cisterns; those of wood, however strong at first, are soon decomposed,
and need repairs. They ought to be erected in the neighbourhood of the
calcining heaps, to save the labour of transport, and so arranged that
the solutions from the higher cisterns may spontaneously flow into the
lower. In this point of view, a sloping terrace is the best situation
for an alum work. In the lowest part of this terrace, and in the
neighbourhood of the boiling-house, there ought to be two or more large
deep tanks, for holding the crude lixivium, and they should be protected
from the rain by a proper shed. Upon a somewhat higher level the
cisterns of the clear lixivium may be placed. Into the highest range of
cisterns the calcined mineral is to be put, taking care to lay the
largest lumps at the bottom, and to cover them with lighter ashes. A
sufficient quantity of water is now to be run over it, and allowed to
rest for some time. The lixivium may then be drawn off, by a stopcock
connected with a pipe at the bottom of the cistern, and run into another
cistern at a somewhat lower level. Fresh water must now be poured on the
partly exhausted schist, and allowed to remain for a sufficient time.
This lixivium, being weak, should be run off into a separate tank. In
some cases a third addition of fresh water may be requisite, and the
weak lixivium which is drawn off may be reserved for a fresh portion of
calcined mineral. In order to save evaporation, it is always requisite
to strengthen weak leys by employing them instead of water for fresh
portions of calcined schist. Upon the ingenious disposition and form of
these lixiviating cisterns much of the economy and success of an alum
work depend. The hydrometer should be always used to determine the
degree of concentration which the solutions acquire.
The lixiviated stone being thus exhausted of its soluble ingredients, is
to be removed from the cisterns, and piled up in a heap in any
convenient place, where it may be left either spontaneously to
decompose, or, after drying, may be subjected to another calcination.
The density of the solution may be brought, upon an average, up to the
sp. gr. of from 1·09 to 1·15. The latter density may always be obtained
by pumping up the weaker solutions upon fresh calcined _mine_. This
strong liquor is then drawn off, when the sulphate of lime, the oxide of
iron, and the earths are deposited. It is of advantage to leave the
liquor exposed for some time, whereby the green vitriol may pass into a
persulphate of iron with the deposition of some oxide, while the
liberated acid may combine with some of the clay present, so as to
increase the quantity of sulphate of alumina. The manufacture of alum is
the more imperfect, as the quantity of sulphate of iron left
undecomposed is greater, and therefore every expedient ought to be tried
to convert the sulphate of iron into sulphate of alumina.
3. _The evaporation of the Schist Lixivium._--As the aluminous liquors,
however well settled at first, are apt, on the great scale, to deposit
earthy matters in the course of their concentration by heat, they are
best evaporated by a surface fire, such as that employed at Hurlett and
Campsie. A water-tight stone cistern must be built, having a layer of
well rammed clay behind the flags or tiles which line its bottom and
sides. This cistern may be 4 or 6 feet wide, 2 or 3 feet deep, and 30 or
40 feet long, and it is covered in by an arch of stone or brickwork. At
one extremity of this tunnel, or covered canal, a fire-grate is set, and
at the other a lofty chimney is erected. The cistern being filled to the
brim with the alum ley, a strong fire is kindled in the reverberatory
grate, and the flame and hot air are forced to sweep along the surface
of the liquor, so as to keep it in constant ebullition, and to carry off
the aqueous parts in vapour. The soot which is condensed in the process
falls to the bottom, and leaves the body of the liquor clear. As the
concentration goes on, more of the rough lixivium is run in from the
settling cistern, placed on a somewhat higher level, till the whole gets
charged with a clear liquor of a specific gravity sufficiently high for
transferring into the proper lead boilers.
At Whitby, the lead pans are 10 feet long, 4 feet 9 inches wide, 2 feet
2 inches deep at the one end, and 2 feet 8 inches deep at the other.
This increase of depth and corresponding slope, facilitates the
decantation of the concentrated lixivium by means of a syphon, applied
at the lower end. The bottom of the pan is supported by a series of
parallel iron bars, placed very near each other. In these lead pans the
liquor is concentrated, at a brisk boiling heat, by means of the flame
of a flue beneath them. Every morning the pans are emptied into a
settling cistern of stone or lead. The specific gravity of the liquor
should be about 1·4 or 1·5, being a saturated solution of the saline
matters present. The proper degree of density must vary, however, with
different kinds of lixivia, and according to the different views of the
manufacturer. For a liquor which consists of two parts of sulphate of
alumina, and one part of sulphate of iron, a specific gravity of 1·25
may be sufficient; but for a solution which contains two parts of
sulphate of iron to one of sulphate of alumina, so that the green
vitriol must be withdrawn first of all by crystallisation, a specific
gravity of 1·4 may be requisite.
The construction of an evaporating furnace well adapted to the
concentration of aluminous and other crude lixivia, is described under
SODA. The liquor basin may be made of tiles or flags puddled in clay,
and secured at the seams with a good _hydraulic_ cement. A mortar made
of quicklime mixed with the exhausted schist in powder, and iron
turnings, is said to answer well for this purpose. Sometimes over the
reverberatory furnace a flat pan is laid, instead of the arched top,
into which the crude liquor is put for neutralisation and partial
concentration. In Germany, such a pan is made of copper, because iron
would waste too fast, and lead would be apt to melt. From this
preparation basin the under evaporating trough is gradually supplied
with hot liquor. At one side of this lower trough, there is sometimes a
door, through which the sediment may be raked out as it accumulates upon
the bottom. Such a contrivance is convenient for this mode of
evaporation, and it permits, also, any repairs to be readily made; but,
indeed, an apparatus of this kind, well mounted at first, will serve for
many years.
In the course of the final concentration of the liquors, it is customary
to add some of the mother waters of a former process, the quantity of
which must be regulated by a proper analysis and knowledge of their
contents. If these mother waters contain much free sulphuric acid, from
the peroxidation of their sulphate of iron, they may prove useful in
dissolving a portion of the alumina of the sediment which is always
present in greater or less quantity.
4. _The precipitation of the Alum by adding Alkaline Salts._--As a
general rule, it is most advantageous to separate, first of all, from
the concentrated clear liquors, the alum in the state of powder or small
crystals, by addition of the proper alkaline matter, and to leave the
mingled foreign salts, such as the sulphate of iron or magnesia, in
solution, instead of trying to abstract these salts by a previous
crystallisation. In this way we not only simplify and accelerate the
manufacture of alum, and leave the mother waters to be worked up at any
convenient season, but we also avoid the risk of withdrawing any of the
sulphate of alumina with the sulphate of iron or magnesia. On this
account, the concentration of the liquor ought not to be pushed so far
as that, when it gets cold, it should throw out crystals, but merely to
the verge of this point. This density may be determined by suitable
experiments.
The clear liquor should now be run off into the precipitation cistern,
and have the proper quantity of sulphate or muriate of potash, or impure
sulphate or carbonate of ammonia added to it. The sulphate of potash,
which is the best precipitant, forms 18·34 parts out of 100 of
crystallised alum; and therefore that quantity of it, or its equivalent
in muriate of potash, or other potash or ammoniacal salts, must be
introduced into the aluminous liquor. Since sulphate of potash takes 10
parts of cold water to dissolve it, but is much more soluble in boiling
water, and since the precipitation of alum is more abundant the more
concentrated the mingled solutions are, it would be prudent to add the
sulphate solution as hot as may be convenient; but, as muriate of potash
is fully three times more soluble in cold water, it is to be preferred
as a precipitant, when it can be procured at a cheap rate. It has, also,
the advantage of decomposing the sulphate of iron present into a
muriate, a salt very difficult of crystallisation, and, therefore, less
apt to contaminate the crystals of alum. The quantity of alkaline salts
requisite to precipitate the alum, in a granular powder, from the
lixivium, depends on their richness in potash or ammonia, on the one
hand, and on the richness of the liquors in sulphate of alumina on the
other; and it must be ascertained, for each large quantity of product,
by a preliminary experiment in a precipitation glass. Here, an aliquot
measure of the aluminous liquor being taken, the liquid precipitant must
be added in successive portions, as long as it causes any cloud, when
the quantity added will be indicated by the graduation of the vessel. A
very exact approximation is not practicable upon the great scale; but,
as the mother waters are afterwards mixed together in one cistern, any
excess of the precipitant, at one time, is corrected by excess of
aluminous sulphate at another, and the resulting alum meal is collected
at the bottom. When the precipitated saline powder is thoroughly settled
and cooled, the supernatant mother water must be drawn off by a pump, or
rather a syphon or stopcock, into a lower cistern. The more completely
this drainage is effected, the more easily and completely will the alum
be purified.
This mother liquor has, generally, a specific gravity of 1·4 at a medium
temperature of the atmosphere, and consists of a saturated solution of
sulphate or muriate of black and red oxide of iron, with sulphate of
magnesia, in certain localities, and muriate of soda, when the soaper’s
salt has been used as a precipitant, as also a saturated solution of
sulphate of alumina. By adding some of it, from time to time, to the
fresh lixivia, a portion of that sulphate is converted into alum; but,
eventually, the mother water must be evaporated, so as to obtain from it
a crop of ferruginous crystals; after which it becomes capable, once
more, of giving up its alum to the alkaline precipitants.
