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These alloys can be further divided into wrought and cast alloy categories, as shown in Table 2.21.1. The
compositions and physical properties of selected wrought copper alloys are given in Table 2.21.2. Copper
and copper alloys are generally classified using a five-digit number according to the unified numbering
system (UNS). Copper alloys C1XXXX to C7XXXX are wrought alloys, and C8XXXX to C9XXXX are cast alloys.
Therefore an alloy manufactured in both wrought and cast forms can have two numbers depending on the
method of manufacture.
The physical properties of copper alloys, such as the melting temperature range, coefficient of thermal
expansion, and the electrical and thermal conductivity, are important for welding, brazing and soldering.
The thermal conductivities of copper and copper alloys shown in Table 2.21.2 indicate that the addition of
alloying elements drastically decreases the conductivity of copper alloys. The conductivity will significantly
affect the welding procedures used for the alloy.
Electrolytic tough-pitch coppers contain minimal impurities and between 0.02 and 0.05% residual oxygen.
It is commonly used for roofing, gutters, downspouts, automobile radiators and gaskets, kettles, vats,
pressure vessels, and distillery and other process equipment. The oxygen in oxygen-bearing copper is
usually present in the form of eutectic cuprous oxide (Cu2O) globules throughout the wrought forms.
Although this condition does not affect mechanical properties or conductivity, it makes ETP copper
susceptible to embrittlement when heated in the presence of hydrogen. Hydrogen rapidly diffuses into the
metal, reducing the oxides and forming steam at the grain boundaries. The metal will rupture when
stressed. When oxygen-bearing coppers are heated to high temperatures, the Cu2O tends to concentrate
in the grain boundaries causing a major reduction in strength and ductility. After working and annealing,
the interdendritic network is destroyed, and the strength is improved. Fusion welding of oxygen-bearing
copper for structural applications is not recommended. Embrittlement will be less severe with a rapid
solid-state welding process such as friction welding. Appropriate silver brazing procedures and soft
soldering can be used successfully to join oxygen-bearing copper.
b
Relative Weldability
Melting
UNS No. Alloy name Nominal composition, % thermal
point, °C a
GTAW GMAW SMAW
conductivity
OCF and ETP coppers
C10200 Oxygen-free copper (OFC) 99.95 Cu 1083 100 G G NR
C11000 Electrolytic tough-pitch copper (ETP) 99.9Cu-0.04O2 1083 100 F F NR
Deoxidised coppers
C12000 Phosphorus-deoxidised copper, low P (DLP) 99.9Cu-0.008P 1083 99 E E NR
C12000 Phosphorus-deoxidised copper, high P (DHP) 99.9Cu-0.02P 1083 87 E E NR
Beryllium coppers
c
C17500 High-conductivity beryllium copper, 0.6% 96.9Cu-0.6Be-2.5Co 1068 53-66 F F F
c
C17000 High-strength beryllium copper, 1.7% 98.3Cu-1.7Be 982 27-33 G G G
c
C17200 High-strength beryllium copper, 1.9% 98.1Cu-1.9Be 982 27-33 G G G
Low-zinc brasses
C21000 Gilding, 95% 95Cu-5Zn 1066 60 G G NR
C22000 Commercial bronze, 90% 90Cu-10Zn 1043 48 G G NR
C23000 Red brass, 85% 85Cu-15Zn 1027 41 G G NR
C24000 Low brass, 80% 80Cu-20Zn 999 36 G G NR
High-zinc brasses
C26000 Cartridge brass, 70% 70Cu-30Zn 954 31 F F NR
C26800 Yellow brass, 66% 65Cu-35Zn 932 30 F F NR
C28000 Muntz metal, 60% 60Cu-40Zn 904 31 F F NR
Tin brasses
C44300 Admiralty brass 71Cu-28Zn-1Sn
d 934 28 F F NR
C46400 Naval brass 60Cu-39.25Zn-0.75Sn
d 899 30 F F NR
Special brasses
C67500 Manganese bronze A 58.5Cu-39Zn-1.4Fe-1Sn-0.1Mn 888 27 F F NR
C68700 Aluminium brass, arsenical 77.5Cu-20.5Zn-2Al (0.06As) 971 26 F F NR
Nickel silvers
C74500 Nickel silver, 65-10 65Cu-25Zn-10Ni 1021 12 F F NR
C75200 Nickel-silver, 65-18 65Cu-17Zn-18Ni 1110 8 F F NR
C75400 Nickel-silver, 65-15 65Cu-20Zn-15Ni 1077 9 F F NR
C75700 Nickel-silver, 65-12 65Cu-23Zn-12Ni 1038 10 F F NR
C77000 Nickel-silver, 55-18 55Cu-27Zn-18Ni 1054 8 F F NR
Phosphor bronzes
C50500 Phosphor bronze, 1.25% E 98.7Cu-1.3Sn (0.2P) 1077 53 G G F
C51000 Phosphor bronze, 5% A 95Cu-5Sn (0.2 P) 1049 18 G G F
