Experimental Researches in Electricity Part 17

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Experimental Researches in Electricity



Experimental Researches in Electricity Part 17


[B] Ibid. p, 24, &c.

551. The instances in which sulphuric acid could not be pa.s.sed though baryta, or baryta through sulphuric acid[A], because of the precipitation of sulphate of baryta, enter within the pale of the law already described (380. 412.), by which liquidity is so generally required for conduction and decomposition. In a.s.suming the solid state of sulphate of baryta, these bodies became virtually non-conductors to electricity of so low a tension as that of the voltaic battery, and the power of the latter over them was almost infinitely diminished.

[A] Philosophical Transactions, 1807, p. 25, &c.

552. The theory I have advanced accords in a most satisfactory manner with the fact of an element or substance finding its place of rest, or rather of evolution, sometimes at one pole and sometimes at the other. Sulphur ill.u.s.trates this effect very well[A]. When sulphuric acid is decomposed by the pile, sulphur is evolved at the negative pole; but when sulphuret of silver is decomposed in a similar way (436.), then the sulphur appears at the positive pole; and if a hot platina pole be used so as to vaporize the sulphur evolved in the latter case, then the relation of that pole to the sulphur is exactly the same as the relation of the same pole to oxygen upon its immersion in water. In both cases the element evolved is liberated at the pole, but not retained by it; but by virtue of its elastic, uncombinable, and immiscible condition pa.s.ses away into the surrounding medium. The sulphur is evidently determined in these opposite directions by its opposite chemical relations to oxygen and silver; and it is to such relations generally that I have referred all electro-chemical phenomena.

Where they do not exist, no electro-chemical action can take place. Where they are strongest, it is most powerful; where they are reversed, the direction of transfer of the substance is reversed with them.

[A] At 681 and 757 of Series VII, will be found corrections of the statement here made respecting sulphur and sulphuric acid. At present there is no well-ascertained fact which proves that the same body can go directly to _either_ of the two poles at pleasure.--_Dec. 1838._

553. _Water_ may be considered as one of those substances which can be made to pa.s.s to _either_ pole. When the poles are immersed in dilute sulphuric acid (527.), acid pa.s.ses towards the positive pole, and water towards the negative pole; but when they are immersed in dilute alkali, the alkali pa.s.ses towards the negative pole, and water towards the positive pole.

554. Nitrogen is another substance which is considered as determinable to either pole; but in consequence of the numerous compounds which it forms, some of which pa.s.s to one pole, and some to the other, I have not always found it easy to determine the true circ.u.mstances of its appearance. A pure strong solution of ammonia is so bad a conductor of electricity that it is scarcely more decomposable than pure water; but if sulphate of ammonia be dissolved in it, then decomposition takes place very well; nitrogen almost pure, and in some cases quite, is evolved at the positive pole, and hydrogen at the negative pole.

555. On the other hand, if a strong solution of nitrate of ammonia be decomposed, oxygen appears at the positive pole, and hydrogen, with sometimes nitrogen, at the negative pole. If fused nitrate of ammonia be employed, hydrogen appears at the negative pole, mingled with a little nitrogen. Strong nitric acid yields plenty of oxygen at the positive pole, but no gas (only nitrous acid) at the negative pole. Weak nitric acid yields the oxygen and hydrogen of the water present, the acid apparently remaining unchanged. Strong nitric acid with nitrate of ammonia dissolved in it, yields a gas at the negative pole, of which the greater part is hydrogen, but apparently a little nitrogen is present. I believe, that in some of these cases a little nitrogen appeared at the negative pole. I suspect, however, that in all these, and in all former cases, the appearance of the nitrogen at the positive or negative pole is entirely a secondary effect, and not an immediate consequence of the decomposing power of the electric current[A].

[A] Refer for proof of the truth of this supposition to 748, 752, &c.--_Dec. 1838._

556. A few observations on what are called the _poles_ of the voltaic battery now seem necessary. The poles are merely the surfaces or doors by which the electricity enters into or pa.s.ses out of the substance suffering decomposition. They limit the extent of that substance in the course of the electric current, being its _terminations_ in that direction: Hence the elements evolved pa.s.s so far and no further.

