dc.identifier.citation |
De Silva, D.S.M, Zeng, X.B., Ungar, G. and Spells, S.J. 2003. Perpendicular and tilted chains in lamellar crystals. Journal of Macromolecular Science-Physics B 42, 915-927. |
en_US |
dc.description.abstract |
Chain tilt and surface disorder were investigated in end-deuterated long n-alkane
C12D25C192H384C12HD24 crystallized from solution and in n-alkane C162H326
crystallized from melt. Small-angle X-ray scattering and infrared spectroscopy were
employed. Extended-chain crystals of C12D25C192H384C12HD24 as-grown from
solution have the molecular axis perpendicular to the lamellar surface, but when
heated, around 908C, they start tilting relative to the layer normal. The tilt increases
gradually to reach 358 just below the melting point. C162H326 crystallized from the melt
at small supercoolings has chains tilted at 358 at the outset, as found previously for all
melt-crystallized long alkanes and polyethylene. However, for the first time in long
alkanes, it is found that when molten C162H326 is supercooled to DT $ 10K; crystals
with perpendicular chains form. At still larger DT, the chains are once-folded, with a
mixed population of tilted and perpendicular chain crystals. The use of Davydov
splitting of the CH2 and CD2 bending vibration of the end-labelled alkane
C12D25C192H384C12HD24 allows independent IR probing of molecular disorder at the
deuterated surface and in the hydrogenous crystal interior. The initially small CD2
splitting and the presence of an additional singlet component indicate a rough surface in
as-grown crystals, with considerable longitudinal interchain disorder. It is estimated
that about 10% of chains are displaced by up to a dozen C-atoms. The increase in
splitting and decrease in absorbance of the singlet, which occur on annealing at
progressively higher temperatures, are evidence of steady improvement in translational surface order, occurring simultaneously with increasing chain tilt angle. From the
above evidence, it is concluded that the absence of tilt in as-grown crystals is not the
result of high surface order, as in the case of shorter odd n-alkanes, but rather of a high
frozen-in longitudinal disorder with chain ends or folds protruding out of or sunken
beneath the crystal surface. It is also concluded that chain tilt only becomes necessary
as the crystal surface becomes translationally more ordered and the crystal–amorphous
interface sharpens. The effect of chain tilt on the Davydov splitting is addressed briefly. |
en_US |