Experimental Researches in Electricity, Volume 1 11 – Faraday · Verses Across
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Experimental Researches in Electricity, Volume 1 11Experimental Researches in Electricity, Volume 1 (part 11)
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Literature · Science
Experimental Researches in Electricity, Volume 1 11
Experimental Researches in Electricity, Volume 1 (part 11)
FaradayEnglish
861. What an enormous quantity of electricity, therefore, is required for the decomposition of a single grain of water! We have already seen that it must be in quantity sufficient to sustain a platina wire 1/104 of an inch in thickness, red-hot, in contact with the air, for three minutes and three quarters (853.), a quantity which is almost infinitely greater than that which could be evolved by the little standard voltaic arrangement to which I have just referred (860. 871.). I have endeavoured to make a comparison by the loss of weight of such a wire in a given time in such an acid, according to a principle and experiment to be almost immediately described (862.); but the proportion is so high that I am almost afraid to mention it. It would appear that 800,000 such charges of the Leyden battery as I have referred to above, would be necessary to supply electricity sufficient to decompose a single grain of water; or, if I am right, to equal the quantity of electricity which is naturally associated with the elements of that grain of water, endowing them with their mutual chemical affinity.
862. In further proof of this high electric condition of the particles of matter, and the identity as to quantity of that belonging to them with that necessary for their separation, I will describe an experiment of great simplicity but extreme beauty, when viewed in relation to the evolution of an electric current and its decomposing powers.
863. A dilute sulphuric acid, made by adding about one part by measure of oil of vitriol to thirty parts of water, will act energetically upon a piece of zinc plate in its ordinary and simple state: but, as Mr. Sturgeon has shown, not at all, or scarcely so, if the surface of the metal has in the first instance been amalgamated; yet the amalgamated zinc will act powerfully with platina as an electromotor, hydrogen being evolved on the surface of the latter metal, as the zinc is oxidized and dissolved. The amalgamation is best effected by sprinkling a few drops of mercury upon the surface of the zinc, the latter being moistened with the dilute acid, and rubbing with the fingers or two so as to extend the liquid metal over the whole of the surface. Any mercury in excess, forming liquid drops upon the zinc, should be wiped off.
The experiment may be made with pure zinc, which, as chemists well know, is but slightly acted upon by dilute sulphuric acid in comparison with ordinary zinc, which during the action is subject to an infinity of voltaic actions. See De la Rive on this subject, Bibliothèque Universelle, 1830, p.391.
864. Two plates of zinc thus amalgamated were dried and accurately weighed; one, which we will call A, weighed 163.1 grains; the other, to be called B, weighed 148.3 grains. They were about five inches long, and 0.4 of an inch wide. An earthenware pneumatic trough was filled with dilute sulphuric acid, of the strength just described (863.), and a gas jar, also filled with the acid, inverted in it. A plate of platina of nearly the same length, but about three times as wide as the zinc plates, was put up into this jar. The zinc plate A was also introduced into the jar, and brought in contact with the platina, and at the same moment the plate B was put into the acid of the trough, but out of contact with other metallic matter.
The acid was left during a night with a small piece of unamalgamated zinc in it, for the purpose of evolving such air as might be inclined to separate, and bringing the whole into a constant state.
865. Strong action immediately occurred in the jar upon the contact of the zinc and platina plates. Hydrogen gas rose from the platina, and was collected in the jar, but no hydrogen or other gas rose from either zinc plate. In about ten or twelve minutes, sufficient hydrogen having been collected, the experiment was stopped; during its progress a few small bubbles had appeared upon plate B, but none upon plate A. The plates were washed in distilled water, dried, and reweighed. Plate B weighed 148.3 grains, as before, having lost nothing by the direct chemical action of the acid. Plate A weighed 154.65 grains, 8.45 grains of it having been oxidized and dissolved during the experiment.
