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  • Chemistry  (32)
  • ATOMIC AND MOLECULAR PHYSICS  (4)
  • 1995-1999  (7)
  • 1990-1994  (18)
  • 1975-1979  (9)
  • 1965-1969  (2)
  • 1
    facet.materialart.
    Unknown
    In:  Other Sources
    Publication Date: 2011-08-16
    Description: The resonance line spectra of ions in the Xe I isoelectronic sequence, consisting of the five transitions to the 5p6 150 ground state from levels with J = 1 in the 5p5 5d and 6s configurations, have been observed for Cs II, Ba III, and La IV. The observations were made with a sliding spark on the 10.7-m normal-incidence vacuum spectrograph at NBS. The resonance transitions from the 5p5 6d and 7s configurations were also observed for these ions, except for that from 5p5 6d 3P1 of Ba III. Several resonance transitions from higher nd and ns levels were also observed. Estimated values for the J = 1 levels of the 5p5 7s configuration of Ce V were obtained by extrapolation. The derived ionization energies in eV are Cs II 23.17(4), Ba III 35.79(6), La IV 45.95(6), Ce V 65.55(25).
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: Optical Society of America; vol. 65
    Format: text
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  • 2
    facet.materialart.
    Unknown
    In:  Other Sources
    Publication Date: 2011-08-16
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: Optical Society of America; vol. 65
    Format: text
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  • 3
    Publication Date: 2011-08-16
    Description: Spectra of Cs III, Ba IV, and La V were photographed in a low-voltage sliding spark on a 10.7 m normal-incidence vacuum spectrograph. These ions are isoelectronic with neutral iodine and display a halogen-like energy level structure. Detailed isoelectronic comparisons, level transition diagrams, and tabular data on the transitions of the ions and percentage compositions of Cs III configurations are presented.
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: Optical Society of America; vol. 66
    Format: text
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  • 4
    Publication Date: 2019-06-27
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: PB80-103773 , Optical Society of America; vol. 69
    Format: text
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1227-1234 
    ISSN: 0887-624X
    Keywords: polyanilines ; derivatives ; chemical synthesis ; oxidation state ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses of parent polyaniline and methyl, methoxy, and ethoxy ortho-substituted polyanilines were performed using the conventional chemical methodology and monitored using the new open-circuit-potential (Voc) profile technique. The intermediate pernigraniline oxidation state was identified and isolated at the Voc maximum (A) during the conventional chemical synthesis of poly(o-methoxyaniline) in the emeraldine oxidation state. The introduction of the substituent on the aniline ring leads to longer polymerization times and lower Voc values. Syntheses in the presence of two different monomers in solution were also investigated and showed preferential polymerization of the monomer with the lowest Voc potential. All polymers produced were characterized by elemental analysis, gel permeation chromatography, UV-VIS spectroscopy, and cyclic voltammetry. The influence of the substituent on the Voc profile and on the polymer characteristics are rationalized in terms of steric and electronic effects. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0959-8103
    Keywords: polyaniline ; pernigraniline oxidation state ; copolymer ; synthesis ; electrochemistry ; 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: Polyaniline was electrochemically synthesized in the emeraldine oxidation state and then converted to the pernigraniline oxidation state by applying an electric potential under optimized conditions. The stability/reactivity of polyaniline in the pernigraniline oxidation state was evaluated in various aqueous media. The products of the reduction of the pernigraniline oxidation state by o-toluidine were analyzed by gel permeation chromatography, ultraviolet-visible and infrared spectroscopies, and cyclic voltammetry. The results are consistent with the synthesis of a diblock copolymer of polyaniline/poly(o-toluidine) and also of some poly(o-toluidine) homopolymer in the emeraldine oxidation state as a side product.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 375-375 
    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
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1629-1646 
    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 purpose of the present work has been to produce knowledge as regards the rheological behavior of polymer matrix in nonwoven fibrous reinforcing structures for composites. The results are expected to contribute toward a better understanding of flow mechanisms in fibrous systems in order to develop better techniques for fabricating elastomer-based composites. Theoretical and experimental analyses have been made of interactions between the structural parameters of the fibrous mats and the flow characteristics of the matrix with systematically varied material and process parameters. In nonwoven mats with fibers laid lengthwise, the flow rate along the fiber direction was found to be significantly higher than the flow rate crosswise to the fiber direction. Nonwoven mats with multidirectionally laid fibers exhibited a practically radial flow front pattern. Nonwoven mats made of coarser fibers showed greater matrix polymer flow rate as compared with finer fibers. The matrix flow distance was proportional to the logarithm of injection time. The decrease of pressure in the mold cavity was linearly proportional to the matrix flow distance. The dependence of permeability on the level of compression of the fibrous structure is in agreement with the results published by other workers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 21 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1693-1704 
    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 new type of mold was developed and tested for structural reaction injection molding (SRIM) of elastomer composites having polymer matrices made from a mixture of two components. These mixtures had short pot lives and relatively high viscosity. Channel systems for polymer feeding and vacuum application were investigated. The mold cavity was provided with up to 24 polymer feeding holes and 38 vacuuming holes. The cavity and channels were made from transparent materials that allowed easy observation and video recording of the polymer matrix flow. In addition, some design parameters were studied such as channel layout. Investigations were carried out on the mechanism of polymer matrix flow and fiber breakage during the formation of fiber-reinforced composites made of non-woven fiber reinforcement structures with considerably longer fiber lengths than reported earlier. Other studies included determination of the effects of fiber type, fiber dimensions, and fiber/matrix v/v ratio on the matrix flow during impregnation. © 1992 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 751-765 
    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 influence of fiber type and fiber-surface properties on matrix flow behavior was investigated using structural reaction injection-molding (SRIM). The influence of fiber type, fiber-surface properties, and matrix type on strength properties in elastomeric composites reinforced with nonwoven fibrous structures was investigated using tensile tests on elastomer composite samples from SRIM and latex coagulation (LC) fabrication methods and the microbond strength method on individual fibers. The fibers used were PET, LLDPE, and p-aramid. Fibers were treated with epoxy, styrene, and isocyanate derivatives, which make the surface chemically reactive. Treatments were also made with NaOH and a copolymer of polyester and polyol ether, causing a change in the fiber surface energy. The matrix types were polyurethane elastomer and natural rubber. The results show that the surface treatments which produced a change in the surface energy influenced the flow rate of the matrix polymer during the composite fabrication process. The treatments resulted in chemically reactive fiber surfaces which improved the fiber-matrix bond strength without affecting the Young's modulus of the composite material. Good correlation was found between bond strength and surface energy including the dispersive component of surface energy in the case of polyurethane elastomer and surface-modified PET fibers. The age of the polyurethane matrix has a marked influence on the bond strength. The fiber volume fraction in composites has a strong influence on the Young's modulus of the elastomer composite. © 1995 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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