C52100 Phosphor bronze, 8% C 92Cu-8Sn (0.2P) 1027 16 G G F
C52400 Phosphor bronze, 10% D 90Cu-10Sn (0.2P) 999 13 G G F
Aluminium bronzes
C61300 Aluminium bronze D, Sn stabilised 89Cu-7Al-3.5Fe (0.35Sn) 1046 14 G E G
C61400 Aluminium bonze D 91Cu-6/8Al-1.5/3.5Fe-1Mn max 1046 17 G E G
C63000 Aluminium bonze E 82Cu-10Al-5Ni-3Fe 1054 10 G G G
Silicon bronzes
C65100 Low-silicon bronze B 98.5Cu-1.5Si 1060 15 E E F
C65500 High silicon bronze A 97Cu-3Si 1027 9 E E F
Cupronickels
C70600 Copper nickel, 10% 88.6Cu-9/11Ni-1.4Fe-1.0Mn 1149 12 E E G
C71500 Copper nickel, 30% 70Cu-30Ni 1238 8 E E E
a
Based on the thermal conductivity of C10200 as 100. Carbon steel has a conductivity of 13 on this scale.
b
E = excellent, G = good, F = fair, NR = not recommended.
c
In the precipitation-hardened condition.
d
Alloys C44300 and C46500 contain a nominal amount of 0.06% As; alloys C44400 and C46600 a nominal amount of 0.06% Sb; and alloys
C44500 and C46700 a nominal amount of 0.06% P.
• Brasses:
Brasses are essentially alloys of copper and zinc, with small amounts of other elements such as lead, tin or
aluminium. Variations in composition will result in the desired colour, strength, ductility, machinability,
corrosion resistance, or a combination of such properties. The portion of the Cu-Zn phase diagram
applicable to commercial brass alloys is shown in Figure 7.1. The solubility of zinc in the FCC α-phase
increases from 32.5% at 903°C to about 39% at 454°C. The β-phase is BCC and undergoes ordering,
indicated by the dot-dash line in Figure 2.21.1. The ordering reaction is so rapid that it cannot be
prevented by quenching. The addition of zinc to copper increases both the strength and ductility of the
alloys. The best combination of strength and ductility is obtained in 70Cu-30Zn brass.
− Alpha brasses: The alpha brasses contain up to 36% Zn and possess relatively good corrosion resistance
and working properties. The colour of alpha brass varies from red to yellow according to the copper
content. The yellow alpha brasses (20 to 36% Zn) combine good strength with high ductility and are
suited for drastic cold-working operations. These brasses are susceptible to stress corrosion cracking
(season cracking) after cold-working, particularly in ammonia atmospheres, and to dezincification. The
most widely used yellow alpha brasses are cartridge brass (70Cu-30Zn) and yellow brass (65Cu-35Zn).
• Bronzes:
The term bronze was originally applied to copper-tin alloys, however, the term is now used for any copper
alloy, with the exception of copper-zinc alloys, that contain up to approximately 12% of the principal
alloying element. Commercial bronzes are primarily alloys of copper and tin, aluminium, silicon or
beryllium. In addition they may contain phosphorus, lead, zinc or nickel.
− Tin bronzes: The tin bronzes are generally referred to as phosphor bronzes since phosphorus is always
present as a deoxidiser in castings. The usual range of phosphorus contents is between 0.01 and 0.5%,
and that of tin between 1 and 11%. The copper-rich portion of the Cu-Sn phase diagram is shown in
Figure 2.21.2. The β-phase forms as a result of a peritectic reaction at 798°C. At 586°C, the β-phase
undergoes a eutectoid reaction to form the eutectoid mixture (α+γ). At 520°C, γ also undergoes a
eutectoid reaction to (α+δ). The diagram also predicts the decomposition of the δ-phase, but this
reaction is so sluggish that the ε-phase is nonexistent in commercial alloys. There is a considerable
decrease in the solubility of tin in the α-phase. The precipitation of the δ- or ε-phases due to this
change in solubility is so slow that, for practical purposes, the solvus line is as indicated by the vertical
dotted line. The phosphor bronzes are characterised by high strength, toughness, high corrosion
resistance, low coefficient of friction, and freedom from stress corrosion cracking. They are used
extensively for diaphragms, bellows, bushings, clutch disks and springs. Zinc is sometimes used to
replace some of the tin. The result is an improvement in the casting properties and toughness, with
little effect on the wear resistance. Lead can be added to tin bronze to improve machinability and wear
resistance.
