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Graft polymer architecture

Variations in the graft polymer architectures are possible by controlling the... [Pg.231]

Recalling the demands on the polymer architecture of a polymer brush and the projected properties in terms of swelling, wetting and friction, as described in the theoretical work, the brush has to consist of linear polymer chains of the same length at high grafting densities. The closest approximation to this can be obtained by the living anionic SIP (LASIP). The experimental difficulties outlined mean that only relatively few examples of LASIP are documented in the literature. [Pg.414]

A number of different types of copolymers are possible with ATRP—statistical (random), gradient, block, and graft copolymers [Matyjaszewski, 2001]. Other polymer architectures are also possible—hyperbranched, star, and brush polymers, and functionalized polymers. Statistical and gradient copolymers are discussed in Chap. 6. Functionalized polymers are discussed in Sec. 3-16b. [Pg.322]

Statistical, gradient, and block copolymers as well as other polymer architectures (graft, star, comb, hyperbranched) can be synthesized by NMP following the approaches described for ATRP (Secs. 3-15b-4, 3-15b-5) [Hawker et al., 2001]. Block copolymers can be synthesized via NMP using the one-pot sequential or isolated macromonomer methods. The order of addition of monomer is often important, such as styrene first for styrene-isoprene, acrylate first for acrylate-styrene and acrylate-isoprene [Benoit et al., 2000a,b Tang et al., 2003]. Different methods are available to produce block copolymers in which the two blocks are formed by different polymerization mechanisms ... [Pg.327]

Edgecombe BD, Stein JA, Frechet JMJ, Xu Z, Kramer EJ. The role of polymer architecture in strengthening polymer— polymer interfaces a comparison of graft, block, and random copolymers containing hydrogen-bonding moieties. Macromolecules 1998 31 1292-1304. [Pg.96]

Among the two ionic polymerization techniques mentioned above, a living anionic polymerization should show the best possible control of polymer architecture and composition. Mono dispersed homopolymers, complex-block, graft, star, and miktoarm architectures have been accessible primarily by anionic polymerization methods [22]. They have been used to grow polymer brushes from various small particles such as silica gels graphite,carbon black, and flat surfaces [23-26]. Recent results have been reported on living anionic polymerizations on clay [27] and silica nanoparticles [28,29]. [Pg.113]

Chapter 4 shows that the range of polymeric structures from enzymatic polymerization can be further increased by combination with chemical methods. The developments in chemoenzymatic strategies towards polymeric materials in the synthesis of polymer architectures such as block and graft copolymers and polymer networks are highlighted. Moreover, the combination of chemical and enzymatic catalysis for the synthesis of unique chiral polymers is discussed. [Pg.158]

Figure 1 Macromolecular architectures linear macromolecular chains (homopolymer, block-copolymer and statistical copolymer [14]), brushed-polymer (= linear chains attached to a polymer-chain brush-polymer, brush-copolymers [14]), star polymer [4], mikto-star-polymer [16], arborescent graft polymer (=repeated grafting of linear chains on a macromolecule [17,18]), dendrimer (= maximally branched, regular polymer [15])... Figure 1 Macromolecular architectures linear macromolecular chains (homopolymer, block-copolymer and statistical copolymer [14]), brushed-polymer (= linear chains attached to a polymer-chain brush-polymer, brush-copolymers [14]), star polymer [4], mikto-star-polymer [16], arborescent graft polymer (=repeated grafting of linear chains on a macromolecule [17,18]), dendrimer (= maximally branched, regular polymer [15])...
The main feature of polymers is their MMD, which is well known and understood today. However, several other properties in which the breadth of distribution are important and influence polymer behavior (see Figure 1) include physical, the classical chain-length distribution chemical, two or more comonomers are incorporated in different fractions topological, polymer architecture may differ (e.g., linear, branched, grafted, cyclic, star or comb-like, and dendritic) structural, comonomer placement may be random, block, alternating, and so on and functional, distribution of chain functions (e.g., all chain ends or only some carry specific groups). Other properties the polymers may disperse (tacticity and crystallite dimensions) are not of the same general interest or cannot be characterized by solution methods. [Pg.224]

To synthesise polymers with unusual properties from existing basic monomers one needs to place the monomer units in ordered arrays rather than at random. Thus polymer architecture control remains an important area of research. Possible structural elements include block, graft and comb copolymers as well as star and dendritic/hyperbranched topographies. Potential for such structures in the surface coatings and adjacent industries include use as... [Pg.19]

I/III. Complex Macromolecular Architectures A. Star and Graft Polymers... [Pg.122]

Enzymes are perfectly equipped to convert substrates into products in high enantio-, regio-, or chemoselectivity, a property that is commonly used in industry to prepare optically active fine-chemical intermediates [5]. More specifically, lipases appeared as ideal catalysts as a result of their high enantioselectivity, broad substrate scope and stability. In addition, lipases are powerful catalysts for the preparation of polyesters, polycarbonates and even polyamides, as is reviewed in Chapters 4 and 5 of this book. Moreover, a variety of different polymer architectures such as block copolymers, graft copolymers etc have been prepared using lipases as the catalyst (see Chapter 12). [Pg.277]


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