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Polymerization Yield (polymerization + yield)
Selected AbstractsSynthesis by a single-step swelling process and characterization of micrometer-sized polychloromethylstyrene/poly(butyl methacrylate) hemispherical composite particles of narrow size distributionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Sigal Baruch-Sharon Abstract Polychloromethylstyrene (PCMS) micrometer-sized particles of narrow size distribution were prepared by the dispersion polymerization of chloromethylstyrene in a mixture of ethanol and dimethyl sulfoxide. Micrometer-sized PCMS/poly(butyl methacrylate) hemispherical composite particles of narrow size distribution were prepared by a single-step swelling process of the uniform PCMS template particles with emulsion droplets of butyl methacrylate (BMA) containing benzoyl peroxide, followed by the polymerization of BMA at 73°C within the swollen template particles. The effects of various polymerization parameters, for example, BMA volume, initiator type and concentration, and toluene as the swelling solvent, on the properties (size and size distribution, morphology, polymerization yield, and composition) of the hemispherical composite particles were elucidated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Water-repellent finishing of cotton fabrics by ultraviolet curingJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008F. Ferrero Abstract Cotton fabrics were water-repellent-finished by radical ultraviolet curing of silicone and urethane acrylates with different formulations. The fabrics were impregnated with undiluted resins and with toluene solutions or water emulsions. Moreover, cationic ultraviolet-curable systems were also investigated, such as an epoxy-functional polysiloxane and mixtures of an epoxy resin with hydroxyl-containing silicone additives. The gel content and polymerization yield were considered for the ultraviolet-curing process evaluation. Water-resistance properties were determined in terms of the contact angle, wettability, moisture adsorption, and water vapor permeability measurements, whereas the morphology and surface composition of treated fabrics were examined with scanning electron microscopy and energy-dispersive X-ray analysis. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Titanium-mediated [CpTiCl2(OEt)] ring-opening polymerization of lactides: A novel route to well-defined polylactide-based complex macromolecular architecturesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2010Nikolaos Petzetakis Abstract Among three cyclopentadienyl titanium complexes studied, CpTiCl2(OEt), containing a 5% excess CpTiCl3, has proven to be a very efficient catalyst for the ring-opening polymerization (ROP) of L -lactide (LLA) in toluene at 130 °C. Kinetic studies revealed that the polymerization yield (up to 100%) and the molecular weight increase linearly with time, leading to well-defined PLLA with narrow molecular weight distributions (Mw/Mn , 1.1). Based on the above results, PS- b -PLLA, PI- b -PLLA, PEO- b -PLLA block copolymers, and a PS- b -PI- b -PLLA triblock terpolymer were synthesized. The synthetic strategy involved: (a) the preparation of OH-end-functionalized homopolymers or diblock copolymers by anionic polymerization, (b) the reaction of the OH-functionalized polymers with CpTiCl3 to give the corresponding Ti-macrocatalyst, and (c) the ROP of LLA to afford the final block copolymers. PMMA- g -PLLA [PMMA: poly(methyl methacrylate)] was also synthesized by: (a) the reaction of CpTiCl3 with 2-hydroxy ethyl methacrylate, HEMA, to give the Ti-HEMA-catalyst, (b) the ROP of LLA to afford a PLLA methacrylic-macromonomer, and (c) the copolymerization (conventional and ATRP) of the macromonomer with MMA to afford the final graft copolymer. Intermediate and final products were characterized by NMR spectroscopy and size exclusion chromatography, equipped with refractive index and two-angle laser light scattering detectors. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1092,1103, 2010 [source] Monitoring ultrathin film photopolymerization of tetra-alkylepoxyporphyrin by UV-Vis spectroscopyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2009Kalle Lintinen Abstract Cationic photopolymerization is a convenient in situ polymerization method for organic thin film preparation. In this work, the polymerization mechanisms is applied for highly viscous cross-linking monomers, using tetra-alkylepoxyporphyrin (TAEP) as a case study. By comparing the UV-Vis spectra of the polymerized sample before and after the unreacted monomers have been dissolved, it is possible to estimate the polymerization yield. An IR spectrum of a reference thick film confirms full polymerization. Scanning fluorescence lifetime microscopy and AFM show the uniformity of the polymer. It was shown that photopolymerization is highly dependent on the substrate nature and requires at best case a 10 min illumination at 90 °C. Thermal polymerization of the same sample requires 10 min heating at 150 °C in dark. It was also shown that TAEP works as a self-sensitizer for cationic photopolymerization. The proposed method is a mild and versatile technique for in situ preparation of thin polymeric films directly from chromophore monomers. