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  • 1
    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: A series of flexible urethane foams was formulated from diisocyanate-terminated polyether prepolymers, using both a polyether diol and an ethylenediamine tetraglycol as extenders. The long-term compression set characteristics and the compression deflection properties of these foams were studied. The swelling effect in a solvent, the free isocyanate content, and the role of a carbon black filler on the flexible urethane foam formulation were also evaluated. It was concluded that the total amount of diisocyanate used in the formulation, rather than a variation in the type of isocyanate, has the greatest influence on molecular structure.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 4081-4088 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements of molecular weight averages and distributions have been made on three samples of narrow molecular size distribution polystyrene with molecular weights from 100, 000 to 400, 000 subjected to 60Co γ irradiation in vacuo for various doses within the pregel region+ G(X), the radiation chemical yield of crosslinking, has been determined as 0.043 ± 0.002 and G(S)/G(X), the ratio of scission to crosslinking, as 0.02; no effect of molecular weight was observed. By comparison with previous experimental results for polystyrene irradiated in air it has been established unequivocally that an oxygen environment leads to enhanced scission at the expense of crosslinking. Literature values of G(X) and G(S)/G(X) are reviewed in the light of these results and explanations are offered to account for major discrepancies.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 1749-1770 
    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 amount of residual n-pentane in expandable polystyrene bead foam (PSBF) has an effect on the strength and dimensional stability of the foam. Data were needed to determine how fast the residual n-pentane could be removed to enhance the properties of PSBF. An experiment was designed to determine the diffusivity of n-pentane through PSBF at various temperatures. Mathematical models based on the appropriate diffusion differential equations were then used to predict n-pentane concentrations in in cylinders of PSBF. The diffusivity of n-pentane through PSBF was found to have a magnitude of 1×10-8 to 1×10-6 cm2/sec and to vary with temperature, foam density, n-pentane concentration, and foam structure.
    Additional Material: 19 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 897-903 
    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 absorption spectra of a series of polyamic acids prepared using various reaction conditions were studied using the ultraviolet (UV), visible, and near-infrared (IR) ranges. The near-IR proved most valuable; the amidization and imidization processes could be followed by observing the change of intensities of the 1950-nm combination amine band and a band at 2300 nm assumed to be a function of the amide group.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 929-939 
    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: Boron trifluoride forms complexes with nitrogen-and oxygen-containing Lewis bases. These acid-base complexes are sometimes added to epoxy resins to accelerate their cure at elevated temperature (120°C-160°C). Several possible processing concerns with the use of boron trifluoride complexes have been investigated. It was shown that each complex can be readily identified by its distinct fluorine-19 NMR spectrum. All of the boron trifluoride complexes are converted to fluoroboric acid under normal epoxy resin cure conditions. The fluoroboric acid is the true catalyst for epoxy resins. Experimental results show that fluoroboric acid does not catalyze the polymerization of an epoxy resin at room temperature. Finally, it was shown that fluoroboric acid is not hydrolyzed to hydrofluoric acid.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2499-2507 
    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: A direct method for preparing deuterated ethylene by reducing acetylene-d2 with chromous ions in a dimethylformamide/deuterium oxide mixture is described. This method gives a good yield of precursor gas of relatively high purity. The gas was polymerized with a Ziegler-type catalyst to produce deuterated polyethylene with sufficient purity and melt flow properties for use in laser fusion studies. A reaction variables study showed that polymerization of deuterated ethylene yields polymers with higher molecular weights than those obtained using normal ethylene. The study also indicated that the deuterium content of the polymer decreases with increasing reaction temperature, thus dictating that the process operates near room temperature. Several mechanical and chemical properties of the deuterated polymer were determined and are reported.
    Additional Material: 7 Ill.
