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Chains Faraday effect

Figure 6.8 Effect of chain transfer to solvent according to Eq. (6.89) for polystyrene at 100°C. Solvents used were ethyl benzene ( ), isopropylbenzene (o), toluene (- ), and benzene (°). [Data from R. A. Gregg and F. R. Mayo, Discuss. Faraday Soc. 2 328 (1947).]... Figure 6.8 Effect of chain transfer to solvent according to Eq. (6.89) for polystyrene at 100°C. Solvents used were ethyl benzene ( ), isopropylbenzene (o), toluene (- ), and benzene (°). [Data from R. A. Gregg and F. R. Mayo, Discuss. Faraday Soc. 2 328 (1947).]...
H. R. Brown. Chain mobihty and pull-out effects in lubrication and friction. Faraday Discuss Chem Sci 98 41-54, 1994. [Pg.624]

Wolstenholme, G. A., and Schulman, J. H. Metal-monolayer interactions in aqueous systems. Part III. Steric effects with branched chain fatty acid monolayers. Trans. Faraday Soc. 47, 788-794 (1951). [Pg.91]

Higgins JS, Roots JE (1985) Effect of entanglement on the single-chain motion of polymer molecules in melt samples observed by neutron scattering. J Chem Soc Faraday Trans II 81 757-767... [Pg.245]

Aveyard R, Binks BP, Mead J. Interfacial tension minima in oil-water-sur-factant systems. Effect of alkane chain length and presence of M-alkanols in systems containing Aerosol OT. J Chem Soc Faraday Trans 1986 82 1755— 1770. [Pg.436]

G. S. Hartley, The Effect of Long-Chain Salts on Indicators The Valence-Type of Indicators and the Protein Error, Trans. Faraday Soc. 30, 444 (1934). [Pg.538]

Ma Y, Zha LY, Hu WB, Reiter G, Han CC (2008) Crystal nucleation enhanced at the diffuse interface of immiscible polymer blends. Phys Rev E 77 061801 Ma Y, Li C, Cai T, Li J, Hu WB (2011) Role of block junctions in the interplay of phase transitions of two-component polymeric systems. J Phys Chem B 115 8853-8857 Nelson PC (2004) Biological physics energy, information, life. Freeman, New York Richards RB (1946) The phase equilibria between a crystalline polymer and solvents. I. The effect of polymer chain length on the solubility and swelling of polymers. Trans Faraday Soc 42 10-28... [Pg.240]

Reactivity of Triatomic Molecules.— The outermost, unpaired electron of the ground state of the NOj molecule lies in the i sa-Su orbital. From the arguments above, this electron is more localized on the N atom than on the 0 atoms. Reaction of NOj with a free radical is therefore likely to form a nitro-compound rather than a nitrite. Inhibition of certain free-radical reactions by NOj may plausibly be attributed to such reaction the inhibition occurs under conditions where addition of a nitro-compound has no effect, but addition of a nitrite catalyses the reaction. Similarly, initiation of chains by H-abstraction by NOj (see, e.g., McDoweU and Thomas, Trans. Faraday Soc., 1950, 46,... [Pg.208]

Doroszkowski, A., and Lamboume, R. 1978. Effect of molecular architecture of long chain fatty acids on the dispersion properties of titanium dioxide in non-aqueous liquids. Faraday Discuss. Chem. Soc. 65 252. [Pg.59]

The effect of polymer chain length on the solubihty and swelling of polymers, Trans. Faraday Soc., 42, 10, 1946. [Pg.693]

TAN Tancrede, P., Patterson, D., and Lam, V.-T., Thermodynamic effects of orientation order in chain-molecule mixtures, J. Chem. Soc., Faraday Trans. II, 71, 985, 1975. [Pg.191]

Lawrence ASC, Al-Mamun MA, McDonald MP (1967) Investigation of Upid-water system. Part 2. Effect of water on the polymorphism of long chain alcohols and adds. J Chem Soc Faraday Trans I 63 2789-2795... [Pg.42]


See other pages where Chains Faraday effect is mentioned: [Pg.287]    [Pg.180]    [Pg.227]    [Pg.13]    [Pg.176]    [Pg.208]    [Pg.443]    [Pg.215]    [Pg.219]    [Pg.191]    [Pg.337]    [Pg.291]    [Pg.836]    [Pg.836]    [Pg.229]    [Pg.3]    [Pg.137]    [Pg.337]    [Pg.229]    [Pg.153]    [Pg.727]   
See also in sourсe #XX -- [ Pg.180 ]




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