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  • 2000-2004
  • 1995-1999  (3)
  • emulsion polymerization  (3)
  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 461-473 
    ISSN: 0887-624X
    Schlagwort(e): calorimetry ; styrene ; kinetics ; emulsion polymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: An automated reaction calorimeter was used to directly monitor the rate of emulsion polymerization of styrene using different emulsifier (sodium lauryl sulfate) and initiator (potassium persulfate) concentrations. By using this technique in conjunction with off-line measurements of the evolution of the particle size distributions, important details of the process were observed. The classical constant rate period (Interval II) often reported for the batch emulsion polymerization of styrene was not seen in this work. Instead, the experimental results suggest that the end of nucleation and the disappearance of monomer droplets take place at approximately the same conversion (36-40%). From the polymerization rate data, important parameters such as the monomer concentration in the polymer particles and the average number of radicals per particle were calculated. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3813-3825 
    ISSN: 0887-624X
    Schlagwort(e): reaction calorimetry ; emulsion polymerization ; kinetics ; styrene ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The emulsion polymerization of styrene was studied using the nonionic surfactant Triton X-405 (octylphenoxy polyethoxy ethanol). Two separate nucleation periods were noted in these polymerizations resulting in bimodal final latex particle size distributions. The partitioning of the surfactant between the phases was found to play the major role in determining the nucleation mechanism(s) in these polymerizations. Although the total concentration of the emulsifier was always added at a level above its critical micelle concentration (CMC) based on the water phase in the recipe, it was found that the portion of the surfactant initially present in the aqueous phase was below its CMC due to the partitioning. This CMC was also found to increase with increasing total surfactant because the distribution of the surfactant (varying ethylene oxide chain length) depended on the partitioning between the phases. Under these conditions, the first of the two nucleation periods was attributed to homogeneous nucleation, while the second was attributed to micellar nucleation. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3813-3825, 1997
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3827-3835 
    ISSN: 0887-624X
    Schlagwort(e): reaction calorimetry ; emulsion polymerization ; n-butyl acrylate ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In the emulsion polymerization of n-butyl acrylate, the nonionic surfactant Triton X-405 (octylphenoxy polyethoxy ethanol) partitions primarily into the aqueous phase leading to nucleation in the presence of micelles and unimodal final latex particle size distributions. Nucleation is accompanied by limited aggregation in the early stages of the reactions with particles being formed in some cases past 50% conversion depending on the experimental conditions. High values of the average number of radicals per particle (n̄ 〉 10) are observed during these reactions which explains a secondary increase in the heat of reaction. This increase was not observed when the initiator (K2S2O8) concentration was reduced from 6.4 to 0.6 mM or the temperature was decreased from 70°C to 60°C; contrary to what was expected, an inverse relationship was observed between the rate of polymerization and the final number of particles for these experiments. This was attributed to more extensive limited aggregation at the higher temperature and initiator concentration. Limited aggregation is thus shown to be an important mechanism in these polymerizations. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3827-3835, 1997
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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