Increase in Adsorption

In formulating an explanation of this enhanced adsorption, there are several features to be accounted for the increase in adsorption occurs without hysteresis the amount of adsorbate involved is relatively small the Kelvin r -values are also small (e.g. for nitrogen, less than 17 A) and the effect is found in a region of relative pressures where, according to the simple tensile strength hypothesis, capillary condensate should be incapable of existence. 

Typical adsorption isotherms are shown in Figs. 16 and 17. Despite the large experimental scatter, a steep increase in adsorption can be seen at low concentrations, followed by a plateau at concentrations exceeding the CMC. Similar behavior has been observed before with model surfactants [49-54] and has also been predicted by modem theories of adsorption [54]. According to Fig. 16, adsorption increases modestly with salinity provided that the calcium ion concentration remains low. The calcium influence, shown in Fig. 17, cannot be explained by ionic strength effects alone but may be due to calcium-kaolinite interactions. 

Vitanov and Popov et al.156 660-662 have studied Cd(0001) electrolyti-cally grown in a Teflon capillary in an aqueous surface-inactive electrolyte solution. The E is independent of ce) and v. The capacity dispersion is less than 5%, and the electrode resistance dispersion is less than 3%. The adsorption of halides increases in the order Cl" < Br" < I".661 A comparison with other electrodes shows an increase in adsorption in the sequence Cd(0001) < pc-Cd < Ag( 100) < Ag(l 11). A linear Parsons-Zobel plot with /pz = 1.09 has been found at a = 0. A slight dependence has been found for the Cit a curves on ce, ( 5%) in the entire region of a. Theoretical C, E curves have been calculated according to the GCSG model. 

In reality one observes the increase in adsorption at 3672 cm despite the fact that at 3498 and 1708 cm" adsporption not only increases, but, on the contrary, decreases as amount of adsorbed H-atoms grows... 

The effects of tin/palladium ratio, temperatnre, pressnre, and recycling were studied and correlated with catalyst characterization. The catalysts were characterized by chemisorption titrations, in situ X-Ray Diffraction (XRD), and Electron Spectroscopy for Chemical Analysis (ESCA). Chemisorption studies with hydrogen sulfide show lack of adsorption at higher Sn/Pd ratios. Carbon monoxide chemisorption indicates an increase in adsorption with increasing palladium concentration. One form of palladium is transformed to a new phase at 140°C by measurement of in situ variable temperature XRD. ESCA studies of the catalysts show that the presence of tin concentration increases the surface palladium concentration. ESCA data also indicates that recycled catalysts show no palladium sulfide formation at the surface but palladium cyanide is present. 

The effects of calcium on polymer-solvent and polymer-surface interactions are dependent on polymer ionicity a maximum intrinsic viscosity and a minimum adsorption density as a function of polymer ionicity are obtained. For xanthan, on the other hand, no influence of specific polymer-calcium interaction is detected either on solution or on adsorption properties, and the increase in adsorption due to calcium addition is mainly due to reduction in electrostatic repulsion. The maximum adsorption density of xanthan is also found to be independent of the nature of the adsorbent surface, and the value is close to that calculated for a closely-packed monolayer of aligned molecules. 

Table III shows that the adsorption densities at the plateau region increase with increasing PVA molecular weight, despite the distribution of molecular weights for each sample. The adsorption density of Vinol 350 is given in parentheses because of the difficulty in establishing its exact value. For the fully hydrolyzed PVA s, which show no specific interactions with polystyrene surfaces, the increase in adsorption density is proportional to the 0.5 power of the molecular weight, in good agreement with theory, which predicts for weak surface interactions under...

HPC exhibited a notable increase in adsorption with increasing NaCl concentration. Entrapment in the interlayer of recovered sodium montmorillonite did not vary with salinity the extent of entrapment was greater with the 4 M.S. HE and HP celluloses than either of the 2.0 M.S. polymers. Mixed ethers of HEC (2 M.S.) containing an anionic (carboxymethyl) or cationic (3-0-2-hydroxypropyltrimethylaramonium chloride) group at 0.4 M.S. levels did not adsorb from fresh water. Adsorption of these polar mixed ethers increased with increasing electrolyte until electrostatic and solvation effects were negated in 0.54N NaCl solutions and the adsorbed amounts typical of a 2 M.S. HEC were observed. Interlayer entrapments comparable to the equivalent M.S. HEC were observed at lower (0.18N) electrolyte concentrations. 

As shown in Figure 4, the increase in adsorption of acetic acid on Pt(lll) occurs in the potential range of 0.15 to 0.3 V, which roughly coincides with position of the current-potential peak of the voltammogram recorded in the same solution. An interdependence can thus be sought between acetic acid adsorption... 

The sharp increase in adsorption in region II marks the onset of surfactant association at the surface through lateral interaction of the hydrocarbon chains. 

In Situ Mossbauer Measurement on Hematite/Divalent Co-57. The adsorption behavior of cobaltous ions on hematite surfaces was essentially the same as that on silica reported by James and Healy (12). Appreciable adsorption begins at about pH 4 followed by an abrupt increase in adsorption between pH 6 and 8. Beyond pH 9, adsorption is practically complete. Emission Mossbauer spectra of Fe-57 arising from the divalent Co-57 ions at the interface between hematite particles and the 0.1 mol/dm3 NaCl solutions of different pH at room temperature are shown in Figure 3 The emission spectra show a marked dependence on the pH of the aqueous phase. No emission lines ascribable to paramagnetic iron species are recognized in... 

Screening by the ions of the diffuse layer, decreasing the mutual repulsion of the dipoles and leading to an increase in adsorption (e.g., the change in adsorption and reorientation ofcoumarin ). 

We see that illuminatioQ can lead both to an increase in adsorptivity (photoadsorption, AN > 0) and to its decrease (photodesorption, AN < 0). This depends on the ratios An/no and Ap/po, i.e., on the relative changes in the surface concentrations of the electron and hole gases due to illumination. 

Fig. 7. Enzyme-coupled assay in which the hydrolase-catalyzed reaction releases acetic acid. The latter is converted by acetyl-CoA synthetase (ACS) into acetyl-CoA in the presence of (ATP) and coenzyme A (CoA). Citrate synthase (CS) catalyzes the reaction between acetyl-CoA and oxaloacetate to give citrate. The oxaloacetate required for this reaction is formed from L-malate and NAD in the presence of L-malate dehydrogenase (l-MDH). Initial rates of acetic acid formation can thus be determined by the increase in adsorption at 340 nm due to the increase in NADH concentration. Use of optically pure (Ry- or (5)-acetates allows the determination of the apparent enantioselectivity i app i81)-...

The adsorption of cobalt (II) at 1.3 X 10"4M Co(ClCh)2 is shown in Figure 2. in the pH range from 1.7 to 12.0. This form of plot, percent adsorption vs. pH or concentration while useful for demonstrating the dramatic increase in adsorption over a narrow pH or concentration range, is however of limited theoretical value. In Figure 3 the cobalt (II) adsorption data are therefore redrawn as log (adsorption density) vs. pH. The vertical dashed lines in Figures 2 and 3 represent the minimum pH for precipitation of 1.3 X 10"4M Co (II) in the absence of adsorption. The plateau of Figure 3 therefore represents adsorbed and precipitated cobalt. 

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