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Ammonium Persulfate (ammonium + persulfate)
Selected AbstractsEcofriendly Solid-State Oxidative Deprotection of 1,3-Dithianes and 1,3-Dithiolanes Using Ammonium Persulfate on Wet Montmorillonite K-10 Clay Support under Microwave Irradiation.CHEMINFORM, Issue 30 2004Nemai C. Ganguly Abstract For Abstract see ChemInform Abstract in Full Text. [source] Synthesis of Poly(3,4-ethylenedioxythiophene) latexes using poly(N -vinylpyrrolidone)-based copolymers as reactive stabilizersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2010Muhammad Mumtaz Abstract The synthesis by oxidative polymerization of well-defined poly(3,4-ethylenedioxythiophene) (PEDOT) nano-objects in the presence of modified and unmodified poly(N -vinylpyrrolidone)-based copolymers used as stabilizers in aqueous media is reported. Ammonium persulfate or a mixture of ammonium persulfate with CuCl2 or CuBr2 was used as oxidants. The effects of several parameters such as the molar mass and the concentration of the stabilizer as well as the nature of the oxidants on the size, morphology, and the conductivity of the PEDOT particles have been investigated. The distribution of the reactive moieties along the copolymer stabilizer backbone was shown to be crucial to get well-defined PEDOT nano-objects. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3841,3855, 2010 [source] One-Pot Three-Step Synthesis of Naphtho[2,3- a]carbazole- 5,13-diones using a Tandem Radical Alkylation,Cyclization, Aromatization Reaction SequenceADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 5 2010Chunyong Ding Abstract A three-step, one-pot tandem reaction including radical nucleophilic alkylation/cyclization/aromatization was developed using 0.3 equivalents of silver(I) acetate (AgOAc) as the catalyst and 2 equivalents of ammonium persulfate [(NH4)2S2O8] as the oxidant. This strategy is highly efficient for the assembly of pentacyclic complex carbazoles from aryl-fused bromobenzoquinones and indol-3-ylpropanoic acid acids in 52,72% overall yields (three steps). This new approach provides a significant improvement over the previously reported methods and would greatly facilitate analog library construction of pentacyclic complex carbazoles and benefit further biological evaluation of these compounds. [source] A fluorescence study on swelling of hydrogels (PAAm) at various cross-linker contentsADVANCES IN POLYMER TECHNOLOGY, Issue 4 2009Demet Kaya Akta Abstract Disk-shaped acrylamide (AAm) gels were prepared from AAm with various N,N,-methylenebisacrylamide (Bis) contents as cross-linker in the presence of ammonium persulfate as an initiator by free-radical cross-linking copolymerization in water. Polyacrylamide (PAAm) gels were dried before using for swelling experiments. Steady-state fluorescence spectrometer was employed during the swelling of PAAm hydrogels in water. Pyranine was introduced as a fluorescence probe. Fluorescence intensity of pyranine from various Bis content gel samples was measured during in situ swelling process. It was observed that fluorescence intensity decreased as swelling has proceeded. Gravimetric and volumetric experiments were also performed. The Li,Tanaka equation was used to determine the swelling time constants, ,c, and cooperative diffusion coefficients, Dc, from intensity, weight, and volume variations during the swelling processes. It was observed that swelling time constants, ,c, increased and diffusion coefficients, Dc, decreased as the cross-linker content was increased. © 2010 Wiley Periodicals, Inc. Adv Polym Techn 28:215,223, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20163 [source] Comparison of poly(o -anisidine) and poly(o -anisidine- co -aniline) copolymer synthesized by chemical oxidative methodJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010J. Longun Abstract In this study, poly(o -anisidine) [POA], poly(o -anisidine- co -aniline) [POA- co -A], and polyaniline [PANi] were chemically synthesized using a single polymerization process with aniline and o -anisidine as the respective monomers. During the polymerization process, p -toluene sulfonic acid monohydrate was used as a dopant while ammonium persulfate was used as an oxidant. N -methyl-pyrolidone (NMP) was used as a solvent. We observed that the ATR spectra of POA- co -A showed features similar to those of PANi and POA as well as additional ones. POA- co -A also achieved broader and more extended UV,vis absorption than POA but less than PANi. The chemical and electronic structure of the product of polymerization was studied using Attenuated Total Reflectance spectroscopy (ATR) and UV,visible spectroscopy (UV,vis). The transition temperature of the homopolymers and copolymers was studied using differential scanning calorimetry and the viscosity average molecular weight was studied by using dilute solution viscometry. