CN107497606A - A kind of regime of agent of phosphorus ore direct flotation roughing - Google Patents
A kind of regime of agent of phosphorus ore direct flotation roughing Download PDFInfo
- Publication number
- CN107497606A CN107497606A CN201710823151.0A CN201710823151A CN107497606A CN 107497606 A CN107497606 A CN 107497606A CN 201710823151 A CN201710823151 A CN 201710823151A CN 107497606 A CN107497606 A CN 107497606A
- Authority
- CN
- China
- Prior art keywords
- agent
- regulators
- phosphorus ore
- direct flotation
- collecting agent
- 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
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/002—Inorganic compounds
-
- 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
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- 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
-
- 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
- B03D2201/02—Collectors
-
- 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
- B03D2201/06—Depressants
-
- 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
- B03D2203/00—Specified materials treated by the flotation agents; specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
- B03D2203/06—Phosphate ores
Abstract
A kind of regime of agent of phosphorus ore direct flotation roughing, first pH regulators and collecting agent are mixed, obtain the mixture of pH regulators and collecting agent;In phosphorus ore direct flotation rougher process, inhibitor is first added, then adds the mixture of pH regulators and collecting agent.The present invention can significantly reduce the collector dosage of phosphorus ore direct flotation roughing, improve the utilization rate of direct flotation collecting agent, reduce floating agent cost.
Description
Technical field
The present invention relates to a kind of technique of the floating and enriching phosphorus concentrate from rock phosphate in powder, and in particular to a kind of by using new
Medicament addition manner improves phosphorus ore direct floatation process and refers to calibration method.
Background technology
At present, domestic application mainly have in the technique of preparing of collophane floatation, scrubbing-desliming technique, gravity separation,
Roasting-digestion process, chemical leaching technologies, photoelectricity selection technology, beneficiation combined method flow, hydrochloric acid decompose mid-low grade collophanite ore system
Take phosphoric acid etc..Floatation is that application is most wide, technology also the most ripe one kind.Mainly have using floatation sorting collophane
Direct flotation technique, reverse floatation process, direct-reverse flotation technique, trans- direct floatation process and bi-anti-symmetric matrix technique.
At present, comparative maturity, the successful key of floatation are to search out the good, collecting performance of selectivity to flotation of phosphate rock technique
The strong collecting agent of energy, next to that searching out selectivity strong gangue mineral and Phosphate minerals inhibitor.
At present, phosphorus ore direct flotation medicament is mainly that oleic acid, aliphatic acid or modified fat are sour and its saponified etc..
In all kinds of documents, phosphorus ore direct flotation medicament order of addition is pH regulators, inhibitor, collecting agent, its collecting agent
Dosage is larger, and utilization rate is limited.
The content of the invention
The technical problem to be solved in the present invention is overcome the deficiencies in the prior art, there is provided a kind of phosphorus ore direct flotation roughing
Regime of agent, change direct flotation roughing medicament addition manner, improve flotation collector utilization rate, reduce the dosage of collecting agent, drop
Low floating agent cost.
It is a kind of regime of agent of phosphorus ore direct flotation roughing that the present invention, which solves the technical scheme that its technical problem uses, first
PH regulators and collecting agent are mixed, obtain the mixture of pH regulators and collecting agent;In phosphorus ore direct flotation rougher process, first add
Inhibitor, then add the mixture of pH regulators and collecting agent.
Specifically include herein below:
(1)Determine additive amount of medicament:According to the normal medicament order of addition of phosphorus ore direct flotation roughing, i.e., first add pH regulators, so
Inhibitor is added afterwards, is eventually adding the order of collecting agent, and the addition of three kinds of medicaments is found out by condition test;
(2)Medicament configuration:Weigh pH regulators and collecting agent, then mix pH regulators and collecting agent, obtain pH regulators and
The mixture of collecting agent;
(3)Medicament addition manner:Inhibitor is first added in phosphorus ore direct flotation rougher process, then adds step(2)Middle configuration
The mixture of pH regulators and collecting agent.
Further, the pH regulators are Na2CO3, at least one of NaOH.The inhibitor is waterglass, acidifying water
At least one of glass, starch etc..The collecting agent is oleic acid, aliphatic acid, modified fat acid, saponification oleic acid, saponified fat
Acid, modified fat acid are at least one of saponified.
