CN111940146A - Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof - Google Patents
Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof Download PDFInfo
- Publication number
- CN111940146A CN111940146A CN202010792050.3A CN202010792050A CN111940146A CN 111940146 A CN111940146 A CN 111940146A CN 202010792050 A CN202010792050 A CN 202010792050A CN 111940146 A CN111940146 A CN 111940146A
- Authority
- CN
- China
- Prior art keywords
- composite
- zinc oxide
- sodium
- temperature
- flotation
- 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.)
- Granted
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 title claims abstract description 123
- 239000002131 composite material Substances 0.000 title claims abstract description 75
- 239000011787 zinc oxide Substances 0.000 title claims abstract description 66
- 238000005188 flotation Methods 0.000 title claims abstract description 47
- 239000003153 chemical reaction reagent Substances 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 36
- 238000000034 method Methods 0.000 claims abstract description 25
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 24
- 239000011734 sodium Substances 0.000 claims abstract description 24
- 235000015424 sodium Nutrition 0.000 claims abstract description 24
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 24
- 238000002156 mixing Methods 0.000 claims abstract description 22
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229960000583 acetic acid Drugs 0.000 claims abstract description 18
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 18
- 239000012362 glacial acetic acid Substances 0.000 claims abstract description 18
- 230000008569 process Effects 0.000 claims abstract description 15
- 239000010705 motor oil Substances 0.000 claims abstract description 13
- 239000002699 waste material Substances 0.000 claims abstract description 13
- 229920002472 Starch Polymers 0.000 claims abstract description 11
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims abstract description 11
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims abstract description 11
- 235000019698 starch Nutrition 0.000 claims abstract description 11
- 239000008107 starch Substances 0.000 claims abstract description 11
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims abstract description 11
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- 229910052979 sodium sulfide Inorganic materials 0.000 claims description 10
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 claims description 10
- 230000003213 activating effect Effects 0.000 claims description 8
- 239000012141 concentrate Substances 0.000 claims description 8
- 238000000227 grinding Methods 0.000 claims description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- 230000001804 emulsifying effect Effects 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 230000035484 reaction time Effects 0.000 claims description 5
- JQJCSZOEVBFDKO-UHFFFAOYSA-N lead zinc Chemical group [Zn].[Pb] JQJCSZOEVBFDKO-UHFFFAOYSA-N 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 2
- 239000003607 modifier Substances 0.000 claims 3
- 238000004090 dissolution Methods 0.000 claims 1
- 238000011084 recovery Methods 0.000 abstract description 12
- 235000014692 zinc oxide Nutrition 0.000 description 52
- 239000011701 zinc Substances 0.000 description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 9
- 229910052725 zinc Inorganic materials 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000007667 floating Methods 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 229940105847 calamine Drugs 0.000 description 3
- 229910052864 hemimorphite Inorganic materials 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000002000 scavenging effect Effects 0.000 description 3
- CPYIZQLXMGRKSW-UHFFFAOYSA-N zinc;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+3].[Fe+3].[Zn+2] CPYIZQLXMGRKSW-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910001425 magnesium ion Inorganic materials 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229910001656 zinc mineral Inorganic materials 0.000 description 1
Images
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
- 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
- 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
- B03D1/001—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
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/018—Mixtures of inorganic and organic 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
- B03D1/02—Froth-flotation processes
-
- 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
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
The invention relates to a low-temperature-resistant zinc oxide ore flotation composite reagent and a preparation method and application thereof, wherein the composite reagent comprises a composite regulator and a composite collecting agent, wherein the composite regulator is prepared from sodium hexametaphosphate, starch and sodium humate in a weight ratio of (5-7: 3-6): 1-3, mixing; the composite collecting agent is formed by mixing octadecylamine, glacial acetic acid, sodium benzyloxyhydroxamate and waste engine oil according to the weight ratio of 5-8: 1-3. The two composite beneficiation reagents are used, desliming is not needed in the flotation process, so that the recovery of fine-fraction zinc oxide is enhanced, and the beneficiation recovery rate of zinc oxide ores can be improved by 5-15%.
Description
Technical Field
The invention relates to the field of mineral processing and comprehensive utilization of mineral resource ores, in particular to a low-temperature-resistant zinc oxide ore flotation composite agent and a preparation method and application thereof.
Background
Zinc oxide is negatively affected by the high slime content and soluble calcium and magnesium ions. In the traditional desliming flotation process of zinc oxide ores, the desliming amount is very difficult to accurately control, the production is extremely unstable, the interference of slime on the zinc oxide flotation cannot be thoroughly eliminated, in addition, part of zinc oxide minerals are removed during desliming, the problems of low zinc oxide recovery rate, poor sorting index and the like are caused, in addition, the traditional beneficiation reagent needs higher operation temperature, the general temperature requirement is higher than 25 ℃, and the flotation operation cannot be carried out in areas with lower temperature or in winter (such as high-altitude mining areas in Yunnan).
