Search results for "Radical polymerization"

Preparation of drug-polymer composites by polymerization in supercritical carbon dioxide: a new method to increase the dissolution rate of bioactive …

2008

Dispersion Copolymerization of Vinyl Monomers in Supercritical Carbon Dioxide.

2003

The thermally initiated free-radical dispersion copolymerization of methyl methacrylate (MMA) and N,N-dimethylacrylamide (DMA) in supercritical carbon dioxide has been studied in the presence of polysiloxane surfactants. The formation of a stable latex seems to be related to the presence of at least one reactive end group in the surfactant macromolecule, thus suggesting that anchoring of the stabilizer to the surface of the growing polymer particles occurs through chemical grafting. In the case of a molar ratio of DMA to MMA lower than 0.40, microspherical copolymer particles with yields ranging from 81 to 97% were collected from batch polymerizations carried out at 65 °C and 23-28 MPa usin…

Thermo- and Light-Responsive Polymers Containing Photoswitchable Azobenzene End Groups

2009

Telechelic thermo- and light-responsive polymers based on poly(oligo(ethylene glycol) methyl ether methacrylate) P(OEGMA) with azobenzene functionalities at the end groups were synthesized. In a reversible addition−fragmentation chain transfer (RAFT) polymerization using a functionalized chain transfer agent (CTA) containing a pentafluorophenyl (PFP) activated ester, oligo(ethylene glycol) methyl ether methacrylate (OEGMA, Mn ∼ 300 g mol−1) could successfully be polymerized with good control over molecular weight, very high conversions, and narrow molecular weight distributions. Polymers derived from this CTA possessed an activated ester at the α-end of the polymer chain as well as a dithio…

Long-Distance Magnetic Interaction of Exchange-Coupled Copper Dimers with Nitronyl Nitroxide and tert-Butyl Nitroxide Radicals

2009

To study long-distance magnetic interactions between exchange-coupled metal centers and coordinated radical moieties, two new homodimetallic Cu(II) complexes held together by the chelating ligand L(nPr) = N,N,N',N'-tetrakis(N-propyl-2-benzimidazolyl)-2-hydroxy-1,3-diaminopropane and additionally bridged by either a nitronyl nitroxide (NIT) or a tert-butyl nitroxide (NOA) radical-substituted benzoate have been prepared. The complexes have been investigated by X-ray crystallography, magnetic susceptibility measurements, electron paramagnetic resonance (EPR) spectroscopy, and density functional theory (DFT) calculations. For comparison additionally the related copper dimer with the bridging di…

Radiation curing of diacrylate glycerolate of bisphenol-A in the presence of an organically modified montmorillonite for the production of flame-resi…

2006

Polymerization of an acrylate derivative of bisphenol-A by ionizing radiation in the presence of an organically modified montmorillonite was carried out in order to produce a flame-retardant composite. The measurement of the thermal effect during irradiation indicates that radiation curing of pure resin and resin-clay mixtures occurred in both cases. Moreover, differential scanning calorimetry and dynamic mechanical thermal analysis showed that a curing completion can be obtained by thermal curing after irradiation with a significant increase of the glass transition temperature. The morphology was investigated by X-ray diffraction and transmission electron microscopy. These have indicated t…

Biocompatible Polymers and Processing Techniques in Drug Delivery and Tissue Engineering

2013

Study of Atrp Process for the Grafting of Vinyl Monomers on PVC and PVDF

2014

STUDY OF ATRP PROCESS FOR THE GRAFTING OF VINYL MONOMERS ON PVC AND PVDF Sonia Lanzalaco, Onofrio Scialdone, Alessandro Galia, Rosalia Mauro, Flavia Lazzano Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, Viale delle Scienze, Palermo e-mail: sonia.lanzalaco@unipa.it ATRP (atom transfer radical polymerization) has been recently used to prepare graft copolymers with regularly-spaced polymer chains from polymeric macroinitiators that have pendant chemical groups containing radically transferable halogen atoms [1]. The halogen atom serves as initiation site for the polymerization of side chains. Furthermore, Matyjaszewsky and Gennaro showed that an externally applied ele…

Polymerizable and polymeric zwitterionic surfactants: 1. Synthesis and bulk properties

1991

Abstract The synthesis of a series of permanently zwitterionic surfactant monomers based on sulphobetaines and the preparation of their polymers is described. Solubilities, thermal properties and bulk structures of the zwitterionic polymers are studied with respect to their molecular architecture, and compared with cationic analogues. The various solubilities of the polymers can be correlated with their molecular geometry, enabling differentiation into distinct classes. This behaviour is paralleled by the observed bulk structures of the polymers where distinct classes of superstructures are present. However, independently of the molecular geometry, no thermal transition could be detected fo…

Cyclodextrins in Polymer Synthesis:  Influence of Acrylate Side Groups on the Initial Rate of Radical Polymerization of Various Acrylate/Methylated β…

2001

Methylated β-cyclodextrin was used to complex the hydrophobic monomers n-propyl acrylate (1), n-butyl acrylate (2), n-pentyl acrylate (3), n-hexyl acrylate (4), and cyclohexyl acrylate (5) respectively yielding the corresponding water-soluble host/guest-complexes 1a−5a. The complexes were polymerized in water by free radical mechanism and the initial polymerization rates (v0) determined. We found that v0 increases as follows:  1a (12.5), 2a (27.5), 3a (44.2), 5a (49.4), 4a (75.8 × 10-6 mol·L-1·s-1). To investigate the influence of the hydrophobic character of the guest monomers on the reaction rate, the water solubilities of the uncomplexed monomers 1−5 were determined by HPLC measurements.…

Core-shell polyacrylate and polystyrene-block-polyacrylate stars

2005

The polymerization of p-(iodomethyl)styrene (PIMS) yields well-defined branched polymers with reactive iodomethyl groups. The branched poly[p-(iodomethyl)styrene] was used as the transfer agent in the iodine mediated radical polymerization of vinyl monomers. The polymerization proceeds in a controlled way and yields polystyrene and poly(t-butyl acrylate) star polymers with reactive groups at the end of their arms. Polymers so obtained were also used to prepare stars with block copolymer arms: polystyrene-block-poly(t-butyl acrylate). The characterization of star structures was performed by NMR and gel permeation chromatography with absolute molar mass detection (MALLS). Preliminary characte…