AT140567B - Process for removing iron from acidic aluminum salt solutions. - Google Patents
Process for removing iron from acidic aluminum salt solutions.Info
- Publication number
- AT140567B AT140567B AT140567DA AT140567B AT 140567 B AT140567 B AT 140567B AT 140567D A AT140567D A AT 140567DA AT 140567 B AT140567 B AT 140567B
- Authority
- AT
- Austria
- Prior art keywords
- salt solutions
- aluminum salt
- removing iron
- acidic aluminum
- iron
- Prior art date
Links
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims description 20
- 229910052742 iron Inorganic materials 0.000 title claims description 9
- 238000000034 method Methods 0.000 title claims description 8
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 title claims description 5
- 230000002378 acidificating effect Effects 0.000 title claims description 4
- 239000012266 salt solution Substances 0.000 title claims description 4
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 9
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 4
- 150000001447 alkali salts Chemical class 0.000 description 3
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 159000000009 barium salts Chemical class 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/68—Aluminium compounds containing sulfur
- C01F7/74—Sulfates
- C01F7/746—After-treatment, e.g. dehydration or stabilisation
- C01F7/748—Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Compounds Of Iron (AREA)
- Removal Of Specific Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Catalysts (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Entfernung von Eisen aus sauren Aluminiumsalzlösungen.
Gemäss Stammpatent Nr. 137319 entfernt man Eisen aus sauren Aluminiumsalzlösungen dadurch, dass man das Eisen mitels ss-Naphthalinsulfosäure oder ihrer löslichen Salze als unlösliches Ferrosalz dieser Säure abscheidet und im Filtrat eisenfreie Aluminiumsalze aufarbeitet. Weiter ist angegeben, dass man die verwendete ss-NaphthaIinsuIfosäure aus ihrem Ferrosalz durch Umsetzen mit Alkalikarbonaten in ihr lösliches Alkalisalz verwandeln und wieder in den Prozess einführen kann. Die Arbeitsweise mit Alkalisalze der ss-Naphthalinsulfosäure ist dann nachteilig, wenn es sich um die Gewinnung von reinem, von Alkalisulfat und Doppelverbindungen freiem Aluminiumsulfat handelt.
Es wurde nun gefunden, dass man diesen Übelstand beseitigen kann durch Verwendung von solchen
Salzen der ss-Naphthalinsulfosäure, deren Metalle Sulfate bilden, die bei gewöhnlicher Temperatur schweroder unlöslich sind. Die entstandenen Sulfate bleiben dann zusammen mit dem unlöslichen Ferrosalz der ss-NaphthaIinsuIfosäure im Rückstand, während das Filtrat nun einzig das Aluminiumsulfat enthält, das seinerseits daraus durch Kristallisation oder Eindampfen leicht in festem Zustand gewinnbar wird.
Als derart zu verwendende Salze kommt neben dem Bariumsalz insbesondere das Calciumsalz der ss-NaphthaIinsuIfosäure in Frage, dessen Löslichkeit in der Hitze einen glatt verlaufenden Umsatz mit dem Ferrosulfat im Ausgangsgemisch gestattet. Diese Salze haben auch den Vorzug ihrer Wiedergewinnung durch Umsetzen der regenerierten Alkalisalze des ss-Naphthalinsulfosäure mit Erdalkalichlorid.
Während im Verfahren des Stammpatentes nur Salze Verwendung finden, die bei gewöhnlicher Temperatur löslich sind, und bei der Rückführung der ss-Naphthalinsulfosäure mit Hilfe von Alkalikarbonaten wiederum Salze erhalten werden, die lösliche Sulfate bilden und infolgedessen mit dem Aluminiumsulfat zusammen in die Endlösung übergehen und sie verunreinigen, wird im vorliegenden Verfahren bei der Rückführung oder Umwandlung der erhaltenen Niederschläge in die Ausgangsstoffe unter Zusatz schwerlöslicher Salze der ss-NaphthaIinsuIfosäure, beispielsweise des Calcium- oder Bariumsalzes, der besondere Vorteil erzielt, dass die entstehenden Niederschläge leichter in die Ausgangsstoffe zurückverwandelt werden können und die bei der Umsetzung erhaltenen Filtrate reine Lösungen darstellen.
Neu und von vorteilhafter Wirkung ist weiter der Umstand, dass, wenn beim Fällen ein Überschuss an Fällungsmittel, der einer vollkommenen Eisenabtrennung zweckdienlich ist, verwendet wird, das unverbrauchte Fällungsmittel bei der Filtration nicht in die Endlösung übergeht, wie es beim Gebrauch löslicher Salze vorkommt, sondern im Filtrationsrückstand verbleibt und gegebenenfalls von dort in den Kreislauf zurückkehrt.
Beispiel :
In 100 Teile der vom Baux ; taufschluss herrührenden schwefelsauren Lösung, enthaltend 25 Teile Aluminiumsulfat und 4 Teile Ferrisulfat, werden 9'5 Teile ss-naphthalinsulfosaures Calcium eingetragen.
Bei zirka 800 C wird unter Rühren Schwefel dioxyd eingeleitet, bis das Eisen vollständig als-naphthalinsulfosaures Eisen ausgefällt ist. Nach Abkühlen auf zirka 10 C wird die Lösung von dem aus ss-naphthalin- sulfosaurem Eisen und Caleiumsulfat bestehenden Niederschlag abfiltriert. Aus dem Filtrat wird durch Kristallisation das Aluminiumsulfat erhalten, welches nur zirka 0'01% Eisen als Verunreinigung enthält.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for removing iron from acidic aluminum salt solutions.
