Part 44

890. Then remove the acid from y, and introduce a drop of the solution of iodide of potassium at x (fig. 75.). Exactly the same set of effects occur, except that when the metallic communication is made at PZ, the electric current is in the opposite direction to what it was before, as is indicated by the arrows, which show the courses of the currents (667.).

891. Now both the solutions used are conductors, but the conduction in them is essentially connected with decomposition (858.) in a certain constant order, and therefore the appearance of the elements in certain places shows in what direction a current has passed when the solutions are thus employed. Moreover, we find that when they are used at opposite ends of the plates, as in the last two experiments (889. 890.), metallic contact being allowed at the other extremities, the currents are in opposite directions. We have evidently, therefore, the power of opposing the actions of the two fluids simultaneously to each other at the opposite ends of the plates, using each one as a conductor for the discharge of the current of electricity, which the other tends to generate; in fact, substituting them for metallic contact, and combining both experiments into one (fig. 76.). Under these circumstances, there is an opposition of forces: the fluid, which brings into play the stronger set of chemical affinities for the zinc, (being the dilute acid,) overcomes the force of the other, and determines the formation and direction of the electric current; not merely making that current pass through the weaker liquid, but actually reversing the tendency which the elements of the latter have in relation to the zinc and platina if not thus counteracted, and forcing them in the contrary direction to that they are inclined to follow, that its own current may have free course. If the dominant action at y be removed by making metallic contact there, then the liquid at x resumes its power; or if the metals be not brought into contact at y but the affinities of the solution there weakened, whilst those active x are strengthened, then the latter gains the ascendency, and the decompositions are produced in a contrary order.

892. Before drawing a final conclusion from this mutual dependence and state of the chemical affinities of two distant portions of acting fluids (916.), I will proceed to examine more minutely the various circumstances under which the re-action of the body suffering decomposition is rendered evident upon the action of the body, also undergoing decomposition, which produces the voltaic current.

893. The use of metallic contact in a single pair of plates, and the cause of its great superiority above contact made by other kinds of matter, become now very evident. When an amalgamated zinc plate is dipped into dilute sulphuric acid, the force of chemical affinity exerted between the metal and the fluid is not sufficiently powerful to cause sensible action at the surfaces of contact, and occasion the decomposition of water by the oxidation of the metal, although it is sufficient to produce such a condition of the electricity (or the power upon which chemical affinity depends) as would produce a current if there were a path open for it (916. 956.); and that current would complete the conditions necessary, under the circumstances, for the decomposition of the water.

894. Now the presence of a piece of platina touching both the zinc and the fluid to be decomposed, opens the path required for the electricity. Its direct communication with the zinc is effectual, far beyond any communication made between it and that metal, (i.e. between the platina and zinc,) by means of decomposable conducting bodies, or, in other words, electrolytes, as in the experiment already described (891.); because, when they are used, the chemical affinities between them and the zinc produce a contrary and opposing action to that which is influential in the dilute sulphuric acid; or if that action be but small, still the affinity of their component parts for each other has to be overcome, for they cannot conduct without suffering decomposition; and this decomposition is found experimentally to re-act back upon the forces which in the acid tend to produce the current (904. 910. &c.), and in numerous cases entirely to neutralize them. Where direct contact of the zinc and platina occurs, these obstructing forces are not brought into action, and therefore the production and the circulation of the electric current and the concomitant action of decomposition are then highly favoured.

895. It is evident, however, that one of these opposing actions may be dismissed, and yet an electrolyte be used for the purpose of completing the circuit between the zinc and platina immersed separately into the dilute acid; for if, in fig. 73, the platina wire be retained in metallic contact with the zinc plate a, at x, and a division of the platina be made elsewhere, as at s, then the solution of iodide placed there, being in contact with platina at both surfaces, exerts no chemical affinities for that metal; or if it does, they are equal on both sides. Its power, therefore, of forming a current in opposition to that dependent upon the action of the acid in the vessel c, is removed, and only its resistance to decomposition remains as the obstacle to be overcome by the affinities exerted in the dilute sulphuric acid.

896. This becomes the condition of a single pair of active plates where metallic contact is allowed. In such cases, only one set of opposing affinities are to be overcome by those which are dominant in the vessel c; whereas, when metallic contact is not allowed, two sets of opposing affinities must be conquered (894.).

897. It has been considered a difficult, and by some an impossible thing, to decompose bodies by the current from a single pair of plates, even when it was so powerful as to heat bars of metal red-hot, as in the case of Hare's calorimeter, arranged as a single voltaic circuit, or of Wollaston's powerful single pair of metals. This difficulty has arisen altogether from the antagonism of the chemical affinity engaged in producing the current with the chemical affinity to be overcome, and depends entirely upon their relative intensity; for when the sum of forces in one has a certain degree of superiority over the sum of forces in the other, the former gain the ascendency, determine the current, and overcome the latter so as to make the substance exerting them yield up its elements in perfect accordance, both as to direction and quantity, with the course of those which are exerting the most intense and dominant action.

