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304 International
Ol'shanskii2004
and18 Morozov
(4) 304–306 doi:10.1533/wint.2004.3288
Selected from Svarochnoe Proizvodstvo 2003 47 (11) 8–11; Reference SP/03/11/8; Translation 3288
A N O L' S H A N S K I I and B P M O R O Z O V
K E Tsiolkovskii Moscow Institute of Aviation Technology
The development of porosity in liquid metal is possible where c is a constant; [H] is the concentration of hydrogen
only if there are suitable conditions for the formation of in the metal of the weld pool.
nuclei of pores. This should be accompanied by a decrease Equation [4] shows that r cr increases with increasing
in the free energy of the system. The total change of the pex . Therefore, the increase of the pressure above the
energy of the system: 1 weld pool can be regarded as a factor, capable of
preventing the generation of the dissolved gas in the
∆Φ = −∆fV + ΣSi σi , [1] form of pores.
The increase of the size of the micronuclei of the pores
in the volume takes place in the liquid metal as a result
where ∆f is the difference of the free energy of the dissolved of diffusion of the dissolved hydrogen. 3
and free gas; V is the volume of the new gas phase; S i is The atomic hydrogen, diffusing into the pores, is
the total surface of the new phase; σj is the surface tension transferred into the molecular form and generates a
at the phase boundary. pressure in the pores, equalised by the external pressure.3
For a gas pore with a radius r, equation [1] has the The amount of hydrogen, diffusing into the nucleus
following form: of the pore from the surrounding liquid metal, can be
determined from the Richardson Equation:
4
∆Φ = − πr 3 ∆f + 4πr 2 σi . [2]
3
∆m = D0
1
∆x
K ( )
pH' 2 − pH2 S ∆t , [5]
Equation [2] indicates that the decrease in the free
energy of the system in the formation of a new phase is where D 0 is the diffusion coefficient at the solidification
proportional to the cube of the radius r and the increase temperature; ∆x is the thickness of the metal; K is a
of the energy. As a result, the losses for the formation of constant; pH 2 is the equilibrium pressure of hydrogen
the phase boundary are proportional to the square of at the temperature of the weld pool; pH′ 2 is the pressure
the radius. Thus, increase of the volume of the pore with of hydrogen in the pore at the temperature of the weld
the radius higher than the critical radius is accompanied by pool; S is the side surfaces of the pore; t is the diffusion
a decrease of the free energy of the system. In this case, time.
the nucleus of the pore becomes stable and capable of Assuming that the pressure of hydrogen in the pore
growth. The hydrogen pressure in the gas bubble is: in the liquid metal is equal to the external pressure:
2σ i pH 2 = pex ,
pH 2 = pex + hρ + , [3]
r
the equation may be presented in the following form:
where p ex is the external pressure of the gas above the
molten metal; h is the height of the column of the metal;
ρ is the density of metal; σ is the surface tension of the ∆m = D0
1
∆x
( )
K pH' 2 − pex S ∆t. [6]
metal at the metal-gas boundary; r is the radius of the
bubble.
The critical radius of the nucleus of the pore, formed Equation [6] shows that there are two regions of
during the generation of hydrogen, dissolved in the diffusion of the gas: p ex < pH 2 – the rate of diffusion of
aluminium pool of liquid metal is:2 the gas into the pores is positive, i.e. the amount of the
gas in the pore increases and the pores grow; p ex > pH′ 2
2σ i 1 – the rate of diffusion of the gas into the pores is negative
rcr = , [4] and the volume of the pores decreases.
c ln [ H ]
Thus, changing pex, with other conditions being equal,
pH 2 it is possible to cause the dissolution of the gas, enclosed
doi:10.1533/wint.2004.3288 Welded joints in aluminium alloys 305
in the pores, and this is accompanied by a decrease in metal, the formation of porosity is caused by the moisture
the volume of the pore by the transfer of gas from the present in the oxide film on the surface of the metal. In this
solution into the pores and by the increase of the volume case, equation [7] has the following form:
of the latter.
In the actual welding conditions, in addition to the
T 1
hydrogen, dissolved in the welded metal, it is also necessary ΣVn = K [ H ]d 1 + . [9]
to take into account the possibility of introduction of 273 pex
additional hydrogen into the weld metal from the surface of
the parent metal and the welding wire and also as a result In the SAP-type material and granulated aluminium,
of dissociation of the water vapours, distributed in the gas. the high gas saturation of the parent metal results in a
If the diffusion removal of hydrogen from the liquid metal situation in which the porosity forms as a result of the
is not taken into account, and the possibility of rising and generation of gas from the parent metal.
removal of parts of the pores is disregarded, the volume of For SAP and granulated aluminium, equation [7] has
hydrogen, generated in the pores, can be determined by the following form:
the following dependence:
T 1
T 1 ΣVn = C [ H ]d 1 + . [10]
ΣVn = ([ H ]0 + [ H ]d − [ H ] p pex ) 1 + , [7] 273 pex
273 pex
The results of experiments with the examination of
Here [H]0 is the concentration of hydrogen in the parent
the variation of the total volume of the pores in relation
metal; [H]d is the additional concentration of the hydrogen
to the argon pressure in the chamber in the welding of
transferred into the pool from the surface of the metal;
aluminium materials show that with an increase in the
[H]p is the equilibrium concentration of hydrogen at the
concentration of the gas in the metal, the suppression
solidification temperature of the metal; T is the melting
of porosity takes place at a higher pressure.
point of the metal.
Figure 1 shows the variation of porosity of welded joints
The dependence [7] shows that the volume of the pores,
in aluminium (type A95, AO) at different pressures. It may
formed in the metal, depends on the initial concentration
be seen that the increase of the hydrogen concentration in
of hydrogen in the liquid metal, the additional
the metal results in an increase of the total volume of the
concentration of hydrogen, transferred into the pool from
pores and of the external pressure at which the porosity is
the surface of the metal, and on the external pressure of
suppressed. The decrease in the porosity in the weld metal
the shielding gas above the molten pool.
with the application of pressure lower than atmospheric is
The external pressure, resulting in the complete
explained by the processes of degassing of the liquid metal.
suppression of porosity in the weld metal, i.e., the total
In welding AMg6 alloy (Fig. 2), the pressure range below
volume of the pores is equal to zero, is determined from
the atmospheric pressure was not characterised by a decrease
equation [7].
of porosity, indicating problems in the processes of degassing
Assuming that pex = pcr, one obtains:
of the metal. These processes are characterised by low
intensity because of the increase of the solubility of
([ H ] + [ H ] )
2 hydrogen in the metal. Increase in the gas pressure decreases
pcr = 0 d
. [8]
[ H ]2p
No porosity
Pressure, MPa
Pressure, MPa
2 The dependence of the total volume of pores in welded 4 The range of optimum pressure resulting in the production
joints in AMg6 aluminium alloys on pressure: 1) after etching; of sound welded joints in aluminium materials: 1) aluminium;
2) etching and holding in air 3 days; 3) etching and holding 2) AMg6 alloys; 3) granulated aluminium; 4) sintered
in water vapours for 3 days. aluminium powder (SAP).
Conclusions