OUTLINES OF MINERALOGY, TRANSLATED FROM THE ORIGINAL, OF Sir TORBERN BERGMAN, KNIGHT OF THE ORDER OF WASA, PROFESSOR OF CHEMISTRY AT UPSAL, &C.
Transcriber’s Note:
New original cover art included with this eBook is granted to the public domain.
By WILLIAM WITHERING, M. D.
MEMBER OF THE ROYAL MEDICAL SOCIETY
AT EDINBURGH.
Itum eſt in viſcera terræ;
Quaſque recondiderat ſtygiiſque admoverat umbris
Effodiunter opes, irritamenta malorum.
Ovid.
BIRMINGHAM:
PRINTED BY PIERCY AND JONES,
FOR T. CADELL, AND G. ROBINSON, LONDON,
J. BALFOUR, AND C. ELLIOTT, EDINBURGH.
M,DCC,LXXXIII.
TRANSLATOR’s PREFACE.
iii
The pleaſure and inſtruction I received
myſelf from this excellent
little work of Profeſſor Bergman, inſpired
me with a wiſh to make it more
generally known to others. A ſyſtem
like this, founded upon the constituent
principles of things, may be improved,
but never can be exploded. Engliſh
names are given, but the Latin ones of
the original are ſtill retained, as an acquaintance
with them will enable the
reader more readily to conſult other
authors. Blank ſpaces are left after
most of the ſpecies, for the convenience
of inſerting any new ones that may occur.
I have added a few new ſpecies,
ivand ſome notes; the utility of which
will be ſufficiently obvious. The table
of metals, at page 71, and the index
at the end, will alſo, I hope, be
conſidered as uſeful additions.
Birmingham,
1ſt September, 1783.
N. B. The centenary (centenarius) of Professor
Bergman is equal to 60 Swediſh grains, or nearly 63
Engliſh grains.
THE AUTHOR’s PREFACE.
v
In compliance with the requeſt of my
learned and amiable friend, the celebrated
Mr. Ferber, I tranſmitted to him a ſlight
ſketch of mineralogy, in which the ſubjects
were arranged according to their conſtituent
or component parts. After peruſing it, he
requeſted my permiſſion to publiſh it. At
firſt I thought it better to ſuppreſs a work
that was ſo imperfect, eſpecially when I conſidered
the number of analyſes that yet remained
to be made. He replied, that a perfect
method was not yet to be expected in a
ſubject ſo extenſive, but that having once
laid a good foundation, I might occaſionally
make ſuch additions and corrections, in new
editions of the work, as future experiments
might render neceſſary. Indeed, I was fully
aware, that the ſyſtem would ſooner be rendered
perfect, if ſubmitted to the inſpection
of other more diſcerning chemiſts, than if the
completion of it reſted upon myſelf only. The
different remarks of others, will correct errors,
viwhich, by a further attention, I might
have amended; but if the intereſt of ſcience
be promoted, no matter by whom.
This little work contains Genera and
Species, except in the appendixes, which,
as not properly belonging to my deſign, contain
Genera only.
The Genera are founded upon the prevalent
component parts; the Species upon
the diverſity of the composition. Varieties
depend upon external appearances, and
therefore are at preſent omitted.
After this manuſcript was ſent away, I
diſcovered two species of ſtannum ſulphuratum
(tin combined with ſulphur), one of which
contains about forty per cent. of ſulphur,
the other only twenty. The firſt has the
appearance of aurum muſivum; the latter
partly reſembles antimonium ſulphuratum
(crude antimony), but does not contain antimony.
Both are contaminated by a ſmall
quantity of copper. I got them from Nerchinſkoi
in Siberia[1].
viiAs to the Terra Ponderosa (heavy
earth), I have long been aware of its great
reſemblance to calx of lead, and have even
lately found a method of precipitating it by
the phlogiſticated alkaly[2]; ſo that I verily
believe it to be of a metallic nature, although
it has never yet been made into a regulus,
and, therefore, I ſtill place it with the
earths, until its ſituation be better aſcertained.
If providence allots me life and health, I
hope, a few years hence, to republiſh this
imperfect ſketch, corrected and enlarged.
OF A NATURAL SYSTEM OF MINERALOGY.
5
§ 1.
The Mineral Kingdom conſiſts of the foſſil
ſubſtances found in the earth. Theſe are
either entirely deſtitute of organic structure, or,
having once poſſeſſed it, poſſeſs it no longer:
ſuch are the petrefactions.
§ 2.
It is requiſite, for the proper diſcrimination of
foſſils, to eſtabliſh certain characters, whereby
they may, at all times, and in all places, be diſtinguiſhed
from one another. The ſcience that
teaches theſe is called Mineralogy.
§ 3.
As in the vegetable kingdom different methods
have been formed upon the roots, the leaves, the
flowers, the fruit, &c. ſo alſo in Mineralogy
6many methods may be deviſed, and there is no
doubt of the utility of contemplating inorganic
bodies in every point of view; for the more compariſons
are multiplied, the more evidently do
reſemblances or differences appear.
§ 4.
But as the chief object of the ſcience is to
render foſſils ſubſervient to the uſes of man, it is
evident that that method muſt be the beſt which
diſplays their component parts: for theſe being
well underſtood, we know what to expect from
them; we accommodate our deſigns to their nature,
and ſpend not our labour and money in
vain attempts inconſiſtent with their inherent
qualities.
§ 5.
There is a power implanted by the creator in
organized bodies, which, upon the acquiſition of
proper nutriment, unfolds and evolves the ſtructure
which before lay concealed in the fecundated
egg or ſeed. Similar veſſels, in each ſpecies, abſorb,
convey, and aſſimilate the nouriſhment in
the ſame manner; ſo that the appearance and
ſtructure remain the ſame, unleſs peculiar cauſes
prevent the accuſtomed courſe of things, and produce
monſters: but this very rarely happens.
Hence it is that the leading features or the external
parts agree with the internal properties,
7and when judiciouſly choſen, form ſufficient characteriſtic
diſtinctions.
§ 6.
But the formation of foſſils is totally different.
Here no ſyſtem of veſſels collects, diſtributes,
ſecretes or changes the concurrent particles, but
they run together by chance, and are ſolely connected
by the power of attraction; they are generally,
too, of different kinds, rare and denſe,
figured and ſhapeleſs, admitting of every poſſible
variety. This general view of the ſubject ſhews
us how little external characters can be depended
on; but we ſhall more particularly conſider the
principal of theſe.
§ 7.
Colour varies exceedingly, as does alſo the
ſize of bodies. We cannot ſufficiently wonder at
the violence done to nature by the ſtudied ſeparation
of earths from ſtones. The conſequence is,
that a ſtone of a certain ſize muſt conſtitute one
genus, whilſt the ſame thing, reduced to powder,
muſt be placed under another genus, which ſhall
not be found even in the ſame claſs.
§ 8.
Hardness not unfrequently varies even in the
ſame ſpecimen. Soft clay dries in the fire, and
at length acquires the hardneſs of flint. Steatites
(ſoap-rock) which may be ſcraped with the nail,
8and many other matters harden in the ſame manner,
and that ſometimes without any notable loſs
of weight; ſo that bodies paſs through every different
degree of hardneſs, without any other change
of their mixture.
§ 9.
Texture, and external form of the particles,
may ſeem at firſt ſight to depend more upon the
conſtituent parts; but a calcareous particle, globular
or ſhapeleſs, is found, upon the moſt ſcrupulous
examination, to poſſeſs the ſame properties
as a piece of ſpar; and in another place I have
clearly ſhewn, that the ſchirl-like, garnet-like,
hyacinthine, twelve-ſided, and other figures, are
not unfrequently formed by nature out of the ſame
materials[3]. And if we are liable to deception
where ſo great a difference in external forms exiſts,
what can we expect from leſs conſtant external
qualities?
§ 10.
Superficial characters are therefore inſufficient.
They cannot even enable us to diſtinguiſh calcareous
from other earths, for the efferveſcence
with acids is a chemical mark, and happens, too,
in matters of very different natures. To paſs
9over other inſtances, let him who is able diſtinguiſh
the plumbum aeratum and plumbum
phoſphoratum (§ 182. § 183.) by external appearances
only!
§ 11.
But let us not altogether deſpiſe external characters:
it is of moment to know and mark
them well[4]. They frequently enable the accuſtomed
eye without troubleſome trials to acquire
a degree of certainty, which wants only a few
ſelect experiments to confirm it. Sometimes alſo
the uſe depends upon external properties, evident
to our ſenſes, as the hardneſs, the colour,
the pellucidity, &c. Theſe therefore may with
propriety be joined to thoſe which point out the
conſtituent principles.
§ 12.
Claſſes, Genera and Species are therefore to
be formed upon the internal nature and compoſition;
the varieties upon the external appearances.
In ſuch a ſyſtem both methods conveniently
agree.
§ 13.
Cronstedt firſt attempted this method, and
with great ſucceſs; but afterwards the liquid
10analyſis, in which the illuſtrious Margraaf took
the lead, better opened the internal ſecrets of
nature; ſo that the excellent work of Cronſtedt
now appears to contain many errors; theſe however
are not to be attributed to any fault in the
author, but to the inſufficiency of his experiments.
The attempts of Mr. Pott by fuſion
have long been known; but theſe however uſeful
in other reſpects, rather tend to confound
than to lay open the component parts of bodies.
§ 14.
In methodizing foſſils, compounds ſhould rank
under the moſt abundant ingredient. Thus let a and
b repreſent the component parts; if the former
be the heavier, the compound muſt be placed
under the genus of that: but this rule admits
of ſeveral exceptions.
§ 15.
Thus, the properties of all ingredients are not
of the same intenſity, if I may be allowed the expreſſion;
ſome are more powerful or efficacious,
ſo as to impreſs the maſs with their own genus
and character, though forming leſs than half the
weight. In ſuch a caſe the qualities are rather
to be conſidered than the quantity, eſpecially if
b ſo far from preponderating hardly ever amounts
to half the weight.
§ 16.
Argillaceous earth (earth of allum) and magneſia
are never found ſeparate, but almoſt always
11mixed with other things ſo that their weight conſtitutes
the ſmaller part of the maſs: therefore if
the above rule (§ 14.) was rigourouſly adhered
to, theſe primitive earths would not be found
amongſt the Genera, which would doubtleſs be
an abſurdity.
§ 17.
The value of a thing muſt likewiſe be conſidered.
Minerals containing gold or ſilver muſt
be ranked with thoſe noble metals although they
hold three, four, or more times the quantity of
heterogeneous matter. Not to mention other
examples, pyrites are placed under the genus
copper although they contain a much greater
quantity of iron. This cuſtom, eſtabliſhed with
the univerſal conſent of mineralogiſts, wants indeed
a natural foundation, but it ſeems uſeful
to miners to retain it; and the more ſo as it
is certain that otherwiſe many minerals would
be to be sought for under ſtrange and improper
titles.
§ 18.
Laſtly, it muſt be remarked, that the ſolid ingredient
determines the genus although the menſtruum
be greater in quantity. Thus in magneſia
vitriolata (Epſom ſalt) the earth gives the
Generic name, although the vitriolic acid be the
more ponderous. The same holds good in gypſum,
allum, &c.
CLASSES OF FOSSILS.
12
§ 19.
Fossils are of four kinds, viz. ſaline,
earthy, inflammable, and metallic; hence ariſe
four claſſes.
§ 20.
Salts, or ſaline ſubſtances are more or
leſs ſapid, and when finely powdered diſſolve
in at leaſt 1000 times their weight of boiling
water. They melt in the fire, which for the
moſt part changes or deſtroys them[5].
§ 21.
Earths are inſipid, not ſoluble in water
in the degree mentioned above (§ 20) though
13perhaps water in Papin’s digeſtor will diſſolve
ſome if not all of them, eſpecially if their ſurface
be greatly increaſed by a previous ſolution
in and precipitation from ſome other menſtruum.
In the chain of nature they are by inſenſible gradation
joined to the ſalts, ſo as not to be diſtinguiſhed
without artificial limits. Their form
is not changed by a moderate heat, nor are they
diſſipated by a violent one. Their ſpecific gravity
is to water, leſs than 5 to 1.
§ 22.
Inflammable foſſils abound with phlogiſton,
do not unite with water, but when pure
diſſolve in oils; expoſed to the fire, they ſmoke,
generally inflame, are for the moſt part conſumed,
and ſometimes totally vaniſh.
§ 23.
Metals when perfect do not diſſolve at all
in water; only a few of them in oils, and then
only when in part deprived of their phlogiſton.
They are the heavieſt of all known ſubſtances,
the lighteſt of them weighing more than ſix
times its bulk of water.
They melt in the fire with a ſhining ſurface,
and in clay veſſels the ſurface is convex.
CLASS I. SALTS.
14
§ 24.
We begin with the nature and properties
of ſaline bodies, for unacquainted with
theſe our knowledge of other bodies muſt be exceedingly
imperfect. Native ſalts are either acid,
alkaline, neutral, earthy or metallic.
§ 25.
Acids may be diſtinguiſhed by their proper
taſte; they efferveſce with mild alkalies; and
change the blue juices of vegetables and tincture
of heliotropium to a red colour[6].
We are acquainted with many ſpecies of acids,
but they are hardly ever found pure in the bowels
of the earth, nor can we expect to find them ſo
when we conſider how ſoon ſuch powerful menſtrua
15muſt meet with ſubſtances to ſaturate them.