866. The hydrogen gas was next transferred to a water-trough and measured; it amounted to 12.5 cubic inches, the temperature being 52°, and the barometer 29.2 inches. This quantity, corrected for temperature, pressure, and moisture, becomes 12.15453 cubic inches of dry hydrogen at mean temperature and pressure; which, increased by one half for the oxygen that must have gone to the anode, i.e. to the zinc, gives 18.232 cubic inches as the quantity of oxygen and hydrogen evolved from the water decomposed by the electric current. According to the estimate of the weight of the mixed gas before adopted (791.), this volume is equal to 2.3535544 grains, which therefore is the weight of water decomposed; and this quantity is to 8.45, the quantity of zinc oxidized, as 9 is to 32.31. Now taking 9 as the equivalent number of water, the number 32.5 is given as the equivalent number of zinc; a coincidence sufficiently near to show, what indeed could not but happen, that for an equivalent of zinc oxidized an equivalent of water must be decomposed.
The experiment was repeated several times with the same results.
867. But let us observe how the water is decomposed. It is electrolyzed, i.e. is decomposed voltaically, and not in the ordinary manner (as to appearance) of chemical decompositions; for the oxygen appears at the anode and the hydrogen at the cathode of the body under decomposition, and these were in many parts of the experiment above an inch asunder. Again, the ordinary chemical affinity was not enough under the circumstances to effect the decomposition of the water, as was abundantly proved by the inaction on plate B; the voltaic current was essential. And to prevent any idea that the chemical affinity was almost sufficient to decompose the water, and that a smaller current of electricity might, under the circumstances, cause the hydrogen to pass to the cathode, I need only refer to the results which I have given (807. 813.) to shew that the chemical action at the electrodes has not the slightest influence over the quantities of water or other substances decomposed between them, but that they are entirely dependent upon the quantity of electricity which passes.
868. What, then, follows as a necessary consequence of the whole experiment? Why, this: that the chemical action upon 32.31 parts, or one equivalent of zinc, in this simple voltaic circle, was able to evolve such quantity of electricity in the form of a current, as, passing through water, should decompose 9 parts, or one equivalent of that substance: and considering the definite relations of electricity as developed in the preceding parts of the present paper, the results prove that the quantity of electricity which, being naturally associated with the particles of matter, gives them their combining power, is able, when thrown into a current, to separate those particles from their state of combination; or, in other words, that the electricity which decomposes, and that which is evolved by the decomposition of a certain quantity of matter, are alike.
869. The harmony which this theory of the definite evolution and the equivalent definite action of electricity introduces into the associated theories of definite proportions and electrochemical affinity, is very great. According to it, the equivalent weights of bodies are simply those quantities of them which contain equal quantities of electricity, or have naturally equal electric powers; it being the ELECTRICITY which determines the equivalent number, because it determines the combining force. Or, if we adopt the atomic theory or phraseology, then the atoms of bodies which are equivalents to each other in their ordinary chemical action, have equal quantities of electricity naturally associated with them. But I must confess I am jealous of the term atom; for though it is very easy to talk of atoms, it is very difficult to form a clear idea of their nature, especially when compound bodies are under consideration.
870. I cannot refrain from recalling here the beautiful idea put forth, I believe, by Berzelius (703.) in his development of his views of the electro-chemical theory of affinity, that the heat and light evolved during cases of powerful combination are the consequence of the electric discharge which is at the moment taking place. The idea is in perfect accordance with the view I have taken of the quantity of electricity associated with the particles of matter.
