Author/Authors :
Joseph A. Gardella Jr.، نويسنده , , Christine M. Mahoney1، نويسنده ,
Abstract :
While many XPS and SIMS studies of polymers have detected and quantified segregation of low surface energy blocks or
components in copolymers and polymer blends [D. Briggs, in: D.R. Clarke, S. Suresh, I.M. Ward (Eds.), Surface Analysis of
Polymers by XPS and Static SIMS, Cambridge University Press, Cambridge, 1998 (Chapter 5).], this paper reports ToF-SIMS
studies of direct measurement of the segment length distribution at the surface of siloxane copolymers. These data allow insight
into the segregation of particular portions of the oligomeric distribution; specifically, in this study, longer PDMS oligomers
segregated at the expense of shorter PDMS chains. We have reported XPS analysis of competitive segregation effects for short
PDMS chains [Macromolecules 35 (13) (2002) 5256]. In this study, a series of poly(ureaurethane)–poly(dimethylsiloxane)
(PUU–PDMS) copolymers have been synthesized containing varying ratios of G-3 and G-9 (G-X describes the average segment
length of the PDMS added), while maintaining a constant overall siloxane weight percentage (10, 30, and 60%). These
copolymers were utilized as model systems to study the preferential segregation of certain siloxane segment lengths to the
surface over others. ToF-SIMS analysis of PUU–PDMS copolymers has yielded high-mass range copolymer fragmentation
patterns containing intact PDMS segments. For the first time, this information is utilized to determine PDMS segment length
distributions at the copolymer surface as compared to the bulk. The results show that longer siloxane segment lengths are
preferentially segregating to the surface over shorter chain lengths. These results also show the importance of ToF-SIMS and
mass spectrometry in the development of new materials containing low molecular weight amino-propyl-terminated siloxanes.
# 2004 Elsevier B.V. All rights reserved.
Keywords :
Polymer surface analysis , Secondary ion mass spectrometry , Oligomer chainlength analysis , Polymer surface molecular weight distribution , Polymer fragmentation mechanisms