Polymers insoluble

Nonaqueous Dispersion Polymerization. Nonaqueous dispersion polymers are prepared by polymerizing a methacryhc monomer dissolved in an organic solvent to form an insoluble polymer in the presence of an amphipathic graft or block copolymer. This graft or block copolymer, commonly called a stabilizer, lends coUoidal stabiUty to the insoluble polymer. Particle sizes in the range of 0.1—1.0 pm were typical in earlier studies (70), however particles up to 15 pm have been reported (71). 

Divinylbenzene. This is a specialty monomer used primarily to make cross-linked polystyrene resins. Pure divinylbenzene (DVB) monomer is highly reactive polymericaHy and is impractical to produce and store. Commercial DVB monomer (76—79) is generally manufactured and suppHed as mixtures of m- and -divinylbenzenes and ethylvinylbenzenes. DVB products are designated by commercial grades in accordance with the divinylbenzene content. Physical properties of DVB-22 and DVB-55 are shown in Table 10. Typical analyses of DVB-22 and DVB-55 are shown in Table 11. Divinylbenzene [1321 -74-0] is readily polymerized to give britde insoluble polymers even at ambient temperatures. The product is heavily inhibited with TBC and sulfur to minimize polymerization and oxidation. 

Polymerization. Chloroprene is normally polymerized with free-radical catalysts in aqueous emulsion, limiting the conversion of monomer to avoid formation of cross-linked insoluble polymer. At a typical temperature of 40°C, the polymer is largely head-to-taH in orientation and trans in configuration, but modest amounts of head-to-head, cis, 1,2, and 3,4 addition units can also be detected. A much more regular and highly crystalline polymer can be made at low temperature (11). Chloroprene can also be polymerized with cationic polymerization catalysts, giving a polymer with... 

Solids may be processed continuously or semicontinuously by pumping slurries or by using lock hoppers. An example is the separation of insoluble polymers by floatation with a variable-density SCF. For liquid feeds, multistage separation may be achieved by continuous counter-current extraction, much like conventional liquid-hquid extraction. The final produces may be recovered from the extract phase by a depressurization, a temperature change, or by conventional distillation. 

Growing ot a polypeptide chain by attachment ot the first aminoadd to an insoluble polymer and attaching successively amirx>acids At the end cleavage of the peptide from the polymer... 

These are all examples of soluble polymers. Combinations of soluble with insoluble polymers have also been reported. Polychloroprene or chlorosulfonated polyethylene was eombined with core-shell polymer particles to give an adhesive with improved cold impact resistance [33]. The fascinating chemistry of chlorosulfonated polyethylene in acrylic adhesives will be further discussed in the section on initiators. In many cases chlorosulfonated polyethylene is chemically attached to the acrylic matrix. 

Catalytic asymmetric dihydroxylation of alkenes with participation of insoluble polymer-bound cinchonine alkaloids 99SLI181. 

Acrylamide readily undergoes polymerization by conventional free radical methods, ionizing radiation, ultrasonic waves, and ultraviolet radiation. The base-cata-lized hydrogen transfer polymerization of acrylamide yields poly-/3-alanine (Nylon 3) a water insoluble polymer that is soluble in certain hot organics. All current industrial production is believed to be by free radical polymerization. 

In a pioneering article, Farrall et al. [61] reported the preparation of fuUy regenerable sulfonium salts anchored to an insoluble polymer and their use in the preparation of epoxides by reaction of their ylides with carbonyl compounds. Their results clearly indicate that... 

A second Boc-protected amino acid is coupled to the first by reaction with DCC. Excess reagents are removed by washing them from the insoluble polymer. 

Robotic peptide synthesizers are now used to automatically repeat the coupling, washing, and deprotection steps with different amino acids. Each step occurs in high yield, and mechanical losses are minimized because the peptide intermediates are never removed from the insoluble polymer until the final step. Using this procedure, up to 25 to 30 mg of a peptide with 20 amino acids can be routinely prepared. 

Polyphenyls Polyphenylene oxide Decompose at 530°C (986°F) infusible, insoluble polymers. Decomposes close to 500°C (932°F) heat cures above 150° C (302°F) to elastomer usable heat range —135-185 C (—211-365°F). 

The furfuryl esters of acrylic and methacrylic acid polymerize via a free-radical mechanism without apparent retardation problems arising from the presence of the furan ring. Early reports on these systems described hard insoluble polymers formed in bulk polymerizations and the cross-linking ability of as little as 2% of furfuryl acrylate in the solution polymerization of methylacrylate121. ... 

The polymerization of nonconjugated diene monomers might be expected to afford polymer chains with pendant unsaturation and ultimately, on further reaction of these groups, crosslinked insoluble polymer networks. Thus, the finding by Butler et a .,, 03, n5 that polymerizations of diallylammonium salts, of general structure 8 [e.g. diallyldimethylammonium chloride (9)] gave linear saturated polymers, was initially considered surprising. 

Hall and Steuck polymerized 2 with a variety of Lewis and Bronsted acids or oxonium salts. The best conditions for the polymerization proved to be the use of phosphorus pentafluoride in methylene chloride solution at -78 °C. Yields of methanol-insoluble polymers ranging from 68 to 84% were obtained with inherent viscosities of 0.26—0.33 dl/g. Lower or higher temperatures gave lower yields. Tetra-hydrofuran as solvent at —78 °C gave 68-92% yields of materials having inherent viscosities of 0.12-0.14 dl/g. No incorporation of tetrahydrofuran into the polymer occurred. 

AGX are also the dominant hemicelluloses in the cell walls of hgnified supporting tissues of grasses and cereals. They were isolated from sisal, corncobs and the straw from various wheat species [4]. A more recent study on corncob xylans [30] showed the presence of a hnear, water-insoluble polymer... 

In addition to the insoluble polymers described above, soluble polymers, such as non-cross-linked PS and PEG have proven useful for synthetic applications. However, since synthesis on soluble supports is more difficult to automate, these polymers are not used as extensively as insoluble beads. Soluble polymers offer most of the advantages of both homogeneous-phase chemistry (lack of diffusion phenomena and easy monitoring) and solid-phase techniques (use of excess reagents and ease of isolation and purification of products). Separation of the functionalized matrix is achieved by either precipitation (solvent or heat), membrane filtration, or size-exclusion chromatography [98,99]. 

Chang, R. K., Price, J. C., and Whitworth, C. W., Enhancement of dissolution rate by incorporation into a water insoluble polymer, polycaprolactone. Drug Dev. Ind. Pharm., 13. 249-256, 1987. 

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