Polyethylene oxide -poly butylene

Poly (ethylene oxide)/poly (butylene oxide) copolymers In polyethylene oxide)-poly(butylene oxide) (PEO-PBO) diblocks with short blocks, unfolded PEO blocks crystallize into lamellar crystals, and the PBO... [Pg.297]

Engineering resins can be combined with either other engineering resins or commodity resins. Some commercially successhil blends of engineering resins with other engineering resins include poly(butylene terephthalate)—poly(ethylene terephthalate), polycarbonate—poly(butylene terephthalate), polycarbonate—poly(ethylene terephthalate), polysulfone—poly (ethylene terephthalate), and poly(phenylene oxide)—nylon. Commercial blends of engineering resins with other resins include modified poly(butylene terephthalate), polycarbonate—ABS, polycarbonate—styrene maleic anhydride, poly(phenylene oxide)—polystyrene, and nylon—polyethylene. [Pg.277]

RAFT polymerization has been used to prepare poly(ethylene oxide)-/ /wA-PS from commercially available hydroxy end-functional polyethylene oxide).4 5 449 Other block copolymers that have been prepared using similar strategies include poly(ethylene-co-butylene)-6/oci-poly(S-eo-MAH), jl poly(ethylene oxide)-block-poly(MMA),440 polyethylene oxide)-Moe -poly(N-vinyl formamide),651 poly(ethylene oxide)-Wot A-poly(NlPAM),651 polyfethylene ox de)-b ock-polyfl,1,2,2-tetrahydroperfluorodecyl acrylate),653 poly(lactic acid)-block-poly(MMA)440 and poly( actic acid)-6focA-poly(NIPAM),4 8-<>54... [Pg.546]

The morphologies of various copolymers composed of polyethylene oxide), PEO, and poly (1,2-butylene oxide), PBut, were recently reviewed by Ryan et al. [61]. The corresponding phase diagrams of PEO-fr-PBut, PBut-fo-PEO-fo-PBut and PEO-fo-PBut-fo-PEO melts are depicted in Fig. 11. In all phase diagrams the semi-crystalline lamellar phase was not attained because of the copolymers low melting points. [Pg.155]

Other polyethers which have found limited application are polyethylene oxides) and some mixed polyester-polyethers such as Peedo-120 (Union Carbide), a diester of poly (1,4-butylene oxide )diol and azelaic acid. [Pg.97]

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]

The decorative laminates described in the previous chapter are made with selected thermosetting resins while resins of this type can be moulded and extruded by methods similar to those outlined in the present and the next chapter the materials employed for these processes predominantly are thermoplastic. Many such plastics can be moulded and extruded under suitable conditions, the most important in terms of quantities used being those that combine properties satisfactory for the purpose with convenience in pro-cessing-especially the polyolefins (polyethylene and polypropylene), poly(vinyl chloride), and styrene polymers and blends. Other plastics with special qualities, such as better resistance to chemical attack, heat, impact, and wear, also are used—including acetals (polyformaldehyde or polyoxymethylene), polyamides, polycarbonates, thermoplastic polyesters like poly(ethylene terephtha-late) and poly(butylene terephthalate), and modified poly(phenylene oxide),... [Pg.136]

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]

Blankenship [3] prepared polyethylene glycol carbamate, (II), as paint thickeners containing poIy(ethyIene oxide-b-propylene oxide-b-ethylene oxide) and either 1,6-hexamethyIene diisocyanate or 4,4 -methyIene bis-(isocyanatocy-clohexane). Polycarbamates were also prepared by Bauer [4] using a block polymer initiated by stearyl alcohol and consisting of poly(ethylene oxide-b-propylene oxide-b-butylene oxide-b-dodecene oxide-b-tetradecene oxide) coupled with the diisocyanate, Desmodur N . [Pg.3]

It was found meanwhile that nearly every slim unbranched polymer chain, such as poly(trimethylene oxide) [224], poly(l,3-dioxolane) [225], poly(tetramethylene oxide) [226], polyethylene imine) [227], poly(3-hydroxy propionate), poly (4-hydroxybutyrate) and poly(6-hydroxyhexanoate) [228,229], poly(butylene succinate) [229], polyadipates [230], nylon-6 [231], and even oligomers of polyethylene [232], form a-CD ICs with channel structures. In all of these cases, inclusion is a heterogeneous process, since the guest polymer and its CD complex are almost insoluble in water. Therefore, extensive sonication had to be applied to accelerate the diffusion process. The polymer was also dissolved in an organic solvent, e.g., nylon-6 in formic acid, and this solution was added to the solution of a-CD [231], Alternatively, a monomer, such as 11-aminoundecanoic acid, was included in a-CD and polymerized to nylon-11 by solid state polycondensation within the channels of the IC. Thus, the IC of nylon-11 was formed under conservation of the crystal packing [233-235],... [Pg.34]

