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Electrolytes Bases Salts

Poly(ethylene oxide) associates in solution with certain electrolytes (48—52). For example, high molecular weight species of poly(ethylene oxide) readily dissolve in methanol that contains 0.5 wt % KI, although the resin does not remain in methanol solution at room temperature. This salting-in effect has been attributed to ion binding, which prevents coagulation in the nonsolvent. Complexes with electrolytes, in particular lithium salts, have received widespread attention on account of the potential for using these materials in a polymeric battery. The performance of soHd electrolytes based on poly(ethylene oxide) in terms of ion transport and conductivity has been discussed (53—58). The use of complexes of poly(ethylene oxide) in analytical chemistry has also been reviewed (59). [Pg.342]

Analysis of the activation energies of charge transport as a function of temperature and concentration shows that a type of corresponding state is attained at concentration 41 characterized by constant critical energies of activation for a given temperature. Electrolytes based on salts with small nonsolvated ions or small Stokes radii attain high 41 and /rmax values, whereas those based on large ions attain only small 41 and /fmax values. [Pg.487]

In conclusion, polymer electrolytes based on phosphazene backbone and containing ether side chains are, after complexation with alkali metal salts, among the highest ionically solvent-free polymer salt complexes, with conductivities in the order of 10" -10" S cm However, these conductivities are still below the value of 10 S cm" which is considered to be the minimum for practical applications. Therefore the design of new polyphosphazenes electrolytes with a higher conductivity and also a higher dimensional stability still remains a challenge for future researchers. [Pg.212]

Solutions of substances that are good conductors of electricity are called electrolytes. Sodium chloride, the major constituent of seawater, is a strong electrolyte. Most salts, as well as strong acids and bases, are strong electrolytes because they remain in solution primarily in ionic (charged) forms. Weak acids and bases are weak electrolytes because they tend to remain in nonionic forms. Pure water is a nonconductor of electricity. [Pg.809]

Subcategory A encompasses the manufacture of all batteries in which cadmium is the reactive anode material. Cadmium anode batteries currently manufactured are based on nickel-cadmium, silver-cadmium, and mercury-cadmium couples (Table 32.1). The manufacture of cadmium anode batteries uses various raw materials, which comprises cadmium or cadmium salts (mainly nitrates and oxides) to produce cell cathodes nickel powder and either nickel or nickel-plated steel screen to make the electrode support structures nylon and polypropylene, for use in manufacturing the cell separators and either sodium or potassium hydroxide, for use as process chemicals and as the cell electrolyte. Cobalt salts may be added to some electrodes. Batteries of this subcategory are predominantly rechargeable and find application in calculators, cell phones, laptops, and other portable electronic devices, in addition to a variety of industrial applications.1-4 A typical example is the nickel-cadmium battery described below. [Pg.1311]

It is known that in the process of electrochemical cycling of tin oxide-based thin films versus lithium metal there are at least two reactions in standard alkylcarbonate electrolyte based on lithium salts [1], The first of them leads to formation of metallic tin on the first cycle ... [Pg.322]

The anodic stability of the AsFe" anion proved to be high. In proper solvents, such as esters rather than ethers, the electrolyte based on this salt can remain stable up to 4.5 V on various cathode surfaces.The combination of cathodic and anodic stability would have made LiAsFe a very promising candidate salt for both lithium and lithium ion batteries had the toxicity not been a source of concern. Instead, it was never used in any commercialized cells but is still frequently used in laboratory tests even today. ... [Pg.73]

As a result, the acid strength of the proton is approximately equivalent to that of sulfuric acid in nonaqueous media. In view of the excellent miscibility of this anion with organic nonpolar materials, Armand et al. proposed using its lithium salt (later nicknamed lithium imide , or Lilm) in solid polymer electrolytes, based mainly on oligomeric or macro-molecular ethers. In no time, researchers adopted its use in liquid electrolytes as well, and initial results with the carbonaceous anode materials seemed promising. The commercialization of this new salt by 3M Corporation in the early 1990s sparked considerable hope that it might replace the poorly... [Pg.74]

New synthetic efforts generated a few structural derivatives of Lilm with longer perfluorinated alkyls such as LiBeti and a lithium salt of an asymmetric imide anion, and the stability of A1 in the electrolytes based on these salts was found to be much improved when compared with those in electrolytes based on Lilm and LiTf.i i s... [Pg.109]

Figure 52. Passivation of A1 substrate in LiBOB-based electrolytes Time-decaying current observed on an A1 electrode at various potentials containing 1.0 M LiBOB in EC/EMC. Inset the dependence of steady-state current density at t= 10 s) on applied potential as obtained on an A1 electrode in electrolytes based on various salts in the same mixed solvent. (Reproduced with permission from ref 155 (Eigure 1). Copyright 2002 The Electrochemical Society.)... Figure 52. Passivation of A1 substrate in LiBOB-based electrolytes Time-decaying current observed on an A1 electrode at various potentials containing 1.0 M LiBOB in EC/EMC. Inset the dependence of steady-state current density at t= 10 s) on applied potential as obtained on an A1 electrode in electrolytes based on various salts in the same mixed solvent. (Reproduced with permission from ref 155 (Eigure 1). Copyright 2002 The Electrochemical Society.)...
Lithium Chelatophosphates. If the work of Barthel et al. and Angell et al. on various borate-based salts could be viewed as the structural modification of a perhalogenated borate salt (LiBF4) that was already used in commercial lithium ion cells, then similar modifications were also carried out on the more popular salt LiPFe. the industry standard of lithium ion cell electrolytes. [Pg.149]

More stringent electrochemical characterizations were carried by Aurbach and co-workers, who comparatively investigated the interfacial properties of the electrolytes based on LiFAP on anode and cathode materials against the benchmark salts LiPFe and LiBeti through various instrumental means, including voltammetry, EIS, FT-IR, and They... [Pg.150]

Another salt that is less sensitive to moisture than LiPFe, LiBF4, was also tested as an electrolyte solute intended for high-temperature applications. Zhang et al. reported that electrolytes based on this salt could allow the lithium ion cells to cycle at temperatures up to 70 Irreversible reactions occurred at temperatures above 80 °C, and the cells lost capacity rapidly, which was accompanied by the rise of cell impedance simultaneously. [Pg.160]

ELECTROLYTE IMBALANCE Improper proportions of acids, bases, salts, and fluids in the body. Electrolytes include the salts sodium, potassium, magnesium, chloride chlorine. They can conduct electricity, and therefore are essential in nerve, muscle, and heart function. [Pg.172]


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