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Immiscible Polymer Blends (immiscible + polymer_blend)
Selected AbstractsEffect of Organic Modification on the Compatibilization Efficiency of Clay in an Immiscible Polymer BlendMACROMOLECULAR RAPID COMMUNICATIONS, Issue 20 2005Suprakas Sinha Ray Abstract Summary: This communication describes the effect of organic modifier miscibility with the matrices, and the effect of the initial interlayer spacing of the organoclay, on the overall morphology and properties of an immiscible polycarbonate/poly(methyl methacrylate) blend. By varying the organic-modifier-specific interactions with the blend matrices at the same time as changing the initial interlayer spacing of the organoclay, different levels of compatibilization were revealed. The evidence for the interfacial compatibilization of the organoclay was assessed by scanning electron microscopy observations and was supported by differential scanning calorimetry analyses. The effect on the level of clay exfoliation was also examined. Differential scanning calorimetry scans of virgin, montmorillonite, and various organically modified montmorillonite-compatibilized 40PC/60PMMA blends [source] Morphology in Immiscible Polymer Blends During Solidification of an Amorphous Dispersed Phase under ShearingTHE CANADIAN JOURNAL OF CHEMICAL ENGINEERING, Issue 6 2002Yves Deyrail Abstract Solidification under shear of dispersed polycarbonate (PC) fibers in copolymer polyethylene-methyl acrylate matrix (EMA) was investigated using a hot optical shear device. First, the deformation of PC droplets and its modeling under isothermal conditions were studied for comprehension purposes. Overall agreement with literature models was found and the main influence of the viscosity ratio has been stressed. Second, the morphology control through dynamic quenching was experimented. It consists of solidifying the amorphous PC dispersed phase under shear flow. Break-up times of PC fibers were taken into account. Shear rate and quenching-time balance was demonstrated. Thus, during dynamic solidification, a fibrillar morphology could be obtained through rapid quenching. Long quenching times allow nodular morphology, whose size depends on the shear rate used. PC rods can be obtained by adjusting the shear rate during dynamic quenching. La solidification sous cisaillement du polycarbonate (PC) dispersé dans une matrice copolymère éthylène-acétate de vinyle (EMA) a été suivie à l'aide d'un microscope et d'une platine de cisaillement chauffante. Dans un premier temps la déformation isotherme de billes de PC pour différentes températures a été étudiée, ainsi que sa modélisation. Une bonne corrélation avec les modèles issus de la littérature a été obtenue. L'importance du rapport des viscosités a été ainsi soulignée. Dans un second temps le contrôle de la morphologie par le procédé de « refroidissement dynamique » a été expérimenté. Celui-ci consiste à solidifier le PC sous cisaillement pendant le refroidissement. Les temps de rupture des fibres de PC ont été considérés et l'importance du couple gradient de cisaillement-temps de refroidissement sur le contrôle de la morphologie a été mis en évidence. Pendant la solidification, un refroidissement rapide permet d'obtenir une morphologie fibrillaire. [source] Formation of a fibrillar morphology of crosslinked epoxy in a polystyrene continuous phase by reactive extrusionPOLYMER ENGINEERING & SCIENCE, Issue 4 2004Françoise Fenouillot An immiscible polymer blend where the dispersed phase is fibrillar was prepared by in situ crosslinking of the minor phase. A model polystyrene/epoxy-amine blend was selected on the basis of rheological (achievement of the fibrillar structure) and reactivity (fast crosslinking) criteria. The system was a polystyrene/diglycidyl ether of bisphenol A (DGEBA)-aminoethyl piperazine (AEP) blend. At the temperature of extrusion, 180°C, the DGEBA is immiscible in PS and heterogeneous material is obtained. The elongational flow imposed by drawing the extrudate at the die exit permitted controlled generation of a fibrillar morphology of the dispersed epoxy phase, with a fiber diameter of 1 ,m and an aspect ratio greater than 100. It was shown that when the amine comonomer was injected into the extruder, its reactivity with DGEBA at high temperature was high enough to ensure partial crosslinking of the epoxy. The fibrils were formed even though the gel point of the epoxy phase was exceeded. However, above a certain critical insoluble fraction that we estimated to be between 45% and 70%, a coarsening of the structure appeared, caused by the decreasing deformability of the domains and their coalescence. Finally, for our system, the crosslinking of the dispersed phase up to 90% of insoluble fraction