Metal vapor pressure

Very high metal vapor pressures are required to... 

For comparable metal-vapor pressures, the most stable hexaboride is that which has the smallest unit ceil SmB is more stable than BaB, which has a larger unit cell. 

The thermal stability of alkali-metal borides is relatively low, which is expected from the high vapor pressures of the corresponding metals at high T. Consequently, the alkali-metal vapor pressure is an important parameter, and synthesis of alkali-metal boride is carried out in isothermal reactors that permit maximum alkali-metal pressure and hence optimum preparation conditions. 

The experimental set-up has been previously described (A). Silicon and germanium metal were vaporized from a vitreous carbon crucible over the temperature range of 1475-1675°C and 1325-1500°C respectively. Tin and lead were vaporized from a molybdenum crucible over a temperature range of 1125-1240°C and 644-742°C respectively. This corresponds to an approximate metal vapor pressure range of 1x10 -1x10 torr for each metal. 

Chemical self-diffusion coefficients, D, as a function of temperature and metal vapor pressure, Pcd were studied in undoped single crystals at high temperatures. The... 

The phase transition region was characterized by confused values of D because of changes due to phase mixture. The value of D was about 3 orders of magnitude faster than that for self-diffusion under the same conditions. It was shown that doubly-ionized interstitial metal atoms were the predominant diffusible defects at high metal vapor pressures. The value of D was found to be almost independent of the metal vapor pressure at high P n-... 

Curium metal has an entropy of vaporization remarkably similar to that of gadolinium, although its vapor pressure is about double that of gadolinium over the measured range [33]. The metal vapor pressure of triply distilled Cm metal has been measured between 1300 and 2000 K and obeys the following relations [33] ... 

The criterion retained up to now in the specifications is not the true vapor pressure, but an associated value called the Reid vapor pressure, RVP. The procedure is to measure the relative pressure developed by the vapors from a sample of motor fuel put in a metallic cylinder at a temperature of 37.8°C. The variations characteristic of the standard method are around 15 millibar in repeatability and 25 millibar in reproducibility. 

It is one of four metals — mercury, cesium, and rubidium — which can be liquid near room temperature and, thus, can be used in high-temperature thermometers. It has one of the longest liquid ranges of any metal and has a low vapor pressure even at high temperatures. 

Significant vapor pressure of aluminum monofluoride [13595-82-9], AIF, has been observed when aluminum trifluoride [7784-18-1] is heated in the presence of reducing agents such as aluminum or magnesium metal, or is in contact with the cathode in the electrolysis of fused salt mixtures. AIF disproportionates into AIF. and aluminum at lower temperatures. The heat of formation at 25°C is —264 kJ/mol(—63.1 kcal/mol) and the free energy of formation is —290 kJ/mol(—69.3 kcal/mol) (1). Aluminum difluoride [13569-23-8] h.3.s been detected in the high temperature equihbrium between aluminum and its fluorides (2). 

Halides. Indium trichloride [10025-83-8] InCl, can be made by heating indium in excess chlorine or by chlorinating lower chlorides. It is a white crystalline soHd, deUquescent, soluble in water, and has a high vapor pressure. InCl forms chloroindates, double salts with chlorides of alkaLi metals, and organic bases. 

Anionic polymerization of vinyl monomers can be effected with a variety of organometaUic compounds alkyllithium compounds are the most useful class (1,33—35). A variety of simple alkyllithium compounds are available commercially. Most simple alkyllithium compounds are soluble in hydrocarbon solvents such as hexane and cyclohexane and they can be prepared by reaction of the corresponding alkyl chlorides with lithium metal. Methyllithium [917-54-4] and phenyllithium [591-51-5] are available in diethyl ether and cyclohexane—ether solutions, respectively, because they are not soluble in hydrocarbon solvents vinyllithium [917-57-7] and allyllithium [3052-45-7] are also insoluble in hydrocarbon solutions and can only be prepared in ether solutions (38,39). Hydrocarbon-soluble alkyllithium initiators are used directiy to initiate polymerization of styrene and diene monomers quantitatively one unique aspect of hthium-based initiators in hydrocarbon solution is that elastomeric polydienes with high 1,4-microstmcture are obtained (1,24,33—37). Certain alkyllithium compounds can be purified by recrystallization (ethyllithium), sublimation (ethyllithium, /-butyUithium [594-19-4] isopropyllithium [2417-93-8] or distillation (j -butyUithium) (40,41). Unfortunately, / -butyUithium is noncrystaUine and too high boiling to be purified by distiUation (38). Since methyllithium and phenyllithium are crystalline soUds which are insoluble in hydrocarbon solution, they can be precipitated into these solutions and then redissolved in appropriate polar solvents (42,43). OrganometaUic compounds of other alkaU metals are insoluble in hydrocarbon solution and possess negligible vapor pressures as expected for salt-like compounds. 

