Chapter 15

1.Extraction of Gold by Washing.—In the early days of gold-washing in California and Australia, when rich alluvial deposits were common at the surface, the most simple appliances sufficed. The most characteristic is the “pan,” a circular dish of sheet-iron or “tin,” with sloping sides about 13 or 14 in. in diameter. The pan, about two-thirds filled with the “pay dirt” to be washed, is held in the stream or in a hole filled with water. The larger stones having been removed by hand, gyratory motion is given to the pan by a combination of shaking and twisting movementsso as to keep its contents suspended in the stream of water, which carries away the bulk of the lighter material, leaving the heavy minerals, together with any gold which may have been present. The washing is repeated until enough of the enriched sand is collected, when the gold is finally recovered by careful washing or “panning out” in a smaller pan. In Mexico and South America, instead of the pan, a wooden dish or trough, known as “batea,” is used.The “cradle” is a simple appliance for treating somewhat larger quantities, and consists essentially of a box, mounted on rockers, and provided with a perforated bottom of sheet iron in which the “pay dirt” is placed. Water is poured on the dirt, and the rocking motion imparted to the cradle causes the finer particles to pass through the perforated bottom on to a canvas screen, and thence to the base of the cradle, where the auriferous particles accumulate on transverse bars of wood, called “riffles.”The “tom” is a sort of cradle with an extended sluice placed on an incline of about 1 in 12. The upper end contains a perforated riddle plate which is placed directly over the riffle box, and under certain circumstances mercury may be placed behind the riffles. Copper plates amalgamated with mercury are also used when the gold is very fine, and in some instances amalgamated silver coins have been used for the same purpose. Sometimes the stuff is disintegrated with water in a “puddling machine,” which was used, especially in Australia, when the earthy matters are tenacious and water scarce. The machine frequently resembles a brickmaker’s wash-mill, and is worked by horse or steam power.In workings on a larger scale, where the supply of water is abundant, as in California, sluices were generally employed. They are shallow troughs about 12 ft. long, about 16 to 20 in. wide and 1 ft. in depth. The troughs taper slightly so that they can be joined in series, the total length often reaching several hundred feet. The incline of the sluice varies with the conformation of the ground and the tenacity of the stuff to be washed, from 1 in 16 to 1 in 8. A rectangular trough of boards, whose dimensions depend chiefly on the size of the planks available, is set up on the higher part of the ground at one side of the claim to be worked, upon trestles or piers of rough stone-work, at such an inclination that the stream may carry off all but the largest stones, which are kept back by a grating of boards about 2 in. apart. The gravel is dug by hand and thrown in at the upper end, the stones kept back being removed at intervals by two men with four-pronged steel forks. The floor of the sluice is laid with riffles made of strips of wood 2 in. square laid parallel to the direction of the current, and at other points with boards having transverse notches filled with mercury. These were known originally as Hungarian riffles.In larger plant the upper ends of the sluices are often cut in rock or lined with stone blocks, the grating stopping the larger stones being known as a “grizzly.” In order to save very fine and especially rusty particles of gold, so-called “under-current sluices” are used; these are shallow wooden tanks, 50 sq. yds. and upwards in area, which are placed somewhat below the main sluice, and communicate with it above and below, the entry being protected by a grating so that only the finer material is admitted. These are paved with stone blocks or lined with mercury riffles, so that from the greatly reduced velocity of flow, due to the sudden increase of surface, the finer particles of gold may collect. In order to save finely divided gold, amalgamated copper plates are sometimes placed in a nearly level position, at a considerable distance from the head of the sluice, the gold which is retained in it being removed from time to time. Sluices are often made double, and they are usually cleaned up—that is, the deposit rich in gold is removed from them—once a week.The “pan” is now only used by prospectors, while the “cradle” and “tom” are practically confined to the Chinese; the sluice is considered to be the best contrivance for washing gold gravels.

1.Extraction of Gold by Washing.—In the early days of gold-washing in California and Australia, when rich alluvial deposits were common at the surface, the most simple appliances sufficed. The most characteristic is the “pan,” a circular dish of sheet-iron or “tin,” with sloping sides about 13 or 14 in. in diameter. The pan, about two-thirds filled with the “pay dirt” to be washed, is held in the stream or in a hole filled with water. The larger stones having been removed by hand, gyratory motion is given to the pan by a combination of shaking and twisting movementsso as to keep its contents suspended in the stream of water, which carries away the bulk of the lighter material, leaving the heavy minerals, together with any gold which may have been present. The washing is repeated until enough of the enriched sand is collected, when the gold is finally recovered by careful washing or “panning out” in a smaller pan. In Mexico and South America, instead of the pan, a wooden dish or trough, known as “batea,” is used.

The “cradle” is a simple appliance for treating somewhat larger quantities, and consists essentially of a box, mounted on rockers, and provided with a perforated bottom of sheet iron in which the “pay dirt” is placed. Water is poured on the dirt, and the rocking motion imparted to the cradle causes the finer particles to pass through the perforated bottom on to a canvas screen, and thence to the base of the cradle, where the auriferous particles accumulate on transverse bars of wood, called “riffles.”

The “tom” is a sort of cradle with an extended sluice placed on an incline of about 1 in 12. The upper end contains a perforated riddle plate which is placed directly over the riffle box, and under certain circumstances mercury may be placed behind the riffles. Copper plates amalgamated with mercury are also used when the gold is very fine, and in some instances amalgamated silver coins have been used for the same purpose. Sometimes the stuff is disintegrated with water in a “puddling machine,” which was used, especially in Australia, when the earthy matters are tenacious and water scarce. The machine frequently resembles a brickmaker’s wash-mill, and is worked by horse or steam power.

In workings on a larger scale, where the supply of water is abundant, as in California, sluices were generally employed. They are shallow troughs about 12 ft. long, about 16 to 20 in. wide and 1 ft. in depth. The troughs taper slightly so that they can be joined in series, the total length often reaching several hundred feet. The incline of the sluice varies with the conformation of the ground and the tenacity of the stuff to be washed, from 1 in 16 to 1 in 8. A rectangular trough of boards, whose dimensions depend chiefly on the size of the planks available, is set up on the higher part of the ground at one side of the claim to be worked, upon trestles or piers of rough stone-work, at such an inclination that the stream may carry off all but the largest stones, which are kept back by a grating of boards about 2 in. apart. The gravel is dug by hand and thrown in at the upper end, the stones kept back being removed at intervals by two men with four-pronged steel forks. The floor of the sluice is laid with riffles made of strips of wood 2 in. square laid parallel to the direction of the current, and at other points with boards having transverse notches filled with mercury. These were known originally as Hungarian riffles.

In larger plant the upper ends of the sluices are often cut in rock or lined with stone blocks, the grating stopping the larger stones being known as a “grizzly.” In order to save very fine and especially rusty particles of gold, so-called “under-current sluices” are used; these are shallow wooden tanks, 50 sq. yds. and upwards in area, which are placed somewhat below the main sluice, and communicate with it above and below, the entry being protected by a grating so that only the finer material is admitted. These are paved with stone blocks or lined with mercury riffles, so that from the greatly reduced velocity of flow, due to the sudden increase of surface, the finer particles of gold may collect. In order to save finely divided gold, amalgamated copper plates are sometimes placed in a nearly level position, at a considerable distance from the head of the sluice, the gold which is retained in it being removed from time to time. Sluices are often made double, and they are usually cleaned up—that is, the deposit rich in gold is removed from them—once a week.

The “pan” is now only used by prospectors, while the “cradle” and “tom” are practically confined to the Chinese; the sluice is considered to be the best contrivance for washing gold gravels.

2.The Amalgamation Process.—This method is employed to extract gold from both alluvial and reef deposits: in the first case it is combined with “hydraulic mining,”i.e.disintegrating auriferous gravels by powerful jets of water, and the sluice system described above; in the second case the vein stuff is prepared by crushing and the amalgamation is carried out in mills.

