CHLORINE, IODINE, BROMINE, FLUORINE.
_The four Halogens, or Producers of Substances like Sea Salt._
Chlorine ([Greek: _chlôros_], green). Symbol, Cl. Combining proportion,
35.5. Specific gravity, 2.44. Scheele termed it dephlogisticated
muriatic acid; Lavoisier, oxymuriatic acid; Davy, chlorine.
The consideration of the nature of this important element introduces to
our notice one of the most original chemists of the eighteenth
century--viz., the illustrious Scheele, who was born at Stralsund, in
1742, and in spite of every obstacle, fighting his "battle of life" with
sickness and sorrow, he succeeded in making some of the most valuable
discoveries in science, and amongst them that of chlorine gas. It was in
the examination of a mineral solid--viz., of manganese--that Scheele
made the acquaintance of a new gaseous element; and in a highly original
dissertation on manganese, in 1774, he describes the mode of procuring
what he termed _dephlogisticated muriatic acid_--a name which is
certainly to be regretted, from its absurd length, but a title which was
strictly in accordance with the then established theory of phlogiston;
and if the latter is considered synonymous with hydrogen, quite in
accordance with our present views of the nature of this element. Scheele
discovered the leading characteristics of chlorine, and especially its
power of bleaching, which is alone sufficient to place this gas in a
high commercial position, when it is considered that all our linen used
formerly to be sent to Holland, where they had acquired great dexterity
in the ancient mode of bleaching--viz., by exposure of the fabric to
atmospheric air or the action of the damps or dews, assisted greatly by
the agency of light. Some idea may be formed of the present value of
chlorine, when it is stated that the linen goods were retained by the
Dutch bleachers for nine months; and if the spring and summer happened
to be favourable, the operation was well conducted; on the other hand,
if cold and wet, the goods might be more or less injured by continual
exposure to unfavourable atmospheric changes. At the present time, as
much bleaching can be done in nine weeks as might formerly have been
conducted in the same number of months; and the whole of the process of
chlorine bleaching is carried on independent of external atmospheric
caprices, whilst the money paid for the process no longer passes to
Holland, but remains in the hands of our own diligent bleachers and
manufacturers.
_First Experiment._
[Illustration: Fig. 130. A. Flask containing the fuming hydrochloric
acid, which is gently boiled by the heat of the spirit lamp. B. Tube
passing to the Wolfe's bottle, containing pumice-stone or asbestos
moistened with sulphuric acid. C. Second tube passing into a dry empty
bottle, which receives the hydrochloric acid gas.]
As Scheele first indicated, chlorine is obtained by the action of the
black oxide of manganese, on "the Spirit of Salt," or hydrochloric acid;
and the most elementary and instructive experiment showing its
preparation can be made in the following manner:--
[Page 130]
Place in a clear Florence oil-flask, to which a cork and bent tube have
been first fitted, some strong fuming hydrochloric acid. Arrange the
flask on a ring-stand, and then pass the bent tube either to a Wolfe's
bottle containing some pumice-stone moistened with oil of vitriol, or to
a glass tube containing either pumice or asbestos wetted with the same
acid. Another glass tube, bent at right angles, passes away from the
Wolfe's bottle into a receiving bottle. (Fig. 130). On the application
of heat, the hydrochloric gas is driven off from its solution in water,
and any aqueous vapour carried up is retained by the asbestos or pumice
stone wetted with oil of vitriol; the application of the latter is
called _drying the gas_--i.e., depriving it of all moisture; sometimes
the salt called chloride of calcium is used for the same purpose, and it
must be understood by the juvenile chemist that gases are not dried like
towels, by exposure to heat, or _by putting them in bladders before the
fire_, as we once heard was actually recommended, but by causing the gas
charged with invisible steam to pass over some substance having a great
affinity for water. The dry hydrochloric gas falls into the bottle, and
displaces the air, being about one-fourth heavier than the latter, and
gradually overflowing from the mouth of the vessel, produces a white
smoke, which is found to be acid by litmus paper, but has no power to
bleach, and is not green; it is, in fact, a combination of one combining
proportion of chlorine with one of hydrogen, and to detach the latter,
and set the chlorine free, it is necessary to convey the hydrochloric
gas to some body which has an affinity for hydrogen. Such a substance is
provided in the use of the black oxide of manganese, which is placed
either in a small flask or in a tube provided with two bulbs, and when
heated with the lamp it separates the hydrogen from the hydrochloric
gas, and forms water, which partly condenses in the second bulb. And now
the gas that escapes is no longer acid and fuming with a white smoke on
contact with the air; but is green, has a strong odour, bleaches, and is
so powerful in its action on all living tissues, that it must be
carefully avoided and not inhaled; if a small quantity is accidentally
inhaled, it produces a violent fit of coughing, which lasts a [Page
131] considerable time, and is only abated by inhaling the diluted
vapour of ammonia, or ether, or alcohol, and swallowing milk and other
softening drinks. (Fig. 131.)
[Illustration: Fig. 131. A. The flask containing the fuming hydrochloric
acid, heated by spirit lamp. B. Tube passing to Wolfe's bottle,
containing the pumice-stone or asbestos wetted with oil of vitriol. C.
Second tube, which passes into a wide-mouthed small flask containing
black oxide of manganese, partly in powder and partly in lump; and the
third tube conveys the chlorine to any convenient vessel. The double
bulb tube, E E, may be substituted for the flask, the oxide of manganese
being contained in the bulb M.--N.B. Any tube may be joined on to
another by a bit of india-rubber tubing, which is tied by string.]
[Illustration: Tube A is joined to tube B by the caoutchouc pipe C, tied
with packthread.]
