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  • Polymer and Materials Science  (74)
  • Biochemistry and Biotechnology  (15)
  • Lunar and Planetary Science and Exploration
  • 1995-1999  (89)
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  • 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: 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.
    Additional Material: 6 Ill.
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  • 2
    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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  • 3
    ISSN: 0173-0835
    Keywords: Two-dimensional polyacrylamide gel electrophoresis ; Protein sequencing ; Amino acid analysis ; Matrix assisted laser desorption ionization-mass spectrometry ; Database ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The master gel of the human myocardial two-dimensional electrophoresis (2-DE) gel database contains about 3300 protein spots characterized in terms of isoelectric point (pI) and molecular mass. A high-performance technique was applied, using large gels (23 × 30 cm). Isoelectric focusing with anodic sample preparation and nonequilibrium running conditions (NEPHGE) was combined with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) in 15% acrylamide gels in the second dimension. The range of pI extends from pH 4.5 to 9.6. Seventy proteins were identified by combinations of amino acid analysis, N-terminal and internal sequencing, immunostaining, matrix assisted laser desorption/ionization-mass spectrometry (MALDI-MS) peptide mass fingerprinting, post-source decay MALDI-MS and ladder sequencing by carboxypeptidase P. The identification of additional proteins, not found in the master gel, was achieved by immunoblotting. Unequivocal identification with high sensitivity and good yield was obtained by combining internal sequencing and MALDI-MS. In-gel digestion, the concentration and purification of peptides in a peptide collecting device, and the improved FRAGMOD program for peptide mass fingerprinting have added to the security and sensitivity of identification. The high-performance human myocardial 2-DE database was built up with proteins detected by the TOPSPOT program. Spots within six sections of the whole pattern are clickable. Protein description includes detailed information about identification, characterization, and links to the related SWISS-PROT, other 2-DE databases and Medline entries. The database is constructed in accordance with four of the rules for a federated database.
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  • 4
    ISSN: 0173-0835
    Keywords: Matrix assisted laser desorption ; ionization-mass spectrometry ; Peptide mass fingerprinting ; Two-dimensional polyacrylamide gel electrophoresis ; Enzymatic in-gel digestion ; Myocardial proteins ; Heat shock protein 27 ; Phosphorylated proteins ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Immunostaining of heat shock protein 27 (Hsp27) protein species on two-dimensional electrophoresis (2-DE) gels with enhanced sensitivity yields 59 spots reacting with anti-Hsp27 antibodies. Recombinant Hsp27 exists in 2-DE as two major protein species which comigrate in the human myocardial pattern with Hsp27 spots C754 and D899 as defined in the heart high-performance 2-DE database (http://www.mdc-berlin.de/∼emu/heart/). Preparative electrophoresis of human myocardial proteins and analysis of the enriched mass range 20-30 kDa by 2-DE revealed eight protein spots (C438, C582, C658, C697, C754, C595, C750) from the human myocardial database and a new spot not previously detected on silver-stained gels. These spots were identified as Hsp27 protein species by enzymatic in-gel-digestion and analysis by matrix assisted laser desorption-ionization (MALDI) peptide mass fingerprinting and, in part, MALDI-post source decay sequencing of single fragments. Possible post-translational modifications were investigated: immunostaining tests with anti-phospho-serine/-threonine/-tyrosine antibodies, although positive for other myocardial proteins, were negative for presumed Hsp27 protein species; likewise, periodate-glycostaining assays and biotinylation screening did not detect modifications in the investigated Hsp27 protein species.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 244 (1997), S. 121-133 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The world-wide production of polyurethanes has exceeded 6 mio. metric tons in 1994. Compared with the produced amounts of large-scale thermoplastics such as PE, PVC, PP and PS, polyurethanes keep the 5th place.Polyurethanes (PUR) are segmented polymers, which can be synthesized from preformed building blocks in a modular unit construction system. The chemical modules and the various possibilities of combination will be discussed here.Tailor-made polyurethane materials can be divided into two main-fields of application: foams and compact PUR.The main constituents of polyurethane materials are diisocyanates and polyols. These key- chemicals are well characterised with respect to their technological, economical and ecological properties. Taking into account the availability, the masses of production and the experiences that have been collected with the PUR main constituents, these PUR precursors seem to be very mature already.In contrast to this, the PUR-materials made from these building blocks still offer numerous novel problem-solutions, resulting from the variability of the diisocyanate-poly-addition reaction: PUR materials are most commonly segmented into several phases. The formation of hard- and softsegments can be easily demonstrated by looking at thermoplastic polyurethanes (TPU). A deeper understanding of this phase separation and the molecular organisation within these materials promises to realize prospectic polymeric architectures with new and improved properties. PUR materials will still be able to offer new answers to future requirements in balancing economical and ecological needs. By looking at the life-cycles of soft and hard-foams, polyurethane-coatings and thermoplastic PUR-elastomers, this contribution will adress the question: “Is PUR-chemsitry still a challenging field?”
