CN108411121A - A method of your antimony electrum is produced by - Google Patents

A method of your antimony electrum is produced by Download PDF

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Publication number
CN108411121A
CN108411121A CN201810259415.9A CN201810259415A CN108411121A CN 108411121 A CN108411121 A CN 108411121A CN 201810259415 A CN201810259415 A CN 201810259415A CN 108411121 A CN108411121 A CN 108411121A
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antimony
electrum
lead
producing
content
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CN108411121B (en
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姚广生
赵俊华
周威
赵海平
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Guangxi Wanshizhi Rare Precious Metal Technology Co ltd
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Guangzhou Wan Shi Zhi Investment Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B11/00Obtaining noble metals
    • C22B11/02Obtaining noble metals by dry processes
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B30/00Obtaining antimony, arsenic or bismuth
    • C22B30/02Obtaining antimony

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  • 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)

Abstract

The invention discloses a kind of methods for your antimony producing electrum by, this method by the way that your antimony raw material is successively added in reverberatory furnace, lead melting furnace, vacuum drying oven, blown by your antimony melting, your antimony removal of impurities, your antimony ash, leading and continue ash blow plus sulphur copper removal and be condensed into lead bullion and etc. electrum is made.This method is directly produced the electrum of high value by your antimony, and technological process is short, advantage of lower cost, high-efficiency environment friendly energy-conservation, is to be initiated in antimony industry, has preferable application value, is worth promoting the use of on a large scale.