Based on the defects of the traditional zinc oxide desliming flotation method, poor low-temperature flotation effect and the like, how to reduce desliming procedures by changing a flotation reagent system on the premise of basically not changing the existing flotation process effectively saves factory building investment and reduces production operation cost, improves the recovery rate of zinc oxide, ensures that the production process is easy to adjust and control, has stable production indexes, and is a problem which needs to be solved urgently at present.
Disclosure of Invention
In order to solve the technical problems, the invention provides a low-temperature-resistant zinc oxide ore flotation composite reagent, and a preparation method and application thereof, which can improve the recovery rate of zinc oxide ore.
The technical scheme of the invention is as follows:
the low-temperature-resistant zinc oxide ore flotation composite reagent comprises a composite regulator and a composite collecting agent, wherein the composite regulator is prepared from sodium hexametaphosphate, starch and sodium humate in a weight ratio of 5-7: 3-6: 1-3, mixing; the composite collecting agent is formed by mixing octadecylamine, glacial acetic acid, sodium benzyloxyhydroxamate and waste engine oil according to the weight ratio of 5-8: 1-3.
Further, the following is performed:
mixing sodium hexametaphosphate, starch and sodium humate according to the weight ratio of 5-7: 3-6: 1-3, stirring for about 10 minutes in a high-speed stirrer, wherein the high speed means that the rotating speed is more than 2000 revolutions per minute, and taking out the mixture to be the composite regulator;
heating 5-8 parts of octadecylamine and 5-8 parts of glacial acetic acid according to the weight ratio until the octadecylamine and the glacial acetic acid are dissolved; then adding 1-3 parts of waste engine oil into the dissolved solution, and ultrasonically stirring and emulsifying; and then adding 1-3 parts of sodium benzyloxyhydroxamate, reacting for 20 minutes, and cooling to normal temperature to obtain the composite collector.
Further, the octadecylamine and the glacial acetic acid are heated to 80-90 ℃ to be dissolved.
Further, the mixture was emulsified by ultrasonic agitation for about 5 minutes.
Further, sodium benzyloxymate was added to the reaction mixture to react for about 30 minutes.
The application of the low-temperature-resistant zinc oxide ore flotation composite reagent comprises the following steps:
grinding raw ore to-0.074 mm, wherein the ore pulp accounts for 75-95%, controlling the concentration of the ore pulp to be about 25%, and adding 100-800 g/t of a composite regulator at an overflow port of a grader, namely adding 800g of a medicament of one ton of ore, so that the composite regulator and the ore pulp fully react;
after the step (2) and the overflow process, adding an activating agent into the pulp mixing barrel to ensure that the reaction time of the activating agent in the ore pulp exceeds 5 minutes;
and (3) after the slurry mixing procedure, adding 200 g/t of composite collecting agent into the first roughing tank of the flotation machine for primary roughing, and carrying out two-time concentration on the obtained roughing product to obtain the qualified zinc oxide concentrate product.
Further, the activating agents are sodium sulfide and sodium carbonate, and the addition amount is 3000-6000g/t of sodium sulfide and 500-1500g/t of sodium carbonate.
Further, the raw ore is lead zinc oxide ore flotation tailings or zinc oxide ore.
A certain amount of waste engine oil is added, stirred and emulsified for 5 minutes by ultrasonic wave, so that the waste engine oil is fully dispersed and floated, and the problems of floating foam running out of a groove, difficult flowing of floating ore pulp and the like caused by foam stickiness in the flotation process can be effectively reduced.
Compared with the prior art, the invention has the following beneficial effects:
(1) the composite regulator and the composite collecting agent of the invention act together synergistically, the two kinds of zinc oxide ore flotation agents are the first kind of composite regulator which is gangue mineral inhibitor, fine mud zinc oxide aggregate and unavoidable ion remover, and Ca in ore pulp is removed in the composite regulator2+、Mg2+The zinc oxide fine particles are selectively agglomerated by the unavoidable ions to form a new carrier, so that the zinc oxide fine particles can more easily act with a collecting agent, and the floating of the fine zinc oxide particles is increased; the second one is low temperature resistant zinc oxide composite collector, under the action of the composite collector, different kinds of beneficiation reagent generate synergistic effect, the low temperature flotation environment of zinc oxide is improved, the composite collector can be used at a low temperature of about 5 ℃, the floating of fine-grained zinc oxide ore is increased, the recovery rate of zinc flotation is improved, and meanwhile, the cost of the beneficiation reagent is reduced by 1/3.
