Patent Application
20100212855
The invention relates to the casting of aluminum alloys, in particular the casting of alloys containing magnesium and/or lithium, sensitive to oxidation.
The oxidation of aluminum alloys in liquid state has detrimental consequences on the casting process. In furnaces and transfer troughs the oxidation of metal initially results in a net metal loss, called loss on ignition. In addition, during casting, too great an oxidation of the molten metal generates surface defects on the ingot cast which have a detrimental effect when the products made are used. These problems are particularly marked in alloys containing magnesium and/or lithium.
The main defect is the vertical fold which is caused by crumpling of the oxide skin on the surface of the sump. In certain cases, and in particular when casting 7xxx alloys, this problem is particularly great because the folds, especially when they are long and deep, easily cause surface cracks. Folds and cracks must generally be eliminated before transforming the ingots obtained during casting. The defects may, for example, be eliminated by machining, which may be a very economically unsatisfactory solution, in terms of both the cost of the operation and the significant metal loss which occurs as a result. In certain cases, the presence of cracking makes the ingot unusable and it has to be remelted.
It has long been known that adding certain elements makes it possible to limit oxidation and to improve the surface quality.
In 1943, U.S. Pat. No. 2,336,512 described the addition of very small quantities of beryllium to aluminum alloys containing magnesium in order to limit oxidation of the molten metal surface.
International application WO 02/30822 described the substitution of beryllium by calcium with the same aim of limiting oxidation.
But the use of additives may cause other problems. Beryllium, for example, is to some extent toxic which has led to its removal from aluminum alloys used as food packaging. Calcium may lead to edge cracking during hot rolling.
It has also been proposed to protect the surface of the molten metal by means of various devices.
U.S. Pat. No. 4,582,118 proposes using a non-reactive and non-combustible, atmosphere, such as for example an atmosphere of argon, helium, neon, krypton, nitrogen or carbon dioxide, for casting aluminum-lithium alloys. But such processes are very expensive to use.
Patent application EP 0 109.170 A1 describes the use of a baffle on the edge of the casting device to sweep the molten metal surface with an inert gas (usually nitrogen and/or argon with or without chlorine or another halogen). But these gases are tricky to use and significantly increase the cost of operations.
The use of carbon dioxide or combustion gas to limit oxidation is also known by C. N. Cochran, D. L. Belitskus and D. L. Kinosz, Metallurgical Transactions B, Volume 8B, 1977, pages 323-331.
Patent application EP 1 964 628 A1 describes a method for producing aluminum ingots in which at least one stage of the process is carried out in an atmosphere containing a fluorinated gas. However, fluorinated gases are tricky to use and carry large safety risks.
U.S. Pat. No. 5,415,220 describes the use of molten salts of lithium chloride and potassium chloride to protect the surface of aluminum-lithium alloys during casting.
But the drawback to using molten salts is the risk of contamination of the molten metal with impurities, as well as the difficulty of using them.
U.S. Pat. No. 7,267,158 describes the forced addition of a wet gas, containing more than 0.005 kg/m3 water on the surface of the molten metal in order to improve the surface quality of the cast ingots. This process has, however, the disadvantage of bringing the water vapor and liquid aluminum into contact with each other, in spite of the dangers of explosion caused by contact between water and liquid aluminum.
In addition, it is known from application EP 0 216 393 A1 that dry air can be used in a treatment ladle for liquid aluminum to prevent hydrogen from penetrating into the molten metal when a treatment gas is injected into the molten metal and causes the oxide coating protecting its surface to burst.
The problem is to find a casting process suitable for most oxidable aluminum alloys, in particular aluminum alloys containing magnesium and/or lithium, which does not have these disadvantages and makes it possible to obtain cast ingots that are free from surface defects and pollution, in complete safety.
A first subject of the invention is a casting process for an aluminum alloy containing at least about 0.1% of Mg and/or at least about 0.1% of Li in which a liquid surface of said alloy is put into contact with a dried gas including at least about 2% of oxygen by volume and with a water partial pressure lower than about 150 Pa throughout most of the solidification process.
A second subject of the invention is the use in a facility for casting aluminum alloys containing at least about 0.1% of Mg and/or at least about 0.1% of Li of a dried gas including at least about 2% of oxygen by volume and with a water partial pressure lower than about 150 Pa on a liquid surface of said aluminum alloy in order to minimize oxidation of it.
The names of alloys follow the rules of The Aluminum Association, known to skilled in the art. The chemical composition of standardized aluminum alloys is defined for example in standard EN 573-3.
Unless otherwise specified, the definitions of European standard EN 12258-1 apply. A “casting facility” is here considered to be all the devices used to transform a metal in unspecified form into a semi-finished product of rough form via the liquid phase. A casting facility may include a number of devices such as one or more furnaces necessary for melting the metal and/or keeping it at a given temperature and/or for operations to prepare the molten metal and adjust the composition, one or more ladles designed to carry out treatment to eliminate impurities that are dissolved or in suspension in the molten metal this treatment may involve filtering the molten metal through a filter medium in a “filtration ladle” or introducing into the bath a “treatment” gas which may be inert or reactive in a “degassing ladle”, a device for solidifying the molten metal (or “casting device), for example by direct chill casting, horizontal casting, continuous casting of wire, continuous casting of strips between cylinders, continuous casting of strips using a belt caster, which may include devices such as a mold (or “ingot mold”), a device for procuring molten metal (or “nozzle”), a cooling system, these various furnaces, tanks and solidification devices being connected to each other by troughs (or “transfer trough”) in which the molten metal can be transported.