Their great abundance and their properties ſhew
their various and indiſpenſible uſes in the œconomy
of nature.
§ 26.
As mineralogy treats of thoſe bodies which are
found under the ſurface of the earth, and as
acids in an uncombined ſtate are not found there,
it would ſeem proper to exclude them; but the
ſame reaſon would likewiſe exclude the primitive
earths, ſome of which have never yet been found
pure. Therefore in a ſyſtem formed upon the
component parts of bodies, a ſhort deſcription of
the principal of theſe is not to be diſpenſed
with, although they hardly ever preſent themſelves
in a ſeparate ſtate.
§ 27.
Vitriolic ACID. When moſt concentrated by
artificial means its ſpecific gravity is 2, 125.
When pure, has neither colour nor ſmell. Cold
ſometimes though very rarely concretes it into a
ſolid form; it may be coagulated by nitrous air.
This as well as the other acids is beſt known from
the compounds it forms with other ſubſtances.
Mr. Vandelli[7] ſays that it is ſometimes mixed
with the ſtreams from the hills in the neighbourhood
of Sienna and Viterbo, raiſed no doubt
16by ſubterranean fires; but in general it is united
to alkalies (§§ 44, 47, 50,) to earths (§§ 58, 59,
63, 67,) to metals (§§ 69, 70, 72, 73,) or to
phlogiſton (§§ 134, 136.)
Phlogiſticated vitriolic ACID (volatile vitriolic
acid) is frequently thrown out by the craters of
volcanoes; its ſmell ſuffocating and penetrating.
The union to phlogiſton and the matter of heat
gives it an aerial form, but does not prevent its
union with water.
§ 28.
Nitrous ACID is by ſome excluded from the
foſſil kingdom, becauſe they ſuppoſe it to be produced
from the putrefaction of organic bodies.
But theſe bodies when deprived of life are again
received amongſt the foſſils, from whence their
more fixed parts were originally derived.
In the moſt concentrated ſtate that art can procure
it, its ſpecific gravity is 1, 580. Colourleſs
when pure; but its ſtrong attraction to phlogiſton
renders particular management neceſſary to
procure it ſo[8]. With different proportions of
phlogiſton it forms phlogiſticated acid and nitrous
air.
17It has never as far as I know been met with
diſengaged, unleſs perhaps in water precipitated
out of the atmoſphere, but is found united to alkalies
(§§ 45, 47, 51 ) or to earths (§§ 60, 64.)
§ 29.
Muriatic ACID (ſpirit of ſalt) is found in
great quantity at and under the ſurface of the
earth. The ſtrongeſt prepared by art hardly attains
a ſpecific gravity of 1, 150. It has a very
peculiar and volatile ſmell. Deprived of its ſuperfluous
water it aſſumes an aerial form, for phlogiſton
ſeems to be one of its conſtituent parts[9].
It has never been found uncombined (unleſs
perhaps like the nitrous acid in water precipitated
from the atmoſphere[10])[11] but united to
alkalies (§§ 46, 49, 52), to earths (§§ 61, 65),
or to metals (§§ 74, 161, 175, 191).
§ 30.
Fluor ACID, is obtained by art; its ſpecific
gravity never exceeds 1,500, it is very volatile.
Its vapours when hot, corrode glaſs; and meeting
with moiſture generate, or at leaſt depoſit
ſiliceous earth. When deprived of its ſuperfluous
water it aſſumes an aerial form[12]. It has
18never been found diſengaged, but united to calcareous
earth forming ſparry fluor[13] (§ 96) and
if I am not miſtaken it enters into the compoſition
of ſiliceous earths.
§ 31.
Arſenical ACID, dry; prepared by art; ſpecific
gravity 3,391; fuſible and fixed in the fire,
until it acquires from the matter of heat ſo much
phlogiſton as is neceſſary to convert it into white
arſenic. In a moiſt air it deliqueſces.
It is not found uncombined, but united to
calx of cobalt (§ 228), and alſo to phlogiſton,
forming a brittle arſenical metal (§ 220), and its
calx (§ 222).
§ 32.
Molybdæna ACID. This is very probably of
metallic origin, though it does not yet appear to
which metal it belongs. Seeing that arſenic, a
brittle metal, by dephlogiſtication only is changed
into an acid, different from all other acids, it
is not improbable that other metals may have
an acid baſis, although their phlogiſton adhering
more ſtrongly has not yet been completely ſeparated.
19How this ſubſtance may be obtained by art
does not belong to this place to deſcribe[14]; but
that the acid got from Molybdæna has a metallic
nature, and as yet has not been perfectly freed
from phlogiſton, is probable from the following
conſiderations. 1, Its taſte is acid and at the
ſame time metallic. 2, Microcoſmic ſalt and
borax are coloured by it, and theſe ſalts are hardly
coloured by any thing but metallic calxes. 3,
Its decompoſition by means of the phlogiſticated
fixed alkaly, which always indicates the preſence
of a metal. 4, Its concrete form, and not deliqueſcing,
analogous to white arſenic. 5, Its ſpecific
gravity 3,460. And very lately M. Hielm
by my perſuaſion attempted the reduction and
obtained a regulus, ſeemingly different from
every other metal, but not yet ſufficiently examined.
§ 33.
An acid conjoined to the calx ponderoſa (ponderous
calx or lime) is nearly allied to the preceding,
but dropped into lime water produces a
different compound, though in a number of
other circumſtances theſe two acids agree. I apprehend
that this is likewiſe of a metallic nature.
20§ 34.
Phoſphoric ACID, evidently exiſts in the animal
kingdom,[15] much more plentifully in the vegetable,
but in the foſſil very rare. Mr. J. G. Gahn
firſt detected it united with lead;[16] but probably
it may be found in many other foſſils. It is fuſible
in the fire. Its ſpecific gravity when deprived
of water 2,687.
§ 35.
Boracic ACID, (acid of borax, or ſedative ſalt.)
Many people ſtill think this to be an artificial
production, but not long ſince Mr. Hoefer[17]
found it in a lake near Sienna in the great dutchy
of Hetruria, and it has long been known to be
united to the foſſil alkaly in native borax. It
acts like an acid, though very feebly. It melts
in the fire and volatilizes with water. Its ſpecific
gravity is 1,480.
§ 36.
Amber ACID, is a concrete ſalt obtained from
amber; it acts like a feeble acid. It is yet doubtful
whether amber be of vegetable origin; many
reckon it foſſil.
21§ 37.
Aerial ACID (fixed air) is not only combined
with water but with many other foſſil ſubſtances,
as alkalies (§§ 54, 56), earths (§§ 62, 66), and
with ſome metals (§§ 71, 183, 192, 217, 234,
243). It floats uncombined in the atmoſphere.
Its ſpecific gravity 0,0018[18].
§ 38.
ALKALIES are known by their peculiar lixivial
taſte, by their vehement attraction to acids,
and by their changing the blue colours of vegetables
to a green. In a pure ſtate, as was before
obſerved of acids, their attraction to other ſubſtances
is ſo ſtrong that they cannot long remain
uncombined; and if other acids were wanting,
the aerial acid, every where preſent in the atmoſphere,
would unite with them: therefore they are
always found in a ſtate of combination, unleſs
prepared by art.
§ 39.
New acids are daily detected, but no additions
have been made to the three ſpecies of alkaly
long ſince known.
§ 40.
Vegetable fixed ALKALY, deprived of every
acid is not found on the face of the earth; but
it is ſometimes met with in combination with the
22vitriolic acid (§ 44) or the muriatic (§ 46), generally
with the nitrous, (§ 45) rarely with the
aerial (§ 54).
§ 41.
Foſſil fixed ALKALY is only found in combination
with acids, rarely with the vitriolic (§ 47)
or nitrous (§ 48), principally with the muriatic
(§ 49) or aerial (§ 55).
§ 42.
Volatile ALKALY is frequently found in clays,
doubtleſs in a mild ſtate, for the help of art is required
to render it cauſtic. It is alſo found united
to the vitriolic (§ 50) and the muriatic acids
(§ 52.)
§ 43.
ACIDS united to alkalies form NEUTRAL
SALTS. Theſe diſſolved in water are no ways
diſturbed by the addition of an alkaly, and generally
by evaporation concrete into cryſtals. If by
proper teſts they ſhew neither acid nor alkaline
properties they are ſaid to be perfect neutrals,
but imperfect when from defect in quantity or
ſtrength of one ingredient the peculiar properties
of the other more or leſs prevail.
We now proceed to conſider the native ſalts of
both kinds.
NEUTRAL SALTS.
23
§ 44.
Alkali vegetabile vitriolatum (tartar of vitriol)
ſeldom occurs ſpontaneouſly, unleſs
where tracts of wood have been burnt down.
§ 45.
Alkali vegetabile nitratum (common nitre)
forms upon the ſurface of the earth where vegetables,
eſpecially when mixed with animal ſubſtances,
putrify. The alkaline baſis previously exiſts
in the plants[19], but the origin of the acid is not
ſo well underſtood: whether it lies concealed in
the vegetable acid, and by means of the putrefactive
proceſs ſufficiently dephlogiſticating it,
is evolved; or whether the purer part of the atmoſpheric
air contains nitrous acid fully ſaturated
with phlogiſton, which[20] upon the alkaly being
ſeparated by the putrefaction is attracted and extricated
by it, and upon loſing its inflammable principle
aſſumes its accuſtomed form. Nature perhaps
operates in both ways; the latter however
ſeems clearly confirmed by a very remarkable
experiment (§ 60.)
24As nitre is annually produced in large quantities,
it cannot but ſometimes be found in ſprings
or wells, as has been obſerved at Berlin[21], London[22],
and elſewhere[23]. Sometimes it abounds
in ſuch quantities that fleſh boiled in theſe waters
turns red.
§ 46.
ALKALI vegetabile ſalitum (digeſtive ſalt) is
ſometimes though rarely met with; generated
perhaps by the deſtruction of animal and vegetable
ſubſtances.
§ 47.
ALKALI minerale vitriolatum (Glauber’s ſalt)
is ſometimes found in waters. Some of the lakes
in Siberia and Astracan contain it, and many
ſprings in other places.
§ 48.
ALKALI minerale nitratum (cubic nitre) rarely
occurs but where maritime plants putrify.
§ 49.
ALKALI minerale ſalitum (common ſalt) plentiful
every where as well in the earth, where it
25forms ſtrata more or leſs thick (ſal gem), as alſo
diſſolved in ſprings and lakes, and in the ſea.
(ſea ſalt.)
§ 50.
ALKALI volatile vitriolatum (vitriolic ammoniac)
is ſcarcely found any where but in places
where the phlogiſticated fumes of vitriolic acid
ariſe from burning ſulphur, and in putrid places
are abſorbed by the volatile alkaly.[24] Thus at
Fahlune the acid vapour from the roaſted minerals
produces this ſalt in the neceſſary houſes. It
is ſometimes alſo formed in the craters of volcanoes.
§ 51.
ALKALI volatile nitratum (nitrous ammoniac)
is generally found along with common nitre.
§ 52.
ALKALI volatile ſalitum (ſal ammoniac or
common ammoniac.) I have examined ſome
from Veſuvius, and ſome from the Solfaterra
near Naples.
26The ſalts hitherto enumerated are perfect neutrals,
thoſe which follow are imperfect (§§ 53, 56.)
§ 53.
ALKALI FOSSIL, only in part ſaturated with
a peculiar acid is called tinkal; after depuration,
borax. It is dug out of the earth in the kingdom
of Thibet[25]. Borax takes nearly an equal weight
of acid before the alkaline properties entirely diſappear[26].
I believe no one has yet found the acid of borax
united either to the vegetable or volatile alkalies.
§ 54.
ALKALI VEGETABILE aeratum (mild vegetable
alkaly) is hardly ever found native, unleſs
in the neighbourhood of woods deſtroyed by fire.
In the year 1774, at Douai in Flanders, a
ſpring was diſcovered ſurrounded by a wall, whoſe
waters, beſides other impregnations, contained
11 grains of vegetable alkaly in a pint[27].
27§ 55.
ALKALI MINERALE aeratum (mild foſſil
alkaly, natron, the nitre of the ancients) is found
plentifully in many places, particularly in Africa
and Aſia, either concreted into chryſtallized ſtrata,
or fallen to a powder; or effloreſcing on old brick
walls, or laſtly, diſſolved in ſprings. It frequently
originates from decompoſed common ſalt. I
am not ignorant that the acid of common ſalt
adheres ſtrongly to its baſis ſo as not to be expelled
by fire; but perhaps the viciſſitudes of the
atmoſphere continually acting for ages, may be
more powerful. In immenſe plains covered over
with this alkaly, ſcarcely any common ſalt is
found upon the ſurface, but the deeper you dig
the more it is contaminated by it, the common
ſalt being yet undecompoſed for want of acceſs
of air.
§ 56.
ALKALI VOLATILE aeratum (mild volatile
alkaly) has been found in pump waters in London[28],
in Lauchſtadt[29], at Frankfort on the Mayne[30],
and copper immerſed therein is ſaid to have been
diſſolved into a blue liquor.
The three alkalies mentioned above as ſaturated
with aerial acid, differ greatly from cauſtic alkalies,
28in the mildneſs of their taſte, in their property
of chryſtallizing, and in their efferveſcing
with acids which expel the aerial acid, but they
ſtill change vegetable blues to greens, though
not ſo powerfully as the cauſtic alkalies do. Therefore,
although the ſubtil aerial acid in other reſpects
gives them neutral properties, yet in this
it does it but imperfectly.
