Chemical Modification of Porous Silicon Surfacewith Polyoxyethylene Groups
Abstract
The fragments of nonionic surfactants Triton X-100, Neonol AF9-10, and Synthanol ALM-10 were grafted on the surface of porous silicon by means of the photoinitiated reaction in presence of iodoform. The materials obtained were studied by means of FTIR spectroscopy and temperature programmed desorption mass spectrometry (TPD MS). A mechanism of thermal decomposition of grafted surfactants, consisting in multistage transformations starting from the destruction of polyoxyethylene chain, was evaluated. The hydrophobic properties and the hydrolytic stability of obtained materials were investigated. Their hydrophobicity can be defined by the nature of grafted surfactant groups and likely depends on the presence of alkyl chains, capable to be packed into the dense hydrophobic structures on the surface.References
Скришевський В.А. Фізичні основи напівпровідникових хімічних сенсорів. Київ: ВПЦ Київський університет, 2006. – 190 с.
Shmygol I.V., Alekseev S.A., Lavrinenko O.Yu. et al. Chemically modified porous silicon for laser desorption/ionization mass spectrometry of ionic dyes // J. Mass Spectrom. – 2009. – V. 44, N 8. – P. 1234–1240.
De Stefano L., Morett L., Rendina I., Rotiroti L. Pesticides detection in water and humic solutions using porous silicon technology // Sens. Actuators B. – 2005. – V. 111–112, N 11. – P. 522–525.
Go E.P, Uritboonthai W., Apon J.V. et al. Selective metabolite and peptide capture/mass detection using fluorous affinity tags // J. Proteome Res. – 2007. – V. 6, N 4. – P. 1492–1499.
Buriak J.M. Organometallic chemistry on silicon and germanium surfaces // Chem. Rev. – 2002. – V. 102, N 5. – P. 1271–1306.
Барабаш Р.Н., Алексеев С.А., Зайцев В.Н., Барбье Д. Устойчивость к окислению и модифицирование винилсиланами пористого кремния // Укр. хим. журн. – 2006. – Т. 72, № 10. – С. 78–84.
Lewis W.G., Shen Z., Finn M.G, Siuzdak G. Desorption/ionization on silicon (DIOS) mass spectrometry: background and application // Int. J. Mass Spectrom. – 2003. – V. 226, N 1. – P. 107–116.
Зайцев В.Н., Халаф В.А., Зайцева Г.Н., Алексеев С.А Полиоксиэтилированный кремнезем для концентрирования фенола из водных растворов // Укр. хим. журн. – 2005. – Т. 71, № 9. – C. 59–64.
Zaitsev V.N., Khalav V.A., Zaitseva G.N. Organosilica composite for preconcentration of phenolic compounds from aqueous solutions // Anal. Bioanal Chem. – 2008. – V. 391, N 4. – P. 1335–1342.
Халаф В.А., Турчин В.О., Зайцев В.Н. Определение 2,4-дихлорфеноксиуксусной кислоты в водных объектах окружающей среды // Методы и объекты химического анализа. – 2009. – Т. 4, № 1. – С. 67–72.
Халаф В.А., Турчин В.О., Гринько А.П., Зайцев В.Н. Твердофазно-экстракционное концентрирование 2,4-дихлорфеноксиуксусной кислоты на кремнеземе с привитыми группами полиоксиэтилированного изооктилфенола // Журн. аналит. химии. – 2009. – Т. 64, № 2. – С. 124–129.
Alekseev S.A., Lysenko V., Zaitsev V.N., Barbier D. Application of infrared interferometry for quantitative analysis of chemical groups grafted onto the internal surface of porous silicon nanostructures // J. Phys. Chem. C. – 2007. – V. 111, N 42. – P. 15217–1522.
Herino R., Bomchil G., Barla K. et al. Porosity and pore size distributions of porous silicon layers // J. Electrochem. Soc. – 1987. – V. 134, N 4. – P. 1994–2000.
Абрамзон А.А. Поверхностно-активные вещества: свойства и применение. – Ленинград: Химия, 1981. – 304 с.
Vadakkan T.J., Mandler D. Surface functionalization of H-terminated silicon surfaces with alcohols using iodoform as an in situ iodinating agent // ChemPhysChem. – 2002. – V. 3, N 11. – P. 973–975.
Butt H.-J., Graf K., Kappl M. Physics and Chemistry of Interfaces. – Weinheim: Wiley-VCH, 2003. – 373 p.
Lysenko V., Vitiello J., Remaki B., Barbier D Gas permeability of porous silicon nanostructures // Phys. Rev. E. – 2004. – V. 70, N 1. – P. 017301 (1–4).
Nakamura M., Song M.-B., Ito M. Etching processing of Si(111) and Si(100) surfaces in an ammonium fluoride solution investigated by in situ ATR-IR // Electrochim. Acta. – 1996. – V. 41, N 5. – P. 681–686.
Alekseev S.A., Zaitsev V.N., Fraissard J. Organosilicas with covalently bonded groups under thermochemical treatment // Chem. Mater. – 2006. – V. 18, N 7. – P. 1981–1987.
Downloads
How to Cite
Issue
Section
License
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.

