CN108842072A - A kind of leaching liquid and extract technology of zinc - Google Patents

A kind of leaching liquid and extract technology of zinc Download PDF

Info

Publication number
CN108842072A
CN108842072A CN201810969985.7A CN201810969985A CN108842072A CN 108842072 A CN108842072 A CN 108842072A CN 201810969985 A CN201810969985 A CN 201810969985A CN 108842072 A CN108842072 A CN 108842072A
Authority
CN
China
Prior art keywords
zinc
leaching
parts
liquid
leaching liquid
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.)
Pending
Application number
CN201810969985.7A
Other languages
Chinese (zh)
Inventor
李百荃
李军
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.)
Zibo Gan Da Environmental Protection Technology Co Ltd
Original Assignee
Zibo Gan Da Environmental Protection Technology Co Ltd
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 Zibo Gan Da Environmental Protection Technology Co Ltd filed Critical Zibo Gan Da Environmental Protection Technology Co Ltd
Priority to CN201810969985.7A priority Critical patent/CN108842072A/en
Publication of CN108842072A publication Critical patent/CN108842072A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/20Obtaining zinc otherwise than by distilling
    • C22B19/22Obtaining zinc otherwise than by distilling with leaching with acids
    • 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

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Electrolytic Production Of Metals (AREA)

Abstract

A kind of leaching liquid and extract technology of zinc, belong to zinc preparation method technical field.It is characterized in that, group becomes the raw material of water and following parts by weight:31.2 ~ 38.6 parts of iron chloride, 49.8 ~ 58.7 parts of sodium chloride, 4.3 ~ 6.2 parts of yttrium chloride, 4.2 ~ 6.7 parts of hydrochloric acid.Leaching step:Zinc concentrate is added to the leaching liquid of zinc, the solid-to-liquid ratio g of zinc concentrate and zinc leaching liquid after broken:L is 1 ~ 3:4~7;It carries out leaching while carrying out electrochemical reduction under agitation, leaching temperature is 40 DEG C ~ 50 DEG C, and leaching time is 2.5h ~ 3h;0.01% ~ 1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 obtains zinc chloride through evaporative crystallization, is back to the reuse of zinc leaching liquid after the steam condensation evaporated.This leaching liquid and extract technology leach the zinc in mine adequately.Leaching liquid used can be recycled after isolating required zinc.