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  • 7
    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: A comprehensive 13C-NMR method for the analysis of composition in the most common commercial polyethylene copolymers has been established. The method covers ethene copolymers with propene, butene-1, hexene-1, octene-1, and 4-methyl pentene-1 in the composition range of 1-10 mol %. The chemical shift assignments and T1 values of the resonances of the copolymers are presented. Results of precision studies and interlaboratory analyses showed that the molar composition could be determined with a relative precision at 2δ of about 6%. This method is being proposed to ASTM as Method X70-8605-2.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 229-239 
    ISSN: 0887-624X
    Keywords: ammonia/ammonium thiocyanate solvent ; cellulose ; dissolution mechanism ; solid state CP/MAS 13C-NMR ; X-ray ; conformation ; hydrogen bonding ; ammonia mercerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ammonia/ammonium thiocyanate (NH3/NH4SCN) is an excellent swelling agent and solvent for cellulose, even at a high degree of polymerization. Because polymorphic conversion in cellulose has been a long-standing, perplexing, troublesome problem, we have undertaken to study that mechanism. Solid state CP/MAS 13C-NMR and X-ray analysis proved to be very useful analytical techniques for the task. It appears that during temperature cycling, specific cellulosic inter- and intramolecular hydrogen-bonds are broken as polymorphic conversion proceeds sequentially from the polymorph I to III, and finally at total solvation to amorphous. This proceeds correspondingly via transformation of the polymorph conformations of CH2OH from trans-gauche, “tg,” to gauche-trans, “gt,” to gauche-gauche, “gg.” © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 241-247 
    ISSN: 0887-624X
    Keywords: ammonia/ammonium thiocyanate solvent ; cellulose ; dissolution mechanism ; conformation ; swelling ; mercerization ; hydrogen bonding ; entropy ; enthalpy ; affinity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a previous article,1 we reported on the interaction of cellulose with NH3/NH4SCN by using solid state CP / MAS 13C-NMR, wide-angle X-ray and other techniques. It appears that during an imposed temperature cycling sequence, specific cellulosic inter- and intramolecular hydrogen bonds are broken as polymorphic conversion and, ultimately, dissolution occurs. Cellulose is converted from the polymorph I to II to III and, finally, to amorphous. We speculate that these changes proceed via transformation of the polymorph conformations of CH2OH from trans-gauche, “tg,” to gauche-trans, “gt,” to gauche-gauche, “gg.” Remarkably, the temperature cycling effectively and rapidly effects these changes, seemingly, by invoking at two different temperatures (22°C and -78°C), a subtle but powerful temperature-related interplay of enthalpic and entropic forces. At the higher of the cycling temperature limits, entropy and van der Waals forces dominate, causing NH3 to partition in favor of the liquid phase. At the lower of the temperature cycling limits, enthalpy dominates and the situation is reversed favoring NH3 partition toward the cellulose, resulting in breakage of inter- and intracellulosic H-bonds by the interpenetrating ammonia to form new H-bonds between cellulose and ammonia, leading ultimately to conformational changes and, ultimately, even dissolution. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 461-491 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study has been made of the mechanical, thermal, and morpholigical characteristics of melt-crystallized isotactic polypropylene containing high levels of the β or pseudohexagonal crystalline form. Different levels of β-form crystallinity were produced in the polymer by blending in low levels of quinacridone dye nucleating agent. Microscopical studies of the crystallization process revealed that both α-form (monoclinic), and β-form spherulites nucleated on the dye particles, with α-spherulite growth commencing at a higher temperature. These observations were able to qualitatively explain the dependence of β-form level on both the nucleant concentration and its state of dispersion in the polymer. Improving the dispersion of the nucleant was found to reduce the level of β-form crystallinity if the nucleant concentration exceeded an optimum level. A new procedure for quantifying the volume fraction of β spherulites in a sample was developed which utilized the technique of selective solvent extraction. From volume-fraction, x-ray, and density data, the pure α and β crystal densities were obtained. Dynamic mechanical measurements-obtained on unoriented specimens containing varying levels of β-form crystallinity showed an increase in the magnitude of the damping in the post-Tg region with increasing β content. High levels of the β form lead to lower values of the modulus and yield stress, and higher values of the elongation at break and impact strength.
    Additional Material: 22 Ill.
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