Polyethylene terephthalate copolymer

NEW POLYETHYLENE TEREPHTHALATE) COPOLYMERS 6.4 TEREPHTHALATE RING SUBSTITUTIONS... 

Komolprasert V, McNeal TP, Begley TH. Effects of gamma- and electron beam irradiation on semi-rigid amorphous polyethylene terephthalate copolymers. hood Addit Contain 2003 20(5) 505 17. 

The suitability of several other membranes for demineralizing saline waters was then investigated. Commercially available membranes of polystyrene, polyethylene terephthalate), copolymer poly (vinyl chloride)-poly (vinyl acetate), rubber hydrochloride, cellulose triacetate, and ethylcellulose were tested. Only the cellulose triacetate and ethylcellulose gave high degrees of desalinization... 

Polyethyleneoxide-co-polypropyleneoxides, dispersants, S 710t Poly(ethylene oxide) film, physical properties of, 10 68It Poly(ethylene oxide) floe, 11 638 Poly(ethylene oxide)-poly(ethylene terephthalate) copolymers, bioresorbable polymers, 3 738 Poly(ethylene oxide) resins, molecular weight of, 10 684-685 Polyethylene oxides, dispersants, S 706t, 710t... 

Polyethylene terephthalate (PET) is a copolymer of ethylene glycol with either terephthalic acid or dimethyl terephthalate. PET is used in packaging applications for soft drinks and mineral water, and for the bottles that are collected by curbside or deposit systems. As it does not thermally deform below about 220° C, PET is also used for trays and dishes for microwave and conventional cooking. 

For most step polymerizations, for example, in the synthesis of polyl hexamethylene adipa-mide) or polyethylene terephthalate), two reactants or monomers are used in the process, and the polymer obtained contains two different kinds of structures in the chain. This is not the case for chain polymerizations, where only one monomer need be used to produce a polymer. However, chain polymerizations can be carried out with mixtures of two monomers to form polymeric products wiht two different structures in the polymer chain. This type of chain polymerization process in which two monomers are simultaneously polymerized is termed a copolymerization, and the product is a copolymer. It is important to stress that the copolymer is not an alloy of two homopolymers hut contains units of both monomers incorporated into each copolymer molecule. The process can be depicted as... 

The same technique was applied to a mixture of polyethylene terephthalate and acrylic acid (34). The polymerizations were followed by looking at the acid number of the product the parameters studied were time, temperature, and monomer content see Fig.9a,b,c. The hydrophilicity, the solubility of the copolymer in benzyl alcohol, aniline, and a mixture of phenol and CHQ3 were increased by graft copolymerization. 

Baramboim and coworkers (42) performed a low temperature copolymerization of a frozen polyethylene terephthalate suspension in acrylic acid, obtaining block copolymers and ternary acid resistant products. 

Terephthalic acid and ethylene glycol polymerize to form the condensation copolymer polyethylene terephthalate. 

Other Polymers. Besides polycarbonates, poly(methyl methacrylate)s, cyclic polyolefins, and uv-curable cross-linked polymers, a host of other polymers have been examined for their suitability as substrate materials for optical data storage, preferably compact disks, in the last years. These polymers have not gained commercial importance polystyrene (PS), poly(vinyl chloride) (PVC), cellulose acetobutyrate (CAB), bis(diallylpolycarbonate) (BDPC), polyethylene terephthalate) (PEL), styrene—acrylonitrile copolymers (SAN), poly(vinyl acetate) (PVAC), and for substrates with high resistance to heat softening, polysulfones (PSU) and polyimides (PI). 

High speed stirring has be claimed by Nozaki for giving block copolymers from polymer-monomer mixtures (775). Among the polymers which have been subjected to such a degradation are addition polymers (polyvinyl chloride, polystyrene, polyacrylamide) as well as cellulose derivatives, phenol-formaldehyde linear condensation products and polyethylene terephthalate. 

In the case of copolymers a calorimetric investigation by Dole and Wunderlich (1959) of the copolyester, polyethylene terephthalate and sebacate) at the 80/20. (80 moles of terephthalate units to 20 of sebacate)... 

The agreement between heats of fusion of the same polymer is excellent in some cases, but very poor in others. Obviously, in the case of polypropylene more work needs to be done before the heat of fusion of this substance will be known with any certainty. Heats of fusion calculated from the copolymer equation, Eq. (6), are uniformly low, except in the case of Rybnikar s data. As pointed out by Dole and Wunderlich (1957) this is probably due to the failure to measure the maximum melting of carefully annealed samples. Thus, Dole and Wunderlich (1959) found that the calorimetrically estimated melting point in the case of the carefully annealed copolyester, the 80/20 polyethylene terephthalate and sebacate, was 240° C, whereas the value calculated from Eq. (6) using the heat of fusion estimated from the calorimetric data of Smith and Dole (1956) was 245° C. The unannealed sample had a melting point of ca. 210°. 

