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Thermoplastic elastomers blend morphology

S. Shahbikian, Phase Morphology Development and Rheological Behavior of Non-plasticized and Plasticized Thermoplastic Elastomer Blends (Ecole Polytechnique, Mraitreal, 2010),... [Pg.869]

Verma, G., et ai, PBT/thermoplastic elastomer blends - Mechanical, morphological, and rheological characterization. Polymer - Plastics Technology and Engineering, 47(10) p. 969. 2008. [Pg.427]

Guo Q, Figueiredo P, Thomann R, Gronski W. Phase behavior, morphology and interfacial structure in thermoset/thermoplastic elastomer blends of polyfpropylene glycol)-type epoxy resin and polystyrene-b-polybutadiene. Polymer 2001 42 10101-10. [Pg.13]

SAXS and WAXS are particularly efficient in the study of amorphous polymers including microstructured materials, hence their use in block copolymers (see also Chapters 6 and 7). The advent of synchotron sources for X-ray scattering provided new information, particularly on the evolution of block copolymer microstructures with time resolution below one second. In particular, the morphology of TPEs is most often studied with these techniques Guo et al. [108] applied SAXS to the analysis of the phase behavior, morphology, and interfacial structure in thermoset/thermoplastic elastomer blends. WAXS is often associated with SAXS and some other methods, such as electron microscopy, and various thermal and mechanical analyses. It is mainly used in studies of the microphase separation [109,110], deformation behavior [111], and blends [112]. [Pg.14]

Sengupta P and Noordermeer J W M (2003) Effects of composition and processing conditions on morphology and properties of thermoplastic elastomer blends of SEBS/PP/oil and of d5mamically vulcanized EPDM/PP/oil, 163 Spring ACS Rub Div Tech Meet, San Francisco, Ga, USA, 149-176. [Pg.30]

Such soft-touch materials are usually TP Vs or thermoplastic elastomers (TPEs) which combine the moldability of thermoplastics in the melt state with elasticity, lower hardness, fracture resistance, and surface characteristics of elastomers. However, plastics and elastomers respond differently to mechanical stress. Hence, both rheological behavior and mechanical strength will to a large extent depend on the morphology of the blend which may change with change in the composition. [Pg.332]

Akhtar, S. Morphology and Physical Properties of Thin Films of Thermoplastic Elastomers from Blends of Natural Ruhher and Polyethylene, Rubber Chem. Technol. 61, 599-583, 1988. [Pg.350]

TPEs from thermoplastics-mbber blends are materials having the characteristics of thermoplastics at processing temperature and that of elastomers at service temperature. This unique combination of properties of vulcanized mbber and the easy processability of thermoplastics bridges the gap between conventional elastomers and thermoplastics. Cross-linking of the mbber phase by dynamic vulcanization improves the properties of the TPE. The key factor that controls the properties of TPE is the blend morphology. It is essential that in a continuous plastic phase, the mbber phase should be dispersed uniformly, and the finer the dispersed phase the better are the properties. A number of TPEs from dynamically vulcanized mbber-plastic blends have been developed by Bhowmick and coworkers [98-102]. [Pg.1055]

Thermoplastic elastomers (TPE), 9 565-566, 24 695-720 applications for, 24 709-717 based on block copolymers, 24 697t based on graft copolymers, ionomers, and structures with core-shell morphologies, 24 699 based on hard polymer/elastomer combinations, 24 699t based on silicone rubber blends, 24 700 commercial production of, 24 705-708 economic aspects of, 24 708-709 elastomer phase in, 24 703 glass-transition and crystal melting temperatures of, 24 702t hard phase in, 24 703-704 health and safety factors related to, 24 717-718... [Pg.942]

The physical interactions in TPE can be characterised by IR spectroscopy. A few examples of such studies are discussed here. Examples of PE based thermoplastic elastomers are NR/PE blends [50, 52]. TPE [49] based on 50/50 NR/LDPE, forms co-continuous morphological structure of both NR and LDPE. Thermal analysis shows that the blend is immiscible and from IR spectra of the 50/50 NR/LDPE blends [53], it is observed, the peaks of NR and PE exist almost in the same positions in the blend with a very little shift (Figure 5.12). The absorption band at 833 cm"1 for cis >C = C in NR (Figure 5.12) is shifted to 836 cm 1. Similarly the peak at 1370 cm"1 (C-H stretching of CH3 group) shifts to 1373 cm"1, while the peak for C=C double bond shifts from 1660 cm"1 to 1658 cm"1, and the band at 1467 cm"1 for -CH2 in LDPE (Figure 5.12) is shifted to 1462 cm 1. The spectra thus confirm that there exist only physical interactions in NR-PE blend. [Pg.188]

Defined diblocks, triblock or multiblock copolymers find important applications in the areas of thermoplastic elastomers, data storage technology [126], and as compatibilizers (e.g. in polymer blends). In thin films these polymers may display different morphologies than in the bulk, which necessitates an accurate analysis. [Pg.143]

Nanocomposite technology using small amounts of silicate layers can lead to improved properties of thermoplastic elastomers with or without conventional fillers such as carbon black, talc, etc. Mallick et al. [305] investigated the effect of EPR-g-M A, nanoclay and a combination of the two on phase morphology and the properties of (70/30w/w) nylon 6/EPR blends prepared by the melt-processing technique. They found that the number average domain diameter (Dn) of the dispersed EPR phase in the blend decreased in the presence of EPR-g-MA and clay. This observation indicated that nanoclay could be used as an effective compatibilizer in nylon 6/EPR blend. X-ray diffraction study and TEM analysis of the blend/clay nanocomposites revealed the delaminated clay morphology and preferential location of the exfoliated clay platelets in nylon 6 phase. [Pg.105]

Block polymers and polymer blends deserve now a great intere because of their multiphase character and their related properties. The thermodynamic immiscibility of the polymeric partners gives rise indeed to a phase separation, the extent of which controls the detailed morphology of the solid and ultimately its mechanical behavior. The advent of thermoplastic elastomers and high impact resins (HIPS or ABS type) illustrates the importance of the industrial developments that this type of materials can provide. In selective solvents, and depending on molecular structure, concentration and temperature, block polymers form micelles which influence the rheological behavior and control the morphology of the material. [Pg.244]


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See also in sourсe #XX -- [ Pg.255 , Pg.256 , Pg.257 ]




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