(2) The composite reagent is added at a proper position, desliming is not needed in the process, the recovery of fine-grained zinc oxide is enhanced, the beneficiation recovery rate of zinc oxide ores is improved, the process is easy to adjust and control in the flotation process, flotation is not affected in a low-temperature environment, the indexes are stable, and the like, and the composite reagent is suitable for the beneficiation of various refractory zinc oxide ores.
(3) The invention reduces desliming process by changing the flotation reagent system on the premise of basically not changing the prior flotation process, can effectively save factory building investment and reduce production and operation cost, can also improve the recovery rate of zinc oxide, and has the advantages of easy adjustment and control of production process and stable production index.
Drawings
FIG. 1 is a schematic process flow diagram of zinc oxide flotation using the low temperature resistant zinc oxide ore flotation composite reagent of the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail with reference to the following embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention. The examples do not specify particular techniques or conditions, and are performed according to the techniques or conditions described in the literature in the art or according to the product specifications. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available by purchase.
Example 1
The low-temperature-resistant zinc oxide ore flotation composite reagent comprises a composite regulator and a composite collector, wherein the composite regulator is formed by mixing sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 5:3: 1; the composite collector is formed by mixing octadecylamine, glacial acetic acid, sodium benzoxyoxime and waste engine oil according to the weight ratio of 8:5:2: 1.
The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent of the embodiment is carried out as follows:
mixing sodium hexametaphosphate, starch and sodium humate according to the weight ratio of 5:3:1, stirring for 10 minutes in a high-speed stirrer, and taking out a mixture which is a composite regulator and is marked as KYS-1.
Heating 8 parts of octadecylamine and 5 parts of glacial acetic acid according to the weight ratio until the octadecylamine and the glacial acetic acid are dissolved; then adding 2 parts of waste engine oil into the dissolved solution, and ultrasonically stirring and emulsifying; and then adding 1 part of sodium benzyloxyhydroxamate, reacting, and cooling to normal temperature to obtain the composite collector which is marked as KYS-2.
The application of the low-temperature-resistant zinc oxide ore flotation composite reagent comprises the following steps:
the method comprises the following steps of (1) aiming at a certain zinc oxide ore in Yunnan, wherein main zinc oxide is heteropolar ore, a small amount of calamine is selected from Zn13.14%, the zinc oxidation rate is 90.14%, the ore grinding fineness is 75% when the ore grinding fineness is-0.074 mm, the raw ore grinding is 75% when the ore grinding fineness is-0.074 mm, the ore pulp concentration is controlled to be 25%, 1000g/t of sodium carbonate and 250 g/t of KYS-1 are added to an overflow port of a classifier, and the KYS-1 and the ore pulp are made to fully react.
And (2) adding 4000 g/t of activator sodium sulfide into the stirring barrel, wherein the reaction time of the sodium sulfide in the ore pulp is ensured to exceed 5 minutes.
And (3) adding 350g/t KYS-2 into a first roughing tank of a flotation machine, performing primary roughing, and performing two times of fine concentration, two times of scavenging and middling recleaning on a roughed product obtained by a conventional process to obtain a qualified zinc oxide concentrate product as shown in figure 1.
The obtained zinc oxide concentrate Zn is 39.16 percent, and the zinc recovery rate is 88.43 percent.
Example 2
The low-temperature-resistant zinc oxide ore flotation composite reagent comprises a composite regulator and a composite collector, wherein the composite regulator is formed by mixing sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 6: 6: 3; the composite collector is formed by mixing octadecylamine, glacial acetic acid, sodium benzoxyoxime and waste engine oil according to the weight ratio of 8: 8:2: 2.
The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent of the embodiment is carried out as follows:
mixing sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 6:3, mixing, stirring for 10 minutes in a high-speed stirrer, and taking out a mixture which is a composite regulator and is marked as KYS-1.
Heating 8 parts of octadecylamine and 8 parts of glacial acetic acid according to the weight ratio until the octadecylamine and the glacial acetic acid are dissolved; then adding 2 parts of waste engine oil into the dissolved solution, and ultrasonically stirring and emulsifying; and then adding 2 parts of sodium benzyloxyhydroxamate, reacting, and cooling to normal temperature to obtain the composite collector which is marked as KYS-2.
