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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 8 (1992), S. 2932-2937 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 7 (1991), S. 62-68 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 4 (1988), S. 668-676 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 4
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 4521-4531 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Small-angle neutron scattering experiments at various contrasts were performed on concentrated mixtures of colloidal spheres differing in size. Both colloidal components consisted of fairly monodisperse silica cores coated with a layer of octadecyl chains. Cyclohexane was used as dispersing medium; variation of the contrast was achieved by using mixtures of 1H -cyclohexane and 2H -cyclohexane. Scattered intensities were measured at three volume fractions up to 0.4, at equal partial volume fractions. The different contrast dependence of the scattering amplitudes of both colloids allowed us to calculate partial structure factors. This was done using a method which has not been reported previously. Describing the intraparticle structures with layered-sphere models, and using a decoupling approximation, three partials were obtained from a system of linear equations. The scattering curves at the various contrasts constitute a consistent data set, at all volume fractions. Although the separate components interact like hard spheres, the partial structure factors in the mixture reflect marked deviations from hard-sphere behavior. Their nature can be qualitatively explained with an attractive interaction between unequal particles. This is confirmed with simple model calculations.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 3250-3253 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Light scattering measurements determined the ratio of the nonequilibrium to equilibrium static structure factor for suspensions of "hard spheres'' undergoing shear flow as a function of volume fraction of the suspended particles, the shear rate, and a limited number of scattering angles. These data are compared with existing theoretical predictions for the static structure factor ratio in the limit of small shear flow rates. We conclude that the existing theories, some which are considered exact at low volume fractions, give increasingly poor estimates of the true structure factor at small scattering angles as the volume fraction increases.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6098-6103 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Increasing the pressure on stable dispersions of sterically stabilized silica particles in toluene induces a phase transition. This transition can also be induced by lowering the temperature. The dispersion separates into two phases with different particle densities. The origin of the phase behavior cannot be explained with the classical Flory-polymer-physics model. Here we attribute the observed behavior to a "local ordering'' or "liquid-crystalline-like phase transition'' of the stabilizing moieties grafted to the particles. Through such an effect we can consistently explain the observed phenomena and particularly the high value of the differential quotient dp/dTtrans =+77 bars/K for the phase transition temperature at which the dispersion separates into two liquid phases of different particle concentrations.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5909-5921 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Small angle neutron scattering (SANS) was used as a probe of the structure factor distortion for concentrated hard-sphere dispersions subjected to steady shear flow. The dispersions consisted of stearically stabilized silica spheres of 40 nm radius suspended in cyclohexane, with volume fractions 0.36〈φ〈0.52. We subjected the dispersions to weak shear flow (Peclet number Pe〈1) in a Couette flow cell, and collected intensity measurements in the flow–vorticity plane. We conducted the experiments using the D11 spectrometer at the Institut Laue-Langevin in Grenoble, France. The data permit a thorough evaluation of the existing theories for the shear-induced distortion of the structure factor. We find that the theories as they stand severely underpredict the distortion at low wave vectors (||k||〈0.1 nm−1), but the theories can be made to qualitatively agree with the data by adjusting Pe in the equations to a higher value. The theories are based on a perturbation expansion that is linear in small Pe, but such an expansion is inadequate for describing our data. We show that the nonequilibrium contribution to the structure factor is proportional to fractional powers of Pe, with the exponent depending on volume fraction φ. The failure of the theories is probably due to their neglect of hydrodynamic interactions, which are important in concentrated dispersions. The distortion of the structure factor is greatest around its first maximum, with significant distortion being exhibited in both the flow and vorticity directions. The peak in the structure factor broadens, indicating that weak shear flow produces a more disordered structure relative to the equilibrium structure. The data reveal that the shear flow results in a decreased concentration of particles in the flow direction. The concentration of particles in the vorticity direction increases when shear flow is applied, and the formation of temporal clusters is probable.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 6865-6869 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Adiabatic calorimetry measurements were made on colloidal silica particles (designated SJ4) coated with a dense layer of octadecyl chains. A dry powder consisting of these particles shows a phase transition at 284 K. This is attributed to an order–disorder transition in the stabilizing chains. Dispersing the particles in toluene shifts this order–disorder transition to lower temperatures. We propose a model in which the organic layer dissolves in the solvent at high temperatures and solidifies at low temperatures. This eutectic model predicts qualitatively correct the phase behavior of such colloidal dispersions. Particularly the pressure dependence of the phase transition is consistent with the model.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 7799-7806 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: When dispersed in a marginal solvent like benzene, sterically stabilized silica particles exhibit an effective attraction. This attraction is due to the interaction of solvent molecules with the stabilizing chains and is modeled by a square-well potential; the well has a depth of ε/kT=L(θ/T−1), σ≤r≤σ+Δ. L is an interaction parameter, θ the theta temperature of the chain–solvent pair, σ the particle diameter and Δ the width of the square well. An expression for the diffusivity of adhesive hard spheres is derived with the help of the general Stokes–Einstein equation. The model allows scaling to one master plot of experimentally determined diffusion coefficients for samples of six volume fractions, at 20 different temperatures and for each sample at three scattering angles. Additional results obtained with the model are discussed as well. Phase separation in the abovementioned silica dispersions occurs at a well depth of about 5 kT.
    Type of Medium: Electronic Resource
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