Description

A kind of leaching liquid and extract technology of zinc
Technical field
A kind of leaching liquid and extract technology of zinc, belong to zinc preparation method technical field.
Background technique
Zinc concentrate be usually by zinc zinc ore or zinc-containing ores through techniques such as broken, ball milling, froth flotations reaching for producing To the higher ore of zinc content of national standard.Alloy can be made with a variety of non-ferrous metals in zinc, wherein most importantly zinc and copper, The brass etc. of the compositions such as tin, zinc, can also be with the composition diecasting alloys such as aluminium, magnesium, copper.Zinc is mainly used for steel, metallurgy, machinery, electricity Gas, chemical industry, light industry, military affairs and medicine and other fields.The preparation method of zinc mainly includes following several at present:1)By marmatite or Zincblende is sintered into zinc oxide in air, is then restored to obtain the final product with charcoal, but the purity of gained zinc is lower;2)By zinc oxide and Coke mixing, heating causes 1373K ~ 1573K in blast furnace, comes out zinc distillation, purity about 98%;But energy consumption is excessively high, 3)With After sulfuric acid leaching is at zinc sulfate, by controlling pH, make zinc be dissolved as zinc sulfate and the hydrolysis of the impurity such as iron arsenic antimony be converted into precipitate into Enter in leached mud, the impurity such as the copper cadmium that zinc powder removes in filtrate is added, then be deposited zinc with electrolysis method, the zinc produced is pure It spends higher(About 99.99%), but this method, the recovery rate of zinc is not high enough, and preparation efficiency is relatively low.
Summary of the invention
The technical problem to be solved by the present invention is to:Overcome the deficiencies of the prior art and provide a kind of high production efficiency, the energy disappears Consume the leaching liquid and extract technology of few zinc.
The technical solution adopted by the present invention to solve the technical problems is:The leaching liquid of the zinc, which is characterized in that group becomes The raw material of water and following parts by weight:31.2 ~ 38.6 parts of iron chloride, 49.8 ~ 58.7 parts of sodium chloride, 4.3 ~ 6.2 parts of yttrium chloride, hydrochloric acid 4.2 ~ 6.7 parts.
Zinc leaching liquid of the invention is suitble to directly quickly be leached from ore, and the zinc powder as seed is being added It afterwards, can more completely leaching separation goes out by the zinc in mineral.Can efficiently, completely by the zinc leaching separation in zinc ore Out.Leaching liquid of the invention can be reused, without discharging of waste liquid, environmental protection and energy saving.
Preferably, group become water and following parts by weight 49.8 ~ 58.7 parts of 31.2 ~ 38.6 parts of raw material iron chloride, sodium chloride, 4.7 ~ 5.4 parts of yttrium chloride, 4.7 ~ 5.7 parts of hydrochloric acid.Preferred zinc leaching liquid proportion can be in the environment of milder faster Complete leaching.
Preferably, the mass ratio of the yttrium chloride and hydrochloric acid is 1:1.05.Preferred proportion can be further improved leaching Efficiency.
A kind of extract technology of zinc, which is characterized in that include the following steps:
1)Zinc concentrate is added to the leaching liquid of any one of claim 1 ~ 3 zinc, zinc concentrate and zinc leaching liquid after broken Solid-to-liquid ratio g:L is 1 ~ 3:4~7;It carries out leaching while carrying out electrochemical reduction under agitation, leaching temperature is 80 DEG C ~ 95 DEG C, leaching time is 2h ~ 3h;
2)0.01% ~ 1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is through evaporative crystallization Zinc chloride is obtained, is back to the reuse of zinc leaching liquid after the steam condensation evaporated.
The present invention provide it is a kind of directly leached by zinc ore, obtain the technique of zinc chloride, zinc chloride can be directly as Product is applied, and zinc chloride can also be given to subsequent process and obtain zinc metal.Key of the invention is leaching liquid, zinc leaching Take liquid be suitble to directly quickly leached from ore, be added as the zinc powder of seed after, can by the zinc in mineral compared with Complete leaching separation goes out.It realizes and efficiently, completely goes out the zinc leaching separation in zinc ore.Leaching liquid of the invention can It reuses, without discharging of waste liquid, environmental protection and energy saving.Preparation process of the invention is not destroyed to remaining element in ore, After leaching zinc out, remaining element is easier to separate and produce.
Preferably, the content of the Zinc in Zinc Concentrates is calculated in mass percent greater than 40%.Technique of the invention is especially suitable Close and continuous two step is carried out to the higher ore of Zn content leach, realize efficient, complete zinc, sulphur content from.
Preferably, step 1)Described in leaching temperature be 80 DEG C ~ 85 DEG C, leaching time be 2.0 h ~ 2.5h.The leaching Condition meets preferred zinc leaching liquid proportion leaching.
Preferably, step 1)The solid-to-liquid ratio g of middle zinc concentrate and zinc leaching liquid:L is 2:5~6.Preferred zinc concentrate and zinc soak Take the solid-to-liquid ratio of liquid that can faster complete to leach.
Preferably, step 2)The amount of middle zinc powder is the 0.5% ~ 1% of Zinc Concentrates Quality.The seed zinc powder of preferred amounts can be faster The completion leaching of speed.
Preferably, step 1)Described in progress electrochemical reduction voltage be the V of 10V ~ 30, electric current be 10 A ~ 100A, institute Electrode is tungsten electrode.Preferred electrochemical reduction condition can preferably cooperate with leaching condition, more efficiently, completely Separation.
Compared with prior art, possessed beneficial effect of the invention is:This leaching liquid and extract technology make in mine Zinc is adequately leached.Leaching liquid used can be recycled after isolating required zinc, and the mine generated It is standby that slag can be used for further made of metal, after extracting zinc, the concentration of residual metallic element double it is even more, Keep the refinement of residual metallic element more convenient.This preparation process is not only able to efficiently prepare zinc metal, and required temperature It spends that lower, energy consumption is smaller, is generated in the process without any exhaust gas, waste residue, waste liquid, energy conservation and environmental protection.