The application of the low-temperature-resistant zinc oxide ore flotation composite reagent comprises the following steps:
aiming at certain lead-zinc oxide ore flotation tailings in Zhaotong of Yunnan, the main zinc minerals in the tailings are calamine and a small amount of hemimorphous ore, the zinc selection grade Zn is 4.92%, the zinc oxidation rate is 96.42%, the grinding fineness is-0.074 mm and accounts for 85%, the concentration of ore pulp is controlled to be 25%, and 500g/t and 300g/t of sodium carbonate KYS-1 are added at an overflow port of a classifier, so that the KYS-1 and the ore pulp fully react.
And (2) adding 5000g/t of activating agent sodium sulfide into the stirring barrel, wherein the reaction time of the sodium sulfide in the ore pulp is ensured to exceed 5 minutes.
And (3) adding 400g/t KYS-2 into a first roughing tank of a flotation machine, performing primary roughing, and performing two times of fine concentration, two times of scavenging and middling recleaning on a roughed product obtained by a conventional process to obtain a qualified zinc oxide concentrate product as shown in figure 1.
The obtained zinc oxide concentrate Zn is 31.33 percent, and the zinc recovery rate is 76.42 percent.
Example 3
The low-temperature-resistant zinc oxide ore flotation composite reagent comprises a composite regulator and a composite collector, wherein the composite regulator is formed by mixing sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 7:6: 3; the composite collector is formed by mixing octadecylamine, glacial acetic acid, sodium benzoxyoxime and waste engine oil according to the weight ratio of 5:5:1: 1.
The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent of the embodiment is carried out as follows:
mixing sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 7:6:3, stirring for 10 minutes in a high-speed stirrer, and taking out a mixture which is a composite regulator and is marked as KYS-1.
Heating 5 parts of octadecylamine and 5 parts of glacial acetic acid according to the weight ratio until the octadecylamine and the glacial acetic acid are dissolved; then adding 1 part of waste engine oil into the dissolved solution, and ultrasonically stirring and emulsifying; and then adding 1 part of sodium benzyloxyhydroxamate, reacting, and cooling to normal temperature to obtain the composite collector which is marked as KYS-2.
The application of the low-temperature-resistant zinc oxide ore flotation composite reagent comprises the following steps:
the method comprises the steps of (1) aiming at some old zinc oxide ores in Yunnan, wherein zinc mainly is calamine and contains a large amount of iron sludge, the selected grade Zn is 8.92%, the zinc oxidation rate is 93.33%, the ore grinding fineness is 85% when the zinc oxide ores are ground to be 0.074mm, the concentration of ore pulp is controlled to be 25, and 1500g/t of sodium carbonate and 500g/t of KYS-1 are added to an overflow port of a classifier, so that the KYS-1 and the ore pulp are fully reacted.
And (2) adding 4500g/t of activating agent sodium sulfide into the stirring barrel, wherein the reaction time of the sodium sulfide in the ore pulp is ensured to exceed 5 minutes.
And (3) adding 550g/t KYS-2 into a first roughing tank of a flotation machine, performing primary roughing, and performing two times of fine concentration, two times of scavenging and middling recleaning on a roughed product obtained by a conventional process to obtain a qualified zinc oxide concentrate product as shown in figure 1.
The zinc oxide concentrate Zn obtained is 25.64 percent, and the zinc recovery rate is 81.43 percent.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.
Claims (8)
1. The low-temperature-resistant zinc oxide ore flotation composite reagent is characterized in that: the composite modifier comprises a composite modifier and a composite collector, wherein the composite modifier is prepared from sodium hexametaphosphate, starch and sodium humate according to a weight ratio of 5-7: 3-6: 1-3, mixing; the composite collecting agent is formed by mixing octadecylamine, glacial acetic acid, sodium benzyloxyhydroxamate and waste engine oil according to the weight ratio of 5-8: 1-3.
2. The preparation method of the low temperature resistant zinc oxide ore flotation composite reagent according to claim 1, characterized in that: the method comprises the following steps:
mixing sodium hexametaphosphate, starch and sodium humate according to the weight ratio of 5-7: 3-6: 1-3, stirring for about 10 minutes in a high-speed stirrer, wherein the high speed means that the rotating speed is more than 2000 revolutions per minute, and taking out the mixture to be the composite regulator;
heating 5-8 parts of octadecylamine and 5-8 parts of glacial acetic acid according to the weight ratio until the octadecylamine and the glacial acetic acid are dissolved; then adding 1-3 parts of waste engine oil into the dissolved solution, and ultrasonically stirring and emulsifying; and then adding 1-3 parts of sodium benzyloxyhydroxamate, reacting for 20 minutes, and cooling to normal temperature to obtain the composite collector.
