Glossary of terms used in the study of ancient metal-working
Part 3 - O to R

Note
- This is the first section of the glossary to get to the completed draft stage. This is not fully checked and corrected but has almost all of the entries that will be in the final version (a few more are likely to be added while working on the other sections). Most of the links have been added but there is no guarrantee that the linked term will be more than the heading at this stage. The section S-Z will be completed next.

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

O

Off-cut
A fragment of metal cut from the main body of an artefact during manufacturing. Often fragments of sheet, rod or bar with visible cut marks. This type of material may be important evidence for the raw metal used, the type(s) of artefact produced, and/or the manufacturing process. As well being preserved in non-ferrous metal working debris, these marks can often be seen in the small fragments of iron associated with iron smithing sites.
Open Hearth Furnace
A furnace of a reverberatory type fired by producer gas and used air preheated using a pair of regenerative heaters. The use of open hearth furnaces was first patented for the melting of glass and metals by Frederick Siemens in 1856, based on the principles set out in Stirling`s patent of 1812, and Nielson's use of hot blast in the coke fire blast furnace.
The 1856 patent outlined the use of two sets of checkerwork firebrick heat exchangers through which the air flowing into, or out of, the furnace passed. One set was heated by the waste gas from the furnace, while the other (hot from a previous heating phase) was used to heat the air going into the furnace. Periodically, the control valves were changed so that the air flow thorugh the furnace and heat exchangers was reversed, the checkerwork that had been cooled by the incoming air now being heated by the exhaust gas, and vice versa.
Initially the furnaces were fuelled by coke, or other solid fuel, but the ash carried over by the air eventually blocked the checkerwork. This problem was eliminated if producer gas was used as the fuel instead of a solid fuel. A further patent in 1861 by both William and Frederick improved the furnace temperature by having a separate pair of checkerworks to preheat the gas as well as the air. Such furnaces were capable of reaching temperatures as high as 1600°C, and thus steel could be melted in them.
Open Hearth Steelmaking
In general, the term covers all methods of making steel using the Siemens Open Hearth.
Following the considerable savings in fuel costs by application of the Siemens regenerative heating method in glassmaking, steelmakers tried to apply the same method to their industry. Initially, open hearths were simply used as more efficient melting furnaces for the production of crucible steel.
In 1864, as a result of their work at Sireuil, Pierre & Emile Martin issued a British patent, through R.A. Brooman, on the melting of cast iron (pig iron) and puddled iron or steel in a Siemens open hearth. This patent described a semi-continuous method with an initial melt of cast iron, to which additional scrap steel and puddled iron or cast iron was added as required to obtain the required composition. In following the year, another patent improving on the method was issued. This outlined a batch process consisting of a single melt that resulted in the steel maker having better control of the composition of the steel. This Siemens-Martin method of steelmaking was widely used through Europe for the next 15 years. Seimens described the Siemens-Martin process as the pig and scrap process. In Britain, from 1865 to 1869 Siemens experimented and developed a method of steelmaking using the open hearth. By 1869 this had progressed to the extend that Siemens was making 75 tons of steel a week at his Landoe works, near Swansea. The method, which Siemens described as the pig and ore method, involved melting cast iron, then adding iron oxide in the form of iron ore, together with some lime and other fluxes. The iron oxide acted as a source of oxygen to decarburize the cast iron. Then as a final step before casting, -spiegeleisen was added to the molten metal it was poured into ladle to be taken to the foundry. In Britain, this was method was known as the "Siemens Open Hearth Process" (or the Acid Open Hearth Process). For further information on this topic see Barraclough 1990.

Related Terms - Basic Steelmaking, Bessemer Steelmaking, Puddling, Refining (cast iron), Steelmaking

Open mould
A form of mould for flat or long object of relatively simple shape in which the top is left open to the air. Examples of the type of object that were cast in open moulds are Bronze Age flat axes, ingot moulds of all periods, cast-iron pigs and fire-backs and probably Roman mirrors.
Order Hardening
A process which hardening of the metal occurs as result of an order-disorder reaction. It is not widely used, but may be important in some noble metals, where the effect can be used to advantage, but may also be detrimental if the metal needs to retain its flexibility.
Ordering
In binary alloys there is a preference for dissimilar atoms to surround each other. Consequently certain alloys, when slowly cooled below a critical ordering temperature, may undergo a transformation in which the atoms organize themselves into regular arrays of alternating atoms over large regions (also call superlattice).
In the gold-copper alloy system there are three ordered alloys corresponding to the compositions Au3Cu, AuCu, and AuCu3. The ordered phases are, in general, harder than the normal or equivalent dis-ordered alloy. Therefore, quenching gold alloys of these compositions from above the critical ordering temperature will keep these alloys in the soft state, rather than harden them. However, the formation of ordered structures over time may lead to embrittlement.
Ordered alloys differ from most intermetallic phases, in that they have a greater composition range and that range tends to increase with decreasing temperature. This gives their phase range in the equilibrium phase diagram a characteristic inverted U-shape.
Ore hearth
A bellows-blown low open-fronted hearth used for lead smelting, in a water-powered smeltmill. Dressed ore (galena, lead sulphide) was mixed with fuel in the hearth, and raked out intermittently onto a sloping 'work-stone' in front of the hearth to partially oxidise the ore; the lead produced in the hearth ran out though channel across the workstone into an iron pot, from which it was ladled into pig moulds. The chemistry was complex, but can be summarised as a double-decomposition between oxidised ore (lead oxide and sulphate) and unoxidised sulphide, producing metallic lead and sulphur dioxide vapour. The 'grey slag' produced was often resmelted in a separate slag hearth. The ore hearth was developed in the mid 16th century; it was partially replaced by the reverberatory furnace in the early 18th century, but remained in use in some areas till till the late 19th century -later 19th century examples developed into enclosed shaft furnaces, blown by pipes from blowing machines. The fuel was initially charcoal, but by the 18th century a mixture of peat and low-grade coal was normally used.
Orthoclase
The potassium rich end member of the alkali feldspars (KAlSi3O8) group of minerals.
Overheating
Heating a metal or alloy to such a high temperature that its properties are impaired.
Oxidation (or Oxidization)
Chemical reaction in which a metal is converted to its oxide, or from one oxidization state to a higher state (that is the equivalent of an increase in the number of oxygen atoms for each metal atom. For example, in the reactions -
2Fe + O2 = 2FeO Metallic Iron to Wüstite
6FeO + O2 = 2Fe3O4Wüstite to Magnetite
4Fe3O4 + 02 = 6Fe2O3Magnetite to Haematite
iron is progressively oxidized from the metal to its highest oxide, haematite. Another way of looking at these reactions is that oxidation occurs every time the cation (the metallic ion) gains a unit of charge, e.g. Fe2+ goes to Fe3+, or alternative that the cation loses an electron (the charge on an electron is negative - e-)
e.g.  Fe3 + e- = Fe2+

Related terms - Reduction, Valency

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
P
PGE
Platinum Group Elements;
Paktong
Corruption of Chinese 'Paitung' used for alloys containing zinc. The other elements are usually copper and nickel; this alloy is synonymous with a nickel silver or German silver.
Panning
A mineral washing process in which the lighter unwanted mineral is removed from the wanted mineral in a shallow vessel (or pan). Panning was used as a prospecting method, and for small-scale ore processing of gold deposits.
Part mould
A semi-permanent mould made of several pieces so that objects with recesses can be cast without destroying the mould each time.
Parkes' Process
The Parkes' process was a cheaper method of extracting silver from lead. An appropriate amount of metallic zinc was added to the molten impure lead. The zinc formed an alloy with the silver, which crystallized out of the melt and floated to the surface where it was skimmed off. The silver was then recovered by heating the alloy in a zinc retort where the zinc evaporated leaving the silver behind,or by dissolving the zinc in acid. The archaeology and archaeometallurgy of this process have not yet been investigated.

