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  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 22 (1994), S. 491-496 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Interfacial effects of a multifunctional additive (MFA), i.e. n-tallow-1,3-propanediamine salt of a carboxylic acid, on carbon black filled rubber have been studied. Surfaces of several normal cure rate carbon blacks were characterized by XPS and vapour-phase chemical derivatization, and the carbon blacks were found to have very few functional groups on their surfaces. The MFA has been found to decompose at ∼120 °C and the decomposition generates a diamine and a carboxylic acid. Bound rubber, determined by o-xylene extraction, was found to decrease with the addition of MFA and a limiting bound rubber value was obtained at the MFA loading which corresponds to a monolayer coverage of the carbon black. The reduction of bound rubber with the addition of MFA is attributed to the release of the occluded rubber within carbon black agglomerates as a result of improved dispersion induced by the MFA. Mechanical properties were found to improve with the addition of MFA and the improvement was again attributed to the dispersing effect of MFA. Optimum mechanical properties were again observed to occur at an MFA loading which approximately corresponds to a monolayer coverage of the carbon black surface.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 17 (1991), S. 177-182 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A method is proposed for obtaining the matrix element SIMS sensitivity factors for III-V compounds of the form ABxC1-x without using standards. This method tests for variation of sensitivities with concentration and, in the case where no strong variation is shown, allows determination of the sensitivity functions by use of samples where the concentrations of two elements vary continuously over a wide range. This method provides a no-standards route to quantification of matrix element concentrations in SIMS depth profiles of layers with graded compositions.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 303-313 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The model of Maxwell et al. (Macromolecules 24, 1629 (1991)) for initiator efficiencies in emulsion polymerization has been extended to take into account the effect of added chain transfer agent (CTA). The model supposes that the rate-determining step for radical entry into latex particles is aqueous-phase propagation of the primary free radicals to a critical chain length z required for entry (forming species such as .MzSO-4, where M is a monomer entity and peroxodisulfate S2O2-8 is the initiator). The effect of CTA on the entry rate is assumed to occur by facilitating the production of aqueous-phase free-radical species (CTA.) by transfer between species such as .MzSO-4 (where n 〈 z) and CTA in the aqueous phase. The CTA. will be formed at a reasonable rate provided the CTA is not too water-insoluble (e.g. C12H25SH); it should also be capable of entering the latex particles rapidly because of its relative insolubility. If the monomer-derived .MnSO-4 tend to suffer aqueous-phase termination rather than entry, the overall rate of entry (and hence initiator efficiency) will be increased. This can explain the accelerating effect of intermediate molecular weight CTA's on emulsion polymerization of monomers such as butadiene, where z is large and hence initiator efficiency is very low in the absence of CTA, because most .MnSO-4 undergo termination rather than entry into the latex particles.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 2049-2063 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two methods are described for experimentally determining the concentrations of monomer in both the aqueous phase and the latex particle phase during partial swelling of latex particles, and therefore also during intervall III of an emulsion polymerization. The ratio of the monomer concentrations in the aqueous phase, both below and at saturation, can be related to the volume fraction of polymer in the latex particles via the Vanzo equation. Comparison of theory and experiments for the methyl acrylate and poly(methyl acrylate-co-styrene) system shows that the monomer partitioning is insensitive to temperature, latex particle radius, polymer composition, polymer molecular weight and polymer cross-linking. Thermodynamic treatment of these and previously published partitioning results shows, at higher volume fractions of polymer, that the conformational entropy of mixing of monomer and polymer is the significant term determining the degree of partial latex particle swelling by monomer. Theoretical predictions of experimental results are quite insensitive to values of the Flory-Huggins interaction parameter and to the latex particle-water interfacial tension. A simple model is developed for the estimation of monomer partitioning which requires only the saturation monomer concentrations in the particle and aqueous phases.
    Additional Material: 12 Ill.
