CHAPTER I.

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A

TEXT-BOOK OF TANNING.

[Illustration:

Pl. I.

_E. & F. N. Spon, London & New York._ "INK-PHOTO." SPRAGUE & CO. LONDON.

LIME PITS AND RINSING TANKS.]

A

TEXT-BOOK OF TANNING:

A TREATISE ON THE

CONVERSION OF SKINS INTO LEATHER,

BOTH PRACTICAL AND THEORETICAL.

BY

HENRY R. PROCTER, F.C.S.,

OF LOWLIGHTS TANNERY;

EXAMINER IN TANNING TO THE CITY AND GUILDS TECHNICAL INSTITUTE.

With 8 Plates and numerous Illustrations.

[Illustration]

E. & F. N. SPON, 125, STRAND, LONDON.

NEW YORK: 35, MURRAY STREET.

1885.

PREFACE.

[Illustration]

The aim of the following handbook is two-fold; to give, in a

compendious form, such a summary of our scientific knowledge as may

be useful to the practical tanner; and such a sketch of manufacturing

processes as may enable the chemist to apply his knowledge to their

improvement. Each may, therefore, find some superfluous matter, for

which his indulgence is asked. The book is an expansion of a short

article which appeared in Spons' 'Encyclopædia of the Industrial Arts,'

and to some extent still bears traces of its origin; and, having been

written under stress of limited leisure, and defective eyesight, is

very far from being so perfect as I should desire. For the sake of

completeness it has been necessary to describe many processes which are

outside the range of my own manufacturing experience, and in doing so

I have generally referred to the sources of my information. Chapters

III. and XXIV. are written by Mr. C. G. Warnford Lock, to whose kind

assistance I am much indebted. It may be well to state in conclusion,

that while the work is not intended for a cram-book for technical

students, it is hoped that it may be an assistance to teachers of the

subject.

HENRY R. PROCTER.

Tynemouth,

_August 1885_.

CONTENTS.

[Illustration]

PAGE

INTRODUCTORY NOTE 1

CHAPTER I.

Anatomical Structure of Hide 2

CHAPTER II.

Chemical Composition of Hide 17

CHAPTER III.

Commercial Tanning Materials 23

CHAPTER IV.

The Chemistry of Tannins 57

CHAPTER V.

Water as used in Tanning 83

CHAPTER VI.

Methods of Chemical Analysis for the Tannery 90

CHAPTER VII.

Sole-leather:--Preparing the Hides 132

CHAPTER VIII.

Sole-leather:--Unhairing Hides 139

CHAPTER IX.

Sole-leather:--Tanning Materials 157

CHAPTER X.

Sole-leather:--Treatment in the Tan-house 169

CHAPTER XI.

Sole-leather:--Treatment in the Shed 179

CHAPTER XII.

Dressing Leather 184

CHAPTER XIII.

Currying 193

CHAPTER XIV.

Enamelled, Patent, or Japanned Leather 203

CHAPTER XV.

Morocco Leather 206

CHAPTER XVI.

Russia Leather 208

CHAPTER XVII.

Chamois or Wash-leather 210

CHAPTER XVIII.

Crown Leather, or Preller's Leather 213

CHAPTER XIX.

Mineral-tanned Leather 218

CHAPTER XX.

Calf-Kid 223

CHAPTER XXI.

Glove-Kid 225

CHAPTER XXII.

Construction and Maintenance of Tanneries 231

CHAPTER XXIII.

Drying-sheds for Leather 243

CHAPTER XXIV.

Commerce, Statistics, and Bibliography 255

Index 275

A

TEXT-BOOK OF TANNING

ETC., ETC.

[Illustration]

INTRODUCTORY NOTE.

Leather manufacture may be broadly divided into two stages: "tanning,"

in which the raw hide is converted into the imputrescible and more or

less flexible material known as "leather"; and "currying," in which

this leather is further manipulated, and treated with fatty matters, to

soften and render it more waterproof, and to improve its appearance.

