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Multiblock copolymers applications

Multiannular nozzle design, 16 8, 9 MultiBatchDS software, 26 1040 Multibladed disk turbines, 15 692-693 Multiblock copolymers, applications of, 24 715-716 MULTICASE, 6 19... [Pg.605]

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]

The A-B type iniferters are more useful than the B-B type for the more efficient synthesis of polymers with controlled structure The functionality of the iniferters can be controlled by changing the number of the A-B bond introduced into an iniferter molecule, for example, B-A-B as the bifunctional iniferter. Detailed classification and application of the iniferters having DC groups are summarized in Table 1. In Eqs. (9)—(11), 6 and 7 serve as the monofunctional iniferters, 9 and 10 as the monofunctional polymeric iniferters, and 8 and 11 as the bifunctional iniferters. Tetrafunctional and polyfunctional iniferters and gel-iniferters are used for the synthesis of star polymers, graft copolymers, and multiblock copolymers, respectively (see Sect. 5). When a polymer implying DC moieties in the main chain is used, a multifunctional polymeric iniferter can be prepared (Eqs. 15 and 16), which is further applied to the synthesis of multiblock copolymers. [Pg.83]

The PPDX-fr-PCL diblock copolymers were recently synthesized [111] and apart from the references already mentioned, only the contribution of Lendlein and Langer [112] deals with chemically similar materials, although structurally quite different since they employed multiblock copolymers of PPDX and PCL with very low molecular weights to prepare shape memory polymers for biomedical applications. [Pg.42]

The actual knowledge of the basic molecular structure property relationships relies mainly on the availability of well defined linear architectures the di, tri- and multiblock copolymers. New and well controlled molecular structures could undoubtedly provide a deep understanding of the behavior of block copolymers and a more efficient mastering of their applications. ... [Pg.212]

Multiblock Copolymers. Replacement of conventional vulcanized mbber is the main application for the polar polyurethane, polyester, and polyamide block copolymers. Like styrenic block copolymers, they can be molded or extmded using equipment designed for processing thermoplastics. Melt temperatures during processing are between 175 and 225°C, and predrying is required scrap is reusable. They are mostly used as essentially pure materials, although some work on blends with various thermoplastics such as plasticized and unplasticized PVC and also ABS and polycarbonate (14,18,67—69) has been reported. Plasticizers intended for use with PVC have also been blended with polyester block copolymers (67). [Pg.19]

The polyetherimide—polysiloxane multiblock copolymers are relatively hard (about 70 on the Shore D scale). Their main application is flame-resistant wire and cable covering (24), where they combine very low flammability with a low level of toxic products in the smoke. This unusual and vital combination of properties justifies their relatively high price, about 37/kg, at a specific gravity of about 1.2. [Pg.20]

Numerous authors took advantage of the reactivity of double bonds towards ozone to prepare a-(0 functional oligomers usable in the synthesis of multiblock copolymers by copolycondensation, or in the synthesis of precursors of surfactants or ionomer resins. Results in this field of investigation are numerous, mainly in terms of industrial applications. [Pg.60]

Defined diblocks, triblock or multiblock copolymers find important applications in the areas of thermoplastic elastomers, data storage technology [126], and as compatibilizers (e.g. in polymer blends). In thin films these polymers may display different morphologies than in the bulk, which necessitates an accurate analysis. [Pg.143]

A completely different approach has been recently developed in that prospect, based on the assumption that "properties similar to those of multiblock copolymers could be reached, in a more versatile manner, by replacing their hard segments by single groupings, provided the molecular characteristics of these groupings promote very strong mutual interactions, at least in the media envisoned for their applications". [Pg.330]

Ilyin, V. V, Bilibin, A. Yu. (2002). Synthesis and Properties of Multiblock-Copolymers Consisting of Flexible and Rigid-Link Blocks / in Materials of the 3-rd Youth School-Conference on Organic Synthesis. Sankt-Petersburg, 230-231. [in Russian]. Germany Patent Application hfo 19907605. 2000. [Pg.182]

Lee HS, Roy A, Lane O, Lee M, McGrath JE. Synthesis and characterization of multiblock copolymers based on hydrophilic disulfonated poly(arylene ether sulfone) and hydrophobic partially fluorinated poly(arylene ether ketone) for fuel cell applications. J Polym Sci Part A Polym Chem 2010 48(l) 214-22. [Pg.206]

Block copolymer self-assembly is a very promising alternative to make cylindrical polymer brushes. These brushes can replace the function and roles of molecular bmshes in many fields however, if the response of the main chain is necessary or in the case of multiblock copolymer side chains, they will fail to satisfy the application. [Pg.225]


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See also in sourсe #XX -- [ Pg.98 ]




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