did not totally stabilize the morphology after the second processing step (injection molding). Polym. Eng. Sci. 44:625,637, 2004. © 2004 Society of Plastics Engineers. [source] Reactively and physically compatibilized immiscible polymer blends: stability of the copolymer at the interfaceMACROMOLECULAR SYMPOSIA, Issue 1 2003Charef Harrats Abstract This paper reports on the interfacial behaviour of block and graft copolymers used as compatibilizers in immiscible polymer blends. A limited residence time of the copolymer at the interface has been shown in both reactive blending and blend compatibilization by preformed copolymers. Polystyrene (PS)/polyamide6 (PA6), polyphenylene oxide (PPO)/PA6 and polymethylmethacrylate (PMMA)/PA6 blends have been reactively compatibilized by a styrene-maleic anhydride copolymer SMA. The extent of miscibility of SMA with PS, PPO and PMMA is a key criterion for the stability of the graft copolymer at the interface. For the first 10 to 15 minutes of mixing, the in situ formed copolymer is able to decrease the particle size of the dispersed phase and to prevent it from coalescencing. However, upon increasing mixing time, the copolymer leaves the interface which results in phase coalescence. In PS/LDPE blends compatibilized by preformed PS/hydrogenated polybutadiene (hPB) block copolymers, a tapered diblock stabilizes efficiently a co-continuous two-phase morphology, in contrast to a triblock copolymer that was unable to prevent phase coarsening during annealing at 180°C for 150 minutes. [source] Nonuniformity of phase structure in immiscible polymer blendsPOLYMER ENGINEERING & SCIENCE, Issue 3 2008Ivan Fortelný This article is focused on the phase structure development in immiscible polymer blends during melt mixing. Nonuniformity of the phase structure, i.e., the coexistence of areas containing particles with markedly different size distribution, was detected in quenched and compression molded samples of a number of various blends prepared by long and intensive mixing in the chamber of a Plasticorder. The same effect was found also for polystyrene/polyamide blends prepared in a twin-screw extruder. It was shown that neglecting nonuniformity of the phase structure can lead to considerable error in evaluation of the effect of system parameters on the blend morphology. The reasons for the effect were discussed and it was found that inhomogeneous flow field in mixers is a plausible explanation of the nonuniform phase structure. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Production of electrically conductive networks in immiscible polymer blends by chaotic mixingPOLYMER ENGINEERING & SCIENCE, Issue 1 2006Dhawal P. Dharaiya A minor polymer was deformed into lamellar and fibrillar morphological forms in a chaotic mixer, which rendered the resultant immiscible blend electrically conductive along the flow direction. This was demonstrated using a blend consisting of 10 wt% polypropylene (PP), polyamide 6 (PA6), and 1 wt% conductive carbon black (CB) particles. It was found that PP-phase containing CB particles deformed into lamellar and fibrillar morphological forms produced continuous networks in the flow direction, and provided conductivity by double percolation. Breakup of PP fibrils into droplets destroyed the continuous conductive networks, although conductivity was sustained purportedly due to migration of CB particles from the bulk to the surface of closely spaced PP droplets. This was augmented by the formation of much smaller PP droplets in the presence of CB particles. On continued mixing, the blend eventually turned into insulator as CB particles migrated from the polymer,polymer interfaces to PA6 phase. POLYM. ENG. SCI., 46:19,28, 2006. © 2005 Society of Plastics Engineers [source] Effect of marangoni stresses on the deformation and coalescence in compatibilized immiscible polymer blendsPOLYMER ENGINEERING & SCIENCE, Issue 10 2002Peter Van Puyvelde The effect of physical compatibilization on the deformation and coalescence of droplets in immiscible polymer blends is discussed. Evidence is provided for the existence of concentration gradients in block copolymers along the interface during deformation. This causes complex changes in droplet shapes during deformation and relaxation. These concentration gradients also result in Marangoni stresses, which stabilize the droplets against deformation and breakup. Coalescence experiments have been performed, varying both the compatibilizer concentration and the shear rate. Existing coalescence models have been evaluated. An empirical extension of Chesters' partially mobile interface model is presented, that treats the effects of Marangoni stresses on the coalescence process as a higher effective viscosity ratio. [source] | ||||||||||