Hydraulic mining has for the most part been confined to the country of its invention, California, and the western territories of America, where the conditions favourable for its use are more fully developed than elsewhere—notably the presence of thick banks of gravel that cannot be utilized by other methods, and abundance of water, even though considerable work may be required at times to make it available. The general conditions to be observed in such workings may be briefly stated as follows: (1) The whole of the auriferous gravel, down to the “bed rock,” must be removed,—that is, no selection of rich or poor parts is possible; (2) this must be accomplished by the aid of water alone, or at times by water supplemented by blasting; (3) the conglomerate must be mechanically disintegrated without interrupting the whole system; (4) the gold must be saved without interrupting the continuous flow of water; and (5) arrangements must be made for disposing of the vast masses of impoverished gravel.The water is brought from a ditch on the high ground, and through a line of pipes to the distributing box, whence the branch pipes supplying the jets diverge. The stream issues through a nozzle, termed a “monitor” or “giant,” which is fitted with a ball and socket joint, so that the direction of the jet may be varied through considerable angles by simply moving a handle. The material of the bank being loosened by blasting and the cutting action of the water, crumbles into holes, and the superincumbent mass, often with large trees and stones, falls into the lower ground. The stream, laden with stones and gravel, passes into the sluices, where the gold is recovered in the manner already described. Under the most advantageous conditions the loss of gold may be estimated at 15 or 20%, the amount recovered representing a value of about two shillings per ton of gravel treated. The loss of mercury is about the same, from 5 to 6 cwt. being in constant use per mile of sluice.In working auriferous river-beds, dredges have been used with considerable success in certain parts of New Zealand and on the Pacific slope in America. The dredges used in California are almost exclusively of the endless-chain bucket or steam-shovel pattern. Some dredges have a capacity under favourable conditions of over 2000 cub. yds. of gravel daily. The gravel is excavated as in the ordinary form of endless-chain bucket dredge and dumped on to the deck of the dredge. It then passes through screens and grizzlies to retain the coarse gravel, the finer material passing on to sluice boxes provided with riffles, supplied with mercury. There are belt conveyers for discharging the gravel and tailings at the end of the vessel remote from the buckets. The water necessary to the process is pumped from the river; as much as 2000 gallons per minute is used on the larger dredges.The dressing or mechanical preparation of vein stuff containing gold is generally similar to that of other ores (seeOre-dressing), except that the precious metal should be removed from the waste substances as quickly as possible, even although other minerals of value that are subsequently recovered may be present. In all cases the quartz or other vein stuff must be reduced to a very fine powder as a preliminary to further operations. This may be done in several ways,e.g.either (1) by the Mexican crusher orarrastra, in which the grinding is effected upon a bed of stone, over which heavy blocks of stone attached to cross arms are dragged by the rotation of the arms about a central spindle, or (2) by the Chilean mill ortrapiche, also known as the edge-runner, where the grinding stones roll upon the floor, at the same time turning about a central upright—contrivances which are mainly used for the preparation of silver ores; but by far the largest proportion of the gold quartz of California, Australia and Africa is reduced by (3) the stamp mill, which is similar in principle to that used in Europe for the preparation of tin and other ores.The stamp mill was first used in California, and its use has since spread over the whole world. In the mills of the Californian type the stamp is a cylindrical iron pestle faced with a chilled cast iron shoe, removable so that it can be renewed when necessary, attached to a round iron rod or lifter, the whole weighing from 600 to 900 ℔; stamps weighing 1320 ℔ are in use in the Transvaal. The lift is effected by cams acting on the under surface of tappets, and formed by cylindrical boxes keyed on to the stems of the lifter about one-fourth of their length from the top. As, however, the cams, unlike those of European stamp mills, are placed to one side of the stamp, the latter is not only lifted but turned partly round on its own axis, whereby the shoes are worn down uniformly. The height of lift may be between 4 and 18 in., and the number of blows from 30 to over 100 per minute. The stamps are usually arranged in batteries of five; the order of working is usually 1, 4, 2, 5, 3, but other arrangements,e.g.1, 3, 5, 2, 4, and 1, 5, 2, 4, 3, are common. The stuff, previously broken to about 2-in. lumps in a rock-breaker, is fed in through an aperture at the back of the “battery box,” a constant supply of water is admitted from above, and mercury in a finely divided state is added at frequent intervals. The discharge of the comminuted material takes place through an aperture, which is covered by a thin steel plate perforated with numerous slits about1⁄50th in. broad and ½ in. long, a certain volume being discharged at every blow and carried forward by the flushing water over an apron or table in front, covered by copper plates filled with mercury. Similar plates are often used to catch any particles of gold that may be thrown back, while the main operation is so conducted that the bulk of the gold may be reduced to the state of amalgam by bringing the two metals into intimate contact under the stamp head, and remain in the battery. The tables in front are laid at an incline of about 8° and are about 13 ft. long; they collect from 10 to 15% of the whole gold; a further quantity is recovered by leading the sands through a gutter about 16 in. broad and 120 ft. long, also lined with amalgamated copper plates, after the pyritic and other heavy minerals have been separated by depositing in catch pits and other similar contrivances.When the ore does not contain any considerable amount of free gold mercury is not, as a rule, used during the crushing, but the amalgamation is carried out in a separate plant. Contrivances of the most diverse constructions have been employed. The most primitive is the rubbing together of the concentrated crushings with mercury in iron mortars. Barrel amalgamation,i.e.mixing the crushings with mercury in rotating barrels, is rarely used, the process being wasteful, since the mercury is specially apt to be “floured” (see below).At Schemnitz, Kerpenyes, Kreuzberg and other localities in Hungary, quartz vein stuff containing a little gold, partly free and partly associated with pyrites and galena, is, after stamping in mills, similar to those described above, but without rotating stamps, passed through the so-called “Hungarian gold mill” or “quick-mill.” This consists of a cast-iron pan having a shallow cylindrical bottom holding mercury, in which a wooden muller, nearly of the same shape as the inside of the pan, and armed below with several projecting blades, is made to revolve by gearing wheels. The stuff from the stamps is conveyed to the middle of the muller, and is distributed over the mercury, when the gold subsides, while the quartz and lighter materials are guided by the blades to the circumference and are discharged, usually into a second similar mill, and subsequently pass over blanket tables,i.e.boards covered with canvas or sacking, the gold and heavier particles becoming entangled in the fibres. The action of this mill is really more nearly analogous to that of a centrifugal pump, as no grinding action takes place in it. The amalgam is cleaned out periodically—fortnightly or monthly—and after filtering through linen bags to remove the excess of mercury, it is transferred to retorts for distillation (see below).Many other forms of pan-amalgamators have been devised. The Laszlo is an improved Hungarian mill, while the Piccard is of the same type. In the Knox and Boss mills, which are also employed for the amalgamation of silver ores, the grinding is effected between flat horizontal surfaces instead of conical or curved surfaces as in the previously described forms.One of the greatest difficulties in the treatment of gold by amalgamation, and more particularly in the treatment of pyrites, arises from the so-called “sickening” or “flouring” of the mercury; that is, the particles, losing their bright metallic surfaces, are no longer capable of coalescing with or taking up other metals. Of the numerous remedies proposed the most efficacious is perhaps sodium amalgam. It appears that amalgamation is often impeded by the tarnish found on the surface of the gold when it is associated with sulphur, arsenic, bismuth, antimony or tellurium. Henry Wurtz in America (1864) and Sir William Crookes in England (1865) made independently the discovery that, by the addition of a small quantity of sodium to the mercury, the operation is much facilitated. It is also stated that sodium prevents both the “sickening” and the “flouring” of the mercury which is produced by certain associated minerals. The addition of potassium cyanide has been suggested to assist the amalgamation and to prevent “flouring,” but Skey has shown that its use is attended with loss of gold.Separation of Gold from the Amalgam.—The amalgam is first pressed in wetted canvas or buckskin in order to remove excess of mercury. Lumps of the solid amalgam, about 2 in. in diameter, are introduced into an iron vessel provided with an iron tube that leads into a condenser containing water. The distillation is then effected by heating to dull redness. The amalgam yields about 30 to 40% of gold. Horizontal cylindrical retorts, holding from 200 to 1200 ℔ of amalgam, are used in the larger Californian mills, pot retorts being used in the smaller mills. The bullion left in the retorts is then melted in black-lead crucibles, with the addition of small quantities of suitable fluxes,e.g.nitre, sodium carbonate, &c.The extraction of gold from auriferous minerals by fusion, except as an incident in their treatment for other metals, is very rarely practised. It was at one time proposed to treat the concentrated black iron obtained in the Ural gold washings, which consists chiefly of magnetite, as an iron ore, by smelting it with charcoal for auriferous pig-iron, the latter metal possessing the property of dissolving gold in considerable quantity. By subsequent treatment with sulphuric acid the gold could be recovered. Experiments on this point were made by Anossow in 1835, but they have never been followed in practice.Gold in galena or other lead ores is invariably recovered in the refining or treatment of the lead and silver obtained. Pyritic ores containing copper are treated by methods analogous to those of the copper smelter. In Colorado the pyritic ores containing gold and silver in association with copper are smelted in reverberatory furnaces for regulus, which, when desilverized by Ziervogel’s method, leaves a residue containing 20 or 30 oz. of gold per ton. This is smelted with rich gold ores, notably those containing tellurium, for white metal or regulus; and by a following process of partial reduction analogous to that of selecting in copper smelting, “bottoms” of impure copper are obtained in which practically all the gold is concentrated. By continuing the treatment of these in the ordinary way of refining, poling and granulating, all the foreign matters other than gold, copper and silver are removed, and, by exposing the granulated metal to a high oxidizing heat for a considerable time the copper may be completely oxidized while the precious metals are unaltered. Subsequent treatment with sulphuric acid renders the copper soluble in water as sulphate, and the final residue contains only gold and silver, which is parted or refined in the ordinary way. This method of separating gold from copper, by converting the latter into oxide and sulphate, is also used at Oker in the Harz.

Hydraulic mining has for the most part been confined to the country of its invention, California, and the western territories of America, where the conditions favourable for its use are more fully developed than elsewhere—notably the presence of thick banks of gravel that cannot be utilized by other methods, and abundance of water, even though considerable work may be required at times to make it available. The general conditions to be observed in such workings may be briefly stated as follows: (1) The whole of the auriferous gravel, down to the “bed rock,” must be removed,—that is, no selection of rich or poor parts is possible; (2) this must be accomplished by the aid of water alone, or at times by water supplemented by blasting; (3) the conglomerate must be mechanically disintegrated without interrupting the whole system; (4) the gold must be saved without interrupting the continuous flow of water; and (5) arrangements must be made for disposing of the vast masses of impoverished gravel.

The water is brought from a ditch on the high ground, and through a line of pipes to the distributing box, whence the branch pipes supplying the jets diverge. The stream issues through a nozzle, termed a “monitor” or “giant,” which is fitted with a ball and socket joint, so that the direction of the jet may be varied through considerable angles by simply moving a handle. The material of the bank being loosened by blasting and the cutting action of the water, crumbles into holes, and the superincumbent mass, often with large trees and stones, falls into the lower ground. The stream, laden with stones and gravel, passes into the sluices, where the gold is recovered in the manner already described. Under the most advantageous conditions the loss of gold may be estimated at 15 or 20%, the amount recovered representing a value of about two shillings per ton of gravel treated. The loss of mercury is about the same, from 5 to 6 cwt. being in constant use per mile of sluice.

In working auriferous river-beds, dredges have been used with considerable success in certain parts of New Zealand and on the Pacific slope in America. The dredges used in California are almost exclusively of the endless-chain bucket or steam-shovel pattern. Some dredges have a capacity under favourable conditions of over 2000 cub. yds. of gravel daily. The gravel is excavated as in the ordinary form of endless-chain bucket dredge and dumped on to the deck of the dredge. It then passes through screens and grizzlies to retain the coarse gravel, the finer material passing on to sluice boxes provided with riffles, supplied with mercury. There are belt conveyers for discharging the gravel and tailings at the end of the vessel remote from the buckets. The water necessary to the process is pumped from the river; as much as 2000 gallons per minute is used on the larger dredges.

