Adsorption magnitude

The values obtained for the parameter a = A (298 K) are not reported in Table 4.9, since absolute adsorption magnitudes are not directly measured by the FTIR methodology [97],... 

Adsorption may in principle occur at all surfaces its magnitude is particularly noticeable when porous solids, which have a high surface area, such as silica gel or charcoal are contacted with gases or liquids. Adsorption processes may involve either simple uni-molecular adsorbate layers or multilayers the forces which bind the adsorbate to the surface may be physical or chemical in nature. 

These effects can be illustrated more quantitatively. The drop in the magnitude of the potential of mica with increasing salt is illustrated in Fig. V-7 here yp is reduced in the immobile layer by ion adsorption and specific ion effects are evident. In Fig. V-8, the pH is potential determining and alters the electrophoretic mobility. Carbon blacks are industrially important materials having various acid-base surface impurities depending on their source and heat treatment. 

The degree of uncertainty of 10 per cent or more, inseparable from estimates of specific surface from adsorption isotherms, even those of nitrogen, may seem disappointing. In fact, however, attainment of this level of accuracy is a notable achievement in a field where, prior to the development of the BET method, even the order of magnitude of the specific surface of highly disperse solids was in doubt. The adsorption method still provides the only means of determining the specific surface of a mass of non-... 

In principle, the use of a suitable adsorptive should also make it possible, as Kamaukhov has pointed out, to reduce the magnitude of the f-correction, which is always a source of some uncertainty. From the Kelvin equation... 

Adsorption on a nonpolar surface such as pure siUca or an unoxidized carbon is dominated by van der Waals forces. The affinity sequence on such a surface generally follows the sequence of molecular weights since the polarizabiUty, which is the main factor governing the magnitude of the van der Waals interaction energy, is itself roughly proportional to the molecular weight. 

FiaaHy, an analysis of the energies of adsorption on many practical polar and nonpolar adsorbents has shown not only that the magnitude of the Op term depends directly upon the polarizabiUty a, but also that the sum of all of the nonspecific terms taken together, ie, + Lp, iacreases... 

Effects of Surfactants on Solutions. A surfactant changes the properties of a solvent ia which it is dissolved to a much greater extent than is expected from its concentration effects. This marked effect is the result of adsorption at the solution s iaterfaces, orientation of the adsorbed surfactant ions or molecules, micelle formation ia the bulk of the solution, and orientation of the surfactant ions or molecules ia the micelles, which are caused by the amphipathic stmcture of a surfactant molecule. The magnitude of these effects depends to a large extent on the solubiUty balance of the molecule. An efficient surfactant is usually relatively iasoluble as iadividual ions or molecules ia the bulk of a solution, eg, 10 to mol/L. 

These mechanisms are characterized by the relative magnitudes of the heats of reaction, solution, or adsorption (see Adsorption, separation). AH useflil drying mechanisms are exothermic. Phosphoms pentoxide is a Class 1 drying agent that reacts with water to form a polyphosphoric acid (2) ... 

Surface Area Determination The surface-to-volume ratio is an important powder property since it governs the rate at which a powder interacts with its surroundings. Surface area may be determined from size-distribution data or measured directly by flow through a powder bed or the adsorption of gas molecules on the powder surface. Other methods such as gas diffusion, dye adsorption from solution, and heats of adsorption have also been used. It is emphasized that a powder does not have a unique surface, unless the surface is considered to be absolutely smooth, and the magnitude of the measured surface depends upon the level of scrutiny (e.g., the smaller the gas molecules used for gas adsorption measurement the larger the measured surface). 

Comparison of the volume/volume composition data with the relative pressure data shows that although C2-C4 hydrocarbons are present to the greatest volume percent, their actual pressures are an order of magnitude lower than the C5 plus hydrocarbons. Hence, the C5 plus hydrocarbons would be adsorbed in preference to the C2-C4 hydrocarbons and would displace them over a number of cycles. It is apparent therefore that the C5 plus hydrocarbons must be considered the primary target gases for pre-adsorption in guard bed systems... 

