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  • Chemistry  (228)
  • Comment; Deposit type; DEPTH, sediment/rock; Description; Japan; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Position; Quantity of deposit; Sample ID; Sediment type; Size; Substrate type; Todoroki_Y
  • Magnetism
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  • 1970-1974  (226)
  • 1935-1939  (4)
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Keywords
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Year
  • 1
    Publication Date: 2023-08-28
    Description: Manganese deposits are abundant in various places in the Oshima Peninsula southwest of Hokkaido. This is particular the case of Todoroki Mine situated about 25 kilometers to the south-east of the Ginzan railway station in Siribesi Province. It consists of manganese beds intermixed with a tertiary volcanic tuff complex overlaying granite.
    Keywords: Comment; Deposit type; DEPTH, sediment/rock; Description; Japan; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Position; Quantity of deposit; Sample ID; Sediment type; Size; Substrate type; Todoroki_Y
    Type: Dataset
    Format: text/tab-separated-values, 9 data points
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 15 (1973), S. 1081-1088 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A procedure for the preparation of about 50 g batches of tRNA from 25 kg E. coli W is described. The method involves phenolic extraction of the cells, batch absorption of the tRNA on DEAE-cellulose, washing the DEAE-cellulose and packing it into a column, elution of the tRNA from the column and precipitation of the tRNA with ethanol. The method is less time and labor consuming than the methods described in the literature and can be carried out with relatively simple equipment.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 17 (1971), S. 272-280 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The kinetics of simultaneous, noncatalytic solid-gas reaction systems has been analyzed in terms of the selectivity and effectiveness factor, based on the unreacted core shrinking model. The reaction systems discussed include the first-order independent, parallel, and consecutive reactions with the simultaneous influences of heat and mass transfer. The effects of various chemical and transport properties on the stability, selectivity, and effectiveness factor of the system are discussed. The pseudosteady state approximation is employed to reduce the mathematical difficulties.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 16 (1970), S. 848-856 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Solid-fluid reactions often involve two or more simultaneous reactions because either the feed contains multiple fluid reactants or the fluid products are reactive with the solid. Three types of simultaneous reactions, independent, parallel, and consecutive, are examined in terms of the selectivity and the effectiveness factor based on the unreacted core shrinking model under isothermal conditions. Criteria for high selectivities are derived, and effects of diffusion and chemical reaction are discussed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 20 (1974), S. 279-284 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Transient sorption rates of allene and methylacetylene in synthetic faujasite (Linde 13X) powder and self-bonded pellets are studied in a constant-volume, constant-pressure system at three temperatures. The intracrystalline diffusion coefficients are found to be in the order of 10-11 cm2/s and the activation energy for diffusion is 4.0 kcal/g-mole.A simple bipore distribution model for transient diffusion in macropores and micropores is presented. It agrees well with the experimental data and quantitatively predicts the macropore diffusion coefficients. The flow in the macropores is found to be in the Knudsen flow regime.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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: Aus der Analyse des E.S.R.-Spektrums einer Probe von Titantrichlorid (Stauffer H) resultieren fünf Elementarsignale, von denen drei 85% des ganzen Spektrums darstellen und eine axiale Symmetrie aufzeigen. Mit Hilfe der Ligandenfeldtheorie und den Ergebnissen der diffusen Reflexion im ultravioletten und sichtbaren Bereich gelangt man zu dem Schluß, daß diese Signale aus inneren Kristallstruktur-Fehlern stammen. Diese Schlußfolgerung stimmt mit verschiedenen experimentellen Beobachtungen überein.
    Notes: Le spectre de résonance paramagnétique électronique d'un échantillon de TiCl3 (Stauffer H) est analysé comme la somme de cinq signaux élémentaires dont trois représentent 85% du total et présentent une symétrie axiale. A l'aide de la théorie du champ cristallin et des résultats d'une étude spectroscopique UV-visible en réflexion diffuse, on arrive à conclure que ces signaux proviennent de défauts internes de la structure cristalline; cette conclusion est en accord avec plusieurs observations expérimentales.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 12 (1973), S. 2423-2430 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absorption and cicular dichroism spectra of the complex of poly-L-lysine (PLL) in the random coil form with methyl orange (MO) have been measured in aqueous solution. A new absorption band is observed at the shorter wavelength compared with that of the free dye. Although MO does not show a formation of dimer or aggregation with an increase in concentration, circular dichroism bands are observed at the wavelength corresponding to the wavelength of the new absorption band. These induced circular dichroism bands may arise from the dimeric MO molecules bound to PLL in the random coil form. The main contribution to the interaction between MO molecules is shown to be the electro static interaction. The observed circular dichroism spectra and the configuration of dimeric MO molecules bound to PLL can be explained by the dipole couping mechanism.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 1383-1390 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectral fragmentation of N-arylsulphonyliminopyridinium betaines has been rationalized using high resolution mass spectrometry as well as deuterium labelling. The most characteristic features are a very facile N—S bond cleavage and skeletal rearrangements accompanied by the expulsion of SO2 from the molecular ion and the [M—1] ion to the corresponding ionized N-aryliminopyridinium betaines and azacarbazoles, respectively. The presence of methyl substituents at the α-position of the pyridine ring has a significant effect on the mode of the fragmentation.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 139 (1970), S. 183-196 
    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: Pfropfcopolymere aus Polyvinylalkohol (PVA) mit Methylmethacrylat (MMA) wurden durch direkte Bestrahlung, Vorbestrahlung und nach der katalytischen Methode mit Kaliumpersulfat hergestellt; außerdem wurde eine Methode verwendet, die keine Katalysatoren benötigt.Nachdem die reinen Pfropfcopolymeren von unaufgepfropften PVA und Homo-PMMA durch erschöpfende, wechselseitige Extraktion isoliert worden waren, wurden die Hydroxylgruppen in den Copolymeren quantitativ acetyliert, damit einerseits osmotische Messungen möglich wurden und andererseits die Zusammensetzung durch hydrolytischen Abbau bestimmt werden konnte. In einem anderen Versuch wurden die aufgepfropften Seitenketten durch oxydative Spaltung der 1.2-Glykol-Bindungen im PVA-Molekül mit Perjodsäure isoliert, und das Molekulargewicht wurde osmometrisch bestimmt. An Hand dieser Ergebnisse wird gezeigt, daß die gebildeten Pfropfcopolymeren aus nur einer Seitenkette und einem Ausgangs-PVA-Molekül bestehen und daß ihre Struktur von den verwendeten Aufpfropfungsmethoden unabhängig ist.
    Notes: Poly(vinyl alcohol) (PVA)/methyl methacrylate (MMA) graft copolymers were prepared by mutual irradiation, pre-irradiation, and by a catalytic method with potassium persulfate (KPS); a technique to prepare graft copolymer using no initiator was also adopted. After pure graft copolymers were isolated from the graft films by vigorous alternate extraction unreacted PVA and homo-PMMA, hydroxyl groups in the copolymers were completely acetylated to carry out osmotic pressure measurements and determine the chemical composition by hydrolysis. Graft branches were separated by cleaving C—C bonds of 1.2-glycol structure in backbone PVA with periodic acid. The chemical structure of the graft copolymers was made clear on the basis of the measured number-average molecular weights of the pure graft copolymer, separated branch and mother PVA molecule, and the chemical composition of the graft copolymer. It was shown that the graft copolymer has only one branch and one mother PVA molecule, irrespective of the grafting methods employed.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 12 (1974), S. 715-718 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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