When the aluminous lixivia contain a great deal of sulphate of iron, it
may be good policy to withdraw a portion of it by crystallisation before
precipitating the alum. With this view, the liquors must be evaporated
to the density of 1·4, and then run off into crystallising stone
cisterns. After the green vitriol has concreted, the liquor should be
pumped back into the evaporating pan, and again brought to the density
of 1·4. On adding to it, now, the alkaline precipitants, the alum will
fall down from this concentrated solution, in a very minute crystalline
powder, very easy to wash and purify. But this method requires more
vessels and manipulation than the preceding, and should only be had
recourse to from necessity; since it compels us to carry on the
manufacture of both the valuable alum and the lower priced salts at the
same time; moreover, the copperas extracted at first from the schist
liquors carries with it, as we have said, a portion of the sulphate of
alumina, and acquires thereby a dull aspect; whereas the copperas
obtained after the separation of the alum is of a brilliant appearance.
5. _The washing, or edulcoration, of the Alum Powder._--This crystalline
pulverulent matter has a brownish colour, from the admixture of the
ferruginous liquors; but it may be freed from it by washing with very
cold water, which dissolves not more than one sixteenth of its weight of
alum. After stirring the powder and the water well together, the former
must be allowed to settle, and then the washing must be drawn off. A
second washing will render the alum nearly pure. The less water is
employed, and the more effectually it is drained off, the more complete
is the process. The second water may be used in the first washing of
another portion of alum powder, in the place of pure water. These
washings may be added to the schist lixivia.
6. _The crystallisation._--The washed alum is put into a lead pan, with
just enough water to dissolve it at a boiling heat; fire is applied, and
the solution is promoted by stirring. Whenever it is dissolved in a
saturated state, it is run off into the crystallising vessels, which are
called _roching_ casks. These casks are about five feet high, three feet
wide in the middle, somewhat narrower at the ends; they are made of very
strong staves, nicely fitted to each other, and held together by strong
iron hoops, which are driven on _pro tempore_, so that they may be
easily knocked off again, in order to take the staves asunder. The
concentrated solution, during its slow cooling in these close vessels,
forms large regular crystals, which hang down from the top, and project
from the sides, while a thick layer or cake lines the whole interior of
the cask. At the end of eight or ten days, more or less, according to
the weather, the hoops and staves are removed, when a cask of apparently
solid alum is disclosed to view. The workman now pierces this mass with
a pickaxe at the side near the bottom, and allows the mother water of
the interior to run off on the sloping stone floor into a proper
cistern, whence it is taken and added to another quantity of washed
powder to be crystallised with it. The alum is next broken into lumps,
exposed in a proper place to dry, and is then put into the finished bing
for the market. There is sometimes a little insoluble basic alum
(subsulphate) left at the bottom of the cask. This being mixed with the
former mother liquors, gets sulphuric acid from them; or, being mixed
with a little sulphuric acid, it is equally converted into alum.
When, instead of potash or its salts, the ammoniacal salts are used, or
putrid urine, with the aluminous lixivia, ammoniacal alum is produced,
which is perfectly similar to the potash alum in its appearance and
properties. At a gentle heat both lose their water of crystallisation,
amounting to 45-1/2 per cent. for the potash alum, and 48 for the
ammoniacal. The quantity of acid is the same in both, as, also, very
nearly the quantity of alumina, as the following analyses will show:
Potash alum. Ammonia alum.
Sulphate of potash 18·34 Sulphate of ammonia 12·88
Sulphate of alumina 36·20 Sulphate of alumina 38·64
Water 45·46 Water 48·48
------ ------
100·00 100·00
------ ------
Or otherwise, Potash alum. Ammonia alum.
1 atom sulphate of potash 1089·07 1 atom sulphate of ammonia 716·7
1 alumina 2149·80 1 alumina 2149·8
24 water 2669·52 24 water 2699·5
------- ------
5938·39 5566·0
------- ------
Or, Potash alum. Ammonia alum.
Alumina 10·82 Alumina 11·90
Potash 9·94 Ammonia 3·89
Sulphuric Acid 33·77 Sulphuric acid 36·10
Water 45·47 Water 48·11
------ ------
100·00 100·00
------ ------
When heated pretty strongly, the ammoniacal alum loses its sulphuric
acid and ammonia, and only the earth remains. This is a very convenient
process for procuring pure alumina. Ammoniacal alum is easily
distinguished from the other by the smell of ammonia which it exhales
when triturated with quicklime. The Roman alum, made from alum stone,
possesses most of the properties of the schist-made alums, but it has a
few peculiar characters: it crystallises always in opaque cubes, whereas
the common alum crystallises in transparent octahedrons. It is probable
that Roman alum is a sulphate of alumina and potash, with a slight
excess of the earthy ingredient. It is permanent when dissolved in cold
water; for after a slow evaporation it is recovered in a cubical form.
But when it is dissolved in water heated to 110° Fahr. and upwards, or
when its solution is heated above this pitch, subsulphate of alumina
falls, and on evaporation octahedral crystals of common alum are
obtained. The exact composition of the Roman alum has not been
determined, as far as I know. It probably differs from the other also in
its water of crystallisation. The Roman alum contains, according to MM.
Thenard and Roard, only 1/2200 of sulphate of iron, while the common
commercial alums contain 1/1000. It may be easily purified by solution,
granulation, crystallisation, and washing, as has been already
explained.
Alum is made extensively in France from an artificial sulphate of
alumina. For this purpose clays are chosen as free as possible from
carbonate of lime and oxide of iron. They are calcined in a
reverberatory furnace, in order to expel the water, to peroxidise the
iron, and to render the alumina more easily acted on by the acid. The
expulsion of the water renders the clay porous and capable of absorbing
the sulphuric acid by capillary attraction. The peroxidation of the iron
renders it less soluble in the sulphuric acid; and the silica of the
clay, by reacting on the alumina, impairs its aggregation, and makes it
more readily attracted by the acid. The clay should, therefore, be
moderately calcined; but not so as to indurate it like pottery ware, for
it would then suffer a species of siliceous combination which would make
it resist the action of acids. The clay is usually calcined in a
reverberatory furnace, the flame of which serves thereafter to heat two
evaporating pans and a basin for containing a mixture of the calcined
clay and sulphuric acid. As soon as the clay has become friable in the
furnace it is taken out, reduced to powder, and passed through a fine
sieve. With 100 parts of the pulverised clay, 45 parts of sulphuric
acid, of sp. gr. 1·45, are well mixed, in a stone basin, arched over
with brickwork. The flame and hot air of a reverberatory furnace are
made to play along the mixture, in the same way as described for
evaporating the schist liquors. See SODA. The mixture, being stirred
from time to time, is, at the end of a few days, to be raked out, and to
be set aside in a warm place, for the acid to work on the clay, during
six or eight weeks. At the end of this time it must be washed, to
extract the sulphate of alumina. With this view, it may be treated like
the roasted alum ores above described. If potash alum is to be formed,
this sulphate of alumina is evaporated to the specific gravity of 1·38;
but if ammonia alum, to the specific gravity of only 1·24; because the
sulphate of ammonia, being soluble in twice its weight of water, will
cause a precipitation of pulverulent alum from a weaker solution of
sulphate of alumina than the less soluble sulphate of potash could do.
The alum stone, from which the Roman alum is made, contains potash. The
following analysis of _alunite_, by M. Cordier, places this fact in a
clear light:--
Sulphate of potash 18·53
Sulphate of alumina 38·50
Hydrate of alumina 42·97
------
100·00
------
To transform this compound into alum, it is merely necessary to abstract
the hydrate of alumina. The ordinary alum stone, however, is rarely so
pure as the above analysis would seem to show; for it contains a mixture
of other substances; and the above are in different proportions.
Alum is very extensively employed in the arts, most particularly in
dyeing, lake making, dressing sheep-skins, pasting paper, in clarifying
liquors, &c. Its purity for the dyer may be tested by prussiate of
potash, which will give solution of alum a blue tint in a few minutes if
it contain even a very minute portion of iron. A bit of nut-gall is also
a good test of iron.
AMADOU. The French name of the spongy combustible substance, called in
German _zunderschwamm_, prepared from a species of agaric, the _boletus
igniarius_, a kind of mushroom, which grows on the trunks of old oaks,
ashes, beeches, &c. It must be plucked in the months of August and
September. It is prepared by removing the outer bark with a knife, and
separating carefully the spongy substance of a yellow brown colour,
which lies within it, from the ligneous matter below. This substance is
cut into thin slices, and beat with a mallet to soften it, till it can
be easily pulled asunder between the fingers. In this state the
_boletus_ is a valuable substance for stopping oozing hemorrhages, and
some other surgical purposes. To convert it into tinder it must receive
a finishing preparation, which consists in boiling it in a strong
solution of nitre; drying it, beating it anew, and putting it a second
time into the solution. Sometimes, indeed, to render it very
inflammable, it is imbued with gunpowder, whence the distinction of
black and brown amadou.
All the puff balls of the lycopodium genus of plants, which have a
fleshy or filamentous structure, yield a tinder quite ready for soaking
in gunpowder water. The Hindoos employ a leguminous plant, which they
call _solu_, for the same purpose. Its thick spongy stem, being reduced
to charcoal, takes fire like amadou.