The preparation method of the acidified sodium silicate:Water glass solution pH is adjusted to 2-4 with sulfuric acid, hydrochloric acid or nitric acid etc., i.e.,
.
The modified fat acid is product of the aliphatic acid after organic reaction, the organic reaction include substitution reaction,
At least one of addition reaction, elimination reaction, redox reaction, esterification etc..
The present invention can significantly reduce the collector dosage of phosphorus ore direct flotation roughing, improve the utilization rate of direct flotation collecting agent,
Reduce floating agent cost.
Embodiment
Below in conjunction with embodiment, the invention will be further described.
In following embodiment and comparative example, the preparation method of the acidified sodium silicate:With sulfuric acid by water glass solution pH
Desired pH value is adjusted to, is produced.
The collecting agent oleic acid, saponified fat acid (C16-C18) it is commercially available prod.
Comparative example 1
This comparative example comprises the following steps:
(1)By phosphorus ore(Containing P2O518.32wt%), it is milled to -400 mesh(-0.038mm)60wt% is accounted for below;
(2)One roughing once purging selection is carried out to the raw ore ground, one roughing adds pH regulators Na2CO33333g/t, suppression
Preparation acidified sodium silicate(pH=2-3)2333g/t, collecting agent saponified fat acid (C16-C18) 1333g/t, flotation time 5 minutes,
Obtain rough concentrate K.After one roughing, collecting agent saponified fat acid (C is added16-C18) 400g/t, flotation time 3 minutes, obtain
K and mine tailing X are swept to scavenger concentrate.
Embodiment 1
The preparation of Mixed Pharmacy I:According to the step of comparative example 1(2)Middle roughing pH regulators Na2CO3With roughing collecting agent saponification fat
Fat acid (C16-C18) mass ratio be 3333:1333 ratio, by pH regulators Na2CO3With roughing collecting agent saponified fat acid point
Do not weigh, be then configured in same container in proportion, obtain mixture-Mixed Pharmacy I of pH regulators and collecting agent.
The preparation of Mixed Pharmacy II:Roughing collector dosage is reduced to 800g/t:Caught according to roughing pH regulators with roughing
Receive agent saponified fat acid (C16-C18) mass ratio be 3333:800 ratio, by pH regulators and roughing collecting agent saponified fat
Acid weighs in proportion respectively, is then configured in same container, obtains mixture-Mixed Pharmacy of pH regulators and collecting agent
Ⅱ。
Scheme one:By phosphorus ore(Containing P2O518.32 wt%), it is milled to 400 mesh(-0.038mm)60wt% is accounted for below;To mill
Broken raw ore carries out one roughing once purging selection, and one roughing adds inhibitor acidified sodium silicate(pH=2-3)2333g/t, mixture
The 1333g/t of medicament I(Calculated according to collector dosage), flotation time 5 minutes, obtain rough concentrate K.After one roughing, add
Collecting agent saponified fat acid (C16-C18) 400g/t, flotation time 3 minutes, obtain scavenger concentrate and sweep K and mine tailing X.
Scheme two:Mixed Pharmacy I is changed to Mixed Pharmacy II, the step of iteration scheme one.Result of implementation such as following table.
Table 1
It is total:“P2O5Grade " column " total " refers to that each product returns calculation head grade by weighted average, to show that raw ore has generation
Table.It is as follows.
As seen from Table 1, saponified fat acid (C in Mixed Pharmacy II16-C18) dosage substantially reduces, and is reducing collecting
Under conditions of agent, gained P2O5Grade and P2O5The rate of recovery can't reduce.
Comparative example 2
This comparative example comprises the following steps:
(1)By phosphorus ore(Containing P2O522.57 wt%), it is milled to -200 mesh(-0.075mm)67.63 wt% are accounted for below;
(2)One roughing once purging selection is carried out to the raw ore ground, one roughing adds pH regulators Na2CO33333g/t, suppression
Preparation acidified sodium silicate(pH=2-3)1066g/t, collecting agent saponification oleic acid 1333g/t, flotation time 5 minutes, obtains rough concentrate
K.After one roughing, collecting agent saponification oleic acid 300g/t is added, flotation time 3 minutes, scavenger concentrate is obtained and sweeps K and mine tailing X.
