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Copolymers with adsorption

In this chapter we consider polymer models with periodic charges. Precisely we consider the copolymer with adsorption model of Section 1.6.3, that is the measure defined by (1.66). This of course includes poljmier... [Pg.69]

On copolymers with adsorption there is a certain amount of literature, see e.g. [Soteros and Whittington (2004)], but we are not aware of clear answers to the questions we have raised in this section. We point out that a coarse graining result is available also for this model, under suitable conditions, and the limit model is a Brownian copolymer with the energy modified by the appearance of a non-disordered local time term such a result has been proven in [Petrelis (2006)] to which we refer for the precise statement. [Pg.149]

By Jensen inequality Vs C V. The subscript s stands for strongly delocalized and the definition is natmally generalized to copolymers and copolymers with adsorption. Note that (/ , h) Vs if and only if /i > logS/c + logM(/ ). [Pg.174]

For general renewal models the recursion is even simpler to write. We consider directly the case of copolymers with adsorption of (1.66), but of... [Pg.183]

Giacomin, G. and Toninelli, F. L. (2006b). The Locahzed Phase of Disordered Copolymers with Adsorption, Alea 1, 149-180. [Pg.236]

Figure 7 shows the results of measurements of adsorption density by Parsonage, etal. [77] on a series of eighteen block copolymers, with poly(2-vinylpyridine) [PVP] anchors and polystyrene [PS] buoys, adsorbed from toluene (selective for PS) of variable molecular weight in each block. The results are presented as the reciprocal square of Eq. 28, that is, as a dimensionless number density of chains ct (d/Rg A)-2. For all but the copolymers of highest asymmetry, Eq. 28 is in good agreement with the data of Fig. 7. The high asymmetry copolymers are in the regime of the data of curves (a) and (c) of Fig. 3 where the large relative size... Figure 7 shows the results of measurements of adsorption density by Parsonage, etal. [77] on a series of eighteen block copolymers, with poly(2-vinylpyridine) [PVP] anchors and polystyrene [PS] buoys, adsorbed from toluene (selective for PS) of variable molecular weight in each block. The results are presented as the reciprocal square of Eq. 28, that is, as a dimensionless number density of chains ct (d/Rg A)-2. For all but the copolymers of highest asymmetry, Eq. 28 is in good agreement with the data of Fig. 7. The high asymmetry copolymers are in the regime of the data of curves (a) and (c) of Fig. 3 where the large relative size...
NR, styrene-butadiene mbber (SBR), polybutadiene rubber, nitrile mbber, acrylic copolymer, ethylene-vinyl acetate (EVA) copolymer, and A-B-A type block copolymer with conjugated dienes have been used to prepare pressure-sensitive adhesives by EB radiation [116-126]. It is not necessary to heat up the sample to join the elastomeric joints. This has only been possible due to cross-linking procedure by EB irradiation [127]. Polyfunctional acrylates, tackifier resin, and other additives have also been used to improve adhesive properties. Sasaki et al. [128] have studied the EB radiation-curable pressure-sensitive adhesives from dimer acid-based polyester urethane diacrylate with various methacrylate monomers. Acrylamide has been polymerized in the intercalation space of montmorillonite using an EB. The polymerization condition has been studied using a statistical method. The product shows a good water adsorption and retention capacity [129]. [Pg.866]

Merrill and Salzman have developed PEO soft segment polyurethanes and indeed have demonstrated minimal adsorption of blood proteins and minimal platelet adhesion on such surfaces121). Nagaoka et al. have studied various methacrylate copolymers with PEO side-chains of varying lengths and showed a direct correlation between minimization of platelet adhesion with increased PEO side-chain length and surface... [Pg.46]

The following plain example might demonstrate the usefulness of the e° data. In benzene (e° = 0.32) polystyrene samples are eluted from a silica column, whereas polymethylmethacrylates and its copolymers are not. In THF (0.57) even PMMA homopolymers leave the column. Hence, THF is strong enough to prevent PMMA from adsorption. In chloroform (0.40) random copolymers with no more than 50%... [Pg.171]

This chapter is organized as follows. The thermodynamics of the critical micelle concentration are considered in Section 3.2. Section 3.3 is concerned with a summary of experiments characterizing micellization in block copolymers, and tables are used to provide a summary of some of the studies from the vast literature. Theories for dilute block copolymer solutions are described in Section 3.4, including both scaling models and mean field theories. Computer simulations of block copolymer micelles are discussed in Section 3.5. Micellization of ionic block copolymers is described in Section 3.6. Several methods for the study of dynamics in block copolymer solutions are sketched in Section 3.7. Finally, Section 3.8 is concerned with adsorption of block copolymers at the liquid interface. [Pg.132]

Anionic surfaces flat adsorption (DADMAC with low or moderate molar mass) partial adsorption (copolymers with low charge density, homo-and copolymers with high molar mass, branched structures) recharge of surfaces, neutralization, stabilization... [Pg.171]

Following this line, Zheligovskaya et al. [55] compared the adsorption properties of copolymers with special adsorption-tuned primary structures (adsorption-tuned copolymers, ATCs) with those of truly random copoly-... [Pg.23]


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See also in sourсe #XX -- [ Pg.36 , Pg.69 , Pg.82 ]




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Copolymers adsorption

With adsorption

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