Albert F. Yee

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Name: Yee,, Albert Fan
Organization: University of Michigan , USA
Department: Macromolecular Science and Engineering Center
Title: Professor(PhD)

TOPICS

Co-reporter:Hua-Gen Peng, Yen Peng Kong and Albert F. Yee
Macromolecules 2010 Volume 43(Issue 1) pp:409-417
Publication Date(Web):November 6, 2009
DOI:10.1021/ma901666v
Relaxation and chain dynamics of polymer nanostructures after release of spatial confinement were studied using line gratings as small as 33 nm on polystyrene surface fabricated by nanoimprint lithography. The temperature for “slumping”—rapid line height relaxation—decreased as the line width diminished for all molecular masses (MWs), but a simple explanation based on enhanced surface mobility fails to explain the results. When MW was low and the structure was large, the line height monitored with an AFM reduced as surface tension overcame the polymer viscosity. Interesting and complex behaviors were observed when the radius of gyration (Rg) of the polymer molecules was not small compared with the dimension of the nanostructure. Careful examination of the surface viscosity shows that confinement of polymer chains into space comparable to or even smaller than its Rg appears to enhance relaxation, which is the major factor for the surprisingly low temperature at which nanostructures of high MW slumps.
Co-reporter:Nanjian Sun;Jianwei Liu;Terry Dull
Journal of Polymer Science Part B: Polymer Physics 2007 Volume 45(Issue 12) pp:1410-1417
Publication Date(Web):3 MAY 2007
DOI:10.1002/polb.21168

This study examines if correlation between a specific molecular motion and the growth and relaxation of nanovoids, which are precursors to crazes, can be established. A novel technique, positronium annihilation lifetime spectroscopy (PALS) synchronized with cyclic stress, is reported. In this technique the positronium annihilation signal was accumulated in sixteen channels corresponding to sixteen phases of the sinusoidal load, which allowed statistically significant data for nanovoid generation and relaxation due to the fluctuating stress to be accumulated. This technique was applied to a series of copolymers of poly(ethylene terephthalate) (PET) and poly(1,4-cyclohexylenedimethylene terephthalate) (PCT). Previous studies have shown that the cyclohexylene rings in the main chain of PCT actively undergo chair-boat-chair conformational transitions in the glassy PCT at around room temperature. The PET-co-PCT series was also chosen for this study because the crazing stress increases systematically with the cyclohexylene content. The synchronized PALS data are consistent with the hypothesis that transient nanovoids generated by the cyclic stress in polymers containing more cyclohexylene rings relax more readily than those with fewer rings. The results also correlate well with the crazing stress in this series of copolymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1410–1417, 2007

Glycine, N-[2-(octyloxy)-5-[(1-oxo-10-undecenyl)amino]benzoyl]-
Benzoic acid, 5-nitro-2-[[11-(phenylmethoxy)undecyl]oxy]-
BENZOIC ACID, 5-NITRO-2-[[11-(PHENYLMETHOXY)UNDECYL]OXY]-, METHYL ESTER
1,3-Benzenedicarboxylic acid, 4,6-bis(octyloxy)-, monomethyl ester
1,3-Benzenedicarboxylic acid, 4,6-bis(octyloxy)-, dimethyl ester
GLYCINE, N-[5-AMINO-2-(OCTYLOXY)BENZOYL]-, ETHYL ESTER
Glycine, N-[5-nitro-2-(octyloxy)benzoyl]-, ethyl ester
Benzene, [[(11-bromoundecyl)oxy]methyl]-
1,3-Benzenedicarboxylic acid, 4,6-dihydroxy-, dimethyl ester