AMALGAM. When mercury is alloyed with any metal, the compound is called
an amalgam of that metal; as, for example, an amalgam of tin, bismuth,
&c.
AMALGAMATION. This is a process used extensively in extracting silver
and gold from certain of their ores, founded on the property which
mercury has to dissolve these metals as disseminated in the minerals,
and thus to separate them from the earthy matters. See MERCURY,
METALLURGY, and SILVER.
AMBER. (_Succin_, Fr.; _Bernstein_, Germ.) A mineral solid, of a yellow
colour of various shades, which burns quite away with flame, and
consists of carbon, hydrogen, and oxygen, in nearly the same
proportions, and the same state of combination, as vegetable resin. Its
specific gravity varies, by my trials, from 1·080 to 1·085. It becomes
negatively and powerfully electrical by friction. When applied to a
lighted candle it takes fire, swells considerably, and exhales a white
smoke of a pungent odour; but does not run into drops. Copal, which
resembles it in several respects, differs in being softer, and in
melting into drops at the flame; and mellite, or honey-stone, which is a
mineral of a similar colour, becomes white when laid on a red-hot coal.
The texture of amber is resino-vitreous, its fracture conchoidal, and
lustre glassy. It is perfectly homogeneous; sufficiently hard to scratch
gypsum, and to take a fine polish. It is, however, scratched by
calcareous spar. When amber is distilled in a retort, crystalline
needles of succinic acid sublime into the dome, and oil of amber drops
from the beak into the receiver. Fossil resins, such as that of
Highgate, found in the London clay formation, do not afford succinic
acid by heat; nor does copal. Amber is occasionally found of a whitish
and brownish colour.
The most interesting fact relative to this vegeto-mineral is its
geological position, which is very characteristic and well determined.
It is found almost uniformly in separate nodules, disseminated in the
sand, clay, or fragments of lignite of the plastic clay, and lignite
formation, situated between the _calcaire grossier_ (crag limestone) of
the tertiary strata above, and the white chalk below. The size of these
nodules varies from a nut to a man’s head; but this magnitude is very
rare in true amber. It does not occur either in continuous beds, like
the chalk flints, nor in veins; but it lies at one time in the earthy or
friable strata, which accompany or include the lignites; at another,
entangled in the lignites themselves; and is associated with the
minerals which constitute this formation, principally the pyrites, the
most abundant of all. The pieces of amber found in the sands, and other
formations evidently alluvial, those met with on the sea-coasts of
certain countries, and especially Pomerania, come undoubtedly from the
above geological formation; for the organic matters found still adhering
to the amber leave no doubt as to its primitive place. Amber does not,
therefore, belong to any postdiluvian or modern soil, since its native
bed is covered by three or four series of strata, often of considerable
thickness, and well characterised; proceeding upwards from the plastic
clay which includes the amber: these are, the crag limestone, the bone
gypsum, with its marls, the marly limestone, the upper marl sandstone,
which covers it, and, lastly, the freshwater or lacustrine formation,
often so thick, and composed of calcareous and siliceous rocks.
The amber bed is not, however, always covered with all these strata; and
it is even rare to see a great mass of one of them above the ground
which contains it; because, were it buried under such strata, it would
be difficult to meet with such circumstances as would lay it
spontaneously open to the day. But by comparing observations made in
different places, relatively to the patches of these formations, which
cover the amber deposits, we find that no other mineral formations have
been ever seen among them except those above detailed, and thus learn
that its geological locality is completely determined.
The proper yellow amber, therefore, or the Borussic, from the country
where it has been most abundantly found, belongs to the plastic clay
formation, intermediate, in England, between the chalk and the London
clay. It is sometimes interposed in thin plates between the layers of
the lignites, but more towards the bark of the fibrous lignites, which
retain the form of the wood, than towards the middle of the trunk of the
tree; a position analogous to that of the resinous matters in our
existing ligneous vegetables. The fibrous lignites which thus contain
amber belong to the dicotyledinous woods. Hence that substance seems to
have been formed during the life of the vegetable upon which it is now
encrusted. It must be remembered that the grounds containing the amber
are often replete with the sulphates of iron, alumina, and lime, or at
least with the pyritous elements of these salts. Some specimens of amber
have a surface figured with irregular meshes, indicating a sort of
shrinkage from consolidation, and consequently a matter that was at one
time fluid, viscid, or merely soft. From optical examination, Dr.
Brewster has concluded amber to be of vegetable origin.
The different bodies included in the amber, distinguishable from its
transparence, demonstrate, indeed, in the most convincing manner, its
primitive state of liquidity or softness. These bodies have long
exercised the skill of naturalists. They are generally insects, or
remains of insects, and sometimes leaves, stalks, or other portions of
vegetables. Certain families of insects occur more abundantly than
others. Thus the _hymenoptera_, or insects with four naked membranaceous
wings, as the bee and wasp, and the _diptera_, or insects with two
wings, as gnats, flies, gadflies, &c.; then come the spider tribe; some
_coleoptera_ (insects with crustaceous shells or elytra, which shut
together, and form a longitudinal suture down the back,) or beetles,
principally those which live on trees; such as the _elaterides_, or
leapers, and the _chrysomelida_. The lepidoptera, or insects with four
membranaceous wings, and pterigostea covered with mail-like scales, are
very rare in amber. We perceive from this enumeration, which results
from the labours of Germar, Schweiger, &c., that the insects enveloped
in this resinous matter are in general such as sit on the trunks of
trees, or live in the fissures of their bark. Hitherto, it has not been
found possible to refer them to any living species; but it has been
observed in general that they resemble more the insects of hot climates
than those of the temperate zones.
The districts where amber occurs in a condition fit for mining
operations are not numerous; but those in which it is met with in small
scattered bits are very abundant. Its principal exploitation is in
Eastern Prussia, on the coasts of the Baltic sea, from Memel to
Dantzick, particularly in the neighbourhood of Konigsberg, along the
shore which runs north and south from Grossdirschheim to Pillau, and in
several other places near Dantzick.
It is collected upon this coast in several ways; 1. In the beds of small
streams which run near the villages, and in rounded fragments without
bark, or in the sand-banks of rivers, in pieces thrown back by the sea,
and rounded by the waves. 2. If the pieces thrown up by the waters are
not numerous, the fishers, clothed in a leather dress, wade into the sea
up to the neck, seek to discover the amber by looking along its surface,
and seize it with bag nets, hung at the end of very long poles. They
conclude that a great deal of amber has been detached from the cliffs by
the sea, when many pieces of lignite (wood coal) are seen afloat. This
mode of collecting amber is not free from danger, and the fishers,
therefore, advance in troops, to lend each other aid in case of
accident; but their success, even thus, is most precarious. 3. The third
method of searching for amber is a real mining operation: it consists in
digging pits upon the borders of the sandy downs, sometimes to a depth
of more than 130 feet. 4. The last mode is by exploring the precipitous
sea cliffs in boats, and detaching masses of loose soil from them with
long poles terminating in iron hooks; a very hazardous employment. They
search the cliffs with great care at the level, where the amber nodules
commonly lie, and loosen the seams with their hooks; in which business
the boats are sometimes broken against the precipices, or sunk by an
avalanche of rubbish.
Amber occurs in Sicily, disseminated in beds of clay and marl, which lie
below the crag limestone. It is accompanied with bitumen; and, though a
scanty deposit, it is mined for sale. The pieces are coated with a kind
of whitish bark, present a variety of colours, and include many insects.
Amber is found in a great many places in the sandy districts of Poland,
at a very great distance from the sea, where it is mixed with cones of
the pine. In Saxony it is met with in the neighbourhood of Pretsch and
Wittemberg, in a bituminous clay mingled with lignite. At the embouchure
of the Jenissey, in Siberia, it occurs likewise along with lignite; as
also in Greenland.
Fine amber is considerably valued for making ornamental objects, and the
coarser kinds for certain uses in chemistry, medicine, and the arts. The
oriental nations prize more highly than the people of Europe trinkets
made of amber; and hence the chief commerce of the Pomeranian article is
with Turkey. The Prussian government is said to draw an annual revenue
of 17,000 dollars from amber. A good piece of a pound weight fetches 50
dollars. A mass weighing 13 pounds was picked up not long since in
Prussia, for which 5000 dollars were offered, and which would bring, in
the opinion of the Armenian merchants, from 30,000 to 40,000 dollars at
Constantinople. At one time it was customary to bake the opaque pieces
of amber in sand, at a gentle heat, for several hours, in order to make
it transparent, or to digest it in hot rapeseed oil, with the same view;
but how far these processes were advantageous does not appear.
When amber is to be worked into trinkets, it is first split on a leaden
plate at a lathe (see GEMS, _Cutting of_), and then smoothed into shape
on a Swedish whetstone. It is polished on the lathe with chalk and
water, or vegetable oil, and finished by friction with flannel. In these
processes the amber is apt to become highly electrical, very hot, and
even to fly into fragments. Hence, the artists work the pieces time
about, so as to keep each of them cool, and feebly excited. The men are
often seized with nervous tremors in their wrists and arms from the
electricity. Pieces of amber may be neatly joined by smearing their
edges with linseed oil, and pressing them strongly together, while they
are held over a charcoal fire. Solid specimens of amber, reported to
have been altogether fused by a particular application of heat, are now
shown in the royal cabinet of Dresden.
