Search results for "plastics"
showing 10 items of 2724 documents
TI: Compatibilization of PA6/rubber blends by using an oxazoline functionalized rubber
2003
The compatibilization of blends of polyamide 6 with a nitrile butadiene rubber has been investigated. The procedure consists of two steps: modification of the nitrile groups of the rubber into oxazoline in the melt through condensation of ethanolamine with formation of a molecule of ammonia, followed by use of the modified rubber as a compatibilizing precursor which is melt mixed with the polyamide to produce the compatibilized blend. The modification reaction has been detected by NMR analysis and a rheological, mechanical and thermomechanical characterization has been carried out on the all the blends. The results indicate that the modification reaction occurs but the conversion of nitrile…
Monte Carlo simulation in polymer physics: Some recent developments
1991
The computer simulation of macromolecular materials has to deal with phenomena on length scales from 1A to 100A, as well as with time scales ranging over many orders of magnitude, and thus still presents a challenge. With suitably coarse-grained models which disregard detailed information on chemical structure nevertheless collective phenomena can be described, such as unmixing of polymer blends, mesophase ordering of block-copolymer melts, “blob formation” in semidilute solutions, etc. Simulations of such models provide a sensitive test of approximate theories and give valuable hints for experiments.
Compatibility of a statistical copolymer P(EMA-co-MMA) with PS and PMMA
1999
The compositions of coexisting phases and the interface widths in blends of a statistical copolymer of poly(ethylmethacrylate-co -methylmethacrylate) (P(EMA 1-x -co-MMA x )) and a deuterated polystyrene (PS(D)) as well as a deuterated poly(methylmethacrylate) (PMMA(D)) have been investigated by neutron reflectometry (NR). Interaction parameters are calculated from the compositions of coexisting phases and the interface width values. Utilizing a novel two dimensional scheme for graphical representation of the interaction parameters, the results are in very good agreement with studies on the interaction parameters for PS/PMMA, PS/PEMA and PEMA/PMMA blends. In particular, χ EMA/MMA deduced fro…
Ultrathin metal films and inorganic clusters via thermodesorption of LB films
1991
Langmuir-Blodgett multilayers of cadmium arachidate and ferric stearate were investigated during heating in order to derive information on processes involved in thermodesorption and on the inorganic microstructures left on the substrate after thermodesorption. We studied these processes by X-ray induced photoelectron spectroscopy (XPS), interference enhanced reflection (IeR), Nomarsky microscopy, electron microprobe analysis and in the case of Fe57-ions by conversion electron Mossbauer spectroscopy (CEMS). Two different mechanisms of desorption were observed. In the case of cadmium arachidate multilayers it is shown that before desorption the film ruptures laterally and then forms droplets.…
Control over Branching Topology by Introducing a Dual Catalytic System in Coordinative Chain Transfer Polymerization of Olefins
2020
Coordinative polymerization brings opportunities for producing well-defined long-chain branched polyolefins specifically by using homogeneous single-site catalysts. Herein, we report a new dual cat...
Hollow Polymeric Capsules from POSS-Based Block Copolymer for Photodynamic Therapy
2016
A novel amphiphilic diblock copolymer, PHEMAPOSS-b-P(DMAEMA-co-CMA), was prepared via reversible addition–fragmentation chain transfer (RAFT) polymerization, where PHEMAPOSS block was first synthesized using a methacrylate monomer based on polyhedral oligomeric silsesquioxane (HEMAPOSS), and PHEMAPOSS was further utilized to prepare the block copolymer via RAFT copolymerization of 2-(dimethylamino)ethyl methacrylate (DMAEMA) and reduction-cleavable coumarin methacrylate (CMA) monomer. PHEMAPOSS-b-P(DMAEMA-co-CMA) could self-assemble in water to form spherical micelles with POSS core and stimuli-responsive shell. The micelles were cross-linked by photodimerization of coumarin, and then hollo…
Poly(styrene-b-methyl methacrylate) block copolymers as compatibilizing agents in blends of poly(styrene-co-acrylonitrile) and poly(2,6-dimethyl-1,4-…
1993
Abstract The compatibilizing effect of the symmetric narrowly distributed block copolymer poly(styrene- b -methyl methacrylate) (P(S- b -MMA)) in blends of high-molecular-weight poly(styrene- co -acrylonitrile) containing 20 wt% (PSAN20) or 43 wt% acrylonitrile (PSAN43) with poly(2,6-dimethyl-1,4-phenylene ether) (PPE) was investigated by dynamic mechanical spectroscopy and transmission electron microscopy. In blends with the PSAN43, P(S- b -MMA) forms spherical micelles in the PPE phase with no dispersing efficiency. In contrast to this, for blends with PSAN20, the block copolymer is located at the phase boundary, causing an extremely fine dispersion of the components. Depending on the loc…
On the Preparation and Characterization of Polyethylene/Polyamide Blends by Melt Processing in the Presence of an Ethylene/Acrylic Acid Copolymer and…
2006
Samples of HDPE and PA6 have been melt-processed in the presence of two new phosphazene compounds, CP-2EPOX and CP-20XA together with an ethylene/acrylic acid copolymer. The blends have been prepared in an industrial twin-screw extruder by using PA6 and PE in weight ratios of 25/75 and 75/25. When used, 5 phr of EAA and 0.2 phr of CP have been added. The materials have been completely characterized from a rheological, morphological, and mechanical point of view. The results indicate that the additives used caused an increase in the rupture tensile properties, of the impact strength and viscosity especially in the PE-rich blend in the presence of CP-2EPOX. This result can be attributed both …
Modelling the Influence of Nanoparticles in the Phase Behaviour of an Epoxy/Polystyrene Mixture, 2
2007
The influences of nanoparticle size and concentration on the thermodynamic behaviour of epoxy/polystyrene blends are evaluated in the framework of Ginzburg's simple analytical theory. Two approaches have been employed: NPEPO (for particles coated with epoxy groups) and NPFEN (for particles coated with phenyl groups). Using NPEPO, the particles are found to prefer the phase richer in epoxy, whereas the opposite occurs for NPFEN. The particles size significantly influences blend compatibility. When the particle radius Rp is about the same size as the radius of gyration R g of PS, the compatibility of blends increases with particle concentration, whereas for R p > R g , higher particle concent…
Ellipsoidal core-shell cylindrical microphases in PS-b -PB-b -PCL triblock copolymers with a crystallizable matrix
1997
Polystyrene-block-polybutadiene-block-poly(e-caprolactone) SBC triblock copolymers with a PCL matrix exhibit microphase separation into three different phases within the spherulitic superstructures. Mixing of the PS-block can occur upon melting of the PCL-block if the molecular weight is low enough. Even though the crystallization takes place well below the PS-glass transition, a deformation of the amorphous microphases into ellipsoidal core-shell cylindrical microdomains is observed by TEM. These copolymers have mechanical properties which are dominated by the PCL (Poly(e-caprolactone)) matrix with an influence of the amorphous blocks.