2009
DOI: 10.1002/app.30629
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Rheology and morphology of high impact polystyrene/ polyethylene blends and the effect of compatibilization on their properties

Abstract: Attempts were made to study rheology and morphology of high impact polystyrene/polyethylene (HIPS/PE) blends. The Effect of compatibilization using styrene-butadiene-styrene copolymer (SBS) and styrene-ethylene-butylene-styrene copolymer (SEBS) on their properties was also studied. The results of linear viscoelastic properties showed negative deviation of viscosity and elasticity from the mixing rules in low HIPS content blends, while positive deviation was observed for high HIPS content blends. The former was… Show more

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Cited by 16 publications
(6 citation statements)
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“…This increase is mainly due to the increase in interfacial elasticity resulting from the decrease in droplet size (or increase in interfacial area). As discussed in the Introduction, similar behavior has been observed in blends compatibilized with diblock or graft copolymers. However, an additional feature is evident in our blends compatibilized with CB, namely, a plateau in G ′ appears at very low frequencies (ω < 0.05 rad/s) which suggests an additional relaxation (with relaxation time larger than 30 min). A possible source for this additional relaxation may come from the interfacial CB network established by interfacial stitching with the PE backbone of the CB being entangled within the PE phase and its PP combs entangled, or hooked, in the PP phases across many interfacial points (see cartoon in Figure ).…”
Section: Resultssupporting
confidence: 81%
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“…This increase is mainly due to the increase in interfacial elasticity resulting from the decrease in droplet size (or increase in interfacial area). As discussed in the Introduction, similar behavior has been observed in blends compatibilized with diblock or graft copolymers. However, an additional feature is evident in our blends compatibilized with CB, namely, a plateau in G ′ appears at very low frequencies (ω < 0.05 rad/s) which suggests an additional relaxation (with relaxation time larger than 30 min). A possible source for this additional relaxation may come from the interfacial CB network established by interfacial stitching with the PE backbone of the CB being entangled within the PE phase and its PP combs entangled, or hooked, in the PP phases across many interfacial points (see cartoon in Figure ).…”
Section: Resultssupporting
confidence: 81%
“…In general, rheological behavior of noncompatibilized immiscible blends is characterized by an extra contribution to the elastic modulus at low frequencies, resulting from interfacial relaxation. This interfacial relaxation process is manifested in the plot of the elastic modulus ( G ′) versus frequency (ω) as a shoulder for blends with droplet-matrix morphologies and as a power law for blends with cocontinuous structures . The addition of a BC compatibilizer further raises the elasticity in the terminal relaxation region due to an increase in interfacial area (or a reduction in domain size). Furthermore, addition of a BC compatibilizer reduces the coarsening rate, characterized by the time evolutions of both the elastic modulus and the specific interfacial area .…”
Section: Introductionmentioning
confidence: 99%
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“…[ 9–11 ] Styrene‐butadiene‐styrene (SBS) terpolymer is most frequently used as compatibilizer for PE with other polymers like PS. [ 12,13 ] Deanin and Chang [ 14 ] investigated that blending SBS with HDPE improved impact strength of the HDPE. However, blending small amount of LDPE in SBS increased hardness, strength without affecting the flexible rubbery properties of SBS.…”
Section: Introductionmentioning
confidence: 99%
“…Reactive compatibilization generates graft or block copolymers in situ during processing, such as maleic anhydride grafted polypropylene (PP‐g‐MAH), [ 10 ] maleic anhydride grafted acrylonitrile‐butadiene‐styrene copolymer (ABS‐g‐MAH), [ 11 ] and so on. On the other hand, nonreactive compatibilization relies on physical entanglement with the substrate, such as polystyrene‐polyethylene(PS‐g‐PE), [ 12 ] polypropylene‐ethylene‐butylene/styrene (PP‐g‐EBS), [ 13 ] and so on. For instance, not only the mechanical performances, [ 14 ] but also the interlaminar shear strength [ 15 ] was efficiently enhanced due to the interface strengthening between CF and resin matrix.…”
Section: Introductionmentioning
confidence: 99%