Polyethylene oxide studies

The very first studies with radiation crosslinked polyethylene oxide (PEO) have shown that SAH is able to substantially reduce the sensitivity of plants to water shortage [7], to promote their growth, particularly, under conditions of water deficiency [8], to improve seedling survival and the final crop [9], These results stimulated a more detailed analysis of the effects of SAH in the water balance of... 

The qualitative thermodynamic explanation of the shielding effect produced by the bound neutral water-soluble polymers was summarized by Andrade et al. [2] who studied the interaction of blood with polyethylene oxide (PEO) attached to the surfaces of solids. According to their concept, one possible component of the passivity may be the low interfacial free energy (ysl) of water-soluble polymers and their gels. As estimated by Matsunaga and Ikada [3], it is 3.7 and 3.1 mJ/m2 for cellulose and polyvinylalcohol whereas 52.6 and 41.9 mJ/m2 for polyethylene and Nylon 11, respectively. Ikada et al. [4] also found that adsorption of serum albumin increases dramatically with the increase of interfacial free energy of the polymer contacting the protein solution. 

The same research group proved the applicability of PEO-silicas to the separation of ribonucleic acids and studied how the log k vs m slopes are affected by the molecular weight of polyethylene oxide, the type of salt used in eluent... 

Yang and coworkers did the most efforts on the development of network polyester based on citric acid. " They investigated the reaction of citric acid with a series of aliphatic diols (from 3-16 carbon chains) and polyether diols such as polyethylene oxide (PEG), in which 1,8-octanediol (POC) and 1,10 decanediol (PDC) have been studied the most. 

The effect of pH in the range studied is completely eliminated by addition of 300,000 MW polyethylene oxide with "collapse" of the data onto a single calibration curve. This competitive adsorption effect will be discussed more fully in section 4. 

Strain-induced crystallization would presumably further improve the ultimate properties of a bimodal network. It would therefore obviously be of considerable importance to study the effect of chain length distribution on the ultimate properties of bimodal networks prepared from chains having melting points well above the very low value characteristic of PDMS. Studies of this type are being carried out on bimodal networks of polyethylene oxide) (55), poly(caprolactone) (55), and polyisobutylene (56). 

MD Simulations and Experimental Study of Structure, Dynamics, and Thermodynamics of Polyethylene oxide) and its Oligomers. 

Short PS macromonmers (DP = 4 or 9) polymerized completely under ROMP conditions. Macromonomers with DP = 14 to 46 invariably led to incomplete polymerization, suggesting that the dense polymacromonomer imposes steric limitations on the polymerization. Heroguez et al. studied the ROMP of polyethylene oxide) macromonomers [111, 112], The macromonomers are prepared from a norbornene derivative according to the following sequence ... 

The periodontal pocket is another site for drug delivery in the oral cavity. Needleman et al. [46] investigated three mucoadhesive polymers (cationic chitosan, anionic xanthan gum, neutral polyethylene oxide) in vitro, using organ cultures, and in vivo in patients on their periodontal and oral mucosa. Of the polymers studied, chitosan displayed the longest adhesion in vitro and on the periodontal pockets, and the shortest adhesion on oral mucosa. 

On the other hand, Connor and Hartland ( ) have reported results of a proton NMR study for a series of polyethylene oxide samples by rotating frame proton relaxation time T p meastirements. Ti was also determined. For their lowest molecular weight sam-... 

Polymer phase-transfer catalysts (also referred to as triphase catalysts) are useful in bringing about reaction between a water-soluble reactant and a water-insoluble reactant [Akelah and Sherrington, 1983 Ford and Tomoi, 1984 Regen, 1979 Tomoi and Ford, 1988], Polymer phase transfer catalysts (usually insoluble) act as the meeting place for two immiscible reactants. For example, the reaction between sodium cyanide (aqueous phase) and 1-bromooctane (organic phase) proceeds at an accelerated rate in the presence of polymeric quaternary ammonium salts such as XXXIX [Regen, 1975, 1976]. Besides the ammonium salts, polymeric phosphonium salts, crown ethers and cryptates, polyethylene oxide), and quaternized polyethylenimine have been studied as phase-transfer catalysts [Hirao et al., 1978 Ishiwatari et al., 1980 Molinari et al., 1977 Tundo, 1978]. 

The kinetics of the reaction of solid sodium iodide with 1-bromooctane were studied with a 95 % RS graft of polyethylene oxide) 6-mer methyl ether on 3 % CL polystyrene as catalyst (51)176). The rates were approximately first order in 1-bromooctane and independent of the amount of excess sodium iodide. The rates varied with the amount of the solid catalyst used, but there was not enough data to establish the exact functional dependence. All experiments employed powdered sodium iodide, magnetic stirring, and 75-150 pm catalyst beads. Thus the variables stirring speed and particle size, which normally are affected by mass transfer and intraparticle diffusion, were not studied. Yanagida 177) favors a mechanism of transfer of the sodium iodide by dissolution in the solvent (benzene) and diffusion to the catalyst particle... 

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