I have also constructed during these experiments many such single-wire

bulbs with or without internal electrode, in which the radiant matter

was projected against, or focused upon, the body to be rendered

incandescent. Fig. 24 illustrates one of the bulbs used. It consists

of a spherical globe L, provided with a long neck n, on the top, for

increasing the action in some cases by the application of an external

conducting coating. The globe L is blown out on the bottom into a very

small bulb b, which serves to hold it firmly in a socket S of

insulating material into which it is cemented. A fine lamp filament f,

supported on a wire w, passes through the centre of the globe L. The

filament is rendered incandescent in the middle portion, where the

bombardment proceeding from the lower inside surface of the globe is

most intense. The lower portion of the globe, as far as the socket S

reaches, is rendered conducting, either by a tinfoil coating or

otherwise, and the external electrode is connected to a terminal of

the coil.

The arrangement diagrammatically indicated in Fig. 24 was found to be

an inferior one when it was desired to render incandescent a filament

or button supported in the centre of the globe, but it was convenient

when the object was to excite phosphorescence.

In many experiments in which bodies of a different kind were mounted

in the bulb as, for instance, indicated in Fig. 23, some observations

of interest were made.

It was found, among other things, that in such cases, no matter where

the bombardment began, just as soon as a high temperature was reached

there was generally one of the bodies which seemed to take most of the

bombardment upon itself, the other, or others, being thereby relieved.

This quality appeared to depend principally on the point of fusion,

and on the facility with which the body was "evaporated," or,

generally speaking, disintegrated--meaning by the latter term not only

the throwing off of atoms, but likewise of larger lumps. The

observation made was in accordance with generally accepted notions. In

a highly exhausted bulb electricity is carried off from the electrode

by independent carriers, which are partly the atoms, or molecules, of

the residual atmosphere, and partly the atoms, molecules, or lumps

thrown off from the electrode. If the electrode is composed of bodies

of different character, and if one of these is more easily

disintegrated than the others, most of the electricity supplied is

carried off from that body, which is then brought to a higher

temperature than the others, and this the more, as upon an increase of

the temperature the body is still more easily disintegrated.

It seems to me quite probable that a similar process takes place in

the bulb even with a homogeneous electrode, and I think it to be the

principal cause of the disintegration. There is bound to be some

irregularity, even if the surface is highly polished, which, of

course, is impossible with most of the refractory bodies employed as

electrodes. Assume that a point of the electrode gets hotter,

instantly most of the discharge passes through that point, and a

minute patch is probably fused and evaporated. It is now possible that

in consequence of the violent disintegration the spot attacked sinks

in temperature, or that a counter force is created, as in an arc; at

any rate, the local tearing off meets with the limitations incident to

the experiment, whereupon the same process occurs on another place. To

the eye the electrode appears uniformly brilliant, but there are upon

it points constantly shifting and wandering around, of a temperature

far above the mean, and this materially hastens the process of

deterioration. That some such thing occurs, at least when the

electrode is at a lower temperature, sufficient experimental evidence

can be obtained in the following manner: Exhaust a bulb to a very high

degree, so that with a fairly high potential the discharge cannot

pass--that is, not a _luminous_ one, for a weak invisible discharge

occurs always, in all probability. Now raise slowly and carefully the

potential, leaving the primary current on no more than for an instant.

At a certain point, two, three, or half a dozen phosphorescent spots

will appear on the globe. These places of the glass are evidently more

violently bombarded than others, this being due to the unevenly

distributed electric density, necessitated, of course, by sharp

projections, or, generally speaking, irregularities of the electrode.

But the luminous patches are constantly changing in position, which is

especially well observable if one manages to produce very few, and

this indicates that the configuration of the electrode is rapidly

changing.

From experiences of this kind I am led to infer that, in order to be

most durable, the refractory button in the bulb should be in the form

of a sphere with a highly polished surface. Such a small sphere could

be manufactured from a diamond or some other crystal, but a better way

would be to fuse, by the employment of extreme degrees of temperature,

some oxide--as, for instance, zirconia--into a small drop, and then

keep it in the bulb at a temperature somewhat below its point of

fusion.

Interesting and useful results can no doubt be reached in the

direction of extreme degrees of heat. How can such high temperatures

be arrived at? How are the highest degrees of heat reached in nature?

By the impact of stars, by high speeds and collisions. In a collision

any rate of heat generation may be attained. In a chemical process we

are limited. When oxygen and hydrogen combine, they fall,

metaphorically speaking, from a definite height. We cannot go very far

with a blast, nor by confining heat in a furnace, but in an exhausted

bulb we can concentrate any amount of energy upon a minute button.