Embodiment 1
The preparation of Mixed Pharmacy I:According to the step of comparative example 2(2)The ratio of middle roughing pH regulators and roughing collecting agent saponification oleic acid
Example 3333:1333, pH regulators and roughing collecting agent saponification oleic acid are weighed in proportion respectively, are then configured at same container
It is interior, obtain Mixed Pharmacy I.
The preparation of Mixed Pharmacy II:Roughing collector dosage is reduced to 800g/t:Caught according to roughing pH regulators with roughing
Receive the mass ratio 3333 of agent saponification oleic acid:800, pH regulators and roughing collecting agent saponification oleic acid are weighed in proportion respectively, so
After be configured in same container, obtain Mixed Pharmacy II;
Scheme one:By phosphorus ore(Containing P2O522.57wt%), it is milled to -200 mesh(-0.038mm)67.63wt% is accounted for below;To mill
Broken raw ore carries out one roughing once purging selection, and one roughing adds inhibitor acidified sodium silicate(pH=2-3)1066g/t, mixture
The 1333g/t of medicament I(Calculated according to collector dosage), flotation time 5 minutes, obtain rough concentrate K.After one roughing, add
Collecting agent saponification oleic acid 300g/t, flotation time 3 minutes, obtains scavenger concentrate and sweeps K and mine tailing X.
Scheme two:Mixed Pharmacy I is changed to Mixed Pharmacy II, the step of iteration scheme one.Result of implementation such as following table.
Table 2
It is total:“P2O5Grade " column " total " refers to that each product returns calculation head grade by weighted average, to show that raw ore has generation
Table.
Saponification oleic acid dosage significantly reduces in Mixed Pharmacy II.
Comparative example 3
This comparative example comprises the following steps:
(1)By phosphorus ore(Containing P2O524.98wt%), it is milled to -200 mesh(-0.075mm)65.77 wt% are accounted for below;
(2)One roughing once purging selection is carried out to the raw ore ground, one roughing adds pH regulators Na2CO33333g/t, suppression
Preparation acidified sodium silicate(pH=2-3)1333g/t, collecting agent saponified fat acid (C16-C18) 1667g/t, flotation time 5 minutes,
Obtain rough concentrate K.After one roughing, collecting agent saponified fat acid (C is added16-C18) 300g/t, flotation time 3 minutes, obtain
K and mine tailing X are swept to scavenger concentrate.
Embodiment 3
The preparation of Mixed Pharmacy I:According to the step of comparative example 3(2)Middle roughing pH regulators and roughing collecting agent saponified fat acid
(C16-C18) mass ratio 3333:1667, pH regulators and roughing collecting agent saponified fat acid are weighed in proportion respectively, then
It is configured in same container, obtains Mixed Pharmacy I.
The preparation of Mixed Pharmacy II:Roughing collector dosage is reduced to 1000g/t:Caught according to roughing pH regulators with roughing
Receive agent saponified fat acid (C16-C18) mass ratio 3333:1000, pH regulators and roughing collecting agent saponified fat acid are distinguished
Weigh, be then configured in same container in proportion, obtain Mixed Pharmacy II.
Scheme one:By phosphorus ore(Containing P2O524.98wt%), it is milled to -200 mesh(-0.075mm)65.77wt% is accounted for below;
One roughing once purging selection is carried out to the raw ore ground, one roughing adds inhibitor acidified sodium silicate(pH=2-3)1333g/t,
The 1667g/t of Mixed Pharmacy I(Calculated according to collector dosage), flotation time 5 minutes, obtain rough concentrate K.After one roughing, then
Add collecting agent saponified fat acid (C16-C18) 300g/t, flotation time 3 minutes, obtain scavenger concentrate and sweep K and mine tailing X.
Scheme two:Mixed Pharmacy I is changed to Mixed Pharmacy II, the step of iteration scheme one.Result of implementation such as following table.Mixture
Saponified fat acid (C in medicament II16-C18) dosage significantly reduces.
Table 3
Claims (7)
1. a kind of regime of agent of phosphorus ore direct flotation roughing, it is characterised in that first pH regulators and collecting agent are mixed, obtain pH tune
Whole dose and the mixture of collecting agent;In phosphorus ore direct flotation rougher process, inhibitor is first added, then adds pH regulators and collecting
The mixture of agent.
