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Latex Particles (latex + particle)
Kinds of Latex Particles Selected AbstractsThe Properties of Covalently Immobilized Trypsin on Soap-Free P(MMA-EA-AA) Latex ParticlesMACROMOLECULAR BIOSCIENCE, Issue 4 2005Kai 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] Morphology of Polymer/Clay Latex Particles Synthesized by Miniemulsion Polymerization: Modeling and Experimental ResultsMACROMOLECULAR REACTION ENGINEERING, Issue 6-7 2010Matej Mi Abstract BA/MMA (90:10,wt.-%) were copolymerized in the presence of two different organomodified clays (C30B and CMA16) and 1.6,2.6,wbm.-% surfactants. The effect of the compatibility of the organoclay in the monomer mixture on the morphology of hybrid polymer/clay particles was determined using TEM. The resulting morphologies were compared with the prediction of a Monte-Carlo simulation that determined the equilibrium morphology of monomer/clay hybrid miniemulsion droplets. The model predicted encapsulated morphologies only when the organoclay presented low clay/monomer and high clay/water interfacial tensions. C30B and CMA16 did not fulfill these conditions and provided a preferential surface location of the platelets on the polymer/water interphase as predicted by the model. [source] Starch- graft -(synthetic copolymer) latexes initiated with Ce4+ and stabilized by amylopectinJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 18 2007Hank De Bruyn Abstract A method is presented for synthesizing surfactant-free latexes comprising starch- graft -(vinyl polymer) starting with a suspension of amylopectin, either native or modified, then using cerium(IV) with either potassium persulfate or glucose to create grafting sites on the starch. Latex particles comprising polystyrene, poly(styrene- co -(n -butyl acrylate)) and poly(vinyl acetate) grafted onto high molecular weight amylopectin were developed, with up to 80% of the starch effectively grafted to the particles. These latexes were colloidally stable against electrolyte (several months in 4 M NaCl). Reaction rates of Ce4+ with simple sugars and polysaccharides were investigated, as well as the gelation mechanism of the latex. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4185,4192, 2007 [source] Synthesis of polybutadiene-based particles via dispersion ring-opening metathesis polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2004Abraham Chemtob Abstract Latex particles based on 1,4-polybutadiene were synthesized via dispersion ring-opening metathesis copolymerization of 1,5-cyclooctadiene with a ,-norbornenyl poly(ethylene oxide) macromonomer. Stable but polydisperse colloidal dispersions in the 50 nm to 10 ,m size range were obtained. In this work, particular attention was paid to the effects of the kinetics of copolymerization on the structure of the graft copolymers formed and on the onset of turbidity. Strategies to prepare monodisperse polybutadiene particles were also designed through the growth of a polybutadiene shell from a well-defined polynorbornene seed. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1154,1163, 2004 [source] Bioinspired Mineralization of Inorganics from Aqueous Media Controlled by Synthetic PolymersMACROMOLECULAR BIOSCIENCE, Issue 2 2007Katarzyna Gorna Abstract The formation of inorganic structures in nature is commonly controlled by biogenic macromolecules. The understanding of mineralization phenomena and the nucleation and growth mechanisms involved is still a challenge in science but also of great industrial interest. This article focuses on the formation and mineralization of two archetypical inorganic materials: zinc oxide and amorphous calcium carbonate (ACC). Zinc oxide is selected as a model compound to investigate the role that polymers play in mineralization. Most of the effort has been devoted to the investigation of the effects of double-hydrophilic block and graft copolymers. Recent work has demonstrated that latex particles synthesized by miniemulsion polymerization, properly functionalized by various chemical groups, have similar effects to conventional block copolymers and are excellently suited for morphology control of ZnO crystals. Latex particles might serve as analogues of natural proteins in biomineralization. The second example presented, ACC, addresses the issue of whether this amorphous phase is an intermediate in the biomineralization of calcite, vaterite, or aragonite. Conditions under which amorphous calcium carbonate can be obtained as nanometer-sized spheres as a consequence of a liquid,liquid phase segregation are presented. Addition of specific block copolymers allows control of the particle size from the micrometer to the submicrometer length scale. The physical