Laws of electro-chemical decomposition.

Laws of electro-chemical decomposition.

In our conceptions and reasonings regarding the forces of nature, we perpetually make use of symbols which, when they possess a high representative value, we dignify with the name of theories. Thus, prompted by certain analogies, we ascribe electrical phenomena to the action of a peculiar fluid, sometimes flowing, sometimes at rest. Such conceptions have their advantages and their disadvantages; they afford peaceful lodging to the intellect for a time, but they also circumscribe it, and by-and-by, when the mind has grown too large for its lodging, it often finds difficulty in breaking down the walls of what has become its prison instead of its home.¹

No man ever felt this tyranny of symbols more deeply than Faraday, and no man was ever more assiduous than he to liberate himself from them, and the terms which suggested them. Calling Dr. Whewell to his aid in 1833, he endeavoured to displace by others all terms tainted by a foregone conclusion. His paper on Electro-chemical Decomposition, received by the Royal Society on January 9, 1834, opens with the proposal of a new terminology. He would avoid the word 'current' if he could.²

He does abandon the word 'poles' as applied to the ends of a decomposing cell, because it suggests the idea of attraction, substituting for it the perfectly natural term Electrodes. He applied the term Electrolyte to every substance which can be decomposed by the current, and the act of decomposition he called Electrolysis. All these terms have become current in science. He called the positive electrode the Anode, and the negative one the Cathode, but these terms, though frequently used, have not enjoyed the same currency as the others. The terms Anion and Cation, which he applied to the constituents of the decomposed electrolyte, and the term Ion, which included both anions and cations, are still less frequently employed.

Faraday now passes from terminology to research; he sees the necessity of quantitative determinations, and seeks to supply himself with a measure of voltaic electricity. This he finds in the quantity of water decomposed by the current. He tests this measure in all possible ways, to assure himself that no error can arise from its employment. He places in the course of one and the same current a series of cells with electrodes of different sizes, some of them plates of platinum, others merely platinum wires, and collects the gas liberated on each distinct pair of electrodes. He finds the quantity of gas to be the same for all. Thus he concludes that when the same quantity of electricity is caused to pass through a series of cells containing acidulated water, the electro-chemical action is independent of the size of the electrodes.³

But before he can apply this measure he must clear his ground of numerous possible sources of error. The decomposition of his acidulated water is certainly a direct result of the current; but as the varied and important researches of MM. Becquerel, De la Rive, and others had shown, there are also secondary actions which may materially interfere with and complicate the pure action of the current. These actions may occur in two ways: either the liberated ion may seize upon the electrode against which it is set free, forming a chemical compound with that electrode; or it may seize upon the substance of the electrolyte itself, and thus introduce into the circuit chemical actions over and above those due to the current. Faraday subjected these secondary actions to an exhaustive examination. Instructed by his experiments, and