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3 M NaCl solution

Figure 6. MAS NMR spectra of illite exchanged in 0.1 M NaCl solutions at 25°c. Spectra collected at = 11.7 T, room temperature, and room humidity ca. 35% RH). Figure 6. MAS NMR spectra of illite exchanged in 0.1 M NaCl solutions at 25°c. Spectra collected at = 11.7 T, room temperature, and room humidity ca. 35% RH).
Jin and Atrens (1987) have elucidated the structure of the passive film formed on stainless steels during immersion in 0.1 M NaCl solution for various immersion times, employing XPS and ion etching techniques. The measured spectra consist of composite peaks produced by electrons of slightly different energy if the element is in several different chemical states. Peak deconvolution (which is a non-trivial problem) has to be conducted, and these authors used a manual procedure based on the actual individual peaks shapes and peak positions as recorded by Wagner et al. (1978). The procedure is illustrated in Figure 2.8 for iron. [Pg.33]

Figure 14. Typical SEM micrographs of pit morphology on the surface of alloy 600 subjected to a constant anodic potential of 0.8 V(Ag/AgCl) for 300s in aqueous 0.1 M Na2S2C>3 + 0.1 M NaCl solution at (a) 25°, (b) 60°, (c) 100°, (d) 150°, (e) 200°, (f) 250°, and (g) 300°C. Reprinted from J. -J. Park and S. -I. Pyun, Pit formation and growth of alloy 600 in CF ion-containing thiosulphate solution at temperatures 298-573 K using fractal geometry, Corros. Sci., 45, p. 995, Copyright 2003, with permission from Elsevier Science. Figure 14. Typical SEM micrographs of pit morphology on the surface of alloy 600 subjected to a constant anodic potential of 0.8 V(Ag/AgCl) for 300s in aqueous 0.1 M Na2S2C>3 + 0.1 M NaCl solution at (a) 25°, (b) 60°, (c) 100°, (d) 150°, (e) 200°, (f) 250°, and (g) 300°C. Reprinted from J. -J. Park and S. -I. Pyun, Pit formation and growth of alloy 600 in CF ion-containing thiosulphate solution at temperatures 298-573 K using fractal geometry, Corros. Sci., 45, p. 995, Copyright 2003, with permission from Elsevier Science.
An illustration of the effect of micelle/nanoparticle volume fraction on contact line motion is found in [57]. They used 0.1 M NaCl solution to reduce the electrical double layer thickness surrounding the NaDS micelle. At a given number concentration of micelles, decreasing the size of each micelle decreases the volume fraction greatly, since the volume of each spherical micelle varies as the third power of the radius. Thus, the addition of electrolyte effectively reduced the micellar volume fraction in the aqueous medium. The authors found that the oil droplet that would otherwise become completely detached from the solid surface, came back to reattach itself to the solid when electrolyte was present. They rationalized this finding as being caused by the inability of the weakened structural disjoining forces to counteract the attraction of the oil drop to the solid surface. [Pg.135]

If you have a class with biochemists, clearly the area of enzyme kinetics is practically mandatory. If biologists are mixed in with the biochemists, osmotic pressure is an important concept to cover carefully and a concept typically not well covered in general chemistry and in most physical chemistry texts or classes. A quick example what is a 2 Osmolar solution of sodium chloride Such concentration units are used when dispensing various saline solutions in hospitals. What is the origin of the unit A 1 M NaCl solution dissociates into two ions that would double the osmotic pressure of a non dissociating solute. Thus, the 1 M solution of NaCl becomes a 2 Osmolar solution. Other examples abound - the bursting pressure of a cell relates to the osmotic pressure of the serum in which the cell finds itself. [Pg.13]

A 0.1 M NaCl solution was placed in contact with a 0.1 M NaN03 solution. Which side of the junction is positive ... [Pg.303]

Molar mass distributions of PDADMAC were also determined by fractionation using dioxane/methanol system [144] and from sedimentation velocity measurements in 1 m NaCl solution [134]. The molar mass calculations were based on the s-M relation [134] ... [Pg.169]

Hectorite (H), barasym SSM-100 (BS) from the Source Clays Repository of the Clay Minerals Society and laponite B (L) from Laporte Industries were used. The clays were exchanged with 1 M NaCl solutions three times, the < 2 mm fraction was separated by centrifugation and stored in 1 M NaCl at 277 K. [Pg.381]

Phosphodiester Linkages The dTpdA and dA dT phosphodiester linkages do not give resolved 3lp spectra for poly(dA-dT) in 1 M NaCl solution (10). It is therefore striking that two partially resolved resonances are observed for this synthetic DNA in 1 M TMA+ solution (Figure 15). The chemical shift separation was 0.42 ppm at 52°C and 0.34 ppm at 67°C. Partially resolved 33P resonances have been reported for 150 base pair (dA-dT)n in the... [Pg.237]