871. In this exposition of the law of the definite action of electricity, and its corresponding definite proportion in the particles of bodies, I do not pretend to have brought, as yet, every case of chemical or electro-chemical action under its dominion. There are numerous considerations of a theoretical nature, especially respecting the compound particles of matter and the resulting electrical forces which they ought to possess, which I hope will gradually receive their development; and there are numerous experimental cases, as, for instance, those of compounds formed by weak affinities, the simultaneous decomposition of water and salts, &c., which still require investigation. But whatever the results on these and numerous other points may be, I do not believe that the facts which I have advanced, or even the general laws deduced from them, will suffer any serious change; and they are of sufficient importance to justify their publication, though much may yet remain imperfect or undone. Indeed, it is the great beauty of our science, CHEMISTRY, that advancement in it, whether in a degree great or small, instead of exhausting the subjects of research, opens the doors to further and more abundant knowledge, overflowing with beauty and utility, to those who will be at the easy personal pains of undertaking its experimental investigation.
872. The definite production of electricity (868.) in association with its definite action proves, I think, that the current of electricity in the voltaic pile: is sustained by chemical decomposition, or rather by chemical action, and not by contact only. But here, as elsewhere (857.), I beg to reserve my opinion as to the real action of contact, not having yet been able to make up my mind as to whether it is an exciting cause of the current, or merely necessary to allow of the conduction of electricity, otherwise generated, from one metal to the other.
873. But admitting that chemical action is the source of electricity, what an infinitely small fraction of that which is active do we obtain and employ in our voltaic batteries! Zinc and platina wires, one-eighteenth of an inch in diameter and about half an inch long, dipped into dilute sulphuric acid, so weak that it is not sensibly sour to the tongue, or scarcely to our most delicate test-papers, will evolve more electricity in one-twentieth of a minute (860.) than any man would willingly allow to pass through his body at once. The chemical action of a grain of water upon four grains of zinc can evolve electricity equal in quantity to that of a powerful thunder-storm (868. 861.). Nor is it merely true that the quantity is active; it can be directed and made to perform its full equivalent duty (867. &c.). Is there not, then, great reason to hope and believe that, by a closer experimental investigation of the principles which govern the development and action of this subtile agent, we shall be able to increase the power of our batteries, or invent new instruments which shall a thousandfold surpass in energy those which we at present possess?
874. Here for a while I must leave the consideration of the definite chemical action of electricity. But before I dismiss this series of experimental Researches, I would call to mind that, in a former series, I showed the current of electricity was also definite in its magnetic action (216. 366. 367. 376. 377.); and, though this result was not pursued to any extent, I have no doubt that the success which has attended the development of the chemical effects is not more than would accompany an investigation of the magnetic phenomena.
_Royal Institution,
December 31st, 1833._
EIGHTH SERIES.
§14. On the Electricity of the Voltaic Pile; its source, quantity, intensity, and general characters. ¶ i. On simple Voltaic Circles. ¶ ii. On the intensity necessary for Electrolyzation. ¶ iii. On associated Voltaic Circles, or the Voltaic Battery. ¶ iv. On the resistance of an Electrolyte to Electrolytic action. ¶ v. General remarks on the active Voltaic Battery.
Received April 7,--Read June 5, 1831.
¶ i. On simple Voltaic Circles.
875. The great question of the source of electricity, in the voltaic pile has engaged the attention of so many eminent philosophers, that a man of liberal mind and able to appreciate their powers would probably conclude, although he might not have studied the question, that the truth was somewhere revealed. But if in pursuance of this impression he were induced to enter upon the work of collating results and conclusions, he would find such contradictory evidence, such equilibrium of opinion, such variation and combination of theory, as would leave him in complete doubt respecting what he should accept as the true interpretation of nature: he would be forced to take upon himself the labour of repeating and examining the facts, and then use his own judgement on them in preference to that of others.
876. This state of the subject must, to those who have made up their minds on the matter, be my apology for entering upon its investigation. The views I have taken of the definite action of electricity in decomposing bodies (783.), and the identity of the power so used with the power to be overcome (855.), founded not on a mere opinion or general notion, but on facts which, being altogether new, were to my mind precise and conclusive, gave me, as I conceived, the power of examining the question with advantages not before possessed by any, and which might compensate, on my part, for the superior clearness and extent of intellect on theirs. Such are the considerations which have induced me to suppose I might help in deciding the question, and be able to render assistance in that great service of removing doubtful knowledge. Such knowledge is the early morning light of every advancing science, and is essential to its development; but the man who is engaged in dispelling that which is deceptive in it, and revealing more clearly that which is true, is as useful in his place, and as necessary to the general progress of the science, as he who first broke through the intellectual darkness, and opened a path into knowledge before unknown to man.