_Second Experiment._
The mode of preparing chlorine, as already given, though very
instructive, is troublesome to perform; a more simple process may
therefore be described:--
Pour some strong hydrochloric acid upon powdered black oxide of
manganese contained in a Florence oil-flask, taking care that the whole
of the black powder is wetted with the acid so that none of it clings to
the bottom of the flask in the dry state to cause the glass to crack on
the application of heat. A cork and bent glass tube is now attached, and
conveyed to the pneumatic trough; on the application of heat to the
mixture in the flask the chlorine is evolved, and may be collected in
stoppered bottles, the first portion that escapes, although it contains
atmospheric air, should be carefully collected in order to prevent any
[Page 132] accident from inhaling the gas, and it will do very well to
illustrate the bleaching power of the gas, and therefore need not be
wasted. The above process may be described in symbols, all of which are
easily deciphered by reference to the table of elements, page 86.
MnO_{2} + 2 HCl = MnCl + 2HO + Cl.
_Third Experiment._
Another and still more expeditious mode of preparing a little chlorine,
is by placing a small beaker glass, containing half an ounce of
chlorinated lime, usually termed chloride of lime or bleaching powder,
carefully at the bottom of a deep and large beaker glass, and then, by
means of a tube and funnel, conveying to the chloride of lime some
dilute oil of vitriol, composed of half acid and half water;
effervescence immediately occurs from the escape of chlorine gas, and as
it is produced it falls over the sides of the small beaker glass into
the large one, when it may be distinguished by its green colour. If a
little gas be dipped out with a very small beaker glass arranged as a
bucket, and poured into a cylindrical glass containing some dilute
solution of indigo, and shaken therewith, the colour disappears almost
instantaneously; and if a piece of Dutch metal is thrown into the beaker
glass it will take fire if enough chlorine has been generated, or some
very finely-powdered antimony will demonstrate the same result. Thus,
with a few beaker glasses, some chloride of lime, sulphuric acid, a
solution of indigo, and a little Dutch metal, the chief properties of
chlorine may be displayed. (Fig. 132.)
[Illustration: Fig. 132. A A. The large beaker glass. B. The small one,
containing the chloride of lime. C. The tube and funnel down which the
dilute sulphuric acid is poured. D D. Sheet of paper over top of large
glass, with hole in centre to admit the tube. E. The little beaker used
as a bucket.]
_Fourth Experiment._
Into a little platinum spoon place a small pellet of the metal sodium,
and after heating it in the flame of a spirit lamp, introduce the metal
[Page 133] into a bottle of chlorine, when a most intense and brilliant
combustion occurs, throwing out a vivid yellow light, and the heat is
frequently so great that the bottle is cracked. After the combustion,
and when the bottle is cool, it is usually lined with a white powder,
which will be found to taste exactly the same as salt, and, in fact, is
that substance, produced by the combination of chlorine, a virulent
poison, with the metal sodium, which takes fire on contact with a small
quantity of water; and hence the use of salt for the preparation of
chlorine gas when it is required on the large scale.
Parts.
Common salt 4
Black oxide of manganese 1
Sulphuric acid 2
Water 2
_Fifth Experiment._
Some Dutch metal, or powdered antimony, or a bit of phosphorus,
immediately takes fire when introduced into a bottle containing chlorine
gas, forming a series of compounds termed chlorides, and demonstrating
by the evolution of heat and light, the energetic character of chlorine,
and that oxygen is not the only supporter of combustion; chlorine gas
has even, in some cases, greater chemical power, because some time
elapses before phosphorus will ignite in oxygen gas, whilst it takes
fire directly when placed in a bottle of chlorine.
_Sixth Experiment._
The weight and bleaching power of chlorine are well shown by placing a
solution of indigo in a tall cylindrical glass, leaving a space at the
top of about five inches in depth. By inverting a bottle of chlorine
over the mouth of the cylindrical glass, it pours out like water, being
about two and a half times heavier than atmospheric air, and then, after
placing a ground glass plate over the top of the glass, the chlorine is
recognised by its colour, whilst the bleaching power is demonstrated
immediately the gas is shaken with the indigo solution.
_Seventh Experiment._
As a good contrast to the last experiment, another cylindrical jar of
the same size may be provided, containing a solution of iodide of
potassium with some starch, obtained by boiling a teaspoonful of
arrowroot with some water; any chlorine left in the bottle (sixth
experiment) may be inverted into the top of this glass and shaken, when
it turns a beautiful purple blue in consequence of the liberation of
iodine by the chlorine, whose greater affinity for the base produces
this result. The colour is caused by the union of the iodine and the
starch, which form together a beautiful purple compound, and thus the
apparent anomaly of destroying and producing colour with the same agent
is explained.
[Page 134]
_Eighth Experiment._
Dry chlorine does not bleach, and this fact is easily proved by taking a
perfectly dry bottle, and putting into it two or three ounces of fused
chloride of calcium broken in small lumps, then if a bottle full of
chlorine is inverted over the one containing the chloride of calcium,
taking the precaution to arrange a few folds of blotting paper with a
hole in the centre on the top of the latter to catch any water that may
run out of the chlorine bottle at the moment it is inverted, the gas
will be dried by contact with the chloride of calcium, and if a piece of
paper, with the word chlorine written on it with indigo, and previously
made hot and dry, is placed in the chlorine, no change occurs, but
directly the paper is removed, dipped in water, and placed in a bottle
of damp chlorine, the colour immediately disappears. (Fig. 133.)
[Illustration: Fig. 133. A A. Dry bottle, containing chloride of
calcium. B. Bottle of chlorine. The arrow indicates the gas. C C. The
blotting-paper, to catch any water from the bottle, B. D. The bottle
closed, and containing the paper.]
This experiment shows that chlorine is only the means to the end, and
that it decomposes water, setting free oxygen, which is supposed to
exert a high bleaching power in its _nascent_ state, a condition which
many gases are imagined to assume just before they take the gaseous
state, a sort of intermediate link between the solid or fluid and the
gaseous condition of matter. The nascent state may possibly be that of
ozone, to which we have already alluded as a powerful bleaching agent.
_Ninth Experiment._
A piece of paper dipped in oil of turpentine emits a dense black smoke,
and frequently a flash of fire is perceptible, directly it is plunged
into a bottle containing chlorine gas; here the gas combines only with
the hydrogen of the turpentine, and the carbon is deposited as soot.
