Cooley's Cyclopaedia of Practical Receipts Volume I Part 264

Sometimes as much cullet as sand is used; but in all cases 1% to 1-1/2% of its weight in carbonate of soda is added with it, besides that ordered in the formula, to compensate for loss of alkali by remelting. Used at the celebrated plate-gla.s.s works at Saint-Gobain, France. The product possesses an amount of excellence which British manufacturers have yet failed to equal.

GLa.s.s, TABLE BOHEMIAN CRYSTAL. Sp. gr. 26 to 28.--

_a._ By a.n.a.lysis:--

1. (M. Berthier.) Silica, 717%; pota.s.sa, 127%; soda, 23%; lime, 103%; alumina, 4%; oxides of iron and manganese (and loss), 26%. Very white, hard, and beautiful table gla.s.s.

2. (Dumas.) Silica, 70%; pota.s.sa, 20%; lime, 4%; alumina, 5%; oxide of iron, 6%; peroxide of manganese, 4%. A beautiful white winegla.s.s.

_b._ Materials used:--

1. Finest sand, 50%; purified potashes, 25%; chalk, 10%; nitre, 2%; crystal cullet, 27%; manganese, a little (say 1/16%). Used in England recently for table gla.s.s.

2. Quartz (hyalin, in powder), 63%; purified potashes, 26%; slaked lime (carefully sifted), 11%; manganese, a little; crystal cullet, at will.

Used in Bohemia.

3. (M. Perdonnet.) Powdered quartz, 44%; carbonate of pota.s.sa, 33%; quicklime (in fine powder), 22%; nitre, 1%; and a very small quant.i.ty of a.r.s.enious acid and peroxide of manganese. Said to be the formula used at Neuwelt for the gla.s.s _a_, 1 (_above_).

_Qual., &c._ These are denoted by its hardness, transparency, h.o.m.ogeneity, strength, and power of resisting the action of water, air, light, and the stronger acids and alkalies. The power of gla.s.s to resist the action of menstrua is readily tried by exposing it to boiling oil of vitriol, and hot but dilute solution of caustic pota.s.sa. Neither of these tests should cause the gla.s.s to lose its transparency or to become dim.

_Swallowed gla.s.s._ Gla.s.s and enamel, both in fragments and in powder, have occasionally been swallowed, with different results. These bodies are insoluble in the fluids of the body, and, consequently, any injurious action they may exert upon the system whilst they are retained in it must entirely depend upon mechanical attrition or irritation. As treatment, we must administer an emetic, and a.s.sist its action by thick mucilaginous liquids, and afterwards have recourse to antiphlogistics, if necessary.

_a.n.a.l._--_a._ A portion of the sample for examination is heated to dull redness, and then suddenly thrown, whilst still hot, into a vessel of cold water. It is next dried, and reduced to fine powder in an agate or hardened-steel mortar.

_b._ 100 gr. of the prepared powder is thoroughly mixed with 200 gr. of pure pota.s.sic hydrate, and the whole is exposed to heat in a silver or platinum crucible or capsule until perfect fusion takes place; when cold, the crucible and its contents are boiled in about half a pint of distilled water; nitric acid is added to the resulting solution, in excess, and the mixture, together with any sediment, is evaporated to dryness, after which the heat is gradually increased to 400 or 500 Fahr.; the dry residuum is next reduced to powder, and digested in water acidulated with nitric acid, until exhausted of soluble matter; the insoluble portion is then carefully dried, gently ignited and weighed. The weight in grains represents the per-centage of silica in the sample examined.

_c._ The mixed liquid and was.h.i.+ngs of _b_ is next acidulated with nitric acid, and treated to a stream of sulphuretted hydrogen, which, if it produces a precipitate, is continued for some time; the precipitate is collected on a very small filter, washed, and dried; the filter with the precipitate next placed in a beaker gla.s.s, and strong fuming nitric acid is cautiously added, drop by drop, until complete solution takes place; after boiling the solution for a few minutes, diluting with distilled water, and allowing it to cool, it is precipitated with sulphuric acid, in excess; this precipitate (sulphate of lead) is washed, dried, slightly ignited in a porcelain crucible, and weighed. The weight in grains, multiplied by 7369, gives the per-centage of oxide of lead or litharge.

