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  • 1
    Electronic Resource
    Electronic Resource
    Rheological behaviour of aqueous solutions of polyvinylalcohol in the presence of some nonionic substances (1979)
    Springer
    Colloid & polymer science 257 (1979), S. 1196-1202 
    Details
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01517244
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  • 2
    Electronic Resource
    Electronic Resource
    Polymerisation von Acrylnitril mit Mg(H2H5)2 (1975)
    Springer
    Colloid & polymer science 253 (1975), S. 345-345 
    Details
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02352184
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  • 3
    Electronic Resource
    Electronic Resource
    Preparation of ABS (acrylonitrile/butadiene/styrene) latexes using hydroperoxide redox initiators (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2463-2477 
    Details
    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: The 80/20 (w/w) azeotropic styrene/acrylonitrile mixture was copolymerized at 35, 50, and 70°C in crosslinked polybutadiene seed latexes of varying particle size (range 113-242 nm) using the t-butyl or cumene hydroperoxide/sodium formaldehyde sulfoxylate dihydrate/EDTA-chelated Fe+2 redox initiator. Other initiators used for comparison were: (1) ammonium persulfate at 70°C; (2) ammonium persulfate/sodium bisulfite redox initiator at 35 and 50°C; (3) oil-soluble, 2,2'-azobis(2,4-dimethylvaleronitrile) at 50°C. The following polymerization parameters were varied systematically: (1) polybutadiene seed latex particle size; (2) monomer/polymer swelling ratio; (3) polymerization temperature; (4) type and concentration of initiator; and (5) mode (and duration) of initiator addition. The following parameters were determined: (1) polymer yield (final conversion); (2) variation of conversion with time; (3) morphology of the latex particles; (4) amount of coagulum; and (5) fraction of styrene/acrylonitrile monomer mixture grafted to the polybutadiene seed latex (defined here as grafting efficiency). For polymerizations using the t-butyl or cumene hydroperoxide/sodium formaldehyde sulfoxylate dihydrate/EDTA-chelated Fe+2 redox initiator, the rates of polymerization were faster, the grafting efficiencies were greater, and the amounts of coagulum were greater at 70°C than at 50 or 35°C. The rates of polymerization were decreased by decreasing the concentration of redox initiator or adding it incrementally. A 1.00/1.00/0.08 (w/w) t-butyl or cumene hydroperoxide/sodium formaldehyde sulfoxylate dihydrate/EDTA-chelated Fe+2 ratio gave reasonable polymerization rates at 35 and 50°C, and a 0.48/1.00/0.07 ratio, at 70°C. The latexes were stabilized during polymerization with 3% (based on seed solids) nonionic Igepal CO-990 at 35°C, and 6% at 50 and 70°C. The grafting efficiency increased with decreasing particle size of the polybutadiene seed latex and decreasing monomer/polymer ratio. The rate of polymerization increased with decreasing monomer/polymer ratio. The monomer/polymer ratio also affected the morphology of the particles; higher values gave inclusions of poly(styrene-co-acrylonitrile) in the polybutadiene particles. There were no significant differences in polymerization kinetics or grafting efficiency between the t-butyl and cumene hydroperoxides.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1990.070410945
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  • 4
    Electronic Resource
    Electronic Resource
    Evaluation of alkylated diphenyl ether disulfonate surfactants in 60 : 40 styrene - butadiene emulsion copolymerization (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 1549-1568 
    Details
    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: Dowfax* 2A1 is a branched C12-alkylated diphenyl ether disulfonate surfactant widely used in industrial emulsion polymerization because of its electrolyte tolerance, stability in concentrated acids and alkalis, oxidation resistance, temperature stability, efficiency in solubilization, and moderate foaming. This surfactant and other similar surfactants were evaluated as emulsifiers in 60 : 40 styrene-butadiene emulsion copolymerizations carried out at 70°C using persulfate ion initiator, and their solution properties were determined. The similar surfactants were Dowfax 3B2 (linear C10-alkylated), XD-8390 (linear C16), XD-8292 (linear C6), XD-8174 (linear C12), and various laboratory monoalkylated and dialkylated variations. Sodium lauryl sulfate, Aerosol MA, and Aerosol OT were used as standards for comparison. The emulsifier concentration required to give a 200-nm particle diameter varied strongly with the degree of alkylation of the emulsifier; the linear C16-monoalkylated diphenyl ether disulfonate emulsifier gave the desired diameter with the lowest concentration. The adsorption isotherms of these emulsifiers on the 60 : 40 styrene - butadiene copolymer particles were determined and correlated with the emulsifier structure. The interfacial tensions between styrene and the aqueous emulsifier solutions were measured and used to calculate the free energies of micellization and adsorption.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1990.070410716
