Covalent and noncovalent functionalisation and solubilisation of nanodiamond

Maitra, Urmimala ; Gomathi, A. ; Rao, C. N. R. (2008) Covalent and noncovalent functionalisation and solubilisation of nanodiamond Journal of Experimental Nanoscience, 3 (4). pp. 271-278. ISSN 1745-8080

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Official URL: http://www.tandfonline.com/doi/abs/10.1080/1745808...

Related URL: http://dx.doi.org/10.1080/17458080802574155

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.

Item Type:Article
Source:Copyright of this article belongs to Taylor and Francis Group.
Keywords:Nanodiamond; Covalent Functionalisation; Solubilisation; Organosilicon; Organotin
ID Code:54832
Deposited On:22 Aug 2011 13:17
Last Modified:22 Aug 2011 13:17

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