CA1054970A - Treatment of aluminium reduction cell linings - Google Patents
Treatment of aluminium reduction cell liningsInfo
- Publication number
- CA1054970A CA1054970A CA225,688A CA225688A CA1054970A CA 1054970 A CA1054970 A CA 1054970A CA 225688 A CA225688 A CA 225688A CA 1054970 A CA1054970 A CA 1054970A
- Authority
- CA
- Canada
- Prior art keywords
- alumina
- reduction cell
- nitrides
- insulation
- cell
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 230000009467 reduction Effects 0.000 title claims abstract description 16
- 229910052782 aluminium Inorganic materials 0.000 title claims description 6
- 239000004411 aluminium Substances 0.000 title claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000003792 electrolyte Substances 0.000 claims abstract description 8
- 150000004767 nitrides Chemical class 0.000 claims abstract description 8
- 150000001247 metal acetylides Chemical class 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims abstract description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims abstract description 3
- 230000000694 effects Effects 0.000 claims abstract description 3
- 238000011084 recovery Methods 0.000 claims abstract 2
- 230000015556 catabolic process Effects 0.000 claims description 2
- 239000012774 insulation material Substances 0.000 claims description 2
- 238000009413 insulation Methods 0.000 claims 4
- 239000000463 material Substances 0.000 abstract description 12
- 150000002222 fluorine compounds Chemical class 0.000 abstract description 3
- 238000006722 reduction reaction Methods 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 101100039010 Caenorhabditis elegans dis-3 gene Proteins 0.000 description 1
- -1 aluminium carbides Chemical class 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000002001 electrolyte material Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
- C25C3/06—Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Processing Of Solid Wastes (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
A B S T R A C T
The alumina linings of electrolytic reduction calls become contaminated with carbides, nitrides and fluorides with continued use of the cell.
A procedure for the recovery of such used alumina linings comprises subjecting the crushed used lining to the action of dry steam in a pressure vessel to effect break down and removal of carbides and nitrides. The thus treated material, which is partially hydrated, is then charged to the electrolyte of an electrolytic reduction cell to recycle both the fluoride and alumina content of the used alumina lining.
The alumina linings of electrolytic reduction calls become contaminated with carbides, nitrides and fluorides with continued use of the cell.
A procedure for the recovery of such used alumina linings comprises subjecting the crushed used lining to the action of dry steam in a pressure vessel to effect break down and removal of carbides and nitrides. The thus treated material, which is partially hydrated, is then charged to the electrolyte of an electrolytic reduction cell to recycle both the fluoride and alumina content of the used alumina lining.
Description
~5~
r~he present invention relates to the treatment of used linings of aluminium reduction cells and to methods of recovering usable materials therefrom.
In an aluminium reduction cell the electrolyte, consiætin~ essentially of alumina 9 dissolved in molten cryolite 7 is co~tained within a cell, having an outer steel shell, lined with carbon. ~he floor of the cell forms the cathode and co~sists of carbon blocks~ Between the cathode floor blocks and the steel shell it is customary to include a layer of highly compactea alumina~ which acts as a thermal and electrical insulation between the cathode blocks and the steel shell.
It i5 well known that the carbo~ lining of a reduc-tion cell becomes increasin~ly permeated with the c~mponents of the electrolyte, including undesired impurities, which build u~
in the electrolyte during prolonged use. In addition to contamination of the carbon lining, the alumina underlayer beGomes permeated by the electrolyte. r~he concentration of the electr~lyte materials in the alumina progressively increases t~wards the i~terface between the alumina and the carbon blocks.
The insulating properties of the alumina layer deteriorate as a result of this permeation by electrolyte materials and, in conse-. ~ .
; ~uence, it is usual to remove and discaxd this alumina layer whenever the carbon lining of the cell is removed for renewal~
~he discarded alumina material is unsuitable for re-use in the , ,.: .
reduction cell lining and, because of its high content of impurities, is unsuitable for direct addition to the electrolyte of another reduction cell, although in additio~ to -the alumi~a, it contains a substantial amount of valuable fluorides.
The principal objection to the addition of the dis-3 carded alumina to a reduction cell is the strong odours which arise when -the material i8 heated after it is added to the solid crust of a reduction cell. We have now discovered that this , ., ~ 54~7~
difficulty may be overcome by subjecting the alumina material to hydration by dry steam under elevated pressure~ ~his has the effect of breaking dow~ the carbides and/or nitrides contained ~ thereinO ~he steam treatment ~ay be continued until the evolu-; 5 tion of hydrocarbons and/or ammonia has ceased. ~ypically a layer of alumina removed from a reduction cell includes up to
r~he present invention relates to the treatment of used linings of aluminium reduction cells and to methods of recovering usable materials therefrom.
