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POLYTETRAMETHYLENE

Uses. Furfural is primarily a chemical feedstock for a number of monomeric compounds and resins. One route produces furan by decarbonylation. Tetrahydrofuran is derived from furan by hydrogenation. Polytetramethylene ether glycol [25190-06-1] is manufactured from tetrahydrofuran by a ring opening polymeri2ation reaction. Another route (hydrogenation) produces furfuryl alcohol, tetrahydrofurfuryl alcohol, 2-methylfuran, and 2-methyltetrahydrofuran. A variety of proprietary synthetic resins are manufactured from furfural and/or furfuryl alcohol. Other... [Pg.78]

As can be seen, most of the furfural produced in this country is consumed as an intermediate for other chemicals. Hydrogenation to furfuryl alcohol is the largest use. Some of the furfuryl alcohol is further hydrogenated to produce tetrahydrofurfuryl alcohol. The next major product is furan, produced by decarbonylation. Furan is a chemical intermediate, most of it is hydrogenated to tetrahydrofuran, which in turn is polymerized to produce polytetramethylene ether glycol (PTMEG). [Pg.79]

Butanediol [110-63-4] (BDO) goes primarily into tetrahydrofuran [109-99-9] (THE) for production of polytetramethylene ether glycol (PTMEG), used ia the manufacture of polyurethane fibers, eg, Du Font s Spandex. THE is also used as a solvent for PVC and ia the production of pharmaceuticals (qv). Lesser amounts of BDO are employed ia the production of polybutylene terephthalate resias and y-butyrolactone. [Pg.473]

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]

Polybutester (10) is a polyether—ester produced by the condensation polymerization of dimethyl terephthalate, polytetramethylene ether glycol [25190-06-17, and 1,4-butanediol [110-63-4]. Polybutester sutures are available in clear, ie, undyed, or blue, ie, melt-pigmented with (phthalocyaninato(2-)) copper. Monofilament polybutester is sold under the trade name Novafil. [Pg.269]

Most of the commercial polymers consist of polyether blocks separated by polyamide blocks. The polyether blocks may be based on polyethylene glycol, polypropylene glycol or, more commonly, polytetramethylene ether glycol. The polyamides are usually based on nylon 11 but may be based on nylons 6 or 66 even a copolymer, e.g. 6/11. [Pg.526]

In 1978 Hiils (Mumcu et al ) described the properties of a block copolymer prepared by condensation of polytetramethylene ether glycol with laurin lactam and decane-1,10-dicarboxylic acid. The materials were introduced as XR3808 and X4006. The polyamide XR3808 is reported to have a specific gravity of 1.02, a yield stress of 24 MPa, a modulus of elasticity of 300 MPa and an elongation of break of 360%. The Swiss company Emser Werke also introduced similar... [Pg.526]

Figures 13.25-13.28 show the ultrahigh resolution separations in chloroform of polystyrene standards, polytetramethylene glycol, urethanes and isocyanates, and epoxy resins, respectively. Multiple column sets of anywhere from two to six columns in series have been used for well over a year with no apparent loss of efficiency. The 500- and 10 -A gels can easily tolerate 15,000 psi or more. In fact, the limiting factor in the number of columns that can be used in series is generally the pump or injector in the FIPLC system. A pump capable of 10,000 psi operation should allow the use of a column bank of 10-12 50-cm columns with a total plate count of 500,000 or more. Figures 13.25-13.28 show the ultrahigh resolution separations in chloroform of polystyrene standards, polytetramethylene glycol, urethanes and isocyanates, and epoxy resins, respectively. Multiple column sets of anywhere from two to six columns in series have been used for well over a year with no apparent loss of efficiency. The 500- and 10 -A gels can easily tolerate 15,000 psi or more. In fact, the limiting factor in the number of columns that can be used in series is generally the pump or injector in the FIPLC system. A pump capable of 10,000 psi operation should allow the use of a column bank of 10-12 50-cm columns with a total plate count of 500,000 or more.
In this review recent theoretical developments which enable quantitative measures of molecular orientation in polymers to be obtained from infra-red and Raman spectroscopy and nuclear magnetic resonance have been discussed in some detail. Although this is clearly a subject of some complexity, it has been possible to show that the systematic application of these techniques to polyethylene terephthalate and polytetramethylene terephthalate can provide unique information of considerable value. This information can be used on the one hand to gain an understanding of the mechanisms of deformation, and on the other to provide a structural understanding of physical properties, especially mechanical properties. [Pg.114]

