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Reduced polymer

Boron also reacts with hydroxyl-containing polymers such as cellulose. When exposed to a flame the boron and hydroxyl groups form a glassy ester that coats the substrate and reduces polymer degradation. A similar type of action has been observed in the boron—alumina tfihydrate system. [Pg.457]

Antiozonants (qv) prevent or reduce polymer degradation by the active ozone molecule. Some antioxidant compounds, such as the /)i7n7-phenylenediamines, are excellent as antiozonants (36). The protection by these compounds is thought to be either a reaction with the ozone before it can react with the surface of the mbber or an aid in reuniting chains severed by ozone (37). [Pg.499]

Synthetic fiber producers have attempted to minimise the tendency for pilling by several methods, one of which is to reduce polymer molecular weight. The resulting lower strength fiber would break away from the fabric surface more readily. Another method for reducing pilling is to notch or etch the fiber surface either before or after incorporation in fabric form. [Pg.460]

An example of an appHcation of hydrocracking is in lubricating oils, where it is used to improve the viscosity index, color, and color stabiHty to reduce polymer formation (storage stabiHty) and to decrease the neutralization number (acidity) (61). [Pg.201]

Figure 7-8H. Special metal disk holder for polymer systems using a smooth disk surface to reduce polymer adherence, and a smooth annuleir sealing area. Usually thick to avoid need for vacuum support and to allow for corrosion attack. By permission, Fike Metal Products Co. Div., Fike Corporation, Inc. Figure 7-8H. Special metal disk holder for polymer systems using a smooth disk surface to reduce polymer adherence, and a smooth annuleir sealing area. Usually thick to avoid need for vacuum support and to allow for corrosion attack. By permission, Fike Metal Products Co. Div., Fike Corporation, Inc.
A review on drag-reducing polymers is given in the literature [1359]. It has been suggested that drag reduction occurs by the interactions between elastic macromolecules and turbulent-flow macrostructures. In turbulent pipe flow, the region near the wall, composed of a viscous sublayer and a buffer layer, plays a major role in drag reduction. [Pg.167]

K. Oh-Kil and C. Ling-Siu. Drag reducing polymers. In The polymeric materials encyclopedia. CRC Press, Inc, Boca Raton, FL,... [Pg.442]

K. W. Smith, L. V. Haynes, and D. F. Massouda. Solvent free oil soluble drag reducing polymer suspension. Patent US 5449732, 1995. [Pg.462]

Aid in the uniform dispersion of additives. Make powdered solids (e.g. particulate fillers with high energy and hydrophilic surface) more compatible with polymers by coating their surfaces with an adsorbed layer of surfactant in the form of a dispersant. Surface coating reduces the surface energy of fillers, reduces polymer/filler interaction and assists dispersion. Filler coatings increase compound cost. Fatty acids, metal soaps, waxes and fatty alcohols are used as dispersants commonly in concentrations from 2 to 5 wt %. [Pg.778]

Sylvester, N.D. and Tyler, J.S. "Dilute Solution Properties of Drag-Reducing Polymers," Ind.Eng.Chem.Prod.Res.Develop.. 1970, 9(4), 548 553. [Pg.668]

Chang, H.D., Darby, R. "Effect of Shear Degradation on the Rheological Properties of Dilute Drag Reducing Polymer Solutions," J. Rheol.. 1983, 27(1), 77-88. [Pg.668]

Drag reducing polymers are susceptible to degradation and consequently find only limited application. However, suspensions of fibres, particularly of asbestos, exhibit drag reducing properties and may be more suitable for prolonged use. [Pg.134]

Mass spectrometer studies of oxidant additions to fluoro- and chlorocarbon gases have demonstrated that the relative reactivity of atoms with unsaturate species in a glow discharge follows the sequence F -- O > Cl > Br (41), Of course, the most reactive species present will preferentially undergo saturation reactions that reduce polymer formation and that may increase halogen atom concentration. Ultimately, determination of the relative reactivity of the plasma species allows prediction of the primary atomic etchants in a plasma of specific composition. [Pg.237]