877. The identity of the force constituting the voltaic current or electrolytic agent, with that which holds the elements of electrolytes together (855.), or in other words with chemical affinity, seemed to indicate that the electricity of the pile itself was merely a mode of exertion, or exhibition, or existence of true chemical action, or rather of its cause; and I have consequently already said that I agree with those who believe that the supply of electricity is due to chemical powers (857.).
878. But the great question of whether it is originally due to metallic contact or to chemical action, i.e. whether it is the first or the second which originates and determines the current, was to me still doubtful; and the beautiful and simple experiment with amalgamated zinc and platina, which I have described minutely as to its results (863, &c.), did not decide the point; for in that experiment the chemical action does not take place without the contact of the metals, and the metallic contact is inefficient without the chemical action. Hence either might be looked upon as the determining cause of the current.
879. I thought it essential to decide this question by the simplest possible forms of apparatus and experiment, that no fallacy might be inadvertently admitted. The well-known difficulty of effecting decomposition by a single pair of plates, except in the fluid exciting them into action (863.), seemed to throw insurmountable obstruction in the way of such experiments; but I remembered the easy decomposability of the solution of iodide of potassium (316.), and seeing no theoretical reason, if metallic contact was not essential, why true electro-decomposition should not be obtained without it, even in a single circuit, I persevered and succeeded.
880. A plate of zinc, about eight inches long and half an inch wide, was cleaned and bent in the middle to a right angle, fig. 73 a, Plate VI. A plate of platina, about three inches long and half an inch wide, was fastened to a platina wire, and the latter bent as in the figure, b. These two pieces of metal were arranged together as delineated, but as yet without the vessel c, and its contents, which consisted of dilute sulphuric acid mingled with a little nitric acid. At x a piece of folded bibulous paper, moistened in a solution of iodide of potassium, was placed on the zinc, and was pressed upon by the end of the platina wire. When under these circumstances the plates were dipped into the acid of the vessel c, there was an immediate effect at x, the iodide being decomposed, and iodine appearing at the anode (663.), i.e. against the end of the platina wire.
881. As long as the lower ends of the plates remained in the acid the electric current continued, and the decomposition proceeded at x. On removing the end of the wire from place to place on the paper, the effect was evidently very powerful; and on placing a piece of turmeric paper between the white paper and zinc, both papers being moistened with the solution of iodide of potassium, alkali was evolved at the cathode (663.) against the zinc, in proportion to the evolution of iodine at the anode. Hence the decomposition was perfectly polar, and decidedly dependent upon a current of electricity passing from the zinc through the acid to the platina in the vessel c, and back from the platina through the solution to the zinc at the paper x.
882. That the decomposition at x was a true electrolytic action, due to a current determined by the state of things in the vessel c, and not dependent upon any mere direct chemical action of the zinc and platina on the iodide, or even upon any current which the solution of iodide might by its action on those metals tend to form at x, was shown, in the first place, by removing the vessel c and its acid from the plates, when all decomposition at x ceased, and in the next by connecting the metals, either in or out of the acid, together, when decomposition of the iodide at x occurred, but in a reverse order; for now alkali appeared against the end of the platina wire, and the iodine passed to the zinc, the current being the contrary of what it was in the former instance, and produced directly by the difference of action of the solution in the paper on the two metals. The iodine of course combined with the zinc.
