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  • Chemistry  (24)
  • CYBERNETICS  (2)
  • Computer Systems
  • 1990-1994  (21)
  • 1970-1974  (4)
  • 1935-1939  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 207 (1993), S. 9-21 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wird ein phänomenologisches Modell vorgestellt, mit dem sich das Entstehen starker Anisotropien der physikalischen Eigenschaften semikristalliner Polymerer nach einachsigem Verstrecken beschreiben 1äßt. Dieses Modell führt die Temperatur als expliziten Parameter in die Orientierungsfunktion ein. Es enthält zwei frei wählbare Parameter, die für jedes Polymere durch Anpassen der experimentellen Daten der Doppelbrechung als Funktion des Verstreckverhältnisses bei einer bestimmten Temperatur ermittelt werden konnen. Die berechneten Werte für Elastizitätsmodul, thermische Leitfähigkeit und Expansibilität parallel und senkrecht zur Streckrichtung stimmen in einem wäiten Bereich des Verstreckverhältnisses und der Temperatur mit den experimentellen Ergebnissen gut überein.
    Notes: A phenomenological model has been proposed to understand the development of strong anisotropy in physical properties of semicrystalline polymers on uniaxial drawing. The proposed model introduces temperature as an explicit parameter in the orientation function. The model contains two free parameters for each polymer which can be evaluated by fitting the experimental data on birefringence versus draw ratio at a particular temperature. The calculated values of elastic moduli, thermal conductivity and expansibility along and perpendicular to the drawing direction over the entire range of draw ratio and a wide range of temperature are in good agreement with experimental values.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3795-3800 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 35 (1990), S. 244-251 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Enhancement of the productivity of xylanase and β-xy-losidase of Aspergillus ochraceus was investigated by multistep mutagenesis. The spores of the wild strain were subjected to UV and N-methyl-N-nitro-N-nitro-soguanidine (NTG). The hyperxylanolytic mutant (NG-13), which showed good clearing on the surface of the xylan-agar plate, secretes xylanase and β-xylosidase at high levels during growth on commercial xylan and on agricultural wastes. Both liquid and solid state cultures were employed in the study for enzyme production. The xylanase from NG-13 was purified to homogeneity by ammonium sulfate precipitation and gel filtration. This purified enzyme showed a pH optimum of 6.0 and was stable in the range of pH 5 to 10. Prolonged stability of the enzyme was observed at 45°C though its activity was maximal at 50°C. The molecular weight of the enzyme was estimated to be 4.3 × 104 by SDS-polyacrylamide gel electrophoresis and 5 × 104 by gel filtration on Sephadex G-75. The kinetic data showed that the Km and Vmax values for xylan were 1 × 10-3M and 19.6 μmol/ min/mg protein, respectively. The enzyme was both more active and thermostable in the presence of K+and was inactivated by thiol reagents such as Hg2+, p-hydroxymercuribenzoate (PHMB), 3′, 5′-dithiobis (2′-nitrobenzoic acid) (DTNB), and N-ethylmaleimide (NEM).
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 163 (1973), S. 37-43 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Substanzpolymerisation von N-Vinylcarbazol (NVC) wurde mit 3d-Metalloxid-Katalysatoren durchgeführt, und die folgende Reaktivitätsreihe für die untersuchten Oxide wurde vorgeschlagen: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm 2} {\rm O}_{\rm 5} {\rm 〉 MnO}_{\rm 2} {\rm 〉 TiO}_{\rm 2} {\rm 〉 Cr}_{\rm 2} {\rm O}_{\rm 3} {\rm 〉 NiO 〉 ZnO 〉 Cu}_{\rm 2} {\rm O 〉 CuO 〉 Co}_{\rm 3} {\rm O}_{\rm 4} {\rm andCoO} $$\end{document} wobei die Oxide des Kupfers und Kobalts nicht wirksam sind. Einige kinetische Untersuchungen wurden mit dem System NVC/MnO2 ausgeführt. Auf Grund der Verzögerung der Polymerisationsgeschwindigkeit bei Gegenwart von Wasser oder Thiophen wurde ein kationischer Mechanismus für die Polymerisation vorgeschlagen. Die Wirkungslosigkeit der Kupfer- und Kobaltoxide als Katalysatoren wurde vorläufig mit der Annahme gedeutet, daß sie eher oxydierend wirken als durch π-Komplex-Bindung. Rühren übt keinen Einfluß auf die Polymerisationsgeschwindigkeit aus.
