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  • Polymer and Materials Science  (31)
  • Analytical Chemistry and Spectroscopy  (5)
  • Physical Chemistry  (5)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 7 (1993), S. 360-362 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The production of carbon clusters (but not fullerenes) from coal-derived material by the use of laser desorption mass spectrometry is described. Benzo(e)pyrene, a standard polynuclear hydrocarbon found in coal tars, also gave carbon clusters despite using low laser power to avoid pyrolysis of target molecules. Positive- and negative-ion spectra of the standard included carbon clusters. These clusters are formed by the laser energy and can be confused with aromatic hydrocarbons of the same nominal masses. They have no relevance for studies of coal structure.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The use of a laser-desorption mass spectrometer to examine a coal liquefaction extract known to contain high-molecular-mass material (from size-exclusion chromatography) has shown the presence of components of molecular mass in excess of 104Da for the first time. The molecules detected differ from each other in molecular mass by a few hundred or a few thousand Da. These preliminary results indicate that the basic coal-structure molecules probably consist of aromatic clusters on a chin, in reasonable agreement with current theories of coal structure.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Molecular masses up to 270 000 u have been observed during matrix-assisted laser desorption mass spectroscopy on a sample of bituminous coal; the major fraction of desorbed ions appeared between m/z values of 800 and 5000. Similar mass distributions have been found in a coal-liquefaction extract and a pyrolysis tar. The highest molecular masses identified in this work far exceed previously reported high molecular masses found in coal-derived products (12 000 u), which were also detected by laser-desorption mass spectrometry.
    Additional Material: 2 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 14 (1970), S. 777-787 
    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 preparation of isotactic and syndiotactic 1,4-polypentadienes with a cis content of at least 70%-75% using i-Bu2AlH/Ti(i-OPr)4 and AlEtCl2/thiophene/Co(acetylacetonate)2 catalysts, respectively, is reported. Physical characterization of the vulcanizates, prepared by a common recipe, involving infrared analysis, DTA, simple stress-strain and swelling measurements, and dynamic mechanical measurements over a frequency range of 2 decades and temperature range of -60°C to +20°C indicated that no isomerization had taken place during vulcanization and that stereoregularity of the polymer chains affected the resultant cure: the isotactic form was found to have a greater crosslink density than the syndiotactic form. Master curves covering an extended frequency range were constructed from the reduced dynamic mechanical data and the calculated quantities - thermal expansion coefficients of free volume and the fractional free volumes at the glass transition temperatures - agree with the accepted values. Glass transition temperatures of the isotactic and syndiotactic polymers are -37°C and -42°C, respectively, and for their vulcanizates, -33°C and -40°C, respectively.
    Additional Material: 9 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 62 (1996), S. 1167-1177 
    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: Blends of aromatic/aliphatic polyamides of varying compositions were extrusion compounded with an impact modifying reactive elastomer and injection molded. The effect of two different twin-screw blending configurations on the physical and mechanical properties of the blends was evaluated. Effects of processing conditions on blend morphology were also examined. The experimental results indicate that the extrusion sequence affects the extent of polyamide matrix-elastomer reaction as well as the morphology. The relationship between blend morphology, blend components structure and reactivity, and processing conditions with ultimate properties is discussed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 159-170 
    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: Carbon dioxide sorption isotherms in poly(methyl methacrylate) (PMMA) and poly(ethyl methacrylate) (PEMA) are reported for pressures up to 20 atm. Temperatures between 35 and 80°C were studied for PMMA and temperatures between 30 and 55°C were studied for PEMA. Typical dual mode sorption isotherms concave to the pressure axis were observed in all cases. The measured Langmuir sorption capacities of both polymers extrapolated to zero at the glass transition (Tg) consistent with the behavior of other glassy polymer/gas systems. Sorption enthalpies for CO2 in the Henry's law mode for PMMA and PEMA are in the same range (-2 to -4 kcal/mole) as has been reported for a variety of other glassy polymers such as poly(ethylene terephthalate), polycarbonate, and polyacrylonitrile. Some of the data suggest that postcasting treatment of the PEMA films left a small amount of residual solvent in the film. the presence of the trace residual solvent during quenching from the rubbery to the glassy state after annealing appears to cause a dilation of the Langmuir capacity and an alteration in the apparent Langmuir affinity constant of the PEMA film. These results suggest the possibility of tailoring physical properties of glassy polymers such as sorptivity, permeability, impact strength, and craze resistance by doping small amounts of selected residuals into polymers prior to quenching to the glassy state from the rubbery state.
