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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 5754-5754 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 3213-3221 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Later-stage unmixing process of a near critical mixture of polybutadiene (PB)/poly(styrene- r-butadiene)(SBR) were examined at real time t and in situ at several temperatures T by time-resolved light scattering method. The magnitude of scattering vector qm(t,T) at which the intensity becomes maximum and the maximum intensity Im(t,T) were analyzed in order to characterize the coarsening processes of the later-stage spinodal decomposition. The variations of Im and qm with t at different T's were found to fall onto master curves on the reduced plots, thus assuring the scaling postulate that the data obtained at different t and T for given mixtures are properly scaled with the temperature-dependent characteristic wave number qm(0,T) and characteristic time tc(T).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 1386-1396 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We presented some experimental results on flow small-angle light scattering ("flow SALS'') of lyotropic polymer liquid crystals which involved real-time, in situ, and simultaneous measurements of mechanical properties and small-angle light scattering (SALS) of a complex structured fluid. The flow-SALS studies were conducted under steady-state Couette flow and during relaxation process occurring after the cessation of the steady-state shear flow. We found the following universal behavior on the structure and properties for two kinds of the liquid crystal systems, i.e., poly(γ-benzyl L-glutamate) in m-cresol and hydroxypropyl cellulose in water. (i) Upon increasing shear rate γ(overdot), the "polydomain'' structure gradually tends to be transformed to the essentially "monodomain'' texture through annihilation of the disclinations. On the top of this general tendency, we found more specific characteristic of the fluid systems with γ(overdot), (ii) at γ(overdot)〈γ(overdot)c, a critical shear rate above which a remarkable shear thinning occurs, the disclinations are more or less uniformly distributed in space, while at γ(overdot)〉γ(overdot)c the disclinations are localized into domains and dispersed in the more or less uniform medium with a high degree of orientation, (iii) the relaxation after cessation of the steady state shear depends on its γ(overdot) before the cessation and is quite different below and above γ(overdot)c, and (iv) the cessation from γ(overdot)〉γ(overdot)c involves formation of the "band texture'' during the relaxation process of the fluids.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 4360-4368 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Cooperative diffusion D of polyacrylamide gels in water was investigated by quasielastic light scattering both under the isotropically swollen state and under the uniaxially stretched and swollen state. The concentration (Ce) dependence of D for the isotropic gels having equilibrium degrees of swelling was measured by systematically changing crosslinking density of gels. The results yielded D=(3.4±0.5)×10−6 C0.76±0.03e cm2/s, in accord with a scaling prediction. For each of the gels prepared and having a given Ce, the uniaxial stretching was applied, and the values D were investigated as a function of extension ratio α and direction β with respect to the stretching direction. The results gave D (α,Ce)=(3.4±0.5)×10−6 αx Cye cm2/s, where x=2/3 for β=0° and −1/4 for β=90°, and y=0.76, independent of α and β. The results clearly indicate that upon increasing α, D increases and decreases, respectively, in the direction parallel and perpendicular to the stretching direction, implying suppression and enhancement of the concentration fluctuations as a result of the network being stiffened and softened in the respective directions.
    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 91 (1989), S. 4369-4379 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Shear-induced homogenization of semidilute solutions of polybutadiene and polystyrene mixtures with nearly critical composition was studied by the flow small-angle light scattering method. The dramatic drop of the homogenizationtemperature ΔTc(S)=Tc(0)−Tc(S) was observed, and studied as a function of shear rate S, where Tc(S) is the homogenization temperature at a given S and Tc(0) is the temperature under the quiescent state. The experimental results showed that ΔTc(S)/Tc(0)=KS0.50±0.02 where the prefactor K was found to be (2.6±0.6)×10−3 for the solutions containing 3.0 wt. % of total polymer weights. This prefactor is much larger than that reported for a case of simple-liquid mixture by 3 or 4 orders of magnitude. The large prefactor is proposed to be due to a long lifetime of the concentration fluctuations in the single-phase state and slow growth rate of the fluctuations in the two-phase state, compared with the corresponding quantities for the simple-liquid mixture. In the shear-induced homogenized state, the light scattered intensity I(qy) perpendicular to the flow direction was found to obey the Ornstein–Zernike equation. The correlation length ξ and the intensity at qy=0, I(0), were found to depend on S, i.e., ξ−2∼S1/2−S1/2c and I(0)−1∼S1/2−S1/2c, and diverge at the critical shear rate Sc. These experimental results on Tc(S), ξ−2 and I(0)−1, suggest the mean-field behavior of the solution of the polymer mixture under shear. The early-stage unmixing behavior after the cessation of the steady-state shear at S〉Sc was also examined, the results of which indicate that the hydrodynamic interaction is suppressed, giving rise to the small mode–mode coupling contribution Dhydro/Dapp=0.2 to 0.45, but is not yet completely screened out. Hence the hydrodynamic interaction cannot be still ignored for this system.
