Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Liquid metals, references

For the purposes of discussion, it is useful to consider the blast furnace as operating in four consecutive zones. At the fourtlr, bottom, zone the oxidation of coke at the tuyeres canres the temperamre to levels in excess of 2100 K. The next zone, which operates in the temperature range 1600-1900 K is where the liquid metal and slag are formed. The second zone, sometimes referred to as the thermal reserve zone, is where the CO2-C reaction to produce CO, the so-called solution reaction mainly occurs, and die reduction of h on is completed. In the first zone, at the top of the furnace, tire primaty reduction of... [Pg.333]

Information on bimetallic corrosion for buried metals may be obtained in Referencesfor embedded metals in References , and for non-aqueous liquids in References (liquid fluorine)and (liquid ammonia). [Pg.231]

Metal/molten salt interfaces have been studied mainly by electrocapillary833-838 and differential capacitance839-841 methods. Sometimes the estance method has been used.842 Electrocapillary and impedance measurements in molten salts are complicated by nonideal polarizability of metals, as well as wetting of the glass capillary by liquid metals. The capacitance data for liquid and solid electrodes in contact with molten salt show a well-defined minimum in C,E curves and usually have a symmetrical parabolic form.8 10,839-841 Sometimes inflections or steps associated with adsorption processes arise, whose nature, however, is unclear.8,10 A minimum in the C,E curve lies at potentials close to the electrocapillary maximum, but some difference is observed, which is associated with errors in comparing reference electrode (usually Pb/2.5% PbCl2 + LiCl + KC1)840 potential values used in different studies.8,10 It should be noted that any comparison of experimental data in aqueous electrolytes and in molten salts is somewhat questionable. [Pg.147]

Certain long-chain alkylammonium salts, notably tricaprylmethyl-ammonium chloride (Aliquat 336-S) and tri-Ao-octylamine hydrochloride (TIOA) are liquids, sometimes referred to as liquid anion exchangers, which can form extractable ion pairs or aggregates with anionic metal complexes in the... [Pg.61]

The details of the development of the EBRD process have been described by Pietsch et al.[187] There are two alternative operation modes in addition to the above continuous non-contact mode. The first one may be referred to as continuous contact atomization. In this mode, liquid metal contacts the bottom surface of the container instead of melt dripping, and then flows continuously from the center to the rim of the container. The second one may be termed discontinuous non-contact atomization. In this mode, the container is first filled by dripping melt while it is rotating at a very low speed of about 3 x 10-3 radians/s. The rotating speed of the container is then enhanced to about 14 radians/s while the metal or alloy is remelted and atomized. More than one focused electron beam may be used to provide energy for melting metal. [Pg.103]

Sodium is produced by an electrolytic process, similar to the other alkali earth metals. (See figure 4.1). The difference is the electrolyte, which is molten sodium chloride (NaCl, common table salt). A high temperature is required to melt the salt, allowing the sodium cations to collect at the cathode as liquid metallic sodium, while the chlorine anions are liberated as chlorine gas at the anode 2NaCl (salt) + electrolysis —> Cl T (gas) + 2Na (sodium metal). The commercial electrolytic process is referred to as a Downs cell, and at temperatures over 800°C, the liquid sodium metal is drained off as it is produced at the cathode. After chlorine, sodium is the most abundant element found in solution in seawater. [Pg.51]

MERCURY. [CAS 7439-97-6, Chemical element, symbol Hg. at. no. 8(1. at. vvt. 21X1.59. periodic table gmup 12. nip —3X.84 C. bp 356.5x C. density 13.546 g/cin (liquid). 14.193 g/cm isolid). Solid mercury has a rhomhohedral crystal structure The element, sometimes referred to as quicksilver, is a silver-while liquid metal at standard conditions. There are seven stable isotopes of mercury. " Hg " Hg through "- Hg. and JHe. and seven radioactive isotope s., Hg through "Tig. l,7Hg. " Hg. and " Hg. With exception of l>JHg (half-life of approximately 130 days) and 1415Hg thalMtl e of approximately 46 daysl. the half-lives of the radioactive isotopes are short, measured in terms ol minutes or hours. [Pg.978]

As the name implies, the phenomenon is based on coating a solid metal with a liquid metal. In our theory, liquid metal (being above its melting temperature) has no covalent bonds and the free electrons essentially provide the cohesive energy. It can be recalled that this was the basis for obtaining the correlation (Fig. 11). Thus, by coating a metal that has a distinct ratio of covalent bond over free electron band with a liquid metal that has only free electrons (no covalent bond) can have no effect whatsoever in the AEi (for these notations refer to Fig. 9) which has to do only with covalent bond. This is the observation of 4.1.3. [Pg.170]