_d._ The filtered liquid from _c_ is evaporated to dryness, and redissolved in water acidulated with hydrochloric acid, and treated with a solution of ammonium chloride, and afterwards with ammonia, in excess; the precipitate (alumina and oxide of iron) is collected, washed, and boiled in a solution of pota.s.sium hydrate; the undissolved portion is collected on a filter, washed with boiling water, ignited, and weighed. This gives the per-centage of peroxide of iron.

_e._ The liquid filtered from the oxide of iron holds the alumina (if any) in solution; a solution of carbonate of ammonium is dropped in; the resulting precipitate is washed, dried, ignited, and weighed. This gives the per-centage of alumina.

_f._ The filtrate from the alumina and oxide of iron (see _d_), after being evaporated to dryness, is redissolved in a large quant.i.ty of distilled water, and is treated with a solution of oxalic acid (a solution of oxalate of ammonium is preferable when no baryta is present); the precipitate is washed, dried, gently ignited, and weighed. The weight of the resulting carbonate of calcium, in grains, multiplied by 56292, gives the per-centage of lime required.

_g._ The filtrate from _f_ is now mixed with carbonate of pota.s.sium, in considerable excess, and boiled for a long time; the resulting precipitate (if any) is then collected on a filter, slightly washed with hot water, dried, and exposed to a full red heat for some time (say 2 hours); the residuum of the calcination is then weighed. This furnishes the per-centage value of the sample in magnesia.

_h._ The filtrate from _f_ is treated with dilute sulphuric acid or the solution of a sulphate, as long as a precipitate falls; the precipitate (sulphate of barytum,) is washed, dried, gently ignited, and weighed. The weight, in grains, multiplied by 6589, gives the per-centage of baryta in the sample.

The above may be varied by gently concentrating the liquid filtered from the precipitate of alumina and oxide of iron (see _d_), and precipitating it with dilute sulphuric acid; the mixed precipitate is exhausted by digestion in water holding chloride of ammonium in solution; the undissolved residuum (sulphate of barytum,) is washed, dried, and otherwise treated as before; whilst the solution with the was.h.i.+ngs is treated with a solution of carbonate of ammonium; the precipitate is carbonate of calcium, which is to be washed, &c., as directed under _f_.

The liquor, &c., filtered from the lime, is lastly tested for magnesia.

(See _g_.)

_i._ A second 100 gr. of the powdered gla.s.s (see _a_) is mixed with 200 gr. of fluor spar, also in powder; the compound is placed in a platinum or leaden capsule, 500 gr. of strong sulphuric acid are added, and the whole cautiously stirred together with a silver stirrer or spoon, care being taken to avoid inhaling the fumes; the heat of a spirit lamp is next applied, and at first is kept at about 212 Fahr., but towards the conclusion of the process is raised to 300 Fahr., or even higher, and is continued for at least 2 hours, or until fumes entirely cease to be evolved; 5 or 6 fl. oz. of distilled water are next poured on the residuary ma.s.s, and, after thorough agitation, the whole is thrown on a filter, more water being at last poured on to wash out any remains of soluble matter; to the filtrate, carbonate of ammonium is added in excess, and after a time the earthy salts are removed by filtration; the filtered liquor is now evaporated to dryness, and ignited to dull redness for 2 or 3 minutes; the residuum (sulphate of pota.s.sium or sodium, or of both), after being weighed (the weight being carefully noted down), is redissolved in distilled water; a solution of chloride of barium is then added as long as it disturbs the liquor, and after a time the whole is again filtered; the filtrate is concentrated by evaporation, and solution of b.i.+.c.hloride of platinum added in excess; the whole is now gently evaporated to dryness, mixed with alcohol, collected on a filter, carefully washed with weak alcohol, dried at a temperature under 212 Fahr., and weighed. The weight, in grains, multiplied by 1940, gives the per-centage of pota.s.sa sought.

