|
| ||
|
|
||
Blend Properties (blend + property)
Selected AbstractsUse of carboxylated nitrile rubber and natural rubber blends as retreading compound for OTR tiresPOLYMER ENGINEERING & SCIENCE, Issue 12 2008Kaushik Pal Ore transportation is one of the important unit operations in a mineral industry. In this study, three raw rubber compounds are prepared in three different blend ratios, and four types of raw rubber samples of pure NR with silica reinforced has been collected from the different tire retreading industries. Blend properties largely depend on the blend ratio and on the blending technique. The improvement in the physical properties such as cure characteristics, mechanical characterization, cross-link density, FTIR, thermal characterization, SEM studies, and dynamic mechanical analysis has been studied in those samples. It has been found that retread rubber made with 80 phr XNBR and 20 phr NR has given the better results when compared with the other samples against all the characterization done. It is also seen that rubber made by the researchers are very good in tough, rigid and these are extremely able to withstand for using as a retread rubber for 35T dump trucks tire when compared with the retread rubber made by the tire retreading industries for different mines in India. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Improving low-density polyethylene/poly(ethylene terephthalate) blends with graft copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008D. E. El-Nashar Abstract Blends of low-density polyethylene (LDPE) and poly(ethylene terephthalate) (PET) were prepared with different weight compositions with a plasticorder at 240°C at a rotor speed of 64 rpm for 10 min. The physicomechanical properties of the prepared blends were investigated with special reference to the effects of the blend ratio. Graft copolymers, that is, LDPE-grafted acrylic acid and LDPE-grafted acrylonitrile, were prepared with ,-irradiation. The copolymers were melt-mixed in various contents (i.e., 3, 5, 7, and 9 phr) with a LDPE/PET blend with a weight ratio of 75/25 and used as compatibilizers. The effect of the compatibilizer contents on the physicomechanical properties and equilibrium swelling of the binary blend was investigated. With an increase in the compatibilizer content up to 7 phr, the blend showed an improvement in the physicomechanical properties and reduced equilibrium swelling in comparison with the uncompatibilized one. The addition of a compatibilizer beyond 7 phr did not improve the blend properties any further. The efficiency of the compatibilizers (7 phr) was also evaluated by studies of the phase morphology (scanning electron microscopy) and thermal properties (differential scanning calorimetry and thermogravimetric analysis). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Blending of NR/BR/EPDM by reactive processing for tire sidewall applications.JOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Abstract Cure incompatibility in NR/BR/EPDM blends is a crucial problem, affecting blend properties. In a previous study, it was demonstrated that the mechanical properties of such blends can be significantly improved by utilizing a reactive processing technique, in which a pretreated EPDM is first prepared by incorporating all compounding ingredients in the EPDM and subsequent preheating, prior to crossblending with premasticated NR/BR. In the present article, the pretreated EPDM-moieties are prepared using two different accelerators, N -cyclohexyl-2-benzothiazole sulfenamide (CBS) and 6-nitro MBTS. The latter was synthesized and applied for the purpose of IR characterization. The infrared (IR) spectra of the pretreated, extracted EPDM demonstrate absorption peaks associated with the IR absorption of the functional groups in the accelerator fragments, attached to the EPDM. NR/BR/EPDM (35/35/30) ternary blends are prepared by reactive mixing of the pretreated EPDM with CBS fragments attached with premasticated NR/BR on a two-roll mill. Their blend morphological features are studied using the atomic force microscopy (AFM) and transmission electron microscopy (TEM) microscopic techniques, in comparison with those of blends prepared by a conventional straight mixing method. Both the tapping mode AFM phase images and TEM micrographs clearly show that reactive mixing leads to more homogeneous blends. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103:2547,2554, 2007 [source] Morphological and fractal studies of polypropylene/poly(ethene-1-octene) blends during melt mixing using scanning electron microscopyPOLYMER INTERNATIONAL, Issue 3 2008Xinhua Xu Abstract BACKGROUND: Polymer blending creates new materials with enhanced mechanical, chemical or optical properties, with the exact properties being determined by the type of morphology and the phase dimension of the blend. In order to control blend properties, morphology development during processing needs to be understood. The formation and evolution of polypropylene/poly(ethylene-1-octene) (PP/POE) blend morphology during blending are qualitatively represented by a series of time-dependent scanning electron microscopy (SEM) patterns. The area diameter and its distribution of dispersed phase domains are discussed in detail. In order to characterize the formation and evolution of phase morphology quantitatively, two fractal dimensions, Ds and Dd, and their corresponding scaling functions are introduced to analyze the SEM patterns. RESULTS: The evolution of the area diameter indicates that the major reduction in phase domain size occurs during the initial stage of melt mixing, and the domain sizes show an increasing trend due to coalescence with increasing mixing times. The distribution in dispersed phase dimension obeys a log-normal distribution, and the two fractal dimensions are effective to describe the phase morphology: Ds for dispersed phase dimension and Dd for the distribution in it. CONCLUSIONS: The fractal dimensions Ds and Dd can be used quantitatively to characterize the evolutional self-similarity of phase morphology and the competition of breakup and coalescence of dispersed phase domains. It is shown that the fractal dimensions and scaling laws are useful to describe the phase morphology development at various mixing times to a certain extent. Copyright © 2007 Society of Chemical Industry [source] Thermally crosslinked polymer blends of polyurethane and chlorobutyl elastomers (sulfur cure)POLYMER INTERNATIONAL, Issue 5 2001B Khatua Abstract Blends of polyurethane with chlorobutyl elastomer prepared by three different blending techniques have been studied in the entire composition range. The properties of the blends showed that the blending technique plays an important role in determining the blend properties. IR spectral analysis revealed that interchain crosslinking is possible in this blend system upon heat treatment. Thermal stability of blends prepared by preheating the preblend was increased and the degradation process was retarded. Extractability of the single phase, by solvent, was also limited significantly in the case of the preheated preblended sample, probably due to phase adhesion. © 2001 Society of Chemical Industry [source] Effect of EPDM on Morphology, Mechanical Properties, Crystallization Behavior and Viscoelastic Properties of iPP+HDPE BlendsMACROMOLECULAR SYMPOSIA, Issue 1 2007Nina Vranjes Abstract Summary: Blends of isotactic polypropylene (iPP) and high density polyethylene (HDPE) with and without ethylene-propylene-diene (EPDM) terpolymer as compatibilizer were systematically investigated to determine the influence of the EPDM on blends properties. The morphology was studied by Scanning Electron Microscopy (SEM). Mechanical properties of investigated systems: tensile strength at break, elongation at break, yield stress and Izod impact strength were determined. Crystallization behavior was determined by Differential Scanning Calorimetry (DSC). Dynamic Mechanical Analysis (DMA) was used to determined the storage modulus (E,), loss modulus (E,), and loss tangent (tan ,). The PP+HDPE blend revealed poor adhesion between PP and HDPE phases. Finer morphology was obtained by EPDM addition in PP+HDPE blends and better interfacial adhesion. Addition of HDPE to PP decreased tensile strength at break, elongation and yield stress. Decrease of tensile strength and yield stress is faster with EPDM addition in PP+HDPE blends. Elongation at break and impact strength was significantly increased with EPDM addition. The addition of EPDM in PP+HDPE blends did not significantly change melting points of PP phase, while melting points of HDPE phase was slightly decreased in PP+HDPE+EPDM blends. The EPDM addition increased the percentage of crystallization (Xc) of PP in PP+HDPE blends. The increase of Xc of HDPE was found in the blend with HDPE as matrix. Dynamical mechanical analysis showed glass transitions of PP and HDPE phase, as well as the relaxation transitions of their crystalline phase. By addition of EPDM glass transitions (Tg) of HDPE and PP phases in PP+HDPE blends decreased. Storage modulus (E,) vs. temperatures (T) curves are in the region between E,/T curves of neat PP and HDPE. The decrease of E, values at 25,°C with EPDM addition in PP+HDPE blends is more pronounced. [source] | ||||||||||