DE1792675A1 - Process for the flotation of ion exchangers - Google Patents
Process for the flotation of ion exchangersInfo
- Publication number
- DE1792675A1 DE1792675A1 DE19681792675 DE1792675A DE1792675A1 DE 1792675 A1 DE1792675 A1 DE 1792675A1 DE 19681792675 DE19681792675 DE 19681792675 DE 1792675 A DE1792675 A DE 1792675A DE 1792675 A1 DE1792675 A1 DE 1792675A1
- Authority
- DE
- Germany
- Prior art keywords
- flotation
- floated
- ion exchangers
- adsorbed
- exchanger
- 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.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J47/00—Ion-exchange processes in general; Apparatus therefor
- B01J47/10—Ion-exchange processes in general; Apparatus therefor with moving ion-exchange material; with ion-exchange material in suspension or in fluidised-bed form
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/008—Organic compounds containing oxygen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/012—Organic compounds containing sulfur
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/014—Organic compounds containing phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Treatment Of Water By Ion Exchange (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Physical Water Treatments (AREA)
Description
Wintershall Aktiengesellschaft, Celle; Kassel, August-Rosterg-HausWintershall Aktiengesellschaft, Celle; Kassel, August-Rosterg-Haus
"Verfahren zur Flotation von Ionenaustauschern""Process for the flotation of ion exchangers"
Zum nicht vorveröffentlichten Stand der Technik gehört ein Verfahren zur Flotation von Ionenaustauschern, welches dadurch gekennzeichnet ist, daß an dem zu flotierenden Austauscher ein amphiphiler Stoff entgegengesetzter Ladung'adsorbiert und daß das Adsorbat durch Einblasen eines Gases, insbesondere Luft, in wäßriger Dispersion ausgeschäumt wird.The state of the art, which has not been previously published, includes a method for the flotation of ion exchangers, which is characterized by is that an amphiphilic substance of opposite charge 'adsorbed on the exchanger to be floated and that the adsorbate is foamed in an aqueous dispersion by blowing in a gas, in particular air.
Dieses Verfahren ist weiter dadurch gekennzeichnet, daß Anionenaustauscher mit quaternärem Stickstoff auf Polystyrol-, Divinyl-, Benzolbasis hei einem pH-Wert niht unter 3 - 4·, Insbesondere bei pH 5 - Ί, mit Fettsäuren, oder deren Seifen, oder Alkalisulfaten oder Sulfonaten der Fettsäuren in Wasser oder in verdünnter wäßriger Lösung flotiert werden, und ferner dadurch, darß Kationenaustauscher mit negativer Aufladung, wie mit SO-,-Wirkgruppen, bei pH-Werten von 1-8 mit primären oder sekundären Aminen oder quaternären Ammoniumverbindungen in Wasser oder wäßrigen Lösungen flotiert werden. ·This process is further characterized in that anion exchangers with quaternary nitrogen based on polystyrene, divinyl, benzene at a pH value not below 3-4, especially at pH 5-, with fatty acids or their soaps, or alkali sulfates or sulfonates the fatty acids are floated in water or in dilute aqueous solution, and furthermore, this means that cation exchangers with negative charge, such as with SO -, - active groups, at pH values of 1-8 with primary or secondary amines or quaternary ammonium compounds in water or aqueous Solutions are floated. ·
Das vorbekannte Verfahren betrifft die Flotation νοΆ Ionenaustauschern aus Lösungen. Ein technisches Interesse besteht an diesem Verfahren besonders dann, wenn die Filtration dieser hochmolekularen Substai<4en Schwierigkeiten bereitet. . .The previously known method relates to the flotation νοΆ ion exchangers from solutions. There is technical interest in this process especially when the filtration of these high molecular weight substances causes difficulties. . .
Iri der Technik besteht aber auch weiter die Aufgabe, Ionenaustauscher aus TrUben, die beispielsweise Gangart enthalten, abzutrennen, damit nach der flotativen Ausscheidung der beladenen Ionenaustauscher die übrigen Feststoffe der Trübe von der Lösung z.B. durch Filtration getrennt werden können.In technology, however, there is still the task of ion exchangers to separate from turbines that contain, for example, gait, so after the flotative separation of the charged ion exchangers the remaining solids of the pulp from the solution e.g. by filtration can be separated.
