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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 1853-1867 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The memory of irradiated polyethylene has been studied with emphasis on the magnitude of the restoration force exerted by the deformed polymer during the process of restoration to the nonstressed state and on the degree of completeness with which restoration occurs. The particular form of the memory effect studied has involved the deformation of the heated polymer followed by “locking-in” of the memory via cooling. Subsequent heating restores the deformed specimen to the undeformed state. The memory effect has been studied under both nontransparency (NT) and transparency (T) deformation conditions. The effects of parameters such as the polymer properties (Tm, density, molecular weight), radiation dose, and deformation and restoration conditions on the degree of restoration and restoration force have been investigated. The results of this study may be summarized as follows. Restoration temperatures equal to or above the crystalline melting point (Tm) of the polymer are required in order to obtain complete restoration. The restoration temperature increases with increasing polymer crystalline melting point. The degree of restoration increases with increasing restoration temperature for NT deformed specimens. T deformed specimens do not begin to restore until the temperature approaches the Tm of the polymer. The restoring force increases with decreasing deformation temperature. NT deformation results in larger restoring forces and faster restoration relative to T deformation. The restoring force increases with increasing radiation dose for both T and NT deformations, the effect being greater for NT deformation. Radiation dose, however, above a minimum value does not affect the degree of restoration. The restoring force increases with increasing polymer initial molecular weight for T deformation.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 143-157 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The radiation crosslinking (via Co60) of both high and low density polyethylene in the presence of several tetrafunctional monomers has been studied to observe the effects of the additives on mechanical and electrical properties. The monomers employed were allyl methacrylate, divinylbenzene, and diallyl maleate. Monomer levels were such that the number of moles presented per number-average mole of polyethylene was 2.2-2.6 for AMA and DVB with Marlex 5003 and 6009, and 9-10 for Marlex 1712. The DAM level was 3-5% of that of the other monomers on the same basis. Gel fractions, tensile strengths (at yield and break) at ambient temperature and tensile strengths, elongations, and moduli measured at a temperature above which no crystallinity remains all undergo more marked changes in the presence of tetrafunctional monomer after only 1-3 Mrad of radiation, regardless of monomer nature. Gels, tensiles, and moduli increase while elongation decreases. The magnitude of the changes depends upon the monomer nature (at the above ratios), the order being AMA〉DVB〉DAM〉 Monomer-free. With increasing does to 8 Mrad, the trends continue. The gel swelling ratios are inversely proportional to the 3/5 power of the crosslink density, as determined by the modulus value in the absence of crystallinity. Straight radiation of monomer-free polyethylene to higher doses not necessarily yield physical properties values attained at the lower doses with additive. The dielectric constant and dissipation factor of monomer-containing crosslinked polyethylene are only slightly affected by the presence of the polyfunctional monomer.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 245-250 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: It has been demonstrated that the use of solvent additives can substantially increase the rate of radiation-induced graft polymerization in the systems polyethylene-styrene, polypropylene-styrene, polyvinyl chloride-styrene, nylon-styrene, polyethylenemethyl acrylate, polypropylene-methyl acrylate, nylon-methyl acrylate. Teflonmethyl acrylate, and polyethylene-tert-butylaminoethyl methacrylate. Two different mechanisms have been shown to be responsible for the observed accelerative effects. One is the incursion of a Trommsdorff effect due to the insolubilization of the growing graft polymer chains in the solvent-monomer medium. The other mechanism is the enhancement in the degree of accessibility of monomer to grafting sites within the polymer brought about by the greater ability of the solvent additive to swell certain base polymers.
    Additional Material: 9 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 16 (1995), S. 845-849 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic bulk polymerization of optically active (2R, 3S)-3,4-epoxy-1,2-O-isopropylidenebutane-1,2-diol (1) and its (2 S, 3 S) diastereomer 2 was studied. Molecular weights and optical activity measurements as well as carbon and proton NMR spectra are reported. The polymers show solvent dependent inversion of the sign of optical rotation. The NMR spectra are consistent with isotactic polymer chains.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 55 (1961), S. 663-673 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The radiation-induced graft polymerization of styrene to low density polyethylene was investigated. It was found that dilution of the styrene monomer with methanol accelerates the rate of graft polymerization with a maximum effect occurring at approximately 70 vol.-% methanol. Both the accelerated and unaccelerated graft polymerizations yield volumetric or homogeneous graft copolymers. Experiments in which n-octane was substituted for methanol as the diluent showed that the accelerative effects of methanol are best explained by the incursion of a Trommsdorff-type effect. The kp2/kt values for the grafting reaction in the various styrene-methanol solutions were calculated. It was found that the kp2/kt term is larger in grafting than in homopolymerization by a factor of 103, and that it increases as the methanol concentration of the monomer solution increases.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 42 (1960), S. 575-578 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 57 (1962), S. 661-667 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gamma radiation-induced surface graft copolymerizations of styrene - acrylonitrile and styrene - methyl acrylate to Teflon were studied. It was observed that the compositions of the various grafted copolymers are richer in the more polar monomer than one would predict from the Lewis-Mayo copolymer composition equation. These results were interpreted in terms of a preferential solvation of the relatively immobile growing graft polymer free radicals by the polar monomers.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 1481-1489 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of radiation graft polymerization of styrene onto cellulose acetate-butyrate is studied over a range of radiation intensities and monomer concentrations. The reaction is diffusion-free under the experimental conditions as shown by the independence of the grafting rate on film thickness. The dependence of the grafting rate on monomer concentration increases from 3/2-order to slightly greater than 5/2-order with increasing radiation intensity. The dependence of the grafting rate on radiation intensity decreases from 1/2-order to 0-order with decreasing monomer concentration. Possible mechanisms for these results are discussed.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 2789-2799 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of propylene oxide (PO) was studied with an initiator prepared by the reaction of (R)-(-)-3,3-dimethyl-1,2-butanediol (1) with aluminium hydride. When mixed with zinc chloride in a 1:1 mole ratio, the initiator was found to be highly reactive and also stereoelective in the polymerization of PO, preferentially incorporating (R)-(+)-PO into the polymer chain. Analysis of the polymer structure by 13C NMR spectroscopy showed that chlorine, hydroxyl and alkoxy end groups, derived from the initiator, were present. Fractionation of poly(propylene oxide) (PPO) in acetone at -30°Cgave about 10% insoluble PPO, shown to be isotactic by 13C NMR. The soluble, largely atactic fraction contained irregular head-to-head (h,h) and tail-to-tail (t,t) structures. In the absence of coinitiator zinc chloride the PPO product was completely soluble in acetone at -30°Cand contained a greater proportion of irregular h,h and t,t structure.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2283-2290 
    ISSN: 0887-624X
    Keywords: epoxide ; bicyclic amide acetal ; 2-oxazoline ; ring-opening polymerization ; zwitterion polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various bicyclic amide acetals were synthesized from the cycloaddition reactions of 2-substituted-2-oxazolines with styrene oxide. Ring-opening polymerization of the bicyclic amide acetals occurred upon heating in the presence of methyl tosylate. Characterization of the bicyclic amide acetals and their polymers was accomplished by NMR and elemental analysis. Vapor pressure osmometry showed the highest polymer molecular weight was only 2,400. The mechanisms for cycloaddition and polymerization are discussed. © 1994 John Wiley & Sons, Inc.
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