CN1051581C - Method and device for preparing stibic white with jamesonite - Google Patents

Method and device for preparing stibic white with jamesonite Download PDF

Info

Publication number
CN1051581C
CN1051581C CN97108157A CN97108157A CN1051581C CN 1051581 C CN1051581 C CN 1051581C CN 97108157 A CN97108157 A CN 97108157A CN 97108157 A CN97108157 A CN 97108157A CN 1051581 C CN1051581 C CN 1051581C
Authority
CN
China
Prior art keywords
alloy
heater
arsenic
furnace
jamesonite
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 - Fee Related
Application number
CN97108157A
Other languages
Chinese (zh)
Other versions
CN1186868A (en
Inventor
孔祥成
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.)
GUANGXIN SMELTERY Co.,Ltd. YUNAN COUNTY
HUANDONG METAL MATERIAL Co.,Ltd.
Original Assignee
HUANDONG INTEGRATED NON-FERROUS METAL CHEMICAL PLANT LIUZHOU CITY
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 HUANDONG INTEGRATED NON-FERROUS METAL CHEMICAL PLANT LIUZHOU CITY filed Critical HUANDONG INTEGRATED NON-FERROUS METAL CHEMICAL PLANT LIUZHOU CITY
Priority to CN97108157A priority Critical patent/CN1051581C/en
Publication of CN1186868A publication Critical patent/CN1186868A/en
Application granted granted Critical
Publication of CN1051581C publication Critical patent/CN1051581C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Abstract

The present invention relates to a method and a device for preparing stibium white from jamesonite, which belongs to the metallurgy field. The present invention is characterized in that after arsenic is oxidized and removed in advance, the stibium white is prepared from the jamesonite under the conditions that an alloy fusant is controlled below 700 DEG C, and a furnace chamber space is controlled to be 150 to 450 DEG C by a special designed oxidizing furnace. The technology has the advantages of short process and high metal recovery rate. The Pb recovery rate and the Ag recovery rate are both larger than 93%, the Sb recovery rate is larger than 80% and is enhanced by 10 to 15% as compared with that of traditional technology. Equipment investment is reduced by more than 60% as compared with that of the traditional technology, and thus, the present invention is easy to realize in industry.