§ 57.
The compounds of earths and acids which poſſeſs
ſolubility mentioned at § 20, are decompoſed
and precipitated by mild, but not by phlogiſticated
alkalies.
§ 58.
TERRA PONDEROSA vitriolata, (heavy
ſpar, marmor metallicum, calk) is placed with
the earths (§ 89.) Terra ponderoſa nitrata i. e.
terra ponderoſa united to the nitrous acid, perhaps
exiſts ſomewhere, but has never been met with;
neither has the terra ponderoſa united to the aerial
acid, yet been found[31]. Terra ponderoſa ſalita
i. e. terra ponderoſa with the muriatic acid Mr.
29Hielm ſays[32] is diſſolved in the waters of the
lake Vettern and its neighbourhood.
§ 59.
CALX vitriolata (gypſum, ſelenite) is not
only found diſſolved in various waters, but alſo
in many places forms immenſe ſtrata. It is
placed by all mineralogiſts amongſt the earths,
but I think improperly. When burnt it generates
heat with water, but in a leſs degree than lime
does.
§ 60.
CALX nitrata (nitre of lime; terrene nitre)
is ſometimes found in water, but very ſparingly.
It is ſaid that the chalk hills in ſome parts of
France become ſpontaneouſly impregnated with
nitrous acid, which may be waſhed out, and after
a certain time they will become impregnated
with it again.
§ 61.
CALX Salita (fixed ammoniac) occurs very
frequently in waters.
§ 62.
CALX aerata (marble, limeſtone, chalk, ſpar)
is very commonly found diſſolved in waters in
conſequence of an exceſs of the aerial acid.
When it greatly abounds, the water is ſaid to
be hard (cruda). By boiling, or by evaporation,
it depoſits ſtreaks or cruſts of calcareous matter.
30Calx aerata is not ſoluble in water without an
exceſs of the ſubtil acid, and therefore might
properly be referred to the earths (§ 21).
§ 63.
MAGNESIA vitriolata (Epſom ſalt) is not
unfrequent in the waters of England, Bohemia,
and other countries. This ſalt is preſently decompoſed
by lime water, which circumſtance
readily diſtinguiſhes it from the alk. min. vitriol.
or Glauber’s ſalt.
§ 64.
MAGNESIA nitrata (magneſia and nitrous
acid) is uſually found together with nitre.
§ 65.
MAGNESIA ſalita (magneſia and muriatic
acid) is found diſſolved in various waters, but
plentifully in ſea water, to which it gives a
diſagreeable bitterneſs.
§ 66.
MAGNESIA aerata (common magneſia) with
an exceſs of aerial acid it becomes ſoluble in
cold water, otherwiſe it is ſcarce ſoluble at all,
and therefore ſhould be claſſed with the earths.
(§ 21.)
31§ 67.
ARGILLA vitriolata (alum) is ſometimes
ſpontaneouſly generated by the decompoſition of
pyrites lodged in clay, or in argillaceous ſchiſtus.
It is found in a ſpring at Steckenitz in Bohemia[33],
in Eaſt Bothnia and elſewhere. What
is commonly called plumoſe alum is not a ſaline
ſubſtance.
ARGILLA (clay) united to the nitrous, muriatic[34],
or aerial acids has not to my knowledge
hitherto been found in any waters.
METALLIC SALTS.
32
§ 68.
The native ſalts belonging to this diviſion,
may be diſtinguiſhed by the phlogiſticated
alkaly which precipitates them all.
The few which have ſaline properties (§ 20.)
we ſhall mention here, referring the reſt to the
mineralized metals.
§ 69.
CUPRUM vitriolatum (vitriol of copper, blue
vitriol) is found in the mines of Herregrund,
Fahlune, and others which contain copper
pyrites.
§ 70.
FERRUM vitriolatum (vitriol of iron, green
vitriol) is formed from the decompoſition of the
more common pyrites.
§ 71.
FERRUM aeratum (iron with aerial acid)
diſſolved by an exceſs of acid in the lighter
chalybeate waters.
33FERRUM nitratum, and ſalitum (iron with
nitrous and muriatic acids) have never yet been
found native.
§ 72.
NICCOLUM vitriolatum (vitriol of Nickel)
ſometimes exiſts from the decompoſition of ſulphureous
ores of Nickel.
§ 73.
ZINCUM vitriolatum (vitriol of zinc, white
vitriol) is ſometimes, though rarely, produced
By the decompoſition of pſeudogalena, or black
Jack, becauſe this ſubſtance does not very
readily decompoſe ſpontaneouſly.
§ 74.
[35]MANGANESIUM ſalitum (manganeſe
united to muriatic acid) exiſts in ſome waters
Mr. Hielm ſays.
Whether manganeſe be ever united to waters
like iron, by means of an exceſs of aerial acid,
we know not.
TRIPLE SALTS.
34
§ 75.
The compound ſalts hitherto enumerated are
ſuch as are compoſed of two ingredients only;
but ſometimes three or more are ſo united as not to
be ſeparated by chryſtallization. The vitriols that
we are acquainted with are hardly ever pure, and
two or three of them ſometimes are joined together.
Sometimes likewiſe it happens that neutral ſalts
join earthy ſalts, and earthy ſalts metallic ones.
I generally diſtinguiſh compound ſalts according
to the number of their principles, whether
the ſame acid be joined to ſeveral baſes, or the
ſame baſis to different acids; or laſtly, whether
ſeveral menſtrua and ſeveral baſes are joined together.
Hence ariſe ſalts triple, quadruple, &c.
which the diligence of after times muſt illuſtrate.
I ſubjoin the moſt remarkable examples of triple
and quadruple native ſalts which have occurred
to me.
§ 76.
ALKALI MINERALE Salitum (common
ſalt) contaminated by magneſia ſalita. The common
35ſalt when pure does not deliqueſce, but this
degree of purity is ſeldom found, and in the native
foſſil production (ſal gem) never.
§ 77.
MAGNESIA vitriolata (Epſom ſalt) contaminated
by ferrum vitriolatum[36] (vitriol of iron.)
§ 78.
ARGILLA vitriolata (alum) native, contaminated
by vitriol of iron. In the aluminous ſchiſtus
it ſometimes effloreſces in a feathery form. Is
this the plumoſe alum of the antients?
§ 78*.
ARGILLA vitriolata (alum) native; contaminated
by ſulphur and vitriolic acid.
At the places about Wedneſbury and Bilſton,
in Staffordſhire, where the coal pits are on fire,
this ſubſtance ſublimes to the ſurface, and may
be collected in conſiderable quantity during dry
or froſty weather. I cannot be certain that this
is a true chemical union, but the eye cannot diſtinguiſh
the parts. Perhaps the ſulphur volatilizes
the alum and ſo becomes intimately mixed with
it. The exceſs of vitriolic acid keeps it in a
deliqueſcent ſtate.
I believe a ſimilar compound ſubſtance
ſublimes at the Solfaterra near Naples. W.
36§ 79.
ARGILLIA vitriolata (alum) native, contaminated
by vitriol of cobalt. In the mines of Herregrund
and Idra this may be ſeen, ſhooting out
into long ſlender filaments. Perhaps this is the
trichites of the Greeks. Diſſolved in water it immediately
betrays the preſence of vitriolic acid,
upon the addition of terra ponderoſa ſalita (muriatic
acid ſaturated with heavy earth.) By the
addition of phlogiſticated alkali a precipitate of
cobalt is thrown down, which makes a blue glaſs
with borax or microcoſmic ſalt.
§ 80.
CUPRUM vitriolatum (vitriol of copper)
contaminated by iron.
§ 81.
FERRUM vitriolatum (vitriol of iron) contaminated
by nickel.
§ 82.
CUPRUM vitriolatum (vitriol of copper) and
vitriol of iron contaminated by zinc. Such is
found at Fahlune.
CLASS II. EARTHS.
37
§ 83.
Before we can underſtand the nature of
earths, we muſt know their component parts.
Thoſe earths which cannot be further decompoſed
we call primitive, and thoſe which conſiſt of two
or more of theſe intimately united, derivative. By
this union we do not mean a mere mechanical
diffuſion, at leaſt not ſuch as can be diſtinguiſhed
by the eye, as is the caſe in ſtones, (ſaxa.)
§ 84.
It is evident that the primitive earths will conſtitute
ſo many natural Genera, and different
mixtures of theſe the Species.
They who would make ſeveral Genera out of
one primitive earth, muſt ſeparate the glaſſy, red,
white, horny ſilver ores, and other different
compoſitions into as many Genera, or elſe act
inconſiſtently with their own principles.
§ 85.
At preſent we only know five primitive earths.
They who reckon fewer, reſt their opinions upon
fanciful metamorphoſes unſupported by faithful
38experiments[37]. As experiments teach us that there
are five primitive earths, it is evident that the
Species ariſing from the mixture of theſe cannot
exceed twenty-four, viz. 10 double (conſiſting of
two earths) 6 triple, 3 quadruple, and the 5
primitive.
Although theſe different mixtures are poſſible,
and probably do exiſt, they have not yet been
all found. The natural compoſitions of acids
with the earths, forming ſubſtances not ſoluble
in 1000 times their weight of boiling water, and
which may be called ſaline earths, muſt be added
to the ſpecies, as they are certainly chemical
combinations.
§ 86.
The primitive earths hitherto detected are,
TERRA PONDEROSA, or
heavy earth.
CALX,
calcareous earth.
MAGNESIA,
magneſia.
ARGILLA,
argillaceous earth.
TERRA SILICEA,
ſiliceous earth.
And we muſt believe theſe to be primitive, until
it ſhall appear by proper experiments that they
may be ſeparated into others ſtill more ſimple, or
changed into one another by art.
39Theſe are firſt to be conſidered in their greateſt
ſimplicity and purity, although nature never
preſents us with ſuch, nor can they even by art be
rendered abſolutely free from all heterogeneous
mixture. Water and aerial acid readily unite
with the four firſt, and when expelled by fire, a
little of the matter of heat is added, and remains
until driven out by a more powerful attraction.
But in this ſtate they poſſeſs a degree of purity
not to be attained by any other known method.
Therefore it is neceſſary to examine them when
ſufficiently burnt in order to diſtinguiſh better
what properties depend upon adhering heterogeneous
matters.
HEAVY EARTH, OR TERRA PONDEROSA.
40
§ 87.
To obtain this as pure as poſſible, the ſpathum
ponderoſum § 89 (heavy ſpar) muſt
be reduced to a fine powder, and with equal parts
of fixed alkaly and charcoal duſt roaſted for an
hour in a covered crucible. Powder the maſs,
and add nitrous or muriatic acid diluted until all
efferveſcence ceaſes, and the liquor be ſenſibly
acid. To this liquor add mild fixed alkaly, and
the heavy earth will be precipitated in a mild
ſtate. If the acids or the alkaline ſalt contain
any vitriolic acid, the heavy ſpar will immediately
be regenerated. What remains undiſſolved by
the acid is heavy ſpar, not decompoſed. The
proceſs may be repeated upon this, but the product
will then contain ſome martial earth and
ſome clay from the crucible, therefore the firſt
part will be the moſt pure.
41§ 88.
TERRA PONDEROSA aerata, (heavy earth)
has a ſpecific gravity of 3, 773[38]. 100 parts of
it contain about 28 of water, 7 of aerial acid, and
65 of pure earth. It efferveſces with acids: with
the vitriolic acid forms heavy ſpar, not ſoluble in
water; with the nitrous and muriatic acids, it
yields chryſtals, not very readily ſoluble; but
with the vegetable acid the chryſtals deliqueſce.
When free from all contamination of acid or
alkaly it ſcarcely melts in the fire, but loſes ³⁵⁄₁₀₀
of its weight. When united with the matter of
heat, (i. e. rendered cauſtic) it diſſolves in 900
times its weight of water; and when this ſolution
is expoſed to the atmoſphere, a cream or cruſt
ſeparates at the top, which efferveſces with acids.
After burning, it unites to acids without efferveſcence;
but heat is produced, and the union is
more tardy than when it is in a mild ſtate[39].
When cauſtic, it expels the volatile alkaly
from ſal ammoniac, and forms a hepar with ſulphur,
the watery ſolution of which is but imperfectly
decompoſed by the nitrous or muriatic acids,
42upon account of the remarkable attraction betwixt
this earth and the acid of the ſulphur, which
it even takes from the vegetable alkaly[40].
When we compare theſe properties with thoſe
which belong to common calcareous earth, mentioned
at (§§ 92, 93), we ſhall readily ſee wherein
they agree, and wherein they differ.
§ 89.
TERRA PONDEROSA vitriolata (heavy
ſpar) is full four times as heavy as an equal bulk
of water. It diſſolves entirely, though ſparingly,
in concentrated boiling vitriolic acid, but the addition
of a ſingle drop of water occaſions a precipitation.
The ſame thing happens to gypſum;
but that requires much leſs acid to diſſolve it, and
the precipitation is made more ſlowly. If the
heavy ſpar contained any ſulphur, it muſt certainly
have appeared when the whole was diſſolved, but
I never could find any thing like it.
Cronstedt, Min. § 18. 2.
Marmor metallicum druſicu § 19 C. Ponderous Spar.
§ 90.
TERRA PONDEROSA vitriolata, impregnated
with bitumen, and mixed with gypſum,
alum, and ſiliceous earth.