557. Metals make admirable poles, in consequence of their high conducting power, their immiscibility with the substances generally acted upon, their solid form, and the opportunity afforded of selecting such as are not chemically acted upon by ordinary substances.

558. Water makes a pole of difficult application, except in a few cases (494.), because of its small conducting power, its miscibility with most of the substances acted upon, and its general relation to them in respect to chemical affinity. It consists of elements, which in their electrical and chemical relations are directly and powerfully opposed, yet combining to produce a body more neutral in its character than any other. So that there are but few substances which do not come into relation, by chemical affinity, with water or one of its elements; and therefore either the water or its elements are transferred and a.s.sist in transferring the infinite variety of bodies which, in a.s.sociation with it, can be placed in the course of the electric current. Hence the reason why it so rarely happens that the evolved substances rest at the first surface of the water, and why it therefore does not exhibit the ordinary action of a pole.

559. Air, however, and some gases are free from the latter objection, and may be used as poles in many cases (461, &c.); but, in consequence of the extremely low degree of conducting power belonging to them, they cannot be employed with the voltaic apparatus. This limits their use; for the voltaic apparatus is the only one as yet discovered which supplies sufficient quant.i.ty of electricity (371. 376.) to effect electro-chemical decomposition with facility.

560. When the poles are liable to the chemical action of the substances evolved, either simply in consequence of their natural relation to them, or of that relation aided by the influence of the current (518.), then they suffer corrosion, and the parts dissolved are subject to transference, in the same manner as the particles of the body originally under decomposition. An immense series of phenomena of this kind might be quoted in support of the view I have taken of the cause of electro-chemical decomposition, and the transfer and evolution of the elements. Thus platina being made the positive and negative poles in a solution of sulphate of soda, has no affinity or attraction for the oxygen, hydrogen, acid, or alkali evolved, and refuses to combine with or retain them. Zinc can combine with the oxygen and acid; at the positive pole it does combine, and immediately begins to travel as oxide towards the negative pole. Charcoal, which cannot combine with the metals, if made the negative pole in a metallic solution, refuses to unite to the bodies which are ejected from the solution upon its surface; but if made the positive pole in a dilute solution of sulphuric acid, it is capable of combining with the oxygen evolved there, and consequently unites with it, producing both carbonic acid and carbonic oxide in abundance.

561. A great advantage is frequently supplied, by the opportunity afforded amongst the metals of selecting a substance for the pole, which shall or shall not be acted upon by the elements to be evolved. The consequent use of platina is notorious. In the decomposition of sulphuret of silver and other sulphurets, a positive silver pole is superior to a platina one, because in the former case the sulphur evolved there combines with the silver, and the decomposition of the original sulphuret is rendered evident; whereas in the latter case it is dissipated, and the a.s.surance of its separation at the pole not easily obtained.

562. The effects which take place when a succession of conducting decomposable and undecomposable substances are placed in the electric circuit, as, for instance, of wires and solutions, or of air and solutions (465, 469.), are explained in the simplest possible manner by the theoretical view I have given. In consequence of the reaction of the const.i.tuents of each portion of decomposable matter, affected as they are by the supervention of the electric current (524.), portions of the proximate or ultimate elements proceed in the direction of the current as far as they find matter of a contrary kind capable of effecting their transfer, and being equally affected by them; and where they cease to find such matter, they are evolved in their free state, i.e. upon the surfaces of metal or air bounding the extent of decomposable matter in the direction of the current.

563. Having thus given my theory of the mode in which electro-chemical decomposition is effected, I will refrain for the present from entering upon the numerous general considerations which it suggests, wishing first to submit it to the test of publication and discussion.

_Royal Inst.i.tution, June 1833._

SIXTH SERIES.

-- 12. _On the power of Metals and other Solids to induce the Combination of Gaseous Bodies._

Received November 30, 1833,--Read January 11, 1834.

