scholarly journals Synthesis of core–shell copper–graphite submicronic particles and carbon nano-onions by spark discharges in liquid hydrocarbons

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
X. Glad ◽  
J. Gorry ◽  
M. S. Cha ◽  
A. Hamdan

AbstractSpark discharge in hydrocarbon liquids is considered a promising method for the synthesis of various nanomaterials, including nanocomposites. In this study, copper–carbon particles were synthesized by generating spark discharges between two Cu electrodes immersed in heptane, cyclohexane, or toluene. The synthesized particles were characterized using scanning electron microscopy, high-resolution transmission electron microscopy, and selected area electron diffraction. Overall, two families of particles were observed: Cu particles (diameter < 10 nm) embedded in a carbon matrix and submicrometric Cu particles encapsulated in a carbon shell. The obtained results indicate that the size distribution of the Cu nanoparticles and the degree of graphitization of the carbon matrix depend on the liquid. Indeed, discharges in heptane lead to Cu particles with diameters of 2–6 nm embedded in a carbon matrix of low graphitization degree, while discharges in toluene result in particles with diameters of 2–14 nm embedded in carbon matrix of high graphitization degree. Based on the obtained experimental results, it is proposed that the Cu nanoparticles are produced in the plasma core where Cu (evaporated from the electrode surface) and carbonaceous species (decomposition of the liquid) are present. When the plasma hits the electrode surface, hot (thousands of Kelvin) Cu particles are ejected from the electrode, and they propagate in the liquid. The propagation of the hot particles in the liquid results in the local evaporation of this liquid, which leads to the formation of a C-shell around each Cu particle. In few cases where the shape of the Cu particle is not spherical, carbon nanoonions are detected between the C-shell and the Cu core. These nanoonions are supposedly formed under the effect of the fluid vortices generated close to the particle surfaces when these latter are ejected into the liquid.

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.


2010 ◽  
Vol 43 (5) ◽  
pp. 990-997 ◽  
Author(s):  
Jie Ma ◽  
Qingsheng Wu

A facile oxides–hydrothermal (O–HT) method is demonstrated to prepare high-purity monazite-type LaPO4nanomaterials. In this approach, La2O3and P2O5powder are first directly used as precursors under additive-free hydrothermal conditions. The as-prepared samples are characterized with X-ray diffraction, Fourier transform IR spectroscopy, thermogravimetry, scanning electron microscopy, transmission electron microscopy (high-resolution TEM, energy dispersive spectroscopy) and selected-area electron diffraction. The typical sample obtained at 433 K in 24 h comprises uniform single-crystal nanofibres with a diameter of ∼15–28 nm and an aspect ratio of 30–50. The influences of treatment time, synthesis temperature and P/La molar ratio are investigated. The phase transition from hexagonal hydrate to monoclinic anhydrous lanthanum phosphate and the growth process of nanofibres are revealed by the experimental results. The formation mechanism of the monoclinic LaPO4is discussed. The result indicates that the P/La ratio does not influence the composition and crystal phase but changes the morphology of the product in the O–HT system.


2013 ◽  
Vol 1513 ◽  
Author(s):  
Toshitaka Ishizaki ◽  
Ryota Watanabe ◽  
Kunio Akedo ◽  
Toshikazu Satoh

ABSTRACTCu nanoparticles capped with fatty acids and amines were developed as low-temperature sintering materials. The fatty acids and amines used were decanoic acid + decyl amine (C10) and oleic acid + oleyl amine (C18), respectively. The synthesized Cu nanoparticles were analyzed using X-ray diffraction, transmission electron microscopy, and thermogravimetric and differential thermal analysis. Because both of the capping layers could be decomposed at temperatures lower than 300°C even under an inert atmosphere, bonding and sintering experiments could be carried out in the absence of oxygen to prevent the oxidation of the Cu nanoparticles. The sintered structures were observed using scanning electron microscopy. The shear strengths of Cu plates bonded using the C18 Cu nanoparticles were larger than those of plates bonded using the C10 Cu nanoparticles. At 300°C, the strength was higher than 30 MPa, and of the same order as ordinary high-temperature solders, even though the processing temperature was low. The resistivity of a film sintered using the C18 Cu nanoparticles was 12 μΩcm at 300°C, which was lower than the values reported in previous studies.


Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 206 ◽  
Author(s):  
James Hower ◽  
Dali Qian ◽  
Nicolas Briot ◽  
Eduardo Santillan-Jimenez ◽  
Madison Hood ◽  
...  