A strong and durable _varnish_ is made by dissolving amber in drying
linseed oil. For this purpose, however, the amber must be previously
heated in an iron pot, over a clear red fire, till it soften and be
semi-liquefied. The oil, previously heated, is to be now poured in, with
much stirring, in the proportion of 10 ounces to the pound of amber;
and after the incorporation is complete, and the liquid somewhat cooled,
a pound of oil of turpentine must be added. Some persons prescribe 2
ounces of melted shellac, though by this means they are apt to deepen
the colour, already rendered too dark by the roasting.
The fine black varnish of the coachmakers is said to be prepared by
melting 16 ounces of amber in an iron pot, adding to it half a pint of
drying linseed oil, boiling hot, of powdered resin and asphaltum 3
ounces each: when the materials are well united, by stirring over the
fire, they are to be removed, and, after cooling for some time, a pint
of warm oil of turpentine is to be introduced.
The _oil of amber_ enters into the composition of the old perfume called
_eau de luce_; and is convertible, by the action of a small quantity of
strong nitric acid, into a viscid mass like shoemakers’ rosin, which has
a strong odour of musk, and, under the name of artificial musk, has been
prescribed, in alcoholic solution, as a remedy against hooping cough,
and other spasmodic diseases.
Acid of amber (_succinic acid_) is a delicate reagent, in chemistry, for
separating red oxide of iron from compound metallic solutions.
AMBERGRIS. (_Ambregric_, Fr.; _Ambra_, Germ.).--A morbid secretion of
the liver of the spermaceti whale (physeter macrocephalus), found
usually swimming upon the sea. It occurs upon the coasts of Coromandel,
Japan, the Moluccas, and Madagascar, and has sometimes been extracted
from the rectum of whales in the South Sea fishery. It has a gray-white
colour, often with a black streak, or is marbled, yellow and black; has
a strong but rather agreeable smell, a fatty taste, is lighter than
water, melts at 60° C. (140° F.), dissolves readily in absolute alcohol,
in ether, and in both fat and volatile oils. It contains 85% of the
fragrant substance called _ambreine_. This is extracted from ambergris
by digestion with alcohol of 0·827, filtering the solution, and leaving
it to spontaneous evaporation. It is thus obtained in the form of
delicate white tufts: which are convertible into ambreic acid by the
action of nitric acid. Ambergris is used in perfumery.
AMIANTHUS. A mineral in silky filaments, called also ASBESTUS.
AMMONIA. A chemical compound, called also _volatile alkali_. This
substance, in its purest state, is a highly pungent gas, possessed of
all the mechanical properties of the air, but very condensable with
water. It consists of 3 volumes of hydrogen and 1 of azote condensed
into two volumes; and hence its density is 0·591, atmospheric air being
1·000. By strong compression and refrigeration it may be liquefied into
a fluid, whose specific gravity is 0·76 compared to water 1·000.
Ammonia gas is composed by weight of 82·53 azote and 17·47 hydrogen in
100 parts. It is obtained by mixing muriate of ammonia, commonly called
sal ammoniac, with quicklime, in a retort or still, applying a moderate
heat, and receiving the gas either over mercury for chemical
experiments, or in water to make liquid ammonia for the purposes of
medicine and the arts. Woulfe’s apparatus is commonly employed for this
condensation.
Ammonia is generated in a great many operations, and especially in the
decomposition of many organic substances, by fire or fermentation. Urine
left to itself for a few days is found to contain much carbonate of
ammonia, and hence this substance was at one time collected in great
quantities for the manufacture of certain salts of ammonia, and is still
used for its alkaline properties in making alum, scouring wool, &c. When
woollen rags, horns, bones, and other animal substances are decomposed
in close vessels by fire, they evolve a large quantity of ammonia, which
distils over in the form of a carbonate. The main source of ammonia now
in this country, for commercial purposes, is the coal gas works. A large
quantity of watery fluid is condensed in their tar pits, which contains,
chiefly ammonia combined with sulphuretted hydrogen and carbonic acid.
When this water is saturated with muriatic acid and evaporated it yields
muriate of ammonia, or sal ammoniac, somewhat impure, which is
afterwards purified by sublimation. See CARBONATE OF AMMONIA and SAL
AMMONIAC.
The soot of chimnies where coal is burned contains both sulphate and
carbonate of ammonia, and was extensively employed, at one time, to
manufacture these salts.
In making water of ammonia on the great scale, a cast iron still should
be preferred, and equal weights of quicklime and sal ammoniac should be
brought to the consistence of a pap, with water, before the heat is
applied. In this case, a refrigeratory worm or globe should be
interposed between the adopter tube of the capital of the still and the
bottles of Woulfe’s apparatus. The muriate of lime, or chloride of
calcium, which is left in the still when the whole ammonia is expelled,
is of no value. Water is capable of condensing easily about one third of
its weight of ammonia gas, or 460 times its bulk. The following table of
the quantity of ammonia in 100 parts by weight of its aqueous
combinations, at successive densities, is the result of very careful
experiments made by me, and recorded in the Philosophical Magazine for
March, 1821.
_Table of Water of Ammonia or Volatile Alkali, by Dr. Ure._
+------+-------+------+-----------+--------+-------------------------+
|Water |Ammonia|Water | Specific | Mean | |
| of | in | in |gravity by |specific| Equivalent primes. |
|0·900.| 100. | 100. |experiment.|gravity.| |
+------+-------+------+-----------+--------+-------------------------+
| 100 |26·500 |73·500| 0·9000 | | |
| 95 |25·175 |74·825| 0·9045 |0·90452 | _Wat. Am._|
| 90 |23·850 |76·150| 0·9090 |0·90909 | 24 + 76, 6 to 1 |
| 85 |22·525 |77·475| 0·9133 |0·91370 | |
| 80 |21·200 |78·800| 0·9177 |0·91838 | 21·25 + 78·75, 7 to 1 |
| 75 |19·875 |80·125| 0·9227 |0·92308 | |
| 70 |18·550 |81·450| 0·9275 |0·92780 | 19·1 + 80·9, 8 to 1 |
| 65 |17·225 |82·775| 0·9320 |0·93264 | 17·35 + 82·65, 9 to 1 |
| 60 |15·900 |84·100| 0·9363 |0·93750 | 15·9 + 84·1, 10 to 1 |
| 55 |14·575 |85·425| 0·9410 |0·94241 | 14·66 + 85·34, 11 to 1 |
| 50 |13·250 |86·750| 0·9455 |0·94737 | 13·60 + 86·40, 12 to 1 |
| 45 |11·925 |88·075| 0·9510 |0·95238 | 11·9 + 88·1, 14 to 1 |
| 40 |10·600 |89·400| 0·9564 |0·95744 | 11·2 + 88·8, 15 to 1 |
| 35 | 9·275 |90·725| 0·9614 |0·96256 | |
| 30 | 7·950 |92·050| 0·9662 |0·96774 | 8·63 + 91·37, 20 to 1 |
| 25 | 6·625 |93·375| 0·9716 |0·97297 | 7 + 93, 25 to 1 |
| 20 | 5·300 |94·700| 0·9768 |0·97826 | 6 + 94, 30 to 1 |
| 15 | 3·975 |96·025| 0·9828 |0·98360 | 4·5 + 95·5, 40 to 1 |
| 10 | 2·650 |97·350| 0·9887 |0·98900 | 3 + 97, 60 to 1 |
| 5 | 1·325 |98·675| 0·9945 |0·99447 | |
+------+-------+------+-----------+--------+-------------------------+
AMMONIAC, gum-resin. This is the inspissated juice of an umbelliferous
plant (the _dorema armeniacum_) which grows in Persia. It comes to us
either in small white tears clustered together, or in brownish lumps,
containing many impurities. It possesses a peculiar smell, somewhat like
that of assafœtida, and a bitterish taste. It is employed in medicine.
Its only use in the arts is for forming a cement to join broken pieces
of china and glass, which may be prepared as follows: Take isinglass 1
ounce, distilled water 6 ounces, boil together down to 3 ounces, and add
1-1/2 ounce of strong spirit of wine;--boil this mixture for a minute or
two; strain it; add, while hot, first, half an ounce of a milky emulsion
of gum ammoniac, and then five drams of an alcoholic solution of resin
mastic. This resembles a substance sold in the London shops, under the
name of _diamond cement_. The recipe was given me by a respectable
dispensing chemist.
AMORPHOUS. _Without shape._ Said of mineral and other substances which
occur in forms not easy to be defined.
ANALYSIS. The art of resolving a compound substance or machine into its
constituent parts. Every manufacturer should so study this art, in the
proper treatises, and schools of Chemistry or Mechanics, as to enable
him properly to understand and regulate his business.
[Illustration: 6]
ANCHOR. (_Ancre_, Fr.; _Anker_, Germ.) An iron hook of considerable
weight and strength, for enabling a ship to lay hold of the ground, and
fix itself in a certain situation by means of a rope called the cable.
