Synthetic polymers cross-linked

Gels of this type can also be used in water and some polar organic solvents. They tend to be more stable than Sephadex, especially under acidic conditions. Polyacrylamides can be used for many biochemical applications involving macromolecules. For separating synthetic polymers, cross-linked polystyrene beads (copolymer of styrene and divinylbenzene) find common application. Again, the beads are swollen before use. Common organic solvents can be used to elute the... 

Nitrile oxide precursors have been prepared by the reaction of an isocyanate and an alkyl nitroacetate. These precursors release alkanol and carbon dioxide when heated, to liberate the highly reactive nitrile oxide species. An improved synthetic procedure has been developed to afford novel cross-linking agents based on difunctional, trifunctional and aliphatic precursors. Application of these agents to polymer cross-linking has been demonstrated (527). 

Cross-linked elastomers (the other main class of polymers studied by ESR) can be pre-strained above Tg to any desired extent (up to fracture) and their orientation stabilised by cooling below Tg before testing. At high pre-strains, strain-induced crystallization may occur providing a morphology essentially similar to that of synthetic fibres Cross-linked polymers may therefore be used to explore in a systematic manner, the role of strain and orientation in rmlecular fracture. 

Cis-l,4-poly(butadienes) are very resistant to abrasion and are therefore used for car tires. Compared to tires of cis-poly(isoprene), they generate less heat in use. This heat causes increased plasticity and decreased elasticity. In cfs-poly(isoprene), the elasticity is preserved by stronger cross-linking of the polymer. Cross-linking raises the glass-transition temperature, however consequently the elasticity of the tires at low temperatures is poor. Thus, cis-poly(butadiene) tires have better elasticity at low temperatures, whereas under normal road conditions they are somewhat poorer in this respect but possess very good wear characteristics. Under normal road conditions, pure cis-l,4-poly(butadiene) tires exhibit poorer road grip than cis-l,4-poly(isoprene) tire rubber is therefore a poly blend of c/s-l,4-poly(butadiene) with natural or synthetic poly(isoprene) or with Buna S. 

Various derivatives have been explored in various studies e.g. in one study three types of cross-linked chitosan polymers were investigated for their adsorption capability for multiple mycotoxins, including allatoxin Bj (AFB,), ochratoxin A (OTA), zearalenone (ZEN), fumonisin B,(FB,), deoxynivalenol (DON) andT-2 toxin (T2). Among these synthetic adsorbents, cross-linked chitosan-glutaraldehyde complex presented the highest adsorption capability for aflatoxin B, (73 %), ochratoxin A... 

Alternatively the ion exchanger may be a synthetic polymer, for example a sulphonated polystyrene, where the negative charges are carried on the —SO3 ends, and the interlocking structure is built up by cross-linking between the carbon atoms of the chain. The important property of any such solid is that the negative charge is static—a part of the solid—whilst the positive ions can move from their positions. Suppose, for example, that the positive ions are... 

A polymer is a macromolecule that is constructed by chemically linking together a sequent of molecular fragments. In simple synthetic polymers such as polyethylene or polystyrer all of the molecular fragments comprise the same basic unit (or monomer). Other poly me contain mixtures of monomers. Proteins, for example, are polypeptide chains in which eac unit is one of the twenty amino acids. Cross-linking between different chains gives rise to j-further variations in the constitution and structure of a polymer. All of these features me affect the overall properties of the molecule, sometimes in a dramatic way. Moreover, or... 

An important application of Eq. (3.39) is the evaluation of M, . Flory et al.t measured the tensile force required for 100% elongation of synthetic rubber with variable crosslinking at 25°C. The molecular weight of the un-cross-linked polymer was 225,000, its density was 0.92 g cm , and the average molecular weight of a repeat unit was 68. Use Eq. (3.39) to estimate M. for each of the following samples and compare the calculated value with that obtained from the known fraction of repeat units cross-linked ... 

EPDM-Derived Ionomers. Another type of ionomer containing sulfonate, as opposed to carboxyl anions, has been obtained by sulfonating ethylene—propjlene—diene (EPDM) mbbers (59,60). Due to the strength of the cross-link, these polymers are not inherently melt-processible, but the addition of other metal salts such as zinc stearate introduces thermoplastic behavior (61,62). These interesting polymers are classified as thermoplastic elastomers (see ELASTOLffiRS,SYNTHETIC-THERMOPLASTICELASTOLffiRS). 

The use of TAG as a curing agent continues to grow for polyolefins and olefin copolymer plastics and mbbers. Examples include polyethylene (109), chlorosulfonated polyethylene (110), polypropylene (111), ethylene—vinyl acetate (112), ethylene—propylene copolymer (113), acrylonitrile copolymers (114), and methylstyrene polymers (115). In ethylene—propylene copolymer mbber compositions. TAG has been used for injection molding of fenders (116). Unsaturated elastomers, such as EPDM, cross link with TAG by hydrogen abstraction and addition to double bonds in the presence of peroxyketal catalysts (117) (see Elastol rs, synthetic). 

Antioxidants. The 1,2-dihydroquinolines have been used in a variety of ways as antioxidants (qv). For example, l,2-dihydro-2,2,4-trimethylquinoline along with its 6-decyl [81045-48-9] and 6-ethoxy [91-53-2] derivatives have been used as antio2onants (qv) and stabilizers (68). A polymer [26780-96-1] of l,2-dihydro-2,2,4-trimethylquinoline is used in resins, copolymers, lubricant oils, and synthetic fibers (69). These same compounds react with aldehydes and the products are useful as food antioxidants (70). A cross-linked polyethylene prepared with peroxides and other monomers in the presence of l,2-dihydro-6-ethoxyquinoline produces polymers with a chemically bonded antioxidant (71). 

Hydrogels, ie, gelatin and agar, have been known for a long time. In the late nineteenth century, Herschel proposed the use of jelly materials on the cornea for the correction of vision (108). In 1960, the use of synthetic hydrogels for contact lenses was proposed and several U.S. patents were obtained for the invention of cross-linked hydrophilic polymers, eg, systems based on 2-hydroxethyl methacrylate [868-77-9] (HEMA) (5) (109—112). 

Isobutjiene was first polymerized ia 1873. High molecular weight polymer was later synthesized at I. G. Farben by decreasiag the polymerization temperature to —75°, but the saturated, unreactive polymer could not be cross-linked iato a useful synthetic elastomer. It was not until 1937 that poly(isobutylene- (9-isoprene) [9010-85-9] or butyl mbber was iavented at the Standard Oil Development Co. (now Exxon Chemical Co.) laboratories (1). 

Blends of isobutylene polymers with thermoplastic resins are used for toughening these compounds. High density polyethylene and isotactic polypropylene are often modified with 5 to 30 wt % polyisobutylene. At higher elastomer concentration the blends of butyl-type polymers with polyolefins become more mbbery in nature, and these compositions are used as thermoplastic elastomers (98). In some cases, a halobutyl phase is cross-linked as it is dispersed in the polyolefin to produce a highly elastic compound that is processible in thermoplastic mol ding equipment (99) (see Elastomers, synthetic-thermoplastic). ... 

Fluoiocaibon elastomeis aie synthetic, noncrystaUine polymers that exhibit elastomeric properties when cross-linked. They are designed for demanding service appHcations in hostile environments characterized by broad temperature ranges and/or contact with chemicals, oils, or fuels. 

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