_k._ The weight of sulphate of pota.s.sium in the ignited residuum in _i_ is calculated from that of the pota.s.sium last found (47 parts of the one being equal to 87 parts of the other), and this weight is deducted from the gross weight of the ignited sulphates; the remainder represents the quant.i.ty of sulphate of sodium present. The weight of the latter, in grains, multiplied by 4367, gives the per-centage of pure soda required.

_Concluding Remarks._ One of the chief points to which the skilful gla.s.s manufacturer directs his attention, is the quality of the materials. Great care is exercised in the selection of the sand for all the finer varieties of gla.s.s. The usual practice is to test it before using it, by exposing it to a very high temperature. The purest sand is that which is the whitest and freest from iron, and which, consequently, suffers the least alteration by this treatment. The alkalies (potash, soda) employed are purified by solution and crystallisation. The red lead and litharge must be pure and absolutely free from oxide of copper (a common contamination), which gives a green tint to the gla.s.s. The former, which is the most costly, is preferable to the finest crystal. Care must also be taken that the lime, clay, &c., are respectively of proper purity; and that the 'cullet,' or broken gla.s.s, which is almost always remelted with the other materials, is of proper quality, and of the same kind as that to which it is added. Pota.s.sa produces a better gla.s.s than soda, although the latter is now very generally employed, from its lower price. It is, however, quite inadmissible as an ingredient in the manufacture of the better cla.s.s of crystal and plate gla.s.s, as, however pure it may be, it imparts to the product a slight greenish tinge more or less destructive of its beauty.

When sulphate of soda (Glauber salt) is used as a source of soda, it is gently calcined to dissipate its water of crystallisation, and requires the addition of about 8% of charcoal to effect its reduction in the melting-pot. Common salt is also employed as a source of soda in the same manner. Sometimes native sulphide of lead (galena) is used to decompose the sulphate of soda, and in lieu of part of the oxide of lead; in which case about 5 parts of the sulphuret are taken for every 9 parts of the calcined sulphate.

To antic.i.p.ate the results of his processes, and to carry out with certainty his various intentions, the gla.s.s manufacturer, perhaps more than any other person, requires the aid of science and experience. All his most essential operations depend on chemical principles. The products of his furnaces are not formed by the mere mechanical admixture of their several ingredients whilst in the state of fusion, but result from the play of delicate affinities which only act under certain conditions, and when the materials are presented to each other in uniform and definite proportions. Chemically speaking, the gla.s.ses are mixed super-silicates of the respective bases which enter into their composition (pota.s.sium, calcium, lead, &c.), and, like all other compounds which are formed by elective attraction, obey the common laws of combination, as developed by Dalton, and now so successfully applied in almost every department of industrial art. It has been shown by the most careful a.n.a.lysis, that in all the more valuable and beautiful commercial gla.s.ses the relative proportions of the materials are conformable to these laws, and that several of them are true atomic compounds, as perfect in this respect as the crystalline bodies commonly denominated salts. In some of the harder gla.s.ses of Bohemia the number of atoms or equivalents of silica are to each of the bases with which it is united, nearly as 5 to 1; whilst in a softer gla.s.s of German manufacture the proportions of the two are found to be as 4 to 1. The celebrated plate gla.s.s of St. Gobain is an atomic compound formed of 1 equivalent of trisilicate of soda united to 1 equivalent of trisilicate of lime, with a small per-centage of alumina in combination with silicic acid, also in atomic proportion. Gla.s.ses in which the ingredients bear no atomic ratio to each other are never h.o.m.ogeneous, but always more or less striated and of unequal colour and refractive power. The absence of atomic proportion between the substances entering into its composition appears to be the only reason why the best English plate and mirror gla.s.s is so greatly inferior to that of France and Germany, that comparison of the two becomes absurd. The only variety of gla.s.s in the production of which the English manufacturer excels is flint gla.s.s or crystal, and here he certainly surpa.s.ses all his numerous compet.i.tors. The subject is doubtless involved in difficulty, owing to the precise temperature necessary to effect the perfect combination of the bases with the silicic acid, varying with the character of the compound, and not being satisfactorily settled by observation or experience. The modifying influence of temperature is shown by the fact that the lower the heat employed in the process, the smaller the quant.i.ty of silica which enters into the composition of the resulting gla.s.s; whilst at higher temperatures a part of the base is dissipated in fumes, until such proportions of base and acid result as are required to produce a permanent atomic compound corresponding to the temperature employed. If the heat is excessive or improperly continued, the loss of base produces an opposite effect, and an opaque, semi-vitrified ma.s.s is formed, resembling 'Reaumur's porcelain.' The quality of the resulting gla.s.s depends on this change being more or less complete. If the furnace yields the right temperature, and the duration of the exposure to its action is neither too short nor too prolonged, nature makes up for the unskilful conduct of the operative, and removes the stumbling blocks which his ignorance had placed in the way of his own attempts at excellence. The proceedings and their results are accidental; but being once obtained, the first are repeated without further trouble or inquiry. This accounts for the same mixture of materials yielding products of different qualities at different times, and in different works, which the operative contents himself with referring to the 'going of the furnace.' The common plan in this country is to regulate the proportions and firing by experience only, rather than by theory and practice combined. Now, although the chemist has much yet to learn on the precise const.i.tution of the gla.s.ses, and although theory may not be able to ensure unvarying success, it is nevertheless certain that, in all cases, it can afford much valuable a.s.sistance in that direction. Indeed, it has been a.s.serted by one of the leading Continental chemists, that ingredients that will yield the proper equivalent proportions in the melting pot cannot produce a bad gla.s.s, if exposed to such a temperature as to permit of perfect combination taking place.

