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  • Articles: DFG German National Licenses  (22)
  • Polymer and Materials Science  (22)
  • nonionic surfactant  (3)
  • 11
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1311-1319 
    ISSN: 0887-6266
    Keywords: polystyrene, chain scission in fracture of ; fracture of glassy polymers, energy consuming micromechanisms ; chain scission mechanism in fracture of polystyrene ; glassy polymers, chain scission and fracture of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The number of chain scissions per unit area that occur during the fracture of partially annealed latex films from Mn ≃ 180,000 g/mol polystyrene particles of about 275 Å radius were measured and correlated to annealing times. A curve with four regimes was found. At short annealing times the curve is nearly flat, in what is called the chain pull-out regime. In the second regime, the number of chains broken per unit area increases with a 0.8 power of annealing time as entanglement of the diffusing polymer chains increases in neighboring host particles. This is in good agreement with Wool's theory which predicts a 0.75 power dependence. Then, after reaching a peak, the number of scissions decreases in the third regime, indicating a change in fracture mechanism. The number of chain scissions increases again in the fourth regime, as final healing of the film interface takes place. Fracture surface analysis reveals a rough surface for short annealing times and a smooth surface for longer annealing times. The number of polymer chain scissions per unit area of fracture surface showed no dependence on initial molecular weights for t ≫ τr where t and τr are annealing and relaxation times, respectively. The number of chain bridges crossing a unit area of interface was suggested as the basic molecular property. © 1992 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1005-1021 
    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 appearance of pseudo-steady states in semicontinuous emulsion copolymerization is studied. Different correlations between the monomer feed rate and the polymerization reaction rate proposed in the literature for homopolymerization systems can be derived from a unified view as presented in this work. The theoretical analysis for copolymerization systems predicts that the individual consumption rates of both monomers involved assume a constant value if the monomer addition rates are kept constant. Different cases for either fixed radical concentration or seeded polymerization with water-soluble or sparingly water-soluble monomers are considered. The assumptions and results of the analysis are tested against experimental data from the seeded copolymerization of vinyl acetate/n-butyl acrylate.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 1649-1662 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The development of supermolecular structure in polystyrene latex particles was investigated by small-angle neutron scattering (SANS). Seed latexes of deuterated polystyrene were swollen with an equal mole-% of protonated styrene monomer, equilibrated, and polymerized to complete conversion. The scattering patterns reflect the extent of supermolecular structure development inside the particle. The data were analyzed by separating the Debye single-chain and spherical scattering form factors. The extent of segregation was found to depend on the relative size of the chains compared with that of the particle, going through a maximum at the ratio Mw/Dw2 of about 0.1, where Dw represents the weight-average diameter of the latex particle. When the chain dimensions are relatively very small, uniform molecular mixing is obtained. The best model for the segregated system is a graduated core-shell supermolecular structure.
    Additional Material: 5 Ill.
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  • 14
    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: Poly(divinylbenzene)/poly(n-butyl acrylate) core/shell latexes were investigated using solid-state 13C-NMR. The (H)T1ρ relaxation time was found to be substantially affected by many of the seeded emulsion polymerization parameters, such as the core/shell ratio, the mode of addition of the second-stage monomer, the addition rate of the second-stage monomer, and the level of conversion of the seed latex at the time of addition of the second-stage monomer. The existence of an interphase region between the core and shell polymers was detected. Maximum interphase region thickness was achieved when the butyl acrylate was added under starved conditions. The thickness of this interphase layer was calculated to be 5-7 nm based on a model proposed by McBriety.1 Solid-state NMR was found to be an excellent spectroscopic technique to probe the interphase region in core/shell latexes. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 911-921 
    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: Dimethyl meta-isopropenyl benzyl isocyanate (TMI®) is a bifunctional monomer possessing a double bond and an isocyanate group. Emulsion terpolymerization of TMI with the acrylic monomers, methyl methacrylate and n-butyl acrylate, was studied. Polymerizations were carried out at 40°C using a redox initiator system in order to minimize the extent of hydrolysis of the isocyanate in the aqueous emulsion environment. The kinetics of the polymerization reaction were investigated. The polymerization rate was found to decrease with increasing TMI concentration. The effects of several preparative variables such as the monomer, surfactant, and initiator concentration on the polymerization kinetics was studied. Several semicontinuous polymerization processes were developed in order to enhance the incorporation of TMI at appreciable rates. These processes also allow us to control the polymer composition, latex particle size, and the locus of isocyanate groups in the latex particle. Process variables such as the mode of initiator addition (batch versus semicontinuous) were found to greatly influence the polymerization behavior. © 1996 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 1 (1990), S. 263-273 
    ISSN: 1042-7147
    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
    Notes: Small-angle neutron scattering studies have been used to clarify several aspects of the internal structure of latexes and subsequent film formation modes. This paper reviews work both around the world and at Lehigh University on those subjects. Two points have been made clear: (1) The appearance of core-shell phenomena in latexes depends on the size of the polymer chain to that of the latex particle; the phenomenon is most marked when the radius of gyration of the chain is about one fifth as big as the latex radius. (2) Strength build-up during film formation depends on the extent of interdiffusion of the chains. For moderate molecular weights, interdiffusion distances of one radius of gyration yield maximum strength. For both moderate (250,000 g/mol) and high (2,000,000 g/mol) molecular weights, full strength was achieved in two hour's annealing time at 144°C.
