Search results for "polymers"
showing 10 items of 3567 documents
Influence of morphology and chemical structure on the inverse response of polypropylene to gamma radiation under vacuum
1999
Abstract In this work the influence of the chemical structure and of the morphology on the gamma-radiation effects on polypropylene based polymers is studied on the basis of a previously discussed kinetic model [1] . For this aim an isotactic polypropylene and a random ethylene–propylene copolymer were irradiated under vacuum at one dose rate and several absorbed doses after well defined solidification conditions. We show that the model is reliable varying both the chemical structure and the morphology of the polypropylene based polymer. An inversion of the response of the material to gamma radiation under vacuum is always observed, and the inversion conditions depend on the irradiation par…
Novel polyolefin materials via catalysis and reactive processing
1998
Recent advances in transition metal catalyzed olefin polymerization and melt processing stimulate the production of new polymers derived from old monomers Modern polyolefin processes do not require polymer purification and give excellent control of molecular and supermolecular polyolefin architectures. Progress in catalyst design and preparation of tailor-made homo-and copolymers is highlighted for isotactic, syndiotactic, atactic and stereoblock polypropylene (PP), novel 1-olefin copolymers, and ethylene copolymers with polar monomers, e.g., CO and acrylics Today polyethylene short-and long-chain-branching is controlled either by uniform ethylene copolymerization with 1-olefins using singl…
Effect of the elongational flow on morphology and properties of polypropylene/graphene nanoplatelets nanocomposites
2018
Abstract In this work the effect of the presence of graphene nanoplatelets (GnP) on the morphology and mechanical properties of polypropylene/GnP nanocomposites has been investigated when these polymer systems are subjected to non-isothermal elongational flow in a melt spinning operation. The presence of the GnP magnifies the effect of the elongational flow. Indeed, the elastic modulus and the tensile strength of nanocomposites increases with the orientation more than that observed for the pure matrix. Moreover, the elongation at break increases at low values of the draw ratio for the nanocomposites, while, the matrix shows the expected decrease in deformability. These effects have been cor…
Gamma radiation induced maleation of polypropylene using supercritical CO 2 : preliminary results
2000
Abstract The charging of maleic anhydride (MA) and dicumyl peroxide (DCP) into polypropylene matrices has been carried out by CO2 in supercritical conditions. The grafting of MA into polymer chains was done through gamma irradiation in CO2 atmosphere (0.1 MPa, 25°C). The grafting was successful and the amount of grafted anhydride was dependent on the amount of MA and DCP charged into the polypropylene matrix. The presence of grafted succinic anhydride was shown by FT-IR spectroscopy and its amount was determined through a calibration curve derived from standard samples. The effect of swelling due to supercritical CO2, maleic anhydride grafting and gamma irradiation on the molecular structur…
Membrane oligo- and polysialic acids
2011
AbstractPolysialic acid (polySia) and oligosialic acid (oligoSia) chains are linear polysaccharides composed of sialic acid monomers. The majority of biological poly/oligoSia chains are bound to membranes. There is a large diversity of membrane poly/oligoSia in terms of chain length, occurrence, biological function, and the mode of membrane attachment. Poly/oligoSia can be anchored to a membrane via a phospholipid (polySia in bacteria), a glycosphingolipid (oligoSia in gangliosides), an integral membrane glycoprotein, or a glycoprotein attached to a membrane via glycosylphosphatidylinositol. In eukaryotic cells, the attachment of a poly/oligoSia chain to the membrane anchor is usually throu…
Structure and dynamics of thin polymer films: a case study with the bond-fluctuation model
2002
Abstract This paper reports Monte Carlo simulation results of a polymer melt of short, non-entangled chains which are embedded between two impenetrable walls. The melt is simulated by the bond-fluctuation lattice model under athermal conditions, i.e. only excluded volume interactions between the monomers and between the monomers and the walls are taken into account. In the simulations, the wall separation is varied from about one to about 15 times the bulk radius of gyration R g . The confinement influences both static and dynamic properties of the films: Chains close to the walls preferentially orient parallel to it. This parallel orientation decays with increasing distances from the wall …
Dipolar Relaxation in Functionalized Poly-p-phenylenes Bearing Ultrastrong Dipoles Perpendicular to the Backbone
2018
Local polymer dynamics are studied in polymers bearing dipoles rigidly attached to the backbone. The compounds are based on cyano-substituted dihydrobenzimidazoles bearing ultrastrong dipole moments (∼12 D per repeat unit) incorporated in a poly-p-phenylene backbone, giving rise to polymers with rigid dipoles perpendicular to the chain. They belong to type B polymers according to the Stockmayer classification. They are ideal model systems for studying rotational isomers in the gas phase and the self-assembly and local dynamics in the solid state. Gas phase calculations (DFT) provided the dipole moments, the energetic barriers, and the backbone conformation as a function of the dipole streng…
Osmotic pressure of catenanes in solution
1989
We propose a nonuniversal scaling for the osmotic pressure in the case of concatenating ring polymers. The size exponent depends on the molecular weight of the catenans. The effect is more significant the shorter and the stiffer the molecules are.
Translocation dynamics of a short polymer driven by an oscillating force
2013
Under the terms of the Creative Commons Attribution 3.0 Unported License.
Solvent-Induced Length Variation of Cylindrical Brushes
2001
Communication: Polymacromonomers with a main chain much larger than the side-chain length adopt the form of cylindrical brush polymers the contour length per mainchain monomer of which depends on the side-chain length. In the present investigation it is demonstrated that the length per monomer also depends on the solvent quality, i.e., the cylinders are shorter in a poor solvent as compared to a good solvent. It is argued that the repulsion of the side chains represents the extension force, which acts against the entropic contraction force of the main chain. Thus, cylindrical brushes may be suitable as responsive materials for sensors, actuators or soft machines.