Cronstedt Min. § 24. Lapis hepaticus. Liver Stone.
43A nucleus of this kind, taken out of a piece of
alum ore from Andrarum in the province of Skone,
yielded, in 100 parts, by analyſis, 33 of ſiliceous
earth, 29 of cauſtic heavy earth, earth of
alum about 5, and quick-lime from 3 to 7, beſides
the water and vitriolic acid. By calculation
it appears, that theſe baſes, together with vitriolic
acid enough to ſaturate them, ought to weigh 71,
which, with the addition of 33, exceeds the amount
of the original 100. This increaſe points out the
difference of a maſs newly chryſtallized, and of
one carefully dried.
§ 91.
When we conſider that the terra ponderoſa
was altogether unknown before the year 1774,
and that many mineralogiſts are even now unacquainted
with it, we cannot wonder that we know
ſo few ſpecies of it. I have ſcarce a doubt but the
terra ponderoſa aerata may be found mixed with
other earths in many ſpecimens, when they come
to be examined by chemical means more accurately
than they could be heretofore. (See
notes to §§ 58 and 88.)
CALCAREOUS EARTH, OR CALX.
44
§ 92.
As calcareous earth united to the aerial acid
is found native, it requires but little trouble
to have it pure. Let ſelected pieces of chalk,
reduced to fine powder, be repeatedly boiled in
pure water: this diſſolves any calx or magneſia
ſalita which it may contain. This done, it
holds no heterogeneous matter but what mechanically
adheres to it, the quantity of which is
generally extremely ſmall. If we deſire to be free
from this likewiſe, diſſolve the waſhed chalk in
diſtilled vinegar, precipitate with volatile alkaly,
and after waſhing the precipitate well, dry it.
§ 93.
The ſpecific gravity of calcareous earth thus
purified, is 2,720. 100 parts of it contain about
34 of aerial acid, 11 of water, and 55 of pure
earth.
Acids unite with it efferveſcing, and a centenary
(centenarius) excites about 22 degrees of
45heat. The vitriolic acid forms gypſum, difficult
to diſſolve, (§ 59). The nitrous and muriatic acids
form deliqueſcent ſalts (§§ 60, 61), and the acetous
acid permanent chryſtals.
Pure calcareous earth does not melt in the fire,
but loſes ⁴⁵⁄₁₀₀ of its weight. It diſſolves in 700
times its weight of water, generating heat[41]. Acids
diſſolve it, producing from a centenary 252 degrees
of heat, but without any efferveſcence. This
laſt circumſtance may be beſt obſerved by immerging
the burnt earth in water, to diſſipate a
part of the heat, which would otherwiſe make the
acid boil. The water likewiſe expels the atmoſpheric
air from the pores of the lime. In this ſituation,
if nitrous or muriatic acid be poured upon
it, and if it was previouſly well burnt, no efferveſcence
will take place. The ſolution proceeds
ſlowly[42], but the ſaturation becomes as perfect as
if the calcareous earth had been in a mild ſtate.
This burnt earth, or lime, expels the volatile
alkaly from ſal ammoniac in a cauſtic ſtate, and
it diſſolves ſulphur; but this compound is ſeparated
upon the addition of any acid, even the
aerial.
§ 94.
Amongſt the native Species of this genus, we
muſt firſt mention the Calxaerata (marble, limeſtone,
46chalk) which conſtitute immenſe ſtrata.
Its chief properties are enumerated above (§ 92).
It is very rarely found entirely free from iron,
which exiſts even in the pureſt Icelandic ſpar, and
indeed in almoſt every foſſil production; upon
which account only the more remarkable impregnations
with iron will be noticed in the following
pages.
Cronstedt Min. §§ 5–12.
§ 95.
CALX aerata (calcareous earth mild), with
more or leſs petroleum. It efferveſces with acids,
and diſſolves; with the vitriolic acid frequently
turning brown. Is fœtid when heated or rubbed.
The oil is not in ſufficient quantity to
be collected, by diſtillation, in drops; it only
fouls the inſide of the veſſels, unleſs a very
great quantity be operated upon. In an open fire
the colour preſently vaniſhes, from the petroleum
drying up. It generally contains a portion
of martial clay.
Cronstedt Min. §§ 22, 23. Lapis ſuillus. Fœtid ſtone.
§ 96.
CALX fluorata (calcareous earth and fluor acid),
when pure, is wholly ſoluble in nitrous and muriatic
acids. Expoſed to heat, below ignition, it
emits a phosphoreſcent light. Fluor acid, dropped
into lime water, precipitates a powder which
47has all the properties of the calx fluorata. It is
ſometimes, but not always, contaminated by a
ſmall proportion of ſiliceous earth and muriatic
acid.
Cronstedt Min. §§ 97–101. Sparry fluor. Blue John.
§ 97.
CALX (calcareous earth) ſaturated with a peculiar
acid, perhaps of a metallic nature (§ 33). In
acids, particularly in the muriatic, it aſſumes a
remarkable yellow colour, but is not very ſoluble.
Cronstedt Min. § 210. Lapis ponderoſus. Tungſten.
§ 98.
CALX aerata (calcareous earth mild), contaminated
by a ſmall proportion of magneſia ſalita.
Magneſia.
§ 99.
CALX aerata (calcareous earth mild) contaminated
by clay.
Argillaceous.
§ 100.
CALX aerata (calcareous earth mild), contaminated
by ſiliceous earth.
Siliceous.
48§ 101.
CALX aerata (calcareous earth mild), contaminated
by clay and ſiliceous earth. (See § 115.)
Cronstedt Min. §§ 25. 28. Calcareous Marle.
§ 102.
CALX aerata (calcareous earth mild), contaminated
by iron and manganeſe. Martial.
Cronstedt Min. §30. See alſo §203. Hæmatites.
103.
There can be no doubt that the four firſt
(§§ 94–97.), if not the laſt (§ 102), are genuine
and diſtinct ſpecies; there is ſome difficulty as to
the reſt, dependent, perhaps, only upon mechanical
mixtures. If the heterogeneous matters can
be diſcerned by the eye, we cannot heſitate to
refer the ſubſtance to the ſaxa (ſtones); but in
theſe the eye cannot diſcern them. Moreover,
we know that the earths have a mutual attraction
to each other, and form combinations more intimate
than mechanical ones. Earth of alum, precipitated
by a cauſtic alkali, and thrown into
lime water, preſently loſes its pellucid and ſpongy
texture, turns white, and condenſes, abſorbing
the lime from the water, and forming an union
not to be ſeparated but by chemical means.
49From theſe conſiderations, I dare not venture
to exclude doubtful ſpecies.
We ſay a thing is contaminated by another, when
the mixture is of the mechanical kind; but when
things are joined by the ſtronger power of attraction,
we ſay they are united.
MAGNESIA.
50
§ 104.
Magnesia, called in the diſpenſatories,
and by apothecaries magneſia alba, is a precipitation
from its union with vitriolic acid, called
Epſom ſalt. If this earthy precipitate be
wanted in the greatest degree of purity, the Epſom
ſalt must be taken chryſtallized, and well depurated,
diſſolved in distilled water, and precipitated
by volatile alkaly. Let the liquor be boiled
for a few minutes, in order that what is kept in
ſolution by the aerial acid may ſubside.
§ 105.
Magneſia, thus obtained, has a ſpecific gravity
of 2,155. 100 parts of it contain about 25 of
aerial acid, 30 of water, and 45 of earth[43]. It
diſſolves in acids, with a violent efferveſcence,
but without heat. It again forms Epſom ſalt, with
the vitriolic acid; with the nitrous acid it chryſtallizes,
but the chryſtals are deliqueſcent; with
the muriatic and vegetable acids it does not chryſtallize,
and after drying, greedily attracts moiſture
from the atmoſphere.
51It does not melt in a moderate heat, but loſes
⁵⁵⁄₁₀₀ of its weight, and then has no attraction for
water; diſſolves ſlowly, even in acids, and that
without efferveſcence, but with ſome degree of
heat. After calcination, it expels the volatile alkaly
from ſal ammoniac, and unites to ſulphur,
though very feebly.
MAGNESIA aerata (common magneſia) is
never found native and unconnected, unleſs in
waters, when it is diſſolved by an exceſs of aerial
acid. (§ 66.)
§ 106.
MAGNESIA aerata (common magneſia) united
with ſiliceous matter. This efferveſces with
acids, and not unfrequently ſtrikes fire with ſteel.
§ 107.
MAGNESIA intimately united with ſiliceous
matter. The ſoluble part is ſlowly taken up by
acids, without efferveſcence.
Cronstedt Min. §§79–83. and perhaps § 102–105
alſo; but I have not yet ſubmitted the aſbeſti to the liquid
analyſis.
Soaprock.Serpentine.
§ 108.
MAGNESIA united to argillaceous, ſiliceous,
and pyritical matters.
M. Monnet diſcovered this, and the next ſpecies.
52§ 109.
MAGNESIA united to argillaceous, ſiliceous,
and pyritical matters, and likewiſe contaminated
by petroleum.
This ſpecies reſembles aluminous ſchiſtus, but upon examination
is found to contain more magneſia than clay.
§ 110.
All the ſpecies, except the firſt, are more or
leſs contaminated by iron, but they do not owe
all their colour to this ſubſtance. The green colours
altogether vaniſh during ignition, and leave
only a white opake maſs.
ARGILLACEOUS EARTH, OR ARGILLA.
53
§ 111.
By earth of alum (argilla) I do not mean common
clay, which is never free from ſiliceous
matter, but a pure clay, unmixed, at leaſt, with
any other earth. It may be readily obtained by
diſſolving Roman or roach alum in diſtilled water,
filtering, and precipitating by mild volatile alkaly.
§ 112.
The ſpecific gravity of this pure clay, or earth
of alum, is 1,305. It diſſolves in acids, with a
little efferveſcence. With the vitriolic acid it
forms alum; with the nitrous, muriatic and vegetable
acids, deliqueſcent ſalts.
When dry, it abſorbs water greedily, becomes
ſoft, and, with a due quantity of water, gains ſuch
a tenacity, that it may be moulded at pleaſure.
This maſs contracts greatly in the fire, from
whence ariſe numerous cracks; and with a due
54degree of heat, it becomes hard enough to ſtrike
fire with ſteel. By this burning it loſes its glutinous
tenacity, and the water is excluded by the
approach of the particles; nor does it again aſſume
its former properties, but by ſolution and precipitation.
It may be diſſolved in the dry way, by means
of fixed alkaline ſalt, as well as in the liquid way,
by acids. The vitriolic acid is better than the
others for this purpoſe, becauſe more eaſily concentrated.
Earth of alum neither diſſolves ſulphur, nor decompoſes
ſal ammoniac.
§ 113.
ARGILLA (argillaceous earth) united to ſiliceous
matter only.
Cronstedt Min. §78. Argilla porcellana. Porcelain
clay.
Pipe clay.
I never examined any clay which did not contain
a large quantity of ſiliceous earth; generally
more than half its weight[44].
55§ 114.
ARGILLA (argillaceous earth) united to ſiliceous
and irony matter.
Cronstedt Min. §§ 87 and 90. Bole. Dye-earth.
Clay.
§ 115.
ARGILLA (argillaceous earth) united to ſiliceous
and calcareous matter.
Cronstedt Min. §25. Marga argillacea. Marle.
§ 116.
ARGILLA (argillaceous earth) united to ſiliceous
earth and magneſia.
Cronstedt Min. §§ 84, 4. B. Terra lemnia.
Its component parts reſemble thoſe of talc,
but differ in their proportions, and are alſo leſs
intimately united.
56§ 116*.
ARGILLA (argillaceous earth) united to ſiliceous,
calcareous, and magneſia earths.
ARGILLA (argillaceous earth) contaminated
by vegetable alkaly and ſulphur, or at leaſt by the
acid of ſulphur.
Cronstedt Min. § 124. 2. b. Minera aluminis romani.
Alum ore.
It certainly contains vitriolic acid[46], and perhaps,
alſo, a ſmall portion of ſulphur. The vegetable
alkaly ſufficiently ſhews its volcanic origin.
§ 118.
ARGILLA (argillaceous earth) contaminated
by ſiliceous matter, pyrites, and petroleum.
Cronstedt Min. § 124. 2. c. Schiſtus aluminaris[47].
Alum ſlate.
57§ 119.
ARGILLA (argillaceous earth) intimately united
with leſs than half its weight of ſiliceous earth,
and a ſmall quantity of mild calcareous earth.
Cronſtedt Min. §§ 43–48. Gemma.
The Gems ſuffer no change under the blowpipe,
with foſſil fixed alkaly, but are diſſolved by
microcoſmic ſalt and borax.
To this head belong
Rubinus, the
ruby;
Saphirus,
ſapphire;
Topazius,
topaz;
Smaragdus,
emerald.
The tourmaline holds a kind of middle place
betwixt the gems and the ſcherle. The colour, in
all of them, is owing to iron.
§ 120.
ARGILLA (argillaceous earth) intimately united
to half its weight of ſiliceous earth (or more),
and a little mild calcareous earth. Scherle.
Cronſtedt Min. §§ 68–71. Granatus et Baſaltes, which
I call Scherle.
The remote varieties of theſe are eaſily diſtinguiſhed,
the near ones difficultly.
58§ 121.
ARGILLA (argillaceous earth) looſely united
to half its weight, or more, of ſiliceous earth, and
a little calcareous earth.
