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  • Polymer and Materials Science  (64)
  • Industrial Chemistry  (15)
  • 1
    ISSN: 0935-9648
    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: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 8 (1996), S. 381-384 
    ISSN: 0935-9648
    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.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 13 (1990), S. 371-375 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A solution of 0.1 M 1,2-dichloroethane in 1 M H2SO4 was anodically converted to CO2, Cl2 and HCIO4 as the main products at smooth platinum. The current efficiency for CO2 exceeds 60% at low current densities, while HClO4 is obtained with about 20% current efficiency. Chlorinated products such as 1,2′,2-trichloroethane are formed in negligible amounts. Platinum plays a distinctive role as anode material and shows a reaction limited anodic prewave. Our experimental findings lead to a mechanism, whereby DCE is initially hydroxylated to form chloroacetaldehyde chlorohydrin which releases HCl and becomes rapidly further oxidized to monochloroacetic acid. The cleavage of the C—C bond proceeds via its anodic decarboxylation. Possible practical applications in the field of anodic water purification and in the direct electrosynthesis of vinyl chloride are discussed.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 673-685 
    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 model nucleating agent for polypropylene crystallization is described. A series of compounds consisting mainly of organocarboxylic acid salts is evaluated as heterogeneous nucleating agent for polypropylene crystallization by measuring their effect upon the polymer supercooling. Sodium benzoate and basic aluminium dibenzoate were among the best nucleating agents found. The nucleating abilities of the various compounds are discussed in terms of their structural features.
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  • 5
    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 effect of cooling, nucleation, and spherulitic growth rates on the properties of polypropylene is discussed briefly. A differential thermal analysis technique is described for evaluating the relative extent of heterogeneous nucleation that occurs in a particular polypropylene composition. The method is based upon a nucleating agent's ability to reduce the relatively large amount of supercooling that occurs upon crystallization of polypropylene. Compounds are shown to vary widely in their effectiveness as heterogeneous nucleating agents in polypropylene. The relationships between the degree of supercooling of a particular polypropylene composition and its relative clarity, tensile properties, density, and morphology are shown.
    Additional Material: 12 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 28 (1977), S. 688-696 
    ISSN: 0947-5117
    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: The corrosion of lead in acid tetrafluoborate electrolytesThe corrosion of 99,985% lead in acid tetrafluoborate electrolytes, predominantly 1 mole/litre HBF4 and 2 mole/litre Pb (BF4)2, was investigated. The corrosion rate in air saturated solution at 20°C is 35 μA/cm2, which corresponds to 1 mm/a. Oxygen corrosion predominates (corrosion is rather reduced under argon). At higher temperatures, corrosion rate increases by an order of magnitude, and acid corrosion has a greater share due to a decrease of hydrogen overvoltage on lead and solubility of oxygen. Cementable additives like Cu++, Sb+++ and Pd++ are found to enhance the initial corrosion rate by up to two orders of magnitude. However, after 10-20 hours, the original value is reestablished. Bi+++ is cemented as well; the resulting acceleration of corrosion is proportional to the additive concentration and decreases but slowly. Oxidants like Fe+++ or quinone accelerate the dissolution of lead as well and are consumed stoichometrically. Reducing agents like Fe++, V+++ or hydroquinone are not able to act as a mediator for air corrosion. Nitrate ions are virtually inert in the given concentration range. Consequences in reference to the lead dissolution secondary battery are discussed. Self discharge in the absence of O2 is very low. On the other hand, it is possible by oxygen corrosion to redissolve lead, which has accumulated on the electrode. In this way, the battery can be brought back to its original state.
    Notes: Die Korrosion von 99,985%igem Blei in tetrafluoborsauren Elektrolyten, insbesondere in einer Lösung von 1 Mol/1 HBF4 + 2 Mol/1 Pb(BF4)2, wurde eingehend untersucht. Bei 20°C beträgt in luftgesättigter Lösung die Korrosionsrate 35 μA/cm2, entsprechend 1,0 mm/a. Da unter Argon die Korrosionsgeschwindigkeit stark zurückgeht, liegt vorwiegend Sauerstoffkorrosion vor. Bei höheren Temperaturen (50°C) kommt wegen der abnehmenden Wasserstofflüberspannung am Blei und der zurückgehenden Sauerstofflöslichkeit dagegen die Säurekorrosion mehr in den Vordergrund, wobei die Korrosionsrate insgesamt um eine Größenordnung steigt. Zementierbare Additive wie Cu++, Sb+++ und Pd++ erhöhen anfänglich die Korrosionsgeschwindigkeit um bis zu zwei Zehnerpotenzen, aber nach 10-20 h hat sich wieder der alte Wert eingestellt. Bi+++ wird ebenfalls zementiert, wobei eine mittlere, zur Additivkonzentration proportionale und zeitlich wenig abnehmende Korrosionsbeschleunigung resultiert. Oxidationsmittel wie Fe+++ und Chinon beschleunigen die Bleiauflösung, wobei sie stöchiometrisch verbraucht werden. Reduktionsmittel wie Fe++, V+++ oder Hydrochinon können nicht als Mediator für die Luftkorrosion wirken. Nitrationen sind im untersuchten Konzentrationsbereich fast inert. Konsequenzen bezüglich des Bleilösungsakkumulators werden diskutiert. Die Selbstentladung in Abwesenheit von O2 ist sehr gering. Andererseits ist es möglich, durch Sauerstoffkorrosion einseitig akkumuliertes Blei wieder in Lösung zu bringen. Auf diese Weise kann die Batterie wieder in den Ausgangszustand zurückgeführt werden.
