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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 2463-2477 
    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
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  • 22
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 465-484 
    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: Atomic force microscopy (AFM) was used to study the interphase regions in rubber-toughened epoxy polymers. The nature of the interphase region was varied by either the adducting of reactive oligomers or by crosslinking the shell polymer on core/shell latex particles. The adducted reactive oligomers were comprised of carboxyl-terminated, butadiene-actrylonitrile copolymers (CTBN) prereacted with either (1) a low molecular weight diglycidyl ether of bisphenol A-based epoxy, which results in an interphase with increased crosslink density, or (2) a high molecular weight epoxy based on the diglycidyl ether of propylene glycol (DEGP), which results in an interphase with decreased crosslink density. The second type of rubber particles is custom-made submicron core/shell latex particles of a poly(butadiene-co-styrene)[P(BS)] core with an acrylate shell. Two acrylate shells were (1) PMMA/AN shell containing 25% acrylonitile and (2) a similar PMMA/AN with 5% divinyl benzene. The toughness of these blends was characterized using linear elastic fracture mechanics. The features on the fracture surfaces were examined using both AFM and FESEM (field emission scanning electron microscopy). AFM was able to detect features not observed in SEM and also to quantify all of the fracture surface features. In particular, the height-to-width ratio of the rim surrounding cavitated particles provided a useful means for determining the ductility of the interphase region. Attempts were made to determine the size of the interphase region using the frictional mode and the tip-adhesion forces. Unfortunately, the results of both approaches are inconclusive at the present time; this is most likely due to the deformation surrounding the rubber particles detected in the fast fracture regions. © 1995 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 23
    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: Composition, molecular weight, and microstructure of the “shell” polymer in core-shell structured latex particles, designed for toughening polycarbonate matrix, should be controlled for enhanced miscibility between the shell polymer and the matrix. Various “shell polymer” systems based on styrene (St) and benzyl methacrylate (BM) were synthesized. Reactivity ratios were determined for (St) and (BM). Chain transfer efficiency studies revealed the susceptibility of styrene to transfer to a chain transfer agent. Benzyl methacrylate was found to have steric and stability factors hindering its tendency to chain transfer with various chain transfer agent. Miscibility tests between P(St/BM) and polycarbonate (PC) indicated different degrees of miscibility, depending upon polymerization conditions. Factors other than molecular weight, such as branching and crosslinking, were found to play a role in the miscibility. Monodisperse poly(n-butyl acrylate) (PBA) seed latex particles of variable degree of crosslinking and particle size were successfully synthesized by batch emulsion polymerization. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 24
    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 synthesis of structured latex particles involved the preparation of a slightly crosslinked poly(n-butyl acrylate) (PBA) seed and a poly(benzyl methacrylate-styrene) [P(BM-St)] shell. It was found that structured core-shell latex particles prepared by semicontinuous monomer addition yielded better coverage of the seed particles than those polymerized by batch and that poly(benzyl methacrylate) yielded better coverage than polystyrene (PS). Polymerizations in the presence and absence of a chain transfer agent indicated that the presence of isooctyl mercaptopropionate (IOMP) causes the second-stage monomer to polymerize as an isolated, single patch of shell material. In the absence of IOMP, smaller patches of shell material are spread throughout the PBA seed surface. The different morphologies obtained under different polymerization conditions were attributed to thermodynamic and kinetic factors such as polymer-polymer interfacial tensions and viscosity effects. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 25
