|
BRIEF HISTORY:
Wrought Iron
dates back to
the ancient Egyptian Empire. Very small blooms of iron were produced in forges
using charcoal. In 500 BC, the
Etruscans were producing 10,000 pounds of iron per year on the western shore of
Italy using short cupolas with bellows made from animal skins to produce the air
source. Once the burn was complete,
the short furnaces made of stone were disassembled and the resulting mass of
iron and impurities were removed and further refined by heating and hammering.
The charcoal making process deforested most of western Italy.
The iron ore was brought to the furnaces on sailing ships.
The extraction method that the Etruscans used was so poor that the
tailings were mined during both world wars to produce steel.
Wrought iron was produced throughout Europe in late BC to early AD.
In the magnificent buildings of the Greeks and Romans, the stones were
held together with butterfly-shaped pieces of iron coated with lead.
The first steel was
produced by the Celts, ca. AD 200. They
cut wrought iron into small strips and stacked the strips in a wrought iron
container with burnt bone and carbon and then heated the iron in a
charcoal-fired furnace for 10-12 hours at high heat.
In the process, carbon was absorbed into the surface of the metal.
They then forge welded the pieces together and produced blades.
This was the forerunner of pattern-welded blades as we know them and
which we erroneously call "Damascus."
Damascus steel was produced in Pakistan about the same time in the form
of Wootz billets and sent to Syria to be made into Damascus blades.
As near as we can tell (since the exact process is unknown), pure iron
ore and carbon were placed in a ceramic crucible and actually melted, producing
carbon steel containing about 1.5% carbon.
The steel was very difficult to forge since it had to be worked at a red
heat. Any hotter and it would
shatter. The Celt's steel process
was copied by the Vikings and Germans to produce pattern-welded steel blades
through about 1050. From then until
about 1400, both countries produced steel blades by family-protected, secret
processes.
During that time period,
they started making their furnaces taller and taller.
At this point they were no longer producing wrought iron.
The iron finally melted, and as it ran down through the charcoal, it
dissolved some of the carbon into the iron.
The resulting iron contained 3-4% carbon, was not forgeable, and was very
brittle. It could only be used for
casted items and was not useful for blades or wagon parts.
Also during this time period, most of the forests in England and Europe
were disappearing because of building and charcoal making.
The King of England ruled at one point that the forests could no longer
be cut for making charcoal. This
forced the steel makers to come up with a process to make coke out of coal by
driving out the volatile oils.
To get wrought iron in
quantity, the English developed a puddling process; they mixed molten cast iron
with molten iron silicate and iron oxide. Iron
silicate is a component of wrought iron. They
called this coal-fired furnace a "finery."
When a worker (the rabbler) stirred this mixture, the iron oxide would
combine with the carbon forming iron and carbon dioxide.
The resulting iron had a much higher melting point and would float to the
top of the puddle. The rabbler would move the pieces into larger lumps weighing
200-300 pounds. Another worker,
using a pair of large tongs and an overhead track, would grab the pieces (called
"blooms") and place them in a press to squeeze out some of the iron
silicate. The pressed blooms would
then be run through a rolling mill and turned into muck bars.
The muck bars were cut into short pieces, wired together, and placed in a
coal-fired soak pit where they were heated to a welding heat.
The muck bars were run through the rolling mill again and turned into a
merchant bar. This process was used
not only throughout Europe but in the eastern United States as well.
To make steel, thin rolled
merchant bars were placed in a coal-fired soak pit, covered with carbon and
burnt bone, and heated at a high temperature for several days.
The carbon would be absorbed into the iron forming blister steel.
The name "blister" comes from the appearance of the bars when
they were removed from the pit-they were covered with "blisters."
The bars were then folded over and re-welded together to be used as
steel. None of the steel was of
very good quality as it had iron silicate inclusions.
England needed good quality
steel to make springs for timepieces so that their fleet could navigate the
oceans. One enterprising Englishman
noticed that glassmakers were able to get very high temperatures in their glass
furnaces. He took pieces of blister steel, placed them in ceramic
crucibles, and set them in a glass furnace.
When the steel melted, iron silicate floated out and the carbon remained,
making a good quality steel. Unfortunately
for him, too many people observed the process and he was unable to keep it
secret and thereby profit from the discovery.
This process was further developed and produced quality steel called
"cast steel" or "crucible steel."
It is still used today to produce small quantities of differing steels.
Many old tools made in the USA are marked "cast steel".
Some mistakenly believe that these tools were "cast" as the
name implies.
Steel making got its
greatest boost when the Bessemer process was developed.
There is a great argument as to whether it was invented in England or the
United States.
Wrought Iron was produced
in quantity by Beyers Steel through 1950 and was used in large construction
projects such as the Grand Coulee Dam because wrought iron is impervious to
rusting. It will only rust down to
the iron silicate and then stop.
Mixing of alloys with iron
occurred in the early 1900's when manganese, chrome, nickel, etc. were added in
gas-fired open hearth furnaces. The
progress of alloying was very slow since it is a hit-or-miss experimental
process. The real push for alloying
metal occurred during WWII when greater strength alloys were required for the
weapons of war. Since then, great
strides have been made in developing different steels.
IRON
& STEEL:
Wrought Iron:
Wrought Iron is pure iron mixed with iron silicate. When rolled through the
mills a few times, its structure takes on the characteristics of wood, having a
definite grain structure. It is forged at a yellow heat. Lower heats will result
in the metal shattering like a wood board unless it has been refined several
times. If it does split, it is easily welded together at a yellow heat. Iron
silicate acts a flux in this process. Holes drilled through wrought iron will
split out lengthwise under load. Therefore, the end where the hole is drilled
should be folded across the grain and forge welded. Since there is no carbon in
wrought iron, it will not burn like carbon steel, even at a yellow heat. Wrought
iron is no longer commercially produced. It can still be found in structures
built a century or more ago. Old bridges have been a good source of wrought
iron.
