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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2021-2030 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Low concentrations of bromine (0.008-0.06M) were used to initiate photopolymerization of MMA in bulk and in diluted (near bulk) systems, the diluents or solvents used being benzene, toluene, dioxane, tetrahydrofuran, carbon tetrachloride, chloroform, methylene chloride, and methanol. Polymerization in bulk follows usual free-radical kinetics. Inert solvents (benzene, toluene) as well as the other solvents used enhance the rate of polymerization MMA even when used in the range of catalytic concentrations (0.04-0.4M). An initiation mechanism involving solvent molecules appears to be predominant in diluted systems.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 203-218 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of MMA was kinetically studied in the presence of visible light (using a 125-W high-pressure mercury vapor lamp with fluorescent coating, without a filter), a THF - bromine charge-transfer complex being used as the photoinitiator. The initiator exponent was 0.5 in bulk polymerization. The monomer exponent varied from about 1.2 to about 2.5, depending on the nature of the solvent used; the initiator exponent also varied in diluted systems, depending on the nature and proportion of the solvent, the variation being from a value of 0.5 in bulk system to zero or almost zero at about 25% (v/v) solvent concentration. Other kinetic parameters, viz., kp2/kt and the activation energy for polymerization, were determined and are reported. Kinetic and other evidence indicates that the photopolymerization takes place by a radical mechanism and termination is bimolecular in nature in bulk systems; in dilute systems, termination by initiator complex assumes predominance, particularly at high solvent concentrations (≥25% v/v).
    Additional Material: 13 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 981-991 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of MMA was carried out under visible light (440 nm) with the use of pyridine-bromine (Py-Br2) charge-transfer (CT) complex as the photoinitiator. Initiator exponent and intensity exponent were 0.5 and 0.43, respectively, and the monomer exponent was found to be dependent on the nature of the solvent or diluent used. The Polymerization was inhibited in the presence of hydroquinone, but oxygen had very little inhibitory effect. An average value of kp2/kt for this polymerization system was 1.19 × 10-2, and the activation energy of photopolymerization was 4.95 kcal/mole. Kinetic data and other evidence indicate that the overall polymerization takes place by a radical mechanism. With Py-Br2 complex as the photoinitiator, the order of polymerizability at 40°C was found to be MMA, EMA ≫ Sty, MA.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 993-1004 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of MMA was done in the presence of visible light (440 nm) with the use of N-bromosuccinimide (NBS) as the photoinitiator. The initiator exponent and intensity exponent were 0.5, and the monomer exponent was found to be unity. The polymerization was inhibited in the presence of hydroquinone. The average kp2/kt for this photopolymerization system was found to be 0.296 × 10-2 and the activation energy of photopolymerization was 4.67 kcal/mole. Kinetic and other evidence indicate that the overall polymerization takes place by a radical mechanism. With NBS as the photoinitiator, the order of polymerizability at 40°C was MMA, EMA ≫ MA ≃ VA, and styrene could not be polymerized under similar conditions.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1407-1419 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Benzophenone (BP)-sensitized photopolymerization of methyl methacrylate (MMA) in near UV/visible light was studied at 40°C using dimethylaniline maleic acid (DMA - MA) combination as the photoinitiator. An instantaneous 1:1 complexation between DMA and MA takes place when they are mixed together in acetonitrile. Also, instantaneous complex formation occurs between DMA and MMA and between MA and MMA when they are dissolved in MMA in low concentrations, separately. Interestingly, when equimolar proportions of DMA and MA are mixed together in MMA, there is indication for further instantaneous complexation between (DMA - MMA) complex and (MA - MMA) complex forming the actual initiating species in the photopolymerization system. Initiator exponent was 0.28 and monomer exponent varied between 0.0 to 1.8 depending on the nature of the solvent and range of dilution used. Analysis of kinetic data indicates a free radical mechanism for the polymerization with initiator-dependent termination. Chain termination via degradative initiator transfer is quite significant; but the degradative effect becomes much less prominent in the higher range of initiator concentration indicating that the reinitiation reaction following the initiator transfer process assumes more proportionate significance as the initiator concentration is increased, probably as a result of higher reinitiation efficiency. Polymers obtained gave evidence for the incorporation of aromatic (amine) end groups in them.