In an aluminium reduction cell the electrolyte, consiætin~ essentially of alumina 9 dissolved in molten cryolite 7 is co~tained within a cell, having an outer steel shell, lined with carbon. ~he floor of the cell forms the cathode and co~sists of carbon blocks~ Between the cathode floor blocks and the steel shell it is customary to include a layer of highly compactea alumina~ which acts as a thermal and electrical insulation between the cathode blocks and the steel shell.
It i5 well known that the carbo~ lining of a reduc-tion cell becomes increasin~ly permeated with the c~mponents of the electrolyte, including undesired impurities, which build u~
in the electrolyte during prolonged use. In addition to contamination of the carbon lining, the alumina underlayer beGomes permeated by the electrolyte. r~he concentration of the electr~lyte materials in the alumina progressively increases t~wards the i~terface between the alumina and the carbon blocks.
The insulating properties of the alumina layer deteriorate as a result of this permeation by electrolyte materials and, in conse-. ~ .
; ~uence, it is usual to remove and discaxd this alumina layer whenever the carbon lining of the cell is removed for renewal~
~he discarded alumina material is unsuitable for re-use in the , ,.: .
reduction cell lining and, because of its high content of impurities, is unsuitable for direct addition to the electrolyte of another reduction cell, although in additio~ to -the alumi~a, it contains a substantial amount of valuable fluorides.
The principal objection to the addition of the dis-3 carded alumina to a reduction cell is the strong odours which arise when -the material i8 heated after it is added to the solid crust of a reduction cell. We have now discovered that this , ., ~ 54~7~
difficulty may be overcome by subjecting the alumina material to hydration by dry steam under elevated pressure~ ~his has the effect of breaking dow~ the carbides and/or nitrides contained ~ thereinO ~he steam treatment ~ay be continued until the evolu-; 5 tion of hydrocarbons and/or ammonia has ceased. ~ypically a layer of alumina removed from a reduction cell includes up to
2~/o ~ in the form of flu~rides and up to 10% of unwanted car~
bides and/or nitrides~ ~hese unwanted carbides and nitrides may be substantially comp]etely eliminated by subjecting the alumina material, after grinding to an appropriate size, to dry steam at a temperature in the range of 120 to 175C and a gauge pressure of 1 to 7 kgs/cm2 in a pressure vessel for about 7 hours. The treated material undergoes a gain in weight of about 7% as a result of hydration of the alumina.
~he th~s treated, partially hydrated material con-; taining valuable fluorides, is suitabLe for use as the alumina feed to a reduction cell either on its o~m or mixed with regular calcined alumina.
In o~e example the alumina insulating material ; 20 removed from a reduction cell was crushed coarsely to particles below 1 cm in size and was treated in open tra~s in a thermally in~ulated pressure vessel, equipped with a pressure gau~e, thermometer and a bleed valve to exhaus-t ammo~ia and hydro- t car~ons. ~he alumina lini~g material was charged in an am~unt ~f about 500 kgs. ~ive steam at a pressure of 105 kg/cm2 was admitted to the vessel and the pressure was maintained u~til the - presence of ammonia or hydrocarbons was not detectable by smell ~; or pe~iodic sampling of the blow-off gases released by opening the bleed valve. The time required to reach this stage is about 7 hours. In this period the content of aluminium carbides and nitrides are substantially completely broken down and a small proportion o~ alumina is hydrated to give a weight increase of _2-' ,:
.. . .
', . : .
~1~5~97~
about ~/o, as noted above.
~ he treated material is then suita~le for direct addition to the electrolyte of an electrolytic reduction cell without any further treatment and in this way the valuable fluoride content of the used alumina lining is recovered in a simple manner.
~ he treatment time required to achieve the required degree of breakdown of carbides and nitrides varies with process conditions 7 particularly with the particle size of the matexial charged to the pressure vessel, the depth of crushed material in the tra~s, the pressure and temperature o~ the steam (which may be to some extent superheated), as well as on the content o~
contaminants in the insulation material. ~owever, appropriate control of process time is extremely simple, since the treatment . .
is effectively completed when the release o~ steam via the bleed valve is ~ longer accompanied by objectionable odours.
In general the treatment requires about 4 to 10 hours, according to circumsta~ces.
.'`'''' ~
.. .. .
.,.~, .
,~ :
~ . .
., .~
~, ~
~.;,. .
. j . ..
.. ; ~ .
t ,i .
. :., v.-; ~;, .. ..
,: ;
; _3_ . , ., ~... . . .
,.~ . . . .
bides and/or nitrides~ ~hese unwanted carbides and nitrides may be substantially comp]etely eliminated by subjecting the alumina material, after grinding to an appropriate size, to dry steam at a temperature in the range of 120 to 175C and a gauge pressure of 1 to 7 kgs/cm2 in a pressure vessel for about 7 hours. The treated material undergoes a gain in weight of about 7% as a result of hydration of the alumina.
