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  • 1
    ISSN: 1040-0397
    Keywords: Liquid-liquid interface ; Ammonium ion ; Nonactin ; Ionophores ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Facilitated ion transfer reactions of the ammonium, potassium, and sodium ions with the ionophores dibenzo-18-crown-6, nonactin, and valinomycin were investigated at the water/ 1, 2-dichloroethane interface. Association constants for the various reactions studied were calculated to determine the selectivity imparted by the ionophores on the transferring ions. Of the ionophores studied, nonactin was found to be the most selective towards the ammonium ion, with a calculated association constant of 14.1.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 7 (1995), S. 714-721 
    ISSN: 1040-0397
    Keywords: Urea ; Liquid-liquid interface ; Enzymatic assay ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The detection of the ammonium ion produced by the enzymatic action of urease on urea is investigated electrochemically by means of Facilitated ion transfer reactions at liquid-liquid micro-interfaces. The urease was used either in a dissolved form (free in aqueous solution) or immobilized onto the surface of an ammonia gas permeable membrane. The sensing structure utilizing the ammonia gas permeable membrane allowed the detection of urea from 200μM to 4mM. Thick film technology was utilized in conjunction with UV excimer laser photoablation techniques to fabricate a inicroelectrode strip sensor for the ammonium ion.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 47 (1960), S. 349-359 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: On pyrolysis at 300° under nitrogen the polythiolcarbamate from methylenebis(4-phenyl isocyanate) and 1,6-hexanedithiol decomposed into carbon dioxide, carbonyl sulfide, 6-mercapto-1-hexene, tetrahydro-2-methyl-1-thiapyran, thiepane, 1,6-hexanedithiol, and an intractable residue. Carbodiimide and amine groups were shown to be intermediates in the formation of the residue. A quantitative study of the degradation indicated that about 80% of the thiolcarbamate groups decomposed by splitting into isocyanate and mercaptan moieties. Further reaction of the isocyanate moiety produced the carbon dioxide and carbodiimide groups. The remaining thiolcarbamate groups formed carbonyl sulfide, and amine and olefin groups, probably by a direct ester type of degradation. The resulting 6-mercapto-1-hexene was the source of the cyclic sulfides.
    Additional Material: 1 Tab.
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of polythiolcarbamates, [ - CONH - X - NHCOS - Y - S]m, have been prepared in which X was either aliphatic or aromatic and Y was a wide variety of aliphatic groups. Synthesis of the polymers by two different methods, the tertiary aminecatalyzed solution polymerization of diisocyanates with dimercaptans and the interfacial polycondensation of bischlorothiolformates and diamines, proved that the polymers had the desired thiolcarbamate structure. Greater yields of lower molecular weight polymers were obtained by the diisocyanate method. Polythiolcarbamates were found to be highly insoluble white powders which tend to decompose in light, in hot solvents, and in aqueous base. They melt somewhat higher than their oxygen analogues, but are less thermally stable.
    Additional Material: 4 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 47 (1960), S. 522-525 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 2317-2328 
    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: Uniform, submicron-diameter polystyrene (PS) and poly(methylmethacrylate) (PMMA) microspheres were dilated by preswelling with pure organic vapors followed by rapid removal of the preswelling penetrant by protracted evacuation of the preswelling chamber to a pressure of 10-3 mm Hg. Aging of the preswollen polymers was carried out both in vacuum and in the presence of various penetrants at sorbed concentrations typically less than 2 wt%. Inferences about relaxations of the polymers were based upon changes in concentrations of the penetrants within the microspheres, at a given temperature and penetrant activity, which result from aging in vacuum or in the presence of penetrant. The kinetics of the relaxations were monitored by probing the expanded glasses with relatively low concentrations of penetrants. In general, the continuous presence of these low concentrations of probe molecules either arrested or retarded the ensuing relaxation as compared with the aging that occurred in vacuum. A series of lower monohydric alcohols, lower n-alkanes, and some other similar penetrants were used as probes to test explicitly and systematically the effects of size and structure of the penetrant contacting the polymer during aging on the decay of excess sorption capacity of the preswollen glassy polymers. Decay of excess sorption in the presence of penetrant was evident only when molecularly small penetrants with interactive functional groups, alcohols for example, were sorbed into preswollen PMMA. This result suggested that the relaxation occurring in the presence of penetrant involved specific interactions between the penetrants and the carbonyl groups in the PMMA.
    Additional Material: 15 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 30 (1996), S. 331-339 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The development of artificial skin substitutes based on cultured cells and biomaterials such as collagen requires an understanding of cellular interactions with the substrate. In this study, human keratinocytes were cultured on the surface of collagen sponges, and confocal laser-scanning microscopy (CLSM) was used to assess both the microstructure of the sponge, and the cell morphology and distribution throughout the sponge. It was found that the pore size increased with increasing depth into the sponge. Both pore size and fiber thickness increased during incubation for up to 10 days at 37°C in culture medium in the absence of cells. This latter effect was not observed when the sponges were incubated in distilled water. Keratinocytes penetrated into the sponge even after only 3 days in culture. By 10 days in culture, the cells had penetrated to the maximum depth that could be examined (120 μm from the sponge surface). In the presence of cells, the inner structure of the collagen sponge had altered after 10 days in culture, with the collagen fibers becoming thicker, and pore geometry less regular. The mechanism responsible for this is unknown at present. Although the presence of the keratinocytes increases distortion of the sponge structure, factors from the medium itself also contribute to this effect. CLSM is a powerful tool for assessing cellular interactions with bioimplants, providing both qualitative and quantitative information. It offers many advantages over scanning electron microscopy (SEM) and histological techniques. CLSM minimizes the time-consuming, extensive preparation of samples required with the latter two methods, and allows noninvasive serial optical sectioning of intact samples. © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 91-94 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The F 1s spectra from fluorine-containing phosphate glasses provide quantitative information about the nature of fluorine bonding that can be used to test structure-composition models. When fluorine is added to an aluminophosphate base glass, AlνF bonds are initially preferred until all available Al sites are filled, after which additional F replaces PνOνP bonds to form PνF sites. In tin phosphate base glasses, the PνOνP bonds are consumed during the initial stages of fluoridation, followed then by the formation of SnνF bonds. The structural insight provided by XPS is complementary to that provided by more conventional "bulk’ spectroscopic probes.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 1657-1674 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation induced solution polymerization of styrene in methylene chloride in a small scale pilot plant utilizing a flow reactor is reported. Both conventional free radical and ionic polymerization have been achieved. With rigorous drying accomplished over molecular sieves the ionic mechanism predominates. Conclusive kinetic evidence as well as polymer properties substantiate radiation induced ionic polymerization for the first time in an engineering pilot plant. The validity of Williams' model is reinforced by this study and a survey of over 100 literature observations.
    Additional Material: 8 Ill.
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