Sodium diagram

Let us consider the formation of sodium chloride from its elements. An energy (enthalpy) diagram (called a Born-Haber cycle) for the reaction of sodium and chlorine is given in Figure 3.7. (As in the energy diagram for the formation of hydrogen chloride, an upward arrow represents an endothermic process and a downward arrow an exothermic process.)... 

To date there is no evidence that sodium forms any chloride other than NaCl indeed the electronic theory of valency predicts that Na" and CU, with their noble gas configurations, are likely to be the most stable ionic species. However, since some noble gas atoms can lose electrons to form cations (p. 354) we cannot rely fully on this theory. We therefore need to examine the evidence provided by energetic data. Let us consider the formation of a number of possible ionic compounds and first, the formation of sodium dichloride , NaCl2. The energy diagram for the formation of this hypothetical compound follows the pattern of that for NaCl but an additional endothermic step is added for the second ionisation energy of sodium. The lattice energy is calculated on the assumption that the compound is ionic and that Na is comparable in size with Mg ". The data are summarised below (standard enthalpies in kJ) ... 

Charge diagrams suggest that the 2-amino-5-halothiazoles are less sensitive to nucleophilic attack on 5-position than their thiazole counterpart. Recent kinetic data on this reactivity however, show, that this expectation is not fulfilled (67) the ratio fc.. bron.c.-2-am.noih.azoie/ -biomoth.azoie O"" (reaction with sodium methoxide) emphasizes the very unusual amino activation to nucleophilic substitution. The reason of this activation could lie in the protomeric equilibrium, the reactive species being either under protomeric form 2 or 3 (General Introduction to Protomeric Thiazoles). The reactivity of halothiazoles should, however, be reinvestigated under the point of view of the mechanism (1690). 

SODIUMCOMPOUNDS - SODIUMHALIDES - SODIUM CHLORIDE] (Vol22) -solubility diagram for [CRYSTALLIZATION] (Vol 7)... 

Orthophosphate salts are generally prepared by the partial or total neutralization of orthophosphoric acid. Phase equiUbrium diagrams are particularly usehil in identifying conditions for the preparation of particular phosphate salts. The solution properties of orthophosphate salts of monovalent cations are distincdy different from those of the polyvalent cations, the latter exhibiting incongment solubiUty in most cases. The commercial phosphates include alkah metal, alkaline-earth, heavy metal, mixed metal, and ammonium salts of phosphoric acid. Sodium phosphates are the most important, followed by calcium, ammonium, and potassium salts. 

Fig. 6. Phase diagram of the Na20—H2O—P20 (sodium orthophosphate) system at 25°C.

The process implications of equation 3 go beyond the weU-known properties (27—29) of NMP to faciUtate S Ar processes. The function of the aminocarboxylate is also to help solubilize the sulfur source anhydrous sodium sulfide and anhydrous sodium hydrogen sulfide are virtually insoluble in NMP (26). It also provides a necessary proton acceptor to convert thiophenol intermediates into more nucleophilic thiophenoxides. A block diagram for the Phillips low molecular weight linear PPS process is shown in Eigure 1. 

Fig. 1. Schematic diagram for the commercial production of potassium from sodium and potassium chloride. EM = electromagnetic.

Fig. 1. Binary soap—water phase diagram for sodium palmitate (4). Courtesy of Academic Press, Ltd.

For sodium palmitate, 5-phase is the thermodynamically preferred, or equiUbrium state, at room temperature and up to - 60° C P-phase contains a higher level of hydration and forms at higher temperatures and CO-phase is an anhydrous crystal that forms at temperatures comparable to P-phase. Most soap in the soHd state exists in one or a combination of these three phases. The phase diagram refers to equiUbrium states. In practice, the drying routes and other mechanical manipulation utilized in the formation of soHd soap can result in the formation of nonequilibrium phase stmcture. This point is important when dealing with the manufacturing of soap bars and their performance. 

Sodium is miscible with many metals in liquid phase and forms alloys or compounds. Important examples ate hsted in Table 9 phase diagrams ate available... 

References 37 and 167 present phase diagrams of sodium with other metals. 

Figure 2 shows a general process flow diagram for almost all production of natural sodium sulfate. Glauber s salt can be converted to anhydrous sodium sulfate by simply drying it in rotary kilns. Direct drying forms a fine, undesirable powder, and any impurities in the Glauber s salt become part of the final product. This process is not used in the United States but is used in other countries. 

