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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 26 (1993), S. 2151-2158 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2341-2349 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The direct silylation of tert-butylphenol formaldehyde resins with N,O-bis(trimethylsily)acetamide (BSA) has allowed a more complete analysis of these resins to be made with proton magnetic resonance (PMR) spectrometry. A quantitative determination of mixtures of the monomer, dimer, trimer, and tetramer may be carried out at 100 MHz.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2103-2119 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The air oxidation of poly-p-xylylene films was studied at temperatures between 125 and 200°C. The oxidation kinetics were obtained from neutron activation (NA) oxygen analyses and infrared (IR) Spectroscopy. A correlation between the NA oxygen analyses and mechanical properties indicated that the amount of oxygen incorporated into these polymers before a significant degradation mechanical properties is about 1000 ppm for poly(dichloro-p-xylylene) and 5000 ppm for poly(monochloro-p-xylylene) or poly-p-xylylene. The activation energy for the oxidation of these polymers was about 30 kcal/mole. Long-term-use (100,000 hr) temperatures were also estimated for each of the poly-p-xylylenes studied. The 100,000-hr maximum continuous-use temperature is 112°C for poly(dichloro-p-xylylene), 72°C for poly(monochloro-p-xylylene), and 57°C for poly-p-xylylene.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 20 (1976), S. 2095-2100 
    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 combination of an extraction technique with proton magnetic resonance spectrometry (PMR) has provided an analytical method for the determination of hydrocarbon mineral oil blended into an impact polystyrene. The amount of extraction time necessary for quantitative removal of the oil has been shown to be dependent on resin particle size. A linear correlation has been found between the weight of the extract obtained from 10.00 g resin and the per cent oil found in the resin.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1619-1632 
    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: Plasma-treated poly-p-xylylene films have been characterized by neutron activation oxygen analysis, internal reflection (IRS) and transmission infrared spectroscopy, transmission electron microscopy (TEM), and surface contact angle measurements. The results indicate that an oxygen plasma roughens the surface and that oxygen is incorporated into the surface. Oxygen is not detected in the bulk of the sample. The infrared transmission spectra exhibited no carbonyl band, but the relative band intensities changed, indicating a change in ring substitution by a loss of chlorine in the chlorinated poly-p-xylylenes. The IRS spectra of the surface of films treated with oxygen plasma did contain carbonyl bands at 1730 and 1640 cm-1. Argon and helium plasmas generally decreased the water contact angle measured on plasma-treated poly-p-xylylene surfaces more than oxygen or nitrogen plasma treatments. Regardless of the plasma utilized, the water contact angles increased with time after the treatment but did not recover to the original level. IRS spectra of the surface of films treated with argon plasma contained carbonyl bands at 1730 and 1695 cm-1. The adhesion of a polyurethane thermosetting material to a poly-p-xylylene surface is greatly improved if a plasma treatment is used prior to the application of the polyurethane. The degree of improvement in adhesion was dependent on the type of plasma and the treatment time.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 1639-1644 
    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: Thin coatings of various polyparaxylylenes were transformed into electrets by corona charging them and then overcoating with more polyparaxylylene to protect the charge layer. For such electrets, the extrapolated ten-year use temperature depended on the thermo-oxidative stability of the polyparaxylylene layer and was greater than 100°C for the most stable electrets. The voltage levels and surface charge densities were always greater than or equal to those of charged Teflon electrets, similar to those used in commercial devices.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 755-764 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High activity ethylene polymerization catalysts have been prepared by the interaction of ethylmagnesium chloride in tetrahydrofuran with high surface area silica, followed by reaction with excess titanium tetrachloride in heptane. The catalysts were tested in ethylene - hexene copolymerization reactions in the presence of AlEt3 at 80°C. For comparison purposes, the copolymerization properties of a similar catalyst prepared without silica were also evaluated. Preparative conditions were identified which provide catalysts that possess high reactivity towards 1-hexane. The silica and the amount of magnesium used in catalyst preparation strongly affect the copolymerization properties of the catalysts. Generally, catalysts prepared with silica showed much higher sensitivity to 1-hexene (effective reactivity ratio r1 = 25-60) while a similar catalyst prepared without silica exhibited an r1 value of 125. Fractionation of the copolymer with a series of boiling solvents showed that all the catalysts exhibit a wide distribution of active centers with respect to reactivity ratios, with the r1 values varying from 5-7 to ca. 200. The width of a the center distribution depends on catalyst composition - it is the narrowest for the catalyst prepared without silica and is the widest for the catalysts with intermediate Ti : Mg ratios.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 1167-1173 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The amount of dibutylmagnesium (DBM) or triethylaluminum (TEAL) that reacted with silica at 55-60°C depended on the silica calcining temperature. Lower silica calcining temperatures resulted in more Mg or Al fixed to the silica surface, indicating greater amounts of DBM or TEAL reacting with the silica. The amount of the metal alkyls butyl(octyl) magnesium ethoxide, ethylaluminum dichloride, tri-n-hexylaluminum, and diethyl(ethyldimethylsilanolato) aluminum that reacted with 600°C calcined silica was also determined. The metal alkyl can react with the silica at two sites, a surface hydroxyl group and a siloxane group. The silica surface hydroxyl groups can be chemically converted to trimethylsilyl groups so that only the siloxane groups are available for attack. After the metal alkyl was reacted with silica, the resulting intermediate was treated with titanium tetrachloride to yield an ethylene polymerization catalyst in the presence of TEAL. When no metal alkyl was employed, titanium tetrachloride reacted only with the silica surface hydroxyl groups to yield a weakly active ethylene polymerization catalyst.
    Additional Material: 2 Ill.
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  • 9
    Publication Date: 1993-04-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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