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Batteries electrolyte

The metallic salts of trifluoromethanesulfonic acid can be prepared by reaction of the acid with the corresponding hydroxide or carbonate or by reaction of sulfonyl fluoride with the corresponding hydroxide. The salts are hydroscopic but can be dehydrated at 100°C under vacuum. The sodium salt has a melting point of 248°C and decomposes at 425°C. The lithium salt of trifluoromethanesulfonic acid [33454-82-9] CF SO Li, commonly called lithium triflate, is used as a battery electrolyte in primary lithium batteries because solutions of it exhibit high electrical conductivity, and because of the compound s low toxicity and excellent chemical stabiUty. It melts at 423°C and decomposes at 430°C. It is quite soluble in polar organic solvents and water. Table 2 shows the electrical conductivities of lithium triflate in comparison with other lithium electrolytes which are much more toxic (24). [Pg.315]

Quaternary Salts. Herbicides paraquat (20) and diquat (59) are the quaternary salts of 4,4 -bipyridine (19) and 2,2 -bipyridine with methyl chloride and 1,2-dibromoethane, respectively. Higher alkylpyridinium salts are used in the textile industry as dye ancillaries and spin bath additives. The higher alkylpyridinium salt, hexadecylpytidinium chloride [123-03-5] (67) (cetylpyridinium chloride) is a topical antiseptic. Amprolium (62), a quaternary salt of a-picohne (2), is a coccidiostat. Bisaryl salts of butylpyridinium bromide (or its lower 1-alkyl homologues) with aluminum chloride have been used as battery electrolytes (84), in aluminum electroplating baths (85), as Friedel-Crafts catalysts (86), and for the formylation of toluene by carbon monoxide (87) (see QuaternaryAA ONiUM compounds). [Pg.336]

Battery electrolytes are concentrated solutions of strong electrolytes and the Debye-Huckel theory of dilute solutions is only an approximation. Typical values for the resistivity of battery electrolytes range from about 1 ohmcm for sulfuric acid [7664-93-9] H2SO4, in lead—acid batteries and for potassium hydroxide [1310-58-3] KOH, in alkaline cells to about 100 ohmcm for organic electrolytes in lithium [7439-93-2] Li, batteries. [Pg.509]

The characteristics for aqueous KOH (97—99) solutions vary somewhat for battery electrolytes when additives are used. Furthermore, potassium hydroxide reacts with many organics and with the carbon dioxide in air to form carbonates. The build-up of carbonates in the electrolyte is to be avoided because carbonates reduce electrolyte conductivity and electrode activity in some cases. [Pg.567]

U.S. Air Force Academy in 1961. He was an early researcher in the development of low-temperature molten salts as battery electrolytes. At that time low temperature meant close to 100 °C, compared to many hundreds of degrees for conventional molten salts. His work led directly to the chloroaluminate ionic liquids. [Pg.3]

The allcylpyridinium cations suffer from being relatively easy to reduce, both chemically and electrochemically. Charles Hussey (Figure 1.3) and I set out a program to predict cations more resistant to reduction, to synthesize ionic liquids on the basis of those predictions, and to characterize them electrochemically for use as battery electrolytes. [Pg.4]

Films on lithium play an important part in secondary lithium metal batteries. Electrolytes, electrolyte additives, and lithium surface treatments modify the lithium surface and change the morphology of the lithium and its current efficiency [93],... [Pg.58]

Table 5 contains a selection of ion-pair association constants, triple ion formation constants, and limiting conductivities for various electrolytes which have been studied in connection with the optimization of battery electrolytes. It shows... [Pg.469]

Salomon and co-workers investigated the role of ligands known to offer cavities with diameters matching the radius of the lithium ion, e.g, 15-crown-5 or the cryp-tand [222] 12-crown-4 (12C4) and derivatives such as l-aza-12-crown-4 (1-A I2C4) and l-benzoaza-12-crown-4 (1-BA-12C4) for various battery electrolytes at moderate concentrations [133-136,217]. [Pg.472]

A 0.2 mol L"1 LiCl/THF solution possesses only very low conductivity of 1.6xl0"6 Scm"1. Addition of N(CH2 CH2NR2)3(R = CF3S02 short nomenclature M6R) yields an increase in conductivity by three orders of magnitude to 1.7 x 10 3 S cm"1. This approach is seemingly especially useful for battery electrolytes, because the transference number of the lithium ion is increased. Conceptually this approach is similar to the use of lith-... [Pg.489]

Table 10 shows a collection of typical battery electrolytes, their conductivities at various temperatures, the concentration of the salt, and references. More examples can be found in Ref. [15] and the literature cited therein... [Pg.490]

Q > A between solid electrolyte/solution or battery electrolyte phases 111.7... [Pg.594]

Rather than natural ores as in Leclanche batteries, electrolytic manganese dioxide (EMD), which is produced by anodic oxidation of Mn ions at graphite electrodes in solutions of manganese salts, is used as the active material for the positive... [Pg.352]

Ionic liquid solvents are non-volatile and non-toxic and are liquids at ambient temperature. Originally, work was concerned with battery electrolytes. These ionic liquids (IL) show excellent extraction capabilities and allow catalysts to be used in a biphasic system for convenient recycling (Holbrey and Seddon, 1999). IFP France has commercialized a dimerization process for butenes using (LNiCH2R ) (AlCU) (where L is PRj) as an IL and here the products of the reaction are not soluble in IL and hence separate out. The catalyst is very active and gives high selectivity for the dimers. [Pg.148]

Carbon/lithium contact in the presence of lithium battery electrolytes can provoke spontaneous ignition. [Pg.165]

Beaker 3 = 100 milliliters of sulfuric acid (new battery electrolyte) [remove metal ion contaminants from PEM surface, and sulfonate the PEM surface]. [Pg.2]

As for studies of ice, a search of the recent proton transfer literature discloses that ice is one of the substances that still generates interest (23, 24) particularly as it relates to membrane proton-transfer problems. Solid battery electrolytes can also involve (25, 26, 27) proton transfers, although these are obviously very slow compared to the kinds of rates that we are used to considering in aqueous inorganic solutions. [Pg.75]


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