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  • Digitale Medien  (5)
  • emulsion polymerization  (4)
  • 21.10.Pc  (1)
Materialart
  • Digitale Medien  (5)
Erscheinungszeitraum
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 273 (1995), S. 999-1007 
    ISSN: 1435-1536
    Schlagwort(e): Surfactants ; polystyrene ; emulsion polymerization ; amphiphilic thiol ; transfer agents
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract Styrene emulsion polymerization has been carried out at 70°C using 2–2′ Azobis (2 methyl, N-(2 hydroxyethyl) propionamide as initiator and thiol-ended surfactants (I) HS-C11 H22- (OCH2 CH2) n OH withn from 17 to 90 units. The kinetics of monomer conversion, the evolution of particle size, particle size distribution, molecular weight, and molecular weight distribution have been studied. After washing the final latex, the incorporation yield of the surfactant moieties in the particles has been measured. Most of the experiments have been carried out in batch; complementary experiments used semi batch or seeded process. In some experiments the two functions of transfer agent and surfactants have been decoupled using either dodecylmercaptan (oil soluble) or thioglycolic acid (water soluble) as transfer agent and the bromine ended precursor of (I) as surfactant. The discussion of the results is chiefly oriented towards both the molecular weight distribution and the incorporation of the surfactant to the latex.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    The European physical journal 334 (1989), S. 133-141 
    ISSN: 1434-601X
    Schlagwort(e): 21.10.−Jx ; 21.10.Pc ; 25.45.−6h
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Proton holes states have been studied up toE x=17 MeV andE x=3.5 MeV in the119In nucleus via the120Sn(d,3He)119In reaction respectively atE d=108.4 MeV andE d=51 MeV. DWBA analysis of angular distributions has allowedl attributions for a large number of new levels and the determination of valence and inner hole strength distributions. The first 1g 9/2, 2p 1/2 and 2p 3/2 levels only exhaust 40%, 60% and 32% of their respective sum rule limits. The missing strengths are shared among several low lying levels and significant higher lying contributions. The 1f strength, not identified in the previous experiments is spread fromE x=1 MeV to about 17 MeV. The low lying levels aroundE x=2.4 MeV could exhaust some 40% of the 1f 5/2 sum rule. The higher lying strength with a flat maximum aroundE x=7.5 MeV could account for the 1f 7/2inner hole strength and the missing 1f 5/2 valence strength. The experimental strength functions compare rather well with the predictions of the quasiparticle-phonon model.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 157-168 
    ISSN: 0887-624X
    Schlagwort(e): emulsion polymerization ; reaction calorimetry ; chain transfer agents ; kinetics ; radical desorption ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The effect of chain transfer agents (CTA) on the emulsion copolymerization of styrene and butyl acrylate was studied in a bench scale 7 L reactor. On-line estimates of conversion were obtained through the joint use of calorimetric measurements and fast gravimetric data. Off-line measurements of partial conversions, molecular weight distribution (MWD), glass transition temperature (Tg), and particle diameter were also performed in order to investigate the effect of two mercaptans (tert-butanethiol and n-dodecanethiol) on both the kinetics of the polymerization process and the microstructure-dependent properties of the copolymer. The obtained experimental results were interpreted in terms of radical desorption and diffusive limitations of the CTA between the oil droplets and the particles. A model has been derived to compute the kinetic constants, the number of radicals per particle, and both the GPC/SEC diagrams and DSC thermograms related to MWD and Tg measurements, respectively. Several batch and semibatch examples are proposed to show that these important variables are satisfactorily fit by the model. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 157-168, 1998
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1559-1572 
    ISSN: 0887-6266
    Schlagwort(e): core-shell ; N-methylol acrylamide ; N-methylol methacrylamide ; N-isobutoxy methyl acrylamide ; butyl acrylate ; polystyrene seed ; latex ; emulsion polymerization ; structured particles ; particle morphology ; functional monomers ; latex films ; phase arrangement ; mechanical properties ; film forming ; scanning electron microscopy ; annealing ; percolation ; coalescence ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polystyrene (PS) (1)/Poly (n-butyl acrylate (BA)/amide type functional monomer) (2) structured latex particles were prepared through emulsion polymerization varying the hydrophilicity of the functional monomer employed. The second-stage polymerization kinetics, the size and morphology of latex particles, and the location of the functional groups in the final latexes were studied, in order to relate them to the thermomechanical properties of films cast from these latexes. It has been shown that, as expected, increasing the hydrophobicity leads to a better homogeneity in the copolymer formed during the second-stage polymerization, while the more hydrophilic functional monomer partly homopolymerizes in a separate phase. However, the functionalization by all the monomers used in this work, prevents the PS seed particles to form a continuous skeleton (percolated network). Further heat treatments at 140°C do not lead to the formation of a continuous PS phase as for pure BA/pure PS two-stage particles. In addition, some thermally induced crosslinking effects are discussed in relation with the functional monomer location within the particles. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 473-479 
    ISSN: 1042-7147
    Schlagwort(e): emulsion polymerization ; steric stabilization ; polymeric transfer agent ; redox system ; polystyrene colloids ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Thiol-ended polyethylene oxide (I) has been prepared from the esterification of thioglycolic acid with monomethylether of polyoxyethylene glycol. Emulsion polymerization of styrene (and, in a few cases, methylmethacrylate as comonomer) was carried out in the presence of I using either water-soluble azo initiator or t-butylhydroperoxide. In the former case, bimodal particle size distribution was obtained while monodisperse latexes could be prepared in the latter case. Then a redox system was formed from I and t-BuOOH so that I was both an initiator and a transfer agent. Good steric stabilization of the latexes was observed. The polyethylene oxide sequence of I was partly incorporated at the surface of the latex particles, but the incorporation yield remained limited (between 7 and 18%). Most of the resdue of I remained in the serum.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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