_Tenth Experiment._
If a lighted taper is plunged into a bottle of chlorine it continues to
burn, emitting an enormous quantity of smoke, for the reason already
explained, and demonstrating the perfection of the atmosphere in which
[Page 135] we live and breathe, and showing that had oxygen gas
possessed the same properties as chlorine, the combustion of compounds
of hydrogen and carbon would have been impossible, in consequence of the
enormous quantity of soot which would have been produced, so that some
other element that would freely enter into combination with it must have
been provided to produce both artificial light and heat. Chlorine is a
gas which cannot be inhaled, and ozone presents the same features, as a
mouse confined for a short time with an excess of ozone soon died; but
ozone is the extraordinary condition of oxygen; the element in the
ordinary state is harmless, and is the one which enters so largely into
the composition of the air we breathe.
_Eleventh Experiment._
When one volume of olefiant gas (prepared by boiling one measure of
alcohol and three of sulphuric acid) is mixed with two volumes of
chlorine, and the two gases agitated together in a long glass vessel for
a few seconds, with a glass plate over the top, which should have a welt
ground perfectly flat, they unite on the application of flame, with the
production of a great cloud of black smoke, arising from the deposited
carbon, whilst a sort of roaring noise is heard during the time that the
flame passes from the top to the foot of the glass. (Fig. 134.)
[Illustration: Fig. 134. Remarkable deposition of carbon during the
combustion of one volume of olefiant gas with two of chlorine.]
_Twelfth Experiment._
Formerly Bandannah handkerchiefs were in the highest estimation, and no
gentleman's toilet was thought complete without one. The pattern was of
the simplest kind, consisting only of white spots on a red or other
coloured ground. These spots were produced in a very ingenious manner by
Messrs. Monteith, of Glasgow, by pressing together many layers of silk
with leaden plates perforated with holes; a solution of chlorine was
then poured upon the upper plate, and pressure being applied it
penetrated the whole mass in the direction of the holes, bleaching out
the colour in its passage. This important commercial result may be
imitated on the small scale by placing a piece of calico dyed with
Turkey red between two thick pieces of board, each of which is [Page
136] perforated with a hole two inches in diameter, and corresponding
accurately when one is placed upon the other. The pieces of board may be
squeezed together in any convenient way, either by weights, strong
vulcanized india-rubber bands or screws, and when a strong solution of
chlorine gas or of chloride of lime is poured into the hole and
percolates through the cloth, the colour is removed, and the part is
bleached almost instantaneously by first wetting the calico with a
little weak acid, and then pouring on the solution of chloride of lime.
On removing and washing the folded red calico it is found to be bleached
in all the places exposed to the solution, and is now covered with white
spots. (Fig. 135.)
[Illustration: Fig. 135. A. Circular hole in the upper piece of wood, a
similar one being perforated in the lower one. B B. The strong
india-rubber bands. The bleaching solution is poured into A.]
IODINE.
Iodine ([Greek: _Iôdês_], violet coloured). Symbol, I; combining
proportion, 127.1; specific gravity, 4.948. Specific gravity of iodine
vapour, 8.716.
In the previous chapter, devoted to the element chlorine, little or
nothing has been said of that inexhaustible storehouse of chlorine,
iodine, and bromine--viz., the boundless ocean. Some one has remarked
that, as it is possible the air may contain a little of everything
capable of assuming the gaseous form, so the ocean may hold in a state
of solution a modicum of every soluble substance, in proof of which we
have lately read of some very important experiments resulting in the
separation of the metal silver from sea water, not certainly in any
profitable quantity, but quite enough to prove its presence in the
ocean.
No elaborate research is necessary to ascertain the presence of
chlorine, when it is remembered that Schafhäutl has calculated, that all
the oceans on the globe contain three millions fifty-one thousand three
hundred and forty-two cubic geographical miles of salt, or about five
times more than the mass of the Alps.
Now, salt contains about 60 per cent. of chlorine gas, and therefore the
bleachers can never stand still for want of it; but iodine is not so
plentiful, and was discovered by M. Courtois, of Paris, in _kelp_, a
substance from which he prepared carbonate of soda, or washing soda; but
as this is now more cheaply prepared from common salt, the kelp is at
present required only for the iodine salts it contains, as also for the
chloride of potassium. Kelp is obtained by burning dried sea-weeds in a
[Page 137] shallow pit; the ashes accumulate and melt together, and this
fused mass broken into lumps forms kelp. The ocean bed no doubt has its
fertile and barren plains and mountains, and amongst the so-called
"oceanic meadows" are to be mentioned the two immense groups and bands
of sea-weed called the Sargasso Sea, which occupy altogether a space
exceeding six or seven times the area of Germany.
The iodine is contained in the largest proportion in the deep sea
plants, such as the long elastic stems of the fucus palmatus, &c. The
kelp is lixiviated with water, and after separating all the
crystallizable salts, there remains behind a dense oily-looking fluid,
called "iodine ley," to which sulphuric acid is added, and after
standing a day or two the acid "ley" is placed in a large leaden retort,
and heated gently with black oxide of manganese. The chlorine being
produced very slowly, liberates the iodine, as already demonstrated in
experiment seven, p. 133, and it is collected in glass receivers.
Iodine, when quite pure and well crystallized, has a most beautiful
metallic lustre, and presents a bluish-black colour, affording an odour
which reminds one at once of the "sea smell."
_First Experiment._
A few grains of iodine placed in a flask may be sublimed at a very
gentle heat, and afford a magnificent violet vapour, which can be poured
out of the flask into a warm bottle. If the bottle is cold the iodine
condenses in minute and brilliant crystals. (Fig. 136.)
[Illustration: Fig. 136. A. Flask containing iodine heated by spirit
lamp. B. Cold flask above to receive the vapour. C C. Sheet of cardboard
to cut off the heat from the spirit lamp.]
_Second Experiment._
Upon a thin slice of phosphorus place a few small particles of iodine;
the heat produced by the combination of the two elements soon causes the
phosphorus to take fire.
