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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 1009-1026 
    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: This paper describes an investigation into the degradation of a purified epoxide based on the diglycidyl ether of bisphenol A hardened with p,p′-diaminodiphenylmethane. The method used was that of hot-wire pyrolysis followed by gas chromatography. Special attention was given to the problem of solid residues formed on the pyrolyzer tube, and evidence was found that these probably contain oligomers. Resonance-stabilized free radicals also appear to be formed, and evidence is found to support the idea of dehydration during degradation, originally put forward by Lee. An attempt, based on first principles, is made to explain the degradation of epoxides, using evidence from previous work as well as that described in this paper.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3195-3214 
    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: This paper contains a description of the use of gas chromatography to examine the pyrolytic degradation of epoxide resins. The method depends on the pyrolysis of the material by use of an electrically heated filament, the difficulties of the method are examined and attempts to overcome them are described. The pyrolytic degradation of a resin based on the glycidyl ether of bisphenol-A hardened with 1,2-diaminoethane and also triethylenetetraamine, is described. An attempt has been made to explain, in terms of possible degradation reactions, the actual compounds detected in the pyrolytic breakdown.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 17 (1955), S. 159-177 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal structure of nylon 6 (—NH (CH2)5CO—)p has been determined by interpretation of the x-ray diffraction patterns given by drawn, rolled fibers. The determination was part of a program to investigate the relation between structure and physical properties, in particular melting point. Nylon 6 melts 50°C. lower than its isomer nylon 66 (—NH (CH2)6NH·CO (CH2)4CO—)p; it had been suggested that this was due to deficient hydrogen-bond formation in nylon 6 crystallites. The unit cell contains eight chemical units (—NH (CH2)5CO—) and is monoclinic with a = 9.56 A., b = 17.24 A., c = 8.01 A., and β = 671/2°. Calculated density = 1.23. Observed density for a drawn monofilament = 1.16. The structure consists of planar chains of CH2 groups and amide groups tilted 7° from the (001) plane. Alternate chains in this plane are oppositely directed, an arrangement which allows all hydrogen bonds to be made perfectly. The hydrogen-bonded sheets of atoms are packed in an “up-and-down” staggered configuration along the c-axis. Distances between atoms in neighboring molecules are all normal van der Waals contact distances. It appears, from a general survey of polyamide melting points published elsewhere, that the determining factor is the number of CH2 groups between the amide “anchor points” - polymers with odd numbers of CH2 groups melt lower than those with even numbers. The present work shows that the odd number of CH2 groups in this polymer does not lead to deficient hydrogenbond formation, and that the lower melting point of nylon 6 as compared with nylon 66 must be ascribed to some other cause, possibly connected with the propagation of vibrations along odd-numbered chain segments.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 8 (1984), S. 125-136 
    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: ‘Oxygen Index’, ‘Rate of Burning and Extent of Burning of Self-supporting Plastics in a Horizontal Position’ and ‘Vertical Flammability’ tests were used for examination of polypropylene copolymer HW 607M and the same copolymer filled with 40% w/w calcium carbonate. Room-scale studies were also carried out using a range of standard ignition sources. In the latter tests, measurements of the levels of smoke generated in the test chamber were monitored continuously, and intermittent measurements were made of the carbon monoxide concentrations. Small-scale testing showed that addition of the filler to the polypropylene raised the limiting oxygen index of the polymer from 17.8 to 20.3, which is only marginally lower than the oxygen concentration in ambient air (20.9); this introduces the possibility of a filled polypropylene which is not ignitable in air. However, the results of the UL94 and ASTM D635 tests did not show significant differences in flammability and rates of vertical and horizontal flame spread as between the two materials, through the unfilled polymer produced extensive burning droplets early in both tests whilst the filled polymer did not. Such droplets can spread fires to floor coverings, so that the filled plastic might be preferable in application. In our laboratory tests, the filled samples gave considerably lower smoke generation than the unfilled ones. At high heat fluxes they generated considerably less smoke than (smaller) unfilled samples containing the same mass of polymer. This suggests that the calcium carbonate has specific smoke-suppressant activity and is not merely acting as a polymer diluent. In larger-scale tests, unfilled samples were readily ignited by a domestic match, whilst the filled samples required an ignition source of 43 kJ (some six times greater than the match source) in order to light them and sustain ignition. The filled polymer did not melt on ignition and there was no lateral spread of flame from the sample. Smoke generation was considerably lower, the average optical density at maximum obscuration being 0.27, compared with 0.84 for the unfilled control. In particular, smoke suppression achieved by use of calcium carbonate at higher heat-flux levels is considerably greater than that expected for an inert diluent.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 9 (1985), S. 167-170 
    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: Smoke and toxic gases (STG) are the main cause of fire deaths. They combine to make escape difficult and to retard rescue work and fire-fighting. The paper reviews advances in the characterization of the STG hazard, and discusses improved materials of construction to meet the new, more stringent safety criteria used by responsible architects and design engineers. Because of the wide choice of safer materials now available at reasonable cost in a number of product areas such as furniture foams and cable insulation, the time is approaching when such materials can be introduced without harming the economics of these industries. Indeed, a convincing demonstration of intrinsic safety could without harming the economics of these industries. Indeed, a convincing demonstration of intrinsic safety could encourage the introduction of improved plastics and other organic materials into a wide range of market applications.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 8 (1984), S. 6-9 
    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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 909-912 
    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 microstructure of polyepichlorohydrin was directly studied by high-field 13C-NMR. Spectral features were found that correspond to different tacticities. By using curve deconvolution techniques, the different tacticities were assigned and quantified.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1541-1545 
    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: Graft copolymerization of collagen with N,N,N′,N′-tetra (2-hydroxypropyl) ethylene diamine methacrylate (THPEDM) was carried out in an aqueous medium using potassium persulfate as the radical initiator. Collagen-g-poly(THPEDM) was characterized by the percent yield and the copper chloride test. The percentage of grafting was determined as functions of concentration of monomer, concentration initiator, reaction time, and temperature.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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