It is an instrument of the greatest importance to the navigator, since
upon its taking and keeping hold depends his safety upon many
occasions, especially near a lee shore, where he might be otherwise
stranded or shipwrecked. Anchors are generally made of wrought iron,
except among nations who cannot work this metal well, and who therefore
use copper. The mode in which an anchor operates will be understood from
inspection of _fig._ 6., where, from the direction of the strain, it is
obvious that the anchor cannot move without ploughing up the ground in
which its hook or fluke is sunk. When this, however, unluckily takes
place, from the nature of the ground, from the mode of insertion of the
anchor, or from the violence of the winds or currents, it is called
_dragging the anchor_. When the hold is good, the cable or the buried
arm will sooner break than the ship will drive. Anchors are of different
sizes, and have different names, according to the purposes they serve;
thus there are, _sheet_, _best bower_, _small bower_, _spare_, _stream_,
and _kedge anchors_. Ships of the first class have seven anchors, and
smaller vessels, such as brigs and schooners, three.
[Illustration: 7]
The manufacture of anchors requires great knowledge of the structure of
iron, and skill in the art of working it. I shall give, here, a brief
notice of the improved system introduced by Mr. Perring, clerk of the
cheque at Plymouth, in which the proportions of the parts are admirably
adapted to the strains they are likely to suffer. In _fig._ 7. A is the
_shank_; B, the _arm_ or _fluke_; C, the _palm_; D, the _blade_; E, the
_square_; F, the _nut_; G, the _ring_; H, the _crown_.
Formerly the shank was made of a number of square iron rods, laid
parallel together in a cylindrical form, and bound by iron hoops. When
they were welded into one bar, the exterior rods could not fail to be
partially burned and wasted by the strong heat. Mr. Perring abated this
evil by using bars of the whole breadth of the shank, and placing them
right over each other, hooping them and welding them together at two
heats into one solid mass. To any one who has seen the working of
puddled iron, with a heavy mill hammer, this operation will not appear
difficult.
He formed the crown with bars similarly distributed with those of the
shank. His mode of uniting the flukes to the crown is probably the most
valuable part of his invention. The bars and half the breadth of the
anchor are first welded separately, and then placed side by side, where
the upper half is worked into one mass, while the lower part is left
disunited, but has carrier iron bars, or _porters_, as these
prolongation rods are commonly called, welded to the extremity of each
portion. The lower part is now heated and placed in the clamping
machine, which is merely an iron plate firmly bolted to a mass of
timber, and bearing upon its surface four iron pins. One end of the
crown is placed between the first of these pins, and passed under an
iron strap; the other end is brought between the other pins, and is bent
by the leverage power of the elongated rods or porters.
Thus a part of the arm being formed out of the crown gives much greater
security that a true union of fibres is effected, than when the junction
was made merely by a short scarf.
The angular opening upon the side opposite B H, _fig._ 7., is filled
with the _chock_, formed of short iron bars placed upright. When this
has been firmly welded, the truss-piece is brought over it. This piece
is made of plates similar to the above, except that their edges are here
horizontal. The truss-piece is half the breadth of the arm; so that when
united to the crown, it constitutes, with the other parts, the total
breadth of the arms at those places.
The shank is now shut upon the crown; the square is formed, and the nuts
welded to it; the hole is punched out for the ring, and the shank is
then fashioned.
The blade is made much in the way above described. In making the palm,
an iron rod is first bent into the approximate form, notching it so that
it may more readily take the desired shape. To one end a _porter_ rod is
fastened, by which the palm is carried and turned round in the fire
during the progress of the fabrication. Iron plates are next laid side
by side upon the rod, and the joint at the middle is broken by another
plate laid over it. When the mass is worked, its under side is filled up
by similar plates, and the whole is completely welded; pieces being
added to the sides, if necessary, to form the angles of the palm. The
blade is then shut on to the palm, after which the part of the arm
attached to the blade is united to that which constitutes the crown. The
smith-work of the anchor is now finished.
The junction, or shutting on, as the workmen call it, of the several
members of an anchor, is effected by an instrument called a _monkey_,
which is merely a mass of iron raised to a certain height, between
parallel uprights, as in the pile engine or vertical ram, and let fall
upon the metal previously brought to a welding heat.
The _monkey_ and the _hercules_, both silly, trivial names, are similar
instruments, and are usually worked, like a portable pile engine, by the
hands of several labourers, pulling separate ropes. Many other modes of
manufacturing anchors have been devised, in which mechanical power is
more extensively resorted to.
The upper end of the shank F (_fig._ 7.) is squared to receive and hold
the stock steadily, and keep it from turning. To prevent it shifting
along, there are two knobs or tenon-like projections. The point of the
angle H, between the arms and the shank, is sometimes called the throat.
The arm B C generally makes an angle of 56° with the shank A; it is
either round or polygonal, and about half the length of the shank.
The _stock_ of the anchor (_fig._ 6.) is made of oak. It consists of two
beams which embrace the _square_, and are firmly united by iron bolts
and hoops, as shown in the figure. The stock is usually somewhat longer
than the shank, has in the middle a thickness about one-twelfth of its
length, but tapers at its under side to nearly one half this thickness
at the extremities. In small anchors the stock is frequently made of
iron; but in this case it does not embrace the anchor, but goes through
a hole made in the square, which is swelled out on purpose.
The weight of anchors for different vessels is proportioned to the
tonnage; a good rule being to make the anchor in hundredweights
one-twentieth of the number of tons of the burden. Thus a ship of 1000
tons would require a sheet anchor of 50 cwts. Ships of war are provided
with somewhat heavier anchors.
Several new forms and constructions of anchors were proposed under Mr.
Piper’s patent of November, 1822, by the adoption of which great
advantages as to strength were anticipated over every other form or
construction previously made.
The particular object was to preserve such a disposition of the fibres
of the metal as should afford the greatest possible strength; in doing
which the crossing or bending of the fibres at the junctions of the
shank, flukes, and crown, where great strength is required, has been
avoided as much as possible, so that the fibres are not disturbed or
injured.
In this respect most anchors are defective; for in connecting the shanks
to the crown-pieces, the grain of the metal is either crossed, or so
much curved, as to strain the fibre, and consequently induce a weakness
where the greatest strength is required. And, further, the very
considerable thicknesses of metal which are to be brought into immediate
contact by means of the hammer in forging anchors upon the old
construction, render it highly probable that faulty places may be left
within the mass, though they be externally imperceptible. Mr. Piper’s
leading principle was, that the fibre of the metal should run nearly
straight in all the parts where strength is particularly required.
[Illustration: 8]
_Fig._ 8. shows an anchor with one tumbling fluke, which passes through
the forked or branched part of the shank. The lower part of this anchor,
answering to the crown, has a spindle through it, upon which the fluke
turns, and a pin is there introduced for the purpose of confining the
fluke when in a holding position. This shank is formed of a solid piece
of wrought iron, the fibres of which run straight, and at the crown
holes are pierced, which merely bulge the metal without bending the
fibres round so as to strain them. The arm and fluke, also, are formed
of one piece punched through without curling or crossing the fibre, and
the spindle which holds the arm to the crown is likewise straight. This
spindle extends some distance on each side of the anchor, and is
intended to answer the purpose of a stock; for when either of the ends
of the spindle comes in contact with the ground, the anchor will be
thrown over into a holding position; or an iron stock may be introduced
near the shackle, instead of these projecting ends. In the descent of
the anchor, the fluke will fall over towards that side which is nearest
the ground, and will there be ready to take hold when the anchor is
drawn forward.
[Illustration: 9]
_Fig._ 9. is another anchor upon the same principle, but slightly varied
in form from the last. In this the forked part of the shank is closer
than in the former, and there are two arms or flukes connected to the
crown-pieces, one of which falls into its holding position as the anchor
comes to the ground, and is held at its proper angle by the other fluke
stopping against the shank.
[Illustration: 10]
_Fig._ 10. represents another variation in the form of these improved
anchors, having two tumbling flukes, which are both intended to take
hold of the ground at the same time. The shank is here, as before, made
without crossing the grain of the iron, and the eyes for admitting the
bolt at the crown and at the shackle are punched out of the solid, not
formed by welding or turning the iron round. In this form a guard is
introduced at the crown, to answer the purpose of a stock, by turning
the flukes over into a holding position. The arms and flukes are made,
as before described, of the straight fibre of the iron punched through,
and the flukes are fixed to the spindle, which passes through the
crown-piece.
[Illustration: 11]
_Fig._ 11. has a shank without any fork, but formed straight throughout;
the guard here is an elongated frame of iron, for the same purpose as a
stock, and is, with the tumbling flukes, fastened to the spindle, which
passes through the crown of the anchor, and causes the flukes to fall
into their holding position.
The principles of these new anchors are considered to consist in shanks
which are made of straight lengths of metal, and finished so that the
fibres of the iron shall not be injured by cross-shuts or uncertain
welding; also each arm and palm is made in one solid piece, and finished
in straight lines, so that the fibres will not be altered, and the
shaft-pin or spindle will also be in one straight line; and this is the
improvement claimed. These anchors being made in separate pieces, give a
great advantage to the workman to execute each part perfectly; for he
will not have such heavy weights to lift when hot, which will render
these anchors much stronger, with less weight; and if any accident
should happen to them, any part may be taken separate from the others to
be repaired, and several of those parts of the anchor which may be
likely to break may be carried on board, in case of accident. This
anchor is so contrived that one of thirty hundred weight may be taken to
pieces and put together again, by one man, in twenty minutes; it may
also be dismounted, and stowed in any part of the ship, in as little
room as straight bars of iron, and speedily put together again.