_Third Experiment._
Heat a brick, and then throw upon it a few grains of iodine; by holding
a sheet of white paper behind, the splendid violet colour of the vapour
is seen to great advantage. It was by the discovery of iodine in the
ashes of sponge--which had long been used as a remedy for goitre, a
remarkable glandular swelling--that this element began to be used for
medical purposes, and the important salt called iodide of potassium is
now used in large quantities, not only in medicine, but likewise for
that most fascinating art, which has made its way steadily, and is now
practised so extensively, under the name of _photography_.
[Page 138]
THE ART OF PHOTOGRAPHY.
It was the great George Stephenson who asked the late Dean Buckland the
posing question, "Can you tell me what is the power that is driving that
train?" alluding to a train which happened to be passing at the moment.
The learned dean answered, "I suppose it is one of your big engines."
"But what drives the engine?" "Oh, very likely a canny Newcastle
driver." "What do you say to the light of the sun?" "How can that be?"
asked Buckland. "It is nothing else," said Stephenson. "It is light
bottled up in the earth for tens of thousands of years; light, absorbed
by plants and vegetables, being necessary for the condensation of carbon
during the process of their growth, if it be not carbon in another form;
and now, after being buried in the earth for long ages in fields of
coal, that latent light is again brought forth and liberated, made to
work--as in that locomotive--for great human purposes."
Such was the opinion of the most original and practical man that ever
reasoned on philosophy; and could he have lived to realize the thorough
adaptation and business use of light in the art of photography, he would
have said, man is only imitating nature, and in producing photographs he
must employ the same agent which in ages past assisted to produce the
coal.
In another part of this elementary work we shall have to consider the
nature of light; here, however, the chemical part only of the process of
photography will be discussed.
Many years ago (in the year 1777) Jenny Lind's most learned countryman,
Scheele, discovered that a substance termed chloride of silver, obtained
by precipitating a solution of chloride of silver with one of salt,
blackened much sooner in the violet rays than in any other part of the
spectrum. He says, "Fix a glass prism at the window, and let the
refracted sunbeams fall on the floor; in this coloured light put a paper
strewed with luna cornua (horn silver or chloride of silver), and you
will observe that this horn silver grows sooner black in the violet ray
than in any of the other rays."
In 1779, Priestley directed especial attention to the action of light on
plants; and the famous Saussure, following up these and other
experiments, determined that the carbonic acid of plants was more
generally decomposed into carbon and oxygen in the blue rays of the
spectrum; these facts probably suggested the bold theory of Stephenson
already alluded to. Passing by the intermediate steps of photography, we
come to the second year of the present century, and find in the Journal
of the Royal Institution a paper by Wedgwood, entitled "An Account of a
Method of Copying Paintings upon Glass, and of making Profiles, by the
Agency of Light upon Nitrate of Silver; with observations, by H. Davy."
Such a paper would lead the reader to suppose that very little remained
to be effected, and that mere details would quickly establish the art;
but in this case the experimentalists were doomed to [Page 139]
disappointment, as, after producing their photographs, they could not
make them permanent; they had not yet discovered the means of _fixing_
the pictures. Nearly fourteen years elapsed, when the subject was again
taken up by Niépcè, of Chalons, with little success, so far as the
fixing was concerned; and twenty-seven years had passed away since the
experiments of Wedgwood and Davy, when, in 1829, Niépcè and Daguerre
executed a deed of co-partnership for mutually investigating the matter.
These names would suggest a rapid progress; but, strange to relate, ten
years again rolled away, the father Niépcè had in the meantime died, and
a new contract was made between the son and M. Daguerre, when, in
January, 1839, the famous discovery was made known to the world, and in
July of the same year the French Government granted a pension for life
of six thousand francs to Daguerre, and four thousand to the son of
Niépcè, who had so worthily continued the experiments commenced by his
father. The triumph of the industrious French experimentalists was not,
however, to be unique; across the Channel another patient and laborious
philosopher had completed on paper precisely the same kind of results as
those obtained by Daguerre on silver plates. Mr. Fox Talbot, in England,
had immortalized himself by a discovery which was at once called the
Talbotype, and for which a patent was secured in 1841. Having thus
hastily sketched a brief history of the art, we may now proceed to the
details of the process.
_First Experiment._
A photogenic drawing, so called, but now termed _a positive copy_, is
prepared by placing some carefully selected paper, which is free from
spots or inequalities (good paper is now made by several English
manufacturers, although some kinds of French paper, such as Cansan's,
are in high repute), in a square white hard porcelain dish containing a
solution of common salt in distilled water, 109 grains of salt to the
pint. The paper is steeped in this solution for ten minutes, and then
taken out and pressed in a _clean_ wooden press, or it should be dabbed
dry on a _clean_ flat surface with a _clean_ piece of white calico,
which may be kept specially for this duty and not used for anything
else, and it is well that all would-be photographers should understand
that neatness and cleanliness are perfectly indispensable in conducting
these processes. If a design were required for the armorial bearings of
the art of photography, it might certainly be most fanciful, but the
motto must be _cleanliness_ and _neatness_, and in preparing paper it
should not be unnecessarily handled, but lifted by the corners only. The
object of dabbing the paper is to prevent the salt accumulating in large
quantities in one part of the paper and the reverse in another, and to
distribute the salt equally through the whole. The paper being now
dried, is called salted paper, and is rendered sensitive when required
by laying it down on a solution of ammonio-nitrate of silver, prepared
by adding ammonia to a solution containing sixty grains of nitrate of
silver to the ounce of distilled water, until the whole of the oxide of
silver is re-dissolved, except [Page 140] a very small portion. A few
drops of nitric acid are also recommended to be added, and after
allowing the solution to stand, it may be poured off quite clear, and is
ready for use either in the bath, or if economy must be rigidly adhered
to, the salted paper may be laid flat on a board, and held in its place
with four pins at the corners, and then just enough to wet the surface
of the paper may be run along the side of a glass spreader, and the
liquid gently drawn over the surface of the salted paper, which is
allowed to dry on a flat surface for a few minutes, and afterwards hung
up by one corner to a piece of tape stretched across the room, until
quite dry, and then placed in a blotting-book fitting into a case which
completely excludes the light. Copying-paper should be made at night, as
the day is then free for all photographic operations requiring an
abundance of light. It will not keep long, and should be used the next
day.
