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  • 1
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been demonstrated that the homogeneity in respect to molecular weight of emulsion copolymers of butadiene and styrene can be increased by the use of certain derivatives of n-dodecyl mercaptan rather than the mercaptan itself. These derivatives decompose and relase n-dodecyl mercaptan at an even rate during the polymerization reaction. Several new derivatives of n-dodecyl mercaptan are described.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 0887-624X
    Keywords: cross-conjugated polymer ; crossed-aldol condensation ; cyclic ketone ; polyketone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Insoluble cross-conjugated polyketones were prepared from terephthalaldehyde and a variety of cycloaliphatic ketones by the crossed-aldol condensation. Elemental analyses and infrared spectra suggest that the polymeric aldol intermediates were not completely dehydrated. Evidence is also presented that suggests conjugate addition of the base to the α,β-unsaturated ketone may occur. Soluble cross-conjugated polyketones were prepared from terephthalaldehyde and 2-indanone, which contains no beta hydrogens, and from cycloaliphatic ketones and 1,2-bis(4-formylphenoxy)ethane, a dialdehyde containing isolated aldehyde groups. It is proposed, therefore, that the lack of solubility in the terephthalaldehyde-based polyketones arises from crosslinking via enolate anions formed at the beta position of the cyclic ketones, which are delocalized through the carbonyl groups of neighboring backbone repeating units. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1755-1760 
    ISSN: 0887-624X
    Keywords: Diels-Alder crosslinking ; polystyrene ; thermally reversible crosslinking ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures of maleimidomethylated polystyrene with difurfuryl adipate or with furfuryl alcohol-esterified poly[styrene-co-(maleic anhydride)] underwent thermally reversible Diels-Alder crosslinking. Reversal of crosslinking occurred rapidly at 150°C. The instability of the furfuryl group, however, limits the practicability of the reaction. © 1992 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 1075-1077 
    ISSN: 0887-624X
    Keywords: anionic polymerization ; polybenzyl-like polymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 461-470 
    ISSN: 0887-624X
    Keywords: kinetics ; polyimides ; thermal cure ; infrared spectroscopy ; DSC ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic mechanism of the thermal cure of a phenylethynyl-terminated imide model compound, 3,4′-bis[(4-phenylethynyl)phthalimido]diphenyl ether (PEPA-3,4′-ODA) and a phenylethynyl-terminated imide oligomer PETI-5 (MW 5000 g/mol) was studied. FTIR was used to follow the cure of the model compound, while thermal analyses (DSC) was used to follow the cure of the PETI-5 oligomer. The changes in IR absorbance of phenylethynyl triple bonds at 2214 cm-1 of PEPA-3,4′-ODA as a function of cure time were detected at 318, 336, 355, and 373°C, respectively. The changes in the glass transition temperature, Tg, of PETI-5 as a function of time were measured at 350, 360, 370, 380, and 390°C, respectively. The DiBenedetto equation was applied to define the relative extent of cure, x, of the PETI-5 oligomer by Tg. For the model compound, the reaction followed first order kinetics, yielding an activation energy of 40.7 kcal/mol as determined by infrared spectroscopy. For PETI-5, the reaction followed 1.5th order, yielding an activation energy of 33.8 kcal/mol for the whole cure reaction, as determined by Tg using the DiBenedetto method. However, the cure process of PETI-5 just below 90% by this method followed first-order kinetics yielding an activation energy of 37.2 kcal/mol. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 461-470, 1998
    Additional Material: 13 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2025-2031 
    ISSN: 0887-624X
    Keywords: poly(propylene glycol) ; poly(methyl methacrylate) ; LiCF3SO3 ; compatibility ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stable to atmospheric moisture, adhesive and transparent polymer electrolytes have been prepared by blending poly(methyl methacrylate) (PMMA) with poly(propylene glycol)-425/LiCF3SO3 complexes. The blending of the polymers has been achieved by a method developed in our laboratory: free radical polymerization of methylmethacrylate in the polyether/salt matrix. A series of polymer blend complexes varying in PMMA content (up to 20% by weight) and oxygen/metal ratios (25, 16, and 8) have been synthesized and their properties studied. All the samples prepared in this study were found to be optically clear unlike the higher molecular weight poly(propylene