properties of novel materials synthesized from concentrated solution and their potential applications as a filler of polymers are also discussed. [source] Retention of airborne latex particles by a bacterial and viral filter used in anaesthesiaANAESTHESIA, Issue 3 2001apparatus We have developed a series of laboratory tests to evaluate the efficiency of a heat and moisture exchanger filter (PallÔ BB25) in retaining latex particles in order to protect allergic patients during anaesthesia. Latex particles were nebulised with cornstarch as a support and collected for assay in a flask, with or without the filter integrated into the experimental circuit. With the Pall BB25 filter in the circuit, no natural latex proteins were detected by measurement of either total protein or antigenic latex proteins. The Pall BB25 filter may represent a useful means of preventing inhalation of latex particles during anaesthesia in susceptible patients. [source] Electrode Reactions of Catechol at Tyrosinase-Immobilized Latex SuspensionsELECTROANALYSIS, Issue 8 2004Patsamon Rijiravanich Abstract Tyrosinase was immobilized on polystyrene latex particles in order to control amounts of the enzyme. The tyrosinase-coated latex particles were composed of the core polystyrene and four successive coating layers: polystyrene sulfonate, polyallylamine, tyrosinase and polyallylamine again, built up by the layer-by-layer technique. They showed catalytic currents for the enzymatic oxidation of catechol to o -quinone. The enzyme activity per particle was evaluated as 2.3×10,7 units from UV absorption of o -quinone. The relation between the catalytic current and the concentration of catechol leads to a Michaelis-Menten type kinetic equation. The layer-by-layer method was found to have a deactivating effect on enzyme catalysis. In spite of this, the catechol oxidation current was larger than the current from free tyrosinase at a common value of enzyme units per volume. This is ascribed to strong adsorption of the latex particles on the electrode, leading to the enhancement of the local concentration of tyrosinase. [source] Using the Aggregation of Latex Polymers in the Fabrication of Reproducible Enzyme ElectrodesELECTROANALYSIS, Issue 17 2003Wibowo Rahmat Abstract An enzyme electrode for glucose is described as a model system to demonstrate a fabrication method using latex aggregation and entrapment of enzyme. Electrosterically-stabilized latex particles synthesized by emulsion polymerization in batch from acrylic acid, methyl methacrylate and butyl acrylate, and glucose oxidase were coagulated together at pH,5.5 with ethanol. A platinum disk electrode dipped in the solution becomes coated with latex/enzyme. The relative thickness of the film and relative amount of enzyme may be controlled by the time the electrode is in contact with the solution. The enzyme was then immobilized by covalent attachment of amine groups to carboxylic moieties in the polymer using 1-ethyl-3(3-dimethylaminopropyl)-carbodiimide hydrochloride and N -hydroxysuccinimide. Five minutes contact with the latex/enzyme solution and subsequent amide coupling, gave electrodes with a reproducibility of 5.7% RSD, a wide dynamic range (0,100,mM) and good storage properties. [source] Separation of cationic polymer particles and characterization of avidin-immobilized particles by capillary electrophoresisELECTROPHORESIS, Issue 5-6 2006Yukihiro Okamoto Abstract Cationic polymer microparticles have received much attention especially in the field of biotechnology, such that their analysis and separation have become important. So far, the separation of cationic polymer particles with different size using CE has not been achieved and the cationic particles migrated as if they are negatively charged, probably due to electrostatic interaction between capillary wall and cationic polymer particles. In this paper, the separation of cationic polymer microparticles by CE was investigated in detail. The separation of cationic particles with different size was achieved in CE by taking into account the interaction between sample particles and the inner surface of capillaries. By employing a poly(vinyl alcohol)-coated capillary, a better size separation of amine-modified latex particles was obtained compared to a Polybrene-coated capillary. It was elucidated that the composition, concentration, and pH of the background solution were also important factors in the separation of colloidal particles to avoid the surface adsorption and the characteristic aggregation of polymer particles. Furthermore, the CE analysis was applied to the characterization of cationic protein-immobilized particles. [source] Modulation of Viscoelasticity and HIV Transport as a Function of pH in a