Description

A method of your antimony electrum is produced by
【Technical field】
The invention belongs to metal smelt technical fields, and in particular to a method of your antimony electrum is produced by.
【Background technology】
In antimony industry, with the consumption of the fluctuation and single antimony raw material in antimony market, the treating capacity of antimony gold raw material is gradual Increase, during antimony pyrometallurgical smelting handles antimony gold raw material, often removes to capture the noble metals such as the gold, silver in raw material using hair antimony, obtain To your antimony containing antimony, gold, silver and other impurities.Your, currently, being typically to be handled using reverberatory furnace antimony, the taste of gold, silver is carried Height obtains rich and honour antimony.But it since this rich and honour antimony is high containing antimony, is easy to influence the rate of recovery of antimony, the country commonly uses chlorination Method extracts noble metal, and technique is cumbersome, high expensive, and application range is not wide, hinders the development of antimony industry processing antimony gold concentrate.
【Invention content】
The present invention is intended to provide a kind of method for your antimony producing electrum by, simple for process, it is suitable for large-scale promotion.
The technical solution adopted in the present invention is:A method of your antimony electrum is produced by, is included the following steps:
(1) according to reverberatory furnace size, your antimony raw material is added in reverberatory furnace in batch, bubble slag is clawed after filling it up with; The main chemical compositions weight percentage ranges of your antimony raw material are:Sb20~80%, Pb2~80%, Fe5~30%, As < 0.5%, S < 0.1%, Au contents > 100g/t, Ag content > 1000g/t;
(2) quartz sand is added to carry out removing iron, it is desirable that the iron content < 0.01% after removal of impurities;
(3) after iron content chemical examination reaches requirement, start air blast ash and blow, mode of operation is against reverberatory furnace inner surface drum Wind plays spark, makes antimony aoxidize and enter dust chamber to gather dust, and when antimony content is 20~30%, stopping ash being blown;
(4) it is added 1#Electrolytic lead waits for 1#After electrolytic lead melting, continue ash and blow, mode of operation is against reverberatory furnace inner surface drum Wind cannot play spark, when antimony reaches 2~8%, stop ash and blow, rich and honour lead is obtained after putting stove.
(5) obtained rich and honour lead is put into lead melting furnace, is warming up to 600 DEG C, after fusing slag is removed in fishing, is cooled to 500 DEG C When fishing go to remove copper dross slag for the first time, when being cooled to 350 DEG C fishing go second to remove copper dross slag;
(6) temperature is controlled at 280~330 DEG C, sulphur is added while stirring, stop stirring after adding 5~10min, Devulcanization copper dross slag is dragged in the case of not heating up;
(7) 620~680 DEG C are warming up to after dragging for slag, blasts compressed air, so that sulphur is oxidized to sulfur dioxide effusion volatilization, puts Stove obtains rich and honour lead after copper removal;
(8) rich and honour lead after copper removal is added in vacuum drying oven, is warming up to 700~800 DEG C under vacuum conditions, allow antimony and lead It volatilizees and is condensed into lead bullion, gold and silver obtains electrum after entering cash register storehouse.
Preferably, the reverberatory furnace is common antimony regulus reverberatory furnace, size is 12~16m2, the grain of your antimony raw material 50~100mm of diameter, and it is 1.5~2.0t that weight, which is added, in every batch of.
Preferably, the quartz sand addition is 2~4 times of iron tramp total amount.
Preferably, described 1#The addition of electrolytic lead is:0.25~0.4t is added by every square metre of stove area.
Preferably, the sulphur calculating that the addition of the sulphur is required when reacting to form cuprous sulfide with copper by sulphur, and mistake Amount 30%.
Preferably, the copper content of rich and honour lead is below 0.5% after the copper removal.
Preferably, the vacuum drying oven vacuum degree is 10~15Pa.
Preferably, silver content in the lead bullion is less than 200g/t, the sum of gold and the content of silver in the electrum Accounting be more than 60%.
Above technical scheme is used, the invention has the advantages that:Your antimony is the present invention produce by rich and honour lead, rich The processes such as precious metals containing lead copper removal and lead antimony separation of gold and silver, are directly produced the electrum of high value by your antimony, and technological process is short, cost phase To relatively low, high-efficiency environment friendly energy-conservation is to be initiated in antimony industry, has preferable application value, is worth promoting the use of on a large scale.
【Specific implementation mode】
The following examples and test example can help those skilled in the art that the present invention is more completely understood, but can not To limit the invention in any way.
Embodiment 1
The main chemical compositions weight percent of your handled antimony raw material is:Sb72.73%, Pb2.06%, Cu1.34%, Fe12.36%, Au contents are that 158.00g/t, Ag content are 2321.50g/t, are handled by following steps:
(1) according to reverberatory furnace size, your antimony raw material is added in reverberatory furnace in batch, bubble slag is clawed after filling it up with; The reverberatory furnace is common antimony regulus reverberatory furnace, size 12m2, 50~100mm of grain size of your antimony raw material, and every batch of Addition weight is 1.5~2.0t;
(2) quartz sand is added to carry out removing iron, the quartz sand addition is 2~4 times of iron tramp total amount, it is desirable that after removal of impurities Iron content < 0.01%;
(3) after iron content chemical examination reaches requirement, start air blast ash and blow, mode of operation is against reverberatory furnace inner surface drum Wind plays spark, makes antimony aoxidize and enter dust chamber to gather dust, and when antimony content is 20~30%, stopping ash being blown;
(4) it is added the 1 of 3~4.8t#Electrolytic lead waits for 1#After electrolytic lead melting, continue ash and blow, mode of operation is against reflection Stove inner surface air blast, cannot play spark, when antimony reaches 2~8%, stop ash and blow, put stove and obtain rich and honour lead.
(5) obtained rich and honour lead is put into lead melting furnace, is warming up to 600 DEG C, after fusing slag is removed in fishing, is cooled to 500 DEG C When fishing go to remove copper dross slag for the first time, when being cooled to 350 DEG C fishing go second to remove copper dross slag;
