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Oxidation copolymer

The method has severe limitations for systems where gradients on near-atomic scale are important (as in the protein folding process or in bilayer membranes that contain only two molecules in a separated phase), but is extremely powerful for (co)polymer mixtures and solutions [147, 148, 149]. As an example Fig. 6 gives a snapshot in the process of self-organisation of a polypropylene oxide-ethylene oxide copolymer PL64 in aqueous solution on its way from a completely homogeneous initial distribution to a hexagonal structure. [Pg.27]

Surface active agents are important components of foam formulations. They decrease the surface tension of the system and facilitate the dispersion of water in the hydrophobic resin. In addition they can aid nucleation, stabilise the foam and control cell structure. A wide range of such agents, both ionic and non-ionic, has been used at various times but the success of the one-shot process has been due in no small measure to the development of the water-soluble polyether siloxanes. These are either block or graft copolymers of a polydimethylsiloxane with a polyalkylene oxide (the latter usually an ethylene oxide-propylene oxide copolymer). Since these materials are susceptible to hydrolysis they should be used within a few days of mixing with water. [Pg.797]

ACPA azobis(4-cyanopentanoic acid) AIBN azobis isobutyronitrile) BPO benzoyl peroxide DVB divinyl benzene, EGA 2-ethylcyano-acrylate HPC hydroxypropyl cellulose MMA methyl methacrylate PAAc polyacrylic acid PEI polyethyleneimine, PEO/PPO polyethylene oxide/polypyropylene oxide copolymer PVME polyvinylmethylether PVP polyvinylpyrrolidone K-30 DMSO dimethylsulfoxide PGA polyglutaraldehyde CMS chloromethylstyrene PMMA-g-OSA polymethylmethacrylate grafted oligostearic acid. [Pg.202]

High modulus blends can be developed by mixing TPU with acetal copolymer (trioxane ethylene oxide copolymers) [242-244]. The highly crystalline acetal forms a second continuous phase. Kumar et al. studied behavior of such blends [245]. TPU retains none of its physical properties after immersion in water at 70°C for three weeks. The hydrolysis resistance of TPU can be improved by blending with polycarbodiimides [246]. Two parts of carbodiimide with TPU offer 87% retention of its strength, 93% of elongation, and 75% of modulus under the same... [Pg.148]

Based on the synthesis of polyphosphazenes and of diblock copolyphosp-hazenes by the living cationic polymerization of phosphoranimines [237,241], the triblock poly(phosphazene-ethylene oxide) copolymer XVIII was synthesized by Allcock [223]. [Pg.212]

Zhu, K. J., Xiangzhou, L., and Shilin, Y., Preparation and properties of D,L-lactide and ethylene oxide copolymer A modifying biodegradable polymeric material, J. Polym. Sei. Part C Polvm. Lett.. 24, 331-337, 1986. [Pg.229]

The pendant hydroxy groups of ethylene oxide-propylene oxide copolymers of dihydroxy and trihydroxy alcohols may be sulfurized to obtain a sulfurized alcohol additive. This is effective as a lubricant in combination with oils and fats [387,533]. The sulfurized alcohols may be obtained by the reaction of sulfur with an unsaturated alcohol. Furthermore, fatty alcohols and their mixtures with carboxylic acid esters as lubricant components [1286] have been proposed. [Pg.14]

X. Chen and S. Dong, Sol-gel-derived titanium oxide/copolymer composite based glucose biosensor. [Pg.551]

Unsaturations of hydroxy-containing compounds are reduced on reaction with nitrile oxides such as tetramethyl terephthalonitrile N,N -dioxide (506) or 1,3,5-triethylbenzene-2,6-dicarbonitrile oxide (507). The reaction of a nitrile oxide with terminal unsaturation, associated with the preparation of a poly-ol from propylene oxide, reduces the mono-ol content of the poly-ol composition. Thus, stirring a solution of an ethylene oxide-propylene oxide copolymer with an OH content of 2.39% and vinyl unsaturation of 3.58% in THF with l,3,5-triethylbenzene-2,6-dicarbonitrile oxide for 1 min results in an effective removal of the terminal unsaturation. [Pg.103]

POLY(STYRENE)-GRAFT-POLY(ETHYLENE OXIDE) COPOLYMERS... [Pg.226]

DE N DRIG RAFT-POL Y(STYRENE)-G RAFT-POL Y(ETHYLENE OXIDE) COPOLYMERS BY TERMINAL GRAFTING... [Pg.230]