Leaving practicability out of consideration, this, then, would be the

means which, in my opinion, would enable us to reach the highest

temperature. But a great difficulty when proceeding in this way is

encountered, namely, in most cases the body is carried off before it

can fuse and form a drop. This difficulty exists principally with an

oxide such as zirconia, because it cannot be compressed in so hard a

cake that it would not be carried off quickly. I endeavored repeatedly

to fuse zirconia, placing it in a cup or arc light carbon as indicated

in Fig. 23. It glowed with a most intense light, and the stream of the

particles projected out of the carbon cup was of a vivid white: but

whether it was compressed in a cake or made into a paste with carbon,

it was carried off before it could be fused. The carbon cup containing

the zirconia had to be mounted very low in the neck of a large bulb,

as the heating of the glass by the projected particles of the oxide

was so rapid that in the first trial the bulb was cracked almost in an

instant when the current was turned on. The heating of the glass by

the projected particles was found to be always greater when the carbon

cup contained a body which was rapidly carried off--I presume because

in such cases, with the same potential, higher speeds were reached,

and also because, per unit of time, more matter was projected--that

is, more particles would strike the glass.

The before mentioned difficulty did not exist, however, when the body

mounted in the carbon cup offered great resistance to deterioration.

For instance, when an oxide was first fused in an oxygen blast and

then mounted in the bulb, it melted very readily into a drop.

Generally during the process of fusion magnificent light effects were

noted, of which it would be difficult to give an adequate idea. Fig.

23 is intended to illustrate the effect observed with a ruby drop. At

first one may see a narrow funnel of white light projected against the

top of the globe, where it produces an irregularly outlined

phosphorescent patch. When the point of the ruby fuses the

phosphorescence becomes very powerful; but as the atoms are projected

with much greater speed from the surface of the drop, soon the glass

gets hot and "tired," and now only the outer edge of the patch glows.

In this manner an intensely phosphorescent, sharply defined line, _l_,

corresponding to the outline of the drop, is produced, which spreads

slowly over the globe as the drop gets larger. When the mass begins to

boil, small bubbles and cavities are formed, which cause dark colored

spots to sweep across the globe. The bulb may be turned downward

without fear of the drop falling off, as the mass possesses

considerable viscosity.

I may mention here another feature of some interest, which I believe

to have noted in the course of these experiments, though the

observations do not amount to a certitude. It _appeared_ that under

the molecular impact caused by the rapidly alternating potential the

body was fused and maintained in that state at a lower temperature in

a highly exhausted bulb than was the case at normal pressure and

application of heat in the ordinary way--that is, at least, judging

from the quantity of the light emitted. One of the experiments

performed may be mentioned here by way of illustration. A small piece

of pumice stone was stuck on a platinum wire, and first melted to it

in a gas burner. The wire was next placed between two pieces of

charcoal and a burner applied so as to produce an intense heat,

sufficient to melt down the pumice stone into a small glass-like

button. The platinum wire had to be taken of sufficient thickness to

prevent its melting in the fire. While in the charcoal fire, or when

held in a burner to get a better idea of the degree of heat, the

button glowed with great brilliancy. The wire with the button was then

mounted in a bulb, and upon exhausting the same to a high degree, the

current was turned on slowly so as to prevent the cracking of the

button. The button was heated to the point of fusion, and when it

melted it did not, apparently, glow with the same brilliancy as

before, and this would indicate a lower temperature. Leaving out of

consideration the observer's possible, and even probable, error, the

question is, can a body under these conditions be brought from a solid

to a liquid state with evolution of _less_ light?

When the potential of a body is rapidly alternated it is certain that

the structure is jarred. When the potential is very high, although the

vibrations may be few--say 20,000 per second--the effect upon the

structure may be considerable. Suppose, for example, that a ruby is

melted into a drop by a steady application of energy. When it forms a

drop it will emit visible and invisible waves, which will be in a

definite ratio, and to the eye the drop will appear to be of a certain

brilliancy. Next, suppose we diminish to any degree we choose the

energy steadily supplied, and, instead, supply energy which rises and

falls according to a certain law. Now, when the drop is formed, there

will be emitted from it three different kinds of vibrations--the

ordinary visible, and two kinds of invisible waves: that is, the

ordinary dark waves of all lengths, and, in addition, waves of a well

defined character. The latter would not exist by a steady supply of

the energy; still they help to jar and loosen the structure. If this

really be the case, then the ruby drop will emit relatively less

visible and more invisible waves than before. Thus it would seem that

when a platinum wire, for instance, is fused by currents alternating

with extreme rapidity, it emits at the point of fusion less light and

more invisible radiation than it does when melted by a steady current,

though the total energy used up in the process of fusion is the same

in both cases. Or, to cite another example, a lamp filament is not

capable of withstanding as long with currents of extreme frequency as

it does with steady currents, assuming that it be worked at the same

luminous intensity. This means that for rapidly alternating currents

the filament should be shorter and thicker. The higher the

frequency--that is, the greater the departure from the steady

flow--the worse it would be for the filament. But if the truth of this

remark were demonstrated, it would be erroneous to conclude that such

a refractory button as used in these bulbs would be deteriorated

quicker by currents of extremely high frequency than by steady or low

frequency currents. From experience I may say that just the opposite

holds good: the button withstands the bombardment better with currents

of very high frequency. But this is due to the fact that a high

frequency discharge passes through a rarefied gas with much greater

freedom than a steady or low frequency discharge, and this will say

that with the former we can work with a lower potential or with a less

violent impact. As long, then, as the gas is of no consequence, a

steady or low frequency current is better; but as soon as the action

of the gas is desired and important, high frequencies are preferable.