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Stability study of inverse suspension copolymerization of 1,1,3,3-tetramethylguandium acrylate and N,N, -methylenebisacrylamideJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010Jie Dong Abstract In a previous study, we synthesized crosslinked P(TMGA- co -MBA) via an inverse suspension copolymerization of 1,1,3,3-tetramethylguandium acrylate (TMGA) and N,N,-methylenebisacrylamide (MBA) and found that the product is a good SO2 sorbent. However, the polymerization stability appeared to be poor under some reaction conditions and is far from being elucidated. In this study, the inverse suspension copolymerization was carried out using cyclohexane as solvent, Span60 as dispersant, and ammonium persulfate (APS) as initiator. The effects of the reaction conditions such as stirring speed, dispersant concentration, and temperature on the polymerization stability and particle size were systematically examined. It is found that the polymerization stability is a strong function of these parameters. Stable crosslinked poly(TMGA- co -MBA) particles from micrometer to millimeter diameters were synthesized under optimized conditions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Preparation and self-assembly of polyaniline nanorods and their application as electroactive actuatorsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Seong Hun Kim Abstract To improve the performance of ion-exchange polymer,metal composite (IPMC) actuators, an electrical pathway material for enhancing the surface adhesion between the membrane and the metal electrodes of the IPMC was studied. As an efficient electrical pathway material, polyaniline nanorods (PANI-NRs) doped with p -toluene sulfonic acid (TSA) were synthesized with a template-free method. The factors affecting polyaniline morphology were studied with various dopant concentrations and oxidant feeding rates. Highly conductive PANI-NRs were formed when they were synthesized with ammonium persulfate at a 5.0 mL/min oxidant feeding rate and doped with 0.125M TSA. The conductivity of the PANI-NRs was 1.15 × 10,1 S/cm, and their diameters and lengths were 120,180 nm and 0.6,2 ,m, respectively. To apply the membrane as an actuator, perfluorosulfonated ionomer (Nafion)/PANI-NR blends were prepared by solution blending and casting. The actuating ability of the three-layered membrane consisting of Nafion/PANI-NR blends was then examined and compared with that of Nafion only. The actuating ability of the IPMC was improved when Nafion/PANI-NRs were used as electrical pathways. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Kinetics of methyl methacrylate grafting polymerization onto flaky aluminum powderJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Hui Liu Abstract With ammonium persulfate (APS) as the initiator, the kinetics of methyl methacrylate (MMA) grafting polymerization onto flaky aluminum powder (Al) was studied. It was found that the experimental apparent grafting polymerization rate, Rg = KC × C × C, was basically consistent with the theoretical result based on the theory of stable polymerization and equivalent activity, Rg = KC × C × CMMA. The activation energy of grafting, homogenous, and total polymerization rate was calculated as 65.1, 35.4, and 37.5 kJ mol,1, respectively. It could be validated that the relationship among these activation energies accorded with the theoretical result of parallel reactions. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Synthesis of higher soluble nanostructured polyaniline by vapor-phase polymerization and determination of its crystal structureJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2009Sambhu Bhadra Abstract Higher soluble nanostructured polyaniline was prepared by vapor-phase polymerization after passing aniline vapor through an aqueous acidic solution of ammonium persulfate (PANI-V). Polyaniline was also synthesized by the conventional oxidative polymerization method (PANI-C) in an aqueous medium for the comparison of its properties with PANI-V. PANI-V exhibited lower conductivity but higher hydrophilicity and higher solubility (2,3 times) in different solvents, such as tetrahydrofuran, N -methyl-2-pyrrolidone, dimethylsulfoxide, N,N -dimethyl formamide, and m -cresol at room temperature compared with that of PANI-C. The thermal stability of PANI-V was higher than that of PANI-C. In-depth investigations of the crystal structures of PANI-C and PANI-V were performed through powder X-ray diffraction analysis. The PANI-V showed a less ordered structure with a lower crystallinity and crystallite size and with a higher d-spacing and interchain separation compared with PANI-C. The unit cell volume of PANI-V was significantly higher with a greater number of atoms in the unit cell than that of PANI-C. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Swelling properties of CMC- g -poly (AAm- co -AMPS) superabsorbent hydrogelJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2009Ali Pourjavadi Abstract A series of biopolymer-based superabsorbent hydrogels based on carboxymethyl cellulose has been prepared by free-radical graft copolymerization of acrylamide and 2-acrylamido-2-methylpropan sulfonic acid (AMPS) in aqueous solution using methylenebisacrylamide as a crosslinking agent and ammonium persulfate as an initiator. The effect of variables on the swelling capacity such as: acrylamide/AMPS weight ratio, reaction temperature, and concentration of the initiator and crosslinker were systematically optimized. The results indicated that with increasing the amount of AMPS, the swelling capacity is increased. FT-IR spectroscopy and scanning electron microscope analysis were used to confirm the hydrogel structure. Swelling measurements of the synthesized hydrogels in different salt solutions indicated considerable swelling capacity. The absorbency under load of the superabsorbent hydrogels was determined by using an absorbency under load tester at various applied pressures. A preliminary swelling and deswelling behaviors of the hydrogels were also studied. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] A study in the uranyl ions uptake on acrylic acid and acrylamide copolymeric hydrogelsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Ghanshyam S. Chauhan Abstract A series of copolymeric hydrogels comprising of acrylic acid and acrylamide and crosslinked with trimethylolpropane triacrylate (TMPTA) were prepared using ammonium persulfate (APS) as initiator. The hydrogels were functionalized further by partial hydrolysis and were characterized by SEM, FTIR, nitrogen analysis, and also by water uptake studies as a function of time, temperature, pH, NaCl, and concentration of sodium dodecyl sulfate (SDS). These hydrogels were used as sorbents for the uranyl ions uptake in the presence of 5% NaCl, which was studied as function of time, temperature, pH, and ion strength. The uranyl uptake was found to be affected both by the structural aspects of the hydrogels as well as by the external environmental factors. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Photoinitiating polymerization to prepare biocompatible chitosan hydrogelsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Xiaohong Hu Abstract Chitosan hydrogels were prepared from water soluble chitosan derivatives (chitosan-MA-LA, CML) by photoinitiating polymerization under the existence of Irgacure2959 and the irradiation of UV light. The CML was obtained by amidation of the amine groups of chitosan with lactic acid and methacrylic acid. Gelation time of the hydrogel could be adjusted within a range of 5,50 min, and controlled by factors such as the degree of MA substitution, initiator concentration, existence of oxygen, and salt. The dry hydrogel adsorbed tens to hundred times of water, forming a highly hydrated gel. The swelling ratio was smaller at the higher degree of MA substitution, higher pH, and higher salt concentration. Rheological test showed that the hydrogel is elastomeric in the measuring frequency range, with a storage modulus and loss modulus of 0.8,7 kPa and 10,100 Pa, respectively. In vitro culture of chondrocytes demonstrated that the cells could normally proliferate in the extractant of the hydrogels, showing no cytotoxicity at lower initiator concentration. By contrast, the extractant of the hydrogel made by the redox initiating system, i.e., ammonium persulfate (APS) and N,N,N,,N,-tetramethylethylenediamine (TEMED), showed apparent cytotoxicity. Thus, the chitosan hydrogels initiated by the Irgacure2959 have better comprehensive properties, in particular better biocompatibility, and are more suitable for biomedical applications. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Grafting emulsion polymerization of glycidyl methacrylate onto leather by chemical initiation systemsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008K. A. Shaffei Abstract The kinetics of the grafting polymerization of glycidyl methacrylate (GMA) onto leather were studied with chemical initiation systems. The results showed that the rate of grafting of GMA onto leather was dependent on different rates in the chemical initiation systems; for ammonium persulfate (AmPS)/acetone sodium bisulfite (ASBS), potassium persulfate (PPS)/ASBS, and sodium persulfate (SPS)/ASBS, the powers were 1.06, 0.48, and 0.43 and 0.63, 0.46, and 0.43, respectively, with respect to the concentration of the emulsifier sodium dodecyl sulfate, whereas the powers were 1.41, 0.70, and 0.81, respectively, with respect to the monomer concentration. The apparent activation energy was calculated for each initiation system and was found to be 180.8, 361.63, and 542.45 kcal for the AmPS/ASBS, PPS/ASBS, and SPS/ASBS systems, respectively. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Synthesis, characterization, and antimicrobial properties of novel quaternary amine methacrylate copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Supriya Punyani Abstract A novel amine methacrylate monomer trimethylolpropane trimethacrylate,piperazine,ethyleneglycol dimethacrylate (TMPTMA-PPZ-EGDMA) was synthesized by amination of trimethylolpropane trimethacrylate (TMPTMA) with excess of piperazine (PPZ) followed by reaction with ethyleneglycol dimethacrylate (EGDMA). Copolymerization of TMPTMA-PPZ-EGDMA with 2-hydroxyethyl methacrylate (HEMA) was carried out by free radical polymerization using ammonium persulfate (APS) and N,N,N,,N,-tetramethyl ethylenediamine (TEMED) as a redox initiator. The copolymers obtained were then quaternized with 1-iodooctane. The monomers were characterized by FTIR and 1H NMR spectral studies. The molecular weights and polydispersity values of the monomers were determined with gel permeation chromatography. Quaternized copolymers containing more than 20% amine methacrylate monomer showed microporosity in the range of 9.9,10.4 ,m. The antibacterial activity of the quaternized copolymers against Escherichia coli and Staphylococcus aureus was studied using UV,vis spectrophotometer and scanning electron microscopy. Quaternized copolymers showed broad-spectrum contact-killing antibacterial properties without releasing any active agent as checked by iodide selective ion meter. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Detection of creatinine enriched on a surface imprinted polystyrene film using FT-ATR-IRJOURNAL OF MOLECULAR RECOGNITION, Issue 5 2006K. Sreenivasan Abstract The surface of polystyrene (PS) was chemically modified by coating a thin layer of polyaniline (PANI) by oxidizing aniline using ammonium persulfate. Affinity sites for creatinine, a clinically relevant molecule, were created in the coated layer by adding creatinine as print molecules during the oxidation. The imprinted layer adsorbed creatinine was compared to non-imprinted surface reflecting the creation of creatinine-specific sites on the surface. The equilibrium was attained rapidly, indicating that a material of this kind is suitable for sensing applications. The adsorbed creatinine on the surface was detected using the technique of Fourier transform attenuated total internal reflection infra red spectroscopy (FT-ATR-IR). The results show that molecularly imprinted surface can enrich molecules of interest and the enriched molecules can be detected using FT-IR. Copyright © 2006 John Wiley & Sons, Ltd. [source] Synthesis of Poly(3,4-ethylenedioxythiophene) latexes using poly(N -vinylpyrrolidone)-based copolymers as reactive stabilizersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2010Muhammad Mumtaz Abstract The synthesis by oxidative polymerization of well-defined poly(3,4-ethylenedioxythiophene) (PEDOT) nano-objects in the presence of modified and unmodified poly(N -vinylpyrrolidone)-based copolymers used as stabilizers in aqueous media is reported. Ammonium persulfate or a mixture of ammonium persulfate with CuCl2 or CuBr2 was used as oxidants. The effects of several parameters such as the molar mass and the concentration of the stabilizer as well as the nature of the oxidants on the size, morphology, and the conductivity of the PEDOT particles have been investigated. The distribution of the reactive moieties along the copolymer stabilizer backbone was shown to be crucial to get well-defined PEDOT nano-objects. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3841,3855, 2010 [source] Modification of multiwall carbon nanotubes via soap-free emulsion polymerization of acrylonitrileJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 10 2010Zhenping Cheng Abstract A novel method for the synthesis of polyacrylonitrile (PAN)-coated multiwall carbon nanotubes (MWCNTs) via a simple soap-free emulsion polymerization is presented for the first time. The polymerization was initiated with conventional anionic ammonium persulfate (APS) at 65 °C. The modification of PAN on MWCNT surfaces was confirmed by Fourier-transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectra (XPS), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), and Raman spectroscopy. It is found that all the surfaces of the MWCNTs were coated by PAN chains, and the PAN coating thickness could be controlled by simply adjusting the polymerization time. The obtained PAN-coated MWCNTs could be well dispersed in water. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2057,2062, 2010 [source] Frontal free-radical copolymerization of urethane,acrylatesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 9 2006Ting Hu Abstract We report the first synthesis of urethane,acrylate copolymers via free-radical frontal polymerization. In a typical run, the appropriate amounts of the reactants (urethane,acrylate macromonomer and 2-hydroxyethyl acrylate) and initiator (ammonium persulfate) were dissolved in dimethyl sulfoxide. Frontal polymerization was initiated by the heating of the wall of the tube with a soldering iron, and the resultant hot fronts were allowed to self-propagate throughout the reaction vessel. Once it was initiated, no further energy was required for the polymerization to occur. The dependence of the front velocity and front temperature on the initiator concentration was investigated. The front temperatures were between 55 and 65 °C, depending on the persulfate concentration. Thermogravimetric analysis indicated that the urethane,acrylate copolymers had higher thermal stability than pure frontally prepared polyurethane. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3018,3024, 2006 [source] Synthesis and characterization of electrically conducting poly(o -/m -toluidine- co - o -/m -aminoacetophenone) copolymersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2004P. Savitha Abstract A series of poly(o -/m -toluidine- co - o -/m -aminoacetophenone) copolymers combining the features of high conductivity and processibility are synthesized and characterized by a number of techniques including 1H NMR; thermogravimetry; IR, Raman, and UV,visible spectroscopy; scanning electron microscopy; and X-ray diffraction. The copolymers are synthesized by the emulsion and inverse emulsion methods using conventional ammonium persulfate and a new oxidant, benzoyl peroxide, respectively. The influence of the polymerization conditions such as the monomer feed ratios, solvent, and the nonsolvent is investigated. The composition of the resulting copolymers is determined by 1H NMR analysis. The conductivity of the copolymers varies with the aminoacetophenone content in the feed and the polymerization conditions. It is interesting that the conductivity of the copolymers is higher than that of the corresponding homopolymers. The results are rationalized on the basis of the effect of the COCH3 substituent on the polymer structure. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4300,4310, 2004 [source] Morphology and temperature responsiveness,swelling relationship of poly(N -isopropylamide,chitosan) copolymers and their application to drug releaseJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2004Chia-Fen Lee Abstract Poly [N -isopropylacrylamide (NIPAAm),chitosan] crosslinked copolymer particles were synthesized by soapless emulsion copolymerization of NIPAAm and chitosan. An anionic initiator [ammonium persulfate (APS)] and a cationic initiator [2,2,-azobis(2-methylpropionamidine)dihydrochloride (AIBA)] were used to initiate the reaction of copolymerization. The chitosan,NIPAAm copolymer synthesized by using