Description

Method and device with preparing stibic white with jamesonite
The invention belongs to field of metallurgy, particularly stibium fire is smelted deleading and arsenic, extracts stibium trioxide.
When adopting pyrorefining, the difficulty or ease that impurity is removed in the antimony mainly are to reach each other the difference of chemical property by these impurity and metallic antimony bonded state to decide.The chemical property of impurity arsenic and antimony is very close, and difficulty is removed, and lead is the most difficult removing then.
Traditional fire refining deleading and arsenic, the technical process of producing stibium trioxide is:
1. at first with mineral aggregate desulfurization in fluidizing furnace;
2. sintering briquetting then;
3. again through the blast furnace roasting reduction, the thick alloy of output;
4. then thick alloy is entered the reverberatory furnace blowing, make plumbous antimony initial gross separation; At this moment, most of antimony voloxidation is reclaimed, and lead then becomes lead bullion;
5. again needle antimony is added the reduction of refining reverberatory furnace;
6. add Na again 2CO 3Impurity such as As are removed in refining, obtain low arsenic lead antimony alloy;
7. add and obtain No. two star metals after phosphoric acid salt removes Pb;
8. once more to the oxygen blast of tertiary air formula oxidized still,, produce qualified stibium trioxide with No. two antimony.
This technical process is long, and especially the weak effect of separation of lead, arsenic because antimony metal needs secondary oxidation can make qualified stibium trioxide, causes metal recovery rate low, stibium trioxide production cost height.
The object of the present invention is to provide technical process short, and the high method and apparatus of metal recovery rate.
The present invention with whole process with preparing stibic white with jamesonite, shortened to for three steps for achieving the above object:
The first step, with common reverberatory furnace with raw ore, soda ash, go back raw coal and mix, with the blowing process direct melting that feeds intake, obtain thick alloy;
Second step, adopt conventional reverberatory furnace basic refining earlier, make arsenic change into the sodium arseniate scum silica frost and remove;
The 3rd step, adopt custom-designed crucible type oxidized still, control suitable condition, the blowing oxidation, the metallic antimony voloxidation, lead is enrichment in residual melt then, draws from process, thus and thus, makes lead thoroughly separate the highly purified stibium trioxide of output with antimony.
Special arrangement of the present invention is characterized in that described body of heater 11 is connected with heat supply chamber 1, and melt is by indirect heating.One air deflector 8 that has a guide duct 3 is installed in this body of heater, and its top is gas tank 4, and its underpart fills alloy melt; Air deflector 8 is equipped with induced exhaust 5 and passes gas tank 4 and communicate with dust chamber 6 through citation damper; Guide duct 3 on the air deflector 8 is communicated with gas tank 4 and melt liquid upper surface.
Technical process of the present invention is simple, facility investment is little, product recovery rate is high, and production cost is low, remarkable in economical benefits, and industrial being easy to realize, is applicable to that the lead antimony alloy that any ratio, any method obtain produces stibium trioxide.
Be further described below in conjunction with accompanying drawing.
Accompanying drawing is the structural representation of apparatus of the present invention crucible type oxidized still.
Accompanying drawing has been described the crucible type oxidized still, and it has a crucible shape body of heater 11, and an air deflector 8 that has a guide duct 3 is installed in this body of heater, and its top is gas tank 4, and its underpart fills alloy melt; Air deflector 8 is equipped with induced exhaust 5 and passes gas tank 4 and communicate with dust chamber 6 through citation damper; Guide duct 3 on the air deflector 8 is communicated with gas tank 4 and melt liquid upper surface; Body of heater 11 has melt intake 2 and communicates with the primary heater unit 13 that fills low arsenic alloy 14, and body of heater 11 has slag-drip opening 9.
Accompanying drawing has been described process implementing process of the present invention, with the low arsenic alloy 14 of fused, introduces in the custom-designed crucible type oxidized still through feeder sleeve 2, and this alloy contains Pb2~92%, and the Sb stable content is between 98~8%; Crucible type oxidation body of heater 11 is connected by indirect heating with heat supply chamber 1, makes the alloy melt temperature-stable below 700 ℃; Control blast channel 7 evenly blasts 900~3000Pa air or oxygen by the alloy surface in stove of the guide duct 3 on furnace roof gas tank 4 and the air deflector 8, makes alloy be in relative static conditions; Adjust air flow rate and pressure, the furnace cavity temperature is remained between 150~450 ℃; Constantly remove the alloy surface coverture from slag-drip opening 9, to keep alloy surface bright and clean; When Sb content less than 8% the time, stop oxygen blast, from drain hole 12 beginning blowings, promptly get and hang down stibium crude lead, and passing on potroom, to extract electricity plumbous, behind the anode sludge melting, circulation enters the oxidized still oxygen blast; Meanwhile, the citation damper that be equipped with at control induced exhaust 5 places is introduced bagroom 6 internal furnace mixed gass with controlled underbalance, obtains meeting the antimonous oxide of national standard, i.e. stibium trioxide through collection.
