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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 13 (1979), S. 676-679 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 22 (1998), S. 239-252 
    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: The gasification behavior for a wide range of polydimethylsiloxane fluids in a nitrogen atmosphere was investigated. Part 1 of this study addressed the measurement of the energy (global heat of gasification) required for the gasification of a wide range of dimenthylsiloxanes. Several significant corrections were required to reconcile measured gasification energy(s) with calculated heat(s) of gasification based on fundamental thermochemical data. The identification of the dominant mode(s) of gasification via the characterization of pyrolysis products provided a firm basis and rationale for understanding and directing efforts at quantifying these correction factors. In Part 2, the gasification products were identified and quantified at various stages of the gasification process corresponding to ignition, fire growth, and steady-state burning. Pyrolysis of methylated siloxanes occurs via two modes: (1) the volatilization of short chain and intermediate chain length species native to the polymer, and (2) the volatilization of short chain and intermediate chain length species resulting from thermal degradation via siloxane rearrangement. The former process is the dominant gasification mechanism for short chain oligomers and low viscosity fluids (η〈10 cS) and the latter process is dominant in all higher molecular weight polymers (η〉100 cS). Both gasification mechanisms are evident in all polymers (η〉20 cS); the dominant mechanism is dependent upon polymer size and distribution thereof, the gasification stage, and the presence of trace catalysts in the polymer. Because of their structural similarity, the combustion of all gasification products emanating from PDMS regardless of the stage of the pyrolysis process or the dominant mode of gasification will result in virtually identical combustion products, i.e. SiO2, CO2, and H2O. Copyright © 1998 John Wiley & Sons, Ltd. This paper was written under the auspices of the US Government and is therefore not subject to copyright in the US.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Plant/Operations Progress 4 (1985), S. 176-180 
    ISSN: 0278-4513
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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: Transient gasification rates and fluid temperatures were measured for polydimethylsiloxane fluids ranging in viscosity from 0.65 cS to 60 000 cS in a nitrogen atmosphere at external radiant fluxes from 20 kW/m2 to 70 kW/m2. A detailed energy balance for each fluid sample was conducted to determine its global heat of vaporization. Two major energy loss corrections were identified and quantified. The absorption of incident radiation by the volatile products from short chain oligomers was measured and found to substantially reduce the incident flux to the sample surface; the energy loss due to re-radiation was determined to be a substantial factor in reducing the net heat flux to the sample for long chain length fluids. Other energy losses, e.g. heat loss to the substrate, were observed but were less significant. The average gasification rate for each fluid increased linearly with increasing external radiant flux. The global heat of gasification increases with an increase in the chain length (molecular weight) for the siloxane oligomers. These agreed well with calculated values. The global heat of gasification for 50 cS fluid is about 1200 kJ/kg and its value remains nearly constant for all higher molecular weight dimethylsiloxanes. Pyrolysis rates for siloxane fluids are very sensitive to trace catalysts. Measurements of the global heat of gasification for ultra-clean polymers resulted in significantly higher values (3000 kJ/kg). The gasification of siloxanes occurs via two modes or combinations thereof: (1) volatilization of molecular species native to the polymer, and (2) volatilization of thermal degradation products. The former process dominates for low molecular weight siloxanes (η〈10 cS) and the latter process dominates for high molecular weight siloxanes (η〉1000 cS). For the intermediate molecular weight siloxanes, both volatilization and degradation processes occur. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 14 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 21 (1997), S. 265-270 
    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: A controlled-atmosphere cone calorimeter was used to investigate the burning of a silicone fluid and two silicone elastomers. The silicone materials were tested at 50 kW/m2 incident heat flux in environments containing 15-30% oxygen. The test results were compared with a high molecular weight hydrocarbon fluid and an ethylene propylene rubber in terms of time to ignition, peak heat release rate and total heat released, carbon monoxide yield and carbon monoxide production rate, and smoke production and smoke production rate. The data from this study show that when materials burn in oxygen-enriched, normal, and vitiated atmospheres, silicone-based materials have a comparatively low peak heat release rate, total heat released, average CO production rate, and average smoke production rate as compared with organic-based materials. The smoke production and smoke production rate of silicone elastomers can be significantly reduced by adding appropriate smoke suppressants and additives. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 541-554 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilute solution parameters were determined for polymethylphenylsiloxamer fractions (5 × 104 〈 M 〈 1.5 × 106) in toluene, cyclohexane, and diisobutylamine (θ ≈ 30.4°C). The data are interpreted by the procedure suggested by Flory and Fox. Minor deviations from theory are noted. Polymers from both cis- and trans-cyclotrisiloxanes were investigated. The major portion of the work, however, was concentrated on fractions derived from the trans form. From the data obtained, a characteristic ratio of dimensions (r02/rof2)½ of 1.56 was determined. The hydrodynamic parameter Φ was determined to be (2.0 ± 0.3) × 1021. The appropriate model for the polymer is indicated to be the impermeable random coil with slight hindrance to rotation about backbone skeletal bonds.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 563-574 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solution parameters for the polymer poly-γ-trifluoro-propylmethylsiloxamer has been determined in cyclohexyl acetate, methyl hexanoate, and ethyl acetate. Interpretation of data follows the theory of Fox and Flory. In contrast to poly-dimethylsiloxane, an increased steric hindrance to rotation about the siloxane bond occurs as evidenced by the characteristic ratio of root-mean-square end to end dimensions, (r02/r0f2)1/2, found to be 1.90 and 1.96 at 25.0 and 72.8°C, respectively. This increase is considered to be primarily due to nearest-neighbor interaction of the polar substituent on the silicon atom. The relation, [η]θ ∝ M1/2, was observed to hold for this polymer system. The hydrodynamic model appropriate for the polymer is a random coil considerably more permeable to solvent flow than is generally reported for linear polymers. The universal parameter φ was determined to be 1.5 × 1021. The effect of temperature on polymer configuration is indicated to be negligible.
    Additional Material: 5 Ill.
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  • 8
    Publication Date: 1979-06-01
    Print ISSN: 0013-936X
    Electronic ISSN: 1520-5851
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
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