Nuc/D =8, in 1 M NaCl solution with the resonance shifting to high field on complex formation (Figure 16). The results demonstrate that the base pairs are intact in the proflavine complex with the synthetic DNA. [Pg.242]

Melting Transition Typical 360 MHz proton NMR spectra of proflavine poly(dA-dT) complexes, Nuc/D = 24 and Nuc/D = 8, in 1 M NaCl solution at temperatures below the midpoint for the dissociation of the complex are presented in Figures 17A and B respectively. The stronger base and sugar resonances can be readily resolved from the weaker proflavine resonances (designated by asterisks) in the presence of excess nucleic acid (Figure 17) so that the resonances of the synthetic DNA and the mutagen can be monitored independently of each other. [Pg.242]

Nucleic Acid Base Resonances The chemical shifts of the nonexchangeable protons in poly(dA-dT), the Nuc/D = 24 complex and the Nuc/D = 8 complex in 1 M NaCl solution are plotted as a function of temperature in Figure 19. The nucleic acid nonexchangeable proton chemical shifts in the duplex state are either unperturbed (adenosine H-8, H-2, and thymidine CH3-5) or shift slightly upfield (thymidine H-6) on complex formation (Figure 19). By contrast, the thymidine H-3 exchangeable proton located in the center of the duplex resonates 0.35 ppm to higher field in the Nuc/D = 8 proflavine complex compared to its position in the... [Pg.242]

Nonexchangeable Proton Spectra Proton spectra of the daunomycin poly(dA-dT) complex in 1 M NaCl, solution have... [Pg.260]

Phosphodiester Linkages The proton noise decoupled lp nmr spectra of the daunomycin poly(dA-dT) complex in 1 M NaCl solution at 67°C have been recorded at 1 antibiotic per 6 base pairs (Nuc/D = 11.8) and 1 antibiotic per A,3 base pairs (Nuc/D = 5.9). Resolved resonances are observed for the complex at both Nuc/D ratios (Figure 32). One of the resonances in the complex exhibits a chemical shift similar to that observed for poly(dA-dT) in 1 M NaCl alone ( 4.1 ppm) at this temperature while the other resonance is shifted downfield by 0.3 ppm in the Nuc/D = 11.8 complex and by 0.45 ppm in the NucD = 5.8 complex (Table XI). The results suggest that daunomycin intercalates at either the dTgdA or dApdT sites, resulting in a downfield shift of the 31p resonance of the corresponding phosphodiester grouping at the intercalation site. [Pg.268]

Figure 4 Metastable pitting rate (k) for 316 stainless steel in 1 M NaCl solution as a function of potential for untreated samples and samples passivated with 20% or 50% nitric acid for 1 hour. (From J. S. Noh, N. J. Laycock, W. Gao, D. B. Wells. Corrosion Sci. 42, 2069 (2000).)... Figure 4 Metastable pitting rate (k) for 316 stainless steel in 1 M NaCl solution as a function of potential for untreated samples and samples passivated with 20% or 50% nitric acid for 1 hour. (From J. S. Noh, N. J. Laycock, W. Gao, D. B. Wells. Corrosion Sci. 42, 2069 (2000).)...
Artificial crevice electrodes have been used to study the effect of dichromate on active dissolution of aluminum. In these experiments, 50 pm thick commercially pure A1 foils were placed between thin plastic sheets and mounted in epoxy. This assembly was fixed against a square cell that accommodated counter and reference electrodes and a trap that allowed for H2 gas collection. A schematic illustration of this cell and electrode is shown in Fig. 9 (36). Crevice corrosion growth experiments were conducted in aerated 0.1 M NaCl solution with additions of either 0.01 or 0.1 M Na2Cr207. Artificial crevice growth experiments were conducted under potentiostatic polarization at potentials ranging from 0 to... [Pg.271]

Figure 11 Cathodic polarization curves on 2024-T3 in actively oxygen-sparged 1 M NaCl solution with (a) dichromate additions and (b) 0.3 vol% peroxide and dichromate additions. (From A. Sehgal, G. S. Frankel, B. Zoofan, S. Rokhlin. J. Electrochem. Soc. 147, 140 (2000).)... [Pg.276]

Potentiodynamic polarization studies [4] on aluminum alloy AA 7075 in air saturated 0.1 M NaCl solution with and without the addition of 1000 ppm each of CeC, P1O3 and YCI3, yielded the polarization curves shown in Fig. 12.1. [Pg.898]

Figure 8.4. Typical normalized retracting force curves (force vs. separation x) measured between BSA-fiinctionalized tip and K-carrageenan in 0.1 M NaCl solution at pH 6.0 (left) and at pH 4.7 (right) (Lee and Huang, unpublished). (See Color Plate.)... Figure 8.4. Typical normalized retracting force curves (force vs. separation x) measured between BSA-fiinctionalized tip and K-carrageenan in 0.1 M NaCl solution at pH 6.0 (left) and at pH 4.7 (right) (Lee and Huang, unpublished). (See Color Plate.)...

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