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  • Polymer and Materials Science  (8)
  • N availability index  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 66 (1982), S. 81-89 
    ISSN: 1573-5036
    Keywords: Extractable organic matter ; N availability index ; Organic matter ; Organic N ; Soil storage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The effect was studied of storage temperature on the index of available soil N wich uses U.V. absorbance of a 0.01M NaHCO3 extract as an indicator. The U.V. absorbance was found to increase at a non-linear rate for four soils stored at temperatures of 50, 75, and 150°C. The change in extract absorbance due to extended soil storage at each of these temperatures was positively correlated to the percent organic matter, percent N, C/N value and concentration of humic substances in soils, but not to the extract absorbance prior to soil storage. These findings were not consistent with room temperature storage data which showed a linear increase in extract absorbance with soil storage time. The change in absorbance for the room temperature case was not related to any of the soil parameters mentioned above. Analysis of a soil stored at 105°C showed an increase in ninhydrin-detectable N, protein N and Kjeldahl N of the NaHCO3 extract, while the apparent molecular weight distribution of extracted organic matter (as determined by gel filtration) showed only a slight change. As a comparison to the NaHCO3 extract, a boiling CaCl2 extract of the same soil was also analyzed; and the absorbance at 260 nm was found to increase in a curvilinear fashion with starage time at 75°C but to less of an extent than was noted with the NaHCO3 extract. Nitrogen availability indexes based on the U.V. absorbance of these extracts, particularly those utilizing the NaHCO3 extract, would be significantly affected by soil storage at elevated temperatures.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 64 (1982), S. 331-341 
    ISSN: 1573-5036
    Keywords: Humic substances ; Molecular weight distribution ; N availability index ; Ninhydrindetectable N ; Relative N uptake ; Soil proteins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Two soil extracts used for chemical indexes for N availability, 0.01M NaHCO3 and boiling 0.01M CaCl2, were analyzed in effort to learn more about the nature of the extracted organic matter (O.M.). The two extracts appeared to remove different fractions of the soil O.M. A study of five soils showed that the C/N value of the NaHCO3 extract (following decarbonation) was significantly higher than that of the total soil O.M.; while the C/N value in the boiling CaCl2 extract was not significantly different from that in the soil O.M. There was also significant variation in C/N values among soils for the boiling CaCl2 extract. The extracts of three soils were analyzed for apparent molecular weight distribution using gel filtration and the results compared to those for base-extracted humic substances. Almost all the molecules in the extracts had apparent molecular weights less than 21,000 daltons while 21 to 47% of the humic substances from the same soils (extracted with 0.5M NaOH) had molecular weights greater than 21,000 daltons. In the boiling CaCl2 extract, 78 to 87% of the humic substances had apparent molecular weights less than 1,000 daltons, whereas with the NaHCO3 extract, 42 to 83% of the humic substances were in the 1,000 to 21,000 dalton range. Forty-three to 92% of the N extracted by the NaHCO3 was in protein form, and 8 to 30% was ninhydrin-detectable. In the boiling CaCl2 extract 25 to 30% of the extracted N was ninhydrin-detectable. For the same 10 soils, ninhydrin-detectable N values of the boiling CaCl2 extract appeared closely related to greenhouse and field relative N uptake, while the ninhydrin-detectable N values of the NaHCO3 extract appeared unrelated to both. The protein N and protein in plus ninhydrin-detectable N values of the NaHCO3 extract were closely related to greenhouse relative N uptake only. The results of this study indicated that specific fractions of the soil O.M. were being extracted by the two solutions and that significant differences existed in the chemical nature of the two extracts.
    Type of Medium: Electronic Resource
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  • 3
    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(methylene disulfide), poly(methylene tetrasulfide), poly(ethylene disulfide), and poly(ethylene tetrasulfide) have been subjected to ultraviolet radiation in vacuum at 50°C. Weight losses during photolysis include both low molecular weight compounds and readily condensable polymeric materials; the latter account for the greater proportion of the weight losses. Carbon monosulfide, isolated as its polymer, and hydrogen sulfide are major photolytic products. Carbon disulfide is a major product from the methylene but not from the ethylene polymers. The tetrasulfide polymers during irradiation from volatile products which on condensation give the original polymer. A mechanism of degradation compatible with these findings is suggested.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2765-2772 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Charge transfer (CT) interaction is described in semiconducting dispersions of TCNQ complex salt \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm Et}_3 {\rm NH}^+ ({\rm TCNQ})_2^{\cdot^{\hskip-3.7pt\hbox{--}}}$\end{document} with and without added TCNQ°, in poly(vinyl acetal) matrices in which the electron-donor moiety is varied. The extent of CT interaction was determined in films and in solution (DMF, acetonitrile, or methylene chloride) through the absorbances at 398 nm (\documentclass{article}\pagestyle{empty}\begin{document}$ {\rm TCNQ}{\ }^{\cdot^{\hskip-3.7pt\hbox{--}}}$\end{document} and TCNQ°) and 857 nm \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm TCNQ}{\ }^{\cdot^{\hskip-3.7pt\hbox{--}}}$\end{document}. Resistivity of the conductive films was related to the stoichiometry of TCNQ species in the films and found to have a minimum at \documentclass{article}\pagestyle{empty}\begin{document}$[{\rm TCNQ}^\circ]/[{\rm TCNQ}{\ }^{\cdot^{\hskip-3.7pt\hbox{--}}}]\simeq 1$\end{document}. Lower resistivities were attained with films having a uniform, densely packed dispersion of microcrystallites which were obtained at a relatively slow solvent removal rate. With this particular complex salt, strong electron-donor polymers are found to be better matrices for semiconductivity.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 1281-1298 
