CHAPTER XXXVII

SAFE CHEMICAL EXPERIMENTS

TWENTIETH-CENTURY “BLACK ART”

AS we stand in the twentieth century and peer curiously down the

corridors of Time, we find at all periods a deep interest in chemical

phenomena.

From the age when wisdom devoted itself in vain to the discovery of an

elixir of life and a method of transmuting the base metals into gold, to

the present day, when scientists pursue their experiments with more

reasonable and far worthier hopes, chemistry appears never to have

suffered any dearth of devotees, despite the fact that in olden times

one had either to occupy a high position or be a man greatly daring if

the Black Art was to be followed without fear of molestation.

To-day matters are different, so that the junior chemist need only

anticipate interference from _materfamilias_--a truly excellent person,

who, however, invariably regards chemical concoctions with hostile

contempt.

The obstacles instanced in the previous paragraph being foreseen,

perhaps no better initiative can be taken than to conciliate the

household deities by the performance of some particular experiment which

has an obviously beneficial result. This might happily be the removal of

ink stains from white linen; and naturally, if no cloth happen to be so

disfigured, some arrangement must be made whereby the ink is

accidentally spilt!

EXPERIMENTS WITH CHLORINE

(1) _Apparatus._--Erect a 4-oz. round-bottom flask about 8 inches above

the table (A, Fig. 1), by clamping its neck in a wooden clip or twisted

stiff iron wire, and fastening this to a firm standard. Introduce three

or four tablespoonfuls of powdered manganese dioxide (obtainable cheaply

in qr. lbs. at most druggists’), and pour over this spirits of salt

until the flask is one-third full. Into the neck now fit a cork provided

with two circular holes, through one of which a stem funnel passes, and

into the other a glass tube fits tightly, being bent at two right

angles, as shown in Fig. 1. The glass tube may be readily bent by

softening it first over a spirit lamp--the flame being colored distinct

yellow when the glass reaches a pliable state. Slide a 4¹⁄₂-inch disc of

paper (B, Fig. 1) on the free limb of the tube, and also soak several

4-inch circles of cardboard in water. These will make satisfactory

covers for the small glass preserve jars, in which the gas is to be

collected.

[Illustration: FIG. 1.--Apparatus for chlorine experiments.]

(2) _Preparation._--Place one jar beneath the glass tube so that the

latter’s orifice reaches nearly to the bottom, and slide the paper disc

down until it covers the mouth of the jar C. On warming the glass flask

gently with a spirit lamp or, if available, Bunsen gas flame, a

greenish-yellow gas is evolved, and gradually expels the air from flask,

tube, and jar, until this latter is filled with heavy chlorine. The

warming is then interrupted whilst the one jar is removed, covered with

a moist cardboard disc, and replaced by another. The heating again

proceeds, and so on until each remaining jar is successively filled.

[Illustration: FIG. 2.--The unalterable postmark.]

_Chlorine Experiments_ (1).--Damp an addressed envelope, received

through the post, by pressing between sheets of wet blotting-paper, and

stand it in a jar of chlorine with the cover replaced (A, Fig. 2). The

writing ink address will soon begin to fade and finally disappear,

whilst the postmark, which has been impressed in indelible printing ink,

remains unaltered. This reaction shows that chlorine possesses the

valuable property of bleaching writing ink. It may be turned to account

in removing stains from cloth by wetting the spoiled material first and

then standing in a vessel containing the yellow gas (Fig. 3). The fabric

must be quite damp, however, as bleaching only proceeds in the presence

of moisture. Coloring matters, other than black ink, are readily removed

by chlorine, as may be strikingly shown by steeping a wet rose blossom

or bunch of violets in a jar of the gas (Fig. 4); the flowers assume a

transparent waxy appearance, that will puzzle any spectator as to their

real identity.

[Illustration: FIG. 3.--Removing stains from linen by means of

chlorine.]

[Illustration: FIG. 4.--The transparent rose.]

_Chlorine Experiments_ (2).--The energetic gas attacks many substances

spontaneously. If thin blotting-paper be soaked in turpentine, drained,

and dropped into a jar of chlorine, the oil takes fire at once, burning

rapidly amid smoky black fumes. Metals are attacked just as readily as

the inflammable oil of turpentine. Powdered antimony metal or iron

filings shaken into a jar of chlorine scintillate brilliantly with the

evolution of thick white fumes. Similarly Dutch metal leaf, used for

gilding cheap picture frames, ignites in the gas; a salt of copper being

precipitated to the bottom of the jar when the action has ceased.