These nicotinoids are appreciably volatile (nicotine vapor pressure, 5.7 Pa at 25°C) and, although colorless Hquids when pure, rapidly darken upon exposure to air. They are highly basic = 1 x 10 , = 1 x 10 ) and readily form salts with acids and many metals. Nicotine sulfate [65-30-5],... 

The vapor pressure, of soHd iodine has been redetermined using the gas current method and by a static method using a flexible metallic diaphragm (27,28). The data from the gas current method are weU represented by equation 2 (27) ... 

More extensive vapor pressure data for lithium and other metals are given ia Ref. 43. To convert kPa to mm Hg, multiply by 7.5. 

Lithium carbonate addition to HaH-Heroult aluminum ceU electrolyte lowers the melting point of the eutectic electrolyte. The lower operating temperatures decrease the solubiHty of elemental metals in the melt, allowing higher current efficiencies and lower energy consumption (55). The presence of Hthium also decreases the vapor pressure of fluoride salts. 

Lithium Iodide. Lithium iodide [10377-51 -2/, Lil, is the most difficult lithium halide to prepare and has few appHcations. Aqueous solutions of the salt can be prepared by carehil neutralization of hydroiodic acid with lithium carbonate or lithium hydroxide. Concentration of the aqueous solution leads successively to the trihydrate [7790-22-9] dihydrate [17023-25-5] and monohydrate [17023-24 ] which melt congmendy at 75, 79, and 130°C, respectively. The anhydrous salt can be obtained by carehil removal of water under vacuum, but because of the strong tendency to oxidize and eliminate iodine which occurs on heating the salt ia air, it is often prepared from reactions of lithium metal or lithium hydride with iodine ia organic solvents. The salt is extremely soluble ia water (62.6 wt % at 25°C) (59) and the solutions have extremely low vapor pressures (60). Lithium iodide is used as an electrolyte ia selected lithium battery appHcations, where it is formed in situ from reaction of lithium metal with iodine. It can also be a component of low melting molten salts and as a catalyst ia aldol condensations. 

Liquid Metals. If operating temperatures rise above 250—300°C, where many organic fluids decompose and water exerts high vapor pressure, hquid metals have found some use, eg, mercury for limited appHcation in turbines sodium, especially its low melting eutectic with 23 wt % potassium, as a hydrauhc fluid and coolant in nuclear reactors and potassium, mbidium, cesium, and gallium in some special uses. 

Eig. 8. Cost of electricity (COE) comparison where represents capital charges, Hoperation and maintenance charges, and D fuel charges for the reference cycles. A, steam, light water reactor (LWR), uranium B, steam, conventional furnace, scmbber coal C, gas turbine combined cycle, semiclean hquid D, gas turbine, semiclean Hquid, and advanced cycles E, steam atmospheric fluidized bed, coal E, gas turbine (water-cooled) combined low heating value (LHV) gas G, open cycle MHD coal H, steam, pressurized fluidized bed, coal I, closed cycle helium gas turbine, atmospheric fluidized bed (AEB), coal J, metal vapor topping cycle, pressurized fluidized bed (PEB), coal K, gas turbine (water-cooled) combined, semiclean Hquid L, gas turbine... 

Most inorganic mercury compounds have very low vapor pressures, and generally do not contribute to high mercury vapor readings. MetaUic mercury is the most potent and troublesome in this respect. Organic mercurials also contribute to mercury vapor readings, possibly by virtue of the presence of extremely small amounts of metallic mercury present as an impurity. 

Reduction to Liquid Metal. Reduction to Hquid metal is the most common metal reduction process. It is preferred for metals of moderate melting point and low vapor pressure. Because most metallic compounds are fairly insoluble in molten metals, the separation of the Hquified metal from a sohd residue or from another Hquid phase of different density is usually complete and relatively simple. Because the product is in condensed form, the throughput per unit volume of reactor is high, and the number and si2e of the units is rninimi2ed. The common furnaces for production of Hquid metals are the blast furnace, the reverberatory furnace, the converter, the flash smelting furnace, and the electric-arc furnace (see Furnaces, electric). 

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