    Additional Material: 11 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 357-366 
    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 molecular basis for fracture was examined using a custom-built Dental Burr Grinding Instrument, which cuts at a depth of 500 nm per pass. A direct miniemulsification method was used to form uniform-sized latex particles from narrow molecular weight distribution, anionically synthesized polystyrenes. Several polystyrenes were examined as a function of molecular weight, and blends were made of high and low molecular weight polystyrenes. In addition, a broad molecular weight polystyrene was included for comparison. These latexes were dried and cleaned, and molded under mild conditions, followed by annealing for various lengths of time at 144°C. The Dental Burr Grinding Instrument measures the total energy required to fracture the sample. The total number of chains undergoing scission per unit volume was determined via GPC before and after the fracture process. Using an energy balance approach, the total number of chains undergoing pullout (from either side of the fracture surfaces) was estimated. In order to obtain a broader picture of the process, data collected by Mohammadi et al., and by Sambasivam et al., were integrated into the analysis. Basically, at very low molecular weights, ca. 32,000 g/mol, substantially 100% pullout occurs. At the midmolecular weight range, about 150,000 to 180,000 g/mol, chain scission and chain pullout contributions to the total energy are approximately equal. For very high molecular weights, the chain scission contribution is about 90%. A scaling relationship is proposed between the molecular weight of the polymer and the fraction of chains undergoing scission. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 367-374 
    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: Film formation from poly(methyl methacrylate) (PMMA) latex and PMMA copolymer latex incorporating N-(iso-butoxymethyl)acrylamide (IBMA) or methacrylic acid (MAA) has been investigated in terms of the development of tensile strength as a function of annealing time and temperature. Tensile strength is developed through a combination of macromolecular interdiffusion and interfacial crosslinking. The relative rates of interdiffusion vs. crosslinking reactions were studied as a function of temperature and the chemical nature and concentration of the IBMA and MAA functional groups. For low concentrations of these two functional monomers it appears that polymer chain interdiffusion between adjacent latex particles during the film formation process dominates the kinetics of strength development. However, at higher IMBA and MAA concentrations, the higher glass transition temperature at the latex particle surface and intraparticle crosslinking hinders interdiffusion, as reflected by differences in the power law exponent values obtained from the log-log dependence of tensile strength on annealing time. The power law exponents were higher in the case of PMMA than for both IBMA- and MAA-containing copolymers. There was a greater influence temperature on the tensile behavior for the MAA copolymer system as compared to the IBMA copolymer. In the interfacially crosslinked latex polymer system, there is competition between the interdiffusion and crosslinking mechanisms in determining the final mechanical strength of films during the annealing process. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 64 (1992), S. 860-860 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 458-463 
    ISSN: 0142-2421
    Keywords: AES ; depth profiling ; ion beam bevelling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: An ion beam technique has been developed that allows the preparation of bevels from semiconducting heteroepitaxial structures with smooth surfaces and very shallow angles between 0.1° and 0.001°. The bevels are used for AES depth profiling of heterostructures by the line scan technique. Comparison of measured and calculated line scans from (Al, Ga)As/GaAs and (Si, Ge)/Si test structures shows the contributions of the electron escape depth and the ion beam mixing to the depth resolution. Application examples are given for semiconductor laser structures where the interesting heterostructures are buried under a thick overlayer. For such structures, the depth profiling by a line scan across the bevel needs much less analysis time than conventional sputter depth profiling. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 8 Ill.
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