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  • Polymer and Materials Science  (3)
  • 1990-1994  (3)
Document type
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Years
Year
  • 1
    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: As predicted by thermodynamic studies of polymer conformation, high molecular weight poly(methyl methacrylate) (PMMA) dissolves cleanly, and at a constant rate, in a 7 : 3 mixture of 1-butanol and acetonitrile, although neither liquid is a solvent for PMMA by itself. Mixtures of other alcohols with acetonitrile also dissolve PMMA. When mixtures with the same fraction of acetonitrile are compared, methanol dissolves PMMA almost twice as fast, ethanol and hexanol at about the same rate, and 2-propanol somewhat more slowly than the 1-butanol mixture with acetonitrile. The measurements of dissolution rate were made using a laser interferometer at 20°C.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 2135-2142 
    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: A series of 17 polymers was etched in the reactive ion-etching (RIE) mode. The etch rates were monitored using a laser interferometer. The gases used were oxygen alone and a mixture of carbon tetrafluoride with oxygen (8% O2). The polymers fell into three groups: the aromatics (polystyrene and derivatives), the aliphatics (methacrylates and vinyl acetate), and the cellulosics (methyl ether and nitrate). In oxygen with a power density of 0.25 W/cm2, the etch rates for the three groups fell in the range of 200-300 nm/min, 350-450 nm/min, and 500-850 nm/min, respectively. The etch rates were also measured at a power density of 0.50 W/cm2. The etch rates at the higher-power density were about 75-80% higher than those at the lower-power density. The etch rate in the fluoride mixture was about half that in the oxygen, all other parameters being the same. Plasticizers that lower the glass transition temperature of polymers based on vinyl chloride, methyl methacrylate, or styrene do not change the etch rate of the polymers very much. There is a slight increase in the rate for polystyrene and a slight decrease in the rate for poly(methyl methacrylate). All the effects of composition on etching rate can be correlated to a first approximation with the molar fractions of carbon and oxygen in the resist. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 765-776 
    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 solution crystallization kinetics and crystal dissolution behavior of three grades of poly (ethylene terephthalate) in N-methyl-2-pyrrolidinone were studied were using turbidimetric and calorimetric methods. The influence of concentration on the equilibrium dissolution temperature was described using Flory's melting point-composition relationship. The effect of the solvent alkyl group was also investigated. N-ethyl-2-pyrrolidinone was found to be a better solvent than N-ethyl-2-pyrrolidinone or N-cyclohexyl-2-pyrrolidinone for poly (ethylene terephthalate). From the calorimetric experiments, it was determined that two crystallization processes (primary and secondary crystallization) were responsible for the total crystallinity. The primary process dominated the early stages of the crystallization process and accounted for the majority of the final crystallinity for lower polymer concentrations. Based on coherent secondary nucleation theory, the effect of the crystallization temperature on the primary crystallization rate constant was quantified in terms of a temperature coefficient. This temperature coefficient was found to be relatively insensitive to PET concentration, PET structural impurities, and solvent alkyl group. © 1993 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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