It should be noted that, due to the strong polarity of the hydroxyl groups on the silica, the initial adsorption of the ethyl acetate on the silica surface is extremely rapid. The individual isotherms for the two adsorbed layers of ethyl acetate are shown in Figure 8. The two curves, although similar in form, are quite different in magnitude. The first layer, which is very strongly held, is complete when the concentration of ethyl acetate is only about l%w/w. At concentrations in excess of l%w/w, the second layer is only just being formed. The formation of the second layer is much slower and the interactions between the solvent molecules with those already adsorbed on the surface are much weaker. 

Agglomerated fine partieles sueli as eatalysts and preeipitates may exhibit internal surfaee areas orders of magnitude greater than that available on the exterior surfaee. Again, if agglomerate partiele size is used as the eharaeteristie dimension, the ealeulated area is that of the external surfaee. If the internal surfaee area is to be ealeulated then additional knowledge of the eonstituent erystal size is required, e.g. via mieroseopy or adsorption. 

In the systems characterized by more complex surface structure, consisting of patches of different size and different magnitude of the boundary field, the properties of adsorption isotherms have been found to depend on the... 

For many metals and alloys the determination of /p is complex, and its magnitude is governed by many factors such as surface finish, rate of formation, alloying constituents, and the presence of those anions, such as halides, that promote localised breakdown. In many instances the attack on passive films by halide ions shows a temperature and concentration dependence similar to the effect of hydrogen ions, i.e. the rate of film dissolution increases with concentration in accordance with a Freundlich adsorption relationship... 

This concept may be invoked to account for electrolyte formation in microcracks in a metal surface or in the re-entrant angle formed by a dust particle and the metal surface. More importantly, it can also explain electrolyte formation in the pores of corrosion product and hence the secondary critical humidity discussed earlier. Ferric oxide gel is known to exhibit capillary condensation characteristic and pore sizes deduced from measurements of its adsorptive capacity are of the right order of magnitude to explain a secondary critical relative humidity as70 7o for rusted steel . 

As with the Langmuir adsorption isotherm, which in shape closely resembles Michaelis-Menten type biochemical kinetics, the two notable features of such reactions are the location parameter of the curve along the concentration axis (the value of Km or the magnitude of the coupling efficiency factor) and the maximal rate of the reaction (Vmax). In generic terms, Michaelis-Menten reactions can be written in the form... 

If the adsorption process is not saturable within the concentration range of the experiment, it becomes a sink claiming a portion of the drug added to the medium—the magnitude of which is dependent on the maximal capacity of the sink ([ 2]) and the affinity of the ligand for the site... 

The rate and mechanism are different on the basal plane and edge sites of carbon. The reactions involving oxygen are two to three orders of magnitude slower on the basal plane than on the edge sites, because of the weak adsorption of oxygen molecules on the basal plane surface [34]. 

The adsorption of gases on solid surfaces proceeds to such an extent that approximately 10 7 gr. is present per cm.2 in the equilibrium state. This is of the same order of magnitude as the strength of the limiting capillary layer of a liquid ( 184), hence it is not improbable, as suggested by Faraday (9) (1884), that the adsorbed gas is sometimes present in the liquid state. The adsorbed amount increases with the pressure and diminishes with rise of temperature. The first effect does not follow a law of simple proportionality, as in the case of the absorption of gases by liquids, rather the adsorbed amount does not increase so rapidly, and the equation ... 

The values of K° seem to confirm the correlations of the earlier field data tnat the adsorption onto sediments does not vary by more than an order of magnitude in systems with low DOC. 

Another case study supporting the AX hydrophilicity scale is the adsorption of terminal diols. Figure 28 shows that adsorption on Au911 is weaker than on Hg912 as expected, while adsorption increases with the number of carbon atoms almost in parallel for the two metals. It is intriguing that the adsorption of 1,4-butanediol at the air/solution interface is weaker than on Hg328 and is of the same order of magnitude as on Au. 

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