The thermal decomposition of commercial silicone grease was carried out in a closed reactor (Swagelok) that was heated at 800 degrees C for 3 h, yielding a SiO2-carbon composite with a BET surface area of 369 m2/g. The bulk conductivity (5.72 x 10(-6) S x cm(-2)) of the SiO2-carbon composite was determined by impedance measurements. The as-prepared SiO2-carbon composite was further annealed at 500 degrees C in air for 2 h, which led to the formation of white paramagnetic silica particles (confirmed by ESR), possessing a surface area of 111 m2/g. The present synthetic technique requires unsophisticated equipment and a low-cost commercial precursor, and the reaction is carried out without a solvent, surfactant, or catalyst. The mechanism for the formation of a porous SiO2-carbon composite from the silicone grease is also presented.
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http://dx.doi.org/10.1021/jp060919q | DOI Listing |
J Nanosci Nanotechnol
March 2020
Department of Chemistry, Keimyung University, Daegu 42601, Korea.
Carbon nanofibers (CNFs) were grown by chemical vapor deposition method on -fiber textiles that Ni and Cu catalysts were pre-deposited via electrophoretic deposition. Carbon nanofibers were oxidized by nitric acid to create hydroxyl group and then coated with silica layer via hydrolysis of TEOS (Tetraethyl orthosilicate). Pyrolytic carbon was coated on the SiO₂/CNFs composite by flowing ethylene gas at 900 °C, and then Ru was dip-coated to prepare Ru/PC/SiO₂/CNFs composite.
View Article and Find Full Text PDFIn this study, carbon nanofibers (CNFs) were grown by chemical vapor deposition on C-fiber textiles that had Ni and Cu catalyst deposited via electrophoretic deposition. Before the CNFs were coated with silica layer via hydrolysis of TEOS (Tetraethyl orthosilicate), the carbon nanofibers were oxidized by nitric acid. Due to oxidation, the hydroxyl group was created on the carbon nanofibers and this was used as an activation site for the SiO2.
View Article and Find Full Text PDFDalton Trans
April 2015
College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei 430072, P. R. China.
Well-dispersed bimetallic Ni-Pt nanoparticles (NPs) with different compositions have been successfully grown on the MIL-96 by a simple liquid impregnation method using NaBH4 as the reducing agent. Powder X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, N2 adsorption-desorption, and inductively coupled plasma-atomic emission spectroscopy measurements were employed to characterize the NiPt/MIL-96. Catalytic activity of NiPt/MIL-96 catalysts was tested in the hydrogen generation from the aqueous alkaline solution of hydrazine at room temperature.
View Article and Find Full Text PDFNanotoxicology
October 2016
a Department of Chemistry and NIS - Nanostructured Interfaces and Surfaces , University of Torino, Italy .
Many studies have shown that the composition of the protein corona dramatically affects the response of cells to nanomaterials (NMs). However, the role of each single protein is still largely unknown. Fibrinogen (FG), one of the most abundant plasma proteins, is believed to mediate foreign-body reactions.
View Article and Find Full Text PDFJ Nanosci Nanotechnol
February 2013
Key Laboratory of Resource Chemistry of Ministry of Education, Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University, Shanghai 200234, PR China.
Ordered mesoporous Al2O3-SiO2-carbon nanocomposites have been synthesized via the direct triblock-copolymer self-assembly route using soluble phenolic resols as polymer precursors, aluminium chloride hexahydrate as an aluminum precursor, tetraethoxysilane as a silica precursor, and Pluronic F127 as a template. Characterization of XRD, N2 sorption isotherms, TEM, solid-state NMR, TG, and NH3-TPD techniques is used to investigate the mesostructure, pore properties, phase composition, metal incorporation state, and acidic properties. Ordered mesoporous nanocomposites have "reinforced concrete"-structured frameworks, in which the oxide and carbon components are microphase separated and homogenously dispersed inside pore walls.
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