CN104831315A - Novel process for recovering antimony from antimony-containing gold concentrate - Google Patents
Novel process for recovering antimony from antimony-containing gold concentrate Download PDFInfo
- Publication number
- CN104831315A CN104831315A CN201510148856.8A CN201510148856A CN104831315A CN 104831315 A CN104831315 A CN 104831315A CN 201510148856 A CN201510148856 A CN 201510148856A CN 104831315 A CN104831315 A CN 104831315A
- Authority
- CN
- China
- Prior art keywords
- antimony
- electrodeposition
- gold concentrate
- press filtration
- novel process
- 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
Links
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Manufacture And Refinement Of Metals (AREA)
Abstract
The invention relates to a new process for recovering antimony from antimony-containing gold concentrate, which comprises the steps of slurrying, leaching, filter pressing and washing, electrodeposition, waste liquid treatment and the like.
Description
Technical field
The present invention relates to a kind of for containing the pretreated novel process of antimony gold concentrate, belong to field of metallurgy and chemical engineering.
Background technology
Antimony (Sb) is a kind of silvery white friable metal; a kind of acid-proof substances at normal temperatures; it is a kind of broad-spectrum metal, is described as " fire extinguishing fp person who has rendered outstanding service ", " strategy metal ", " metallic hard agent ", " protective material of fluorescent tube, electron tube ".
At present, in gold smelting enterprise production process, antimony is a kind of harmful element, and this element exists not only affects quality product to roasting, affects Cyanide Leaching index, reduces Au, Ag rate of recovery.And the production method of existing metallic antimony, pyrogenic process and the large class of wet method two, antimony pyrometallurgical smelting method can be divided into mainly contain precipitation melting and roast-reduction melting, the defect mainly SO of antimony pyrometallurgical smelting
2seriously polluted, administer difficulty, the rate of recovery is low, in smelting process, because returning charge is many, causes the direct yield of metal and the rate of recovery all not satisfactory, and the technico-economical comparison that impact is smelted greatly have impact on the economic benefit of enterprise.
And also there is a lot of problem in existing antimony hydrometallurgy method: 1) in sodium sulphite leaching-thioantimonious acid sodium solution electrodeposition method, the accumulation of sodium sulfate, Sulfothiorine, S-WAT and schlippe's salt is serious, greatly and more numerous and diverse, current efficiency is low, and power consumption is high for liquid waste disposal amount; 2) hydrogen reduction method of Sodium thioantimonite leach liquor is feasible technically, but this method exists, and reduction rate is slow, antimony method bonding reacts the problems such as tube wall; 3) FeCl
3in leaching-electrodeposition method, solution impurity accumulating rate is very fast, and costly and loss is very fast, electrodeposition control condition is harsh for anion-exchange membrane; As, Au separation difficulty in leached mud, production cost is high; 4) the water diluting soln that chloride-hydrolysis processing requirement is a large amount of, acid consumption is high, water consumption is large, reagent consumption is large, and antimony recovery is low, and wastewater discharge is large.
Summary of the invention
The object of this invention is to provide a kind of efficient golden antimony separating technology containing antimony gold concentrate, while raising gold recovery, reclaim antimony element, the features such as this technique possesses stable working simultaneously, operability is high, labour intensity is low, economic benefits.
The technical scheme that the present invention solves the problems of the technologies described above is as follows:
Containing the novel process reclaiming antimony in antimony gold concentrate, comprise the steps:
(1) pulp: will be placed in surge tank in proportion and size mixing containing antimony gold concentrate, water, electrodeposition lean solution, control concentration of sizing mixing is 55 ~ 60wt%, so that when lower step adds catholyte, sodium sulfide solution, sodium hydroxide solution in leaching, be convenient to control to leach pulp density.
