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Adsorption species

After adsorption, species may diffuse on the surface or, eventually, become absorbed in the bulk. Due to collisions between adsorbed species of different kinds the actual reaction step can occur. Of course, this step requires that some energetic and spatial constraints have to be fulfilled. The result of the reaction step is the formation of a product molecule. This product can be either an intermediate of the reaction or its final output. [Pg.389]

When the ammonio-ion on H-EDTA-MOR is heated and evacuated at hi er temperature (Figure 6B-6D), the adsorption species were changed to secondary amines. The deformation bands of ammonio-ion are shifted to lower wave number NH2 deformation bands build up at 1600 cm, together with CH2N defo rmation band at 1442 cm. The intensities of OH deformation bands (1370 cm , 1324 cm ) are decreased with increasing evacuation temperature. The... [Pg.273]

In order to characterize the adsorption species on mineral surface, DDTC is oxidized into the dimmer by adding definite H2O2 into the DDTC solution, which then is extracted by cyclohexane to determine its UV spectrum. As seen from the UV spectrum in Fig. 4.33, there are three UV absorbance peaks at 230 nm, 261 nm, 280 nm respectively. The maximum absorbance peak is at 230 nm, the next peak is at 260 nm, and the weak peak is at 280 nm. The peak at 230 nm can serve as a characteristic absorbance peak, and the peak at 260nm results from absorbance overlapping of diethyl dithiocarbamate and its dimmer. [Pg.96]

In this section, the application of differential multipulse and Square Wave Voltammetric techniques to strongly adsorpted species is treated. Special detail is paid to SWV, since it is the most important technique. Differential Staircase... [Pg.536]

This point can be appreciated more quantitatively after consideration of an important (but simple) model of transport-controlled adsorption kinetics, the film diffusion process.34 35 This process involves the movement of an adsorptive species from a bulk aqueous-solution phase through a quiescent boundary layer ( Nemst film ) to an adsorbent surface. The thickness of the boundary layer, 5, will be largest for adsorbents that adsorb water strongly and smallest for aqueous solution phases that are well stirred. If j is the rate at which an... [Pg.166]

Laser-induced desorption of CO and CO+ from Pt(l 11) is observed by Fukutani et al. [12]. Upon laser irradiation on the CO-saturated Pt(l 1 1) surface at X = 193 nm with a laser fluence of 4mJ/cm2 for 10, 20, and 30 min, the on-top CO decreases gradually in RAIRS intensity, as shown in Fig. 12b-d, respectively. The effects of laser irradiation are clearly demonstrated in the difference spectra shown in Fig. 12. On-top CO decreases, while bridge CO remains unchanged. Neutral CO desorbed from the surface is clearly observed by the REMPI method. In addition to neutral species, CO+ ion desorption is also observed. Figure 19 displays the evolution of the desorption yield as a function of accumulated incident photon numbers at X = 193 nm with a laser fluence of 5.6 mJ/cm2 after a CO exposure of 2 L. Decay rates of the desorption intensity represented by an exponential decay are identical for neutral and ion species within the experimental error and the cross section s is 3 x 10 19 cm2. This result suggests that neutral CO molecules and CO+ ions are desorbed from the same adsorption species. [Pg.308]

For the ethane/carbon dioxide mixture in MCM-41, lAST gives good predictions for the mixture adsorption at low and moderate pressures, but exhibits some deviations at high pressures. This non-ideal behaviour might be due to the chemical dissimilarity of the adsorptive species, which will be taken into account in subsequent GCMC simulations. Nevertheless, lAST gives very accurate selectivity results for this mixture over the whole pressure range. [Pg.692]

