according to the quantity of wool or stuff to be dyed, and according to
the shade to which they are to be brought, is to be diffused in a bath
of water as soon as it begins to grow warm. The bath is then heated till
it be ready to boil, and the wool or stuff is passed through it without
any other preparation, except keeping that longest in, which is to have
the deepest shade. A fine gridelin, bordering upon violet, is thereby
obtained; but this colour has no permanence. Hence archil is rarely
employed with any other view than to modify, heighten, and give lustre
to the other colours. Hellot says, that having employed archil on wool
boiled with tartar and alum, the colour resisted the air no more than
what had received no preparation. But he obtained from herb archil
(_l’orseille d’herbe_) a much more durable colour, by putting in the
bath some solution of tin. The archil thereby loses its natural colour,
and assumes one approaching more or less to scarlet, according to the
quantity of solution of tin employed. This process must be executed in
nearly the same manner as that of scarlet, except that the dyeing may be
performed in a single bath.
Archil is frequently had recourse to for varying the different shades
and giving them lustre; hence it is used for violets, lilacs, mallows,
and rosemary flowers. To obtain a deeper tone, as for the deep _soupes
au vin_, sometimes a little alkali or milk of lime is mixed with it. The
suites of this browning may also afford agates, rosemary flowers, and
other delicate colours, which cannot be obtained so beautiful by other
processes. Alum cannot be substituted for this purpose; it not only does
not give this lustre, but it degrades the deep colours.
The herb-archil is preferable to the archil of Auvergne, from the
greater bloom which it communicates to the colours, and from the larger
quantity of colouring matter. It has, besides, the advantage of bearing
ebullition. The latter, moreover, does not answer with alum, which
destroys the colour; but the herb archil has the inconvenience of dyeing
in an irregular manner, unless attention be given to pass the cloth
through hot water as soon as it comes out of the dye.
Archil alone is not used for dyeing silk, unless for lilacs; but silk is
frequently passed through a bath of archil, either before dyeing it in
other baths or after it has been dyed, in order to modify different
colours, or to give them lustre. Examples of this will be given in
treating of the compound colours. It is sufficient here to point out how
white silks are passed through the archil bath. The same process is
performed with a bath more or less charged with this colour, for silks
already dyed.
Archil, in a quantity proportioned to the colour desired, is to be
boiled in a copper. The clear liquid is to be run off quite hot from the
archil bath, leaving the sediment at the bottom, into a tub of proper
size, in which the silks, newly scoured with soap, are to be turned
round on the skein-sticks with much exactness, till they have attained
the wished-for shade. After this they must receive one beetling at the
river.
Archil is in general a very useful ingredient in dyeing; but as it is
rich in colour, and communicates an alluring bloom, dyers are often
tempted to abuse it, and to exceed the proportions that can add to the
beauty without at the same time injuring in a dangerous manner the
permanence of the colours. Nevertheless, the colour obtained when
solution of tin is employed, is less fugitive than without this
addition: it is red, approaching to scarlet. Tin appears to be the only
ingredient which can increase its durability. The solution of tin may be
employed, not only in the dyeing bath, but for the preparation of the
silk. In this case, by mixing the archil with other colouring
substances, dyes may be obtained which have lustre with sufficient
durability.
We have spoken of the colour of the archil as if it were natural to it;
but it is, really, due to an alkaline combination. The acids make it
pass to red, either by saturating the alkali, or by substituting
themselves for the alkali.
The lichen which produces archil is subjected to another preparation, to
make turnsole (litmus). This article is made in Holland. The lichen
comes from the Canary Islands, and also from Sweden. It is reduced to a
fine powder by means of a mill, and a certain proportion of potash is
mixed with it. The mixture is watered with urine, and allowed to suffer
a species of fermentation. When this has arrived at a certain degree,
carbonate of lime in powder is added, to give consistence and weight to
the paste, which is afterwards reduced into small parallelopipeds that
are carefully dried.
The latest researches on the lichens, as objects of manufacture, are
those of Westring of Stockholm. He examined 150 species, among which he
found several which might be rendered useful. He recommends that the
colouring matter should be extracted in the places where they grow,
which would save a vast expense in curing, package, carriage, and waste.
He styles the colouring substance itself cutbear, persio, or turnsole;
and distributes the lichens as follows:--1st. Those which left to
themselves, exposed to moderate heat and moisture, may be fixed without
a mordant upon wool or silk; such are the L. _cinereus_, _æmatonta_,
_ventosus_, _corallinus_, _westringii_, _saxatilis_, _conspassus_,
_barbatus_, _plicatus_, _vulpinus_, &c.
2. Those which develop a colouring matter fixable likewise without
mordant, but which require boiling and a complicated preparation; such
are the lichens _subcarneus_, _dillenii_, _farinaceus_, _jubatus_,
_furfuraceus_, _pulmonareus_, _cornigatus_, _cocciferus_, _digitatus_,
_ancialis_, _aduncus_, &c. Saltpetre or sea-salt are requisite to
improve the lustre and fastness of the dye given by this group to silk.
3. Those which require a peculiar process to develop their colour; such
as those which become purple through the agency of stale urine or
ammonia. Westring employed the following mode of testing:--He put three
or four drachms of the dried and powdered lichen into a flask; moistened
it with three or four measures of cold spring water; put the stuff to be
dyed into the mixture, and left the flask in a cool place. Sometimes he
added a little salt, saltpetre, quicklime, or sulphate of copper. If no
colour appeared, he then moistened the lichen with water containing one
twentieth of sal ammoniac, and one tenth of quicklime, and set the
mixture aside in a cool place from eight to fourteen days. There
appeared in most cases a reddish or violet coloured tint. Thus the
_lichen cinereus_ dyed silk a deep carmelite, and wool a light
carmelite; the _l. physodes_ gave a yellowish-gray; the _pustulatus_, a
rose red; _sanguinarius_, gray; _tartareus_, found on the rocks of
Norway, Scotland, and England, dyes a crimson-red. In Jutland, cutbear
is made from it, by grinding the dry lichen, sifting it, then setting it
to ferment in a close vessel with ammonia. The lichen must be of the
third year’s growth to yield an abundant dye; and that which grows near
the sea is the best. It loses half its weight by drying. A single person
may gather from twenty to thirty pounds a day in situations where it
abounds. No less than 2,239,685 pounds were manufactured at
Christiansand, Flekkefiort, and Fakrsund, in Norway, in the course of
the six years prior to 1812. Since more solid dyes of the same shade
have been invented, the archil has gone much into disuse. Federigo, of
Florence, who revived its use at the beginning of the fourteenth
century, made such an immense fortune by its preparation, that his
family became one of the grandees of that city, under the name of
Oricellarii, or Rucellarii. For more than a century Italy possessed the
exclusive art of making archil, obtaining the lichens from the islands
of the Mediterranean. According to an official report of 1831, Teneriffe
furnished annually 500 quintals (cwts.) of lichen; the Canary Isles,
400; Fuerta Santura, 300; Lancerot, 300; Gomera, 300; isle of Ferro,
800. This business belonged to the crown, and brought it a revenue of
1500 piastres. The farmers paid from 15 to 20 reals for the right to
gather each quintal. At that time the quintal fetched in the London
market 4_l._ sterling.
Archil is perhaps too much used in some cloth factories of England, to
the discredit of our dyes. It is said, that by its aid one third of the
indigo may be saved in the blue vat; but the colour is so much the more
perishable. The fine soft tint induced upon much of the black cloth by
means of archil is also deceptive. One half-pound of cutbear will dye
one pound of woollen cloth. A crimson red is obtained by adding to the
decoction of archil a little salt of tin (muriate), and passing the
cloth through the bath, after it has been prepared by a mordant of tin
and tartar. It must be afterwards passed through hot water.
ARDENT SPIRIT. Alcohol of moderate strength.
AREOMETER OF BAUMÉ. This scale is much used by the French authors.
Specific Gravity Numbers corresponding with Baumé’s Areometric Degrees.