Reversibly Crosslinked HydrogelADVANCED FUNCTIONAL MATERIALS, Issue 18 2009Julie I. Jay Abstract Materials that respond to physiological stimuli are important in developing advanced biomaterials for modern therapies. The reversibility of covalent crosslinks formed by phenylboronate (PBA) and salicylhydroxamate (SHA) has been exploited to provide a pH-responsive gel for application to the vaginal tract. Dynamic rheology reveals that the gel frequency-dependent viscoelastic properties are modulated by pH. At pH 4.8 the viscous component dominates throughout most of the frequency range. As the pH increases, the characteristic relaxation time continues to increase while the G,Plateau levels off above pH 6. At pH 7.5, the elastic component dominates throughout the frequency sweep and is predominately independent of frequency. Particle tracking assesses the transport of both fluorescently labeled HIV-1 and 100-nm latex particles in the PBA,SHA crosslinked gel as a function of pH. At pH 4.8 the ensemble-averaged mean squared displacement at lag times greater than three seconds reveals that transport of the HIV-1 and 100-nm particles becomes significantly impeded by the matrix, exhibiting diffusion coefficients less than 0.0002,µm2 s,1. This pH-responsive gel thus displays properties that have the potential to significantly reduce the transport of HIV-1 to susceptible tissues and thus prevent the first stage of male-to-female transmission of HIV-1. [source] Synthesis of Light-Diffracting Assemblies from Microspheres and Nanoparticles in Droplets on a Superhydrophobic Surface,ADVANCED MATERIALS, Issue 22 2008Vinayak Rastogi Aqueous suspension droplets of monodisperse latex or latex and gold nanoparticles mixtures assume spherical shape on superhydrophobic substrates. The drying sessile droplets serve as macroscopic templates for assembling microspheres into closed-packed structures. Upon illumination, the supraparticles display discrete colored rings because of the periodic arrangement of latex particles in the surface layer. The physical origin of the colored patterns is explained in detail. [source] The application of distance distribution functions to structural analysis of core,shell particlesJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007Oleksandr O. Mykhaylyk The structure of core,shell latex particles of polymethylmethacrylate (the core) and polyurethane (the shell) have been investigated by methods of small-angle X-ray scattering (SAXS) and atom-force microscopy. A set of SAXS patterns has been obtained using contrast variation method. Indirect methods have been used to follow the evolution of distance distribution functions from SAXS for lattices in various sucrose solutions over a range of solution density, yielding structural parameters of the particles such as core size, shell thickness and density of the polymers including density deviations within the particle's core and shell. A model for an ensemble of core,shell particles with a normal distribution of average electron density of both the core and the shell has been developed to fit the distance distribution functions using a random search algorithm. The effects of nanophase separation in the polyurethane is estimated using Monte Carlo simulations of the distance distribution functions where the phase-separated polyurethane is represented by spherical truncated cones in a shell simulating the location of hard and soft polyurethane blocks, respectively. [source] Development of a homologous expression system for rubber oxygenase RoxA from Xanthomonas sp.JOURNAL OF APPLIED MICROBIOLOGY, Issue 3 2010N. Hambsch Abstract Aims:, Natural rubber (poly-[cis -1,4-isoprene]) can be cleaved into 12-oxo-4,8-dimethyltrideca-4,8-diene-1-al by rubber oxygenase A (RoxA) isolated from Xanthomonas sp. RoxA is a novel type of dihaem dioxygenase with unknown cleavage mechanism of the rubber carbon backbone. Analysis of mutant RoxA after mutagenesis could be a way to investigate the function of selected amino acids of RoxA during catalysis. Unfortunately, expression of functional RoxA in recombinant Escherichia coli or in recombinant ,-Proteobacteria such as Pseudomonas putida was not possible in our hands. Therefore, expression of recombinant RoxA in the homologous host, Xanthomonas, was performed. Methods and Results:, A transformation system via electroporation was established, and a conjugation system was optimized for Xanthomonas sp. Inactivation of the chromosomal roxA gene by insertional mutagenesis resulted in inability of Xanthomonas sp. to produce active RoxA and to utilize rubber as a sole source of carbon and energy. When an intact copy of roxA was cloned under control of a rhamnose-inducible promoter in a broad host range vector and