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  • Physics  (552)
  • 1975-1979  (256)
  • 1970-1974  (296)
  • 1950-1954
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1213-1224 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthetic details of solution polymerization in benzene and bulk polymerization of vinylferrocene are reported. In benzene solutions, with azobisisobutyronitrile (AIBN) as the initiator, small yields of low-polydispersity low molecular weight (M̄n ≃ 5000) polyvinylferrocene is obtained. However, high yields can be obtained by continuous or multiple AIBN addition. Higher molecular weight polymers and binodal polymers can be obtained as the monomer concentration is increased. In bulk polymerizations, yields of 80% can be obtained. The molecular weight increases as temperature decreases from 80 to 60°C in bulk polymerizations, and an increasing amount of insoluble polymer results. The soluble portion is often binodal, the higher molecular weight node consisting of an increasingly branched structure. Lower molecular weight polymer was readily fractionated into narrow fractions from benzene-methanol systems, but higher molecular weight polymer proved impossible to fractionate into narrow fractions due to branching.
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acrylonitrile (AN) was graft-polymerized onto gelatinized cationic starch (CS) possessing diethylaminoethyl ether groups by cerium (IV) initiation to give stable latexlike copolymer dispersions. Dispersions of the latex copolymers, having up to 50% grafted polyacrylonitrile (PAN), air- and heat-dry on glass to clear, adhesive films. Sonification of up to 8% dispersions at 20 Khz reduced their viscosities from 1500-3000 cP to 15-40 cP. Scanning electron microscopy revealed that both nonsonified and sonified dispersions consist of ball-like particles measuring about 0.05-0.15 μ in diameter when dry. The films are formed by coalescence of these particles. The degree to which AN grafts onto CS at ambient temperature is related to the nitrogen content of CS, gelatinization time of CS at 95°C, sequence of AN and cerium(IV) addition, concentration of cerium (IV), concentration of AN, and severity of reaction agitation. Number-average molecular weight values of PAN were about 106 when grafting was conducted under stirring and about 5 × 105 when conducted under shaking action.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 445-454 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fundamental vibrational frequencies of an isolated chain of cis-1,4-polybutadiene have been calculated. Infrared and polarized Raman data are used in the force constant refinement routine. The assignments of the vibrational frequencies are discussed in terms of the potential energy distribution.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1683-1690 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkaline hydrolysis of model carbamates, polyurethanes, and poly(urethane-ureas) has been investigated. The model carbamates were based upon phenyl, benzyl, and cyclohexyl isocyanates. The polyurethanes and poly(urethane-ureas) were prepared from tolylene diisocyanate (TDI), xylylene diisocyanate (XDI), and 4,4′-dicyclohexylmethane diisocyanate (H12MDI) and a poly(oxyethylene)glycol of 6000 molecular weight. Pseudo-first-order rate constants of hydrolysis were obtained in aqueous pyridine solution at 110°C, and second-order rate constants were obtained in aqueous KOH solution for the model biscarbamates. Pseudo-first-order rate constants of hydrolysis were obtained in alcoholic KOH solution for the polyurethanes and poly(urethane-ureas). The hydrolysis of the model carbamates showed that the stability increased in the following manner: phenyl 〈 benzyl 〈 cyclohexyl. The pseudo-first-order rate constants were dependent upon the pKb of the corresponding amines. The hydrolysis of the polyurethanes and poly(urethane-ureas) showed that the stability increased in the following manner: aromatic 〈 aralkyl 〈 cycloaliphatic. It was shown that polyurethanes are more susceptible to alkaline hydrolysis than to acidic hydrolysis.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1619-1643 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of propylene oxide (PO) with tetrahydrofuran (THF) in dichloroethane (DCE) has been studied at -10, 0, +10, and +20°C. The reactions were initiated by triphenylmethyl cations associated with the following gegenions: PF6-, SbF6-, and AsF6-. The overall energies of activation (Eα of PO and Ea of THF) obtained with the three gegenions increase as one passes from PF6- to AsF6- then to SbF6-, though the magnitude of the increase in each case is not substantial. On the other hand, the associated frequency factors A show a considerable variation with the gegenion. The bimodal distributions of the molecular weights, obtained by GPC with the copolymer produced from reactions initiated with triphenylmethyl hexafluorophosphate, show that the proportions of the lower molecular weight component (L) decrease as the solvent is changed from DCE to toluene, and this is even more marked when bulk polymerization conditions are adopted. The proportions of the higher molecular weight component (H) however increase, as does its molecular weight. The GPC molecular weight distributions of the copolymers initiated with triphenylmethyl hexafluorophosphate in DCE to which water has been added, show that the molecular weight of component H decreases with increasing concentration of water, while that of component L remains practically unchanged at a value of 308. This corresponds to an average degree of polymerization (DP) of 4 to 5. The NMR and infrared spectra of copolymers prepared in the presence of still higher initial water concentrations indicate that the PO-based polymer segments are present in excess of those required for a 1:1 copolymer.