DE2251442A1 - Electrolytic detoxication of cyanide using V4A anode - and adding copper salt in small amt to prevent electrolytic dissolution of anode, for economy - Google Patents

Electrolytic detoxication of cyanide using V4A anode - and adding copper salt in small amt to prevent electrolytic dissolution of anode, for economy

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Publication number
DE2251442A1
DE2251442A1 DE19722251442 DE2251442A DE2251442A1 DE 2251442 A1 DE2251442 A1 DE 2251442A1 DE 19722251442 DE19722251442 DE 19722251442 DE 2251442 A DE2251442 A DE 2251442A DE 2251442 A1 DE2251442 A1 DE 2251442A1
Authority
DE
Germany
Prior art keywords
anode
electrolytic
cyanide
detoxication
economy
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
Application number
DE19722251442
Other languages
German (de)
Other versions
DE2251442C3 (en
DE2251442B2 (en
Inventor
Helmut Dr Rer Nat Reuther
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Keramchemie 5433 Siershahn De GmbH
Original Assignee
GEWERK KERAMCHEMIE
GEWERKSCHAFT KERAMCHEMIE 5433 SIERSHAHN
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by GEWERK KERAMCHEMIE, GEWERKSCHAFT KERAMCHEMIE 5433 SIERSHAHN filed Critical GEWERK KERAMCHEMIE
Priority to DE19722251442 priority Critical patent/DE2251442C3/en
Publication of DE2251442A1 publication Critical patent/DE2251442A1/en
Publication of DE2251442B2 publication Critical patent/DE2251442B2/en
Application granted granted Critical
Publication of DE2251442C3 publication Critical patent/DE2251442C3/en
Expired legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D3/00Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
    • A62D3/10Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by subjecting to electric or wave energy or particle or ionizing radiation
    • A62D3/11Electrochemical processes, e.g. electrodialysis
    • A62D3/115Electrolytic degradation or conversion
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/46Treatment of water, waste water, or sewage by electrochemical methods
    • C02F1/461Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
    • C02F1/467Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
    • C02F1/4672Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D2101/00Harmful chemical substances made harmless, or less harmful, by effecting chemical change
    • A62D2101/20Organic substances
    • A62D2101/26Organic substances containing nitrogen or phosphorus
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D2101/00Harmful chemical substances made harmless, or less harmful, by effecting chemical change
    • A62D2101/40Inorganic substances
    • A62D2101/45Inorganic substances containing nitrogen or phosphorus
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/16Nitrogen compounds, e.g. ammonia
    • C02F2101/18Cyanides

Abstract

A continuous or stationary process is used in Cu salt is added to the electrolyte in an amt. of 50-150 (100) mg/l Cu2+; A residual content of 0.5 g/l CN' can be achieved at 65% current yield. The addn. of 400 mg/l. CuSO4.5H2O is partic pref. Salts of Ag, Au and other more noble metals are also effective, but costlier.

Description

Verfahren zur elektrochemischen Entgiftung von cyanidhaltigen Wässrigen Lösungen In Anpassung an die jeweiiigen Gegebenheiten sind chemische, elektrochemische und katalytische Verfahren für die Entgiftung von cyanidhaltigen Lösungen Lösungen bekannt und Kombinationen solcher Verfahren.Process for the electrochemical detoxification of cyanide-containing water Solutions In adaptation to the respective conditions are chemical, electrochemical and catalytic processes for the detoxification of solutions containing cyanide known and combinations of such processes.

Der Erfindung liegt die Aufgabenstellung zugrunde, das in chemischer Hinsicht hochresistente V4A-Materlal als Werkstoff für die Anoden bei der elektrochemischen Entgiftung von Cyanid zu ver-enden.The invention is based on the object that in chemical Highly resistant V4A material as material for the anodes in the electrochemical Detoxification of cyanide to end.

Gegenstand der Erfindung ist ein \Terfahrc-n zur elektrolytischen Entgiftung von Cyanid, dadurch gekennzeichnet, daß als Anodenmaterial VA-Material verwendet zirka und dem Elektrolyten Kupf ersalze in Mengen von 50 mg Cu2+ pro Liter bis 150 mg Gu2+ pro Liter zugeset'zt werden.The subject of the invention is a \ Terfahrc-n for electrolytic Detoxification of cyanide, characterized in that VA material is used as the anode material uses approximately and the electrolyte copper salts in quantities of 50 mg Cu2 + per liter up to 150 mg Gu2 + per liter can be added.