(2) leach: the ore pulp in step (1) surge tank extremely leaches the airtight stirred leaching tank in workshop by pump delivery, add the catholyte that electrodeposition workshop returns wherein and pulp density is adjusted to 50wt%, following current afterwards enters in leaching vat and leaches, in leaching vat, add Na
2s and NaOH solution, keep Na in ore pulp
2s concentration is 50g/L, NaOH concentration is 20g/L;
(3) press filtration washing: the slurries after having leached in step (2) are from flowing into medial launder, ore slurry pump is sent into two high-efficient diaphragm pressure filter and is carried out a press filtration by medial launder pump, the filtrate adding secondary press filtration according to the ratio of ore pulp and washings volume ratio 2:1 is washed, gained filter cake is pumped into secondary pressure filter washing and filter pressing after sizing mixing, washing water are the new water that the ratio being 2:1 according to ore pulp and water volume ratio adds, filter cake send baking cyaniding workshop to extract gold and silver, a filtrate pumping press filtration reuse after sizing mixing;
(4) electrodeposition: enter electrodeposition workshop as electrodeposition mother liquor after the filtrate essence filter in step (3) after a press filtration, adopt diaphragm electrodeposition to improve electrodeposition efficiency, electrical integration two sections carries out, adopt carbon steel cathodes plate and carbon steel palisade positive plate, without the need to adding extra ionogen, antimony is separated out at negative electrode, manually beats exhaustion of yin pole antimony, washes away electrodeposition solution on negative electrode antimony and soluble salt with hot water;
(5) liquid waste disposal: the lean solution part after the electrodeposition in step (4) is used for sizing mixing, another part enters acidifying groove, use sulfuric acid to be adjusted to pH=1, filter the antimony sulfide precipitation produced in acidization, filtrate enters effluent treatment plant reuse after treatment.
The invention has the beneficial effects as follows: leach by high density, overcome the restriction of conventional wet stibium smelting technology electrodeposition to high antimony raw material containing antimony liquid circulation collection, solve traditional smeltery roasting-cyanidation technology to the restriction containing antimony gold concentrate raw material, simultaneously stability and the continuity of this technique by adopting high-efficiency appliance, process procedure technical indicator to control ensure that technique.
Leaching mechanism of the present invention is as follows:
Alkaline leaching has the features such as selectivity good and separable gold and silver, lead, copper, zinc, is applicable to process many metals antimony sulfide ore, and the antimony sulfide in concentrate and weisspiessglanz are easily and Na
2s reacts, and generates water-soluble cpds Sodium thioantimonite (Na
3sbS
3), react as follows:
Sb
2S
3+3Na
2S=2Na
3SbS
3;
Sb
2O
3+6Na
2S+3H
20=2Na
3SbS
3+6NaOH;
Work as Na
2during S quantity not sufficient, NaOH also can rise and dissolve Sb
2s
3effect, react and be:
Sb
2S
3+6NaOH=3Na
2S+2H
3SbO
3;
Electrowinning principle: SbS occurs at negative electrode
3 3-be reduced into the reaction of metal
SbS
3 3-+3e→Sb+3S
2-
The reaction generating oxygen and water is there is at anode:
4OH
—4e→2H
20+O
2↑
Total reaction is:
2Na
3SbS
3+6NaOH=2Sb+6Na
2S+3H
20+3/2O
2↑
On the basis of technique scheme, the present invention can also do following improvement.
Further, in described step (2), extraction time is 1-3 hour.
The beneficial effect of above-mentioned further scheme is adopted to be ensure the leaching completely of antimony element.
Further, described in step (4), electric effusion antimony content is for being greater than 50g/L, and electrodeposition flow is 10.5m/h.
Further, in step (4), one section of electrodeposition current density controls at 9000A/ ㎡, and two sections of electrodeposition current densities control at 4500A/ ㎡.
Accompanying drawing explanation
Fig. 1 is present invention process schema;
Embodiment
Be described principle of the present invention and feature below in conjunction with example, example, only for explaining the present invention, is not intended to limit scope of the present invention.
Containing the novel process reclaiming antimony in antimony gold concentrate, comprise the steps:
(1) pulp: get 10kg and be placed in surge tank size mixing containing antimony gold concentrate, 4L water, 4L electrodeposition lean solution;
(2) leach: the ore pulp in step (1) surge tank extremely leaches the airtight stirred leaching tank in workshop by pump delivery, add the catholyte that 1L electrodeposition workshop returns wherein, following current afterwards enters in leaching vat and leaches, and adds the Na of 800ml 15wt% in leaching vat
2the NaOH solution of S solution and 200ml 20wt%, keeps Na in ore pulp by potentiometric determination sodium sulfide content and determination of acid-basetitration sodium hydrate content
2s concentration is 50g/L, NaOH concentration is 20g/L, leaches 2 hours;
(3) press filtration washing: the slurries after having leached in step (2) are from flowing into medial launder, ore slurry pump is sent into two high-efficient diaphragm pressure filter and is carried out a press filtration by medial launder pump, the filtrate adding secondary press filtration according to the ratio of ore pulp and washings volume ratio 2:1 is washed, gained filter cake is pumped into secondary pressure filter washing and filter pressing after sizing mixing, washing water are the new water that the ratio being 2:1 according to ore pulp and water volume ratio adds, filter cake send baking cyaniding workshop to extract gold and silver, a filtrate pumping press filtration reuse after sizing mixing;
(4) electrodeposition: enter electrodeposition workshop as electrodeposition mother liquor after the filtrate essence filter in step (3) after a press filtration, adopt diaphragm electrodeposition to improve electrodeposition efficiency, electrical integration two sections carries out, adopt carbon steel cathodes plate, electric effusion antimony content is for being greater than 50g/L, electrodeposition flow is 10.5m/h, one section of electrodeposition current density controls at 9000A/ ㎡, two sections of electrodeposition current densities control at 4500A/ ㎡, antimony is separated out at negative electrode, manually beat exhaustion of yin pole antimony, wash away electric effusion on negative electrode antimony and soluble salt with hot water;
(5) liquid waste disposal: the lean solution part after the electrodeposition in step (4) is used for sizing mixing, another part enters acidifying groove, use sulfuric acid to be adjusted to pH=1, filter the antimony sulfide precipitation produced in acidization, filtrate enters effluent treatment plant reuse after treatment.
