The electromotive forces E of the amalgam cells {Li x Hg 1-x | LiCl (m) | AgCl | Ag} and {Li x Hg 1-x | LiBr (m) | AgBr | Ag} have been measured as a function of the mole fraction x of Li metal in amalgams and of the molalities m of LiCl as well as LiBr at T = 298.15 K. For LiCl, the solvents invest
Thermodynamics of the solubility of barium nitrate in the mixed solvent, ethanol + water, and the related ion-association
โ Scribed by M. Aghaie; H. Aghaie; A. Ebrahimi
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 114 KB
- Volume
- 135
- Category
- Article
- ISSN
- 0167-7322
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๐ SIMILAR VOLUMES
The electromotive force E of the amalgam cell {K x Hg 1-x |KCl(m)|AgCl|Ag} has been measured as a function of the mole fraction x of K metal in amalgams and of the molality m of KCl in (ethylene glycol + water), (acetonitrile + water), and (1,4dioxane + water) solvent mixtures containing up to 0.8 m
The standard potential of the (Ag, AgCl) electrode E o , the standard second ionization constant of sulfuric acid K 2 , and the standard association constant of the ion pair [MgSO 4 ] o , K in {0.03226 CO(NH 2 ) 2 + 0.96774 H 2 O} at five temperatures from 278.15 K to 318.15 K were determined from p
The potential differences E of the cells Pt|H 2 |H 2 Ph(m 1 ) + KHPh(m 2 ) + KCl(m 3 ) in Z|AgCl|Ag and Pt|H 2 |H 2 Ph(m 1 ) + KHPh(m 2 ) + KCl(m 3 ) in Z|Hg 2 Cl 2 |Hg have been measured at T = 298.15 K in mixtures Z = (W + S) of water (W) with cosolvents S = propylene carbonate (PC) and S = ethyle
The electromotive force (e.m.f.) E of the cell Pt|H 2 (p)|HCl(m) in Z|AgCl|Ag in {glycerol (G) + water (W)} solvents, Z = (G + W), up to glycerol mass fraction w G = 0.7 has been measured within the temperature range from 273.15 K to 313.15 K at HCl molalities up to 0.1 mol โข kg -1 . On this basis,