It is found that those gla.s.ses which contain a predominance of alkali are acted on by water, and when this is in great excess they are perfectly soluble in that fluid. Ordinary flint gla.s.s is affected by long coction in water, whilst crown gla.s.s, which contains less alkali, is unaltered by that trial. Gla.s.s which contains any considerable quant.i.ty of lead is acted on by sulphuretted hydrogen. This is the cause of the surface of flint gla.s.s, under certain circ.u.mstances, becoming opaque and iridescent.

Gla.s.ses made of silica and alkali alone are incapable of permanently resisting the action of water. The addition of lime or oxide of lead appears to be necessary to give them this quality. Gla.s.ses that have a slight greenish or bluish tint may be often whitened, or rendered colourless, by exposure to light and air. This arises from the peroxidation of the iron, to whose protoxide they owe their tint. Other gla.s.ses become purpled by exposure, owing to the peroxidation of the manganese.

Different colours are communicated to gla.s.s by the addition of metallic oxides. Thus, oxide of manganese gives an amethyst; oxide of cobalt, a blue; oxide of iron, a brown; black oxide of copper, a green; oxide of gold, a purple; suboxide of copper, a ruby-red; oxide of tin, a white; oxide of silver, a yellow, &c. These substances are either added to the melted contents of the gla.s.s-pot, as in preparing artificial gems, &c., or they are applied in a thin layer to the surface of the object, which is then heated until fusion of the coloured compound occurs, as in enamelling and painting on gla.s.s.

