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Redox Initiator (redox + initiator)
Terms modified by Redox Initiator Selected AbstractsInduction of chemical and moisture resistance in Saccharum spontaneum L fiber through graft copolymerization with methyl methacrylate and study of morphological changesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009Balbir Singh Kaith Abstract In this article, morphological modification of Saccharum spontaneum L, a natural fiber through graft copolymerization with methylmethacrylate using ferrous ammonium sulfate,potassium per sulfate redox initiator has been reported. Different reaction parameters such as reaction temperature, time, initiator molar ratio, monomer concentration, pH and solvent were optimized to get maximum graft yield (144%). The graft copolymers thus formed were characterized by Fourier transform infrared, scanning electron microscopy, X-ray diffraction and thermogravimetric, differential thermal analysis, and differential thermogravimetric techniques. Graft copolymer has been found to be more moisture resistant and also showed higher chemical and thermal resistance. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Effect of polymerization method on structure and properties of cationic polyacrylamideJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Yinghua Shen Abstract Acrylamide and 2-(methacryloyloxy)ethyltrimethylammonium chloride (AM/MADQUAT) copolymers were synthesized by solution and inverse microemulsion polymerization using (NH4)2S2O8/NaHSO3 as redox initiator at the same feed mole ratio, and their microstructure, such as sequence distribution and composition distribution, was calculated from monomer reactivity ratios of different polymerization methods. The results show that charge distribution is more uniform for copolymer prepared in inverse microemulsion than that in solution, and copolymer composition distribution is close to unity, and maintains approximately at the feed ratio. Furthermore, the influence of the two structures of cationic polyacrylamides on kaolinite floc size and effective floc density, reduction of Zeta potential and floc compressive yield stress had been investigated at pH 7. The results show that the kaolinite floc size and effective floc density are strongly dependent upon copolymer microstructure, with greater floc size and lower effective floc density being observed for copolymer prepared in inverse microemulsion than for that in solution. Copolymer microstructure has a marked effect on the Zeta potential, whose reduction in the magnitude was much greater in the presence of copolymer prepared in inverse microemulsion than that in solution. Greater compressive yield stress was achieved for the strong flocs produced by copolymer prepared in inverse microemulsion than for the weak flocs produced by that in solution. The difference in flocs compressive yield stress may be attributed to flocs structure. Therefore, in this article, a correlation between the cationic polyacrylamide structure and flocculation property for kaolinite suspension was established. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Ceric ammonium sulfate/sodium disulfite initiated grafting of acrylamide on to Cassia reticulata seed gumJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Vandana Singh Abstract Ceric ammonium sulfate/sodium disulfite redox system was evaluated for the poly(acrylamide) (PAM) grafting on to Cassia reticulata (CR) seed gum. Grafting conditions were optimized and the maximum %Grafting (%G) and %Efficiency (%E) achieved were 152 and 97.2%, respectively, using [disulfite] 0.005M; [ceric ammonium sulfate] 0.026M; [acrylamide] 0.11M; [gum] 0.125 g/25mL at 40 ± 0.2°C. Representative CR-grafted gum (CRPAM) was characterized by Fourier transform infrared spectrometry (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Under identical conditions, the redox initiator could result 142.6 %G and 91.2 %E on to guar gum (GG). Various physical properties of the CR gum/grafted CR gum, such as viscosity, water retention, and saline retention, were studied and compared with GG/grafted GG to find out the potential industrial use of CR gum and PAM- grafted -CR gum. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Synthesis of a cellulose-grafted polymeric support and its application in the reductions of some carbonyl compoundsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Poonam K. Dhiman Abstract The reduction of carbonyl compounds by borohydride supported on a cellulose,anion exchange resin is known. The synthesis of a graft copolymer of cellulose and poly(4-vinyl pyridine) [CellO- g -poly(4-VP)] has been carried out with ceric ions as a redox initiator. A postgrafting treatment of CellO- g -poly(4-VP) with sodium borohydride has produced CellO- g -poly(4-VP) borane, a polymer-supported reducing agent. Optimum conditions pertaining to the maximum percentage of grafting have been evaluated as a function of the concentrations of the initiator, monomer, and nitric acid, amount of water, time, and temperature. The maximum percentage of grafting (585%) has been obtained with 0.927 mol/L of 4-vinyl pyridine and 0.018 mol/L of ceric ammonium nitrate in 120 min at 45°C. The polymeric support, CellO- g -poly(4-VP) borane, has been used for reduction reactions of different carbonyl compounds such as benzaldehyde, cyclohexanone, crotonaldehyde, acetone, and furfural. The graft copolymer has been characterized with IR and thermogravimetric analysis. The grafted cellulose has been found to be thermally stable. The reduced products have been characterized with IR and NMR spectral methods. The reagent has been reused for the reduction of a fresh carbonyl compound, and it has been observed that the polymeric reagent reduces the compounds successfully but with a little lower product yield. © 2007 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] Room-temperature RAFT copolymerization of 2-chloroallyl azide with methyl acrylate and versatile applications of the azide copolymersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2010Guang Li Abstract A new vinyl azide monomer, 2-chlorallyl azide (CAA), has been synthesized from commercially available reagent in one step. The reversible addition fragmentation chain transfer (RAFT) copolymerization of CAA with methyl acrylate (MA) was carried out at room temperature using a redox initiator, benzoyl peroxide (BPO)/N,N -dimethylaniline (DMA), in the presence of benzyl 1H -imidazole-1-carbodithioate (BICDT). The polymerization results showed that the process bears the characteristics of controlled/living radical polymerizations, such as the molecular weight increasing linearly with the monomer conversion, the molecular weight distribution being narrow, and a linear relationship existing between ln([M]0/[M]) and the polymerization time. Chain extension polymerization was performed successfully to prepare block copolymer. Furthermore, the azide copolymers were functionalized by CuI -catalyzed "click" reaction with alkyne-containing poly(ethylene glycol) (PEG) to yield graft copolymers with hydrophilic PEG side chains. Surface modification of the glass sheet was successfully achieved via the crosslinking reaction of the azide copolymer under UV irradiation at ambient temperature. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1348,1356, 2010 [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] Investigation of redox initiators for free radical frontal polymerizationPOLYMER INTERNATIONAL, Issue 8 2009Huan Yu Abstract BACKGROUND: The reaction temperature for frontal polymerization (FP) initiated by redox initiators can be greatly decreased compared with FP initiated by peroxide initiator and disulfide initiator. We report the synthesis of poly(hydroxyethyl acrylate)s via free radical FP using benzoyl peroxide (BPO)/N,N -dimethylaniline (DMA) and ammonium persulfate (APS)/N,N,N,,N,-tetramethylethylenediamine (TMEDA) couples as redox initiators at ambient pressure. RESULTS: The results show that unlike the phenomenon of bubbles and ,fingers' when using BPO alone, a self-sustaining and stable front can be obtained when the [DMA]/[BPO] ratio is higher than 1 (mol/mol). A slight increase of the DMA (or TMEDA) reductant concentration causes a marked decrease of front temperature to 53 °C (or 61 °C). CONCLUSION: We investigated the effects of the ratio of the oxidant to the reductant and the initiator and monomer concentrations on certain parameters of FP: formation of bubbles, front velocity and front temperature. This opens the way to the potential development of FP using more appropriate monomers with low boiling points. Copyright © 2009 Society of Chemical Industry [source] Silane reduction of onium saltsAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 3 2010James V. Crivello Abstract Novel redox initiators for cationic polymerizations were developed consisting of an onium salt together with a SiH functional silane or siloxane. The reduction of the onium salt by the silane is catalyzed by noble metal complexes or certain transition metal compounds and takes place spontaneously at room temperature. The redox reaction of the onium salt with the silane results in the liberation of a strong Brønsted acid that can be subsequently used to initiate cationic polymerizations. Typical onium salts that have been employed in these redox initiator systems are diaryliodonium salts, triarylsulfonium salts and S,S -dialkyl- S -phenacylsulfonium salts. Studies of the effects of variations in the structures of the onium salt, the silane and the type of noble metal catalyst were carried out. In principle, the redox initiator systems are applicable to all types of cationically polymerizable monomers and oligomers, including the ring-opening polymerizations of such heterocyclic monomers as epoxides and oxetanes and, in addition, the polymerization of vinyl monomers such as vinyl ethers, N -vinylcarbazole and styrenic monomers. The use of these novel initiator systems for carrying out commercially attractive crosslinking polymerizations for coatings, composites and encapsulations is discussed. Copyright © 2009 John Wiley & Sons, Ltd. [source] | ||||||||||