Cronstedt Min. §§ 108–112. Zeolithus. Zeolite.
There is a great affinity betwixt this and Scherle;
but in the zeolite, the component parts cohere
ſo looſely, that acids attach and ſeparate them
without their being previouſly treated with alkalies;
but this is not the caſe with the ſcherles.
Zeolite, contaminated by magneſia, I have not
yet examined.
§ 122.
ARGILLA (argillaceous earth) intimately united
to a large proportion of ſiliceous earth, and a
ſmall proportion of magneſia.
Cronstedt Min. §§ 93–96. Mica. Talcum.[48]Glimmer.
Talc.
SILICEOUS EARTH, OR TERRA SILICEA.
59
§ 123.
This, like the other primitive earths, is ſeldom
found pure. In order to have it ſo, reduce
clear quartz chryſtals into powder; melt it with
four times the weight of fixed alkaly; diſſolve the
whole in water; precipitate by a large quantity
of ſtrong acid; carefully waſh and dry the precipitate.
The acid muſt be uſed in a ſuperfluous quantity,
that any other earths contained may be diſſolved.
§ 124.
The ſpecific gravity of this earth, is 1,975.
The particles, when firſt precipitated, occupy, in
water, at leaſt twelve times the ſpace that they
do when dried; ſo that, when ſufficiently fine,
they may remain ſuſpended therein; nay, when
vehemently heated in a cloſe veſſel, they may be
diſſolved. No acid, except that of fluor ſpar
60(§ 30) has any action upon this earth. Fixed alkalies
unite with it in the liquid way, but in the dry
way they ſeize it with great vehemence, and convert
twice their weight of it into a permanent transparent
glaſs. Such is its affinity to alkalies, that
it imparts to clay, which is always loaded with it,
the power of ſeparating ſome of the acid from nitre
and common ſalt. When pure, it is refractory
in the fire.
Although ſiliceous earth is not altogether ſimple,
yet, in mineralogy, it muſt be conſidered
as primitive, until deciſive experiments ſhew us
from which of the preceding earths it is derived[49].
§ 125.
TERRA SILICEA (ſiliceous earth) united to
very ſmall quantities of calcareous and argillaceous
earth.
Cronstedt Min. § 51. Quartzum. Quartz.
§ 126.
TERRA SILICEA (ſiliceous earth) united to
argillaceous earth.
Cronstedt Min. § 58. Calcedonius. Chalcedony.
And perhaps the Opal. The Hydrophanus is
only a variety of theſe.
61Whether the carnelian, and other ſiliceæ, of finer
or coarſer texture, belong to this or the preceding
ſpecies I cannot yet determine with certainty.
§ 127.
TERRA SILICEA (ſiliceous earth), united
to an argillaceous and highly martial earth.
Cronstedt Min. §§ 64, 65. Jaſpis. Jaſper.
§ 128.
TERRA SILICEA (ſiliceous earth), loaded
with martial earth.
Martial.
Cronstedt Min. § 53.
This ſpecies is often called jaſper, but improperly,
becauſe it contains no argillaceous
earth.
§ 129.
TERRA SILICEA (ſiliceous earth), united
to argillaceous and a ſmall quantity of calcareous
earth.
Cronstedt Min. § 63. Petroſilex. Chert.
§ 130.
TERRA SILICEA (ſiliceous earth) united
to argillaceous earth and a little magneſia.
Cronstedt Min. §66. Feldſpathum. Feld ſpat.
62§ 131.
TERRA SILICEA (ſiliceous earth), united
to magneſia, mild calcareous earth, fluor ſpar and
alſo to the calxes of copper and iron. Chryſopraſius.
I have not examined this, but inſert it
upon the experiments of Mr. Achard.
To determine accurately the ſpecies of earths
is the moſt difficult part of mineralogy, for innumerable
analyſes yet remain to be made. But
that which now ſeems intricate and obſcure will
become plain and eaſy when experiments have
been ſufficiently multiplied.
CLASS III. INFLAMMABLES, OR BITUMINA.
63
§ 132.
To this head we refer all foſſils containing
phlogiſton in ſuch great abundance, that
under proper management they are inflammable.
The Genera are obviouſly very few, and
accurately ſpeaking there is only one Genus. But
ſince phlogiſton is so very ſubtle as not by itſelf
to become the object of our ſenſes, it will perhaps
be adviſeable to conſider its more ſimple
combinations as Genera: this has long been done
ſo far as reſpects the metals, by univerſal conſent.
SULPHUR.
64
§ 133.
This name may be given to any acid coagulated
by phlogiſton into a ſolid form.
If all metals conſist of certain radical acids ſaturated
with phlogiſton, as is highly probable,
and with reſpect to arſenic is indubitably proved;
then metals ought to find a place here. But until
this theory be eſtabliſhed by numerous experiments,
we ſhall only rank under this head
the compounds which have not a metallic nature.
§ 134.
PHLOGISTON ſaturated with vitriolic acid.
Cronstedt, Min. § 151. Common Brimſtone. Sulphur.
§ 135.
PHLOGISTON ſaturated with aerial acid.
Cronstedt Min. § 154. A. plumbago. Black-lead.
The true compoſition of this has been detected
by Mr. Scheele.
65§ 136.
PHLOGISTON united to the acid of vitriol
and of molybdæna; or what amounts to the ſame,
ſulphur joined to the acid of molybdæna.
Cronstedt Min. § 154. b. c. Molybdæna. Molybdæna.
The acid of molybdæna has never yet been obtained
quite free from phlogiſton (§ 32). If this
acid be of a metallic origin, molybdæna is a mineralized
metallic ſubſtance, and ſhould be placed
with the other minerals.
PETROLEUM.
66
§ 137.
Phlogiston occurs alſo in the foſſil kingdom,
combined in an oily form; but many
ſuppose this derived from the vegetable kingdom.
§ 138.
PETROLEUM pure and ſelected.
Cronstedt Min. §§ 147–150. Naptha. Rock oil.
§ 139.
PETROLEUM joined to argillaceous earth.
Cronstedt Min. §§ 157–160. Lithantrax. Pit Coal.
§ 140.
PETROLEUM united to acid of amber.
Cronstedt Min. §§ 133–146. Succinum. Amber.
Many contend that amber has a vegetable origin;
but as the point is not very well determined;
and as it is found amongſt foſſils, I ſtill retain it
here.
67§ 141.
Ambergriſe, according to the aſſertion of Mr.
Aublett, is nothing more than the juice of a
tree inſpiſſated by evaporation into a concrete
form. This tree grows in Guyana, and is called
Cuma, but has not been inveſtigated by any botaniſt.
Pieces of this tree are ſaid to be carried down
into the rivers by heavy rains, and the ſpecimens
examined by Mr. Rouelle had the odour and
principal qualities of amber[50]. Rumphius,
long ſince, mentioned a tree called Nanarium,
whoſe juice reſembled amber[51].
DIAMOND.
68
§ 142.
At firſt ſight I may ſeem to have acted erroneouſly,
by ſeparating this from the other
gems, and inſerting it here; but after due conſideration,
I know not where to place it better.
It has never yet been decompoſed by the liquid
analyſis[52]; and when expoſed to the fire in an open
veſſel, it is wholly conſumed, burning with a
lambent flame. This deflagration, though ſlow,
ſhews decidedly its affinity to the inflammables:
beſides, in the focus of a burning glaſs, it leaves
traces of ſoot[53]. When further experiments teach
us better, I ſhall willingly correct my error.
CLASS IV. METALS.
69
§ 143.
I have before mentioned the great affinity betwixt
metallic and inflammable ſubſtances
(§ 133). Zinc and arſenic stand, as it were, upon
the borders betwixt them; for these, in proper
circumſtances, burn with a very evident flame.
All the metallic ſubſtances contain phlogiſton, and
when, to a certain degree, deprived of it, fall into
a powder like an earth; but their attractions for
phlogiſton are different. Moſt of them, when
melted in a common way, and expoſed to the air,
have an earthy cruſt formed upon the ſurface, which
cannot again be reduced to metal without the addition
of ſome inflammable matter. The baſe
metals, eleven in number, have this property:
but the noble metals, platina, gold and ſilver, are
ſo firmly connected to the phlogiſton, that they
never calcine under fuſion, however long continued;
and after being changed into a calx in the
liquid way, when melted in the fire, they re-aſſume
their metallic form, without any other phlogiſton
than what is contained in the matter of heat.
Quickſilver holds a kind of middle place; for,
like the baſe metals, it may be calcined, though
70not readily; and like the noble ones, it may be
reduced by heat alone.
I have placed each diviſion of the metals in the
order of their specific gravities.
Thoſe metals, which are found in a perfect metallic
ſtate, are called native; thoſe united to acids,
or to ſulphur, are ſaid to be mineralized; and
thoſe which are only deprived of their phlogiſton,
calciform[54].
The ſpecific gravity of this metal, when pure,
is 19,640. Aqua regia diſſolves it; but
except the dephlogiſticated muriatic acid, and in
certain circumſtances the nitrous, no ſimple acid
acts upon it, unleſs it has been previouſly calcined[56].
The quantity of phlogiſton neceſſarily
taken away in the ſolution of 100 parts of gold, I
eſtimate at about 394; whilſt the ſame quantity of
ſilver, loſes by ſolution in the nitrous acid, 100[57].
Gold retains the phlogiſton neceſſary to its metallic
form, more obſtinately than any other metal,
except, perhaps, platina. It melts and calcines
in the focus of a burning glaſs at 1301 degrees of
heat.
§ 145.
AURUM nativum (gold native) united to ſilver.
Native.
73I do not know that gold has ever yet been found
perfectly pure.
§ 146.
AURUM nativum (gold native) united to copper.
Native.
§ 147.
AURUM nativum (gold native) united to ſilver
and copper.
Native.
§ 148.
AURUM nativum (gold native) united to ſilver,
copper, and iron.
Native.
§ 149.
AURUM (gold), mineralized by ſulphur, by
means of iron.
Pyritical.
Cronstedt Min; § 166. a. Pyrites aureus.
But ſome doubt may be made about the mineralization
of gold[58].
74§ 150.
AURUM (gold) mineralized by ſulphur, together
with ſilver, lead, and iron.
Its ſpecific gravity is 18,000[60], when very
pure. It diſſolves in aqua regia, and the
loſs of phlogiſton during the ſolution, according
to the experiments hitherto made may be expreſſed
76by 756. Beſides the muriatic acid, which
when dephlogiſticated diſſolves every metal, no
acid acts upon platina without it has undergone a
previous calcination. It ſeems to retain its phlogiſton
more obſtinately than any other metal.
To melt it requires a heat greater than that at
which iron melts.
§ 152.
PLATINA native united to iron. Native.
Cronstedt Min. § 179.
I believe it has never been found quite free
from iron, but this can be ſeparated by art[61].
ARGENTUM, OR SILVER.
77
§ 153.
Its ſpecific gravity is 10,552. The nitrous
acid readily diſſolves it, the vitriolic muſt be
boiling hot; the muriatic attracts its calx very
ſtrongly, but cannot remove its phlogiſton and
therefore cannot diſſolve it in its metallic ſtate.
The quantity of this phlogiſton which cauſes
the difference betwixt its metallic and its calciform
ſtate I before expreſſed as 100 in 100
parts of ſilver. But the force with which it retains
this portion of its phlogiſton is leſs than that
of gold; that is, it occupies the third place in a
ſeries of all the metals. It melts at 1000 degrees
of heat.
§ 154.
ARGENTUM nativum (ſilver native) united
to gold. Native.
§ 155.
ARGENTUM nativum (ſilver native), united
to copper. Native.
78§ 156.
ARGENTUM nativum (ſilver native), united
both to gold and copper. Native.
§ 157.
ARGENTUM nativum (ſilver native), united
to iron. Native.
§ 158.
ARGENTUM nativum (ſilver native), united
to arſenic. Native.
The arſenic hardly exceeds ⁶⁄₁₀₀.
§ 159.
ARGENTUM nativum (ſilver native), united
to antimony. Native.
When melted, it ſmokes but has no ſmell of
arſenic.
§ 160.
ARGENTUM nativum (ſilver native), united
to arſenic and iron. Native.
79The three metallic ingredients are nearly in
equal proportions.
All the ſpecies hitherto mentioned have metallic
properties and appearances. The contaminating
matters are ſometimes extremely ſmall,
but not to be neglected when they exceed ¹⁄₃₀₀
part of the maſs.
§ 161.
ARGENTUM (ſilver) mineralized by the vitriolic
and muriatic acids. Hornlike.
Cronstedt Min. §177. Minera argenti cornea. Horn-ſilver.
Mr. Woulfe[62], detected the preſence of the
vitriolic acid. The ſilver ſeldom exceeds ⁷⁰⁄₁₀₀. I
know not whether it is ever altogether free from
vitriolic acid.
§ 162.
ARGENTUM (ſilver), mineralized by the
vitriolic and muriatic acids, and ſulphur.
I doubt whether this be a diſtinct ſpecies,
ſince the ſulphur and the ſalts ſcarcely admit of
any other than a mechanical union.
80§ 163.
ARGENTUM (ſilver), mineralized by
ſulphur. Glaſſy.
Cronstedt Min. § 169. Minera argenti vitrea.
It ſometimes contains ⁷³⁄₁₀₀ of ſilver, or more.
§ 164.
ARGENTUM (ſilver), mineralized by ſulphur
and iron. Marcaſitical.
Cronstedt Min. § 176, 10. Pyrites argenteus.