564. The conclusion at which I have arrived in the present communication may seem to render the whole of it unfit to form part of a series of researches in electricity; since, remarkable as the phenomena are, the power which produces them is not to be considered as of an electric origin, otherwise than as all attraction of particles may have this subtile agent for their common cause. But as the effects investigated arose out of electrical researches, as they are directly connected with other effects which are of an electric nature, and must of necessity be understood and guarded against in a very extensive series of electro-chemical decompositions (707.), I have felt myself fully justified in describing them in this place.

565. Believing that I had proved (by experiments hereafter to be described (705.),) the constant and definite chemical action of a certain quant.i.ty of electricity, whatever its intensity might be, or however the circ.u.mstances of its transmission through either the body under decomposition or the more perfect conductors were varied, I endeavoured upon that result to construct a new measuring instrument, which from its use might be called, at least provisionally, a _Volta-electrometer_ (739.)[A].

[A] Or Voltameter.--_Dec. 1838._

566. During the course of the experiments made to render the instrument efficient, I was occasionally surprised at observing a deficiency of the gases resulting from the decompositions of water, and at last an actual disappearance of portions which had been evolved, collected, and measured.

The circ.u.mstances of the disappearance were these. A gla.s.s tube, about twelve inches in length and 3/4ths of an inch in diameter, had two platina poles fixed into its upper, hermetically sealed, extremity: the poles, where they pa.s.sed through the gla.s.s, were of wire; but terminated below in plates, which were soldered to the wires with gold (Plate V. fig. 56.). The tube was filled with dilute sulphuric acid, and inverted in a cup of the same fluid; a voltaic battery was connected with the two wires, and sufficient oxygen and hydrogen evolved to occupy 4/5ths of the tube, or by the graduation, 116 parts. On separating the tube from the voltaic battery the volume of gas immediately began to diminish, and in about five hours only 13-1/2 parts remained, and these ultimately disappeared.

567. It was found by various experiments, that this effect was not due to the escape or solution of the gas, nor to recombination of the oxygen or hydrogen in consequence of any peculiar condition _they_ might be supposed to possess under the circ.u.mstances; but to be occasioned by the action of one or both of the poles within the tube upon the gas around them. On disuniting the poles from the pile after they had acted upon dilute sulphuric acid, and introducing them into separate tubes containing mixed oxygen and hydrogen, it was found that the _positive_ pole effected the union of the gases, but the negative pole apparently not (588.). It was ascertained also that no action of a sensible kind took place between the positive pole with oxygen or hydrogen alone.

568. These experiments reduced the phenomena to the consequence of a power possessed by the platina, after it had been the positive pole of a voltaic pile, of causing the combination of oxygen and hydrogen at common, or even at low, temperatures. This effect is, as far as I am aware, altogether new, and was immediately followed out to ascertain whether it was really of an electric nature, and how far it would interfere with the determination of the quant.i.ties evolved in the cases of electro-chemical decomposition required in the fourteenth section of these Researches.

569. Several platina plates were prepared (fig. 57.). They were nearly half an inch wide, and two inches and a half long: some were 1/200dth of an inch, others not more than 1/600dth, whilst some were as much as 1/70th of an inch in thickness. Each had a piece of platina wire, about seven inches long, soldered to it by pure gold. Then a number of gla.s.s tubes were prepared: they were about nine or ten inches in length, 5/8ths of an inch in internal diameter, were sealed hermetically at one extremity, and were graduated. Into these tubes was put a mixture of two volumes of hydrogen and one of oxygen, at the water pneumatic trough, and when one of the plates described had been connected with the positive or negative pole of the voltaic battery for a given time, or had been otherwise prepared, it was introduced through the water into the gas within the tube; the whole set aside in a test-gla.s.s (fig. 58.), and left for a longer or shorter period, that the action might be observed.