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  • 5
    Electronic Resource
    Electronic Resource
    A polymer thin-film technique to study the micromorphology of core/shell latexes (1987)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2595-2603 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of poly(styrene)/poly(styrene-co-acrylonitrile) core-shell latexes were synthesized by seeded emulsion polymerization. The dried latex was dissolved in toluene and then cast on the surface of water to form a very thin film (60-90 nm). Phase separation in the thin film was studied by transmission electron microscopy (TEM). Electron micrographs of these thin films yielded fine structure and interesting morphology that was unattainable by ultramicrotoming of the corresponding compression-molded specimens. Glass transition temperatures and percent grafted polystyrene were correlated with the TEM results. As grafting increases, mixing of the two phases improves, with the resulting Tg value being between the two Tg's of poly(styrene) and poly(styrene-co-acrylonitrile).
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1987.080250924
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  • 6
    Electronic Resource
    Electronic Resource
    Emulsion polymerization of vinyl acetate using a polymerizable surfactant. I. Kinetic studies (1992)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2619-2629 
    Details
    ISSN: 0887-624X
    Keywords: emulsion polymerization, vinyl acetate ; emulsion polymerization, polymerizable surfactant ; emulsion polymerization, kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polymerizable surfactant, sodium dodecyl allyl sulfosuccinate (TREM LF-40; Henkel) and its nonpolymerizable counterpart were used in comparative studies of the emulsion polymerization of vinyl acetate. The conversion-time behavior differed for the two surfactants; the TREM LF-40 showed a decrease in the polymerization rate with increasing concentration while its hydrogenated derivative showed the opposite behavior, the rate increasing with increasing surfactant. Particle size analysis revealed a decreasing particle size with increasing surfactant concentration for both series of reactions. An explanation for the seemingly ambiguous results obtained for the polymerizable surfactant was sought by examining the reactivity of its vinyl group in copolymerization with vinyl acetate and its allylic group in a chain transfer reaction. The results suggest that both the copolymerization and chain transfer reactions can lead to the observed reduction in polymerization rate with increasing TREM LF-40 concentration. © 1992 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1992.080301216
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  • 7
    Electronic Resource
    Electronic Resource
    Emulsion polymerization of vinyl acetate using a polymerizable surfactant. II. Polymerization mechanism (1992)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2631-2644 
    Details
    ISSN: 0887-624X
    Keywords: emulsion polymerization, vinyl acetate ; emulsion polymerization, polymerizable surfactant ; emulsion polymerization, latex characterization ; emulsion polymerization, competitive growth seeded polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of growth of latex particles in the emulsion polymerization of vinyl acetate using a polymerizable surfactant, sodium dodecyl allyl sulfosuccinate (TREM LF-40; Henkel) was investigated. Both the aqueous phase and the particle/water interface were found to be loci for the copolymerization of TREM LF-40 with vinyl acetate. Competitive growth experiments using TREM LF-40 and its nonpolymerizable derivative were conducted to separate the effects of aqueous phase and particle surface. Particle size analysis of the seeded and unseeded polymerizations coupled with kinetic results suggested that the reactions at the particle/water interface are more important and that the particle size of the latexes is a key parameter controlling the polymerization rate through copolymerization and chain transfer to the polymerizable surfactant at the particle surface. A decrease in particle size lead to an increase in the amount of TREM LF-40 polymerized at the particle surface and to a decrease in polymerization rate. © 1992 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1992.080301217
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  • 8
    Electronic Resource
    Electronic Resource
    Multicomponent latex IPN materials. I. Morphology control (1997)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2193-2206 