The dressing or mechanical preparation of vein stuff containing gold is generally similar to that of other ores (seeOre-dressing), except that the precious metal should be removed from the waste substances as quickly as possible, even although other minerals of value that are subsequently recovered may be present. In all cases the quartz or other vein stuff must be reduced to a very fine powder as a preliminary to further operations. This may be done in several ways,e.g.either (1) by the Mexican crusher orarrastra, in which the grinding is effected upon a bed of stone, over which heavy blocks of stone attached to cross arms are dragged by the rotation of the arms about a central spindle, or (2) by the Chilean mill ortrapiche, also known as the edge-runner, where the grinding stones roll upon the floor, at the same time turning about a central upright—contrivances which are mainly used for the preparation of silver ores; but by far the largest proportion of the gold quartz of California, Australia and Africa is reduced by (3) the stamp mill, which is similar in principle to that used in Europe for the preparation of tin and other ores.

The stamp mill was first used in California, and its use has since spread over the whole world. In the mills of the Californian type the stamp is a cylindrical iron pestle faced with a chilled cast iron shoe, removable so that it can be renewed when necessary, attached to a round iron rod or lifter, the whole weighing from 600 to 900 ℔; stamps weighing 1320 ℔ are in use in the Transvaal. The lift is effected by cams acting on the under surface of tappets, and formed by cylindrical boxes keyed on to the stems of the lifter about one-fourth of their length from the top. As, however, the cams, unlike those of European stamp mills, are placed to one side of the stamp, the latter is not only lifted but turned partly round on its own axis, whereby the shoes are worn down uniformly. The height of lift may be between 4 and 18 in., and the number of blows from 30 to over 100 per minute. The stamps are usually arranged in batteries of five; the order of working is usually 1, 4, 2, 5, 3, but other arrangements,e.g.1, 3, 5, 2, 4, and 1, 5, 2, 4, 3, are common. The stuff, previously broken to about 2-in. lumps in a rock-breaker, is fed in through an aperture at the back of the “battery box,” a constant supply of water is admitted from above, and mercury in a finely divided state is added at frequent intervals. The discharge of the comminuted material takes place through an aperture, which is covered by a thin steel plate perforated with numerous slits about1⁄50th in. broad and ½ in. long, a certain volume being discharged at every blow and carried forward by the flushing water over an apron or table in front, covered by copper plates filled with mercury. Similar plates are often used to catch any particles of gold that may be thrown back, while the main operation is so conducted that the bulk of the gold may be reduced to the state of amalgam by bringing the two metals into intimate contact under the stamp head, and remain in the battery. The tables in front are laid at an incline of about 8° and are about 13 ft. long; they collect from 10 to 15% of the whole gold; a further quantity is recovered by leading the sands through a gutter about 16 in. broad and 120 ft. long, also lined with amalgamated copper plates, after the pyritic and other heavy minerals have been separated by depositing in catch pits and other similar contrivances.

When the ore does not contain any considerable amount of free gold mercury is not, as a rule, used during the crushing, but the amalgamation is carried out in a separate plant. Contrivances of the most diverse constructions have been employed. The most primitive is the rubbing together of the concentrated crushings with mercury in iron mortars. Barrel amalgamation,i.e.mixing the crushings with mercury in rotating barrels, is rarely used, the process being wasteful, since the mercury is specially apt to be “floured” (see below).

At Schemnitz, Kerpenyes, Kreuzberg and other localities in Hungary, quartz vein stuff containing a little gold, partly free and partly associated with pyrites and galena, is, after stamping in mills, similar to those described above, but without rotating stamps, passed through the so-called “Hungarian gold mill” or “quick-mill.” This consists of a cast-iron pan having a shallow cylindrical bottom holding mercury, in which a wooden muller, nearly of the same shape as the inside of the pan, and armed below with several projecting blades, is made to revolve by gearing wheels. The stuff from the stamps is conveyed to the middle of the muller, and is distributed over the mercury, when the gold subsides, while the quartz and lighter materials are guided by the blades to the circumference and are discharged, usually into a second similar mill, and subsequently pass over blanket tables,i.e.boards covered with canvas or sacking, the gold and heavier particles becoming entangled in the fibres. The action of this mill is really more nearly analogous to that of a centrifugal pump, as no grinding action takes place in it. The amalgam is cleaned out periodically—fortnightly or monthly—and after filtering through linen bags to remove the excess of mercury, it is transferred to retorts for distillation (see below).

Many other forms of pan-amalgamators have been devised. The Laszlo is an improved Hungarian mill, while the Piccard is of the same type. In the Knox and Boss mills, which are also employed for the amalgamation of silver ores, the grinding is effected between flat horizontal surfaces instead of conical or curved surfaces as in the previously described forms.

One of the greatest difficulties in the treatment of gold by amalgamation, and more particularly in the treatment of pyrites, arises from the so-called “sickening” or “flouring” of the mercury; that is, the particles, losing their bright metallic surfaces, are no longer capable of coalescing with or taking up other metals. Of the numerous remedies proposed the most efficacious is perhaps sodium amalgam. It appears that amalgamation is often impeded by the tarnish found on the surface of the gold when it is associated with sulphur, arsenic, bismuth, antimony or tellurium. Henry Wurtz in America (1864) and Sir William Crookes in England (1865) made independently the discovery that, by the addition of a small quantity of sodium to the mercury, the operation is much facilitated. It is also stated that sodium prevents both the “sickening” and the “flouring” of the mercury which is produced by certain associated minerals. The addition of potassium cyanide has been suggested to assist the amalgamation and to prevent “flouring,” but Skey has shown that its use is attended with loss of gold.

Separation of Gold from the Amalgam.—The amalgam is first pressed in wetted canvas or buckskin in order to remove excess of mercury. Lumps of the solid amalgam, about 2 in. in diameter, are introduced into an iron vessel provided with an iron tube that leads into a condenser containing water. The distillation is then effected by heating to dull redness. The amalgam yields about 30 to 40% of gold. Horizontal cylindrical retorts, holding from 200 to 1200 ℔ of amalgam, are used in the larger Californian mills, pot retorts being used in the smaller mills. The bullion left in the retorts is then melted in black-lead crucibles, with the addition of small quantities of suitable fluxes,e.g.nitre, sodium carbonate, &c.

The extraction of gold from auriferous minerals by fusion, except as an incident in their treatment for other metals, is very rarely practised. It was at one time proposed to treat the concentrated black iron obtained in the Ural gold washings, which consists chiefly of magnetite, as an iron ore, by smelting it with charcoal for auriferous pig-iron, the latter metal possessing the property of dissolving gold in considerable quantity. By subsequent treatment with sulphuric acid the gold could be recovered. Experiments on this point were made by Anossow in 1835, but they have never been followed in practice.

Gold in galena or other lead ores is invariably recovered in the refining or treatment of the lead and silver obtained. Pyritic ores containing copper are treated by methods analogous to those of the copper smelter. In Colorado the pyritic ores containing gold and silver in association with copper are smelted in reverberatory furnaces for regulus, which, when desilverized by Ziervogel’s method, leaves a residue containing 20 or 30 oz. of gold per ton. This is smelted with rich gold ores, notably those containing tellurium, for white metal or regulus; and by a following process of partial reduction analogous to that of selecting in copper smelting, “bottoms” of impure copper are obtained in which practically all the gold is concentrated. By continuing the treatment of these in the ordinary way of refining, poling and granulating, all the foreign matters other than gold, copper and silver are removed, and, by exposing the granulated metal to a high oxidizing heat for a considerable time the copper may be completely oxidized while the precious metals are unaltered. Subsequent treatment with sulphuric acid renders the copper soluble in water as sulphate, and the final residue contains only gold and silver, which is parted or refined in the ordinary way. This method of separating gold from copper, by converting the latter into oxide and sulphate, is also used at Oker in the Harz.

Extraction by Means of Aqueous Solutions.—Many processes have been suggested in which the gold of auriferous deposits is converted into products soluble in water, from which solutions the gold may be precipitated. Of these processes, two only are of special importance, viz. the chlorination or Plattner process, in which the metal is converted into the chloride, and the cyanide or MacArthur-Forrest process, in which it is converted into potassium aurocyanide.

