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  • Articles  (495)
  • Polymer and Materials Science  (310)
  • Chemical Engineering  (162)
  • Engineering  (23)
  • Life and Medical Sciences
  • 1980-1984  (495)
  • 1940-1944
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (495)
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  • Articles  (495)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 509-519 
    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 deterioration of polyolefin, poly(ethylene terephthalate), and polyamide films under soil burial conditions extending up to 32 months has been investigated. Based on changes in their elongation at break, the films can be ranked in order of increasing sensitivity to degradation: Polyester ≃ polypropylene 〈 low-density polyethylene ≃ high-density polyethylene 〈 nylon 6.6. The degraded nylon 6.6 and polyethylene films were characterized by infrared and luminescence spectroscopy and scanning electron microscopy, as well as by wet analysis for hydroperoxides. From a comparison with the well-known oxidative sensitivity of nylon 6.6 in oxygenated water at slightly elevated temperatures, the rapid deterioration of nylon 6.6 film during soil burial was also concluded to be an oxidative process. The somewhat smaller, but significant, embrittlement of the polyethylenes studied could not be simply explained by thermal oxidation (with only trace oxidation products detectable) or microbiological attack (deterioration being unaffected by surface activation to enhance wettability).
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 7 (1983), S. 79-88 
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: There are two major fire processes, an understanding of which is essential for effective fire safety design: (1) the conditions under which a combustible material may become involved in flaming combustion, and (2) the rate at which such a material, once involved, will provide an output of heat, smoke, toxic gases, etc., which can endanger people and property. The first process may be regarded as covering both ignition and spread of fire on materials; its complement is the way in which fire may become extinguished. It is necessary for such processes to bring in a characteristic of the basic combustion reaction which, directly or indirectly, expresses the reactivity of the combustion process. Thus pilot ignition is usually associated with an approximate surface fuel temperature. More basically, it is associated with a critical flow rate of volatiles and a critical heat loss from the flame, the latter being influenced by ambient oxygen and temperatures conditions as well as heat lost and gained by the fuel itself. The most important factor governing the production of dangerous product is the rate at which volatiles first (fuel controlled fires) and later air (air controlled fires) are fed into the flames. The reactivity is of less importance, although it may be one of the factors which control combustion efficiency. In general, the more efficient is the combustion the more heat is produced, but the less smoke and toxic gases are produced. Some of the main advances in the above areas are reviewed in this paper.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 39-46 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Thermoplastic interpenetrating polymer networks, IPN's, are defined as combinations of two physically crosslinked polymers. A styrene-b-ethylene-co-butylene-b-styrene (SEBS) triblock elastomer was combined with an ionomer prepared from a random copolymer of styrene, methacrylic acid, and isoprene (90/10/1 by volume), and subsequently neutralized. Two subclasses of the thermoplastic IPN's were identified. A sequential polymerization method yielded the chemically blended thermoplastic IPN's (CBT IPN's). Melt blending of the separately synthesized polymers produced the mechanically blended thermoplastic IPN's (MBT IPN's). Stress-strain and Rheovibron characterization revealed that the CBT IPN's exhibited greater tensile strength and higher elongation at break, but lower moduli than the MBT IPN materials of the same overall composition. Analysis of moduli data with the theories of Takayanagi, Davies, Budiansky, and Kerner disclosed more equal dual phase continuity for the MBT IPN's than the CBT IPN's at each composition. The low modulus of the more rubbery CBT IPN compositions was attributed to a decrease in the effective chain end-to-end distance between crosslinks in the elastomeric (EB) center block, brought about by the synthetic method.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 86-92 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: An experimental investigation into the performance in general and the melting behavior in particular of a single screw extruder running with a low density polyethylene power has been carried out and the results compared with those for a granular feedstock of low density polyethylene having similar melt properties. It was found that the tendency was for the output rate, pressure generated and specific power consumption to be lower for the powders, and that the removal of barrel heating near the feed hopper increased these parameters. Two melting mechanisms were observed in powder extrusion; one being the classic “Maddock” type, and the other such that the solid bed and melt pool were in reversed positions relative to the Maddock case. There was a trend for this latter mechanism to operate with low screw speeds, shallow channels and full heating. Melt initiation occurred nearer the feed end and melting was completed much more quickly with powders. An explanation of the mechanisms is proposed which is based on the observation of early melt initiation, and the industrial practices of feed zone cooling and increasing feed pressure generation to improve the performance of extruders running with powders are seen to be consistent with this proposition.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3719-3728 
