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X cations

Fig. 3.1 The plot of parameter D vs. parameter N. The plot contains elements (x), cations without homoatomic bonding ( ), anions without homoatomic bonding (O), cations with homoatomic bonding ), anions with homoatomic bonding (O), and ideal structures +). The definitions of some of the ideal structures are as follows, ideal rutile the oxygen positions of the ideal... Fig. 3.1 The plot of parameter D vs. parameter N. The plot contains elements (x), cations without homoatomic bonding ( ), anions without homoatomic bonding (O), cations with homoatomic bonding ), anions with homoatomic bonding (O), and ideal structures +). The definitions of some of the ideal structures are as follows, ideal rutile the oxygen positions of the ideal...
The Gibbs energy of an electroneutral system is independent of the electrostatic potential. In fact, when substituting into Eq. (3.7) the electrochemical potentials of the ions contained in the system and allowing for the electroneutrality condition, we can readily see that the sum of aU terms jZjF f is zero. The same is true for any electroneutral subsystem consisting of the two sorts of ion and (particularly when these are produced by dissociation of a molecule of the original compound k into x+ cations and x anions), for which... [Pg.38]

A state of dynamic equilibrium exists between the ionized and the non-ionized molecules (XY (non-ionized molecule) X+ (cation) + Y (anion)). The process of electrolytic dissociation is reversible. [Pg.605]

E = S, Se X = I, Br) cation.20 Whether this cation really forms in solutions, especially in low-polar solvents, is difficult to prove. It has been shown, however, that the calculated NBO charge distribution on [LE-X]+ can be of great help in predicting the most likely product, at least among [LE-EL]2+ dications, C.-T. spoke , and T-shaped hypervalent adducts.21,22 In fact, these three types of products can formally derive from a nucleophilic attack of the appropriate nucleophile on the [LE-X]+ cation at the chalcogen or the halogen site. [Pg.478]

Interlayer X cations Ko vyNao leBuo os Ko.89Nao 06 0.05 K0.9Na0.05... [Pg.324]

Table 5.62 lists the chemical compositions of natural feldspars, taken from Deer et al. (1983). Feldspar chemistry is solved on a 32-oxygen anhydrous basis, corresponding to four formula units. The X cation summation is quite close to the stoichiometric value (4) the Z cations are also close to the theoretical value (16). [Pg.347]

Many binary compounds (those with only 2 elements) contain more than 1 cation or anion. The general binary compound can be written CW, in which the subscripts mean the compound has x cations and y anions. In this case, the solubility equation is... [Pg.93]

Attempts have been made to treat selective ion solvation in mixed solvents as ligand exchange reactions [36 e]. We express ion X (cation or anion) existing in solvent A by XA and in solvent B by XB,-. Here, nf=ri if the molecular size of A is very different from that of B or if A is unidentate and B is bidentate (e.g. PC and DME in the solvation of Li+). Otherwise, it is usual that n=n. Then, the ligand exchange reaction in the mixture of A and B will proceed as follows with the increase in the concentration of B ... [Pg.52]

Cation Siting in Linde X. Cation siting for the Na+ and K+exchanged forms of hydrated Linde X has been determined by x-ray analysis (9, 10) (Table IV). The cations located by x-ray analysis are distributed over three different sites (I, I, and II) on the threefold axes. These cations bind onto the framework such that the closest cation-oxygen distances are approximately equal to the sum of their ionic radii. The linear relationships in Figure 5 indicate that the Li+ Na+ Ag+ K+, and Tl+ exchanged forms have an approximately similar distribution of those cations which are strongly bound to the framework. This has been found by x-ray... [Pg.100]

FIGURE 2. A plot of the average bond lengths, , of the XOn coordination polyhedra observed for silicate and oxide crystals vs the Pauling bond strength, s, of the X—O bond. The Roman numeral superscript denotes the coordination number of the X-cation... [Pg.105]

Similar calculations have yet to be completed for molecules with the main group X-cations for rows in the periodic table beyond the second. Nonetheless, it was found6 that the observed bond length data for the main group cations for all six rows of the periodic table correlate with s in six separate but essentially parallel trends similar to those displayed in Figure 2. In a search for a parameter that would rank all of the bond length data in a single trend, a bond order parameter p = s/r was defined where r =... [Pg.107]

FIGURE 5. A scatter diagram of resonance bond numbers, n, calculated for the individual bonds in ten silicate crystals vs the observed bond lengths where r is the row number of the X-cation... [Pg.108]

NH3 is similar to H2O in that they both possess large dipole moments and are both small molecules. The presence of NH3 in a zeolite is chemically similar to the presence of H2O in a zeolite. Therefore, the hydrated cation distribution in zeolites is probably more typical of NH3 adsorption in zeolites than the dehydrated cation distribution. According to Breck (18), for hydrated zeolite X, cations are found in sites SI, SI, SII, and SIV. Of these sites, SI, SII, and SIV would all be adsorption lattice solution sites. The cationic and anionic lattice solution sites (in the supercavity of NaX) are illustrated in Figure 8. For NH3, the subscript J1 will refer to SII sites, the subscript J2 will refer to SI sites, and J3 will refer to SIV sites. The anionic sites are two and are (l) in the center U-membered ring of the connecting frame and (2) near the center of the 0(2)—0(1)—0(l) triad of oxygen atoms. For NH3, the subscript il will refer to the first anionic site the subscript i2 will refer to the second anionic site. [Pg.20]

Table 1. Limiting equivalent conductivities (X °cation (T=25 °C) ) of quaternary ammonium ions [39]... Table 1. Limiting equivalent conductivities (X °cation (T=25 °C) ) of quaternary ammonium ions [39]...
X °cation=34.8 S-cm2-mol 1 was obtained for the cation C8H16N+. Data in Table 1 show that this limiting equivalent conductivity fits onto a single line with those of the other quaternary ammonium salts of the homologues series. [Pg.132]

Electronic spectra of [M(CNR)4(RNHC=CNHR)X]+ cations in methanol exhibit two major visible absorptions, with the higher energy absorption (Amax 340-360 nm) more intense (e = 15,000 M l cm-1) than the... [Pg.67]

Cationic surfactant S+ Counterion X Cationic inorganic l+ S1 XI+ electrostatic force SBA-1 (cubic Pm3n), SBA-2 (hex-cubic), SBA-3 (hex), zirconia (lam, hex), titanium dioxide (hex), zinc phosphate... [Pg.477]

The above argument may be restated m the followmg way Suppose that one mole of KC1 is dissolved in V liters of solution Owmg to dissociation there are (1 - x) undissociated moles, x cations and anions, the total number of individuals being (x + x), where (1 + x) is identical -with van t Hoff s factor t Now suppose that the 10ns and the undissociated molecules obey the gas law If w, is the osmotic pressure of either of the 10ns and the osmotic pressure of the molecules it follows on the above assumption that—... [Pg.206]


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See also in sourсe #XX -- [ Pg.124 , Pg.189 , Pg.201 , Pg.261 ]




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Zeolite X cations

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