Part 46

938. Dilute sulphuric acid, sp. gr. 1.25, was put into the cell A, and a strong solution of caustic potassa into the cell B; they mingled slowly through the paper, and at last a thick crust of sulphate of potassa formed on the side of the paper next to the alkali. A plate of clean platina was put into each cell and connected with a delicate galvanometer, but no electric current could be observed. Hence the contact of acid with one platina plate, and alkali with the other, was unable to produce a current; nor was the combination of the acid with the alkali more effectual (925.).

939. When one of the platina plates was removed and a zinc plate substituted, either amalgamated or not, a strong electric current was produced. But, whether the zinc were in the acid whilst the platina was in the alkali, or whether the reverse order were chosen, the electric current was always from the zinc through the electrolyte to the platina, and back through the galvanometer to the zinc, the current seeming to be strongest when the zinc was in the alkali and the platina in the acid.

940. In these experiments, therefore, the acid seems to have no power over the alkali, but to be rather inferior to it in force. Hence there is no reason to suppose that the combination of the oxide formed with the acid around it has any direct influence in producing the electricity evolved, the whole of which appears to be due to the oxidation of the metal (919.).

941. The alkali, in fact, is superior to the acid in bringing a metal into what is called the positive state; for if plates of the same metal, as zinc, tin, lead, or copper, be used both in the acid or alkali, the electric current is from the alkali across the cell to the acid, and back through the galvanometer to the alkali, as Sir Humphry Davy formerly stated . This current is so powerful, that if amalgamated zinc, or tin, or lead be used, the metal in the acid evolves hydrogen the moment it is placed in communication with that in the alkali, not from any direct action of the acid upon it, for if the contact be broken the action ceases, but because it is powerfully negative with regard to the metal in the alkali.

Elements of Chemical Philosophy, p. 149; or Philosophical Transactions, 1826, p. 403.

942. The superiority of alkali is further proved by this, that if zinc and tin be used, or tin and lead, whichsoever metal is put into the alkali becomes positive, that in the acid being negative. Whichsoever is in the alkali is oxidized, whilst that in the acid remains in the metallic state, as far as the electric current is concerned.

943. When sulphuretted solutions are used (930.) in illustration of the assertion, that it is the chemical action of the metal and one of the ions of the associated electrolyte that produces all the electricity of the voltaic circuit, the proofs are still the same. Thus, as Sir Humphry Davy has shown, if iron and copper be plunged into dilute acid, the current is from the iron through the liquid to the copper; in solution of potassa it is in the same direction, but in solution of sulphuret of potassa it is reversed. In the two first cases it is oxygen which combines with the iron, in the latter sulphur which combines with the copper, that produces the electric current; but both of these are ions, existing as such in the electrolyte, which is at the same moment suffering decomposition; and, what is more, both of these are anions, for they leave the electrolytes at their anodes, and act just as chlorine, iodine, or any other anion would act which might have been previously chosen as that which should be used to throw the voltaic circle into activity.

Elements of Chemical Philosophy, p. 148.

944. The following experiments complete the series of proofs of the origin of the electricity in the voltaic pile. A fluid amalgam of potassium, containing not more than a hundredth of that metal, was put into pure water, and connected, through the galvanometer with a plate of platina in the same water. There was immediately an electric current from the amalgam through the electrolyte to the platina. This must have been due to the oxidation only of the metal, for there was neither acid nor alkali to combine with, or in any way act on, the body produced.

945. Again, a plate of clean lead and a plate of platina were put into pure water. There was immediately a powerful current produced from the lead through the fluid to the platina: it was even intense enough to decompose solution of the iodide of potassium when introduced into the circuit in the form of apparatus already described (880.), fig. 73. Here no action of acid or alkali on the oxide formed from the lead could supply the electricity: it was due solely to the oxidation of the metal.

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946. There is no point in electrical science which seems to me of more importance than the state of the metals and the electrolytic conductor in a simple voltaic circuit before and at the moment when metallic contact is first completed. If clearly understood, I feel no doubt it would supply us with a direct key to the laws under which the great variety of voltaic excitements, direct and incidental, occur, and open out new fields of research for our investigation.

