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Polyesteramide

This is often a convenient route to produce polyesteramides. [Pg.226]

Some 50 years later, in the 1990s Bayer produced their BAK polyesteramides by co-reacting either hexamethylene diamine or e-caprolactam with adipic acid and butane glycol. These materials do have sufficient regularity to be crystallisable and are of interest as biodegradable plastics and are discussed further in Chapter 31. [Pg.529]

A further approach is used by Bayer with their polyesteramide BAK resins. A film grade, with mechanical and thermal properties similar to those of polyethylene is marketed as BAK 1095. Based on caprolactam, adipic acid and butane diol it may be considered as a nylon 6-co-polyester. An injection moulding grade, BAK 2195, with a higher melting point and faster crystallisation is referred to as a nylon 66-co-polyester and thus presumably based on hexamethylene diamine, adipic acid and butane diol. [Pg.882]

Anodier ordered polyesteramide is polyester containing a small amount of diamides (amide units of uniform length) ... [Pg.147]

PAs have also been copolymerized with other polymer systems and, in particular", with polyesters and poly ethers. In the copoly esteramides the crystallinity is decreased by copolymerization, as the crystalline structure of the amide unit is very different from the ester unit. However, alternating polyesteramides behave as homopolymers with a glass ttansition temperature and a melting temperature intermediate to the polyester and the PA polymer (Figs. 3.10 and 3.11).23,24 Polyesters, such as PBT and PET, modified with a small amount of diamide are also copolymers that have a high order.24,73... [Pg.189]

Aliphatic hyperbranched polyesters, 56 Aliphatic isocyanate adducts, 202 Aliphatic isocyanates, 210, 225 Aliphatic polyamides, 138 Aliphatic polyesteramides, 56 Aliphatic polyesters, 18, 20, 29, 32, 87 degradable, 85 hyperbranched, 114-116 melting points of, 33, 36 structure and properties of, 40-44 syntheses of, 95-101 thermal degradation of, 38 unsubstituted and methyl-substituted, 36-38... [Pg.576]

Silylated diamines, 156, 187-188 Silylated monomers, 72 Silylation, distillation and, 338 6NT6 alternating polyesteramide, synthesizing, 189-190 6,6 -linked polymers, 480 Size exclusion chromatography (SEC) analyses, 90, 490 Slabstock foam, 233-234 Slow monomer addition, 57 Small-angle neutron scattering (SANS), 282... [Pg.601]

Muscat D, van Benthem RATM (2001) Hyperbranched Polyesteramides - New Dendritic Polymers. 212 41-80... [Pg.236]

Many diols and polyols like 1, 4-butanediol and hydroxy-terminated polyesters or polyethers or polyesteramides are used for reaction with diisocyanates commercially. [Pg.202]

Figure 6.2 The polyesteramide structure proposed by Gaymans and co-workers E, ester group A, amide group [21]. Reprinted from Polymer, 38, van Bennekom, A. C. M. and Gaymans, R. J., Amide-modified polybutylene terephthalate structure and properties, 657-665, Copyright (1997), with permission from Elsevier Science... Figure 6.2 The polyesteramide structure proposed by Gaymans and co-workers E, ester group A, amide group [21]. Reprinted from Polymer, 38, van Bennekom, A. C. M. and Gaymans, R. J., Amide-modified polybutylene terephthalate structure and properties, 657-665, Copyright (1997), with permission from Elsevier Science...
Other, rigid-rod monomers can be incorporated into PET, to increase chain stiffness, and therefore the Tg (Figure 6.5). A prime example of such a rigid copolyester is a multi-ring poly(ethylene terephthalate-imide) [43], As was the case with the polyesteramides of Gaymans, the imide-containing diol monomer, A,A-bis[p-(2-hydroxyethoxycarbonyl)phenyl]-biphenyl-3,3,4,4-tetracarboxy-diimide, was preformed prior to polycondensation, where this monomer is free... [Pg.252]


See other pages where Polyesteramide is mentioned: [Pg.294]    [Pg.306]    [Pg.307]    [Pg.481]    [Pg.528]    [Pg.529]    [Pg.882]    [Pg.799]    [Pg.8]    [Pg.18]    [Pg.28]    [Pg.29]    [Pg.56]    [Pg.189]    [Pg.189]    [Pg.189]    [Pg.576]    [Pg.119]    [Pg.313]    [Pg.20]    [Pg.249]    [Pg.250]    [Pg.250]    [Pg.486]    [Pg.858]   
See also in sourсe #XX -- [ Pg.154 ]

See also in sourсe #XX -- [ Pg.154 ]

See also in sourсe #XX -- [ Pg.135 ]

See also in sourсe #XX -- [ Pg.37 ]




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Biodegradable polyesteramides

Biodegradable polymers polyesteramides

Polyesteramide BAK resins

Polyesteramide copolymers

Polyesteramides

Polyesteramides

Polyesteramides (PEAs)

Polyesteramides applications

Polyesteramides biodegradation

Polyesteramides processing

Polyesteramides producers

Polyesteramides properties

Polyesteramides, melting point

Silicone aliphatic polyesteramides

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