[Illustration: Fig. 137. A. The glass spreader with cork handle. B. The
silver solution clinging to rod and paper by capillary attraction. C C C
C. Four pins holding down the paper on a board.--N.B. The spreader is
made of glass rod three-eighths thick.]
A piece of lace, a skeleton leaf, a sharp engraving on thin paper, and
above all things, a negative photograph on glass or paper, is easily
copied by placing the prepared paper with the prepared side (carefully
protected from the light) upwards on any flat surface, such as plate
glass; upon this is arranged the bit of lace or the negative photograph
with the face or picture downwards, another bit of plate glass is then
placed over it, and weights arranged at the corners; after exposure to
the sun's rays for thirty minutes, more or less (according to the
dullness or bright aspect of the day), the picture is brought into a
dark room and examined by the light of a candle or by the light from a
window covered with yellow calico, and after placing a paper weight on
one corner of the lace, or [Page 141] negative picture, or copying
paper, it may be carefully lifted in one part, and if the copy is
sufficiently dark, is ready for fixing, but if it is faint the lifted
corner is carefully replaced, the upper glass is laid on, and the
picture again exposed to the light. Should the position of the lace or
negative be changed during the examination, re-exposure is useless, and
would only produce a double and confused picture, as it would be
impossible to lay the lace or the negative exactly in the same place
again on the copying paper.
The manipulations just described are much facilitated by using a
copying-frame or press, which consists of a square wooden frame with a
thick plate-glass window; upon this are placed the negative picture and
the copying paper, and the two are brought in close contact by means of
a board at the back pressed by a hand-screw. (Fig. 138.) After the
photogenic drawing or positive copy is taken, it is fixed by being
placed in a solution of hyposulphite of soda, consisting of one fluid
ounce of saturated solution to eight of water. The saturated solution of
hyposulphite of soda is conveniently kept in a large bottle for use, and
in order to improve the colour a very little chloride of gold is added
to the fixing solution, the picture must now be thoroughly washed,
dried, and pressed.
[Illustration: Fig. 138. The back of the copying-frame, showing the
hand-screw and pressure-board. The plate glass inside is set in the base
of the frame, and is of course the part exposed to the light.]
_Second Experiment._
Another mode of preparing the copying paper, called albumen paper, is to
take the whites of four eggs, and four ounces of distilled water
containing one hundred and sixty grains of chloride of ammonium; these
are beaten up with a fork or a bundle of feathers, and as the froth is
produced it is skimmed off by a silver spoon into another basin, or a
beaker glass, and being allowed to settle for twelve hours it is
strained through fine muslin, and is ready for use. The best paper is
floated on the surface of this liquid for three minutes, taken out, and
dried at once on a hot plate.
In floating paper one corner is first laid down, and care taken not to
enclose any air bubbles, which would prevent the fluid wetting the
paper, whilst the remainder of the paper is slowly laid upon the surface
of the fluid.
The albumen paper is excited by laying it for five minutes on a solution
of nitrate of silver, seventy-two grains to the ounce of water, [Page
142] and when dry it will keep for three days. This copying paper is
used in the same manner as the last, and fresh eggs only must be used in
its preparation, because stale ones soon cause the copy to change and
blacken all over from the liberation of sulphur, which unites with the
silver. The colour of the copy is sometimes improved by a solution of
hot potash, and by dipping the well-washed picture, after the use of the
hyposulphite of soda, in a very dilute solution of hydrosulphuret of
ammonia.
_Third Experiment._
In the Daguerreotype process, a silver plate, after being thoroughly
cleaned and polished, is exposed to the vapour of iodine, and is thus
rendered so sensitive that it may be at once exposed in the camera. In
the Talbotype process, the same principle is apparent, and paper is
prepared by first covering its surface with iodide of silver, which is
afterwards rendered sensitive to the action of light by means of an
excess of nitrate of silver, as follows:--
One side of a sheet of selected Cansan's paper is first covered (by
means of a spreader) with a solution of nitrate of silver (thirty grains
to the ounce of water), hung up in a dark room and dried; it is then
immersed in a solution of iodide of potassium of five hundred grains to
a pint of distilled water, for five or ten minutes, and immediately
changes to a yellow colour in consequence of the precipitation of the
yellow iodide of silver; it is then well washed with plenty of water,
and being dried, may be kept for any length of time, and is called
"iodized paper." Light has no action whatever upon it. To render the
paper sensitive, three solutions are prepared in separate bottles, and
marked 1, 2, 3.
No. 1, contains a solution of nitrate of silver, fifty grains to the
ounce of water.
No. 2, glacial acetic acid.
No. 3, a saturated solution of gallic acid.
With respect to No. 3, Mr. William Crookes has shown, that when a
saturated solution of gallic acid is required in large quantities, that
it is better to dissolve at once two ounces of gallic acid in six ounces
of alcohol (60° over proof); to hasten solution, the flask may be
conveniently heated by immersion in hot water; when cold it should be
filtered, mixed with half a drachm of glacial acetic acid, and preserved
in a stoppered bottle for use; so prepared it will keep unaltered for a
considerable length of time. The gallic acid is not precipitated from
this solution by the addition of water; consequently, if in any case
desirable, the development of a picture may be effected with a much
stronger bath than the one usually employed. To obtain a solution of
about the same strength as a saturated aqueous solution, such as No. 3,
half a drachm of the alcoholic solution is mixed with two ounces of
water; but for my particular purpose, says Mr. Crookes, referring to the
wax-paper process, "I prefer a weaker bath, which is prepared by mixing
half a drachm with ten ounces of water." In either case it [Page 143]
will be found necessary to add solution of nitrate of silver in small
quantities, as the developing picture seems to require it.
