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Title: | Covalent and noncovalent functionalisation and solubilisation of nanodiamond |
Authors: | Maitra, Urmimala Gomathi, A Rao, C N R |
Keywords: | nanodiamond covalent functionalisation solubilisation organosilicon organotin Nanoscale Diamond Immobilization Chemistry Chemistry |
Issue Date: | 2008 |
Publisher: | Taylor & Francis Ltd |
Citation: | Journal of Experimental Nanoscience 3(4), 271-278 (2008) |
Abstract: | Covalent functionalisation of nanodiamond has been carried out by employing several methods. One of them involves the reaction of acid-treated nanodiamond with thionyl chloride followed by reaction with a long-chain aliphatic amine to produce the amide derivative. The second method involves reaction of acid-treated nanodiamond with an organosilicon or organotin reagent such as hexadecyltrimethoxysilane, dibutyldimethoxytin, and perfluoro-octyltriethoxysilane. The products of covalent functionalisation produce excellent dispersions in CCl4 and toluene. SiO2- and SnO2- covered nanodiamond are obtained by heating the nanodiamond coated with the organosilane and the organotin reagents, respectively. By interaction of nanodiamond with surfactants such as sodium bis(2-ethylhexyl) sulphosuccinate (AOT), Triton X-100 (TX-100), polyvinyl alcohol (PVA), cetyltrimethylammonium bromide (CTAB), and tert-octylphenoxy poly(oxyethylene) ethanol (IGEPAL) gives good dispersions in water, the best dispersion with the lowest surfactant concentration being obtained with IGEPAL. |
Description: | Restricted Access |
URI: | https://libjncir.jncasr.ac.in/xmlui/10572/330 |
Other Identifiers: | 1745-8080 |
Appears in Collections: | Research Papers (Prof. C.N.R. Rao) |
Files in This Item:
File | Description | Size | Format | |
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J. Expt. Nanosci 27.pdf Restricted Access | 975.11 kB | Adobe PDF | View/Open Request a copy |
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