Gla.s.s is FORMED or FAs.h.i.+ONED into articles by the processes of blowing, casting, drawing, rolling, or spreading. In the process of BLOWING GLa.s.s the workman begins by collecting a proper quant.i.ty of gla.s.s in a soft, pasty state, at the end of his blow-pipe (an iron tube, five or six feet in length, terminated by a mouth-piece of wood), which he then commences blowing through, by which the lump is expanded into a kind of flask, susceptible of having its form modified by the position in which it is held, and the velocity of rotation continually given to the iron tube. If an open-mouthed vessel is to be made, an iron rod, called a 'pontil' or 'puntil,' is dipped into the gla.s.s-pot and applied to the bottom of the flask, to which it thus serves as a handle, the blow-pipe being removed by the application of a cold iron to the neck. The vessel is now re-heated, and the aperture enlarged, and the vessel otherwise altered in figure by the aid of a few simple tools until completed. It is then detached, and carried to the 'annealing oven,' where it undergoes slow and gradual cooling during many hours. In this way bottles, flasks, carboys, and an almost infinite variety of other articles, are formed. The large circular tables of CROWN-GLa.s.s are made by a joint process of BLOWING and SPREADING. The globular flask at first produced, transferred from the blow-pipe to the 'pontil,' is suddenly made to a.s.sume the form of a flat disc by the centrifugal force of the rapid rotatory movement given to the rod. SPREAD or BROAD GLa.s.s is formed into sheets in a nearly similar manner. PLATE-GLa.s.s is cast upon a flat metal table, and, after very careful annealing, is ground and polished by suitable machinery. TUBES are made by rapidly drawing out a hollow cylinder; and from these a great variety of useful small apparatus are constructed with the help of a lamp and blowpipe, or, still better, the bellows-table of the barometer-maker.

GLa.s.s BEADS are made from small tubes chopped into pieces of suitable lengths, which are stirred first in a mixture of sand and wood-ashes, in the cold, and afterwards in an iron pan over the fire until they a.s.sume a rounded form. SMALL TUBES are bent in the flame of a spirit lamp or gas-jet, and cut by a file, a scratch being made, and the two portions pulled or broken asunder in a way easily learned by a few trials. LARGE TUBES require the heat of a powerful blowpipe and lamp, or that of a furnace.

The following hints respecting the MANAGEMENT OF GLa.s.s may prove useful to the inexperienced:--

ANNEALING. The process of annealing gla.s.s has been briefly referred to before. The extreme brittleness of imperfectly annealed wrought gla.s.s may generally be remedied on the small scale by immersing the articles in a bath of oil, or a concentrated solution of chloride of calcium, or common salt, and heating the whole gradually and cautiously to the boiling-point, and letting it again cool--the slower the better. By this treatment the gla.s.s will be enabled to bear any alterations of temperature between the two extremes to which it has been exposed.

BLOWING. By the ingenious art of GLa.s.s-BLOWING and GLa.s.s-DRAWING, as practised on the small scale, with a blowpipe lamp furnace, a variety of articles of ornament and utility may be made, their number being limited only by the ingenuity of the artist. The details of the various operations are, however, too lengthy to describe here.

CLEANING. 1. Windows, looking-gla.s.ses, &c., may be quickly cleaned as follows:--Dip a slightly moistened rag or flannel into whiting, fuller's earth, wood-ashes, or rotten-stone, in impalpable powder, with which smear the gla.s.s, and wipe it off with a dry, soft cloth. This does well when the surface is very dirty. In other cases, a little thumb blue, whiting, or chalk, in fine powder, tied up in muslin, may be dusted on the gla.s.s, which should then be cleaned off with chamois leather. This gives a fine polish.

2. The vessel to be cleansed, is filled, or, if large, rinsed, with a moderately dilute solution of permanganate of potash, contact being prolonged till a film of hydrated manganic oxide has been deposited; the solution is then poured away, and the gla.s.s vessel rinsed with some strong hydrochloric acid.

CUTTING. Gla.s.s may be easily cut with a common well-hardened steel file, provided it be moistened with oil of turpentine, or plunged under water.

It may be also perforated with a common steel brad-awl in the same way.

GLa.s.s VESSELS, as bottles and tubes, may be readily cut or shortened by placing a heated iron ring over the spot, or a piece of loose string or cotton dipped in oil of turpentine and set on fire, and immediately on the withdrawal of either applying cold water to the part. Gla.s.s vessels or tubes thus treated will generally crack round, and may be readily divided into two parts. In this manner a common Florence oil-flask may be converted into an evaporating dish and a funnel. By a little practice a crack may be led in almost any direction, or a new one made, by the point of a red-hot poker or a spring coal (an ignited crayon of prepared charcoal). The parts may then be separated by a little force or a smart rap, and the divided edges smoothed by the flame of a blowpipe, or by grinding them with powdered emery and water on a flat stone. In this way many broken articles in gla.s.s may be converted into others scarcely less useful.

