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Block polymerization

A -isopropyl acrylamide (N1PA VI) copolymerization by RAFT 529 JV-isopropyl acrylamide (Ml PAV1) polymerization block copolymers 543, 546 with dithiocarbamale photmnitiaior 465... [Pg.615]

The precipitated silica (J. Crosfield Sons) was heated in vacuo at 120° for 24h. before use. Two grades of surface areas 186 and 227 m g l (BET,N2), were used during this project. Random copolymers, poly(methyl methacrylates) and polystyrene PS I were prepared by radical polymerization block polymers and the other polystyrenes were made by anionic polymerization with either sodium naphthalene or sodium a methylstyrene tetramer as initiator. The polymer compositions and molecular weights are given in Table I. [Pg.298]

Controlled expansion alloys, 13 520-522 Controlled flavor release systems, 11 528, 543-553, 554-555 characteristics of, ll 544t demand for, 11 555 developments in, 11 558 elements of, 11 555-557 extrusion encapsulation for, 11 550 key aspects of, 11 556t morphologies of, 11 545 Controlled free-radical polymerization, block copolymers, 7 646 Controlled humidity drying, ceramics processing, 5 655-656 Controlled indexing, 18 241 Controlled initiation, 14 268-269 Controlled laboratory studies, in... [Pg.214]

The book consists of four articles reviewing the literature based on the authors own experiences over the last decade in this field. It does not claim to be exhaustive nor to provide complete coverage of the very extensive literature in this field. Instead, it focuses on the currently intense areas of research namely living polymerization, block copolymer synthesis, synthesis of dendrimers and finally macroporous thermosets. Hopefully, this volume will not only serve as a book on the design of macromolecular architectures but also as a source of inspiration to produce polymers combining several functional properties. [Pg.248]

The arms are block copolymers which may or not have the same composition and molecular weight but differ with respect to the polymeric block which is attached to the central point. [Pg.75]

Figure 16.23. Proton image of the polymer in a crosslinked silicone polymeric block that contains in situ precipitated silica filler. Figure 16.23. Proton image of the polymer in a crosslinked silicone polymeric block that contains in situ precipitated silica filler.
In addition to the sequential living polymerizations, block copolymers may be synthesized by various reactions of end-functionalized polymers. The method may be subdivided into two classes, as discussed in Section III. A. Most of the examples via living cationic polymerizations are based on vinyl ethers, and Fig. 8 lists the second monomers used in these vinyl ether-based block copolymers. Similar syntheses based on the inifer methods are discussed elsewhere [1,3]. [Pg.396]

Back-biting reaction occurring during cationic polymerization of lactams is detrimental to preparation of block copolymers of two different lactams by sequential polymerization. Block copolymers can be obtained only in those systems in which the rate of polymerization of the second monomer is much higher than the rate of chain transfer to polymer resulting in transamidation [219]. [Pg.520]

Block copolymers are made of two or more chemically distinct sequences, or polymeric blocks (see Fig. 13-1) (Molau 1971 Aggarwal 1976 Folkes 1985 Bates and Fredrickson 1990) The simplest type of block copolymer is the diblock, which contains a sequence of type A monomers covalently bonded to a sequence of type B monomers. A triblock... [Pg.594]

Topological Asymmetry. The arms of the star are block copolymers that may have the same molecular weight and composition but differ with respect to the polymeric block that is covalently attached to the core of the star. [Pg.575]

Keywords Review, Copolymer, Controlled/living radical polymerization, Block, Graft, Gradient, Statistical... [Pg.7]

Recent advances in polymer synthetic chemistry have allowed the development of elegant and more complicated architectural polymers. This has been driven predominantly by the development of various controlled polymerization methodologies, particularly in the area of free radical polymerization [45-49]. This has equipped the polymer chemist with a rich and abundant synthetic toolbox. In general, these architectural polymers are based on the principle of being able to sequentially add different polymeric blocks with defined molecular weight into a single polymer chain [50]. The synthesis of block copolymers is particularly suited to the combination of two different polymerization techniques. This can be quite easily achieved by the use of a bifunctional initiator and is an elegant synthetic... [Pg.329]

Since the anionically polymerized block copolymers are relatively expensive they have been more frequently used in blends with engineering than commodity resins. Owing to miscibility of styrene blocks with PPE, the SBS and SEBS are natural tougheners for this polymer. However, for blending with PEST, PC, POM or PA, the copolymer should be modified by incorporation of acidic, acid anhydride, or epoxy moieties. [Pg.36]


See other pages where Block polymerization is mentioned: [Pg.730]    [Pg.85]    [Pg.157]    [Pg.213]    [Pg.24]    [Pg.176]    [Pg.152]    [Pg.135]    [Pg.248]    [Pg.114]    [Pg.33]    [Pg.105]    [Pg.362]    [Pg.144]    [Pg.123]    [Pg.49]    [Pg.113]    [Pg.330]    [Pg.330]    [Pg.175]    [Pg.11]    [Pg.137]    [Pg.174]    [Pg.330]   
See also in sourсe #XX -- [ Pg.255 ]

See also in sourсe #XX -- [ Pg.480 ]




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