    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 97 (1992), S. 6855-6863 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The unmixing process via spinodal decomposition of poly(styrene-ran-butadiene) (SBR)/polyisoprene (PI) mixtures was investigated by the time-resolved light-scattering method to see how it is affected by the temperature of phase separation T and by the molecular weight of PI with that of SBR fixed. Time changes in the wave number qm(t;T) and intensity Im(t;T) at the peak of the scattering function were followed to explore the coarsening process in the later stage of spinodal decomposition. For each mixture the observed changes at different T were reduced to a master curve when plotted against a reduced time τ. This finding is consistent with the scaling postulate by Langer et al. and Chou and Goldburg. The master curves for mixtures with different PI molecular weights were divergent, showing the phenomenon called the N branch. However, it was possible to bring them to a master curve when τ was multiplied by a shift factor depending on the average number of entanglements per chain. The dependence was weaker than that predicted theoretically by Onuki.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 679-689 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Spinodal decomposition of off-critical mixtures of poly(styrene–random–butadiene) copolymer with polyisoprene or polybutadiene was investigated as a function of the composition w of the mixtures and of the phase separation temperature T by time-resolved light scattering. The coarsening behavior of the mixtures was characterized in terms of the time change of the maximum intensity Im and that of the magnitude of the scattering vector qm at which the intensity becomes maximum. It was found that the time changes of Im and qm for the off-critical mixtures studied here are effectively pinned at a certain time defined here as the "pinning'' time. This spontaneous pinning of the growth of the unmixing structure was found to occur earlier when w is biased toward 0 or 1 at a given T and when the phase separation temperature is raised at a given w, for these systems which seemingly have upper critical solution temperature behavior.
    Type of Medium: Electronic Resource
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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. 2463-2472 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Small-angle x-ray scattering from the segmental density fluctuations of a starblock copolymer with a given arm number n of 6 as well as that of a linear diblock copolymer (corresponding to the starblock copolymer with n=1) were studied in both ordered and disordered states. In the ordered state the characteristic wavelength (D) of the fluctuations for the copolymer with n=6 was found to have the same temperature (T) dependence as that for the diblock copolymer, where n=1, i.e., D∼T−1/3. In the disordered state, the theoretical spectrum of the fluctuations was found to essentially agree with the experimental results. The thermodynamic interaction parameter (χ) between the dissimilar monomers was also determined as a function of T from the fluctuation spectrum in the disordered state. The results show a significant n dependence.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 6177-6190 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Our previous work on time evolution of the interfacial structure for a near critical mixture of polybutadiene and polyisoprene undergoing the spinodal decomposition (SD) [T. Hashimoto, M. Takenaka, and H. Jinnai, J. Appl. Crystallogr. 24, 457 (1991)] was extended to explore the behavior as a function of temperature T, again using the time-resolved light scattering method. The study involved the investigation of the time evolutions of various characteristic parameters such as the wave number qm(t;T ) of the dominant mode of the concentration fluctuations, the maximum scattered intensity Im(t;T ), the scaled structure factor F(x;T ), the interfacial area density Σ(t;T ), and the characteristic interfacial thickness tI(t;T ) from the early-to-late stage SD, where t refers to time after the onset of SD and x refers to the reduced scattering vector defined by x=q/qm(t;T ); q is the magnitude of the scattering vector. The results confirm the model previously proposed at a given T over a wider temperature range corresponding to the quench depth ΔT=T−Ts =5.5–34.5 K, or εT=(χ−χs)/χs =4.50×10−2 to 2.79×10−1, where Ts is the spinodal temperature, and χ and χs are the Flory interaction parameters at T and Ts, respectively. This blend is noted to have a phase diagram of the lower critical solution temperature type.
    Type of Medium: Electronic Resource
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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. 5874-5881 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A semidilute solution of a polymer mixture with a nearly critical composition was studied by using the small-angle light scattering method as a model system to study ordered structures and critical phenomena of mixtures under shear flow. The experimental studies revealed that there are five regimes in the shear-rate dependence of the concentration fluctuations of the solution, as discussed in the text, including the regime in which the "shear-induced homogenization'' takes place. The results were interpreted, as much as possible, with the theories developed for binary mixtures of simple liquids and, when necessary, with a theory proposed here for polymer systems. Unique features of polymer dynamics in comparison with the dynamics for the critical mixtures of simple liquids were presented in the text, e.g., the shear-rate (S) dependence of the cutoff wave number being proposed to be given by qc,S∼(Dcξ20)−1/4 S1/4 rather than qc,S∼(6πη/kBT)1/3S1/3 for the simple liquids.
    Type of Medium: Electronic Resource
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