Authors: Raji Heyrovska
Arrhenius theory of partial dissociation of electrolytes rose to its heights and fame when he was awarded the Nobel Prize (1903). While the theory was still being developed to account for the non-ideal properties of electrolytes at higher concentrations, it was unfortunately replaced by Lewis’ empirical concepts of activity and activity coefficients. With the near success of the Debye-Huckel theory of inter-ionic interactions for very dilutions, the latter was erroneously extended over the next few decades by extended parametrical equations to higher concentrations assuming complete dissociation at all concentrations. This eventually turned solution theory into a mere catalogue of parameters. Therefore, the present author abandoned it all and started systematically analyzing the available experimental data as such. She found that with the degrees of dissociation and ‘surface’ and ‘bulk’ hydration numbers obtained from vapor pressure data, properties of electrolytes could be explained quantitatively over the whole concentration range, using simple mathematical equations.
Comments: 18 pages
Unique-IP document downloads: 340 times
Vixra.org is a pre-print repository rather than a journal. Articles hosted may not yet have been verified by peer-review and should be treated as preliminary. In particular, anything that appears to include financial or legal advice or proposed medical treatments should be treated with due caution. Vixra.org will not be responsible for any consequences of actions that result from any form of use of any documents on this website.
Add your own feedback and questions here:
You are equally welcome to be positive or negative about any paper but please be polite. If you are being critical you must mention at least one specific error, otherwise your comment will be deleted as unhelpful.