_All dealings with chlorine should be conducted in a well

ventilated--even draughty--room, and care must be taken not to inhale

the gas._ It corrodes animal tissues just as eagerly as it attacks

turpentine and metals. The gas is very heavy, however, and is therefore

the less difficult to keep under control.

_Niter Paper._--Touch-paper burns quickly, surely, and without flame. It

is prepared by soaking thin tissue paper with a saturated solution of

saltpeter in weak vinegar, and when dry feels rough and crisp to the

touch. Moreover, it burns with a rather pleasant smell. The

advertisement scheme of bygone days, wherein a lighted match was placed

on a particular spot of a paper sheet, and thence the name of the

advertised commodity gradually burnt itself out over the surface, was a

modification of this preparation (Fig. 5). The name or design is simply

drawn with a pointed stump of wood dipped repeatedly in the saltpeter

solution, and the starting-point marked conspicuously by a cross or

black spot. When dry a match is applied to this mark. If there is a

tendency for other parts of the paper than the design itself to burn, a

short immersion in dilute alum solution, when the saltpeter lines have

dried, may be resorted to.

[Illustration: FIG. 5.--A niter paper experiment.]

_Electric Fire._--This compound is in no way of an electric nature,

except that it burns rapidly with brilliant blue illumination. The

constituents are flowers of sulphur, saltpeter, and antimony, four parts

of the former being intermingled with ten parts of powdered saltpeter,

and then one-seventh the total quantity of powdered antimony finally

added. Thorough mixing by gentle stirring must be insured. A good method

of firing the powder is to pack it round a twist of touch-paper in a

small mustard tin, threading the fuse (A, Fig. 6) through a hole in the

lid, so that it may be lighted easily. The mixture burns not only

brightly, but with intense heat--sufficient to melt the thin iron of the

inclosing tin.

[Illustration: FIG. 6.--Lighting electric fire.]

[Illustration: FIG. 7.--A sodium or potassium experiment.]

_The Lightest Element._--Hydrogen is a gas at ordinary temperature, and

has the honor of being the lightest element, for all practical purposes,

known. For this reason it finds wide employment in filling balloons and

airships. The most common methods of preparation consist of decomposing

water or an acid in their several constituents, either by the influence

of electricity or the reaction of a metal. For instance, if a pea’s bulk

of sodium or potassium metal be thrown into a basin of water, A, Fig. 7,

(the experimenter should not bend directly over the vessel), a violent

reaction ensues, the metal decomposes and hustles round the surface as

though in feverish excitement, and in the case of potassium a purple

flame springs up spontaneously. The sodium may also be ignited if it is

thrown on to a floating piece of blotting-paper, or if the water be

thickened with starch. This metal burns with a yellow flame, or rather

colors the hydrogen flame yellow.

[Illustration: FIG. 8.--An interesting hydrogen experiment.]

Preparing hydrogen by the foregoing method is inconvenient and expensive

if any quantity is to be collected, and so in this case the following

plan is usually adopted:--Support a flask (A, Fig. 8), and place zinc

chips (B) in it to the depth of about ¹⁄₄ inch. Fit the mouth with a

cork, through which passes a delivery tube (C) and a “thistle” funnel

(D), dipping nearly to the level of the zinc. When the gas is required,

dilute sulphuric acid--one part oil of vitriol to ten parts water--is

poured down the funnel until the flask is about one-third filled (E).

Five or ten minutes should be allowed after bubbling has commenced

before an attempt is made to light the gas at the delivery tube, as

otherwise air from the flask may be intermingled in the exact proportion

to cause a bad explosion. _No danger need be feared if several minutes

are allowed for the air to be thoroughly dispelled, or, as an additional

measure of safety, a damp towel_ (F) _is wrapped round the flask to

prevent scattering of the glass in the event of a mishap._ The glass

delivery tube should have been softened in a spirit flame and drawn to

a fine point where the hydrogen issues. The gas will be found to burn

with an almost colorless flame.

If a glass tube (A) of larger bore than the delivery pipe be slid over

this latter while the gas burns, a peculiar musical note is

produced--hollow-sounding and shrill (Fig. 9). It is caused by the rapid

succession of slight explosions which constitute the combustion of

hydrogen.

[Illustration: FIG. 9.--A musical flame.]

