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  • Chemistry  (345)
  • Magnetism
  • Nederland
  • P ligands
  • 1965-1969  (150)
  • 1960-1964  (124)
  • 1955-1959  (71)
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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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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: The enthalpy change accompanying the double helix-coil transition of polyriboadenylic acid (poly A) in aqueous solution has been measured optically and calorimetrically in the pH range 5.7-4.5. The course of this cooperative transition was followed optically by measuring changes in ultraviolet absorption as a function of temperature at different pH values, and calorimetrically by determining the heat capacity of the solution through the transition region. From the latter measurements, the enthalpy of transition was calculated. It is shown, that ΔH is dependent on pH as it is expected from the influence of protonation of the double helix of poly A.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 1296-1304 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Darstellung der freien Farbsäuren des Betanins und Betanidins wird beschrieben, ihre Bruttoformeln werden erörtert. Beide Verbindungen sind optisch aktiv. Sie spalten mit starker Natronlauge in der Hitze etwa 1/3 ihres Stickstoffes als Ammoniak ab. Quantitative Decarboxylierungsversuche und potentiometrische Titration weisen für das Glucosid wie für das Aglykon auf drei Carboxylgruppen, von denen eine durch eine basische Gruppe neutralisiert zu sein scheint, und eine schwach saure (phenolische) Gruppe hin. Beim oxydativen Abbau des Betanidins wurde L-Asparaginsäure erhalten.
    Additional Material: 2 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 2761-2776 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dehydro-digallussäure (I) und Valoneasäure-dilacton (II) erleiden mit Alkalien eine Spaltung an der Diphenyläther-Brücke, die keine Hydrolyse ist. Anhand zahlreicher Modellsubstanzen wird festgestellt, daß diese neuartige Spaltung von Diphenyläthern offenbar an das Vorliegen von 3 vicinalen, freien Hydroxygruppen an einem der beiden Phenylreste gebunden ist. Die Spaltung ist eine innere Disproportionierung; als Mechanismus wird eine β-(oder vinyloge β-)Eliminierung diskutiert. - Sieben einseitig hydroxyl-substituierte Diphenyläther wurden neu dargestellt.
    Additional Material: 3 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 102 (1969), S. 2158-2159 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 556-557 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 7
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Cultivation of Norcardia sp., Mycobacterium phlei, and Candida lipolytica in inorganic salt solution containing n-alkanes C10-C20 as solo carbon and energy source was investigated. Generation times of 0.5-7.0 hr were typical during the exponential growth phase. The final cell concentrations (dry weight) were usually 9-26 g/l with n-alkane mixtures ranging from n-decane through n-eicosane. A linear dependence was found between the production of cell mass and the consumption of n-alkanes. The rest concentration of n-alkanes in the cell mass is in all experiments smaller than 0.5% (w/w). Cell yields were Ysub 60-142% and for Ye 50-97% based on n-alkane utilization. In one case, with the Nocardia NBZ 23, the substrate specifity on hydrocarbons and on a n-alkane mixture C10-C20 was studied. The cell mass recovered from the fermentations contained 47.8-57.7% carbon, 5.6-9.95% nitrogen, 7.2-9.4% hydrogen, 35-62% crude protein, and 6-36% lipid. Cellular protein and lipid synthesized by an organism is influenced by the type of nitrogen source. The amino acid, glucosamine, muramic acid, 2,6-diaminopimelinic acid, and fatty acid distribution in organisms grown on n-alkanes compared with a corresponding fermentation on glucose as sole carbon source were also estimated.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 9 (1958), S. 383-390 
    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 Rest Potentials and the Cathodic Polarizations of Active Chrome and a Chrome Iron Alloy in Sulfuric AcidThe cathodic polarization curves and the rest potentials of active chrome and a chrome iron alloy (25,6 pct chrome) were measured in dependance of the pH-value of the electrolyte. The behavior of the rest potential deviates from that of the hydrogen electrode. By means of the factors α and β they can be explained for the deposition of hydrogen as well as for the dissolution of metal. The equation of the rest potential is \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm o} = {\rm B} - \frac{{0,058}}{{2\,\alpha + \beta }} \cdot {\rm p}_{\rm H} $$\end{document} where B is a constant factor. The sum 2 α - β is usually greater than 1.In the range of the pH-values investigated the cathodic polarization curves of the deposition of hydrogen are parallel. The exchange currents calculated from the logarithmic representation of the polarization curves rise with increasing concentration of the acid and increasing content of chrome in the alloy. The evaluation of the experimental results was carried out according to theroretical principles which had been applied successfully before.
    Notes: An aktivem Chrom und einer Eisen Chrom-Legierung mit 25,6%; Cr wurden in Abhängigkeit vom pH-Wert die Ruhepotentiale gemessen und kathodische Polarisationskurven aufgenommen. Die Ruhepotentiale zeigen ein gegenüber der reversiblen Wasserstoffelektrode abweichendes Verhalten, das mit Hilfe der Durchtrittsfaktoren α und ß für die H2-Entwicklung und für die Metallauflösung gedeutet werden kann. Es gilt für das Ruhepotential \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm V}_{\rm o} = {\rm B} - \frac{{0,058}}{{2\,\alpha + \beta }} \cdot {\rm p}_{\rm H} $$\end{document} mit B =const. Die Summe 2α+β ist in der Regel 〉 1.Die kathodischen Polarisationskurven der H2-Entwicklung verlaufen im untersuchten pH-Bereich parallel. Die aus der logarithmischen Darstellung ermittelten Ausgleichsströme, die der Korrosion entsprechen, steigen mit wachsender Säure-konzentration und mit wachsendem Cr-Gehalt der Eisen-Chrom-Legierung stark an. Die Auswertung der Versuchsergebnisse erfolgte nach den in letzter Zeit mit gutem Erfolg verwendeten kinetischen Ansätze.
