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Poly ethyl ether ketone

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)... [Pg.959]

Whereas UL 94 delivers only a classification based on a pass-and-fail system, LOI can be used to rank and compare the flammability behavior of different materials. In Figure 15.2 the increasing LOI values are presented for different polymers as an example POM = poly(oxymethylene), PEO = poly(ethyl oxide), PMMA = poly(methyl methacrylate), PE = polyethylene), PP, ABS, PS, PET = polyethylene terephthalate), PVA = poly(vinyl alcohol), PBT, PA = poly(amide), PC, PPO = poly(phenylene oxide), PSU, PEEK = poly(ether ether ketone), PAEK = poly(aryl ether ketone), PES, PBI = poly(benzimidazole), PEI = poly(ether imide), PVC = poly(vinyl chloride), PBO = poly(aryl ether benzoxazole), PTFE. The higher the LOI, the better is the intrinsic flame retardancy. Apart from rigid PVC, nearly all commodity and technical polymers are flammable. Only a few high-performance polymers are self-extinguishing. Table 15.1 shows an example of how the LOI is used in the development of flame-retarded materials. The flame retardant red phosphorus (Pred) increases... [Pg.391]

The acid-base Nafion composite membranes include blends of Nafion with polypyrrole (PPy) [98-104], polybenzimidazole (PBI) [105-107], poly (propyleneoxide) (PPO) [108, 109], polyfurfuryl alcohol (PFA) [110], poly(vinyl alcohol) (PVA) [111-115], sulfonated phenol-formaldehyde (sPF) [116], polyvinylidene fluoride (PVdF) [117-122], poly(p-phenylene vinylene) (PPV) [123], poly(vinyl pyrrolidone) (PVP) [124] polyanifine (PANI) [125-128], polyethylene (PE) [129], poly(ethylene-terephtalate) [130], sulfated p-cyclodextrin (sCD) [131], sulfonated poly(ether ether ketone) (sPEEK) [132-135], sulfonated poly(aryl ether ketone) (sPAEK) [136], poly(arylene ether sulfone) (PAES) [137], poly(vinylimidazole) (PVl) [138], poly(vinyl pyridine) (PVPy) [139], poly (tetrafluoroethylene) (PTFE) [140-142], poly(fluorinated ethylene-propylene) [143], sulfonated polyhedral oligomeric silsesquioxane (sPOSS) [144], poly (3,4-ethylenedioxythiophene) (PEDT) [145, 146], polyrotaxanes (PR) [147], purple membrane [148], sulfonated polystyrene (PSSA) [149, 150], polystyrene-b-poly(ethylene-ran-butylene)-bpolystyrene (SEES) [151], poly(2-acrylamido-2-methyl-l-propanesulphonic acid-co-l,6-hexanediol propoxylate diacrylate-co-ethyl methacrylate) (AMPS) [152], and chitosan [31]. A binary PVA/chitosan [153] and a ternary Nafion composite with PVA, polyimide (PI) and 8-trimethoxy silylpropyl glycerin ether-1,3,6-pyrenetrisulfonic acid (TSPS) has also been reported [154]. [Pg.129]

Four poly(ether ketone)s obtained from 2,2-bis[4-(4-fluorobenzoyl)-phenyl]-1,1,1,3,3,3-hexafluoropropane (9) or 2,2-bis[4-(4-fluorobenzoyl)-phenyl]propane (10) with Bisphenol AF (1) or Bisphenol A (4) are all soluble in chloroform, benzene, THF, and aprotic polar solvents such as DMF, DMAc, and NMP.15 Poly(ether ketone) from 9 and 1, which has the highest fluorine content, dissolves easily in ethyl acetate. [Pg.139]

