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Bound ammonia water

Table VII presents a summary of calorimetric measurements of the differential heat of adsorption of ammonia, water, and carbon dioxide on the sodium form of ZSM-5 zeolite. Ammonia adsorption at 416 K (97.147) shows that NaZSM-5 zeolite is weakly acidic, whereas CO adsorption (147) indicates that in addition there are some weak basic sites. It should be noted that of the two samples studied with ammonia adsorption one was 70% H exchanged and the sodium content of the other was not given. Water adsorption on NaZSM-5 displayed unusual behavior, with a steep increase in the differential heat of adsorption at high surface coverages (166). An adsorption mechanism was proposed to explain these findings in which adsorption occurs first on the hydrophilic sites, consisting of sodium cations and framework anions where water molecules are bound by dipole-field interactions. Further adsorption takes place near these sites through weak interaction with zeolite surfaces, and when the number of water molecules close to these sites exceeds a certain value, they tend to reorient by forming clathrate-like struc-... Table VII presents a summary of calorimetric measurements of the differential heat of adsorption of ammonia, water, and carbon dioxide on the sodium form of ZSM-5 zeolite. Ammonia adsorption at 416 K (97.147) shows that NaZSM-5 zeolite is weakly acidic, whereas CO adsorption (147) indicates that in addition there are some weak basic sites. It should be noted that of the two samples studied with ammonia adsorption one was 70% H exchanged and the sodium content of the other was not given. Water adsorption on NaZSM-5 displayed unusual behavior, with a steep increase in the differential heat of adsorption at high surface coverages (166). An adsorption mechanism was proposed to explain these findings in which adsorption occurs first on the hydrophilic sites, consisting of sodium cations and framework anions where water molecules are bound by dipole-field interactions. Further adsorption takes place near these sites through weak interaction with zeolite surfaces, and when the number of water molecules close to these sites exceeds a certain value, they tend to reorient by forming clathrate-like struc-...
It is common practice to consider the traditional Werner octahedral complex ions [MlLNle]" [M = Co(III), Rh(III), Ir(III), Cr(III), Ru(III), Pt(IV) LN = donor atom of unidentate or polydentate ammine or amine] as well as square-planar [M(LN)4p [M = Pt(II), Pd(II)] as kinetically inert compounds. Bound ammonia is generally less labile than bound water, and it has been suggested that this observation can be related to the presence of an extra and exposed electron pair in water. This may make it more sensitive to electrophilic groups in the solvation sheath, which could assist its dissociation from the metal ion (274). If we take the stance of assigning lability as a property of the ligand in such complexes, then ammonia and amines in general can be... [Pg.147]

Cobalt phthalo absorbed bound water, bound ammonia. [Pg.219]

It has been shown in recent years that definitive solvation numbers may be obtained for certain metal cations in water, methanol , liquid ammonia , N, N-dimethylformamide 2 and dimethyl sulphoxide by use of NMR-techniques. For the Mg+ in liquid ammonia the unexpected solvation number of 5 has been found . In methanol six solvent molecules were found associated, with each magnesium ion in the primary solvation sphere. Since only one Lorentzian signal was observed for bound ammonia, the exchange between non equivalent ammonias must be rapid. The most important factor in the formation of the pentaammoniated magnesium ion has been assumed to be rather strong ion pairing, which is known to occur in liquid ammonia . [Pg.34]

Still another type of adsorption system is that in which either a proton transfer occurs between the adsorbent site and the adsorbate or a Lewis acid-base type of reaction occurs. An important group of solids having acid sites is that of the various silica-aluminas, widely used as cracking catalysts. The sites center on surface aluminum ions but could be either proton donor (Brpnsted acid) or Lewis acid in type. The type of site can be distinguished by infrared spectroscopy, since an adsorbed base, such as ammonia or pyridine, should be either in the ammonium or pyridinium ion form or in coordinated form. The type of data obtainable is illustrated in Fig. XVIII-20, which shows a portion of the infrared spectrum of pyridine adsorbed on a Mo(IV)-Al203 catalyst. In the presence of some surface water both Lewis and Brpnsted types of adsorbed pyridine are seen, as marked in the figure. Thus the features at 1450 and 1620 cm are attributed to pyridine bound to Lewis acid sites, while those at 1540... [Pg.718]

