MICROHARDNESS UNDER STRAIN - 2 - MICROHARDNESS BEHAVIOR DURING STRESS-INDUCED POLYMORPHIC TRANSITION IN BLOCK-COPOLYMERS OF POLY(BUTYLENE TEREPHTHALATE)
Aa. Apostolov et al., MICROHARDNESS UNDER STRAIN - 2 - MICROHARDNESS BEHAVIOR DURING STRESS-INDUCED POLYMORPHIC TRANSITION IN BLOCK-COPOLYMERS OF POLY(BUTYLENE TEREPHTHALATE), Journal of macromolecular science. Physics, B37(4), 1998, pp. 543-555
In addition to homopoly(butylene terephthalate) (homo-PBT), the microh
ardness technique was applied to its multiblock copolymers for examina
tion of the stress-induced polymorphic transition. Drawn and annealed
at 170 degrees C for 6 h with fixed ends in a vacuum, bristles of poly
(ether ester) (PEE) having PET as hard segments and poly(ethylene oxid
e) (PEO) with molecular weight 1000 as soft segments (PBT/PEO = 57/43
wt%) were characterized with respect to their microhardness H at vario
us stages of tensile deformation. A sharp H decrease (by 20%) in a nar
row deformation interval (2-4%) due to the stress-induced alpha double
left right arrow beta polymorphic transition is observed followed by
an increase and decrease of H. The transition is registered at much hi
gher relative tensile deformations (between 25% and 30%) compared with
the case of homo-PBT. This is explained by the presence of a very sof
t amorphous phase of PEG, which deforms first. The same phase, disting
uished by low viscosity in which the PET crystallites are ''floating,'
' is the reason for the very low H values measured (between 25 and 35
MPa, depending on the amount of alpha- and beta-modifications). The st
ress-induced polymorphic transition in copolymers of PET with PEO is d
emonstrated for the first time, also supporting the recently proposed
concept of the microhardness depression effect.