Table 2 contains the characteristics of the amic ester-aryl ether copolymers including coblock type, composition, and intrinsic viscosity. Three series of copolymers were prepared in which the aryl ether phenylquinoxaline [44], aryl ether benzoxazole [47], or aryl ether ether ketone oligomers [57-59] were co-re-acted with various compositions of ODA and PMDA diethyl ester diacyl chloride samples (2a-k). The aryl ether compositions varied from approximately 20 to 50 wt% (denoted 2a-d) so as to vary the structure of the microphase-separated morphology of the copolymer. The composition of aryl ether coblock in the copolymers, as determined by NMR, was similar to that calculated from the charge of the aryl ether coblock (Table 2). The viscosity measurements, also shown in Table 2, were high and comparable to that of a high molecular weight poly(amic ethyl ester) homopolymer. In some cases, a chloroform solvent rinse was required to remove aryl ether homopolymer contamination. It should also be pointed out that both the powder and solution forms of the poly(amic ethyl ester) copolymers are stable and do not undergo transamidization reactions or viscosity loss with time, unlike their poly(amic acid) analogs. Table 2 contains the characteristics of the amic ester-aryl ether copolymers including coblock type, composition, and intrinsic viscosity. Three series of copolymers were prepared in which the aryl ether phenylquinoxaline [44], aryl ether benzoxazole [47], or aryl ether ether ketone oligomers [57-59] were co-re-acted with various compositions of ODA and PMDA diethyl ester diacyl chloride samples (2a-k). The aryl ether compositions varied from approximately 20 to 50 wt% (denoted 2a-d) so as to vary the structure of the microphase-separated morphology of the copolymer. The composition of aryl ether coblock in the copolymers, as determined by NMR, was similar to that calculated from the charge of the aryl ether coblock (Table 2). The viscosity measurements, also shown in Table 2, were high and comparable to that of a high molecular weight poly(amic ethyl ester) homopolymer. In some cases, a chloroform solvent rinse was required to remove aryl ether homopolymer contamination. It should also be pointed out that both the powder and solution forms of the poly(amic ethyl ester) copolymers are stable and do not undergo transamidization reactions or viscosity loss with time, unlike their poly(amic acid) analogs.
Glycidyl methacrylate High density polyethylene Isotactic copolymer of styrene and p-methyl styrene Isotactic poly(ethyl methacrylate) Isotactic poly(methyl methacrylate) Isotactic polystyrene Low density polyethylene Linear low density polyethylene Maleic anhydride Poly(4-methyl pentene) Random copolymer of phenyl ether and phenyl ketone... [Pg.285]

Toluene/ethanol Ethyl cellulose (EC) poly(vinyl chloride-co-isobutyl vinyl ether) (PVC-IBVE) poly(4-tert-butyl styrene) (PTBS) polystyrene (PS) poly(vinyl methyl ketone) (PVMK)... [Pg.342]

In the last twenty years, many polymers have been used to make polymer nanocomposites. Thermoplastic polymers include nylon, polyaniline (PANI), " poly(s-caprolactone), polycarbonate (PC), polyether ether ketone (PEEK), polyethylene (PE), poly(ethyl acrylate) (PEA), polyisoprene (PI), polylactide (PLA), poly(methyl methacrylate) (PMMA), " polypropylene (PP), polypyrrole (PPy)," polystyrene (ps)/ i i7,27,30,49-64 poiy inyl acetate) (PVAc), poly(vinyl alcohol) (PVA), poly(vinyl chloride) (PVC) and thermoplastic polyurethane (TPU), and thermosets include Bakelite, butadiene rubber, epoxy,polydimethylsiloxane (PDMS), polyurethane (PU), styrene-butadiene rubber (SBR) and unsaturated polyester resin. [Pg.143]

Poly(isobutyl vinyl ether) 2-Propanol, methyl ethyl ketone, meth- Methanol, acetone ylene chloride, aromatic hydrocarbons... [Pg.75]

Judging from the number of incorrect names that appear in the chemical literature, it s probably safe to say that relatively few practicing organic chemists are fully conversant with the rules of organic nomenclature. Simple hydrocarbons and monofunctional compounds present few difficulties because the basic rules for naming such compounds are logical and easy to understand. Problems, however, are often encountered with polyfunctional compounds. Whereas most chemists could correctly identify hydrocarbon 1 as 3-ethyl-2,5-dimethylheptane, rather few could correctly identify poly functional compound 2. Should we consider 2 as an ether As an ethyl ester As a ketone As an alkeae It is, of course, all four, but it has only one correct name ethyl 3-(4-methoxy-2-oxo-3-cyclohexenyl)propanoate. [Pg.1285]

Ethyl acetate [79-20-9] is a colorless, neutral liquid that is partially miscible with water and has a pleasant, fruity odor. It has a good solvency for cellulose nitrate, cellulose ethers, chlorinated rubber, poly(vinyl acetate), vinyl chloride copolymers, polyacrylates, polystyrene, fats, oils, and many natural and synthetic resins (alkyd resins, saturated polyesters, ketone resins). Cellulose acetate is, however, dissolved only in the presence of small amounts of ethanol. Poly(vinyl chloride) is insoluble. [Pg.363]


See other pages where Poly ethyl ether ketone is mentioned: [Pg.190]    [Pg.190]    [Pg.347]    [Pg.170]    [Pg.167]    [Pg.360]    [Pg.360]    [Pg.234]    [Pg.315]    [Pg.167]    [Pg.1817]    [Pg.167]    [Pg.369]    [Pg.1604]    [Pg.367]    [Pg.142]    [Pg.299]    [Pg.461]    [Pg.377]    [Pg.377]    [Pg.274]    [Pg.461]    [Pg.513]    [Pg.1305]    [Pg.99]    [Pg.764]   
See also in sourсe #XX -- [ Pg.126 , Pg.500 , Pg.796 ]




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Ether ethylic

Ethers ethyl ether

Ethers ketones

Ethyl ether

Ethyl ketones

Poly ethers

Poly ethyl

Poly ketone

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