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Block copolymers derivatives

Block Copolymers Derived from Macroinitiators Recent Advances of Synthesis, Properties, and Applications... [Pg.755]

Additionally, some properties unique to both systems may result. The majority of homopolymer blends are immiscible with one another and often experience poor interfacial adhesion between the separate phases. Since block copolymers are covalently linked together, macroscopic incompatibility at the interface is minimized. The macroscopic incompatibility of a two-polymer blend may be eliminated by the addition of a block copolymer derived from the two systems. Hence, copolymers can be used to strengthen blends of immiscible polymers by serving as emulsifiers (7-9). [Pg.159]

SuPAES). In common with the previously mentioned PEMs, initial SuPAES materials (see Section 3.3.2.1 for later work on block copolymer derivatives of SuPAES) had a statistical distribution of sulfonic acid groups along the polymer backbone. However, instead of using postsulfonation techniques, sulfonic acid groups were introduced via direction copolymerization that is, suitable sulfonic acid precursor groups were introduced into one of the monomers (13). The advantages of this method are threefold ... [Pg.144]

Those block copolymers, derived from more than two monomers, that also exhibit statistical block sequence arrangements are named according to the principles of Rule 2.1. [Pg.375]

Imide block copolymers derived from PAEH have been investigated as a means of modifying self-adhesion properties of semi-rigid polyimides, e.g. [Pg.107]

Bazan [1] prepared cationic conjugated flexible block copolymer derivatives, (IV), containing alkyl substituents along the main chain that disrupted extended-rod stmcture formation. These were then used in optoelectronic devices and biosensors. [Pg.450]

Styrenic block copolymers derive their useful properties from their ability to form distinct styrene (hard phase) and diene (rubber phase) domains, with well defined morphologies. To achieve this requires an unusual degree of control over the polymerization. The polymerization must yield discrete blocks of a uniform and controlled size, and the interface between the blocks must be sharp. This is best achieved by so-called living polymerization. For a polymerization to be classified as truly living, it is generally accepted that it must meet several criteria [3] ... [Pg.465]

Block Copolymers between the Same Family of Monomers. Block copolymers derived from the same family of monomers (Figure 16) are obtained relatively easily, because the two monomers can normally be polymerized with common initiating systems and under similar reaction conditions. [Pg.489]

Naka K., Nakamura T., Okhi A., Maeda S. Aggregates of amphiphilic block copolymers derived from poly((A-acylimido)ethylene) and their complexes with lipase in water. Polymer J. 1995 27(11) 1071-1078. [Pg.741]

ZYLAR series of alloys of brittle polymer, ductile polymer and rubbery polymer are available from Novacor Chemicals, Inc. The components are brittle polymer, styrene (70 wt%) and methyl methacrylate (30 wt%) (Novacor s NAS30) ductile polymer, block copolymer derived from styrene (75 wt%) and butadiene (25 wt%) and rubbery polymer, a tapered polymer derived from styrene (43 wt%) and butadiene (57 wt%). No specific gamma stabilizers were added to these polymer alloys. [Pg.848]

In the second group of monomers are 5-cyano-6-phenylnorbom-2-ene (Ueshima 1974) and ran5-5-carbomethoxy-6-ferrocenylnorbom-2-ene. In the latter case fluorescence quenching studies have been made as for the polymers and block copolymers derived from 81 (Albagli 1992b, 1993). [Pg.311]

Wright ER, Conticello VP. Self-assembly of block copolymers derived from elastin-mimetic polypeptide sequences. Adv Drug Delivery Rev 2002 54 1057-1073. [Pg.450]

Block copolymers exhibit outstanding potential for a variety of applications as a result of their self-assembly into supramolecular structures (see Chapter 1, Section 1.2.5). However, the exploration of metal-containing multiblock materials was only begun in the early 1990s. Block copolymers derived from the living anionic polymerization of vinylferrocene were already mentioned in Section 2.2.1.1. In this section, side-chain metal-containing block copolymers are surveyed. Examples of block copolymers with metals in the main chain will be discussed in Chapter 3 (Section 3.3.8) and Chapter 7 (Section 7.2.3). [Pg.62]

E. N. Peters, TelecheUc polyisobutylene and block copolymer derivatives, U.S. Patent... [Pg.380]

In contrast, very little attention has been paid to block copolymers derived from two hard components. This type of copolymer could include glassy-glassy, glass-crystal, or crystal-crystal morphologies. Block copolymers such as these may also give rise to novel materials with improved properties over those of the homopolymer counterparts. [Pg.959]

Inoue, H., Block copolymers derived from azobiscyanopentanoic acids XI. Properties of silicone-PMMA block copolymers prepared via polysiloxane(azobiscyano-pentanamides), J. Appl. Polym. ScL, 35, 2039 (1988). [Pg.934]

Guldin S, Docampo P, StefikM, KamitaG, Wiesner U, Snaith HJ, Steiner U (2012) Layer-by-layer formation of block-copolymer-derived Ti02 for solid-state dye-sensitized solar cells. Small 8 432 40... [Pg.2039]

Binder, W.H. and Gruber, H. (2000) Block copolymers derived from photoreactive 2-oxazolines. 1. Synthesis and miceUization behavior. Macromol. Chem. Phys., 201(9), 949-957. [Pg.230]

The synthesis of block copolymers of controlled structures is most conventionally accomplished through the use of living anionic polymerization. One can easily imagine, however, desirable block copolymers derived from monomers which are inert to anionic polymerization conditions, or which do not share any common mode of polymerization. In a recent series of papers (24-34), Richards and coworkers have addressed this problem in a general way, and have developed methods which convert one kind of active center into another. Within the context of cyclic ether polymerizations, Richards has focused on the preparation of block copolymers of styrene and tetrahydrofuran (THF) several methods of accomplishing this copolymerization are described in the following paragraphs. [Pg.436]

Polystyrene Block Copolymer Derived From it Before (B) and After (C) Hexane Extraction and the Hexane Extract (D). [Pg.451]

Polystyrene Block Copolymer Derived from it (B), and the Polystyrene Obtained After Degrading the Copolymer with Sulfuric Acid (C). [Pg.454]

Classes of Block Copolymer-Derived Hybrid Nanomaterials. 276... [Pg.260]

This mechanism represents a novel type of living polymerization in that the polymer "dies after each addition of a monomer tmit. The chain "lives and grows only as long as monomer is present to be activated by the catalyst. However, block copolymers derived from the addition of other monomers (e.g., isoprene) via this mechanism have not yet been rqwrted. Breaks in the fused ring structure may occur by cationic 1 2 or 1,4 initiation. [Pg.141]


See other pages where Block copolymers derivatives is mentioned: [Pg.757]    [Pg.759]    [Pg.761]    [Pg.763]    [Pg.66]    [Pg.99]    [Pg.183]    [Pg.353]    [Pg.293]    [Pg.17]    [Pg.223]    [Pg.33]    [Pg.122]    [Pg.697]    [Pg.22]    [Pg.179]    [Pg.97]    [Pg.197]    [Pg.111]    [Pg.260]    [Pg.265]    [Pg.514]    [Pg.397]   
See also in sourсe #XX -- [ Pg.100 ]




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Copolymers, block 2-oxazoline derived

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