+-----------------------------------------+---------------------------+
| Liquids denser than Water. | Less dense than Water. |
+------+------+------+------+------+------+------+------+------+------+
| | Spe- | | Spe- | | Spe- | | Spe- | | Spe- |
| De- |cific | De- |cific | De- |cific | De- |cific | De- |cific |
|grees.|gravi-|grees.|gravi-|grees.|gravi-|grees.|gravi-|grees.|gravi-|
| | ty. | | ty. | | ty. | | ty. | | ty. |
+------+------+------+------+------+------+------+------+------+------+
| 0 |1·0000| 26 |1·2063| 52 |1·5200| 10 |1·0000| 36 |0·8488|
| 1 |1·0066| 27 |1·2160| 53 |1·5353| 11 |0·9932| 37 |0·8439|
| 2 |1·0133| 28 |1·2258| 54 |1·5510| 12 |0·9865| 38 |0·8391|
| 3 |1·0201| 29 |1·2358| 55 |1·5671| 13 |0·9799| 39 |0·8313|
| 4 |1·0270| 30 |1·2459| 56 |1·5833| 14 |0·9733| 40 |0·8295|
| 5 |1·0340| 31 |1·2562| 57 |1·6000| 15 |0·9669| 41 |0·8249|
+------+------+------+------+------+------+------+------+------+------+
| 6 |1·0411| 32 |1·2667| 58 |1·6170| 16 |0·9605| 42 |0·8202|
| 7 |1·0483| 33 |1·2773| 59 |1·6344| 17 |0·9542| 43 |0·8156|
| 8 |1·0556| 34 |1·2881| 60 |1·6522| 18 |0·9480| 44 |0·8111|
| 9 |1·0630| 35 |1·2992| 61 |1·6705| 19 |0·9420| 45 |0·8066|
| 10 |1·0704| 36 |1·3103| 62 |1·6889| 20 |0·9359| 46 |0·8022|
+------+------+------+------+------+------+------+------+------+------+
| 11 |1·0780| 37 |1·3217| 63 |1·7079| 21 |0·9300| 47 |0·7978|
| 12 |1·0857| 38 |1·3333| 64 |1·7273| 22 |0·9241| 48 |0·7935|
| 13 |1·0935| 39 |1·3451| 65 |1·7471| 23 |0·9183| 49 |0·7892|
| 14 |1·1014| 40 |1·3571| 66 |1·7674| 24 |0·9125| 50 |0·7849|
| 15 |1·1095| 41 |1·3694| 67 |1·7882| 25 |0·9068| 51 |0·7807|
+------+------+------+------+------+------+------+------+------+------+
| 16 |1·1176| 42 |1·3818| 68 |1·8095| 26 |0·9012| 52 |0·7766|
| 17 |1·1259| 43 |1·3945| 69 |1·8313| 27 |0·8957| 53 |0·7725|
| 18 |1·1343| 44 |1·4074| 70 |1·8537| 28 |0·8902| 54 |0·7684|
| 19 |1·1428| 45 |1·4206| 71 |1·8765| 29 |0·8848| 55 |0·7643|
| 20 |1·1515| 46 |1·4339| 72 |1·9000| 30 |0·8795| 56 |0·7604|
+------+------+------+------+------+------+------+------+------+------+
| 21 |1·1603| 47 |1·4476| 73 |1·9241| 31 |0·8742| 57 |0·7656|
| 22 |1·1692| 48 |1·4615| 74 |1·9487| 32 |0·8690| 58 |0·7526|
| 23 |1·1783| 49 |1·4758| 75 |1·9740| 33 |0·8639| 59 |0·7487|
| 24 |1·1875| 50 |1·4902| 76 |2·0000| 34 |0·8588| 60 |0·7449|
| 25 |1·1968| 51 |1·4951| | | 35 |0·8538| 61 |0·7411|
+------+------+------+------+------+------+------+------+------+------+
ARGILLACEOUS EARTH. The earth of clay, called in chemistry alumina,
because it is obtained in greatest purity from alum.
ARGOL. Crude _tartar_; which see.
ARMS. Weapons of war. See FIRE-ARMS for an account of this manufacture.
ARRACK. A kind of intoxicating beverage made in India, by distilling the
fermented juice of the cocoa-nut, the palmyra tree, and rice in the
husk.
ARROW ROOT. The root of the _maranta arundinacea_, a plant which grows
in the West Indies, furnishes, by pounding in mortars and elutriation
through sieves, a peculiar species of starch, commonly but improperly
called arrow root. It is reckoned more nourishing than the starch of
wheat or potatoes, and is generally also freer from peculiar taste or
flavour. The fresh root consists, according to Benzon, of 0·07 of
volatile oil; 26 of starch (23 of which are obtained in the form of
powder, while the other 3 must be extracted from the parenchyma in a
paste by boiling water); 1·58 of vegetable albumen; 0·6 of a gummy
extract; 0·25 of chloride of calcium; 6 of insoluble fibrine; and 65·6
of water.
The import duty upon arrow root from our own colonies, is 1_s._ per
cwt.; from foreign parts, 2_d._ per lib. In 1835, 987,966 lbs. were
imported, of which only 6267 were exported; leaving 895,406 for home
consumption. The total revenue derived that year from arrow root, was
518_l._ See STARCH.
ARSENIC. This metal occurs native, in the state of oxide, and also
combined with sulphur under the improper name of _yellow_ and _red
arsenic_, or orpiment and realgar. Arsenic is associated with a great
many metallic ores; but it is chiefly extracted from those of cobalt, by
roasting, in which case the white oxide of arsenic, or, more correctly,
the arsenious acid is obtained. This acid is introduced occasionally in
small quantities into the materials of flint glass, either before their
fusion, or in the melting pot. It serves to peroxidize the iron oxide in
the sand, and thereby to purify the body of the glass; but an excess of
it makes the glass milky.
_Scheele’s green_ is a combination of this arsenious acid with oxide of
copper, or an arsenite of copper, and is described under this metal.
_Arseniate of potash_ is prepared, in the small way, by exposing to a
moderate heat in a crucible, a mixture of equal parts of white arsenic
and nitre in powder. After fusion, the crucible is to be cooled; the
contents being dissolved in hot water, and the solution filtered, will
afford regular crystals on cooling. According to M. Berzelius, they are
composed of arsenic acid, 63·87; potash, 26·16; and water, 9·97. It is
an acidulous salt, and is hence usually called the binarseniate, to
denote that its composition is 2 atoms of arsenic acid, and 1 of potash.
This article is prepared upon the great scale, in Saxony, by melting
nitre and arsenious acid together in a cylinder of cast-iron. A neutral
arseniate also is readily formed, by saturating the excess of acid in
the above salt with potash; it does not crystallize. The acid arseniate
is occasionally used in calico printing, for preventing certain points
of the cotton cloth from taking on the mordant; with which view it is
mixed up with gum water and pipe clay into a paste, which is applied to
such places with a block.
The extraction of arsenic from the cobalt ores, is performed at
Altenberg and Reichenstein, in Silesia, with an apparatus, excellently
contrived to protect the health of the smelters from the vapours of this
most noxious metallic sublimate.
[Illustration: 20]
[Illustration: 23]
_Figs._ 20. to 23. represent the arsenical furnaces at Altenberg. _Fig._
20. is a vertical section of the poison tower; _fig._ 21., a
longitudinal section of the subliming furnace A, with the adjoining
vault B, and the poison tower in part at _n_; _fig._ 22., the transverse
section of the furnace A, of _fig._ 21.; _fig._ 23., ground plan of the
furnace A, where the left half shows the part above, and the right the
part below the muffle or oblong retort; B´ is the upper view, B´´ the
ground plan of the vault B, of _fig._ 21.; _m_, _n_, the base of the
poison tower. In the several figures the same letters denote the same
objects: _a_ is the muffle; _b_ is its mouth for turning over the
arsenical schlich, or ground ore; _c c c_, fire draughts or flues; _d_,
an aperture for charging the muffle with fresh schlich; _e_, the smoke
chimney; _f_, two channels or flues for the ascent of the arsenious
fumes, which proceed to other two flues _g_, and then terminate both in
_h_, which conducts the fumes into the vault B. They issue by the door
_i_, into the conduit _k_, thence by _l_ into the spaces _m_, _n_, _o_,
_p_, _q_, _r_, of the tower. The incondensable gases escape by the
chimney, _s_. The cover _t_, is removed after completion of the
process, in order to push down the precipitate into the lower
compartments.
[Illustration: 22 21]
The arsenious schlichs, to the amount of 9 or 10 cwt. for one operation
(1 _roast-post_, or roasting round), are spread 2 or 3 inches thick upon
the bottom of the muffle, heated with a brisk fire to redness, then with
a gentler heat, in order to oxidize completely, before subliming, the
arsenical ore. With this view the air must have free entrance, and the
front aperture of the muffle must be left quite open. After 11 or 12
hours, the calcined materials are raked out by the mouth of the muffle,
and fresh ones are introduced by the openings indicated above, which are
closed during the sublimation.
The arsenious acid found in these passages, is not marketable till it be
re-sublimed in large iron pots, surmounted with a series of sheet iron
drums or cast-iron cylinders, upon the sides of which the arsenic is
condensed in its compact glassy form. The top cylinder is furnished with
a pipe, which terminates in a condensing chamber.
[Illustration: 24]
_Figs._ 24, 25. represent the arsenic refining furnaces at Reichenstein.
_Fig._ 24. shows at A, a vertical section of the furnace, the kettle,
and the surmounting drums or cylinders; over B it is seen in elevation;
_fig._ 25. is a ground plan of the four fireplaces. _a_ is the grate;
_b_, the ash pit; _c_, the openings for firing; _d_, the fire-place;
_e_, iron pots or kettles which are charged with the arsenious powder;
_f_, the fire flues proceeding to the common chimney _g_; _h_, iron
cylinders; _i_, caps; _k_, pipes leading to the poison vent _l_; _m_,
openings in the pipes for introducing the probing wires.
[Illustration: 25]
The conduct of the process is as follows:--The pot is filled nearly to
its brim with 3-1/2 cwt. of the arsenic meal, the cylinders are fitted
on by means of their handles, and luted together with a mixture of loam,
blood, and hair; then is applied first a gentle, and after half an hour,
a strong fire, whereby the arsenic is raised partly in the form of a
white dust, and partly in crystals; which, by the continuance of the
heat, fuse together into a homogeneous mass. If the fire be too feeble,
only a sublimate is obtained; but, if too violent, much of the arsenic
is volatilized into the pipes. The workmen judge by the heat of the
cylinders whether the operation be going on well or not. After 12 hours
the furnace is allowed to cool, provided the probe wires show that the
sublimation is over. The cylinders are then lifted off, and the
arsenious glass is detached from their inner surface. According to the
quality of the poison-flour, it yields from 3/4 to 7/8 of its weight of
the glass or enamel. Should any dark particles of metallic arsenic be
intermixed with the glass, a fresh sublimation must be had recourse to.