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  • 7
    ISSN: 0947-5117
    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
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 46 (1995), S. 447-459 
    ISSN: 0947-5117
    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: Korrosion von vorbehandeltem Aluminium nach der kathodischen ElektrotauchlackierungDie Kathodische Elektrotauchlackierung (KTL) ist seit nahezu zwei Jahrzehnten bei der industriellen Abscheidung von Grundierungen auf Stahl gut eingeführt. Epoxidharze ergeben optimale Resultate. Es besteht ein zunehmender Bedarf, dieselbe Technik für Aluminium anzuwenden, speziell für die Mischbauweise Eisen/Aluminium bei Autokarosserien. Allerdings kann dieses Metall durch die OH- -Ionen angegriffen werden, die bei der kathodischen Elektrolyse von Wasser gemäß H2O + e- → ½ H2 + OH entstehen. Die. Al2O · xH2O Schutzschicht kann sich langsam auflösen als Aluminat, und dann reagiert das Al-Metall schnell mit Wasser unter Bildung des dreifachen Volumens an Wasserstoff, wobei die oxidische Schicht wiederhergestellt wird. Demgemäß ist die Bruttoreaktion für die kathodische Korrosion des Al gegeben durch: Al + 2H2O + e- → AlO2- + 2H2.Es ist zu erwarten, daß die Änderungen an der Phasengrenze Al/AlOOH/Lack und die Akkumulation von hydrolisiertem Aluminat im Überzug unter anderem auch das Korrosionsschutzverhalten der Lackschichten beeinflussen könnten. Eine systematische Untersuchung des Einfusses von vier verschiedenen technischen Epoxidharzen von BASF Lacke & Farben AG (l)-(4) mit ihren individuellen Pigmentsystemen, wobei das eine für den Lack 3 frei von Bleisilikat war, wurde unternommen. Sieben verschiedene Aluminium (Legierungs) Substrate warden verwendet. Die Art der Vorbehandlung war in den meisten Fällen eine Zinkphosphatierung. Drei Standard-Korrosionstests für die konventionelle Korrosion (KK) und eine für Filiformkorrosion (FFK) wurden angewandt und standardmäßig ausgewertet. Der verschärfte Freibewitterungs-Korrosionstest dauerte 360 Tage.Es wurde gefunden, daß die Korrosionsschutzwirksamkeit für die KK hauptsächlich durch das Harz beeinflußt wurde, wobei sie in der folgenden Reihenfolge abnahm: \documentclass{article}\pagestyle{empty}\begin{document}$$ (4) 〉 (2) 〉 (1),\,(3). $$\end{document}Der Einfluß des Substrats war nicht sehr ausgeprägt, aber ein relatives Optimum konnte erkannt werden mit Al Mg 0.4 Si 1.2 mit Gelbchromatierung und Bonazinc 2000® und mit Al Mg 1.5 Si 0.5 Cu 4.0 mit Gelbchromatierung (mit einer Ausnahme). Die Reihenfolge der Wirksamkeit gegen die FFK änderte sich wie folgt: \documentclass{article}\pagestyle{empty}\begin{document}$$ (2) 〉 (3) 〉 〉 (1),\,(4), $$\end{document} und zinkphosphatiertes Al Mg 3 war allen anderen Substraten überlegen. Die analytisch bestimmte Geschwindigkeit der kathodischen Korrosion für unpigmentierte Lacke korrelierte nicht mit diesen Resultaten, und dies konnte indikativ sein für spezifische Pigmenteffekte. Zusammenfassend kann man sagen, daß these systematische Untersuchung auf der Basis von praktischen Systemen und Korrosionstestmethoden einen Weg aufzeigt für die Optimierung der KTL auf Aluminium.