§ 165.
ARGENTUM (ſilver), mineralized by ſulphur
and lead. Potters.
Cronstedt Min. § 176, 8. Galena.
The ſilver is only a few half ounces in a hundred
weight.
§ 166.
ARGENTUM (ſilver), mineralized by ſulphur
and arſenic. Red.
Cronstedt Min. § 170. Minera argenti rubra.
81It contains about ⁷⁰⁄₁₀₀ of ſilver. Iron is frequently
preſent, as in moſt other ſpecies but
not always.
§ 167.
ARGENTUM (ſilver), mineralized by ſulphur,
arſenic, and iron. Glittering.
Cronstedt Min. § 172.
I have examined ſome ſpecimens from Saxony
which ſometimes contain no ſilver. May
we not therefore ſuppoſe that the ſilver is native
and not mineralized?
§ 168.
ARGENTUM (ſilver), mineralized by ſulphur,
arſenic, iron and cobalt.
The ſilver is ſometimes more than ⁵⁰⁄₁₀₀.
§ 169.
ARGENTUM (ſilver), mineralized by ſulphur,
arſenic, copper and iron. White ore.
Cronstedt Min. § 171. Minera argenti alba.
The proportion of ſilver varies much, ſometimes
it is ¹⁰⁄₁₀₀ or more.
82§ 170.
ARGENTUM (ſilver), mineralized by ſulphur,
arſenic, copper, iron, and antimony. Grey ore.
Cronstedt Min. § 173. 6. Minera argenti griſea. In
the province of Dal[63].
It contains ²⁴⁄₁₀₀ of copper, ſeldom ⁵⁄₁₀₀ ſilver.
§ 171.
ARGENTUM (ſilver), mineralized by ſulphur,
arſenic, antimony and iron. Plumoſe.
Cronstedt Min. §173. 5. Federertz of the
Germans[64].
It ſeldom contains more than a few half
ounces of ſilver in the hundred weight.
It is abſurd to found ſpecies upon the differences
of the matrix: theſe ought to be conſidered
elſewhere.
HYDRARGYRUM, OR QUICKSILVER.
83
§ 172.
Its ſpecific gravity is 14,110. It has been
erroneouſly ranked among the brittle metals,
for at 654 degrees below 0 it freezes[65],
and then ſpreads under the hammer like lead.
But as ſuch an extreme degree of cold rarely
happens unleſs artificially produced, we ceaſe
to wonder why it is always liquid or rather
melted.
Nitrous acid diſſolves it readily, vitriolic acid
requires to be aſſiſted by a boiling heat; muriatic
acid does not act upon it all, unleſs previouſly
deprived of as much phlogiſton as in
100 parts may be called 74. The attractive
power wherewith it retains this portion of phlogiſton
occupies the fourth place in the ſeries;
that is, it holds it leſs ſtrongly than the noble but
more ſtrongly than the baſe metals.
84§ 173.
HYDRARGYRUM nativum (quickſilver native).
Native.
Cronstedt Min. § 217.
Whether it be entirely free from every metallic
contamination I have not yet tried.
§ 174.
HYDRARGYRUM (quickſilver), united to
ſilver. Amalgamated.
Cronstedt Min. § 217.
§ 175.
HYDRARGYRUM (quickſilver), mineralized
by muriatic and vitriolic acids. Hornlike.
Mineralogy owes the diſcovery of this to Mr.
Woulfe. Phil. Tranſ.
§ 176.
HYDRARGYRUM (quickſilver), mineralized
by ſulphur. Cinnabarine.
Cronstedt Min. § 218. Cinnabaris.
85§ 177.
HYDRARGYRUM (quickſilver), mineralized
by ſulphur and iron. Martial.
I am doubtful whether this be a diſtinct ſpecies.
The iron perhaps is only mechanically
diffuſed.
§ 178.
HYDRARGYRUM (quickſilver), mineralized
by ſulphur and copper. Cuprous.
Cronstedt Min. § 219.
PLUMBUM , OR LEAD .
86
§ 179.
Its ſpecific gravity is 11,352, greater than
that of any other of the baſe metals. The
nitrous acid perfectly diſſolves it; the muriatic
more difficultly; the vitriolic hardly at all, for
the vitriol of lead being inſoluble in water incruſts
the metal, and prevents its ſolution. After
calcination the weakeſt vegetable acids diſſolves
it, and acquire a ſweet taſte. The phlogiſton
neceſſary to be taken away in order that
it may diſſolve may be called 43, which is leſs
than that of any other metal. Hence we underſtand
why the calx of lead may be reduced with a
very minute quantity of inflammable matter.
With reſpect to the force wherewith it retains
this phlogiſton it occupies the tenth place. It
melts at 595 degrees of heat.
87§ 180.
PLUMBUM nativum (lead), though many
mineralogiſts doubt whether it has ever yet
been found. Native.
§ 181.
PLUMBUM (lead), mineralized by vitriolic
acid. Vitriol of.
Originating from the decompoſition of Galena.
It is rarely met with. It was firſt obſerved by
Mr. Monnet. It does not efferveſce with acids.
It may be reduced by the blowpipe upon charcoal.
§ 181*.
PLUMBUM (lead), mineralized by vitriolic
acid and iron.
Exiſting in immenſe quantity in the iſland
of Angleſea. It does not reduce with the blowpipe
upon charcoal, but melts to a black
glaſs[66]. W.
88§ 182.
PLUMBUM (lead), mineralized by the acid
of phoſphorus. Phoſphorated.
This was diſcovered by Mr. Gahn. It does
not efferveſce with acids. It melts upon charcoal
with the blowpipe, but is not perfectly
reduced.
§ 183.
PLUMBUM (lead), mineralized by the aerial
acid. Aerated.
Cronstedt Min. § 185.
It efferveſces with acids, and is readily reduced
upon charcoal[67].
§ 184.
PLUMBUM (lead), mineralized by ſulphur. Sulphurated.
Cronstedt Min. § 187.
§ 185.
PLUMBUM (lead), mineralized by ſulphur
and ſilver. Galena.
Cronstedt Min. § 188.
89§ 186.
PLUMBUM (lead), mineralized ſulphur,
with ſilver and iron.
Cronstedt Min. § 189.
§ 187.
PLUMBUM (lead), mineralized by ſulphur,
with ſilver and antimony. Radiated.
Cronstedt Min. § 190.
CUPRUM , OR COPPER .
90
§ 188.
Its ſpecific gravity is 8,876. Nitrous acid diſſolve
it readily, muriatic acid ſlowly, and the
vitriolic requires intenſe boiling. The phlogiſton,
ſeparated in the ſolution of 100 parts, may be expreſſed
by 312. The weakeſt vegetable acids act
upon it, eſpecially after calcination, and ſo do alkalies,
the volatile alkaly eſpecially. With reſpect
to the power with which it retains the phlogiſton,
copper holds the eighth place. It melts with
1450 degrees of heat.
§ 189.
CUPRUM nativum (copper native). Native.
Cronstedt Min. § 193.
It’s rarely found without ſome alloy of gold,
ſilver or iron; but I have not yet fully examined
it.
91§ 190.
CUPRUM calciforme (copper), ſimply deprived
of its phlogiſton. Calciform.
Cronstedt Min. § 195.
§ 191.
CUPRUM (copper), mineralized by muriatic
acid and argillaceous earth. Micaceous.
Mr. Werner, in his tranſlation of Cronſtedt’s
Mineralogy, part 1, page 217, has deſcribed it
accurately, and kindly ſent me a ſpecimen of it,
which I analyſed[68].
§ 192.
CUPRUM (copper), mineralized by the aerial
acid. Aerated.
Cronstedt Min. §§ 194, 196. b. 3.
Mr. Fontana firſt pointed out its true compoſition.
It contains about ⅔ of copper, ⅓ or ¼ of
aerial acid, and a little water[69].
92§ 193.
CUPRUM (copper), mineralized by ſulphur. Vitreous.
Cronstedt, Min. § 197. Minera cupri vitrea; a common,
but improper name.
It generally contains ſome alloy of iron.
§ 194.
CUPRUM (copper), mineralized by ſulphur,
and a ſmall proportion of iron.
Cronstedt Min. § 198, b. Minera cupri lazurea.
By a ſmall proportion of iron, I mean leſs than
the weight of the copper; by a large proportion,
more. This contains from 40 to 50 per cent. of
copper.
§ 195.
CUPRUM (copper), mineralized by ſulphur,
and a large proportion of iron. Pyritical.
Cronstedt Min. § 198. Pyrites Cupri.
The quantity of copper varies greatly, but ſeldom
exceeds ⁴⁰⁄₁₀₀.
93§ 196.
CUPRUM (copper), mineralized by ſulphur,
iron and arſenic. Grey.
Cronstedt Min. § 198. a. Pyrites cupri griſeus.
This frequently contains an alloy of ſilver. The
copper rarely exceeds ⁶⁰⁄₁₀₀.
FERRUM , OR IRON .
94
§ 197.
Its ſpecific gravity is 7,800. All the acids
readily diſſolve it; but the vitriolic muſt be
diluted, otherwiſe it may be boiled almoſt to dryneſs,
without effecting it. The phlogiſton, diſlodged
from centenary of ductile iron, may, as
experiments now ſtand, be called 342; and this
is ſo feebly retained, that this metal, with a few
others, holds the eleventh, or loweſt place in the
ſeries.
It requires an intenſe degree of heat to fuſe it,
viz. 1601, if the uſual compariſon betwixt the
mercurial thermometer, and the metallic one of
Mortimer, be true. Iron is red hot at 1050
degrees of heat.
§ 198.
FERRUM nativum (iron) native. Native.
95It can hardly be doubted, but that the great
maſs of iron, brought by Pallas, from Siberia,
into Europe, is the product of nature. Its compoſition
reſembles that of forged iron; for 100
parts of it yield, by means of the muriatic acid,
49 cubic inches of inflammable air; and from
many experiments upon ductile iron, that is found
to yield from 48 to 51[70].
§ 199.
FERRUM nativum (iron) native, united to
arſenic. Arſenical.
Cronstedt Min. § 243. B. Miſspickel.
§ 200.
FERRUM (iron), with the power of attracting
other iron. Loadſtone.
Cronstedt Min. § 211. b. Magnes.
The cauſe of this property is yet unknown.
§ 201.
FERRUM (iron), with phlogiſton enough to
render it magnetic. Magnetic.
Cronstedt Min. §§ 212, 213.
96But the quantity of phlogiſton is far ſhort of that
which is neceſſary to render it ductile, for a centenary
hardly contains more than three cubic
inches of inflammable air.
§ 202.
FERRUM calciforme (iron calciform), ſimply
deprived of phlogiſton. Ochrous.
Cronstedt Min. §§ 202–206. Bloodſtone.
§ 203.
FERRUM (iron), mineralized by aerial acid,
calcareous earth, and manganeſe. White.
Cronstedt Min. § 20. Minera ferri alba.
§ 204.
FERRUM (iron), mineralized by ſulphur. Pyritical.
Cronstedt Min. § 152. Pyrites.
§ 205.
FERRUM (iron) intimately united to a new
brittle metal[71], or to a peculiar modification of
iron, rendering it brittle when cold. Cold-ſhort.
In cold-ſhort iron, a brittle metal exiſts, readily
uniting to ductile iron, by the aſſiſtance of heat,
but rendering it brittle when cold. This ſubſtance,
diſſolved in acids, forms Pruſſian blue with
phlogiſticated alkaly, but it is not magnetic: it
97affords a white calx, richer in phlogiſton than the
yellow calx of good iron.
I hope, by more experiments, ſoon to become
better acquainted with it.
§ 206.
FERRUM calciforme (iron calciform), phlogiſticated
in a peculiar manner. Blue.
Cronstedt Min. § 208. Cæruleum Berolinenſe nativum.
Clay and mould are sometimes coloured ſuperficially
by a dilute blue, and ſometimes the former,
when newly dug up, is found to acquire this colour
upon expoſure to the air. It is evident that
the baſis of this colour is an irony matter, full of
phlogiſton; for, by ignition upon a charcoal fire,
it flames, turns red, and becomes magnetic.
With a gentle heat it becomes green, but when
melted gives black ſcoriæ.
Alkalies, as well as acids, diſſolve it, and the
colour vaniſhes, but appears again, if precipitated
from the former by acids, and from the latter by
alkalies; but it has then a greenish caſt, and ſoon
becomes white. This white ſediment, immerſed
in an infuſion of galls, or of tea, recovers its former
colour.
From what has been ſaid, it appears that this
colour, although analogous to the artificial Pruſſian
blue, differs from it in its intensity, in the mode
of its production, and in various properties. It
keeps its colour in water, but turns black with oil.
STANNUM , OR TIN .
98
§ 207.
Its ſpecific gravity is 7,264. Vitriolic, muriatic,
acetous acids, and aqua regia, diſſolve it, but
the nitrous, eſpecially when ſtrong, attacks it ſo
violently, that it ſoon reduces it to the ſtate of an
inſoluble calx.
The quantity of phlogiſton it loſes by ſolution,
may be called 114; and this it retains with a force
that gives it the ninth place in the ſeries. It melts
eaſier than any metal, except quickſilver, viz. at
415 degrees.
§ 208.
STANNUM nativum (tin). Native.
This I have not ſeen. Some doubts are entertained
of its true nature, and, perhaps, not without
reaſon.
99§ 208*.