The following is the product in cwts. of arsenious acid, at Altenberg
and Reichenstein, in Silesia, in the years
+------------------+-----+-----+-----+-----+-----+-----+-----+-----+
| |1825.|1826.|1827.|1828.|1829.|1830.|1831.|1832.|
+------------------+-----+-----+-----+-----+-----+-----+-----+-----+
|White arsenic in a| | | | | | | | |
|glassy state | 2632| 1703| 2686| 1900| 2070| 2961| 3337| 2730|
|Sublimed arsenic | | | | | | | | |
|in powder | - | 27| 33| 31| 30| 44| 69| 38|
|Yellow arsenical | | | | | | | | |
|glass | 112| 11| 56| - | 86| 313| 60| 219|
|Red arsenical | | | | | | | | |
|glass | 3| - | - | - | 28| | | |
+------------------+-----+-----+-----+-----+-----+-----+-----+-----+
ARTESIAN WELLS. Under this name is designated a cylindrical perforation,
bored vertically down through one or more of the geological strata of
the earth, till it passes into a porous gravel bed containing water,
placed under such incumbent pressure as to make it mount up through the
perforation, either to the surface or to a height convenient for the
operation of a pump. In the first case, these wells are called spouting
or overflowing. This property is not directly proportional to the depth,
as might at first sight be supposed, but to the subjacent pressure upon
the water. We do not know exactly the period at which the borer or sound
was applied to the investigation of subterranean fountains, but we
believe the first overflowing wells were made in the ancient French
province of Artois, whence the name of Artesian. These wells, of such
importance to agriculture and manufactures, and which cost nothing to
keep them in condition, have been in use, undoubtedly, for several
centuries in the northern departments of France, and the north of Italy;
but it is not more than 50 or 60 years since they became known in
England and Germany. There are now a great many such wells in London and
its neighbourhood, perforated through the immensely thick bed of the
London clay, and even through some portions of the subjacent chalk. The
boring of such wells has given much insight into the geological
structure of many districts.
The formation of artesian wells depends on two things, essentially
distinct from each other: 1. On an acquaintance with the physical
constitution, or nature, of the mineral structure of each particular
country; and, 2. On the skilful direction of the processes by which we
can reach the water level, and of those by which we can promote its
ascent in the tube. We shall first treat of the best method of making
the well, and then offer some general remarks on the other subjects.
The operations employed for penetrating the soil are entirely similar to
those daily practised by the miner, in boring to find metallic veins;
but the well excavator must resort to peculiar expedients to prevent the
purer water, which comes from deep strata, mingling with the cruder
waters of the alluvial beds near the surface of the ground, as also to
prevent the small perforation getting eventually filled with rubbish.
The cause of overflowing wells has been ascribed to a variety of
circumstances. But, as it is now generally admitted that the numerous
springs which issue from the ground proceed from the infiltration of the
waters progressively condensed in rain, dew, snow, &c. upon the surface
of our globe, the theory of these interior streamlets becomes by no
means intricate; being analogous to that of syphons and water jets, as
expounded in the treatises of physics. The waters are diffused, after
condensation, upon the surface of the soil, and percolate downwards,
through the various pores and fissures of the geological strata, to be
again united subterraneously in veins, rills, streamlets, or expanded
films, of greater or less magnitude, or regularity. The beds traversed
by numerous disjunctions will give occasion to numerous interior
currents in all directions, which cannot be recovered, and brought to
the day; but when the ground is composed of strata of sand, or gravel
very permeable to water, separated by other strata nearly impervious to
it, reservoirs are formed to our hand, from which an abundant supply of
water may be spontaneously raised. In this case, as soon as the upper
stratum is perforated, the waters may rise, in consequence of the
hydrostatic pressure upon the lower strata, and even overflow the
surface in a constant stream, provided the level from which they proceed
be proportionally higher.
The sheets of water occur principally at the separation of two
contiguous formations; and, if the succession of the geological strata
be considered, this distribution of the water will be seen to be its
necessary consequence. In fact, the lower beds are frequently composed
of compact sandstone or limestone, and the upper beds of clay. In level
countries, the formations being almost always in horizontal-beds, the
waters which feed the artesian wells must come from districts somewhat
remote, where the strata are more elevated, as towards the secondary and
transition rocks. The copious streams condensed upon the sides of these
colder lands may be therefore regarded as the proper reservoirs of our
wells.
[Illustration: 26]
_Fig._ 26. represents the manner in which the condensed water of the
heavens distributes itself under the surface of our globe. Here we have
a geological section, showing the succession of the several formations,
and the sheets or laminæ of water that exist at their boundaries, as
well as in their sandy beds. The figure shows also very plainly that the
height to which the water reascends in the bore of a well depends upon
the height of the reservoir which supplies the sheet of water to which
the well is perforated. Thus the well A, having gone down to the aqueous
expanse A A, whose waters of supply are derived from the percolation M,
will afford rising waters, which will come to the surface; whilst in the
well B, supplied by the sheet P, the waters will spout above the
surface, and in the well C they will remain short of it. The same figure
shows that these wells often traverse sheets of water, which rise to
different heights. Thus, in the well C there are five columns of
ascending waters, which rise to heights proportional to the points
whence they take their origin. Several of these will be spouting or
overflowing, but some will remain beneath the surface.
[Illustration: 27]
The situation of the intended well being determined upon, a circular
hole is generally dug in the ground, about 6 or 8 feet deep, and 5 or 6
feet wide. In the centre of this hole the boring is carried on by two
workmen below, assisted by a labourer above, as shown in _fig._ 27.
[Illustration: 28 29]
The handle (_fig._ 28.) having a female screw in the bottom of its iron
shank, with a wooden bar or rail passing through the socket of the
shank, and a ring at top, is the general agent to which all the boring
implements are to be attached. A chisel (_fig._ 29.) is first employed,
and connected to this handle by its screw at top. If the ground is
tolerably soft, the weight of the two workmen bearing upon the cross
bar, and occasionally forcing it round, will soon cause the chisel to
penetrate; but if the ground is hard or strong, the workmen strike the
chisel down with repeated blows, so as to peck their way, often changing
their situation by walking round, which breaks the stones, or other hard
substances, that may happen to obstruct its progress.
The labour is very considerably reduced, by means of an elastic wooden
pole, placed horizontally over the well, from which a chain is brought
down, and attached to the ring of the handle. This pole is usually made
fast at one end, as a fulcrum, by being set into a heap of heavy loose
stones; at the other end the labourer above gives it a slight up and
down vibrating motion, corresponding to the beating motion of the
workmen below, by which means the elasticity of the pole in rising lifts
the handle and pecker, and thereby very considerably diminishes the
labour of the workmen. See _fig._ 27.
[Illustration: 30 31 32]
When the hole has been thus opened by a chisel, as far as its strength
would permit, the chisel is withdrawn, and a sort of cylindrical auger
(_fig._ 30.) attached to the handle (_fig._ 28.), for the purpose of
drawing up the dirt or broken stones which have been disturbed by the
chisel. A section of this auger is shown in _fig._ 31., by which the
internal valve will be seen. The auger being introduced into the hole,
and turned round by the workman, the dirt or broken stones will pass
through the aperture at bottom (shown at _fig._ 32.), and fill the
cylinder, which is then drawn up, and discharged at the top of the
auger, the valve preventing its escape at bottom.
[Illustration: 33 34 35 36 37]
In order to penetrate deeper into the ground, an iron rod, as _a_,
_fig._ 33., is now to be attached to the chisel, _fig._ 29., by screwing
on to its upper end, and the rod is also fastened to the handle, _fig._
28., by screwing into its socket. The chisel having thus become
lengthened, by the addition of the rod, it is again introduced into the
hole; and the operation of pecking or forcing it down, is carried on by
the workmen as before. When the ground has been thus perforated, as far
as the chisel and its rod will reach, they must be withdrawn, in order
again to introduce the auger, _fig._ 30., to collect and bring up the
rubbish; which is done by attaching it to the iron rod, in place of the
chisel. Thus as the hole becomes deepened, other lengths of iron rods
are added, by connecting them together, as _a b_ are in _fig._ 34. The
necessity of frequently withdrawing the rods from the holes, in order to
collect the mud, stones, or rubbish, and the great friction produced by
the rubbing of the tools against its sides, as well as the lengths of
rods augmenting in the progress of the operation, sometimes to the
extent of several hundred feet, render it extremely inconvenient, if not
impossible, to raise them by hand. A tripedal standard is, therefore,
generally constructed by three scaffolding poles tied together, over the
hole, as shown _fig._ 27., from the centre of which a wheel and axle, or
a pair of pully blocks is suspended, for the purpose of hauling up the
rods, and from which hangs the fork, _fig._ 35. This fork is to be
brought down under the shoulder, near the top of each rod, and made fast
to it by passing a pin through two little holes in the claws. The rods
are thus drawn up, about seven feet at a time, which is the usual
distance between each joint, and at every haul a fork, _fig._ 36., is
laid horizontally over the hole, with the shoulders of the lower rod
resting between its claws, by which means the rods are prevented from
sinking down into the hole again, while the upper length is unscrewed
and removed. In attaching and detaching these lengths of rod, a wrench,
_fig._ 37., is employed, by which they are turned round, and the screws
forced up to their firm bearing.