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  • 6
    ISSN: 0006-3525
    Keywords: gastrin ; lipo-gastrin derivatives ; cholecystokinin-B/gastrin receptor ; molecular modeling ; ligand binding sites ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Double-tailed lipo-tetragastrin derivatives of increasing fatty acid chain length were used to identify the minimum size of the fatty acid moieties (≥C10) that restricts the access to the CCK-B/gastrin (CCK: cholecystokinin) receptor via a membrane-bound pathway. Then dimyristoyl-mercaptoglycerol/maleoyl-gastrin adducts of increasing peptide chain length were synthesized to define the minimal peptide size required for receptor binding affinities comparable to those of underivatized gastrin peptides despite anchorage of the lipid tails in the membrane bilayer. The experimental results indicated that most of the little-gastrin sequence, i.e., 2-17, is needed for optimal interaction of the molecule with the binding cleft of the receptor. From these data experimentally based restraints could be derived for docking of lipo-gastrin onto a CCK-B/gastrin receptor model applying molecular dynamics simulations and energy minimizations. In the receptor-bound state some of the secondary structure elements of gastrin as determined by nmr analysis of gastrin-peptides in low dielectric constant media are retained. The N-terminal gastrin portion interacts in a more or less extended conformation with the receptor surface, and upon a sharp kink at the Ala-Tyr dipeptide portion the C-terminal pentapeptide amide part inserts deeply into the helix bundle. Besides Arg-57 on top of helix 1 of the receptor, for which no potential interaction with the ligand could be detected, the other amino acid residues identified by mutagenesis studies as involved in gastrin recognition were found to interact with the C-terminal portion of gastrin. Even taking into account the strong limitations of such a model system, it represents an interesting tool for rationalizing the experimental results of the extensive structure-function studies performed previously on gastrin and to delineate more precisely the putative ligand binding site on the extracellular face of the receptor. © 1997 John Wiley & Sons, Inc. Biopoly 41: 799-817, 1997
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  • 7
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ensemble calculations employing restraints developed from 1H-nmr were used to examine the conformational states of the two microcystins LR and LY. Despite the fast “flip-flop” dynamics about the N-methyl-dehydroalanine residue and adjacent residues, the main conformational characteristics of the cyclic heptapeptides consist of a compact ring formed by five of the seven amino acid residues with expulsion of a dipeptide portion out of the plane and the unnatural C20 β-amino acid (2S. 3S. 8S, 9S)-3-amino-9-methoxy-2, 6, 8-trimethyl-10-phenyldeca-4. 6-dienoic acid pointing upward from the ring. This structure of microcystin LR shows high degrees of similarity with the energy-minimized structure of nodularin, a cyclic pentapeptide of identical inhibitory potency against protein phosphatases 1 and 2A. Comparison of these structures with those of the less toxic LY variant and with the structurally unrelated okadaic acid, known as potent inhibitor of the protein phosphatases 1 and 2A, allowed us to propose a rational binding mode of this structural diverse set of natural inhibitors. © 1995 John Wiley & Sons, Inc.
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  • 8
    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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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 27 (1996), S. 345-349 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Ultrafeine ZrO2 - Pulver durch Laserverdampfung: Herstellung und EigenschaftenUltrafeine oxidische Pulver werden durch Co2-Laserverdampfung aus grobem ZrO2-Pulver oder kompakten ZrO2-Stangen hergestellt.Die 10.6 μm-Strahlung im Leistungsbereich von 1 bis 4 kW wird durch einen quergeströmten CO2-Laser erzeugt, der in cw-und Pw-Betrieb arbeitet.Die Verdampfungsrate ist abhängig von der relativen Lage der Fokalebene zur Oberfläche des ZrO2-Pulvers, der Laserintensität und der eingekoppelten Energie.Bei einer Laserintensität von 4.2 · 105 Wcm-2 erreicht man eine optimale Verdampfungsrate von 130 g · h-1 (cw-Betrieb des Lasers).Das hergestellte Pulver besteht aus sphärischen Partikeln; deren Durchmesser variiert im Bereich von 5 bis 200 nm und kann durch die Verfahrensparameter beeinflußt werden. Die spezifische Oberfläche ist einstellbar von 10 bis 30 m2 · g-1.Das Pulver aus unstabilisiertem Zirkonium besitzt einen sehr hohen Anteil tetragonaler Phase. Im Fall von chemisch stabilisiertem Zirkonium kann sich die Zusammensetzung während des Verdampfungsprozesses und der Rekondensation ändern.