Bei der "Säurelaugung" von Uranerzen, wie von z.B. Autunit oder Chalkolit, fällt eine Trübe an, welche neben einer uranhaltigen Lösung vom pH-Wert etwa 2 noch viel Gangart und Schwebstoffe in sehr feiner Verteilung enthält. Eb iet üblich, die Gewinnung des Uran aus dieserDuring the "acid leaching" of uranium ores such as Autunit or Chalcolite, a turbidity occurs, which is next to a uranium-containing solution with a pH value of around 2, there is still a lot of gait and very fine suspended matter Distribution contains. It is common practice to extract the uranium from this
9845/151?9845/151?
Lösung nach Klärung und anschließendem Durchlauf durch Ionenaustauscher durchzuführen. Die Klärung vor der Uranabtrennung ist eine . der schwierigen und kostspieligen Stufen in der Aufbereitung der Uranerze.Carry out solution after clarification and subsequent passage through ion exchanger. The clarification before the uranium separation is one. the difficult and costly stages in the processing of uranium ores.
Es ist möglich, mittels des sog. "resin-in-pulp"-Prozesses auch ungeklärte Lauge aufzubereiten. Dabei wird der Ionenaustauscher in grober Form in Drahtkörben in einem horizontalen Strom ungeklärter Laugelösung vertikal hin- und herbewegt. Ablagerungen suspendierter Feststoffe auf dem Harz sind dabei zu vermeiden. Dieses Verfahren 1st schwierig zu handhaben und die vollständige Erfassung des Uran in der Lauge ist nicht gewährleistet. Außerdem sind, wegen der Notwendigkeit, sehr große Austauschergranulate'zu verwenden, Austauschgeschwindigkeit und Austauscherkapazität stark herabgesetzt. Diese Schwierigkeiten können durch das Verfahren der Erfindung vermieden werden.It is possible to use the so-called "resin-in-pulp" process, also unexplained Prepare lye. The ion exchanger is coarse in wire baskets in a horizontal stream of unclarified caustic solution moved vertically back and forth. Avoid deposits of suspended solids on the resin. This procedure is 1st difficult to handle and the full capture of the uranium in the Lye is not guaranteed. In addition, because of the necessity, to use very large exchanger granules, exchange speed and exchange capacity greatly reduced. These difficulties can be avoided by the method of the invention.
Die technische Durchführung des Verfahrens der Erfindung in Fortentwicklung des Verfahrens nach der Patentanmeldung P I7 67 260.Ö wird durch folgendes Ausführungsbeispiel erläutert:The technical implementation of the method of the invention in further development of the method according to the patent application P I7 67 260.Ö explained by the following exemplary embodiment:
1 kg gemahlenes uranhaltiges Mineral mit einem Gehalt von 1,5 % Uran (17,6 g U-zOg) wird mit 10 1 ver'dünnter Schwefelsäure (ca. 8 g/l H2SO^) solange unter leichtem Erwärmen digeriert, bis das gesamte Uran in Lösung gegangen ist. Nach dem Abkühlen der Trübe auf Zimmertemperatur besitzt diese einen pH-Wert von etwa jj· Der pH-Wert wird dann mit Natronlauge auf 5 eingestellt, wozu ungefähr 20 ml 1-normaler NaOH erforderlich sind. Danach werden etwa 500 g Anionenaustauscher in der Sulfatform, und zwar das Handelsprodukt Dowex-2-Sulfat in die Trübe eingerührt und unter ständiger Durchmischung mit einem langsam laufenden Rührer der Austauscher mit Uran in Form des UO2(SO^)2-Ions beladen. Kationische Verunreinigungen werden dabei vom Austauscher nicht aufgenommen, so daß eine sehr hohe Selektivität in Bezug auf das Uran erreicht wird. Die Beladung des Austauschers beträgt etwa 0,25 Milll-Äquivalente pro Gramm.1 kg of ground uranium-containing mineral with a content of 1.5 % uranium (17.6 g U-zOg) is digested with 10 1 diluted sulfuric acid (approx. 8 g / l H 2 SO ^) with gentle heating until all of the uranium has gone into solution. After the pulp has cooled to room temperature, it has a pH value of about jj · The pH value is then adjusted to 5 with sodium hydroxide solution, which requires about 20 ml of 1 normal NaOH. Then about 500 g of anion exchanger in the sulfate form, namely the commercial product Dowex-2 sulfate, are stirred into the pulp and the exchanger is loaded with uranium in the form of the UO 2 (SO ^) 2 ion with constant mixing with a slow-speed stirrer. Cationic impurities are not absorbed by the exchanger, so that a very high selectivity with regard to the uranium is achieved. The loading of the exchanger is about 0.25 milliliters per gram.