Glove-kid, and certain other leathers, however, are not tanned at all,

but "tawed," or prepared with a mixture in which alum and salt are

the most active ingredients; chamois, "shammy," or "wash" leather, is

produced by fulling with oil alone, and many leathers can scarcely be

said to be curried, although more or less oil is used in the final

processes of "finishing" or "dressing." The first subject to be treated

of in this work will be the operation of tanning, properly so called,

taking for example the tannage of sole- and belting-leather. This

demands thorough explanation, in both its practical and theoretical

aspects, not only because it is one of the most important branches of

the trade, but because the principles involved are those which equally

underlie all other tanning methods. The next to be dealt with will

be the modifications of the process which are necessary in tanning

the more flexible leathers used for boot-uppers, hose-pipes, and

saddlery purposes; then the currying of these leathers; and finally,

the manufacture of moroccos, Russian, and japanned leathers, calf- and

glove-kid, &c.

CHAPTER I.

ANATOMICAL STRUCTURE OF HIDE.

Before speaking of actual processes of manufacture, it is necessary to

devote some attention to the structure and chemical constitution of

hide or skin, which forms the raw material. Although a great variety

of skins are employed in tanning, they are all constituted on the same

general type, and an anatomical description of the hide of the ox will

apply almost equally to those of the calf, sheep, and goat; but from

differences in thickness and closeness of texture, their practical uses

differ widely. Fig. 1 shows a section of ox-hide, cut parallel with the

hair, magnified about 50 diam.: _a_, epithelial layer or _epidermis_,

consisting of horny layer above, and _rete malpighi_ below; _b_, _pars

papillaris_, and _c_, _pars reticularis_ of _corium_, _derma_, or true

skin; _d_, hairs; _e_, sebaceous or fat-glands; _f_, sudoriferous or

sweat-glands; _g_, opening of ducts of sweat-glands; _h_, _erectores

pili_ muscles, for erecting the hair.

The fresh hide consists of 2 layers: an outer, the epidermis; and an

inner, the true skin. The epidermis is very thin as compared with the

true skin which it covers, and is entirely removed preparatory to

tanning; it nevertheless possesses important functions. It is shown in

Fig. 1 at _a_, and more highly magnified in Fig. 2. Its inner mucous

layer _b_, the _rete malpighi_, which rests upon the true skin _c_, is

soft, and composed of living nucleated cells, which are elongated in

the deeper layers, and gradually become flattened as they approach the

surface, where they dry up, and form the horny layer _a_. This last

is being constantly worn away, and thrown off as dead scales of skin;

and as constantly renewed from below, by the continued multiplication

of the cells. It is from this epithelial layer that the hair, as well

as the sweat- and fat-glands, are developed. It will be seen in Fig. 1

that each hair is surrounded by a sheath, which is continuous with the

epidermis. In embryonic development, a small knob of cells forms on the

under side of the epidermis, and this enlarges, and sinks deeper into

the true skin, while the root of the young hair is formed within it;

this is shown in Fig. 3, _a b_. Smaller projections also form on the

stalk of the knob, and in due time produce the sebaceous glands. The

process of development of the sudoriferous glands is very similar to

that of the hairs. There is a great analogy between this process and

that of the ordinary renewal of hair in the adult animal. At _d_^1

Fig. 1, is seen an old and worn-out hair. It is shrunken and elongated,

and is almost ready to fall out. It will be noticed that its sheath or

follicle projects somewhat below the hair to the right. This is the

first production of a young hair, and is quite analogous to the knob of

epithelium which has been described as forming the starting-point of a

hair in embryo. At _d_^2, the same process is seen further advanced,

the young hair being already formed, and growing up into the old

sheath. At _d_^3, it is complete, the old hair having fallen out, and

the young one having taken its place.

[Illustration: Fig. 1.]

[Illustration: Fig. 2.]

[Illustration: Fig. 3.]