Alternatively, if teUurium dioxide is the product desired, the sodium teUurite solution can be neutralized in a controUed fashion with sulfuric acid. As the pH is lowered, precipitates containing impurities such as lead and sUica that form ate filtered off. At pH 5.6 the solubUity of teUurous acid teaches a minimum and essentiaUy aU of the teUurium precipitates (>98%). After filtration and drying, commercial teUurium dioxide is obtained. A diagram for the process of deteUurizing of slimes and recovering teUurium products is shown in Figure 1. 

Sodium thiosulfate, either the anhydrous salt, Na2S202, or the crystalline pentahydrate, is commonly referred to as hypo or crystal hypo. When a concentrated sodium thiosulfate solution (50—60 wt %) is cooled to <48° C, the pentahydrate, containing 63.7% Na2S202, crystallines in monoclinic transparent prisms as shown in the equiUbrium phase diagram (Fig. 1). The monohydrate [55755-19-6] and the heptahydrate [36989-91-0] are also known. 

Fig. 4. Modified Arrhenius diagram of the ionic conductivity of sodium chloride. Tis in Kelvin, O is in ((n-cm)...

Fig. 2. Flow diagram for the production of sodium chromate, sodium dichromate, and chromic acid flake and crystals.

FIG. 2-29 Enthalpy-concentration diagram for aqueous sodium hydroxide at 1 atm. Reference states enthalpy of liquid water at 32 F and vapor pressure is zero partial molal enthalpy of infinitely dilute NaOH solution at 64 F and 1 atm is zero. [McCahe, Trans. Am. Inst. Chem. Eng., 31, 129(1935).]... 

Vanadium-Sodium Compounds Most Corrosive. Physical property data for vanadates, phase diagrams, laboratory experiments, and numerous field investigations have shown that the sodium vanadates are the lowest melting compounds and are the most corrosive to metals and refractories. These compounds are thought to form by either the vapor phase reaction of NaCI and V2O5 or by the combination of fine droplets of these materials upon the cooler parts of combustion equipment. 

An example of a process using O2 to oxidize HiS is the Stretford process, which is licensed by the British Gas Corporation. In this process the gas stream is washed with an aqueous solution of sodium carbonate, sodium vanadate, and anthraquinone disulfonic acid. Figure 7-9 shows a simplified process diagram of the process. 

As may be seen from the diagram, silver in highly alkaline solution corrodes only within a narrow region of potential, provided complexants are absent. It is widely employed to handle aqueous solutions of sodium or potassium hydroxides at all concentrations it is also unaffected by fused alkalis, but is rapidly attacked by fused peroxides, which are powerful oxidising agents and result in the formation of the AgO ion Table 6.6 gives the standard electrode potentials of silver systems. 

Silica is only decomposed by those metals which have a high affinity for oxygen as indicated by the Ellingham diagram (Fig. 18.4). On this basis, molten sodium should be compatible with silica ... 

Fig. 5. Tentative mixed potential model for the sodium-potassium pump in biological membranes the vertical lines symbolyze the surface of the ATP-ase and at the same time the ordinate of the virtual current-voltage curves on either side resulting in different Evans-diagrams. The scale of the absolute potential difference between the ATP-ase and the solution phase is indicated in the upper left comer of the figure. On each side of the enzyme a mixed potential (= circle) between Na+, K+ and also other ions (i.e. Ca2+ ) is established, resulting in a transmembrane potential of around — 60 mV. This number is not essential it is also possible that this value is established by a passive diffusion of mainly K+-ions out of the cell at a different location. This would mean that the electric field across the cell-membranes is not uniformly distributed.

Sodium reduction development directions, 336 diluted melts, 331-332 of K-Salt, 327-328 principals, 326 Solid-phase interaction mechanism, 34-37 niobium oxyfluorides, 26-31 tantalum oxyfluorides, 32-34 Solubility diagrams (NH4)5Nb3OF18, 22 K2NbF7 in HF solutions, 14 K2TaF7 in HF solutions, 14 RbsNbjOF,, 22-23 Solubility of peroxides, 307 Specific conductivity, 153, 164 Spontaneous polarization, 223 Structural characteristics for X Me=8, 61,... 

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