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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 2049-2065 
    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: Small particles (ca. 700 A.) in an SB-R latex can be agglomerated (aggregation and coalescence) to the large size and heterogeneous distribution required for fluid high solids latex. This agglomeration is promoted by high molecular weight materials such as polyvinyl methyl ether (PVM). The mechanism of this agglomeration has been investigated. The effects of controlled variations in the amounts of PVM, electrolyte, soap and latex solids content were determined using statistically designed experiments. The agglomeration was found to differ from Smoluchowski kinetics in that it could best be described by the relationship: (1/n) = (1/n0) + at - bt2 where n = particle number, t = time and a and b are constants. The agglomeration rates were about 1011 to 1012 times slower than the theoretical Smoluchowski rapid coagulation rate. Increases in PVM, soap, and latex solids increased the agglomeration rate. The agglomerations were self-limiting and reached equilibria the level of which increased with increases in PVM and decreased with increases in soap. Regression equations relating the effects of the controlled variables on the agglomeration rate and the equilibria states are derived and presented graphically. The particle size distribution of the final latex was significantly correlated, with that expected from theoretical collision theory.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 311-318 
    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: Differential scanning calorimetry (DSC) and infrared spectroscopy (IR) have been used to study the crosslinked epoxy system tetraglycidyl-4,4′-diaminodiphenyl methane cured with diaminodiphenyl sulfone. Samples cured at various temperatures were soaked in distilled water for extended periods or irradiated with 0.5 Me V electrons and 60Co gamma. DSC results show that the standard-cured (137°C for 2 h and 160°C for 5 h) dry samples have a Tg around 190°C and a large exothermic reaction at about 260°C. The latter is attributed to further reaction of curing agent with the epoxide rings. The exothermic energy is about 124 cal/g for an uncured specimen, 42 cal/g for standard cured specimen, and 20 cal/g for soaked samples containing 4% H2O. The exothermic energy is shown to decrease monotonically with the ionizing radiation dosage. IR results show a reduction in the intensity of the epoxide band as the exothermic energy is decreased.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 35 (1903), S. 420-423 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 32 (1902), S. 174-180 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 851-863 
    ISSN: 0887-624X
    Keywords: polymerization ; kinetics ; free radical ; transfer ; photolysis ; propagation ; rate coefficients ; termination ; EPR ; copolymerization ; initiation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The problems of determining reliable, well-characterized values of kinetic parameters in free-radical polymerizations are discussed. The origins of the fact that experimental determinations of rate coefficients of ostensibly identical systems often result in quite different values being reported can be ascribed to subtle mechanistic assumptions made in data interpretation, which are considered in detail. A series of recommendations to assist in overcoming these problems, and to highlight their origins, are presented, with emphasis placed on new techniques including those employing laser photolysis and EPR.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 759-775 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several masked isocyanates were prepared with variations in both the type of isocyanate and masking group. They were characterized by elemental analysis and NMR spectroscopy, and their unblocking temperatures were determined. In general, higher unblocking temperatures were obtained using acyclic and cyclic aliphatic isocyanates and fluorinated phenols. Those with unblocking temperatures in the range of 120-180°C were incorporated into MY 720/DDS epoxy resin prior to cure. Highly fluorinated variations were incompatible with the resin. IR and DSC analyses showed that residual functional groups in the epoxy resin reacted with the masked isocyanates. Reductions in moisture absorption as high as 65% were obtained depending on the masked isocyanate. DMA studies showed that the Tg of the epoxy resin is lowered by incorporation of the masked isocyanate but the elastic modulus (E′) is relatively unchanged at temperatures below Tg.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1235-1248 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Blocking the hydroxyl, amine, and epoxide functional groups of cured MY720/DDS epoxy thin films with various fluorinated aromatic reagents reduces the equilirium moisture absorption by as much as 75%. The blocking reactions were temperature-, time-, and diffusion-dependent. 2,4-Difluorophenyl isocyanate was a more effective blocking reagent than trifluoromethylphenyl isocyanates (i.e., ortho-, meta-, and para-) due to its higher reactivity. Among the trifluoromethylphenyl isocyanates, meta-trifluoromethylphenyl isocyanate exhibited the greatest extent of reaction based on the reduction of IR peaks at 3400 and 904 cm-1, presumably due to the slightly poorer inductive effect inherent in meta-trifluoromethylphenyl isocyanate, permitting a greater extent of diffusion into the bulk polymer. Pentafluorobenzoyl chloride was a more efficient blocking reagent compared to the fluorinated aromatic isocyanates. DSC thermogram data indicated that reaction of pentafluorobenzoyl chloride at 90°C for 2 days with the epoxy groups was essentially complete. The treated films were stable to hydrolysis even after immersion in distilled water at room temperature for 2 months as measured by IR spectroscopy.
    Additional Material: 9 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 2609-2618 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was found that the amount of water absorbed at room temperature in cured tetraglycidyl-4,4′-diaminodiphenyl methane/diaminodiphenyl sulfone epoxy resins increases as the curing time or temperature increases while the amount of tetrahydrofuran-soluble extractables and the room temperature density decreases. These data suggest that the free volume increases with the extent of cure and the resins become more accessible to water. While the driving force for water absorption is the electrostatic attraction between water and the functional groups in the epoxy, the results suggest that equilibrium H2O absorption is determined primarily by unoccupied volume of the epoxy resin.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3355-3362 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several cellulose derivatives were synthesized and characterized by IR and 1H-NMR spectroscopy. The positions of substitution in these derivatives were confirmed using solid state 13C-NMR spectroscopy techniques.
    Additional Material: 3 Ill.
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