was transferred to Xanthomonas sp., high expression levels of functional RoxA in the presence of rhamnose were obtained. Conclusions and Significance and Impact of the Study:, Purification of recombinantly expressed RoxA was simplified because of drastically shortened fermentation times and because separation of RoxA from remaining rubber latex particles was not necessary with rhamnose-induced cultures. About 6 mg purified RoxA were obtained from 1 l of cell-free culture fluid. Purified recombinant RoxA was highly active and revealed comparable spectral properties as RoxA purified from the wild type. The results of our study are the methodical basis for molecular biological manipulation in Xanthomonas sp. and will simplify investigation into the biochemical mechanisms by which rubber can be biodegraded in the environment by this novel extracellular dihaem dioxygenase RoxA. [source] Effect of acrylic core,shell rubber particles on the particulate flow and toughening of PVCJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2009M. R. Moghbeli Abstract Different types of acrylic core,shell rubber particles with a poly(butyl acrylate) (PBA) core and a grafted poly(methyl methacrylate) (PMMA) shell were synthesized. The average size of acrylic core,shell latex particles ranged from 100 to 170 nm in diameter, having the core gel content in the range of 35,80%. The melt blending behavior of the poly(vinyl chloride) (PVC) and the acrylic core,shell rubber materials having different average particle sizes and gel contents was investigated in a batch mixing process. Although the torque curves showed that the particulate flow of the PVC in the blends was dominant, some differences were observed when the size and gel content of the particles varied. This behavior can be attributed to differences in the plasticizing effect and dispersion state of various types of core,shell rubber particles, which can vary the gelatin process of the PVC in the mixing tool. On the other hand, the highest toughening efficiency was obtained using core,shell rubber particles with the smallest particle size (i.e., 100 nm). The results showed that increasing the gel content of the core,shell impact modifiers with the same particle size improved the particle dispersion state in the PVC matrix. The toughening efficiency decreased for the blends containing 100 and 170 nm rubber particles as the gel content increased. Nevertheless, unexpected behavior was observed for the blends containing 140 nm rubber particles. It was found that a high level of toughness could be achieved if the acrylic core,shell rubber particles as small as 100 nm had a lower gel content. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Using anionic polymerizable surfactants in ultrasonically irradiated emulsion polymerization to prepare polymer nanoparticlesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Yuhui He Abstract An ionic polymerizable surfactant, sodium sulfopropyl-laurylmaleate (M12), was synthesized and used as an emulsifier, an initiator, and a comonomer in ultrasonically irradiated emulsion polymerization. FTIR spectra and gravimetric method results indicated that copolymers P(Styrene-M12) and P(Butylacrlate-M12) were prepared successfully by ultrasonically irradiated emulsion polymerization and the composition of M12 elevated with the increasing concentration of M12 added. TEM photographs of P(St-M12) showed that the nanoparticles with small diameters (20,45 nm) were prepared. With the increase of M12 concentration, the particle size became smaller and the size distribution became wider. The P(BA-M12) particles size was also small (<100 nm) but the size distribution was wide due to the high reactivity of BA. Because surfmer M12 was chemically bonded with the latex particles, the stability of the copolymer latex prepared by ultrasonically irradiated emulsion polymerization was much better than that of the homopolymer latex (PSt or PBA) prepared by the same way. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Effect of the carboxylic acid monomer type on the emulsifier-free emulsion copolymerization of styrene and butadieneJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007Mahdi Abdollahi Abstract Carboxylated styrene,butadiene rubber latexes were prepared through the emulsifier-free emulsion copolymerization of styrene and butadiene with various carboxylic acid monomers. The effects of various carboxylic acid monomers on the particle formation process were investigated. The type of carboxylic acid monomer strongly affected the particle nucleation. The number of particles and thus the polymerization rate increased with the increasing hydrophobicity of the carboxylic acid monomers. There was a significant difference