[Illustration: 38]
The boring is sometimes performed for the first sixty or a hundred feet,
by a chisel of 2-1/2 inches wide, and cleared out by a gouge of 2-1/4
diameter, and then the hole is widened by a tool, such as is shown at
_fig._ 38. This is merely a chisel, as _fig._ 29., four inches wide, but
with a guide, _a_, put on at its lower part, for the purpose of keeping
it in a perpendicular direction; the lower part is not intended to peck,
but to pass down the hole previously made, while the sides of the chisel
operate in enlarging the hole to four inches. The process, however, is
generally performed at one operation, by a chisel of four inches wide,
as _fig._ 29., and a gouge of three inches and three quarters, as _fig._
30.
It is obvious, that placing and displacing the lengths of rod, which is
done every time that the auger is required to be introduced or
withdrawn, must, of itself, be extremely troublesome, independent of the
labour of boring, but yet the operation proceeds, when no unpropitious
circumstances attend it, with a facility almost incredible. Sometimes,
however, rocks intercept the way, which require great labour to
penetrate; but this is always effected by pecking, which slowly
pulverises the stone. The most unpleasant circumstance attendant upon
this business is the occasional breaking of a rod into the hole, which
sometimes creates a delay of many days, and an incalculable labour in
drawing up the lower portion.
When the water is obtained in such quantities and of such quality as may
be required, the hole is dressed or finished by passing down it a
diamond chisel, funnel mouthed, with a triangular bit in its centre;
this makes the sides smooth previous to putting in the pipe. This chisel
is attached to rods, and to the handle, as before described; and, in its
descent, the workmen continually walk round, by which the hole is made
smooth and cylindrical. In the progress of the boring, frequent veins of
water are passed through; but, as these are small streams, and perhaps
impregnated with mineral substances, the operation is carried on until
an aperture is made into a main spring, which will flow up to the
surface of the earth. This must, of course, depend upon the level of its
source, which, if in a neighbouring hill, will frequently cause the
water to rise up, and produce a continued fountain. But if the altitude
of the distant spring happens to be below the level of the surface of
the ground where the boring is effected, it sometimes happens that a
well of considerable capacity is obliged to be dug down to that level,
in order to form a reservoir, into which the water may flow, and whence
it must be raised by a pump; while, in the former instance, a perpetual
fountain may be obtained. Hence, it will always be a matter of doubt, in
level countries, whether water can be procured, which would flow near to
or over the surface; if this cannot be effected, the process of boring
will be of little or no advantage, except as an experiment to ascertain
the fact.
In order to keep the strata pure, and uncontaminated with mineral
springs, the hole is cased, for a considerable depth, with a metallic
pipe, about a quarter of an inch smaller than the bore. This is
generally made of tin (though sometimes of copper or lead) in convenient
lengths; and, as each length is let down, it is held by a shoulder
resting in a fork, while another length is soldered to it; by which
means a continuous pipe is carried through the bore, as far as may be
found necessary, to exclude land springs, and to prevent loose earth or
sand from falling in, and choking the aperture.
Mr. John Good, of Tottenham, who had been extensively employed in boring
the earth for water, obtained a patent, in Aug. 1823, for certain
improved implements contrived by him to facilitate his useful labours; a
description of which cannot fail to be interesting.
[Illustration: 39 40 41 42]
The figures annexed exhibit these ingenious tools; _fig._ 39. is an
auger, to be connected by the screw-head to the length of rods by which
the boring is carried on. This auger is for boring in soft clay or sand;
it is cylindrical, and has a slit or opening from end to end, and a bit,
or cutting-piece at bottom. When the earth is loose or wet, an auger of
the same form is to be employed, but the slit or opening reduced in
width, or even without a slit or opening. A similar auger is used for
cutting through chalk; but the point or bit at bottom should then
project lower, and, for that purpose, some of these cylindrical augers
are made with moveable bits, to be attached by screws, which is
extremely desirable in grinding them to cutting edges. _Fig._ 40. is a
hollow conical auger, for boring loose sandy soils; it has a spiral
cutting edge coiled round it, which, as it turns, causes the loose soil
to ascend up the inclined plane, and deposit itself in the hollow
within. _Fig._ 41. is a hollow cylinder or tube, shown in section, with
a foot-valve, and a bucket to be raised by a rod and cord attached at
the top; this is a pumping tool, for the purpose of getting up water and
sand that would not rise by the auger. When this cylinder is lowered to
the bottom of the bore, the bucket is lifted up by the rod and cord, and
descends again by its own gravity, having a valve in the bucket, opening
upwards, like other lift pumps; which, at every stroke, raises a
quantity of water and sand in the cylinder equal to the stroke; the
ascent and descent of the bucket being limited by a guide-piece at the
top of the cylinder, and two small knobs upon the rod, which stop
against the cross-guide. _Fig._ 42. is a tool for getting up broken
rods. It consists of a small cylindrical piece at bottom, which the
broken rod slips through when it is lowered, and a small catch with a
knife-edge, acted upon by a back-spring. In rising, the tool takes hold
of the broken rod, and thereby enables the workmen at top to draw it up.
Another tool for the same purpose, is shown at _fig._ 43., which is like
a pair of tongs; it is intended to be slidden down the bore, and for the
broken rod to pass between the two catches, which, pressed by
back-springs, will, when drawn up, take fast hold of the broken rod.
[Illustration: 43 44 45 46]
_Fig._ 44. is a tool for widening the hole, to be connected, like all
the others, to the end of the length of rods passed down the bore; this
tool has two cutting-pieces extending on the sides at bottom, by which,
as the tool is turned round in the bore, the earth is peeled away.
_Fig._ 45. is a chisel, or punch, with a projecting piece to be used for
penetrating through stone; this chisel is, by rising and falling, made
to peck the stone, and pulverize it; the small middle part breaking it
away first, and afterwards the broad part coming into action. _Fig._ 46.
is another chisel, or punching tool, twisted on its cutting edge, which
breaks away a greater portion of the stone as it beats against it.
[Illustration: 47 48 49]
The manner of forcing down lengths of cast-iron pipe, after the bore is
formed, is shown at _fig._ 47.; the pipe is seen below in the socket, at
the end of which a block is inserted; and from this block a rod extends
upwards, upon which a weight at top slides. To this weight cords are
shown to be attached, reaching to the top of the bore; where the workmen
alternately raise the weight and let it fall, which, by striking upon
the block in its middle, beats down the pipe by a succession of strokes;
and when one length of pipe has, by these means, been forced down,
another length is introduced into the socket of the former. Another
tool for the same purpose is shown at _fig._ 48., which is formed like
an acorn; the raised part of the acorn strikes against the edge of the
pipe, and by that means, it is forced down the bore. When it happens
that an auger breaks in the hole, a tool similar to that shown at _fig._
49. is introduced; on one side of this tool a curved piece is attached,
for the purpose of a guide, to conduct it past the cylindrical auger;
and at the end of the other side is a hook, which, taking hold of the
bottom edge of the auger, enables it to be drawn up.
[Illustration: 50 51 52]
Wrought iron, copper, tin, and lead pipes, are occasionally used for
lining the bore; and as these are subject to bends and bruises, it is
necessary to introduce tools for the purpose of straightening their
sides. One of these tools is shown at _fig._ 50., which is a bow, and is
to be passed down the inside of the pipe, in order to press out any
dents. Another tool, for the same purpose, is shown at _fig._ 51., which
is a double bow, and may be turned round in the pipe for the purpose of
straightening it all the way down; at _fig._ 52., is a pair of clams,
for turning the pipe round in the hole while driving.
[Illustration: 53 54]
When loose stones lie at the bottom of the hole, which are too large to
be brought up by the cylindrical auger, and cannot be conveniently
broken, then it is proposed to introduce a triangular claw, as _fig._
53., the internal notches of which take hold of the stone, and as the
tool rises, bring it up. For raising broken rods, a tool like _fig._ 54.
is sometimes employed, which has an angular claw that slips under the
shoulder of the rod, and holds it fast while drawing up.
[Illustration: 55 56]
In raising pipes, it is necessary to introduce a tool into the inside of
the pipe, by which it will be held fast. _Fig._ 55. is a pine-apple tool
for this purpose; its surface is cut like a rasp, which passes easily
down into the pipe, but catches as it is drawn up; and by that means
brings the pipe with it. _Fig._ 56. is a spear for the same purpose,
which easily enters the pipe by springing; at the ends of its prongs
there are forks which stick into the metal as it is drawn up, and
thereby raise it.
These are the new implements, for which the patent was granted. In the
process of boring, there does not appear to be any thing new proposed;
but that these several tools are to be employed for boring, packing, and
otherwise penetrating, raising the earth, and extracting broken or
injured tools. There are also suggestions for employing long buckets,
with valves opening upward in their bottoms, for the purpose of drawing
water from these wells when the water will not flow over the surface;
also lift pumps, with a succession of buckets for the same purpose. But
as these suggestions possess little if any novelty, it cannot be
intended to claim them as parts of the patent.
ASPHALTUM. Native bitumen, so called from the lake Asphaltites.
