[0001] This invention relates to a process for producing an Al-Si alloy from concentrates
containing the corresponding oxides, even if chemically combined with each other in
the form of alumino-silicates. For example, in the case of leucites, which is the
most important case especially for Italy, a large number of processes have been developed
during the last 50 years fro recovering alumina and alkalies, including experiments
in pilot plants and sometimes on an industrial scale.
[0002] The results have always been negative for technical or economical reasons. The known
processes of the art are as follows:
- attacking with HNO3 + HCl (Italian patent 536,793), this being . negative because of the high cost of
the acid and because of material problems;
- attacking with CaO at 1000-1400°C (French patent 527,066);
- attacking with hot NaNO3 in solution, under pressure;
- attacking with Ca(OH)2 under pressure in order to recover KOH (French patent 556,994).
[0003] The most recent proposals relate to processes involving attack by H
2S0
4, HCl or alkali. However, at the same time the parametallurgical processes are making
progress, these tending to recover the components of an alkaline (or alkaline earth)
silico-aluminous concentrate in metal form as an Al-Si alloy, together with the alkaline
oxide by virtue of its volatilisation. The use of conventional electric furnaces has
not yet given promising technical and economical results because of the low metal
recovery and high energy consumption.
[0004] It has surprisingly been found that the aforesaid difficulties and drawbacks can
be obviated using the process according to the present invention, by which the metals
Al and Si can be simultaneously reduced and alloyed into an alloy with high process
yields, because of the high contact surface of the reaction phases.
[0005] With regard to the chemical reactions, the chemical-physical energy necessary to
break the formation bond of leucite or Al and Si oxides is provided both by direct
reduction with the carbon and by the energy associated with the Al-Si solution in
liquid phase, which subtracts Si and Al as they become formed, thus lowering the activity
of the reaction products. The alkaline oxides contained in the silico-aluminous concentrates
are recovered separately.
[0006] The present invention relates to a process for producing a metal alloy from the metal
oxides either in individual form or chemically combined with each other, by reducing
the oxides by means of a carbon-based reducing agent in the presence of a plasma arc
burner in a shaft reactor filled with reducing material of suitable size, and is characterised
in that the individual or chemically combined oxides are oxides essentially of aluminium
and silicon, with oxides of alkaline and/or alkaline earth metals, the reduction reaction
taking place at a temperature exceeding 2000°C, the product obtained being an alloy
of aluminium and silicon.
[0007] According to the invention, the alkaline and/or alkaline earth metal oxides are separated
at the top of the shaft reactor.
[0008] The invention is described in greater detail hereinafter with reference to the accompanying
drawing, which represents a sectional view of a shaft or reactor which can be used
in accordance with the present invention.
[0009] On the accompanying drawing, a shaft reactor 1 is filled with a reducing agent 2,
preferably coke.
[0010] A blast furnace charger 3 is mounted at the top of the reactor 1, directly above
the reactor itself, and is arranged to be continuously filled with coke to a predetermined
level. In order to automatically obtain this predetermined level in the mouth 4 of
the blast furnace charger 3, two level indicators 5, 6 are installed, to interact
with filling members, not shown. A pipe 7, connected to a condenser 8, emerges from
the top of the reactor 1.
[0011] The material to be treated, containing silicon and aluminium oxide, is fed through
the inlet 9 either alone or in combination with the reducing material, which may also
be fed through 10.
[0012] There is also a plasma arc burner 11 with a feed pipe 12, and on the base of the
reactor 1 there are mounted tapping means 13 for the slag, and tapping means 14 for
the liquid metal.
[0013] The following occurs during operation. The material to be treated is subjected to
air blasting in the reaction zone of the reactor 1, where together with the reducing
agent it becomes rapidly heated and reacts to form the liquid and gaseous reduction
products. The liquid products consist of an Al + Si alloy, and slag deriving from
slagging agents either added separately during the operation or mixed with the material
containing the metal oxides, a certain quantity of ash originating from the reducing
agent also being produced. The gaseous product consists of unreacted alkaline oxides
and reduction gas, of which the composition depends on the reducing agent used.
[0014] The liquid reduction products are collected on the base of the shaft and can be discharged
through the tapping holes 13, 14, whereas the gaseous products, essentially alkaline
oxides, rise upwards through the shaft and are extracted through the pipe 7.
[0015] The coke in the shaft forms a permeable layer, through which the reaction products
pass respectively towards the base and towards the top of the shaft, and in this respect
the coke has the following purposes:
a) to form a large reaction surface for the contact of all the reaction phases;
b) to hold back all the fine grain material which passes through this layer;
c) if necessary, to act as a reducing agent and thus ensure that the reduction conditions
exist from one end to the other of the shaft;
d) to prevent the evolved oxide vapours from becoming condensed, this being attained
by virtue of the fact that the top of the shaft and the top of the blast furnace are
protected by coke. To ensure that the condition of point (d) is satisfied, coke is
fed into the reactor by way of level regulators 5, 6. Furthermore, as stated heretofore,
the entire coke layer is maintained at a temperature of about 10000C or higher.
[0016] In addition, it is preferable to use a gaseous or liquid hydrocarbon or a solid coal
as the reducing agent.
[0017] The reaction gas which leaves the shaft is made to pass through the condenser 8,
in which it is separated, and the metal oxides contained in it are condensed and discharged
from 15.
[0018] The remaining gas, consisting mainly of carbon monoxide and gaseous hydrogen, leaves
the condenser at 16 and can be used for various purposes.
[0019] The process according to the invention is further illustrated with reference to the
following example, which is,given by way of non-limiting example only.
EXAMPLE
[0020] The material containing a leucite concentrate had the following composition: (in
terms of its main elements)
20-23% A1203
50-53% SiO2
20-21% K20
max. 0.80% as Fe
remainder: oxides of various metals
[0021] The following consumption of reducing agent, slagging agents and electricity was
determined per ton of treated material:
- reducing agent 100 kg of dried coke 300 kg of pit coal
- electricity 4 kWh
[0022] The following products were obtained per ton of starting material:
- 300 kg of alloy containing 30-35% Al and 65-70% Si
- 190 kg of potassium oxide.