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Cross-linked elastomers applications

Rubber base adhesives can be used without cross-linking. When necessary, essentially all the cross-linking agents normally used in the vulcanization of natural rubber can be used to cross-link elastomers with internal double carbon-carbon bonds. A common system, which requires heat to work, is the combination of sulphur with accelerators (zinc stearate, mercaptobenzothiazole). The use of a sulphur-based cross-linking system with zinc dibutyldithiocarbamate and/or zinc mercaptobenzothiazole allows curing at room temperature. If the formulation is very active, a two-part adhesive is used (sulphur and accelerator are placed in two separate components of the adhesive and mixed just before application). [Pg.640]

The process that makes the chemistry, properties, and applications of elastomers so different from other polymers is cross-linking with sulfur, commonly called vulcanization. The modem method of cross-linking elastomers involves using a mixture of sulfur and some vulcanization accelerator. Those derived from benzothiazole account for a large part of the market today. Temperatures of 100-160°C are typical. [Pg.331]

Methods for detecting whether peroxy compound have been used for cross-linking elastomers have been reviewed. An important application of dialkyl peroxides is as initiators of cross-linking and graft polymerization processes. The success of both processes depends on the ability of the peroxide to produce free radicals and the ability of the free radicals for H-abstraction from a relevant donor substrate. A method for evaluating this ability consists of inducing thermal decomposition of the peroxide dissolved in a mixture of cyclohexane and MSD (225). The free radical X" derived from the... [Pg.706]

Another application would be to minimize the swelling of a cross-linked elastomer in contact with a solvent. In this case, of course, one would be looking for a polymer giving the largest mismatch with the solubility parameters of the solvent to which the elastomer was to be exposed. [Pg.33]

The use of these monomers for radiation cross-linking of polyethylene has been suggested [66]. With benzophenone as a photosensitizer, atactic as well as isotactic polypropylene is crosslinked with allyl acrylate by UV radiation. In this process both types of double bonds react [67]. Elastomers such as ethylene-vinyl acetate copolymer have been cross-linked with this monomer on a roller mill at 150°C using dicumyl peroxide as the initiator. Such cross-linked elastomers exhibit little or no swelling with aromatic solvents or chloroform after 24 hr at 30°C, conditions under which the uncured elastomers ordinarily dissolve [68]. Despite these interesting applications for such monomers, the bulk of the commercially produced allyl methacrylate finds application as a synthetic intermediate rather than as a monomer. [Pg.306]

Thermoplastic elastomers, as they are called, are constructed according to a similar principle. They are block copolymers in which a flexible block Tq < application temperature) occurs between two rigid blocks (Tq > application temperature). The different blocks are mutually incompatible. The rigid blocks form physical cross-links. At the application temperature, the material behaves as a cross-linked elastomer. At higher temperatures, the rigid blocks are also above the glass-transition temperature, the physical cross-links are lost, and the material can be deformed like a thermoplast. [Pg.424]

The hard sequence enables further physical cross-linking. The applications of such triblock thermoplastic elastomers are for seal, 0-rings, shafts, for aeronautics (shuttles), and for the automotive industry (oil-resistant tubing). [Pg.100]

In order to produce a rubbery material the polymer must have a flexible baekbone, be suffieiently irregular in structure to be non-crystalline and also contain a site for cross-linking. These are of course requirements applicable equally to any potential elastomer whether or not it contains fluorine. [Pg.379]

Elastomeric composition for dynamic application of cross-linked E-plastomers has been made with filer-reinforced systems which contain a metal salt (typically zinc) of an alpha, beta unsaturated acid. These additives improve the tensile and tear strength of the elastomer and are cured with a peroxide cure system. These cross-linked articles are suitable for dynamic loading applications such as belting, including power transmission and flat belting. [Pg.172]

After almost half a century of use in the health field, PU remains one of the most popular biomaterials for medical applications. Their segmented block copolymeric character endows them with a wide range of versatility in tailoring their physical properties, biodegradation character, and blood compatibility. The physical properties of urethanes can be varied from soft thermoplastic elastomers to hard, brittle, and highly cross-linked thermoset material. [Pg.236]

Obviously, there exists severe interplastics competition, e.g. PP vs. ABS, clarified PP vs. PS, PA, PVC, HDPE and PS (Table 10.7). A wide range of cross-linked and thermoplastic elastomer applications, from footware to automotive parts and toothbrushes, are adopting new metallocene-catalysed polyolefin elastomers (POEs). These low-density copolymers of ethylene and octene were first accepted as impact modifiers for TPOs, but now displace EPDM, (foamed) EVA, flexible PVC, and olefinic thermoplastic vulcanisates (TPVs). Interpolymer competition may also result from... [Pg.715]

The Material of the Example. Poly(ether ester) (PEE) materials are thermoplastic elastomers. Fibers made from this class of multiblock copolymers are commercially available as Sympatex . Axle sleeves for automotive applications or gaskets are traded as Arnitel or Hytrel . Polyether blocks form the soft phase (matrix). The polyester forms the hard domains which provide physical cross-linking of the chains. This nanostructure is the reason for the rubbery nature of the material. [Pg.172]

Silicones are frequently used in transdermal drug delivery. Recently, the use of loosely cross-linked silicone elastomer blends for this application was surveyed.537 The mechanisms of controlled drug release in the silicone-based systems have been studied,538 as silicones are evaluated for relatively new protein drug-delivery systems.5... [Pg.680]

SS-LINKED POLYMERS ARE USED in a wide variety of aerospace, automotive, building construction, and consumer product applications. Not all paints, adhesives, composites, and elastomers are cross-linked, but cross-linking systems are often used in these applications when resistance to solvents, resistance to high temperatures, and high mechanical performance are required. These important properties can be traced directly to the three-dimensional interconnected molecular network that is characteristic of cross-linked systems. [Pg.1]

Diamine curatives were the first cross-linking agents for fluorocarbon mbbers. They are corrosive to mild steel molds and have been replaced in many applications by the bisphenol or other more recent cure systems. Nevertheless, some diamines are still used for food-contact applications of fluorocarbon mbbers and in zinc-free cures of halobutyl mbbers for pharmaceutical stoppers. Methylene dianiline and triethylene tetramine are cross-linking agents for ethylene—acrylic elastomers. [Pg.225]


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See also in sourсe #XX -- [ Pg.503 ]




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