While the catalytic reduction of PPEs is powerful, it is necessary to work at high temperatures and with a stainless-steel autoclave, which may not always be practical. Weder et al. reported an alternative way to reduce dialkoxy-sub-stituted PPEs [81]. Treating the PPEs with a mixture of tosylhydrazide and tripropylamine at elevated temperatures gave the reduced species in high yield and excellent purity (Scheme 14). The purported intermediate is diimine, formed by elimination of Ar-S02-H from the hydrazide. Diimine reduces the triple bonds to give the fully reduced polymer. Attempts to utilize the diimine method to reduce dialkyl PPEs, however, failed perhaps due to the more massive steric shielding by the alkyl groups in these polymers. [Pg.45]

The corrosion behavior of zinc-coated steel electrodes electrochemically modified by polypyrrole [311] and zinc electrode in solution containing reducing polymer (Polyox WSR-301) [312] was investigated. [Pg.748]

Fig. 6. 500 MHz H HRMAS NMR spectra of FMOC-Ala-Ile-Asp-Wang swollen with DMF- 7 and spun at 5 kHz. Spectra were obtained without (a) and with (b) using a ID TOCSY variant54 to reduce polymer signals. Note the substantially reduced signals arising from polystyrene in the aromatic (6.5-7.5 ppm) and aliphatic (1.5-2.5 ppm) regions. Fig. 6. 500 MHz H HRMAS NMR spectra of FMOC-Ala-Ile-Asp-Wang swollen with DMF- 7 and spun at 5 kHz. Spectra were obtained without (a) and with (b) using a ID TOCSY variant54 to reduce polymer signals. Note the substantially reduced signals arising from polystyrene in the aromatic (6.5-7.5 ppm) and aliphatic (1.5-2.5 ppm) regions.
By introducing the reduced polymer network density, p, and the re-defined reduced temperature, t, the isobar is written in a simple form... [Pg.17]

The important bacterial storage material poly-hydroxybutyric acid is related metabolically and structurally to the lipids. This highly reduced polymer is made up of D-(3-hydroxybutyric acid units in ester linkage, about 1500 residues being present per chain. The structure is that of a compact right-handed coil with a twofold screw axis and a pitch of 0.60 nm.a Within bacteria it often occurs in thin lamellae 5.0 nm thick. Since a chain of 1500 residues stretches to 440 nm, there must be 88 folds in a single chain. Present in both cytoplasmic granules and in membranes,b polyhydroxybutyrate can account for as much as 50% of the total carbon of some bacterial In E. coli and many other bacteria polyhydroxybutyrate is present in a lower molecular mass form bound to calcium polyphosphates, proteins, or other macromolecules.d e It has also been extracted from bovine serum albumin and may be ubiquitous in both eukaryotes and prokaryotes.d/e The polymer may function in formation of Ca2+ channels in membranes.b/d... [Pg.1200]

Evans AP (1974) A new drag-reducing polymer with improved shear stability for non-aqueous systems J Appl Polym Sci 18 1919... [Pg.159]

Forame PC, Hansen RJ, Little RC (1972) Observations of early turbulence in the pipe flow of drag reducing polymer solutions AIChE J 18 213... [Pg.159]

Fortuna G, Hanratty TJ (1972) The influence of drag reducing polymers on the viscous sublayer J Fluid Mech 53 575... [Pg.160]

Greene HL, Mostardi RF, Wokes RF (1980) Effects of drag reducing polymers on initiation of arteriosclerosis Polym Eng Sci 20 499... [Pg.160]


See other pages where Reduced polymer is mentioned: [Pg.28]    [Pg.193]    [Pg.60]    [Pg.482]    [Pg.169]    [Pg.17]    [Pg.323]    [Pg.327]    [Pg.152]    [Pg.173]    [Pg.422]    [Pg.14]    [Pg.180]    [Pg.158]    [Pg.229]    [Pg.154]    [Pg.428]    [Pg.238]    [Pg.58]    [Pg.145]    [Pg.4]    [Pg.218]    [Pg.218]    [Pg.106]    [Pg.107]    [Pg.109]    [Pg.112]   


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