in the polymerization rate per particle. The results showed that particle nucleation and growth were dependent on the hydrophilic nature of the carboxylic acid monomers. The average particle diameter of the carboxylated styrene,butadiene rubber latexes in the dry state was obtained through some calculations using direct measurements of the average particle diameter in the monomer-swollen state by a dynamic light scattering technique. Several parameters, such as the polymerization rate, number of latex particles per unit of volume of the aqueous phase, and polymerization rate per particle, were calculated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Miniemulsion polymerization of a fluorinated acrylate copolymer: Kinetic studies and nanolatex morphology characterizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Qinghua Zhang Abstract A stable fluoroacrylate copolymer emulsion was successfully prepared by miniemulsion polymerization with fluoroacrylate, lauryl methylacrylate, and methyl methacrylate as monomers. Extremely hydrophobic fluoroacrylate, instead of conventional cosurfactants, was used as a reactive cosurfactant to stabilize the miniemulsions. The results indicated that fluoroacrylate retarded Ostwald ripening and allowed the production of stable miniemulsions. The chemical compositions of the copolymer were studied with Fourier transform infrared and 1H-NMR. The average composition of the copolymers prepared with miniemulsions was in good agreement with the feed ratio according to 1H-NMR from the integration ratios corresponding to typical protons of the individual monomers. The particle size distribution and morphology of the latex particles were determined with laser particle analysis and transmission electron microscopy. The particle size of the latex underwent no change in the process of miniemulsion polymerization, but the particle size distributions were broader than those of conventional emulsion polymerization. The effects of various reaction parameters, including the temperature and concentrations of the emulsifier and initiator, on the miniemulsion polymerization were also investigated, and the polymerization rate and conversion increased with increasing concentrations of nonylphenol polyethoxylate (with an average of 40 ethylene oxide units per molecule), cetyltrimethylammonium, and 2,2,-azobisisobutyronitrile. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 641,647, 2007 [source] Effect of an anionic monomer on the pickering emulsion polymerization stabilized by titania hydrosolJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 21 2009Xiaomei Song Abstract Polystyrene (PS) nanocomposite particles with high titania content are prepared by Pickering emulsion polymerization. A self-made titania hydrosol modified by an anionic monomer sodium styrene sulfonate (NaSS) is used as a stabilizer and photocatalyst. The stability of the emulsion system is greatly improved by the electrostatic interaction between negatively charged NaSS and positively charged titania nanoparticles. The nanocomposite spheres with the diameter of around 120 nm are highly charged, indicating titania-rich surfaces of latex particles. It is also proven by the field-emission transmission electron microscope and field-emission scanning electron microscope images. The well-defined core-shell structure of the obtained PS/titania composite particles is confirmed by the formation of fragile hollow titania nanospheres after thermogravimetric analysis tests. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5728,5736, 2009 [source] Synthesis of stimuli-responsive macroazoinitiators and their use as an inistab toward hairy polymer latex particlesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 13 2009Syuji Fujii Abstract Stimuli-responsive macroazoinitiators with central azo unit have been synthesized by atom transfer radical polymerization (ATRP) of 2-(dimethylamino)ethyl methacrylate or 2-(diethylamino)ethyl methacrylate in 2-propanol at 25 °C. The mean degree of polymerization of the polymer chains besides the azo group was fixed between 25 and 60. 1H NMR, gel permeation chromatography, UV-Vis spectrophotometer, and surface tensiometer were used to characterize the stimuli-responsive macroazoinitiators in terms of their chemical structure, molecular weight, polydispersity, and pH-responsive behavior, respectively. Eventually, dispersion polymerization of styrene using the poly[2-(diethylamino)ethyl methacrylate] (PDEA) macroazoinitiator as an inistab (initiator + stabilizer) in 2-propanol medium was conducted. Near-monodisperse 98 nm polystyrene (PS) latex particles with pH-responsive PDEA hair were successfully synthesized. The PS latex particles with the PDEA hair can be dispersed in acidic aqueous media where the PDEA hair was protonated and was solvated, and can be flocculated in basic aqueous media where the PDEA hair was deprotonated and was precipitated. This dispersion-flocculation cycle was reversible. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3431,3443, 2009 [source] Synthesis and characterization of synthetic polymer colloids colloidally stabilized by cationized starch oligomersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 7 2009Marianne Gaborieau Abstract A method is developed for anchoring enzymatically degraded cationized starch as electrosteric stabilizers onto synthetic latices, using cerium(IV) to create free-radical grafting sites on the starch. Direct anchoring of debranched starch onto a poly(methyl methacrylate) seed latex yields a latex stabilized by well-defined oligosaccharides. Using ,-amylase to randomly cleave starch to form (1,4)-,-glucans, and a comonomer, N -isopropyl acrylamide (NIPAM), whose corresponding polymer exhibits a lower critical solution temperature (LCST), creates a means to synthesize block (or graft) oligomers of oligosaccharide and synthetic polymer, which are water soluble at room temperature. Above 30 °C, they become amphiphilic and form self-emulsifying nanoparticles (sometimes termed "frozen micelles") from which a synthetic latex is grown after addition of methyl methacrylate, the collapsed NIPAM-containing entities functioning as a type of in situ seed. This synthesis of stable synthetic latex particles is shown to have a high grafting efficiency. The starch fragments were characterized by 1H solution-state NMR before grafting, and 13C solid-state cross-polarization magic-angle spinning (CP-MAS) NMR was used to characterize the starch oligomers actually grafted on the final latex. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1836,1852, 2009 [source] Block copolymer preparation by atom transfer radical polymerization under emulsion conditions using a nanoprecipitation techniqueJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2008Delphine Chan-Seng Abstract Living-radical polymerization of acrylates were performed under emulsion atom transfer radical polymerization (ATRP) conditions using latexes prepared by a nanoprecipitation technique previously employed and optimized for the polymerization of styrene. A macroinitiator of poly(n -butyl acrylate) prepared under bulk ATRP was dissolved in acetone and precipitated in an aqueous solution of Brij 98 to preform latex particles, which were then swollen with monomer and heated. Various monomers (i.e. n -butyl acrylate, styrene, and tert -butyl acrylate) were used to swell the particles to prepare homo- and block copolymers from the poly(n -butyl acrylate) macroinitiator. Under these conditions latexes with a relatively good colloidal stability were obtained. Furthermore, amphiphilic block copolymers were prepared by hydrolysis of the tert -butyl groups and the resulting block copolymers were characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). The bulk morphologies of the polystyrene- b -poly(n -butyl acrylate) and poly(n -butyl acrylate)- b -poly(acrylic acid) copolymers were investigated by atomic force microscopy (AFM) and small angle X-ray scattering (SAXS). © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 625,635, 2008 [source] Cagelike polymer microspheres with hollow core/porous shell structuresJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2007Xiaodong He Abstract Submicron-scaled cagelike polymer microspheres with hollow core/porous shell were synthesized by self-assembling of sulfonated polystyrene (PS) latex particles at monomer droplets interface. The swelling of the PS latex particles by the oil phase provided a driving force to develop the hollow core. The latex particles also served as porogen that would disengage automatically during polymerization. Influential factors that control the morphology of the microspheres, including the reserving time of emulsions, polymerization rate, and the Hildebrand solubility parameter and polarity of the oil phase, were studied. A variety of monomers were polymerized into microspheres with hollow core/porous shell structure and microspheres with different diameters and pore sizes were obtained. The polymer microspheres were characterized by scanning electron microscopy, transmission electron microscopy, optical microscopy, and Fourier transform infrared spectroscopy. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 933,941, 2007 [source] Highly magnetic latexes from submicrometer oil in water ferrofluid emulsionsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 8 2006Franck Montagne Abstract The synthesis of functionalized submicrometer magnetic latex particles is described as obtained from a preformed magnetic emulsion composed of organic ferrofluid droplets dispersed in water. Composite (polystyrene/,-Fe2O3) particles were prepared according to a two-step procedure including the swelling of ferrofluid droplets with styrene and a crosslinking agent (divinyl benzene) followed by seeded emulsion polymerization with either an oil-soluble [2,2,-azobis(2-isobutyronitrile)] or water-soluble (potassium persulfate) initiator. Depending on the polymerization conditions, various particle morphologies were obtained, ranging from asymmetric structures, for which the polymer phase was separated from the inorganic magnetic phase, to regular core,shell morphologies showing a homogeneous encapsulation of the magnetic pigment by a crosslinked polymeric shell. The magnetic latexes were extensively characterized to determine their colloidal and magnetic properties. The desired core,shell structure was efficiently achieved with a given styrene/divinyl benzene ratio, potassium persulfate as the initiator, and an amphiphilic functional copolymer as the ferrofluid droplet stabilizer. Under these conditions, ferrofluid droplets were successfully turned into superparamagnetic polystyrene latex particles, about 200 nm in size, containing a large amount of iron oxide (60 wt %) and bearing carboxylic surface charges. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2642,2656, 2006 [source] Synthesis of an alkali-swellable emulsion and its effect on the rate of polymer diffusion in poly(vinyl acetate-butyl acrylate) latex filmsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2005Jung Kwon Oh Abstract We describe the synthesis and characterization of a weakly cross-linked poly(methacrylic acid- co -ethyl acrylate) alkali-swellable emulsion (ASE), as well as an investigation of its influence on the rate of polymer diffusion in latex films. The films examined were formed from poly(vinyl acetate- co -butyl acrylate) latex particles containing a small amount of acrylic acid as a comonomer. Polymer diffusion rates were monitored by the energy transfer technique. We found that the presence of the ASE component, either in the acid form or fully neutralized by ammonia or sodium hydroxide, had very little effect on the polymer diffusion rate. However, in the presence of 2 wt % NH4 -ASE, there was a small but significant increase in the polymer diffusion rate. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5632,5642, 2005 [source] Determination of the extent of incorporation of a reactive surfactant in polystyrene latex particles via GPCJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2005Zhen Lai The reactive surfactant HITENOL BC20 (polyoxyethylene alkylphenyl ether ammonium sulfate containing 20 units of ethylene oxide) was used in emulsion polymerizations of styrene with potassium persulfate as initiator. A new method to determine the amount of chemically bound surfactant was developed using GPC combined with UV detection as shown in the figure. Comparing this GPC method with the serum replacement/FTIR method reveals it to be a relatively simple and more effective means of characterization. [source] Microemulsion copolymerization of styrene and acrylonitrile with n -butanol as the cosurfactantJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 1 2005Yuanchang Shi Abstract The microemulsion copolymerization of styrene and acrylonitrile in an n -butanol/cetyltrimethylammonium bromide/oil/water microemulsion system was studied. The solubilization sites of the two monomers were determined with an NMR technique. The results showed that the solubilization behaviors of the two monomers were quite different. Most of the styrene was solubilized in the palisade layer of the microemulsion, whereas the acrylonitrile had an equilibrium distribution in the aqueous phase and palisade layer of the microemulsion. The reactivity ratios of styrene and acrylonitrile in the microemulsion system were different from those in other media. The effect of the monomer feed composition on the copolymerization kinetics was investigated, and the mechanism of nucleation of the latex particles was examined. The experimental results showed that the copolymerization loci were changed from the microemulsion droplets to the aqueous phase when the concentration of acrylonitrile in the monomer feed reached approximately 80%; this could be further proved by the effect of the monomer feed composition on the copolymerization kinetics. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 203,216, 2005 [source] Fluorescent polymer particles by emulsion and miniemulsion polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2003Frédéric Tronc Abstract We describe the synthesis and characterization of latex particles labeled with a brightly fluorescent yellow dye (HY) based on the benzothioxanthene ring structure. Three dye derivatives were synthesized with different spacers connecting the HY nucleus to a methacrylate group. For one of the dyes (HY2CMA, rA), we show that the reactivity ratios with styrene (rA = 0.71, rB = 0.25) and butyl methacrylate (rA = 0.87, rB = 0.14) should lead to random dye incorporation if the amount of dye in the feed is small. Seeded emulsion polymerization fails to lead to significant dye incorporation unless large amounts of nonionic surfactant are present. In contrast, miniemulsion polymerization worked well to yield latex particles of polystyrene, poly(butyl methacrylate), and poly(methyl methacrylate) with high monomer conversion and essentially quantitative dye incorporation. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 766,778, 2003 [source] Polymerizable benzophenone derivatives for labeling vinyl acetate-butylacrylate latex particlesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2002Jung Kwon Oh Abstract We describe the synthesis and characterization of three new polymerizable benzophenone derivatives [2-acryloxy-5-methyl benzophenone (8), 4,-dimethylamino-2-acryloxy-5-methyl benzophenone (9), and 4,-dimethylamino-2-(,-acryloxyethyl)oxy-5-methyl benzophenone (10)]. We show that these monomers can successfully be incorporated into vinyl acetate (VAc) copolymer latex particles. These particles were prepared by semicontinuous emulsion polymerization and mini-emulsion polymerization of VAc with butylacrylate (BA) for VAc/BA = 4/1 by weight. The two monomers 9 and 10 bearing the 4,-dimethylamino group satisfy the important spectroscopic criteria required of a dye to serve as an acceptor chromophore for nonradiative energy transfer from phenanthrene (Phe) as the donor. Their UV absorption spectra suggest significant overlap with the emission spectrum of Phe, which can be incorporated into P(VAc- co -BA) latex through copolymerization with 9-acryloxymethyl Phe (2). In addition, these chromophores provide a window in their absorption spectra for excitation of the Phe chromophore at 300 nm. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3001,3011, 2002 [source] Microemulsion polymerization of styrene stabilized by sodium dodecyl sulfate and short-chain alcoholsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 19 2001Chorng-Shyan Chern Abstract Styrene microemulsion polymerizations with different short-chain alcohols [n -CiH2i+1OH (CiOH), where i = 4, 5, or 6] as the cosurfactant were investigated. Sodium dodecyl sulfate and sodium persulfate (SPS) were used as the surfactant and initiator, respectively. The desorption of free radicals out of latex particles played an important role in the polymerization kinetics. An Arrhenius expression for the radical desorption rate coefficient was obtained from the polymerizations at temperatures of 50,70 °C. The polymerization kinetics were not very sensitive to the alkyl chain length of alcohols compared with the temperature effect. The maximal polymerization rate in decreasing order was C6OH > C4OH > C5OH. This was related to the differences in the water solubility of CiOH and the structure of the oil,water interface. The feasibility of using a water-insoluble dye to study the particle nucleation mechanisms was also evaluated. The parameters chosen for the study of the particle nucleation mechanisms include the cosurfactant type (CiOH), the SPS concentration, and the initiator type (oil-soluble 2,2,-azobisisobutyronitrile versus water-soluble SPS). © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3199,3210, 2001 [source] Surfactant characteristics of polystyrene/poly(ethylene oxide) macromonomers in aqueous solution and on polystyrene latex particles: Two-step emulsion polymerizationsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 16 2001Sebastien Gibanel Abstract Macromonomers were synthesized by anionic "living" polymerization. They comprised a poly(ethylene oxide) hydrophilic block and a hydrophobic block or sequence terminated with an unsaturation. The surface activity properties of these materials (critical micelle concentration and parking area) were determined, and the values were compared and discussed in terms of the molecular structure of these new surfactants. Some of the macromonomers were employed as emulsifiers in two-step emulsion polymerizations. The data obtained were discussed while taking into account the different chemical structures of the macromonomers and the efficiency of these species as emulsifiers in the polymerization recipes. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2767,2776, 2001 [source] | ||||||||||||||||||||||||||||||||||