ASSAY and ASSAYING. (_Coupellation_, Fr.; _Abtreiben auf der capelle_,
Germ.) This is the process by which the quality of gold and silver
bullion, coin, plate, or trinkets is ascertained with precision, or by
which the quantity of either or both these precious metals is determined
in any given alloy. It is, therefore, a case of chemical analysis, in
which peculiar methods are employed to attain the object in view with
accuracy and dispatch. Assaying has been also extended of late years, to
determine the quantity of palladium and platina in certain bullion and
gold dust brought from Brazil.
The art of assaying gold and silver _by the cupel_, is founded upon the
feeble affinity which these metals have for oxygen, in comparison with
copper, tin, and the other cheaper metals; and on the tendency which the
latter metals have to oxidize rapidly in contact with lead at a high
temperature, and sink with it into any porous earthy vessel in a thin
glassy or vitriform state. The porous vessel may be made either of
wood-ashes, freed from their soluble matter by washing with water; or,
preferably, of burned bones reduced to a fine powder.
The lead added to the silver or gold to be assayed, serves chiefly to
dissolve the oxidized copper, whence it appears that the quantity of
lead requisite for silver assays, ought to be directly proportional to
the quantity which the silver and copper would separately require. It
has been found by experiment, that 16 parts of lead are quite sufficient
to pass 1 of copper through the cupel; and that 3/10 of lead presents
the most suitable proportion for passing one of silver. From these
principles, however, if we should always regard the dose of lead to be
employed for any alloy as being equal to (16 × C) + (3/30 × S) we should
certainly commit an error. The phenomena of cupellation is of a more
complex nature. Long practice and delicate trials alone can guide to the
proper quantity of lead to be employed for every various state of the
alloy. The following Table contains the results of M. D’Arcet’s
elaborate experiments upon this subject:--
+---------------+--------+-------------+
| Alloy. |Lead for|Ratio of the |
+-------+-------+ 1 of |Copper to the|
|Silver.|Copper.| Alloy. | Lead. |
+-------+-------+--------+-------------+
| 1000 | 0 | 3/10| 0 |
| 950 | 50 | 3 | 1 : 60 |
| 900 | 100 | 7 | 1 : 70 |
| 800 | 200 | 10 | 1 : 50 |
| 700 | 300 | 12 | 1 : 40 |
| 600 | 400 | 14 | 1 : 35 |
| 500 | 500 |16 or 17| 1 : 32 |
| 400 | 600 |16 -- 17| 1 : 26·7 |
| 300 | 700 |16 -- 17| 1 : 22·9 |
| 200 | 800 |16 -- 17| 1 : 20 |
| 100 | 900 |16 -- 17| 1 : 17·8 |
| 0 | 1000 |16 -- 17| 1 : 16 |
+-------+-------+--------+-------------+
Bismuth may be used as a substitute for lead in cupellation; two parts
of it being nearly equivalent to three of lead. But its higher prices
will prevent its general introduction among assay masters.
We begin this assay process by weighing, in a delicate balance, a
certain weight of the metallic alloy; a gramme (= 15·444 gr.) is usually
taken in France, and 12 grains in this country. This weight is wrapped
up in a slip of lead foil or paper, should it consist of several
fragments. This small parcel, thus enveloped, is then laid in a watch
glass or a capsule of copper, and there is added to it the proportion of
lead suited to the quality of alloy to be assayed; there being less
lead, the finer the silver is presumed to be. Those who are much in the
habit of cupellation can make good guesses in this way; though it is
still guess work, and often leads to considerable error, for if too much
lead be used for the proportion of baser metal present, a portion of the
silver is wasted; but if too little, then the whole of the copper, &c.
is not carried off, and the button of fine silver remains more or less
impure. The most expert and experienced assayer by the cupel, produces
merely a series of approximate conjectural results, which fall short of
chemical demonstration and certainty in every instance. The lead must
be, in all cases, entirely free from silver, being such as has been
revived from pure litharge; otherwise errors of the most serious kind
would be occasioned in the assays.
The best cupels weigh 12-1/2 grammes, or 193 grains. The cupels allow
the fused oxides to flow through them as through a fine sieve, but are
impermeable to the particles of metals; and thus the former pass readily
down into their substance while the latter remain upon their surface; a
phenomenon owing to the circumstance of the glassy oxides moistening, as
it were, the bone-ash powder, whereas the metals can contract no
adherence with it. Hence also the liquid metals preserve a hemispherical
shape in the cupels, as quicksilver does in a cup of glass, while the
fused oxide spreads over, and penetrates their substance, like water. A
cupel may be regarded, in some measure, as a filter permeable only to
certain liquids.
If we put into a cupel, therefore, two metals, of which the one is
unalterable in the air, the other susceptible of oxidizement, and of
producing a very fusible oxide, it is obvious that, by exposing both to
a proper degree of heat, we shall succeed in separating them. We should
also succeed, though the oxide were infusible, by placing it in contact
with another one, which may render it fusible. In both cases, however,
the metal from which we wish to part the oxides must not be volatile; it
should also melt, and form a button at the heat of cupellation; for
otherwise it would continue disseminated, attached to the portion of
oxide spread over the cupel, and incapable of being collected.
The furnace and implements used for assaying in the Royal Mint and the
Goldsmiths’ Hall, in the city of London, are the following:--
[Illustration: 58 59]
A A A A, _fig._ 58., is a front elevation of an assay furnace; _a a_, a
view of one of the two iron rollers on which the furnace rests, and by
means of which it is moved forward or backward; _b_, the ash-pit; _c c_
are the ash-pit dampers, which are moved in a horizontal direction
towards each other for regulating the draught of the furnace; _d_, the
door, or opening, by which the cupels and assays are introduced into the
muffle; _e_, a moveable funnel or chimney by which the draught of the
furnace is increased. B B B B, _fig._ 59., is a perpendicular section
of _fig._ 58.; _a a_, end view of the rollers; _b_ the ash-pit; _c_ one
of the ash-pit dampers; _d_ the grate, over which is the plate upon
which the muffle rests, and which is covered with loam nearly one inch
thick; _f_ the muffle in section representing the situation of the
cupels; _g_ the mouth-plate, and upon it are laid pieces of charcoal,
which during the process are ignited, and heat the air that is allowed
to pass over the cupels, as will be more fully explained in the sequel;
_h_ the interior of the furnace, exhibiting the fuel.
The total height of the furnace is 2 feet 6-1/2 inches; from the bottom
to the grate, 6 inches; the grate, muffle, plate, and bed of loam, with
which it is covered, 3 inches; from the upper surface of the grate to
the commencement of the funnel _e_, _fig._ 58., 21-1/2 inches; the
funnel _e_, 6 inches. The square of the furnace which receives the
muffle and fuel is 11-3/4 inches by 15 inches. The external sides of the
furnace are made of plates of wrought iron, and are lined with a 2-inch
fire-brick.
[Illustration: 60]
C C C C, _fig._ 60., is a horizontal section of the furnace over the
grate, showing the width of the mouth-piece, or plate of wrought iron,
which is 6 inches, and the opening which receives the muffle-plate.
[Illustration: 61]
_Fig._ 61. represents the muffle or pot, which is 12 inches long, 6
inches broad inside; in the clear 6-3/4: in height 4-1/2 inside measure,
and nearly 5-1/2 in the clear.
[Illustration: 62]
_Fig._ 62., the muffle-plate, which is of the same size as the bottom of
the muffle.
[Illustration: 63]
_Fig._ 63. is a representation of the sliding-door of the mouth-plate,
as shewn at _d_, in _fig._ 58.
[Illustration: 64]
_Fig._ 64., a front view of the mouth-plate or piece, _d_, _fig._ 58.
[Illustration: 65]
_Fig._ 65., a representation of the mode of making, or shutting up with
pieces of charcoal, the mouth of the furnace.
_Fig._ 66., the teaser for cleaning the grate.
[Illustration: 66 67 68]
_Fig._ 67., a larger teaser, which is introduced at the top of the
furnace, for keeping a complete supply of charcoal around the muffle.
_Fig._ 68., the tongs used for charging the assays into the cups.
[Illustration: 69]
_Fig._ 69. represents a board of wood used as a register, and is divided
into 45 equal compartments, upon which the assays are placed previously
to their being introduced into the furnace. When the operation is
performed, the cupels are placed in the furnace in situations
corresponding to these assays on the board. By these means all confusion
is avoided, and without this regularity it would be impossible to
preserve the accuracy which the delicate operations of the assayer
require.
[Illustration: 70 71 72]
I shall now proceed to a description of a small assay furnace, invented
by Messrs. Anfrye and d’Arcet, of Paris. They term it, _Le Petit
Fourneau à Coupelle_. _Fig._ 70. represents this furnace, and it is
composed of a chimney or pipe of wrought iron _a_, and of the furnace B.
It is 17-1/2 inches high, and 7-1/4 inches wide. The furnace is formed
of three pieces; of a dome A; the body of the furnace B; and the ash-pit
C, which is used as the base of the furnace, _fig._ 70. and 71. The
principal piece, or body of the furnace, B, has the form of a hollow
tower, or of a hollow cylinder, flattened equally at the two opposite
sides parallel to the axis, in such a manner that the horizontal section
is elliptical. The foot which supports it is a hollow truncated cone,
flattened in like manner upon the two opposite sides, and having
consequently for its basis two ellipses of different diameters; the
smallest ought to be equal to that of the furnace, so that the bottom of
the latter may exactly fit it. The dome, which forms an arch above the
furnace, has also its base elliptical, whilst that of the superior
orifice by which the smoke goes out preserves the cylindrical form. The
tube of wrought iron is 18 inches long and 2-1/2 inches diameter, having
one of its ends a little enlarged, and slightly conical, that it may be
exactly fitted or jointed upon the upper part of the furnace dome _d_,
_fig._ 70. At the union of the conical and cylindrical parts of the
tube, there is placed a small gallery of iron, _e_, _fig._ 70, 71. See
also a plan of it, _fig._ 72. This gallery is both ingenious and useful.