Related terms - Pattinson process, Zinc smelting

Parting
Noble metals can be separated from base metals by liquidation of the metal with lead, then cupellation of the lead, however, this does not separate silver from gold. To remove silver from gold a method of parting has to be used. This was by either acid parting, or the salt cementation process, and later by sulphur parting. For full discussion of the history of parting see Rampage and Craddock 2000.
Acid parting
Although weak organic acids could improve the colour of gold containing copper, these would not remove silver, so that silver-rich gold would remain a pale colour. The removal of silver required the use of strong acids (hydrochloric and nitric in particular). Acid parting only became possible when strong mineral acids became generally available. The distillation is thought to have been first used during the eleventh or twelfth centuries in Europe, although it is some evidence that they were used by the 10th century in the Islamic world.
The method is not mentioned by Theophilus, but various 16th century European metallurgical treatises and handbooks describe the method in some detail; they suggest that it was not a cost effective alternative to salt parting. However, it seems likely that it became more widely used by the end of the 16th century and during the 17th century.
Antimony Parting
See sulphur and sulphide parting.
Salt Cementation Parting
Until the discovery of strong mineral acids salt cementation parting was the main method used to refine gold. The literature would suggest that there were a number of different variations on the process, but the essentials were the use of common salt cement and the presence of alumino-silicate ceramics preferably with an appreciable iron oxide content (in the form of an earthenware container, and possibly the addition of crushed brick or earthenware powder to the salt cement).
The impure gold was beaten into thin sheets, or was granulated to produce fine grains, or was naturally in the form as an ore. The gold was interleaved with layers of 'cement' formed of either salt or a mixture of slightly moistened ground up alumino-silicate material (burnt clay - old pot or tile) and salt (NaCl) in a sealed clay vessel. On heating the salt would react with the alumino-silicates of the burnt clay together with the water or urine, used to moisten the cement, to liberate volatile hydrogen chloride or chlorine gas. This gas, in turn, reacts with the silver at the surface of gold to form volatile silver chloride (AgCl), which was absorbed by the alumino-silicate in the 'cement'.
The process had to be carried out at as high as a temperature possible to speed the diffusion process. But the temperature was limited by either the melting points of either the alloy, or of the active reagents if no carrier medium was used. If the gold alloy melted, or the temperature rose very close to its melting point, the foil would ball up. This would reduce the surface area available for attack and increase the diffusion distances, thus slowing the reaction. If no carrier material (brick or pottery dust) was used, the gold would sink through a simple salt cement if the temperature rose too close to the melting point of salt (804 oC).
At the end of the process the gold would be melted into small ingots that could be tested for purity and if found to be of low purity these could be forged into foils so that the parting process could be repeated. The spent cement would be smelted with lead, which would be cupelled to recover the silver.

Various versions of the process have been described in the ancient literature, with the addition of other salts such green vitriol (hydrated ferrous sulphate), salt-petre (potassium nitrate) in addition to common salt. However, the presence of large amounts of nitrates in the mixture would result in the loss of gold as the combination of hydrochloric and nitric acid will dissolve the gold as well as the silver.
Although widely used until the 18th century, the process was largely forgotten and the distinctive debris from the process is rarely identified, as the sherds do not have the vitrified internal surfaces typical of used crucibles. However, parting vessels do have a distinctive purple tinge due to the presence of silver chloride.

See Craddock 1995 216-219 and Bayley 2001, Rampage & Craddock 2000 for more information.

Related terms - Depletion Gilding
Sulphur and sulphide parting
Finely divided impure gold could be treated with elemental sulphur. All other metals would react with the sulphur to form sulphides. The process had to be carried out at a low temperature as sulphur is easily evaporated. The process could be carried out at higher temperatures if antimony sulphide (Sb2S3)was used. Parting using antimony sulphide was misleadingly known as the antimony process.
There is no evidence that either sulphur or sulphide parting was used in antiquity, although sulphur was reacted with a mixture of copper and silver to form niello. The advantage of sulphur parting was that it was much quicker than salt parting. It was also believed to give much purer gold, but it was a more expensive process. In addition, it was more difficult to recover the silver - the sulphide had to be treated with iron filings.

The first definite European reference to the use of sulphur refining is in Theophilus. It was used either when refined gold was required quickly, or where gold of a higher purity than normal was required, i.e. to form hollow-ware vessels.

Surprising, the first definite Islamic reference appears as late as the 14th century. Care has to taken with some translations, as some authors seem to have translated terms for sulphate compounds as sulphides (Rampage and Craddock p 36).
Patina
The surface layer formed by reaction with environment over time. However, a patina may be formed artificially by chemical means for artistic effects, or to fake an ancient appearance.
Pattern
Pattern Welding
The technique of producing a pattern on a blade or other ferrous artefact by the welding together of two or more types of iron or steel.

From the second century AD some Roman swords were made with a patterned core fabricated by twisting and welding together several rods of low carbon iron and phosphoritic iron. Steel cutting edges were then welded on to this complex composite core. The resulting complete blade would be etched to reveal the complex pattern of welds. It is likely that these blades were regarded as high status objects, considering it would have taken about 70 hours to manufacture a sword (Anstee & Biek), and that they were recorded as being given as gifts. Even so, it is likely that they were mechanically inferior to a weapon made with a plain low-carbon iron core as examination of the swords has revealed that the welds were often poorly executed, with many slag inclusions, and even voids, at the welds between the various decorative components (Tylecote & Gilmour 1986, Gilmour and Salter 1998).

In the early period the cutting edges do not appear to have been hardened, but later the cutting edges were quenched. By the tenth century the number of pattern-welded swords decreased, as swords forged from more uniform steel replaced them. Pattern welded inserts were also used in seaxs (large single edged knives) and spearheads

The technique of pattern welding reappeared much later as European craftsmen tried to imitate the patterns seen in watered-steel (Damascus Steel) artefacts made from a single piece of crucible steel. The technique was thus described as damascening, in reference to the steel swords and artefacts sold through Damascus. The technique is still used to this day to produce the intricate patterns of very high quality shotguns.

