based on Ultra Small Angle Scattering (USAXS) by micro structural elements causing phase related effects like refraction and total reflection at a few minutes of arc as the refractive index of X-rays is nearly unity. The extraordinary refraction contrast of inner surfaces is far beyond absorption effects and hence especially useful for materials of low absorption or mixed phases, showing similar X-ray absorption properties. Crack orientation and fibre-matrix debonding in plastics, polymers, ceramics and metal-matrix-composites after cyclic loading and hydro thermal aging can be visualized. By combining the refraction technique with the computed tomography technique the three dimensional imaging of the micro structure of the materials is obtained. In most cases the investigated inner surface and interface structures correlate to mechanical properties. Recent results with a sub-micrometer resolution will be presented.

Sign in / Sign up

Export Citation Format

Share Document