Cyclohexylenedimethylene terephthalate

Fibres are also available from poly-(l,4-cyclohexylenedimethylene terephthalate) and are marketed as Kodar (Kodak) and Vestan (Hills). 

Poly(l,4-cyclohexylenedimethylene terephthalate) (PCT) finds some niche applications in the packaging market as amorphous, clear, extrusion, or injectionmolding material for films and bottles. 

See also PBT degradation structure and properties of, 44-46 synthesis of, 106, 191 Polycaprolactam (PCA), 530, 541 Poly(e-caprolactone) (CAPA, PCL), 28, 42, 86. See also PCL degradation OH-terminated, 98-99 Polycaprolactones, 213 Poly(carbo[dimethyl]silane)s, 450, 451 Polycarbonate glycols, 207 Polycarbonate-polysulfone block copolymer, 360 Polycarbonates, 213 chemical structure of, 5 Polycarbosilanes, 450-456 Poly(chlorocarbosilanes), 454 Polycondensations, 57, 100 Poly(l,4-cyclohexylenedimethylene terephthalate) (PCT), 25 Polydimethyl siloxanes, 4 Poly(dioxanone) (PDO), 27 Poly (4,4 -dipheny lpheny lpho sphine oxide) (PAPO), 347 Polydispersity, 57 Polydispersity index, 444 Poly(D-lactic acid) (PDLA), 41 Poly(DL-lactic acid) (PDLLA), 42 Polyester amides, 18 Polyester-based networks, 58-60 Polyester carbonates, 18 Polyester-ether block copolymers, 20 Polyester-ethers, 26... 

CHDA CHDM DMCD EG IPA N NDA PCT PCTA PCTG PET PETG TMCD TPA cis/trans-1,4-cyclohexanedicarboxylic acid cis/trans-1,4-cyclohexanedimethanol dimethyl cis/trans-1,4-cyclohexanedicarboxylate ethylene glycol isophthalic acid dimethyl 2,6-naphthalenedicarboxylate 2,6-naphthalenedicarboxylic acid poly(1,4-cyclohexylenedimethylene terephthalate) dibasic-acid-modified PCT copolyester glycol-modified PCT copolyester poly(ethylene terephthalate) CHDM-modified PET copolyester c .S / ra .v-2,2,4,4-tetramethyl-l,3-cyclobutancdiol terephthalic acid... 

PCT describes a polyester composition prepared from CHDM and DMT (or TPA). The abbreviation PCT is thus derived from the technical name for the polymer, i.e. poly(l,4-cyclohexylenedimethylene terephthalate), or PCT. This material is a highly crystalline, high-melting polyester, with the following structure ... 

The primary crystalline polymer based on CHDM is the terephthalate, poly(1,4-cyclohexylenedimethylene terephthalate) (PCT). This polyester was originally developed for fiber applications but has since found wider utility as a reinforced polymer for injection molding and (when copolymerized with a small amount of isophthalic acid) as a material for crystallized food packaging trays. The key property of PCT which sets it apart from other thermoplastic polyesters in these latter applications is its melting point. 

Minnick, L. A. and Seymour, R. W., Poly(l,4-cyclohexylenedimethylene terephthalate) with improved melt stability, US Patent 5 428 086, 1995. 

Minnick, L. A., Reinforced molding composition based on poly(l,4-cyclohexylenedimethylene terephthalate) having improved crystallization characteristics, US Patent 4 859 732, 1988. 

Photodegradation of Poly(Ethylene Terephthalate) and Poly(Ethylene/1,4-Cyclohexylenedimethylene Terephthalate)... 

Hill, A.J., Winhold, S Stack, G.M., Tant, M.R. (1996) Effect of copolymer composition on free volume and gas permeability in polyethylene terephthalate) -poly(l,4 cyclohexylenedimethylene terephthalate) copolymers . Eur. Polym. J. 32(7), 843. 

Poly( 1,4-cyclohexylenedimethylene terephthalate-c< -1,4-cyclohexyl-enedimethylene 2,6-naphthalate) (P(CT-c< -CN)) copolymers behave similarly with respect to crystallization behavior than poly(ethylene-co-butyl-ene 2,6-naphthalate) copolymers. Poly(ethylene 2,6-naphthalate-co-l,4-cyclohexylenedimethylene 2,6-naphthalate) (P(EN-co-CN)) copolymers do not crystallize in the middle of copolymer composition, whereas poly-(hutylene 2,6-naphthalate-c< -1,4-cyclohexylenedimethylene 2,6-naphthalate) (P(BN-co-CN)) and poly(hexamethylene 2,6-naphthalate-co-l,4-cy-clohexylenedimethylene 2,6-naphthalate) (P(HN-c< -CN)) copolymers exhibit clear melting and crystallization peaks. This behavior indicates that both P(BN-co-CN) and P(HN-co-CN) copolymers exhibit a co-crystallization behavior. P(BN-co-CN) copolymers exhibit a eutectic melting and isodimorphic co-crystallization. 

Jeong YG, Jo WH, Lee SC. Synthesis and isodi-morphic cocrystallization behavior of poly( 1,4-cyclohexylenedimethylene terephthalate-co-1, 4-cyclohexylenedimethylene 2,6-naphthalate) copolymers. J Polym Sci Part B Polym Phys 2004 42(l) 177-87. 

Other aromatic polyesters which have been commercialised include poly(l,4-cyclohexylenedimethylene terephthalate) (PCT used in the production of circuit board components and automotive applications) and the clear, amorphous, polymer poly(l,4-cyclohexylenedimethylene terephthalate-co-isophthalate). 

Various copolymers based on this chemistry have also been commercialised, including poly(ethylene-co-l,4-cyclohexylenedimethylene terephthalate) and poly(l,4-cyclohexylenedimethylene terephthalate-co-isophthalate). Both of these types are largely amorphous, clear, polymers. 

A few studies have been made on the thermal degradation of poly(l,4-cyclohexylenedimethylene terephthalate) [84—86], although these have little to say concerning the likely breakdown mechanism. Assuming the same process is applied here as in straight-chain poly(alkylene terephthalate)s, the process might be deduced as follows [NB (CgHjo) denotes the 1,4-cyclohexyl moiety in the polymer backbone] ... 

It is thus anticipated that the small-molecule breakdown products will be l,4-bis(methylene)cyclohexane and 4-methylenecyclohex-anemethanol. Such by-products have been found in the pyrolysis of the copolymer poly(ethylene- o-l,4-cyclohexylenedimethylene terephthalate) [87]. 

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