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Poly ethylene-2,6-naphthalene

Properties and Applications of Poly(Ethylene 2,6-Naphthalene), its Copolyesters and Blends... [Pg.323]

Stewart, M. E., Cox, A. J. and Naylor, D. M., Reactive processing of poly(ethylene-2,6-naphthalene dicarboxylate)/poly(ethyleneterephthalate) blends, Polymer, 34, 4060-4067 (1993). [Pg.334]

Biaxially Oriented Poly(Ethylene 2,6-Naphthalene) Films Manufacture, Properties and Commercial Applications... [Pg.335]

DSC and DTA. They can be used to confirm suspicious glass transitions revealed by DSC and most important, they can further quantify molecular mobility associated with sub-glass transitions. For example, DSC analysis of poly (ethylene 2,6-naphthalene dicarboxylate) (PEN) only revealed the presence of a glass transition around 112 °C (Hardy et al., 2001). DMA analysis of the same sample, however, revealed two secondary relaxations below this glass transition (Hardy et al., 2001). In the case of humic materials, it is not uncommon for DSC to fail to detect clear thermal transitions due to their heterogeneous nature, which contributes to overlap/ broadening or washout of thermal transitions. As such,TMA and DMA represent powerful, complementary tools to DSC. [Pg.823]

Hardy, L., Stevenson, I., Boiteux, G., Seytre, G., and Schonhals, A. (2001). Dielectric and dynamic mechanical relaxation behaviour of poly(ethylene 2,6 naphthalene dicarboxyl-ate). I. Amorphous films. Polymer 42(13), 5679-5687. [Pg.831]

Hashimoto et al. [132] studied the fluorescence of the MCLC polyesters, poly[(ethylene terephthalate)-co-(p-oxybenzoate)], 66, and poly[(ethylene 2,6-naphthalene dicarboxylate)-co-(/ -oxybenzoate)], 67. The fluorescence of 66, both at relatively high concentration (5 x 10 3 mol dm-3) in hexafluoro-2-propanol,... [Pg.185]

PB PBI PBMA PBO PBT(H) PBTP PC PCHMA PCTFE PDAP PDMS PE PEHD PELD PEMD PEC PEEK PEG PEI PEK PEN PEO PES PET PF PI PIB PMA PMMA PMI PMP POB POM PP PPE PPP PPPE PPQ PPS PPSU PS PSU PTFE PTMT PU PUR Poly(n.butylene) Poly(benzimidazole) Poly(n.butyl methacrylate) Poly(benzoxazole) Poly(benzthiazole) Poly(butylene glycol terephthalate) Polycarbonate Poly(cyclohexyl methacrylate) Poly(chloro-trifluoro ethylene) Poly(diallyl phthalate) Poly(dimethyl siloxane) Polyethylene High density polyethylene Low density polyethylene Medium density polyethylene Chlorinated polyethylene Poly-ether-ether ketone poly(ethylene glycol) Poly-ether-imide Poly-ether ketone Poly(ethylene-2,6-naphthalene dicarboxylate) Poly(ethylene oxide) Poly-ether sulfone Poly(ethylene terephthalate) Phenol formaldehyde resin Polyimide Polyisobutylene Poly(methyl acrylate) Poly(methyl methacrylate) Poly(methacryl imide) Poly(methylpentene) Poly(hydroxy-benzoate) Polyoxymethylene = polyacetal = polyformaldehyde Polypropylene Poly (2,6-dimethyl-l,4-phenylene ether) = Poly(phenylene oxide) Polyp araphenylene Poly(2,6-diphenyl-l,4-phenylene ether) Poly(phenyl quinoxaline) Polyphenylene sulfide, polysulfide Polyphenylene sulfone Polystyrene Polysulfone Poly(tetrafluoroethylene) Poly(tetramethylene terephthalate) Polyurethane Polyurethane rubber... [Pg.939]

Polymers that have bulky repeat units can have multiple secondary relaxations. If more than one secondary relaxation is found, then the slowest one has to be the JG relaxation, assuming that the latter is resolved. Excellent illustrations of this scenario are found by dielectric relaxation studies of aromatic backbone polymers such as poly(ethylene terephthalate) (PET) and poly(ethylene 2,6-naphthalene dicarboxylate) (PEN) [43]. The calculated To from the parameters, n and xa, of the a-relaxation are in good agreement with the experimental value of %jq obtained either directly from the dielectric loss spectra or from the Arrhenius temperature dependence of xjg in the glassy state extrapolated to Tg. The example of PET is shown in Fig. 46. [Pg.554]

The search for basic principles to guide the development of more effective barrier materials based on condensation polymerization is ongoing. Advanced polyesters such as poly(ethylene 2,6-naphthalene dicarboxylate) or PEN have been reported to have as much as 5 times lower permeability than conventional PET however, proprietary considerations have prevented the publication of complete details concerning such materials. [Pg.8]

Poly(ethylene-2,6-naphthalene dicarboxylate) (PEN) with MDPE and/or PP... [Pg.55]

This chapter covers fundamental and applied research on polyester/clay nanocomposites (Section 31.2), which includes polyethylene terephthalate (PET), blends of PET and poly(ethylene 2,6-naphthalene dicarboxy-late) (PEN), and unsaturated polyester resins. Section 31.3 deals with polyethylene (PE) and polypropylene (PP)-montmorillonite (MMT) nanocomposites, including blends of low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and high density polyethylene (HDPE). Section 31.4 analyzes the fire-retardant properties of nanocomposites made of high impact polystyrene (HIPS), layered clays, and nonhalogenated additives. Section 31.5 discusses the conductive properties of blends of PET/PMMA (poly (methyl methacrylate)) and PET/HDPE combined with several types of carbon... [Pg.585]

Cheng SZD, Wunderlich B. (1985) Glass Transition and Melting Behavior of Poly(ethylene-2,6-naphthalene Dicarboxylate). Macromolecules 21 789-797. [Pg.703]

Sato O, Aral K, Shirai M. Hydrolysis of poly (ethylene terephthalate) and poly(ethylene 2,6-naphthalene dicarboxylate) using water at high temperature Effect of proton on low ethylene glycol yield. Catal Today 2006 111 297-301. [Pg.291]


See other pages where Poly ethylene-2,6-naphthalene is mentioned: [Pg.165]    [Pg.165]    [Pg.704]    [Pg.65]    [Pg.1159]    [Pg.1423]    [Pg.717]    [Pg.275]    [Pg.634]    [Pg.790]    [Pg.864]    [Pg.866]    [Pg.4761]    [Pg.87]    [Pg.133]    [Pg.1322]    [Pg.208]    [Pg.8426]    [Pg.13]    [Pg.103]    [Pg.117]    [Pg.130]    [Pg.139]    [Pg.149]    [Pg.164]    [Pg.176]    [Pg.185]   


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