In Asia two traditions of forming patterned blades arose by development of the piling technique using dissimilar types of iron. In Japan, low and high carbon steel components were welded together, then forged out, folded and welded back on itself repeatedly, to form finely layered steel. On quenching this produced alternate layers of pearlite and martensite, which were revealed by etching and polishing. In Southeast Asia, a similar technique developed in Malaysia and Bali but in this case the patterns were formed due to the use of steel containing a little nickel (pamur). This could be from meteoritic iron from the Prambana meteorite (now in the Kraton Gardens, Surakarta), or smelted from nickel rich iron ore, possibly from Sulawesi, in the Celebes Isles, (Craddock 1995, 273)

Related terms: Damascened, Damascus Steel, Watered-Steel, Wootz

Pattinson Process
A 19th century development of the cupellation process for extracting silver from lead, depending on the principle that, when molten lead crystallises, the silver concentrates in the remaining liquid while the crystals are silver-poor. The process was conducted in a row of cast-iron pans, each holding 6-10 tons of molten lead, and heated by a coal fire. Lead was introduced to a pan at the centre of the row, melted, and allowed to cool to crystallisation point. The crystals were scooped out with a perforated ladle, and passed to the next pan in one direction, while the remaining liquid lead was ladled out to the next pan in the other direction. The process was repeated in each pan, the crystals being passed in the opposite direction to the remaining liquid, so that the silver content was progressively enriched in the liquid. The silver-rich lead from the end pan, containing up to 200-300 oz/ton, was then treated by cupellation.
The Pattinson process was gradually replaced by the Parkes' process after its introduction in 1852.
Pearlite
A constituent structure that can be found in iron containing more than 0.15% carbon consisting of alternating parallel lamellae of ferrite (Fe) and cementite (Fe3C). It forms by the eutectoid decomposition of austenite.  It is a product of slow to moderate rate cooling but may appear in conjunction with martensite and troostite, or bainite and troostite when the rate of quenching is not high enough to form the fully quenched morphology, or in regions of lower carbon content in inhomogeneous steels. Often in more slowly cooled, or reheated steels the pearlitic structure has degenerated or spheroidised to some extent.

Related term - Sorbite

Peritectic
An isothermal reaction in which one solid phase reacts with a liquid of a different composition to form a new solid phase. The new phase may consume all of the liquid to form a totally new solid. The formation of the beta phase in the bronze system is an example.
Peritectoid
A peritectoid is the solid-state version of the peritectic reaction. It is an isothermal process in which two solid phases react to form a new solid phase. For example, a peritectoid reaction occurs in the copper-tin (bronze) system, at 65% copper. On cooling from above about 580 ºC. the intermetallic Cu3Sn, and solid solution gamma, react producing a new phase, Cu4Sn.
As such solid-state reactions are largely diffusion controlled they often only occur to a limited extent, or may be completely suppressed by rapid cooling.
Pewter
Ancient pewter is an alloy of tin and lead, much used in Roman times, and from the Medieval to the 18th century. The poisonous nature of lead has resulted in the replacement of lead with antimony, although antimony is also inadvisable in high amounts for cooking utensils. Roman pewter appears to have included three different binary tin lead alloys, the groups covering the range 30 to 50%, 69% to 80% and greater than 90% tin. The first group would seem to correspond to Pliny's 50-50 alloy, but the second has a higher tin content (nearer to 3 tin to 1 lead) than Pliny's second alloy of two tin to one lead. ( Pollard 1983 and Hughes 1980)
Some Romano-British and medieval pewter has been found to contain an appreciable amount of copper (( Pollard 1983 and Brownsword and Pitt).
  Modern lead-free pewter is basically tin with variable amounts of copper and/or antimony to harden the metal or alter the casting characteristics. Such alloys may contain between 0.5-2.5% copper, and 0-10% antimony
Phase
A single component of the chemical assembly having a common physical and crystallographic state. 
For example - water, ice and steam are all different phases although they have the same chemical formula. Silver in solid solution with gold is also a single phase no matter what the composition, as there is complete solid solution between the two metals. On the other hand, copper will only dissolve to a limited extent in silver and vice versa. Thus most silver-copper alloys consist of two distinct finely dispersed phases - copper with a very little silver in solution, and silver with a little copper in solution.
Phase diagram (equilibrium)
A diagram with axes of temperature and composition describing the different phases that will be present in a chemical system or alloy at equilibrium at a given composition and temperature. A binary phase diagram consists of two elements. A ternary system consists of three elements; these are often plotted as a triangular diagram with temperature as contour lines.

Related Terms: Ternary diagram, TTT-curve

Phosphoric iron
Iron with sufficient phosphorus present to increase the hardness of the metal. As well as increasing the hardness, phosphorus also increases the rate of work hardening of the metal, and its brittleness. In 17th-18th century Britain, phosphoric iron was referred to as 'cold-short', since it tended to crack during cold forging, but was preferred for nailmaking due to its hardness. Phosphorus also increases the drawability of low-carbon wrought iron, phosphoric iron being used for the wires of musical instruments (Goodway 1999 [JHMS, 33.2, 104-5]
The presence of phosphoritic iron may be revealed under the microscope by excessive grain size (when little or no carbon is present) and/or ghost structures when some carbon is present in the metal.
Phosphorus ghosting
In metallography of iron artefacts, regions in which differential relief develops during polishing and etching due to phosphorus segregation in the ferrite. These bands, which can cross the grain structure, are often best observed by moving the sample slightly off focus.
Piece-mould
As part mould
Pig
In the earliest period of British cast iron production (16th century), one of the products of the blast furnace was a large central ingot with small ingots run off it. This was thought to look like a sow and sucking piglets. The smaller ingots were termed pigs. Now the term has been widened to apply to any similar shaped metal ingot destined to be broken up and remelted, although most commonly applied to iron and lead.
Pig boiling
See Puddling
Pig iron
Cast iron ingots: Pigs of cast iron - or more generally broken cast iron ready to be remelted. See above.
Piled (steel)
A method of improving the mechanical properties of iron and steel, in which the metal is forged out, folded back on itself and the resulting 'pile' of metal is welded together. This process may be repeated several times so that the final metal consists of many fine layers.
Piling was used to homogenise steel produced by carburising strips of iron. Because the carbon has to diffuse into the metal from the surface it is difficult to produce homogeneous steel of any great thickness. If carried out successfully the piling process reduces the final thickness of each original strip to a fine lamination, while migration of carbon at welding heat further homogenises the carbon content. Thus, although exactly the same methods are used as in damascening (forging, folding and welding) the results and aims are different. The aim was to produce a more uniform consistent structure, whereas, damascening through the use of two different types of iron or steel deliberately produces a decorative pattern. The aim of piling (although not always achieved) was to produce a macro- and microscopically homogeneous steel, whereas, the aim of damascening was to produce a steel that behaved in a uniform manner in the bulk, but was patterned on the small scale. The production of 'shear steel', the highest-quality British product before the development of crucible steel, was essentially a large-scale version of piling, though given the thickness of the blister steel bar raw material, micro-homogeneity could not be achieved (Barraclough 1984, 45-6 and 65-7).
Additional comment
Although, it is absolutely clear that some artefacts have been made by this technique, it is likely that some that been identified as having been made by this technique are, in fact, the result of either fortuitous banding, or the side effect of other parts of the manufacturing process. (In due course there will be another page added discussing problems associated with the identification of piling and weld lines).
Pinchbeck
Gold coloured brass, invented by Christopher Pinchbeck, a watchmaker of Fleet Street, London, in 1725. Probably made by melting copper and imported spelter (zinc). Later the term was widely used for all gold coloured brasses, and became a synonym for any cheap imitation. Thornton, J. 2000, 311
Placer deposits
Placer deposits form by the release of dense minerals (or metals in case of gold) by weathering of a primary ore body, and concentration by the action of water. The most important placer deposits are of gold and tin (the latter in the form of cassiterite), although locally magnetite may be concentrated in black sands sufficiently for them to be used as an ore. Often, the deposits are associated with the rivers flowing over a newly exposed landscape, rather than the present river or beach systems. Thus, the alluvial 'stream' tin deposits of Devon and Cornwall were buried several metres below the river level. As well as alluvial deposits in river and stream valleys, placer deposits include eluvial deposits weathered out from primary ores but only moved downslope by weathering and soil creep processes.
Plating
The technique of applying a thin surface layer of one metal over another for decorative, aesthetic, or anti-corrosive purposes. Plating may be applied by a number of different means -
Diffusion bonded plating
Diffusion plating involves bringing the plating metal into intimate contact with the metal to be coated at elevated temperatures, by application of pressure or by mechanical working. The main use of this technique was for the production of Sheffield Plate - silver-covered copper sheet. Diffusion bonding was also used to produce the mokume multi-layer decorative metals used in Japan.
Dip or Hot Dip
In this technique the objects to be plated were dipped in a hot bath of the molten plating metal. This technique was used in the Iron Age to simultaneously plate and braze iron horse fittings rings; examples of this technique have been found at Gussage All Saints and Maiden Castle in Dorset, and Yarnton in Oxfordshire.
Other examples of hot dipping to protect iron sheet from corrosion are tin plating and zinc-coated galvanized iron
Electro-plating
Electroplating uses an electric current to deposit the metal from solution on to the object to be plated, which acts as the cathode of the cell. The process was invented by Weiner Siemens in Germany, in 1842. His brother, Karl Wilhelm, introduced the process to Britain in 1843, where he sold it to James Elkington. This new electro-plating industry rendered the Sheffield plate industry obsolete by the latter part of the 19th century
Gilding
A method of putting a thin layer of high carat gold on a less expensive substrate. This includes a number of methods that are given in more detail in the section on gilding - Depletion gilding, Foil gilding, Leaf gilding, Mercury or fire gilding.
Vapour deposition
A modern technique in which the object to be plated is put in a vacuum chamber and the metal is thermally vaporized and deposited on the surface as a thin film. Widely used to deposit aluminium on a wide variety of surfaces.
Wiping
In this technique the metal object to be coated was fluxed and heated. The rod of the plating metal was rubbed over the areas to be plated. This technique was typically used for the decorative application of low melting point 'white' metal alloys.
Platinum
Metallic element atomic number 78, atomic weight 195.09, mp 1772 oC, specific gravity 21.45. First discovered by Western Science in South America by Ulloa in 1735, but had been used previously by the natives of Ecuador and Colombia. Finds are known particularly from La Tolita dating to the last centuries B.C. The metal is malleable and ductile, however, its high melting point, well above the temperatures attainable in any medieval or earlier furnace, made it very difficult to consolidate the native metal. Hence, the early South American artefacts were of platinum sintered with gold.
In the 19th century AD an attempt was made to establish a Russian coinage based on platinum coming from the Urals. In this case, the metal was consolidated by sintering the metal at high temperature and pressure. This early attempt at powder metallurgy was soon abandoned due to technical difficulties.
Native platinum is usually alloyed with some iron. Sometimes there is sufficient iron present for the metal to be magnetic. Platinum was used in early scientific instruments since its coefficient of expansion is very similar to soda-lime glass.
Related terms - Platinum Group Elements, PGE inclusions
Platinum Group Elements
The group of elements whose characteristics are similar to platinum, in that they have high densities and melting points, and are unreactive. These elements are iridium, osmium, palladium, rhodium, and ruthenium
Platinum Group Element Inclusions
Platinum group element inclusions occur as small silver-grey or steely coloured particles in alluvial gold. These were much harder than the surrounding gold and caused problems to jewellery makers. Osmium-iridium inclusions found in the California placer gold were used to make the hard-wearing Osmiroid pen tips until quite recently, due to their high hardness.
It has recently been realised that the classical term, adamas, must have been referring, in part, to PGE inclusions, as Pliny noted that - from Rampage and Craddock 2000, 240, referring to the interpretation of the text suggested independently by Ogden 1977 and Nicollini 1990.
Powder Metallurgy
Powder metallurgy is a set of methods used, initially, to produce metal components by sintering of pre-formed shaped powder compacts by the application of heat and pressure.
The technique was first developed to deal with refractory and reactive metals. More recently, the method has been applied to oxides and other ceramic materials. Also, it has been use to try to make alloys with finely divided and uniform microstructures which can niow be produced by any other means.
Poling
A process designed to reduce the oxygen content of molten copper. This is carried out by plunging a pole of wood into a bath of molten copper. The distillation of volatiles in the wood results in the evolution of hydrogen and other reducing gases. These, in turn, reduce any copper oxide present in the molten metal.
Polycrystalline
Consisting of many individual crystalline grains. Most metals are polycrystalline solids.
Precipitation
The process by which a minor phase or component comes out of solution due to a chemical or physical change. For example -
'Iron carbo-nitrides may precipitate as small acicular particles in ferrite subject to prolonged heating in air.'
Precipitate
A small particle of a specific metallurgical phase that has formed out of solution. For example -
'The aging of aluminium copper may harden the metal due to the formation of small coherent CuAl3 precipitates.'
Prill
A small droplet of metal that has solidified from the melt. Prills are often the result of splashes of metal lost during casting operations, or are trapped in slag during a variety of metallurgical processes but in particular smelting or assaying.
According to the Shorter Oxford Dictionary, the word originally was used in Cornwall to describe the richer pieces of copper ore remaining after the leaner ore had been removed by cobbing. Later it was used to describe the globule of metal obtained on assaying the ore by cupellation. Hence, its present wider use to describe small metallic droplets.
Proeutectoid
For an alloy with a composition away from the eutectoid composition a phase will precipitate before the eutectoid component can be described as the proeutectoid phase or component. In the case of a hypoeutectoid steel, ferrite will start to form on the austenite grain boundaries at temperature above the eutectoid temperature. This grain boundary ferrite can be described as proeutectoid ferrite to distinguish it from the eutectoid ferrite of the eutectoid pearlite.
Pseudomorph
One phase copying the morphology characteristic of another phase. Typically, as a result of corrosion, one material or phase mimics the form of the replaced original. Pseudomorphic replacement of organic materials is common on iron artefacts and can occur on copper alloys and silver/copper alloys as well.
Proeutectoid
When an alloy of composition away from the exact eutectoid composition is cooled, particles of the first phase to precipitate are described as proeutectoid. For example, on cooling a 0.6 % carbon steel from a temperature where the structure is fully austenitic proeutectoid ferrite will start growing before the eutectoid reaction produces pearlite.
Puddling
As the production of coke pig for forge use took off from the 1740s onwards, there were increasing attempts to find a cast-to-wrought iron conversion process that was larger-scale and less labour-intensive than the finery, and that obviated dependence on charcoal and water-power and the craft skill of the finers. Many of these involved attempts to use the coal-fuelled reverberatory furnace, either in conjunction with or as replacement for the finery, although, the most successful process until the late 1780s, 'stamping and potting', involved heating granulated iron (broken up by stamping) in sealed pots with decarburising fluxes. In the late 1780s, however, Henry Cort's puddling process was developed, and rapidly took over complete dominance; Cort's main innovation was the use of grooved rolls to form the decarburised iron into bars. In this process a charge of cold cast iron was melted in a reverberatory puddling furnace with a sand bed. The air draught into the furnace was then controlled to produce oxidising conditions, while the molten iron was stirred with iron tools through the furnace door. As the carbon content dropped, the iron became increasingly 'pasty', and was manipulated into large balls. These were removed from the furnace, hammered and passed through grooved rollers to consolidate the metal and form it rapidly into bars of uniform section. The mechanical working of the iron at the various stages was an important aspect of the process.
In Cort's process the cast iron reacted with silica in the sand bottom to form a fayalitic slag. This resulted in a considerable loss of metal. This so-called 'dry' puddling was later replaced by 'wet' puddling. In the wet process, the floor of the furnace incorporated iron oxide in the form of iron scale or roasted slag rich in iron oxides; also material rich in iron oxides was added as part of the charge. The effect of this was to reduce the losses of iron caused by slag formation and more importantly to aid the decarburisation as the iron oxide reacted with the carbon in the molten cast iron to form carbon monoxide. The wet process was also known as 'pig boiling' from the strength of the reaction.
(Tylecote 1992, 126-129)
Puddling furnace
A reverberatory furnace used for converting cast iron into wrought iron, using a stirring or 'puddling' action in the later stages when the iron becomes pasty.