The present invention compares with prior art and has the following advantages:
1. technical process is short, and operation is easily gone, and can realize automatic or semi-automatic;
2. metal recovery rate height, Pb, Ag metal yield all>93%, Sb metal recovery rate>80% improves 10~15% than the traditional technology Sb rate of recovery; Pb, g metal yield improve>5%;
3. the finished product are highly processed goods, and finished product appreciate 17% than No. two antimony of tradition, and tooling cost reduces by 10~15%;
4. smelting process SO 2Discharging reduces more than 50%, and directly smelting process reduces arsenic dirt, and the workshop labor condition is improved;
5. this traditional technology of facility investment reduces more than 60%, and industrial being easy to realized;
6. end product quality is being better than traditional technology aspect regular crystal ratio, the particle uniformity coefficient;
7. the present invention is applicable to leaded antimony sulfide ore or the antimony oxide ore that can not produce No. two antimony with two steps of conventional method.
Embodiment:
Below for adopting 17M 2The reverberatory furnace direct melting and arsenic removal, use 14.4M 2The implementation data of crucible type oxidized still; Oxidized still uses when containing the alloy of Sb<40%, and 120 tons of monthly output stibium trioxides are suitably kept Sb and produced 250 tons of stibium trioxides at 35~45% o'clock per month.
Embodiment 1:
The raw material of handling is a jamesonite, and composition is: (%) elements Pb Sb As S Fc Ag content 27.34 23.46 1.09 20.14 9.32 800g/T
Technical qualification: 1300 ℃ of caustic fusion temperature of reaction; 620 ℃ of oxidized still interalloy melt temperatures, 250 ℃ of furnace cavity temperature.
Reaction alloy ingredient: (%) elements Pb Sb As Ag content 54.03 42.96 1.53 1.68kg/T slag compositions: (%) elements Pb Sb Na 2Alloy ingredient after the 1.2 1.5 22.0 refining arsenic removals of S content: (%) elements Pb Sb As Ag content 57.53 41.04 0.02 1.70kg/T bag collections get the antimonous oxide composition: (%) element sb 2O 3Pb As whiteness 325 order percent of pass content 99.52 0.15 0.04 92 100 lead bullion compositions: (%) elements Pb Sb Ag content 90.28 8.15 2.63kg/T embodiment 2: the raw material of processing is a jamesonite, and composition is: (%)
Elements Pb Sb As S Fe Ag
Content 30.16 22.83 1.23 20.05 10.64 850g/T
Technical qualification: 1300 ℃ of caustic fusion temperature of reaction; 650 ℃ of oxidized still interalloy melt temperatures, 280 ℃ of furnace cavity temperature.
Reaction alloying constituent: (%) elements Pb Sb As Ag content 57.01 39.89 1.61 1.52kg/T slag compositions: (%) elements Pb Sb Na 2Alloy ingredient after the 1.3 1.22 25.0 refining arsenic removals of S content: (%) elements Pb Sb As Ag content 56.77 39.21 0.018 1.61kg/T bag collections get the antimonous oxide composition: (%) element sb 2O 3Pb As whiteness 325 order percent of pass content 99.63 0.12 0.04 93 100 lead bullion compositions: (%) elements Pb Sb Ag content 89.68 9.13 2.42kg/T embodiment 3: the raw material of processing is a jamesonite, and composition is: (%) elements Pb Sb As S Fe Ag content 28.26 24.17 1.31 24.58 11.03 886g/T
Technical qualification: 1350 ℃ of caustic fusion temperature of reaction; 680 ℃ of oxidized still interalloy melt temperatures, 300 ℃ of furnace cavity temperature.
Reaction alloying constituent: (%) elements Pb Sb As Ag content 54.24 42.48 1.45 1.60kg/T slag compositions: (%) elements Pb Sb Na 2Alloy ingredient after the 1.8 0.8 32.0 refining arsenic removals of S content: (%) elements Pb Sb As Ag content 57.94 38.85 0.019 1.79kg/T bag collections get the antimonous oxide composition: (%) element sb 2O 3Pb As whiteness 325 order percent of pass content 99.58 0.10 0.039 94 100 lead bullion compositions: (%) elements Pb Sb Ag content 91.02 7.66 2.67kg/T embodiment 4: the raw material of processing is low plumbous antimony ore, and composition is: (%)
Elements Pb Sb As S Fe Si Ca
Content 1.51 47.26 0.83 18.2 4.2 9.7 6.8
Technical qualification: 1350 ℃ of caustic fusion temperature of reaction; 680 ℃ of oxidized still interalloy melt temperatures, 300 ℃ of furnace cavity temperature.
Reaction alloying constituent: (%) elements Pb Sb As content 2.14 95.47 0.76 slag compositions: (%) elements Pb Sb Na 2S content 1.4 1.7 28.0 alloys are after adjusting composition and arsenic removal: (%) elements Pb Sb content 38.00 60.50 bag collections get the antimonous oxide composition: (%) element sb 2O 3Pb As whiteness 325 order percent of pass content 99.78 0.067 0.008 94 100 lead bullion compositions: (%) elements Pb Sb content 91.02 7.66

