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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3813-3825 
    ISSN: 0887-624X
    Keywords: reaction calorimetry ; emulsion polymerization ; kinetics ; styrene ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 461-473 
    ISSN: 0887-624X
    Keywords: calorimetry ; styrene ; kinetics ; emulsion polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3837-3846 
    ISSN: 0887-624X
    Keywords: reaction calorimetry ; emulsion copolymerization ; styrene ; n-butyl acrylate ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Emulsion copolymerizations of styrene and n-butyl acrylate were conducted at 70°C using varying amounts of Triton X-405 (octyl phenoxy polyethoxyethanol) as emulsifier. The kinetic behavior was found to vary widely depending on the emulsifier concentration. Unimodal particle size distributions were produced at the lowest (4.2 mM) and the highest levels (12.5 mM, 16.2 mM) of emulsifier while at intermediate levels (6.3 mM and 8.4 mM) bimodal distributions were produced; these were reflected in the reaction kinetics. These results were attributed to the surfactant partitioning behavior in the system which led to homogeneous/coagulative nucleation at the lowest level to homogeneous/coagulative nucleation followed by micellar nucleation at the intermediate levels to micellar nucleation at the highest levels. Although the added surfactant levels were all well above that required to exceed its CMC in the aqueous phase, the substantial partitioning into the oil phase lead to conditions well below the CMC of the portion of the surfactant present in the aqueous phase for the lowest and the intermediate levels of the Triton X-405. Consequences of this partitioning were seen in a semibatch reaction where all the surfactant was initially present in the aqueous phase; in this case, too many particle were nucleated leading to massive coagulation due to insufficient surfactant being available to stabilize the particles. © John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3837-3846, 1997
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 9 (1895), S. 291-294 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 137 (1924), S. 39-55 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wurde die Auflösungsgeschwindigkeit der flüssigen Natriumamalgame in alkalischen und in sauren Lösungen untersucht.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 137 (1924), S. 56-65 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Reaktionsgeschwindigkeit in heterogenen Systemen ist als Summe zweier Größen aufzufassen, deren eine für die gegebene Reaktion konstant und die andere der Rührgeschwindigkeit proportional ist. Der Proportionalitätsfaktor ist von der Rührvorrichtung abhängig und zwar wird er schon durch geringe Änderungen dieser deutlich beeinflußt.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 69 (1936), S. 2087-2097 
    ISSN: 0365-9631
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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