According to parent patent no. 137319, iron is removed from acidic aluminum salt solutions by separating the iron with β-naphthalenesulfonic acid or its soluble salts as the insoluble ferrous salt of this acid and working up iron-free aluminum salts in the filtrate. It is also stated that the β-naphthalenesulfonic acid used can be converted from its ferrous salt into its soluble alkali salt by reaction with alkali metal carbonates and reintroduced into the process. The procedure with alkali salts of β-naphthalenesulfonic acid is disadvantageous when it is a matter of obtaining pure aluminum sulfate free of alkali sulfate and double compounds.
It has now been found that this inconvenience can be overcome by using them
Salts of β-naphthalene sulfonic acid, the metals of which form sulfates which are sparingly or insoluble at ordinary temperature. The sulphates formed then remain in the residue together with the insoluble ferrous salt of the β-naphthalenesulfonic acid, while the filtrate now only contains the aluminum sulphate, which in turn can easily be obtained in a solid state by crystallization or evaporation.
As salts to be used in this way, in addition to the barium salt, the calcium salt of β-naphthalenesulfonic acid, in particular, whose solubility in the heat allows smooth conversion with the ferrous sulfate in the starting mixture is possible. These salts also have the merit of being recovered by reacting the regenerated alkali salts of β-naphthalenesulfonic acid with alkaline earth chloride.
While in the process of the parent patent only salts are used that are soluble at ordinary temperature, and when the ß-naphthalenesulfonic acid is recycled with the help of alkali carbonates, salts are again obtained that form soluble sulfates and consequently merge with the aluminum sulfate into the final solution and they contaminate, the particular advantage achieved in the present process when recirculating or converting the precipitates obtained into the starting materials with the addition of sparingly soluble salts of β-naphthaIinsulfonic acid, for example the calcium or barium salt, is that the precipitates formed can be more easily converted back into the starting materials the filtrates obtained in the reaction are pure solutions.
Another new and beneficial effect is the fact that if an excess of precipitating agent, which is useful for complete iron separation, is used during the felling process, the unused precipitating agent does not pass into the final solution during the filtration, as occurs when using soluble salts, but remains in the filtration residue and possibly returns from there into the cycle.
Example:
In 100 parts of the Baux; The sulfuric acid solution resulting from the digestion and containing 25 parts of aluminum sulphate and 4 parts of ferric sulphate, 9'5 parts of ß-naphthalenesulphonic acid calcium are introduced.
At about 800 C, sulfur dioxide is introduced with stirring until the iron has completely precipitated as naphthalenesulfonic iron. After cooling to about 10 ° C., the solution is filtered off from the precipitate consisting of ß-naphthalene sulfonic acid iron and calcium sulfate. The aluminum sulfate is obtained from the filtrate by crystallization, which contains only about 0.01% iron as an impurity.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEG83083D DE570376C (en) | 1932-07-09 | 1932-07-09 | Removal of iron from acidic aluminum salt solutions |
| DEG85573D DE619018C (en) | 1932-07-09 | 1933-05-20 | Removal of iron from acidic aluminum salt solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT140567B true AT140567B (en) | 1935-02-11 |
Family
ID=33565846
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT137319D AT137319B (en) | 1932-07-09 | 1933-07-01 | Process for removing iron from acidic aluminum salt solutions. |
| AT140567D AT140567B (en) | 1932-07-09 | 1934-05-12 | Process for removing iron from acidic aluminum salt solutions. |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT137319D AT137319B (en) | 1932-07-09 | 1933-07-01 | Process for removing iron from acidic aluminum salt solutions. |
Country Status (7)
| Country | Link |
|---|---|
| AT (2) | AT137319B (en) |
| BE (2) | BE397337A (en) |
| CH (2) | CH169038A (en) |
| DE (2) | DE570376C (en) |
| FR (2) | FR757907A (en) |
| GB (2) | GB399772A (en) |
| NL (2) | NL35278C (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3148024A (en) * | 1962-10-29 | 1964-09-08 | Universal Oil Prod Co | Process for removing iron from an inorganic aluminum salt solution |
-
0
- BE BE403216D patent/BE403216A/xx unknown
-
1932
- 1932-07-09 DE DEG83083D patent/DE570376C/en not_active Expired
-
1933
- 1933-05-20 DE DEG85573D patent/DE619018C/en not_active Expired
- 1933-07-01 AT AT137319D patent/AT137319B/en active
- 1933-07-03 BE BE397337D patent/BE397337A/xx unknown
- 1933-07-04 FR FR757907D patent/FR757907A/en not_active Expired
- 1933-07-04 NL NL65882A patent/NL35278C/xx active
- 1933-07-06 GB GB19176/33A patent/GB399772A/en not_active Expired
- 1933-07-07 CH CH169038D patent/CH169038A/en unknown
-
1934
- 1934-05-12 AT AT140567D patent/AT140567B/en active
- 1934-05-15 CH CH174868D patent/CH174868A/en unknown
- 1934-05-17 FR FR44872D patent/FR44872E/en not_active Expired
- 1934-05-18 NL NL69480A patent/NL37350C/xx active
- 1934-05-22 GB GB15301/34A patent/GB422318A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL35278C (en) | 1935-04-15 |
| BE403216A (en) | |
| FR757907A (en) | 1934-01-08 |
| DE570376C (en) | 1933-02-15 |
| DE619018C (en) | 1935-09-20 |
| CH169038A (en) | 1934-05-15 |
| GB399772A (en) | 1933-10-12 |
| NL37350C (en) | 1936-01-15 |
| BE397337A (en) | 1933-08-31 |
| AT137319B (en) | 1934-04-25 |
| GB422318A (en) | 1935-01-09 |
| FR44872E (en) | 1935-04-24 |
| CH174868A (en) | 1935-01-31 |
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