    Notes: Ultrafine oxide powders were produced by CO2 laser evaporation of coarse ZrO2 powder or compact stabilized ZrO2 materialThe 10.6μm radiation in the power range 1-4kW was generated by a transversal flow Co2 laser which can oscillate in cw and pw operationThe vaporization rate depends on the relative position of the focal plane to the surface of the ZrO2 powder, the laser intensity and the supplied energy input.At a laser intensity of 4.2 · 105 Wcm-2 the optimum vaporization rate is 130 g · h-1 (cw-operation of the laser).The produced powders consist of spherical particles; their diameters vary in the range from 5 to 200 nm can be controlled by the process conditions. The surface area (BET) is adjustable from 10 to 30 m2 · g-1.The powders of unstabilized zirconia show an unusual high content of the tetragonal phase. In case of chemically stabilized zirconia the composition can change during the process of evaporation and recondensation.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 29 (1998), S. 97-130 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Valve Materials for Combustion EnginesAn overview is being given on production numbers, requirements and properties of valve materials. Their development from the beginning till today's state of the art is reviewed with a focus on Chromium-Manganese-Nitrogen-alloys. Valve materials are grouped by the criteria of density - heavy, lightweight - and alloying elements. The multiple stresses of the material in the valve are being met with a few standardised grades and specific ways of manufacture. The path of the material from bar stock to the finished valve is being followed. Engine development in the past decades increased the load on the valves which could be met by continuously developing their structural strength. Also the strength of all valve materials could be raised to nominal strength above 1100 Mpa by applying specific methods. Higher strength at the surface is being effectuated by work hardening effects. The technology to increase reliability of hollow valves and new aspects of valve seat facing including residual stress is explicitly discussed. General aspects of alloy utilisation is followed by a discussion of lightweight valve materials as Titanium alloys, intermetallic Titaniumaluminide alloys and ceramic materials, spec. Silicon Nitride, which all have a potential as forthcoming valve materials capable of reducing fuel consumption of the engines.
    Notes: Nach einem Überblick über Produktionszahlen, allgemeine Anforderungen und Eigenschaften von Ventilen für Verbrennungsmotoren, wird in einem Rückblick die Werkstoffentwicklung für die Ventilstähle von den ersten Anfängen bis zum heutigen Stand aufgezeigt. Schwerpunktmäßig wird die Gruppe der Chrom-Mangan-Stickstoff-Stähle behandelt. Daneben werden die Ventilwerkstoffe geordnet nach schweren und leichten und innerhalb dieser Gruppen nach Legierungsmerkmalen beschrieben. Es wird über die vielfältigen Werkstoffanstrengungen am Ventil informiert, die mit wenigen genormten Werkstoffgüten und speziellen Fertigungsverfahren problemlos mit niedrigsten Fehlerraten beherrscht werden. Der Weg des Werkstoffes vom Halbzeug bis zum fertigen Ventil wird in allen Schritten verfolgt. Die in den letzten Dekaden forcierte Motorenentwicklung führte zu verschärften Betriebsbedingungen auch für die Ventile, die mit einer kontinuierlichen Weiterentwicklung bestehender Werkstoffgüten und Verbesserungen der Gestaltsfestigkeit der Ventile aufgefangen wurden. In diesem Zusammenhang werden spezielle Lösungen zur Festigkeitssteigerung aller Ventilwerkstoffe bis in den Bereich von über 1100 MPa erläutert, die nach bekannten metallkundlichen Gesetzen ermöglicht wurden. Als wesentliches Prinzip werden ortsabhängig, besonders an der Oberfläche, erhöhte Festigkeits- und Verschleißeigenschaften zur Optimierung der Gestalts- und Betriebsfestigkeit eingesetzt. Über Entwicklungen zur Technologie der Hohlventile und von erweiterten Lösungen beim Auftragschweißen von Ventilsitzen im Zusammenhang mit Eigenspannungen wird ausführlich berichtet. Einer kurzen allgemeinen Betrachtung zum Legierungsaufwand der wichtigsten Ventilwerkstoffe folgt ein Kapitel über Titan, Intermetallische Verbindungen und Keramik, die möglicherweise als zukünftige leichte Ventilwerkstoffe Verwendung finden können.
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