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6095,6103, 2009 [source] Dispersion polymerization of styrene in carbon dioxide stabilized by copolymers of poly(propylene glycol) methacrylate and 2-(perfluorooctyl)ethyl methacrylateJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 23 2003Lunhan Ding Abstract The dispersion polymerization of styrene in carbon dioxide with a series of copolymers of poly(propylene glycol) methacrylate (PPGMA) and 2-(perfluorooctyl)ethyl methacrylate (FOEMA) as the polymerization dispersants was examined. It was demonstrated that PPGMA and FOEMA copolymers and polymers containing 52,100% FOEMA could be used as effective dispersants for the polymerization, and the composition of the copolymeric dispersant had a dramatic effect on both the polymerization yield and the morphology of the resulting polystyrene. The effects of the concentrations of the copolymeric dispersants, the concentrations of the monomer, and the reaction pressure were also investigated. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3804,3815, 2003 [source] Preparation and characterization of soluble terpolymers from m -phenylenediamine, o -anisidine, and 2,3-xylidineJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2001Xin-Gui Li Abstract A series of terpolymers were synthesized by the chemical oxidative polymerization of m -phenylenediamine (MPD), o -anisidine (AS), and 2,3-xylidine (XY) in hydrochloride aqueous medium. The yield, intrinsic viscosity, and solubility of the terpolymers were studied by changing the MPD/AS/XY molar ratio from 100/0/0 to 53/39/8 to 0/100/0. It was discovered that the MPD/AS/XY terpolymers exhibit a higher polymerization yield and better solubility than MPD/AS and MPD/XY bipolymers having the same MPD molar content. The as-prepared MPD/AS/XY terpolymer bases were characterized by Fourier transform infrared, ultraviolet,visible, 1H NMR, and high-resolution solid-state 13C NMR spectroscopies; wide-angle X-ray diffraction; and thermogravimetry. The results suggested that the oxidative polymerization from MPD, AS, and XY is exothermic, and the resulting terpolymers are more easily soluble in some organic solvents than MPD homopolymer. The copolymer obtained was a real terpolymer containing MPD, AS, and XY units, and the actual MPD/AS/XY molar ratio calculated by solid-state 13C NMR spectra of the polymers is very close to the feed ratio, although the AS content calculated on the basis of the 1H NMR spectrum of the soluble part of the polymer is higher than the feed AS content. The terpolymers and MPD homopolymer exhibit a higher polymerization yield and much higher intrinsic viscosity and are more amorphous than the AS homopolymer. At a fixed MPD content of 70 mol %, the terpolymers exhibit an increased thermostability and activation energy of the major degradation in nitrogen and air with an increasing AS content. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3989,4000, 2001 [source] Cyclodextrins in Polymer Synthesis: Enzymatic Polymerization of a 2,6-Dimethyl- , -Cyclodextrin/2,4-Dihydroxyphenyl-4,-Hydroxybenzylketone Host-Guest Complex Catalyzed by Horseradish Peroxidase (HRP)MACROMOLECULAR BIOSCIENCE, Issue 8 2003Lorenzo Mejias Abstract This paper reports the enzymatic polymerization of the inclusion complex 2,4-dihydroxyphenyl-4,-hydroxybenzylketone/2,6-dimethyl- , -cyclodextrin by horseradish peroxidase (HRP) in aqueous media. The structure of the complex was determined by means of NOESY-NMR and crystallographic analysis (indicating an orthorhombic structure). The enzymatic polymerization of the uncomplexed 2,4-dihydroxyphenyl-4,-hydroxybenzylketone yields oligomers with molecular weights up to in organic-aqueous media, but because of its poor solubility in aqueous systems, no polymerization is observed if water is used as solvent. An increase of the availability of the ketone in solution is achieved by complexing it with random-methylated , -cyclodextrin in water. We found that the use of methylated , -cyclodextrin in equimolar concentration to the monomer increases the polymerization yield and the average molecular weight. The polymers formed were analyzed by GPC and ATR-FTIR techniques. Representation from X-ray diffraction analysis of the 