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  • 5
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; isotachophoresis ; oligomer ; free radical ; aqueous phase ; styrene ; termination ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The concentrations and probable nature of charged oligomers formed by aqueous-phase termination in the persulfate-initiated emulsion polymerization of styrene were measured by isotachophoresis. Isotachophoresis has some advantages over other techniques (e.g., GPC, UV spectroscopy) in that it separates species according to their molecular weight, geometry, and charge. The charged water-soluble oligomeric species were detected in experiments in which particles were nucleated in a surfactant-free environment. Identification of the moieties present was made by comparison with model compounds. Evidence was found for bimolecular combination as a major mechanism of termination in the aqueous phase, although the possibility of disproportionation could not be ruled out. The species formed in the aqueous phase under saturated monomer conditions were found to be subject to further reaction towards the end of polymerization. The surface adsorption characteristics of the compounds formed were compared with those of known surfactants and showed good agreement with the assumptions in the model of Maxwell et. al. [Macromolecules, 24, 1629 (1991)] for initiator efficiencies in emulsion polymerization. The relatively large concentrations of nonradical aqueous-soluble oligomeric compounds demonstrate conclusively that initiator efficiencies are not 100%, as is often assumed in such systems. © 1993 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 605-630 
    ISSN: 0887-624X
    Keywords: free radical ; exit ; emulsion ; polymerization ; model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The exit or desorption of free radicals from latex particles is an important kinetic process in an emulsion polymerization. This article unites a successful theory of radical absorption (i.e., initiator efficiency), based on propagation in the aqueous phase being the rate determining step for entry of charged free radicals, with a detailed model of radical desorption. The result is a kinetic scheme applicable to true “zero-one” systems (i.e., where entry of a radical into a latex particle already containing a radical results in instantaneous termination), which is still, with a number of generally applicable assumptions, relatively simple. Indeed, in many physically reasonable limits, the kinetic representation reduces to a single rate equation. Specific experimental techniques of particular significance and methods of analysis of kinetic data are detailed and discussed. A methodology for both assessing the applicability of the model and its more probable limits, via use of known rate coefficients and theoretical predictions, is outlined and then applied to the representative monomers, styrene and methyl methacrylate. A detailed application of the theory and illustration of the methodology of model discrimination via experiment is contained in the second article of this series. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 631-649 
    ISSN: 0887-624X
    Keywords: free radical ; exit ; emulsion ; polymerization ; experiment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In emulsion polymerizations, desorption (exit) from latex particles of monomeric radical species that arise from transfer can be an important determinant of the overall kinetics. An examination of various methodologies for the testing of postulated free radical exit mechanisms is made. These utilize the model descriptions for the exit process presented in the accompanying article of Casey et al., employing data consisting of conversion as a function of time for the approach to steady state polymerization conditions. Experimental data are presented on the exit rate coefficients as a function of such experimental parameters as: particle size, monomer concentration, and aqueous-phase free-radical concentration for a series of styrene polymerizations at 50°C, where the average number of free radicals per particle (n̄) never exceeds 0.5. It is demonstrated for these systems that while the conversion/time dependence from a single run, under conditions sensitive to exit, is insensitive to mechanistic assumptions as to the fate of desorbed free radicals, the variation of the exit rate coefficient with particle size so obtained suggests a second order dependence on n̄, implying complete re-entry of desorbed free radicals under all conditions studied. Once the monomeric radicals have re-entered, they are more likely to remain inside the particle where they will either propagate or undergo termination rather than re-escape. The article also presents an estimate for the rate coefficient at 50°C of the first propagation step of the monomeric radical subsequent to transfer. The conclusions drawn here for seeded systems should prove useful for study of particle nucleation mechanisms, when exit is particularly likely in small, newly formed, particles. © 1994 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 22 (1994), S. 497-501 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Oxygen plasma and ultra violet (UV) ozone treatments have been used to oxidize the surfaces of batches of natural wool fibres and woven cloths. The changes in surface composition and chemistry induced by these treatments have been followed using X-ray photoelectron spectroscopy (XPS).Oxidation of surface proteinaceous di-sulphide sulphur to sulphonic acid groups (—SO3H) containing S(6+) is shown to occur for both treatments. However, oxidation at levels of approximately 90% is apparent for the UV ozone treatment which is significantly higher than levels achieved using oxygen plasmas (30%). Both treatments also lead to oxidation of surface carbon species. The data presented indicate that the UV ozone treatment used is capable of producing surface sulphur and carbon chemistry of the type usually obtained industrially by wet chemical methods which have the disadvantage of producing chlorinated effluent.
    Additional Material: 5 Ill.
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