The extreme lightness of hydrogen, as well as its combustibility, is

well illustrated by blowing a soap bubble. Connect a clay pipe with the

glass delivery tube by means of a length of india-rubber tubing, and

provide this latter with a small clip--tie-clip, for example--so that

the gas supply may be shut off at will (Fig. 10). Let the hydrogen pass

for a minute or so, to clear air out of the clay pipe, and then, having

shut off the gas, dip the pipe bowl into soap-suds. Next open the clip

until the hydrogen has blown the bubble large enough, and then shut off,

shaking the shimmering globe free. It will rise very quickly, just like

an unballasted balloon, and if a lighted taper be applied to its surface

it will explode to annihilation with a loud report.

[Illustration: FIG. 10.--To explode a soap bubble.]

[Illustration: FIG. 11.--Freezing a flask of ammonia to a block of

wood.]

_Spirits of Hartshorn._--Commercial ammonia is actually an aqueous

solution of the gas, which dissolves to an abnormal extent in water.

When it has been absorbed as much as possible the liquid weighs only

22.25 as much as an equal bulk of water, owing, of course, to the

latter’s association with a compound far lighter than itself. So great

is the energy of solution that heat is dissipated from the liquid as

absorption proceeds. Conversely, if the gas be dispelled by blowing air

through strong liquor ammoniac, heat is rapidly absorbed at the expense

of surrounding objects. To show this, stand a small flask in a pool of

water on a wood block, and having about half filled the flask with fresh

ammonia, blow into this through a glass tube connected with the mouth by

a length of rubber tubing (Fig. 11). No long time should elapse before

enough heat has been abstracted from the water to convert it into ice,

so that the flask is frozen firmly to the wood.

Another demonstration of water’s avidity for ammonia gas is afforded by

the following performance. Erect one large flask (A) in an inverted

position, so that the distance between its neck and the table is several

inches greater than its own height. Some distance away, as shown in Fig.

12, erect a small 4-oz. flask (B), and half fill it with a mixture of

four parts sal-ammoniac to three parts slaked lime (C). Fit the neck

with a cork and a delivery tube, which has been so bent as to pass

through a stopper in the mouth and reach nearly to the bottom of a jar

(D) packed with quicklime (E).

Another glass tube (F) issues from this chamber--but only from just

below the cork’s under surface--and passes upwards into the orifice of

the large flask. A square of paper (G, in Fig. 12) is pushed over the

glass tube and presses against the mouth of the flask.

[Illustration: FIG. 12.--To prove water’s affection for ammonia.]

If now the mixture in the 4-oz. flask be warmed, ammonia gas is

produced, and having been robbed of moisture by the quicklime through

which it passes, travels upwards, and collects in the large inverted

flask. When the action has continued for a little while, stop the

heating and remove the delivery tube, and bring an open spirits of salt

bottle near the inverted flask’s mouth. If dense white fumes are

immediately formed, the flask is known to be filled with ammonia gas,

and must be corked up.

[Illustration: FIG. 13.--A novel fountain.]

Beneath this container is next stood another large flask filled with red

litmus solution (A) and fitted with a stopper, through which pass two

glass tubes (M and N, in Fig. 13). One of these (N) is bent outwards,

and extends only just inside the flask’s neck, whilst the other is long

enough to reach from the bottom of the lower flask almost to the top of

that holding the ammonia. Instead of red litmus solution, a liquid made

by boiling red cabbage leaves in water, and adding _just enough_ vinegar

to dispel entirely the bluish coloration, may be used with equal

success.

The position then is that two flasks--of which the upper (B) holds

ammonia gas, whilst the lower retains a pink solution--are supported one

above the other, their necks approaching and joined by a glass tube (M).

A second glass tube (N) also emerges from just above the surface of the

pink liquid, and is bent outwards from the flask, so that it may be held

in the mouth. When this is blown through, the pink water is forced up

the connecting tube (M) and sprays out, fountain-like, within the upper

flask. Moreover, as the ammonia is so rapidly absorbed by the incoming

water, this continually ascends to fill the vacuum, which tends to form

as the gas is dissolved. The fountain continues to play when the blowing

has ceased, and further, although the spray presents a reddish tinge on

entering the flask, it immediately turns blue as the ammonia dissolves

(C, Fig. 13). This reaction indicates the alkalinity of ammonia, such

substances being capable of neutralizing acids, which redden solutions

of vegetable blues.

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