STANNUM ſulphuratum (tin), mineralized by
ſulphur. Sulphurated.
STANNUM calciforme (tin) calciform, contaminated
by iron. Calciform.
VISMUTUM , OR BISMUTH .
100
§ 210.
The heaviest of all the brittle metals that follow
it, its ſpecific gravity being 9,670.
Nitrous acid, and aqua regia diſſolve it perfectly.
The vitriolic acid muſt be boiled nearly to dryneſs
before it acts upon it, and the muriatic acid
only attacks its calx. The quantity of phlogiſton
which reſists the action of menſtrua, is expreſſed by
57; and its power of retaining it ranks it in the ſeventh
place. It melts at the heat of 494 degrees.
§ 211.
VISMUTUM nativum (biſmuth). Native.
Cronstedt Min. § 222.
§ 212.
VISMUTUM calciforme (biſmuth). Calciform.
Cronstedt Min. § 223.
101I am not able to ſay whether this is merely deprived
of its phlogiſton, or whether it is not alſo
mineralized by aerial acid.
§ 213.
VISMUTUM (biſmuth) mineralized by ſulphur. Sulphurated.
Cronstedt Min. § 224.
§ 214.
VISMUTUM (biſmuth) mineralized by ſulphur
and iron. Pyritical.
Cronstedt Min. § 225.
NICCOLUM , OR NICKEL .
102
§ 215.
The regulus, when depurated, has a ſpecific
gravity of 9,000, or more; but the common
regulus, obtained by the firſt reduction, little
exceeds 7,000. Aqua regia, and nitrous acid,
diſſolve it perfectly; muriatic acid, ſlowly; vitriolic
acid, not without boiling almoſt to dryneſs
and the acetous acid does not act upon it, unleſs
in a calciform ſtate. The quantity of phlogiſton
ſeparated by ſolution, may be called 156; and this
it retains with a force about equal to that with
which iron retains its phlogiſton (§ 197).
The heat neceſſary to melt it, is about equal to
that which gold requires; but when depurated,
it is almoſt as difficult to melt as iron.
The properties of it are more fully examined
elſewhere[72].
103§ 216.
NICCOLUM nativum (nickel) native, united
to iron and arſenic. Native.
It ſometimes, perhaps, contains cobalt. As it
contains neither ſulphur nor mineralizing acid,
and is perfectly in its metallic form, it muſt be
called native, although joined to other metals.
§ 217.
NICCOLUM aeratum (nickel) mineralized by
aerial acid. Aerated.
Cronstedt Min. § 255.
§ 218.
NICCOLUM (nickel) mineralized by ſulphur,
arſenic, cobalt, and iron. Mineralized.
Cronstedt Min. § 256. Cuprum Nicolai. Kupfer nickel.
ARSENICUM , OR ARSENIC .
104
§ 219.
The ſpecific gravity of the radical acid, is
3,391; of white arſenic, 3,706; of its glaſſy
ſtate, 5,000; and its regulus, 8,308. Aqua
regia, and muriatic acid, diſſolve it perfectly;
the vitriolic acid requires boiling; the acetous
acts only upon its calx: the nitrous acid not only
takes away as much phlogiſton as may be expreſſed
by 109, deprived of which the regulus is reduced
to the ſtate of a calx, but in a large quantity, aſſiſted
by a proper degree of heat, it at length so
far dephlogiſticates this calx, as to leave the acid
of arſenic alone. Theſe phænomena are well
worthy of obſervation, as they ſeem to lay open
the nature of metals in general. From analogy,
it is probable that every metal contains a radical
acid of a peculiar nature, which, with a certain
quantity of phlogiſton, is coagulated into a metallic
calx; but with a larger quantity, ſufficient to
ſaturate it, forms a compleat metal. The radical
acid retains the coagulating phlogiſton much more
105ſtrongly than that which is neceſſary to the ſaturation.
But different metallic acids retain both
with different degrees of attraction. Hence the
noble metals cannot be calcined in the dry way;
it is only by acid menſtrua that they can be
brought into that form; but all the others loſe
their ſaturating phlogiſton in the fire, though
with more or leſs difficulty. I have diſtinctly
obſerved eleven different degrees of reſiſtance:
thus, gold may be precipitated by all the other
metals, except perhaps platina, which I think
may thus be explained. The calx of gold having
the greateſt attraction for phlogiſton, takes
it from all other metals, and thus loſing its ſolubility
falls down in a metallic ſtate. Therefore
gold in the ſeries of metals, occupies at leaſt
the ſecond place. Platina is precipitated by all,
but leſs evidently than gold. To this therefore,
I think we muſt give the firſt place, and so on
of the others as I have remarked in the character
of each metal. As nickel, cobalt, iron, manganeſe
and zinc, do not precipitate one another,
they are put together in the laſt and eleventh
place[73].
In order to obtain the radical acids we muſt
ſeparate them from the coagulating phlogiſton.
If the induſtry of chemiſts ever effects this, I am
confident that metallurgy will be wonderfully
elucidated. This therefore is a taſk to which
106our labours muſt be directed. I know that analogy
muſt be cautiously trusted, but it at leaſt
leads us to new experiments. Hitherto this operation
has only ſucceeded with arſenic; and it is
worth notice, that this metal which holds the
fifth place with reſpect to its quantity of phlogiſton,
ſhould be inferior to all others with regard
to the attraction by which the coagulating
quantity is retained.
Arſenic melts, but the moment it ſuffers heat
enough to melt it, it volatilizes, unleſs it be firſt
calcined. The regulus thrown upon a plate of
iron properly heated, preſently takes fire and calcines,
diffuſing a ſmell like garlic[74].
§ 220.
ARSENICUM nativum (arſenic), native, united
to iron. Native.
Cronstedt Min. § 239.
I have never found it free from martial impregnation.
§ 221.
ARSENICUM nativum (arſenic), native, united
to ſilver.
107§ 222.
ARSENICUM calciforme (arſenic), deprived
of phlogiſton. Calciform.
Cronstedt Min. § 240.
§ 223.
ARSENICUM (arſenic), mineralized by ſulphur. Yellow.
Cronstedt Min. § 241. Auripigmentum.Riſigallum.
§ 224.
ARSENICUM (arſenic), mineralized by ſulphur
and iron. Pyritical.
Cronstedt Min. § 243. A. Pyrites arſenicalis.
COBALTUM , OR COBALT .
108
§ 225.
Its ſpecific gravity is 7,700. Nitrous acid and
aqua regia readily diſſolve it. The vitriolic
acid requires to be boiled nearly to dryneſs.
The muriatic and acetous acids do not act upon
it unleſs previouſly calcined. 270 expreſſes the
quantity of ſaturating phlogiſton, which it retains
with the ſame force that iron does. Common
regulus melts in the ſame heat that copper does,
but when well purified it is hardly eaſier to melt
than iron.
§ 226.
COBALTUM nativum (cobalt), native and
united to arſenic. Native.
Cronstedt Min. § 249.
§ 227.
COBALTUM calciforme (cobalt). Calciform.
Cronstedt Min. § 247.
It is found variouſly mixed, principally with
arſenic, iron and copper, but whether mechanically
or by a more intimate union I know not.
109§ 228.
COBALTUM (cobalt), mineralized by acid
of arſenic. Red.
Cronstedt Min. § 248.
The ſmall ſpecimens that I have been able to
examine point out ſuch a compoſition[75].
§ 229.
COBALTUM (cobalt), contaminated by iron
and vitriolic acid. Vitriolic.
Cronstedt Min. § 250.
§ 230.
COBALTUM (cobalt), mineralized by ſulphur,
arſenic and iron. Glanz-cobalt.
Cronstedt Min. § 251.
§ 231.
COBALTUM (cobalt), mineralized by ſulphur,
arſenic, iron and nickel. Kupfernickel.
Cronstedt Min. § 252.
ZINCUM OR ZINC .
110
§ 232.
Its ſpecific gravity is 6,862. All the acids
diſſolve it readily and with efferveſcence,
which denotes its very lax union with the inflammable
principle, as was remarked before
(§ 219). 182 expreſſes the quantity of phlogiſton
it loſes in ſolution. It melts in a heat of
699 degrees; and if the heat be a little increaſed
it takes fire; and diſſipates in white flowers[76].
§ 233.
ZINCUM calciforme (zinc), calciform ſimply
deprived of its phlogiſton. Calciform.
Cronstedt Min. § 228. A. Lapis calaminaris.
It is almost always mixed with clay or calciform
iron.
111§ 234.
ZINCUM (zinc), mineralized by aerial acid. Aerated.
Cronstedt Min. § 228. A. 1.
§ 235.
ZINCUM (zinc) with aerial acid and mixed
with ſiliceous matter. Siliceous.
D. A. Born ſent me chryſtals of this ſpecies,
which expoſed to the fire gave out aerial acid,
but they were not wholly ſoluble in acids.
§ 236.
ZINCUM (zinc), mineralized by ſulphur and
iron. Black jack.
Cronstedt Min. §§ 229. 230. Pſeudogalena.
ANTIMONIUM OR ANTIMONY .
112
§ 237.
Its ſpecific gravity is 6,860. Aqua regia diſſolves
it well; vitriolic acid requires boiling;
muriatic and acetous acids act hardly at all upon
it, unleſs previouſly calcined. The nitrous acid
corrodes it ſo as to prevent the ſolution. The
phlogiſton it loſes in ſolution is expreſſed by 120,
and with reſpect to the force wherewith it retains
this, it ſtands in the ſixth place. It melts at a
heat of 809 degrees.
§ 238.
ANTIMONIUM nativum (antimony). Native.
Cronstedt Min. § 238.
113§ 239.
ANTIMONIUM (antimony), mineralized by
ſulphur. Sulphurated.
Cronstedt Min. § 234.
§ 240.
ANTIMONIUM (antimony) mineralized by
ſulphur and arſenic. Red.
Cronstedt Min. § 235.
MANGANESIUM , OR MANGANESE .
114
§ 241.
Its ſpecific gravity is 6,850. This new metal
is ſoluble in all the acids, and is ſo readily deprived
of its ſaturating phlogiſton that with iron
and ſome others it ſtands the loweſt in the ſeries.
227 expreſſes the quantity of phlogiſton
it loſes in ſolution. It is very difficult to melt,
more ſo than iron.
§ 242.
MANGANESIUM calciforme (manganeſe)
ſimply deprived of phlogiſton. Calciform.
Cronstedt Min. § 114.
115§ 243.
MANGANESIUM (manganeſe) mineralized
by aerial acid.
Aerated.
Cronstedt Min. § 115. 1. a.
APPENDIX THE FIRST. — Salts with Salts. — Salts with Earths. — Salts with Inflammables. — Salts with Metals. — Earths with Earths. — Earths with Inflammables. — Earths with Metals. — Inflammables with Inflammables. — Inflammables with Metals. — Metals with Metals. — Salts with Earths and Inflammables. — Salts with Earths and Metals. — Salts with Inflammables and Metals. — Earths with Inflammables and Metals. — Salts with Earths, Inflammables, and Metals.
116
§ 244.
In the preceding pages only the more ſimple
combinations occur, whoſe principles are either
chemically united or at leaſt ſo ſubtly interwoven
that the texture appears perfectly homogeneous.
But if two or more of theſe ſpecies,
forming little diſtinct maſſes are cemented
together, theſe mechanical mixtures, diſcernible
by the eye ought to conſtitute a new ſeries,
to be diſtinguiſhed by their component parts as
the others were by their firſt principles or chemical
elements. Such compoſitions may well
be excluded from the preſent work, but upon
account of their extenſive phyſical, œconomical
and metallurgical uſes, I propoſe to give a ſlight
ſketch of them here, enumerating the more remarkable
Genera.
§ 245.
In a general view it appears that not only
ſeveral ſpecies cemented together may be referred
to this place, but likewiſe thoſe which are mechanically
diffuſed in a powdery or an earthy form.
117§246.
From the laws of combination it is evident,
that according to the arrangement of foſſils into
four claſſes, there can be only TEN Genera compoſed
of two, FOUR of three, and ONE of four conſtituent
parts. And although ſo many have not
yet been detected, yet it is better to mention them
here as the induſtry of a future age will probably
diſcover more. The ſpecies are formed from
the differences of the more ſimple ſpecies and
their component parts.
§ 247.
This compoſition can hardly ever conſtitute a
genus, if it muſt be made in a dry and concrete
form; for excepting gypſum, the other native
ſalts readily diſſolve in water, and by evaporation
are ſo mixed together as not readily to be diſcerned
by the eye. Yet the foſſil alkaly mixed
with common ſalt will perhaps find a place here.
The contents of mineral waters may likewiſe
be referred here, ſince every material difference
in them depends upon the particles diſſolved.
118
§ 248.
This mixture is hardly to be found but where
bits of gypſum are concreted to matters of an
earthy nature.
§ 249.
May perhaps be found in volcanoes.
§ 250.
If gypſum forms the matrix of any metal, it
muſt be placed here.
§ 251.
To this head belong moſt of the ſaxa (ſtones),
enumerated by Mr. Cronſtedt, which form the
immenſe bulk of mountains, and deſerve our particular
attention, in order that, being better acquainted
with the nature and ſtructure of the ſhell
of the earth, we may be able to point out the coverings
of minerals, and convert them all to our
uſe.
119
§ 252.
Lumps of mountain pitch are frequently connected
with ſtones, and ſulphureous matters are
found diffuſed through earthy materials.
§ 253.