Upon it are placed the cupels, which are thus annealed during the
ordinary work of the furnace, that they may be introduced into the
muffle, when it is brought into its proper degree of heat. A little
above this gallery is a door _f_, by which, if thought proper, the
charcoal could be introduced into the furnace; above that there is
placed at _g_ a throttle valve, which is used for regulating the draught
of the furnace at pleasure. Messrs. Anfrye and d’Arcet say, that, to
give the furnace the necessary degree of heat so as to work the assays
of gold, the tube must be about 18 inches above the gallery, for
annealing or heating the cupels. The circular opening _h_, in the dome,
_fig._ 70., and as seen in the section, _fig._ 71., is used to introduce
the charcoal into the furnace: it is also used to inspect the interior
of the furnace, and to arrange the charcoal round the muffle. This
opening is kept shut during the working of the furnace, with the
mouth-piece, of which the face is seen at _n_, _fig._ 71.
The section of the furnace, _fig._ 71., presents several openings, the
principal of which is that of the muffle; it is placed at _i_; it is
shut with the semicircular door _m_, _fig._ 70., and seen in the section
_m_, _fig._ 71. In front of this opening, is the table or shelf, upon
which the door of the muffle is made to advance or recede; the letter
_q_, _fig._ 71., shows the face, side, and cross section of the shelf,
which makes part of the furnace. Immediately under the shelf, is a
horizontal slit, _l_, which is pierced at the level of the upper part of
the grate, and used for the introduction of a slender rod of iron, that
the grate may be easily kept clean. This opening is shut at pleasure, by
the wedge represented at _k_, _fig._ 70. and 71.
Upon the back of the furnace is a horizontal slit _p_, _fig._ 71, which
supports the fire-brick, _s_, and upon which the end of the muffle, if
necessary, may rest; _u_, _fig._ 71., is the opening in the furnace
where the muffle is placed.
[Illustration: 73]
The plan of the grate of the furnace is an ellipse: _fig._ 73. is a
horizontal view of it. The dimensions of that ellipsis determine the
general form of the furnace, and thickness of the grate. To give
strength and solidity to the grate, it is encircled by a bar or hoop of
iron. There is a groove in which the hoop of iron is fixed. The holes of
the grate are truncated cones, having the greater base below, that the
ashes may more easily fall into the ash-pit. The letter _v_, _fig._ 71.,
shows the form of these holes. The grate is supported by a small bank or
shelf, making part of the furnace, as seen at _a_, _fig._ 71.
The ash-pit, C, has an opening _y_ in front, _fig._ 71.; and is shut
when necessary by the mouth-piece _r_, _fig._ 70. and 71.
To give strength and solidity to the furnace, it is bound with hoops of
iron, at _b_, _b_, _b_, _b_, _fig._ 70.
[Illustration: 74 75 76]
_Figs._ 74. 75. 76. are views of the muffle.
_Fig._ 77. is a view of a crucible for annealing gold.
[Illustration: 77 78 79 80]
_Figs._ 78. 79. 80. are cupels of various sizes, to be used in the
furnace. They are the same as those used by assayers in their ordinary
furnaces.
[Illustration: 81 82]
_Figs._ 81. and 82. are views of the hand-shovels, used for filling the
furnace with charcoal; they should be made of such size and form as to
fit the opening _h_, in _figs._ 70. and 71.
The smaller pincers or tongs, by which the assays are charged into the
cupels, and by which the latter are withdrawn from the furnace, as well
as the teaser for cleaning the grate of the furnace, are similar to
those used in the British Mint.
In the furnace of the Mint above described, the number of assays that
can be made at one time, is 45. The same number of cupels are put into
the muffle. The furnace is then filled with charcoal to the top, and
upon this are laid a few pieces already ignited. In the course of three
hours, a little more or less, according to circumstances, the whole is
ignited; during which period, the muffle, which is made of fire-clay, is
gradually heated to redness, and is prevented from cracking; which a
less regular or more sudden increase of temperature would not fail to
do: the cupels, also, become properly annealed. All moisture being
dispelled, they are in a fit state to receive the piece of silver or
gold to be assayed.
The greater care that is exercised in this operation, the less liable is
the assayer to accidents from the breaking of the muffle; which it is
both expensive and troublesome to fit properly into the furnace.
The cupels used in the assay process, are made of the ashes of burnt
bones (phosphate of lime). In the Royal Mint, the cores of ox-horn are
selected for this purpose; and the ashes produced are about four times
the expense of the bone-ash, used in the process of cupellation upon the
large scale. So much depends upon the accuracy of an assay of gold or
silver, where a mass of 15lbs. troy in the first, and 60lbs. troy in the
second instance, is determined by the analysis of a portion not
exceeding 20 troy grains, that every precaution which the longest
experience has suggested, is used to obtain an accurate result. Hence
the attention paid to the selection of the most proper materials for
making the cupels.
The cupels are formed in a circular mould made of cast steel, very
nicely turned, by which means they are easily freed from the mould when
struck. The bone-ash is used moistened with a quantity of water,
sufficient to make the particles adhere firmly together. The circular
mould is filled, and pressed level with its surface; after which, a
pestle or rammer, having its end nicely turned, of a globular or convex
shape, and of a size equal to the degree of concavity wished to be made
in the cupel for the reception of the assay, is placed upon the ashes in
the mould, and struck with a hammer until the cupel is properly formed.
These cupels are allowed to dry in the air for some time before they are
used. If the weather is fine, a fortnight will be sufficient.
An assay may prove defective for several reasons. Sometimes the button
or bead sends forth crystalline vegetations on its surface with such
force, as to make one suppose a portion of the silver may be thrown out
of the cupel. When the surface of the bead is dull and flat, the assay
is considered to have been too hot, and it indicates a loss of silver in
fumes. When the tint of the bead is not uniform, when its inferior
surface is bubbly, when yellow scales of oxide of lead remain on the
bottom of the cupel, and the bead adheres strongly to it, by these signs
it is judged that the assay has been too cold, and that the silver
retains some lead.
Lastly, the assay is thought to be good if the bead is of a round form,
if its upper surface is brilliant, if its lower surface is granular and
of a dead white, and if it separates readily from the cupel.
After the lead is put into the cupel, it gets immediately covered with a
coat of oxide, which resists the admission of the silver to be assayed
into the melted metal; so that the alloy cannot form. When a bit of
silver is laid on a lead bath in this predicament, we see it swim about
for a long time without dissolving. In order to avoid this result, the
silver is wrapped up in a bit of paper; and the carburetted hydrogen
generated by its combustion, reduces the film of the lead oxide, gives
the bath immediately a bright metallic lustre, and enables the two
metals readily to combine.
As the heat rises, the oxide of lead flows round about over the surface,
till it is absorbed by the cupel. When the lead is wasted to a certain
degree, a very thin film of it only remains on the silver, which causes
the iridescent appearance, like the colours of soap-bubbles; a
phenomenon, called by the old chemists, fulguration.
When the cupel cools in the progress of the assay, the oxygenation of
the lead ceases; and, instead of a very liquid vitreous oxide, an
imperfectly melted oxide is formed, which the cupel cannot absorb. To
correct a cold assay, the temperature of the furnace ought to be raised,
and pieces of paper ought to be put into the cupel, till the oxide of
lead which adheres to it, be reduced. On keeping up the heat, the assay
will resume its ordinary train.
Pure silver almost always vegetates. Some traces of copper destroy this
property, which is obviously due to the oxygen which the silver can
absorb while it is in fusion, and which is disengaged the moment it
solidifies. An excess of lead, by removing all the copper at an early
stage, tends to cause the vegetation.
The brightening is caused by the heat evolved, when the button passes
from the liquid to the solid state. Many other substances present the
same phenomenon.
In the above operation it is necessary to employ lead which is very
pure, or at least free from silver. That kind is called _poor lead_.
It has been observed at all times, that the oxide of lead carries off
with it, into the cupel, a little silver in the state of an oxide. This
effect becomes less, or even disappears, when there is some copper
remaining; and the more copper, the less chance there is of any silver
being lost. The loss of silver increases, on the other hand, with the
dose of lead. Hence the reason why it is so important to proportion the
lead with a precision which, at first sight, would appear to be
superfluous. Hence, also, the reason of the attempts which have, of late
years, been made to change the whole system of silver assays, and to
have recourse to a method exempt from the above causes of error.
M. d’Arcet, charged by the Commission of the Mint in Paris, to examine
into the justice of the reclamations made by the French silversmiths
against the public assays, ascertained that they were well founded; and
that the results of cupellation gave for the alloys between 897 and 903
thousandths (the limits of their standard coin) an inferior standard, by
from 4 to 5 thousandth parts, from the standard or title which should
result from the absolute or actual alloy.
