Linear polyethylene oxide

COMPARISON OF FOUR COMMERCIAL LINEAR AQUEOUS SIZE EXCLUSION COLUMNS AND FOUR SETS OF COMMERCIAL POLYETHYLENE OXIDE (PEO) STANDARDS FOR AQUEOUS SIZE EXCLUSION CHROMATOGRAPHY OF POLYVINYLPYRROLIDONE AND PEO... 

TABLE 17.8 Separation Efficiency of Four Linear Columns in Water and Water/Methanol for Polyethylene Oxide Standards... 

The chemical and physical properties of the polymers obtained by these alternate methods are identical, except insofar as they are affected by differences in molecular weight. In order to avoid the confusion which would result if classification of the products were to be based on the method of synthesis actually employed in each case, it has been proposed that the substance be referred to as a condensation polymer in such instances, irrespective of whether a condensation or an addition polymerization process was used in its preparation. The cyclic compound is after all a condensation product of one or more bifunctional compounds, and in this sense the linear polymer obtained from the cyclic intermediate can be regarded as the polymeric derivative of the bifunctional monomer(s). Furthermore, each of the polymers listed in Table III may be degraded to bifunctional monomers differing in composition from the structural unit, although such degradation of polyethylene oxide and the polythioether may be difficult. Apart from the demands of any particular definition, it is clearly desirable to include all of these substances among the condensation... 

On addition of polyethylene oxide of M.W. 300,000 at a concentration of 0.025 g liter , it is seen that a single calibration curve is obtained, independent of NaCl concentration. (It should be noted, however, that at very low NaCl concentration, less than about 0.005 M, the curve still appears at lower elution voliames). This curve is not linear but does exhibit fairly good resolution. It is likely that the effect of polyethylene oxide... 

Figures 6, 7 and 9 show calibration curves using two multi-column combinations and illustrate the degree of "optimization obtained in this system. The mobile phases for Figures 6 and 7 contained 0.025 g polyethylene oxide and ion exclusion and adsorption effects should therefore be largely eliminated. Figure 6 shows that reasonably good resolution can be obtained with a combination of five columns but does exhibit some loss of peak separation at the low cuid high MW ends. In Figure 7 the effect of adding a sixth column of small pore size is illustrated and it is seen that resolution at the low MW end is thereby somewhat improved. This calibration curve is effectively linear with a change of slope at 500,000 MW. It should provide a useful aqueous GPC system for MW and MWD determination of nonionic polyacrylamides.

The high-density polyethylene is linear and can be manufactured by (i) coordination polymerisation of monomer by triethyl aluminium and tritanium chloride, (ii) polymerisation with supported Metal Oxide Catalysts. Such as chromium or molybdenum oxides supported over alumina-silica bases. 

Aqueous SEC Experiments. Aqueous SEC separations were carried out at ambient temperature using two column sets of MicroPak TSK PW Type gel which were investigated for linearity of molecular weight calibration curve using polyethylene glycol (PEG) and polyethylene oxide (PEO) narrow MWD standards. Columns were matched in pore volume as closely as possible to promote linearity of the molecular weight calibration cuiA e. Column set A consisted... 

Figure i A. Calibration curves using a series of narrow MWD polyethylene oxide standards for MicroPak TSK PW column sets. Linear least squares fit for log (MW) vs. elution volume. Column set A MicroPak TSK 3000PW + LOOOPW + 5000PW + 6000PW. 

Based on the results obtained to date, which have been summarized above for several different semicrystalline polymers— linear and low density (branched) polyethylene, polytrimethylene oxide, polyethylene oxide and cis polyisoprene—it is concluded that the relatively fast segmental motions, as manifested in Tq, are independent of all aspects of the crystallinity and are the same as the completely amorphous polymer at the same temperature. Furthermore, it has previously been shown that for polyethylene, the motions in the non-crystalline regions are essentially the same as those in the melts of low molecular weight ii-alkanes. (17)... 

Proton NMR relaxation parameters have also been determined for polyethylene ( ) and polyethylene oxide (39) in the melting region. The apparent contradiction between the proton spin-lattice relaxation parameter for a high molecular weight linear polyethylene sample at its melting point, with the relaxation measurements, has previously been pointed out. (17) This discrepancy is still maintained with the more detailed results reported here for both types of polyethylene. For the proton relaxation a small, but distinct, discontinuity is reported at the melting teirperature. (38)... 

In the present work the limiting value of the linewidths for polyethylene oxide increases from 135 Hz in the melt above 70°C, to the range 300-350 Hz in the crystalline state at room temperature. As is indicated in Table I, the resonant linewidths for linear polyethylene increase substantially upon crystallization and attain values in the range 500-900 Hz at 45°C and 57.9 MHz. 