    Details
    ISSN: 0887-624X
    Keywords: multicomponent ; latex ; interpenetrating polymer networks ; IPN ; core/shell ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of novel structured latex particles with interpenetrating polymer network (IPN) cores and glassy SAN shells were developed in an attempt to investigate the feasibility of these polymers as both toughening and damping agents in thermoplastics. The IPN cores were composed of one impact part (polybutadiene based) and one damping part (acrylic based, with Tg around +10°C). The particle morphologies of these polymers were determined by TEM. The glass transitions and mechanical behavior of the polymers were characterized from DMS. The effect of different components on the final core/shell particle morphologies and mechanical properties was studied. The mechanical behavior of core/shell particles with IPN cores was also compared with that of separate core/shell and multilayered core/shell particles. In addition, normal core/shell synthesis (rubbery part first then the glassy part) and inverted core/shell synthesis (glassy part first then the rubbery part) were performed to provide another access for morphology control. It was found that the core/shell latex particles with poly(butyl acrylate) based copolymers are more miscible than poly(ethylhexyl methacrylate)-based copolymers. The high grafting efficiency of poly(butyl acrylate) plays an important role in governing phase miscibility. The latex particles synthesized by the inverted core/shell mode showed higher miscibility than the normal synthesized ones. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2193-2206, 1997
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Preparation and morphological characterization of microscopic composite particles (1991)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 857-867 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monodisperse microscopic poly (methyl methacrylate)/polystyrene composite particles of 1-10 μm diameter were prepared by seeded emulsion polymerization of styrene in poly (methyl methacrylate) seed particles which were initially prepared by dispersion polymerization. The resulting composite particles were characterized by transmission and scanning electron microscopy. The unique morphology of the composite particles comprised three types of polystyrene domains embedded in a continuous poly (methyl methacrylate) matrix: the dispersed “internal” domains in the interior, the interconnected “subsurface” domains that from a crust beneath the surface, and the separated “surface” domains at the surface. In addition to thermodynamics and kinetics, the phase separation in composite particles is affected by polymerization mechanism. The complicated particle morphology found is attributed to the coexistence of bulk polymerization and emulsion polymerization (radical absorption and desorption) mechanisms. An explanation of the formation of the observed morphology is proposed. With varying poly (methyl methacrylate)/styrene ratio, the internal viscosity and the competition between the two polymerization mechanisms resulted in a series of interesting morphologies.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1991.080290610
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  • 10
    Electronic Resource
    Electronic Resource
    Anionic dispersion polymerization of styrene. I. Investigation of parameters for preparation of uniform micron-size polystyrene particles with narrow molecular weight distribution (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2633-2649 
    Details
    ISSN: 0887-624X
    Keywords: dispersion polymerization ; polystyrene ; steric stabilizer ; poly(styrene-block-polybutadiene) ; tetrahydrofuran ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anionic dispersion polymerization in a hexane medium has been applied to the synthesis of monodisperse polystyrene particles in the size range of 1.41-6.16 μm, and having narrow molecular weight distributions Mw/Mn of 1.02-1.28. sec-Butyllithium was used as the initiator. Polystyrene-block-polybutadiene diblock copolymer containing 23% polystyrene block, (i.e., Stereon 730A) with a molecular weight of 147,000 g/mol and a polydispersity of 1.05, was found to be a suitable steric stabilizer for the preparation of micron-size polystyrene particles with narrow size distribution. Tetrahydrofuran (THF) was used as a promoter for obtaining narrow molecular weight distributions. However, this study revealed that the addition of small amounts of THF as promoter broadened the particle size distribution. High solids content polystyrene dispersions were also prepared without using any promoter by both batch and/or multi-addition monomer processes. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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