The hair itself is covered with a layer of overlapping scales, like

the slates on a roof, but of irregular form. These give it a serrated

outline at the sides, strongly developed in wool. Within these scales,

which are sometimes called the "hair cuticle," is a fibrous substance,

which forms the body of the hair; and sometimes, but not always, there

is also a central and cellular pith, which is mostly transparent,

though under the microscope it frequently appears black and opaque,

from the optical effect of imprisoned air. On boiling or long soaking

in water, alcohol, or turpentine, these air-spaces become saturated

with the liquid, and then appear transparent.

The fibrous part of the hair is made up of long spindle-shaped cells,

and contains the pigment which gives the hair its colour. The hair

of the deer differs from that of most other animals in being almost

wholly formed of polygonal cells, which, in white hairs, are usually

filled with air. At its base, the hair swells into a bulb, which is

hollow, and rests on a sort of projecting knob of the _corium_, called

the hair-papilla. This has blood-vessels and nerves, and supplies

nourishment to the hair. The hair-bulb is composed of round, soft

cells, which multiply rapidly; as they grow, they press upward through

the hair-sheath, become elongated and hardened, and form the hair. In

dark hairs, both the cells of the hair itself and those of its follicle

or sheath are strongly pigmented, but the hair much the more so, and

hence the bulb has usually a distinct dark form. The dark-haired

portions of a hide from which the hair has been removed by liming

still remain coloured, from the pigmented cells of the hair-sheaths,

which can only be got out completely by bating and scudding. The

cells outside the bulb, shown at _f_, in Fig. 4, pass upwards as they

grow, and form a distinct coating around the hair, which is called

the "inner root-sheath." This again consists of 2 separate layers,

of which the inner is "Huxley's," the outer, "Henle's." They arise

from the same cells in the base of the hair; but in the inner layer,

these remain polygonal and nucleated, while in the outer, they become

spindle-shaped and without nuclei. The inner root-sheath does not

extend to the surface of the skin, but dies away below the sebaceous

glands. This figure represents an ox-hair root, mag. 200 diam.: _a_,

fibrous substance of hair; _b_, hair cuticle; _c_, inner root-sheath;

_d_, outer root-sheath; _e_, dermic coat of hair-sheath; _f_, origin of

inner sheath; _g_, bulb; _h_, papilla.

[Illustration: Fig. 4.]

Outside the inner root-sheath is a layer of nucleated cells, continuous

with those of the epidermis, and of the same character. This is the

"outer root-sheath," and is shown at _d_, Fig. 4. This, together with

the whole of the epidermis, is covered next the _corium_ with an

exceedingly fine membrane, called the "hyaline" or glassy layer. It

is possible that this forms the very thin buff-coloured "grain" of

tanned leather, which evidently is of different structure from the rest

of the _corium_, since, if it gets scraped off before tanning, the

exposed portion of the _pars papillaris_ remains nearly white, instead

of colouring. The whole of the hair-sheath is enclosed in a coating of

elastic and connective-tissue fibres, which are supplied with nerves

and blood-vessels, and form part of the _corium_. Near the opening of

the hair-sheaths to the surface of the skin, the ducts of the sebaceous

or fat-glands (_e_, Fig. 1), pass into them, and secrete a sort of

oil to lubricate the hair. The glands themselves are formed of large

nucleated cells, arranged somewhat like a bunch of grapes; one is shown

highly magnified in Fig. 5: _a_, sebaceous gland; _b_, hair-stem; _c_,

part of _erector pili_ muscle. The upper and more central cells are

most highly charged with fat, which is shown by the darker shading.

[Illustration: Fig. 5.]

As already remarked, the sudoriferous or sweat-glands are also derived

from the epidermis layer. They are shown at _f_, Fig. 1, and on a

larger scale (200 diam.) in Fig. 6: _a_, windings laid open in making

section; they consist, in the ox and sheep, of a large wide tube,

sometimes slightly twisted. In this, they differ considerably from

those of man, which form a spherical knot of extremely convoluted

tube. The walls of these glands are formed of longitudinal fibres of

connective tissue of the _corium_, lined with a single layer of large

nucleated cells, which secrete the perspiration. The ducts, which are

exceedingly narrow, and with walls of nucleated cells like those of

the outer hair-sheaths, sometimes open directly through the epidermis,

as shown at _g_, Fig. 1, but more frequently into the orifice of a

hair-sheath, just at the surface of the skin. Each hair is provided

with a slanting muscle (_h_, Fig. 1), called the _arrector_ or _erector

pili_, which is contracted by cold or fear, and causes the hair to

"bristle," or stand on end; by forcing up the attached skin, it

produces the effect known as "goose-skin." The muscle, which is of the

unstriped or involuntary kind, passes from near the hair-bulb to the

epidermis, and just under the sebaceous glands, which it compresses.

[Illustration: Fig. 6.]

The _corium_ or true skin is principally composed of interlacing

bundles of white fibres, of the kind known as "connective tissue";

these are composed of fibrils of extreme fineness, cemented together

by a substance of different composition from the fibres themselves.

This may be demonstrated by steeping a small piece of hide for some

days in a stoppered bottle in lime-, or baryta-water, in which the

inter-fibrillar substance is soluble, and then teasing a small fragment

of the fibre with needles on a glass microscope-slide, and examining

with a power of at least 200-300 diam. In the middle portion of the

skin, these bundles of fibre are closely interwoven; but next the

body, they gradually become looser and more open, forming the _pars

reticularis_ (or netted part); and the innermost layer is a mere

network of loose membrane, generally loaded with masses of fat-cells,

and hence called adipose tissue.

It is this adipose tissue which is removed in the "fleshing" process.

On the other hand, the outermost layer, just beneath the epidermis,

is exceedingly close and compact, the fibre-bundles that run into it

being separated into their elementary fibrils, which are so interlaced

that they can scarcely be recognised. This is the _pars papillaris_,

and forms the lighter-coloured layer, called (together with its very

fine outer coating) the "grain" of leather. It is in this part that the

fat-glands are embedded, while the hair-roots and sweat-glands pass

through it into the looser tissue beneath.

Besides the connective-tissue fibres, the skin contains a small

proportion of fine yellow fibres, called "elastic" fibres. If a thin

section of hide be soaked for a few minutes in strong acetic acid, and

then examined under the microscope, the white connective-tissue fibres

become swollen and transparent, and the yellow fibres may then be seen,

as they are scarcely affected by the acid. The hair-bulbs and sweat-

and fat-glands are also rendered distinctly visible.

The nerves of the skin are very numerous, each hair being supplied

with fibres passing into both the papilla and sheath. They also

pass into the skin papillæ. They cannot readily be seen, without

special preparation, and, so far as is known, exercise no influence

on the tanning process. "Breaking the nerve" is a technical term,

which signifies a thorough stretching and softening of the skin, but

has nothing to do with nerves properly so called. The blood- and

lymph-vessels are, from the present point of view, somewhat more

important. They may often be seen in sections, and are lined with

nucleated cells, similar to those of the glands. These are surrounded

by coatings of unstriped muscular fibre, running both around and

lengthways, and also by connective-tissue fibres. In the arteries, the

muscular coating is much stronger than in the veins.

It may be thought that the space devoted to a discussion of the

anatomical structure of the skin is disproportionately large;

but there can be no doubt that, in order to make improvements,

nothing is of more importance than a clear conception, even to the

smallest details, of the materials and causes to be dealt with. The

illustrations are from actual specimens, and enable the various parts

of the hide to be identified under the microscope.

As this instrument is a most useful means of investigation in the

tanning industry, and one likely to be of increasing importance, it

will be well, before proceeding further, to say a few words, both on

the selection of a suitable instrument, and on its manipulation in

general.

To do useful work, it is not necessary to possess a very elaborate

or expensive instrument, but it is essential that the microscope be

well made and good of its kind. As high powers are often required in

the examination, both of hide sections and of ferments, which are the

principal objects of investigation in a tannery, it is of the first

importance that the fine adjustment should be perfectly steady, without

vibration or backlash. This, in the writer's experience, is never the

case with cheap microscopes, in which the fine adjustment is made by

a screw at the side of the tube moving the nose by means of a lever.