(6) temperature is controlled at 280~330 DEG C, sulphur is added while stirring, stop stirring after adding 5~10min, Devulcanization copper dross slag is dragged in the case of not heating up;
(7) 620~680 DEG C are warming up to after dragging for slag, blasts compressed air, so that sulphur is oxidized to sulfur dioxide effusion volatilization, puts Stove obtains rich and honour lead after copper removal;
(8) rich and honour lead after copper removal is added in vacuum drying oven, is warming up to 700~800 DEG C under vacuum conditions, allow antimony and lead It volatilizees and is condensed into lead bullion, gold and silver obtains electrum after entering cash register storehouse.
By being produced according to above step, the silver content in the lead bullion of output is less than 200g/t, mainization of electrum Learning composition by weight percent is:Sb0.8%, Au20.48%, Ag40.95%, Pb0.5%, Cu37.05%, Fe0.17%, gold It is more than 60% with the accounting of the sum of the content of silver.The electrum directly outer can be sold or further extract proof gold and fine silver, be sold outside Gold, silver haggle over coefficient height, and copper can also valuate.
Embodiment 2
The main chemical compositions weight percent of your handled antimony raw material is:Sb65.38%, Pb2.60%, Cu1.88%, Fe21.54%, Au contents are that 356.00g/t, Ag content are 4321.15g/t, are handled by following steps:
(1) according to reverberatory furnace size, your antimony raw material is added in reverberatory furnace in batch, bubble slag is clawed after filling it up with; The reverberatory furnace is common antimony regulus reverberatory furnace, size 16m2, 50~100mm of grain size of your antimony raw material, and every batch of Addition weight is 1.5~2.0t;
(2) quartz sand is added to carry out removing iron, the quartz sand addition is 2~4 times of iron tramp total amount, it is desirable that after removal of impurities Iron content < 0.01%;
(3) after iron content chemical examination reaches requirement, start air blast ash and blow, mode of operation is against reverberatory furnace inner surface drum Wind plays spark, makes antimony aoxidize and enter dust chamber to gather dust, and when antimony content is 20~30%, stopping ash being blown;
(4) it is added the 1 of 4~6.4t#Electrolytic lead waits for 1#After electrolytic lead melting, continue ash and blow, mode of operation is against reflection Stove inner surface air blast, cannot play spark, when antimony reaches 2~8%, stop ash and blow, put stove and obtain rich and honour lead.
(5) obtained rich and honour lead is put into lead melting furnace, is warming up to 600 DEG C, after fusing slag is removed in fishing, is cooled to 500 DEG C When fishing go to remove copper dross slag for the first time, when being cooled to 350 DEG C fishing go second to remove copper dross slag;
(6) temperature is controlled at 280~330 DEG C, sulphur is added while stirring, stop stirring after adding 5~10min, Devulcanization copper dross slag is dragged in the case of not heating up;
(7) 620~680 DEG C are warming up to after dragging for slag, blasts compressed air, so that sulphur is oxidized to sulfur dioxide effusion volatilization, puts Stove obtains rich and honour lead after copper removal;
(8) rich and honour lead after copper removal is added in vacuum drying oven, is warming up to 700~800 DEG C under vacuum conditions, allow antimony and lead It volatilizees and is condensed into lead bullion, gold and silver obtains electrum after entering cash register storehouse.
By being produced according to above step, the silver content in the lead bullion of output is less than 200g/t, mainization of electrum Learning composition by weight percent is:Sb0.85%, Au23.2%, Ag49.5%, Pb0.62%, Cu25.6%, Fe0.2%, gold with The accounting of the sum of the content of silver is more than 60%.The electrum directly outer can be sold or further extract proof gold and fine silver, sell outside gold, Silver haggles over coefficient height, and copper can also valuate.
Embodiment 3
The main chemical compositions weight percent of your handled antimony raw material is:Sb67.39%, Pb2.48%, Cu1.27%, Fe20.52%, Au contents are that 326.58g/t, Ag content are 3988.14g/t, are handled by following steps:
(1) according to reverberatory furnace size, your antimony raw material is added in reverberatory furnace in batch, bubble slag is clawed after filling it up with; The reverberatory furnace is common antimony regulus reverberatory furnace, size 16m2, 50~100mm of grain size of your antimony raw material, and every batch of Addition weight is 1.5~2.0t;
(2) quartz sand is added to carry out removing iron, the quartz sand addition is 2~4 times of iron tramp total amount, it is desirable that after removal of impurities Iron content < 0.01%;
(3) after iron content chemical examination reaches requirement, start air blast ash and blow, mode of operation is against reverberatory furnace inner surface drum Wind plays spark, makes antimony aoxidize and enter dust chamber to gather dust, and when antimony content is 20~30%, stopping ash being blown;
(4) it is added the 1 of 4~6.4t#Electrolytic lead waits for 1#After electrolytic lead melting, continue ash and blow, mode of operation is against reflection Stove inner surface air blast, cannot play spark, when antimony reaches 2~8%, stop ash and blow, put stove and obtain rich and honour lead.
(5) obtained rich and honour lead is put into lead melting furnace, is warming up to 600 DEG C, after fusing slag is removed in fishing, is cooled to 500 DEG C When fishing go to remove copper dross slag for the first time, when being cooled to 350 DEG C fishing go second to remove copper dross slag;
(6) temperature is controlled at 280~330 DEG C, sulphur is added while stirring, stop stirring after adding 5~10min, Devulcanization copper dross slag is dragged in the case of not heating up;
(7) 620~680 DEG C are warming up to after dragging for slag, blasts compressed air, so that sulphur is oxidized to sulfur dioxide effusion volatilization, puts Stove obtains rich and honour lead after copper removal;
(8) rich and honour lead after copper removal is added in vacuum drying oven, is warming up to 700~800 DEG C under vacuum conditions, allow antimony and lead It volatilizees and is condensed into lead bullion, gold and silver obtains electrum after entering cash register storehouse.
By being produced according to above step, the silver content in the lead bullion of output is less than 200g/t, mainization of electrum Learning composition by weight percent is:Sb0.82%, Au20.69%, Ag47.08%, Pb0.48%, Cu30.66%, Fe0.25%, Gold and the accounting of the sum of the content of silver are more than 60%.The electrum directly outer can be sold or further extract proof gold and fine silver, outside That sells gold, silver haggles over coefficient height, and copper can also valuate.