    Notes: The bulk polymerization of N-Vinylcarbazole (NVC) is carried out using some 3 d-metal oxides as catalysts and the following order of reactivity is suggested for the various metal oxides studied: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm 2} {\rm O}_{\rm 5} {\rm 〉 MnO}_{\rm 2} {\rm 〉 TiO}_{\rm 2} {\rm 〉 Cr}_{\rm 2} {\rm O}_{\rm 3} {\rm 〉 NiO 〉 ZnO 〉 Cu}_{\rm 2} {\rm O 〉 CuO 〉 Co}_{\rm 3} {\rm O}_{\rm 4} {\rm andCoO} $$\end{document} the oxides of copper and cobalt being ineffective. Some kinetic studies are carried out with the NVC/MnO2 system. Endorsed by the observed retardation of the rate in the presence of water and thiophene a cationic mechanism is suggested for the polymerization. The incapability of the oxides of Cu and Co to act as good catalysts is tentatively explained by supposing that they act as oxidizing rather than π-complexing polymerization catalysts. Stirring does not show any influence on the rate of polymerization.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 151 (1972), S. 121-125 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Störung der Metachromasie eines an einem Polyanion gebundenen Farbstoffs durch Cetylpyridiniumchlorid (CPCl) wurde quantitative abgeschätzt, indem die in der wässerigen Schicht verbliebenen Farbstoffmengen nach Schütteln der metachromatischen Lösung mit Tetrachlorkohlenstoff in An- und Abwesenheit von CPCl ermittelt wurden. Die Aufhebung der Metachromasie wurde außerdem aus der konduktometrischen Titration der Farbstoff/Polyanion-Lösung mit CPCl ermittelt. CPCl verdrängt die Farbstoffionen von den Polyanionen beinahe stöchiometrisch, was bei Natriumchlorid nicht der Fall ist. Dieses besondere Verhalten von CPCl wird seiner Neigung zur Bildung hydrophober Bindungen zugeschrieben. Es wurden Methylenblau und Kristallviolett als Farbstoffe sowie Chondroitinschwefelsäure und Heparin als Polyanionen verwendet
    Notes: The disturbance of metachromasia of a dye/polyanion system by cetyl pyridinium chloride (CPCl) has been estimated quantitatively from the difference of the amounts of dye left in the aqueous layer after carbon tetrachloride extraction of the metachromatic solution in the presence and absence of CPCl, as well as from conductometric titration of the dye/polyanion solution with CPCl. Results show that CPCl, unlike sodium chloride, displaces the dye ions from the polyanions almost stoichiometrically. This special behaviour of CPCl has been assigned to its tendency to form hydrophobic bonds. As dyes methylene blue and crystal violet, as polyanions chondroitin sulfate and heparin have been used.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 737-747 
    ISSN: 0887-6266
    Keywords: Crystallization ; melting ; morphology ; thermoplastic polyimide ; New-TPI ; PMDA ; 33BAPB ; polarizability ; SAXS ; lamellar thickness ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization, melting, and morphology of a thermoplastic polyimide (New-TPI) containing pyromellitic dianhydride (PMDA) and 3,3'-bis(4-aminophenoxy) biphenyl diamine (33BAPB) moieties have been studied. This material showed a glass transition temperature (Tg) of 250°C, an equilibrium melting temperature (T°m) of 406°C and a heat of fusion (ΔH) for 100% crystallinity of 6.38 kJ/mol. Measurements of the crystallization bulk rate (by DSC) and spherulite growth rate (by optical microscopy) indicated that the maximum crystallization temperature was about 320°C and the crystallization growth process was three-dimensional under thermal nucleation (the Avrami exponent n ca. 4). The rate of nucleation density was estimated to decrease with increasing temperature, and the product of two crystal surface free energies σeσo was calculated to be 1176 erg2/cm4. The meltgrown spherulite consistently showed a Maltese cross pattern with negative birefringence under cross-polars. The calculation of polarizability along the three unit cell axes suggested that the crystal b axis may be along the spherulite growth (radial) direction. Two scattering maxima were seen in small-angle x-ray scattering (SAXS) profiles. The dominant peak indicated a long period of ca. 20 nm which varied as a function of crystallization temperature. The weak peak at a d-spacing of 2.5 nm was independent of temperature and has been attributed to the chemical repeat distance determined by Okuyama et al. (indexed as 001). The lamellar thickness lc, estimated by the correlation function analysis of the SAXS data, was found to be similar to that determined by the Scherrer analysis of the 001 reflection peak. © 1994 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1375-1385 
    ISSN: 0887-6266
    Keywords: liquid crystalline aromatic copolymers, solid state order in ; copolymers, wholly aromatic, nature of order in solid state of ; solid state order in aromatic liquid crystalline random copolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two different models of order in the solid state of wholly aromatic liquid crystalline copolymers (ALCPs), namely the nonperiodic layer (NPL) model of Windle et al. and the paracrystalline lattice (PCL) model of Biswas and Blackwell, have been analyzed with respect to experimental and theoretical observations. The NPL model proposes the formation of ordered domains by matching random sequences between adjacent chains while the PCL model relies on the presence of conformational correlations between adjacent monomers, without explicit sequence matching, to form ordered domains. The presence of three-dimensional order in the quenched state of ALCPs has been reported previously. The initial stages of crystallization are very likely to be assisted by the presence of small sequence matched domains. However, the probabilities for the formation of NPL domains having sizes comparable to those observed experimentally in the quenched state are extremely small. The PCL model, on the other hand, is not hampered by probability statistics and also provides a better fit to the experimental wide-angle x-ray scattering data along the fiber (Z) axis. The reported calorimetric data on ALCPs are also inconsistent with the presence of significant motion between chains, which is required for the NPL crystal to grow during the process of annealing. In contrast, the observation of a slow crystallization process, which converts the quenched hexagonal phase to the ordered orthorhombic phase, is adequately described by the PCL model as occurring via local conformational changes and small axial shifts between adjacent monomers. The observations from dielectric relaxation, nuclear magnetic resonance and dynamical mechanical spectroscopy studies also favor the PCL model over the NPL model of order in the solid state of ALCPs. © 1992 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1703-1710 
    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: PVC modified by Cl displacement reaction with meta-aminophenol (MAP), bisphenol A (BISA), and phenolphthalein (PHEN) has been converted into phosphoric acid cation exchange resins. These resins have been characterized in regard to their structure, ion exchange properties, and thermal stability. The ion exchange capacities fall into the range 5.5-8.0 (meq/g) for the resins. The overall thermal stability is considerably higher than that for the corresponding sulfonic acid resins, as well as for the PVC-MAP, PVC-BIS A, and PVC-PHEN condensates. The resins exhibit ca. 4-6% capacity losses under isothermal hydrolytic cleavage at 100°C for 24 h.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 1685-1692 
    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 group of poly(N-vinylcarbazole) pendant polysulfones has been prepared by reacting it with benzene, toluene, p-chlorobenzene- and p-nitrobenzenesulfonyl chloride and N-methyl carbazole, 3,6-disulfonyl chloride by the Friedel Crafts reaction. Carbazole-based backbone polysulfones have also been prepared by the reaction of N-methyl carbazole, 3,6-disulfonyl chloride and biphenyl, naphthalene, anthracene, and carbazole in presence of anhydrous aluminum chloride. The various sulfone polymers, thus prepared, have been structurally characterized by elemental analysis and IR spectroscopy. Detailed analyses of thermal stability, dielectric, and conductivity characteristics have revealed certain significant differences between these two types of sulfone polymers.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1575-1580 
    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 aqueous polymerization of pyrrole with varying FeCl3/Py mol ratio produces black insoluble powders. IR characterization reveals the shifting of the N—H stretching band to higher frequency with increasing FeCl3 amount in the feed composition due to lowering of intermolecular H-bonding. SEM shows a spongy texture of the polymer. TGA indicates the initial decomposition temperatures (180°-237°C) to be somewhat dependent on the FeCl3/Py feed ratio. DSC suggests the glass-transition temperature to be in the range 160-170°C for the polymers prepared with various feed compositions. The conductivity is also dependent on the FeCl3/Py feed composition and levels off at a value of ∼3 ohm-1cm-1. © 1994 John Wiley & Sons, Inc.
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