570. The following result may be given as an ill.u.s.tration of the phenomenon to be investigated. Diluted sulphuric acid, of the specific gravity 1.336, was put into a gla.s.s jar, in which was placed also a large platina plate, connected with the negative end of a voltaic battery of forty pairs of four-inch plates, with double coppers, and moderately charged. One of the plates above described (569.) was then connected with the positive extremity, and immersed in the same jar of acid for five minutes, after which it was separated from the battery, washed in distilled water, and introduced through the water of the pneumatic trough into a tube containing the mixture of oxygen and hydrogen (569.). The volume of gases immediately began to lessen, the diminution proceeding more and more rapidly until about 3/4ths of the mixture had disappeared. The upper end of the tube became quite warm, the plate itself so hot that the water boiled as it rose over it; and in less than a minute a cubical inch and a half of the gases were gone, having been combined by the power of the platina, and converted into water.

571. This extraordinary influence acquired by the platina at the positive pole of the pile, is exerted far more readily and effectively on oxygen and hydrogen than on any other mixture of gases that I have tried. One volume of nitrous gas was mixed with a volume of hydrogen, and introduced into a tube with a plate which had been made positive in the dilute sulphuric acid for four minutes (570.). There was no sensible action in an hour: being left for thirty-six hours, there was a diminution of about one-eighth of the whole volume. Action had taken place, but it had been very feeble.

572. A mixture of two volumes of nitrous oxide with one volume of hydrogen was put with a plate similarly prepared into a tube (569. 570.). This also showed no action immediately; but in thirty-six hours nearly a fourth of the whole had disappeared, i.e. about half of a cubic inch. By comparison with another tube containing the same mixture without a plate, it appeared that a part of the diminution was due to solution, and the other part to the power of the platina; but the action had been very slow and feeble.

573. A mixture of one volume olefiant gas and three volumes oxygen was not affected by such a platina plate, even though left together for several days (640. 641.).

574. A mixture of two volumes carbonic oxide and one volume oxygen was also unaffected by the prepared platina plate in several days (645, &c.).

575. A mixture of equal volumes of chlorine and hydrogen was used in several experiments, with plates prepared in a similar manner (570.).

Diminution of bulk soon took place; but when after thirty-six hours the experiments were examined, it was found that nearly all the chlorine had disappeared, having been absorbed, princ.i.p.ally by the water, and that the original volume of hydrogen remained unchanged. No combination of the gases, therefore, had here taken place.

576. Reverting to the action of the prepared plates on mixtures of oxygen and hydrogen (570.), I found that the power, though gradually diminishing in all cases, could still be retained for a period, varying in its length with circ.u.mstances. When tubes containing plates (569.) were supplied with fresh portions of mixed oxygen and hydrogen as the previous portions were condensed, the action was found to continue for above thirty hours, and in some cases slow combination could be observed even after eighty hours; but the continuance of the action greatly depended upon the purity of the gases used (638.).

577. Some plates (569.) were made positive for four minutes in dilute sulphuric acid of specific gravity 1.336: they were rinsed in distilled water, after which two were put into a small bottle and closed up, whilst others were left exposed to the air. The plates preserved in the limited portion of air were found to retain their power after eight days, but those exposed to the atmosphere had lost their force almost entirely in twelve hours, and in some situations, where currents existed, in a much shorter time.

578. Plates were made positive for five minutes in sulphuric acid, specific gravity 1.336. One of these was retained in similar acid for eight minutes after separation from the battery: it then acted on mixed oxygen and hydrogen with apparently undiminished vigour. Others were left in similar acid for forty hours, and some even for eight days, after the electrization, and then acted as well in combining oxygen and hydrogen gas as those which were used immediately after electrization.

579. The effect of a solution of caustic pota.s.sa in preserving the platina plates was tried in a similar manner. After being retained in such a solution for forty hours, they acted exceedingly well on oxygen and hydrogen, and one caused such rapid condensation of the gases, that the plate became much heated, and I expected the temperature would have risen to ignition.

580. When similarly prepared plates (569.) had been put into distilled water for forty hours, and then introduced into mixed oxygen and hydrogen, they were found to act but very slowly and feebly as compared with those which had been preserved in acid or alkali. When, however, the quant.i.ty of water was but small, the power was very little impaired after three or four days. As the water had been retained in a wooden vessel, portions of it were redistilled in gla.s.s, and this was found to preserve prepared plates for a great length of time. Prepared plates were put into tubes with this water and closed up; some of them, taken out at the end of twenty-four days, were found very active on mixed oxygen and hydrogen; others, which were left in the water for fifty-three days, were still found to cause the combination of the gases. The tubes had been closed only by corks.

