Grafting of hyperbranched cyclotriphosphazene polymer onto silica nanoparticle and carbon black surfaces

The surface grafting of hyperbranched cyclotriphosphazene polymer onto silica nanoparticles and carbon black was investigated. The grafting of hyperbranched cyclotriphosphazene polymer onto these surfaces was achieved by the repeated reactions of hexachlorocyclotriphosphazene with hexamethylenediami...

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Veröffentlicht in:Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2008-06, Vol.46 (12), p.4218-4226
Hauptverfasser: Wei, Gang, Sasage, Nozomu, Kusanagi, Yusuke, Fujiki, Kazuhiro, Yamauchi, Takeshi, Tsubokawa, Norio
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container_issue 12
container_start_page 4218
container_title Journal of polymer science. Part A, Polymer chemistry
container_volume 46
creator Wei, Gang
Sasage, Nozomu
Kusanagi, Yusuke
Fujiki, Kazuhiro
Yamauchi, Takeshi
Tsubokawa, Norio
description The surface grafting of hyperbranched cyclotriphosphazene polymer onto silica nanoparticles and carbon black was investigated. The grafting of hyperbranched cyclotriphosphazene polymer onto these surfaces was achieved by the repeated reactions of hexachlorocyclotriphosphazene with hexamethylenediamine from surface amino groups and sodium carboxylate groups, respectively. The percentage of grafting onto silica and carbon black surfaces exceeded 760 and 390%, respectively. However, it proved difficult to achieve the theoretical growth of cyclotriphosphazene polymer from these surfaces because of steric hindrance. The introduction of sulfonic acid groups was successfully achieved by the reaction of terminal chlorophosphazene groups of the hyperbranched polymer-grafted silica and carbon black with sulfanilic acid. The content of sulfonic acid groups introduced onto silica and carbon black surfaces was 4.98 mmol/g and 5.70 mmol/g, respectively. The sulfonated cyclotriphosphazene polymer-grafted carbon black was extremely hydrophilic, yielding stable colloidal dispersions in polar solvents. The sulfonated cyclotriphosphazene polymer-grafted silica and carbon black showed ionic conductivity, with the conductance increasing exponentially with increasing relative humidity and temperature. This study may offer important leads in the application of silica nanoparticles and carbon black in polymeric membranes for fuel cells.
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The grafting of hyperbranched cyclotriphosphazene polymer onto these surfaces was achieved by the repeated reactions of hexachlorocyclotriphosphazene with hexamethylenediamine from surface amino groups and sodium carboxylate groups, respectively. The percentage of grafting onto silica and carbon black surfaces exceeded 760 and 390%, respectively. However, it proved difficult to achieve the theoretical growth of cyclotriphosphazene polymer from these surfaces because of steric hindrance. The introduction of sulfonic acid groups was successfully achieved by the reaction of terminal chlorophosphazene groups of the hyperbranched polymer-grafted silica and carbon black with sulfanilic acid. The content of sulfonic acid groups introduced onto silica and carbon black surfaces was 4.98 mmol/g and 5.70 mmol/g, respectively. The sulfonated cyclotriphosphazene polymer-grafted carbon black was extremely hydrophilic, yielding stable colloidal dispersions in polar solvents. 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Part A, Polymer chemistry</title><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><description>The surface grafting of hyperbranched cyclotriphosphazene polymer onto silica nanoparticles and carbon black was investigated. The grafting of hyperbranched cyclotriphosphazene polymer onto these surfaces was achieved by the repeated reactions of hexachlorocyclotriphosphazene with hexamethylenediamine from surface amino groups and sodium carboxylate groups, respectively. The percentage of grafting onto silica and carbon black surfaces exceeded 760 and 390%, respectively. However, it proved difficult to achieve the theoretical growth of cyclotriphosphazene polymer from these surfaces because of steric hindrance. The introduction of sulfonic acid groups was successfully achieved by the reaction of terminal chlorophosphazene groups of the hyperbranched polymer-grafted silica and carbon black with sulfanilic acid. The content of sulfonic acid groups introduced onto silica and carbon black surfaces was 4.98 mmol/g and 5.70 mmol/g, respectively. The sulfonated cyclotriphosphazene polymer-grafted carbon black was extremely hydrophilic, yielding stable colloidal dispersions in polar solvents. The sulfonated cyclotriphosphazene polymer-grafted silica and carbon black showed ionic conductivity, with the conductance increasing exponentially with increasing relative humidity and temperature. 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The grafting of hyperbranched cyclotriphosphazene polymer onto these surfaces was achieved by the repeated reactions of hexachlorocyclotriphosphazene with hexamethylenediamine from surface amino groups and sodium carboxylate groups, respectively. The percentage of grafting onto silica and carbon black surfaces exceeded 760 and 390%, respectively. However, it proved difficult to achieve the theoretical growth of cyclotriphosphazene polymer from these surfaces because of steric hindrance. The introduction of sulfonic acid groups was successfully achieved by the reaction of terminal chlorophosphazene groups of the hyperbranched polymer-grafted silica and carbon black with sulfanilic acid. The content of sulfonic acid groups introduced onto silica and carbon black surfaces was 4.98 mmol/g and 5.70 mmol/g, respectively. The sulfonated cyclotriphosphazene polymer-grafted carbon black was extremely hydrophilic, yielding stable colloidal dispersions in polar solvents. 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subjects Applied sciences
carbon black
dispersions
Exact sciences and technology
hyperbranched
Inorganic and organomineral polymers
ionic conductivity
nanoparticles
Physicochemistry of polymers
Preparation
silicas
title Grafting of hyperbranched cyclotriphosphazene polymer onto silica nanoparticle and carbon black surfaces
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