Specific embodiment
The present invention will be further described combined with specific embodiments below, and wherein embodiment 1 is best implements.
Embodiment 1
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 2:5.6;It carries out leaching while carrying out electrochemical reduction under agitation, electrification The voltage for learning reduction is 15 V, and electric current 50A, electrode used is tungsten electrode;Leaching temperature is 80 DEG C, leaching time 2h; The leaching liquid of zinc, which is characterized in that group becomes the raw material of water and following parts by weight:35.2 parts of iron chloride, 54.7 parts of sodium chloride, chlorine Change 5.1 parts of yttrium, 5.2 parts of hydrochloric acid;
2)0.61% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is obtained through evaporative crystallization Zinc chloride is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 0.001%.
Embodiment 2
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 2:5;It carries out leaching under agitation while carrying out electrochemical reduction, electrochemistry The voltage of reduction is 15V, and electric current 30A, electrode used is tungsten electrode;Leaching temperature is 85 DEG C, leaching time 2.5h;Zinc Leaching liquid, which is characterized in that group become water and following parts by weight raw material:33.2 parts of iron chloride, 55.7 parts of sodium chloride, chlorination 5.4 parts of yttrium, 5.7 parts of hydrochloric acid;
2)1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 obtains chlorine through evaporative crystallization Change zinc, is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 0.001%.
Embodiment 3
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 2:6;It carries out leaching under agitation while carrying out electrochemical reduction, electrochemistry The voltage of reduction is 25 V, and electric current 70A, electrode used is tungsten electrode;Leaching temperature is 80 DEG C, and leaching time is 2 h;Zinc Leaching liquid, which is characterized in that group become water and following parts by weight raw material:37.6 parts of iron chloride, 51.8 parts of sodium chloride, chlorination 4.7 parts of yttrium, 4.7 parts of hydrochloric acid;
2)0.5% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is obtained through evaporative crystallization Zinc chloride is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 0.001%.
Embodiment 4
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 1:7;It carries out leaching under agitation while carrying out electrochemical reduction, electrochemistry The voltage of reduction is 10V, and electric current is 10 A, and electrode used is tungsten electrode;Leaching temperature is 90 DEG C, leaching time 3h;Zinc Leaching liquid, which is characterized in that group become water and following parts by weight raw material:31.2 parts of iron chloride, 58.7 parts of sodium chloride, chlorination 4.3 parts of yttrium, 4.2 parts of hydrochloric acid;
2)0.1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is obtained through evaporative crystallization Zinc chloride is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 0.004%.
Embodiment 5
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 3:4;It carries out leaching under agitation while carrying out electrochemical reduction, electrochemistry The voltage of reduction is 30 V, and electric current 100A, electrode used is tungsten electrode;Leaching temperature is 95 DEG C, leaching time 2.8h; The leaching liquid of zinc, which is characterized in that group becomes the raw material of water and following parts by weight:38.6 parts of iron chloride, 49.8 parts of sodium chloride, chlorine Change 6.2 parts of yttrium, 6.7 parts of hydrochloric acid;
2)0.01% ~ 1% 0.5% ~ 1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 warp Evaporative crystallization obtains zinc chloride, is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 0.005%.
Comparative example 1
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 2:5.6;It carries out leaching while carrying out electrochemical reduction under agitation, electrification The voltage for learning reduction is 15 V, and electric current 50A, electrode used is tungsten electrode;Leaching temperature is 40 DEG C, and leaching time is 2.5h;The leaching liquid of zinc, which is characterized in that group becomes the raw material of water and following parts by weight:35.2 parts of iron chloride, sodium chloride 54.7 Part, 5.2 parts of hydrochloric acid;
2)0.61% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is obtained through evaporative crystallization Zinc chloride is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 39.4%.
Comparative example 2
1)Zinc concentrate is added to the leaching liquid of zinc, it is 43.2% that the content of Zinc in Zinc Concentrates, which is calculated in mass percent, after broken.Zinc The solid-to-liquid ratio g of concentrate and zinc leaching liquid:L is 2:5.6;It carries out leaching while carrying out electrochemical reduction under agitation, electrification The voltage for learning reduction is 15 V, and electric current 50A, electrode used is tungsten electrode;Leaching temperature is 40 DEG C, and leaching time is 2.5h;The leaching liquid of zinc, which is characterized in that group becomes the raw material of water and following parts by weight:54.7 parts of iron chloride, sodium chloride 35.2 Part, 5.1 parts of yttrium chloride, 5.2 parts of hydrochloric acid;
2)0.61% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is obtained through evaporative crystallization Zinc chloride is back to the reuse of zinc leaching liquid after the steam condensation evaporated;
Detecting the Zn content in filter residue Y1 is 28.4%.
The above described is only a preferred embodiment of the present invention, being not that the invention has other forms of limitations, appoint What those skilled in the art changed or be modified as possibly also with the technology contents of the disclosure above equivalent variations etc. Imitate embodiment.But without departing from the technical solutions of the present invention, according to the technical essence of the invention to above embodiments institute Any simple modification, equivalent variations and the remodeling made, still fall within the protection scope of technical solution of the present invention.