Poly(ethylene oxide) polymers and poly(ethylene oxide/propylene oxide) copolymers with iminodipropionitrile (139) or iminodiacetonitrile end groups were used as ligands in the palladium-catalyzed oxidation of higher olefins (1-octene to 1-hexadecene) at 50-70 °C with atmospheric air or 1-3 bar O2. In an ethanol/water mixture 88 % yield of 2-hexanone and 92 % yield of 2-hexadecanone was obtained in 4 and 2 h, respectively, with a... [Pg.212]

Chen, E.-T., Duo, Y.-Q., Luo, S.-G., Luo, Y.-J., and Tan, H.-M., Novel Segmented Thermoplastic Polyurethane Elastomers Based on Tetrahydrofuran/Ethylene Oxide Copolymers as High Energetic Propellant Binders, Propellants, Explosives, Pyrotechnics, Vol. 28, 2003, pp. 7. [Pg.111]

Both end groups can be determined quantitatively. A second side reaction is the transacetalization. Here a poly(oxymethylene) cation attacks an oxygen of a poly(oxymethylene) chain with formation of an oxonium ion that decomposes. Through continued cleavage and recombination of poly(oxymethylene) chains one obtains polymers which are chemically and molecularly largely homogeneous. For the case of a trioxane/ethylene oxide copolymer the following reaction scheme can be formulated ... [Pg.209]

Alexandridis P, Athanassiou V, Eukuda S, Hatton TA. Surface activity of polyfethylene oxide)-f>tock-poly(propylene oxide)-f>tock-poly(ethylene oxide) copolymers. Langmuir 1994 10 2604-2612. [Pg.30]

Antistatic Compositions. Antistatic properties can be imparted to ABS polymers by coating the surface of the resin with surfactants or by incorporating surfactants into the resin by kneading. Further, it has been proposed to admix an epihalohydrin polymer or an ethylene oxide copolymer. [Pg.221]

Compositions of ABS polymers that contain a special ethylene oxide copolymer have been developed, which do not suffer from these drawbacks. The ethylene oxide copolymer consists of ethylene oxide and 1-naphthyl glycidyl ether. The copolymer a should have a high refractive index of more than 1.50. The presence of this copolymer in the ABS resin composition gives a product of remarkably improved surface appearance when the composition is subjected to injection molding. In addition, the resin composition has an excellent antistatic property (23). [Pg.222]

Y. Matoba, Y. Shimizu, K. Miura, S. Kitano, T. Sakashita, and H. Tanaka, Antistatic resin blends comprising ABS graft copolymers and ethylene oxide copolymers, US Patent 5556916, assigned to Daiso Co. Ltd. (Osaka, JP), September 17,1996. [Pg.258]

The selective oxidation of cellulose to dialdehyde by sodium periodate is well known. It has been postulated by Criegee (74) and by Waters (73) that this reaction proceeds by a free radical mechanism. Toda (76) and Morimoto, Okada, Okada, and Nakagawa (77) have concluded that sodium periodate oxidation should initiate graft polymerization. They succeeded in grafting methyl methacrylate and acrylonitrile onto cellulose substrates, such as rayon and paper. A similar procedure is recommended in a patent of Chemische Werke Huels (78) to graft vinyl monomers onto cotton, polyethylene oxide, copolymers of vinyl chloride-vinyl acetate, and others. [Pg.127]

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]

Preparation and Properties of Poly(arylene oxide) Copolymers... [Pg.242]

Poly(arylene oxide) copolymers were prepared by simultaneous and sequential oxidation of 1 1 mixtures of 2, 6-dimethylphenol (DMP), 2-methyl-6-phenylphenol (MPP), and 2,6-diphenylphenol (DPP), and methods were developed for determination of their structure. DMP and DPP yielded either random copolymers or block copolymers with crystallizable DMP and DPP blocks, depending on the order of oxidation and reaction conditions. Four types of copolymers were produced from MPP and DPP random copolymers, block copolymers with crystallizable DPP blocks, short block copolymers with DPP segments too short to permit crystallization, and mixed block copolymers containing DPP blocks and randomized MPP-DPP segments. Redistribution is so facile in the DMP-MPP system that only random copolymers were obtained, even on oxidation of a mixture of the two homopolymers. [Pg.242]


See other pages where Oxidation copolymer is mentioned: [Pg.381]    [Pg.198]    [Pg.8]    [Pg.211]    [Pg.505]    [Pg.46]    [Pg.46]    [Pg.72]    [Pg.254]    [Pg.228]    [Pg.230]    [Pg.319]    [Pg.280]    [Pg.98]    [Pg.36]    [Pg.39]    [Pg.8]    [Pg.149]    [Pg.381]    [Pg.295]    [Pg.301]    [Pg.243]    [Pg.245]    [Pg.247]   


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