ETCHING ON GLa.s.s has been already noticed under the head of Etching.

GILDING OF GLa.s.s. Gold chloride is dissolved in boiling water; the solution is filtered, and the filtrate so far diluted, that 200 cubic centimetres contain 00648 gram of the metal, and it is then made alkaline with soda. The reducing agent is alcohol saturated with marsh gas; this is diluted with its own volume of water. 25 cubic centimetres of this solution are mixed with the alkaline gold chloride solution, and this mixture is poured between the perfectly well-cleaned plate to be gilded, and another sheet of gla.s.s placed at a distance of 3 mm. under the first.

After two to three hours' rest the gilding is effected. The plate is removed and washed. ('Dingler's Journal.')

GRINDING. This, on the large scale, like gla.s.s-cutting, forms a distinct occupation. On the small scale, gla.s.s may be roughed or ground by friction with powdered emery and water and a flat rubber of wood; care being taken that the article, if a plate, is laid on a perfectly flat surface, or, if hollow, is supported by a core of cement or plaster. The frosted appearance of ground gla.s.s is given to the panes of windows by gently dabbing the gla.s.s over with a piece of glazier's putty, stuck on the ends of the fingers. When applied with a light and even touch, the resemblance is considerable. Another method is to dab the gla.s.s over with thin white paint, or flour paste, by means of a brush, but the effect is much inferior to the above.

GLa.s.s, PACKING. This subject will be considered under the general head of PACKING.

WRITING ON GLa.s.s may be performed by a piece of French chalk or crayons prepared for the purpose; or even with a common pen held nearly perpendicular. Indian ink, or, when the article will be exposed to damp, sh.e.l.l-lac ink or varnish, thickened with a little Vermillion, or lampblack, is best adapted to this purpose. Common ink is not sufficiently opaque.

GLa.s.s, TO PREVENT THE CRACKING OF, BY BOILING WATER. When new, all gla.s.s and earthenware should be placed in cold water in a saucepan, and after some hours the saucepan containing the vessel or vessels, should be placed over the fire, until the water reaches the boiling point.

=Gla.s.s.= This term was applied by the older chemists to various substances to which a vitreous appearance has been given by heat. Thus we have 'GLa.s.s OF ANTIMONY,' 'GLa.s.s OF BORAX,' &c. It is now obsolete.

=Gla.s.s, Iridescent.= The inventor of the process by which this beautiful variety of gla.s.s is made is M Clemandot.

The 'Chemical News' states that the principle observed in its manufacture consists in submitting the gla.s.s articles to the action of dilute hydrochloric, sulphuric, or other acid, under a pressure of from two to six atmospheres. M Clemandot claims to be able to imitate the nacreous films which are seen on ancient gla.s.s which has been exposed to combined atmospheric influences for thousands of years.

=Gla.s.s, Pow'dered.= _Syn._ VITRUM PULVERISATUM, L. _Prep._ Heat the gla.s.s red hot, throw it into cold water, dry, and powder it. Used to filter acids, and glued upon paper as a polis.h.i.+ng powder; also to wear down corns upon the feet, after the feet have been well soaked, and dried.

=Gla.s.s, Sol'uble.= _Syn._ WATER GLa.s.s; VITRUM SOLUBILE, L. An impure alkaline silicate. _Prep._ Silica, 1 part; carbonate of pota.s.sium or of sodium, 2 parts; fused together.

Carbonate of sodium (dry), 54 parts; carbonate of pota.s.sium (dry), 70 parts; silica, 192 parts; as last. Soluble in boiling water, yielding a fine, transparent, semi-elastic varnish.

Carbonate of pota.s.sium (dry), 10 parts; powdered quartz (or sand free from iron and alumina), 15 parts; charcoal 1 part; fused together. Soluble in 5 or 6 times its weight of boiling water; and the filtered solution, evaporated to dryness, yields a transparent gla.s.s, permanent in the air.