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  • 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: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 4 (1949), S. 639-664 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of polyisobutene, polyisoprene, polybutadiene, GR-S, and polyethylene, weighing about 25 to 50 mg., were pyrolyzed in a vacuum of about 10-6mm. of mercury in a specially designed apparatus at temperatures ranging between 300 to 475°C. The volatile products of pyrolysis were separated into four fractions: (IV) gaseous, volatile at -196°; (IIIA) liquid, at -75°, (IIIB) liquid, at 25°; and (II) waxlike fraction, volatile at the temperature of pyrolysis. The gaseous fraction was analyzed in the mass spectrometer and was found to consist in all cases of CH4. The liquid fraction, IIIA, was analyzed similarly and was found to give a mass spectrum characteristic for any given polymer. A molecular weight determination of the waxlike fraction by the micro freezing point-lowering method, showed it to vary from 543 to 739, depending on the polymer from which the fraction was obtained. It is shown that the method of pyrolytic fractionation of high molecular weight polymers, in conjunction with mass spectrometer analysis of the more volatile fractions, can serve as a means of identifying the polymers.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 19 (1956), S. 373-377 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A brief experimental investigation was made of the copolymerization of twelve alkoxysilanes with monochlorostyrene, vinyl chloride, and acrylonitrile. These new monomers include vinyltrimethoxy-, vinyltriethoxy-, vinyltriisoproxy-, vinylmethyldiethoxy-, vinylethyldiethoxy-, and vinylphenyldiethoxy-silanes as well as allyl-, propenyl-, 2-butenyl-, Δ3-cyclohexenyl-, 6-triethoxysilylbicyclo [2.2.1]heptane-2, and α-chlorovinyl-triethoxysilanes. No copolymerization took place with monochlorostyrene. In the copolymerizations with vinyl chloride, and with acrylonitrile, the reactivity ratio r2 was assumed to be zero and the value of r1 determined.
    Additional Material: 3 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: Equilibrium and kinetic studies of the sorption and desorption of water vapor by poly(acrylic acid), poly(sodium acrylate), sodium carboxy methyl cellulose, methyl cellulose, and a series of poly(methyl acrylate) hydrolyzates in acid and sodium salt forms were made at 30°C. It was found, as expected, that equilibrium sorption increased and was greater for polymers containing strong-electrolyte type substituents than for those containing an equivalent number of weakly ionizable units. In general, the diffusion is somewhat slower than in the case of water-insoluble polymers. It was also found that water solubility of a polymer does not per se result in anomalous water sorption. In Methocel, for example, water diffusion is both Fickian and concentration-independent. All of the results, particularly those on the poly(methyl acrylate) hydrolyzates which ranged from completely water-soluble to insoluble systems, support the following conclusion: For water-soluble polymers both anomalous diffusion and relatively high glass temperatures are associated with high concentrations along polymer chains of very polar or ionic groups, such as —OH, —COOH, and CO2-Na+. Presumably both the anomalies and high transition temperatures are associated with restricted segmental mobility resulting from strong chain-chain interactions which originate in the highly polar and ionic, water-solubilizing chain substituents.
    Additional Material: 8 Ill.
