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  • Wiley-Blackwell  (11)
  • 1995-1999  (2)
  • 1970-1974  (9)
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 315 (1973), S. 629-639 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Experimentell ermittelte UV-, ESR- und elektrochemische Daten arylsubstituierter Anthracene werden an Hand von Modellrechnungen und Literaturdaten diskutiert. Dabei kann gezeigt werden, daß diese Eigenschaften im wesentlichen durch die Molekülgeometrie, hier repräsentiert durch Verdrillungswinkel, bestimmt werden. Ein spezifischer Einfluß der Arylsubstituenten auf die elektronischen Eigenschaften des Grundkörpers konnte nicht nachgewiesen werden.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 316 (1974), S. 75-86 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Möglichkeiten der quantenchemischen Berechnung thermodynamischer Gleichgewichtsdaten für die Elektronentransferlumineszenz- bzw. Elektronentransferlöschreaktionen zwischen aromatischen π-Elektronensystemen in Lösung werden diskutiert und derartige Berechnungen für einige Systeme durchgeführt. Die kleine Enthalpie dieser Reaktionen ergibt sich als Summe der wesentlich größeren negativen Enthalpie einer hypothetischen Gasphasenreaktion und positiven Änderung der Solvatationsenthalpie. Ferner wird die Möglichkeit untersucht, durch LFE-Beziehungen die Freie Reaktionsenthalpie aus quantenchemisch berechneten Größen vorauszusagen. Es zeigt sich, daß dies nur in kleinen Gruppen verwandter Substanzen möglich ist.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1097-1115 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Studies have been made of the secondary relaxation processes in the solid state of a number of polymers containing aromatic groups in the polymer chain. The polymers investigated include one, polystyrene, with the aromatic group in side-chain positions, and six high polymers in which phenylene rings lie in the main backbone chain. In polystyrene, wagging and torsional motions of the side chain phenyl rings give rise to a low-temperature δ-relaxation which is centered at 33°K (1.7 Hz) and which has an activation energy of about 2.3 kcal/mol. Most of the polymers with phenylene rings in the main chain exhibit a low-temperature relaxation in the temperature region from 100°-200°K. This relaxation process is centered at 159°K (0.54 Hz) in poly-p-xylylene, at 162°K (0.67 Hz) in polysulfone, and at 165°K (1.24 Hz) in poly(diancarbonate). In poly(2,6-dimethyl-p-phenylene oxide), two overlapping low-temperature relaxations are found, one in the range 125-140°K and the other near 277°K (ca. 1 Hz). The low-temperature secondary relaxation process in all of these polymers is believed to be associated with local reorientational motion of the phenylene, or substituted phenylene, rings or with combined motion of the phenylene rings and nearby chain units. For these low temperature relaxation processes, the activation energy is about 10 kcal/-mole. The temperature location of the relaxation appears to depend on the specific units to which the phenylene rings are attached and on steric and polar effects caused by substituents on the ring. In the poly-p-xylylenes the relaxation is shifted to much higher temperatures by a single Cl substitution on the ring but remains at essentially the same temperature position when dichlorosubstitution is made. The effects of water on the magnitude and temperature location of the observed low temperature relaxations, as well as the implications of the study for other polymers containing aromatic groups in their backbone chains, are discussed.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1291-1294 
    ISSN: 0887-6266
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: No abstract.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1235-1245 
    ISSN: 0887-6266
    Schlagwort(e): PMMA ; mechanical properties ; ionomer precursor polymer ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Rigid-rigid blends made of ionomer and ionomer precursor polymer, based on poly(methyl methacrylate) (PMMA), have been investigated. Two series of blends have been prepared for studying mechanical properties. In one series, dynamic mechanical properties were determined over a wide range of temperatures. As the weight fraction of the ionomer was increased, there was a modest increase of modulus at ambient temperature and a very large increase in the rubbery modulus at elevated temperatures above the glass transition temperature of PMMA. In a second series of tests, tensile stress-strain measurements, made at an ambient temperature, were carried out over a wide range of blend compositions. For all blends tested, the mechanical properties exhibited a synergistic enhancement, i.e., average values of modulus, strength and fracture energy were all higher than expected based on the rule of mixtures. Measurements of fracture toughness also exhibited synergy, with a maximum value, higher than the value of either blend component, being attained in blends containing about 30 wt % of the PMMA ionomer. These results are interpreted in terms of a higher resistance to fracture of the more chain-entangled ionomer phase and good interfacial adhesion between the two components of the blend. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1235-1245, 1998
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 13 (1973), S. 51-58 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Existing dynamic mechanical relaxation data on two polymers containing aromatic groups in the backbone chain, viz., polyimide PI, and poly(2,6-dimethyl-p-phenylene oxide), PDMPO, are reviewed and new data bearing on specimen purity and water content are presented. It is demonstrated that three separate relaxation processes are normally present in both polymers in the temperature range from about 100-400°K. The lowest temperature relaxation, designated γ, occurs in the 100-180°K range and is considered to arise from limited rotational oscillation of some phenylene rings about the 1,4 axis. Another relaxation process, designated β arises from the presence of water in the polymer. Its strength increases with increase of water content, its activation energy is about 10-12 kcal/mole, and it occurs in the 180-190°K range at 1 Hz. A higher strength secondary glass relaxation process, designated β*, occurs in the 280-400°K range at usual measuring frequencies (1 Hz to 104 Hz). This relaxation is thought to be associated with the combined reorientational motion, of rings and connecting atoms of the monomer unit in “defect” regions, or regions of poor chain packing. As such, its position is affected by sample history. Both polymers also show a rise in damping in the high temperature region indicative of additional main chain motions. In addition to the above relaxations, PDMPO shows a δ-relaxation below liquid nitrogen temperatures, associated with onset of Me rotation and PI shows an additional small relaxation near 500°K.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 14 (1974), S. 801-805 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Fatigue tests under reversed tension-compression have been made on polystyrene specimens in both the unnotched and notched condition. For the notched specimens subject to a stress amplitude of 2500 psi, the log of the fatigue life was found to be a linear function of the log of the notch size. From the data, it was possible to determine an inherent flaw size for polystyrene subject to alternating loading and this value is compared to corresponding values obtained from static tests. Fracture surfaces were examined by scanning electron microscopy and the changes produced by notching are discussed.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 1319-1350 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Fracture response of polyimide and polysulfone in tension under superimposed hydrostatic pressures up to 100,000 psi is presented. The influence of hydrostatic pressure and the pressure medium on the specific surface energy γ is determined by utilizing the Griffith theory of brittle fracture. For polyimide as well as for polysulfone, γ is found to increase with increasing pressure. Furthermore, for polysulfone at any given pressure level, the value of γ is found to be lower in heptane medium than in kerosene. Heptane is known to be a stress-cracking agent for polysulfone. Fracture surface of the tested tensile specimens is examined by using a scanning electron microscope. The observed fracture features are correlated with the macroscopic deformation behavior and also with the effects of the pressure medium used. In polyimide, the region of crack initiation narrows down from a very broad region at atmospheric pressure to almost a point source along the outer periphery of the specimen at 100,000 psi. In addition, polyimide undergoes a transition in the nature of fracture response between 80,000 to 100,000 psi, and this is clearly indicated in the scanning electron micrographs. In polysulfone, the crack propagation appears to be faster when heptane is used as the pressure medium than when kerosene is used. The penetration of the medium into the specimens can be observed on the micrographs. Several scanning electron micrographs of the fracture surface suggest the possibility of a significant temperature rise in the specimen during fracture. This increase in the specimen temperature is roughly estimated from the stored elastic energy released upon fracture.
    Zusätzliches Material: 34 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 519-526 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Significant improvements in the fatigue life of polystyrene can be realized by increase in molecular weight. In this investigation, samples of polystyrene of varying molecular weight were subject to alternating cycles of axial tension and compression at a test speed of 1600 rpm. One set of fatigue tests was made on samples machined from commercial whole polymer rod. A second set of samples was prepared from a PS standard having an average molecular weight of 160,000 and a narrow molecular weight distribution. A third set of samples had a high average molecular weight of 860,000. For a whole polymer, the S-log N curves tended to have the same general shape as for metals, and the endurance limit appeared to be about 1400 psi. The test results show that the average fatigue life, at any given stress amplitude, is significantly increased by increase in molecular weight. For example, the average life of the high molecular weight standard at any given stress level was found to be more than tenfold that of the low molecular weight standard.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new interpretation - based on a reevaluation of the spectroscopic properties of products 16 to 27 - is proposed for the reaction of diphenyl-cyclopropen-one 14 and -thione 15 with ketene-A, N-diacetals 8 to 13 (A = R2N, RO and RS) originally reported by Sauer & Krapf. It is concluded that the previous structural assignments (see the a-structures), made on the assumption of a prevailing “C,C-insertion” reaction, must be rcplaced as follows: (1) All the “secondary adducts” are, in fact, derivatives (amides and lactams) of 2,3-diphenyl-penta-2, 4-dienoic acid and thioacid (structures 16b to 24b); (2) the “isomerization products”, differ from the latter only in the configuration of the α,β-double bond (structures 25b and 26b); (3) the common “hydrolysisproduct” is α,β-diphenyl-γ-methyl-γ-hydroxy-Δα-butenolide (27b), The above cyclopropenone-ketcneacetal reactions represent, therefore, cases of “C, N-insertion”.This is rationalized with a reaction scheme, in which the “acylide” structure of the “primary adducts” plays a role.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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