Search results for "Copolymer"
showing 10 items of 1003 documents
Improvement of the photo-stability of polystyrene-block-polybutadiene-block-polystyrene through carbon nanotubes
2015
Abstract The photo-stability of Polystyrene-Polybutadiene-Polystyrene (SBS) based nanocomposites containing bare multi-walled carbon nanotubes (CNTs) and carbon nanotubes bearing carboxylic functional groups (CNTs-COOH) in comparison to that of pristine SBS has been studied. The photo-oxidation of pristine SBS occurs through crosslinking reactions and oxidized species formation and both these processes begin at early stage of exposure. The formation of crosslinking, formerly in polybutadiene phase, assessed by spectroscopical (FTIR), mechanical, dynamic mechanical and rheological analysis, leads to occurrence of internal mechanical stresses in the solid state and the SBS samples become prem…
Solubilisation of Chlorinated oils in triblock copolymers-surfactant mixed aggregates
2006
Solubilization of oils in aqueous solution of star-like block copolymer with thermo- and pH-sensitive features
2010
Triblock SEBS/DVB crosslinked and sulfonated membranes: Fuel cell performance and conductivity
2021
[EN] A set of styrene-ethylene-butylene-styrene triblock copolymer (SEBS) membranes with 10 or 25 wt.% divinyl-benzene (DVB) as a crosslinking agent were prepared and validated. Physicochemical characterization revealed suitable hydrolytic and thermal stability of photo-crosslinked membranes containing 25%wt. DVB and post-sulfonated. These compositions were evaluated in H2/O2 single cells, and electrical and proton conductivities were furtherly assessed. The membranes with the milder post-sulfonation showed greater proton conductivity than those with excessive sulfonation. In terms of electrical conductivity, a universal power law was applied, and the values obtained were low enough for bei…
Triblock copolymers, mesogels and deformation behavior in poor solvents
2007
A fundamental distinction between the mesophases formed by ABA triblock copolymers and by AB diblock copolymers is the bridging of A domains by B blocks. The ABA mesophases form physically crosslinked networks characterized by non-uniform spatial distribution of high-functionality crosslinks. The swelling of these networks by selective solvents gives rise to novel "mesogels". Three theoretical aspects of these systems, focusing on the lamellar case, are considered: i) The SCF theory of the equilibrium fraction of bridging chains in mesophases formed by a melt of ABA triblock copolymers. ii) The swelling equilibrium and the deformation behavior of mesogels swollen by a selective solvent for …
Critical micellisation density: a SAS structural study of the unimer–aggregate transition of block-copolymers in supercritical CO2
2000
In this paper we report a SANS investigation of micelle formation by fluorocarbon-hydrocarbon block copolymers in supercritical CO2 (scCO2) at 313K. A sharp unimer-micelle transition is obtained due to the tuning of the solvating ability of scCO2 by profiling pressure. At high pressure the copolymer is in a monomeric state with a random coil structure. By lowering the pressure aggregates are formed with the hydrocarbon segments forming the core and the fluorocarbon segments forming the corona of spherical aggregates. This aggregateunimer transition is driven by the gradual penetration of CO2 molecules toward the core of the aggregate and is critically related to the density of the solvent, …
Gelchromatographie. 9. Mitt.: Polymethacrylatgele1
1970
Der Einflus der Herstellungsbedingungen auf die gelchromatographischen Eigenschaften von Polymethylmethacrylatgelen, die mit Glykoldimethacrylat vernetzt sind, wurde untersucht. Homogen-vernetzende Copolymerisation fuhrt zu Gelen mit Ausschlusmolekulargewichten bis ca. 6000. Durch Copolymerisation in Gegenwart von Inertkomponenten entstehen heterogene Strukturen. Durch heterogen-vernetzende Copolymerisation konnen Gele mit Ausschlusmolekulargewichten, die formal 1010 und mehr entsprechen, erhalten werden. Die Anderung der Vernetzerkonzentration und des Solvatationsvermogens der Inertkomponente erlaubt es, die Ausschlusmolekulargewichte der Gele in weiten Grenzen zu variieren. Die Polymerisa…
Order-disorder-and order-order-transitions in AB and ABC block copolymers: description by a simple model
1996
Based on the description of AB-block copolymers as micellar structures given by Semenov, the phase diagram of AB-diblock copolymers is calculated taking the homogeneously mixed system as a reference state. The predicted value (χN)c = 10.385 for a symmetric AB-diblock copolymer compares very well to the result of the original Random Phase Approximation theory (10.495). The simplicity of the model allows its extension to predict order-order transitions in ABC-triblock copolymers.
A POLYCARBOXYLIC/AMINO FUNCTIONALIZED HYALURONIC ACID DERIVATIVE FOR THE PRODUCTION OF pH SENSIBLE HYDROGELS IN THE PREVENTION OF BACTERIAL ADHESION …
2014
A graft copolymer derivative of hyaluronic acid bearing pendant amino and short polymethacrylate portions (HA-EDA-BMP-MANa) has been employed for the production of a pH sensible vancomycin releasing hydrogel and studied in vitro to test its potential anti adhesive property against Staphylococcus aureus colonization. The copolymer obtained through atom transfer radical polymerization bears chargeable (carboxyl and amino groups) portions and it could be formulated as a hydrogel at a concentration of 10% w/v. The HA-EDA-BMP-MANa hydrogels, produced at three different pH values (5, 6 and 7, respectively), were formulated with or without the addition of vancomycin (2% w/v). The vancomycin releas…
Dilute and semi dilute solutions of block copolymers in water, near-critical and super-critical CO2: a small angle scattering study of the monomer–ag…
2002
Abstract Small angle neutron (SANS) and X-ray (SAXS) Scattering measurements on aggregate formation of block copolymers in water and in near-critical and supercritical CO2 are reported here. Time Resolved SAXS (TR-SAXS) has also been performed in the supercritical region. Experiments have been carried out for a series of different thermodynamic conditions, changing the solvent density by profiling the pressure at constant temperature. A sharp transition between monomers dissolved as random coils and micelles characterized by a solvo-philic shell and a solvo-phobic core occurs when the solvent density reaches the critical micellization value. This is easily shown in the case of scCO2.