Poly(butylene terephthalate) (PBT) [also called polytetramethylene terephthalate (PTMT)] Poly(ethylene terephthalate) (PET)... [Pg.1279]

Polyethylene adipate Polyethylene suberate Polyethylene azelate Polyethylene sebacate Polyethylene decamethylate Polytetraunethylene succinate Polytetramethylene adipate Polytetramethylene sebacate Polyhexamethylene sebacate Poly-2,2-dimethyItrimethylene succinate... [Pg.140]

Figure 6. Relationship between Tm and the biodegradability of polyesters by R> delemar (a) and R> arrhizus (b) lipases, and PEA-degrading enzyme from Penicillium sp. strain ll+-3 (c). PESu polyethylene suberate PEAz polyethylene azelate PESE polyethylene sebacate PEDe polyethylene decamethylate PBS polytetramethyl-ene succinate PBA polytetramethylene adipate PBSE polytetra-methylene sebacate PHSE polyhexamethylene sebacate PPL poly-propiolactone. Figure 6. Relationship between Tm and the biodegradability of polyesters by R> delemar (a) and R> arrhizus (b) lipases, and PEA-degrading enzyme from Penicillium sp. strain ll+-3 (c). PESu polyethylene suberate PEAz polyethylene azelate PESE polyethylene sebacate PEDe polyethylene decamethylate PBS polytetramethyl-ene succinate PBA polytetramethylene adipate PBSE polytetra-methylene sebacate PHSE polyhexamethylene sebacate PPL poly-propiolactone.
A calibration curve was obtained from C-NMR spectra of a series of polytetramethylene ether (PTME)-THF/CH3N02 solutions at... [Pg.237]

Figure 1 shows the proton noise-decoupled C-NMR spectrum of a polytetrahydrofurein (polytetramethylene ether glycol, PTMEG) dissolved in THF. In this spectrum the carbons numbered 1, 2 and 3 which cure a to the oxygen appear at lower field them the 6-carbons labeled as 4, 5 and 6. The carbon atoms in the polymer are clearly resolved from the corresponding carbons of the THF monomer. The fact that carbons 3 and 4 near the hydroxyl end-groups can be easily identified shows the excellent resolution of this technique. [Pg.239]

The effect of carboxylate and/or sulfonate ion incorporation on the physical and blood contacting properties of polyurethanes was studied by Cooper and collaborators [476-478]. Specifically, propyl sulfonate and ethyl carboxylate groups were grafted onto polytetramethylene oxide-based polyurethanes. Carboxylate polymers had no statistically significant effect on canine ex vivo blood contact response, but propyl sulfonate incorporation significantly reduced platelet deposition for very short blood contact times. [Pg.40]

Ti and Zr containing polytetramethylene oxide (PTMO) ceramic hybrid materials have lately been prepared by a sol-gel technique [61, 62]. Trialkoxy silane capped organic oligomer (PTMO or polyarylene ether sulfones) backbones with titanium isopropoxide or Zr-(n-propoxide) are used in this process ... [Pg.104]


See other pages where POLYTETRAMETHYLENE is mentioned: [Pg.1010]    [Pg.795]    [Pg.795]    [Pg.233]    [Pg.365]    [Pg.185]    [Pg.738]    [Pg.787]    [Pg.384]    [Pg.395]    [Pg.487]    [Pg.472]    [Pg.100]    [Pg.212]    [Pg.220]    [Pg.572]    [Pg.598]    [Pg.109]    [Pg.745]    [Pg.745]    [Pg.745]    [Pg.745]    [Pg.896]    [Pg.110]    [Pg.110]    [Pg.140]   


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PTMEG (polytetramethylene ether

PTMO (polytetramethylene oxide

Polytetrahydrofuran (Polytetramethylene Glycols)

Polytetramethylene adipate polyol

Polytetramethylene adipate polyol PTMA)

Polytetramethylene ether

Polytetramethylene ether (PTME

Polytetramethylene ether glycol

Polytetramethylene ether glycol PTMEG)

Polytetramethylene glycol

Polytetramethylene glycol PTMG)

Polytetramethylene oxide

Polytetramethylene oxide polyurethanes

Polytetramethylene terephthalate

Polytetramethylene-terephthalate PTMT)

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