Many procedures have been studied for detoxification of aflatoxkis, including heat and treatment with ammonia, methylamine, or sodium hydroxide coupled with extraction from an acetone—hexane—water solvent system. Because ki detoxification it is important to free the toxki from cellular constituents to which it is bound, a stabifi2ation of protekis uskig a tanning compound such as acetaldehyde (qv) or glutaraldehyde may be a solution to the problem (98). [Pg.480]

The number and kinds of atoms in a molecule can also be shown in a molecular formula. For example, the water molecule is symbolized H20. In this molecular formula, H means hydrogen atom, O means oxygen atom, and the subscript 2 following H indicates there are two hydrogen atoms bound to the single oxygen atom. The molecular formula of ammonia, NH3, indicates that one molecule of ammonia contains one atom of nitrogen (N) and... [Pg.31]

Because ammonia is the solvent, the solvated species is known as an ammoniate. The solvent molecules are not always bound in the solid in the same way. For example, some solids may contain water of hydration, but in other cases the water may be coordinated to the metal ion. In classifying materials as hydrates or ammoniates, the mode of attachment of the solvent is not always specified. [Pg.338]

A. Analysis of Wastewater and Natural Waters. The presence of certain anions in wastewater effluents can cause deterioration of natural water systems. Phosphorous and nitrogen can be present in several chemical forms in wastewaters. Phosphorous is usually present as phosphate, polyphosphate and organically-bound phosphorus. The nitrogen compounds of interest in wastewater characterization are ammonia, nitrite, nitrate and organic nitrogen. Analyses are often based on titrimetric, and colorimetric methods (3). These methods are time consuming and subject to a number of interferences. Ion Chromatography can be used to determine low ppm concentrations of these ions in less than thirty minutes with no sample preparation. [Pg.236]

Chemically bound nitrogen in coal is converted to NH in the gasifier and the ammonia ends up in the "gas liquor" (water) phase. After extraction of the tar acids in the Phenosolvan process, the liquor is steam-stripped to remove the NH which is then purified. [Pg.32]

Hydrotreat to reduce organically bound nitrogen, sulfur, and oxygen to ammonia, hydrogen sulfide, and water, respectively. [Pg.208]

For a given surfactant, the ability to form a single-phase w/o microemulsion is a function of the type of oil, nature of the electrolyte, solution composition, and temperature (54-58). When microemulsions are used as reaction media, the added reactants and the reaction products can also influence the phase stability. Figure 2.2.4 illustrates the effects of temperature and ammonia concentration on the phase behavior of the NP-5/cyclohexane/water system (27). In the absence of ammonia, the central region bounded by the two curves represents the single-phase microemulsion region. Above the upper curve (the solubilization limit), a water-in-oil microemulsion coexists with an aqueous phase, while below the lower curve (the solubility limit), an oil-in-water water microemulsion coexists with an oil phase. It can be seen that introducing ammonia into the system results in a shift of the solubilization... [Pg.158]


See other pages where Bound ammonia water is mentioned: [Pg.31]    [Pg.74]    [Pg.311]    [Pg.33]    [Pg.220]    [Pg.318]    [Pg.33]    [Pg.362]    [Pg.49]    [Pg.257]    [Pg.1613]    [Pg.134]    [Pg.592]    [Pg.21]    [Pg.227]    [Pg.162]    [Pg.26]    [Pg.1150]    [Pg.29]    [Pg.116]    [Pg.244]    [Pg.82]    [Pg.230]    [Pg.234]    [Pg.59]    [Pg.29]    [Pg.396]    [Pg.120]    [Pg.226]    [Pg.621]    [Pg.197]    [Pg.92]    [Pg.164]    [Pg.7]    [Pg.219]    [Pg.79]   
See also in sourсe #XX -- [ Pg.214 ]




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