The foregoing is only preferred embodiment of the present invention, not in order to limit the present invention, within the spirit and principles in the present invention all, any amendment done, equivalent replacement, improvement etc., within the protection domain that all should be included in invention.
Claims (4)
1., containing the novel process reclaiming antimony in antimony gold concentrate, comprise the steps:
(1) pulp: by containing antimony gold concentrate, water, to be placed in surge tank in proportion from the electrodeposition lean solution of electrodeposition room and to size mixing, the concentration that controls to size mixing is 55 ~ 60wt%;
(2) leach: the ore pulp in step (1) surge tank extremely leaches the airtight stirred leaching tank in workshop by pump delivery, add the catholyte that electrodeposition workshop returns wherein and pulp density is adjusted to 50wt%, following current afterwards enters in leaching vat and leaches, in leaching vat, add Na
2s and NaOH solution, keep Na in ore pulp
2s concentration is 50g/L, NaOH concentration is 20g/L;
(3) press filtration washing: the slurries after having leached in step (2) are from flowing into medial launder, ore slurry pump is sent into two high-efficient diaphragm pressure filter and is carried out a press filtration by medial launder pump, the filtrate adding secondary press filtration according to the ratio of ore pulp and washings volume ratio 2:1 is washed, gained filter cake is pumped into secondary pressure filter washing and filter pressing after sizing mixing, washing water are the new water that the ratio being 2:1 according to ore pulp and water volume ratio adds, filter cake send baking cyaniding workshop to extract gold and silver, a filtrate pumping press filtration reuse after sizing mixing;
(4) electrodeposition: enter electrodeposition workshop as electrodeposition mother liquor after the filtrate essence filter purification in step (3) after a press filtration, adopt diaphragm electrodeposition to improve electrodeposition efficiency, electrical integration two sections carries out, adopt carbon steel cathodes plate and carbon steel palisade positive plate, without the need to adding extra ionogen, antimony is separated out at negative electrode, manually beats exhaustion of yin pole antimony, washes away electrodeposition solution on negative electrode antimony and soluble salt with hot water;
(5) liquid waste disposal: the lean solution part after the electrodeposition in step (4) is used for sizing mixing, another part enters acidifying groove, use sulfuric acid to be adjusted to pH=1, filter the antimony sulfide precipitation produced in acidization, filtrate enters effluent treatment plant reuse after treatment.
2. a kind of novel process containing reclaiming antimony in antimony gold concentrate according to claim 1, it is characterized in that, in described step (2), extraction time is 1-3 hour.
3. a kind of novel process containing reclaiming antimony in antimony gold concentrate according to claim 1, it is characterized in that, described in step (4), electrodeposition mother liquor antimony content is for being greater than 50g/L, and electrodeposition flow is 10.5m
3/ h.
