CN110142131A - A kind of separation method of high-As and high-S tin rough concentrate - Google Patents
A kind of separation method of high-As and high-S tin rough concentrate Download PDFInfo
- Publication number
- CN110142131A CN110142131A CN201910301246.5A CN201910301246A CN110142131A CN 110142131 A CN110142131 A CN 110142131A CN 201910301246 A CN201910301246 A CN 201910301246A CN 110142131 A CN110142131 A CN 110142131A
- Authority
- CN
- China
- Prior art keywords
- tin
- tons
- concentrate
- agent
- separation method
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B1/00—Conditioning for facilitating separation by altering physical properties of the matter to be treated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B5/00—Washing granular, powdered or lumpy materials; Wet separating
- B03B5/02—Washing granular, powdered or lumpy materials; Wet separating using shaken, pulsated or stirred beds as the principal means of separation
- B03B5/04—Washing granular, powdered or lumpy materials; Wet separating using shaken, pulsated or stirred beds as the principal means of separation on shaking tables
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B7/00—Combinations of wet processes or apparatus with other processes or apparatus, e.g. for dressing ores or garbage
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B9/00—General arrangement of separating plant, e.g. flow sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/02—Froth-flotation processes
- B03D1/025—Froth-flotation processes adapted for the flotation of fines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/007—Modifying reagents for adjusting pH or conductivity
Abstract
The present invention relates to a kind of separation methods of high-As and high-S tin rough concentrate.The separation method includes the following steps: S1: prescreening ore grinding;S2: it sizes mixing;S3: FLOTATION SEPARATION;S4: Gravity separation;S5: FLOTATION SEPARATION.The present invention uses prescreening-closed circuit grinding, not only effectively prevents easy cross of cassiterite and crushes, but also ensure that pozzuolite mineral floating removes feed particle size;Using the floatability difference between pyrite, mispickel and cassiterite, in acidic environment, sulfoarsenic mineral is activated using activator, sulfoarsenic mineral is removed by flotation, effectively reduces Tin concentrate sulphur arsenic excessive problem;It is sorted by multistage shaking table and tin-lead soldering, keeps Tin concentrate and tin time concentrate product structure distribution more reasonable.The Tin concentrate tin grade that beneficiation method of the invention obtains is greater than 45%, the tin rate of recovery and is greater than 85%, and tin time concentrate tin grade is greater than the technical indicator that 4%, the tin rate of recovery is greater than 11%, and Tin concentrate sulphur arsenic meets the quality standard requirement.
Description
Technical field
The present invention relates to technical field of beneficiation, more particularly, to a kind of separation method of high-As and high-S tin rough concentrate.
Technical background
As China's placer tin ore resources gradually reduce, stannum-contained multi-metal sulphide ore becomes the main source of tin.However, such
The universal sulfur content of tin resource is higher, and sulphide ore floatability differs greatly, and ore properties are sufficiently complex, causes Tin concentrate sulphur arsenic etc. miscellaneous
Prime element content be difficult to meet Tin concentrate quality standard (YS/T 339-2011): tin grade > 40%, sulfur grade < 1.20%,
The requirement of arsenic grade < 0.80%.Tin product selling price is not only influenced, it is unfavorable also to cause for subsequent smelting deep processing.
Currently, tin rough concentrate separation method mainly has gravity treatment, flotation and floating-weight process integration, selecting process is gradually
Develop towards efficient, easy direction, selects factory rules and regulations mould enlarged, production management fining.Significantly, since tin-polymetallic
Sulphide ore takes different degrees of inhibition in preamble sulphide ore sorting operation, for sulfoarsenic minerals such as pyrite, mispickel, therefore
Suppression sulfoarsenic mineral how is solved, is the key that floatation desulphurization.
Zhao Shu (thick Tin concentrate dressing process research and industrial production relevant issues are inquired into, " mineral products comprehensive utilization ", and 2011
(05): 48-52. it) has studied and " floating-weight-magnetic " and " weight-magnetic-is floating " process flow processing tin rough concentrate is respectively adopted, although obtaining
Preferable expanding test index, but technique is related to multiple ore grinding, process is tediously long, and cumbersome, inconvenience promotes and applies.
