Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Copolyesters, production

Eastman, Eastar BIO GP Copolyester Product Data Sheet, 2001. http //www. eastman.com. [Pg.134]

Eastman, Eastar Bio GP and Ultra Copolyester, product data sheet, July, 2001 and May,... [Pg.30]

Thermoplastic copolyester elastomers are generally block copolymers produced from short-chain aUphatic diols, aromatic diacids, and polyalkjlene ether-diols. They are often called polyesterether or polyester elastomers. The most significant commercial product is the copolymer from butane-l,4-diol, dimethyl terephthalate, and polytetramethylene ether glycol [25190-06-1J, which produces a segmented block copolyesterether with the following stmcture. [Pg.301]

Uses. Approximately 70% of the U.S. production is used to make poly(tetramethylene ether glycol) [25190-06-1] (PTMEG), also known as poly-THE, which is used in the production of urethane elastomers, polyurethane fibers (ether-based spandex), and copolyester—ether elastomers. PTMEG is also the fastest growing use (see PoLYETPiERS, TETRAHYDROFURAn). The remaining production is used as a solvent for the manufacture of poly(vinyl chloride) cements and coating, precision magnetic tape, a reaction solvent in the production of pharmaceuticals, and other miscellaneous uses. [Pg.429]

The principal solvolysis reactions for PET are methanolysis with dimethyl terephthalate and ethylene glycol as products, glycolysis with a mixture of polyols and BHET as products, and hydrolysis to form terephthalic acid and ethylene glycol. The preferred route is methanolysis because the DMT is easily purified by distillation for subsequent repolymerization. However, because PET bottles are copolyesters, the products of the methanolysis of postconsumer PET are often a mixture of glycols, alcohols, and phthalate derivatives. The separation and purification of the various products make methanolysis a cosdy process. In addition to the major product DMT, methanol, ethylene glycol, diethylene glycol, and 1,4-cyclohexane dimethanol have to be recovered to make the process economical.1... [Pg.533]

Aromatic copolyesters, 13 372 Aromatic diacyl peroxides, 14 283 Aromatic diisocyanates, urethanes obtained from, 25 462—463 Aromatic epoxies, 10 347-348 Aromatic ethers, 10 574 Aromatic fluorocarbon production, global, 11 871-872... [Pg.70]

With the exception of ethylene vinyl acetate added in the 1980 s, the list of materials and polymers approved as packaging for food irradiated products has remained static for decades. This article supplies details of the approved list, which includes such polymers as polyethylene terephthalate and polyvinyl chloride. The article provides an update on the latest proactive move to expand the list of packaging materials and polymers approved for the irradiation of foods. The expanded list would include ethylene vinyl alcohol, PVC film, ionomers, nylon 66, 6/12 and copolyesters among others. [Pg.90]

An additional example of applying SSP to co-polyester production has been outlined in a US patent [59], This discloses the production of co-polyesters based on terephthalic acid and with up to 12% bis-(hydroxy ethoxy phenyl)sulfone co-monomer content. Additional patents exist concerning the SSP of other copolyesters [60, 61]. [Pg.238]

Copolyesters (such as BIOMAX ) which combine aromatic esters with aliphatic esters or other polymer units (e.g. ethers and amides) provide the opportunity to adjust and control the degradation rates. These added degrees of freedom on polymer composition provide the opportunity to rebalance the polymer to more specifically match application performance in physical properties, while still maintaining the ability to adjust the copolyesters to complement the degradation of natural products for the production of methane or humic substances. Since application performance requirements and application specific environmental factors and degradation expectations vary broadly, copolyesters are, and will continue to be, an important class of degradable polyesters. [Pg.606]

Cl in conjunction with a direct exposure probe is known as desorption chemical ionization (DCI). [30,89,90] In DCI, the analyte is applied from solution or suspension to the outside of a thin resistively heated wire loop or coil. Then, the analyte is directly exposed to the reagent gas plasma while being rapidly heated at rates of several hundred °C s and to temperatures up to about 1500 °C (Chap. 5.3.2 and Fig. 5.16). The actual shape of the wire, the method how exactly the sample is applied to it, and the heating rate are of importance for the analytical result. [91,92] The rapid heating of the sample plays an important role in promoting molecular species rather than pyrolysis products. [93] A laser can be used to effect extremely fast evaporation from the probe prior to CL [94] In case of nonavailability of a dedicated DCI probe, a field emitter on a field desorption probe (Chap. 8) might serve as a replacement. [30,95] Different from desorption electron ionization (DEI), DCI plays an important role. [92] DCI can be employed to detect arsenic compounds present in the marine and terrestrial environment [96], to determine the sequence distribution of P-hydroxyalkanoate units in bacterial copolyesters [97], to identify additives in polymer extracts [98] and more. [99] Provided appropriate experimental setup, high resolution and accurate mass measurements can also be achieved in DCI mode. [100]... [Pg.349]

Statistical copolymerization of ethylene glycol and 1,4-butanediol with dimethyl ter-ephthalate results in products with improved crystallization and processing rates compared to poly(ethylene terephthalate). Polyarylates (trade names Ardel, Arylon, Durel), copolymers of bisphenol A with iso- and terephthalate units, combine the toughness, clarity, and proce-sibility of polycarbonate with the chemical and heat resistance of poly(ethylene terephthalate). The homopolymer containing only terephthalate units is crystalline, insoluble, sometimes infusible, and difficult to process. The more useful copolymers, containing both tere- and isophthalate units, are amorphous, clear, and easy to process. Polyarylates are used in automotive and appliance hardware and printed-circuit boards. Similar considerations in the copolymerization of iso- and terephthalates with 1,4-cyclohexanedimethanol or hexa-methylene diamine yield clear, amorphous, easy-to-process copolyesters or copolyamides,... [Pg.141]


See other pages where Copolyesters, production is mentioned: [Pg.156]    [Pg.158]    [Pg.99]    [Pg.188]    [Pg.156]    [Pg.158]    [Pg.99]    [Pg.188]    [Pg.186]    [Pg.609]    [Pg.722]    [Pg.432]    [Pg.20]    [Pg.26]    [Pg.27]    [Pg.31]    [Pg.75]    [Pg.103]    [Pg.108]    [Pg.152]    [Pg.152]    [Pg.153]    [Pg.174]    [Pg.83]    [Pg.104]    [Pg.138]    [Pg.160]    [Pg.161]    [Pg.172]    [Pg.21]    [Pg.273]    [Pg.489]    [Pg.594]    [Pg.188]    [Pg.137]    [Pg.159]    [Pg.242]    [Pg.226]    [Pg.139]    [Pg.310]    [Pg.74]    [Pg.11]   
See also in sourсe #XX -- [ Pg.1100 ]




SEARCH



Copolyesters

Polyethylene Terephthalate-Based Copolyester—Eastman Chemical Products

© 2024 chempedia.info