Home About us Contact
|
Home About us Contact | ||
|
|
||
Immiscible Blends (immiscible + blend)
Selected AbstractsThe 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] A comparative study of dispersing a polyamide 6 into a polypropylene melt in a Buss Kneader, continuous mixer, and modular intermeshing corotating and counter-rotating twin screw extrudersPOLYMER ENGINEERING & SCIENCE, Issue 4 2008Keungjin Shon We have made a study of the development of phase morphology of an immiscible blend(75/25)(polypropylene,polyamide-6) for different types of continuous mixers including (i) Buss Kneader, (ii and iii) modular intermeshing corotating and counter-rotating twin screw extruders, and (iv) NEX-T Kobelco Continuous Mixer. Comparisons are made using different screw configurations for each machine. Generally, in comparison of the different machines, the intermeshing counter-rotating twin screw extruder produced the finest dispersed morphology. Using a droplet breakup kinetic model, we interpreted the blend dispersed phase droplet breakdown rate and coalescence rate. In comparison with our earlier study of the continuous mixing of agglomerates of CaCO3 particles the polymer droplet breakup rate was smaller than that of the particle agglomerates and the coalescence rates of droplets were many times greater than the particle reagglomerates rates. 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] Mixing immiscible blends in an intermeshing counter-rotating twin screw extruderADVANCES IN POLYMER TECHNOLOGY, Issue 2 2006Ramesh Potluri Abstract Domain size of 10% dispersed polystyrene in polyethylene was followed in a 34-mm intermeshing counter-rotating twin screw extruder. Variables studied included the effects of barrel temperature, screw speed, viscosity ratio of dispersed-to-continuous phase, and parallel melt versus preblended solids feeds. After steady state was achieved, die samples were quenched for later photomicrographing. The extruder was then stopped and quenched, with subsequent pulling of the screws. From 7 to 12 additional samples were taken along the 18/1 L/D extruder for determination of the mechanism of dispersion and dispersed phase domain size by optical microscopy. At low temperatures, the polystyrene tended to fracture with sharp edges. The fine particles formed in the initial breakup underwent no further size reduction. At higher temperatures, fractured segments had rounder edges, but the size of the small domains remained constant throughout the axial length. There was some evidence of flocculation and coalescence prior to exit through the die. © 2006 Wiley Periodicals, Inc. Adv Polym Techn 25: 81,89, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20065 [source] Dynamic rheological and morphological study of the compatibility of thermoplastic polyurethane/ethylene,octene copolymer blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Jin Yang Abstract Two grafted ethylene,octene copolymers [POEs; i.e., POE-g-maleic anhydried (MAH) and aminated POE (denoted by POE-g-NH2) were used as compatibilizers in immiscible blends of thermoplastic polyurethane (TPU) and POE. The effects of the compatibilizers on the dynamic rheological properties and morphologies of the TPU/POE blends were investigated. The characteristic rheological behaviors of the blends indicated that the strong interactions between the two phases were due to the compatibilization. Microstructural observation confirmed that the compatibilizers were located at the interface in the blends and formed a stable interfacial layer and smaller dispersed phase particle size. Compared with POE- g -MAH, POE- g -NH2 exhibited a better compatibilization effect in the TPU/POE blends. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Morphology and electrical properties of carbon black filled LLDPE/EMA compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Ping Zhou Abstract The morphology and electrical properties of linear low density polyethylene (LLDPE)/poly (ethylene-methyl arylate) (EMA) blends filled with carbon black (CB) are investigated in this work. Comparing to LLDPE/CB composite, the higher percolation threshold of EMA/CB composite is attributed to the good interaction between EMA and CB. However, carbon black is found to locate preferentially in the LLDPE phase of LLDPE/EMA immiscible blends from the characterization of SEM and electrical properties, which greatly decreases the percolation threshold of the composites. The viscosity of the two polymers is the key factor to determine the distribution of CB instead of interfacial energy in this system. This suggests a method to control the distribution of CB in the immiscible blends by choosing the viscosity ratio of polymer blend. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 487,492, 2007 [source] Design of Blends with an Extremely Low Viscosity Ratio between the Dispersed and Continuous Phases.MACROMOLECULAR SYMPOSIA, Issue 1 2007Dependence of the Dispersed Phase Size on the Processing Parameters Abstract Summary: This work deals with the development of the dispersed phase morphology in immiscible blends of poly(ethylene glycol)/polyamide 66 (PEG/PA) with an extremely low viscosity ratio. The blends were obtained, under different operating conditions, by melt blending in an internal mixer. The objective was to examine the influence of the main processing parameters on the particles size of the minor phase (PEG). A model was elaborated to describe the dependence of the particle size on interfacial tension, PEG concentration, shear rate and viscosity ratio between the two blend components. [source] Solubility islands for polymer blends , a new option to homogenize incompatible polymers?MACROMOLECULAR SYMPOSIA, Issue 1 2003Attila R. Imre Abstract Experimental results of liquid-liquid phase equilibrium in a polydisperse blend of two polyalkylsiloxane are presented here. The UCST has an unusual pressure dependence: pressure induced miscibility at moderate pressures and pressure induced immiscibility at higher pressures, above a double critical point. The cloud point curve has two maxima in (concentration, temperature) as well as in (concentration, pressure) space. Approaching the double critical point, the high and low pressure branches of the cloud point curve merge and in a certain stage of this merging, they form a miscibility island located inside the two-phase region. Islands of this kind can give us a new tool to mix virtually immiscible blends. [source] Melt processed microporous films from compatibilized immiscible blends with potential as membranesPOLYMER ENGINEERING & SCIENCE, Issue 4 2002M. Xanthos Microporous flat films with potential as membranes were produced via melt processing and post-extrusion drawing from immiscible polypropylene/polystyrene blends containing a compatibilizing copolymer. The blends were first compounded in a co-rotating twin-screw extruder and subsequently extruded through a sheet die to obtain the precursor films. These were uniaxially drawn (100%,500%) with respect to the original dimensions to induce porosity and then post-treated at elevated temperatures to stabilize the resultant structure, which consisted of uniform microcracks in the order of a few nanometers in width. The effects of blend composition and extrusion process parameters on surface and cross-sectional porosity and solvent permeability of the prepared films are presented and related to specific microstructural features of the films before and after drawing. Finite element modeling of the stretching operation in the solid state yielded a successful interpretation of the blend response to uniaxial tension that resulted in microcrack formation. Comparison of some of the novel microporous structures of this work with commercial membranes prepared by solvent-based phase inversion processes suggests comparable pore size and porosity ranges, with narrower pore size distribution. [source] Evolution of structure in the softening/melting regime of miscible polymer mixingPOLYMER ENGINEERING & SCIENCE, Issue 6 2001Heidi E. Burch Structure development in the softening/melting processing regime is investigated using the model miscible blend poly(styrene-co-acrylonitrile) (SAN)/poly(methyl methacrylate) (PMMA). Feed materials of four different particle sizes are compounded to study their effects upon structure development. Fourier-transform infrared spectroscopy is used to help determine the normalized sample variance, a quantitative measure of mixing. The normalized sample variance is determined both as a function of sample size and as a function of feed particle size in an effort to assess the characteristic size scale(s) present in the blend at short mixing times. Results of these experiments indicate that the distribution of size scales in the softening regime is at least bimodal. Optical examination of pigmented mixtures reveals that this multimodality is due to the operation of the Scott/Macosko sheeting mechanism of morphology development, which was previously shown to be active in immiscible blends. This is contrary to the currently accepted laminar mixing model, which postulates the formation of a striated mixture while ignoring the softening/melting regime. [source] | ||||||||||