Nowadays, the sieving matrices most employed in CSE are polymer solutions that under suitable conditions may form a transient mesh or sieving matrix that provide the size-based separation of charged biopolymers. The polymer solutions can be formulated with linear acrylamide and N-substituted acrylamide polymers, cellulose derivatives, polyethylene oxide, and its copolymers or with a variety of polymers, such as polyvinylpyrrolidone (PVP), polyethylene oxide (PEO), and hydroxypropyl cellulose(HPC), which do not necessitate the preventive coating of the capillary wall due to their ability to dynamically coat the inner surface of the capillary, resulting in suppressed EOE and sample interactions with the capillary wall. 

The principal polyolefins are low-density polyethylene (ldpe), high-density polyethylene (hope), linear low-density polyethylene (lldpe), polypropylene (PP), polyisobutylene (PIB), poly-1-butene (PB), copolymers of ethylene and propylene (EP), and proprietary copolymers of ethylene and alpha olefins. Since all these polymers are aliphatic hydrocarbons, the amorphous polymers are soluble in aliphatic hydrocarbon solvents with similar solubility parameters. Like other alkanes, they are resistant to attack by most ionic and most polar chemicals their usual reactions are limited to combustion, chemical oxidation, chlorination, nitration, and free-radical reactions. 

Because of the presence of ether groups and terminal hydroxyl groups, polyethylene oxide (PEO) is also soluble in water. Likewise, polyvinyl alcohol (PVA), which contains a hydroxyl group on most of the alternate carbon atoms in the linear chain, is soluble in water. 

Figure 3. Linear dependence of the apparent bimolecular rate constant of living polyethylene oxide propagation on the fraction of free ions a with cryptates as counterions in THF at 20°C K + 222 ( ) with + [222] ( ) + [ ] ) with 4>kBCs + [ ] -...

Film -use of microbial polysaccharides [MICROBIAL POLYSACCHARIDES] (Vol 16) -cellulose esters m [CELLULOSE ESTERS - ORGANIC ESTERS] (Vol 5) -drying of [DRYING] (Vol 8) -by extrusion [PLASTIC PROCESSING] (Vol 19) -ITOPE [OLEFIN POLYMERS - POLYETHYLENE - HIGH DENSITY POLYETHYLENE] (Vol 17) -from LDPE [OLEFIN POLYMERS - POLYETHYLENE - LOW DENSITY POLYETHYLENE] (Vol 17) -of LLDPE [OLEFIN POLYMERS - POLYETHYLENE - LINEAR LOW DENSITY POLYETHYLENE] (Vol 17) -of polyethylene oxide) [POLYETHERS - ETHYLENE OXIDE POLYMERS] (Vol 19) -of polystyrene [STYRENE PLASTICS] (Vol 22) -m printing processes [PRINTING PROCESSES] (Vol 20)... 

The effects of longer and shorter side chains on the epoxide compared to PBO are shown in Table VII. Polyethylene oxide led to a small improvement in impact strength and melt flow rate, but the heat distortion temperature was decreased. Polypropylene oxide and polyhexene-1 oxide had enhancing effects similar to and even a bit greater than those of PBO. Polyphenylglycidyl ether appeared to be inert when added to modified CPVC. Finally, in this application, the linear PTHF was harmful to properties. 

Recently, a new class of inhibitors (nonionic polymer surfactants) was identified as promising agents for drug formulations. These compounds are two- or three-block copolymers arranged in a linear ABA or AB structure. The A block is a hydrophilic polyethylene oxide) chain. The B block can be a hydrophobic lipid (in copolymers BRIJs, MYRJs, Tritons, Tweens, and Chremophor) or a poly(propylene oxide) chain (in copolymers Pluronics [BASF Corp., N.J., USA] and CRL-1606). Pluronic block copolymers with various numbers of hydrophilic EO (,n) and hydrophobic PO (in) units are characterized by distinct hydrophilic-lipophilic balance (HLB). Due to their amphiphilic character these copolymers display surfactant properties including ability to interact with hydrophobic surfaces and biological membranes. In aqueous solutions with concentrations above the CMC, these copolymers self-assemble into micelles. 

Linear viscoelastic measurements using infrared dichroism on the compatible blend polyethylene oxide) and poly(methyl methacrylate) were reported by Zawada et al. [139]. Unlike Monnerie and coworkers [127], who reported seeing only orientation in the PMMA component, and none in the PEO, Zawada et al. observed alignment in the PEO. However, since the PEO was of lower molecular weight (as was the case for Monnerie and coworkers), its relaxation timescales were substantially faster than the PMMA. This may explain the lack of any measurable orientation by Monnerie and coworkers, who studied quenched samples, since their preparation may have allowed the PEO to relax prior to testing. 

The mechanism of separation with linear polymers is as follows. At a certain polymer concentration known as the entanglement threshold, the individual polymer strands begin to interact with each other, leading to a meshlike structure within the capillary. This allows DNA separation to take place. Many of the common polymers are cellulose derivatives, such as hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, and methylcellulose. Other applicable polymers include linear polyacrylamide, polyethylene oxide, agarose, polyvinyl pyrrolidone, and poly-N. Ar-dimethylacrylamide. High-resolution separation up to 12,000 bp has been reported using entangled polymer solutions. 

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