Als besonders vorteilhaft'hat sich ein Zusatz von 400 mg CuSO4.5H2O pro Liter eriesen.It is particularly advantageous to add 400 mg of CuSO4.5H2O per liter.

Es ist auBerordentlich überraschend, daß durch Zusatz so kleiner ?iengen an Kupfersalzen die elektrolytische Auflösung der V4A-Anoden unter Stromfluß vermieden werden kann, daß eine Ausgestaltung zu einem wirtschaftlichen technischen Verfahren möglich ist, bei dem geeignete Anoden im Elektrolyten selbst erhalten werden können.It is extraordinarily surprising that they are so smaller by adding them Avoided electrolytic dissolution of the V4A anodes with copper salts under current flow It can be that an embodiment becomes an economical technical process is possible in which suitable anodes can be obtained in the electrolyte itself.

Selbstverständlich können auch Salze des Silbers, des Goldes und anderer edlerer Metalle für das erfindungsgemäße Verfahren ver--endet werden, die jedoch teurer sind als die Salze des Kupfers.Of course, salts of silver, gold and others can also be used nobler metals are used for the process according to the invention, but these are more expensive than the salts of copper.

Bekannt sind die Verwendung von Magnetit als Anodenmaterial, der Zusatz von o,2 % Kupfer oder anderer edlerer Metalle zu grunde metallen für-Elektrolysen, desgleichen die Herstellung von Zementkupfer durch Ausfällung vermittels Eisen.The use of magnetite as an anode material, the additive, is known from o, 2% copper or other noble metals to basic metals for electrolysis, likewise the production of cement-copper by precipitation with iron.

Überraschenderweise wird beim erfindungsge£oäßen Verfahren eine qinreichende Haftfetigkeit des feinpulvrigen Kupfers auf dem Anodenrnaterial für die Durchführung der elektrolytischen Entgiftung nach dem erfindungsgemäßen Verfahren erzielt. Das ist um o überraschender, da bei der Elektrolyse auch noch abgeschiedenes feinpulvrie Kupfer in Lösung geht und leer abgeschieden wird und keine unlösliche nichtleitende Sperrschichten erzeugt erden.Surprisingly, the method according to the invention is sufficient Adhesion of the finely powdered copper to the anode material for the implementation the electrolytic detoxification achieved by the method according to the invention. That is all the more surprising, since fine powder also deposited during the electrolysis Copper goes into solution and is deposited empty and not insoluble non-conductive Ground barriers created.

Die V4A-Anoden zeigen bei der Durchführung der Elektrolyse gemäß Patentanspruch keinerlei Gewichtsabnahme, auch über lange Zeiträume hin eg nicht.The V4A anodes show when carrying out the electrolysis according to claim no weight loss whatsoever, even over long periods of time, eg not.

Das vorschlagsgemäße Verfahren kann mit der sei elektrolytischen Oxydationen üblicnen Stromausbeute von 65 % bis zu einem Restgehalt von o,) g/l CN im burcnlaufverfahren oder im Standverfahren durengefünrt @erden. Daran kann chemische Restentgiftung angeschlossen @erden.The proposed method can be with electrolytic oxidations Usual current yield of 65% up to a residual content of 0.1 g / l CN in the burnt-out process or in the stand procedure durengefünrt @erden. This can be used to detoxify chemical residues connected @ground.

Selbstverständlich können dem Elektrolyten aucn noch Kupfersalzmengen über 150 mg Cu2+ pro Liter zugesetzt werden.Of course, the electrolyte can also contain amounts of copper salt more than 150 mg Cu2 + per liter are added.