Thus, the adsorption of CO on active ZrOa catalysts led to the formation of various types of adsorption species of CO having different reactivities toward Ha, and these species were found to play a significant role in the hydrogenation of CO. Moreover, it is likely that CO is adsorbed on the active surface sites of low coordination and that an electron transfer from the other surface sites to this CO species leads to the formation of the dimeric adsorbed species (CO)a. These dimeric species react, step by step, with CO molecules from the gas phase to from a relatively stable cyclic polymer species of (CO)s and then (CO) ", Such adsorbed CO species easily react with hydrogen and are also activated through the dissociative adsorption of hydrogen on surface sites of low coordination or the coordina-tively unsaturated surface sites on the catalyst. [Pg.154]

Activated carbon fibers (ACFs) offer a choice of other carbon forms for VOC removal. As discussed earlier, the narrow diameter of the fibers provides ready access of adsorptive species to the adsorbent surface. The incorporation of ACF into permeable forms such as felt, paper, and rigid monoliths helps to surmount the disadvantages of using loose fibers. Rigid ACF composites have been prepared at the University of Kentucky and examined for their potential for the removal of low concentrations of VOCs [31]. [Pg.17]

Y. Mori, K. Uemura, and K. Shimanoe, Adsorption species of transtion metal ions on silicon wafer in SC-1 solution, J. Electrochem. Soc. 142, 3104, 1995. [Pg.490]

Finally he showed the reaction to be inhibited by H2S and that this coincided with a substantial change in the secondary ion spectra due to strong H2S adsorption (species detected were HS", H2S, SO, S02, and PtS" ). [Pg.108]

Since very large surface areas are usually needed, the solids used should be highly porous.1 The extent of surface involved can be estimated from measurements of adsorptive capacity. With n-butyl amine as adsorptive,2 for an example, the total volume occupied by one molecule (as liquid) is 1.65 X 10-22 cm.3 The area occupied by one molecule is approximately the two-thirds power of the volume, or 3.0 X 10-16 cm.2 An efficient adsorbent in contact with a gas phase may hold a volume of adsorbate equal to as much as 1.0% of the particle volume (silica gel has an even larger capacity). One cm.3 of such an adsorbent would thus present a surface area of 18 square meters, equivalent to about 5.5 X 106 square feet per cubic foot of particle volume. The precise value of the surface area will vary with the adsorptive species used for the measurement (B12). [Pg.150]

Treatment with acids It is well known that certain components in Raney alloys, e.g., NiAl or NiAla, are difficult to dissolve with NaOH. However, they can be dissolved by aqueous solutions of a-hydroxy acids. Selective elimination of Al, together with the removal of disordered Ni results in an improved precursor Ni catalyst, denoted as the acid-treated RNi (RNiA). Thus, treatment of a conventional RNiH (6% Al) with a solution of glycolic acid (GA) or TA at pH 3.5 and 100"C yields RNiA(GA) or RNiA(TA) with an Al content less than 3%. "Soft" TA modification (pH 5 0"C) does not eliminate Al, but nevertheless gives MNi with a better e.d.a. thain RNiH (Table 1). The optimum modifying conditions stated in the early studies (pH 3.5-5 100 C) thus not only provide the favorable adsorption species (i.e., TAHNa) but also partly remove the N-regions by corrosion with acid (a one pot preparation of TA-MRNiA). [Pg.217]

Simons s pioneering efforts anticipated the need for a detailed examination of pore connectivity in carbons. This issue continues to be in need of careful experimental assessment [171-174]. For example. Figure 1.9 reproduces the approach proposed by Ldpez-Ramdn et al. [174] The smaller adsorptive species probes all the pores, and its adsorption isotherm yields the complete PSD. The larger species is excluded from the smaller pores and also from the larger pore that is shielded by the smaller pores. So the PSD obtained using the larger species is (i) zero for pores that are smaller than the molecules of that species and... [Pg.19]

The adsorption species was concluded to be GaCH3 under monolayer growth conditions, as detected by a real time optical monitoring method/" A possible reaction of GaCH3 with ASH3 was proposed, as shown in Equation (2). [Pg.9]