Carbon
steels:
Most carbon steels contain less than 1.5% carbon. Mild steel, as we once knew
it, was labeled 1018-1020 and contained .18% and .20% carbon respectively. Today
this is only true for steels smaller than 1/4" thick and over 4" in
width. Most of the hot-rolled steel today is made from scrap and is categorized
as A-36, having a guaranteed tensile strength of 65,000 psi. Since it contains
numerous other alloys, the carbon content can vary up to .29% at which level it
is not very suitable for forging. Metal with that carbon content develops black
hardness which results in cracking and breaking. A-36 is also made in a
continuous pour process. As a result, it contains inclusions which will cause it
to split when you work with it.
Sulfur
or Lead is added to low carbon steel to improve machineability. This is usually
found in cold-drawn mild steels and is no good for forging at all as it has a
tendency to crumble at forging temperatures. It is usually designated as 1118 or
11L18.
The
more carbon added to the iron, the stronger the tensile strength until it
becomes brittle. The optimum strength is achieved at .40% to .45% carbon. In
order to achieve hardness, the steel has to be heated to a cherry red, quenched
in warm salt brine, and then tempered.
Carbon
steels with a carbon content of .60% to 1.4% are designated as W-1, W-2, etc.
The "W" indicates that they can be hardened in water. This is somewhat
misleading as only small pieces such as chisels and punches can be safely
hardened in water. When water boils, it causes steam bubbles which result in
uneven cooling, causing cracking on larger pieces of carbon steel. Most of the
time, the coolant used is warm salt brine. With the best quench, the depth of
the hardness goes in less that 1/4" leaving the core soft. The cherry red
color of the core can be observed in a dark area with no outside lighting.
Blacksmiths of old used a blackened bucket to find this red color.
For people who
are colorblind, this temperature occurs when the steel is no longer
magnetic.
Tempering:
Once the steel is quenched, it has to be tempered using heat. This is done by
first cleaning the piece down to bright metal and then slowly heating it,
watching for the color of the metal to change. The proper temper is reached
according to the chart below and then the metal is further cooled in water.
|
Straw
yellow
|
lathe
tools, milling cutters
|
| bronze
to dark purple |
chisels
and punches |
| blue |
woodworking
tools |
| dark
blue |
springs |
Alloy steels:
Since carbon steels can only be hardened to a depth of 1/4", large pieces
of hardened steel were not available to industry. The most important alloying
metal is chrome. Chrome does two things: It allows for deeper hardening and for
increased resistance to deforming at elevated temperatures. Other metals that
improve strength and deep hardening are molybdenum, vanadium, nickel, and
tungsten. Since we now have deep hardening during quenching, we can no longer
use water or brine because the cooling is too fast and high stresses in the
metal cause cracking or breakage. We must now quench with oil or air. Quenching
oils are organic and specifically developed for quenching. Motor oil can be used
but fumes from the oil are toxic and results are not predictable since quenching
rates are unknown.
Some useful steels that blacksmiths can find at
the local junkyard:
| Car & Truck
springs--flat, round, coiled |
Referred to as 5160 which is
a chrome steel with 0.5% carbon, 1.0% manganese, 0.3% silicon, 0.6%
chrome |
| Large truck axles (for good
hammer heads) |
Referred to as 4140 which is
steel with 0.4% carbon, 1.0% manganese, 0.2% silicon, 1.0% chrome, 0.2%
molybdenum |
| Bessemer Process
(for Sir Henry Bessemer): Industrial process for the manufacture of
steel from molten pig iron. The principle involved is that of oxidation
of the impurities in the iron by the oxygen of air that is blown through
the molten iron; the heat of oxidation raises the temperature of the
mass and keeps it molten during operation. The process is carried on in
a large container called the Bessemer converter, which is made of steel
and has a lining of silica and clay or of dolomite. The capacity is from
8 to 30 tons of molten iron; the usual charge is 15 or 18 tons. The
converter is egg-shaped. At its narrow upper end it has an opening
through which the iron to be treated is introduced and the finished
product is poured out. The wide end, or bottom, has a number of
perforations (tuyères) through which the air is forced upward into the
converter during operation. The container is set on pivots (trunnions)
so that it can be tilted at an angle to receive the charge, turned
upright during the “blow,” and inclined for pouring the molten steel
after the operation is complete. As the air passes upward through the
molten pig iron, impurities such as silicon, manganese, and carbon unite
with the oxygen in the air to form oxides; the carbon monoxide burns off
with a blue flame and the other impurities form slag. Dolomite is used
as the converter lining when the phosphorus content is high; the process
is then called basic Bessemer. The silica and clay lining is used in the
acid Bessemer, in which phosphorus is not removed. In order to provide
the elements necessary to give the steel the desired properties, another
substance (often spiegeleisen, an iron-carbon-manganese alloy) is
usually added to the molten metal after the oxidation is completed. The
converter is then emptied into ladles from which the steel is poured
into molds; the slag is left behind. The whole process is completed in
15 to 20 min. The Bessemer process was superseded by the open-hearth
process. Columbia Encyclopedia, 6th edition, 2001
Encyl.
information did not appear in the
SOFA article but is added for the
reader's convenience.
|
|