This genus contains the peculiar matrices of
metals, a judicious conſideration of which would
be particularly uſeful to miners.
§ 254.
Perhaps, in ſome places, ſulphureous matters
are found mixed with mountain pitch.
§ 255.
If plumbago (black-lead) or common ſulphur,
ſhall ever be found mixed with metallic ſubſtances,
ſuch ſpecies muſt ſtand under this genus.
120
§ 256.
We know that ſome metals, in the boſom of
the earth, are almoſt always mixed, whilſt others
are rarely, or never, found together. A more
accurate knowledge of theſe things, would illuſtrate
phyſical geography, as well as metallurgy.
We now proceed to the more compound genera.
§ 257.
This genus can hardly ever occur but in countries
formerly expoſed to ſubterranean fires.[77]
§ 258.
To be expected amongſt volcanic productions.
121
§259.
To be ſought for in the productions of volcanoes.
§ 260.
Obvious amongſt the productions of volcanoes,
otherwiſe extremely rare.
§ 261.
Hardly to be expected but in volcanic mountains.
APPENDIX THE SECOND. — Saline Calcareous Earth with an organic Form . — Saline Iron with an organic Form . — Mild Calcareous Earth with an organic Form . — Clay with an organic Form . — Siliceous Earth with an organic Form . — Earth organic. — Petroleum impregnating organic Bodies . — Silver with an organic Form . — Quickſilver in an organic Form . — Copper with an organic Form . — Iron with an organic Form . — Zinc with an organic Form .
122
§ 262.
Foſſils externally reſembling animals or
vegetables, originate from foreign matters,
which by ſome peculiar proceſs are changed in the
boſom of the earth, or are ſo impregnated by mineral
particles gradually occupying the place of
thoſe which have putrified, that they no longer
reſemble organic ſubſtances, except in figure.—Theſe
are commonly called Petrefactions.
§ 263.
The harder ſhells of animals expoſed to the
weather, are not always exempt from deſtruction;
for their gelatinous matter being gradually deſtroyed
by putrefaction, they become brittle, and
in a manner calcined. In leſs expoſed ſituations,
ſome of them preſerve the nature of their materials,
but acquire a ſpar-like texture.
§ 264.
We muſt carefully diſtinguiſh betwixt the foreign
bodies themſelves, changed or petrified, and
their impreſſions upon the ſurrounding matrices.
123Sometimes the body is entirely deſtroyed, forming
a cavity in the ſurrounding matter, and this
cavity afterwards is filled with other materials.
Nuclei, or kernels, are likewiſe found, formed
within the cavities of the harder ſhells, and bearing
the form of their internal ſurface.
§ 265.
I am far from thinking the knowledge of petrefactions
is barren and uſeleſs. We may, and
ought, to conſider them as medals depoſited by
the hand of nature, in memory of the more remarkable
changes on the ſurface of the earth, and
from which the time and order of the work may,
in ſome meaſure, be judged of, whilſt other monuments
are ſilent. Theſe, being properly interpreted,
ſhew us their native ſituations in the
former ſtate of the ſurface of the earth, and teach
us the unbounded empire of the ſea, and the conſequent
changes. By them we learn to diſtinguiſh
the ancient and modern foundations of the mineral
kingdom; for thoſe which are not formed of
petrefactions, and never contain them, are doubtleſs
of greater antiquity than animals or vegetables;
and, laſtly, by their figure they ſhew us the inhabitants
of our globe, eſpecially thoſe of the
greateſt depths of the ocean.
§ 266.
Mr. Cronstedt has admirably arranged the
petrefactions; we think it right, therefore, to retain
his method. The Genera are built upon the
124Genera of foſſils, and arranged like the four claſſes
thereof; the ſpecies upon their ſpecies, and the
varieties upon the organic ſubſtances that have
been changed. The following are the Genera
hitherto diſcovered.
§ 267.
Gypſeous petrefactions are very rare.
§ 268.
Human bodies have ſometimes been found indurated
and penetrated by vitriol of iron; so likewiſe
have plants, their roots eſpecially. In the
open air they moulder away.
§ 269.
This conſtitutes the ſubſtance of moſt petrefactions.
125
§ 270.
It is remarkable, that petrefactions found in
clay are compreſſed, although, in ſubjacent calcareous
ſtrata, they preſerve their natural figure.
Similar compreſſed petrefactions are alſo found
in the marly ſchiſtus.
§ 271.
Siliceous petrefactions are ſometimes met with,
but, in general, this material forms only nuclei
(§ 264). Trunks of trees are ſometimes found
changed into agate. The celebrated Ferber
has ſeen petrefactions in chert and jaſper, and the
illuſtrious Born mentions corallines (porpitæ) in
ſinople or martial jaſper.
§ 272.
Animals and vegetables are reſolved by putrefaction
into an earth, which may be regarded as
forming a peculiar genus, until every appearance
of organization being obliterated, at length it
comes to be conſidered as common earth.
126
§ 273.
Wood, penetrated by indurated petroleum,
forms a remarkable variety of coal.
§ 274.
Native ſilver is ſometimes inherent in petrefactions,
but never, to my knowledge, conſtitutes the
ſubſtance of them, unleſs mineralized with copper
and ſulphur.
§ 275.
When mineralized by ſulphur, it ſometimes,
though very rarely, conſtitutes petrefactions.
§ 276.
Bones and teeth are ſometimes found replete
with the blue calx of copper. Bits of copper
pyrites often ſtick in petrefactions, but ſeldom
conſtitute their whole ſubſtance. I have some
such from Norway, in a matrix of magnetical iron
ore.
127
§ 277.
Calciform iron ſometimes is found in the ſhape
of roots and branches of trees. When mineralized
by ſulphur, it frequently exiſts in petrefactions,
but ſeldom conſtitutes the whole maſs.
§ 278.
I have ſeen pſeudo-galena (black jack), in the
form of coral.
§ 279.
Some modern writers, as well as Mr. Cronstedt,
place the productions of volcanoes in
an appendix by themſelves; but, I think, to no
good purpoſe. Things formed by the hand of
nature, whether by a liquid or a dry proceſs, muſt
not be diſjoined; for ſhe frequently avails herſelf
of both methods in one and the ſame inſtance.
And, indeed, the origin of many things is ſo very
doubtful, every veſtige thereof being obliterated,
that even an Œdipus could not with certainty determine
how they were produced. And, on the
other hand, many aſſert, that almoſt the whole of
the mineral kingdom is the product of fire. To
128avoid error, therefore, it is better to claſs foſſil ſubſtances
according to their conſtituent parts, which
proper experiments will lay open to us; for we
can seldom know their origin or formation.
Homogeneous ſubſtances joined together, but
not primitive, will find a place among the ſtones,
or elſewhere, in the firſt appendix.
1. In this tranſlation they are introduced in their proper
places. W.
2. There is no difficulty in doing this: either the foſſil, or
the vegetable fixed alkaly phlogiſticated, precipitate the terra
ponderoſa, inſtantly and entirely, out of the nitrous, muriatic,
or vegetable acids. W.
4. Conſult particularly Profeſſor Werner’s treatiſe on the external
characters of foſſils printed in German in the year 1774.
5. The latter part of this definition does not apply perfectly
well to ſome of the ſimple ſalts. I ſhall therefore
offer another, given by Dr. Cullen, viz. “Saline bodies
are ſapid, miſcible with water, and not inflammable.”
I am ſenſible too that this definition is not perfectly unexceptionable,
ſince it has been found that vol. alkaly in an
aerial ſtate is in a certain degree inflammable. W.
6. As the tincture of heliotropium is the niceſt known teſt
of the preſence of an acid, it may not be amiſs to mention
that it may be had from dyers under the name of litmus.
It is very cheap, and generally requires to be greatly diluted
with diſtilled water before it can be uſed. W.
8. The moſt highly coloured and fuming nitrous acid may
readily be rendered colourleſs by boiling it haſtily in an open
veſſel. Part of the acid flies off, carrying the ſuperabundant
phlogiſton along with it, in the form of nitrous air. W.
18. It is found in a ſeparate ſtate in large quantities in ſome
of our mines and wells, and is called the choak damp. In
the famous Grotto del Cano too it exiſts tolerably pure. W.
23. Dr. Home, in his eſſay on bleaching, ſays it is found
in coal mines in this iſland, and a friend aſſures me that he
has obtained it from the water iſſuing out of coal pits. W.
24. As volatile alkaly may be obtained in large quantities
from pit coal, and produced by proceſſes not dependant upon
putrefaction, there is reaſon to believe that the vitriolic
ammoniac may be formed in ſeveral ways not noticed by the
author. W.
26. From ſome experiments lately made I found that both
tinkal and purified borax, required twice their weight of
ſedative ſalt, to neutralize them perfectly ſo that they would
no longer change vegetable blues to a green. W.
31. I have lately diſcovered a ſpecimen of Terra Ponderosaaerata got out of a mine in this kingdom. It is
very pure, and in a large maſs. As this ſubſtance is a new
acquiſition to mineralogy, and may be turned to uſeful
purpoſes in Chemiſtry, I intend ſhortly to preſent a more
particular account of it to the Royal Society. W.
34. I found it in conſiderable quantity in the Nevil Holt
water, when I analyzed it ſix years ago; and it is probable
that the Ballycaſtle water in Ireland, likewiſe contains it. W.
35. In the original the word is MAGNESIUM, but it is here
changed, by the advice of Dr. Swediar and the concurrence
of profeſſor Bergman to MANGANESIUM, in order to prevent
confuſion from its ſimilarity to Magneſia. W.
38. The author ſpeaks here of ſuch as he obtained by precipitation
from acids, but the nativeTerra Ponderosaaerata (ſee note at page 28) has a ſpecific gravity of nearly
4, 338. W.
44. Profeſſor Bergman does not here ſeem to be ſufficiently
aware of the difference between our Devonſhire pipe clay,
and that which is uſed in the manufacture of porcelain. The
former, in an open fire, burns to a blueiſh grey, or pidgeon
colour; the latter remains white. The former ſeems to be the
ſame as the Cologne and Maeſtricht pipe clay, of Cronſtedt,
§78; the latter is a decayed Feldſpath, and conſequently,
according to our author, (§ 130) contains magneſia. Our
porcelain clay, likewiſe, has quartz, chryſtals, and mica
mixed with it, parts of the granite which it originally compoſed.
Before it is uſed the quartz is ſeparated, but the
mica remains. I am indebted to my friend Mr. Watt for
theſe obſervations. W.
45. I have taken the liberty to add this ſpecies upon our
author’s own authority. See Bergman Diff. de Lithomarga,
page 13.
48. It is probable, that in another edition, the author may
ſee reaſon to ſeparate the mica from the talc; as ſome experiments
I have made, though yet too imperfect for publication,
ſeem to indicate the neceſſity of ſuch a meaſure. W.
51. Dr. Swediar lately preſented a paper to the Royal
Society, from which it appears highly probable that Ambergriſe
is nothing but the indurated fæces of the Sperma Ceti
whale, who feeds upon the cuttle fiſh. He has found the
beaks of that fiſh intermixed with the ambergriſe, in the
form of black ſpots. W.
55. The degrees of heat here expreſſed, are according to
Farenheit’s ſcale.
By ſaturating phlogiſton, Profeſſor Bergman means to expreſs
the proportionate quantities taken away from each metallic
ſubſtance, when diſſolved by means of acids, and of
courſe reduced to a calciform ſtate. The laſt column only
expreſſes their attractions to this part of their phlogiſton, not
to that which ſtill remains united to them in a calciform
ſtate. W.
60. From ſome late experiments made upon platina by the
Count de Sikengen, and publiſhed in German by profeſſor
Succow, it appears that the ſpecific gravity of pure platina
is 21,000. When perfectly pure and in its metallic ſtate it
was not calcined by deflagration with nitre, it did not admit
of being hardened or ſoftened by tempering, like ſteel
or other metals; it was drawn into a wire ¹⁄₁₉₄₀ of a line in
diameter; this wire admitted of being flattened, and had
more ſtrength than a wire of gold or ſilver of the ſame ſize.
This platina is not fuſible by the ſtrongeſt fire, but melts in
the focus of a burning glaſs; its colour white, ſhining like
fine ſilver.
From conſidering the very intereſting experiments of the
Count de Sikengen, I apprehend the following method to obtain
pure and malleable platina will be found a good one.
Diſſolve the grains of native platina that are leaſt magnetic,
in aqua regia. Precipitate the iron by means of phlogiſticated
fixed alkaly. Then precipitate whatever elſe will
fall, by cauſtic vegetable alkaly. Saturate the liquor with
cauſtic foſſil alkaly, and ſet it by to chryſtallize. The yellow
chryſtals thus obtained are to be hammered together at a
welding heat, and the metallic parts will unite. W.
63. This reference is not to be found in the Engliſh
edition of Cronſtedt. I imagine it ſhould be § 174. 6.
where it is called the Dal Falertz. W.
64. In this reference too I ſuſpect a miſtake. It ought
I believe to be 173, 6. W.
65. Some late experiments made at Hudſon’s Bay ſeem to
prove that Quickſilver congeals and becomes malleable at
39 degrees below 0. See Lond. Med. Journal, page 205,
for the year 1783. W.
66. When I introduce a new ſpecies I repeat the preceding
number, with the addition of an aſteriſk, rather
than break in upon the order of the author’s numbers. I
intend ſhortly to publiſh an exact analyſis of this ſubſtance.
W.