Surprisingly, the present inventors noted that when put into contact with a dried gas including at least about 2% of oxygen by volume and with a water partial pressure of less than about 150 Pa, a liquid aluminum surface undergoes little oxidization, which makes it possible to produce castings that are free from unacceptable surface defects. This result is surprising because it is commonly accepted that, on the contrary, the moisture contained in the air makes it possible to limit oxidation of aluminum alloys in liquid state.
In a first embodiment of the invention, this surprising effect is made use of in a casting process.
The process according to the invention is useful only for highly oxidable aluminum alloys, containing at least about 0.1% of Mg and/or at least about 0.1% of Li. The process according to the invention is particularly useful for alloys of the 2XXX, 3XXX, SXXX, 6XXX, 7XXX or 8XXX families, especially when these alloys do not contain a deliberate addition of beryllium and/or calcium. The process according to the invention is particularly advantageous for alloys containing less than 3 ppm of beryllium or even less than 1 ppm of beryllium and/or less than 15 ppm of calcium or even less than 5 ppm of calcium. Examples of alloys for which the process according to the invention is particularly advantageous are, in the 2XXX family of alloys, alloys AA2014, AA2017, AA2024, AA2024A, AA2027, AA2139, AA2050, AA2195, AA2196, AA2098, AA2198, AA2214, AA2219 and AA2524, in the 3XXX family of alloys, alloys AA3003, AA3005, AA3104 and AA3915, in the 5XXX family of alloys, alloys AA5019, AA5052, AA5083, AA5086, AA5154, AA5182, AA5186, AA5383, AA5754 and AA5911, and in the 7XXX family of alloys, alloys AA7010, AA7020, AA7040, AA7140, AA7050, AA7055, AA7056, AA7075, AA7449, AA7450, AA7475, AA7081, AA7085, AA7910, and AA7975.
The dried gas must contain at least about 2% of oxygen by volume and have a water partial pressure lower than about 150 Pa, preferably lower than 100 Pa and preferably still lower than 70 Pa. In a particularly advantageous embodiment, the water partial pressure is even less than 30 Pa, preferably less than 5 Pa and even more preferably less than 1 Pa. The water partial pressure of a gas is also known by the name of vapor pressure. The pressure partial of a perfect gas i in a mixture of perfect gases of total pressure P is defined as the pressure which would be exerted by the molecules of gas i if this gas occupied on its own all the volume available to the mixture. The dewpoint of a gas is the temperature at which, the gas becomes saturated with water vapor, the current barometric conditions remaining unchanged. It may also be defined as the temperature at which the steam pressure would be equal to the saturating vapor pressure. A water partial pressure of 150 Pa corresponds to a dewpoint of −17.9° C. and to a quantity of water of 0.0013 kg/m3 at this temperature. A water partial pressure of 100 Pa corresponds to a dewpoint of −22.6° C. and to a quantity of water of 0.0009 kg/m3 at this temperature. A water partial pressure of 70 Pa corresponds to a dewpoint of −26.5° C. and to a quantity of water of 0.0006 kg/m3 at this temperature.
The dried gas also advantageously includes at least one gas chosen from air, helium, argon, nitrogen, carbon dioxide, carbon monoxide, natural gas combustion products, methane, ethane, propane, natural gas, organic fluorinated compounds, organic chlorinated compounds. Adding carbon dioxide to the dried gas can in certain cases improve the antioxidant effect. In one embodiment of the invention, the dried gas includes between 1 and 10% of CO2 by volume. However, as this is a limited effect and as adding CO2 costs money, the CO2 content of the dried gas is less than 1% by volume or even less than 0.1% by volume in another advantageous embodiment of the invention. In an advantageous embodiment of the invention, said dried gas is primarily air dried by any suitable means to reach the desired water partial pressure.
According to the invention the dried gas is put into contact with a liquid surface of aluminum alloy during most of the solidification process of said alloy. The gas is preferably brought into contact with the surface in order to establish an atmosphere above this surface whose water content is substantially equal to that of the dried gas, i.e. in order to avoid significant diffusion of water vapor coming from the ambient air in said atmosphere.
So when this contact is made using a flow of dried gas, it is advantageous for this flow to be sufficient in relation to the liquid surface subjected to the dried flow in order to establish said atmosphere. If this flow is too low, the composition of said atmosphere may be too greatly influenced by the external atmosphere and its water content may no longer correspond to the desired content.