(3)Chlorination or Plattner Process.—In this process moistened gold ores are treated with chlorine gas, the resulting gold chloride dissolved out with water, and the gold precipitated with ferrous sulphate, charcoal, sulphuretted hydrogen or otherwise. The process originated in 1848 with C. F. Plattner, who suggested that the residues from certain mines at Reichenstein, in Silesia, should be treated with chlorine after the arsenical products had been extracted by roasting. It must be noticed, however, that Percy independently made the same discovery, and stated his results at the meeting of the British Association (at Swansea) in 1849, but the Report was not published until 1852. The process was introduced in 1858 by Deetken at Grass Valley, California, where the waste minerals, principally pyrites from tailings, had been worked for a considerable time by amalgamation. The process is rarely applied to ores direct; free-milling ores are generally amalgamated, and the tailings and slimes, after concentration, operated upon. Three stages in the process are to be distinguished: (i) calcination, to convert all the metals, except gold and silver, into oxides, which are unacted upon by chlorine; (ii.) chlorinating the gold and lixiviating the product; (iii.) precipitating the gold.The calcination, or roasting, is conducted at a low temperature in some form of reverberatory furnace. Salt is added in the roasting to convert any lime, magnesia or lead which may be present, into the corresponding chlorides. The auric chloride is, however, decomposed at the elevated temperature into finely divided metallic gold, which is then readily attacked by the chlorine gas. The high volatility of gold in the presence of certain metals must also be considered. According to Egleston the loss may be from 40 to 90% of the total gold present in cupriferous ores according to the temperature and duration of calcination. The roasted mineral, slightly moistened, is introduced into a vat made of stoneware or pitched planks, and furnished with a double bottom. Chlorine, generally prepared by the interaction of pyrolusite, salt and sulphuric acid, is led from a suitable generator beneath the false bottom, and rises through the moistened ore, which rests on a bed of broken quartz; the gold is thus converted into a soluble chloride, which is afterwards removed by washing with water. Both fixed and rotating vats are employed, the chlorination proceeding more rapidly in the latter case; rotating barrels are sometimes used. There have also been introduced processes in which the chlorine is generated in the chloridizing vat, the reagents used being dilute solutions of bleaching powder and an acid. Munktell’s process is of this type. In the Thies process, used in many districts in the United States, the vats are rotating barrels made, in the later forms, of iron lined with lead, and provided with a filter formed of a finely perforated leaden grating running from one end of the barrel to the other, and rigidly held in place by wooden frames. Chlorine is generated within the barrel from sulphuric acid and chloride of lime. After charging, the barrel is rotated, and when the chlorination is complete the contents are emptied on a filter of quartz or some similar material, and the filtrate led to settling tanks.After settling the solution is run into the precipitating tanks. The precipitants in use are: ferrous sulphate, charcoal and sulphuretted hydrogen, either alone or mixed with sulphur dioxide; the use of copper and iron sulphides has been suggested, but apparently these substances have achieved no success.In the case of ferrous sulphate, prepared by dissolving iron in dilute sulphuric acid, the reaction follows the equation AuCl3+ 3FeSO4= FeCl3+ Fe2(SO4)3+ Au. At the same time any lead, calcium, barium and strontium present are precipitated as sulphates; it is therefore advantageous to remove these metals by the preliminary addition of sulphuric acid, which also serves to keep any basic iron salts in solution. The precipitation is carried out in tanks or vats made with wooden sides and a cement bottom. The solutions are well mixed by stirring with wooden poles, and the gold allowed to settle, the time allowed varying from 12 to 72 hours. The supernatant liquid is led into settling tanks, where a further amount of gold is deposited, and is then filtered through sawdust or sand, the sawdust being afterwards burnt and the gold separated from the ashes and the sand treated in the chloridizing vat. The precipitated gold is washed, treated with salt and sulphuric acid to remove iron salts, roughly dried by pressing in cloths or on filter paper, and then melted with salt, borax and nitre in graphite crucibles. Thus prepared it has a fineness of 800-960, the chief impurities usually being iron and lead.Charcoal is used as the precipitant at Mount Morgan, Australia. Its use was proposed as early as 1818 and 1819 by Hare and Henry; Percy advocated it in 1869, and Davis adopted it on the large scale at a works in Carolina in 1880. The action is not properly understood; it may be due to the reducing gases (hydrogen, hydrocarbons, &c.) which are invariably present in wood charcoal. The process consists essentially in running the solution over layers of charcoal, the charcoal being afterwards burned. It has been found that the reaction proceeds faster when the solution is heated.Precipitation with sulphur dioxide and sulphuretted hydrogen proceeds much more rapidly, and has been adopted at many works. Sulphur dioxide, generated by burning sulphur, is forced into the solution under pressure, where it interacts with any free chlorine present to form hydrochloric and sulphuric acids. Sulphuretted hydrogen, obtained by treating iron sulphide or a coarse matte with dilute sulphuric acid, is forced in similarly. The gold is precipitated as the sulphide, together with any arsenic, antimony, copper, silver and lead which may be present. The precipitate is collected in a filter-press, and then roasted in muffle furnaces with nitre, borax and sodium carbonate. The fineness of the gold so obtained is 900 to 950.4.Cyanide Process.—This process depends upon the solubility of gold in a dilute solution of potassium cyanide in the presence of air (or some other oxidizing agent), and the subsequent precipitation of the gold by metallic zinc or by electrolysis. The solubility of gold in cyanide solutions was known to K. W. Scheele in 1782; and M. Faraday applied it to the preparation of extremely thin films of the metal. L. Eisner recognized, in 1846, the part played by the atmosphere, and in 1879 Dixon showed that bleaching powder, manganese dioxide, and other oxidizing agents, facilitated the solution. S. B. Christy (Trans. A.I.M.E., 1896, vol. 26) has shown that the solution is hastened by many oxidizing agents, especially sodium and manganese dioxides and potassium ferricyanide. According to G. Bodländer (Zeit. f. angew. Chem., 1896, vol. 19) the rate of solution in potassium cyanide depends upon the subdivision of the gold—the finer the subdivision the quicker the solution,—and on the concentration of the solution—the rate increasing until the solution contains 0.25% of cyanide, and remaining fairly stationary with increasing concentration. The action proceeds in two stages; in the first hydrogen peroxide and potassium aurocyanide are formed, and in the second the hydrogen peroxide oxidizes a further quantity of gold and potassium cyanide to aurocyanide, thus (1) 2Au + 4KCN + O2+ 2H2O = 2KAu(CN)2+ 4KOH + H2O2; (2) 2Au + 4KCN + 2H2O2= 2KAu(CN)2+ 4KOH. The end reaction may be written 4Au + 8KCN + 2H2O + O2= 4KAu(CN)2+ 4KOH.The commercial process was patented in 1890 by MacArthur and Forrest, and is now in use all over the world. It is best adapted for free-milling ores, especially after the bulk of the gold has been removed by amalgamation. It has been especially successful in the Transvaal. In the Witwatersrand the ore, which contains about 9 dwts. of gold to the metric ton (2000 ℔), is stamped and amalgamated, and the slimes and tailings, containing about 3½ dwts. per ton, are cyanided, about 2 dwts. more being thus extracted. The total cost per ton of ore treated is about 6s., of which the cyaniding costs from 2s. to 4s.The process embraces three operations: (1) Solution of the gold; (2) precipitation of the gold; (3) treatment of the precipitate.The ores, having been broken and ground, generally in tube mills, until they pass a 150 to 200-mesh sieve, are transferred to the leaching vats, which are constructed of wood, iron or masonry; steel vats, coated inside and out with pitch, of circular section and holding up to 1000 tons, have come into use. The diameter is generally 26 ft., but may be greater; the best depth is considered to be a quarter of the diameter. The vats are fitted with filters made of coco-nut matting and jute cloth supported on wooden frames. The leaching is generally carried out with a strong, medium, and with a weak liquor, in the order given; sometimes there is a preliminary leaching with a weak liquor. The strengths employed depend also upon the mode of precipitation adopted, stronger solutions (up to 0.25% KCN) being used when zinc is the precipitant. For electrolytic precipitation the solution may contain up to 0.1% KCN. The liquors are run off from the vats to the electrolysing baths or precipitating tanks, and the leached ores are removed by means of doors in the sides of the vats into wagons. In the Transvaal the operation occupies 3½ to 4 days for fine sands, and up to 14 days for coarse sands; the quantity of cyanide per ton of tailings varies from 0.26 to 0.28 ℔, for electrolytic precipitation, and 0.5 ℔ for zinc precipitation.The precipitation is effected by zinc in the form of bright turnings, or coated with lead, or by electrolysis. According to Christy, the precipitation with zinc follows equations 1 or 2 according as potassium cyanide is present or not:(1) 4KAu(CN)2+ 4Zn + 2H2O = 2Zn(CN)2+ K2Zn(CN)4+ Zn(OK)2+ 4H + 4Au;(2) 2KAu(CN)2+ 3Zn + 4KCN + 2H2O = 2K2Zn(CN)4+ Zn(OK)2+ 4H + 2Au;one part of zinc precipitating 3.1 parts of gold in the first case, and 2.06 in the second. It may be noticed that the potassium zinc cyanide is useless in gold extraction, for it neither dissolves gold nor can potassium cyanide be regenerated from it.The precipitating boxes, generally made of wood but sometimes of steel, and set on an incline, are divided by partitions into alternately wide and narrow compartments, so that the liquor travels upwards in its passage through the wide divisions and downwards through the narrow divisions. In the wider compartments are placed sieves having sixteen holes to the square inch and bearing zinc turnings. The gold and other metals are precipitated on the under surfaces of the turnings and fall to the bottom of the compartment as a black slime. The slime is cleaned out fortnightly or monthly, the zinc turnings being cleaned by rubbing and the supernatant liquor allowed to settle in the precipitating boxes or in separate vessels. The slime so obtained consists of finely divided gold and silver (5-50%), zinc (30-60%), lead (10%), carbon (10%), together with tin, copper, antimony, arsenic and other impurities of the zinc and ores. After well washing with water, the slimes are roughly dried in bag-filters or filter-presses, and then treated with dilute sulphuric acid, the solution being heated by steam. This dissolves out the zinc. Lime is added to bring down the gold, and the sediment, after washing and drying, is fused in graphite crucibles.5.Electrolytic Processes.—The electrolytic separation of the gold from cyanide solutions was first practised in the Transvaal. The process, as elaborated by Messrs. Siemens and Halske, essentially consists in the electrolysis of weak solutions with iron or steel plate anodes, and lead cathodes, the latter, when coated with gold, being fused and cupelled. Its advantages over the zinc process are that the deposited gold is purer and more readily extracted, and that weaker solutions can be employed, thereby effecting an economy in cyanide.In the process employed at the Worcester Works in the Transvaal, the liquors, containing about 150 grains of gold per ton and from 0.08 to 0.01% of cyanide, are treated in rectangular vats in which is placed a series of iron and leaden plates at intervals of 1 in. The cathodes, which are sheets of thin lead foil weighing 1½ ℔ to the sq. yd., are removed monthly, their gold content being from 0.5 to 10%, and after folding are melted in reverberatory furnaces to ingots containing 2 to 4% of gold. Cupellation brings up the gold to about 900 fine. Many variations of the electrolytic process as above outlined have been suggested. S. Cowper Coles has suggested aluminium cathodes; Andreoli has recommended cathodes of iron and anodes of lead coated with lead peroxide, the gold being removed from the iron cathodes by a brief immersion in molten lead; in the Pelatan-Cerici process the gold is amalgamated at a mercury cathode (see also below).