Claims (2)

1. with the method for preparing stibic white with jamesonite, belong to the field of metallurgy of stibium fire refining deleading and arsenic, it is characterized in that: whole process with preparing stibic white with jamesonite was divided into for three steps:
The first step: with common reverberatory furnace with raw ore, soda ash, go back raw coal and mix, with the blowing process direct melting that feeds intake, obtain thick alloy;
Second step: adopt conventional reverberatory furnace basic refining earlier, make arsenic change into the sodium arseniate scum silica frost and remove;
The 3rd step: by custom-designed crucible type oxidized still, with the low arsenic alloy (14) of fused, in feeder sleeve (2) was introduced custom-designed crucible type oxidized still, this alloy contained Pb2~92%, and the Sb stable content is between 98~8%; Crucible type oxidation body of heater (11) is connected by indirect heating with heat supply chamber (1), makes the alloy melt temperature-stable below 700 ℃; Control blast channel (7) evenly blasts 900~3000Pa air or oxygen by guide duct (3) alloy surface in stove on furnace roof gas tank (4) and the air deflector (8), makes alloy be in relative static conditions; Adjust air flow rate and pressure, the furnace cavity temperature is remained between 150~450 ℃; Constantly remove the alloy surface coverture from slag-drip opening (9), to keep alloy surface bright and clean; When Sb content less than 8% the time, stop oxygen blast, from drain hole (12) beginning blowing, promptly get and hang down stibium crude lead, and passing on potroom, to extract electricity plumbous, behind the anode sludge melting, circulation enters the oxidized still oxygen blast; Meanwhile, control induced exhaust (5) citation damper locating to be equipped with is introduced bagroom (6) internal furnace mixed gas with controlled underbalance, obtains meeting the antimonous oxide of national standard, i.e. stibium trioxide through collection.
2. realize the described device of claim 1 for one kind, it has a crucible type body of heater (11) to have melt intake (2) to communicate with the primary heater unit that fills low arsenic alloy (14) (13), and have a slag-drip opening (9) that is higher than the molten alloy liquid level, have the drain hole (12) of discharging low antimony alloy under the crucible type oxidized still, it is characterized in that: body of heater (11) is connected with heat supply chamber (1); One air deflector (8) that has guide pipe (3) is installed in the body of heater, and its top is gas tank (4), and its underpart fills alloy melt; Air deflector (8) is equipped with induced exhaust (5) and passes gas tank (4) and communicate with dust chamber (6) through outer air-valve; Guide duct (3) on the air deflector (8) is communicated with gas tank (4) and melt liquid upper surface.
CN97108157A 1997-07-18 1997-07-18 Method and device for preparing stibic white with jamesonite Expired - Fee Related CN1051581C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN97108157A CN1051581C (en) 1997-07-18 1997-07-18 Method and device for preparing stibic white with jamesonite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN97108157A CN1051581C (en) 1997-07-18 1997-07-18 Method and device for preparing stibic white with jamesonite

Publications (2)

Publication Number Publication Date
CN1186868A CN1186868A (en) 1998-07-08
CN1051581C true CN1051581C (en) 2000-04-19

Family

ID=5170179

Family Applications (1)

Application Number Title Priority Date Filing Date
CN97108157A Expired - Fee Related CN1051581C (en) 1997-07-18 1997-07-18 Method and device for preparing stibic white with jamesonite

Country Status (1)

Country Link
CN (1) CN1051581C (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101935766B (en) * 2010-08-31 2012-06-27 河南豫光金铅股份有限公司 Method and device for smelting jamesonite by bottom-blowing pool
CN102974669B (en) * 2012-11-30 2014-12-24 宁波思明汽车科技有限公司 Fusible alloy recycling method for pipe forming
CN103540761B (en) * 2013-10-22 2015-12-02 株洲鼎端装备股份有限公司 High temperature continuous smelting platform furnace
CN104372381B (en) * 2014-10-28 2017-08-08 江西瑞林装备有限公司 Lead potroom and lead electrolytic method
CN104495923B (en) * 2014-12-30 2015-11-11 耒阳市焱鑫有色金属有限公司 The high-grade stibium trioxide volatilization furnace of a kind of long lifetime durable lead antimony alloy
CN106643157B (en) * 2016-11-30 2019-02-12 湖南娄底华星锑业有限公司 A kind of antimony powder smelting furnace
CN108913915A (en) * 2018-07-19 2018-11-30 湖南腾驰环保科技有限公司 A kind of arsenic trioxide restores to obtain the technique of elemental arsenic

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1072963A (en) * 1991-12-03 1993-06-09 沈阳市中兴冶金实用技术研究所 The preparation method of low-arsenic pure antimony
CN1103895A (en) * 1994-08-27 1995-06-21 周磊 Method for prodn. of antimony sesquioxide powder using antimony oxide ore or antimony ore containing sulphur and oxygen