581. The act of combination always seemed to diminish, or apparently exhaust, the power of the platina plate. It is true, that in most, if not all instances, the combination of the gases, at first insensible, gradually increased in rapidity, and sometimes reached to explosion; but when the latter did not happen, the rapidity of combination diminished; and although fresh portions of gas were introduced into the tubes, the combination went on more and more slowly, and at last ceased altogether. The first effect of an increase in the rapidity of combination depended in part upon the water flowing off from the platina plate, and allowing a better contact with the gas, and in part upon the heat evolved during the progress of the combination (630.). But notwithstanding the effect of these causes, diminution, and at last cessation of the power, always occurred. It must not, however, be unnoticed, that the purer the gases subjected to the action of the plate, the longer was its combining power retained. With the mixture evolved at the poles of the voltaic pile, in pure dilute sulphuric acid, it continued longest; and with oxygen and hydrogen, of perfect purity, it probably would not be diminished at all.

582. Different modes of treatment applied to the platina plate, after it had ceased to be the positive pole of the pile, affected its power very curiously. A plate which had been a positive pole in diluted sulphuric acid of specific gravity 1.336 for four or five minutes, if rinsed in water and put into mixed oxygen and hydrogen, would act very well, and condense perhaps one cubic inch and a half of gas in six or seven minutes; but if that same plate, instead of being merely rinsed, had been left in distilled water for twelve or fifteen minutes, or more, it would rarely fail, when put into the oxygen and hydrogen, of becoming, in the course of a minute or two, ignited, and would generally explode the gases. Occasionally the time occupied in bringing on the action extended to eight or nine minutes, and sometimes even to forty minutes, and yet ignition and explosion would result. This effect is due to the removal of a portion of acid which otherwise adheres firmly to the plate [A].

[A] In proof that this is the case, refer to 1038.--_Dec. 1838._

583. Occasionally the platina plates (569.), after being made the positive pole of the battery, were washed, wiped with filtering-paper or a cloth, and washed and wiped again. Being then introduced into mixed oxygen and hydrogen, they acted apparently as if they had been unaffected by the treatment. Sometimes the tubes containing the gas were opened in the air for an instant, and the plates put in dry; but no sensible difference in action was perceived, except that it commenced sooner.

584. The power of heat in altering the action of the prepared platina plates was also tried (595.). Plates which had been rendered positive in dilute sulphuric acid for four minutes were well-washed in water, and heated to redness in the flame of a spirit-lamp: after this they acted very well on mixed oxygen and hydrogen. Others, which had been heated more powerfully by the blowpipe, acted afterwards on the gases, though not so powerfully as the former. Hence it appears that heat does not take away the power acquired by the platina at the positive pole of the pile: the occasional diminution of force seemed always referable to other causes than the mere heat. If, for instance, the plate had not been well-washed from the acid, or if the flame used was carbonaceous, or was that of an alcohol lamp trimmed with spirit containing a little acid, or having a wick on which salt, or other extraneous matter, had been placed, then the power of the plate was quickly and greatly diminished (634. 636.).

585. This remarkable property was conferred upon platina when it was made the positive pole in sulphuric acid of specific gravity 1.336, or when it was considerably weaker, or when stronger, even up to the strength of oil of vitriol. Strong and dilute nitric acid, dilute acetic acid, solutions of tartaric, citric, and oxalic acids, were used with equal success. When muriatic acid was used, the plates acquired the power of condensing the oxygen and hydrogen, but in a much inferior degree.

586. Plates which were made positive in solution of caustic pota.s.sa did not show any sensible action upon the mixed oxygen and hydrogen. Other plates made positive in solutions of carbonates of pota.s.sa and soda exhibited the action, but only in a feeble degree.






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