Related terms - Cast Iron, Puddling, Refining, Wrought Iron

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Q
Quartation
Quartation is a stage in the parting process in which additional copper or silver is added to gold to be refined. The method does not seem to be extensively used until acid parting became the main method of refining silver from gold, although it use is mentioned by 16th century writers. The process is also known as graduation.
In the early accounts gold was refined by parting in the normal way, then a large amount of copper was added, and the metal parted again. Later, it became standard to add silver rather than copper.
Although, it seems counter-intuitive that the addition of extra impurities should help in refining gold, it became the standard method for acid parting. It is doubtful whether the method was particularly beneficial when used in conjunction with salt cementation, as in that case the reaction proceeded as a gas/solid phase interaction, and transport through the narrow pores formed in relatively pure gold alloys would be rapid at the temperatures involved. However, the method was helpful when salt cementation was replaced by acid parting. Because acid parting was carried out at low temperatures, it was necessary to have larger pores and shorter diffusion distances for the method to be effective. The addition of extra silver, which was subsequently dissolved by the acid, resulted in a more open and reactive structure.
Quench
The act of quickly cooling a metal or alloy by plunging it into cold water, brine or oil. In some alloy systems the effect of quenching is to form non-equilibrium meta-stable phases with very different properties from those of a more slowly cooled alloy. This is particularly important for formation of martensite in steels, but also in high tin bronzes.
In other alloy systems quenching has little effect other than preventing grain growth and additional surface oxidisation during cooling. However, in some gold alloys it can prevent embrittlement associated with the formation of ordered alloys.
The martensitic transformation occurs by a shear transform rather than a diffusion-controlled transformation, therefore, the metal is left in a highly stressed condition after a simple quench. It is normal in modern metallurgical practise to gently heat or temper steel after quenching to relieve these stresses, and adjust the metals properties to those required for its intended function.
The rate at which heat is removed from the metal is critical to the resultant properties; see Quench agitation, critical diameter, media, and severity (below) for further discussion of the topic.
Quench, agitation
The more vigorously the work piece is agitated in the quench bath, the more severe the quench will be. See Quench severity.
Quench, critical diameter
It takes longer for the temperature to drop in the centre of an object than near the surface due to the time it takes for the heat to be conducted to the surface. Considering a steel bar with uniform composition, the quench rate may be sufficient for the surface to be fully martensitic, but because the centre of the bar has cooled more slowly it may be only partially martensitic, or possibly totally pearlitic steel, depending on the diameter of the bar. The critical diameter for a given alloy is given as the diameter of a bar so that the centre of the bar has a structure of 50/50% martensite and pearlite when given an ideal quench. In practice, the critical diameter is determined by the Jominy test.
The importance of the critical diameter is that it is a measure of the hardenability of a steel. The larger the critical diameter, the easier it would be to form martensite, to greater depth, with a less severe quench. Most early steels were of low hardenability.
Quench hardening
The hardening of steel by plunging it at a red heat (the austenite field) into cold liquid such as water, brine, or oil. The structure is converted to martensite, or bainite, depending a combination of the composition of the steel and the quench rate. At lower quench rates, combinations of martensite, bainite, troostite and pearlite may form, and the relative proportion of these components that are likely to form is described by the TTT curve.
Hardenability DI
Hardenability is one of the most important properties of a steel. It is a measure of how easy it is to convert austenite to martensite on quenching. The ease of this conversion is controlled by a number of factors, the most of important of which is composition. The shape of the object in terms of the thickness of section and the grain size of the metal will also determine if the metal can be fully transformed to martensite.
Composition - the effects of
Carbon:
In ancient European steels the only element that has an appreciable effect on the hardenability of steel is carbon. At low carbon contents it is impossible to cool the metal rapidly enough for avoid the formation of pearlite (the pearlite curve on the TTT diagram is well to the left). With increasing carbon content the TTT curve is pushed to the right, so that it is possible to cool the metal without passing through a regime in which pearlite would be formed.

An additional effect of increasing the carbon content of a steel is to drop the temperature of Ms and Mf, the start and finish of the martensitic transformation. With sufficient carbon the Mf is less than room temperature, so that not all the austenite will transform on quenching. This is termed retained austenite. On tempering, this retained austenite will transform to martensite or bainite depending on the temperature. These changes can start at the same sort of temperatures required to set hot mounting thermo-resins; for this reason only cold setting resins should be used to mount samples from artefacts that may contain quenched steels.

Other elements:

Manganese (Mn), silicon (Si), nickel (Ni), chromium (Cr) and molybdenum (Mo) will all move the pearlite curve of the TTT diagram to the right, thus, making it easier to avoid the formation of pearlite before reaching the start of the martensite transformation. However, none of these elements occur in any appreciable quantity in most early western steels, although, nickel may be concentrated at weld lines up to levels of 1% or more. Some crucible steels and associated material from the Middle East and South Asia can contain low but appreciable amounts of manganese (up to 0.3%). However, this is insufficient to aid the reliable formation of martensite.
As with carbon, the addition of manganese will drop the Ms temperature. With a 1.0% carbon steel the effect of the addition of 6% manganese is to drop the Ms far below room temperature, so that the austenitic structure is effectively stable. This effect was only discovered and used in the second half of the 19th century with the discovery and production of spiegeleisen (1848). Tylecote 1992, 165.
Section thickness
For a given severity of quench, the rate at which the temperature can be reduced is a function of the thickness of the section. A thick-sectioned blade will cool more slowly than a thin one, as it will take longer for the heat of the metal at the centre to be conducted to the surface.
Grain Size
Austenite grain size has an important effect on the hardenability of steel, in that it controls the number of potential nucleation sites for pearlite. Pearlite prefers to nucleate on the austenite grain boundaries and grow out into the centre of the austenite grain. Steel with a small grain size will have a much greater area of austenite grain boundary per unit volume than one with a larger grain size. Thus, the probability of pearlite formation and growth in the time it takes to cool the steel to the Ms temperature is much higher for a fine-grained steel than one with a larger grain size. That is, it is more difficult to harden a fine-grained steel than a coarse grained one.
Related terms: Grain size, Control of grain size
Quench, Media
Brine
Brine will give a more severe quench than pure water as the additions of salt will increase the boiling point of the liquid thus preventing the thermal insulating effect of a layer of steam for longer. However, when boiling does occur it is as a series of small explosions in the liquid close to the metal, resulting in the violent agitation of the liquid
Oil
Oil is more viscous than either brine or water, therefore, the surface bubbles formed at the surface of the hot metal are much more difficult to remove. With a slower cooling rate the quench is likely to be more even than in the case of pure water.
Water
Water was widely used to quench metals as it is widely available and has a very good thermal capacity (the ability of a given weight of the material to absorb heat). However, when a piece of steel is plunged into water, the water at the surface boils generating a layer of poorly conducting steam. As some areas will act as nucleation centres for steam bubbles, these will cool more slowly than other adjacent regions, resulting in an uneven microstructure.
(Reed-Hill, 1973. 708-709)
Quench, severity
The medium in which an object is quenched, and the degree of the movement of the metal in the medium control the rate of cooling. The rate of cooling, the H value is given by the table below. By measuring the critical diameter of test piece, the H value and using charts it is possible to calculate the ideal critical diameter for that material - that is a measure of its hardenability.