In the course of these experiments a great many trials were made with

all kinds of carbon buttons. Electrodes made of ordinary carbon

buttons were decidedly more durable when the buttons were obtained by

the application of enormous pressure. Electrodes prepared by

depositing carbon in well known ways did not show up well; they

blackened the globe very quickly. From many experiences I conclude

that lamp filaments obtained in this manner can be advantageously used

only with low potentials and low frequency currents. Some kinds of

carbon withstand so well that, in order to bring them to the point of

fusion, it is necessary to employ very small buttons. In this case the

observation is rendered very difficult on account of the intense heat

produced. Nevertheless there can be no doubt that all kinds of carbon

are fused under the molecular bombardment, but the liquid state must

be one of great instability. Of all the bodies tried there were two

which withstood best--diamond and carborundum. These two showed up

about equally, but the latter was preferable, for many reasons. As it

is more than likely that this body is not yet generally known, I will

venture to call your attention to it.

It has been recently produced by Mr. E.G. Acheson, of Monongahela

City, Pa., U.S.A. It is intended to replace ordinary diamond powder

for polishing precious stones, etc., and I have been informed that it

accomplishes this object quite successfully. I do not know why the

name "carborundum" has been given to it, unless there is something in

the process of its manufacture which justifies this selection. Through

the kindness of the inventor, I obtained a short while ago some

samples which I desired to test in regard to their qualities of

phosphorescence and capability of withstanding high degrees of heat.

Carborundum can be obtained in two forms--in the form of "crystals"

and of powder. The former appear to the naked eye dark colored, but

are very brilliant; the latter is of nearly the same color as ordinary

diamond powder, but very much finer. When viewed under a microscope

the samples of crystals given to me did not appear to have any

definite form, but rather resembled pieces of broken up egg coal of

fine quality. The majority were opaque, but there were some which were

transparent and colored. The crystals are a kind of carbon containing

some impurities; they are extremely hard, and withstand for a long

time even an oxygen blast. When the blast is directed against them

they at first form a cake of some compactness, probably in consequence

of the fusion of impurities they contain. The mass withstands for a

very long time the blast without further fusion; but a slow carrying

off, or burning, occurs, and, finally, a small quantity of a

glass-like residue is left, which, I suppose, is melted alumina. When

compressed strongly they conduct very well, but not as well as

ordinary carbon. The powder, which is obtained from the crystals in

some way, is practically non-conducting. It affords a magnificent

polishing material for stones.

The time has been too short to make a satisfactory study of the

properties of this product, but enough experience has been gained in a

few weeks I have experimented upon it to say that it does possess some

remarkable properties in many respects. It withstands excessively high

degrees of heat, it is little deteriorated by molecular bombardment,

and it does not blacken the globe as ordinary carbon does. The only

difficulty which I have found in its use in connection with these

experiments was to find some binding material which would resist the

heat and the effect of the bombardment as successfully as carborundum

itself does.

I have here a number of bulbs which I have provided with buttons of

carborundum. To make such a button of carborundum crystals I proceed

in the following manner: I take an ordinary lamp filament and dip its

point in tar, or some other thick substance or paint which may be

readily carbonized. I next pass the point of the filament through the

crystals, and then hold it vertically over a hot plate. The tar

softens and forms a drop on the point of the filament, the crystals

adhering to the surface of the drop. By regulating the distance from

the plate the tar is slowly dried out and the button becomes solid. I

then once more dip the button in tar and hold it again over a plate

until the tar is evaporated, leaving only a hard mass which firmly

binds the crystals. When a larger button is required I repeat the

process several times, and I generally also cover the filament a

certain distance below the button with crystals. The button being

mounted in a bulb, when a good vacuum has been reached, first a weak

and then a strong discharge is passed through the bulb to carbonize

the tar and expel all gases, and later it is brought to a very intense

incandescence.

When the powder is used I have found it best to proceed as follows: I

make a thick paint of carborundum and tar, and pass a lamp filament

through the paint. Taking then most of the paint off by rubbing the

filament against a piece of chamois leather, I hold it over a hot

plate until the tar evaporates and the coating becomes firm. I repeat

this process as many times as it is necessary to obtain a certain

thickness of coating. On the point of the coated filament I form a

button in the same manner.