The mode of assay shows, in fact, that an ingot, experimentally composed
of 900 thousandths of fine silver, and 100 thousandths of copper,
appears, by cupellation, to be only, at the utmost, 896 or 897
thousandths; whereas fine silver, of 1000 thousandths, comes out nearly
of its real standard. Consequently a director of the Mint, who should
compound his alloy with fine silver, would be obliged to employ 903 or
904 thousandths, in order that, by the assay in the laboratory of the
Mint, it should appear to have the standard of 900 thousandths. These 3
or 4 thousandths would be lost to him, since they would be disguised by
the mode of assay, the definitive criterion of the quantity of silver,
of which the government keeps count from the coiner of the money.
From experiments subsequently made by M. d’Arcet, it appears that silver
assays always suffer a loss of the precious metal, which varies,
however, with the standard of the alloy. It is 1 thousandth for fine
silver,
4·3 thousandths for silver of 900 thousandths,
4·9 -- for -- of 800 --
4·2 -- for -- of 500 --
and diminishes thereafter, progressively, till the alloy contains only
100 thousandths of silver, at which point the loss is only 0·4.
Assays requested by the Commission of the Paris Mint, from the assayers
of the principal Royal Mints in Europe, to which the same alloys,
synthetically compounded, were sent, afforded the results inscribed in
the following table.
+----------------------+----------+-----------------------------+
| | | Standards found for the |
| | Cities | Mathematical Alloys. |
|Names of the Assayers.|where they+---------+---------+---------+
| | reside. |950 mill.|900 mill.|800 mill.|
+----------------------+----------+---------+---------+---------+
|F. de Castenhole, Mint| | | | |
|Assayer |Vienna |946·20 |898·40 |795·10 |
|A. R. Vervaëz, Ditto |Madrid |944·40 |893·70 |789·20 |
|D. M. Cabrera, Assayer| | | | |
|in Spain |Ditto |944·40 |893·70 |788·60 |
|Assayer |Amsterdam |947·00 |895·00 |795·00 |
|Mr. Bingley, Assay | | | | |
|Master |London |946·25 |896·25 |794·25 |
|Mr. Johnson, Assayer |Ditto |933·33 |883·50 |783·33 |
|Inspector of the Mint |Utrecht |945·00 |896·50 |799·00 |
|Assayer of the Mint |Naples |945·00 |891·00 |787·00 |
|Assayer of Trade |Ditto |945·00 |891·00 |787·00 |
|Assayer of the Mint |Hamburgh |946·13/72|897·41/72|798·44/72|
|Ditto |Altona |942·1/4 |894·00 |790 |
+----------------------+----------+---------+---------+---------+
These results, as well as those in still greater numbers, obtained from
the ablest Parisian assayers, upon identical alloys of silver and
copper, prove that the mode of assay applied to them brings out the
standard too low; and further, that the quantity of silver masked or
disguised, is not uniform for these different eminent assay masters. An
alloy, for example, at the standard of 900 thousandths is judged at
M.
the Mint of Paris to have a standard of 895·6
At that of Vienna -- 898·4
-- Madrid -- 893·7
-- Naples -- 891·0
The fact thus so clearly made out of a loss in the standard of silver
bullion and coin, merits the most serious attention; and it will appear
astonishing, perhaps, that a thing recurring every day, should have
remained for so long a time in the dark. In reality, however, the fact
is not new; as the very numerous and well-made experiments of Tillet
from 1760 to 1763, which are related in the memoirs of the Academy of
Sciences, show, in the silver assays, a loss still greater than that
which was experienced lately in the laboratory of the Commission of the
French Mint. But he thought that, as the error was common to the nations
in general, it was not worth while or prudent to introduce any
innovation.
A mode of assaying, to give, with certainty, the standard of silver
bullion, should be entirely independent of the variable circumstances of
temperature, and the unknown proportions of copper, so difficult to
regulate by the mere judgment of the senses. The process by the humid
way, recommended by me to the Royal Mint in 1829, and exhibited as to
its principles before the Right Honourable John Herries, then Master, in
1830, has all the precision and certainty we could wish. It is founded
on the well-known property which silver has, when dissolved in nitric
acid, to be precipitated in a chloride of silver quite insoluble, by a
solution of sea salt, or by muriatic acid; but, instead of determining
the weight of the chloride of silver, which would be somewhat uncertain
and rather tedious, on account of the difficulty of drying it, we take
the quantity of the solution of sea salt which has been necessary for
the precipitation of the silver. To put the process in execution, a
liquor is prepared, composed of water and sea salt in such proportions
that 1000 measures of this liquor may precipitate, completely, 12 grains
of silver, perfectly pure, or of the standard 1000, previously dissolved
in nitric acid. The liquor thus prepared, gives, immediately, the true
standard of any alloy whatever, of silver and copper, by the weight of
it which may be necessary to precipitate 12 grains of this alloy. If,
for example 905 measures have been required to precipitate the 12 grains
of alloy, its standard would be 905 thousandths.
The process by the humid way is, so to speak, independent of the
operator. The manipulations are so easy; and the term of the operation
is very distinctly announced by the absence of any sensible nebulosities
on the affusion of sea salt into the silver solution, while there
remains in it 1/2 thousandth of metal. The process is not tedious, and
in experienced hands it may rival the cupel in rapidity; it has the
advantage over the cupel of being more within the reach of ordinary
operators, and of not requiring a long apprenticeship. It is
particularly useful to such assayers as have only a few assays to make
daily, as it will cost them very little time and expense.
By agitating briskly during two minutes, or thereby, the liquid rendered
milky by the precipitation of the chloride of silver, it may be
sufficiently clarified to enable us to appreciate, after a few moments
of repose, the disturbance that can be produced in it by the addition of
1000 of a grain of silver. Filtration is more efficacious than
agitation, especially when it is employed afterwards; it may be
sometimes used; but agitation, which is much more prompt, is generally
sufficient. The presence of lead and copper, or any other metal, except
mercury, has no perceptible influence on the quantity of sea salt
necessary to precipitate the silver; that is to say, the same quantity
of silver, pure or alloyed, requires for its precipitation a constant
quantity of the solution of sea salt.
Supposing that we operate upon a gramme of pure silver, the solution of
sea salt ought to be such that 100 centimetres cube may precipitate
exactly the whole silver. The standard of an alloy is given by the
number of thousandths of solution of sea salt necessary to precipitate
the silver contained in a gramme of the alloy.
When any mercury is accidentally present, which is, however, a rare
occurrence, it is made obvious by the precipitated chloride remaining
white when exposed to daylight, whereas when there is no mercury
present, it becomes speedily first grey and then purple. Silver so
contaminated must be strongly ignited in fusion before being assayed,
and its loss of weight noted. In this case, a cupel assay must be had
recourse to.
_Preparation of the Normal Solution of Sea Salt, when it is measured by
Weight._--Supposing the sea salt pure as well as the water, we have only
to take these two bodies in the proportion of 0·5427 k. of salt to
99·4573 k. of water, to have 100 k. of solution, of which 100 grammes
will precipitate exactly one gramme of silver. But instead of pure salt,
which is to be procured with difficulty, and which besides may be
altered readily by absorbing the humidity of the air, a concentrated
solution of the sea salt of commerce is to be preferred, of which a
large quantity may be prepared at a time, to be kept in reserve for use,
as it is wanted. _Instruction de Gay Lussac._
_Preparation of the Normal Solution of Sea Salt, when measured by
Volume._--The measure by weight has the advantage of being independent
of temperature, of having the same degree of precision as the balance,
and of standing in need of no correction. The measure by volume has not
all these advantages; but, by giving it sufficient precision, it is more
rapid, and is quite sufficient for the numerous daily assays of the
mint. This normal solution is so made, that a volume equal to that of
100 grammes of water, or 100 centimetres cube, at a determinate
temperature, may precipitate exactly one gramme of silver. The solution
may be kept at a constant temperature, and in this case the assay stands
in want of no correction; or if its temperature be variable, the assay
must be corrected according to its influence. These two circumstances
make no change in the principle of the process, but they are
sufficiently important to occasion some modifications in the apparatus.
Experience has decided the preference in favour of applying a correction
to a variable temperature.
We readily obtain a volume of 100 cubic centimetres by means of a
_pipette_, _fig._ 83., so gauged that when filled with water up to the
mark _a_, _b_, and well dried at its point, it will run out, at a
continuous efflux, 100 grammes of water at the temperature of 15 C. (59
Fah.). We say purposely at one efflux, because after the cessation of
the jet, the pipette may still furnish two or three drops of liquid,
which must not be counted or reckoned upon. The weight of the volume of
the normal solution, taken in this manner with suitable precautions,
will be uniform from one extreme to another, upon two centimetres and a
half, at most, or to a quarter of a thousandth, and the difference from
the mean will be obviously twice less, or one half. Let us indicate the
most simple manner of taking a measure of the normal solution of sea
salt.
[Illustration: 83 84]
After having immersed the beak _c_ of the pipette in the solution, we
apply suction by the mouth, to the upper orifice, and thereby raise the
liquid to _d_ above the circular line _a b_. We next apply neatly the
forefinger of one hand to this orifice, remove the pipette from the
liquid, and seize it as represented in _fig._ 84. The mark _a b_ being
placed at the level of the eye, we make the surface of the solution
become exactly a tangent to the plane _a b_. At the instant it becomes a
tangent, we leave the beak _c_ of the pipette open, by taking away the
finger that had been applied to it, and without changing any thing else
in the position of the hands, we empty it into the bottle which should
receive the solution, taking care to remove it whenever the efflux has
run out.
