F. Fally et al., QUANTIFICATION OF THE FUNCTIONAL-GROUPS PRESENT AT THE SURFACE OF PLASMA POLYMERS DEPOSITED FROM PROPYLAMINE, ALLYLAMINE, AND PROPARGYLAMINE, Journal of applied polymer science, 56(5), 1995, pp. 597-614
The surface chemistry of plasma-deposited films created from amine-fun
ctionalized saturated (propylamine) and unsaturated (allylamine and pr
opargylamine) precursors has been investigated by high-energy resoluti
on XPS, chemical derivatization, elemental analysis, and HREELS. XPS r
esults show that nitrogen-rich deposits are obtained from unsaturated
precursors at low power or at high power in the postdischarge region.
Quantitative information on the chemical groups in the polymers is obt
ained by simulating the XPS C1s and N1s core levels and by performing
derivatization reactions. The proportion of primary amine functions de
duced from tagging reactions with pentafluorobenzaldehyde in the liqui
d phase and with 4-trifluoromethylbenzaldehyde in the vapor phase vari
es between 10 and 33%. These groups are converted into imine (more tha
n 50%) in polypropylamine and polyallylamine, while imine and nitrile
functions were found in polypropargylamine. HREELS has allowed us to d
istinguish between different nitrogen-containing functionalities prese
nt at the extreme surface of the polymers. The comparison of the HREEL
S and TIR spectra shows that the chemical composition at the extreme s
urface of the samples is representative of that of the bulk. To explai
n the conversion of the chemical groups in the plasma, polymerization
mechanisms are proposed for each of the monomers. (C) 1995 John Wiley
and Sons, Inc.