A much more satisfactory arrangement is that in which the whole body

of the microscope is raised or lowered by a screw in a pillar at the

back of the stand on which it slides. A rack for the coarse adjustment

is useful, but not essential. If a sliding tube only is provided, it

must be tight enough not to slip, but must move easily up and down

with a sort of screwing movement. A mechanical stage is not at all

necessary, and for most purposes one of black glass is better as well

as cheaper. The diaphragm for regulating the light should be as near

level with the surface of the stage as possible, and when examined with

a low power should appear in the centre of the field. For research work

on the minuter ferments, an achromatic condenser and the finest oil-

or water-immersion lenses are necessary, but directions for this are

beyond the scope of the present work. It may, however, be mentioned

that Prof. Flügge,[A] a first-class authority on the subject,

especially recommends Abbé's illuminating apparatus as made by Zeiss.

[Footnote A: "Fermente und Mikroparasiten," Leipzig, 1883.]

A frequent defect in cheap English microscopes is that the mirror for

substage illumination does not bring the rays of a lamp to a focus

exactly on the slide, but frequently some inches above it. This may be

to a great extent overcome by the use of a bulls'-eye condenser between

the lamp and the microscope. Another defect is that sometimes the

centre of the mirror is not in a line with that of the microscope body.

The objectives (or lenses at the lower end of the microscope) are the

most important part of the instrument, and however good it may be in

all other respects, if these are defective the whole is useless. The

most useful lenses for our purpose, if only two are to be selected, are

a 1-in., magnifying about 50 diam., and a 1/4-in., magnifying about 200

to 400, according to the eye-piece; a 1/8-in. giving, say, twice this

magnification will be needed to see the smaller bacteria distinctly,

but it is possible just to see even the small putrefaction bacteria

with a really fine 1/4-in. In any case, the highest power should be as

perfect and of as large an angle as attainable. A good 1/4-in. should

resolve _Pleurosigma angulatum_ with direct light, and should show the

movement of the granules of protoplasm in the round corpuscles which

are present in saliva. In using the latter test, it must be remembered

that the motion only lasts a very short time on a cold slide.

About 5_l._ is the very least for which a microscope can be obtained

which is suitable for tanners' use; where it can be afforded, a better

one is advisable.

Without disparaging other makers, it may be mentioned that the writer

has generally used both the eye-pieces and objectives of Dr. Hartnack

of Potsdam; and that they are moderate in price, at least for the dry

combinations, and perfectly satisfactory for all technical purposes.

Numbers 2, 5, and 8 objectives with No. 3 eye-piece, are sufficient

for all ordinary work. If only 2 objectives are to be obtained, Nos.

3 and 7 would be perhaps the best selection. It is always better

to use objectives on the stand, and with the eye-pieces for which

they are intended, but in case Hartnack's objectives are used on an

English stand (which is easily done by means of an adaptor ring), it

is important to remember that they are constructed to work with a

shorter tube than that customary on English microscopes, and that they

will not perform well if its length is much more than 6 in.; these

objectives are not provided with a movable adjustment for thickness

of cover-glasses, which for technical purposes is not required, and

in inexperienced hands is apt to prove troublesome. Extra-thin covers

must therefore always be used. Where this adjustment is provided, the

object must be accurately focused, and then, maintaining this focus

with the fine focusing-screw, the collar must be cautiously turned till

the best definition is obtained. Practically it will be best to make

this adjustment accurately once for all, and to take care to use covers

selected of a uniform thickness.