Claims (9)

1. a kind of leaching liquid of zinc, which is characterized in that group becomes the raw material of water and following parts by weight:31.2 ~ 38.6 parts of iron chloride, 49.8 ~ 58.7 parts of sodium chloride, 4.3 ~ 6.2 parts of yttrium chloride, 4.2 ~ 6.7 parts of hydrochloric acid.
2. a kind of leaching liquid of zinc according to claim 1, it is characterised in that:Group becomes the raw material of water and following parts by weight 31.2 ~ 38.6 parts of iron chloride, 49.8 ~ 58.7 parts of sodium chloride, 4.7 ~ 5.4 parts of yttrium chloride, 4.7 ~ 5.7 parts of hydrochloric acid.
3. a kind of leaching liquid of zinc according to claim 1, it is characterised in that:The mass ratio of the yttrium chloride and hydrochloric acid It is 1:1.05.
4. a kind of extract technology of zinc, which is characterized in that include the following steps:
1)Zinc concentrate is added to the leaching liquid of any one of claim 1 ~ 3 zinc, zinc concentrate and zinc leaching liquid after broken Solid-to-liquid ratio g:L is 1 ~ 3:4~7;It carries out leaching while carrying out electrochemical reduction under agitation, leaching temperature is 80 DEG C ~ 95 DEG C, leaching time is 2h ~ 3h;
2)0.01% ~ 1% zinc powder of Zinc Concentrates Quality is added, filtrate X1 and filter residue Y1 is obtained by filtration;Filtrate X1 is through evaporative crystallization Zinc chloride is obtained, is back to the reuse of zinc leaching liquid after the steam condensation evaporated.
5. a kind of extract technology of zinc according to claim 4, it is characterised in that:The content of the Zinc in Zinc Concentrates with Mass percentage is greater than 40%.
6. a kind of extract technology of zinc according to claim 4, it is characterised in that:Step 1)Described in leaching temperature be 80 DEG C ~ 85 DEG C, leaching time is 2h ~ 2.5h.
7. a kind of extract technology of zinc according to claim 4, it is characterised in that:Step 1)Middle zinc concentrate and zinc leaching liquid Solid-to-liquid ratio g:L is 2:5~6.
8. a kind of extract technology of zinc according to claim 4, it is characterised in that:Step 2)The amount of middle zinc powder is zinc concentrate The 0.5% ~ 1% of quality.
9. a kind of extract technology of zinc according to claim 4, it is characterised in that:Step 1)Described in progress electrochemistry also Former voltage is the V of 10V ~ 30, and electric current is 10 A ~ 100A, and electrode used is tungsten electrode.
CN201810969985.7A 2018-08-24 2018-08-24 A kind of leaching liquid and extract technology of zinc Pending CN108842072A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810969985.7A CN108842072A (en) 2018-08-24 2018-08-24 A kind of leaching liquid and extract technology of zinc

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810969985.7A CN108842072A (en) 2018-08-24 2018-08-24 A kind of leaching liquid and extract technology of zinc

Publications (1)

Publication Number Publication Date
CN108842072A true CN108842072A (en) 2018-11-20

Family

ID=64189266

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810969985.7A Pending CN108842072A (en) 2018-08-24 2018-08-24 A kind of leaching liquid and extract technology of zinc

Country Status (1)