Flat good fortune first (comprehensive recovery experiment of old factory's tin rough concentrate association tungsten sulphur, " Modern Mineral ", 2014,30 (08): 34-
36+39.) have studied the process flow of use " ore grinding-floats sulphur-fubai tungsten " synthetical recovery sulphur, tungsten and tin from tin rough concentrate.By
Used waterglass to size mixing in the technique, sulphide mineral flotation removing be not thorough, in addition float Tungsten tailing (as Tin concentrate) not into
Row deep processing processing, causes Tin concentrate sulfur grade exceeded, for tin grade less than 30%, synthetical recovery index is undesirable.
Therefore, developing a kind of separation method for high-As and high-S tin rough concentrate and reaching Tin concentrate quality criteria requirements has
Important research significance and economic value.
Summary of the invention
It is tediously long that there are processes it is an object of the invention to overcoming the separation method of tin rough concentrate in the prior art, operates numerous
Trivial, inconvenience promotes and applies, and synthetical recovery index undesirable defect or deficiency provide a kind of separation of high-As and high-S tin rough concentrate
Method.The present invention is using " floating-weight " process integration, and separation obtains Tin concentrate and tin time concentrate, separating technology from tin rough concentrate
Simply, tin product structure is reasonable, and Tin concentrate sulphur arsenic is met the requirements of the standard.
In order to achieve the above-mentioned object of the invention, the present invention adopts the following technical scheme:
A kind of separation method of high-As and high-S tin rough concentrate, includes the following steps:
S1: prescreening ore grinding: after tin rough concentrate prescreening, oversize repeats ore grinding-screening operation, until tin is thick
Concentrate is -0.25mm grade;
S2: it sizes mixing: tin rough concentrate obtained by S1 is modulated to ore pulp, and it is 5~6 that regulator, which is added, to adjust pH;The ore pulp
Concentration is 28~32%;
S3: 80~100 g tons of activator, 100~120 g tons of collecting agent, foaming agent FLOTATION SEPARATION: are added into ore pulp
20~30 g tons are done one roughing;Be added 30~40 g tons of collecting agent, 10~20 g tons of foaming agent do once purging selection;It is added
20~30 g tons of collecting agent, 10~15 g tons of foaming agent do secondary scan;It is selected that roughing foam does blank three times;Obtain sulphur essence
Mine and floating sulphur tailing;
S4: Gravity separation: doing shaking table roughing for floating sulphur tailing, obtains Tin concentrate, medium tin ore, tailing and tin time concentrate, so
Shaking table is made to medium tin ore afterwards to scan, and is obtained Tin concentrate, tin time concentrate and tailings, is respectively scanned shaking table roughing and shaking table
Tin concentrate, tin time concentrate and tailings are corresponding to be merged, and Tin concentrate, shaking table tin time concentrate and shaking table tailing are obtained;
S5: FLOTATION SEPARATION: being milled to -0.074mm for shaking table tailing and account for 85%, controls pulp density 28~32%, successively plus
Enter 80~120 g tons of Inorganic regulator, 70~110 g tons of supplementary catching agent, 500~700 g tons of collecting agent, foaming agent 15
~25 g tons are done one roughing;25~35 g tons of supplementary catching agent, 180~220 g tons of collecting agent, foaming agent 8~12 is added
G ton do once purging selection;15~25 g tons of supplementary catching agent of addition, 120~180 g tons of collecting agent, 8~12 grams of foaming agent/
Ton does secondary scan;It is selected that roughing foam does blank three times;Floating Tin concentrate and floating tailing are obtained, floating Tin concentrate is incorporated to tin time essence
Mine.
The present invention uses prescreening-closed circuit grinding, not only effectively prevents easy cross of cassiterite and crushes, but also ensure that pozzuolite
Mineral floating removes feed particle size;Using the floatability difference between pyrite, mispickel and cassiterite, in acidic environment, use
Activator activates sulfoarsenic mineral, removes sulfoarsenic mineral by flotation, effectively reduces Tin concentrate sulphur arsenic excessive problem;Pass through
Multistage shaking table sorts and tin-lead soldering, keeps Tin concentrate and tin time concentrate product structure distribution more reasonable.
The Tin concentrate tin grade that beneficiation method of the invention obtains is greater than 45%, the tin rate of recovery and is greater than 85%, tin time concentrate
Tin grade is greater than the technical indicator that 4%, the tin rate of recovery is greater than 11%, and Tin concentrate sulphur arsenic meets the quality standard requirement.
Preferably, it is sieved in S1 using 0.25mm sieve.
Preferably, regulator described in S2 is one or more of sulfuric acid or oxalic acid.