(3)Chlorination or Plattner Process.—In this process moistened gold ores are treated with chlorine gas, the resulting gold chloride dissolved out with water, and the gold precipitated with ferrous sulphate, charcoal, sulphuretted hydrogen or otherwise. The process originated in 1848 with C. F. Plattner, who suggested that the residues from certain mines at Reichenstein, in Silesia, should be treated with chlorine after the arsenical products had been extracted by roasting. It must be noticed, however, that Percy independently made the same discovery, and stated his results at the meeting of the British Association (at Swansea) in 1849, but the Report was not published until 1852. The process was introduced in 1858 by Deetken at Grass Valley, California, where the waste minerals, principally pyrites from tailings, had been worked for a considerable time by amalgamation. The process is rarely applied to ores direct; free-milling ores are generally amalgamated, and the tailings and slimes, after concentration, operated upon. Three stages in the process are to be distinguished: (i) calcination, to convert all the metals, except gold and silver, into oxides, which are unacted upon by chlorine; (ii.) chlorinating the gold and lixiviating the product; (iii.) precipitating the gold.

The calcination, or roasting, is conducted at a low temperature in some form of reverberatory furnace. Salt is added in the roasting to convert any lime, magnesia or lead which may be present, into the corresponding chlorides. The auric chloride is, however, decomposed at the elevated temperature into finely divided metallic gold, which is then readily attacked by the chlorine gas. The high volatility of gold in the presence of certain metals must also be considered. According to Egleston the loss may be from 40 to 90% of the total gold present in cupriferous ores according to the temperature and duration of calcination. The roasted mineral, slightly moistened, is introduced into a vat made of stoneware or pitched planks, and furnished with a double bottom. Chlorine, generally prepared by the interaction of pyrolusite, salt and sulphuric acid, is led from a suitable generator beneath the false bottom, and rises through the moistened ore, which rests on a bed of broken quartz; the gold is thus converted into a soluble chloride, which is afterwards removed by washing with water. Both fixed and rotating vats are employed, the chlorination proceeding more rapidly in the latter case; rotating barrels are sometimes used. There have also been introduced processes in which the chlorine is generated in the chloridizing vat, the reagents used being dilute solutions of bleaching powder and an acid. Munktell’s process is of this type. In the Thies process, used in many districts in the United States, the vats are rotating barrels made, in the later forms, of iron lined with lead, and provided with a filter formed of a finely perforated leaden grating running from one end of the barrel to the other, and rigidly held in place by wooden frames. Chlorine is generated within the barrel from sulphuric acid and chloride of lime. After charging, the barrel is rotated, and when the chlorination is complete the contents are emptied on a filter of quartz or some similar material, and the filtrate led to settling tanks.

After settling the solution is run into the precipitating tanks. The precipitants in use are: ferrous sulphate, charcoal and sulphuretted hydrogen, either alone or mixed with sulphur dioxide; the use of copper and iron sulphides has been suggested, but apparently these substances have achieved no success.

In the case of ferrous sulphate, prepared by dissolving iron in dilute sulphuric acid, the reaction follows the equation AuCl3+ 3FeSO4= FeCl3+ Fe2(SO4)3+ Au. At the same time any lead, calcium, barium and strontium present are precipitated as sulphates; it is therefore advantageous to remove these metals by the preliminary addition of sulphuric acid, which also serves to keep any basic iron salts in solution. The precipitation is carried out in tanks or vats made with wooden sides and a cement bottom. The solutions are well mixed by stirring with wooden poles, and the gold allowed to settle, the time allowed varying from 12 to 72 hours. The supernatant liquid is led into settling tanks, where a further amount of gold is deposited, and is then filtered through sawdust or sand, the sawdust being afterwards burnt and the gold separated from the ashes and the sand treated in the chloridizing vat. The precipitated gold is washed, treated with salt and sulphuric acid to remove iron salts, roughly dried by pressing in cloths or on filter paper, and then melted with salt, borax and nitre in graphite crucibles. Thus prepared it has a fineness of 800-960, the chief impurities usually being iron and lead.

Charcoal is used as the precipitant at Mount Morgan, Australia. Its use was proposed as early as 1818 and 1819 by Hare and Henry; Percy advocated it in 1869, and Davis adopted it on the large scale at a works in Carolina in 1880. The action is not properly understood; it may be due to the reducing gases (hydrogen, hydrocarbons, &c.) which are invariably present in wood charcoal. The process consists essentially in running the solution over layers of charcoal, the charcoal being afterwards burned. It has been found that the reaction proceeds faster when the solution is heated.

Precipitation with sulphur dioxide and sulphuretted hydrogen proceeds much more rapidly, and has been adopted at many works. Sulphur dioxide, generated by burning sulphur, is forced into the solution under pressure, where it interacts with any free chlorine present to form hydrochloric and sulphuric acids. Sulphuretted hydrogen, obtained by treating iron sulphide or a coarse matte with dilute sulphuric acid, is forced in similarly. The gold is precipitated as the sulphide, together with any arsenic, antimony, copper, silver and lead which may be present. The precipitate is collected in a filter-press, and then roasted in muffle furnaces with nitre, borax and sodium carbonate. The fineness of the gold so obtained is 900 to 950.

4.Cyanide Process.—This process depends upon the solubility of gold in a dilute solution of potassium cyanide in the presence of air (or some other oxidizing agent), and the subsequent precipitation of the gold by metallic zinc or by electrolysis. The solubility of gold in cyanide solutions was known to K. W. Scheele in 1782; and M. Faraday applied it to the preparation of extremely thin films of the metal. L. Eisner recognized, in 1846, the part played by the atmosphere, and in 1879 Dixon showed that bleaching powder, manganese dioxide, and other oxidizing agents, facilitated the solution. S. B. Christy (Trans. A.I.M.E., 1896, vol. 26) has shown that the solution is hastened by many oxidizing agents, especially sodium and manganese dioxides and potassium ferricyanide. According to G. Bodländer (Zeit. f. angew. Chem., 1896, vol. 19) the rate of solution in potassium cyanide depends upon the subdivision of the gold—the finer the subdivision the quicker the solution,—and on the concentration of the solution—the rate increasing until the solution contains 0.25% of cyanide, and remaining fairly stationary with increasing concentration. The action proceeds in two stages; in the first hydrogen peroxide and potassium aurocyanide are formed, and in the second the hydrogen peroxide oxidizes a further quantity of gold and potassium cyanide to aurocyanide, thus (1) 2Au + 4KCN + O2+ 2H2O = 2KAu(CN)2+ 4KOH + H2O2; (2) 2Au + 4KCN + 2H2O2= 2KAu(CN)2+ 4KOH. The end reaction may be written 4Au + 8KCN + 2H2O + O2= 4KAu(CN)2+ 4KOH.

The commercial process was patented in 1890 by MacArthur and Forrest, and is now in use all over the world. It is best adapted for free-milling ores, especially after the bulk of the gold has been removed by amalgamation. It has been especially successful in the Transvaal. In the Witwatersrand the ore, which contains about 9 dwts. of gold to the metric ton (2000 ℔), is stamped and amalgamated, and the slimes and tailings, containing about 3½ dwts. per ton, are cyanided, about 2 dwts. more being thus extracted. The total cost per ton of ore treated is about 6s., of which the cyaniding costs from 2s. to 4s.

The process embraces three operations: (1) Solution of the gold; (2) precipitation of the gold; (3) treatment of the precipitate.

The ores, having been broken and ground, generally in tube mills, until they pass a 150 to 200-mesh sieve, are transferred to the leaching vats, which are constructed of wood, iron or masonry; steel vats, coated inside and out with pitch, of circular section and holding up to 1000 tons, have come into use. The diameter is generally 26 ft., but may be greater; the best depth is considered to be a quarter of the diameter. The vats are fitted with filters made of coco-nut matting and jute cloth supported on wooden frames. The leaching is generally carried out with a strong, medium, and with a weak liquor, in the order given; sometimes there is a preliminary leaching with a weak liquor. The strengths employed depend also upon the mode of precipitation adopted, stronger solutions (up to 0.25% KCN) being used when zinc is the precipitant. For electrolytic precipitation the solution may contain up to 0.1% KCN. The liquors are run off from the vats to the electrolysing baths or precipitating tanks, and the leached ores are removed by means of doors in the sides of the vats into wagons. In the Transvaal the operation occupies 3½ to 4 days for fine sands, and up to 14 days for coarse sands; the quantity of cyanide per ton of tailings varies from 0.26 to 0.28 ℔, for electrolytic precipitation, and 0.5 ℔ for zinc precipitation.

The precipitation is effected by zinc in the form of bright turnings, or coated with lead, or by electrolysis. According to Christy, the precipitation with zinc follows equations 1 or 2 according as potassium cyanide is present or not:

(1) 4KAu(CN)2+ 4Zn + 2H2O = 2Zn(CN)2+ K2Zn(CN)4+ Zn(OK)2+ 4H + 4Au;

(2) 2KAu(CN)2+ 3Zn + 4KCN + 2H2O = 2K2Zn(CN)4+ Zn(OK)2+ 4H + 2Au;

one part of zinc precipitating 3.1 parts of gold in the first case, and 2.06 in the second. It may be noticed that the potassium zinc cyanide is useless in gold extraction, for it neither dissolves gold nor can potassium cyanide be regenerated from it.