883. When this experiment was made with pieces of zinc amalgamated over the whole surface (863.), the results were obtained with equal facility and in the same direction, even when only dilute sulphuric acid was contained in the vessel c (fig. 73.). Whichsoever end of the zinc was immersed in the acid, still the effects were the same: so that if, for a moment, the mercury might be supposed to supply the metallic contact, the inversion of the amalgamated piece destroys that objection. The use of unamalgamated zinc (880.) removes all possibility of doubt.
The following is a more striking mode of making the above elementary experiment. Prepare a plate of zinc, ten or twelve inches long and two inches wide, and clean it thoroughly: provide also two discs of clean platina, about one inch and a half in diameter:--dip three or four folds of bibulous paper into a strong solution of iodide of potassium, place them on the clean zinc at one end of the plate, and put on them one of the platina discs: finally dip similar folds of paper or a piece of linen cloth into a mixture of equal parts nitric acid and water, and place it at the other end of the zinc plate with the second platina disc upon it. In this state of things no change at the solution of the iodide will be perceptible; but if the two discs be connected by a platina (or any other) wire for a second or two, and then that over the iodide be raised, it will be found that the whole of the surface beneath is deeply stained with evolved iodine.--Dec. 1838.
884 When, in pursuance of other views (930.), the vessel c was made to contain a solution of caustic potash in place of acid, still the same results occurred. Decomposition of the iodide was effected freely, though there was no metallic contact of dissimilar metals, and the current of electricity was in the same direction as when acid was used at the place of excitement.
885. Even a solution of common salt in the glass c could produce all these effects.
886. Having made a galvanometer with platina wires, and introduced it into the course of the current between the platina plate and the place of decomposition x, it was affected, giving indications of currents in the same direction as those shown to exist by the chemical action.
887. If we consider these results generally, they lead to very important conclusions. In the first place, they prove, in the most decisive manner, that metallic contact is not necessary for the production of the voltaic current. In the next place, they show a most extraordinary mutual relation of the chemical affinities of the fluid which excites the current, and the fluid which is decomposed by it.
888. For the purpose of simplifying the consideration, let us take the experiment with amalgamated zinc. The metal so prepared exhibits no effect until the current can pass: it at the same time introduces no new action, but merely removes an influence which is extraneous to those belonging either to the production or the effect of the electric current under investigation (1000.); an influence also which, when present, tends only to confuse the results.
889. Let two plates, one of amalgamated zinc and the other of platina, be placed parallel to each other (fig. 74.), and introduce a drop of dilute sulphuric acid, y, between them at one end: there will be no sensible chemical action at that spot unless the two plates are connected somewhere else, as at PZ, by a body capable of conducting electricity. If that body be a metal or certain forms of carbon, then the current passes, and, as it circulates through the fluid at y, decomposition ensues.
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.
915. Returning to the consideration of the source of electricity (878. &c.), there is another proof of the most perfect kind that metallic contact has nothing to do with the production of electricity in the voltaic circuit, and further, that electricity is only another mode of the exertion of chemical forces. It is, the production of the electric spark before any contact of metals is made, and by the exertion of pure and unmixed chemical forces. The experiment, which will be described further on (956.), consists in obtaining the spark upon making contact between a plate of zinc and a plate of copper plunged into dilute sulphuric acid. In order to make the arrangement as elementary as possible, mercurial surfaces were dismissed, and the contact made by a copper wire connected with the copper plate, and then brought to touch a clean part of the zinc plate. The electric spark appeared, and it must of necessity have existed and passed before the zinc and the copper were in contact.
916. In order to render more distinct the principles which I have been endeavouring to establish, I will restate them in their simplest form, according to my present belief. The electricity of the voltaic pile (856. note) is not dependent either in its origin or its continuance upon the contact of the metals with each other (880. 915.). It is entirely due to chemical action (882.), and is proportionate in its intensity to the intensity of the affinities concerned in its production (908.); and in its quantity to the quantity of matter which has been chemically active during its evolution (869.). This definite production is again one of the strongest proofs that the electricity is of chemical origin.