Country Link
CN (1) CN108842072A (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1197766A (en) * 1998-03-20 1998-11-04 水志良 Reclamation method and equipment of zinc chloride from zinc-containing organic waste liquid
CN101090983A (en) * 2004-10-21 2007-12-19 安格洛操作有限公司 Leaching process in the presence of hydrochloric acid for the recovery of a value metal from an ore
CN103589873A (en) * 2013-11-27 2014-02-19 郴州市金贵银业股份有限公司 Method for recovering valuable metals from silver-zinc slag
CN105779774A (en) * 2016-04-22 2016-07-20 王树立 Lead concentrate and zinc anode mud combined recycling method
CN105936979A (en) * 2016-07-06 2016-09-14 广东新生环保科技股份有限公司 Lead recovery agent for lead-containing wastes and application method thereof
CN106011474A (en) * 2016-05-24 2016-10-12 郴州市金贵银业股份有限公司 Silver-zinc crust wet process comprehensive recovery method
CN106222431A (en) * 2016-08-30 2016-12-14 北京矿冶研究总院 Method for comprehensively recovering rare and dispersed noble metals from smelting furnace slag

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1197766A (en) * 1998-03-20 1998-11-04 水志良 Reclamation method and equipment of zinc chloride from zinc-containing organic waste liquid
CN101090983A (en) * 2004-10-21 2007-12-19 安格洛操作有限公司 Leaching process in the presence of hydrochloric acid for the recovery of a value metal from an ore
CN103589873A (en) * 2013-11-27 2014-02-19 郴州市金贵银业股份有限公司 Method for recovering valuable metals from silver-zinc slag
CN105779774A (en) * 2016-04-22 2016-07-20 王树立 Lead concentrate and zinc anode mud combined recycling method
CN106011474A (en) * 2016-05-24 2016-10-12 郴州市金贵银业股份有限公司 Silver-zinc crust wet process comprehensive recovery method
CN105936979A (en) * 2016-07-06 2016-09-14 广东新生环保科技股份有限公司 Lead recovery agent for lead-containing wastes and application method thereof
CN106222431A (en) * 2016-08-30 2016-12-14 北京矿冶研究总院 Method for comprehensively recovering rare and dispersed noble metals from smelting furnace slag

Similar Documents

Publication Publication Date Title
Anderson The metallurgy of antimony
Dvořák et al. Hydrometallurgical recovery of zinc from hot dip galvanizing ash
CA2860614C (en) Recovering lead from a mixed oxidized material
CN104789783B (en) Process for selective efficient copper extraction and comprehensive recovery from lead copper matte
CN104928483B (en) Method for comprehensively recovering silver, selenium, tellurium and copper from copper telluride residues
CN108624759B (en) Method for comprehensively recovering valuable metals from white smoke
CN106566928A (en) Method used for selective high-efficiency extraction of copper and bismuth from high-copper bismuth slag
CN101560670A (en) High nickel matte refining method
CN104630826A (en) Technique for recovering tin from tin anode sludge
CN106381399B (en) A method of recycling tellurium from high tellurium slag charge
CN111647754A (en) Comprehensive utilization method of zinc-containing dust and sludge in steel plant
CN103695636A (en) Preparation method of electrolytic manganese dioxide
CN104017991A (en) Process for efficiently and selectively separating copper in lead copper matte
CN104263948A (en) Method for recovering sliver from silver-bearing waste liquor
CN105200242B (en) A kind of method that cadmium is reclaimed from containing arsenic refining lead oxygen bottom blown furnace cigarette ash
CN106498181A (en) Green metallurgy extraction method for lead-zinc oxide ore
CN109402410B (en) Method for enriching precious metals through iron matte acid slag pretreatment
CN100586617C (en) Method for recycling and preparing ultra-fine zinc dust from zinc dust containing material
CN104805301B (en) Method for producing zinc ingots by using hot-dip galvanizing slag for wet smelting and zero discharge of waste residues
CN113481371A (en) Method for efficiently recovering antimony, bismuth, copper and silver from silver separating slag of lead anode slime
CN109971945A (en) A kind for the treatment of process of coarse tin decoppered slag
CN116411169B (en) Comprehensive utilization method of leadless hot galvanizing scum
CN105018726B (en) A kind of lead zinc mineral intergrowth processing method
CN111575500A (en) Method for treating zinc-containing dangerous solid waste and zinc ore by combining chlorination roasting with ammonia process electrodeposition
CN108977656A (en) A kind of lixiviation process preparation process of Zinc in Zinc Concentrates and sulphur

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20181120