Search results for "Radical polymerization"
showing 10 items of 184 documents
A continuous reaction system to investigate dispersion polymerization of vinyl monomers in supercritical carbon dioxide
2006
A laboratory-scale continuous reaction system using a stirred tank reac- tor was assembled in our laboratory to study the dispersion polymerization of vinyl monomers in supercritical carbon dioxide (scCO2). The apparatus was equipped with a suitable downstream separation section to collect solid particles entrained in the effluent stream from the reactor, whose monomer concentration could be measured online with a gas chromatograph. The dispersion polymerization of methyl methacry- late in scCO2 was selected as a model process to be investigated in the apparatus. The experiments were performed at 65 8C and 25 MPa with 2,2 0 -azobisisobutyroni- trile as the initiator and a reactive polysilox…
Polymerization of vinylidene fluoride with perfluoropolyether surfactants in supercritical carbon dioxide as a dispersing medium
2006
The heterogeneous polymerization of vinylidene fluoride (VDF) was investigated at 50 °C with supercritical carbon dioxide (scCO 2 ) as a dispersing medium and diethylperoxidicarbonate as an initiator in the presence of different perfluoropolyether surfactants. When FLK 7004A ammonium carboxylate salts were used at a 5% (w/w) concentration with respect to VDF, with an initial pressure of 31-45 MPa and with an olefin concentration of about 5.5 mol/L, monomer conversions up to 63% were obtained, corresponding to a final solid content higher than 200 g/L, and the polymer was collected at the end of the process in the form of a white powder completely composed of microspheres. The effects of the…
Polyreactions in ordered systems: Polymerization of octadecyl methacrylate in monolayers at the gas–water interface
1977
The ultraviolet-initiated polymerization of octadecyl methacrylate (ODMA, octadecyl 2-methyl-2-propenoate) as a monomolecular layer at the gas-water interface was studied. The polymerization was carried out at 27°C at the nitrogen-water interface; air inhibits the polymerization. At 27°C the ODMA monolayer exhibits three different states which were characterized by surface pressure-area diagrams and by surface potential measurements. The ODMA monolayer was polymerized under constant surface pressure in the range between 0 and 10 dyne/cm. The polymerization was followed by recording the contraction of the film. The conversion was determined by comparison of the area per monomer unit during p…
Spherical and rod-like colloids with polymer-brush surfaces
2008
In this paper, we describe a strategy to overcome incompatibility of colloidal particles and polymer coils as well as immiscibility of spherical and rod-shaped nanoparticles. Two new types of model colloids are presented, colloidal nanospheres with hairy surfaces (spherical brushes) and polymacromonomers to represent cylindrical brushes. The spherical brushes are synthesized from polyorganosiloxane-μ-gels of diameter 20 nm by grafting onto anionically prepared polystyrene macromonomers of molecular weight M w=5000 g/mol. On average, each sphere has a surface layer of 200 polymer chains. Compatibility of spherical nanoparticles with polymer coils was probed by turbidity of as-cast films as w…
Cyclodextrins in polymer synthesis: free radical polymerization of cyclodextrin complexes with oxazoline-functionalized vinyl monomers as guest molec…
2000
The synthesis of five new oxazoline functionalized vinyl monomers N-[4-(4′,5′-dihydrooxazol-2-yl)phenyl]acrylamide (3 a), N-[4-(4′,5′-dihydrooxazol-2-yl)phenyl]-2-methylacrylamide (3 b), N-{10-[4-(4′,5′-dihydrooxazol-2-yl)phenylcarbamoyl]decyl}-2-acrylamide (5 a), N-{10-[4-(4′,5′-dihydrooxazol-2-yl)phenylcarbamoyl]decyl}-2-methylacrylamide (5 b) and N-[4-(4′,5′-dihydrooxazol-2-yl)-phenyl]-4-vinylbenzamide (7) is described. With an equimolar amount of 2,6-dimethyl-β-cyclodextrin (DMCD) these monomers formed hydrophilic inclusion complexes 3 a,b-DMCD, 5 a,b-DMCD and 7-DMCD. These complexes were polymerized radically in an aqueous medium. Resulting polymers P-(3 a, b), P-(5 a, b) and P-(7) pre…
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.
Functional Diblock Copolymers for the Integration of Triboluminescent Materials into Polymer Matrices
2008
This work describes the synthesis and use of new diblock copolymers to integrate functional inorganic particles into a polymer matrix. These diblock copolymers were synthesized by nitroxide-mediated polymerization (NMP) from styrene and two styrene-like monomers with protected functional groups for the later connection to the functional inorganic material. It was possible to keep the polydispersity of the block copolymers around or below 1.2 and to preset the length of the functional block to about 20 monomers or 10 mol-% of monomers. The groups for the surface functionalization (amino groups or chelating ligands) were obtained in their free form by polymer analogous reactions. As an exampl…
Liquid Crystals from Polymer-Functionalized TiO2 Nanorod Mesogens
2008
In this work, we functionalized TiO2 nanorods with dopamine-functionalized diblock copolymers. After functionalization, they are well dispersible in organic solvents. Light scattering proves that t...
Novel Amphiphilic Styrene-Based Block Copolymers for Induced Surface Reconstruction
2008
This paper describes the synthesis of amphiphilic block copolymers by living radical polymerization (NMP) of new styrene-like monomers. The polar monomers (ethylene oxide side chains and free hydroxyl- or amino-groups after deprotection) were polymerized in a “protected form” to adjust the solubility of the monomers. In this way high molar mass polymers with a narrow polydispersity (around or below 1.2) were accessible. In the bulk state hydrophobic and hydrophilic domains demix. By exposing thin films of these polymers to vacuum (air) or alternatively to water or a hydrophilic surface it becomes possible to switch the surface polarity reversibly between contact angles of about 105° and 83°…
Copolymerization of methacryloyl-terminated PMMA macromonomers with methyl methacrylate
1992
Methacryloyl-terminated macromonomers (MM) of polymethylmethacrylate (PMMA) of two different molecular weights were prepared by group transfer polymerization (GTP). They were copolymerized with methyl methacrylate (MMA) by radical polymerization using toluene as the solvent. The relative reactivity of the MM, 1/r1, decreases with increasing initial MM concentration. This is interpreted as a consequence of the increasing viscosity of the reaction medium leading to an increasing diffusion control of the MM addition. At a constant weight ratio of MMA to MM the reactivity of the longer macromonomer is higher than of the shorter one. Increasing the molar ratio [MMA]/[MM], i.e. increasing the ave…