High-power objectives of wide angle (which condition is essential to

good defining power) necessarily work extremely close to the object,

and it is always best to use the thinnest cover-glasses which can be

got. Even then, with such glasses as Hartnack's No. 8, unless the

sections are very thin, it will be impossible to examine their lower

parts; and one of the greatest difficulties of microscopic research

is to obtain them thin enough. It will be obvious, from what has

been said, that the greatest care is needed to avoid screwing the

objective down on the cover, and so breaking one or both of them. One

way to avoid this is to screw down as close as possible to begin with,

and then focus upwards. Another plan, when the object on the slide

is small, is to keep continuously moving the slide gently with the

fingers, while looking into the tube. It is then easy to notice when

the dust and small particles on the slide come into focus, and if the

point should happen to be overstepped the contact will generally be

felt before serious damage is done.

Illumination is one of the most important points in practical

microscopy. With powers of not less than 1/2-in. focus, objects may

generally be examined by light thrown upon them from above by a

bulls'-eye condenser, or by good daylight. In this case they need not

be transparent; and the plan is often convenient for a mere surface

examination. In examining bodies illuminated in this way, prominences

often appear as hollows and _vice versâ_, by a sort of optical

illusion, which, once established, is very difficult to overcome. By

remembering the direction of the light, and that this appears reversed

in the microscope, it is easy to decide the truth.

For all finer work and higher powers, and most generally with the low

powers also, it is necessary to render the object transparent, and to

examine it by light transmitted from the mirror below the stage.

Good daylight is least trying to the eyes. Where artificial light must

be used, that of a small paraffin lamp is best; and a blue chimney,

or blue glass interposed between the stage and mirror, or lamp and

microscope, spares the sight, and makes it easier to distinguish

colours. The light should be sufficient, but not too dazzling. Work

should never be prolonged after the least strain is felt, nor should

the microscope be used for some little time after a meal. It is well to

accustom oneself to keep both the eyes open while observing.

If it be required to see how far the cellular structures of the hide,

such as hair-sheaths and fat-glands, are affected or destroyed in any

stage of liming or bating, the following ready method may be employed.

If a strip of hide be cut 2/3 through from the grain side, as shown

at _a_ in Fig. 7, and the flap be turned down, and held between the

finger and thumb, the fibrous tissue will be put on the stretch, and

will then allow a moderately thin shaving (including the grain and

parts immediately below it) to be cut by a sharp razor. The hide

should be held in the positions shown, and a steady drawing cut be

made from flesh to grain, the razor being steadied on the tip of

the forefinger, and its hollow surface flooded with water. If the

thin section be now placed on a glass slide, moistened with a drop of

water, and examined on the microscope under a strong light from above,

with a 1-in. objective, the fat-glands will be seen as yellow masses,

embedded in the white fibrous tissue. If a drop of a mixture of equal

vols. of strong acetic acid, glycerin, and water be used to moisten the

section, the fibrous tissue will become quite transparent, and whatever

remains of the cellular tissue will be easily visible, and may even be

studied under tolerably high powers if covered with a thin glass, and

lighted by the mirror from below. (The cover-glass must be carefully

cleaned by rubbing with a linen handkerchief, and placed in position

with a pair of tweezers, one side being supported by a needle, which is

gradually withdrawn, so as to avoid air-bubbles.) Care must be taken

that this mixture does not touch the brass-work of the microscope; even

the vapour is apt to tarnish, so that the preparation must not remain

longer than necessary on the microscope. The same method is applicable

for ascertaining the completeness of the tannage of leather, and to

decide whether the hide fibre is really tanned, or only dyed. Actually

tanned leather is unaffected by the acetic acid, but raw or only

stained hide swells and becomes transparent.

[Illustration: Fig. 7.]

To prepare the very thin sections necessary for detailed study of the

hide, more complicated methods are required. Small slips of hide, not

exceeding 1/4 in. wide, and cut exactly across the lie of the hair,

are placed first in weak alcohol (equal parts methylated spirit and

water), and, after a few hours, are removed into strong methylated

spirit. It is then kept for some days in absolute alcohol, which must

be repeatedly changed, until the hide is hard enough to give fine

shavings, and may be cut either when held as above described, between

cork or pith, or when embedded in paraffin wax. This is accomplished

by placing the piece of hide in a little paper-box and covering it

with melted paraffin (candle), which is just beginning to stiffen. The

piece of hide may be fixed in position with a needle, which must of

course be withdrawn before cutting. When hard, the paraffin is shaved

away till the object is exposed, when it may be cut. The razor must be

wet with alcohol, and the section be made exactly in the plane of the

hair-roots, which may be seen with a hand-lens. (The use of a microtome

for hide-sections is rarely successful, as it is almost impossible to

fix the fragment of hide so that it is cut exactly with the hairs.)

