z-logo
Premium
Mechanical properties of glass bead‐ and wollastonite‐filled isotactic‐polypropylene composites modified with thermoplastic elastomers
Author(s) -
Balkan Onur,
Demirer Halil
Publication year - 2010
Publication title -
polymer composites
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.577
H-Index - 82
eISSN - 1548-0569
pISSN - 0272-8397
DOI - 10.1002/pc.20953
Subject(s) - materials science , composite material , microstructure , elastomer , thermoplastic elastomer , toughness , thermoplastic polyurethane , tacticity , composite number , acicular , copolymer , polymer , polymerization
Mechanical properties of the isotactic‐polypropylene/glass bead (iPP/GB) and iPP/wollastonite (iPP/W) composites modified with thermoplastic elastomers, the poly(styrene‐ b ‐ethylene‐ co ‐butylene‐ b ‐styrene) copolymer (SEBS) and corresponding block copolymer grafted with maleic anhydride (SEBS‐ g ‐MA), were investigated. An increase in toughness of iPP with the elastomers was associated with a decrease in rigidity and strength. Mechanical performance of iPP increased more with acicular W than with spherical GB due to reinforcing effect of W. Comparing the (iPP/GB)/SEBS and (iPP/W)/SEBS composites having the separate microstructure, strength and toughness values of the iPP/GB and iPP/W composites increased more with SEBS‐ g ‐MA at the expense of rigidity due to the core‐shell microstructure with strong interfacial adhesion. Moreover, the iPP/W composite exhibited superior mechanical performance with 2.5 and 5 vol% of SEBS‐ g ‐MA because of a positive synergy between the core‐shell microstructure and reinforcing effect of acicular W. The extended models revealed that the elastomer and filler particles in the (iPP/GB)/SEBS and (iPP/W)/SEBS composites acted individually due to the separate microstructure. However, the rigid GB and W particles encapsulated with the thick elastomer interlayer ( R 0 / R 1 = 0.91) in the (iPP/GB)/SEBS‐ g ‐MA and (iPP/W)/SEBS‐ g ‐MA composites acted like neither big elastomer particles nor like individual rigid particles, inferring more complicated failure mechanisms in the core‐shell composites. POLYM. COMPOS., 31:1285–1308, 2010. © 2010 Society of Plastics Engineers

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom