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  • Polymer and Materials Science  (438)
  • Lunar and Planetary Science and Exploration  (47)
  • 1
    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: This paper is concerned with the ring opening of the uretdione group in presence of nucleophilic partners and of the technological significance of this reaction. It is shown that at temperatures from 100° to 120°C both polyesters containing hydroxyl groups and low-molecular weight compounds carrying Zerewitinow-active hydrogen atoms react in solution as well as in the molten state with free NCO groups of uretdione diisocyanates by the diisocyanate polyaddition process. Under these conditions no opening of the uretdione ring occurs.These results give rise to the use of uretdione diisocyanates for chain extensions yielding polyuretdione polyurethanes. Reactions with blocking agents (e.g. ε-caprolactam) result in new types of blocked uretdione and blocked polyuretdione polyurethanes. It is shown that the four-membered rings are split completely at temperatures from 140° to 180°C. Compounds containing hydroxyl groups which are available in the reaction mixture react with the latent NCO groups of the uretdiones to form urethanes. By selection and combination of suitable starting compounds crystalline, high-melting polyuretdione polyurethane powders of good milling properties can be obtained. The new syntheses of technical usefulness yield non-polluting polyurethane powder coatings for application by electrostatic spraying.
    Notes: Die Ringöffnung der Uretdiongruppe in Gegenwart von nukleophilen Reaktionspartner und die technische Bedeutung dieser Reaktionsind Gegenstand der vorliegenden Arbeit. Die Untersuchungen machen deutlich, daß hydroxylgruppenhaltige Polyester und niedermolekulare Zerewitinow-aktive Wasserstofftome tragende Verbindungen sich bei Temperaturen von 100-120°C in Lösung, aber auch in der Schmelze mit den freien NCO-Gruppen der Uretdiondiisocyanate nach dem Diisocyanat-Polyadditionsver-faren umsetzen lassen, ohne daß nennenswerte Uretdionringöffnung eintritt. Auf Grund dieser Erkenntnis können mit den Uretdiondiisocyanaten Kettenverlängerungen zu Poly-uretdionpolyurethanen durchgeführt werden. Durch Umsetzung mit Blockierungsmitteln (z.B.ε-Caprolactam) werden neuartige blockierte Uretdione und blockierte Polyuretdion-polyurethane erhalten. Es wird nachgewiesen, daß die Vierringe im Temperaturbereich von 140-180°C vollständig aufspalten. Gleichzeitig vorliegende hydroxylgruppenhaltige Verbindungen reagieren mit den latenten NCO-Gruppen der Uretdione unter Urethanbildung. Durch geeignete Wahl und Kombinatio der Asgangsverbindungen lassen sich kristalline, hochschmelzende, gut mahlbare Polyuretdionpolyurethanpulver gewinnen. Die neuen technisch verwertbaren Synthesen führen zu umweltfreundlichen, lösungsmittel-freien Verfahen der elektrostatischen Pulverbeschichtung.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The η3, η2, η2-dodeca-2(E), 6(E), 10(Z)-trien-1-yl-nickel(II) complexes [Ni(C12H19)]X (X = SbF6, O3SCF3) were treated in toluene with amorphous aluminium trifluoride (which was prepared from AlEt3 and BF3 · OEt2) in a mole ratio 1 : 10 to 20, forming a highly active catalyst for the 1,4-cis polymerization of butadiene. This catalyst is comparable in its activity and selectivity, and in the molar mass distribution of the polybutadiene, with the technical nickel catalyst Ni(O2CR)2/BF3ċOEt2/AlE3 developed by Bridgestone Tire Company thirty years ago. The existence of the C12-allynickel(II) cation [Ni(C12H19)]+ on the AlF3 support could be proved by FAB mass spectroscopic measurements. In agreement with our reaction model for the allyl nickel complex catalyzed butadiene polymerization, it is concluded that the technical nickel catalyst in its effective structure can be described as a polybutadienylnickel(II) complex co-ordinated to a polymeric fluoroaluminate anion via a fluoride bridge.
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  • 3
    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: Metallocen-Katalysatoren eröffnen neue Wege zur Synthese von Olefinoligomeren und -polymeren, deren Molekulargewichte und Schmelzpunkte in weiten Bereichen variieren. Einige wichtige Besonderheiten bei der Herstellung von Oligomeren, von wachsartigen sowie von hochmolekularen Polymeren durch Metallocen-Katalyse werden hier behandelt. Am Beispiel der Oligomerisation von Hexen wird ein einfaches kinetisches Modell entwickelt, das geeignet erscheint, den Reaktionsverlauf und die resultierende Oligomerenverteilung beim Einsatz von Metallocen-Katalysatoren zu beschreiben. Die Herstellung von Propylenpolymeren mit niedrigen und hohen Molekulargewichten durch Metallocen-Katalyse wird hinsichtlich der Reaktionsbedingungen und der Produkteigenschaften mit bekannten Prozessen verglichen. Ferner wurde der Einfluß von verschiedenen Unregelmäßigkeiten der Polymerketten, wie Kettenenden, Regioirregularitäten und Comonomersegmenten auf die Schmelzpunkte untersucht.
    Notes: Metallocenes offer new synthetic routes to olefin oligomers and polymers covering a wide range of molecular weights and melting points. This paper deals with some important features of the preparation of oligomers, wax-like polymers as well as highmolecular-weight polymers via metallocene catalysis. Taking the oligomerization of hexene as an example, a simple kinetic scheme is established, which is suitable to describe the course of the reaction and the resulting oligomer distribution with metallocenes as catalysts. For low and high-molecular-weight polymers, the metallocene route to polypropylene is compared to existent processes in terms of reaction conditions and product properties. An attempt is made to separate the effect of different chain defects like chain ends, regioirregularities and comonomers on the melting point.
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Small- and wide-angle x-ray scattering is used for structural characterization of amylose solutions and gets. Recently published coordinates determined by x-ray fiber structure analysis and electron diffraction [A. Imberty and S. Perez: (1988) Biopolymers, Vol. 27. pp. 1205-1212: H. C. Wu and A. Sarko (1978) Carbohydrate Research, Vol. 6.1, pp. 7-40]. X-ray crystallography [W. Hinrichs & W. Saenger (1990) Journal of the American Chemical Society, Vol. 112. pp. 2789-2796], and theoretically calculated atomic coordinates for energy-minimized conformers of amylose molecules in solution and crystals served to simulate small- and wide-angle x-ray scattering curves. The simulation of scattering curves renders possible a quick screening and detection of special features in experimental curves and the decision of whether they are significant or not. The scattered intensities of the models were calculated using the atomic scattering factors and van der Waals radii within the framework of the improved cube method [J. J. Müller (1983) Journal of Applied Crystallography, Vol. 16, pp. 74-82]. All model data and the scattering curves are stored for a fast information retrieval in the database OBIOSCAT controlled by the ORACLE management system.In the context of a mixture of diflerent structures existing in an amylose solution or gel, theparallel-stranded left-handed B-form double helices (Imberty and Perez) do not scatter in a way that is significantly different from that of the parallel-stranded right-handed duplex proposed by Wu and Sarko. The structure of the energy-minimized left-handed parallel-stranded double helix is very similar to that of the canonical B form, but energy-minimized right-handed duplexes with parallel or antiparallel strands have structures that produce new scattering features. Up to now, such features have not been experimentally detected. Extended or collapsed single helices, too, can be discriminated by their scattering features from double helices for scattering vectors larger than 5 nm-1, and the energy-minimized left-handed single helices are nearly identical with the V-forms experimentally found in fibres [G. Rappenecker and P. Zugenmaier (1981) Carbohydrate Research, Vol. 89, pp. 11-19.].Because the investigated amylose gels contain crystallites. The growing of V- and B-form nanocrystallites up to dimensions of 20 nm was simulated with atomic resolution. The scattering curves of independently scattering nunocrystals hold information about crystallite shape, size, surrounding, and the structure, factors of the asymmetric unit in the unit cell, hence, they differ remarkably from the recently published fiber-structure factors and provide this structure information at an early stage of crystallization.Experimental scattering data of wheat amylose recorded during the gelation process can explained by a remarkable amount of V-helices with 6-12 glucopyranosyl residues in solution at 70°C. Extended single helices probably exist also under these conditions. A mixture of independently scattering V- and B-form nanocrystallites is detectable in freshly cooled samples (40°C), and pure B-form nanocrystallites embedded in a matrix of an electron density comparable to that in the crystallites exist together with amorphous material afterjve weeks of aging at 21°C. From the scattering of the amylose sample during the gelation process it follows that Gidley's gelation model [M. J. Gidley (1989) Macromolecules, Vol. 22, pp. 351-358], which assumes crystallization during the phase separation, is prejerred to the model proposed by Miles et al. [M. J. Miles, V. J. Morris, and S. G. Ring (1985) Carbohydrate Research, Vol. 135, pp. 257-269], where crystallization is preceded by phase separation. © 1995 John Wiley & Sons, Inc.
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  • 5
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 289-298 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3603-3611 
    ISSN: 0887-624X
    Keywords: PVA ; acrylic acid ; methacrylic acid ; 2-vinyl-4,4-dimethyl-azlactone ; acrylamides ; GPC ; light scattering ; photochemistry ; contact lenses ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(vinyl alcohol) (PVA) was partially modified by polymer analogous reaction with acrylic and methacrylic acid and with 2-vinyl-4,4-dimethyl-azlactone to obtain water-soluble polymers with pendant (meth)acrylate and acrylamide groups. Aqueous solutions of these polymers were crosslinked by UV-irradiation within seconds to form transparent networks with potential for use in contact lenses. The water content of these hydrogels was studied as a function of polymer molecular weight, the acetate, (meth)acrylate, and methacrylamide contents and irradiation conditions. The hydrogels showed good mechanical properties, even at low crosslinker (〈5 mol %) and high water contents (60-80%). The formation kinetics and stability of aggregates, investigated by combined GPC/light-scattering measurements of samples annealed and/or stored at different temperatures (-20 to 100°C), give insight into PVA secondary structures. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3603-3611, 1997
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 421-427 
    ISSN: 0887-6258
    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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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2669-2681 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymers of α-chloroacrylate (MCA), 1-chloroethyl methacrylate (1CEMA), 2-chloroethyl methacrylate (2CEMA), 2,2,2-trichloroethyl methacrylate (trCEMA) and 1,2,2,2-tetrachloroethyl methacrylate (teCEMA) were γ-irradiated at 77 K. The primary radicals were generated by the abstraction of chlorine. They decay or change into chain end radicals upon warming up to room temperature.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1589-1598 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical generation after γ-irradiation at 77 K and radical reactions during temperature increase are discussed for the polymers poly(2-chloroethyl methacrylate) and poly(1,2,2,2-tetrachloroethyl methacrylate), mixed with triallylisocyanurate (TAIC). After the radiation interaction radicals are generated in the ester alkyl side groups of the polymer by chlorine abstraction in both polymer/TAIC mixtures. Radical transfer to TAIC occurs during temperature increase to produce allyl radicals. Hence, the high radiation sensitivity of chlorine-containing polymers is combined with the reactivity of allyl radicals of TAIC in such polymer-TAIC mixtures.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2755-2764 
    ISSN: 0887-624X
    Keywords: acrylated silicones ; radical photocrosslinking ; polymerization kinetics ; oxygen effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photoinduced radical crosslinking of silicones containing pendant acrylate and methacrylate groups has been investigated with calorimetric and ESR measurements. Oxygen very strongly influences this process, which leads to a prolonged induction period and a pseudo first-order termination reaction between polymer radicals and oxygen. Kinetically, such reaction steps are responsible for light intensity and monomer exponents, both of unity. In the absence of oxygen, second-order processes take place between polymer and primary radicals. The results of conversion-time and reaction-rate time measurements using stationary irradiations and postpolymerization experiments agree with the corresponding kinetic expressions. Long-lived polymer radicals and their decay have also been determined with ESR techniques. Long-chain spacer groups, which link the unsaturated ester moiety at the silicone backbone, increase the crosslinking rate. The final conversions of the double bonds exceed high values in each case. © 1992 John Wiley & Sons, Inc.
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