917. As volta-electro-generation is a case of mere chemical action, so volta-electro-decomposition is simply a case of the preponderance of one set of chemical affinities more powerful in their nature, over another set which are less powerful: and if the instance of two opposing sets of such forces (891.) be considered, and their mutual relation and dependence borne in mind, there appears no necessity for using, in respect to such cases, any other term than chemical affinity, (though that of electricity may be very convenient,) or supposing any new agent to be concerned in producing the results; for we may consider that the powers at the two places of action are in direct communion and balanced against each other through the medium of the metals (891.), fig. 76, in a manner analogous to that in which mechanical forces are balanced against each other by the intervention of the lever (1031.).
918. All the facts show us that that power commonly called chemical affinity, can be communicated to a distance through the metals and certain forms of carbon; that the electric current is only another form of the forces of chemical affinity; that its power is in proportion to the chemical affinities producing it; that when it is deficient in force it may be helped by calling in chemical aid, the want in the former being made up by an equivalent of the latter; that, in other words, the forces termed chemical affinity and electricity are one and the same.
919. When the circumstances connected with the production of electricity in the ordinary voltaic circuit are examined and compared, it appears that the source of that agent, always meaning the electricity which circulates and completes the current in the voltaic apparatus, and gives that apparatus power and character (947. 996.), exists in the chemical action which takes place directly between the metal and the body with which it combines, and not at all in the subsequent action of the substance so produced with the acid present. Thus, when zinc, platina, and dilute sulphuric acid are used, it is the union of the zinc with the oxygen of the water which determines the current; and though the acid is essential to the removal of the oxide so formed, in order that another portion of zinc may act on another portion of water, it does not, by combination with that oxide, produce any sensible portion of the current of electricity which circulates; for the quantity of electricity is dependent upon the quantity of zinc oxidized, and in definite proportion to it: its intensity is in proportion to the intensity of the chemical affinity of the zinc for the oxygen under the circumstances, and is scarcely, if at all, affected by the use of either strong or weak acid (908.).
Wollaston, Philosophical Transactions, 1801, p. 427.
920. Again, if zinc, platina, and muriatic acid are used, the electricity appears to be dependent upon the affinity of the zinc for the chlorine, and to be circulated in exact proportion to the number of particles of zinc and chlorine which unite, being in fact an equivalent to them.
921. But in considering this oxidation, or other direct action upon the METAL itself, as the cause and source of the electric current, it is of the utmost importance to observe that the oxygen or other body must be in a peculiar condition, namely, in the state of combination; and not only so, but limited still further to such a state of combination and in such proportions as will constitute an electrolyte (823.). A pair of zinc and platina plates cannot be so arranged in oxygen gas as to produce a current of electricity, or act as a voltaic circle, even though the temperature may be raised so high as to cause oxidation of the zinc far more rapidly than if the pair of plates were plunged into dilute sulphuric acid; for the oxygen is not part of an electrolyte, and cannot therefore conduct the forces onwards by decomposition, or even as metals do by itself. Or if its gaseous state embarrass the minds of some, then liquid chlorine may be taken. It does not excite a current of electricity through the two plates by combining with the zinc, for its particles cannot transfer the electricity active at the point of combination across to the platina. It is not a conductor of itself, like the metals; nor is it an electrolyte, so as to be capable of conduction during decomposition, and hence there is simple chemical action at the spot, and no electric current.
I do not mean to affirm that no traces of electricity ever appear in such cases. What I mean is, that no electricity is evolved in any way, due or related to the causes which excite voltaic electricity, or proportionate to them. That which does appear occasionally is the smallest possible fraction of that which the acting matter could produce if arranged so as to act voltaically, probably not the one hundred thousandth, or even the millionth part, and is very probably altogether different in its source.
