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  • 1
    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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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2391-2401 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 220 MHz NMR spectra of sample of poly-p-isopropyl-α-methylstyrene prepared through anionic (A) and cationic (B) polymerizations are studied. Peaks at τ values of 9.07, 9.41, and 9.71 are assigned to isotactic (i), heterotactic (h), and syndiotactic (s) α-methyl triads, respectively. From the α-methyl triads and the β-proton tetrads it is found that polymer A deviates little from Bernoullian statistics and that first-order Markov configurational statistics applies to polymer B. Isopropyl methine and methyl proton resonances are also analyzed in terms of the configurational statistics of the polymer. Resonances of the phenyl protons are assigned with increasing field to s, h, i meta and ortho protons.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 271-288 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerizations at -10 to +20°C of propylene oxide (PO) with tetrahydrofuran (THF) were carried out in 1,2-dichloroethane (DCE) under dry, inert atmospheric conditions. Reactions were initiated by triphenylmethyl hexafluorophosphate (TPM-HFP) and subsequently followed by vapor-phase chromatography. Vacuum-dried residual copolymer products (RCP) were analyzed by gel-permeation chromatography (GPC), vapor-pressure osmometry (VPO) and nuclear magnetic resonance spectrometry (NMR). Attempts to homopolymerize THF in equimolar mixtures of DCE and THF at THF/TPMHFP ratios of 1:1 × 10-3 proved futile, while the homopolymerization of PO under identical operating conditions took place quite readily. Copolymerizations of PO-THF mixtures were easily carried out with high and often complete consumption of both monomers though, more often than not, THF was the principal residual monomer at the end of the 24 hr reaction period since, under no circumstances could additional THF be polymerized when the PO charged was completely consumed. Linearity of plots of -ln (C0/C) versus time showed the reactions to be first order with respect to both PO and THF concentrations. Influence of temperature reveals, via Arrhenius plots and overall activation energies (16.0 kcal/mole for PO and 13.0 kcal/mole for THF), that the initiator system functions similarly to other reported systems. Reactivity ratios (0.26 for PO and 0.80 for THF) indicate that monomer units tend to alternate along the chains rather than form extended segments of a given kind. This is supported by NMR analyses of RCP samples. Bimodal GPC distributions observed in the present study suggest that the copolymerization reaction may be proceeding by either a dual mechanism or a two-step process.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 193-203 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of styrene with two catalyst systems consisting of Al(C2H5)3 in combination with ZrCl4 or ZrCl3 has been studied. The rate of polymerization with catalyst concentration was first-order with ZrCl4 system and second-order with ZrCl3 system, but at higher catalyst concentrations in both cases, the rate progressively decreases and finally attains a low value. The rate of polymerization is, however, proportional to the square of the monomer concentration in both the cases. The overall energy of activation was 10.9 kcal./mole and 6.45 kcal./mole in these systems. The polymers obtained with ZrCl4 were of lower molecular weights as compared to those obtained with ZrCl3. The polymers in both the cases had amorphous character.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1983-1991 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The equilibrium anionic polymerization of α-methylstyrene in p-dioxane, with potassium as initiator, has been investigated at 5, 15, 25, and 40°C by using high-vacuum techniques. The comparison of these results with those obtained previously for the equilibrium polymerization of α-methylstyrene in tetrahydrofuran revealed that, although the values of ΔG1c, the free-energy change upon the polymerization of 1 mole of liquid monomer to 1 bases-mole of liquid amorphous polymer of infinite chain length, are the same for both systems, there is a distinct effect of the solvent. This effect is reflected in the value of monomer equilibrium concentration and its variation with polymer concentration and is explained in terms of a solvent-monomer and solvent-polymer interaction parameter.
    Additional Material: 3 Ill.
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