The precipitating boxes, generally made of wood but sometimes of steel, and set on an incline, are divided by partitions into alternately wide and narrow compartments, so that the liquor travels upwards in its passage through the wide divisions and downwards through the narrow divisions. In the wider compartments are placed sieves having sixteen holes to the square inch and bearing zinc turnings. The gold and other metals are precipitated on the under surfaces of the turnings and fall to the bottom of the compartment as a black slime. The slime is cleaned out fortnightly or monthly, the zinc turnings being cleaned by rubbing and the supernatant liquor allowed to settle in the precipitating boxes or in separate vessels. The slime so obtained consists of finely divided gold and silver (5-50%), zinc (30-60%), lead (10%), carbon (10%), together with tin, copper, antimony, arsenic and other impurities of the zinc and ores. After well washing with water, the slimes are roughly dried in bag-filters or filter-presses, and then treated with dilute sulphuric acid, the solution being heated by steam. This dissolves out the zinc. Lime is added to bring down the gold, and the sediment, after washing and drying, is fused in graphite crucibles.

5.Electrolytic Processes.—The electrolytic separation of the gold from cyanide solutions was first practised in the Transvaal. The process, as elaborated by Messrs. Siemens and Halske, essentially consists in the electrolysis of weak solutions with iron or steel plate anodes, and lead cathodes, the latter, when coated with gold, being fused and cupelled. Its advantages over the zinc process are that the deposited gold is purer and more readily extracted, and that weaker solutions can be employed, thereby effecting an economy in cyanide.

In the process employed at the Worcester Works in the Transvaal, the liquors, containing about 150 grains of gold per ton and from 0.08 to 0.01% of cyanide, are treated in rectangular vats in which is placed a series of iron and leaden plates at intervals of 1 in. The cathodes, which are sheets of thin lead foil weighing 1½ ℔ to the sq. yd., are removed monthly, their gold content being from 0.5 to 10%, and after folding are melted in reverberatory furnaces to ingots containing 2 to 4% of gold. Cupellation brings up the gold to about 900 fine. Many variations of the electrolytic process as above outlined have been suggested. S. Cowper Coles has suggested aluminium cathodes; Andreoli has recommended cathodes of iron and anodes of lead coated with lead peroxide, the gold being removed from the iron cathodes by a brief immersion in molten lead; in the Pelatan-Cerici process the gold is amalgamated at a mercury cathode (see also below).

Refining or Parting of Gold.—Gold is almost always silver-bearing, and it may be also noticed that silver generally contains some gold. Consequently the separation of these two metals Is one of the most important metallurgical processes. In addition to the separation of the silver the operation extends to the elimination of the last traces of lead, tin, arsenic, &c. which have resisted the preceding cupellation.

The “parting” of gold and silver is of considerable antiquity. Thus Strabo states that in his time a process was employed for refining and purifying gold in large quantities by cementing or burning it with an aluminous earth, which, by destroying the silver, left the gold in a state of purity. Pliny shows that for this purpose the gold was placed on the fire in an earthen vessel with treble its weight of salt, and that it was afterwards again exposed to the fire with two parts of salt and one of argillaceous rock, which, in the presence of moisture, effected the decomposition of the salt; by this means the silver became converted into chloride.The methods of parting can be classified into “dry,” “wet” and electrolytic methods. In the “dry” methods the silver is converted into sulphide or chloride, the gold remaining unaltered; in the “wet” methods the silver is dissolved by nitric acid or boiling sulphuric acid; and in the electrolytic processes advantage is taken of the fact that under certain current densities and other circumstances silver passes from an anode composed of a gold-silver alloy to the cathode more readily than gold. Of the dry methods only F. B. Miller’s chlorine process is of any importance, this method, and the wet process of refining by sulphuric acid, together with the electrolytic process, being the only ones now practised.The conversion of silver into the sulphide may be effected by heating with antimony sulphide, litharge and sulphur, pyrites, or with sulphur alone. The antimony, orGuss und Fluss, method was practised up till 1846 at the Dresden mint; it is only applicable to alloys containing more than 50% of gold. The fusion results in the formation of a gold-antimony alloy, from which the antimony is removed by an oxidizing fusion with nitre. The sulphur and litharge, orPfannenschmied, process was used to concentrate the gold in an alloy in order to make it amenable to “quartation,” or parting with nitric acid. Fusion with sulphur was used for the same purpose as the Pfannenschmied process. It was employed in 1797 at the St Petersburg mint.The conversion of the silver into the chloride may be effected by means of salt—the “cementation” process—or other chlorides, or by free chlorine—Miller’s process. The first process consists essentially in heating the alloy with salt and brickdust; the latter absorbs the chloride formed, while the gold is recovered by washing. It is no longer employed. The second process depends upon the fact that, if chlorine be led into the molten alloy, the base metals and the silver are converted into chlorides. It was proposed in 1838 by Lewis Thompson, but it was only applied commercially after Miller’s improvements in 1867, when it was adopted at the Sydney mint. Sir W. C. Roberts-Austen introduced it at the London mint; and it has also been used at Pretoria. It is especially suitable to gold containing little silver and base metals—a character of Australian gold—but it yields to the sulphuric acid and electrolytic methods in point of economy.The separation of gold from silver in the wet way may be effected by nitric acid, sulphuric acid or by a mixture of sulphuric acid andaqua regia.Parting by nitric acid is of considerable antiquity, being mentioned by Albertus Magnus (13th cent.), Biringuccio (1540) and Agricola (1556). It is now rarely practised, although in some refineries both the nitric acid and the sulphuric acid processes are combined, the alloy being first treated with nitric acid. It used to be called “quartation” or “inquartation,” from the fact that the alloy best suited for the operation of refining contained 3 parts of silver to 1 of gold. The operation may be conducted in vessels of glass or platinum, and each pound of granulated metal is treated with a pound and a quarter of nitric acid of specific gravity 1.32. The method is sometimes employed in the assay of gold.Refining by sulphuric acid, the process usually adopted for separating gold from silver, was first employed on the large scale by d’Arcet in Paris in 1802, and was introduced into the Mint refinery, London, by Mathison in 1829. It is based upon the facts that concentrated hot sulphuric acid converts silver and copper into soluble sulphates without attacking the gold, the silver sulphate being subsequently reduced to the metallic state by copper plates with the formation of copper sulphate. It is applicable to any alloy, and is the best method for parting gold with the exception of the electrolytic method.The process embraces four operations: (1) the preparation of an alloy suitable for parting; (2) the treatment with sulphuric acid; (3) the treatment of the residue for gold; (4) the treatment of the solution for silver.It is necessary to remove as completely as possible any lead, tin, bismuth, antimony, arsenic and tellurium, impurities which impair the properties of gold and silver, by an oxidizing fusion,e.g.with nitre. Over 10% of copper makes the parting difficult; consequently in such alloys the percentage of copper is diminished by the addition of silver free from copper, or else the copper is removed by a chemical process. Other undesirable impurities are the platinum metals, special treatment being necessary when these substances are present. The alloy, after the preliminary refining, is granulated by being poured, while molten, in a thin stream into cold water which is kept well agitated.The acid treatment is generally carried out in cast iron pots; platinum vessels used to be employed, while porcelain vessels are only used for small operations,e.g.for charges of 190 to 225 oz. as at Oker in the Harz. The pots, which are usually cylindrical with a hemispherical bottom, may hold as much as 13,000 to 16,000 oz. of alloy. They are provided with lids, made either of lead or of wood lined with lead, which have openings to serve for the introduction of the alloy and acid, and a vent tube to lead off the vapours evolved during the operation. The bullion with about twice its weight of sulphuric acid of 66° Bé is placed in the pot, and the whole gradually heated. Since the action is sometimes very violent, especially when the bullion is treated in the granulated form (it is steadier when thin plates are operated upon), it is found expedient to add the acid in several portions. The heating is continued for 4 to 12 hours according to the amount of silver present; the end of the reaction is known by the absence of any hissing. Generally the reaction mixture is allowed to cool, and the residue, which settles to the bottom of the pot, consists of gold together with copper, lead and iron sulphates, which are insoluble in strong sulphuric acid; silver sulphate may also separate if present in sufficient quantity and the solution be sufficiently cooled. The solution is removed by ladles or by siphons, and the residue is leached out with boiling water; this removes the sulphates. A certain amount of silver is still present and, according to M. Pettenkofer, it is impossible to remove all the silver by means of sulphuric acid. Several methods are in use for removing the silver. Fusion with an alkaline bisulphate converts the silver into the sulphate, which may be extracted by boiling with sulphuric acid and then with water. Another process consists in treating a mixture of the residue with one-quarter of its weight of calcined sodium sulphate with sulphuric acid, the residue being finally boiled with a large quantity of acid. Or the alloy is dissolved inaqua regia, the solution filtered from the insoluble silver chloride, and the gold precipitated by ferrous chloride.The silver present in the solution obtained in the sulphuric acid boiling is recovered by a variety of processes. The solution may be directly precipitated with copper, the copper passing into solution as copper sulphate, and the silver separating as a mud, termed “cement silver.” Or the silver sulphate may be separated from the solution by cooling and dilution, and then mixed with iron clippings, the interaction being accompanied with a considerable evolution of heat. Or Gutzkow’s method of precipitating the metal with ferrous sulphate may be employed.The electrolytic parting of gold and silver has been shown to be more economical and free from the objections—such as the poisonous fumes—of the sulphuric acid process. One process depends upon the fact that, with a suitable current density, if a very dilute solution of silver nitrate be electrolysed between an auriferous silver anode and a silver cathode, the silver of the anode is dissolved out and deposited at the cathode, the gold remaining at the anode. The silver is quite free from gold, and the gold after boiling with nitric acid has a fineness of over 999.Gold is left in the anode slime when copper or silver are refined by the usual processes, but if the gold preponderate in the anode these processes are inapplicable. A cyanide bath, as used in electroplating, would dissolve the gold, but is not suitable for refining, because other metals (silver, copper, &c.) passing with gold into the solution would deposit with it. Bock, however, in 1880 (Berg- und hüttenmännische Zeitung, 1880, p. 411) described a process used at the North German Refinery in Hamburg for the refining of gold containing platinum with a small proportion of silver, lead or bismuth, and a subsequent patent specification (1896) and a paper by Wohlwill (Zeits. f. Elektrochem., 1898, pp. 379, 402, 421) have thrown more light upon the process. The electrolyte is gold chloride (2.5-3 parts of pure gold per 100 of solution) mixed with from 2 to 6% of the strongest hydrochloric acid to render the gold anodes readily soluble, which they are not in the neutral chloride solution. The bath is used at 65° to 70° C. (150° to 158° F.), and if free chlorine be evolved, which is known at once by its pungent smell, the temperature is raised, or more acid is added, to promote the solubility of the gold. The bath is used with a current-density of 100 ampères per sq. ft. at 1 volt (or higher), with electrodes about 1.2 in. apart. In this process all the anode metals pass into solution except iridium and other refractory metals of that group, which remain as metals, and silver, which is converted into insoluble chloride; lead and bismuth form chloride and oxychloride respectively, and these dissolve until the bath is saturated with them, and then precipitate with the silver in the tank. But if the gold-strength of the bath be maintained, only gold is deposited at the cathode—in a loose powdery condition from pure solutions, but in a smooth detachable deposit from impure liquors. Under good conditions the gold should contain 99.98% of the pure metal. The tank is of porcelain or glazed earthenware, the electrodes for impure solutions are ½ in. apart (or more with pure solutions), and are on the multiple system, and the potential difference at the terminals of the bath is 1 volt. A high current-density being employed, the turn-over of gold is rapid—an essential factor of success when the costliness of the metal is taken into account. Platinum and palladium dissolved from the anode accumulate in the solution, and are removed at intervals of, say, a few months by chemical precipitation. It is essential that the bath should not contain more than 5% of palladium, or some of this metal will deposit with the gold. The slimes are treated chemically for the separation of the metals contained in them.Authorities.—Standard works on the metallurgy of gold are the treatises of T. Kirke Rose and of M. Eissler. The cyanide process is especially treated by M. Eissler,Cyanide Process for the Extraction of Gold, which pays particular attention to the Witwatersrand methods; Alfred James,Cyanide Practice; H. Forbes Julian and Edgar Smart,Cyaniding Gold and Silver Ores. Gold milling is treated by Henry Louis,A Handbook of Gold Milling; C. G. Warnford Lock,Gold Milling; T. A. Rickard,Stamp Milling of Gold Ores. Gold dredging is treated by Captain C. C. Longridge inGold Dredging, and hydraulic mining is discussed by the same author in hisHydraulic Mining. For operations in special districts see J. M. Maclaren,Gold(1908); J. H. Curle,Gold Mines of the World; Africa: F. H. Hatch and J. A. Chalmers,Gold Mines of the Rand; S. J. Truscott,Witwatersrand Goldfields Banket and Mining Practice; Australasia: D. Clark,Australian Mining and Metallurgy; Karl Schmeisser,Goldfields of Australasia; A. G. Charleton,Gold Mining and Milling in Western Australia; India: F. H. Hatch,The Kolar Gold-Field.

