Microfluidic system based on porous silicon.
SUMMARY OF MAIN RESULTS
1.
Covalent immobilization of alkanes on porous silicon
was successfully performed. It was demonstrated that due to high porous silicon
activity no catalysts needed for covalent immobilization of alkanes.
2.
Two main pathways of silicon-surface modification were
studied:
a)
silicon hydrosilylation
, R = C8H17,
C16H33
Scheme (A) b)
silanisation of partly-oxidized silicon
, R = CH3,
C8H17 Scheme
(B) 3.
By DRIFT, FTIR and TPD-MS methods covalent nature (not
adsorption) of chemical bond between silicon and alkane chain was proved.
4.
Conditions that may give stable for chromatography
application particles postulated
MAIN
CONCLUSIONS It was demonstrated
that pathway (A) is suitable for fresh porous silicon only, but pathway (B)
acceptable for most porous silicon samples. Complete
substitution of surface Si-H groups does not observed in any cases neither in
hydrosilylation reaction nor in porous silicon oxidation. Partly oxidized
silicon containing Si-H bonds is inactive in hydrosilylation reaction (A). Since unstable
silicon framework is protected by siloxane layers, materials obtained by
silanisation according to the scheme (B) can be more stable in common
chromatography environment then those obtained by scheme (A). Due to poor
stability of Si-Si bond partial oxidation on porous silicon surface is needed,
but this oxidation may increase size of silicon crystals and decrease
permeability of the membrane, so optimal conditions leading to stable but
suitable for chromatography silicon-base phase should be found.
Publications
Study of Porous Silicon Nanostructures as Hydrogen Reservoirs
Lysenko, V.; Bidault, F.; Alekseev, S.; Zaitsev, V.; Barbier, D.; Turpin, C.;
Geobaldo, F.; Rivolo, P.; Garrone, E.;
J. Phys. Chem. B. ;
(Article); 2005; 109(42);
19711-19718.