THERMOCHEMICAL INVESTIGATIONS OF THE SYSTEMS USEFUL FOR LITHIUM BATTERY CONSTRUCTION .2. SOLUTION ENTHALPIES OF LICLO4 IN 1,2-DIMETHOXYETHANE PLUS GAMMA-BUTYROLACTONE MIXTURES AND OF LICLO4, NAI AND N,N-DIMETHYLACETAMIDE IN 1,2-DIMETHOXYETHANE PLUS PROPYLENE CARBONATE MIXTURES AT 298.15 K
A. Piekarska et H. Piekarski, THERMOCHEMICAL INVESTIGATIONS OF THE SYSTEMS USEFUL FOR LITHIUM BATTERY CONSTRUCTION .2. SOLUTION ENTHALPIES OF LICLO4 IN 1,2-DIMETHOXYETHANE PLUS GAMMA-BUTYROLACTONE MIXTURES AND OF LICLO4, NAI AND N,N-DIMETHYLACETAMIDE IN 1,2-DIMETHOXYETHANE PLUS PROPYLENE CARBONATE MIXTURES AT 298.15 K, Thermochimica acta, 288(1-2), 1996, pp. 63-71
Solution enthalpies of LiClO4 in 1,2-dimethoxyethane + gamma-butyrolac
tone (1,2-DME + gamma BL) mixtures and of LiClO4, NaI and N,N-dimethyl
acetamide in 1,2-DME + propylene carbonate (PC) mixtures have been mea
sured. The molar enthalpies of solution, Delta(sol)H(m) of the examine
d electrolytes as a function of the mixed solvent composition exhibit
a distinct minimum within the range of high 1,2-DME content, similar t
o those observed earlier for LiBF4 and LiPF6 solutions in 1,2-DME + ga
mma-BL mixtures while the dissolution enthalpy of DMA runs monotonousl
y within the same range of the mixed solvent compositions. The presenc
e of the Delta(sol)H(m) minimum of the salts is explained as a resulta
nt of energetic effects of interactions in the solution, connected wit
h the ionic association of the salt, the 1,2-DME + cation complex form
ation and changes in a composition of the ionic solvation shells