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Melt Rheology (melt + rheology)
Selected AbstractsRheological and Thermal Properties of Polylactide/Silicate Nanocomposites FilmsJOURNAL OF FOOD SCIENCE, Issue 2 2010Jasim Ahmed ABSTRACT:, Polylactide (DL)/polyethylene glycol/silicate nanocomposite blended biodegradable films have been prepared by solvent casting method. Rheological and thermal properties were investigated for both neat amorphous polylactide (PLA-DL form) and blend of montmorillonite (clay) and poly (ethylene glycol) (PEG). Melt rheology of the PLA individually and blends (PLA/clay; PLA/PEG; PLA/PEG/clay) were performed by small amplitude oscillation shear (SAOS) measurement. Individually, PLA showed an improvement in the viscoelastic properties in the temperature range from 180 to 190 °C. Incorporation of nanoclay (3% to 9% wt) was attributed by significant improvements in the elastic modulus (G,) of PLA/clay blend due to intercalation at higher temperature. Both dynamic modulii of PLA/PEG blend were significantly reduced with addition of 10% PEG. Rheometric measurement could not be conducted while PLA/PEG blends containing 25% PEG. A blend of PLA/PEG/clay (68/23/9) showed liquid-like properties with excellent flexibility. Thermal analysis of different clay loading films indicated that the glass transition temperatures (Tg) remained unaffected irrespective of clay concentration due to immobilization of polymer chain in the clay nanocomposite. PEG incorporation reduced the,Tg of the blend (PLA/PEG and PLA/PEG/clay) significantly. Both rheological and thermal analysis data supported plasticization and flexibility of the blended films. It is also interesting to study competition between PLA and PEG for the intercalation into the interlayer spacing of the clay. This study indicates that PLA/montmorillonite blend could serve as effective nano-composite for packaging and other applications. [source] Characterization of Ethylene Copolymers with Liquid Chromatography and Melt Rheology MethodsMACROMOLECULAR SYMPOSIA, Issue 1 2009Yefim Brun Abstract Summary: Melt rheology and polymer chromatography methods were applied to characterize molecular heterogeneities in products of free radical copolymerization of ethylene with methyl acrylate and vinyl acetate comonomers performed in continuously stirred tank and tubular reactors. We found that the ethylene,vinyl acetate copolymers made in both reactors had similar linear viscoelastic properties typical to branched products of the high pressure process. But the ethylene,methyl acrylate copolymers obtained in the tubular reactor had unusually high melt viscosity at low shear rate and much lower onset of shear thinning despite the narrower molecular weight distribution and the lower overall amount of long-chain branches compare to their autoclave counterparts with similar average molecular weight and chemical composition. Using interaction polymer chromatography method called gradient elution at critical point of adsorption we found that ethylene-acrylate copolymers from the tubular reactor had very broad chemical composition distribution, which was consistent with a significant difference in reactivity ratios between ethylene and acrylate comonomers. Such chemical composition heterogeneity can be a reason for the observed unusual rheological properties of these copolymers. [source] Melt rheology of HDPE/EVA blends: The effects of blend ratio, compatibilization, and dynamic vulcanizationPOLYMER ENGINEERING & SCIENCE, Issue 4 2010Biju John The melt rheological behavior of high-density polyethylene (HDPE)/ethylene vinyl acetate (EVA) blends has been examined with reference to the effect of blend ratio, shear stress, and temperature. The HDPE/EVA blends exhibit pseudoplastic behavior, and the observed rheological behavior of the blends was correlated with the extrudate morphology. The experimental values of the viscosity were compared with the theoretical models. The effect of maleic- and phenolic-modified PE compatibilizers on the viscosity of H70 blend was analyzed and found that compatibilization did not significantly increase the viscosity. The effect of dynamic vulcanization and temperature on the viscosity was also analyzed. The activation energy of the system decreased with increase in EVA content in the system. The phase continuity and phase inversion points of the blends were theoretically predicted and compared with the experimental values. The melt flow index (MFI) values of the blends were also determined and found that the MFI values decreased with increase in EVA content in the system. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers [source] Simulation of polymer melt processingAICHE JOURNAL, Issue 7 2009Morton M. Denn Abstract Polymer melt processing requires an integration of fluid mechanics and heat transfer, with unique issues regarding boundary conditions, phase change, stability and sensitivity, and melt rheology. Simulation has been useful in industrial melt processing applications. This brief overview is a personal perspective on some of the issues that arise and how they have been addressed. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Advances in modeling of polymer melt rheologyAICHE JOURNAL, Issue 3 2007Ronald G. Larson First page of article [source] A solid-state NMR study of phase structure, molecular interactions, and mobility in blends of citric acid and paracetamolJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 5 2009S. Schantz Abstract Citric acid anhydrate (CAA) and paracetamol (PARA), prepared as crystalline physical mixtures and as amorphous blends, were studied using 13C solid-state cross polarization magic angle spinning (CPMAS) NMR. Amorphous blends showed significant line broadening from the conformational distribution as compared to the crystalline samples. Also, chemical shift variations were observed between crystalline and amorphous blends, which were attributed to differences in intermolecular interactions. Averaging of proton rotating-frame spin-lattice relaxation times (T1,) probed via different 13C sites in the amorphous blends confirmed molecular level mixing. For some, initially amorphous, sample compositions the onset of crystallization was evident directly from spectra and from the significantly longer T1, relaxations. Thus, crystallization caused phase separation with properties of the two phases resembling those of pure CAA and PARA, respectively. 13C spectra of amorphous 50/50 (w/w, %) CAA/PARA recorded from above the glass transition temperature broadened as the temperature increased to a maximum at T,,,Tg,+,33 K. This was the result of a dynamic interference between the line narrowing techniques being applied and the time scale of molecular reorientation in the miscible melt. The derived average correlation time was found to correspond well with previous results from melt rheology. We conclude that the underlying reasons for physical instability (i.e., crystallization from the miscible melt, including molecular interactions and dynamics) of this class of amorphous binary mixtures can be effectively evaluated using NMR spectroscopy. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 98:1862,1870, 2009 [source] Biodegradable Polylactide and Its Nanocomposites: Opening a New Dimension for Plastics and CompositesMACROMOLECULAR RAPID COMMUNICATIONS, Issue 14 2003Suprakas Sinha Ray Abstract The academic and industrial aspects of the preparation, characterization, mechanical and materials properties, crystallization behavior, melt rheology, and foam processing of pure polylactide (PLA) and PLA/layered silicate nanocomposites are described in this feature article. Recently, these materials have attracted considerable interest in polymer science research. PLA is linear aliphatic thermoplastic polyester and is made from agricultural products. Hectorite and montmorillonite are among the most commonly used smectite-type layered silicates for the preparation of nanocomposites. Smectites are a valuable mineral class for industrial applications because of their high cation exchange capacities, surface area, surface reactivity, adsorptive properties, and, in the case of hectorite, high viscosity, and transparency in solution. In their pristine form, they are hydrophilic in nature, and this property makes them very difficult to disperse into a polymer matrix. The most common way to overcome this difficulty is to replace interlayer cations with quaternized ammonium or phosphonium cations, preferably with long alkyl chains. In general, polymer/layered silicate nanocomposites are of three different types: (1) intercalated nanocomposites, in which insertion of polymer chains into the layered silicate structure occurs in a crystallographically regular fashion, regardless of polymer to layered silicate ratio, with a repeat distance of few nanometer; (2) flocculated nanocomposites, in which intercalated and stacked silicate layers are sometimes flocculated due to the hydroxylated edge,edge interactions between the silicate layers; (3) exfoliated nanocomposites, in which individual silicate layers are uniformly distributed in the polymer matrix by average distances that totally depend on the layered silicate loading. This new family of composite materials frequently exhibits remarkable improvements in its material properties when compared with those of virgin PLA. Improved properties can include a high storage modulus both in the solid and melt states, increased flexural properties, a decrease in gas permeability, increased heat distortion temperature, an increase in the rate of biodegradability of pure PLA, and so forth. Illustration of the biodegradability of PLA and various nanocomposites. [source] Molecular, rheological, and crystalline properties of low-density polyethylene in blown film extrusionPOLYMER ENGINEERING & SCIENCE, Issue 12 2007Khokan Kanti Majumder The molecular weight and its distribution, degree of long chain branching and cooling rate strongly influence crystallinity during processing, which in turn determines the processability and the ultimate properties of the blown film. Generally a decrease in the number of branches and molecular weight of the polymer and the cooling rate results in an increase of the crystallinity. Length of the main chain and extent of branching in low-density polyethylene (LDPE) are also factors that affect melt rheology and film crystallinity. Long chain branched polyethylene is suitable in the blown film process due to its better melt strength for bubble stability. The objective of this article is to describe the effect of molecular properties (e.g. molecular weight and its distribution, degree of long chain branching etc) of LDPE on film crystallinity at different cooling rates of blown film extrusion. Two different grades of LDPE were selected to investigate molecular characteristics, crystallinity, and rheology. The resins were processed in a blown film extrusion pilot plant using four different cooling rates. Molecular, rheological, and crystalline properties of the resins were key parameters considered in this study. POLYM. ENG. SCI., 47:1983,1991, 2007. © 2007 Society of Plastics Engineers [source] | |||||||||||||