Search results for "Phase"
showing 10 items of 6344 documents
Phase identification of triphenylene-based discotic monomer and its main chain polymers
1998
Abstract A monomer, 2,3,6,7,10,11-hexakispentyloxy triphenylene (HPT) possesses a triphenylene core as a discotic mesogen. Polymers containing this discotic mesogen have been studied using wide-angle X-ray and electron diffraction. HPT is known to show a discotic liquid crystal phase, noted as Dho (h for hexagonal bidimensional lattice, o for ordered molecular spacing in each column). In this paper, however, HPT liquid crystalline phases, heated up from the crystalline state and cooled down from the isotropic state, were characterized in the diameter dimensions. In addition. the diameters of the columns are close to a parameter of two separate crystals. A core orientation was, therefore, pr…
Phase Behavior of Polymer-Containing Systems: Recent Advances Through Computer Simulation
2011
Nanoscale Blends between Immiscible Polymers via Simultaneous Non-Interfering Polymerisation
2005
An important topic in polymer science seeks to improve the performances of polymer blends using nanoscale phase segregation. Here, blends between polystyrene and polycaprolactone are realised by a chemical route. The non-interfering character of the radical polymerisation of styrene and the lanthanide halide initiated ring-opening polymerisation of caprolactone is assessed. The molecular weights range from 2 000 to 3 500 for polycaprolactone and up to 140 000 for polystyrene, with reasonable polydispersity indexes. From calorimetry measurements, it is shown that polystyrene and low molecular weight polycaprolactone are immiscible. The morphology of the blends between the two immiscible poly…
Block Copolymers Build-up of Electron and Hole Transport Materials
2004
In this article we describe the synthesis of various monomers modified with triphenyl-1,3,5-triazine side groups as electron transport moieties. By nitroxide-mediated polymerization with a TEMPO unimer it was possible to obtain polymers with a narrow polydispersity. Furthermore, by living radical polymerization block copolymers were obtained from these monomers. Therefore, microphase separated structures are accessible which possess hole conducting moieties in one phase and electron conducting moieties in the other phase.
Crystallization kinetics in relation to polymer processing
1993
Phase distribution of quenched samples has been determined by a deconvolution procedure of WAXS spectra in a wide range of cooling rates. The informations collected together with isothermal and DSC results provide a very wide set of data on the crystallization kinetics of polymers relevant which covers conditions encountered in most polymer processing operations. They have been compared with predictions of a non-isothermal crystallization model assuming two independent and parallel crystallization processes competing during solidification.
Antibacterial chitosan-based blends with ethylene–vinyl alcohol copolymer
2010
Abstract This study reports for the first time about the formulation, morphology, water barrier and the antimicrobial activity of high and low molecular weight chitosonium-acetate based solvent-cast blends with ethylene–vinyl alcohol (EVOH) copolymers. The blends based on the low molecular weight chitosan grade showed enhanced phase morphology, transparency, enhanced water barrier properties, up to 86% water permeability reduction compared to pure chitosonium-acetate films, as well as excellent antimicrobial activity. When the fraction of low molecular weight chitosan exceeded the phase inversion in the blend, phase segregation became noticeable but good interfacial adhesion was still obser…
Hydrogen-Bonded Aggregates of Oligoaramide−Poly(ethylene glycol) Block Copolymers
2010
Rod−coil copolymers with an oligomeric rod aggregate on a nanometer length scale, which is important for many applications like e.g. organic photovoltaics. However, this aggregation behavior and the driving forces such as hydrogen bonding and π−π interactions, as well as the role of side groups, are not yet fully understood. Here, we investigated these noncovalent interactions in oligo(p-benzamide)−poly(ethylene glycol) (OPBA−PEG) copolymers using solid-state NMR supported by wide-angle X-ray scattering (WAXS), differential scanning calorimetry (DSC), and polarization optical microscopy (POM). It was found that longer OPBAs form layered β-sheet-like aggregates and that these are stabilized …
Role of Solvent Compatibility in the Phase Behavior of Binary Solutions of Weakly Associating Multivalent Polymers
2021
AbstractCondensate formation of biopolymer solutions, prominently those of various intrinsically disordered proteins (IDPs), is determined by “sticky” interactions between associating residues, multivalently present along the polymer backbone. Using a ternary mean field “stickers-and-spacers” model, we demonstrate that if sticker association is of the order of a few times the thermal energy, a delicate balance between specific binding and non-specific polymer-solvent interactions gives rise to a particularly rich ternary phase behavior under physiological circumstances. For a generic system represented by a solution comprising multi-associative scaffold and client polymers, the difference i…
Transmission of mechanical energy through polymeric liquid crystals and their blends
1988
Molecular composites, also called polymeric liquid crystals (PLC), are contrasted with the traditional composites; the name heterogeneous composites is proposed for the latter. Advantages of blending PLCs with ordinary engineering polymers are discussed. Results reported for blends of poly(ethylene terepthalate) (PET) with a PLC containing sequences of PET and p-hydroxybenzoic acid (PHB) include thermophysical properties, melt rheology, mechanical properties of solid blends, and scanning electron microscopy of fracture surfaces. A model called the island model was developed to explain the results: One assumes that the lines of force as well as propagating cracks tend to concentrate in the p…
Small angle X-ray scattering from amorphous polymers arising from heterogeneities
1973
The small angle X-ray scattering of glassy polymers (PET, PC, PVC, PMMA) and of polymer melts (PE) was studied. The dependence of the intensity scattered at small angles on the sample treatment suggests that neither the inherent structure of the pure polymer phase nor microholes are the origin of the scattering. In agreement with all experimental facts the scattering can be attributed to foreign particles such as for instance stabilizers in the polymer matrix. The consequence of this result is discussed with respect to the nodular structure of the amorphous phase and with respect to structural models of the amorphous phase. The nodular structure is not related to regions of different densit…