Polystyrene salts

Furthermore, the entropy change ASj ° for the dissociation of the alkaline earth polystyrene salts Is substantially less... 

Table II. Propagation by Living Polystyrene Salts in Various Solvents at 25°C.

Li et al. employed LbL self-assembly to construct multilayered films on top of nonwoven PCL fibers. The multilayered film consisted of gelatin and polystyrene salt. The top layer was further coated with calcium phosphate. The fabricated scaffold was tested for its potential in bone tissue engineering. Results indicated an enhanced cell proliferation for the LbL-assembled scaffolds (Li et al., 2008). Zhang et al. (2005) employed LbL fabrication technique to form multilayers consisting of type I collagen and hyaluronic acid and were able to generate fibrous multilayered structures that supported the attachment of chondrosarcoma cells. 

Water is softened by removing calcium and magnesium ions from hard water in exchange for sodium ions at sites on cation-exchange resin. Water softeners typically use a gel polystyrene sulfonate cation-exchange resin regenerated with a 10% salt brine solution (25). 

The monomer 4-styrenesulfonic acid was prepared by dehydrohalogenation of -bromoethjibenzene—sulfonyl chloride. The potassium salt can be polymerized in aqueous solution (222). The sulfonation of cross-linked polystyrene beads is being carried out in industry with concentrated sulfuric acid. 

Some commercial durable antistatic finishes have been Hsted in Table 3 (98). Early patents suggest that amino resins (qv) can impart both antisHp and antistatic properties to nylon, acryUc, and polyester fabrics. CycHc polyurethanes, water-soluble amine salts cross-linked with styrene, and water-soluble amine salts of sulfonated polystyrene have been claimed to confer durable antistatic protection. Later patents included dibydroxyethyl sulfone [2580-77-0] hydroxyalkylated cellulose or starch, poly(vinyl alcohol) [9002-86-2] cross-linked with dimethylolethylene urea, chlorotria2ine derivatives, and epoxy-based products. Other patents claim the use of various acryUc polymers and copolymers. Essentially, durable antistats are polyelectrolytes, and the majority of usehil products involve variations of cross-linked polyamines containing polyethoxy segments (92,99—101). 

Fig. 8. The stabiUty and instabiUty regions of a polystyrene latex with added aluminum salt at different pH values (17).

Anionic hydrophobic Sodium polystyrene sulfonate 0.1-0.3 M salt/buffer, pH 7-9 with 20% methanol... 

In nonrigid ionomers, such as elastomers in which the Tg is situated below ambient temperature, even greater changes can be produced in tensile properties by increase of ion content. As one example, it has been found that in K-salts of a block copolymer, based on butyl acrylate and sulfonated polystyrene, both the tensile strength and the toughness show a dramatic increase as the ion content is raised to about 6 mol% [10]. Also, in Zn-salts of a butyl acrylate/acrylic acid polymer, the tensile strength as a function of the acrylic acid content was observed to rise from a low value of about 3 MPa for the acid copolymer to a maximum value of about 15 MPa for the ionomer having acrylic acid content of 5 wt% [II]. Other examples of the influence of ion content on mechanical properties of ionomers are cited in a recent review article [7],... 

Strongly basic anion exchange resins, e.g. a cross-linked polystyrene containing quaternary ammonium groups, are largely ionised in both the hydroxide and the salt forms. Some of their typical reactions may be represented as ... 

Block or graft copolymem can be obtained by cationic polymerization of THF with macromolecular initiators. The recommended groups for the initiation are the dioxolenium cation, the acyl cation and the super acid ester, each of which can be introduced into the backbone polymer by reaction with silver salts of strong acids. Introduction of the dioxolenium group into polystyrene was carried out by the following route32 ... 

The kinetics of polymerization and conductometric studies of barium polystyrene with one active end-group per chain were reported by De Groof et al. 79,80). Formation of an unconventional anionic species, Ba2 +, (CH(Ph)CH2—)j, had to be postulated to account for the results. The existence of such a species is supported by the recent study of the kinetics of polymerization of lithium polystyrene performed in the presence of barium polystyrene endowed with two active endgroups 78). The polymerization of the lithium salt is retarded by the presence of the barium salt, and the retardation is accounted for by the formation of the inert aggregated anions,... 

Barium and strontium salts of polystyrene with two active end-groups per chain were prepared by Francois et al.82). Direct electron transfer from tiny metal particles deposited on a filter through which a THF solution of the monomer was percolated yields the required polymers 82). The A.max of the resulting solution depends on the DPn of the formed oligomers, being identical with that of the salt of polymers with one active end-group per chain for DPn > 10, but is red-shifted at lower DPn. Moreover, for low DPn, (<5), the absorption peak splits due to chromophor-chromophor interaction caused by the vicinity of the reactive benzyl type anions. 

The order of reactivities could be also reversed by a change of solvent. For example, in THF styrene is more reactive than butadiene towards salts of polystyryl anions, whereas in hydrocarbon solvents butadiene is more reactive than styrene towards lithium polystyrene. This reversal of reactivities presumably is caused by a change in the mechanism of propagation. The monomers react directly with carbanions in THF, but become coordinated to Li+ in hydrocarbon solvents. 

This polymeric oxocarbenium salt readily initiates the cationic ring opening polymerization of oxolane to produce a polystyrene-polyTHF block copolymer. Molecular weight control is provided, polydispersity is narrow and compositional heterogeneity is small59). 

Suspension Polymerization. Water is the suspending phase. Inorganic salts and vigorous agitation prevent coalescence and agglomeration. The reaction mode is batch. The largest use of suspension polymerization is for the manufacture of expandable polystyrene beads. 

The first study utilizing this method was reported by Schuller in 1966 [65]. Schuller used polystyrene latex beads that were spread on a salt-containing aqueous subphase in order to keep the particles at the interface. tt-A plots of the floating particles were determined, which showed several phase regions with reproducible transition points. The author determined the particle diameters from the A-value, at which a steep rise in the isotherm occurred. Moreover, Schuller also spread millimeter-sized Styropor particles and found isotherms of similar shape [66]. By taking pictures at different surface pressure, he was able to correlate the shape with different states of order in the monolayer. Shortly after that. 

Serizawa and Akashi [95] analyzed the monolayer adsorption of polystyrene latex particles with cationic polyvinylamine grafted on their surface, while Serizawa et al. [96,97] used commercial anionic latex particles. Both types of particles were adsorbed on polyelectrolyte-coated substrates previously prepared by alternating adsorption of cationic and anionic polyelectrolytes such as polyallylamine hydrochloride (PAH) and polystyrene sulfonate sodium salt (PSS) according to the method described by Decher [164]. Using... 

Particle separation can be characterized by the separation factor, Rp, which is the ratio of eluant to particle elution volumes, or, by the difference in elution voliame, AV, between particle and eluant marker turbidity peaks. For polystyrene monodisperse standards, a linear relationship occ irs between the log of the particle diameter and AV, with a series of parallel lines resulting for different concentration of either salt or surfactant below its critical micelle concentration (IT>18,19) The separation factor has also been shown to be independent of eluant... 

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