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  • Physics  (54)
  • Wiley-Blackwell  (54)
  • Cambridge University Press
  • 1985-1989  (54)
  • 1960-1964
  • 1955-1959
  • 1
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: IR specular reflectance spectra with respect to hydrogen peroxide formation during uncatalyzed and Cu (oxide)-catalyzed oxidation of isotactic Polypropylene films have been measured as function of time and temperature (90-130°C). Energies of activation for the various cases have been obtained. The originally proposed kinetic scheme based on oxygen-absorption measurements has been modified in order to accommodate the spectroscopical results. The amount of ROOH groups present at any time on the polymer is very small, indicating relatively slow rates of ROOH formation and fast rates of their decomposition. The kinetic scheme fits well the experimental data. However, the reasons for the variations of the relevant energies of activation obtained for the catalyzed oxidation in absence and presence of the main volatile reaction products, H2O and CO2, are not yet understood, i.e., the mechanism needs further investigations.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 479-488 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of power and substrate temperature on the chemical composition of inductively coupled RF plasma-polymerized films of acrylonitrile was monitored by ESCA. At a substrate temperature of 20°C a minimum in nitrogen content as a function of power was observed for films deposited in the coil region. A maximum was observed for a substrate temperature of 150°C. When power was increased from 1 to ∼50 W a linear increase in nitrogen content was observed in the tail region at both substrate temperatures. A step function observed in the C1s and N1s core-level spectra is discussed in terms of extensive unsaturation being present in the films.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 507-515 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The surface aspects of plasma polymers derived from ferrocene, dimethylaminomethylferrocene, and vinylferrocene were studied by electron spectroscopy for chemical applications. From a consideration of the ESCA peak area ratios it is apparent that ferrocene and vinylferrocene maintain a carbon-to-iron ratio characteristic of the “monomer”, whereas dimethylaminomethylferrocene plasma polymer is richer in iron than its monomer.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1771-1785 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements of saturated liquid densities and ethylene solubilities in ethylene - polyethylene systems up to 26.1 MPa and 493.1 K were obtained using a new variable-volume static cell after a careful investigation of the influence of inhibitors of polymerization of ethylene under experimental conditions.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2043-2061 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new series of polyhalogenated, principally polybrominated polyamides have been prepared either by polymerization in a melt-phase process at high temperature or by a low-temperature solution process. The polymers were obtained from perchloroterephthaloyl-, perbromoterephthaloyl-, and 2,5-dibrometerephthaloyl dichlorides and tetrabromophthalic anhydride with aromatic and aliphatic diamines. They were characterized by elemental analysis, infrared spectroscopy, intrinsic viscosities, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and flame-resistance testing.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2225-2232 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Water-in-oil (w/o) microemulsions of methyl methacrylate (MMA), acrylic acid (AA), sodium acrylamidostearate (NaAAS), and water were investigated. MMA, AA, and NaAAS could be terpolymerized in these microemulsions. For a composition of 54% MMA, 34% AA, 2% NaAAS, and 10% H2O, polymers of high molecular weights of about 1,000,000 were obtained between 3.5 to 24% polymer conversion. The system became a transparent gel when conversion exceeded 36%. Transparent solid terpolymer containing water up to 16% were also obtained after fully polymerizations of certain compositions.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 87-106 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Plasma polymerization of tetra fluoroethylene (TFE), perfluoro-2-butyl-tetrahydrofuran (PFBTHF), ethylene, and styrene were investigated in various combinations of monomer flow rates and discharge wattages for the substrate temperature range of -50 to 80°C. The polymer deposition rates can be generally expressed by k0 = Ae-bt, where k0 is the specific deposition rate given by k0 = (deposition rate)/(mass flow rate of monomer), A is the preexponential factor representing the extrapolated value of k0 at zero absolute temperature, and b is the temperature-dependence coefficient. It was found that the value of b is not dependent on the condensibility of monomer but depends largely on the group of monomer; that is, perfluorocarbons versus hydrocarbons. The values of A are dependent on domains of plasma polymerization. In the energy deficient region A is given by A = α(W/FM)n, where α is the proportionality constant, W is discharge wattage, FM is the mass flow rate, and n is close to unity. In the monomer deficient region A becomes a constant. The kinetic equation is discussed in view of the bicyclic rapid step-growth polymerization mechanisms.
    Additional Material: 16 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1997-2003 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of butadiene by lithium-based initiators in aliphatic hydrocarbon solvents in the presence of dipiperidinoethane gives a highly 1,2 structure. This system was studied to determine the factors that govern the structure. The effect of this complexing agent on the kinetics of propagation, the microstructure of the polymer, and the ultraviolet spectrum of the active chain end was measured. The results suggest that more than one solvated species form, all giving highly 1,2 polymer structures, but that a solvate containing one chain end with one dipiperidinoethane molecule is the principal reacting species which gives close to 100% 1,2 structure. This reacting center has a high proportion of trans-structure in the allyllic ion, únlike most complexed active chain ends, which are often highly cis. It is this transstructure in the ion that is thought to be responsible for the polymer structure.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 981-995 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterogeneous grafting on polyvinylchloride suspended in water was carried out using N-butyl-3-mercaptopropionamide as nucleophile. Over 50% graft was obtained by using a small amount of solvent as a swelling agent and tricapryl methyl ammonium chloride as a phase transfer catalyst. Elemental analysis of the grafted polymer shows that the chlorine displaced from the polymers is replaced by the thio-amide group. The above conclusion is supported by NMR and IR analysis. The kinetics of the chlorine displacement from PVC by the thio amide group obeys the Shell progressive mechanism. The rate at which an individual spherical particle reacts depends on the diffusion through the reacted layer. The grafted polymer is soluble in tetrahydrofuran or nitrobenzene. The films obtained from the grafted material are brittle due to excessive internal hydrogen bonding. The electrostatic charge which is a characteristic surface phenomena in PVC is diminished in the grafted polymer which may be due to the existence of the amide group near the surface. The amide groups attached to the side chains on the polymer may participate in various reactions, e.g., with epoxy resins. IR analysis of the cured film indicates the disappearance of the oxiran band at 913 cm-1 and an increase in the hydroxyl band around 3300 cm-1. Thus, grafting of amide groups on PVC enables us to further modify PVC by epoxy resins.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 1031-1041 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The first 200-400 nm of crosslinked epoxy resin adjacent to an aromatic polyamide (aramid) surface were characterized by internal reflection spectroscopy (IRS) using an aramid-coated IRS element. The crosslinking kinetics and final crosslinked state of an anhydride-cured epoxy resin were strongly affected by the aramid surface, which produced a localized increase in the rate of anhydride consumption and a decrease in the yield of ester products. An aromatic amine-cured epoxy resin was less affected by the aramid surface. Unidirectional aramid fiber:epoxy composites were examined by dynamic mechanical analysis (DMA), and differential scanning calorimetry (DSC). The chemical changes detected spectroscopically were shown to correlate with mechanical and thermal transition data obtained by DMA and DSC. These results are rationalized on the basis of the effect of absorbed moisture in the aramid on the crosslinking chemistry.
    Additional Material: 8 Ill.
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