    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: Morphology, stress-strain properties, and grafting have been investigated in highly phase-separated polyurethane (PU)-poly(n-butyl methacrylate) (PBMA) mixtures as a function of the sequence of formation of the components, both linear (l) and crosslinked (x), in the presence of each other. In the range of 0.3-0.7 weight fraction of PU, a morphology of PBMA particles in a PU matrix results. Particle size depends on matrix viscosity at the time of PBMA formation, decreasing as viscosity increases. The PBMA (l) particles are spherical; PBMA (x) particles are irregular in shape when formed in a fluid medium but tend to become spherical as the delay time before the onset of their formation is increased. Grafting, decreasing with increasing delay time, is observed between PBMA (l) particles and the PU (x) or PU (l) matrix. The grafting results from transesterification between BMA and the polyol precursors to the PU. Two families of mechanical properties are found, depending generally more on particle shape than size. Systematic trends of property values through a series of samples of constant composition, but increasing delay times, are observed with greater variation in the series with PBMA (x) particles; the trends are explainable in terms of matrix immobilization by the particles.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 507-517 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photodegradation of thin films of poly-α-methylstyrene by near ultraviolet radiation has been studied in vacuum at 27 and 115°C. Changes taking place during photolysis were followed by a determination of monomer formation by ultraviolet spectroscopy, residue molecular weight through a measurement of intrinsic viscosity, and volatile products by mass spectroscopy. Gross features of the photolysis include random chain scission in the polymer with subsequent depolymerization of the radicals formed to yield small amounts of monomer; the kinetic chain length is on the order of 15 in the temperature range studied. Quantum yields at 27°C. for chain scission and monomer formation are 1 × 10-3 and 7 × 10-3, respectively. At 115°C. the quantum yields are 2 × 10-2 and 0.5. Small quantities of hydrogen, CO2, CO, and a number of hydrocarbons were liberated during irradiation. An approximate one-to-one correlation between the number of main chain scissions and CO2 + CO molecules evolved was found, suggesting the occurrence of chain scission at weak linkages involving oxygen.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 2373-2379 
    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(methyl methacrylate) has been photolyzed with 2537 A. radiation in dioxane and in methylene chloride at about 25°C. in the presence and absence of air. In degassed solutions, quantum yields for random scission are only slightly affected by either intensity or polymer concentration. Oxygen is an apparent inhibitor for photodegradation. The inhibiting and sensitizing effects of a variety of added solutes, including aromatic hydrocarbons, aliphatic dienes, and ketones were investigated; the behavior is similar whether or not oxygen is present. The results are best explained on the basis of an electronic energy transfer mechanism involving the lowest excited triplet levels of the polymer and the added solutes.
    Additional Material: 2 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2303-2311 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Apparent quantum yields for the random scission of poly(α-methylstyrene) in solution by 2537 A. radiation were shown to be solvent-dependent, indicating that processes other than the direct photolysis of the polymer are taking place. Quantum yields on the order of 10-3 scissions per quantum absorbed by the polymer were found in benzene, dioxane, cyclohexane, and methylene chloride and about 0.2 in chloroform and carbon tetrachloride; the quantum yields were unaffected by oxygen. In carbon tetrachloride, the quantum yields decreased slightly with increasing polymer concentration. Ethanol and cyclohexane were inhibitors for the photolysis in carbon tetrachloride, while the latter solvent acted as a sensitizer in cyclohexane. By comparison with model compounds irradiated in carbon tetrachloride, it was shown that an early step in the photolysis of poly(α-methylstyrene) in this solvent involves reaction with a main-chain methylene group and eventual substitution with a trichloromethyl group.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 2085-2092 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thin films of poly(methyl acrylate) at room temperature have been photodegraded in air and in vacuum by radiation from a low-pressure mercury source. Changes in intrinsic viscosities, ultraviolet absorption, and volatile products were followed as a function of the energy absorbed. Crosslinking occurs in both air and vacuum, but at a slower rate in air. The apparent quantum yield for random scission in air was 0.013 scissions per quantum absorbed. In air, carbonyl groups are formed along the backbone chain. Most of the volatile products studied appear to orginate from the ester groups in the polymer; formaldehyde, methanol, and methyl formate evolved at a constant rate for doses up to at least 2 × 1020 quanta/g.; quantum yields for each were determined. Carbon dioxide forms in amounts increasing exponentially with dose. Small amounts of carbon monoxide, methane, and hydrogen were detected qualitatively, but monomer was not observed. A mechanism compatible with these findings is suggested.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 4 (1966), S. 771-774 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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