The surface tensions of amine-, hydroxyl-, and methyl-terminated poly(dimethylsiloxane) (PDMS) oligomers with molecular weights ranging from 1000 to 75 000 are measured by pendant drop tensiometry. The surface tension increases with molecular weight for the methyl-terminated polymers, decreases with molecular weight for the amine-terminated polymers, and is nearly independent of molecular weight for the hydroxyl-terminated polymers. This behavior is attributed to differences in surface tension of the end groups and the repeat unit of the chain ( . -
The depletion of alkylamine terminal groups at the vacuum-polymer interface is measured for a,@-difunctional poly(dimethylsi1oxane) oligomers by X-ray photoelectron spectroscopy. The driving force for this depletion is the high relative surface energy of the amine terminal groups compared to that of the low surface energy poly(dimethylsi1oxane) backbone. The degree of surface end group depletion, within the maximum sampling depth probed (ca. 7 nm), is found to be on the order of 40% for a 960 molecular weight oligomer and decreases slightly with an increase in the oligomer molecular weight. Angle-dependent measurements are applied to determine end-group concentration depth profiles. End-group depletion is largest at the shallowest sampling depths and decays rapidly toward the bulk. The decay profiles cannot be explained by simple monotonic decay functions, consistent with the expected effects of connectivity between the end groups and the chain backbone, but the data are insufficient to prove whether the profiles are oscillatory in nature, as expected from theoretical considerations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.