The “parting” of gold and silver is of considerable antiquity. Thus Strabo states that in his time a process was employed for refining and purifying gold in large quantities by cementing or burning it with an aluminous earth, which, by destroying the silver, left the gold in a state of purity. Pliny shows that for this purpose the gold was placed on the fire in an earthen vessel with treble its weight of salt, and that it was afterwards again exposed to the fire with two parts of salt and one of argillaceous rock, which, in the presence of moisture, effected the decomposition of the salt; by this means the silver became converted into chloride.

The methods of parting can be classified into “dry,” “wet” and electrolytic methods. In the “dry” methods the silver is converted into sulphide or chloride, the gold remaining unaltered; in the “wet” methods the silver is dissolved by nitric acid or boiling sulphuric acid; and in the electrolytic processes advantage is taken of the fact that under certain current densities and other circumstances silver passes from an anode composed of a gold-silver alloy to the cathode more readily than gold. Of the dry methods only F. B. Miller’s chlorine process is of any importance, this method, and the wet process of refining by sulphuric acid, together with the electrolytic process, being the only ones now practised.

The conversion of silver into the sulphide may be effected by heating with antimony sulphide, litharge and sulphur, pyrites, or with sulphur alone. The antimony, orGuss und Fluss, method was practised up till 1846 at the Dresden mint; it is only applicable to alloys containing more than 50% of gold. The fusion results in the formation of a gold-antimony alloy, from which the antimony is removed by an oxidizing fusion with nitre. The sulphur and litharge, orPfannenschmied, process was used to concentrate the gold in an alloy in order to make it amenable to “quartation,” or parting with nitric acid. Fusion with sulphur was used for the same purpose as the Pfannenschmied process. It was employed in 1797 at the St Petersburg mint.

The conversion of the silver into the chloride may be effected by means of salt—the “cementation” process—or other chlorides, or by free chlorine—Miller’s process. The first process consists essentially in heating the alloy with salt and brickdust; the latter absorbs the chloride formed, while the gold is recovered by washing. It is no longer employed. The second process depends upon the fact that, if chlorine be led into the molten alloy, the base metals and the silver are converted into chlorides. It was proposed in 1838 by Lewis Thompson, but it was only applied commercially after Miller’s improvements in 1867, when it was adopted at the Sydney mint. Sir W. C. Roberts-Austen introduced it at the London mint; and it has also been used at Pretoria. It is especially suitable to gold containing little silver and base metals—a character of Australian gold—but it yields to the sulphuric acid and electrolytic methods in point of economy.

The separation of gold from silver in the wet way may be effected by nitric acid, sulphuric acid or by a mixture of sulphuric acid andaqua regia.

Parting by nitric acid is of considerable antiquity, being mentioned by Albertus Magnus (13th cent.), Biringuccio (1540) and Agricola (1556). It is now rarely practised, although in some refineries both the nitric acid and the sulphuric acid processes are combined, the alloy being first treated with nitric acid. It used to be called “quartation” or “inquartation,” from the fact that the alloy best suited for the operation of refining contained 3 parts of silver to 1 of gold. The operation may be conducted in vessels of glass or platinum, and each pound of granulated metal is treated with a pound and a quarter of nitric acid of specific gravity 1.32. The method is sometimes employed in the assay of gold.

Refining by sulphuric acid, the process usually adopted for separating gold from silver, was first employed on the large scale by d’Arcet in Paris in 1802, and was introduced into the Mint refinery, London, by Mathison in 1829. It is based upon the facts that concentrated hot sulphuric acid converts silver and copper into soluble sulphates without attacking the gold, the silver sulphate being subsequently reduced to the metallic state by copper plates with the formation of copper sulphate. It is applicable to any alloy, and is the best method for parting gold with the exception of the electrolytic method.

The process embraces four operations: (1) the preparation of an alloy suitable for parting; (2) the treatment with sulphuric acid; (3) the treatment of the residue for gold; (4) the treatment of the solution for silver.

It is necessary to remove as completely as possible any lead, tin, bismuth, antimony, arsenic and tellurium, impurities which impair the properties of gold and silver, by an oxidizing fusion,e.g.with nitre. Over 10% of copper makes the parting difficult; consequently in such alloys the percentage of copper is diminished by the addition of silver free from copper, or else the copper is removed by a chemical process. Other undesirable impurities are the platinum metals, special treatment being necessary when these substances are present. The alloy, after the preliminary refining, is granulated by being poured, while molten, in a thin stream into cold water which is kept well agitated.

The acid treatment is generally carried out in cast iron pots; platinum vessels used to be employed, while porcelain vessels are only used for small operations,e.g.for charges of 190 to 225 oz. as at Oker in the Harz. The pots, which are usually cylindrical with a hemispherical bottom, may hold as much as 13,000 to 16,000 oz. of alloy. They are provided with lids, made either of lead or of wood lined with lead, which have openings to serve for the introduction of the alloy and acid, and a vent tube to lead off the vapours evolved during the operation. The bullion with about twice its weight of sulphuric acid of 66° Bé is placed in the pot, and the whole gradually heated. Since the action is sometimes very violent, especially when the bullion is treated in the granulated form (it is steadier when thin plates are operated upon), it is found expedient to add the acid in several portions. The heating is continued for 4 to 12 hours according to the amount of silver present; the end of the reaction is known by the absence of any hissing. Generally the reaction mixture is allowed to cool, and the residue, which settles to the bottom of the pot, consists of gold together with copper, lead and iron sulphates, which are insoluble in strong sulphuric acid; silver sulphate may also separate if present in sufficient quantity and the solution be sufficiently cooled. The solution is removed by ladles or by siphons, and the residue is leached out with boiling water; this removes the sulphates. A certain amount of silver is still present and, according to M. Pettenkofer, it is impossible to remove all the silver by means of sulphuric acid. Several methods are in use for removing the silver. Fusion with an alkaline bisulphate converts the silver into the sulphate, which may be extracted by boiling with sulphuric acid and then with water. Another process consists in treating a mixture of the residue with one-quarter of its weight of calcined sodium sulphate with sulphuric acid, the residue being finally boiled with a large quantity of acid. Or the alloy is dissolved inaqua regia, the solution filtered from the insoluble silver chloride, and the gold precipitated by ferrous chloride.

The silver present in the solution obtained in the sulphuric acid boiling is recovered by a variety of processes. The solution may be directly precipitated with copper, the copper passing into solution as copper sulphate, and the silver separating as a mud, termed “cement silver.” Or the silver sulphate may be separated from the solution by cooling and dilution, and then mixed with iron clippings, the interaction being accompanied with a considerable evolution of heat. Or Gutzkow’s method of precipitating the metal with ferrous sulphate may be employed.

The electrolytic parting of gold and silver has been shown to be more economical and free from the objections—such as the poisonous fumes—of the sulphuric acid process. One process depends upon the fact that, with a suitable current density, if a very dilute solution of silver nitrate be electrolysed between an auriferous silver anode and a silver cathode, the silver of the anode is dissolved out and deposited at the cathode, the gold remaining at the anode. The silver is quite free from gold, and the gold after boiling with nitric acid has a fineness of over 999.