H ValueQuench conditionsAgitation
0.20Poor Oil QuenchNone
0.35Good Oil QuenchModerate
0.50Very Good Oil QuenchGood
0.70Strong Oil QuenchViolent
1.00Poor Water QuenchNone
1.50Very Good Water QuenchStrong
2.00Brine QuenchNone
5.00Brine QuenchViolent
Infinity Ideal Quench 

Quench, Slack
A slack quench is one in which not all the structure was converted to the quenched microstructure. In the case of steel, this means that the quenched structure was not fully martensitic, but there may be some ferrite or pearlite present.
A slack quenched structure may be deliberately produced by the use of a delayed or interrupted quench. On the other hand, a piece of steel may have been accidentally slack quenched due to the carbon content being lower than anticipated, and hence it becomes impossible to quench the metal in that particular thickness of section quickly enough to produce a fully hardened structure.
Not all non-fully martensitic structures are slack quenched as in very high carbon steels, where Mf can drop to well below room temperature, resulting in even fully water quenched micro-structures retaining some austenite.
Quenched structures
Non-equilibrium metastable structures or phases formed by quenching in water or oil. The most common quenched products are martensite and bainite in steels and martensite in high-tin bronzes. Quenching may also be used to suppress ordering reactions, especially in gold alloys, and some ancient texts refer to this practice to avoid embrittlement.
Quern stones
In archaeometallurgy, stones used for grinding ore preparatory to dressing or smelting, or for grinding slag to release trapped prills of metal.
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

R

Rabble
An iron rod bent at the end used to stir the molten cast iron during puddling, to ball up the refined iron produced in the process into blooms. The blooms would then be forged and rolled into bars of wrought iron.
Probably, the term originally came from the French word - râble , meaning rake. It was first used to describe the shovel used by charcoal burners to tend the covering of the burning charcoal clamp, and was later applied to puddling.

Related Terms - Puddling, Refining (cast iron)

Raising
The method of producing hollow-ware (dishes and bowls etc) by hammering an initially flat sheet of metal over a curved stake. In raising the metal is struck on the convex side of the form with a curved faced-hammer compressing and thickening the walls of the vessel as the overall diameter of the vessel is reduced and the edges are 'raised' above the centre. The diameter of the initial blank is much larger than the diameter of the finished article; typically the starting blank has a diameter equivalent to the combined dimensions of the average diameter and the height of the finished form and is of relatively thin sheet. The thickening of the metal at the rim is often increased further by caulking the edge. So that, starting with a 0.9 mm thick blank the rim may end up 2 to 3 mm thick, and the vessel is less likely to distort during use.
The raising process is usually preceded by a `blocking out` or `hollowing` process in which the sheet is forged into a shallow dish-shaped form by hammering from what will become the inside of the vessel against a concave depression in a wooden block.

Related Terms: blocking, caulking, dishing, hollowing, sinking

Reaction Solder
A method of soldering gold in which the joint was covered with a mixture consisting of powdered copper compound, such as azurite, malachite or chrysocolla, and an organic compound, then heated. The carbon rich compound reduced the copper in the mixture to metallic copper. This copper dissolved in the gold forming a small region on the surface of the join with a lower melting point. If the temperature was high enough a solder (metal-liquid-metal) joint would form. Prolonged heating would result in the copper diffusing into the body of the gold, leaving little or no external evidence of the use of solder. The technique was extensively used to produce Anglo-Saxon gold jewellery.

Sometimes the technique is misleadingly called diffusion soldering - the solid-state diffusion of copper away from the join is a secondary effect.

Related Term - brazing, diffusion bonding, solder

Reamer
A tool for cleaning out a hole bored by a drill, auger, or cast-in, in the case of hollow-cast objects. Iron cannon were cast hollow until the 18th century, and finished by reaming the bore; a reamer with steel-edged cutters has been recovered from Stream furnace, Sussex
Recovery
The mechanical deformation (cold working) of a metal will increase its strength, hardness, and electrical resistance, and will decrease its ductility. Recovery is the term used to describe the tendency for these properties to recover to the original values without any obvious change to the deformed crystal grain structure. This may occur slowly at room temperature, or more quickly as the temperature is increased.
Recovery is the first stage of the annealing cycle after cold working. It occurs before recrystallization and grain growth. It occurs, largely, through the elimination or rearrangement of the vacancies and dislocations introduced into the crystal lattice of the metal during working. Many of these processes follow an Arrhenius type law. That is, they are time-temperature dependent with the rate of recovery increasing with temperature in an exponential manner.
Related terms - Annealing, Arrhenius, Cold working, Dislocation, Ductility, Dynamic Recovery, Grain Growth, Hot Working, Recrystallization, Vacancy
Dynamic Recovery
Dynamic recovery occurs when a recovery type process occurs during deformation. It is often strongly temperature dependent and may extend the deformation possible with some metals. But recrystallization, which occurs at higher temperatures, is the main process that occurs during hot working.
Recrystallization
Generally, a change from one grain structure to another with a lower overall energy, without a change in crystal type. Recrystallization normally occurs during an anneal after cold work, as it softens the metal so that further working mechanical deformation can occur in the next cycle of cold work. It is also the main mechanism by which the mechanical properties of the metal recover during deformation in hot working.
    Recrystallization is a nucleation and growth process, that is, it is temperature controlled. In pure metals the rate of recrystallization may become measurable at temperatures as low as a third of the absolute melting point of the metal (0.3Tm). The presence of small quantities of solute atoms can have a marked effect on the recrystallization temperature; for example the addition of 0.01 atomic percent tin to high purity copper will raise the recrystallization temperature by 180oC. With alloys the recrystallization temperature is typically 0.5Tm
    The final recrystallized grain size, for a given temperature, is a function of the number of nucleation centres and the length of time that recrystallization and grain growth has been possible, and the density of pinning features such as second phase precipitates or inclusions. Nucleation occurs in the regions of high lattice strain. These are near slip-line intersections, deformation twin intersections, and the original grain boundaries. The number of these features will increase with increasing deformation, but at low strain there will be very few sites with sufficiently high dislocation density to form nuclei for new grains. Thus the recrystallized grain size tends to decrease with increasing deformation as nucleation predominates over growth, whereas at low strains with few nucleation centres grain growth predominates.
   The aim of a recrystallization anneal is to complete primary recrystallization but to keep the grain size as small as possible, as large grain sizes are detrimental to the mechanical properties of metals.

Recrystallization - critical strain
Below a critical strain, no or very few nucleation centres will be created. Annealing metal that has not been deformed beyond the critical strain will result in detrimental secondary recrystallization.
Recrystallization - Primary
Primary recrystallization is the term used to describe the replacement of the original deformed grains with new grains. It is complete when all the deformed original grains have been replace by new strain-free grains.
Recrystallization - Secondary
Once primary recrystallization is completed continued annealing, or annealing at higher temperature than intended, will result in a second wave of grain growth with some of the grains with favourable orientations growing at the expense of others. In general, large grains will grow at the expense of smaller. It is possible that boundaries of these grains will not stopped by inclusions and second phases in the way that grains are during primary recrystallization resulting in abnormally large grains.
Recrystallization - Temperature
As recrystallization is a thermally activated process, the rate of recrystallization roughly doubles with every 10oC. So there is not, in fact, a fixed temperature at which recrystallization starts, but because the process is so strongly temperature controlled, below a certain temperature primary recrystallization is never completed. The recrystallization temperature is usually defined as the lowest temperature at which primary recrystallization is completed in a reasonable time (typically 1 hour).