4. a kind of novel process containing reclaiming antimony in antimony gold concentrate according to claim 1 and 2, it is characterized in that, in step (4), one section of electrodeposition current density controls at 9000A/ ㎡, and two sections of electrodeposition current densities control at 4500A/ ㎡.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510148856.8A CN104831315A (en) | 2015-03-31 | 2015-03-31 | Novel process for recovering antimony from antimony-containing gold concentrate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510148856.8A CN104831315A (en) | 2015-03-31 | 2015-03-31 | Novel process for recovering antimony from antimony-containing gold concentrate |
Publications (1)
Publication Number | Publication Date |
---|---|
CN104831315A true CN104831315A (en) | 2015-08-12 |
Family
ID=53809503
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510148856.8A Pending CN104831315A (en) | 2015-03-31 | 2015-03-31 | Novel process for recovering antimony from antimony-containing gold concentrate |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104831315A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106480319A (en) * | 2016-10-26 | 2017-03-08 | 山东国大黄金股份有限公司 | A kind of method of the immersion cleaning treatment hydrogen containing tail gas synthetical recovery antimony of alkali containing antimony |
CN107641818A (en) * | 2017-11-04 | 2018-01-30 | 山东恒邦冶炼股份有限公司 | A kind of technique for producing mao antimony |
CN105951146B (en) * | 2016-05-06 | 2018-04-03 | 燕山大学 | A kind of preparation method of antimony trisulfide film |
CN107988488A (en) * | 2017-11-24 | 2018-05-04 | 江苏盐城环保科技城重金属防治研究中心 | A kind of method of hydrometallurgic recovery mercury antimony in antimony ore mine tailings from mercury |
CN108285984A (en) * | 2017-12-20 | 2018-07-17 | 甘肃招金贵金属冶炼有限公司 | A method of improving the rate of recovery of cyaniding containing antimony gold concentrate |
CN106367780B (en) * | 2016-08-31 | 2018-08-28 | 北京矿冶研究总院 | Method for producing antimony by rotational flow electrodeposition of antimony-containing solution |
CN109881004A (en) * | 2019-04-01 | 2019-06-14 | 山东恒邦冶炼股份有限公司 | A method of reducing gold grade in hair antimony leachate |
CN110257627A (en) * | 2019-07-08 | 2019-09-20 | 湖南辰州矿业有限责任公司 | A kind of method that gold sulphide concentrate removes antimony, lead |
CN110629042A (en) * | 2019-11-05 | 2019-12-31 | 湖南工业大学 | Method for leaching antimony oxide material by tartaric acid system and producing metallic antimony by electrodeposition |
CN111074303A (en) * | 2020-01-19 | 2020-04-28 | 北京科技大学 | Method for separating antimony and gold by crude antimony non-anode-residue electrolysis |
CN112811524A (en) * | 2020-12-28 | 2021-05-18 | 大连博融新材料有限公司 | Electrolytic reduction antimony removal method for electrodeposited copper modified carbon fiber felt electrode |
CN113621827A (en) * | 2021-08-24 | 2021-11-09 | 昆明理工大学 | Method for synchronously recovering gold and value-added utilizing antimony from antimony-containing gold ore |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101565174A (en) * | 2009-06-05 | 2009-10-28 | 永兴县鑫泰银业有限责任公司 | Method for extracting refined tellurium from tellurium-contained smelting slag |
CN101775619A (en) * | 2010-03-26 | 2010-07-14 | 中南大学 | Clean metallurgical method for bismuth or antimony by wet process |
CN102912125A (en) * | 2012-10-29 | 2013-02-06 | 云南锡业集团有限责任公司研究设计院 | Method for separating lead and antimony in antimony-containing lead concentrates |
CN104278154A (en) * | 2014-09-30 | 2015-01-14 | 北京矿冶研究总院 | Method for pretreating antimony-containing gold concentrate |
-
2015
- 2015-03-31 CN CN201510148856.8A patent/CN104831315A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101565174A (en) * | 2009-06-05 | 2009-10-28 | 永兴县鑫泰银业有限责任公司 | Method for extracting refined tellurium from tellurium-contained smelting slag |
CN101775619A (en) * | 2010-03-26 | 2010-07-14 | 中南大学 | Clean metallurgical method for bismuth or antimony by wet process |
CN102912125A (en) * | 2012-10-29 | 2013-02-06 | 云南锡业集团有限责任公司研究设计院 | Method for separating lead and antimony in antimony-containing lead concentrates |
CN104278154A (en) * | 2014-09-30 | 2015-01-14 | 北京矿冶研究总院 | Method for pretreating antimony-containing gold concentrate |
Non-Patent Citations (2)
Title |
---|
锡矿山矿务局: ""硫化锑精矿的湿法冶金"", 《有色金属》 * |
靳冉公等: ""碱性硫化钠浸出含锑金精矿过程中金锑行为"", 《有色金属(冶炼部分)》 * |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105951146B (en) * | 2016-05-06 | 2018-04-03 | 燕山大学 | A kind of preparation method of antimony trisulfide film |
CN106367780B (en) * | 2016-08-31 | 2018-08-28 | 北京矿冶研究总院 | Method for producing antimony by rotational flow electrodeposition of antimony-containing solution |
