TY - JOUR
T1 - Wood fiber reinforced multicomponent, multiphase PP composites
T2 - Structure, properties, failure mechanism
AU - Sudár, András
AU - Burgstaller, Christoph
AU - Renner, Károly
AU - Móczó, János
AU - Pukánszky, Béla
N1 - Publisher Copyright:
© 2014 Elsevier Ltd.
PY - 2014/10/8
Y1 - 2014/10/8
N2 - Polypropylene (PP) was reinforced with wood flour and impact modified with elastomers to increase stiffness and impact resistance simultaneously. Elastomer was added in 0, 5, 10 and 20. wt%, while wood content changed from 0 to 60. wt% in 10. wt% steps. Structure and adhesion were controlled by the addition of functionalized (maleated) polymers. Composites were homogenized in a twin-screw extruder and then injection molded to tensile bars. The results showed that composite structure is determined by the relative strength of adhesion and shear forces prevailing during processing. Structure can be controlled by the application of functional polymers within limits. Although embedding is favored by thermodynamics and further promoted by coupling, de-encapsulation occurs at the large shear stresses of injection molding even in the presence of a functionalized elastomer. Composite properties depend on composition, increasing elastomer content results in decreasing stiffness and strength. Model calculations showed that the elastomer does not contribute to load bearing, average stress in the matrix increases with increasing elastomer content. Local stresses and adhesion define the initiation of deformation processes around wood particles, which start at the same stress irrespectively of elastomer content. Local processes determine the mechanism of failure and composite strength independently of their mechanism.
AB - Polypropylene (PP) was reinforced with wood flour and impact modified with elastomers to increase stiffness and impact resistance simultaneously. Elastomer was added in 0, 5, 10 and 20. wt%, while wood content changed from 0 to 60. wt% in 10. wt% steps. Structure and adhesion were controlled by the addition of functionalized (maleated) polymers. Composites were homogenized in a twin-screw extruder and then injection molded to tensile bars. The results showed that composite structure is determined by the relative strength of adhesion and shear forces prevailing during processing. Structure can be controlled by the application of functional polymers within limits. Although embedding is favored by thermodynamics and further promoted by coupling, de-encapsulation occurs at the large shear stresses of injection molding even in the presence of a functionalized elastomer. Composite properties depend on composition, increasing elastomer content results in decreasing stiffness and strength. Model calculations showed that the elastomer does not contribute to load bearing, average stress in the matrix increases with increasing elastomer content. Local stresses and adhesion define the initiation of deformation processes around wood particles, which start at the same stress irrespectively of elastomer content. Local processes determine the mechanism of failure and composite strength independently of their mechanism.
KW - A: Polymer-matrix composites (PMCs)
KW - A: Recycling
KW - B: Interfacial strength
KW - Bumper material
KW - C: Damage mechanics
UR - http://www.scopus.com/inward/record.url?scp=84907051370&partnerID=8YFLogxK
U2 - 10.1016/j.compscitech.2014.08.018
DO - 10.1016/j.compscitech.2014.08.018
M3 - Article
AN - SCOPUS:84907051370
SN - 0266-3538
VL - 103
SP - 106
EP - 112
JO - Composites Science and Technology
JF - Composites Science and Technology
ER -