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Emulsion Polymerization Technique (emulsion + polymerization_technique)

Distribution by Scientific Domains
Polymers and Materials Science100%

Selected Abstracts

Synthesis and Characterization of Degradable p(HEMA) Microgels: Use of Acid-Labile Crosslinkers

MACROMOLECULAR BIOSCIENCE, Issue 4 2007
Volga Bulmus
Abstract New divinyl-functionalized acetal-based crosslinkers were synthesized as building elements to form acid-labile microgel particles for controlled-release applications. The synthesized crosslinkers underwent hydrolysis at slightly acidic pHs in less than 1 h while they were stable at neutral pHs for longer times. HEMA was copolymerized with the crosslinkers via an inverse emulsion polymerization technique using a redox initiator system at room temperature to form crosslinked, colloidal p(HEMA) microgels. Microgels in diameters ranging from 150 to 475 nm with narrow distribution could be produced. The crosslinking density and the diameter of the microgels were found to be controlled by monomer/crosslinker feed ratio. The microgels demonstrated a pH-dependent cleavage behavior that mimicked the pH-dependent hydrolysis profile of the acid-labile crosslinkers. Model biomacromolecules, i.e., Rhodamine B-labeled dextran and BSA were efficiently loaded into the microgels. The release of the biomolecules from p(HEMA) microgels was also found to be controllable by the pH of the environment similar to the particle degradation. The protein released from the microgels was observed to retain its structural stability. [source]

The Properties of Covalently Immobilized Trypsin on Soap-Free P(MMA-EA-AA) Latex Particles

MACROMOLECULAR BIOSCIENCE, Issue 4 2005
Kai Kang
Abstract Summary: The covalent immobilization of trypsin onto poly[(methyl methacrylate)- co -(ethyl acrylate)- co -(acrylic acid)] latex particles, produced by a soap-free emulsion polymerization technique, was carried out using the carbodiimide method. The catalytic properties and kinetic parameters, as well as the stability of the immobilized enzyme were compared to those of the free enzyme. Results showed that the optimum temperature and pH for the immobilized trypsin in the hydrolysis of casein were 55,°C and 8.5, both of which were higher than that of the free form. It was found that Km (Michaelis constant) was 45.7 mg,·,ml,1 and Vmax (maximal reaction rate) was 793.0 ,g,·,min,1 for immobilized trypsin, compared to a Km of 30.0 mg,·,ml,1 and a Vmax of 5,467.5 ,g,·,min,1 for free trypsin. The immobilized trypsin exhibited much better thermal and chemical stabilities than its free counterpart and maintained over 63% of its initial activity after reusing ten times. TEM photograph of latex particles after trypsin immobilization. [source]

Emulsion copolymerization of styrene and sodium styrene sulfonate: kinetics, monomer reactivity ratios and copolymer properties

POLYMER INTERNATIONAL, Issue 1 2009
Dhamodaran Arunbabu
Abstract BACKGROUND: The synthesis of poly[styrene- co -(sodium styrene sulfonate)], poly(S- co -NaSS), with a high loading of sulfonate groups is of current interest owing to its potential use in numerous areas. A series of these copolymers with various sulfonate loads were synthesized using the emulsion polymerization technique with a study of the copolymerization kinetics, monomer reactivity ratio and copolymer properties. RESULTS: The copolymerization kinetics are significantly enhanced with an increase of NaSS feed in the polymerization. Monomer reactivity ratios were determined from NMR data by employing the Fineman,Ross and Kelen,Tüdös methods. Styrene (r1) and NaSS (r2) reactivity ratios are 0.5 and 10, respectively. The colloidal particle size of the copolymers depends upon the NaSS composition. The thermal stability of the copolymers is greatly enhanced with higher NaSS content in the copolymer backbone. Higher glass transition temperatures are observed for the copolymers with higher NaSS content. CONCLUSION: The reactivity ratio values suggest that styrene prefers to form copolymers whereas NaSS produces homopolymers. It is also found that styrene copolymerization with NaSS is only twice as fast as homopolymerization. In contrast, NaSS homopolymerization is ten times faster than NaSS copolymerization with styrene. The NaSS content in the copolymer backbone affects the thermal stability and the glass transition of the copolymers. Copyright © 2008 Society of Chemical Industry [source]

Coloration of monodispersed polystyrene nanoparticles prepared via the RAFT reaction

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 3 2006
Ju Sung Kim
Abstract Highly monodispersed polystyrene (PS) nanoparticles were prepared via the reversible addition fragmentation transfer (RAFT) living radical emulsion polymerization technique using a sur-iniferter, 4-(2-hydroxyethyl)piperazine-1-carbodithioicacid benzylether (HPCB). The monodispersed nanoparticles were colored by various methods, namely random and block copolymeriztion, the end group reaction and the adsorption method. For the coloration of the block and random copolymer monodispersed nanoparticles, a color pre-monomer was previously synthesized with a vinyl functional site. Dynamic light scattering and scanning electron microscopy were the main tools used to analyze the size and distribution of the prepared nanoparticles. Copyright © 2006 John Wiley & Sons, Ltd. [source]