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Polyethyleneoxide

The physical properties of commercial alkoxysilanes are provided in Table 1. Two classes of silane esters have very distinct properties and are generally considered apart from alkoxysilanes. Sdatranes are compounds derived from trialkanolamines and have siHcon—nitrogen coordination. These are generally hydrolytically stable and have unique physiological properties (3). A second special class of monomeric esters are cycHc diesters of polyethyleneoxide glycols designated sila-crowns, which have appHcation as catalysts (4). Neither silatranes nor sila-crowns are considered herein. [Pg.36]

Charge-transfer complexes Dioxane, pyridine, polyvinyl, pyrrolid one, poly-2-vinvyl pyridine, polyethyleneoxide [4]... [Pg.179]

Fig. 3 a-c. Summary of data from different laboratories, obtained by surface force measurement, on the average layer thickness L as a function of tethered chain length for flat, tethered layers constructed by adsorption of amphiphilic polymers on mica. Adapted from Ref. 21. (a) Data of reference 20 on poly-tert-butylstyrene chains anchored by adsorbing blocks of poly-2-vinylpyridine. (b) Data of references 11 and 12 on polystyrene chains anchored by adsorbing blocks of poly-2-vinylpyridine. (c) Data of references 13 and 14 on polystyrene chains anchored by adsorbing zwitterionic groups [13] or by small adsorbing blocks of polyethyleneoxide [14]... [Pg.39]

Associations can be of physical nature too. Chitosan blends with hydrophilic polymers including polyvinylalcohol, polyethyleneoxide and poly-vinylpyrrohdone, were investigated as candidates for oral gingival delivery systems. Chitosan blends were superior to chitosan alone in terms of comfort, ease of processing, film quality, and flexibihty [325]. [Pg.195]

This behavior shows that the dimensions of these polymers are independent of pH, ionic strength (in the ranges studied) and presence or absence of Tergitol or polyethyleneoxide. This result is of considerable help in interpretation of GPC behavior since in the absence of polymer-glass substrate interactions, the molecular weight calibration curves (log MW vs. elution volume) should be independent of pH, ionic strength or the two nonionic surfactants investigated. [Pg.269]

Alcohols. Higher aliphatic alcohols with polyethyleneoxide and poly-propyleneoxide are particularly effective at reducing the gas content of drilling solutions [1442]. [Pg.321]

The most important additives are polyethyleneoxide, polypropyleneoxide, and polybutyleneoxide. They are also referred to as polyalkylene glycols, but this name is correct strictly for derivatives of 1,2-diols. [Pg.329]

Polymer grafting can be used to alter chemical and physical properties of a homopolymer. For example, Sawhney and Hubbell [18] grafted polyethyleneoxide to poly L-lysine to enhance biocompatibility of polylysine and improve the polylysine-alginate capsules. Stevenson and Sefton [19] modified alginate by grafting it with hydroxyalkyl methacrylate, again to improve the biocompatibility and to allow for polymerization by means of y-irradiation. Covalently modified (co)-polymers have not been evaluated in this study. [Pg.56]

Polyethyleneoxide-co-polypropyleneoxides, dispersants, S 710t Poly(ethylene oxide) film, physical properties of, 10 68It Poly(ethylene oxide) floe, 11 638 Poly(ethylene oxide)-poly(ethylene terephthalate) copolymers, bioresorbable polymers, 3 738 Poly(ethylene oxide) resins, molecular weight of, 10 684-685 Polyethylene oxides, dispersants, S 706t, 710t... [Pg.731]

Hyperbranched polyesteramides, partially or fully functionalized with fluoroalkyl chains, are expected to be valuable additives for numerous applications. A fully functionalized derivative could be considered to be a unimolecular micelle (like the polyethyleneoxide functionalized analogue) suitable for, e. g., extractions in organic media. An idealized example is shown in Fig. 27. [Pg.75]

Another class of polymers capable of stabilizing Au NPs through physisorption is amphiphilic block copolymers. Initial reports describe the formation of Au NPs in the presence of different amounts of diblock copolymers like PS-P2VP (polystyrene-block -poly-2-vinylpyridine) [111] or PS-PEO (polystyrene-block-polyethyleneoxide) [112]. [Pg.155]

However, according to Little (1969), polyethyleneoxide solutions of different molecular weights gave the same drag reduction when their concentration was proportional to the critical concentration at each molecular weight (i.e., the computed concentration for the polymer coils to touch each other). Kinnier obtained similar results but used the concept of equivalent concentrations . He found that to have equal drag reduction for different molecular weight polymer solutions, one has to have equal volumes of polymer based upon the hydrodynamic sphere considerations. [Pg.113]