[Illustration: 12]
The anchor (_fig._ 12.) patented by Mr. Brunton, in February, 1822, has
its stock introduced at the crown part, for the purpose of turning it
over into a holding position. The shank is perforated through the solid,
in two places, with elliptical apertures, for the purpose of giving it a
greater stability, and more effectually resisting the strain to which
the anchor may be subjected. The stock is a cylindrical iron rod, held
at its extremities by lateral braces, which are bolted to the shank.
_Fig._ 12. shows the form of the anchor. The shank is seen upright, with
one of the flukes projecting in its front; the horizontal iron stock is
at bottom; and the oblique braces are bolted to both shank and stock.
The ends of the stock, from the shoulder, are formed dove-tailed, and
oval in the vertical direction, and are protruded through apertures in
the braces, also oval, but in the horizontal direction, and counter
sunk. When the ends of the stock have been thus introduced through the
holes, the braces are securely bolted to the shank; the ends of the
stock are then spread, by hammering into the counter-sunk holes of the
braces, and by that means they are made firm.
An anchor of this description is considered by the patentee to possess
considerable advantage, particularly in point of stability, over the
ordinary construction of anchors, and is economical, inasmuch as a less
weight of metal will give, upon this plan, an equal degree of strength.
An ingenious form of anchor was made the subject of a patent, by
Lieutenant Rodgers, of the Royal Navy, in 1828, and was afterwards
modified by him in a second patent, obtained in August, 1829. The whole
of the parts of the anchor are to be bound together by means of iron
bands or hoops, in place of bolts or pins.
[Illustration: 13 14 15 16]
_Fig._ 13. is a side view of a complete anchor, formed upon his last
improved construction, and _fig._ 14., a plan of the same; _fig._ 15.,
an end view of the crown and flukes, or arms; _fig._ 16. represents the
two principal iron plates, _a_, _a_, of which the shank is constructed,
but so as to form parts of the stump arms to which the flukes are to be
connected.
The crown piece is to be welded to the stump piece, _c c_, _fig._ 16.,
as well as to the end _l_ of the centre piece _h h_, and the scarfs _m
m_ are to be cut to receive the arms or flukes. Previously, however, to
uniting the arms or flukes with the stump arms, the crown and throat of
the anchor are to be strengthened, by the application of the crown slabs
_n n_, _fig._ 16., which are to be welded upon each side of the crown,
overlapping the end of the pillar _h_, and the throat or knees of the
stump arms and the crown piece. The stump arms are then to be
strengthened in a similar manner, by the thin flat pieces _p p_, which
are to be welded upon each side. The palms are united to the flukes in
the usual way, and the flukes are also united to the stump arms by means
of the long scarfs _m m_. When the shank of the anchor has been thus
formed, and united with the flukes, the anchor smith’s work may be said
to be complete.
[Illustration: 17]
Another of the improvements in the construction of anchors, claimed
under this patent, consists in a new method of affixing the stock upon
the shank of the anchor, which is effected in the following manner: in
_fig._ 14. the stock is shown affixed to the anchor; in _fig._ 17. it is
shown detached. It may be made either of one or two pieces of timber, as
may be found most convenient. It is, however, to be observed that the
stock is to be completed before fitting on to the shank. After the stock
is shaped, a hole is to be made through the middle of it, to fit that
part of the shank to which it is to be affixed. Two stock plates are
then to be let in, one on each side of the stock, and made fast by
counter sunk nails and straps, or hoops; other straps or hoops of iron
are also to be placed round the stock, as usual.
In place of nuts, formed upon the shank of the anchor, it is proposed to
secure the stock by means of a hoop and a key, shown above and below J,
in _fig._ 14. By this contrivance, the stock is prevented from going
nearer to the crown of the anchor than it ought to do, and the key
prevents it from sliding towards the shackle.
Since fitting the stock to the shank of an anchor, by this method,
prevents the use of a ring, as in the ordinary manner, the patentee says
that he in all cases substitutes a shackle for the ring, and which is
all that is required for a chain cable; but, when a hempen cable is to
be used, he connects a ring to the usual shackle, by means of a joining
shackle, as in _figs._ 13. and 14.
Mr. Rodgers proposes, under another patent, dated July, 1833, to alter
the size and form of the palms; having found from experience that
anchors with small palms will not only hold better than with large ones,
but that the arms of the anchor, even without any palms, have been found
to take more secure hold of the ground than anchors of the old
construction, of similar weight and length. He has, accordingly, fixed
upon one-fifth of the length of the arm, as a suitable proportion for
the length or depth of the palm. He makes the palms, also, broader than
they are long or deep.
ANIMÉ. A resin of a pale brown yellow colour, transparent and brittle.
It exudes from the courbaril of Cayenne, a tree which grows also in
various parts of South America. It occurs in pieces of various sizes,
and it often contains so many insects belonging to living species, as to
have merited its name, as being animated. It contains about a fifth of
one per cent. of a volatile oil, which gives it an agreeable odour.
Alcohol does not dissolve the genuine animé, as I have ascertained by
careful experiments; nor does caoutchoucine; but a mixture of the two,
in equal parts, softens it into a tremulous jelly, though it will not
produce a liquid solution. When reduced to this state, the insects can
be easily picked out, without injury to their most delicate parts.
The specific gravity of the different specimens of animé which I tried,
varied from 1·054 to 1·057. When exposed to heat, in a glass retort over
a spirit flame, it softens, and, by careful management, it may be
brought into liquid fusion, without discolouration. It then exhales a
few white vapours, of an ambrosiacal odour, which being condensed in
water, and the liquid being tested, is found to be succinic acid.
_Author._
It is extensively used by the varnish makers, who fuse it at a pretty
high heat, and in this state combine it with their oils, or other
varnishes.
ANKER. A liquid measure of Amsterdam, which contains 32 gallons English.
ANNEALING or NEALING. (_Le recuit_, Fr.; _das anlassen_, Germ.) A
process by which glass is rendered less frangible; and metals, which
have become brittle, either in consequence of fusion, or long-continued
hammering, are again rendered malleable. When a glass vessel is allowed
to cool immediately after being made, it will often sustain the shock of
a pistol-bullet, or any other blunt body falling into it from a
considerable height; while a small splinter of flint, or an angular
fragment of quartz, dropped gently into it, makes it sometimes
immediately, sometimes after a few minutes, fly to pieces with great
violence. This extreme fragility is prevented by annealing, or placing
the vessels in an oven, where they take several hours or even some days
to cool. Similar phenomena are exhibited in a higher degree by
glass-tears, or Prince Rupert’s drops. They are procured by letting
drops of melted glass fall into cold water. Their form resembles that of
a pear, rounded at one extremity, and tapering to a very slender tail at
the other. If a part of the tail be broken off, the whole drop flies to
pieces with a loud explosion; and yet the tail of a drop may be cut away
by a glass-cutter’s wheel, or the thick end may be struck smartly with
a hammer, without the fear of sustaining any injury. When heated to
redness, and permitted to cool gradually in the open air, they lose
these peculiarities, and do not differ sensibly from common glass.
The properties of unannealed glass depend on a peculiar structure,
extending uniformly through its whole substance; and the bursting of a
glass drop by breaking off the tail, or of an unannealed glass vessel,
by dropping a piece of flint into it, arises from a crack being thus
begun, which afterwards extends its ramifications in different
directions throughout the glass.
When metals have been extended to a certain degree under the hammer,
they become brittle, and incapable of being further extended without
cracking. In this case the workman restores their malleability by
annealing, or heating them red-hot. The rationale of this process seems
to be, that the hammering and extension of the metal destroy the kind of
arrangement which the particles of the metal had previous to the
hammering; and that the annealing, by softening the metal, enables it to
recover its original structure.
Of late years a mode has been discovered of rendering cast iron
malleable, without subjecting it to the action of puddling. The process
is somewhat similar to that employed in annealing glass. The metal is
kept for several hours at a temperature a little below its fusing point,
and then allowed to cool slowly. In this manner vessels are made of cast
iron which can sustain considerable violence, without being broken. See
STEEL, softening of.
ANNOTTO. (_Rocou_, or _roucou_, Fr.; _orleans_, Germ.) A somewhat dry
and hard paste, brown without, and red within. It is usually imported in
cakes of two or three pounds weight, wrapped up in leaves of large
reeds, packed in casks, from America, where it is prepared from the
seeds of a certain tree, the _bixa orellana_, of Linnæus.
The pods of the tree being gathered, their seeds are taken out and
bruised; they are then transferred to a vat, which is called the
steeper, where they are mixed with as much water as covers them. Here
the substance is left for several weeks, or even months; it is now
squeezed through sieves placed above the steeper, that the water
containing the colouring matter in suspension may return, into the vat.
The residuum is preserved under the leaves of the anana (pine-apple)
tree, till it becomes hot by fermentation. It is again subjected to the
same operation, and this treatment is continued till no more colour
remains.
The substance thus extracted is passed through sieves, in order to
separate the remainder of the seeds, and the colour is allowed to
subside. The precipitate is boiled in coppers till it be reduced to a
consistent paste; it is then suffered to cool, and dried in the shade.
Instead of this long and painful labour, which occasions diseases by the
putrefaction induced, and which affords a spoiled product, Leblond
proposes simply to wash the seeds of annotto till they be entirely
deprived of their colour, which lies wholly on their surface; to
precipitate the colour by means of vinegar or lemon juice, and to boil
it up in the ordinary manner, or to drain it in bags, as is practised
with indigo.
The experiments which Vauquelin made on the seeds of annotto imported by
Leblond, confirmed the efficacy of the process which he proposed; and
the dyers ascertained that the annotto obtained in this manner was worth
at least four times more than that of commerce; that, moreover, it was
more easily employed; that it required less solvent; that it gave less
trouble in the copper, and furnished a purer colour.
Annotto dissolves better and more readily in alcohol than in water, when
it is introduced into the yellow varnishes for communicating an orange
tint.
The decoction of annotto in water has a strong peculiar odour, and a
disagreeable taste. Its colour is yellowish-red, and it remains a little
turbid. An alkaline solution renders its orange-yellow clearer and more
agreeable, while a small quantity of a whitish substance is separated
from it, which remains suspended in the liquid. If annotto be boiled in
water along with an alkali, it dissolves much better than when alone,
and the liquid has an orange hue.
The acids form with this liquor an orange-coloured precipitate, soluble
in alkalies, which communicate to it a deep orange colour. The
supernatant liquor retains only a pale yellow hue.
When annotto is used as a dye, it is always mixed with alkali, which
facilitates its solution, and gives it a colour inclining less to red.
The annotto is cut in pieces, and boiled for some instants in a copper
with its own weight of crude pearl ashes, provided the shade wanted do
not require less alkali. The cloths may be thereafter dyed in this bath,
either by these ingredients alone, or by adding others to modify the
colour; but annotto is seldom used for woollen, because the colours
which it gives are too fugitive, and may be obtained by more permanent
dyes. Hellot employed it to dye a stuff, prepared with alum and tartar;
but the colour acquired had little permanence. It is almost solely used
for silks.
For silks intended to become aurora and orange, it is sufficient to
scour them at the rate of 20 per cent. of soap. When they have been well
cleansed, they are immersed in a bath prepared with water, to which is
added a quantity of alkaline solution of annotto, more or less
considerable according to the shade that may be wanted. This bath should
have a mean temperature, between that of tepid and boiling water.
When the silk has become uniform, one of the hanks is taken out, washed,
and wrung, to see if the colour be sufficiently full; if it be not so,
more solution of annotto is added, and the silk is turned again round
the sticks: the solution keeps without alteration.
When the desired shade is obtained, nothing remains but to wash the
silk, and give it two beetlings at the river, in order to free it from
the redundant annotto, which would injure the lustre of the colour.
When raw silks are to be dyed, those naturally white are chosen, and
dyed in the annotto bath, which should not be more than tepid, or even
cold, in order that the alkali may not attack the gum of the silk, and
deprive it of the elasticity which it is desirable for it to preserve.
What has been now said regards the silks to which the aurora shades are
to be given; but to make an orange hue, which contains more red than the
aurora, it is requisite, after dyeing with annotto, to redden the silks
with vinegar, alum, or lemon juice. The acid, by saturating the alkali
employed for dissolving the annotto, destroys the shade of yellow that
the alkali had given, and restores it to its natural colour, which
inclines a good deal to red.
For the deep shades, the practice at Paris, as Macquer informs us, is to
pass the silks through alum; and if the colour be not red enough, they
are passed through a faint bath of brazil wood. At Lyons, the dyers who
use carthamus, sometimes employ old baths of this ingredient for dipping
the deep oranges.
When the orange hues have been reddened by alum, they must be washed at
the river; but it is not necessary to beetle them, unless the colour
turns out too red.
Shades may be obtained also by a single operation, which retain a
reddish tint, employing for the annotto bath a less proportion of alkali
than has been pointed out.
Guhliche recommends to avoid heat in the preparation of annotto. He
directs it to be placed in a glass vessel, or in a glazed earthen one;
to cover it with a solution of pure alkali; to leave the mixture at rest
for 24 hours; to decant the liquor, filter it, and add water repeatedly
to the residuum, leaving the mixture each time at rest for two or three
days, till the water is no longer coloured; to mix all these liquors,
and preserve the whole for use in a well-stopped vessel.
He macerates the silk for 12 hours in a solution of alum, at the rate of
an eighth of this salt for one part of silk, or in a water rendered
acidulous by the aceto-citric acid above described; and he wrings it
well on its coming out of this bath.
Silk thus prepared is put into the annotto bath quite cold. It is kept
in agitation there till it has taken the shade sought for; or the liquor
may be maintained at a heat far below ebullition. On being taken out of
the bath, the silk is to be washed and dried in the shade.
For lighter hues, a liquor less charged with colour is taken; and a
little of the acid liquid which has served for the mordant may be added,
or the dyed silk may be passed through the acidulous water.
We have seen the following preparation employed for cotton velvet:--one
part of quicklime, one of potash, two of soda.
Of these a ley is formed, in which one part of annotto is dissolved; and
the mixture is boiled for an hour and a half. This bath affords the
liveliest and most brilliant auroras. The buff (chamois) fugitive dye is
also obtained with this solution. For this purpose only a little is
wanted; but we must never forget, that the colours arising from annotto
are all fugitive.
Dr. John found in the pulp surrounding the unfermented fresh seeds,
which are about the size of little peas, 28 parts of colouring resinous
matter, 26·5 of vegetable gluten, 20 of ligneous fibre, 20 of colouring
extractive matter, 4 formed of matters analogous to vegetable gluten and
extractive, and a trace of spicy and acid matters.
The Gloucestershire cheese is coloured with annotto, in the proportion
of one cwt. to an ounce of the dye.
When used in calico-printing, it is usually mixed with potash or ammonia
and starch.
It is an appropriate substance for tingeing varnishes, oils, spirits,
&c.
The import duty upon annotto is 1_s._ per cwt. for flag, and 4_s._ for
other sorts. In 1834, 252,981 lbs. were imported; and in 1835, 163,421
lbs. The revenue from this drug in these two years, was 180_l._ and
98_l._ respectively.
ANTHRACITE, from ανθραξ, coal, is a species of coal found in the
transition rock formation, and is often called stone coal. It has a
grayish black, or iron black colour, an imperfectly metallic lustre,
conchoidal fracture, and a specific gravity of from 1·4 to 1·6, being,
therefore, much denser than the coal of the proper coal measures. It
consists wholly of carbon, with a small and variable proportion of
iron, silica, and alumina. It is difficult to kindle in separate masses,
and burns when in heaps or grates without smell or smoke, leaving
sometimes an earthy residuum. It has been little explored or worked in
the old world; but is extensively used in the United States of America,
and has become of late years a most valuable mineral to that country,
where it is burned in peculiar grates, adapted to its difficult
combustion. In Pennsylvania the anthracite coal formation has been
traced through a tract many miles in width, and extending across the two
entire counties of Luzerne and Schuylkill. At Maunch Chunk, upon the
Lehigh, 800 men were employed so far back as 1825, in digging this coal.
In that year 750,000 bushels were dispatched for Philadelphia. It is
worked there with little cost or labour, being situated on hills from
300 to 600 feet above the level of the neighbouring rivers and canals,
and existing in nearly horizontal beds, of from 15 to 40 feet in
thickness, covered by only a few feet of gravelly loam. At Portsmouth,
in Rhode Island, an extensive stratum of this coal has been worked, with
some interruptions, for 20 years; and more recently a mine of anthracite
has been opened at Worcester, in Massachusetts, at the head of the
Blackstone canal. It has been of late employed in South Wales, for
smelting iron, and in a cupola blast furnace, by Mr. Crane.
ANTIGUGGLER. A small syphon of metal, which is inserted into the mouths
of casks, or large bottles, called carboys, to admit air over the liquor
contained in them, and thus to facilitate their being emptied without
agitation or a guggling noise.
ANTIMONY. (_Antimoine_, Fr.; _Spiessglanz_, or _Spiessglass_, Ger.) The
only ore of this metal found in sufficient abundance to be smelted, is
the sulphuret, formerly called crude antimony. It occurs generally in
masses, consisting of needles closely aggregated, of a metallic lustre,
a lead-gray colour, inclining to steel-gray, which is unchanged in the
streak. The needles are extremely brittle, and melt even in the flame of
a candle, with the exhalation of a sulphureous smell. The powder of this
sulphuret is very black, and was employed by women in ancient times to
stain their eyebrows and eyelids. This ore consists in 100 parts of
72·86 metal, and 27·14 sulphur. Specific gravity from 4·13 to 4·6.
The veins of sulphuret of antimony occur associated with gangues of
quartz, sulphate of barytes, and carbonate of lime; those of Allémont
occur in the numerous fissures of a mica schist, evidently primitive.
In treating the ore to obtain the metal, the first object is to separate
the gangue, which was formerly done by filling crucibles with the mixed
materials, placing them on the hearth of an oven, and exposing them to a
moderate heat. As the sulphuret easily melts, it ran out through a hole
in the bottom of the crucible into a pot placed beneath, and out of the
reach of the fire. But the great loss from breakage of the crucibles,
has caused another method to be adopted. In this the broken ore, being
sorted, is laid on the bottom of a concave reverberatory hearth, where
it is reduced.
