Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Intrinsic Molecular Mobility and Toughness of Polymers I, 2005, p.1-33
Ort / Verlag
Berlin, Heidelberg: Springer Berlin Heidelberg
Erscheinungsjahr
2005
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
By way of introduction to the subject of this Volume1
this contribution reviews the effects of the most prominent properties of macromolecules (their enormous
length, strong elastic anisotropy in axial and lateral directions and high segmental mobility) and
of their characteristic dimensions on the elementary molecular deformation mechanisms of thermoplastic
polymers. The competition between these mechanisms has a determinant influence on the different
failure modes (crazing, creep, yielding and flow, fracture through crack propagation). The main part
is devoted to an analysis of failure in creep. The micro-morphological approach is further developed
and compared to criteria derived from visco-elastic theory with representative equations. Small angle
X-ray analysis of the formation of fibrillar structures in amorphous polymers SAN and PC identifies
three distinct regimes associated to fluid-like behaviour and disentanglement by forced reptation
at low and moderate stresses (or high temperatures) and chain-scission dominated craze initiation
(at low temperatures and high stresses), respectively. In semi-crystalline polymers similar differences
are found: homogeneous creep at high stresses mostly involving the plastic deformation and break-up
of crystal lamellae as opposed to the formation of craze-like structures due to the disentanglement
of chains at low stresses. This review focuses on the important dual role of molecular mobility,
to be at the origin of time-dependent properties of polymer materials, especially of their toughness,
and to influence without exception all damage mechanisms which limit the strength and durability of
polymer components.