2. the regime of agent of phosphorus ore direct flotation roughing according to claim 1, it is characterised in that including herein below:
(1)Determine additive amount of medicament:According to the normal medicament order of addition of phosphorus ore direct flotation roughing, i.e., first add pH regulators, so
Inhibitor is added afterwards, is eventually adding the order of collecting agent, and the addition of three kinds of medicaments is found out by condition test;
(2)Medicament configuration:Weigh pH regulators and collecting agent, then mix pH regulators and collecting agent, obtain pH regulators and
The mixture of collecting agent;
(3)Medicament addition manner:Inhibitor is first added in phosphorus ore direct flotation rougher process, then adds step(2)Middle configuration
The mixture of pH regulators and collecting agent.
3. the regime of agent of phosphorus ore direct flotation roughing according to claim 1 or 2, it is characterised in that the pH regulators
For Na2CO3, at least one of NaOH.
4. the regime of agent of phosphorus ore direct flotation roughing according to claim 1 or 2, it is characterised in that the inhibitor is
At least one of waterglass, acidified sodium silicate, starch.
5. the regime of agent of phosphorus ore direct flotation roughing according to claim 1 or 2, it is characterised in that the collecting agent is
Oleic acid, aliphatic acid, modified fat acid, saponification oleic acid, saponified fat acid, modified fat acid are at least one of saponified.
6. the regime of agent of phosphorus ore direct flotation roughing according to claim 1 or 2, it is characterised in that the acidifying water glass
The preparation method of glass:Water glass solution pH is adjusted to 2-4 with sulfuric acid, hydrochloric acid or nitric acid etc., produced.
7. the regime of agent of phosphorus ore direct flotation roughing according to claim 1 or 2, it is characterised in that the modified fat
Acid is product of the aliphatic acid after organic reaction, and the organic reaction includes substitution reaction, addition reaction, elimination reaction, oxygen
Change at least one of reduction reaction, esterification.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710823151.0A CN107497606A (en) | 2017-09-13 | 2017-09-13 | A kind of regime of agent of phosphorus ore direct flotation roughing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710823151.0A CN107497606A (en) | 2017-09-13 | 2017-09-13 | A kind of regime of agent of phosphorus ore direct flotation roughing |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107497606A true CN107497606A (en) | 2017-12-22 |
Family
ID=60695392
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710823151.0A Pending CN107497606A (en) | 2017-09-13 | 2017-09-13 | A kind of regime of agent of phosphorus ore direct flotation roughing |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107497606A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111036410A (en) * | 2019-11-27 | 2020-04-21 | 东北大学 | Method for removing magnesium from phosphate ore by flotation through chelating inhibitor PBTCA |
CN111451001A (en) * | 2020-03-10 | 2020-07-28 | 中国地质科学院矿产综合利用研究所 | Medium-low grade mixed collophanite flotation separation reagent system and application thereof |
CN113117882A (en) * | 2019-12-30 | 2021-07-16 | 有研资源环境技术研究院(北京)有限公司 | Pre-flotation method for low-grade phosphorite in high sesquioxide |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104043535A (en) * | 2014-06-28 | 2014-09-17 | 中蓝连海设计研究院 | Phosphorite obverse and reverse flotation method without sodium carbonate in whole process |
CN104624379A (en) * | 2014-12-29 | 2015-05-20 | 中蓝连海设计研究院 | Obverse and reverse flotation method of low-grade silica-calcia bearing collophane |
CN104801427A (en) * | 2015-05-11 | 2015-07-29 | 中蓝连海设计研究院 | Direct and reverse flotation technique for high-magnesium low-grade phosphorus ore coarse grains |
CN104907183A (en) * | 2015-07-03 | 2015-09-16 | 武汉工程大学 | Silica-calcia low-grade collophanite positive and inverse floatation process |
CA2849653A1 (en) * | 2014-04-23 | 2015-10-23 | Richard A. Pilon | Organics removal from sedimentary phosphate ore |
-
2017