922. It might at first be supposed that a conducting body not electrolytic, might answer as the third substance between the zinc and the platina; and it is true that we have some such capable of exerting chemical action upon the metals. They must, however, be chosen from the metals themselves, for there are no bodies of this kind except those substances and charcoal. To decide the matter by experiment, I made the following arrangement. Melted tin was put into a glass tube bent into the form of the letter V, fig. 78, so as to fill the half of each limb, and two pieces of thick platina wire, p, w, inserted, so as to have their ends immersed some depth in the tin: the whole was then allowed to cool, and the ends p and w connected with a delicate galvanometer. The part of the tube at x was now reheated, whilst the portion y was retained cool. The galvanometer was immediately influenced by the thermo-electric current produced. The heat was steadily increased at x, until at last the tin and platina combined there; an effect which is known to take place with strong chemical action and high ignition; but not the slightest additional effect occurred at the galvanometer. No other deflection than that due to the thermo-electric current was observable the whole time. Hence, though a conductor, and one capable of exerting chemical action on the tin, was used, yet, not being an electrolyte, not the slightest effect of an electrical current could be observed (947.).
923. From this it seems apparent that the peculiar character and condition of an electrolyte is essential in one part of the voltaic circuit; and its nature being considered, good reasons appear why it and it alone should be effectual. An electrolyte is always a compound body: it can conduct, but only whilst decomposing. Its conduction depends upon its decomposition and the transmission of its particles in directions parallel to the current; and so intimate is this connexion, that if their transition be stopped, the current is stopped also; if their course be changed, its course and direction change with them; if they proceed in one direction, it has no power to proceed in any other than a direction invariably dependent on them. The particles of an electrolytic body are all so mutually connected, are in such relation with each other through their whole extent in the direction of the current, that if the last is not disposed of, the first is not at liberty to take up its place in the new combination which the powerful affinity of the most active metal tends to produce; and then the current itself is stopped; for the dependencies of the current and the decomposition are so mutual, that whichsoever be originally determined, i.e. the motion of the particles or the motion of the current, the other is invariable in its concomitant production and its relation to it.
924. Consider, then, water as an electrolyte and also as an oxidizing body. The attraction of the zinc for the oxygen is greater, under the circumstances, than that of the oxygen for the hydrogen; but in combining with it, it tends to throw into circulation a current of electricity in a certain direction. This direction is consistent (as is found by innumerable experiments) with the transfer of the hydrogen from the zinc towards the platina, and the transfer in the opposite direction of fresh oxygen from the platina towards the zinc; so that the current can pass in that one line, and, whilst it passes, can consist with and favour the renewal of the conditions upon the surface of the zinc, which at first determined both the combination and circulation. Hence the continuance of the action there, and the continuation of the current. It therefore appears quite as essential that there should be an electrolyte in the circuit, in order that the action may be transferred forward, in a certain constant direction, as that there should be an oxidizing or other body capable of acting directly on the metal; and it also appears to be essential that these two should merge into one, or that the principle directly active on the metal by chemical action should be one of the ions of the electrolyte used. Whether the voltaic arrangement be excited by solution of acids, or alkalies, or sulphurets, or by fused substances (476.), this principle has always hitherto, as far as I am aware, been an anion (943.); and I anticipate, from a consideration of the principles of electric action, that it must of necessity be one of that class of bodies.
925. If the action of the sulphuric acid used in the voltaic circuit be considered, it will be found incompetent to produce any sensible portion of the electricity of the current by its combination with the oxide formed, for this simple reason, it is deficient in a most essential condition: it forms no part of an electrolyte, nor is it in relation with any other body present in the solution which will permit of the mutual transfer of the particles and the consequent transfer of the electricity. It is true, that as the plane at which the acid is dissolving the oxide of zinc formed by the action of the water, is in contact with the metal zinc, there seems no difficulty in considering how the oxide there could communicate an electrical state, proportionate to its own chemical action on the acid, to the metal, which is a conductor without decomposition. But on the side of the acid there is no substance to complete the circuit: the water, as water, cannot conduct it, or at least only so small a proportion that it is merely an incidental and almost inappreciable effect (970.); and it cannot conduct it as an electrolyte, because an electrolyte conducts in consequence of the mutual relation and action of its particles; and neither of the elements of the water, nor even the water itself, as far as we can perceive, are ions with respect to the sulphuric acid (848.).
