Search results for "copolymer"
showing 10 items of 1003 documents
Small angle scattering study of poly(methylmethacrylate)-block-poly(ethylene oxide) block co-polymer in aqueous solution
2005
A combined Small Angle X ray (SAXS) and Neutron (SANS) Scattering study of aqueous solutions of a symmetric block copolymer consisting of poly(methyl methacrylate) (PMMA) and poly(ethylene oxide) (PEO) moieties is presented. The polymer forms slightly polydisperse spherical micelles in a wide range of concentration (0.03 – 6.7 w/V) and temperature (20°C ≤ T ≤ 65°C). A good description of the SANS data is obtained using a polydisperse core-shell model with a structure factor for a modified hard sphere potential. By increasing the concentration at constant T we observed a decrease of the aggregation number and an increase of solvation of PEO groups in the shell, opposite to what happens by in…
New copolymers graft of α,β-poly(N-2-hydroxyethyl)-d,l-aspartamide obtained from atom transfer radical polymerization as vector for gene delivery
2012
Abstract New cationic α,β-poly(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) graft copolymers were synthesized by ATRP, using diethylamino ethyl methacrylate (DEAEMA) as monomer for polymerization, yielding polycations (PHEA-pDEAEMA) able to condense DNA. Then, consecutive ATRP conditions were set up on PHEA-pDEAEMA to obtain copolymers containing also hydrophilic chains (PHEA-IB-pDMAEMA-pPEGMA) able to improve biocompatibility of polyplexes and to provide them stealth properties. Agarose gel studies showed that the copolymers effectively condensed plasmid DNA to form polyplexes. Light scattering studies were used to analyze the size and the ζ -potential of these polyplexes, showing that cop…
The effect of macromolecular architecture of ethylene copolymers with multi-alkenylsilsesquioxane on morphological, rheological and dynamic mechanica…
2021
Abstract The influence of the degree and the way of incorporation of multi-alkenylsilsesquioxane into the polymer chain on morphological, rheological and dynamic mechanical parameters were determined. It was found that POSS incorporated into the polymer chain was located outside the crystalline structure of lamella in amorphous phase. The incorporation of POSS-6-2 as a pendant group resulted in significant increase of separation of macromolecules. The key factor in rheological and dynamic mechanical behavior of copolymers turned out to be the way of POSS incorporation into the polymer chain. The incorporation of POSS into the polymer chain as a pendant group resulted in decreased relaxation…
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…
Influence of PVP/VA copolymer composition on drug–polymer solubility
2015
In this study, the influence of copolymer composition on drug-polymer solubility was investigated. The solubility of the model drug celecoxib (CCX) in various polyvinylpyrrolidone/vinyl acetate (PVP/VA) copolymer compositions (70/30, 60/40, 50/50 and 30/70 w/w) and the pure homopolymers polyvinylpyrrolidone (PVP) and polyvinyl acetate (PVA) was predicted at 25 °C using a thermal analysis method based on the recrystallization of a supersaturated amorphous dispersion (recrystallization method). These solubilities were compared with a prediction based on the solubility of CCX in the liquid monomeric precursors of PVP/VA, N-vinylpyrrolidone (NVP) and vinyl acetate (VA), using the Flory-Huggins …
Preparation of Polymer-Supported Polyazamacrocycles. The Role of the Polymeric Matrix in the Preparation of Polymer-Supported Polyazamacrocycles
2000
Different approaches have been studied for the preparation of resins containing different polyazamacrocycles. Preparation of monolithic resins by polymerization of vinylic derivatives of the corresponding macrocycles is shown to be a more versatile strategy for this purpose. The use of energy-dispersive analysis by X-ray has revealed to be a very useful tool for the rapid evaluation of the interaction of those materials with both anions and cations and has allowed the corresponding selectivity trends to be obtained in a fast and simple way. Important effects of the polymeric matrix are observed in some cases.
Diene/polar monomer copolymers, compatibilisers for polar/non-polar polymer blends. A controlled block copolymerisation with a single-site component …
2002
A well-controlled two-step process, the polymerisation of isoprene or isoprene/hex-1-ene copolymerisation followed by e-caprolactone polymerisation, affords trans-polyisoprene or (trans-polyisoprene/hex-1-ene copolymer)–poly(e-caprolactone) diblocks of various lengths. The single component initiator is an allylsamarocene compound. An atomic force microscopy study shows that these copolymers are efficient compatibilisers for poly(e-caprolactone) and polyisoprene blends. Poly(e-caprolactone) chain growth from Sm–polyisoprene chain.
Critical micellization density: A small-angle-scattering structural study of the monomer-aggregate transition of block copolymers in supercriticalCO2
2000
In this paper we report a small-angle neutron-scattering investigation of micelle formation by the fluorocarbon-hydrocarbon block copolymer, polyvinyl acetate-b-poly (1,1,2,2-tetrahydroperfluoro-octyl acrylate) in supercritical CO{sub 2} (scCO{sub 2}) at 313 K. At high pressure the copolymer is in a monomeric state with a random coil structure, while at low pressure the polymer forms spherical aggregates stable in a wide range of thermodynamic conditions. By profiling pressure, a sharp monomer-micelle transition is obtained due to the tuning of the solvating ability of scCO{sub 2}. We confirm the previous finding that this aggregate-monomer transition is driven by the gradual penetration of…
Über die anionische polymerisation von acrolein. Polymere acroleine. 34. Mitt.1
1967
Acrolein wurde mit Lithium-, Natrium- oder Kaliumcyanid in Tetrahydrofuran bzw.in Toluol polymerisiert. Die Abhangigkeit der Polymerisationsgeschwindigkeit und der Struktur der Polymeren von Reaktionsmedium, Temperatur und Gegenion wurde untersucht. Unterhalb -10°C polymerisiert Acrolein mit Natriumcyanid nur uber die CO. Doppelbindung. Es entstehen hochmolekulare, losliche Poly-3,4-acroleine. Oberhalb -10°C wird dagegen auch Polymerisation uber die Vinylgruppe beobachtet. Die Kurve fur die Abhangigkeit der Polymerisationsgeschwindigkeit von der Reaktionstemperatur durchlauft Extremwerte. Es wird ein Mechanismus aufgestellt, der die jeweilige Struktur des Polymeren als Ergebnis von Gleichge…
Thermal behavior of ethylene copolymers with di- and tri-alkenylsilsesquioxane comonomers synthesized by post-metallocene catalysts
2020
AbstractThis paper reported thermal properties of ethylene copolymers with di- and tri-alkenylsilsesquioxanes (POSS) synthesized by bis(phenoxy-imine) Ti, Zr, V, and V salen-type complexes. Ethylene copolymers with multi-alkenyl POSS obtained by such complexes contain multi-alkenyl POSS incorporated into the polymer chain as a side group. They were characterized by different thermal behavior depending on the kind of multi-alkenyl POSS comonomer, and type of the catalyst used, as well as polymerization conditions and thus the structure of the copolymer chain. Ethylene/POSS copolymers differed in incorporation of POSS into the polymer chain, content of specific unsaturation groups, and molecu…