A brief qualitative evaluation of CO2 adsorption selectivity in MOFs is the direct observation on differences in uptakes between separated gases under given conditions, usually based on the single-component adsorption isotherms. These isotherms can also be used to quantitatively estimate the adsorption selectivity. If adsorption species are presented at low loadings, namely within the Henry s regime, the adsorption selectivity for an equimolar mixture is close to the ratio of the Henry s constants for each species. At non-dilute loadings, however, more information is required to estimate multi-component adsorption. One common approach is to use ideal adsorbed solution theory (lAST) to predict multi-component adsorption isotherms and selectivity based on the single-component adsorption isotherms [60], This approximate theory is known to work accurately in many porous materials. [Pg.89]

The derivation in Section HI demonstrates that the absolute molar entropy of charge-transfer adsorption species can be obtained, in a rigorous way, from the combination of AN and ANji data. According to Eq. (62), the absolute molar entropy of hydrogen and OH species can be obtained from ... [Pg.43]

Alternatively, one can perform a full analysis of the laser-induced transients measured at several concentrations of charge-transfer adsorption species. In this way, one can characterize both... [Pg.54]

As aforementioned, surface structure effects on adsorption are well known in electrochemistry. A typical example is CO adsorption on low-index singleplatinum surfaces. For CO, three different adsorption geometries exist on-top, bridge-bonded, and multibonded. The relative population of each adsorption species and the surface structure of adsorbate layer are dependent on the surface structure and metal (see for instance Refs. [19-21]... [Pg.984]

The separation of the tested adsorptive species from electroactive non-adsorptive compounds in biological samples can be realized by medium exchange (e.g., by the flow injection method [171] or by electrode transfer [157, 158]. The scheme of this procedure is illustrated in Fig. 67. The extent of the interference depends on relative adsorbabil-ities of all species, on their bulk concentration, the choice of the accumulation potential and pH values of the solution. The electrocata-lytic activity of adsorbed substances is favorable for lowering the detection limit. For example, metal complexes of the Pt group extremely enhance the reduction of hydrogen ions in acidic and neutral aqueous media. Thus, the detection limit of these metals is decreased down to 10- " M [172, 173]. [Pg.128]

The dissociation adsorption of N2 is supported by many experimental results (i) Only NH and N were detected after N2 and H2 were adsorbed on dual-promoter iron catalyst at reaction temperature and 101.3kPa and vacuumed at 200°C (ii) N2 adsorption state has never been found by XPS detection. Heat desorption data provided by Toyashima and Xiamen University showed that N2 is not the main adsorption species under the conditions of ammonia S3mthesis at 400°C-450°C (iii) ErtP° provides a powerful support for the dissociation adsorption of N2 by the following results from energy spectroscopy ... [Pg.90]

Table 3.19 Adsorption species of H2 on reduced catalysts derived from different iron oxides as precursor... Table 3.19 Adsorption species of H2 on reduced catalysts derived from different iron oxides as precursor...
HREELS High-Resolution Electron Energy Loss Spectroscopy adsorption species... [Pg.545]

When relating the surface nature and surface structure of catalyst according to the adsorption capacity of solid surface, it is indispensable to understand the relationship between the probe-molecule and the metal elements on surface, including adsorption species and stoichiometry of the probe-molecule, both of which are closely related. [Pg.580]


See other pages where Adsorption species is mentioned: [Pg.272]    [Pg.358]    [Pg.141]    [Pg.371]    [Pg.448]    [Pg.167]    [Pg.168]    [Pg.182]    [Pg.300]    [Pg.732]    [Pg.154]    [Pg.231]    [Pg.267]    [Pg.12]    [Pg.213]    [Pg.261]    [Pg.737]    [Pg.4636]    [Pg.52]    [Pg.238]    [Pg.48]    [Pg.75]    [Pg.235]    [Pg.237]    [Pg.514]    [Pg.642]   
See also in sourсe #XX -- [ Pg.75 , Pg.90 , Pg.235 , Pg.236 , Pg.545 , Pg.580 , Pg.642 , Pg.794 ]




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