In addition, it is in general not necessary to put all the liquid surface of aluminum alloy available into contact with the dried gas, as illustrated by
A liquid surface of aluminum alloy is kept in contact with the dried gas during most of the solidification process. Therefore, while it is not necessary to bring a liquid surface into contact with the dried gas as soon as the molten metal is introduced into the casting device, it is preferable to do this as soon as a stationary mode is established. For example, in the case of direct chill casting, it is preferable to do it at least at the beginning of the descent of the dummy bottom, or at least at the start of casting of a zone which will not be cut during later operations. It is possible to vary the flow of dried gas during casting, in particular if surface defects appear. So an increase in the flow of dried gas makes it possible in certain cases to make folds in the cast product disappear. Contact between the liquid surface and the dried gas can possibly be removed before the end of casting, in particular when one reaches a zone which will be cut during following operations.
The present invention applies to various casting processes and preferably to a casting process chosen from direct chill casting, horizontal casting, continuous casting of wire, continuous casting of strips between cylinders, and continuous casting of strips using a belt caster.
The process known to skilled in the art as “direct chill casting” or “DC casting”, is a preferred process within the context of this invention. In this process an aluminum alloy is cast in an ingot mould with a dummy bottom while moving the dummy bottom vertically and continuously so as to maintain a substantially constant level of molten metal during solidification of the alloy, the solidified faces being directly cooled with water.
The process according to the invention is particularly advantageous for the casting of plates and billets by direct chill cooling. The process according to the invention is particularly advantageous for the casting of large-sized plates, in particular those of section greater than 0.5 m2.
Many devices allow dried gas to be brought into contact according to the invention with a liquid surface of an aluminum alloy. In the case of direct chill casting, the device may be integrated into an ingot mould or fixed to the latter in order to introduce the dried gas from the edge of the liquid surface towards its center, positioned above the liquid surface so as to introduce the dried gas substantially perpendicularly to the liquid surface, fixed around a molten metal injector so as to introduce the dried gas from the center of the liquid surface towards its edge and/or from the edge towards the center or it may be made up by any combination of these devices.
An advantageous device for procuring gas in the case of direct chill casting is illustrated in
The dried gas from the casting process according to the invention can also be used in other parts of a casting plant on a liquid surface of aluminum alloy containing at least about 0.1% of Mg and/or at least about 0.1% of Li, in order to minimize oxidation. A casting facility includes several other devices in which liquid surfaces of aluminum alloy are in contact with the atmosphere. The dried gas can therefore advantageously be used to limit the oxidation of the liquid surface of alloys in a furnace, in particular a smelting or holding furnace, in a treatment tank such as a filtration ladle or a degassing ladle or in a trough such as a transfer trough. For these uses, conditions of using the dried gas and/or a composition of aluminum alloy similar to those described in the process according to the invention, in particular concerning the procurement of dried gas, are preferably used.
The products obtained by a process according to the invention and/or a use according to the invention can as an option be wrought in particular by rolling, spinning and/or forging, particularly in order to obtain sheets and sections.
The invention makes it possible to cast the most oxidable aluminum alloys, in particular aluminum alloys containing magnesium and/or lithium, without using additives such as beryllium and/or calcium and without using expensive devices and/or gases, to obtain cast ingots free from surface defects and pollution, in complete safety.
In this example, oxidation of the molten metal was measured by thermogravimetric analysis. In these tests, a crucible containing the molten metal is held at a controlled temperature. This crucible contains about 5 kg of metal, and has a diameter of 100 mm. The significant size of these experiments, which makes it possible to take macroscopic effects into account, may explain differences with experiments carried out on very small quantities often reported in former art. The mass of the sample is continuously weighed. The increase in weight is due to oxidation of the molten metal. A diagram illustrating this experiment is presented in
Three alloys were studied: alloys AA7449, AA2196 and AA5182. The conditions of the various tests are summarized in table 1. In all tests, the beryllium and calcium content were similar and less than 1 ppm and 10 ppm respectively.
a is a photograph of the surface obtained after the test in the case of test 7 (ambient air). A large amount of oxidation is observed, leading to oxidation products in the characteristic dark-colored cauliflower shape.
Plates of rectangular section 446 mm×2160 mm made of alloy AA7449 were DC-cast using AlTiC refining. The length of the plates obtained ranged between 900 mm and 4000 mm. The beryllium content of the alloy was less than 1 ppm and the calcium content was less than 15 ppm.
The dried gas was dry air whose water partial pressure was 60 Pa, in certain cases containing 5% of CO2 by volume.
Table 2 describes the conditions of the various tests carried out and the results obtained.
The effect of the dry air was shown on several occasions: during test 22, bringing a liquid surface into contact with dry air made it possible to make the deep folds disappear. In the same way, in test 23, the presence of dry air made it possible as of the start of the test to obtain a satisfactory surface quality for the plates cast (some short (˜40 mm) vertical and shallow folds). In addition, for this test it was observed that the increase in the flow of dry air made it possible to make the folds disappear. The effect of the presence of CO2 in the dried gas on the surface quality is, if it exists, of second order as compared with the effect of the water partial pressure. So for test 23, a satisfactory result was obtained in the absence of CO2.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0900780 | Feb 2009 | FR | national |
| Number | Date | Country | |
|---|---|---|---|
| 61286594 | Dec 2009 | US |