− Silicon bronzes: The copper-rich portion of the Cu-Si phase diagram is shown in Figure 2.21.3. The
solubility of copper in the α-phase is 5.3% at 852°C, and decreases with temperature. The eutectoid
reaction at 554°C is very sluggish, so that commercial silicon bronzes, that generally contain less than 5%
silicon, are single-phase alloys. Silicon bronzes are the strongest of the work-hardenable copper alloys.
They have mechanical properties comparable to those of mild steel and corrosion resistance comparable
to that of copper. The Si-bronzes are used for tanks, pressure vessels, marine construction and hydraulic
pressure lines.
− Aluminium bronzes: The Cu-rich portion of the Cu-Al system is shown in Figure 2.21.4. The maximum
solubility of aluminium in the α-phase is approximately 9.5% at 566°C. The β-phase undergoes a
eutectoid reaction at 566°C to form the (α+γ2) mixture. Most commercial aluminium bronzes contain
between 4 and 11% aluminium. Those alloys containing up to 7.5% aluminium are usually single-phase,
while those containing between 7.5 and 11% aluminium are two-phase alloys. Other elements such as
iron, nickel, manganese and silicon are frequently added to aluminium bronzes. The single-phase
aluminium bronzes show good cold-working properties and good strength combined with corrosion
resistance to atmospheric and water attack. They are used for condenser tubes, corrosion-resistant
vessels, nuts and bolts, and protective sheathing in marine applications. The dual-phase aluminium
bronzes can be heat treated to obtain structures similar to those in steel. Figure 2.21.5(a) shows the
structure of primary α and granular eutectoid (α+γ2), representative of an as-cast 10% aluminium bronze.
Figure 2.21.5. Structures of aluminium bronze. (a) As-cast 10% Al-bronze showing primary α and granular
eutectoid, (b) furnace-cooled Al-bronze showing lamellar eutectoid, and (c) quenched Al-bronze showing a
martensitic β structure.
− Beryllium bronze: The solubility of Be in the α-phase decreases from 2,1% at 866°C to less than 0,25%
at room temperature. Such a change in solubility is always indicative of age-hardening possibilities.
The optimum mechanical properties are obtained in an alloy containing approximately 2% beryllium. A
typical heat treatment cycle for this alloy would be a solution anneal at 790°C, followed by water
quenching, cold-working, and finally an aging heat treatment at 315°C. Aging allows the precipitation
of very fine γ-phase particles throughout the α matrix. Beryllium bronzes are used for parts requiring a
combination of excellent formability in the soft condition with high yield strength and creep resistance
in the hardened condition (many springs); parts requiring corrosion resistance, high strength and
relatively high electrical conductivity (contact bridges, surgical instruments, diaphragms, bolts and
screws); and hard parts that will wear well against hardened steel (firing pins, dies, nonsparking tools).
• Nickel silvers:
These are essentially ternary alloys of copper, nickel and zinc. Commercial alloys are produced with the
following range of compositions: copper 50 to 70%, nickel 5 to 30%, and zinc 5 to 40%. The nickel silver
alloys containing more than 60% copper are single-phase alloys that show only fair hot-working properties,
but are ductile and easily worked at room temperature. The addition of nickel to Cu-Zn alloys gives it a
pleasing silver-blue colour and good corrosion resistance to food chemicals, water and the atmosphere.
These alloys make excellent base metals for plating with chromium, nickel or silver. They are used for
rivets, screws, zippers and costume jewellery.
The nickel silvers containing between 50 and 60% copper are dual phase (α+β) alloys. They can be readily
hot-worked and are less susceptible to stress corrosion cracking than binary Cu-Zn alloys of the same Zn
content. Typical applications of the dual-phase nickel silvers include springs and contacts in telephone
equipment, resistance wire, and surgical and dental equipment.
2.21.2.4 Porosity:
At the typical weld pool temperatures that have been measured in weld pools of gas tungsten arc welded
copper (1350°C at 100 A, and 1890°C at 450 A) the affinity of copper for oxygen is low, while it does not
Much of the porosity to which fusion welds in copper are subject has been ascribed to the steam reaction.
