Experimental Researches in Electricity, Volume 1

by Michael Faraday

997. It is evident, therefore, that when ordinary zinc is used in a voltaic arrangement, there is an enormous waste of that power which it is the object to throw into the form of an electric current; a consequence which is put in its strongest point of view when it is considered that three ounces and a half of zinc, properly oxidized, can circulate enough electricity to decompose nearly one ounce of water, and cause the evolution of about 2100 cubic inches of hydrogen gas. This loss of power not only takes place during the time the electrodes of the battery are in communication, being then proportionate to the quantity of hydrogen evolved against the surface of any one of the zinc plates, but includes also all the chemical action which goes on when the extremities of the pile are not in communication.

998. This loss is far greater with ordinary zinc than with the pure metal, as M. De la Rive has shown[208]. The cause is, that when ordinary zinc is acted upon by dilute sulphuric acid, portions of copper, lead, cadmium, or other metals which it may contain, are set free upon its surface; and these, being in contact with the zinc, form small but very active voltaic circles, which cause great destruction of the zinc and evolution of hydrogen, apparently upon the zinc surface, but really upon the surface of these incidental metals. In the same proportion as they serve to discharge or convey the electricity back to the zinc, do they diminish its power of producing an electric current which shall extend to a greater distance across the acid, and be discharged only through the copper or platina plate which is associated with it for the purpose of forming a voltaic apparatus.

999. All these evils are removed by the employment of an amalgam of zinc in the manner recommended by Mr. Kemp[209], or the use of the amalgamated zinc plates of Mr. Sturgeon (863.), who has himself suggested and objected to their application in galvanic batteries; for he says, "Were it not on account of the brittleness and other inconveniences occasioned by the incorporation of the mercury with the zinc, amalgamation of the zinc surfaces in galvanic batteries would become an important improvement; for the metal would last much longer, and remain bright for a considerable time, even for several successive hours; essential considerations in the employment of this apparatus[210]."

1000. Zinc so prepared, even though impure, does not sensibly decompose the water of dilute sulphuric acid, but still has such affinity for the oxygen, that the moment a metal which, like copper or platina, has little or no affinity, touches it in the acid, action ensues, and a powerful and abundant electric current is produced. It is probable that the mercury acts by bringing the surface, in consequence of its fluidity, into one uniform condition, and preventing those differences in character between one spot and another which are necessary for the formation of the minute voltaic circuits referred to (998.). If any difference does exist at the first moment, with regard to the proportion of zinc and mercury, at one spot on the surface, as compared with another, that spot having the least mercury is first acted on, and, by solution of the zinc, is soon placed in the same condition as the other parts, and the whole plate rendered superficially uniform. One part cannot, therefore, act as a discharger to another; and hence all the chemical power upon the water at its surface is in that equable condition (949.), which, though it tends to produce an electric current through the liquid to another plate of metal which can act as a discharger (950.), presents no irregularities by which any one part, having weaker affinities for oxygen, can act as a discharger to another. Two excellent and important consequences follow upon this state of the metal. The first is, that the full equivalent of electricity is obtained for the oxidation of a certain quantity of zinc; the second, that a battery constructed with the zinc so prepared, and charged with dilute sulphuric acid, is active only whilst the electrodes are connected, and ceases to act or be acted upon by the acid the instant the communication is broken.

1001. I have had a small battery of ten pairs of plates thus constructed, and am convinced that arrangements of this kind will be very important, especially in the development and illustration of the philosophical principles of the instrument. The metals I have used are amalgamated zinc and platina, connected together by being soldered to platina wires, the whole apparatus having the form of the couronne des tasses. The liquid used was dilute sulphuric acid of sp. gr. 1.25. No action took place upon the metals except when the electrodes were in communication, and then the action upon the zinc was only in proportion to the decomposition in the experimental cell; for when the current was retarded there, it was retarded also in the battery, and no waste of the powers of the metal was incurred.

1002. In consequence of this circumstance, the acid in the cells remained active for a very much longer time than usual. In fact, time did not tend to lower it in any sensible degree: for whilst the metal was preserved to be acted upon at the proper moment, the acid also was preserved almost at its first strength. Hence a constancy of action far beyond what can be obtained by the use of common zinc.

1003. Another excellent consequence was the renewal, during the interval of rest, between two experiments of the first and most efficient state. When an amalgamated zinc and a platina plate, immersed in dilute sulphuric acid, are first connected, the current is very powerful, but instantly sinks very much in force, and in some cases actually falls to only an eighth or a tenth of that first produced (1036.). This is due to the acid which is in contact with the zinc becoming neutralized by the oxide formed; the continued quick oxidation of the metal being thus prevented. With ordinary zinc, the evolution of gas at its surface tends to mingle all the liquid together, and thus bring fresh acid against the metal, by which the oxide formed there can be removed. With the amalgamated zinc battery, at every cessation of the current, the saline solution against the zinc is gradually diffused amongst the rest of the liquid; and upon the renewal of contact at the electrodes, the zinc plates are found most favourably circumstanced for the production of a ready and powerful current.

1004. It might at first be imagined that amalgamated zinc would be much inferior in force to common zinc, because, of the lowering of its energy, which the mercury might be supposed to occasion over the whole of its surface; but this is not the case. When the electric currents of two pairs of platina and zinc plates were opposed, the difference being that one of the zincs was amalgamated and the other not, the current from the amalgamated zinc was most powerful, although no gas was evolved against it, and much was evolved at the surface of the unamalgamated metal. Again, as Davy has shown[211], if amalgamated and unamalgamated zinc be put in contact, and dipped into dilute sulphuric acid, or other exciting fluids, the former is positive to the latter, i.e. the current passes from the amalgamated zinc, through the fluid, to the unprepared zinc. This he accounts for by supposing that "there is not any inherent and specific property in each metal which gives it the electrical character, but that it depends upon its peculiar state—on that form of aggregation which fits it for chemical change."

1005. The superiority of the amalgamated zinc is not, however, due to any such cause, but is a very simple consequence of the state of the fluid in contact with it; for as the unprepared zinc acts directly and alone upon the fluid, whilst that which is amalgamated does not, the former (by the oxide it produces) quickly neutralizes the acid in contact with its surface, so that the progress of oxidation is retarded, whilst at the surface of the amalgamated zinc, any oxide formed is instantly removed by the free acid present, and the clean metallic surface is always ready to act with full energy upon the water. Hence its superiority (1037.). 1006. The progress of improvement in the voltaic battery and its applications, is evidently in the contrary direction at present to what it was a few years ago; for in place of increasing the number of plates, the strength of acid, and the extent altogether of the instrument, the change is rather towards its first state of simplicity, but with a far more intimate knowledge and application of the principles which govern its force and action. Effects of decomposition can now be obtained with ten pairs of plates (417.), which required five hundred or a thousand pairs for their production in the first instance. The capability of decomposing fused chlorides, iodides, and other compounds, according to the law before established (380. &c.), and the opportunity of collecting certain of the products, without any loss, by the use of apparatus of the nature of those already described (789. 814. &c.), render it probable that the voltaic battery may become a useful and even economical manufacturing instrument; for theory evidently indicates that an equivalent of a rare substance may be obtained at the expense of three or four equivalents of a very common body, namely, zinc: and practice seems thus far to justify the expectation. In this point of view I think it very likely that plates of platina or silver may be used instead of plates of copper with advantage, and that then the evil arising occasionally from solution of the copper, and its precipitation on the zinc, (by which the electromotive power of the zinc is so much injured,) will be avoided (1047.).