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1072963A (en) * 1991-12-03 1993-06-09 沈阳市中兴冶金实用技术研究所 The preparation method of low-arsenic pure antimony
CN1103895A (en) * 1994-08-27 1995-06-21 周磊 Method for prodn. of antimony sesquioxide powder using antimony oxide ore or antimony ore containing sulphur and oxygen

Also Published As

Publication number Publication date
CN1186868A (en) 1998-07-08

Similar Documents

Publication Publication Date Title
CN103421955B (en) Zinc leaching slag treatment method
CN1800423A (en) Process for producing antimony white using slag from lead anode mud processing
CN101078052A (en) Method for synthetically reclaiming iron and non-ferrous metal from solid waste of iron and steel plant
US4489046A (en) Method for working-up arsenic-containing waste
CN101321880B (en) Method and apparatus for lead smelting
CN111893310A (en) Harmless recycling treatment method for solid hazardous waste
CN105803205B (en) A kind of energy-efficient secondary lead smelting technique
CN1270235A (en) Process for treating low-grade anode mud
CN1051581C (en) Method and device for preparing stibic white with jamesonite
CN203559108U (en) System for simultaneously smelting lead and zinc
US5178667A (en) Dry process for refining zinc sulfide concentrates
CN1142300C (en) Dearsenicating method during smelting lead-antimony alloy
CN1325672C (en) Lead smelting method and apparatus implementing the same
CN108893621A (en) A kind of method of pyro-refining lead bullion
CN212247151U (en) Jet smelting electric heating reduction furnace
CN109487097B (en) Feeding device and method for refining and deironing crude antimony
AU594370B2 (en) Recovery of volatile metal values from metallurgical slags
CN105838894A (en) Process for treating copper dross through oxygen enrichment top-blowing smelting-settling separation
CN101280364B (en) Method for producing high-stibium crude lead
CN101654744A (en) Reverberatory furnace pyrorefining method of crude copper with high arsenic and antimony
CN1420186A (en) Process for separating zinc and lead from metallurgic furnace dust
CN219793074U (en) Comprehensive recovery and harmless treatment device for valuable metal elements of copper smelting slag
CN1279193C (en) High iron slag type formulation in top blowing sinking smelting furnace tin-making process
CN115852162B (en) Smelting method of high zinc melt molten pool reducing slag and zinc and application thereof
CN103233243A (en) Production method of electrolytic metal manganese

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
CI01 Publication of corrected invention patent application

Correction item: Co-applicant

Correct: Huandong Integrated Non-Ferrous Metal Chemical Plant, Liuzhou City

False: Zhengzhou link joint non ferrous metal chemical plant

Number: 27

Page: 46

Volume: 14

ERR Gazette correction

Free format text: CORRECT: CO-APPLICANT; FROM: ZHENGZHOU CITY HUANDONG LIANHE NON-FERROUS METAL CHEMICAL PLANT TO: LIUZHOU CITY HUANDONG LIANHE NON-FERROUS METAL CHEMICAL PLANT

C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: YUNAN COUNTY GUANGXIN SMELTING CO., LTD.

Free format text: FORMER OWNER: KONG XIANGCHENG

C41 Transfer of patent application or patent right or utility model
C56 Change in the name or address of the patentee

Owner name: LIUZHOU CITY HUANDONG BEER MATERIAL CO., LTD.

Free format text: CHANGE FOR CO-PATENTEE; FORMER NAME OR ADDRESS: LIUZHOU CITY HUANDONG LIANHE NON-FERROUS METAL CHEMICAL PLANT

CP03 Change of name, title or address

Address after: 545005 Guangxi Liuzhou City Liuzhou Road nine km

Co-patentee after: HUANDONG METAL MATERIAL Co.,Ltd.

Co-patentee before: HUANDONG INTEGRATED NON FERROU

TR01 Transfer of patent right

Effective date of registration: 20031210

Address after: 527100, both towns of Yunan County in Guangdong province are rushing to learn mountain

Co-patentee after: HUANDONG METAL MATERIAL Co.,Ltd.

Patentee after: GUANGXIN SMELTERY Co.,Ltd. YUNAN COUNTY

Address before: 537100, room 4, No. 410 West Central Road, Yunan, Guangdong

Co-patentee before: HUANDONG METAL MATERIAL Co.,Ltd.

Patentee before: Kong Xiangcheng

C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20000419

Termination date: 20090818