In addition, it is responsible for the intergranular embrittlement and cracking of the HAZ in tough-pitch
copper welds made by the oxyacetylene process. Hydrogen generated by the combustion of the acetylene
diffuses into the HAZ and reacts with Cu2O. The steam nucleates at the grain boundaries and causes the
observed failures.
The effect of nitrogen additions to argon shielding gas on porosity for two materials (OFCH and ETP copper)
is shown in Figure 2.21.6. It is sometimes stated that nitrogen is insoluble in liquid copper, whereas the
results in Figure 2.21.6 clearly indicate a significant degree of nitrogen absorption. The use of argon-
nitrogen mixtures is desirable in the GMAW of copper to increase the heat input rate. Addition of strong
nitride-formers, such as titanium and aluminium, makes it possible to produce sound welds in such
atmospheres.
Figure 2.21.6. The effect of the nitrogen content of argon-nitrogen atmospheres of total pressure 1 atm on the
porosity of gas metal arc welds in OFHC copper.
Figure 2.21.7 shows the effect of hydrogen additions for the same materials and welding parameters as in
Figure 2.21.6. The ETP copper is more severely affected by hydrogen than the OFHC type, as would be
expected from equation (2.21.1). However, note the difference in scale of both porosity and gas additions
in Figures 2.21.6 and 2.21.7. The slope of the line for OFHC copper in Figure 2.21.7 is the same as that for
ETP copper in Figure 2.21.6. The effect of water vapour is shown in Figure 2.21.8. In this case there is little
difference between the two materials, suggesting that the water vapour is dissociating into hydrogen and
oxygen in the arc and recombining in the liquid metal. These results support the view that, in the absence
of deoxidants, the steam reaction is a potent cause of porosity in copper welds.
The effect of oxygen is shown in Figure 2.21.9. Up to a partial pressure of 0.1 atm, oxygen reduces the
amount of porosity. Above this level, porosity increases again. Carbon dioxide has a similar effect. The
amount of oxygen present in the shielding gas due to atmospheric contamination is certainly below 0.1 atm
partial pressure, so this element is not likely to promote porosity in copper welds.
Cracking in the HAZ of copper welded by the oxyacetylene process may be prevented by the addition of
between 0.02 and 0.10% phosphorus to the plate material. However, the weld metal itself is rarely free
from porosity, and as a result, the tensile strength of as-welded oxyacetylene welds in phosphorus
deoxidised copper is substantially lower than that of the parent metal. Gas welds in copper are frequently
hammered or rolled to remove distortion, and this treatment improves their tensile strengths.
Inert gas shielded welding does not cause porosity in the base metal, whether or not it contains
phosphorus. The weld metal itself, however, is grossly porous unless it is deoxidised. Phosphorus is not
adequate for this purpose, and a combination of either silicon and manganese, or titanium and aluminium,
Welding Metallurgy NSW700
Study Theme 2.21- Page | 11
is added to filler wires and electrodes. Even using such powerful deoxidants, porosity may still occur in
SMAW, particularly at restarts. Phosphorus-deoxidised plate is usually specified for GTAW or GMAW.
Shielding gases are argon, helium or nitrogen, the latter being used where higher heat input rates are
required. There is little difference between argon and nitrogen shielding as regards the incidence of
porosity, but helium-shielded welds appear to be somewhat less sensitive to this type of defect. Tunnelling
porosity, which is associated with turbulence in the weld pool, may occur in GMAW if the current is too
high (over 350 A for nitrogen shielding, and over 450 A for argon shielding).
Figure 2.21.7. The effect of the hydrogen content of argon-hydrogen atmospheres of total pressure 1 atm on the
porosity of gas metal arc welds in copper.
Figure 2.21.8. The effect of water vapour in argon shielding gas on the porosity of gas metal arc welds in copper.
Figure 2.21.9. The effect of the oxygen content of argon-oxygen mixtures at a total pressure of 1 atm on the porosity
of gas metal arc welds in copper.
Copper alloys containing deoxidising elements - aluminium bronze, tin bronze and silicon copper - are not
subject to porosity and may be welded without special additions to the filler metal. Cupronickels, however,
suffer from the same type of porosity as commercially pure copper and require deoxidised electrodes.