Nach vollständiger Beladung, die in etwa 10-15 Minuten erreicht ist, wird die Trübe in eine Schwimmeschine übergeführt, 0,25 g Na-Oleat zugegeben und durch Belüftung das Austauscherharz vollständig ausflo-After a full load, which is reached in about 10-15 minutes, the pulp is transferred to a floating machine, 0.25 g Na oleate added and the exchange resin flowed out completely through ventilation.
009845/151?009845/151?
tiert. Aus dem als Konzentrat vorliegenden Harz wird das Uran mit einer schwach sauren NaCl-Lösurig eluiert. Das aus diesem Eluat als Uranat gefällte Uran liegt sehr rein vor. Das abgetrennte Austauscherharz wird nach überführung in die Sulfat-Form in das Verfahren zur erneuten Verwendung zurückgeführt.animals. The uranium is made from the resin, which is available as a concentrate a weakly acidic NaCl solution. That from this eluate Uranium precipitated as uranium is very pure. The separated exchange resin becomes part of the process after it has been converted into the sulphate form returned for reuse.
009845/151?009845/151?
Claims (4)
FD-JH/schp• December 27, 1968
FD-JH / schp
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681792675 DE1792675A1 (en) | 1968-09-30 | 1968-09-30 | Process for the flotation of ion exchangers |
BE733317D BE733317A (en) | 1968-09-30 | 1969-05-20 | |
NL6907899A NL6907899A (en) | 1968-09-30 | 1969-05-22 | |
FR6917894A FR2019144A1 (en) | 1968-09-30 | 1969-05-30 | Recovery of ion exchange resins by flotation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681792675 DE1792675A1 (en) | 1968-09-30 | 1968-09-30 | Process for the flotation of ion exchangers |
Publications (2)
Publication Number | Publication Date |
---|---|
DE1792675A1 true DE1792675A1 (en) | 1970-11-05 |
DE1792675C3 DE1792675C3 (en) | 1974-05-30 |
Family
ID=5707502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19681792675 Granted DE1792675A1 (en) | 1968-09-30 | 1968-09-30 | Process for the flotation of ion exchangers |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE733317A (en) |
DE (1) | DE1792675A1 (en) |
FR (1) | FR2019144A1 (en) |
NL (1) | NL6907899A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4830738A (en) * | 1986-09-23 | 1989-05-16 | British Nuclear Fuels Plc | Separation of matter by floatation |
-
1968
- 1968-09-30 DE DE19681792675 patent/DE1792675A1/en active Granted
-
1969
- 1969-05-20 BE BE733317D patent/BE733317A/xx unknown
- 1969-05-22 NL NL6907899A patent/NL6907899A/xx unknown
- 1969-05-30 FR FR6917894A patent/FR2019144A1/en not_active Withdrawn
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4830738A (en) * | 1986-09-23 | 1989-05-16 | British Nuclear Fuels Plc | Separation of matter by floatation |
Also Published As
Publication number | Publication date |
---|---|
BE733317A (en) | 1969-11-20 |
DE1792675C3 (en) | 1974-05-30 |
NL6907899A (en) | 1970-04-01 |
FR2019144A1 (en) | 1970-06-26 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
SH | Request for examination between 03.10.1968 and 22.04.1971 | ||
C3 | Grant after two publication steps (3rd publication) | ||
E77 | Valid patent as to the heymanns-index 1977 | ||
EHV | Ceased/renunciation |