APS as the initiator showed a homogeneous morphology and exhibited the characteristic of a lower critical solution temperature (LCST). The copolymer synthesized by using AIBA as an initiator showed a core,shell morphology, and the characteristic of LCST was insignificant. The LCST of the chitosan,NIPAAm copolymer depended on the morphology of the copolymer particles. In addition, the chitosan,NIPAAm copolymer particles were processed to form copolymer disks. Then, the effect of various variables such as the chitosan/NIPAAm weight ratio, the concentration of crosslinking agent, and the pH values on the swelling ratio of chitosan,NIPAAm copolymer disks were investigated. Furthermore, caffeine was used as the model drug to study the characteristics of drug loading of the chitosan,NIPAAm copolymer disks. Variables such as the chitosan/NIPAAm weight ratio and the concentration of the crosslinking agent significantly influenced the behavior of caffeine loading. Two factors (pore size and swelling ratio) affected the behavior of caffeine release from the chitosan,NIPAAm copolymer disks. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3029,3037, 2004 [source] Macroporous molecularly imprinted monolithic polymer columns for protein recognition by liquid chromatographyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 17-18 2010Jinxiang Liu Abstract Macroporous cytochrome c (cyc)-imprinted monolithic polyarylamide columns were prepared, and applied for the template protein recognition by HPLC. With cyc (18.8,mg) as template, the imprinted monolithic materials were in situ polymerized in an HPLC column tube, with methacrylamide (450,mg), methacrylic acid (15.8,mg), piperazine diacrylamide (720,mg) and ammonium sulfate (390,mg) dissolved in 5,mL of phosphate buffer (pH 7.4), initiated by ammonium persulfate and TEMED. After the reaction, cyc was removed with acetic acid (10%, v/v) containing 10%,w/v SDS. The non-imprinted monolithic column was prepared under the same procedure except without cyc. Retention of cyc and its competitive protein, lysozyme (lys), on molecular-imprinting polymer (MIP) and non-imprinted polymer columns was studied. When the pH value of mobile phase was 4.0, on MIP column, the retention factors of cyc and lys were 2.0 and 1.3, respectively. However, those on non-imprinted polymer column were very similar, both as 1.1. Even in competitive environment, a mixture of cyc and lys could be separated on MIP column under gradient elution, with resolution as 1.2. These results indicate that protein-imprinted monolithic polymer columns could offer obvious affinity and specific recognition to the template protein. [source] A Scalable Route to Highly Functionalized Multi-Walled Carbon Nanotubes on a Large ScaleMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 8 2008Xianhong Chen Abstract A scalable and solvent-free chemical process to obtain highly functionalized and dispersible multi-walled carbon nanotubes is reported. Highly functionalized multi-walled carbon nanotubes have been prepared using in situ generated aryl diazonium salts in the presence of ammonium persulfate and 2,2,-azoisobutyronitrile by solvent-free techniques. In the Raman spectra of the resulting materials, characteristic peaks, the D- and G-bands, are shifted by about 10 cm,1 to lower frequencies. At the same time, the relative intensity ratios between the D- and G-bands increase in comparison to that in the spectrum of the purified product. Fourier-transform infrared spectroscopy reveals the presence of the functional groups on the surface. Transmission electron microscopy images directly confirm the significant build-up of sidewall organic moieties on the treated materials. The weight loss of various functional moieties determined by thermogravimetry,differential scanning calorimetry analysis is about 18,33%. The dispersibility of the functionalized materials in solvents, such as chloroform, tetrahydrofuran, and water, is obviously improved. [source] Study on Superabsorbent Composite, 14MACROMOLECULAR MATERIALS & ENGINEERING, Issue 12 2006Preparation of Poly(acrylic acid)/Organo-attapulgite Composite Hydrogels, Swelling Behaviors in Aqueous Electrolyte Solution Abstract Summary: Organo-attapulgite (organo-APT) was prepared by modifying APT using four quaternary ammonium salts with various lengths of the alkyl group, including (octyl)trimethylammonium bromide (OTMABr) and (stearyl)trimethylammonium chloride (STMACl), etc. A