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of water vapor on the rate of diffusion of organic molecules has been studied at 40°C. by the sorption method for the systems water-acetone-polyvinyl acetate, water-carbon tetrachloride-polyvinyl acetate, water-acetone-cellulose acetate (37.9% acetyl) and water-benzene-polystyrene. For the first three systems the rate of diffusion of the organic vapor is markedly faster for the mixture of water and organic vapor than for the pure organic vapor. With polyvinyl acetate, the rate of diffusion of 80 mm. of acetone is increased about 25-fold if 36 mm. of water vapor is mixed with the acetone. Diffusion of the larger carbon tetrachloride molecule is accelerated by water even more than is acetone. Water vapor at a pressure of 36 mm. causes about a 30-fold increase in the rate of diffusion of 80 mm. of acetone into cellulose acetate even though the diffusion of acetone itself into cellulose acetate is anomalous. With polystyrene the presence of water vapor causes no acceleration of the diffusion of benzene which is the expected result since, in contrast to the other two polymers, polystyrene sorbs only very small amounts of water. It is concluded that the marked effect of water vapor on the diffusion of organic vapors into polyvinyl acetate and cellulose acetate involves (a) a rapid diffusion of water into the polymer and (b) more rapid diffusion of the organic vapor into the “water plasticized” polymer than into the dry polymer.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 34 (1959), S. 741-760 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Although crystallization under stress occurs in nearly all synthetic fiber making, giving fine fibrillar fiber structures, it has been relatively little studied; and the literature, centered mainly round coarser spherulitic crystallization, does not take us very far in understanding it. However, a simple experiment shows that it is very important. If a filament of amorphous polyethylene terephthalate is stretched over a hot plate between two roller moving at different speeds, stretching can take place either without crystalization at low tension, or with considerable crystallization at high tension, at the same temperature and speed, simply according to the method of starting the machine. A model visco-elastic theory based on Maxwell's equation is, therefore, developed to describe this behaviour using the simplest possible assumptions. Further experiments then show that this simple and partly empirical theory fits the observed behaviour of polyethylene terephthalate reasonably well, and the simple assumptions made, therefore, seem to give a first approximation to the course of strain induced crystallization. They correspond with the idea of exremely rapid crystallization from a nucleus to a small structural unit, the density of nucleation being dependent on the stress. Parallel work on the streching of spherulitic structures is then mentioned, and it is finally suggested that stress induction and rapid growth to a small structural unit may be common to both spherulitic crystallization under internal stresses, and fibrillar crystallization under an externally applied stress.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 37 (1959), S. 313-315 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. S31 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 26 (1998), S. 30-38 
    ISSN: 0142-2421
    Keywords: XPS ; AES ; CoAg granular film ; CoPt alloy ; magnetoresistance ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The chemical state of Co, Ag and Pt in giant magnetoresistive CoAg granular films sandwiched between Pt layers is studied using high-resolution x-ray photoelectron spectroscopy. Measurements were carried out as a function of depth for samples deposited at different temperatures and containing different amounts of Co. In all samples Ag is found to segregate at the surface to form an AgPt alloy. The depth profiles are consistent with the deposited Co concentration modified by preferential sputtering. No variation of the chemical state for Co or Ag in the CoAg layer is found for different deposition conditions. However, small amounts of Pt do affect the Co 3d electrons. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 892-898 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The mechanism of oxidation of copper at the alloy/film interface, and the subsequent migration of copper ions in barrier-type films, has been examined for anodizing of an Al - 1.5 wt.% Cu alloy with a prior chemical polishing treatment. Both chemical polishing and anodizing result in formation of a thin layer of alloy at the alloy/film interface, of ∼2 nm thick, that is highly enriched in copper. The layer is present immediately beneath the different types of film formed by chemical polishing and subsequent anodizing, and contains in both cases ∼6 × 1019 Cu atoms m-2. The amount of copper contained within the enriched layer of alloy is not significantly dependent upon the anodizing voltage. During anodic film growth, both aluminium and copper ions are incorporated into the film at the alloy/film interface, on average in their alloy proportions. However, the film is depleted in copper relative to the alloy because copper ions in the film migrate faster than Al3+ ions and, on reaching the film/electrolyte interface, are ejected directly to solution. The mechanism of oxidation of copper is proposed to depend upon the formation, through prior oxidation of aluminium, of copper-rich clusters in the enriched layer of alloy at the alloy/film interface. Individual clusters are oxidized only on achieving a critical size. Consequently, copper is incorporated into the film discontinuously both in time and in position along the alloy/film interface. The films contain a high population density of flaws, which affects the film composition, the uniformity of ionic current, the faradaic efficiency of film growth, and the detailed distributions of copper ions within the films. However, the general features of film growth are compatible with the usual growth mechanism of anodic alumina, with transport numbers of Al3+ and O2-/OH- ions of ∼0.4 and ∼0.6, respectively.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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