Search results for "blend"
showing 10 items of 421 documents
Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange
2017
Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…
Effect of the Components Molar Mass and of the Mixing Conditions on the Compatibilization of PE/LCP Blends by PE-g-LCP Copolymers
1999
The rheology, morphology, and mechanical properties of blends of high-density polyethylene (HDPE) with a semiflexible liquid crystalline copolyester (SBH) were studied in order to assess the compatibilizing ability of added PE-g-SBH copolymers, and its dependence on the molar mass of the PE matrix, and on the technique used for blend preparation. The PE-g-SBH copolymers were synthesized as described in previous articles, either by the polycondensation of the SBH monomers in the presence of a functionalized PE sample containing free carboxyl groups, or by reactive blending of the latter polymer with preformed SBH. Two samples of HDPE having different molar masses, and two samples of SBH with…
Compatibilization of blends of polyethylene with a semirigid liquid crystalline polymer by PE-g-LCP copolymers
1997
The blends of thermoplastics with liquid crystalline polymers show, in general, poor properties because of the lack of adherence between the two phases. The use of ad hoc synthesized copolymers containing the monomer units of the two polymers has been recently considered by some of us for blend compatibilization, and the results appear promising. In this work, new PE-g-LCP copolymers, prepared either by the synthesis of the LCP in the presence of a functionalized PE, or by reactive blending of the latter polymer with preformed LCP, have been employed as compatibilizing additives for blends of PE with a semirigid LCP. The morphology and the rheological and mechanical properties of the ternar…
PLLA/PLA scaffolds prepared via Thermally Induced Phase Separation (TIPS): tuning of properties and biodegradability
2008
Foams for tissue engineering applications were prepared via thermally induced phase separation (TIPS). Poly-L-Lactic Acid (PLLA) and blends of PLLA with PLA in different proportions were used (100/0, 90/10, 75/25, 50/50, 0/100 PLLA/PLA wt/wt) starting from ternary systems where dioxane was the solvent and water the non-solvent. Morphology was evaluated by Scanning Electron Microscopy (average pore size and interconnection) and the void fraction was measured by means of Hg porosimetry. Foams apparent density was also evaluated (porosity ranges from 87% to 92%). Biodegradability was estimated in a body mimicking fluid. Results show that structure and morphology (in terms of average pore size …
Effect of stress and temperature on the thermomechanical degradation of a PE-LD/OMMT nanocomposites
2014
Thermomechanical degradation of nanocomposites is a topical issue that has not been fully investigated as demonstrated by the low number of papers available in the literature regarding this spe- cific aspect. In particular, with regards to low density polyethylene/clay nanocomposites, the degrada- tion behavior is very complex since it involves the degradation paths of both the polymer matrix and the organomodified nanoclay. In the present work, the effects of mechanical stress and temperature on the thermomechanical behavior of PE-LD/organomodified clay nanocomposites and the degradation paths were investigated by rheological, FT-IR and mechanical methods. The results have shown that the t…
Compatibilization of polyethylene/polyamide 6 blend nanocomposite films
2015
Polymer blends of incompatible components need to undergo compatibilization, in order to give rise to a blend with good physical properties. At the same way, polymer/clay nanocomposites show this problem because of different chemical nature of the polymer matrix and of the clay. Compatibilization is therefore more necessary if an incompatible polymer blend is filled with an organomodified clay in order to give a final material with good properties. In this work, a polyethylene/polyamide 6 blend filled with an organomodified clay has been compatibilized with a maleic anhydride grafted SEBS (styrene-ethylene-butylene-styrene) copolymer and a glicidylmethacrylate-ethylene copolymer. The result…
Neutron reflectometry studies on the interfacial width between polystyrene and various poly(alkylmethacrylates)
1999
From neutron reflectometry we have obtained the interfacial width (typically 2-8 nm) between incompatible polymers above the glass transition temperatures. The investigated polymer bilayers consist of a deuterated polystyrene top layer and various poly(alkylmethacrylates) as a bottom layer. We obtained interesting effects of the length of the alkyl group on the interfacial width. Using mean-field theory we calculate Flory-Huggins-Stavermann interaction parameters X from the interfacial width a I data. These results are compared with investigations of the interfacial width between deuterated poly(methylmethacrylate) and respective polyalkyl-methacrylates.
Relative strength of H-bonding groups on biodegradable polymer-based blends in solution
2006
The intermolecular hydrogen bonding interactions between poly(3-hydroxybutyrate) and poly(styrene-co-vinyl phenol) copolymers with mutual solvent epichlorohydrin were thoroughly investigated by steady-state fluorescence and viscosity techniques. Fluorescence spectroscopy along with viscosity technique was used to asses the intermolecular hydrogen bonding between poly-(3-hydroxybutyrate) and its blends with five copolymer samples of styrene–vinyl phenol, containing different proportions of vinyl phenol but similar average molecular weight and polydispersity index. In the case of very low OH contents (2–4 mol %), as expected, both components of poly(3-hydroxybutyrate) and poly(styrene-co-4-vi…
Radiation grafting functionalization of poly (vinylidene fluoride) to compatibilize its blends with polyolefin ionomers
1998
Blends of a crystalline vinylidene fluoride copolymer (PVDF) and a polyolefin ionomer were produced by melt mixing and characterized by a variety of techniques to examine the effect of increasing the level of salt formation on morphology. The PVDF component was also grafted with methacrylic acid by irradiating the polymer powder and subsequently treating it with an aqueous monomer solution. The effect of neutralizing the acid in both polymer components to produce the corresponding zinc salt was also investigated. Compatibilization was accomplished by the addition of zinc acetyl acetonate (ZnAcAc) to the mixture. This increased the viscosity of the polyolefin ionomer phase, comparable to tha…
The role of the disposition of the recycled polymer on the properties of films for greenhouses coverage
2010
Multilayer films, by using postconsumer materials in the central layer, i.e., multilayer composition: virgin polyethylene/postconsumer polymer/virgin polyethylene, allows to get a film for greenhouses coverage with good mechanical properties and photo-oxidation resistance, similar to that of the films made from virgin material and certainly better than the photo-oxidation resistance of the film made melt blending the virgin polyethylene and the postconsumer polymer. Moreover, the disposition of the postconsumer polymer containing oxygenated groups only in the central layer determines a significant slowdown of the photo-oxidation process of the multilayer film although faster than of the pri…