Gold is left in the anode slime when copper or silver are refined by the usual processes, but if the gold preponderate in the anode these processes are inapplicable. A cyanide bath, as used in electroplating, would dissolve the gold, but is not suitable for refining, because other metals (silver, copper, &c.) passing with gold into the solution would deposit with it. Bock, however, in 1880 (Berg- und hüttenmännische Zeitung, 1880, p. 411) described a process used at the North German Refinery in Hamburg for the refining of gold containing platinum with a small proportion of silver, lead or bismuth, and a subsequent patent specification (1896) and a paper by Wohlwill (Zeits. f. Elektrochem., 1898, pp. 379, 402, 421) have thrown more light upon the process. The electrolyte is gold chloride (2.5-3 parts of pure gold per 100 of solution) mixed with from 2 to 6% of the strongest hydrochloric acid to render the gold anodes readily soluble, which they are not in the neutral chloride solution. The bath is used at 65° to 70° C. (150° to 158° F.), and if free chlorine be evolved, which is known at once by its pungent smell, the temperature is raised, or more acid is added, to promote the solubility of the gold. The bath is used with a current-density of 100 ampères per sq. ft. at 1 volt (or higher), with electrodes about 1.2 in. apart. In this process all the anode metals pass into solution except iridium and other refractory metals of that group, which remain as metals, and silver, which is converted into insoluble chloride; lead and bismuth form chloride and oxychloride respectively, and these dissolve until the bath is saturated with them, and then precipitate with the silver in the tank. But if the gold-strength of the bath be maintained, only gold is deposited at the cathode—in a loose powdery condition from pure solutions, but in a smooth detachable deposit from impure liquors. Under good conditions the gold should contain 99.98% of the pure metal. The tank is of porcelain or glazed earthenware, the electrodes for impure solutions are ½ in. apart (or more with pure solutions), and are on the multiple system, and the potential difference at the terminals of the bath is 1 volt. A high current-density being employed, the turn-over of gold is rapid—an essential factor of success when the costliness of the metal is taken into account. Platinum and palladium dissolved from the anode accumulate in the solution, and are removed at intervals of, say, a few months by chemical precipitation. It is essential that the bath should not contain more than 5% of palladium, or some of this metal will deposit with the gold. The slimes are treated chemically for the separation of the metals contained in them.

Authorities.—Standard works on the metallurgy of gold are the treatises of T. Kirke Rose and of M. Eissler. The cyanide process is especially treated by M. Eissler,Cyanide Process for the Extraction of Gold, which pays particular attention to the Witwatersrand methods; Alfred James,Cyanide Practice; H. Forbes Julian and Edgar Smart,Cyaniding Gold and Silver Ores. Gold milling is treated by Henry Louis,A Handbook of Gold Milling; C. G. Warnford Lock,Gold Milling; T. A. Rickard,Stamp Milling of Gold Ores. Gold dredging is treated by Captain C. C. Longridge inGold Dredging, and hydraulic mining is discussed by the same author in hisHydraulic Mining. For operations in special districts see J. M. Maclaren,Gold(1908); J. H. Curle,Gold Mines of the World; Africa: F. H. Hatch and J. A. Chalmers,Gold Mines of the Rand; S. J. Truscott,Witwatersrand Goldfields Banket and Mining Practice; Australasia: D. Clark,Australian Mining and Metallurgy; Karl Schmeisser,Goldfields of Australasia; A. G. Charleton,Gold Mining and Milling in Western Australia; India: F. H. Hatch,The Kolar Gold-Field.

GOLD AND SILVER THREAD.Under this heading some general account may be given of gold and silver strips, threads and gimp used in connexion with varieties of weaving, embroidery and twisting and plaiting or lace work. To this day, in many oriental centres where it seems that early traditions of the knowledge and the use of fabrics wholly or partly woven, ornamented, and embroidered with gold and silver have been maintained, the passion for such brilliant and costly textiles is still strong and prevalent. One of the earliest mentions of the use of gold in a woven fabric occurs in the description of the ephod made for Aaron (Exod. xxxix. 2, 3), “And he made the ephod of gold, blue, and purple, and scarlet, and fine twined linen. And they did beat the gold into thin plates, and cut it into wires (strips), to work it in the blue, and in the purple, and in the scarlet, and in the fine linen, with cunning work.” This is suggestive of early Syrian or Arabic in-darning or weaving with gold strips or tinsel. In both theIliadand theOdysseyallusion is frequently made to inwoven and embroidered golden textiles. Assyrian sculpture gives an elaborately designed ornament upon the robe of King Assur-nasir-pal (884B.C.) which was probably an interweaving of gold and coloured threads, and testifies to the consummate skill of Assyrian or Babylonian workers at that date. From Assyrian and Babylonian weavers the conquering Persians of the time of Darius derived their celebrity as weavers and users of splendid stuffs. Herodotus describesthe corselet given by Amasis king of Egypt to the Minerva of Lindus and how it was inwoven or embroidered with gold. Darius, we are told, wore a war mantle on which were figured (probably inwoven) two golden hawks as if pecking at each other. Alexander the Great is said to have found Eastern kings and princes arrayed in robes of gold and purple. More than two hundred years later than Alexander the Great was the king of Pergamos (the third bearing the name Attalus) who gave much attention to working in metals and is mentioned by Pliny as having invented weaving with gold, hence the historic Attalic cloths. There are several references in Roman writings to costumes and stuffs woven and embroidered with gold threads and the Graeco-Romanchryso-phrygiumand the Romanauri-phrygiumare evidences not only of Roman work with gold threads but also of its indebtedness to Phrygian sources. The famous tunics of Agrippina and those of Heliogabalus are said to have been of tissues made entirely with gold threads, whereas the robes which Marcus Aurelius found in the treasury of Hadrian, as well as the costumes sold at the dispersal of the wardrobe of Commodus, were different in character, being of fine linen and possibly even of silken stuffs inwoven or embroidered with gold threads. The same description is perhaps correct of the reputedly splendid hangings with which King Dagobert decorated the early medieval oratory of St Denis. Reference to these and many such stuffs is made by the respectively contemporary or almost contemporary writers; and a very full and interesting work by Monsieur Francisque Michel (Paris, 1852) is still a standard book for consultation in respect of the history of silk, gold and silver stuffs.

From indications such as these, as well as those of later date, one sees broadly that the art of weaving and embroidering with gold and silver threads passed from one great city to another, travelling as a rule westward. Babylon, Tarsus, Bagdad, Damascus, the islands of Cyprus and Sicily, Constantinople, Venice and southern Spain appear successively in the process of time as famous centres of these much-prized manufactures. During the middle ages European royal personages and high ecclesiastical dignitaries used cloth and tissues of gold and silver for their state and ceremonial robes, as well as for costly hangings and decoration; and various names—ciclatoun, tartarium, naques or nac, baudekin or baldachin (Bagdad) and tissue—were applied to textiles in the making of which gold threads were almost always introduced in combination with others. The thin flimsy paper known as tissue paper is so called because it originally was placed between the folds of gold “tissue” (or weaving) to prevent the contiguous surfaces from fraying each other. Under the articles dealing with carpets, embroidery, lace and tapestry will be found notices of the occasional use in such productions of gold and silver threads. Of early date in the history of European weaving are rich stuffs produced in Southern Spain by Moors, as well as by Saracenic and Byzantine weavers at Palermo and Constantinople in the 12th century, in which metallic threads were freely used. Equally esteemed at about the same period were corresponding stuffs made in Cyprus, whilst for centuries later the merchants in such fabrics eagerly sought for and traded in Cyprus gold and silver threads. Later the actual manufacture of them was not confined to Cyprus, but was also carried on by Italian thread and trimming makers from the 14th century onwards. For the most part the gold threads referred to were of silver gilt. In rare instances of middle-age Moorish or Arabian fabrics the gold threads are made with strips of parchment or paper gilt and still rarer are instances of the use of real gold wire.

In India the preparation of varieties of gold and silver threads is an ancient and important art. The “gold wire” of the manufacturer has been and is as a rule silver wire gilt, the silver wire being, of course, composed of pure silver. The wire is drawn by means of simple draw-plates, with rude and simple appliances, from rounded bars of silver, or gold-plated silver, as the case may be. The wire is flattened into strip, tinsel or ribbon-like form, by passing fourteen or fifteen strands simultaneously, over a fine, smooth, round-topped anvil and beating each as it passes with a heavy hammer having a slightly convex surface. Such strips or tinsel of wire so flattened are woven into Indiansoniri, tissue or cloth of gold, the web or warp being composed entirely of golden strips, andruperi, similar tissue of silver. Other gold and silver threads suitable for use in embroidery, pillow and needlepoint lace making, &c., consist of fine strips of flattened wire wound round cores of orange (in the case of silver, white) silk thread so as to completely cover them. Wires flattened or partially flattened are also twisted into exceedingly fine spirals and much used for heavy embroideries. Spangles for embroideries, &c., are made from spirals of comparatively stout wire, by cutting them down ring by ring, laying each C-like ring on an anvil, and by a smart blow with a hammer flattening it out into a thin round disk with a slit extending from the centre to one edge. The demand for many kinds of loom-woven and embroidered gold and silver work in India is immense, and the variety of textiles so ornamented is also very great, chief amongst which are the golden or silvery tinsel fabrics known as kincobs.

Amongst Western communities the demand for gold and silver embroideries and braid lace now exists chiefly in connexion with naval, military and other uniforms, masonic insignia, court costumes, public and private liveries, ecclesiastical robes and draperies, theatrical dresses, &c.

The proportions of gold and silver in the gold thread for the woven braid lace or ribbon trade varies, but in all cases the proportion of gold is exceedingly small. An ordinary gold braid wire is drawn from a bar containing 90 parts of silver and 7 of copper, and plated with 3 of gold. On an average each ounce troy of a bar so plated is drawn into 1500 yds. of wire; and therefore about 16 grains of gold cover 1 m. of wire.


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