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Interaction of (3-Aminopropyl)triethoxysilane With Late ArN2 Afterglow: Application to Nanoparticles Synthesis
From results of in situ FTIR absorption and optical emission spectroscopy, the interaction of (3‐aminopropyl)triethoxysilane (APTES) with late ArN2 afterglow is shown to occur mainly with N atoms. They react preferentially with carbon from CHx groups in the precursor, leading to the synthesis of CN...
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Published in: | Plasma processes and polymers 2016-07, Vol.13 (7), p.698-710 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | From results of in situ FTIR absorption and optical emission spectroscopy, the interaction of (3‐aminopropyl)triethoxysilane (APTES) with late ArN2 afterglow is shown to occur mainly with N atoms. They react preferentially with carbon from CHx groups in the precursor, leading to the synthesis of CN bonds. No production of NH radical is observed, demonstrating the lack of direct reaction between active nitrogen and APTES. The NH2 group is not affected by the afterglow. One of the CC bonds of the propylamine group in the APTES is likely broken. These nanoparticles present secondary amides due to reactions with active nitrogen. They are amorphous and react in air to produce a salt.
The synthesis of nanoparticles by interaction between a late ArN2 afterglow (3‐aminopropyl)triethoxysilane, a organosilicon compound containing one amine functional group, is shown to lead to an amorphous material containing amide functional groups produced by nitrogen atoms of the afterglow. |
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ISSN: | 1612-8850 1612-8869 |
DOI: | 10.1002/ppap.201500201 |