    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: Hydrophilic three-dimensional methacrylate polymer networks (hydrogels) were prepared from 2-hydroxyethyl methacrylate (HEMA) monomer and tetraethylene glycol dimethacrylate (TEGDMA) as crosslinker. The nature and states of water in these hydrogels were studied by differential thermal analysis and pulse NMR relaxation spectroscopy. The thermal studies showed no endotherm peak for ice melting in the lower water content (bound water region); there are two endotherms peaks for higher water content hydrogels near 0°C. The amounts of bound water, intermediate water, and bulklike (free) water in the hydrogels were determined from a quantitative analysis of the endotherms of the water melting transitions. The water structure ordering in the hydrogels were discussed in terms of the fusion entropy and enthalpy obtained from the endotherm. Nuclear magnetic relaxation spectroscopy was also used to understand the mobilities of the water protons in the hydrogels and the interaction of water molecules with the gel networks. The measured spin-lattice relaxation time (T1) values for water protons in the hydrogels are greatly reduced compared to that of liquid water. The measured values of spin-spin relaxation times (T2) of water protons in the hydrogels are approximately 10 times less than that of T1 and are almost constant in the region of bound water content. Beyond the bound water content region in the hydrogels, the T2 values rapidly increase as the water content increases.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1941-1949 
    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 adhesive bond of allyl 2-cyanoacrylate between steel substrates has been analyzed and compared to that of ethyl 2-cyanoacrylate. Mechanical strength as well as thermomechanical, calorimetric, thermogravimetric, and dynamic mechanical response was observed. It was demonstrated that the allyl 2-cyanoacrylate bonds exhibit improved temperature resistance owing to the formation of heat-induced crosslinks in the adhesive layer, resulting in much improved lap-shear strengths. Scanning electron microscopy of the fracture surfaces showed that plastic deformation occurred in the allyl 2-cyanoacrylate adhesive after thermal aging, while interfacial and brittle failure dominated all other cases.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 1011-1024 
    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 curing reaction of tetraglycidyl diaminodiphenyl methane (TGDDM) with diaminodiphenyl sulfone (DDS) has been investigated using differential scanning calorimetry, Fourier transform IR spectroscopy, and ESR spin trapping techniques. A mechanism has been proposed, and the cure kinetics has been obtained at 177°C. The major conclusion is that cure proceeds mainly through chain extension, while crosslinking occurs through the reaction of hydroxyl groups with epoxides, resulting in formation of ether linkages.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1269-1276 
    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: Uncrosslinked cis-trans polybutadiene films were prepared on ultraclean glass microscope slides by uniform dipping. The samples were stored in different environments prior to evaluation of surface oxidation by dynamic contact angle using the Wilhelmy plate method and by X-ray photoelectron spectroscopy (XPS). Storage conditions evaluated were: (1) laboratory air at 20°C and 30% relative humidity; (2) vacuum at 0.1 torr; (3) distilled water equilibrated with air; and (4) degassed distilled water. XPS and contact angle analysis indicate that samples exposed to air undergo significant surface oxidation within 8 h. Exposure of polybutadiene to air-equilibrated water results in slower oxidation. Samples stored in degassed water demonstrated less surface oxidation. Vacuum-stored samples demonstrated the least surface oxidation. Dynamic contact angle measurements demonstrated that receding contact angles are more sensitive to changes in surface oxidation than are advancing contact angles, as expected. Changes in surface wetting characteristics are readily observed after only 1 h in laboratory air, although XPS analysis does not show evidence of oxidation within 4 h of air storage.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 715-724 
    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: Poly(ethylene terephthalate) fabric was degraded under rapid heating conditions and the solid residue characterized by diffuse reflectance infrared spectroscopy. Fabric samples with and without flame retardant were pyrolyzed in air or nitrogen and spectra-recorded after various percentage weight changes. Dominant species included carboxylic acid end groups and linear anhydrides, based on infrared absorbances before and after chemical treatments of the residues. Vinyl benzoate end groups were clearly precluded, as were cyclic anhydrides. Diffuse reflectance spectra were also compared with spectra obtained by transmission infrared on conventional KBr discs prepared from the same residue. The former technique was shown to be superior to the pressed disc method for the tough residues obtained by thermolysis.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2131-2131 
    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
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