898. Water has generally been the substance, the decomposition of which has been sought for as a chemical test of the passage of an electric current. But I now began to perceive a reason for its failure, and for a fact which I had observed long before (315. 316.) with regard to the iodide of potassium, namely, that bodies would differ in facility of decomposition by a given electric current, according to the condition and intensity of their ordinary chemical affinities. This reason appeared in their re-action upon the affinities tending to cause the current; and it appeared probable, that many substances might be found which could be decomposed by the current of a single pair of zinc and platina plates immersed in dilute sulphuric acid, although water resisted its action. I soon found this to be the case, and as the experiments offer new and beautiful proofs of the direct relation and opposition of the chemical affinities concerned in producing and in resisting the stream of electricity, I shall briefly describe them.

899. The arrangement of the apparatus was as in fig. 77. The vessel v contained dilute sulphuric acid; Z and P are the zinc and platina plates; a, b, and c are platina wires; the decompositions were effected at x, and occasionally, indeed generally, a galvanometer was introduced into the circuit at g: its place only is here given, the circle at g having no reference to the size of the instrument. Various arrangements were made at x, according to the kind of decomposition to be effected. If a drop of liquid was to be acted upon, the two ends were merely dipped into it; if a solution contained in the pores of paper was to be decomposed, one of the extremities was connected with a platina plate supporting the paper, whilst the other extremity rested on the paper, e, fig. 81: or sometimes, as with sulphate of soda, a plate of platina sustained two portions of paper, one of the ends of the wires resting upon each piece, c, fig. 86. The darts represent the direction of the electric current (667.).

900. Solution of iodide of potassium, in moistened paper, being placed at the interruption of the circuit at x, was readily decomposed. Iodine was evolved at the anode, and alkali at the cathode, of the decomposing body.

901. Protochloride of tin, when fused and placed at x, was also readily decomposed, yielding perchloride of tin at the anode (779.), and tin at the cathode.

902. Fused chloride of silver, placed at x, was also easily decomposed; chlorine was evolved at the anode, and brilliant metallic silver, either in films upon the surface of the liquid, or in crystals beneath, evolved at the cathode.

903. Water acidulated with sulphuric acid, solution of muriatic acid, solution of sulphate of soda, fused nitre, and the fused chloride and iodide of lead were not decomposed by this single pair of plates, excited only by dilute sulphuric acid.

904. These experiments give abundant proofs that a single pair of plates can electrolyze bodies and separate their elements. They also show in a beautiful manner the direct relation and opposition of the chemical affinities concerned at the two points of action. In those cases where the sum of the opposing affinities at x was sufficiently beneath the sum of the acting affinities in v, decomposition took place; but in those cases where they rose higher, decomposition was effectually resisted and the current ceased to pass (891.).

905. It is however, evident, that the sum of acting affinities in v may be increased by using other fluids than dilute sulphuric acid, in which latter case, as I believe, it is merely the affinity of the zinc for the oxygen already combined with hydrogen in the water that is exerted in producing the electric current (919.): and when the affinities are so increased, the view I am supporting leads to the conclusion, that bodies which resisted in the preceding experiments would then be decomposed, because of the increased difference between their affinities and the acting affinities thus exalted. This expectation was fully confirmed in the following manner.

906. A little nitric acid was added to the liquid in the vessel r, so as to make a mixture which I shall call diluted nitro-sulphuric acid. On repeating the experiments with this mixture, all the substances before decomposed again gave way, and much more readily. But, besides that, many which before resisted electrolyzation, now yielded up their elements. Thus, solution of sulphate of soda, acted upon in the interstices of litmus and turmeric paper, yielded acid at the anode and alkali at the cathode; solution of muriatic acid tinged by indigo yielded chlorine at the anode and hydrogen at the cathode; solution of nitrate of silver yielded silver at the cathode. Again, fused nitre and the fused iodide and chloride of lead were decomposable by the current of this single pair of plates, though they were not by the former (903.).

907. A solution of acetate of lead was apparently not decomposed by this pair, nor did water acidulated by sulphuric acid seem at first to give way (973.).