Oxygen-free copper (OFHC) has excellent ductility and is readily joined by welding, brazing or soldering. Arc
welds in oxygen-bearing coppers (ETP) are not very satisfactory, as they usually contain defects and at best
have undesirably high electrical resistance due to the use of deoxidised filler metal. Cold pressure welding
is applicable to rod and is used to make cold joints in electrical conductors. Appropriate silver brazing
procedures and soft soldering can be used successfully to join oxygen-bearing copper. The process
generally used for joining copper in electrical conductors is thermit welding, using a mixture of copper
oxide and aluminium for the exothermic reaction. The mixture is held in a graphite crucible, with a steel
Welding Metallurgy NSW700
Study Theme 2.21- Page | 13
disc covering the exit hole. It is ignited and in a very short time a pool of molten copper is formed, which
melts the retaining disc and flows out into a mould surrounding the joint. The liquid copper has sufficient
superheat to melt the joint faces and produce sound welds. A collar of metal is left around the joint for
strength and to ensure good electrical conductivity.
Figure 2.21.10. Joint designs for GTAW and SMAW of commercial coppers.
• For GTAW of sections greater than 3.2 mm in thickness, preheating of the base material is required.
Typical preheat temperatures and recommended welding conditions for GTAW of copper are shown in
Table 2.21.5. These conditions should serve as a guide for establishing welding procedures, and should
be adjusted to produce the desired weld bead shape in any particular application.
The interpass temperature is the same as the preheat temperature.
• The travel speed should be controlled to provide optimal bead shape. Excessive welding speeds result
in welds that are very convex in shape, causing underfill along the edges of the joint and very poor
fusion on subsequent weld passes.
• Recommended joint preparations for GMAW of commercial coppers are shown in Figure 2.21.11. A
square-groove joint is recommended for single-pass GMAW of copper up to 3 mm in thickness, or for
one-pass-per-side welding of copper sections of up to 6 mm thick. A copper backing bar should be used
in joints with no root opening, and a grooved copper backing bar in joints with root openings of up to
1.6 mm. Single V-groove joints are recommended for section thicknesses between 3 and 13 mm. Filler
metal shall be deposited from one side using multiple passes. The root shall then be back gouged to
sound metal before the last pass is welded from the back of the joint. When the section thickness
exceeds 13 mm, double V-grooves or double U-groove joints shall be used. Whenever possible,
welding shall be performed by depositing multiple passes, alternating between opposite sides of the
joint to control distortion.
• For sections greater than 6.4 mm in thickness, preheating of the base material is required. Typical
preheat temperatures and recommended welding conditions for GMAW of copper are shown in Table
2.21.6. These conditions should serve as a guide for establishing welding procedures, and should be
adjusted to produce smoothly contoured welds that blend smoothly with the base metal.
• The forehand welding technique is recommended for welding in the flat position. For vertical welding,
upward progression should be used.
• In order to avoid excessive porosity when welding oxygen-free copper (UNS number C10200), heating
and welding cycles should be kept as short as possible.
Shielding gas
Workpiece Root opening (with Electrode Current Preheat
Weld types for butt joints Root face (grooved Cu Gas flow rate Voltage Travel speed Number of passes
thickness Cu backing) diameter (DCEP) temperature
backing)
Square groove
3.2 mm 3.2 mm 0 mm 1.6 mm Ar 15 L/min 310 A 27 V 0.75 m/min None 1
(Cu backing)
Square groove
3.2 mm 3.2 mm 0-1.6 mm 1.6 mm Ar or 75Ar-25He 15-16.5 L/min 325-350 A 28-33 V ⋅⋅⋅ None 1
(grooved Cu backing)
6.4 mm 6.4 mm 0 mm 2.4 mm Ar 15 L/min 460 A 26 V 0.50 m/min 95°C 2
Square groove
6.4 mm 6.4 mm 0 mm 2.4 mm Ar 15 L/min 500 A 27 V 0.50 m/min 95°C 1
75°-90° single V-groove 6.4 mm 3.2 mm 0-3.2 mm 1.6 mm Ar or 75Ar-25He 15-16.5 L/min 400-425 A 32-36 V ⋅⋅⋅ 200-260°C 2
(grooved Cu backing) 12.7 mm 0-3.2 mm 0-3.2 mm 1.6 mm Ar or 75Ar-25He 15-16.5 L/min 425-450 A 35-40 V ⋅⋅⋅ 425-480°C 4
9.5 mm 4.8 mm 0 mm 2.4 mm Ar 15 L/min 500 A 27 V 0.35 m/min 200°C Special sequence
90° single V-groove 9.5 mm 4.8 mm 0 mm 2.4 mm Ar 15 L/min 550 A 27 V 0.35 m/min 200°C Special sequence
(grooved Cu backing) 12.7 mm 6.4 mm 0 mm 2.4 mm Ar 15 L/min 540 A 27 V 0.30 m/min 200°C Special sequence
12.7 mm 6.4 mm 0 mm 2.4 mm Ar 15 L/min 600 A 27 V 0.25 m/min 200°C Special sequence