The slices may now be stained by placing them in a watch-glass with

water and a few drops of the logwood or picrocarmine staining-mixtures

sold by opticians, and afterwards either examined in glycerin, or,

after soaking some hours in absolute alcohol, may be transferred to

clove-oil, and afterwards to a slide, and covered with a drop of

dammar varnish or Canada balsam dissolved in chloroform. The sections

moistened with glycerin may also be mounted in Farrant's solution

or glycerin jelly, under a cover-glass for permanent preservation.

If picrocarmine be used, the connective-tissue fibres (gelatinous

fibres) and the nuclei of the cells will be coloured red, and the cells

themselves of both epidermis and glands, together with the muscles and

elastic fibres, will be yellow.

Franz Kathreiner, who has made very elaborate researches on skin, and

the changes which take place in it during the processes of tanning,

employs a mixture of osmic and chromic acids for hardening, and at the

same time staining the tissue. This mixture was first used by a German

histologist with whose name I am not acquainted, in a research on the

internal organs of hearing, and was applied by Kathreiner in 1879 to

the investigation of skin, and communicated by him to the writer in

the autumn of that year. His method is briefly as follows. The pieces

of hide to be examined must, if salted, be well washed, or if dry, be

thoroughly softened. For the study of hide in its unaltered and natural

condition, it is essential that it be quite fresh, and taken from the

animal as soon as possible after death. In any case the _Panniculus

adiposus_ or fatty layer is, as far as possible, removed with scissors,

the hair cut short, and the skin cut up into little pieces of 3-4

millimetres wide by 10-12 millimetres long (about 1/8 in. by 1/2 in.);

the hair must lie exactly across these pieces.

They are then placed for 4-8 days, according to the thickness of the

hide, in about 12 times their volume of a solution consisting of

0·2 parts osmic acid.[B]

0·5 " chromic acid.

200·0 " water.

[Footnote B: Solution of osmic acid is best preserved in sealed tubes

in the dark. If obtained in solution it is rarely of full strength,

for which allowance may have to be made. Care must be taken to avoid

inhaling its fumes, which are very irritating to the eyes and to the

respiratory organs, producing severe catarrh.]

This solution must be kept from dust and light, in a glass stoppered

bottle, and in a cool place. On removing the hide-pieces from this

solution, they are placed in about 12 times their volume of absolute

alcohol for 4-8 days, during which time the spirit must be at least 3

times renewed. The sections are cut with a razor flooded with absolute

alcohol, so that the thin shavings float without friction upon it. The

hide-pieces may be held either between soft cork, or, as is generally

preferable, simply between the forefinger and thumb as shown in Fig.

7. The cut must be made exactly parallel with the direction of the

hair roots, and from the grain towards the flesh; and the sections

cannot possibly be too thin. After lying for 1/2-1 hour in absolute

alcohol, the sections are soaked till quite clear in clove oil (which

must be pale and of the purest kind), and may then be mounted in dammar

varnish, or solution of Canada balsam.

In these sections, fat and the oily contents of the fat glands are

stained black, and the limits of the cells both of these glands and of

other elements of the hide (_rete malpighi_, hair-bulb, &c.) are made

very distinct, so as to be capable of the most delicate investigation

under the highest powers; but the beginner will learn most easily to

recognise the different tissues by studying at first some sections

stained with picrocarmine as before described. The method is admirably

adapted for the study of hide as affected by the limes and bates.

A Text-book of Tanning A treatise on the conversion of skins into leather, both practical and theoretical. · 第 1 / 24 章