In connexion with this part of the subject refer now to Series XI. 1164, Series XII. 1343-1358, and Series XIII. 1621. &c.--Dec. 1838.

947. We seem to have the power of deciding to a certain extent in numerous cases of chemical affinity, (as of zinc with the oxygen of water, &c. &c.) which of two modes of action of the attractive power shall be exerted (996.). In the one mode we can transfer the power onwards, and make it produce elsewhere its equivalent of action (867. 917.); in the other, it is not transferred, but exerted wholly at the spot. The first is the case of volta-electric excitation, the other ordinary chemical affinity: but both are chemical actions and due to one force or principle.

948. The general circumstances of the former mode occur in all instances of voltaic currents, but may be considered as in their perfect condition, and then free from those of the second mode, in some only of the cases; as in those of plates of zinc and platina in solution of potassa, or of amalgamated zinc and platina in dilute sulphuric acid.

949. Assuming it sufficiently proved, by the preceding experiments and considerations, that the electro-motive action depends, when zinc, platina, and dilute sulphuric acid are used, upon the mutual affinity of the metal zinc and the oxygen of the water (921. 924.), it would appear that the metal, when alone, has not power enough, under the circumstances, to take the oxygen and expel the hydrogen from the water; for, in fact, no such action takes place. But it would also appear that it has power so far to act, by its attraction for the oxygen of the particles in contact with it, as to place the similar forces already active between these and the other particles of oxygen and the particles of hydrogen in the water, in a peculiar state of tension or polarity, and probably also at the same time to throw those of its own particles which are in contact with the water into a similar but opposed state. Whilst this state is retained, no further change occurs; but when it is relieved, by completion of the circuit, in which case the forces determined in opposite directions, with respect to the zinc and the electrolyte, are found exactly competent to neutralize each other, then a series of decompositions and recompositions takes place amongst the particles of oxygen and hydrogen constituting the water, between the place of contact with the platina and the place where the zinc is active; these intervening particles being evidently in close dependence upon and relation to each other. The zinc forms a direct compound with those particles of oxygen which were, previously, in divided relation to both it and the hydrogen: the oxide is removed by the acid, and a fresh surface of zinc is presented to the water, to renew and repeat the action.

950. Practically, the state of tension is best relieved by dipping a metal which has less attraction for oxygen than the zinc, into the dilute acid, and making it also touch the zinc. The force of chemical affinity, which has been influenced or polarized in the particles of the water by the dominant attraction of the zinc for the oxygen, is then transferred, in a most extraordinary manner, through the two metals, so as to re-enter upon the circuit in the electrolytic conductor, which, unlike the metals in that respect, cannot convey or transfer it without suffering decomposition; or rather, probably, it is exactly balanced and neutralized by the force which at the same moment completes the combination of the zinc with the oxygen of the water. The forces, in fact, of the two particles which are acting towards each other, and which are therefore in opposite directions, are the origin of the two opposite forces, or directions of force, in the current. They are of necessity equivalent to each other. Being transferred forward in contrary directions, they produce what is called the voltaic current: and it seems to me impossible to resist the idea that it must be preceded by a state of tension in the fluid, and between the fluid and the zinc; the first consequence of the affinity of the zinc for the oxygen of the water.

951. I have sought carefully for indications of a state of tension in the electrolytic conductor; and conceiving that it might produce something like structure, either before or during its discharge, I endeavoured to make this evident by polarized light. A glass cell, seven inches long, one inch and a half wide, and six inches deep, had two sets of platina electrodes adapted to it, one set for the ends, and the other for the sides. Those for the sides were seven inches long by three inches high, and when in the cell were separated by a little frame of wood covered with calico; so that when made active by connexion with a battery upon any solution in the cell, the bubbles of gas rising from them did not obscure the central parts of the liquid.

952. A saturated solution of sulphate of soda was put into the cell, and the electrodes connected with a battery of 150 pairs of 4-inch plates: the current of electricity was conducted across the cell so freely, that the discharge was as good as if a wire had been used. A ray of polarized light was then transmitted through this solution, directly across the course of the electric current, and examined by an analysing plate; but though it penetrated seven inches of solution thus subject to the action of the electricity, and though contact was sometimes made, sometimes broken, and occasionally reversed during the observations, not the slightest trace of action on the ray could be perceived.