Fly ash from the combustion of eastern Kentucky Fire Clay coal in a southeastern United States pulverized-coal power plant was studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). TEM combined with elemental analysis via energy dispersive X-ray spectroscopy (EDS) showed that rare earth elements (REE; specifically, La, Ce, Nd, Pr, and Sm) were distributed within glassy particles. In certain cases, the REE were accompanied by phosphorous, suggesting a monazite or similar mineral form. However, the electron diffraction patterns of apparent phosphate minerals were not definitive, and P-lean regions of the glass consisted of amorphous phases. Therefore, the distribution of the REE in the fly ash seemed to be in the form of TEM-visible nano-scale crystalline minerals, with additional distributions corresponding to overlapping ultra-fine minerals and even true atomic dispersion within the fly ash glass.


2013 ◽  
Vol 829 ◽  
pp. 152-156 ◽  
Author(s):  
Hamed Sadabadi ◽  
Adeleh Aftabtalab ◽  
Shirzad Zafarian ◽  
Shilpa Chakra ◽  
K. Venkateswara Rao ◽  
...  

Copper oxide nanoparticles have been received attraction due to their unique properties and potential future applications. In present work nanostructure Copper (II) oxide (CuO) spherical nanoparticle synthesized by solution combustion method and the influence of different fuel and condition on the properties of CuO particle was investigated. Crystalline phase and size indicated by applying XRD and particle size distribution studied further using DLS. Scanning electron microscopy (SEM) was used for morphological study and EDAX analysis shows composition of CuO particles. Nanostructure of copper (II) oxide particle studied further by Transmission electron microscopy (TEM) and selected area electron diffraction (SAED) applied for detail study on crystalline structure of particles.


2010 ◽  
Vol 8 (5) ◽  
pp. 1027-1033 ◽  
Author(s):  
Junhao Zhang ◽  
Yuhui Wu ◽  
Jia Zhu ◽  
Shaoxing Huang ◽  
Dongjing Zhang ◽  
...  

AbstractSelf-assembled CdS architectures with flower-like structures have been synthesized by a mixed solvothermal method using ethylene glycol and oleic acid as the mixed solvent at 160°C for 12 h. The results of X-ray diffraction (XRD) patterns, field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) images indicate that the product exists as the hexagonal wurtzite phase and conatins of larger numbers of flower-like CdS architectures with diameters of 1.8–3 μm. The selected-area electron diffraction (SAED) pattern and the high resolution transmission electron microscope (HRTEM) image reveal that the grain has better crystallinity. The optical properties of flower-like CdS architectures were also investigated by ultraviolet-visable (UV-vis) and photoluminescence spectroscopy at room temperature. A strong peak at 490 nm is shown in the UV-vis absorption, while an emission at 486 nm and another strong emission at 712 nm are shown in the PL spectrum.


2013 ◽  
Vol 101 (1) ◽  
pp. 7-12 ◽  
Author(s):  
R. Gupta ◽  
S. K. Gupta ◽  
S. K. Aggarwal

Abstract Nanoparticles of thorium oxalate were synthesized by the reaction of thorium nitrate and ammonium oxalate by the microemulsion method. The Th02 nanoparticles were obtained by heating thorium oxalate nanoparticles at 500 °C in air. The oxalate and oxide nanoparticles of thorium were characterized by transmission electron microscopy (TEM), X-ray powder diffraction (XRD), thermogravimetric analysis (TGA) and selected area electron diffraction (SAED). X-ray diffraction studies showed the mono-phasic nature of the powder thoria. The particle size was obtained from X-ray line broadening (~l0 nm) and transmission electron microscopy (~l0 nm). Dynamic light scattering (DLS) was used to calculate the average grain size of the particles. SAED confirmed the nanocrystalline nature of thoria particles. High resolution transmission electron microscopy (HRTEM) was also carried out to understand the morphology of the system. The monodisperse nanoparticles of thoria are promising for future reactor technologies.


2009 ◽  
Vol 24 (1) ◽  
pp. 192-197 ◽  
Author(s):  
G.M. Cheng ◽  
Y.X. Tian ◽  
L.L. He

The orientation relationship (OR) and the interfacial structure between Nb solid solution (Nbss) precipitates and α-Nb5Si3 intermetallics have been investigated by transmission electron microscopy (TEM). The OR between Nbss and α-Nb5Si3 was determined by selected-area electron diffraction analyses as (222)Nb//(002)α and . High-resolution TEM images of the Nbss/α-Nb5Si3 interface were presented. Steps existed at the interface that acted as centers of stress concentration and released the distortion of lattices to decrease the interfacial energy. In addition, the interfacial models were proposed based on the observed OR to describe the atomic matching of the interface. The distribution of alloying elements at the Nbss/α-Nb5Si3 interface has also been investigated, and Hf was enriched at the interface to strengthen the grain boundary.


Sign in / Sign up

Export Citation Format

Share Document