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Flory-Huggins X parameter

The role of the solvent in polymer adsorption has been the subject of much discussion. For example, theories have made predictions about the effect of the polymer/solvent interaction (i.e. Flory Huggins x parameter) on adsorption. For many systems, x parameters had already been tabulated so that a number of adsorption studies focused attention on this parameter. In spite of much effort, available data are ambiguous, sometimes verifying and sometimes contradicting the trends predicted by theory. [Pg.53]

Hammers, W. E. De Ligny, C. L., "Determination of the Flory-Huggins X Parameter, the Heat of Dilution, and the Excess Heat Capacity of Some Alkanes in Polydimethylsiloxane by Gas Chromatography," J. Polym. Sci., Polym. Phys. Ed., 12, 2065 (1974). [Pg.172]

As well as the above quoted studies this method has also been used to study the interaction between poly(vinylidene fluoride) and poly(methyl methacrylate) , between poly(ethylene oxide) and the hydroxy ether of bisphenol A ° , and between poly(ethylene oxide) and a poly(ether sulphone) The above equations have also been reformulated in terms of the equation-of-state theory to obtain the interaction energy, which is concentration independent rather than the Flory-Huggins X parameter which is composition dependent. [Pg.149]

Calculate the steric interaction energy between the two spheres given in problem 1. Use Table 10.7 for the value of the relevant Flory-Huggins x parameter. [Pg.489]

Figure 4.5 Measurements of effective Flory-Huggins x parameter for deuterated polystyrene-poly(vinylmethylether) blends (Han et al, 1988) as a function of l/T. The temperature range is typically 100-150 °C, and the numbers near each set of data indicate the volume fraction of polystyrene. The observed linear dependence on 1/r provides the physical conclusion that first-order perturbation theory is a satisfactory treatment of attractive interactions here. Figure 4.5 Measurements of effective Flory-Huggins x parameter for deuterated polystyrene-poly(vinylmethylether) blends (Han et al, 1988) as a function of l/T. The temperature range is typically 100-150 °C, and the numbers near each set of data indicate the volume fraction of polystyrene. The observed linear dependence on 1/r provides the physical conclusion that first-order perturbation theory is a satisfactory treatment of attractive interactions here.
Here Xeff(q) is a wavevector-dependent generalization of the Flory-Huggins X parameter [78]. For q-> 0, Eq. (34) yields... [Pg.194]

Here we rather focus on effects of external surfaces (e.g. hard walls) on polymer blends. In general, one expects that the forces between the wall and monomers of type A will differ from those between the wall and monomers of type B, as it generally occurs at the surfaces of small-molecule mixtures as well [365]. For polymer mixtures that are partially compatible, the interactions in the bulk (as described by the Flory-Huggins x-parameter) must be relatively small, however, since the entropy of mixing is down by a factor of N (for simplicity, the following discussion is restricted to a symmetric mixture, Na = Nb = N). However, there is no reason that the difference of wall-A and wall-B forces is similarly small [125]. Thus one may expect rather pronounced surface enrichment effects in polymer mixtures [125], Indeed some experimental evidence for this prediction has been found [37, 38, 126, 127]. [Pg.287]

Flory-Huggins x parameter, and the volume fraction of the A block, Z. The structure-property relationship for coil-coil diblock copolymer systems is relatively well understood both experimentally [14-19] and theoretically [20-23]. Chain stretching normal to the interface leads to a positive deviation of the scaling exponent [14]. For example, scaling behavior for a conven-... [Pg.66]

Due to the tendency for the Flory-Huggins x parameter to be positive, miscibility between high-molar-mass polymers is rare. If homopolymers are involved, miscibility requires some kind of specific interactions of which hydrogen bonding is the... [Pg.294]

The Flory-Huggins X parameter has been one of the most widely used quantities, characterizing a variety of polymer-solvent and polymer-polymer interactions. It is a unitless number. Sometimes the Flory-Huggins parameter is written Xi,2< sometimes just plain x- While the original theory proposed that x-y be concentration independent, many polymer-solvent systems exhibit increases ofxi with polymer concentration (21). In that case the analytical representation of the experimentally found concentration dependence can be written as a power series,... [Pg.84]

An important parameter in the theory of diluted polymers, polymer mixtures, and block copolymers is the Flory-Huggins x parameter, as it determines the propensity of the system to mix or de-mix. In DPD, the x parameter is taken into account by systematically varying the conservative interaction parameter between unlike particles, whilst the repulsion between like particles remains unchanged to maintain a homogeneous compressibility. Hence, for a mixture of A and B particles one has aAA = aBB and aAB = (Iaa + Groot and Warren [24] argued on the basis of the DPD... [Pg.564]

The most advanced theoretical studies of micelle formation are based on numerical versions of the SCFT [32-35, 297] of polymers, and such an approach has been worked out by Cavallo et al. [125]. Since the same approach has previously been used to study interfacial properties in polymer blends and compared to corresponding bond fluctuation model simulations, the translation factor from the interaction parameter e of the simulation to the Flory-Huggins x parameter of the SCFT is already known, and is not an adjustable parameter. SCFT predicts that for large enough N, the distribution P nab) at the CMC should only depend on the ratio ab/A /. Figure 24 demonstrates that, at least in the range of sizes 48 < IV < 128,... [Pg.318]

The excess free energy of the mixture (relative to a pure polymer) is written as the sum of an entropy of mixing term, and an enthalpy term. In the latter, only a reduced energy parameter e enters, which is related to the Flory-Huggins x parameter... [Pg.360]

Observations on the interfacial retardation, decay of retardation with distance from the filler, effect of filler size, and the dependence on Flory-Huggins x parameter are in quantitative agreement with the theory. Additional data on the effect of crosslink density indicate that cohesive failure of elastomer at low cross-linking and non-Gaussian network statistics and/or failure at high crosslinking must be taken into consideration. [Pg.273]

The bare interactions are related to the dimensionless Flory-Huggins X-parameters through... [Pg.253]

SHI Shiomi, T., Tohyama, M., Endo, M., Sato, T., and hnai, K., Dependence of Flory-Huggins X-parameters on the copolymer composition for solutions of poly(methyl methacrylate-ran-n-butyl methacrylate) in cyclohexanone, J. Polym. Sci., Part B Polym. Phys., 34, 2599, 1996. [Pg.348]


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See also in sourсe #XX -- [ Pg.73 ]




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