Returning again to the solutions marked 1, 2, 3, the numbers will assist
the memory in mixing the proportions of each. If the paper is required
to be used _at once_, a drachm of each may be mixed together and spread
over the iodized paper (of course, in a dark room), which is then
transferred to a clean blotting-book of white bibulous paper, and being
placed in the paper-holder may be taken to the camera and exposed at
once. If the paper is not required to be used immediately, the solutions
are mixed in the proportions of the numbers--viz., one of No. 1, two of
No. 2, three of No. 3; and in making the mixture, it is advisable to
keep a measure specially for No. 3, the gallic acid, or else the
measure, if used for the three solutions, will have to be washed out
every time, which is very troublesome, particularly where water is not
plentiful.
If the excited paper is required to be kept some hours before use, No. 3
must be added in still larger proportion, as much as ten or even twenty
measures of No. 3 to two of No. 2, and one of No. 1, being used, and
even this large dilution is frequently insufficient to prevent the paper
spoiling in hot weather; therefore if the temperature is high, too much
reliance must not be placed on this paper, as it is peculiarly
disappointing, after walking some miles to romantic and beautiful
scenery, to find, when developing the pictures in the evening, that the
paper used was all spoilt before exposure; and it will be seen presently
that when the excited paper is to be carried about for use, it is better
to adopt the wax-paper process.
After the excited iodized paper is exposed in the camera--and the time
of exposure cannot be taught, as that speciality is only acquired by
experience, and may vary from five to thirty minutes, or even more--the
invisible picture is developed and rendered visible, not by exposure to
the vapour of mercury, as in Daguerre's process with silver plates, but
by a mixture of one of No. 1 with four of No. 3. The development is
carefully watched by looking through the negative placed before a
lighted candle, and the time of development may vary from ten to thirty
minutes, and all the time the picture must be kept wet with the
solution, so that it is better perhaps to make a bath of the solution
and lay the picture on its surface than to pour the liquid over the
picture. After the development is matured, the picture is now washed in
clean water, and fixed temporarily, if required, by immersion in a bath
containing 200 grains of bromide of potassium in one pint of water, or
permanently by the hyposulphite of soda, made by mixing one part of a
saturated solution with five or ten of water, or one ounce of the salt
to six or twelve of water; but, as before mentioned, it is better to
keep a Winchester quart full of a saturated solution of hyposulphite of
soda, and then it is always ready for use instead of employing the
weights and scales, and continually weighing out portions of the salt.
The picture after fixing is thoroughly washed with water, and being
[Page 144] dried is now placed between the folds of a wax book--_i.e._,
some leaves of blotting-paper are kept saturated with white wax, and
when a picture is placed between them, and a hot iron passed over the
outside sheet, the wax enters the pores of the paper, and after removing
any excess of wax by passing the picture through a book of bibulous
paper, over which the hot flat iron is passed, the negative picture at
last is ready for use, and any number of positive copies may be taken
from it, as already described in the first experiment, page 139.
This mode of manipulation is called the Talbotype, and before dismissing
the subject another process of iodizing the paper may be explained.
To a solution of nitrate of silver of twenty, thirty, or fifty grains to
the ounce of water, a sufficient number of the crystals of iodide of
potassium is added, first to produce the yellow iodide of silver, and
then to dissolve it, so that the yellow precipitate appears with a small
quantity, and disappears with an excess of the iodide. If this solution
is spread over sheets of paper, and these latter then placed in a bath
of water, the iodide of silver is precipitated on the surface, and after
plenty of washing to remove the excess of iodide of potassium, the paper
may be dried, and will keep for any length of time without change. This
paper may be excited, exposed, developed, fixed, and waxed, as already
explained.
_Fourth Experiment. The Wax-paper Process._
This mode of taking negative photographs begins where the talbotype
ends--viz., by _first_ waxing the paper perfectly and evenly, as already
explained, Cansan's negative paper being preferred. The wax paper is now
well soaked in a bath, made by dissolving one hundred grains of iodide
of potassium, six grains of cyanide of potassium, four grains of
fluoride of potassium, ten grains of bromide of potassium, ten grains of
chloride of sodium, in one pint of fresh whey, with the addition of a
little alcohol and a few grains of iodine. When soaked in this solution
for about one hour, the paper is taken out and hung up to dry.
N.B. With respect to iodizing the wax paper, it is almost better to
obtain it ready prepared, and then every sheet may be relied on. Mr.
Melhuish, of Blackheath and Holborn, supplies it in any quantity, and
his paper never fails; the operator has then only to perform the
sensitizing and developing processes. To render the iodized paper
sensitive it is immersed for about six minutes in a bath containing a
solution of nitrate of silver (thirty-five grains to the ounce of water,
with forty drops of glacial acetic acid); the paper is now removed, and
washed in two trays of common clear rain-water or distilled water, and
is then dried off between folds of blotting-paper.
This process may be performed on the previous evening by the light of a
candle, or by day in a room lit by one window covered with four
thicknesses of yellow calico, and after the paper is dry it will keep
for three [Page 145] weeks or a month, and may be exposed in a camera
with a three-inch lens of eighteen-inch focus, with the inch diaphragm,
on a bright day from five to fifteen minutes; in bad weather the
exposure must be longer. The picture may be carried home and rendered
visible or developed by immersion in a bath containing a saturated
solution of gallic acid, and as the developing continues, a few drops of
the sensitizing solution of nitrate of silver and glacial acetic acid
may be added. Finally, the picture is fixed by immersion for a quarter
of an hour in a solution of hyposulphite of soda (four ounces of the
crystal to one pint of water, or one part of the saturated solution to
eight of water), and being well washed, is then dried, hung before the
fire to melt the wax, and is now ready to print from.