953. The large electrodes were then removed, and others introduced which fitted the ends of the cell. In each a slit was cut, so as to allow the light to pass. The course of the polarized ray was now parallel to the current, or in the direction of its axis (517.); but still no effect, under any circumstances of contact or disunion, could be perceived upon it.

954. A strong solution of nitrate of lead was employed instead of the sulphate of soda, but no effects could be detected.

955. Thinking it possible that the discharge of the electric forces by the successive decompositions and recompositions of the particles of the electrolyte might neutralize and therefore destroy any effect which the first state of tension could by possibility produce, I took a substance which, being an excellent electrolyte when fluid, was a perfect insulator when solid, namely, borate of lead, in the form of a glass plate, and connecting the sides and the edges of this mass with the metallic plates, sometimes in contact with the poles of a voltaic battery, and sometimes even with the electric machine, for the advantage of the much higher intensity then obtained, I passed a polarized ray across it in various directions, as before, but could not obtain the slightest appearance of action upon the light. Hence I conclude, that notwithstanding the new and extraordinary state which must be assumed by an electrolyte, either during decomposition (when a most enormous quantity of electricity must be traversing it), or in the state of tension which is assumed as preceding decomposition, and which might be supposed to be retained in the solid form of the electrolyte, still it has no power of affecting a polarized ray of light; for no kind of structure or tension can in this way be rendered evident.

956. There is, however, one beautiful experimental proof of a state of tension acquired by the metals and the electrolyte before the electric current is produced, and before contact of the different metals is made (915.); in fact, at that moment when chemical forces only are efficient as a cause of action. I took a voltaic apparatus, consisting of a single pair of large plates, namely, a cylinder of amalgamated zinc, and a double cylinder of copper. These were put into a jar containing dilute sulphuric acid, and could at pleasure be placed in metallic communication by a copper wire adjusted so as to dip at the extremities into two cups of mercury connected with the two plates.

When nitro-sulphuric acid is used, the spark is more powerful, but local chemical action can then commence, and proceed without requiring metallic contact.

957. Being thus arranged, there was no chemical action whilst the plates were not connected. On making the connexion a spark was obtained, and the solution was immediately decomposed. On breaking it, the usual spark was obtained, and the decomposition ceased. In this case it is evident that the first spark must have occurred before metallic contact was made, for it passed through an interval of air; and also that it must have tended to pass before the electrolytic action began; for the latter could not take place until the current passed, and the current could not pass before the spark appeared. Hence I think there is sufficient proof, that as it is the zinc and water which by their mutual action produce the electricity of this apparatus, so these, by their first contact with each other, were placed in a state of powerful tension (951.), which, though it could not produce the actual decomposition of the water, was able to make a spark of electricity pass between the zinc and a fit discharger as soon as the interval was rendered sufficiently small. The experiment demonstrates the direct production of the electric spark from pure chemical forces.

It has been universally supposed that no spark is produced on making the contact between a single pair of plates. I was led to expect one from the considerations already advanced in this paper. The wire of communication should be short; for with a long wire, circumstances strongly affecting the spark are introduced.

958. There are a few circumstances connected with the production of this spark by a single pair of plates, which should be known, to ensure success to the experiment. When the amalgamated surfaces of contact are quite clean and dry, the spark, on making contact, is quite as brilliant as on breaking it, if not even more so. When a film of oxide or dirt was present at either mercurial surface, then the first spark was often feeble, and often failed, the breaking spark, however, continuing very constant and bright. When a little water was put over the mercury, the spark was greatly diminished in brilliancy, but very regular both on making and breaking contact. When the contact was made between clean platina, the spark was also very small, but regular both ways. The true electric spark is, in fact, very small, and when surfaces of mercury are used, it is the combustion of the metal which produces the greater part of the light. The circumstances connected with the burning of the mercury are most favourable on breaking contact; for the act of separation exposes clean surfaces of metal, whereas, on making contact, a thin film of oxide, or soiling matter, often interferes. Hence the origin of the general opinion that it is only when the contact is broken that the spark passes.

See in relation to precautions respecting a spark, 1074.--Dec. 1838.