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Ternary Blends (ternary + blend)
Selected AbstractsAn experimental study of morphology and rheology of ternary Pglass-PS-LDPE hybridsPOLYMER ENGINEERING & SCIENCE, Issue 6 2003Peter C. Guschl Ternary blends of low-density polyethylene (LDPE), polystyrene (PS), and a low Tg tin-based phosphate glass (Pglass) were prepared at compositions ranging from 0,50 vol% Pglass in which either LDPE or PS was the continuous matrix phase. Differential scanning calorimetry was used to investigate the phase behavior of the pure components, PS-LDPE blends and binary Pglass-polymer hybrids. Interesting steady-shear and transient rheology was observed for the hybrids. In particular, the steady shear viscosity curves for the hybrids of ,Pglass , 30% exhibited unusual, four-region flow behavior, similar to that of liquid crystalline polymers. Two Newtonian plateaus at low ( , 0.1 s,1) and moderate (0.4 , , s,1) shear rates connected by two distinct shear-thinning regimes were apparent. This observed rheology is ascribed to a unique composite morphology of these multi-component systems. Rheological data on the binary Pglass-polymer systems suggest that the presence of the Pglass within both PS and LDSE contributes significantly to this unusual behavior, perhaps because of the interfacial behavior between the phases. Micrographs obtained via scanning electron microscopy reveal preferential placement of the Pglass phase dispersed within the PS-phase and surrounding the LDPE phase. Optical shearing data confirmed the evolution of this microstructure under specific shear conditions. [source] Synergistic sex pheromone components of the grey-spotted tussock moth, Orgyia ericaeENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 3 2010Guo-Fa Chen Abstract The grey-spotted tussock moth, Orgyia ericae Germar (Lepidoptera: Lymantriidae), is an important pest of deciduous trees and woody scrublands in northern China. In a field trapping experiment conducted during the flight of the first generation of 2009, synthetic (Z)-6-heneicosen-11-one, a common Orgyia spp. sex pheromone component, attracted O. ericae males. Gas chromatography-mass spectrometry analyses (full scan or selected ion-monitoring mode) of pheromone gland extracts from females revealed the presence of a major, a minor, and a trace component, i.e., (6Z,9Z)-heneicosa-6,9-diene, (6Z,9Z)-tricosa-6,9-diene, and (Z)-6-heneicosen-11-one, respectively. Field experiments during the flight of the second generation showed that (6Z,9Z)-tricosa-6,9-diene, the minor component, was inactive alone or in any combination with the other two components, whereas (6Z,9Z)-heneicosa-6,9-diene and (Z)-6-heneicosen-11-one were weakly attractive when tested individually. However, traps baited with a binary blend of (6Z,9Z)-heneicosa-6,9-diene and (Z)-6-heneicosen-11-one caught seven-fold more moths than any other treatment (except the ternary blend), indicating a strong synergistic interaction between the two components. The analytical and field trapping data suggested that (6Z,9Z)-heneicosa-6,9-diene and (Z)-6-heneicosen-11-one are likely the key sex pheromone components of female O. ericae. This synergistic blend will be useful as an efficient monitoring tool, and possible control tool, to combat this economically and ecologically important forest defoliator. [source] Flame-retardant action of red phosphorus/magnesium oxide and red phosphorus/iron oxide compositions in recycled PETFIRE AND MATERIALS, Issue 5 2006F. Laoutid Abstract Red phosphorus was combined with metallic oxides Fe2O3 and MgO to improve the fire properties of recycled PET. Both Fe2O3 and MgO act as co-synergist agents at a total loading of 5 wt%. The analysis by diffraction X of the char formed during combustion shows that transformation of Fe2O3 to Fe3O4 occurs. Fe2O3 favours the oxidation and improves the effectiveness of red phosphorus. It is suggested that MgO interacts with acidic end groups of PET and forms a thermal stable residue. The thermal decomposition of recycled PET containing red phosphorus combined with Fe and Mg oxides was studied by thermal analysis and leads to an increase in char formation. While the incorporation of Fe2O3 in this ternary blend maintains the mechanical properties of PET, the reactivity of MgO leads to a brittle material. The use of reinforcements (talc and glass fibres) to mechanically stabilize the char formed during combustion