Claims (9)

1. a kind of method for your antimony producing electrum by, which is characterized in that include the following steps:
(1) according to reverberatory furnace size, your antimony raw material is added in reverberatory furnace in batch, bubble slag is clawed after filling it up with;
(2) quartz sand is added to carry out removing iron, it is desirable that the iron content < 0.01% after removal of impurities;
(3) after iron content chemical examination reaches requirement, start air blast ash and blow, mode of operation is to be risen against reverberatory furnace inner surface air blast Spark, makes antimony aoxidize and enters dust chamber to gather dust, and when antimony content is 20~30%, stops ash and blows;
(4) it is added 1#Electrolytic lead waits for 1#After electrolytic lead melting, continuing ash and blow, mode of operation is opposite reverberatory furnace inner surface air blast, Spark cannot be played, when antimony reaches 2~8%, stops ash and blows, rich and honour lead is obtained after putting stove.
(5) obtained rich and honour lead is put into lead melting furnace, is warming up to 600 DEG C, after fusing slag is removed in fishing, is dragged for when being cooled to 500 DEG C It goes to remove copper dross slag for the first time, is dragged for when being cooled to 350 DEG C and go to remove copper dross slag second;
(6) temperature is controlled at 280~330 DEG C, sulphur is added while stirring, stopped stirring after adding 5~10min, do not rising Devulcanization copper dross slag is dragged in the case of temperature;
(7) 620~680 DEG C are warming up to after dragging for slag, blasts compressed air, so that sulphur is oxidized to sulfur dioxide effusion volatilization, puts stove and obtain Rich and honour lead after to copper removal;
(8) rich and honour lead after copper removal is added in vacuum drying oven, is warming up to 700~800 DEG C under vacuum conditions, allow antimony and lead volatility And it is condensed into lead bullion, gold and silver obtains electrum after entering cash register storehouse.
2. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that your antimony raw material Main chemical compositions weight percentage ranges are:Sb20~80%, Pb2~80%, Fe5~30%, As < 0.5%, S < 0.1%, Au content > 100g/t, Ag content > 1000g/t.
3. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the reverberatory furnace is normal Antimony regulus reverberatory furnace, size are 12~16m2, 50~100mm of grain size of your antimony raw material, and every batch of addition weight is 1.5~2.0t.
4. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the quartz sand is added Amount is 2~4 times of iron tramp total amount.
5. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the 1# electrolytic leads Addition is:0.25~0.4t is added by every square metre of stove area.
6. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the addition of the sulphur Amount sulphur required when reacting to form cuprous sulfide with copper by sulphur calculates, and excessive 30%.
7. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that rich and honour after the copper removal The copper content of lead is below 0.5%.
8. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the vacuum drying oven vacuum Degree is 10~15Pa.
9. a kind of method for your antimony producing electrum by as described in claim 1, which is characterized in that the silver in the lead bullion Content is less than 200g/t, and the golden accounting with the sum of the content of silver is more than 60% in the electrum.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109306409A (en) * 2018-09-30 2019-02-05 蒙自矿冶有限责任公司 A kind of processing method of the high tin copper master alloy containing antimony
CN117344158A (en) * 2023-10-17 2024-01-05 昆明理工大学 Method for separating and purifying antimony and enriching gold and silver from noble antimony alloy