series of composite hydrogels, poly(acrylic acid)/organo-APT, from acrylic acid (AA), and organo-APT was prepared by aqueous polymerization, using N,N, -methylenebisacrylamide (MBA) as a crosslinker and ammonium persulfate (APS) as an initiator. The organification and organification degree of APT as well as the corresponding composites were characterized by FTIR, TGA, and XRD. The effects of the length of the alkyl group for different quaternary ammonium salts, organification degree of APT, and organo-APT content on water absorbency and swelling behaviors in various electrolyte solutions were investigated in this study. Equilibrium water absorbency strongly depends on chain length of the alkyl group of quaternary ammonium salts, organification degree of APT as well as organo-APT content. Longer alkyl group, higher organification degree, and proper organo-APT content are of benefit for the improvement of equilibrium water absorbency. Equilibrium water absorbency in distilled water for PAA/APT was enhanced from 350.1 to 562.1 g,·,g,1 after 10 wt.-% organo-APT, modified with STMACl for the highest degree, was introduced. The kind of cation is the key factor influencing equilibrium water absorbency of these composite hydrogels in electrolyte solutions. Organification of APT could enhance responsiveness of the corresponding composite hydrogel to electrolyte solutions. Schematic structure of PAA/organo-APT composite in a dry state (left) and in a swollen state (right). [source] Synthesis of PEDOT Nanoparticles and Vesicles by Dispersion Polymerization in Alcoholic MediaMACROMOLECULAR RAPID COMMUNICATIONS, Issue 17 2006Muhammad Mumtaz Abstract Summary: The synthesis of PEDOT nanoparticles and vesicles by dispersion polymerization in a methanol/water mixture (3/2, v/v) is reported, using either ammonium persulfate or iron(III) p -toluenesulfonate as oxidants and , -EDOT-PEO as a reactive stabilizer. The influence of the oxidant as well as the , -EDOT-PEO molar mass and concentration on the core-shell particle morphology and conductivity properties have been investigated. PEDOT particles with conductivities up to 1.5,×,10,2 S,·,cm,1 have been obtained in high yield. TEM image of PEDOT vesicles prepared using PEO-based stabilizers of 25,000 g,·,mol,1 in water/methanol mixture (2:3 v/v) at room temperature using ammonium persulfate as an oxidant. [source] Nanoscaled Polyaniline Fibers Prepared by Ferric Chloride as an OxidantMACROMOLECULAR RAPID COMMUNICATIONS, Issue 5 2006Lijuan Zhang Abstract Summary: Nanoscaled polyaniline (PANI) fibers with 17,30 nm in diameter were successfully prepared by oxidation polymerization using ferric hydrochloride (FeCl3,·,6H2O) as an oxidant in the presence of p -toluenesulfonic acid (p -TSA), , -naphthalenesulfonic acid (, -NSA), and camphorsulfonic acid (CSA) as the dopants. The resulting nanofibers show smaller diameter, higher crystallinity and conductivity (10,1 S,·,cm,1) compared with the nanofibers oxidized by ammonium persulfate (APS), which may be due to the lower oxidation/reduction potential of FeCl3. SEM images of the PANI nanofibers prepared by oxidation polymerization using ferric hydrochloride as an oxidant. [source] Novel Method of Producing Polymer Gels in Aqueous Solution Using UV IrradiationMACROMOLECULAR RAPID COMMUNICATIONS, Issue 16 2004Fumiyoshi Ikkai Abstract Summary: We developed a novel method of producing polymer gels in aqueous solution using UV irradiation. Persulfates were effective photosensitive initiators of polymerization and/or gelation of acryloyl-type monomers/polymers. The gelation was confirmed by an abrupt increase in light scattering intensity, ,I(q),T, at the gelation point. The gelation method entails significant advantages: it does not need any cross-linkers, temperature control (heating), and additives except the persulfate. The UV irradiation time dependence of light scattering intensity, ,I(q),T, for pre-gel solutions containing N -isopropylacrylamide (NIPAm) and/or ammonium persulfate (APS). [source] Study on superabsorbent composite XXV.POLYMER COMPOSITES, Issue 4 2010Synthesis, characterization, swelling behaviors of poly(acrylic acid- co - N -acryloylmorpholine)/attapulgite superabsorbent composites In this work, a novel poly(acrylic acid- co - N -acryloylmorpholine)/attapulgite superabsorbent composite was prepared by graft copolymerization among acrylic acid, N -acryloylmorpholine and attapulgite in aqueous solution, using N,N, -methylenebisacrylamide as a crosslinker and ammonium persulfate as an initiator. The result from FTIR spectra showed that OH of attapulgite participated in graft copolymerization with acrylic acid and N -acryloylmorpholine. Proper monomer ratio and atapulgite content could form a loose surface, and improve reswelling ability and initial swelling rate. The buffer action of the COOH and COO, groups in the superabsorbent composite keeps the water absorbency a rough constant in the pH range of 4.4,9.6. Both polarity and structure of an organic solvent are responsible for the phase transition point of the superabsorbent composite. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers [source] The preparation and properties of dextrin-graft-acrylic acid/montmorillonite superabsorbent nanocompositePOLYMER COMPOSITES, Issue 7 2009Xin Ding A novel superabsorbent nanocomposite was synthesized through intercalation polymerization of partially neutralized acrylic acid, gelatinized dextrin, and an organic-montmorillonite powder using N,N -methylenebisacrylamide as a crosslinker, Span-60 as a dispersant, and ammonium persulfate together with sodiumsulfite as a type of mixed redox initiator. Effects of the amount of them on water absorbency of the superabsorbent were investigated. The structure and the morphology of the nanocomposite were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and transmission electron microscopy analysis. The blood compatibility of the composite was primarily measured. The results show that the acrylic acid monomer was successfully intercalated into the organic-montmorillonite layers and bonded with them. The superabsorbent nanocomposite synthesized under optimal conditions with an organic-montmorillonite powder content of 5 wt% exhibit an absorption of 725.3 g/g in distilled water and favorable blood compatibility. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Preparation and characterization of biodegradable waterabsorbent PAN/SS nanocompositePOLYMER COMPOSITES, Issue 11 2008Bijayashree Samal Polyacrylonitrile (PAN)/sodium silicate (SS) nanocomposite was prepared via nonconventional emulsion method using an in situ developed transition metal complex Cu(II)/glycine taking ammonium persulfate (APS) as initiator, with a novel motive of converting hydrophobic homopolymer PAN into hydrophilic nano material via nanotechnology by the inclusion of SS to the homopolymer. UV,visible spectral analysis was carried out which revealed various interactions between the in situ developed complex with other reaction components. The formation of the PAN/SS nanocomposite was confirmed by infrared spectra (IR). Furthermore, as evidenced by transmission electron microscopy (TEM), the composite so obtained was found to have nano scale structure. X-ray diffraction (XRD) was carried out suggesting that the silicate layers were exfoliated during the polymerization process. An increase in the thermal stability for the developed nanocomposite was recorded by thermogravimetric analysis (TGA). Surprisingly, it was also found that the PAN/SS nanocomposite showed considerable amount of waterabsorbency and was biodegradable as tested by activated sludge and cultured media and further confirmed by scanning electron microscopy (SEM). POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers [source] Preparation of polyaniline,polypyrrole composite sub-micro fibers via interfacial polymerizationPOLYMER COMPOSITES, Issue 1 2008Shuangxi Xing Polyaniline,polypyrrole (PANI,PPy) composite sub-micro fibers were prepared via interfacial polymerization of aniline and pyrrole using ammonium persulfate (APS) as oxidant. Carbon tetrachloride was used as the organic solvent to dissolve the monomers and APS was dissolved in HCl aqueous solution. The reaction was carried out at the interface formed by the two above solutions. Scanning electron microscopy, Fourier transformation infrared spectra and differential thermal analysis were conducted to characterize the morphology, structure and thermostability of the resulting composites. Dodecyl benzene sulfonic acid was also used as medium to make comparison with that using HCl in the reaction system. The guidance of the formation of the PANI nanofibers at the first step and the interaction between PANI and PPy were considered as the drive forces to yield the composite sub-micro fibers. POLYM. COMPOS., 29:22,26, 2008. © 2007 Society of Plastics Engineers [source] | |||||||||||||