Preferably, activator described in S3 is copper sulphate or copper chloride.
Copper ion can activate sulfoarsenic mineral, be removed sulfoarsenic mineral by flotation, and it is super to effectively reduce Tin concentrate sulphur arsenic
Mark problem
Preferably, collecting agent described in S3 is butyl xanthate or butyl xanthate and methyl isobutyl carbinol xanthate mixture.
It is further preferable that the mass ratio of butyl xanthate or butyl xanthate and methyl isobutyl carbinol is 1 in the mixture:
1
Preferably, foaming agent described in S3 is terpenic oil.
Preferably, Inorganic regulator described in S5 is calgon.
Preferably, supplementary catching agent described in S5 is tributyl phosphate.
Preferably, collecting agent described in S5 is Salicyl Hydroximic Acid.
Preferably, sequentially added in S5 100 g tons of Inorganic regulator, 90 g tons of supplementary catching agent, 600 grams of collecting agent/
Ton, 20 g tons of foaming agent do one roughing;30 g tons of supplementary catching agent, 200 g tons of collecting agent, 10 g tons of foaming agent is added
Do once purging selection;Be added 20 g tons of supplementary catching agent, 150 g tons of collecting agent, 10 g tons of foaming agent do secondary scan.
Compared with prior art, the invention has the following beneficial effects:
1. using prescreening-closed circuit grinding, not only effectively prevents easy cross of cassiterite and crush, but also ensure that pozzuolite mineral
Flotation removing feed particle size.
2. in acidic environment, activating sulphur using activator using the floatability difference between pyrite, mispickel and cassiterite
Arsenic mineral is removed sulfoarsenic mineral by flotation, effectively reduces Tin concentrate sulphur arsenic excessive problem.
3. sorting by multistage shaking table and tin-lead soldering, make Tin concentrate and tin time concentrate product structure distribution more adduction
Reason.
The Tin concentrate tin grade that beneficiation method of the invention obtains is greater than 45%, the tin rate of recovery and is greater than 85%, tin time concentrate
Tin grade is greater than the technical indicator that 4%, the tin rate of recovery is greater than 11%, and Tin concentrate sulphur arsenic meets the quality standard requirement.
Detailed description of the invention
Fig. 1 is the process flow chart that Examples 1 to 4 provides.
Specific embodiment
Below with reference to embodiment, the present invention is further explained.These embodiments are merely to illustrate the present invention rather than limitation
The scope of the present invention.Test method without specific conditions in lower example embodiment usually according to this field normal condition or is pressed
The condition suggested according to manufacturer;Used raw material, reagent etc., unless otherwise specified, being can be from the business such as conventional market
The raw materials and reagents that approach obtains.The variation for any unsubstantiality that those skilled in the art is done on the basis of the present invention
And replacement belongs to scope of the present invention.
The present invention by taking the tin rough concentrate of factory's output is selected in Inner Mongol as an example, essential mineral group become cassiterite, pyrite, mispickel and
Quartz etc..Tin grade is 9.60% in rough concentrate, sulfur grade 3.80%, arsenic grade 1.39%.The step of according to embodiment
It is separated with dosing listed by table 1.
Embodiment 1
The present embodiment provides a kind of separation methods of high-As and high-S tin rough concentrate.Such as Fig. 1, specific steps and each substance dosage
Following and table 1.
By tin rough concentrate, using prescreening-closed circuit grinding, (after tin rough concentrate prescreening, oversize repeats to grind
Mine-screening operation), it is milled to -0.25mm;Adjusting pulp density is 30%;Sulfuric acid is added and adjusts pH values of pulp to 6;According to listed by table 1
Dosing operation, flotation (one roughing, once purging selection, it is secondary scan, that roughing foam does blank three times is selected) obtain sulphur
Concentrate and floating sulphur tailing, floating sulphur tailing obtain Tin concentrate, tin time concentrate and shaking table tail after shaking table (shaking table roughing, shaking table are scanned)
Mine;Shaking table tailing is subjected to FLOTATION SEPARATION: shaking table tailing being milled to -0.074mm and accounts for 85%, controls pulp density 30%, successively
Be added 100 g tons of calgon, 90 g tons of tributyl phosphate, 600 g tons of Salicyl Hydroximic Acid, 20 g tons of foaming agent do one
Secondary roughing;Be added 30 g tons of tributyl phosphate, 200 g tons of Salicyl Hydroximic Acid, 10 g tons of foaming agent do once purging selection;It is added
20 g tons of tributyl phosphate, 150 g tons of Salicyl Hydroximic Acid, 10 g tons of foaming agent do secondary scan;Roughing foam does empty three times
Bai Jingxuan;Floating Tin concentrate and floating tailing are obtained, floating Tin concentrate is incorporated to tin time concentrate.