A simple method to measure the membrane permeability to specific molecules has been presented by G. Battaglia and coworkers [141], The authors encapsulated highly hydrophilic 3,3, 3//-phosphinidynetris-benzenesulfonic acid (PH) into polyethylene oxidc)-co-poly(butylene oxide) (EB) vesicles and monitored its reaction with 5,5/-dithiobis-2-nitrobenzoic acid (DTNB) penetrating the membrane from the exterior. The reaction rate (amount of the formed product as a function of time after DTNB addition) measured with IJV/Vis was directly correlated to the permeability of the permeating molecule. A comparison of these results with the permeability of egg yolk phosphatidylcholine (PC) vesicles showed that EB membranes have a more selective permeability toward polar molecules than the phospholipids membranes. Also in this case the permeability appeared to depend on the membrane thickness as predicted by Fick s first law. [Pg.135]

PHA blends with poly(vinyl alcohol) (PVA) are interesting materials whose miscibility depends on the composition and the PVA tacticity [178]. PHB is claimed to be miscible with polyethylene glycol [179] and with poly D-lactide [180] its miscibility with polyethylene oxide depends on the blend composition [181]. Immiscible, but well-compatible blends of PHB, were prepared with poly(butylene succinate-co-butylene adipate) and poly(butylene succinate-co-caprolactone) [182]. [Pg.468]

Botelho G, Queiros A, Gijsman P. Thermo-oxidative studies of poly(ether-esters) 1. copolymer of poly(butylene terephthalate) and polyethylene oxide. Polym Degrad Stab 2000 67 13-20. [Pg.414]

The effect of the amorphous component on the crystallization ability of the crystallizable polymer has been examined for some miscible blends. An improvement of poly( -caprolactone) (PCL) crystallization has been observed in blends with chlorinated polyethylene (CPE) [20], while for poly(ethylene oxide)/poly(ethyl methacrylate) (PEO/PEMA) [21], PCL/SAN [22], and poly(butylene therephthalate)/polyarylate (PBT/ PAr) [23] blends, the crystallization ability is markedly reduced. [Pg.291]

Polymers that crystallize in a temperature interval well removed from T, but whose growth rates do not display maxima, also present problems with respect to the existence of the 111-11 transition. Polymers in this category include poly(butylene terephthalate),(200) poly(trimethylene terephthalate),(201) poly(pivalolactone), (202,203) one study of poly(methylene oxide),(204) linear polyethylene over a slightly more extended temperature range (205,205a) and a set of reports for isotactic poly(propylene).(206-210)... [Pg.130]

Cruz-Pinto JJC, Carvalho MBS, Ferreira JEA (1994) The kinetics and mechanism of polyethylene photo-oxidation. Angew Makromol Chem 216 113—133 Darwin PRK, Abdefilah A, Elise D, Josefina LC, Sebastian MG (2003) Synthesis, characterization, and properties of poly(ethylene terephthalate)/poly(l, 4-butylene succinate) block copolymers. Polymer 44 1321—1330... [Pg.13]

Stackman [29] carried out a study to find systems suitable for reducing the flammability of polyethylene terephthalate (PET) and poly-1,4-butylene terephthalate (PBT) while retaining the chemical and physical properties of the original polymers. The additives used were phosphine oxides, phosphonates and phosphates and their activity was assessed by means of an oxygen index test. Most of the phosphorus esters were found to be volatile under the blending conditions and both the halogenated phosphorus esters and halogenated derivatives of phosphorus oxide proved to be ineffective as flame retardants. [Pg.80]

The chemical modification of homopolymers such as polyvinylchloride, polyethylene, poly(chloroalkylene sulfides), polysulfones,poly-chloromethylstyrene, polyisobutylene, polysodium acrylate, polyvinyl alcohol, polyvinyl chloroformate, sulfonated polystyrene block and graft copolymers such as poly(styrene-block-ethylene-co-butylene-block-styrene), poly(1,4-polybutadiene-block ethylene oxide), star chlorine-telechelic polyisobutylene, poly(lsobutylene-co-2,3-dimethy1-1,3-butadiene), poly(styrene-co-N-butylmethacrylate) cellulose, dex-tran and inulin, is described. [Pg.425]