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  • Polymer and Materials Science  (44)
  • 1980-1984  (31)
  • 1970-1974  (13)
  • 1925-1929
  • 1920-1924
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2065-2072 
    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: For the rapid identification of additives such as antioxidant, ultraviolet absorber, and slipping agent, polypropylene containing such additives was heated in a tube connected directly to the inlet system of a mass spectrometer. The vapor of the additives evaporating out of the polypropylene was led to the reservoir and then submitted to mass spectrometry to give spectra for identification.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 1749-1759 
    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: Nuclear magnetic resonance absorption spectra of linter cellulose containing various amounts of water were studied to clarify the relation between the amount of absorbed water in cellulose fiber and the molecular motion in such a cellulose-water system. An amorphous cellulose sample was used for the sake of comparison. The changes in line width and second moment of the spectra were measured at various temperatures. From the variation with temperature of the first-derivative curves and the second moments, it has been inferred that the proton movement of absorbed water changes markedly over the approximate range 180°-200°K and that the absorbed water lowers the glass transition temperature of cellulose to room temperature.
    Additional Material: 13 Ill.
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  • 3
    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: Large excesses of a chain transfer agent, carbon tetrachloride, were introduced to a recipe for the mutual radiation grafting of styrene to cellulose acetate film. The effect of the carbon tetrachloride on the molecular characteristics as well as the reverse osmosis and time dependent mechanical properties of resulting graft copolymers was determined. Extremely short side chains were generated as a consequence of the high concentrations of chain transfer agent and the composite results further suggest that the morphology of the grafted films is best described as “destructured” or internally plasticized consequent to grafting in the presence of CCl4. Reverse osmosis fluxes increased with percent graft; salt rejection was high and unaffected by per cent graft up to 40% graft; and the tensile creep under wet conditions was significantly retarded by the grafting. These effects were shown to accrue from grafting per se by control experiments involving α-methylstyrene which will not propagate to form a polymer under these conditions. These results are compared and contrasted with earlier work on grafting in the absence of CCl4 where long side chains of polystyrene were generated resulting in a structuring of the polymer involving domains of polystyrene-rich material and domains of cellulose acetate rich polymer.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1629-1638 
    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: Blends of poly(ethylene terephthalate) (PET) and a copolyester of bisphenol A-terephthaloylisophthaloyl (PAr) (2:1:1) have been studied both before and after transesterification. The physical blends exhibit phase separation in their amorphous states: a pure PET phase and a mixed PAr-rich phase. In spite of this phase separation, PET crystallinity in blends, normalized to PET fraction, surprisingly goes through a maximum at 25% PAr content. The transesterfied copolymers are noncrystallizable and exhibit a single Tg between those of starting polymers, PET and PAr.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2929-2936 
    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: Reverse osmosis separation for 23 phenollic derivatives was examined by an anionic charged composite membrane. The solute permeation was carried out in single-solute aqueous solution (200 mg/L) under applied pressure of 3.92-7.85 MPa at 25°C. The correlation between the solute rejection and polar parameters for phenolic derivatives has been investigated. For p-alkylphenols, the solute rejection increased with molecular weight and/or molecular branching. In undissociated state, the rejection of phenolic derivatives was closely related with the Taft's number and the Hammett's number of substituents. Also rejections of phenolic derivatives depended upon the pH value of feed soultion and the polar effect of substituted groups. For example, rejections of aminophenols showed the minimum value at a certain pH value and on either side of the minimum point, the rejection of aminophenol increased. From these facts, the main factors in reverse osmosis serparation by an anionic composite membrane were discussed.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2513-2520 
    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: Gel permeation chromatography, using polystyrene gel and tetrahydrofuran as solvent, has been applied to hydroxybenzophenones, esters of salicylic acid, alkylphenols, alkylated methylenediphenols, and phenol-formaldehyde condensation products. The difference between the calculated molecular volume of these phenolic compounds and that obtained by actual determination with GPC has been ascribed to tetrahydrofuran solvation of the phenolic hydroxyl group. Furthermore, it has become clear that THF solvation is affected by the steric hindrance of ortho-substituted phenol and by inactivation of the phenolic hydroxyl group resulting from internal hydrogen bonding.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3069-3076 
    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 recrystallization of amorphous cellulose at various relative humidities was studied to clarify the relation between the amount of adsorbed water in cellulose and the molecular motion by the DSC method. The initial recrystallization kinetics of amorphous cellulose at various relative humidities were observed on the basis of the exothermic peak between 380° and 470°K in a DSC curve. The recrystallization occurred easily by conditioning at higher than 80% R.H., but hardly by conditioning at lower than 65% R.H. These facts suggest that the conformation of cellulose seems to be easily changeable if cellulose has a moisture regain which is approximately comparable to capillary water. When the Avrami equation was applied to the slope of calorific value versus conditioning time at higher than 80% R. H., it also appeared that the mode of recrystallization growth of amorphous cellulose exposed to water vapor is one-dimensional.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 3161-3170 
    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: Two kinds of ethylene-1-butene copolymers that were produced by the different procedures, that is, the slurry and the high-pressure polymerizations, were characterized by differential scanning calorimetry (DSC) and carbon-13 nuclear magnetic resonance (13C-NMR) spectroscopy. The melting points of both copolymers were found to be different in spite of the same 1-butene content. It was deduced that this phenomenon depended upon the subtly different chain structures between these two copolymers from the tetrad monomer sequence analysis by 13C-NMR method. In addition, the behavior of the composition fractionation by temperature rising elution technique was also considered to be affected by the chain structures.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 16 (1982), S. 851-860 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: To study the effect of fluoride on the physicochemical properties of carbonate-containing apatites, two series of fluoridated CO3 apatites with various fluoride contents were synthesized at 80°C and pH 7.4. The a-axis dimensions of these apatites decreased with the increase of both fluoride and carbonate contents. The crystallinity of the apatites showed similar patterns of variation with the degree of fluoridation irrespective of carbonate content. These patterns appear analogous to the complex pattern of the fluoridated hydroxyapatites previously reported. In contrast to this unexpected crystallinity phenomena, the apparent solubility of fluoridated CO3 apatites in acetate buffer solutions at pH 4.0 and 6.0 and 37°C decreased monotonically with increasing degree of fluoridation and approached that of fluoridated hydroxyapatites at high fluoride content. Dissolution rate of fluoridated CO3 apatite pellets at pH 4.0 also showed a simple decrease with increasing degree of fluoridation and was extremely sensitive to acid at low fluoride content.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 18 (1984), S. 427-434 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A Ni-45 wt % Ti (Ni-50 at % Ti) alloy was cast into molds of magnesia and silica investments by use of a dental argon-arc pressure casting machine with a copper crucible. The castings exhibited shape memory properties. The shape recovery process was sharper in the specimens cast in magnesia investment molds than in those cast in silica (phosphate-bonded) investment molds. The latter casting had a hard region of the periphery, suggesting that shape recovery process may be affected by reaction of molten metal with silica. Furthermore, the alloy possessed the adequate mechanical properties for consideration as crown-and-bridge prostheses.
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