    Additional Material: 11 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 12 (1961), S. 560-569 
    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: Observations concerning primary and secondary passivationPotentiostatic and galvanostatic measurements in sulphuric acid electrolytes have been carried out on high-purity ironchrome alloys with chromium contents ranging from 5 to 70 per cent., as well as on high-purity chromium. These measurements were supplemented by the examination of passivation curves, using the galvanostatic insertion method.The passivation currents thus measured were found to differ considerably from the values known so far. The newly found values can be calculated with the aid of an approximation formula as a function of the chromium content. Apart from the “primary” passivation, it was possible, in the concentration range from about 10 to about 40 per cent. Cr, also to observe the „secondary“ passivation which is likewise governed by the current (i) / time (t) law characteristic for passivation generally: (i - i0) t = const. As this phenomenon is greatly dependent on the pH value of the electrolyte and on the presence of complex-forming substances, it is suggested that the phenomenon might be explained by the formation, due to hydrolysis of a second passivation layer.It is assumed that, in the state of “primary passivation” the alloys are covered by a very thin film comparable to that of passive chromium, and that this film is then covered by a “secondary” passivation layer of greater thickness, similar to the iron passivation layer.In the zone of primary passivation, the alloys are anodically dissolved over the whole area whilst, the zone of secondary passivation, strong pit corrosion can be observed.
    Notes: Es wurden an sehr reinen Eisen-Chrom-Legierungen mit Cr-Gehalten von 5 bis 70% sowie an reinstem Chrom potentionstatische und galvanostatische Messungen in Schwefelsäureelektrolyten durch geführt, die durch die Untersuchung von Passivierungskurven nach der galvanostatischen Einschaltmethode ergänzt wurden.Für die Passivierungsstrommengen wurden Werte gefunden, die von den bisher bekannten erheblich abweichen. Die neu ermittelten Werte lassen sich in Abhängigkeit von Cr-Gehalt der Legierungen durch eine Näherungsformel berechnen. Neben der „primären“ konnte im Konzentrationsbereich von etwa 10 bis 40% Cr auch die „sekundäre“ Passivierung beobachtet werden, für die ebenfalls das die Passivierung kennzeichnende Strom(i)-Zeit(t)-Gesetz (i-i0) = const. gilt. Wegen der starken Abhängigkeit dieses Vorganges von pH-Wert des Elektrolyten und der Anwesenheit von Komplexbildnern wird zu dessen Erklärung die hyrolysebedingte Bildung einer zweiten Passivschicht vor geschlagen.Es wird angenommen, daß die Legierungen im „primärpassiven“ Zustand mit einer sehr dünnen Schicht belegt sind, die mit derjenigen des passiven Chroms vergleichbar ist und auf der sich bei der „sekundären“ Passivierung eine dickere zweite Schicht aufbaut die einer Eisenpassivschicht ähnelt.Im primärpassiven Gebiet werden die Legierungen auf der ganzen Fläche anodisch aufgelöst, während im sekundärpassiven Bereich starke Lochfraßbildung beobachtet wird.
    Additional Material: 21 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 16 (1965), S. 952-958 
    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: Observations on corroded parts of a stationary 10 MW gas turbineThe present contribution to the problem of high-temperature corrosion deals with the observations made on parts of the combustion chamber of a gas turbine driven by heavy oil. The corrosion phenomena encountered are mainly due to the hot combustion gases. Temporarily reducing conditions and the effects of sulphur lead, mainly to a reduction of the Cr content of the base material through the formation of sulphides and carbides and thus to a higher corrosion rate under oxidising condition.By way of experiment, the behaviour of six different heat-resistant materials of high strength at high temperatures was tested under normal working condition. The nickel-based alloy NiCr20Ti was found to show a lower corrosion rate than the materials with fe contents.
    Notes: Der vorliegende Beitrag zum Problem der Hochtemperaturkorrosion beschreibt die an Brennkammerteilen einer mit Schweröl betriebenen Gasturbine gemachten Beobachtungen. Es handelt sich vor wiegend um einen Angriff durch die heißen Brenngase. Zeitweise reduzierende Bedingungen und die Einwirkung von Schwefel führen vor allem zu einer Cr-Verarmung der Grundmasse durch Sulfid- und Carbidbildung und damit zu einem beschleunigten Angriff unter oxydierenden Bedingungen.Versuchsweise wurde das Verhalten von 6 verschiedenen hitzebeständigen und warmfesten Werkstoffen unter Betriebsbedingungen geprüft. Dabei zeigte die Ni-Basis Legierung NiCr20Ti einen schwächeren Angriff als die Fe- haltigen Materialien.
    Additional Material: 13 Ill.
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