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 93-104 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two surface analysis techniques (Rutherford backscattering and surface composition by analysis of neutral and ion impact radiation) have been applied to the study of interfacial copper transport in the oxidation of polyethylene films over copper surfaces. Analysis of films oxidized several thousand hours at 40, 57, and 87°C shows maximum concentrations of copper species in the polymer matrix of ∼0.1M extending to depths of several thousand angstroms. These results, together with previous infrared spectroscopic studies, allow some significant conclusions and hypotheses to be drawn as regards the roles of heterogeneous and homogeneous catalytic processes which occur in the thermal-oxidative degradation of polyethylene-copper systems.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 427-432 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular mobility in an interpenetrating polymeric network (IPN) based on crosslinked polyurethane (1) and styrene-divinylbenzene copolymer (2) was studied by broad-line NMR spectroscopy and reversed gas chromatography. NMR and infrared investigations show the absence of chemical interaction between the two constituent networks. For an IPN in the temperature range -196 to 120°C transition regions corresponding to the individual networks and to an intermediate region were found, the latter being characterized by an additional transition at 25-60°C (NMR spectroscopy) and 44-78°C (gas chromatography). The existence of an intermediate region, presumably of loosely packed structure, leads to a shift in the beginning of the temperature transition in IPN to lower temperature and to a decrease in activation energies of relaxation in comparison with the individual networks. The activation energies in IPN are decreased with increasing weight fraction of the second network.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 3233-3248 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerization of vinyl cyclohexane and α-methyl vinyl cyclohexane with acrylonitrile in the presence of a complexing agent AlEtCl2 results in the formation of alternate copolymers. In the copolymerization of vinyl cyclohexane with acrylonitrile the copolymer composition depends on the ratio of acrylonitrile to AlEtCl2. If this ratio is unity, alternating copolymers of the composition 1:1 are formed; with a ratio greater than unity statistical copolymers that contain more than 50% acrylonitrile units are produced. The 1H-NMR spectroscopy measurements indicate that the interaction between the comonomers and the complexing agent leads to the formation of ternary donor-acceptor complexes of equimolar composition. The equilibrium constants of these complexes at -60°C have been determined. The effects of temperature, nature of solvent and dilution on the yield, and composition of the copolymers of vinyl cyclohexane with acrylonitrile formed have been studied. By lowering the temperature the yield of copolymers increases but their composition remains equimolar. An increase in the polarity of the medium results in an increase in copolymer yield, whereas the yield decreases if the reaction is conducted in a donor-solvent medium. Dilution of the reaction mixture disrupts the alternation of units in the macrochain of copolymers. The kinetic pecularities of copolymerization have been investigated. The linear dependence of the copolymerization rate on the product of comonomer concentration is observed. The rate of copolymerization is proportional to the square root of the incident light intensity. Various additions of radical type and irradiation accelerate the process of copolymerization. The mechanism of alternating copolymerization of vinyl cyclohexane monomers with acrylonitrile in the presence of AlEtCl2 is discussed in terms of homopolymerization of the comonomer complex.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2047-2057 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The importance of nonexclusion effects in the GPC behavior of several stationary phases was investigated with DMF, 0.01M LiBr, as the mobile phase. Various low MW solutes and narrow MWD polymers, encompassing a wide range of polarities, were studied. The elution of the polymers was examined in terms of “universal calibration” behavior. Styragel and silanized glass both exhibit affinity for apolar polymers in DMF; for the former substrate this effect shows a strong inverse dependence on MW. As a consequence, application of polystyrene calibration curves to GPC analysis of more polar polymers with these substrates leads to overestimations of MW parameters. These errors are not corrected when universal calibration procedures are used. Ideal exclusion chromatography is exhibited by a number of polymers on untreated porous glass substrates. However, polymers with strong hydrogen-bonding functionality appear to be susceptible to marked adsorption in this system.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 961-972 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermosetting arylimides were prepared by reaction of sulfone ether diamines with maleic anhydride followed by chemical imidization of the intermediate polyamic acid with acetic anhydride/sodium acetate. These arylimides could be thermally cured to afford heat stable systems possessing high glass transition temperatures (Tg) and moderate to high modulus plateaus above the Tg, depending upon the molecular weight between maleimide sites. The addition type curing process alleviates problems associated with the fabrication of other polyimide systems, since volatiles are not liberated and lowviscosity, high-solids solutions can be prepared in common organic solvents. Thermal, mechanical, adhesive and fabrication characteristics are reported for the sulfone-based arylimides, which indicate utility in spectrum of high-temperature applications.
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