It will be seen that I here agree with Sir Humphry Davy, who has experimentally supported the opinion that acids and alkalies in combining do not produce any current of electricity. Philosophical Transactions, 1826, p. 398.
926. This view of the secondary character of the sulphuric acid as an agent in the production of the voltaic current, is further confirmed by the fact, that the current generated and transmitted is directly and exactly proportional to the quantity of water decomposed and the quantity of zinc oxidized (868. 991.), and is the same as that required to decompose the same quantity of water. As, therefore, the decomposition of the water shows that the electricity has passed by its means, there remains no other electricity to be accounted for or to be referred to any action other than that of the zinc and the water on each other.
927. The general case (for it includes the former one (924.),) of acids and bases, may theoretically be stated in the following manner. Let a, fig. 79, be supposed to be a dry oxacid, and b a dry base, in contact at c, and in electric communication at their extremities by plates of platina pp, and a platina wire w. If this acid and base were fluid, and combination took place at c, with an affinity ever so vigorous, and capable of originating an electric current, the current could not circulate in any important degree; because, according to the experimental results, neither a nor b could conduct without being decomposed, for they are either electrolytes or else insulators, under all circumstances, except to very feeble and unimportant currents (970. 986.). Now the affinities at c are not such as tend to cause the elements either of a or b to separate, but only such as would make the two bodies combine together as a whole; the point of action is, therefore, insulated, the action itself local (921. 947.), and no current can be formed.
928. If the acid and base be dissolved in water, then it is possible that a small portion of the electricity due to chemical action may be conducted by the water without decomposition (966. 984.); but the quantity will be so small as to be utterly disproportionate to that due to the equivalents of chemical force; will be merely incidental; and, as it does not involve the essential principles of the voltaic pile, it forms no part of the phenomena at present under investigation.
It will I trust be fully understood, that in these investigations I am not professing to take an account of every small, incidental, or barely possible effect, dependent upon slight disturbances of the electric fluid during chemical action, but am seeking to distinguish and identify those actions on which the power of the voltaic battery essentially depends.
929. If for the oxacid a hydracid be substituted (927.),--as one analogous to the muriatic, for instance,--then the state of things changes altogether, and a current due to the chemical action of the acid on the base is possible. But now both the bodies act as electrolytes, for it is only one principle of each which combine mutually,--as, for instance, the chlorine with the metal,--and the hydrogen of the acid and the oxygen of the base are ready to traverse with the chlorine of the acid and the metal of the base in conformity with the current and according to the general principles already so fully laid down.
930. This view of the oxidation of the metal, or other direct chemical action upon it, being the sole cause of the production of the electric current in the ordinary voltaic pile, is supported by the effects which take place when alkaline or sulphuretted solutions (931. 943.) are used for the electrolytic conductor instead of dilute sulphuric acid. It was in elucidation of this point that the experiments without metallic contact, and with solution of alkali as the exciting fluid, already referred to (884.), were made.
931. Advantage was then taken of the more favourable condition offered, when metallic contact is allowed (895.), and the experiments upon the decomposition of bodies by a single pair of plates (899.) were repeated, solution of caustic potassa being employed in the vessel v, fig. 77. in place of dilute sulphuric acid. All the effects occurred as before: the galvanometer was deflected; the decompositions of the solutions of iodide of potassium, nitrate of silver, muriatic acid, and sulphate of soda ensued at x; and the places where the evolved principles appeared, as well as the deflection of the galvanometer, indicated a current in the same direction as when acid was in the vessel v; i.e. from the zinc through the solution to the platina, and back by the galvanometer and substance suffering decomposition to the zinc.
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Experimental Researches in Electricity, Volume 1 12