CN106480319A (en) * | 2016-10-26 | 2017-03-08 | 山东国大黄金股份有限公司 | A kind of method of the immersion cleaning treatment hydrogen containing tail gas synthetical recovery antimony of alkali containing antimony |
CN107641818A (en) * | 2017-11-04 | 2018-01-30 | 山东恒邦冶炼股份有限公司 | A kind of technique for producing mao antimony |
CN107988488A (en) * | 2017-11-24 | 2018-05-04 | 江苏盐城环保科技城重金属防治研究中心 | A kind of method of hydrometallurgic recovery mercury antimony in antimony ore mine tailings from mercury |
CN108285984A (en) * | 2017-12-20 | 2018-07-17 | 甘肃招金贵金属冶炼有限公司 | A method of improving the rate of recovery of cyaniding containing antimony gold concentrate |
CN109881004A (en) * | 2019-04-01 | 2019-06-14 | 山东恒邦冶炼股份有限公司 | A method of reducing gold grade in hair antimony leachate |
CN109881004B (en) * | 2019-04-01 | 2021-01-29 | 山东恒邦冶炼股份有限公司 | Method for reducing gold grade in crude antimony leaching solution |
CN110257627A (en) * | 2019-07-08 | 2019-09-20 | 湖南辰州矿业有限责任公司 | A kind of method that gold sulphide concentrate removes antimony, lead |
CN110629042A (en) * | 2019-11-05 | 2019-12-31 | 湖南工业大学 | Method for leaching antimony oxide material by tartaric acid system and producing metallic antimony by electrodeposition |
CN110629042B (en) * | 2019-11-05 | 2021-11-26 | 湖南工业大学 | Method for leaching antimony oxide material by tartaric acid system and producing metallic antimony by electrodeposition |
CN111074303A (en) * | 2020-01-19 | 2020-04-28 | 北京科技大学 | Method for separating antimony and gold by crude antimony non-anode-residue electrolysis |
CN111074303B (en) * | 2020-01-19 | 2021-03-05 | 北京科技大学 | Method for separating antimony and gold by crude antimony non-anode-residue electrolysis |
CN112811524A (en) * | 2020-12-28 | 2021-05-18 | 大连博融新材料有限公司 | Electrolytic reduction antimony removal method for electrodeposited copper modified carbon fiber felt electrode |
CN113621827A (en) * | 2021-08-24 | 2021-11-09 | 昆明理工大学 | Method for synchronously recovering gold and value-added utilizing antimony from antimony-containing gold ore |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104831315A (en) | Novel process for recovering antimony from antimony-containing gold concentrate | |
CN104046785B (en) | The treatment process of a kind of waste and old copper iron base diamond cutter head | |
CN101775619B (en) | Clean metallurgical method for bismuth or antimony by wet process | |
CN101760757B (en) | Method for producing lead by executing electrolysis and alkaline leaching on lead sulfate material | |
CN102766765B (en) | Zinc oxide powder recycling method | |
JP5069173B2 (en) | Method for recovering copper from minerals | |
CN105543485A (en) | Method for separating and recovering valuable metals from copper anode slime | |
JP2009235519A (en) | Method for recovering metal from ore | |
CN102994747A (en) | Technology for recovering metallic copper from high-lead copper matte | |
CN103924095B (en) | Novel method for recovering cadmium from copper-cadmium slag | |
CN104017991A (en) | Process for efficiently and selectively separating copper in lead copper matte | |
CN108384959A (en) | A kind of preparation method of electrolytic zinc | |
CN109971962B (en) | Treatment process for copper, mercury, selenium, lead and gold and silver in copper smelting lead filter cake | |
CN105967153A (en) | Technology for recovering tellurium from high-tellurium slag | |
CN103498053A (en) | Method for separating base metals and noble metals in copper anode slime | |
CN108034825B (en) | The method that wet process extracts gold and silver from the earth of positive pole | |
CN104087971B (en) | Method for treating lead matte | |
JP2009167451A (en) | Method for electrolytically extracting copper | |
CN112680603A (en) | Method for leaching cobalt by using low-cost medicament instead of sodium metabisulfite | |
CN103937975A (en) | Method for directly extracting silver from wet method zinc smelting flotation silver concentrates | |
CN104451205A (en) | Indium extraction method capable of efficiently removing iron | |
CN103397182B (en) | Method for efficiently recycling bismuth from monomer bismuth ore | |
JP6172526B2 (en) | Adjustment method of copper concentration of chlorine leachate in nickel chlorine leaching process | |
CN111041212A (en) | Gold leaching method for copper anode mud | |
RU2510669C2 (en) | Method of extracting noble metals from wastes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
EXSB | Decision made by sipo to initiate substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20150812 |
|
RJ01 | Rejection of invention patent application after publication |