[0001] This invention relates to a process for producing an AI-Si alloy from leucite by
reducing the corresponding oxides contained therein. In the case of leucites, of which
there is a large availability in Italy, a large number of processes have been developed
during the last 50 years for 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 HN03+HCI (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 NaN03 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, HCI or alkali. However, at the same time the pyrometallurgical 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] From US―A―3661561 is known a process for producing, in a blast furnace, an aluminium-silicon
alloy from a charge containing carbon, an aluminium-silicon ore and pure oxygen, where
the temperature in the reduction zone of the furnace ranges from about 2050°C to about
2500°C.
[0005] 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 oxides
of AI and Si can be simultaneously reduced and the so obtained metals are alloyed
into an alloy with high process yields, because of the high contact surface of the
reaction phases.
[0006] With regard to the chemical reactions, the chemical-physical energy necessary to
break the formation bond of leucite or AI and Si oxides is provided both by direct
reduction with the carbon and by the energy associated with the AI-Si solution in
liquid phase, which subtracts Si and AI as they become formed, thus lowering the activity
of the reaction products.
[0007] The alkaline oxides contained in the silico-aluminous concentrates are recovered
separately.
[0008] The present invention relates to a process for producing an aluminium-silicon alloy
from an aluminium-silicon ore with a carbon-containing reducing material at a temperature
of 2000°C and over, characterized in that the aluminium-silicon ore to be reduced
is leucite and said ore is injected in particulate form into a plasma-arc burner positioned
in the bottom section of a shaft-furnace filled with solid carbon-containing reducing
material exclusively, the expected molten Si-Al alloy and the slags are separately
collected at the bottom of said shaft furnace, the vapour of the unreacted alkali
metal- and alkaline earth-metal oxides and the exhaust gases being vented at the top
of said furnace.
[0009] 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.
[0010] On the accompanying drawing, a shaft reactor 1 is filled with a reducing agent 2,
preferably coke.
[0011] 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.
[0012] 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.
[0013] 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.
[0014] 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 AI+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.
[0015] 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.
[0016] 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) 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 1000°C or higher.
[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% AI203
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% AI and 65-70% Si
-190 kg of potassium oxide.