~he th~s treated, partially hydrated material con-; taining valuable fluorides, is suitabLe for use as the alumina feed to a reduction cell either on its o~m or mixed with regular calcined alumina.
In o~e example the alumina insulating material ; 20 removed from a reduction cell was crushed coarsely to particles below 1 cm in size and was treated in open tra~s in a thermally in~ulated pressure vessel, equipped with a pressure gau~e, thermometer and a bleed valve to exhaus-t ammo~ia and hydro- t car~ons. ~he alumina lini~g material was charged in an am~unt ~f about 500 kgs. ~ive steam at a pressure of 105 kg/cm2 was admitted to the vessel and the pressure was maintained u~til the - presence of ammonia or hydrocarbons was not detectable by smell ~; or pe~iodic sampling of the blow-off gases released by opening the bleed valve. The time required to reach this stage is about 7 hours. In this period the content of aluminium carbides and nitrides are substantially completely broken down and a small proportion o~ alumina is hydrated to give a weight increase of _2-' ,:
.. . .
', . : .
~1~5~97~
about ~/o, as noted above.
~ he treated material is then suita~le for direct addition to the electrolyte of an electrolytic reduction cell without any further treatment and in this way the valuable fluoride content of the used alumina lining is recovered in a simple manner.
~ he treatment time required to achieve the required degree of breakdown of carbides and nitrides varies with process conditions 7 particularly with the particle size of the matexial charged to the pressure vessel, the depth of crushed material in the tra~s, the pressure and temperature o~ the steam (which may be to some extent superheated), as well as on the content o~
contaminants in the insulation material. ~owever, appropriate control of process time is extremely simple, since the treatment . .
is effectively completed when the release o~ steam via the bleed valve is ~ longer accompanied by objectionable odours.
In general the treatment requires about 4 to 10 hours, according to circumsta~ces.
.'`'''' ~
.. .. .
.,.~, .
,~ :
~ . .
., .~
~, ~
~.;,. .
. j . ..
.. ; ~ .
t ,i .
. :., v.-; ~;, .. ..
,: ;
; _3_ . , ., ~... . . .
,.~ . . . .
Claims
1. A procedure for the recovery of valuable components from the used alumina insulation of an aluminium reduction cell which comprises the steps of crushing the used insulation, subjecting the used insulation to dry steam at a pressure in the range of 1 to 7 kgs/cm2 and a temperature of 120 to 175°C in a pressure vessel for a time sufficient to effect substantially complete breakdown of contained carbides and nitrides and adding the thus treated partially hydrated alumina insulation material to the electrolyte of an aluminium reduction cell without further treatment whereby the alumina and fluoride content of the used alumina insulation is recycled.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1877374 | 1974-04-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1054970A true CA1054970A (en) | 1979-05-22 |
Family
ID=10118174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA225,688A Expired CA1054970A (en) | 1974-04-29 | 1975-04-28 | Treatment of aluminium reduction cell linings |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS5339245B2 (en) |
| AU (1) | AU8062175A (en) |
| CA (1) | CA1054970A (en) |
| CH (1) | CH594745A5 (en) |
| ES (1) | ES437060A1 (en) |
| FR (1) | FR2268877A1 (en) |
| IT (1) | IT1037724B (en) |
| NL (1) | NL7505082A (en) |
| NO (1) | NO751515L (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58119651A (en) * | 1982-01-11 | 1983-07-16 | Nippon Telegr & Teleph Corp <Ntt> | Semiconductor device and manufacture thereof |
-
1975
- 1975-04-26 ES ES437060A patent/ES437060A1/en not_active Expired
- 1975-04-28 CA CA225,688A patent/CA1054970A/en not_active Expired
- 1975-04-28 NO NO751515A patent/NO751515L/no unknown
- 1975-04-29 CH CH547475A patent/CH594745A5/xx not_active IP Right Cessation
- 1975-04-29 FR FR7513358A patent/FR2268877A1/en not_active Withdrawn
- 1975-04-29 IT IT22850/75A patent/IT1037724B/en active
- 1975-04-29 NL NL7505082A patent/NL7505082A/en unknown
- 1975-04-29 AU AU80621/75A patent/AU8062175A/en not_active Expired
- 1975-04-30 JP JP5244775A patent/JPS5339245B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS50151711A (en) | 1975-12-05 |
| NO751515L (en) | 1975-10-30 |
| ES437060A1 (en) | 1977-01-16 |
| JPS5339245B2 (en) | 1978-10-20 |
| CH594745A5 (en) | 1978-01-31 |
| FR2268877A1 (en) | 1975-11-21 |
| NL7505082A (en) | 1975-10-31 |
| IT1037724B (en) | 1979-11-20 |
| AU8062175A (en) | 1976-11-04 |
| DE2519080A1 (en) | 1975-10-30 |
| DE2519080B2 (en) | 1976-12-23 |
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