GB958355A - Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor - Google Patents

Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor

Info

Publication number
GB958355A
GB958355A GB29895/59A GB2989559A GB958355A GB 958355 A GB958355 A GB 958355A GB 29895/59 A GB29895/59 A GB 29895/59A GB 2989559 A GB2989559 A GB 2989559A GB 958355 A GB958355 A GB 958355A
Authority
GB
United Kingdom
Prior art keywords
groups
anion
gold
alkyl groups
carbon atoms
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
Application number
GB29895/59A
Inventor
Norman Frank Kember
Anthony Arthur Bueggs
Ronald Alfred Wells
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.)
National Research Development Corp UK
Original Assignee
National Research Development Corp UK
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 National Research Development Corp UK filed Critical National Research Development Corp UK
Priority to GB472/64A priority Critical patent/GB958356A/en
Priority to GB29895/59A priority patent/GB958355A/en
Publication of GB958355A publication Critical patent/GB958355A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G7/00Compounds of gold
    • C01G7/003Preparation involving a liquid-liquid extraction, an adsorption or an ion-exchange
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J41/00Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
    • B01J41/04Processes using organic exchangers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J41/00Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
    • B01J41/04Processes using organic exchangers
    • B01J41/05Processes using organic exchangers in the strongly basic form
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G5/00Compounds of silver
    • C01G5/003Preparation involving a liquid-liquid extraction, an adsorption or an ion-exchange
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • C08F8/32Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20Treatment or purification of solutions, e.g. obtained by leaching
    • C22B3/42Treatment or purification of solutions, e.g. obtained by leaching by ion-exchange extraction
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

Gold and/or silver values are recovered from a gold and/or silver bearing aqueous cyanide liquor by treatment with one or more anion-exchange mixed base resins containing base groups of the type -CH2NRR0, where R and R0 are each an alkyl group which may be the same or different having at least 3 carbon atoms, such alkyl groups being branched or unbranched, the branch not being in the one or two carbon position of the groups, and from 1 to 35% of quaternary groups of the type -CH2NR1R2R3, where R1, R2 and R3 are alkyl groups which may be the same or different and which contain either two or three carbon atoms, and then eluting the gold and/or silver values from the resin, preferably by means of an aqueous or polar organic solvent solution of an alkali metal or ammonium thiocyanate. The anion-exchange resins may be based upon a cross-linked polystyrene e.g. a polystyrene obtained by using 1% to 5% of divinyl benzene or other cross-linking agent. Such a resin may be converted into an anion-exchange resin by chloromethylation (using chloromethyl ether in the presence of catalyst) followed by amination with one or more secondary amines RR0NH and one or more tertiary amines R1R2R3N. The alkyl groups R, R0 in the secondary amines should be those required in the main anion-exchange group -CH2NRR0, and R1, R2, R3 in the tertiary amines should be those required in -CH2NR1R2R3. Specifications 808,909, 808,910 and 958,356 are referred to.ALSO:An N-methano dialkylamine anion-exchange mixed base resin containing base groups of the type -CH2NRR0 and from 1 to 35% of quater nary groups of the type -CH2NR1R2R3 where R and R0 are each alkyl groups, the same or different, having at least three carbon atoms, said alkyl groups being unbranched or branched, the branch not being in the one or two carbon position of the groups, and R1, R2 and R3 are alkyl groups which may be the same or different and which contain either two or three carbon atoms is used to recover gold and silver values (see Division C1). Preferably R and R0 should have at least four carbon atoms. The resin may be based on a cross-linked polystyrene, such as a modified polystyrene obtained by using 1 to 5% of divinyl-benzene as a cross-linking agent. Such resins are preferably converted into the required anion-exchange resins by first halomethylating e.g. chloromethylating using chloromethyl ether in the presence of stannic chloride, the more volatile reaction products boiling below 53 DEG C. being removed by fractional distillation during the early stages of the chloromethylation, and then aminating with one or more secondary amines RR0NH and one or more tertiary amines R1R2R3N. The amination, which may be performed with or without water, is preferably carried out in the presence of a polystyrene swelling agent such as dioxane or chlorobenzene. In the examples chloromethylated polystyrene beads are treated with di-n-butylamine and either triethylamine or tri-n-propylamine. Specifications 808,909, 808,910 and 958,356 are referred to.
GB29895/59A 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor Expired GB958355A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB472/64A GB958356A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor
GB29895/59A GB958355A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB29895/59A GB958355A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor

Publications (1)

Publication Number Publication Date
GB958355A true GB958355A (en) 1964-05-21

Family

ID=10298923

Family Applications (2)

Application Number Title Priority Date Filing Date
GB472/64A Expired GB958356A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor
GB29895/59A Expired GB958355A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB472/64A Expired GB958356A (en) 1959-09-02 1959-09-02 Improvements in or relating to the recovery of gold and silver from aqueous cyanide liquors and to anion exchange resins therefor

Country Status (1)

Country Link
GB (2) GB958356A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0046025A2 (en) * 1980-08-07 1982-02-17 Commonwealth Scientific And Industrial Research Organisation Selective extraction of gold

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2166140B (en) * 1984-10-27 1989-06-07 Ion Exchange Novel adsorbents for use in the purification of water and other chemicals and a process for preparing same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0046025A2 (en) * 1980-08-07 1982-02-17 Commonwealth Scientific And Industrial Research Organisation Selective extraction of gold
EP0046025A3 (en) * 1980-08-07 1982-03-10 Commonwealth Scientific And Industrial Research Organization Selective extraction of gold

Also Published As

Publication number Publication date
GB958356A (en) 1964-05-21

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