glycol)-2000 (PPG-2000) system which required a minimum salt concentration to compatibilize a specific amount of PMMA with PPG. The mechanisms by which the salt holds the otherwise incompatible polymers together in a single phase have been investigated by FT-IR. Our studies show a weak coupling of the ether oxygens in the PPG with the ester groups of the PMMA through the lithium cations. Discrete changes has been observed in the FT-IR spectrum of PMMA when doped with the lithium salt hitherto unnoticed with other dopants. Gel permeation chromatography results of the PMMA samples isolated from the solid electrolytes indicate the molecular weight to vary between 43000 and 121000 with relatively narrow distributions, 1.6-2.0. The ionic conductivities of the polymer blend electrolytes were fairly high (10-5 S/cm) at room temperature. The PMMA neither significantly influenced the Tg of the blend complexes nor effected the ionic conductivities drastically. The ionic conductivity as a function of temperature followed the empirical Vogel-Tammann-Fulcher equation. The blending of PMMA with PPG/LiCF3SO3 complexes was found to impart good adhesiveness to the solid electrolytes while making them stable to atmospheric moisture. © 1992 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 45 (1992), S. 993-996 
    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: Polymeric substrates containing salicylidenimine ligands as discrete units can be obtained by reacting chloromethylated divinylbenzene styrene copolymer with amines, followed by condensation with salicylaldehyde. Polymer-supported Schiff base iron (III) complexes have been prepared and their IR spectra and Mössbauer spectra measured. Catalytic activity of supported complexes have been tested using decomposition of hydrogen peroxide as a model reaction.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 1691-1700 
    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: In a continuation of previously reported work of the effect on cotton cellulose of ethyleneurea crosslinking agents modified with ring substituents of varying hydrogen-bonding capabilities, accessibilities of the cellulosic hydroxylic protons to exchange with deuterium oxide vapor were determined by means of infrared spectroscopy. In analyzing these values with respect to previously reported data on physical properties of the treated fabrics, it was found that accessibility to deuterium oxide did not correlate with moisture regain of the resin-treated samples as has been reported for physically modified celluloses. It appears that the different resins did have some effect on the structure of water adsorbed by the fiber and also that the solvent affected the manner in which the resins attached themselves to the cellulose and eliminated water from the structure. Values of accessibility were not found to correlate well with crease recovery, although a weak trend was indicated. Accessibility was found to decrease as the infrared band for ring stretching decreased.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 4279-4297 
    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: An infrared absorption spectroscopy study of the curing (gelation and postcure) kinetics of a high (4.7) epoxide/hydroxyl group-ratio diglycidyl ether of bisphenol A (DGEBA)-mixed anhydride epoxy resin system is reported. Peak assignments to molecular vibrational modes are given for the range 400-4000 cm-1, and the optical density behavior of all peaks during reaction is discussed in detail. Chemical reaction was found to follow consecutive-step addition esterification and simultaneous addition etherification. Epoxide hydroxyl-group and carboxylic acid dimer hydrogen bonding was found to occur. The gelation phase of reaction is complex, exhibiting rapid initial hydroxyl-anhydride reactions followed by S-shaped kinetics approaching an incompletely reacted limit. Postcure exhibits functional group kinetic behavior similar to that occurring in low epoxide/hydroxyl group-ratio bisphenol A epoxy resin-phthalic anhydride systems and produces similar final chemical structures. The reaction behavior of low and high epoxide/hydroxyl group-ratio bisphenol A epoxy resin-anhydride systems arises from an hydroxyl group-limited inhomogeneous reaction mechanism involving bisphenol A epoxy resin molecular aggregates. The importance of free hydroxyl group content is discussed.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 389-391 
    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: Myrcene-maleic anhydride Diels-Alder adduct and the corresponding diacid were used as monomers for unsaturated polyesters. The polyesters exhibited air-drying properties on cross-linking with styrene.
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