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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 427-431 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    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: Formation of dimeric carboxylic acid functional groups observed at the film-substrate interface of ethyl acrylate/methacrylic acid (EA/MAA) and butyl acrylate / methyl meth-acrylate / methacrylic acid (BA/MMA/MAA) latex films prepared on a high surface tension substrate, such as liquid mercury, is observed when sodium dioctyl sulfosuccinate (SDOSS) is employed as the synthetic emulsifier. To address the acid species assembled at this interface due to the inability of SDOSS to effectively alleviate interfacial tension and to assess the orientation and spatial configuration of acid groups species at the interface, polarized attenuated total reflectance, Fourier-transform infrared spectroscopy (ATR FT-IR) is employed. It is found that the acid dimer rings adopt an average “on-edge” configuration at the interface with the hydrogen-bonded rings perpendicular to the film-mercury interface. This configuration serves to provide not only the necessary interfacial acid-dimer layer, but also facilitates favorable ring-ring interactions between groups of opposite polarity on adjacent rings. This study indicates that the on-edge configuration may also serve to reduce unfavorable interactions between the polar acid functionality and the less polar components present in the bulk of the coalesced latexes. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 56 (1995), S. 387-395 
    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: In an effort to establish to what extent transient effects prior to coalescence may influence mobility, distribution, and orientation of surfactant molecules after coalescence, poly(n-butyl acrylate) (n-BA) and polystyrene (Sty) were polymerized independently and mixed in a 5 : 1 ratio. It appears that if a mixture of the n-BA and Sty latex particles is allowed to stabilize prior to coalescence, the time of stabilization may have a significant effect not only on the distribution of SDOSS surfactant molecules across the coalesced film, but also on their orientation changes depending upon the stage of coalescence and the water front moving toward the surface. The coalescence of latex films was conducted under gaseous nitrogen and at 60% relative humidity. While the water front moves from the film-substrate upward, during this process, various segments of the surfactant molecule change their orientation. Near the F-A interface, hydrophobic segments are being reoriented from parallel to perpendicular, whereas preferentially parallel orientation exhibit hydrophylic SO-3 Na+ segments. When water molecules, however, diffuse out of the film, the surfactant molecules have no preferred orientation. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1887-1892 
    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: This study focuses on the behavior of sodium dioctylsulfosuccinate (SDOSS) in 50/50 w/w % polystyrene/poly(butyl acrylate) (p-Sty/p-BA) latex films. Specifically, mobility and orientation are examined in the context of the film formation by the use of dynamic mechanical thermal analysis and attenuated total reflectance (ATR) Fourier transform infrared (FT-IR) spectroscopy. While for the homopolymer blends of p-Sty and p-BA, two Tg values resulting from a phase separation of p-Sty and p-BA phases are observed, only a single Tg is detected for a copolymer of the same mixture, indicating a single phase within the film. ATR FTIR spectroscopic data indicate that the phase separation of p-Sty and p-BA blends does not occur uniformly across the film. After coalescence, p-Sty particles produce a significant degree of stratification at approximately 1.6 μm from the film surface. At this depth, the polystyrene rings assume preferentially parallel orientation to the film surface. At the same time, the hydrophilic groups of SDOSS surfactant (SO-3Na+) are oriented preferentiallyparallel to the surface. Under high relative humidity conditions, water is able to diffuse into the film and swells the surface layers, thus causing them to expand. As a result, the top, predominately poly-n-BA surface becomes “thicker», and p-Sty phase appears to be near 2.3 μm from the surface. The polystyrene rings maintain their preferential parallel orientation to the surface, but the hydrophilic groups of SDOSS are able to diffuse into the film with the water uptake and are thus not present at the filmair interface. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1733-1740 
    ISSN: 0887-6266
    Keywords: polyesters ; pigment dispersion ; acid-base interaction ; dispersion rheology ; adsorption ; chain configuration ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rheological properties have been measured for solutions of polyesters containing quantities of inorganic and organic pigments. Complex behavior patterns were simplified by computing the effective volume fraction of dispersed solids, taking in account the thickness of polymer layers adsorbed on pigment surfaces. The dimension of interphases created by the adsorbed polymers was rationalized by applying principles of specific interaction between polymers and pigment surfaces. The parameters of specific interaction were obtained from inverse gas chromatographic data. Pigment sedimentation data were used to identify a range of specific interactions best suited to stabilize dispersions of the solids. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 695-703 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Blends of poly(3-hydroxybutyrate) (PHB) and ethyl cellulose (EtC) were prepared by compression molding of solution cast films. The two components were not miscible but the blends showed ‘mechanical compatibility’. Two PHB/EtC blends (80/20 and 50/50 (w/w in all cases)) were selected for biodegradation experiments in activated sludge and in enzymatic solution of PHB-depolymerase from Pseudomonas lemoignei and from Aureobacterium saperdae. Blend morphology was quite different: blend 80/20 was composed of a matrix of impinging PHB spherulites with dispersed EtC inclusions, whereas blend 50/50 was constituted of two continuous phases with interpenetrated domains. Both blends biodegraded in activated sludge, but only blend 80/20 was attacked by PHB-depolymerases from P. lemoignei and A. saperdae. From weight loss, thickness and composition measurements after different exposure times and from scanning electron microscopy of the biodegraded blend surface it was concluded that in blend 80/20 biodegradation of the PHB matrix caused concomitant release in the medium of the embedded EtC particles. The results on PHB/EtC (50/50) after sludge exposure demonstrated that in this blend the PHB phase - thanks to its interconnected domains - was continuously accessible to microbial attack, leaving a highly cavitated ethyl cellulose structure after PHB consumption. The lack of biodegradation of blend 50/50 in enzymatic solution was tentatively attributed to changes of surface hydrophobicity induced by large amounts of EtC, which disfavored enzyme binding.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 1207-1215 
    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: This article, part VII in a series of latex studies, focuses on the effect of ethyl acrylate/methacrylic acid (EA/MAA) latex stability on the exudation of sodium dioctyl sulfosuccinate (SDOSS) surfactant molecules after coalescence. It is found that “aging” of the latex aqueous suspension causes excessive exudation of the surfactant molecules to the film-air interface. Upon exudation to the surface, the surfactant SO3- Na+ hydrophilic heads assemble in preferentially normal-to-the-surface directions, whereas hydrophobic aliphatic tails are randomly burred in the latex surface. ATR FT-IR spectroscopy and a particle size analysis are utilized to elucidate the effects of flocculation and coalescence on the surfactant mobility in latex films. It appears that flocculation, prior to coalescence, enhances exudation and mobility of the surfactant molecules. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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