    Additional Material: 10 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 30 (1985), S. 4099-4111 
    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: A polyamide-epichlorohydrin resin used to shrink-resist wool [Hercosett 125 (Hercules Inc.)] was separated by ultrafiltration into fractions A, B, and C (in the approximate proportions 60, 40, and 2 by weight), which correspond to the three peaks in size exclusion chromatograms (SEC). Viscosity, spectra, and SEC results as well as results of experiments on the reaction of the parent polyamino-polyamide (PAA) with epichlorohydrin indicated that fraction A was high-molecular-weight crosslinked material whereas fraction B was essentially uncrosslinked. Fraction C was minor impurity, possibly a mixture containing a triazine, and it was also found in the PAA from which the original resin was prepared. High-resolution proton NMR spectra of the Hercosett 125 indicated that chlorohydrin or epoxy groups were absent, and thus confirmed an earlier 13C-NMR study that only azetidinium reactive groups were present. Two reactions are believed to occur in Hercosett 125 on storage: hydrolysis of azetidinium to dihydroxypropyl groups and hydrolysis of backbone amides. The small differences in the properties of wool treated with either A or B fractions, and those of wool treated with unfractionated Hercosett 125, were related to the extent of crosslinking before and after curing. As the extent of crosslinking increased, the amount of staining by an anionic dye decreased, and the shrink resistance improved slightly.
    Additional Material: 4 Ill.
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  • 8
    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: A series of prepolymers containing terminal blocked isocyanate groups was prepared by reaction of isocyanate-terminated prepolymers [derived from a poly(propylene oxide) diol (MW = 2000) or a triol (MW = 3000) and different diisocyanates] with various blocking agents. Their curing rates with a polyepoxide crosslinking agent were measured to assess their suitability for a delayed-cure durable-press treatment for wool. The curing rates varied over a wide range, but commonly used blocking groups such as phenols, caprolactam, β-diketones, and alcohols were not sufficiently reactive for the intended application, although others, e.g., oximes and certain blocking agents containing a basic center such as N,N-diethylhydroxylamine, hydroxypyridines, and hydroxyquinolines, had the required reactivity. Blocking by 1,3-dipolar cycloaddition of nitrones was examined, but the reactivities were too low. Prepolymers containing blocked aromatic isocyanates were more reactive than those containing blocked aliphatic isocyanates. Difunctional butanone oxime-blocked pre-polymers cured slightly more slowly than analogous trifunctional prepolymers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acrylate esters of seven n-1,1-dihydroperfluoroalkanols have been synthesized. The esters are: 1,1-dihydroperfluoroethyl-; 1,1-dihydroperfluoropropyl-; 1,1-dihydroperfluorobutyl-; 1,1-dihydroperfluoropentyl-; 1,1-dihydroperfluorohexyl-; 1,1-dihydroperfluorooctyl-; and 1,1-dihydroperfluorodecyl acrylates. Since these alcohols were difficult to esterify using conventional procedures, acrylyl chloride or acrylic acid plus perfluoroacetic anhydride have been empolyed in this work.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 32 (1992), S. 441-445 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Different hexameric forms of insulin have been crystallized from a variety of conditions. In the presence of 1% phenol, 1.0 M sodium chloride, and at a pH of 8.5, a rhombohedral form is produced with two monomers in the asymmetric unit, space group R3, a = 79.92 Å and c = 40.39 Å. The structure has been solved and refined, using data between 8.0 and 2.5 Å resolution, to a residual of 0.157. Each of the monomers adopts an R conformation, that is residues B1-B8 are α-helical. As a result of the T to R transition, an elliptical cavity is created between symmetry-related monomers and is occupied by a phenol molecule. A region of density within bonding distance to one of the zinc ions has been interpreted as an additional phenol molecule.
    Additional Material: 3 Ill.
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