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II International Symposium on Carbon for Catalysis ABSTRACTS

II International Symposium on Carbon for Catalysis ABSTRACTS

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OP-I-23<br />

polyfuncti<strong>on</strong>al surface cover were found. It was established, that carrying out chemical<br />

reacti<strong>on</strong>s <strong>on</strong> the diam<strong>on</strong>d surface permit us to grow carb<strong>on</strong> atoms m<strong>on</strong>olayers, <strong>for</strong> instance via<br />

reacti<strong>on</strong>s: ≡C–Н + CCl 4 → ≡C–СН 2 Cl + HCl, ≡C–СН 2 Cl + CH 4 → ≡C–СН 2 CH 3 + HCl<br />

By treatment of diam<strong>on</strong>d powders with volatile halogenides (TiCl 4 , VCl 5 , CrCl 3 ) surface<br />

metal-c<strong>on</strong>taining groups are <strong>for</strong>med that give us opportunities to per<strong>for</strong>m surface synthesis <strong>for</strong><br />

further chemical modificati<strong>on</strong>.<br />

Covalent grafting, i.e. surface interacti<strong>on</strong> with various substances-modificators, is of<br />

main interest in diam<strong>on</strong>d surface chemical modificati<strong>on</strong>. This modificati<strong>on</strong> provides a basis<br />

<strong>for</strong> fundamentally new spatial structures creati<strong>on</strong> <strong>on</strong> its base. Native cover polyfuncti<strong>on</strong>ality<br />

of ND prohibit from selective surface modificati<strong>on</strong>. As a result preliminary surface<br />

m<strong>on</strong>ofuncti<strong>on</strong>alizati<strong>on</strong> is needed. One of the most effective procedures of ND functi<strong>on</strong>al<br />

cover unificati<strong>on</strong> c<strong>on</strong>sists in hydrogen stream treatment at 800 o C 5 hours. As a result of this<br />

hydride group’s layer is <strong>for</strong>med <strong>on</strong> the diam<strong>on</strong>d powder surface. This layer <strong>for</strong>mati<strong>on</strong> causes<br />

the reducti<strong>on</strong> of diam<strong>on</strong>d surface reacti<strong>on</strong> capacity. For its activati<strong>on</strong> and electrophile center<br />

creati<strong>on</strong> it is subjected to halogenati<strong>on</strong>. Photo- and thermochemical halogenati<strong>on</strong> is<br />

inc<strong>on</strong>venient because of free halogens and high temperatures utilizati<strong>on</strong>. Liquid phase<br />

chlorinati<strong>on</strong> with SO 2 Cl 2 in benzene and chlorine in carb<strong>on</strong> tetrachloride in arg<strong>on</strong> ambient is<br />

more attractive. In the first case azobisisobutir<strong>on</strong>itrile was used <strong>for</strong> initializati<strong>on</strong> and in the<br />

sec<strong>on</strong>d – light irradiati<strong>on</strong>. Both variants of chlorinati<strong>on</strong> yielded in completely full surface<br />

hydrogen atoms substituti<strong>on</strong>. However, hydrolytic instability of chlorinated diam<strong>on</strong>d surface<br />

should be c<strong>on</strong>sidered. Interacti<strong>on</strong> of chlorinated ND powder with butyllithium,<br />

octadecyllithium and others resulted in alkyl groups grafting <strong>on</strong>to the diam<strong>on</strong>d surface.<br />

Phenyl groups were grafted to the surface via reacti<strong>on</strong> with phenyllithium. Reacti<strong>on</strong> of<br />

chlorinated ND with sodium cyanide yielded in surface cyanide groups grafting.<br />

Various physicochemical methods were used to characterize modified ND: IR- and<br />

Auger-spectroscopy, XPS, EELS, NMR-H1, ESR, electr<strong>on</strong> microscopy etc.<br />

Method development and c<strong>on</strong>diti<strong>on</strong>s discovering <strong>for</strong> m<strong>on</strong>ofuncti<strong>on</strong>al cover creati<strong>on</strong> <strong>on</strong><br />

ND surface, <strong>on</strong> the <strong>on</strong>e hand, can result in their more efficiently utilizati<strong>on</strong>, because ND<br />

applicati<strong>on</strong> is restrained by n<strong>on</strong>reproductivity and instability of their physicochemical<br />

characteristics. On the other hand this may lead to creati<strong>on</strong> of fundamentally new materials<br />

<strong>for</strong> biomedical applicati<strong>on</strong> (nanoparticles <strong>for</strong> directi<strong>on</strong>al drug carry in vivo, chromatographic<br />

sorbents <strong>for</strong> HPLC etc.). In latter case sorbents based <strong>on</strong> modified porous ND cakes with<br />

highly developed specific surface together with thin size distributed nanoporoues are<br />

promising.<br />

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