2,6-dimethyl- , -cyclodextrin/2,4-dihydroxyphenyl-4,-hydroxybenzylketone host-guest complex (3). [source] Ring-opening metathesis polymerization of cyclododecene using an electrochemically reduced tungsten-based catalystAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 8 2004Solmaz Karabulut Abstract The ring-opening metathesis polymerization of cyclododecene using an electrochemically reduced tungsten-based catalyst (WCl6e,AlCH2Cl2) is described. In addition, the influence of reaction conditions on the polymerization yield was determined. The resulting polymer has been characterized by NMR, IR, gel permeation chromatography and differential scanning calorimetry. The glass transition temperature and melting point of the polydodecenamer are 19.6°C and 70.0°C respectively. Furthermore, cyclododecene has been polymerized into a low-molecular-weight polymer (12.0 × 103) with a polydispersity of 2.06 in high yields (94%). IR and NMR analysis indicate that the polydodecenamer has a high trans content (60%). Copyright © 2004 John Wiley & Sons, Ltd. [source] Facile High-Yield Synthesis of Polyaniline Nanosticks with Intrinsic Stability and Electrical ConductivityCHEMISTRY - A EUROPEAN JOURNAL, Issue 33 2008Xin-Gui Li Prof. Abstract Chemical oxidative polymerization at 15,°C was used for the simple and productive synthesis of polyaniline (PAN) nanosticks. The effect of polymerization media on the yield, size, stability, and electrical conductivity of the PAN nanosticks was studied by changing the concentration and nature of the acid medium and oxidant and by introducing organic solvent. Molecular and supramolecular structure, size, and size distribution of the PAN nanosticks were characterized by UV/Vis and IR spectroscopy, X-ray diffraction, laser particle-size analysis, and transmission electron microscopy. Introduction of organic solvent is advantageous for enhancing the yield of PAN nanosticks but disadvantageous for formation of PAN nanosticks with small size and high conductivity. The concentration and nature of the acid medium have a major influence on the polymerization yield and conductivity of the nanosized PAN. The average diameter and length of PAN nanosticks produced with 2,M HNO3 and 0.5,M H2SO4 as acid media are about 40 and 300,nm, respectively. The PAN nanosticks obtained in an optimal medium (i.e., 2,M HNO3) exhibit the highest conductivity of 2.23,S,cm,1 and the highest yield of 80.7,%. A mechanism of formation of nanosticks instead of nanoparticles is proposed. Nanocomposite films of the PAN nanosticks with poly(vinyl alcohol) show a low percolation threshold of 0.2,wt,%, at which the film retains almost the same transparency and strength as pure poly(vinyl alcohol) but 262,000 times the conductivity of pure poly(vinyl alcohol) film. The present synthesis of PAN nanosticks requires no external stabilizer and provides a facile and direct route for fabrication of PAN nanosticks with high yield, controllable size, intrinsic self-stability, strong redispersibility, high purity, and optimizable conductivity. [source] Poly(ethylene glycol)-based amphiphilic model conetworks: Synthesis by RAFT polymerization and characterizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2008Mariliz Achilleos Abstract Poly(ethylene glycol) (PEG)-containing quasi-model amphiphilic polymer conetworks (APCNs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization using ,,,-bis(2-cyanoprop-2-yl dithiobenzoate)-PEG as a bifunctional RAFT macrochain transfer agent (macro-CTA) and stepwise additions of a hydrophobic monomer and a crosslinker (crosslinker: macro-CTA = 10:1, reaction time 24 h). Three different types of monomers, methyl methacrylate (MMA), n -butyl acrylate and styrene, were employed as the hydrophobic monomers, whereas ethylene glycol dimethacrylate, ethylene glycol diacrylate and 1,4-divinylbenzene served as the respective crosslinkers. PEG homopolymer hydrophilic quasi-model networks were also prepared by RAFT-polymerizing the three crosslinkers directly onto the two active ends of the PEG-based macro-CTA. From the three ABA triblock copolymers prepared, the MMA-containing one was obtained at the highest polymerization yields. The crosslinking yields of the three ABA triblock copolymers with the corresponding crosslinkers were higher than those of the PEG-based macro-CTA with the same crosslinkers. The degrees of swelling (DSs) of all conetworks were measured in water and in tetrahydrofuran (THF). The DSs of the APCNs in THF were higher than those in water, whereas the reverse was true for the DSs of the hydrophilic homopolymer networks. Finally, the aqueous DSs of the APCNs were lower than those of the corresponding hydrophilic homopolymer networks. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7556,7565, 2008 [source] | |||||||||||||