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De Boer

J. H. de Boer, Electron Emission and Adsorption Phenomena, Macmillan, New York, 1935. [Pg.224]

The total interaction between two slabs of infinite extent and depth can be obtained by a summation over all atom-atom interactions if pairwise additivity of forces can be assumed. While definitely not exact for a condensed phase, this conventional approach is quite useful for many purposes [1,3]. This summation, expressed as an integral, has been done by de Boer [8] using the simple dispersion formula, Eq. VI-15, and following the nomenclature in Eq. VI-19 ... [Pg.232]

A useful approach to the phenomenon of adsorption is from the point of view of the adsorption time, as discussed by de Boer [4]. Consider a molecule in the... [Pg.601]

Van der Waals Equations of State. A logical step to take next is to consider equations of state that contain both a covolume term and an attractive force term, such as the van der Waals equation. De Boer [4] and Ross and Olivier [55] have given this type of equation much emphasis. [Pg.623]

An interesting alternative method for formulating f/(jt) was proposed in 1929 by de Boer and Zwikker [80], who suggested that the adsorption of nonpolar molecules be explained by assuming that the polar adsorbent surface induces dipoles in the first adsorbed layer and that these in turn induce dipoles in the next layer, and so on. As shown in Section VI-8, this approach leads to... [Pg.629]

The characteristic isotherm concept was elaborated by de Boer and coworkers [90]. By accepting a reference from a BET fit to a standard system and assuming a density for the adsorbed film, one may convert n/rim to film thickness t. The characteristic isotherm for a given adsorbate may then be plotted as t versus P/P. For any new system, one reads t from the standard r-curve and n from the new isotherm, for various P/P values. De Boer and co-work-ers t values are given in Table XVII-4. A plot of t versus n should be linear if the experimental isotherm has the same shape as the reference characteristic isotherm, and the slope gives E ... [Pg.633]

Finally, it is perfectly possible to choose a standard state for the surface phase. De Boer [14] makes a plea for taking that value of such that the average distance apart of the molecules is the same as in the gas phase at STP. This is a hypothetical standard state in that for an ideal two-dimensional gas with this molecular separation would be 0.338 dyn/cm at 0°C. The standard molecular area is then 4.08 x 10 T. The main advantage of this choice is that it simplifies the relationship between translational entropies of the two- and the three-dimensional standard states. [Pg.646]

Sing (see Ref. 207 and earlier papers) developed a modification of the de Boer r-plot idea. The latter rests on the observation of a characteristic isotherm (Section XVII-9), that is, on the conclusion that the adsorption isotherm is independent of the adsorbent in the multilayer region. Sing recognized that there were differences for different adsorbents, and used an appropriate standard isotherm for each system, the standard isotherm being for a nonporous adsorbent of composition similar to that of the porous one being studied. He then defined a quantity = n/nx)s where nx is the amount adsorbed by the nonporous reference material at the selected P/P. The values are used to correct pore radii for multilayer adsorption in much the same manner as with de Boer. Lecloux and Pirard [208] have discussed further the use of standard isotherms. [Pg.667]

Fig. 2.26 Comparison of a number of standard isotherms of nitrogen at 77 K, plotted as n/n against pip . O, Shnll x, Pierce , de Boer el , Cranston and Inkley. ... Fig. 2.26 Comparison of a number of standard isotherms of nitrogen at 77 K, plotted as n/n against pip . O, Shnll x, Pierce , de Boer el , Cranston and Inkley. ...
The hysteresis loops to be found in the literature are of various shapes. The classification originally put forward by de Boer S in 1958 has proved useful, but subsequent experience has shown that his Types C and D hardly ever occur in practice. Moreover in Type B the closure of the loop is never characterized by the vertical branch at saturation pressure, shown in the de Boer diagrams. In the revised classification presented in Fig. 3.5, therefore. Types C and D have been omitted and Type B redrawn at the high-pressure end. The designation E is so well established in the literature that it is retained here, despite the interruption in the sequence of lettering. [Pg.116]

BroekhofF and de Boer have addressed themselves to the same problem, putting forward an analysis based on an expression for the chemical potential of the adsorbed him as a function of its thickness t. The status of the de Boer treatment has been discussed in some detail by Everett and Haynes. ... [Pg.125]

As Everett points out, however, the analogy of a pore as a narrownecked bottle is over-specialized, and in practice a series of interconnected pore spaces rather than discrete bottles is more likely. The progress of capillary condensation and evaporation in pores of this kind (cf. Fig. 3.13) has been discussed by de Boer, and more recently by Everett. ... [Pg.129]

A new classification of hysteresis loops, as recommended in the lUPAC manual, consists of the four types shown in the Figure below. To avoid confusion with the original de Boer classification (p. 117), the characteristic types are now designated HI, H2, H3 and H4 but it is evident that the first three types correspond to types A, E and B, respectively, in the original classification. It will be noted that HI and H4 represent extreme types in the former the adsorption and desorption branches are almost vertical and nearly parallel over an appreciable range of gas uptake, whereas in the latter they are nearly horizontal and parallel over a wide range of relative pressure. Types H2 and H3 may be regarded as intermediate between the two extremes. [Pg.287]

J. R. J. van Asperen de Boer, Ph.D. Dissertation, University of Amsterdam, Central Research Laboratory for Objects of Arts and Science, Amsterdam, 1970. [Pg.430]

Refining. KroU-process hafnium sponge and electrowon hafnium do not meet the performance requirements for the two principal uses of hafnium metal. Eurther purification is accompHshed by the van Arkel-de Boer, ie, iodide bar, process (18) and by electron beam melting. [Pg.442]

The iodide or van Arkel-de Boer process is a volatilization process involving transfer of an involatile metal as its volatile compound. It is used for the purification of titanium. The reaction of iodine gas with impure titanium metal at 175°C yields gaseous titanium iodide and leaves the impurities in the sohd residue. [Pg.169]

High purity zirconium was first produced by van Arkel and de Boer in 1925. They vaporized zirconium tetraiodide [13986-26-0] into a bulb containing a hot tungsten filament which caused the tetraiodide to dissociate, depositing zirconium on the filament. [Pg.426]


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Van Arkel-de Boer

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