In the case of the polyesters Smith and Dole s (1956) study of the monomeric analogs of polyethylene terephthalate, namely, dimethyl and diethyl terephthalate, in which they found 39.5 and 26.6 cal g-1 for the heats of fusion, respt., was of aid in supporting their conclusion that Edgar and Hill s (1952) estimate of the heat of fusion of polyethylene terephthalate from the use of the copolymer Eq. (6), namely 11.5 cal g-1, must be definitely too low. It should be pointed out that Edgar and Hill were also uncertain as to the correctness of the value 11.5 cal g-1. 

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... 

MC MDI MEKP MF MMA MPEG MPF NBR NDI NR OPET OPP OSA PA PAEK PAI PAN PB PBAN PBI PBN PBS PBT PC PCD PCT PCTFE PE PEC PEG PEI PEK PEN PES PET PF PFA PI PIBI PMDI PMMA PMP PO PP PPA PPC PPO PPS PPSU Methyl cellulose Methylene diphenylene diisocyanate Methyl ethyl ketone peroxide Melamine formaldehyde Methyl methacrylate Polyethylene glycol monomethyl ether Melamine-phenol-formaldehyde Nitrile butyl rubber Naphthalene diisocyanate Natural rubber Oriented polyethylene terephthalate Oriented polypropylene Olefin-modified styrene-acrylonitrile Polyamide Poly(aryl ether-ketone) Poly(amide-imide) Polyacrylonitrile Polybutylene Poly(butadiene-acrylonitrile) Polybenzimidazole Polybutylene naphthalate Poly(butadiene-styrene) Poly(butylene terephthalate) Polycarbonate Polycarbodiimide Poly(cyclohexylene-dimethylene terephthalate) Polychlorotrifluoroethylene Polyethylene Chlorinated polyethylene Poly(ethylene glycol) Poly(ether-imide) Poly(ether-ketone) Polyethylene naphthalate Polyether sulfone Polyethylene terephthalate Phenol-formaldehyde copolymer Perfluoroalkoxy resin Polyimide Poly(isobutylene), Butyl rubber Polymeric methylene diphenylene diisocyanate Poly(methyl methacrylate) Poly(methylpentene) Polyolefins Polypropylene Polyphthalamide Chlorinated polypropylene Poly(phenylene oxide) Poly(phenylene sulfide) Poly(phenylene sulfone)... 

Fig. 14. Apparent weight distributions calculated from the translational diffusion coefficient distributions corresponding to low-mass (O) and high-mass ( ) copolymer segmented polyethylene terephthalate-co-caprolactone) (PET-PCL) containing 13% PET in tetrahydrofuran (THF) at 25 °C...

Oxirane/cyclic acid anhydride alternating copolymers of controlled molecular weight with a narrow molecular weight distribution were found by Aida et al. [188,189] to be formed under mild conditions when copolymerising ethylene oxide and phthalic anhydride in the presence of the (tpp)AlCl-quater-nary phosphonium salt catalyst system. The copolymerisation carried out with (tpp)AlCl alone proceeded very slowly, and the product was not polyethylene terephthalate) but contained ether linkages in considerable amount. The development of the living character and the tendency towards alternation of the copolymerisation when using the aluminium porphyrin catalyst, coupled with a quaternary salt, have been postulated [188,189] to be due to the formation of... 

Copolymers of polyethylene terephthalate (PET) with nonaromatic acids, poly(ethylene ethers) or hydroxy acids have been blended with starch to produce compostable products such as fibers and films.60 Starch contents up to 80% by weight are claimed. 

Vinylidene Chloride Copolymer Latex. Vinylidene chloride polymers are often made in emulsion, but usually are isolated, dried, and used as conventional resins. Stable latices have been prepared and can be used diiecdy for coatings (171—176). The principal applications for these materials are as barrier coatings on paper products and, more recently, on plastic films. The heat-seal characteristics of VDC copolymer coatings are equally valuable in many applications. They are also used as binders for paints and nonwoven fabrics (177). The use of special VDC copolymer latices for barrier laminating adhesives is growing, and the use of vinylidene chloride copolymers in flame-resistant carpet backing is well known (178—181). VDC latices can also be used to coat polyethylene terephthalate) (PET) bottles to retain carbon dioxide (182). 

Seven families of thermoplastics exceed a billion pounds per year in the United States polyethylenes, polypropylene, PVC, polystyrene and its copolymers, polyethylene terephthalate, acrylonitrile-butadiene-styrene (ABS) and nylon (Table 15.2). 

---