of ternary blend with Fe2O3 entails a further decrease in heat release rate, nevertheless impact resistance of the material decreases dramatically. Copyright © 2005 John Wiley & Sons, Ltd. [source] Near IR Sensitization of Organic Bulk Heterojunction Solar Cells: Towards Optimization of the Spectral Response of Organic Solar CellsADVANCED FUNCTIONAL MATERIALS, Issue 2 2010Markus Koppe Abstract The spectroscopic response of a poly(3-hexylthiophene)/[6,6]-phenyl-C61 -butyric acid methyl ester (P3HT/PCBM)-based bulk heterojunction solar cell is extended into the near infrared region (NIR) of the spectrum by adding the low bandgap polymer poly[2,6-(4,4-bis-(2-ethylhexyl)-4H -cyclopenta[2,1- b;3,4- b´]-dithiophene)- alt -4,7-(2,1,3-benzothiadiazole)] [PCPDTBT] to the blend. The dominant mechanism behind the enhanced photosensitivity of the ternary blend is found to be a two-step process: first, an ultrafast and efficient photoinduced charge transfer generates positive charges on P3HT and PCPDTBT and a negative charge on PCBM. In a second step, the positive charge on PCPDTBT is transferred to P3HT. Thus, P3HT serves two purposes. On the one hand it is involved in the generation of charge carriers by the photoinduced electron transfer to PCBM, and, on the other hand, it forms the charge transport matrix for the positive carriers transferred from PCPDTBT. Other mechanisms, such as energy transfer or photoinduced charge transfer directly between the two polymers, are found to be absent or negligible. [source] Influence of processing conditions and physicochemical interactions on morphology and fracture behavior of a clay/thermoplastic/thermosetting ternary blendJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010M. Hernandez Abstract This study provides information on the mechanical behavior of epoxy-poly(methyl methacrylate) (PMMA)-clay ternary composites, which have been prepared using the phase separation phenomenon of PMMA and the introduction of organophilic-modified montmorillonites (MMTs), the continuous matrix being the epoxy network. Two dispersion processing methods are used: a melt processing without any solvent and an ultrasonic technique with solvent and a high-speed stirrer. TEM analysis shows that phase separation between PMMA and the epoxy network was obtained in the shape of spherical nodules in the presence of the clay in both process methods used. Nanoclay particles were finely dispersed inside thermosetting matrix predominantly delaminated when ultrasonic blending was used; whereas micrometer-sized aggregates were formed when melt blending was used. The mechanical behavior of the ternary nanocomposites was characterized using three-point bending test, dynamic mechanical analysis (DMA), and linear elastic fracture mechanics. The corresponding fracture surfaces were examined by scanning electron microscopy to identify the relevant fracture mechanisms involved. It was evidenced that the better dispersion does not give the highest toughness because ternary nanocomposites obtained by melt blending present the highest fracture parameters (KIc). Some remaining disordered clay tactoids seem necessary to promote some specific toughening mechanisms. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] The totally miscible in ternary hydrogen-bonded polymer blend of poly(vinyl phenol)/phenoxy/phenolicJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2009Shiao-Wei KuoArticle first published online: 28 MAY 200 Abstract The individual binary polymer blends of phenolic/phenoxy, phenolic/poly(vinyl phenol) (PVPh), and phenoxy/PVPh have specific interaction through intermolecular hydrogen bonding of hydroxyl,hydroxyl group to form homogeneous miscible phase. In addition, the miscibility and hydrogen bonding behaviors of ternary hydrogen bond blends of phenolic/phenoxy/PVPh were investigated by using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy, and optical microscopy. According to the DSC analysis, every composition of the ternary blend shows single glass transition temperature (Tg), indicating that this ternary hydrogen-bonded blend is totally miscible. The interassociation equilibrium constant between each binary blend was calculated from the appropriate model compounds. The interassociation equilibrium constant (KA) of each individually binary blend is higher than any self-association equilibrium constant (KB), resulting in the hydroxyl group tending to form interassociation hydrogen bond. Photographs of optical microscopy show this ternary blend possess lower critical solution temperature (LCST) phase diagram. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Compatibilization of Polyamide-6/Polyarylate Blends by Means of an IonomerMACROMOLECULAR MATERIALS & ENGINEERING, Issue 8 2005Aritz Retolaza Abstract Summary: Polyamide-6 (PA6)/polyarylate of bisphenol A (PAr) blends rich in PA6 and modified with an additional 15% poly[ethylene- co -(methacrylic acid)] partially neutralized with zinc (PEMA-Zn) as a compatibilizer were obtained by melt mixing. Their phase structure, morphology, and mechanical performance were compared with those of the corresponding binary blends. The ternary blends were composed of a PA6 amorphous matrix and a dispersed PAr-rich phase in which reacted PA6 and PEMA-Zn were present. Additionally, minor amounts of a crystalline PA6 phase, and a PEMA-Zn phase were also present. The chemical reactions observed led to a clear decrease in the dispersed particle size when PEMA-Zn was added, indicating compatibilization. Consequently, the mechanical behavior of the blends with PEMA-Zn improved, leading, mainly in the case of the blend with 10% PAr, to significant increases in both ductility and impact strength with respect to those of the binary blends. These increases were more remarkable than the slight decrease in stiffness as a consequence of the rubbery nature of the compatibilizer. Cryogenically fractured surface of the PA6/PAr-PEMA-Zn 70/30-15 ternary blend. [source] Ternary miscibility in blends of three polymers with balanced binary interactionsPOLYMER ENGINEERING & SCIENCE, Issue 3 2003E. M. Woo This study demonstrates and discusses ternary miscibility in a three-polymer blend system based on balanced binary interactions. A truly miscible ternary blend comprising poly(,-caprolactone) (PCL), poly(benzyl methacrylate) (PBzMA), and poly(vinyl methyl ether) (PVME), was discovered and reported. Miscibility with phase homogeneity (excluding the PCL crystalline domain) in a wide composition range has been demonstrated using criteria of thermal transition behavior, cloud point, and microscopy characterization. At ambient temperature, the three-polymer ternary system is completely miscible within the entire composition range (i.e., no immiscibility loop). However, at slightly elevated temperatures above the ambient. phase separation readily occurred in this originally miscible ternary blend. A quite low "lower critical solution temperature" (LCST) near 75°C was found for the ternary blend, which is much lower than any of those for the binary pairs. Balanced interactions with no offsetting ,, among the three binary pairs were a key factor leading to a ternary miscible system. [source] A lithium ionomer of poly(ethylene-co-methacrylic acid) copolymer as compatibilizer for blends of poly(ethylene terephthalate) and high density polyethylenePOLYMER ENGINEERING & SCIENCE, Issue 11 2002A. Retolaza Blends of 75/25 poly(ethylene terephthalate) (PET)/high density polyethylene (HDPE) containing poly(ethylene-co-methacrylic acid) partially neutralized with lithium (PEMA-Li) were obtained by direct injection molding in an attempt (i) to ameliorate the poor performance of the binary blend and (ii) to find the best compatibilizer content. The presence of PEMA-Li caused a nucleation effect on PET, and a decrease in the crystalline content of HDPE. The compatibilizing effect of PEMA-Li was due to the combined effects of interaction at the interface and chemical reactions. The ternary blends showed a complex morphology, with two dispersed HDPE and PEMA-Li phases that contained a small internal dispersed phase, probably of PET. The compatibilizing effect of PEMA-Li was clearly shown by means of an impressive increase in the ductility and to a minor extent in the impact strength. The highest property improvement (ductility increase 1450%) appeared upon the addition of 45% PEMA-Li with respect to the HDPE phase, but taking into account the recycling interest, the ternary blend with the addition of roughly 22.5% PEMA-Li appears to be the most attractive. [source] Toughening of recycled polystyrene used for TV backsetJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Xiaoting Fu Abstract The recycled polystyrene (rPS) was toughened with ethylene-octylene copolymer thermoplastic elastomer (POE) and high-density polyethylene (HDPE) with various melt flow index (MFI), compatibilized by styrene-butadiene-styrene copolymer (SBS) to enhance the toughness of rPS for use as TV backset. The rPS/POE binary blends exhibited an increased impact strength with 5,10 wt % POE content followed by a decrease with the POE content up to 20 wt %, which could be due to poor compatibility between POE and rPS. For rPS/POE/SBS ternary blends with 20 wt % of POE content, the impact strength increased dramatically and a sharp brittle-ductile transition was observed as the SBS content was around 3,5 wt %. Rheological study indicated a possible formation of network structure by adding of SBS, which could be a new mechanism for rPS toughening. In rPS/POE/HDPE/SBS (70/20/5/5) quaternary blends, a fibril-like structure was observed as the molecular weight of HDPE was higher (with lower MFI). The presence of HDPE fibers in the blends could not enhance the network structure, but could stop the crack propagation during fracture process, resulting in a further increase of the toughness. The prepared quaternary blend showed an impact strength of 9.3 kJ/m2 and a tensile strength of 25 MPa, which can be well used for TV backset to substitute HIPS because this system is economical and environmental friendly. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Increasing recyclability of PC, ABS and PMMA: Morphology and fracture behavior of binary and ternary blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Jan Rybnicek Abstract Binary and ternary blends of PC, ABS, and PMMA were studied. The blends were produced from original and recycled materials by melt mixing in a wide range of compositions. Instrumented Charpy impact testing, tensile testing, rheology investigations, and electron microscopy were carried out to determine the relationship between the deformation and fracture behavior, blend composition, morphology, and processing parameters. Resistance against unstable crack propagation was evaluated using the concepts of J -integral and crack-tip-opening displacement (CTOD). The transition from ductile elastic-plastic to brittle-linear elastic fracture behavior was observed in the case of PC/ABS/PMMA blend at 10% of PMMA. Reprocessing had only a slight influence on the deformation and fracture behavior of the recycled blends. The blends produced from recycled materials proved to be competitive with the original pure materials. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Structures and properties of ternary blends of recycled poly(ethylene terephthalate)/bisphenol-A polycarbonate/(E/nBA/GMA)JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Yong Peng Abstract Recycled poly(ethylene terephthalate)/bisphenol-A polycarbonate/PTW (ethylene, butylacrylate (BA), and glycidylmethacrylate (E/nBA/GMA) terpolymer) were blended in different sequence through low temperature solid state extrusion (LTSSE) was studied. R-PET/PC blends were toughened by PTW, resulting in the improvement of impact strengths. In tensile test, the (PC/PTW)/r-PET blends made by mixing r-PET with the preblend of PC/PTW had noticeable strengthening effect on its tensile properties, which was not impaired by the rubber content due to its strain-hardening occurred following its necking at the constant load. Morphological study by scanning electron microscopy (SEM) was in conformity with the mechanical result. For the (PC/PTW)/r-PET blends, the PC particles were well embedded in the PET matrix and the smooth morphology exhibited. The DSC thermographs for heating and cooling run indicated that the crystallinity of PET rich phase was affected by different blending sequence. In the FTIR test, the different absorption intensity of PC aromatic carbonate carbonyl band was clearly illustrated. The results indicated different blending sequence led to different blending effect. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Dynamic mechanical properties and morphology of high-density polyethylene/CaCO3 blends with and without an impact modifierJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Yu-Lin Yang Abstract Dynamic mechanical analysis and differential scanning calorimetry were used to investigate the relaxations and crystallization of high-density polyethylene (HDPE) reinforced with calcium carbonate (CaCO3) particles and an elastomer. Five series of blends were designed and manufactured, including one series of binary blends composed of HDPE and amino acid treated CaCO3 and four series of ternary blends composed of HDPE, treated or untreated CaCO3, and a polyolefin elastomer [poly(ethylene- co -octene) (POE)] grafted with maleic anhydride. The analysis of the tan , diagrams indicated that the ternary blends exhibited phase separation. The modulus increased significantly with the CaCO3 content, and the glass-transition temperature of POE was the leading parameter that controlled the mechanical properties of the ternary blends. The dynamic mechanical properties and crystallization of the blends were controlled by the synergistic effect of CaCO3 and maleic anhydride grafted POE, which was favored by the core,shell structure of the inclusions. The treatment of the CaCO3 filler had little influence on the mechanical properties and morphology. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3907,3914, 2007 [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] Evaluation of the Effectiveness of New Compatibilizers Based on EBAGMA-LDPE and EBAGMA-PET Masterbatches for LDPE/PET BlendsMACROMOLECULAR MATERIALS & ENGINEERING, Issue 3 2010Aida Benhamida Abstract The present paper is aimed to evaluate the efficiency of two masterbatches, i.e., EBAGMA/LDPE (MB1) and EBAGMA/PET (MB2) with 50/50 w/w composition, prepared by melt mixing and used as new compatibilizers for blends of LDPE/PET. The morphology, the mechanical and the thermal properties of LDPE/PET/MB1 and LDPE/PET/MB2 ternary blends have been investigated. Morphological investigation by SEM of LDPE/PET/MB1 ternary blends showed a finer dispersion of PET in LDPE matrix with a better interfacial adhesion compared to those of both LDPE/PET/MB2 and binary LDPE/PET blends. The results also indicated a substantial improvement in both elongation at break and impact strength, while the Young's modulus decreased. Moreover, the thermal properties showed a decrease of the crystallization phenomena of PET in LDPE/PET/MB1 blend, thus confirming the good dispersion of PET particles into the continuous phase of LDPE matrix, leading to the conclusion that MB1 could be an efficient compatibilizer for LDPE/PET system. [source] The effect of interface characteristics on the static and dynamic mechanical properties of three-component polymer alloysPOLYMER COMPOSITES, Issue 3 2002I. Fisher The effect of interfacial characteristics on the structure-property relationships of ternary polymer alloys and blends comprising polypropylene (PP), ethylene-vinyl alcohol copolymer (EVOH) and glass beads (GB) or fibers (GF) was investigated. The systems studied were based on a binary PP/EVOH immiscible blend, representing a blend of a semi-crystalline apolar polymer with a semi-crystalline highly polar copolymer. The ternary systems studied consisted of filler particles encapsulated by EVOH, with some of the minor EVOH component separately dispersed within the PP matrix. Modification of the interfacial properties was done using silane coupling agents for the EVOH/glass interface and compatibilization using a maleic anhydride grafted PP (MA-g-PP) for the PP/EVOH interface. Both glass fillers increased the dynamic modulus and decreased the damping of the neat polymers and of their binary blends, especially in the rubbery region. GF has a more profound effect on both the modulus and the damping. Glass surface treatments and compatibilization have only a marginal effect on the dynamic mechanical behavior of the ternary blends. Yet, compatibilization shifted the polymers' TgS to higher temperatures. Both glass fillers increased the elastic modulus of the binary blends, where GF performed better than GB as a reinforcing agent. GF slightly increased the strength of the binary blends while, GB reduced it. Both fillers reduced the ductility of the binary blends. The blends' mechanical properties were related to the morphology and their components' crystallinity. The compatibilizer increases both stiffness and strength and reduces deformability. [source] Compatibilization of PP/PAE blends by means of the addition of an ionomerPOLYMER ENGINEERING & SCIENCE, Issue 8 2010A. Granado Minor amounts of poly(ethylene- co -methacrylic acid) ionomer neutralized with Zn (PEMA-Zn) were added in the melt state to blends of polypropylene (PP) with up to 40% of poly(amino ether) (PAE) resin. Given the good barrier characteristics of PAE, it is a good candidate to improve the poor barrier properties of PP. However, PP/PAE blends were found to be almost fully immiscible, with a large dispersed phase size