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 10 (1985), S. 391-402 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The azeotropic 80:20 styrene-acrylonitrile mixture was polymerized in 190nm- and 300nm-diameter monodisperse polystyrene seed latexes by batch, batch-with-equilibrium-swelling, and semi-continuous polymerization. Polystyrene seed latexes were used to determine the degree of grafting of the substrate as well as the styrene-acrylonitrile copolymer. The Arrhenius plot of log (polymerization rate) of the seeded batch copolymerizations with reciprocal temperature comprised two linear regions with a sharp inflection point at 65°C. Specific volume measurements showed that the Tg of the monomer-swollen styrene-acrylonitrile copolymer was also 65°C. The final latex comprised the original seed particles grown to a larger size and, in some cases, a new crop of particles formed during the polymerization. The critical factor determining the formation of new particles was the surface area of the seed latex: at or above 226 m2/dl, new particles were not formed; at or below 179 m2/dl, a new crop of particles was nucleated, the number increasing with decreasing surface area. The degree of grafting of the polystyrene seed substrate was greater for the smaller particle size seed latex, and increased exponentially with increasing seed surface area. The amount of grafted styrene-acrylonitrile copolymer determined the stability of the grafted particles in acetone, a good solvent for the copolymer. Dynamic mechanical spectroscopy showed that the continuous phase was either the polystyrene substrate (Tg 104°C) or the styrene-acrylonitrile copolymer phase (Tg 120°C) except where the degree of grafting was high, in which case, the Tg was intermediate between the two values. Electron microscopy of thin film sections stained with ruthenium tetroxide confirmed which phase was continuous and showed interpenetrating networks for those systems of intermediate Tg.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 26
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1501-1514 
    ISSN: 0887-6266
    Keywords: multicomponent ; latex ; interpenetrating polymer networks ; IPN ; core/shell ; damping ; loss area ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The integrals of the linear loss shear modulus vs. temperature (loss area, LA) and linear tan δ vs. temperature (tan δ area, TA) were characterized for various core/shell latex particles with synthetic rubber, poly(butadiene-stat-styrene) [P (Bd/S), 90/10], and interpenetrating polymer networks (IPN) as the cores. The IPN cores were composed of P(Bd/S) (Tg ≃ - 70°C) and an acrylate based copolymer (Tg around 10°C) for potential impact and damping improvement in thermoplastics. Poly(styrene-stat-acrylonitrile) (SAN, 72/28) was the shell polymer for all these polymers. Under the same loading, for both toughening and damping controls, among the IPN core/shell, blend of separate core/shell, and multilayered core/shell polymers, the IPN core/shell polymers were the best dampers. However, the other core/shell polymers also showed higher LA values than P(Bd/S)/SAN core/shell polymer. A comparison of LA values via a group contribution analysis method was made, the effect of particle morphology and phase continuity on damping being studied. Inverted core/shell latex particles (glassy polymer SAN was synthesized first) showed much higher LA and TA values than normal core/shell ones (rubbery polymer was synthesized first). Models for maximum LA and TA behavior are proposed. The damping property was essentially controlled by the phase miscibility and morphology of the core/shell latex particles. The LA values for each peak in these multiphase materials provided some indication of the several fractional phase volumes. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1501-1514, 1997
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 27
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Emulsionspolymerisation und -copolymerisation von Styren mit und ohne Emulgator sowie mit und ohne Saatlatex wurde untersucht. Die Saatlatices wurden durch Emulsionspolymerisation ohne Emulgator (bei Polystyren) bzw. in Gegenwar eines anionischen Emugators (bei Polybutadien und Butadien-α-Methylstyren-Copolymer) hergestellt. Die kinetischen Untersuchungen und Teilchengrößenbestimmungen zeigten die entscheidende Bedeutung der Verteilung der Emulgatormoleküle und der polaren Gruppen in der Polymer-Wasser-Grenzfläche für den Teilchenbildungsprozeß.
    Notes: The emulsion polymerization and copolymerization of styrene with or without emulsifiers, seeded or not, was investigated. The seed latex was prepared by emulsion polymerization without emulsifiers (for polystyrene), or in the presence of anionic emulsifiers (for polybutadiene and butadiene-α-methyl-styrene copolymer). The kinetic studies and particle size measurements proved the crucial role of the distribution of emulsifier molecules and of the polar groups at the polymer-water interface on particle formation.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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