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  • Chemistry  (17)
  • GEOPHYSICS
  • 1980-1984  (17)
  • 1960-1964
  • 1983  (6)
  • 1982  (11)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4471-4476 
    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: This paper further illustrates the applicability of multiple internal reflectance infrared spectroscopy to the analysis of near-surface photooxidation. The results are compared with transmission infrared spectra to evaluate compositional gradients resulting from photooxidation and the influence of oxygen diffusion. The sample was a solvent-cast film of atactic, narrow distribution polystyrene, Mw of 100,000, that had been drawn to a ratio of 3.0 at 110°C by solid state coextrusion. Irradiation of these thin films, ∼25μm thickness, was performed on exposure to air at 35°C for periods of up to 6 h using a mercury source emitting at 254 nm. On photooxidation, a board peak appears at 3200-3500 cm-1, attributable to hydroperoxide formation. The most dramatic increase in the infrared spectra is found for a carbonyl band at 1730 cm-1. It appears to result from an aromatic acid group since it is shifted to 1660 cm-1 on immersion of the oxidized polystyrene films in aqueous ammonium hydroxide. It is confirmed that the photooxidation of polystyrene occurs preferentially at the surface and that this reaction rate is greatly reduced in the drawn polystyrene film.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 1109-1116 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 solvent has an influence on the homogeneity of the poly(vinyl methyl ether)-polystyrene, PVME-PS blends Prepared by drying cosolutions. This influence has been analyzed in terms of the competition among polymer-polymer and polymer-solvent interactions. Model solutions have been prepared in which intermoleeular interactions correspond to the interactions in this blend and in some of the cosolutions. These interactions in the model solutions have been detected and identified by applying Rummens' method. The 13C NMR spectra have been determined for PVME and for styrene oligomer dissolved in n-alkanes, cyclohexane, diethyl ether, isopropyl methyl ether, diisopropyl ether, and chloroform, and for PVME dissolved in benzene, toluene, and cumene. The chemical shifts have been plotted against the parameter g2 = [(n22 - 1)/(n22 + 1)]2, where n2 is the refractive index of the solvent. If the structural segment represented by certain carbon and some solvent has an interaction that is stronger than dispersive, the chemical shift for this carbon will deviate from the line formed by its shifts in n-alkane solutions, these deviations indicate characters and intensities of the intermoleeular interactions. Results indicate that cyclohexane exhibits weak interactions with both of the polymers and does not interfere with their mutual interaction, leading to a compatible blend. Results also suggest that benzene and toluene interact in the PVME in the same manner as PS. This leads to a gradual increase of the number of polymer-polymer interactions as the concentration of the polymers is increased by solvent removal, resulting in a compatible blend. Chloroform apparently interacts more strongly with PVME than with PS but interacts strongly enough with both to restrict interaction among the two polymers. As the concentration of polymers in the cosolution is increased, PS forms a separate phase. This leads to an inhomogeneous blend when the solvent is evaporated.
    Additional Material: 6 Ill.
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  • 3
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 intermolecular interaction, IMI, leading to the compatibility of polystyrene, PS, and poly (2,6-dimethyl-1,4-phenylene oxide), PPO, has been identified by analyzing the IMI of the model compounds of low molecular weight; cumene, styrene oligomer, 2,6-dimethyl phenol, and its trimer. The IMI has been detected and identified applying Rummens' method for the analysis of the solvent-induced changes in NMR chemical shifts. The results indicate that the driving force in the formation of the compatible blend of PS and PPO is the π-hydrogen bond between the electrodeficient methyl groups in PPO and π-orbitals in PS. There were no indications that n-hydrogen bonds are formed between ring hydrogens of PS and the oxygen in PPO.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 521-529 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 annealing characteristics of highly-oriented, high density polyethylene (HDPE) fibers extruded at 90°C to constant extrusion draw ratios (EDR) of 5.8 to 30 have been studied using small-(SAXS) and wide-angle (WAXD) x-ray diffraction, differential scanning calorimetry (DSC), thermal shrinkage and tensile tests. The thermal stability in macroscopic properties, such as transparency, sample dimension, and tensile modulus, remarkably increases with the sample EDR. However, the folded chain crystals within microfibrils sensitively reorganize on annealing at ≥ 110°C, even when the macroscopic properties exhibit no significant changes at high EDR's. Although the EDR has a minor effect on the reorganizability of the fold chain crystals, it has a major influence on the SAXS intensity and the extended chain crystalline component detected by WAXD for both unannealed and annealed extrudates. This specific crystalline component has an improved thermal stability and enhances the thermal stability of macroscopic properties at higher EDR. The fibers extruded at 90°C in this study and those prepared at 134°C in a prior study, exhibit significantly different melting behavior after annealing and for long period vs. EDR relationships. These facts combined with the independent observations of the effect of annealing and extrusion temperatures on the consequent long period strongly suggest that annealing during extrusion plays an important role in determining the microstructure of extrudates, especially for extrusion near the ambient melting point of the polymer.
    Additional Material: 11 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 519-520 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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
    Additional Material: 1 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 3227-3233 
    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: Studies have been made of the near surface photooxidation of atactic polystyrene films prepared in the absence of air. The samples were photooxidized on exposure to air at two frequencies, 254 and 365 nm, using a calibrated mercury irradiation source with filters. Most studies were made at 40°C and as a function of irradition time with the reactions characterized by changes in molecular weight and composition. The former was evaluated by gel permeation chromatography and the latter by transmission Fourier transform infrared spectroscopy and by multiple-internal-reflectance infrared spectra using different angles and different crystals to evaluate compositions as a function of film depth. Species identified in photooxidation include the generation of hydroperoxides and the appearance of carbonyl bands with the latter identified by the spectral shift asociated with the exposure of the photooxidized polystyrene surface to ammonia. These results suggest that principal products of near-surface oxidation of polystyrene are carboxylic acids.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 1439-1445 
    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 surface contact angle of glycerol and of water on polystyrene (PS) films has been found to depend on the extent of uniaxial draw for atactic PS. The contact angle depends on direction for the smooth films of PS drawn by solid state coextrusion. Results as a function of draw ratio to values over 4 on these noncrystalline PS samples, Mw = 6 × 105, have also been interrelated with other measures of orientation such as the anisotropy of surface and bulk properties measured, respectively, by dichroic reflectance infrared spectroscopy and by birefringence.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 81-85 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phenol and five acyclic isomeric compounds have been investigated using electron impact and field ionization techniques, mass analysed ion kinetic energy spectrometry and collision induced dissociation mass analysed ion kinetic energy spectrometry. The kinetic energy release data corresponding to the elimination of carbon monoxide from the molecular ions show that at least two structures of the reactant ion are involved. The electron impact and field ionization collision induced dissociation mass analysed ion kinetic energy spectra indicate that under electron impact conditions, the phenol ion partially isomerizes to another ion structure. An isomerization of about 40% to the structure of cis-2-hexen-4-yn-1-al is in good accordance with the spectral data.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 331-334 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Translational energy release measurments on metastable ions are used in the comparison of the structures of isomeric ions. Metastable ions, m2+, formed from m1+ ions as the result of a high energy process in the ion source are compared with isomeric metastable ions formed as daughters from fragmentation of metastable m1+ ions in a field. In the case of o-, m- and p-nitrophenol the structure of the [C5H5O]+ ions formed from [C6H5O]+ ions by these two independent methods is different as verified by comparison of the behaviour of [C5H5O]+ ions formed from several other compounds.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 94 (1982), S. 220-221 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract.Das vollständige Manuskript dieser Zuschrift erscheint in: Angew. Chem. Suppl. 1982, 513-522
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