and a brittle mechanical behavior. Upon PEMA-Zn addition, the dispersed particle size clearly decreased from diameters of several microns to diameters mostly below 0.5 ,m, indicating that compatibilization occurred. This compatibilization was due to the presence of PEMA-Zn in the two phases of the blends and was additionally proven by the large decrease observed in the interfacial tension. Further, the fine morphology led to an enhancement in the unnotched impact strength of the ternary blends and of their ductile behavior (elongation at break 30- to 40-fold that of the corresponding binary blends). POLYM. ENG. SCI., 50:1512,1519, 2010. © 2010 Society of Plastics Engineers [source] Effect of an epoxy octasilsesquioxane on the thermodegradation of an epoxy/amine systemPOLYMER INTERNATIONAL, Issue 1 2010Belén Montero Abstract Polyhedral oligomeric silsesquioxanes (POSS®) can be added to thermoplastic and thermostable polymers to obtain hybrid materials with only a minor tendency to suffer ignition. The aim of the work reported was to analyse the influence of an octafunctional POSS® in the pyrolysis of an epoxy/amine system as well as during the combustion process. Thermal degradation of the modified materials, with respect to the unmodified ones, was analysed using thermogravimetric analysis. As the content of POSS® increased the stability improved and the char/ceramic yields were higher. The Kissinger,Akahira,Sunose method was applied to the modified blends and it showed a decrease in the activation energy with POSS® content. Empirical kinetic models, as well as generalized master plots, were applied to explain the degradation mechanism for ternary blends. The limiting oxygen index parameter was measured to analyse the fire retardancy effect of POSS®: it increased from 24.3 to 25.4% with the addition of 2.5 wt% of POSS®. The mechanism of thermal degradation of the hybrid materials based on an epoxy resin is affected by the presence of the octaepoxy POSS®. Only small amounts of POSS® are necessary to enhance the combustion resistance of the system. Copyright © 2009 Society of Chemical Industry [source] On the linear correlation between microhardness and mechanical properties in polar polymers and blendsPOLYMER INTERNATIONAL, Issue 8 2003E Giménez Abstract The tensile elastic modulus (E), yield stress (,Y) and microhardness (MH) of neat and binary and ternary blends of glassy semicrystalline ethylene,vinyl alcohol copolymer (EVOH), a glassy amorphous polyamide and a semicrystalline nylon-containing ionomer covering a broad range of properties were examined. The tests were carried out on dry and water-equilibrated samples to produce stiffer and softer materials, respectively. From the results, more accurate linear correlations were found to describe adequately the microhardness, modulus and yield stress of these strongly self-associated polymers through hydrogen bonding. Copyright © 2003 Society of Chemical Industry [source] Morphology and properties of ternary polyamide 6/polyamide 66/elastomer blendsPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 1 2003D. Tomova Abstract The aim of the work presented is to evaluate the mechanisms and phase interactions in ternary blends based on different polyamides and functionalised elastomers, and to establish a correlation between the morphology controlled by the specific binary interactions, and physical and technological properties, respectively. The properties of the ternary system polyamide 6/polyamide 66/ elastomer depend on the specific blend morphology which is determined mainly by the differences of the surface tension of the components. A phase-in-phase structure was observed by microscopic study (AFM) in the ternary polyamide 6/polyamide 66/elastomer blends with maleic anhydride grafted ethene-octene copolymer, and a "quasi" phase-in-phase structure in blends with maleic anhydride grafted ethene-propene-diene copolymer as the elastomer phase. An incorporation of polyamide inside of the elastomer particles was observed in the first case due to the difunctionality of polyamide 66. This type of morphology causes an increased elongation at break and toughness of these blends. In comparison to the binary polyamide based blends the ternary blends show an increased elastic modulus, elongation at break and yield stress as well as a high impact strength at low temperatures up to ,20,°C. Copyright © 2003 John Wiley & Sons, Ltd. [source] | |||||||||||||