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Ionic screening

A complementary study of steel/steel contacts (100Cr6) [47] used an oscillation wear and friction tester to screen ionic liquids in the boundary lubrication regime at 30, 100 and 170°C at 200 N load. Results are summarized as follows (i) some promising ionic liquids gave lower friction and wear at all temperatures, compared to reference lubricants, (ii) chemical structures of ionic liquids have a high impact on their physico-chemical as well as on tribological properties and (iii) careful selection of both cation and anion, as a tailor-made ionic liquid, enables adaptation of ionic liquid structures to specific applications. [Pg.255]

Wood, N., Ferguson, J. L., Nimal Gunaratne, H. Q., Seddon, K. R., Goodacre, R., Stephens, G. M. Screening ionic liquids for use in biotransformations with whole microbial cells. Green Chemistry 2011,13,1843-1851. [Pg.418]

The ernes of ionic surfactants are usually depressed by tire addition of inert salts. Electrostatic repulsion between headgroups is screened by tire added electrolyte. This screening effectively makes tire surfactants more hydrophobic and tliis increased hydrophobicity induces micellization at lower concentrations. A linear free energy relationship expressing such a salt effect is given by ... [Pg.2583]

Here (log cmc) is tire log cmc in tire absence of added electrolyte, is related to tire degree of counterion binding and electrostatic screening and c- is tire ionic strengtli (concentration) of inert electrolyte. Effects of added salt on cmc are illustrated in table C2.3.7. [Pg.2583]

The correlation functions of the partly quenched system satisfy a set of replica Ornstein-Zernike equations (21)-(23). Each of them is a 2 x 2 matrix equation for the model in question. As in previous studies of ionic systems (see, e.g.. Refs. 69, 70), we denote the long-range terms of the pair correlation functions in ROZ equations by qij. Here we apply a linearized theory and assume that the long-range terms of the direct correlation functions are equal to the Coulomb potentials which are given by Eqs. (53)-(55). This assumption represents the mean spherical approximation for the model in question. Most importantly, (r) = 0 as mentioned before, the particles from different replicas do not interact. However, q]f r) 7 0 these functions describe screening effects of the ion-ion interactions between ions from different replicas mediated by the presence of charged obstacles, i.e., via the matrix. The functions q j (r) need to be obtained to apply them for proper renormalization of the ROZ equations for systems made of nonpoint ions. [Pg.338]

A from the surface the density is typically constant and equal to the bulk value. In strong unscreened electric fields several authors [137-140] report a phase transition towards a ferroelectric crystalline state in their simulations. However, it should be kept in mind that these systems, because of the absence of ionic screening, are rather unphysical in nature. [Pg.359]

R. D. Coalson, A. Duncan. Systematic ionic screening theory of macroions. J Chem Phys 97 5653-5661, 1992. [Pg.848]

When starting our first experiments with available ionic liquids, in screening programs to identify suitable systems, we encountered several difficulties such as pH shifts or precipitation. More generally, the following aspects should be taken into account when ionic liquids are used with biocatalysts ... [Pg.338]

In order to broaden the field of biocatalysis in ionic liquids, other enzyme classes have also been screened. Of special interest are oxidoreductases for the enan-tioselective reduction of prochiral ketones [40]. Formate dehydrogenase from Candida boidinii was found to be stable and active in mixtures of [MMIM][MeS04] with buffer (Entry 12) [41]. So far, however, we have not been able to find an alcohol dehydrogenase that is active in the presence of ionic liquids in order to make use of another advantage of ionic liquids that they increase the solubility of hydrophobic compounds in aqueous systems. On addition of 40 % v/v of [MMIM][MeS04] to water, for example, the solubility of acetophenone is increased from 20 mmol to 200 mmol L ... [Pg.342]

The agreement is satisfactory, except in the cases where there are deviations from additivity. This fact is a verification of our treatment and of the correctness of our screening constants, for the arbitrary selection of only one ionic radius in a series of salts showing additivity in inter-atomic distances is permitted, and our screening constants fixed four radii independently. [Pg.266]

For sphalerite and wurtzite, for example, the discussion of partial ionic character as described above for molyde-nite leads to the resultant average charges +0.67 for sulfur and—0.67 for zinc. The distribution of the sulfur atoms is calculated to be 12% S2 (quadricovalent), 50 percent S+, 32 percent S°, 6 percent S-, 0.2% S2-. The observed bond length 2.34 A with the sulfur radius 1.03 A and the Schomaker-Stevenson correction 0.05 A leads to 5 = 1.36 A for zinc (quadricovalent Zn2-). The increase by 0.05 A over the value 1.309 A for sp3 bonds of Zn° is reasonable as the result of screening of the nucleus by the extra electrons. [Pg.619]

Note that when the concentration of added salt is very low, Debye length needs to be modified by including the charge contribution of the dissociating counterions from the polyelectrolytes. Because the equilibrium interaction is used, their theory predicts that the intrinsic viscosity is independent of ion species at constant ionic strength. At very high ionic strength, the intrachain electrostatic interaction is nearly screened out, and the chains behave as neutral polymers. Aside from the tertiary effect, the intrinsic viscosity will indeed be affected by the ionic cloud distortion and thus cannot be accurately predicted by their theory. [Pg.105]


See other pages where Ionic screening is mentioned: [Pg.96]    [Pg.107]    [Pg.96]    [Pg.21]    [Pg.41]    [Pg.330]    [Pg.338]    [Pg.96]    [Pg.107]    [Pg.96]    [Pg.21]    [Pg.41]    [Pg.330]    [Pg.338]    [Pg.172]    [Pg.242]    [Pg.575]    [Pg.592]    [Pg.1739]    [Pg.2219]    [Pg.2225]    [Pg.172]    [Pg.427]    [Pg.97]    [Pg.339]    [Pg.557]    [Pg.579]    [Pg.46]    [Pg.42]    [Pg.805]    [Pg.154]    [Pg.37]    [Pg.405]    [Pg.184]    [Pg.271]    [Pg.261]    [Pg.280]    [Pg.301]    [Pg.310]    [Pg.317]    [Pg.450]    [Pg.104]    [Pg.103]   
See also in sourсe #XX -- [ Pg.312 , Pg.315 , Pg.316 ]

See also in sourсe #XX -- [ Pg.45 ]




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