    Notes: Cathodic deposition of paint (CDP) is Well introduced for the industrial coating of primers onto steel since nearly two decades. Epoxy resins provide optimum results. There is an increasing demand to apply the same technique for aluminium, especially for mixed constructions Fe/Al in motor car bodies. However, this metal may be attacked by the OH--ions, generated by the cathodic electrolysis of water according to: H2O + e- → ½ H2 + OH-. The Al2O3 · xH2O protecting layer may dissolve slowly as aluminate and Al-metal then reacts rapidly with water to generate the threefold volume of hydrogen under the reestablishment of the oxide layer. Thus, the overall reaction for this cathodic corrosion of Al is given by: Al + 2H2O + e- → AlO2- + 2H2.It can be foreseen, that the changes at the phase boundary Al, AlOOH/paint and the accumulation of hydrolysed aluminate in the coating may influence, among other, the corrosion protection behavior of the paint layers. A systematic study of the influence of four different industrial epoxy resins from BASF Lacks & Farben AG (1)-(4) with their individual pigment systems, the one for paint (3) to be free of lead silicate, was undertaken. Seven different aluminium (alloy) substrates were employed. Their pretreatment modes were mostly due to zincphosphatation. Three standard corrosion tests for conventional corrosion, (CC) and one for filiform corrosion (FFC) were employed and evaluated, as usual. The accelerated open air corrosion test lasted 360 days.It was found, that for CC the corrosion protection capability was predominantly influenced by the resin, and it decreased in the following order: \documentclass{article}\pagestyle{empty}\begin{document}$$ (4) 〉 (2) 〉 (1),\,(3). $$\end{document}The effect of the substrate was not very pronounced, but a relative optimum could be seen with Al Mg 0.4 Si 1.2-chromate pretreatment and Bonazinc 2000® and with Al Mg 1.5 Si 0.5 Cu 4.0-chromate pretreatment (with one exception). The ranking for FFC changed to: \documentclass{article}\pagestyle{empty}\begin{document}$$ (2) 〉 (3) 〉 〉 (1),\,(4), $$\end{document}, and zincphosphated Al Mg 3 was superior over all the other substrates. The analytically determined rate of cathodic corrosion for unpigmented paints did not correlate to these results, and this may be indicative for specific pigment effects. In conclusion, this systematic study reveals, on the basis of practical systems and corrosion test methods, a way for the optimization of CDP on aluminium.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 2 (1968), S. 51-63 
    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: With the aid of an electrochemical initiated reaction of pure acrylonitrile in the presence of 0,1-1% water and of small concentrations of quaternary ammonium salts, an oligomeric, yellow, in acetone soluble compound was obtained with a molecular weight of 1000-3000. The high current-yield - up to 100 g/Ah, this means that per electrontransfer up to two polymeric molecules were obtained -, the low molecular weight, the independence of molecular weight of current density, the insensitivity to oxygen, and experiments of copolymerization with styrene indicate that the oligomer is formed at the cathode by an anionic mechanism. The influence of electrolyte structure, of cathode material, of current density, of water concentration, of convection, and of temperature on the formation of the oligomer has been investigated. A proposal of the structure of the oligomeric acrylonitrile has been made.
    Notes: Durch eine elektrolytisch gestartete Reaktion von reinem Acrylnitril in Gegenwart von 0,1 bis 1% Wasser und in Anwesenheit geringer Mengen eines quartären Ammoniumsalzes wurde ein oligomeres, acetonlösliches, gelbgefärbtes Produkt erhalten, dessen Molgewicht zwischen 1000 und 3000 liegt. Die hohe Stromausbeute - sie erreichte 100g/Ah, d. h. es wurden pro Elektronentransfer bis zu 2 Polymermoleküle gebildet -, das niedere Molgewicht, die Unabhängigkeit des Molgewichts von der Stromdichte, die Unempfindlichkeit gegen Sauerstoff sowie Co-polymerisationsversuche mit Styrol lassen darauf schließen, daß das Oligomere an der Kathode durch einen anionischen Mechanismus entstehen muß. Der Einfluß der Art des Leitsalzes, der Kathode, der Stromdichte, der Wasserkonzentration, der Konvektion und der Temperatu auf die Oligomerenbildung wurden untersucht. Ein Strukturvorschlag wird zur Diskussion gestellt.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 227 (1995), S. 101-110 
    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: Ein Cellulose- Austauscher wurde aus “o-Aminophenol-Cellulose” durch Diazotieren und Kuppeln mit Diaminodibenzo-17-krone-5 hergestellt. Die Verteilungskoeffizienten für Ca2+, Sr2+, Ba2+, Na+ und K+ wurden in Wasser/Methanol-Mischungen als Funktion des Wassergehaltes bestimmt. Die Trennung von Ca2+, Na+ und K+ und die Fraktionierung der Calciumisotope 48Ca und 40Ca wurde untersucht. Der Anreicherungsfaktor ε = 4.9 · 10-3 für 48Ca2+ ist merklich größer als der für Kationenaustauscher mit SO3H-Gruppen gefundene, aber niedriger als der in der Literatur für bestimmte Kryptanden angegebene Wert.
    Notes: A new cellulose exchanger was synthesized from “o-aminophenolcellulose” by diazotation and coupling with diaminodibenzo-17-crown-5. The distribution coefficients for Ca2+, Sr2+, Ba2+, Na+ and K+ were determined in water/methanol mixtures as a function of the water content. Separation of Ca2+, Na+ and K+ and fractionation of the calcium isotopes 48Ca and 40Ca were investigated. The enrichment factor ε = 4.9 · 10-3 for 48Ca2+ is appreciably higher than that found for cation exchange resins with —SO3H groups, but lower than that reported for certain cryptands.
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