_Fifth Experiment. Albumen on Glass Process._
Albumen is the scientific name for the white of egg, of which four
ounces by measure are mixed with one ounce and a half of distilled
water, and after being whisked to a froth, are removed by a spoon into
another basin or a beaker glass, and allowed to stand for several hours
and then filtered. Mr. Crookes has recommended a very ingenious, simple,
and useful filter. (Fig. 139.) He says: "This simple and inexpensive
piece of apparatus, which any instrument maker or glass-blower can
supply at a few hours' notice, will be found invaluable in almost every
photographic process on glass. The sponge has this great advantage over
all other kinds of filters, that thick gelatinous liquids--_e.g._,
honey, albumen, gelatine, meta-gelatine, or the various preservative
syrups--flow through it with the utmost readiness; whilst at the same
time dust, air bubbles, or froth, and dried particles floating in the
liquid, are effectually kept back, and if fitted with stoppers,
collodion might be filtered in it; or if the ends were fitted together
with a bit of flexible pipe, the stoppers might be dispensed with
altogether.
[Illustration: Fig. 139. A B. Glass tube, bent as in picture. C. Piece
of damp sponge squeezed into the head of the tube. Any liquid poured in
at B will flow through the sponge until it has attained the same level
in A.]
Having poured the albumen on a perfectly clean glass plate, taking care
to have sufficient to run freely over the surface of the glass, the
excess is then gently drained off and the plate turned so as to have the
coated side downwards; it is then fixed in a sling made by taking a
stout bit of string about three feet long, which is doubled and knotted
at the fold, leaving the two ends free; two small triangles or stirrups
of silver wire looped at one corner are now tied on to the ends of the
string, and these form a support for the opposite edges of the glass
plate to rest on; the two strings are knotted together at a [Page 146]
convenient distance from the stirrups to prevent the glass slipping out,
and the plate is now rotated rapidly over a heated metallic surface,
such as an iron box containing some burning charcoal or the _warming
pan_, care being taken to avoid dust as much as possible, and to use
only the whites of new-laid eggs. (Fig. 140.) The glass plate, covered
with dry albumen, is now iodized to a straw colour by exposure over a
box containing iodine, as in the Daguerreotype process, and is
sensitized by immersion for three or four minutes in a bath containing a
solution of nitrate of silver (twenty-five grains to an ounce of water);
the plate is afterwards washed in distilled water and left to dry
spontaneously, of course in a darkened room. The plates may then be
placed ready for use in a very ingenious tin box devised by Mr. Crookes,
which keeps them perfectly light-tight even in the sun, and at the same
time is less bulky than the ordinary wooden ones. It is made of tin
plate, the cover sliding tight over the top, and more than half way down
the sides; light is further excluded by means of an outer jacket of tin,
which is soldered to the box a little below the centre. The cover thus
slides between the case and the jacket, and renders injury to the plates
by the entrance of light an impossibility. (Fig. 141.)
[Illustration: Fig. 140. A. Loop for finger. B. The knot which prevents
the stirrups of silver wire, C C, slipping off the corners of the glass
plate. D D. The opposite corners of the glass plate on which the
stirrups are placed.]
[Illustration: Fig. 141. A A. Tin box, with partitions to hold glass
plates, B B. The outer jacket, between which and the box, A, the lid or
cover, C, slides.]
The sensitive albumenized glass plate is exposed in the camera from
fifteen to thirty minutes, and developed (much in the same way as the
paper pictures) with one ounce of a saturated [Page 147] solution of
gallic acid containing ten or fifteen drops of the sensitizing solution.
The plate is usually placed on a levelling stand, and the solution
poured on the glass plate; the development is slow, and may be quickened
sometimes by the application of heat.
The picture is fixed by immersion for a short time in a bath containing
one part of a saturated solution of hyposulphite of soda in eight of
water. The pictures produced by this process are exquisitely defined,
provided always the camera is well focussed, and to assist this
operation a magnifying glass may be employed. After removal from the
hyposulphite of soda the plate is well washed with water, and being
allowed to dry spontaneously, is now ready to print from.
_Sixth Experiment. The Collodion on Glass Process._
The glass plates for this, as well as the albumen on glass process,
should be cleaned by rubbing them over first with a mixture of Tripoli
powder and ammonia, which is washed off under a tap, and the glass being
drained is rubbed dry and polished with a clean calico duster kept
exclusively for this purpose.
The iodized collodion is now poured on, and the excess returned to the
bottle. Collodion can be made very easily, but if prepared without due
precautions, it cannot be used afterwards, and reminds one of the old
story of the enthusiastic son, who, when asking his father's permission
to espouse the beloved, enumerated amongst her other accomplishments,
the fact that she _could_ make a pudding, and was answered by the bluff
question, "But can you eat it afterwards?" So it is with collodion: a
great deal of messing and loss of time is saved by purchasing it of the
various makers, amongst whom may be specially noticed Mr. Richard
Thomas, of 10, Pall Mall, who has devoted the whole of his attention to
the preparation of this important photographic chemical, and with a
success which his numerous patrons can well testify. The collodion is
sold either mixed with the iodizing solution, or the two can be obtained
separately, with directions on the bottles as to the quantities to be
mixed together.
The plate covered with the iodized collodion is quickly transferred to a
bath containing a solution prepared in the following manner:--Dissolve
four ounces of nitrate of silver in eight ounces of water, and to this
add twenty grains of iodide of potassium in one ounce of water; shake
them together, and then pour the whole into fifty-six ounces of
distilled water, and in half an hour add one ounce of alcohol and half
an ounce of ether; agitate the whole and filter the next morning. The
collodion plate is kept in this solution for a certain period, only
learnt by experience, and should be occasionally lifted out to see if a
uniform transparency is obtained; say that the immersion may be
continued for five minutes, it is now ready for the camera, and may be
exposed from about one to two minutes, or more if the light is
deficient; the time of exposure is also a matter of _practice_, mere
directions can be of no use in this stage of the process.
The picture is developed on a levelled stand, with a solution of three
[Page 148] grains of pyrogallic acid in three ounces of water, to which
sixty drops of glacial acetic acid have been added. When fully developed
the plate is washed with water and fixed with a solution of hyposulphite
of soda, consisting of one part of the saturated solution to eight of
water, again thoroughly but gently washed, so as not to endanger the
separation of the film from the glass; it is allowed to dry
spontaneously, and being coated with amber varnish (a solution of amber
in chloroform) is now ready to print from. (Fig. 123.) It is, perhaps,
hardly necessary to add, that the sensitizing and developing processes
must be performed in a dark room.
