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Pure polyethylene oxide

Nonionic, hydrophilic Polyethylene oxide, polyethylene glycol Polyviny alcohol, hydroxyethyl cellulose, polyacrylamide Pure water 0.1-0.2 M salt/buffer, pH 7... [Pg.364]

The block-polymers containing a middle block of polystyrene and two blocks of polyethylene oxide have some unusual properties. They are soluble in methyl ethyl ketone and cannot be precipitated from this solvent by methanol. Addition of water produces a slight cloudiness but still no precipitation although the block polymer is not soluble in pure water. The polymer is also soluble in benzene, but addition of water to this solution causes its precipitation. On the other hand, neither homopolystyrene nor homo-polyethylene oxide or their mixtures are precipitated from benzene solution by addition of water. This strange behaviour is explained by Richards and Szwarc (45) in terms of hydrogen bonding which depends on the chemical potential of water in the aqueous layer and therefore also in the benzene solution. [Pg.298]

Polyethylene. The action of ozone on polyethylene was studied in the temperature range from 25° to 109° C. The reaction was followed qualitatively and quantitatively by infrared spectra. The products appeared to be of the same nature as those of O2 oxidations of polyethylene 2)—i.e., the formation of aldehydic and ketonic groups as indicated by the appearance of a strong absorption band in the region of 5.9 microns, and the existence of hydroxyl groups as shown by the 2.9-micron band. Polyethylene is readily oxidized in the presence of ozone, as even short period ozonizations carried out at temperatures as low as 25° C. yielded considerable concentrations of carbonyl and hydroxyl groups. Pure O2 oxidations did not yield comparable results until the reaction temperature was raised approximately... [Pg.169]

Studies of novolac-type resins (phenolic polyethylene oxide blends) show by C NMR that a blend of 30 70 composition leads to a ca 2 ppm high freqnency shift compared to a pure phenolic resin. This is ascribed by the anthors to increased hydrogen bonding . [Pg.367]

This is confirmed by the work of Christiansen and Craig [11], Oliver and Jenson [12], and Yoo [13]. These investigators found that the thermal conductivities of dilute aqueous solutions of Carbopol-934, carboxymethyl cellulose (CMC), polyethylene oxide, and polyacrylamide are no more than 5 percent lower than those of pure water at corresponding temperature. However, Bellet et al. [14] observed substantial decreases in the thermal conductivity measurements for much higher concentrations of aqueous solutions of Carbopol-960 and CMC (i.e., beyond 10 to 15 percent by weight). Lee and Irvine [15] reported that the thermal conductivity of aqueous polyacrylamide solutions was dependent on the shear rate. [Pg.739]

The demarcation line between (7) and (8) is not absolute, even in the same flow apparatus. Islam and co-workers studied the effect of inertia [136], as characterized by Re (1), on the scission of polyethylene oxide (PEO) in cross-slot devices. As shown in Fig. 11, in a 50 50 aqueous glycerol mixture 10pure water (910 [Pg.152]

Brown, et al. [74] measured Dg from PFGMR for dextran (M = 44 kDa, = 64.2 kDa) in water, for c up to 250 g/L, as seen in Fig. 1. Brown and the same collaborators [75] also measured Dg of of narrow molecular weight distribution (M /M E (1.02,1.20)) polyethylene oxides in water, as seen in Fig. 2. Polymer molecular weights were in the range 73-661 kDa polymer concentrations reached 70 g/1. Data were fit both to a pure v = 1) and a stretched exponential in c the simple exponentials (which gives excellent fits) are shown. [Pg.316]

For nonionic polymers pure water can often be used as eluant, although a low ionic strength is a good safety measure and adds a degree of reproducibility to the system. Polyethylene oxide and polyethylene glycol are characteristic of this sample category. [Pg.40]

Nonionie, hydrophilie polyethylene oxide polyethylene glycol pure water pure water... [Pg.41]

The possibility of using aluminum nitride (AIN) nanopowders as flame retardant additive was studied [25]. Concentration of the nanopowder AIN incorporated in a polyethylene matrix was 0.1 0.25 0.75 1.5 and 3 wt%. The incorporation of 1.5 wt% AIN in a polyethylene matrix caused the significant increase in the temperature of the beginning of oxidation of 33 °C (to 183 °C) in comparison with pure polyethylene (150 °C) and in the onset temperature of the intensive weight loss of 15 °C (to 375 °C) against 360 °C for pure polyethylene. The resulting effect is explained by the influence of nanoparticles on the microstructural characteristics of polyethylene. Nanoparticles are the crystallization centers and participate in the formation of fine-grained structure. [Pg.4]

TABLE 9. Influeiice of Sulfur-Containing Compounds (0.1%) on the Oxidation of Pure Polyethylene and Polyethylene Containing Carbon Black [41]... [Pg.119]

Polymer electrolytes are used in lithium ion rechargeable batteries. Pure polymer electrolyte systems include polyethylene oxide (PEO), polymethylene-polyethylene oxide (MPEG), or polyphosphazenes. Chlorinated PVC blended with a terpoly-mer comprising vinylidene chloride/acrylonitrile/methyl methacrylate can make a good polymer electrolyte. Rechargeable lithium ion cells use solid polymer electrolytes. Plasticized polymer electrolytes are safer than liquid electrolytes because of a reduced amount of volatiles and flammables. The polymer membrane can condnct lithinm ions. The polymer membrane acts as both the separator and electrolyte [7],... [Pg.171]


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Polyethylene oxide

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