Tin grade is 45.80% in finally obtained Tin concentrate, and the tin rate of recovery is 85.57%, and sulfur-bearing 0.24% contains arsenic
0.10%, tin grade is 4.50% in tin time concentrate, and the tin rate of recovery is 8.50%.
Embodiment 2
The present embodiment provides a kind of separation methods of high-As and high-S tin rough concentrate.Such as Fig. 1, specific steps and each substance dosage
Following and table 1.
By tin rough concentrate, using prescreening-closed circuit grinding, (after tin rough concentrate prescreening, oversize repeats to grind
Mine-screening operation), it is milled to -0.25mm;Adjusting pulp density is 30%;Sulfuric acid is added and adjusts pH values of pulp to 5;According to listed by table 1
Dosing operation, flotation (one roughing, once purging selection, it is secondary scan, that roughing foam does blank three times is selected) obtain sulphur
Concentrate and floating sulphur tailing, floating sulphur tailing obtain Tin concentrate, tin time concentrate and shaking table tailing after shaking table;Shaking table tailing is floated
Choosing separation: being milled to -0.074mm for shaking table tailing and account for 85%, controls pulp density 30%, sequentially add 80 grams of calgon/
Ton, 70 g tons of tributyl phosphate, 500 g tons of Salicyl Hydroximic Acid, 25 g tons of foaming agent do one roughing;Tricresyl phosphate fourth is added
35 g tons of ester, 220 g tons of Salicyl Hydroximic Acid, 12 g tons of foaming agent do once purging selection;25 g tons of tributyl phosphate, water is added
180 g tons of poplar hydroximic acid, 12 g tons of foaming agent do secondary scan;It is selected that roughing foam does blank three times;Obtain floating Tin concentrate
With floating tailing, floating Tin concentrate is incorporated to tin time concentrate.
Tin grade is 45.80% in finally obtained Tin concentrate, and the tin rate of recovery is 85.90%, and sulfur-bearing 0.23% contains arsenic
0.078%, tin grade is 4.11% in tin time concentrate, and the tin rate of recovery is 8.80%.
Embodiment 3
The present embodiment provides a kind of separation methods of high-As and high-S tin rough concentrate.Such as Fig. 1, specific steps and each substance dosage
Following and table 1.
By tin rough concentrate, using prescreening-closed circuit grinding, (after tin rough concentrate prescreening, oversize repeats to grind
Mine-screening operation), it is milled to -0.25mm;Adjusting pulp density is 30%;Oxalic acid is added and adjusts pH values of pulp to 6;According to listed by table 1
Dosing operation, flotation (one roughing, once purging selection, it is secondary scan, that roughing foam does blank three times is selected) obtain sulphur
Concentrate and floating sulphur tailing, floating sulphur tailing obtain Tin concentrate, tin time concentrate and shaking table tailing after shaking table;Shaking table tailing is floated
Choosing separation: being milled to -0.074mm for shaking table tailing and account for 85%, controls pulp density 30%, sequentially add 120 grams of calgon/
Ton, 110 g tons of tributyl phosphate, 700 g tons of Salicyl Hydroximic Acid, 15 g tons of foaming agent do one roughing;Tricresyl phosphate fourth is added
35 g tons of ester, 220 g tons of Salicyl Hydroximic Acid, 8 g tons of foaming agent do once purging selection;25 g tons of tributyl phosphate, water is added
180 g tons of poplar hydroximic acid, 8 g tons of foaming agent do secondary scan;It is selected that roughing foam does blank three times;Obtain floating Tin concentrate and
Floating tailing, floating Tin concentrate are incorporated to tin time concentrate.
Tin grade is 46.72% in finally obtained Tin concentrate, and the tin rate of recovery is 85.60%, and sulfur-bearing 0.23% contains arsenic
0.091%, tin grade is 4.25% in tin time concentrate, and the tin rate of recovery is 9.20%.
Embodiment 4
The present embodiment provides a kind of separation methods of high-As and high-S tin rough concentrate.Such as Fig. 1, specific steps and each substance dosage
Following and table 1.
By tin rough concentrate, using prescreening-closed circuit grinding, (after tin rough concentrate prescreening, oversize repeats to grind
Mine-screening operation), it is milled to -0.25mm;Adjusting pulp density is 30%;Oxalic acid is added and adjusts pH values of pulp to 5;According to listed by table 1
Dosing operation, flotation (one roughing, once purging selection, it is secondary scan, that roughing foam does blank three times is selected) obtain sulphur
Concentrate and floating sulphur tailing, floating sulphur tailing obtain Tin concentrate, tin time concentrate and shaking table tailing after shaking table;Shaking table tailing is floated
Choosing separation: being milled to -0.074mm for shaking table tailing and account for 85%, controls pulp density 30%, sequentially add 110 grams of calgon/
Ton, 100 g tons of tributyl phosphate, 650 g tons of Salicyl Hydroximic Acid, 20 g tons of foaming agent do one roughing;Tricresyl phosphate fourth is added
30 g tons of ester, 210 g tons of Salicyl Hydroximic Acid, 10 g tons of foaming agent do once purging selection;20 g tons of tributyl phosphate, water is added
160 g tons of poplar hydroximic acid, 10 g tons of foaming agent do secondary scan;It is selected that roughing foam does blank three times;Obtain floating Tin concentrate
With floating tailing, floating Tin concentrate is incorporated to tin time concentrate.
Tin grade is 45.50% in finally obtained Tin concentrate, and the tin rate of recovery is 86.10%, and sulfur-bearing 0.22% contains arsenic
0.063%, tin grade is 4.13% in tin time concentrate, and the tin rate of recovery is 9.18%.
1 Examples 1 to 4 floating agent dosage of table (g ton tin rough concentrate)
The above is that particular example embodiment of the invention is not departing from this hair for those skilled in the art
Under bright principle, several improvement and rhetoric can also be made.In fact, the scope of the present invention by the attached claims and its
Equivalents.
Claims (10)
1. a kind of separation method of high-As and high-S tin rough concentrate, which comprises the steps of:
S1: prescreening ore grinding: after tin rough concentrate prescreening, oversize repeats ore grinding-screening operation, until tin rough concentrate
For -0.25mm grade;
S2: it sizes mixing: tin rough concentrate obtained by S1 is modulated to ore pulp, and it is 5~6 that regulator, which is added, to adjust pH;The pulp density
It is 28~32%;
S3: FLOTATION SEPARATION: into ore pulp be added 80~100 g tons of activator, 100~120 g tons of collecting agent, foaming agent 20~
30 g tons are done one roughing;Be added 30~40 g tons of collecting agent, 10~20 g tons of foaming agent do once purging selection;Collecting is added
20~30 g tons of agent, 10~15 g tons of foaming agent do secondary scan;It is selected that roughing foam does blank three times;Obtain iron concentrate and
Floating sulphur tailing;
S4: Gravity separation: doing shaking table roughing for floating sulphur tailing, obtains Tin concentrate, medium tin ore, tailing and tin time concentrate, then right
Medium tin ore makees shaking table and scans, and obtains Tin concentrate, tin time concentrate and tailings, the tin essence for respectively scanning shaking table roughing and shaking table
Mine, tin time concentrate and tailings are corresponding to be merged, and Tin concentrate, shaking table tin time concentrate and shaking table tailing are obtained;
S5: FLOTATION SEPARATION: shaking table tailing is milled to -0.074mm and accounts for 85%, pulp density 28~32% is controlled, sequentially adds nothing
80~120 g tons of machine regulator, 70~110 g tons of supplementary catching agent, 500~700 g tons of collecting agent, foaming agent 15~25
G ton do one roughing;25~35 g tons of supplementary catching agent of addition, 180~220 g tons of collecting agent, 8~12 grams of foaming agent/
Ton does once purging selection;Be added 15~25 g tons of supplementary catching agent, 120~180 g tons of collecting agent, 8~12 g tons of foaming agent do
It is secondary to scan;It is selected that roughing foam does blank three times;Floating Tin concentrate and floating tailing are obtained, floating Tin concentrate is incorporated to tin time concentrate.
2. separation method according to claim 1, which is characterized in that sieved in S1 using 0.25mm sieve.
3. separation method according to claim 1, which is characterized in that regulator described in S2 is one of sulfuric acid or oxalic acid
Or it is several.
4. separation method according to claim 1, which is characterized in that activator described in S3 is copper sulphate or copper chloride;S3
Described in collecting agent be butyl xanthate or butyl xanthate and methyl isobutyl carbinol xanthate mixture.
5. separation method according to claim 4, which is characterized in that butyl xanthate or butyl xanthate and first in the mixture
The mass ratio of base isobutyl carbinol is 1:1.
6. separation method according to claim 1, which is characterized in that foaming agent described in S3 is terpenic oil.
7. separation method according to claim 1, which is characterized in that Inorganic regulator described in S5 is calgon.
8. separation method according to claim 1, which is characterized in that supplementary catching agent described in S5 is tributyl phosphate.
9. separation method according to claim 1, which is characterized in that collecting agent described in S5 is Salicyl Hydroximic Acid.
10. separation method according to claim 1, which is characterized in that sequentially add 100 g tons of Inorganic regulator, auxiliary in S5
Help 90 g tons of collecting agent, 600 g tons of collecting agent, 20 g tons of foaming agent do one roughing;30 g tons of supplementary catching agent of addition,
200 g tons of collecting agent, 10 g tons of foaming agent do once purging selection;Be added 20 g tons of supplementary catching agent, 150 g tons of collecting agent,
10 g tons of foaming agent are done secondary scan.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910301246.5A CN110142131A (en) | 2019-04-15 | 2019-04-15 | A kind of separation method of high-As and high-S tin rough concentrate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910301246.5A CN110142131A (en) | 2019-04-15 | 2019-04-15 | A kind of separation method of high-As and high-S tin rough concentrate |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110142131A true CN110142131A (en) | 2019-08-20 |
Family
ID=67588830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910301246.5A Pending CN110142131A (en) | 2019-04-15 | 2019-04-15 | A kind of separation method of high-As and high-S tin rough concentrate |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110142131A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111632745A (en) * | 2020-04-28 | 2020-09-08 | 西北矿冶研究院 | Mineral processing technology for cracked rock type copper oxide tin ore |
CN114433347A (en) * | 2022-01-27 | 2022-05-06 | 江苏北矿金属循环利用科技有限公司 | Comprehensive recycling method for valuable components in zinc smelting high-sulfur slag |
CN115055286A (en) * | 2022-05-05 | 2022-09-16 | 中国矿业大学(北京) | Method for promoting cassiterite medicament collecting effect |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3347098A1 (en) * | 1983-12-27 | 1985-07-04 | Klöckner-Humboldt-Deutz AG, 5000 Köln | Process and apparatus for the separation of impurities in materials, especially in tin ore |
CN101767056A (en) * | 2010-01-28 | 2010-07-07 | 广西大学 | Method for mixed selection and re-purification of cassiterite and sulfide ores |
CN101920222A (en) * | 2010-08-19 | 2010-12-22 | 云南锡业集团(控股)有限责任公司 | Improved method for cleaning tin rough concentrate |
CN104624389A (en) * | 2015-01-09 | 2015-05-20 | 临武县南方矿业有限责任公司 | Gravitation separation tailing cassiterite flotation method |
CN106622639A (en) * | 2016-12-23 | 2017-05-10 | 云南锡业股份有限公司卡房分公司 | Ore concentration technique for tin sulphide ore rough concentrate |
US9694367B2 (en) * | 2013-10-10 | 2017-07-04 | Titanium Corporation, Inc. | Method for producing a zirconium concentrated product from froth treatment tailings |
-
2019
- 2019-04-15 CN CN201910301246.5A patent/CN110142131A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3347098A1 (en) * | 1983-12-27 | 1985-07-04 | Klöckner-Humboldt-Deutz AG, 5000 Köln | Process and apparatus for the separation of impurities in materials, especially in tin ore |
CN101767056A (en) * | 2010-01-28 | 2010-07-07 | 广西大学 | Method for mixed selection and re-purification of cassiterite and sulfide ores |
CN101920222A (en) * | 2010-08-19 | 2010-12-22 | 云南锡业集团(控股)有限责任公司 | Improved method for cleaning tin rough concentrate |