908. The increase of intensity or power of the current produced by a simple voltaic circle, with the increase of the force of the chemical action at the exciting place, is here sufficiently evident. But in order to place it in a clearer point of view, and to show that the decomposing effect was not at all dependent, in the latter cases, upon the mere capability of evolving more electricity, experiments were made in which the quantity evolved could be increased without variation in the intensity of the exciting cause. Thus the experiments in which dilute sulphuric acid was used (899.), were repeated, using large plates of zinc and platina in the acid; but still those bodies which resisted decomposition before, resisted it also under these new circumstances. Then again, where nitro-sulphuric acid was used (906.), mere wires of platina and zinc were immersed in the exciting acid; yet, notwithstanding this change, those bodies were now decomposed which resisted any current tending to be formed by the dilute sulphuric acid. For instance, muriatic acid could not be decomposed by a single pair of plates when immersed in dilute sulphuric acid; nor did making the solution of sulphuric acid strong, nor enlarging the size of the zinc and platina plates immersed in it, increase the power; but if to a weak sulphuric acid a very little nitric acid was added, then the electricity evolved had power to decompose the muriatic acid, evolving chlorine at the anode and hydrogen at the cathode, even when mere wires of metals were used. This mode of increasing the intensity of the electric current, as it excludes the effect dependent upon many pairs of plates, or even the effect of making any one acid stronger or weaker, is at once referable to the condition and force of the chemical affinities which are brought into action, and may, both in principle and practice, be considered as perfectly distinct from any other mode.

909. The direct reference which is thus experimentally made in the simple voltaic circle of the intensity of the electric current to the intensity of the chemical action going on at the place where the existence and direction of the current is determined, leads to the conclusion that by using selected bodies, as fused chlorides, salts, solutions of acids, &c., which may act upon the metals employed with different degrees of chemical force; and using also metals in association with platina, or with each other, which shall differ in the degree of chemical action exerted between them and the exciting fluid or electrolyte, we shall be able to obtain a series of comparatively constant effects due to electric currents of different intensities, which will serve to assist in the construction of a scale competent to supply the means of determining relative degrees of intensity with accuracy in future researches.

In relation to this difference and its probable cause, see considerations on inductive polarization, 1354, &c.--Dec. 1838.

910. I have already expressed the view which I take of the decomposition in the experimental place, as being the direct consequence of the superior exertion at some other spot of the same kind of power as that to be overcome, and therefore as the result of an antagonism of forces of the same nature (891. 904.). Those at the place of decomposition have a re-action upon, and a power over, the exerting or determining set proportionate to what is needful to overcome their own power; and hence a curious result of resistance offered by decompositions to the original determining force, and consequently to the current. This is well shown in the cases where such bodies as chloride of lead, iodide of lead, and water would not decompose with the current produced by a single pair of zinc and platina plates in sulphuric acid (903.), although they would with a current of higher intensity produced by stronger chemical powers. In such cases no sensible portion of the current passes (967.); the action is stopped; and I am now of opinion that in the case of the law of conduction which I described in the Fourth Series of these Researches (413.), the bodies which are electrolytes in the fluid state cease to be such in the solid form, because the attractions of the particles by which they are retained in combination and in their relative position, are then too powerful for the electric current. The particles retain their places; and as decomposition is prevented, the transmission of the electricity is prevented also; and although a battery of many plates may be used, yet if it be of that perfect kind which allows of no extraneous or indirect action (1000.), the whole of the affinities concerned in the activity of that battery are at the same time also suspended and counteracted.

Refer onwards to 1705.--Dec. 1838.

911. But referring to the resistance of each single case of decomposition, it would appear that as these differ in force according to the affinities by which the elements in the substance tend to retain their places, they also would supply cases constituting a series of degrees by which to measure the initial intensities of simple voltaic or other currents of electricity, and which, combined with the scale of intensities determined by different degrees of acting force (909.), would probably include a sufficient set of differences to meet almost every important case where a reference to intensity would be required.

912. According to the experiments I have already had occasion to make, I find that the following bodies are electrolytic in the order in which I have placed them, those which are first being decomposed by the current of lowest intensity. These currents were always from a single pair of plates, and may be considered as elementary voltaic forces.

Iodide of potassium (solution). Chloride of silver (fused). Protochloride of tin (fused). Chloride of lead (fused). Iodide of lead (fused). Muriatic acid (solution). Water, acidulated with sulphuric acid.

913. It is essential that, in all endeavours to obtain the relative electrolytic intensity necessary for the decomposition of different bodies, attention should be paid to the nature of the electrodes and the other bodies present which may favour secondary actions (986.). If in electro-decomposition one of the elements separated has an affinity for the electrode, or for bodies present in the surrounding fluid, then the affinity resisting decomposition is in part balanced by such power, and the true place of the electrolyte in a table of the above kind is not obtained: thus, chlorine combines with a positive platina electrode freely, but iodine scarcely at all, and therefore I believe it is that the fused chlorides stand first in the preceding Table. Again, if in the decomposition of water not merely sulphuric but also a little nitric acid be present, then the water is more freely decomposed, for the hydrogen at the cathode is not ultimately expelled, but finds oxygen in the nitric acid, with which it can combine to produce a secondary result; the affinities opposing decomposition are in this way diminished, and the elements of the water can then be separated by a current of lower intensity.

914. Advantage may be taken of this principle to interpolate more minute degrees into the scale of initial intensities already referred to (909. 911.) than is there spoken of; for by combining the force of a current constant in its intensity, with the use of electrodes consisting of matter, having more or less affinity for the elements evolved from the decomposing electrolyte, various intermediate degrees may be obtained.