Related terms - Annealing, Grain Growth, Grain Size, Recovery, Strain
Red Heat
See Heat - red
Reduction
Chemical reaction in which a metal is transformed from its oxide or sulphide to the metallic form, or from one oxide to another with a lower number of oxygen atoms for each metal atom. For example the series of transformations -
6Fe2O3 = 4Fe3O4 + 02 Haematite to Magnetite
2Fe3O4 = 6FeO + O2 Magnetite to Wüstite
2FeO = Fe + O2 Wüstite to Metallic Iron
the oxides of iron (going left to right) are successively reduced through to metallic iron. Each individual stage is still a reduction, eg Magnetite to Wüstite even when both reactant and the products are oxides.
Another way of looking at reduction is that it occurs when a cation (the metallic ion) loses a unit of charge, e.g. Fe3+ goes to Fe2+, or alternatively that the Fe ion gains an electron (the charge on an electron is negative - e-)
Fe3 + e- = Fe2+

Related terms - Oxidization, Valency

Refining
Refining is the separation of a metal from its impurities. As such it is applied to a wide range of different processes for the different metals.
Copper
The copper that was produced by the last stage of the smelting process was, in general, rather impure (black copper with copper content as low as 90%). This had a high iron content, which would have to be reduced by two stage refining process if the copper was to be useable for most purposes. This was done by first an oxidizing process to convert the metallic iron in the metal to iron oxide (usually magnetite), and then a reducing process (poling) to remove the excessive amount of oxygen introduced by the iron removal stage.
Refining black copper
The magnetite would float on top of the metal where it could either be slagged by the addition of silica and tapped off, or the pasty magnetite could be physically scrapped off the top of the liquid metal to form a high magnetite smithing hearth bottom type slag. Unfortunately, the tapped refining slag would be difficult to distinguish from other of copper smelting slags, or even iron smelting slag - however the presence of a significant amount of partially digested crushed quartz fragments is often an indicator of a copper smelting or refining slag.
The high magnetite smithing hearth bottoms, or skulls, have been recorded rarely from archaeological contexts. This is almost certainly because the number of sites on which refining occurs would be limited as -
  • Either the slag would be produced on the original smelting site, where the small amount of such slag produced would be swamped by the much large amount of 'normal' smelting slag. Thus not easily recovered and recorded.
  • Or the refining occurred away from the smelting site, that is, the copper was traded as black copper ingots. In this case, the slag might be mistaken as a slightly unusual iron smithing slag.
Poling
This was the final stage of the refining process designed to reduce the oxygen content of copper to a reasonable level. It was carried out by plunging a pole of wood into a bath of molten copper this produces hydrogen and other reducing gases by the distillation of the wood. These in turn reduce any copper oxide present.
Alloying copper with tin or zinc would also deoxidise the metal but at the expense of loss of expensive alloying element to slag or vapour. It is, therefore, more economical to pole the metal before alloying.
Silver
The main method of separating silver from the majority of its impurities was by cupellation of the impure metal with lead. However, cupellation would not separate gold from silver.
Gold
Cupellation
Cupellation was used to separate gold from those alloys containing copper but as silver is not oxidized during the cupellation process, it would not separate gold from silver. Thus, if high purity gold was required for jewellery, or coinage the metal would have to be further refined by parting.
Mercury amalgam refining
In the classical period mercury amalgamation refining was used to recover and refine gold from worn out gold embroideries and gold leaf gilding. Gold dissolves in the mercury to form a pasty amalgam. The majority of the mercury was remove by squeezing the mixture chamois leather leaving the amalgam behind. The gold was then recovered by heating amalgam so that the remaining mercury was lost by evaporation.
The same technique was later used to recover finely divided gold from crushed ore.
Parting
To get rid of silver from gold it was necessary to use a parting technique. The earliest of the heated the impure gold with salt in combination with other chemicals to convert the silver to silver chloride which diffused out of the metal. This method appears to be first used to produce the gold for the Lydian coinage produced at Sardis in the 6th century BC (Rampage and Craddock 2000).
Later other parting methods were used to treat impure gold alloys; these included acid, and the antimony or sulphide parting.

Relate term - Parting
Iron
Bloomery iron and steel did not undergo a specific refining process other than by forging and possibly folding and welding to break up the slag inclusions and homogenize the metal.
However, as the major use of iron was in the malleable form, the majority of cast iron was (re)fined to wrought iron by oxidizing carbon, and when present the silicon, out of the metal. Initially in Britain, this was carried out in the finery forge using the Walloon process where both a finery and chafery hearth were used. After Henry Cort's use of the reverberatory furnace to convert the iron and grooved rolls to convert the resultant bloom to bar, the puddling process generally replaced the finery forge.
Refinery
The refinery was a separate hearth used to convert grey cast iron into white cast iron prior to its conversion to wrought iron in the finery and chafery.
   With the introduction of the coke fired blast furnace the silicon content of cast iron increased. This resulted in the production of grey cast iron rather than white, as was normally the case with the charcoal-fired blast furnace. Grey cast iron was more difficult to refine, because the silicon had to be oxidized before the carbon could be removed. The carbon in grey cast iron was in the form of graphite was more difficult to oxidize than when it was combined with iron in the form of cementite, as in white cast iron. To solve this problem, an additional step in the fining process was added, in which the grey cast iron was heated under oxidizing conditions until the silicon was removed and the metal was converted to white cast iron.

Related term - Chafery, Finery, Puddling, Running-out fire

Refractory
The term either describes the heat resisting properties of a material, or the heat resistant objects such as tuyeres, crucibles, and furnace and hearth linings. A refractory material must have the following properties.

A high melting point
It is likely that much of the history of metallurgy has been controlled by the improvement of the properties of refractories. Although most copper alloy metallurgy can be carried out in the temperature range in which common clay-base refractories are adequate, the same is not true for the production of steel and cast iron.
Chemically inert with respect to the charge
At high temperatures the slag produced can attack some furnace linings extremely aggressively. This was particularly true in the 19th and 20th centuries with the development of the basic steel making. The normal silica refractories were attacked and destroyed rapidly by the basic (calcium-rich) slag needed to reduce the phosphorus content of the steel.
Mechanical strength and dimensional stability at high temperatures.
In the case of crucibles, the material must be able to support the weight of the molten metal and be able to be picked up without excess deformation at the pouring temperature. In the case of furnace linings they must be able to support the weight of the material above them without slumping.
Thermal shock resistance
Crucibles, in particular, have to with stand large thermal shocks when the crucible is removed from the furnace for pouring. Furnace linings have to withstand thermal stresses imposed by thermal gradients within the furnace lining.
Thermal conductivity
Ideally crucibles and muffles should have high conductivity, whereas, furnace linings should have low conductivity. However, conductivity of crucible refractory was not factor that would have been considered important until recently, the other factors being much more important. Similarly, for furnace linings the requirement for low thermal conductivity was not an overriding factor, although reducing the overall thermal losses through the furnace walls would have been important.
The difference between the thermal conductivity of modern refractories and those used in the past has not always been considered in some experimental reconstructions of early smelting processes. The use of different refractory materials can have a major effect on the thermal losses and thus on the blowing and rate of fuel use required to run a smelt.