There is no doubt that such a button--properly prepared under great

pressure--of carborundum, especially of powder of the best quality,

will withstand the effect of the bombardment fully as well as anything

we know. The difficulty is that the binding material gives way, and

the carborundum is slowly thrown off after some time. As it does not

seem to blacken the globe in the least, it might be found useful for

coating the filaments of ordinary incandescent lamps, and I think that

it is even possible to produce thin threads or sticks of carborundum

which will replace the ordinary filaments in an incandescent lamp. A

carborundum coating seems to be more durable than other coatings, not

only because the carborundum can withstand high degrees of heat, but

also because it seems to unite with the carbon better than any other

material I have tried. A coating of zirconia or any other oxide, for

instance, is far more quickly destroyed. I prepared buttons of diamond

dust in the same manner as of carborundum, and these came in

durability nearest to those prepared of carborundum, but the binding

paste gave way much more quickly in the diamond buttons: this,

however, I attributed to the size and irregularity of the grains of

the diamond.

It was of interest to find whether carborundum possesses the quality

of phosphorescence. One is, of course, prepared to encounter two

difficulties: first, as regards the rough product, the "crystals,"

they are good conducting, and it is a fact that conductors do not

phosphoresce; second, the powder, being exceedingly fine, would not be

apt to exhibit very prominently this quality, since we know that when

crystals, even such as diamond or ruby, are finely powdered, they lose

the property of phosphorescence to a considerable degree.

The question presents itself here, can a conductor phosphoresce? What

is there in such a body as a metal, for instance, that would deprive

it of the quality of phosphorescence, unless it is that property which

characterizes it as a conductor? for it is a fact that most of the

phosphorescent bodies lose that quality when they are sufficiently

heated to become more or less conducting. Then, if a metal be in a

large measure, or perhaps entirely, deprived of that property, it

should be capable of phosphorescence. Therefore it is quite possible

that at some extremely high frequency, when behaving practically as a

non-conductor, a metal or any other conductor might exhibit the

quality of phosphorescence, even though it be entirely incapable of

phosphorescing under the impact of a low-frequency discharge. There

is, however, another possible way how a conductor might at least

_appear_ to phosphoresce.

Considerable doubt still exists as to what really is phosphorescence,

and as to whether the various phenomena comprised under this head are

due to the same causes. Suppose that in an exhausted bulb, under the

molecular impact, the surface of a piece of metal or other conductor

is rendered strongly luminous, but at the same time it is found that

it remains comparatively cool, would not this luminosity be called

phosphorescence? Now such a result, theoretically at least, is

possible, for it is a mere question of potential or speed. Assume the

potential of the electrode, and consequently the speed of the

projected atoms, to be sufficiently high, the surface of the metal

piece against which the atoms are projected would be rendered highly

incandescent, since the process of heat generation would be

incomparably faster than that of radiating or conducting away from the

surface of the collision. In the eye of the observer a single impact

of the atoms would cause an instantaneous flash, but if the impacts

were repeated with sufficient rapidity they would produce a

continuous impression upon his retina. To him then the surface of the

metal would appear continuously incandescent and of constant luminous

intensity, while in reality the light would be either intermittent or

at least changing periodically in intensity. The metal piece would

rise in temperature until equilibrium was attained--that is until the

energy continuously radiated would equal that intermittently supplied.

But the supplied energy might under such conditions not be sufficient

to bring the body to any more than a very moderate mean temperature,

especially if the frequency of the atomic impacts be very low--just

enough that the fluctuation of the intensity of the light emitted

could not be detected by the eye. The body would now, owing to the

manner in which the energy is supplied, emit a strong light, and yet

be at a comparatively very low mean temperature. How could the

observer call the luminosity thus produced? Even if the analysis of

the light would teach him something definite, still he would probably

rank it under the phenomena of phosphorescence. It is conceivable that

in such a way both conducting and non-conducting bodies may be

maintained at a certain luminous intensity, but the energy required

would very greatly vary with the nature and properties of the bodies.

These and some foregoing remarks of a speculative nature were made

merely to bring out curious features of alternate currents or electric

impulses. By their help we may cause a body to emit _more_ light,

while at a certain mean temperature, than it would emit if brought to

that temperature by a steady supply; and, again, we may bring a body

to the point of fusion, and cause it to emit _less_ light than when

fused by the application of energy in ordinary ways. It all depends on

how we supply the energy, and what kind of vibrations we set up: in

one case the vibrations are more, in the other less, adapted to affect

our sense of vision.

Experiments with Alternate Currents of High Potential and High Frequency A Lecture Delivered before the Institution of Electrical Engineers, London · 第 5 / 9 段