If after filling the pipette by suction, any one should find a
difficulty in applying the forefinger fast enough to the upper orifice,
without letting the liquid run down below the mark _a b_, he should
remove the pipette from the solution with its top still closed with his
tongue, then apply the middle finger of one of his hands to the lower
orifice; after which he may withdraw his tongue, and apply the
forefinger of the other hand to the orifice previously wiped. This mode
of obtaining a measure of normal solution of sea salt is very simple,
and requires no complex apparatus; but we shall indicate another
manipulation still easier, and also more exact.
In this new process the pipette is filled from the top like a bottle,
instead of being filled by suction, and it is moreover fixed. _Fig._ 85.
represents the apparatus. D and D´ are two sockets separated by a stop
cock R. The upper one, tapped interiorly, receives, by means of a cork
stopper L, the tube T, which admits the solution of sea salt. The lower
socket is cemented on to the _pipette_; it bears a small air-cock R´,
and a screw plug V, which regulates a minute opening intended to let the
air enter very slowly into the pipette. Below the stop-cock R´, a silver
tube N, of narrow diameter, soldered to the socket, leads the solution
into the _pipette_, by allowing the air, which it displaces, to escape
by the stop-cock R´. The screw plug, with the milled head V´, replaces
the ordinary screw by which the key of the stop-cock may be made to
press, with more or less force, upon its conical seat.
[Illustration: 85 86]
_Fig._ 86. represents, in a side view, the apparatus just described. We
here remark an air-cock R, and an opening _m_. At the extremity Q of the
same figure, the conical pipe T enters, with friction. It is by this
pipe that the air is sucked into the pipette, when it is to be filled
from its beak.
[Illustration: 87]
The _pipette_ is supported by two horizontal arms H K (_fig._ 87.)
moveable about a common axis A A, and capable of being drawn out or
shortened by the aid of two longitudinal slits. They are fixed steadily
by two screw nuts _e e´_, and their distance may be varied by means of
round bits of wood or cork interposed, or even by opposite screw nuts _o
o´_. The upper arm H is pierced with a hole, in which is fixed, by the
pressure of a wooden screw _v_, the socket of the _pipette_. The
corresponding hole of the lower arm is larger; and the beak of the
_pipette_ is supported in it by a cork stopper L. The apparatus is fixed
by its tail-piece P, by means of a screw to the corner of a wall, or any
other prop.
The manner of filling the pipette is very simple. We begin by applying
the fore-finger of the left hand to the lower aperture _c_; we then open
the two stop-cocks R and R´. Whenever the liquor approaches the neck of
the _pipette_, we must temper its influx, and when it has arrived at
some millimetres above the mark _a b_, we close the two stop-cocks, and
remove our forefinger. We have now nothing more to do than to regulate
the _pipette_; for which purpose the liquid must touch the line _a b_,
and must simply adhere externally to the beak of the _pipette_.
[Illustration: 88]
This last circumstance is easily adjusted. After taking away the finger
which closed the aperture _c_ of the _pipette_, we apply to this orifice
a moist sponge _m_, _fig._ 88., wrapped up in a linen rag, to absorb the
superfluous liquor as it drops out. This sponge is called the
handkerchief (_mouchoir_), by M. Gay Lussac. The _pipette_ is said to be
wiped when there is no liquor adhering to its point exteriorly.
For the convenience of operating, the handkerchief is fixed by friction
in a tube of tin plate, terminated by a cup, open at bottom to let the
droppings flow off into the cistern C, to which the tube is soldered. It
may be easily removed for the purpose of washing it; and, if necessary,
a little wedge of wood, _o_, can raise it towards the _pipette_.
To complete the adjustment of the _pipette_, the liquid must be made
merely to descend to the mark _a_, _b_. With this view, and whilst the
handkerchief is applied to the beak of the _pipette_, the air must be
allowed to enter very slowly by unscrewing the plug V, _fig._ 85.; and
at the moment of the contact the handkerchief must be removed, and the
bottle F, destined to receive the solution, must be placed below the
orifice of the _pipette_, _fig._ 88. As the motion must be made rapidly,
and without hesitation, the bottle is placed in a cylinder of tin-plate,
of a diameter somewhat greater, and forming one body with the cistern
and the handkerchief. The whole of this apparatus has for a basis a
plate of tinned iron, moveable between two wooden rulers R R, one of
which bears a groove, under which the edge of the plate slips. Its
traverses are fixed by two abutments _b b_, placed so that when it is
stopped by one of them, the beak of the _pipette_ corresponds to the
centre of the neck of the bottle, or is a tangent to the handkerchief.
This arrangement, very convenient for wiping the _pipette_ and emptying
it, gives the apparatus sufficient solidity, and allows of its being
taken away, and replaced without deranging any thing. It is obvious that
it is of advantage, when once the entry of the air into the _pipette_
has been regulated by the screw V, to leave it constantly open, because
the motion from the handkerchief to the bottle is performed with
sufficient rapidity to prevent a drop of the solution from collecting
and falling down.
[Illustration: 89]
_Temperature of the Solution._--After having described the manner of
measuring by volume the normal solution of the sea salt, we shall
indicate the most convenient means of taking the temperature. The
thermometer is placed in a tube of glass T, _fig._ 89., which the
solution traverses to arrive at the _pipette_. It is suspended in it by
a piece of cork, grooved on the four sides to afford passage to the
liquid. The scale is engraved upon the tube itself, and is repeated at
the opposite side, to fix the eye by the coincidence of this double
division at the level of the thermometric column. The tube is joined
below to another narrower one, through which it is attached by means of
a cork stopper B, in the socket of the stop-cock of the _pipette_. At
its upper part it is cemented into a brass socket, screw-tapped in the
inside, which is connected in its turn by a cock, with the extremity,
also tapped, of the tube above T, belonging to the reservoir of the
normal solution. The corks employed here as connecting links between the
parts of the apparatus, give them a certain flexibility, and allow of
their being dismounted and remounted in a very short time; but it is
indispensable to make them be traversed by a hollow tube of glass or
metal, which will hinder them from being crushed by the pressure they
are exposed to. If the precaution be taken to grease them with a little
suet and to fill their pores, they will suffer no leakage.
_Preservation of the Normal Solution of Sea Salt in metallic
Vessels._--M. Gay Lussac uses for this purpose a cylindrical vessel or
drum of copper, of a capacity of about 110 litres, having its inside
covered with a rosin and wax cement.
_Preparation of the Normal Solution of Sea Salt, measuring it by
Volume._--If the drum contains 110 litres, we should put only 105 into
it, in order that sufficient space may be left for agitating the liquor
without throwing it out. According to the principle that 100 centimetres
cube, or 1/10 of a litre of the solution should contain enough of sea
salt to precipitate a gramme of pure silver; and, admitting moreover,
13·516 for the prime equivalent of silver, and 7·335 for that of sea
salt, we shall find the quantity of pure salt that should be dissolved
in the 105 litres of water, and which corresponds to 105 × 10 = 1050
grammes of silver, to be by the following proportion:--
13·516 : 7·335 ∷ 1050 gramm. : x = 569·83 gr.
And as the solution of the sea salt of commerce, formerly mentioned,
contains approximately 250 grammes per kilogramme, we must take 2279·3
grammes of this solution to have 569·83 gram. of salt. The mixture being
perfectly made, the tubes and the _pipette_ must be several times washed
by running the solution through them, and putting it into the drum. The
standard of the solution must be determined after it has been well
agitated, supposing the temperature to remain uniform.
To arrive more conveniently at this result, we begin by preparing two
_decimes_ solutions; one of silver, and another of sea salt.
The decime solution of silver is obtained by dissolving 1 gramme of
silver in nitric acid, and diluting the solution with water till its
volume become a litre.
The decime solution of sea salt may be obtained by dissolving 0·543
grammes of pure sea salt in water, so that the solution shall occupy a
litre; but we shall prepare it even with the normal solution which we
wish to test, by mixing a measure of it with 9 measures of water; it
being understood that this solution is not rigorously equivalent to that
of silver, and that it will become so, only when the normal solution
employed for its preparation shall be finally of the true standard.
Lastly, we prepare beforehand several stoppered phials, in each of which
we dissolve 1 gramme of silver in 8 or 10 grammes of nitric acid. For
brevity’s sake we shall call these tests.
Now to investigate the standard of the normal solution, we must transfer
a _pipette_ of it into one of these test phials; and we must agitate the
liquors briskly to clarify them. After some instants of repose, we must
pour in 2 thousandths of the _decime_ solution of sea salt, which, we
suppose, will produce a precipitate. The normal liquor is consequently
too feeble; and we should expect this, since the sea salt employed was
not perfectly pure. We agitate and add 2 fresh thousandths, which will
also produce a precipitate. We continue thus by successive additions of
2 thousandths, till the last produces no precipitation. Suppose that we
have added 16 thousandths: the last two should not be reckoned, as they
produced no precipitate; the preceding two were necessary, but only in
part; that is to say, the useful thousandths added are above 12 and
below 14, or otherwise they are on an average equal to 13.
Thus, in the condition of the normal solution, we require 1013 parts of
it to precipitate one gramme of silver, while we should require only
1000. We shall find the quantity of concentrated solution of sea salt
that we should add, by noting that the quantity of solution of sea salt,
at first employed, viz. 2279·3 grammes, produced a standard of only 987
thousandths = 1000 - 13; and by using the following proportion: