Polyester block copolymers

Polyolefin Polyester Block copolymers of styrene and butadiene or styrene and isoprene Block copolymers of styrene and ethylene or styrene and butylene Poly(vinyl chloride) and poly(vinyl acetate) ... 

Multiblock Copolymers. Replacement of conventional vulcanized mbber is the main appHcation 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 requited scrap is reusable. They are mostiy 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). 

Polyester block copolymers can be defined as (AB) -type alternating multiblock copolymers composed of flexible aliphatic polyester or polyether blocks (A-type blocks) and rigid high-melting aromatic-aliphatic polyester blocks IB-type blocks) (Formula 2.2). 

In a similar way, polyester block copolymers were obtained by reacting acid chloride-terminated polyesters with hydroxy-terminated polyethers,401 or by reacting polyester-containing polymer mixtures with coupling agents such as diisocyanates.402... 

Polyester-based urethane sealants, 22 36 Polyester block copolymers, commercial, 24 707-708... 

A related product is formed from the analogous reaction using hydroxyl-terminated PEO with aromatic diacids to form a segmented aromatic polyester block copolymer that is sold under the trade name Hytrel. 

Arnitel Polyester block copolymer with polyester DSM... 

Ecdel Polyester block copolymer with polyether Eastman Kodak... 

Fig. 10. Internal energy changes as a function of deformation for oriented LDPE (I) and stress softened thermo-elastoplastic polyurethanes with 50% (2) and 42 % (3) hard phase content and polyether-polyester block copolymer with 48% hard phase content (4). The dotted curves 1 and 2 represent intramolecular energy changes for the corresponding polymers119 ...

Block copolymers characterised by different backbone structures of well-defined block lengths have been obtained from oxiranes and other heterocyclic monomers in the presence of catalysts that are effective at bringing about living polymerisations. Aida et al. [127,188,189,195,196] applied aluminium porphyrins and Teyssie et al. [125,197,198] applied bimetallic /i-oxoalkoxidcs for block copolymerisations in systems involving oxirane lactone, oxirane oxirane/cyclic acid anhydride, and oxirane/cyclic acid anhydride lactone as block forming units and obtained respective polyether polyester and polyester polyester block copolymers. Such copolymers seem to be of exceptionally wide potential utility [53]. 

A procedure for the slow and sustained release of the growth hormone inhibitor Lanreotide is described. The method entails incorporating Lanreotide to the isocitric acid lactone component on the backbone of a polyester block copolymer using sodium hydroxide as the saponification agent. 

In the present chapter, the current status of enzymatic polyester synthesis is described. For information on the enzymatic synthesis of chiral polyesters and polyester block copolymers using enzymatic polymerizations please refer to Chapters 11 and 12 respectively. 

PA/PET blends polyamide-polyester block copolymer Maresca Shafer, 1988... 

Jeong B, Lee DS, Shon J-i, Bae YH, Kim SW. Thermoreversible gelation of poly(ethylene oxide) biodegradable polyester block copolymers. J Polym Sci A 1999 37 751-760. 

The principal mechanism of temperature-sensitive polymers is the sharp transition from coil to globule in water on heating, indicating a change from a hydrophilic state (coil) below the lower critical solution temperature (LCST) to a hydrophobic state (globule) above the LCST. Representative temperature-sensitive polymers include A -isopropylacrylamide (NIPAAm), its copolymers (LCST 30-50°C) [108, 124-127], polyester block copolymers (20-100°Q [97, 128], and elastin-like polypeptides (27-40°C) [129-131]. To achieve both spatial and temporal control in conjunction with local temperature increases (2-5°C), the LCST of a given polymer can be tailored through its comonomer composition, hydrophilic-hydrophobic balance, stereochemistry [125-127,132], and the addition of salts and surfactants [133]. These thermosensitive polymers with controlled LCSTs (around body temperature) can be applied to specific applications (e.g., tumor treatment). 

Despite successful results from in vitro studies, however, the clinical applications of systems that are based on polyNlPAAm may be limited, becanse poly-NIPAAm is nondegradable and insoluble. In addition, a major problem of polyNIPAAm-based drug deUvery systems is that thermal treatment is required for controlled destabilization of the micelles and concurrent drug release, which is not always feasible in clinical situations. Therefore, to overcome the disadvantages of polyNIPAAm, controlled biodegradable systems that use polyester block copolymers as thermosensitive polymers have been investigated. 

R. J. Kumpf, D. A. Wicks, D. K. Nerger, H. Pielartzik, and R. Wehrmann. Poly(arylether)/liquid crystalhne polyester block copolymers and a process for their production. US Patent 5 618 889, assigned to Bayer Corporation (Pittsburgh, PA), April 8, 1997. 

The wide applicability of aluminum porphyrin initiators (1) leads to a variety of tailored block copolymers such as polymethacrylate-polyether and polymethacrylate-polye-ster, as well as polymethacrylate-polymethacrylate and polymethacrylate-polyacrylate, that can be synthesized by sequential living polymerization of the corresponding monomers.- For example, when 1,2-epoxypropane (11, R = Me) is added to a polymerization mixture of methyl methacrylate (21, R = Me) with la at 100% conversion of 21, the polymerization of 11 takes place from the enolate growing end (32 ) to give a narrow MWD polymethacrylate-polyether block copolymer having an alcoholate growing terminal (Table 4). Likewise, the aluminum enolate species (32 ) can also react with lactones (14,15), thereby allowing the formation of a poly(methyl methacrylate)-polyester block copolymer with narrow MWD. 

How can polyurethane-polyamide and polyamide-polyester block copolymers be formed Explain and show chemical reactions. 

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