In this account, the new oxidation states are introduced in the format of a short, but it is hoped complete, summary covering the literature until late 1980. Some of the topics were reviewed previously, but the articles soon became out-dated because of the rapid growth of the fields. Best known are the discussion of gold(II) compounds (23) and the early presentation of gold(V) complexes (5). Gold clusters have been included in the leading reference texts on gold chemistry (77, 85), and the -1 state appeared in a recent summary on liquid metals and liquid semiconductors (39). [Pg.240]

Various types of reference electrodes are used for permanent embedment in concrete. Some fall into the category of double junction electrodes of the second kind and are therefore reference electrodes in the true sense. Others are simply a piece of metal or another material put into the concrete. Although stable and accurate, SCE is not used for permanent embedment in concrete, mainly because it contains a liquid metal, which makes it difficult to manufacture in a rugged form. In addition, environmental reasons make it undesirable for permanent use in the field (poisonous mercury and mercury compounds). [Pg.26]

Experiments by Chuang and Miller (34) confirm good performance of 1 and 2 metallic, surface-treated CMR and 1 Hy-Pak at liquid rates of the order of 0.3 to 0.8 gpm/ft2 with an aqueous system. Their experiments also showed inferior performance when surface treatment was inadequate. This gives support to the metallic values listed in Table 8.6, but emphasizes that surface-treated and oxidized metal refer to proper conditioning of packing surfaces. [Pg.515]

In general, there are many open questions concerning liquid-metal heat transfer, and the reader is referred to Refs. 13 and 23 for more information. [Pg.307]

Figure 6.2. Experimental contact angles for pure liquid metal/oxide systems (taken from references given in the figure) versus calculated values of molar fraction of oxygen in the liquid metal caused by dissolution of the oxide. From (Eustathopoulos and Drevet 1998) [17]. Figure 6.2. Experimental contact angles for pure liquid metal/oxide systems (taken from references given in the figure) versus calculated values of molar fraction of oxygen in the liquid metal caused by dissolution of the oxide. From (Eustathopoulos and Drevet 1998) [17].
Table 7.10. Wetting by Cu of metal-like carbides in a high vacuum at 1100°C(Ramqvist 1965). The equilibrium molar fraction of carbide metal Me dissolved in Cu, X c(Cu), is calculated from equation (7.16). Data for AG (reference state pure liquid metal Me) come from (Rosenqvist 1983) except for Mo2C and HfC (Kubaschewski and Alcock 1979). Data for AHMe(Cu) come from (Niessen et al. 1983). Table 7.10. Wetting by Cu of metal-like carbides in a high vacuum at 1100°C(Ramqvist 1965). The equilibrium molar fraction of carbide metal Me dissolved in Cu, X c(Cu), is calculated from equation (7.16). Data for AG (reference state pure liquid metal Me) come from (Rosenqvist 1983) except for Mo2C and HfC (Kubaschewski and Alcock 1979). Data for AHMe(Cu) come from (Niessen et al. 1983).
McGonigal, P. J. A Generalized Relation Between Reduced Density and Temperature for Liquids with Special Reference to Liquid Metals. J. Phys. Chem. 66, 1686 (1962). [Pg.94]

The reference electrode (RE) shown in Fig. 4 provides a fixed constant potential to the solution. A liquid containing reference electrode with a stable potential, such as a silver/silver chloride electrode, is used for this purpose. As will be discussed in the next section, an inert metal such as platinum or gold can also be used. The electrical circuit for the operation of the two FET elements and the differential output measurement is shown in Fig. 4. [Pg.155]


See other pages where Liquid metals, references is mentioned: [Pg.188]    [Pg.188]    [Pg.385]    [Pg.387]    [Pg.566]    [Pg.178]    [Pg.354]    [Pg.127]    [Pg.145]    [Pg.284]    [Pg.45]    [Pg.277]    [Pg.81]    [Pg.119]    [Pg.350]    [Pg.362]    [Pg.334]    [Pg.385]    [Pg.547]    [Pg.526]    [Pg.115]    [Pg.387]    [Pg.101]    [Pg.541]    [Pg.376]    [Pg.101]    [Pg.168]    [Pg.334]    [Pg.67]    [Pg.236]    [Pg.236]   
See also in sourсe #XX -- [ Pg.477 ]




SEARCH



Liquid metals, heat transfer references

Liquid reference

© 2024 chempedia.info