[Illustration: 18 19]
_Figs._ 18. 19. represent a wind or flame furnace, for the reduction of
antimony. The hearth is formed of sand and clay solidly beat together,
and slopes from all sides towards the middle, where it is connected with
the orifice _a_, which is closed with dense coal-ashes; _b_ is the air
channel up through the bridge; _c_, the door for introducing the
prepared ore, and running off the slags; _d_, the bridge; _e_, the
grate; _f_, the fire or fuel-door; _g_, the chimney. With 2 or 3 cwt. of
ore, the smelting process is completed in from 8 to 10 hours. The metal
thus obtained is not pure enough, but must be fused under coal dust, in
portions of 20 or 30 pounds, in crucibles, placed upon a reverberatory
hearth.
To obtain antimony free from iron, it should be fused with some
antimonic oxide in a crucible, whereby the iron is oxidized and
separated. The presence of arsenic in antimony is detected by the garlic
smell, emitted by such an alloy when heated at the blow-pipe; or,
better, by igniting it with nitre in a crucible; in which case,
insoluble antimonite and antimoniate of potash will be formed along with
soluble arseniate. Water digested upon the mixture, filtered, and then
tested with nitrate of silver, will afford the brown-red precipitate
characteristic of arsenic acid.
According to Berthier, the following materials afford, in smelting, an
excellent product of antimony: 100 parts of sulphuret; 60 of
hammerschlag (protoxide of iron from the shingling or rolling mills); 45
to 50 of carbonate of soda; and 10 of charcoal powder. From 65 to 70
parts of metallic antimony or regulus should be obtained. Glauber salts
may be used instead of soda. For another mode of smelting antimony, at
Malbosc, in the department of Ardèche, in France, see LIQUATION.
In the works where antimonial ores are smelted, by means of tartar
(argol), the alkaline scoriæ, which cover the metallic ingots, are not
rejected as useless, for they hold a certain quantity of antimonial
oxide in combination; a property of the potash flux, which is propitious
to the purity of the metal. These scoriæ, consisting of sulphuret of
potassium and antimonite of potash, being treated with water, undergo a
reciprocal decomposition; the elements of the water act on those of the
sulphuret, and the resulting alkaline hydro-sulphuret re-acts on the
antimonial solution, so as to form a species of _kermes mineral_, which
precipitates. This is dried, and sold at a low price as a veterinary
medicine, under the name of _kermes_, by the dry way.
Metallic antimony, as obtained by the preceding process, is the antimony
of commerce, but is not absolutely pure; containing frequently minute
portions of iron, lead, and even arsenic; the detection and separation
of which belong to the sciences of chemistry and pharmacy. Antimony is a
brittle metal, of a silvery white colour, with a tinge of blue, a
lamellar texture, and crystalline fracture. When heated at the blowpipe,
it melts with great readiness, and diffuses white vapours, possessing
somewhat of a garlic smell. If thrown in this melted state on a sheet of
flat paper, the globule sparkles, and bursts into a multitude of small
spheroids, which retain their incandescence for a long time, and run
about on the paper, leaving traces of the white oxide produced during
the combustion. When this oxide is fused with borax, or other vitrifying
matter, it imparts a yellow colour to it. Metallic antimony, treated
with hot nitric acid and in a concentrated state, is converted into a
powder, called antimonious acid, which is altogether insoluble in the
ordinary acid menstrua; a property by which the chemist can separate
that metal from lead, iron, copper, bismuth, and silver. According to
Bergman, the specific gravity of antimony is 6·86; but Haidinger makes
the Swedish native metal only 6·646. The alchemists had conceived the
most brilliant hopes of this metal; the facility with which it is
alloyed with gold, since its fumes alone render this most ductile metal
immediately brittle, led them to assign to it a royal lineage, and to
distinguish it by the title of _regulus_, or the little king.
Its chief employment now is in medicine, and in making the alloys called
type metal, stereotype metal, music plates, and Britannia-metal; the
first consisting of 6 of lead and 2 of antimony; the second of 6 of lead
and 1 of antimony; the third of lead, tin, and antimony; and the fourth
also of lead, tin, and antimony, with occasionally a little copper and
bismuth.--For Glass of antimony, see PASTES.
ANTISEPTICS. Substances which counteract the spontaneous decomposition
of animal and vegetable substances. These are chiefly culinary salt,
nitre, spices, and sugar, which operate partly by inducing a change in
the animal or vegetable fibres, and partly by rendering the aqueous
constituent unsusceptible of decomposition. See PROVISIONS, CURING OF.
ANVIL. A mass of iron, having a smooth and nearly flat top surface of
steel; upon which blacksmiths, and various other artificers, forge
metals with the hammer. The common anvil is usually made of seven
pieces: 1, the core, or body; 2, 3, 4, 5, the four corner pieces which
serve to enlarge its base; 6, the projecting end, which has a square
hole for the reception of the tail or shank of a chisel on which iron
bars may be cut through; and 7, the beak, or horizontal cone round which
rods or slips of metal may be turned into a circular form, as in making
rings. These 6 pieces are welded separately to the first, or core, and
then hammered into an uniform body. In manufacturing large anvils two
hearths are needed, in order to bring each of the two pieces to be
welded, to a proper heat by itself; and several men are employed in
working them together briskly in the welding state, by heavy swing
hammers. The steel facing is applied by welding in the same manner. The
anvil is then hardened by heating it to a cherry red, and plunging it
into cold water; a running stream being preferable to a pool or cistern.
The facing should not be too thick a plate, for, when such, it is apt to
crack in the hardening. The face of the anvil is now smoothed upon a
grindstone, and finally polished with emery and crocus, for all delicate
purposes of art.
The blacksmith, in general, sets his anvil loosely upon a wooden block,
and in preference on the root of an oak. But the cutlers and file-makers
fasten their anvils to a large block of stone; which is an advantage,
for the more firmly and solidly this tool is connected to the earth, the
more efficacious will be the blows of the hammer on any object placed
upon it.
AQUAFORTIS. Nitric acid, somewhat dilute, was so named by the alchemists
on account of its strong solvent and corrosive operation upon many
mineral, vegetable, and animal substances. See NITRIC ACID.
AQUA REGIA. The name given by the alchemists to that mixture of nitric
and muriatic acids which was best fitted to dissolve gold, styled by
them the king of the metals. It is now called _nitro-muriatic acid_.
AQUA VITÆ. The name very absurdly given to alcohol, when used as an
intoxicating beverage. It has been the _aqua mortis_ to myriads of the
human race; and will, probably, ere long destroy all the native tribes
of North America and Australia.
ARCHIL. A violet red paste used in dyeing, of which the substance called
_cudbear_ in Scotland (from _Cuthbert_, its first preparer in that
form), is a modification. Two kinds of archil are distinguished in
commerce, the _archil_ plant of the Canaries, and that of Auvergne. The
first is most esteemed: it is prepared from the _lichen rocellus_, which
grows on rocks adjoining the sea in the Canary and Cape de Verde
Islands, in Sardinia, Minorca, &c., as well as on the rocks of Sweden.
The second species is prepared from the _lichen parellus_, which grows
on the basaltic rocks of Auvergne.
There are several other species of lichen which might be employed in
producing an analogous dye, were they prepared, like the preceding, into
the substance called _archil_. Hellot gives the following method for
discovering if they possess this property. A little of the plant is to
be put into a glass vessel; it is to be moistened with ammonia and
lime-water in equal parts; a little muriate of ammonia (sal ammoniac) is
added; and the small vessel is corked. If the plant be of a nature to
afford a red dye, after three or four days, the small portion of liquid,
which will run off on inclining the vessel, now opened, will be tinged
of a crimson red, and the plant itself will have assumed this colour. If
the liquor or the plant does not take this colour, nothing need be hoped
for; and it is useless to attempt its preparation on the great scale.
Lewis says, however, that he has tested in this way a great many mosses,
and that most of them afforded him a yellow or reddish brown colour; but
that he obtained from only a small number a liquor of a deep red, which
communicated to cloth merely a yellowish-red colour.
Prepared archil gives out its colour very readily to water, ammonia, and
alcohol. Its solution in alcohol is used for filling spirit-of-wine
thermometers; and when these thermometers are well freed from air, the
liquor loses its colour in some years, as Abbé Nollet observed. The
contact of air restores the colour, which is destroyed anew, in vacuo,
in process of time. The watery infusion loses its colour, by the
privation of air, in a few days; a singular phenomenon, which merits new
researches.
The infusion of archil is of a crimson bordering on violet. As it
contains ammonia, which has already modified its natural colour, the
fixed alkalies can produce little change on it, only deepening the
colour a little, and making it more violet. Alum forms in it a
precipitate of a brown red; and the supernatant liquid retains a
yellowish-red colour. The solution of tin affords a reddish precipitate,
which falls down slowly; the supernatant liquid retains a feeble red
colour. The other metallic salts produce precipitates which offer
nothing remarkable.
The watery solution of archil applied to cold marble, penetrates it,
communicating a beautiful violet colour, or a blue bordering on purple,
which resists the air much longer than the archil colours applied to
other substances. Dufay says, that he has seen marble tinged with this
colour preserve it without alteration at the end of two years.