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN87102039A (en) * 1987-06-15 1988-12-28 张宏君 Antimony, gold smelting technology
KR20010077490A (en) * 2000-02-03 2001-08-20 김동진 Recovering method of valuable metal from antimony containing waste
CN103194605A (en) * 2013-03-21 2013-07-10 中南大学 Treatment method for polymetallic alloy formed by arsenic-lead-antimony and noble metal
CN104120273A (en) * 2014-07-28 2014-10-29 蒙自矿冶有限责任公司 Method for recycling lead, sliver and copper by taking noble lead as raw material
CN104120270A (en) * 2014-07-29 2014-10-29 湖南辰州矿业股份有限公司 One-step technique for separating antimony from gold and lead in gold-containing antimony oxide smoke dust
CN107312935A (en) * 2017-06-30 2017-11-03 郴州市金贵银业股份有限公司 A kind of processing method of reducing slag after lead anode slurry melting

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN87102039A (en) * 1987-06-15 1988-12-28 张宏君 Antimony, gold smelting technology
KR20010077490A (en) * 2000-02-03 2001-08-20 김동진 Recovering method of valuable metal from antimony containing waste
CN103194605A (en) * 2013-03-21 2013-07-10 中南大学 Treatment method for polymetallic alloy formed by arsenic-lead-antimony and noble metal
CN104120273A (en) * 2014-07-28 2014-10-29 蒙自矿冶有限责任公司 Method for recycling lead, sliver and copper by taking noble lead as raw material
CN104120270A (en) * 2014-07-29 2014-10-29 湖南辰州矿业股份有限公司 One-step technique for separating antimony from gold and lead in gold-containing antimony oxide smoke dust
CN107312935A (en) * 2017-06-30 2017-11-03 郴州市金贵银业股份有限公司 A kind of processing method of reducing slag after lead anode slurry melting

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
华一新主编: "《有色金属概论(第二版)》", 31 August 2007 *
李亮等: "真空条件下含银铅锑多元合金中锑的蒸发行为研究", 《真空科学与技术学报》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109306409A (en) * 2018-09-30 2019-02-05 蒙自矿冶有限责任公司 A kind of processing method of the high tin copper master alloy containing antimony
CN109306409B (en) * 2018-09-30 2021-07-20 蒙自矿冶有限责任公司 Treatment method of antimony-containing high-tin high-copper alloy
CN117344158A (en) * 2023-10-17 2024-01-05 昆明理工大学 Method for separating and purifying antimony and enriching gold and silver from noble antimony alloy

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Registration number: Y2021450000028

PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A method for producing gold and silver alloys from precious antimony

Granted publication date: 20200522

Pledgee: Guangxi Beibu Gulf Bank Co.,Ltd. Baise branch

Pledgor: Guangxi wanshizhi rare precious metal Technology Co.,Ltd.

Registration number: Y2024980016988