The earliest refractories were made from local clays. These may have been modified to improve their properties usually by the addition of quartz rich sand, but where available graphite was used. Eventually, some clays (high kaolin fire-clays) were discovered to make particularly good refractories. So that production became centralized in a few centres and the crucible exported over large distances as is shown by the import of large number of Hessian crucibles, manufactured in what is now Germany, into England during the 17th and 18th centuries. The introduction of the blast furnace required the use of refractories with high silica content to withstand the higher temperatures involved. These were either in the form of natural high purity sandstones with low iron content, or later silica bricks that contain more than 96% silica. To deal with basic slag or higher temperatures refractories based on magnesite MgO or dolomite (Ca.Mg)CO3 were used.
Regenerative Heating
A regenerative heater was a fuel saving device fitted to a furnace, consisting of two sets of chambers filled with a checker-work of firebricks. One chamber is heated by the hot waste gas from the furnace, while the other, heated in the preceding cycle, is used to heat the incoming cold air and gas(fuel). After a period the air flow through the furnace and chambers is reversed, so that the chambers change their rôles.
The idea was based on the idea patented by Stirling in 1812, and fully developed by Frederick Siemens between 1856 and 1861. The earlier versions used coal and other solid fuels, but there was a tendency for the ash carried over by the airflow to block the firebrick checkers. The use of producer gas as a fuel eliminated this problem. The use of regenerative heaters allowed the furnaces, both to run using less fuel, and at higher temperatures.
William Siemens applied the use of the regenerative heater to steel making and developed the Open Hearth method of steel making, which was used extensively in Britain

Related term - Hot blast

Relief Polishing
During sample preparation for metallography, there is a tendency for the softer phases in a sample to be preferentially removed by the abrasive paste. Normally this effect is not wanted, but may be helpful in revealing phosphorus ghost structures in phosphoritic irons.
Repoussé
A design is raised on the front side of the metal by hammering from the back surface. The front side is supported with a soft material such as pitch during the repoussé stage, so that large areas of metal compared with the thickness of the sheet was deformed (unlike chasing).
Related terms - Chasing, Tracer.
Retained Austenite
With high-carbon steels the Mf temperature can be reduced to well below ambient temperatures. If such a material is not tempered after quenching, some of the structure will remain as austenite. Retained austenite is rarely seen in examples of archaeological or historical steels as most early steels are either not quenched sufficiently fast, or are tempered. However, retained austenite has been observed in a few Medieval Iranian ultra-high carbon steels.
Retort
A vessel with a long turned down neck used to distil materials by volatilisation. Originally, applied to chemical apparatus, but also furnaces in which metals were purified or smelted by volatilisation - mercury and zinc. The term was also applied to the oven in which coal gas was heated to produce coal gas and coke.
Reverberatory furnace
The name comes from the verb, to reverberate - to beat back or reflect, thus, a reverbatory furnace is one in which the flame or heat is reflected back on to the charge.
This has the effect that fuel is separated from the charge as the heat is reflected down onto the charge from the roof. The furnace is of the induced draught type with a tall chimney at one end and a firebox at the other. It needs a long-flame fuel such as coal or wood (not charcoal or coke) to transfer the heat towards the near-horizontal roof. Used for remelting cast iron, bronze and bell metal. Often known as an 'air furnace' and latterly used for puddling, steel-making and non-ferrous smelting.
Riser
When metal is poured into a mould air has to be displaced. A riser is a vent that lets out any trapped air, and thus, allows the metal to enter the mould more easily. Generally, situated on the opposite side of the mould from the feeder. When the metal is seen in the riser, pouring is stopped. The use of risers appears to be a late development in casting technology as the is no evidence for the use of risers with early stone and metal moulds, or clay investment or part-moulds.
Comment The introduction of the use of risers must have been associated with the development of large castings requiring the use of casting pits. However, although the feeder arrangement of moulds is often discussed in the archaeometallurgical literature, the use of risers is rarely discussed or illustrated.
Riveting
The method of joining metal sheets by metal pegs passing through aligned holes previously cut in the sheets and hammering down the ends. Riveting can be performed hot or cold. The term hot or cold referring to the temperature of the rivet when it is closed. The advantage of hot riveting being that the joint is tightened further by the thermal contraction of the rivet on cooling.
Rolling
The hand-powdered rolls were first used to emboss narrow strips for coins and to flatten and thin soft metals like gold and lead. But the development of the machinery capable of thinning work hardening metals and alloys required the improvement of the materials for the rolls and the their supporting structures as well as the increased power available in the post-medieval period.
It is likely that the early rolling mill technology came from the sltting mill, and Tylecote 1990 (249) quotes C.S. Smith's reference to the earliest description of a rolling mill of 1568 for the preparation lead window 'cames'. Clearly the use of rolls to form metal was of interest at this period, as in 1496 Leonardo da Vinci drew a design for a rolling mill.

Related terms - Slitting

Roasting
Another term used for the heating of materials either in open heaps or simple kilns. Ores may be roasted either under oxidising conditions, or very limited reducing conditions. Roasting was used to drive off water (both any chemically combined water, as well as any general dampness), decompose carbonates, and break up the ore to make it more permeable to gases. Roasting may be used to partially convert sulphides to oxides prior to forming a matte.

Related terms - Calcine, Dead Roast.

Rockwell Hardness Test
The Rockwell hardness testing method uses either a steel ball (Rockwell B) or a diamond cone having an angle of 120o (Rockwell C). It is used for rapid testing but the results are not directly comparable to Vickers Pyramid numbers. A disadvantage of the Rockwell test is single test-head cannot be used over the whole range of materials from soft copper and brass to very hard materials such as nitrided surfaces.
Related Terms - Brinell Hardness, Vickers Pyramid Number
Runner
In a casting the runner is a passage connecting the sprue to the ingate of the mould. A runner is normally horizontal or near horizontal, and helps control the flow of the metal into the mould.
Related terms - Cope, Drag, Feeder, Gate, Riser, Sand Casting, Sprue
Running-out fire
The introduction of coke-fired blast furnace meant that the iron produced had a higher silicon content than was the case with the charcoal-fire blast furnace. As silicon is more reactive than carbon, it protects the carbon from oxidization until most of the silicon has been removed, and thus extending the time required to complete the refining process. In addition, high silicon cast irons tend solidify as grey cast iron rather than white. Grey cast iron is more difficult to convert than white iron. The running-out fire was a method of overcoming these problems. It was a hearth into which the liquid iron from the blast furnace could be tapped. It had a series of tuyeres that blew air down on to the surface of the pool of metal oxidizing the silicon to slag; the resulting low silicon could then be converted as before.
Related terms - Finery, Puddling, Refinery.
Rutile
Titanium dioxide. TiO2. A common accessory mineral in many rocks, in particular it is associated with placer magnetite iron ores.
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

This first draft completed 9th January 2005
Minor updates 13th November, 2005

Terms added, pattern, 1-01-06, definition to be completed.

Chris Salter, Oxford Materials Characterisation Service.

Comments, and suggestions for additions, may be sent to Chris Salter, Oxford Materials Characterisation Service, Oxford Materials, Sandy Lane, Yarnton, Oxon, OX5 1PF, UK.