US9694367B2 (en) * | 2013-10-10 | 2017-07-04 | Titanium Corporation, Inc. | Method for producing a zirconium concentrated product from froth treatment tailings |
CN104624389A (en) * | 2015-01-09 | 2015-05-20 | 临武县南方矿业有限责任公司 | Gravitation separation tailing cassiterite flotation method |
CN106622639A (en) * | 2016-12-23 | 2017-05-10 | 云南锡业股份有限公司卡房分公司 | Ore concentration technique for tin sulphide ore rough concentrate |
Non-Patent Citations (5)
Title |
---|
中国科学技术情报研究所《有所金属技术新进展》编辑组: "《有色金属技术新进展》", 31 July 1984, 北京:科学技术文献出版社 * |
刘殿文 等: "《氧化铜矿浮选技术》", 31 May 2009, 北京:冶金工业出版社 * |
孙传尧 等: "《复杂难处理矿石选矿技术-全国选矿学术会议论文集》", 31 October 2009, 北京:冶金工业出版社 * |
雷霆 等: "《锡冶金》", 31 December 2013, 北京:冶金工业出版社 * |
黄礼煌: "《浮选》", 31 March 2018, 北京:冶金工业出版社 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111632745A (en) * | 2020-04-28 | 2020-09-08 | 西北矿冶研究院 | Mineral processing technology for cracked rock type copper oxide tin ore |
CN114433347A (en) * | 2022-01-27 | 2022-05-06 | 江苏北矿金属循环利用科技有限公司 | Comprehensive recycling method for valuable components in zinc smelting high-sulfur slag |
CN114433347B (en) * | 2022-01-27 | 2024-03-22 | 江苏北矿金属循环利用科技有限公司 | Comprehensive recycling method for valuable components of zinc smelting high-sulfur slag |
CN115055286A (en) * | 2022-05-05 | 2022-09-16 | 中国矿业大学(北京) | Method for promoting cassiterite medicament collecting effect |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2017101078A4 (en) | Beneficiation method for high-clay mixed lead-zinc oxide-sulfide ore | |
CN101537388B (en) | Separation method for bismuth-molybdenum-copper-sulfide mixed concentrate | |
CN101585017B (en) | Ore-selecting method of difficultly-selected copper zinc sulphur ore | |
CN106170343B (en) | A kind of beneficiation method of chalcopyrite | |
CN102489407B (en) | Mineral processing method for recycling scheelite/molybdenum oxide ores from molybdenum sulfide flotation tailings | |
CN102029220B (en) | Separating flotation method of low-grade complex lead-antimony-zinc | |
CN106076600B (en) | A kind of beneficiation method of low-grade difficult scheelite | |
CN107899740A (en) | A kind of high arsenic-bearing pyrite concentrate pozzuolite separation ore-sorting technique containing magnetic iron ore | |
CN105013603B (en) | A kind of beneficiation method of copper nickel sulfide mineral | |
CN101549322A (en) | Process of using sulphur lead-zinc containing tailings to prepare sulphur iron ore concentrate | |
CN103551245B (en) | Complex multi-metal micro fine particle sulphide ore is carried out to the beneficiation method of synthetical recovery | |
CN111495788B (en) | Method for intelligently and preferentially selecting copper-blue-containing copper sulfide ore by X-ray | |
CN105903552A (en) | Beneficiation method for effectively recovering extremely-fine-particle molybdenum ore | |
CN110142131A (en) | A kind of separation method of high-As and high-S tin rough concentrate | |
CN111940118B (en) | Recovery method of secondary copper-containing low-grade copper-sulfur ore | |
CN102151607A (en) | Joint magnetic flotation sorting method for complex magnetic pyrite copper-containing pyrite ore | |
CN110170381A (en) | A kind of beneficiation method recycling cassiterite from tin copper mineral intergrowth | |
CN111841826B (en) | Beneficiation method for high-calcium carbonate type low-grade scheelite | |
CN105289834A (en) | Zinc and sulfur separation beneficiation method for pyrrhotite-rich zinc sulfide ore | |
US5925862A (en) | Process for the recovery of cobalt from ores containing metal sulfides | |
CN109604071A (en) | It is a kind of to reduce the stanniferous method for floating of troilite | |
CN105214849B (en) | A kind of beneficiation method for improving scheelite concentration process concentrate grade | |
CN103909008B (en) | A kind of ore dressing group technology reclaiming sulfur ferrum from Pb-Zn tailings | |
CN102896038A (en) | Flotation method for re-cleaning lead zinc ore and sulfur concentrate after preferable mixing separating | |
CN105772215A (en) | Mineral processing method of separating sulfur concentrates from selected pyrite tailings |
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 |
Application publication date: 20190820 |
|
RJ01 | Rejection of invention patent application after publication |