[Illustration: Fig. 142. A. Glass or gutta-percha bath to hold the
sensitizing solution. B. Glass, with piece cemented on the end to hold
the prepared glass plate, C, whilst dipped in the bath, A. The plate C
has a cross in one corner to show prepared side.]
[Illustration: Fig. 143. First effect of peripatetic photography on the
rural population.]
[Page 149]
BROMINE.
Bromine ([Greek: _brômos_], a bad odour). Symbol, Br. Combining
proportion, 80. Specific gravity, 2.966.
In a previous portion of this work, the connexion between chlorine,
iodine, and bromine has been pointed out; and as we have to notice the
colour of the element bromine, the chromatic union of the triad may be
alluded to. These elements present very nearly all the colours of the
spectrum:
Bromine red to orange.
Chlorine yellow to green.
Iodine blue, indigo, violet.
These three elements also furnish examples of the three conditions of
matter; iodine being a solid, bromine a fluid, chlorine a gas; the
relation of their combining proportions is also curious: as might be
expected, the fluid bromine takes an intermediate position, and
(according to the axiom that half the sum of the extremes is equal to
the mean) by dividing the combining proportions of iodine and chlorine,
and adding them together, we have, as nearly as possible, the combining
proportion of bromine:
Chlorine 35 ÷ 2 = 17.75
Iodine 126 ÷ 2 = 63
-----
80.75
The combining proportion of bromine is 80, but 80.75 is so near, that it
may reasonably be conjectured future experiments will reduce the number
of the three elements, and may prove that they are only modifications of
a single one. This is the only kind of alchemy which is tolerated in the
nineteenth century, and any philosopher who will reduce the number of
elements, and prove that some of them are only modifications of others,
will achieve a renown that must transcend the _éclat_ of all previous
discoverers.
Bromine was discovered by Balard, in 1826, and, like chlorine and
iodine, is a constituent of sea water. The chief source of bromine is a
mineral spring at Kreutznach, in Germany. The process by which it is
obtained offers a good example of chemical affinity; the water of the
mineral spring is evaporated, all crystallizable salts removed, and a
current of chlorine gas passed through the remaining solution, which
changes to a yellow colour, in consequence of the liberation of the
bromine by the combinations of chlorine with the bases previously united
with the former; the liquid is then shaken with ether, which dissolves
out the bromine. In the next place, the etherial solution is agitated
with strong solution of potassa, and is thus obliged to part with the
bromine which is converted into bromate of potassa; this is ultimately
changed by fusion to bromide of potassium; and by distillation with
black oxide of manganese and sulphuric acid, the bromine is finally
obtained. Six [Page 150] processes are therefore necessary before the
small quantity of bromine contained in the mineral spring-water, is
separated.
_First Experiment._
Bromine is a very heavy fluid, which should be preserved by keeping it
in a bottle covered with water; when required, a few drops may be
removed by means of a small tube, and dropped into a warm bottle, which
is quickly filled with the orange-red vapour. If some phosphorus is
placed in a deflagrating spoon, and exposed to the action of bromine
vapour, it takes fire spontaneously.
_Second Experiment._
Powdered antimony sprinkled into the vapour of bromine immediately takes
fire.
_Third Experiment._
A burning taper immersed in a bottle containing the vapour of bromine is
gradually extinguished.
_Fourth Experiment._
Liquid bromine exposed to a freezing mixture of ice and salt, or reduced
to a temperature of about eight degrees below zero, solidifies into a
yellowish-brown, brittle, crystalline mass.
_Fifth Experiment._
A solution of indigo shaken with a small quantity of the vapour of
bromine is quickly bleached. Many substances, when brought in contact
with liquid bromine, combine with explosive violence, and therefore
experiments with liquid bromine are not recommended, as all the most
instructive and conclusive results can be obtained by the use of the
vapour of bromine, which is easily procured by allowing a few drops to
fall into a warm, dry bottle.
Bromine, as already mentioned, is used in the art of photography.
FLUORINE.
Symbol, F. Combining proportion, 19.
This singular element seems almost to embody the ancient idea of the
alchemists, being a sort of _alkahest_, or universal solvent; or in
plainer language, its affinities for other bodies are so powerful, that
it attacks every substance (not even excepting gold), at the moment of
its liberation, and combines therewith, so that its isolation has not
yet been effected. Chemists who assert that they have been able to
obtain fluorine in the elementary condition, pronounce it to be a gas
which possesses the colour of chlorine; but the experiments, as hitherto
conducted, render that statement extremely doubtful.
[Page 151]
The only interesting fact connected with fluorine, is the remarkable
property of attacking glass and other silicious bodies, belonging to its
combination with hydrogen gas, called hydrofluoric acid. This acid is
easily obtained and used by placing some powdered fluorspar in a leaden
tray six inches square and two inches deep. If sulphuric acid is now
mixed with the powdered spar, so as to form a thin paste, and heat
applied, the vapour of the hydrofluoric acid quickly rises, and can be
employed to etch a glass plate upon which a drawing may have been
previously traced by scratching away the wax, with which it is first
coated. By heating the glass plate before a fire, a sufficient quantity
of wax is soon melted on to it by merely rubbing the wax against the
glass plate; any excess should be avoided, if a well-executed drawing is
required to be etched on its surface. (Fig. 144.)
[Illustration: Fig. 144. A A A. The glass plate, with the waxed side
downwards, placed on the leaden tray containing the fluorspar and
sulphuric acid. B. Spirit lamp.]
The wax plate must not remain too long over the leaden tray, as the heat
is apt to melt the wax, when the acid not only attacks those parts from
which the wax has been removed by the etching needle, but also the
surface of the glass generally, and thus the clearness of the design is
spoilt. After exposure--and it is as well to prepare two or three glass
plates for the experiment--the wax is quickly removed by rubbing and
washing with oil of turpentine, and the design (beautifully etched into
the glass) is then apparent.