- 2017-09-13 CN CN201710823151.0A patent/CN107497606A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2849653A1 (en) * | 2014-04-23 | 2015-10-23 | Richard A. Pilon | Organics removal from sedimentary phosphate ore |
CN104043535A (en) * | 2014-06-28 | 2014-09-17 | 中蓝连海设计研究院 | Phosphorite obverse and reverse flotation method without sodium carbonate in whole process |
CN104624379A (en) * | 2014-12-29 | 2015-05-20 | 中蓝连海设计研究院 | Obverse and reverse flotation method of low-grade silica-calcia bearing collophane |
CN104801427A (en) * | 2015-05-11 | 2015-07-29 | 中蓝连海设计研究院 | Direct and reverse flotation technique for high-magnesium low-grade phosphorus ore coarse grains |
CN104907183A (en) * | 2015-07-03 | 2015-09-16 | 武汉工程大学 | Silica-calcia low-grade collophanite positive and inverse floatation process |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111036410A (en) * | 2019-11-27 | 2020-04-21 | 东北大学 | Method for removing magnesium from phosphate ore by flotation through chelating inhibitor PBTCA |
CN111036410B (en) * | 2019-11-27 | 2021-03-23 | 东北大学 | Method for removing magnesium from phosphate ore by flotation through chelating inhibitor PBTCA |
CN113117882A (en) * | 2019-12-30 | 2021-07-16 | 有研资源环境技术研究院(北京)有限公司 | Pre-flotation method for low-grade phosphorite in high sesquioxide |
CN113117882B (en) * | 2019-12-30 | 2022-11-04 | 有研资源环境技术研究院(北京)有限公司 | Pre-flotation method for low-grade phosphorite in high sesquioxide |
CN111451001A (en) * | 2020-03-10 | 2020-07-28 | 中国地质科学院矿产综合利用研究所 | Medium-low grade mixed collophanite flotation separation reagent system and application thereof |
CN111451001B (en) * | 2020-03-10 | 2021-05-11 | 中国地质科学院矿产综合利用研究所 | Medium-low grade mixed collophanite flotation separation reagent system and application thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104084315B (en) | Beneficiation method for separating fluorite and tungsten through flotation | |
CN105435953B (en) | Beneficiation method for molybdenum-containing low-grade mixed copper ore | |
CN101844110B (en) | Sulfide ore flotation layered silicate mineral inhibitor | |
CN100500299C (en) | Phosphate rock floating process | |
CN107497606A (en) | A kind of regime of agent of phosphorus ore direct flotation roughing | |
CN103331212B (en) | Carbonate phosphorite reverse flotation collecting agent and preparation method thereof | |
CN110369152B (en) | Flotation process for micro-fine particle phosphorite | |
CN102513221A (en) | Carbonate phosphorite reverse flotation combined collecting agent and preparation method thereof | |
CN109821661A (en) | A kind of low alkali of high sulfur-lead-zinc ore is without sulfuric acid floatation process | |
CN105597946A (en) | Comprehensive recovery method for tungsten accompanying fluorite resources | |
CN109453891A (en) | A kind of high sesquialter collophane spiral chute floats process integration again | |
CN103691567A (en) | Flotation separation method of fluorite and dolomite in acidic conditions | |
CN105880007B (en) | A kind of separation method of tennantite and galena | |
CN105013616A (en) | Method for separating molybdenum concentrate and lead-sulfur concentrate from molybdenum-lead-sulfur mixed concentrate | |
CN110653075A (en) | Flotation method for copper minerals in seawater medium | |
CN108456153A (en) | Cinnamyl group hydroximic acid and preparation method thereof and the application in floatation of tungsten mineral | |
CN107309075A (en) | Collophane beneficiation method | |
CN103157558A (en) | Beneficiation method of recovering sulfur from copper sulfide ore flotation tailings | |
CN102744159B (en) | A kind of method for floating improving copper sulfide ore mineral processing index | |
CN101972711B (en) | Flotation process for charcoal clay-containing pyrite | |
CN101844106B (en) | Combined and staged separation method for weathered phosphoric ore | |
CN102205269A (en) | Concentration method of molybdenum-tungsten oxide mixed rough concentrate | |
CN103464289B (en) | A kind of method that low-grade phosphate ore mesosilicic acid slaine is deviate from | |
CN115957894A (en) | Phosphogypsum whitening and purifying process | |
CN108714484A (en) | A kind of method for floating of high carbonaceous copper cobalt sulfide ore |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20171222 |