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 921-930 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of MMA was carried out in presence of visible light (440 nm), quinoline-bromine charge-transfer complex being used as the photoinitiator. The initiator exponent was observed to be 0.5 up to 0.014 M initiator concentration; when chloroform was used as the solvent, the monomer exponent was found to be unity. The polymerization was inhibited in presence of hydroquinone but little inhibitory effect was observed in the presence of air. An average value of k2p/kt for this photopolymerization system was found to be (1.08 ± 0.22) × 10-2. Kinetic and other evidence indicates that the overall polymerization takes place by a radical mechanism.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1531-1539 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Low concentrations (0.001-0.03M) of chlorine easily induce photopolymerization of MMA at 40°C. Kinetic data indicate that polymerization follows a radical mechanism involving complexation of monomer by the initiator and initiation takes place through radical generation during photodecomposition of the initiator-monomer complex. Termination appears to take place bimolecularly. The kp2/kt value for MMA polymerization at 40°C was found to be 0.83 × 10-2. Rates of chlorine-initiated photopolymerization were found to decrease in the order MMA, EMA ≫ VA, Sty 〉 MA.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1743-1758 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of MMA was carried out at 40°C in diluted systems by use of quinolinebromine (Q-Br2) charge-transfer complex as the initiator and chloroform, carbon tetrachloride, chlorobenzene, dioxane, THF, acetone, benzene, toluene, quinoline, and pyridine as solvents. The results showed variable monomer exponents ranging from 1 to 3. For chloroform, carbon tetrachloride, and chlorobenzene, the monomer exponent observed was unity; for other solvents used, the value of the same exponent was much higher (between 2 and 3). Initiation of polymerization is considered to take place through radicals generated in the polymerization systems by the photodecomposition of (Q-Br2)-monomer complex (C) formed instantaneously in situ on addition of the Q-Br2 complex in monomer. The kinetic feature of high monomer exponent is considered to be due to higher order of stabilization of the initiating complex (C) in presence of the respective solvents. In the presence of the retarding solvents, very low or zero initiator exponents were also observed, depending on the nature and concentration of the solvents used. The deviation from the square-root dependence of rate on initiator concentration becomes higher at high solvent and initiator concentrations in general. This novel deviation is explained on the basis of initiator termination, probably via degradative chain transfer involving the solvent-modified initiating complexes and the propagating radicals.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 375-386 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of photopolymerization of MMA at 40°C with the use of iodine as the photoinitiator was studied. At low range of iodine concentration (〈 0.0004M), the rate of polymerization was proportional to square root of iodine concentration and the monomer exponent was 2.5, while at a higher range of iodine concentration, (0.0005-0.002M) the initiator exponent and monomer exponent were zero and 3.6-3.8 (i.e., close to 4), respectively. The chain-transfer constant of iodine at 40°C was found to be 6.0. Polymerization was found to be largely inhibited in the presence of relatively high concentrations of iodine (〉 0.005M) and also in presence of hydroquinone. Kinetic and other data indicate a radical mechanism of polymerization involving complexation of monomer molecules with iodine prior to radical generation, and termination is believed to take place bimolecularly at low iodine concentrations and unimolecularly, involving reaction with iodine, at high iodine concentrations (initiator termination).
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 2119-2127 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of MMA with the use of H2O2 as the photoinitiator under visible light at 30°C was studied. Kinetic features in bulk monomer and in the presence of different diluents differ significantly. Usual free radical kinetics with square-root dependence of rate on initiator, indicating bimolecular termination of chain radicals, were observed for bulk polymerization. On dilution with various solvents polymerization was found to be retarded to different (usual and more than usual) extents, the observed monomer exponent value being much higher than unity in many cases. This deviation from normal kinetics has been interpreted in terms of the predominance of degradative initiator transfer in the diluted systems.
    Additional Material: 8 Ill.
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