Apparent molar volume, heat capacity, and conductance of lithium bis(trifluoromethylsulfone)imide in Glymes and other aprotic solvents

Journal of Solution Chemistry

Volumn 27, Issue 2, 1998, Pages 151-182

  Brouillette, Dany ^a   Perron, Gérald ^a   Desnoyers, Jacques E ^a  

^a INRS EMT   (Canada)

Author keywords

Acetonitrile; n(ethylene glycol) dimethyl ether; Apparent molar heat capacities; Apparent molar volumes; LiClO4; Lithium batteries; Lithium bis(trifluoromethylsulfone)imide; Propylene carbonate; Tetraethylsulfamide; butyrolactone

Indexed keywords

EID: 0038979361     PISSN: 00959782     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1022609407560     Document Type: Article

References (47)

1. M. Armand, J. Y. Sanchez, M. Gauthier, and Y. Choquette, in Electrochemistry of Novel Materials. J. Lipkowski and P. N. Ross, eds. (VCH Publishers, New York, 1994), p. 65.
2. M. Salomon, J. Solution Chem. 22, 715 (1993).
3. A. Webber, J. Electrochem. Soc. 138, 2586 (1991).
4. G. Perron, D. Brouillette, and J. E. Desnoyers, Electrochem. Soc. Extended Abstr. 95, 147 (1995).
5. C. L. Matthias, P. M. Shah, and M. L. Kronenberg, Electrochem. Soc. Extended Abstr. 95, 141 (1995).
6. L. A. Dominey, V. R. Koch, and T. Blakley, Electrochim. Acta 37, 1551 (1991).
7. J. E. Desnoyers and C. Jolicoeur, in Comprehensive Treatise of Electrochemistry, B. E. Conway, J. O'M. Bockris, and E. Yeager, eds. (Plenum, New York, 1983), Chap. 1.
8. J. F. Côté, J. E. Desnoyers, and J.-C. Justice, J. Solution. Chem. 25, 113 (1996).
9. G. Perron, L. Couture, D. Lambert, and J. E. Desnoyers, J. Electroanal. Chem. 355, 277 (1996).
10. G. Perron, D. Brouillette, and J. E. Desnoyers, Can. J. Chem. 75, 1608 (1997).
11. P. Picker, P.-A. Leduc, P. R. Philip, and J. E. Desnoyers, J. Chem. Thermodyn. 3, 631 (1971).
12. J. E. Desnoyers, C. De Visser, G. Perron, and P. Picker, J. Solution. Chem. 5, 605 (1976).
13. R. C. Weast, ed., Handbook of Chemistry and Physics, 70th edn. (CRC Press, Boca Raton, Florida, 1990).
14. P. Picker, E. Tremblay, and C. Jolicoeur, J. Solution Chem. 3, 377 (1974).
15. H. S. Harried and B. B. Owen, The Physical Properties of Electrolytic Solutions, 3rd edn. (Reinhold, New York, 1958).
16. J.-F. Côté, D. Brouillette, J. E. Desnoyers, J.-F. Rouleau, J.-M. St-Arnaud, and G. Perron, J. Solution Chem. 25, 1163 (1996).
17. R. H. Erlich, and A. I. Popov, J. Am. Chem. Soc. 93, 5620 (1971).
18. V. Gutmann. The donor-Acceptor Approach to Molecular Interactions, (Plenum, New York, 1978).
19. K. Burger, Solvation, Ionic and Complex Formation Reactions in Non-aqueous Solvents (Elsevier Scientific Pub. Co., Budapest, 1983).
20. V. Gutmann, Electrochim. Acta 21, 661 (1976).
21. H. Erlich, E. Roach, and A. I. Popov, J. Am. Chem. Soc. 92, 4909 (1970).
22. U. Mayer, V. Gutmann, and W. Gerger, Monatsh. Chem. 106, 1235 (1975).
23. V. Gutmann, Coord. Chem. Rev. 18, 225 (1976).
24. M. Zábransky, V. Rüzicka, Jr., V. Majer, and E. S. Domalski, Heat Capacity of Liquids: Vols. I, II (Woodbury, (J. of Phys. and Chem. Ref. Data, Monograph 6 (ACS) 1996).
25. M. Zábransky, V. Rüzicka, Jr., V. Majer, and E. S. Domalski, Heat Capacity of Liquids: Vols. I, II (Woodbury, (J. of Phys. and Chem. Ref. Data, Monograph 6 (ACS) 1996).
26. D. R. Lide, Handbook of Organic Solvents, (CRC Press, Boca Raton, FL, 1995).
27. R. Schmid, J. Solution Chem. 12, 135 (1983).
28. Barthel, ed., Eldar Data Bank, (Phys. Chemie, Berlin, 1990).
29. G. W. Canters, J. Am Chem. Soc. 94, 5230 (1972).
30. M. A. Villamañan, C. Casanova, G. Roux-Desgranges, and J.-P. Grolier, Thermochim. Acta 52, 279 (1982).
31. L. M. Trejo, M. Costas, and D. Patterson, J. Chem. Soc. Faraday, Trans. 87, 3001 (1991).
32. W. J. Wallace, and A. L. Mathews, J. Chem. Eng. Data 9, 267 (1964).
33. R. L. McGee, J. Chem. Eng. Data 28, 305 (1983).
34. D. Fish, and J. Smid, Electrochim. Acta 37, 2043 (1992).
35. G. Perron, G. Trudeau, and J. E. Desnoyers, Can. J. Chem. 65, 1402 (1987).
36. I. Davidson, G. Perron, and J. E. Desnoyers, Can. J. Chem. 59, 2212 (1981).
37. J. Peleteiro, C.A. Tovar, R. Escudero, E. Carballo, J. L. Legido, and L. Roma J. Solution Chem. 22, 1005 (1993).
38. P. Svejda, M. A. Siddiqi, G. Hahn, and N. Christoph, J. Chem. Eng. Data 35, 47 (1990).
39. P. T. Tomkins and P. J. Turner, J. Chem. Eng. Data 21, 153 (1976).
40. J.-C. Justice, J. Solution Chem. 20, 1017 (1991).
41. J. Barthel, H. J. Gores, G. Scheer, and R. Wachter, Top. Curr. Chem. 111, 3 (1983).
42. J. Barthel, R. Gerber, and H.-J. Gores, Ber. Bunsenges. Phys. Chem. 88, 616 (1984).
43. J. F. Casteel and E. S. Amis, J. Chem. Eng. Data 17, 55 (1972).
44. U. Makoto, I. Kazuhiko, and M. Shoichiro, J. Electrochem. Soc. 141, 2989 (1994).
45. G. Perron, A. Hardy, J.-C. Justice, and J. E. Desnoyers, J. Solution Chem. 22, 1159 (1993).
46. M. Grotthus, Tilloch's Phil. Mag. 25, 334 (1806).
47. A. Reger, E. Peled, and E. Gileadi, J. Phys. Chem. 83, 873 (1979).