Polymethylmethacrylate (PMMA) Polyisodecylmethacrylate Polyacrylic acid (PAA) Polyacrylamide (PAAm) Hydrolyzed polyacrylamide Glyoxylyzed polyacrylamide Polyisobutylene (PIB) Polyethyleneoxide (PEO) Polystyrene Polystyrenesulfonate Polyethylenimine (PEI) Polyvinylalcohol (PVA) Polyvinylpyrrolidone (PVP) Poly-cw-isoprene (PCIP)... [Pg.121]

Within this group, the linear polymers have been most intensively studied and researched. The main area of interest lies in water-soluble polymers. However, there have also been many studies into organic solutions, although there exist problems with odor and toxicity in the case of analytical studies. Among the water-soluble additives, tests were made especially on polyethyleneoxide (PEO), polyacrylamide and the coacrylates (PAAm, PAAm/AAcNa), polyacrylic add (PAA), guar gum (GG), carboxymethylcellulose (CMC) and sodium salts, as well as hydroxyethylcellulose (HEC). From these tests, PEO proved to be the most effective flow improver, followed closely by PAAm, which is somewhat more stable than PEO in turbulent flow. [Pg.124]

Kinnier JW (1970) A correlation between friction reduction and molecular size for the flow of dilute aqueous polyethyleneoxide solutions in pipes Thesis, Y. S. Naval Postgraduate School... [Pg.161]

The same electron transfer was investigated in a polyethyleneoxide film known to be a polymer electrolyte capable of transporting ions. The electron transfer mechanism was analyzed to take place by both static and dynamic mechanisms,33) the electron transfer distance was estimated to be 1.7 nm, and the dynamic rate constant was 4.6 x 106 M 1s 1, which is two orders of magnitude lower than that in an aqueous solution. [Pg.167]

Blends of polyphenylenevinylene with water-soluble polymers have been prepared by mixing solutions of the sulfonium precursor with polyethyleneoxide, hydroxy-propylcellulose and polyvinylmethylether317). Polyethyleneoxide forms spherulites which impose a spherulitic texture to the polyphenylenevinylene that is retained after transformation. As a result of this open network, high conductivities are reached at only 10% conducting polymer. [Pg.36]

During decompose the long range water structure changes can be studied by the polyethyleneoxide derivatives too. At the turbidity point Tr the organic phase con-... [Pg.147]

Diacyllipid-polyethyleneoxide conjugates have been introduced into the controlled drug delivery area as polymeric surface modiLers for liposomes (Klibanov et al., 1990). Being incorporated into the liposome membrane by insertion of their lipidic anchor into the bilayer, such molecules can ster-ically stabilize the liposome against interaction with certain plasma proteins in the blood that results in signiLcant prolongation of the vesicle circulation time. The diacyllipid-PEO molecule itself represents a characteristic amphiphilic polymer with a bulky hydrophilic (PEO) portion and a very short but extremely hydrophobic diacyllipid part. Typically, for other PEO-containing amphiphilic block... [Pg.359]

Finally, the method was applied to determine the Ce(IV) concentration during the polymerisation of polyethyleneoxide. A mixture of linear... [Pg.334]

Core ingredient Poly(alkylene oxide), polyethyleneoxide, polymethyleneoxide,... [Pg.219]

Fig. 22. Phase image of a thin film of a hydrogenated polybutadiene-polyethyleneoxide blockcopolymer (3700-2900 g/mol) on mica. The film was crystallised at 38 C close to a triple line caused by dewetting. Courtesy of G. Reiter [275]... Fig. 22. Phase image of a thin film of a hydrogenated polybutadiene-polyethyleneoxide blockcopolymer (3700-2900 g/mol) on mica. The film was crystallised at 38 C close to a triple line caused by dewetting. Courtesy of G. Reiter [275]...

See other pages where Polyethyleneoxide is mentioned: [Pg.559]    [Pg.329]    [Pg.211]    [Pg.211]    [Pg.159]    [Pg.50]    [Pg.307]    [Pg.92]    [Pg.215]    [Pg.220]    [Pg.516]    [Pg.268]    [Pg.272]    [Pg.415]    [Pg.188]    [Pg.219]    [Pg.41]    [Pg.104]    [Pg.107]    [Pg.124]    [Pg.128]    [Pg.327]    [Pg.335]    [Pg.507]    [Pg.197]   
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