Beispiel: 22,5 1 einer bösung mit 10 g/l CN wurden im Standverfahren bis auf einen Restgehalt von 180 mg/l ON entgiftet. Die Gesamtmenge an oxidierter Cyanid betrug somit 221 g.Example: 22.5 l of a solution with 10 g / l CN were used in the standing process detoxified to a residual content of 180 mg / l ON. The total amount of oxidized The cyanide was thus 221 g.

flektrolysedaten: Zellenpannung 2,3 V Stromstärke 100 A Llektrolysedauer 6 Std. 40 Min.Flectrolysis data: Cell voltage 2.3 V, current 100 A, duration of electrolysis 6 hours 40 minutes

Elektrodenabstand 27 mm Hieraus ergibt sich für die Entgiftung von einem Kilogramm Cyanid ein Leistungsbedarf von 6,8 KW. Electrode spacing 27 mm This results in the detoxification of one kilogram of cyanide requires 6.8 KW of power.

Es @urden 393 mg Kupfersulfat pro Liter Lösung zugesetzt, was einer Konzentration von ca. 100 mg/1 Cu2+ entspricht.393 mg of copper sulfate per liter of solution were added, which is a Concentration of approx. 100 mg / 1 Cu2 + corresponds.

Claims (2)

PatentansprücheClaims 1. Verfahren zur elektrolytischen Entgiftung von Cyanid im Durchlaufverfahren oder im Standverfahren, d ad u r c h g e k e n n z e i c h n e t, daß als Anodenmaterial VA-Material verwendet wird und dem Elektrolyten Kupfersalze in Mengen von 50 mg Cu2+ pro Liter bis 150 mg Cu2+ pro Liter zugesetzt werden.1. Process for the electrolytic detoxification of cyanide in a continuous process or in the standing procedure, d ad u r c h e k e n n n n n e i n e t that as anode material VA material is used and the electrolyte is copper salts in amounts of 50 mg Cu2 + per liter up to 150 mg Cu2 + per liter can be added. 2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß dem Elektrolyten 100 mg Cu2+ pro Liter zugesetzt werden.2. The method according to claim 1, characterized in that the electrolyte 100 mg Cu2 + per liter can be added.
DE19722251442 1972-10-20 1972-10-20 Process for the electrolytic detoxification of cyanide Expired DE2251442C3 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19722251442 DE2251442C3 (en) 1972-10-20 1972-10-20 Process for the electrolytic detoxification of cyanide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19722251442 DE2251442C3 (en) 1972-10-20 1972-10-20 Process for the electrolytic detoxification of cyanide

Publications (3)

Publication Number Publication Date
DE2251442A1 true DE2251442A1 (en) 1974-04-25
DE2251442B2 DE2251442B2 (en) 1979-05-17
DE2251442C3 DE2251442C3 (en) 1980-01-10

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Family Applications (1)

Application Number Title Priority Date Filing Date
DE19722251442 Expired DE2251442C3 (en) 1972-10-20 1972-10-20 Process for the electrolytic detoxification of cyanide

Country Status (1)

Country Link
DE (1) DE2251442C3 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4218916A1 (en) * 1992-06-10 1993-12-16 Heraeus Elektrochemie Process for electrolytic detoxification or regeneration of an aqueous solution containing cyanide and device for carrying out the process
DE102011081805A1 (en) 2011-08-30 2013-02-28 Akretia Gmbh Electrolytic refining of metals from solid starting material containing metal to be refined, comprises contacting starting material with cyanide-containing leaching solution, electrolytically depositing metal, and partially reacting cyanide

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3429156C2 (en) * 1984-08-08 1994-06-23 Teves Gmbh Alfred Circuit arrangement for monitoring and controlling an anti-lock brake system

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4218916A1 (en) * 1992-06-10 1993-12-16 Heraeus Elektrochemie Process for electrolytic detoxification or regeneration of an aqueous solution containing cyanide and device for carrying out the process
DE102011081805A1 (en) 2011-08-30 2013-02-28 Akretia Gmbh Electrolytic refining of metals from solid starting material containing metal to be refined, comprises contacting starting material with cyanide-containing leaching solution, electrolytically depositing metal, and partially reacting cyanide

Also Published As

Publication number Publication date
DE2251442C3 (en) 1980-01-10
DE2251442B2 (en) 1979-05-17

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8327 Change in the person/name/address of the patent owner

Owner name: KERAMCHEMIE GMBH, 5433 SIERSHAHN, DE

8339 Ceased/non-payment of the annual fee