3. The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent according to claim 2, characterized by comprising the following steps: heating octadecylamine and glacial acetic acid to 80-90 ℃ for dissolution.
4. The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent according to claim 2, characterized by comprising the following steps: ultrasonic stirring and emulsifying for about 5 minutes.
5. The preparation method of the low-temperature-resistant zinc oxide ore flotation composite reagent according to claim 2, characterized by comprising the following steps: adding sodium benzyloxymate to react for about 30 minutes.
6. Use of the low temperature resistant zinc oxide ore flotation composite reagent according to any one of claims 1 to 5, characterized in that: the method comprises the following steps:
grinding raw ore to-0.074 mm, wherein the ore pulp accounts for 75-95%, controlling the concentration of the ore pulp to be about 25%, and adding 100-800 g/t of a composite regulator into an overflow port of a classifier to enable the composite regulator to fully react with the ore pulp;
after the step (2) and the overflow process, adding an activating agent into the pulp mixing barrel to ensure that the reaction time of the activating agent in the ore pulp exceeds 5 minutes;
and (3) after the slurry mixing procedure, adding 200 g/t of composite collecting agent into the first rough concentration tank of the flotation machine, performing primary rough concentration, and performing two times of fine concentration on the obtained rough concentration product to obtain the qualified zinc oxide concentrate product.
7. Use according to claim 6, characterized in that: the activating agents are sodium sulfide and sodium carbonate, and the addition amount is 3000-6000g/t of sodium sulfide and 500-1500g/t of sodium carbonate.
8. Use according to claim 6, characterized in that: the raw ore is lead zinc oxide ore flotation tailings or zinc oxide ore.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202010792050.3A CN111940146B (en) | 2020-08-08 | 2020-08-08 | Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202010792050.3A CN111940146B (en) | 2020-08-08 | 2020-08-08 | Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN111940146A true CN111940146A (en) | 2020-11-17 |
| CN111940146B CN111940146B (en) | 2022-07-12 |
Family
ID=73332938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202010792050.3A Active CN111940146B (en) | 2020-08-08 | 2020-08-08 | Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN111940146B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116116568A (en) * | 2023-01-10 | 2023-05-16 | 保山金厂河矿业有限公司 | Beneficiation method for efficiently recycling valuable components from low-grade zinc oxide ores |
| CN116899742A (en) * | 2023-08-08 | 2023-10-20 | 昆明理工大学 | A foam controlled flotation method for fine-grained zinc oxide ore |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4253614A (en) * | 1979-07-05 | 1981-03-03 | The New Jersey Zinc Company | Flotation of non-sulfide zinc materials |
| CN102489412A (en) * | 2011-12-26 | 2012-06-13 | 昆明理工大学 | Method for activating calamine in flotation process |
| CN102974446A (en) * | 2012-12-11 | 2013-03-20 | 中国地质科学院矿产综合利用研究所 | Oolitic hematite dressing method |
| CN103071596A (en) * | 2013-01-22 | 2013-05-01 | 昆明理工大学 | Method for recycling fine and superfine cassiterites from oxidized lode tin mud tailings |
| CN103240167A (en) * | 2013-04-27 | 2013-08-14 | 昆明冶金研究院 | Lead and zinc separating method for high-oxidation-rate low-grade lead-zinc oxide ores |
| CN105689150A (en) * | 2016-04-15 | 2016-06-22 | 中南大学 | Lead-zinc oxide ore flotation inhibitor and application thereof |
| CN109482352A (en) * | 2018-09-28 | 2019-03-19 | 昆明理工大学 | A kind of irony zinc oxide ore beneficiation method of sulfuric acid preactivating |
-
2020
- 2020-08-08 CN CN202010792050.3A patent/CN111940146B/en active Active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4253614A (en) * | 1979-07-05 | 1981-03-03 | The New Jersey Zinc Company | Flotation of non-sulfide zinc materials |
| CN102489412A (en) * | 2011-12-26 | 2012-06-13 | 昆明理工大学 | Method for activating calamine in flotation process |
| CN102974446A (en) * | 2012-12-11 | 2013-03-20 | 中国地质科学院矿产综合利用研究所 | Oolitic hematite dressing method |
| CN103071596A (en) * | 2013-01-22 | 2013-05-01 | 昆明理工大学 | Method for recycling fine and superfine cassiterites from oxidized lode tin mud tailings |
| CN103240167A (en) * | 2013-04-27 | 2013-08-14 | 昆明冶金研究院 | Lead and zinc separating method for high-oxidation-rate low-grade lead-zinc oxide ores |
| CN105689150A (en) * | 2016-04-15 | 2016-06-22 | 中南大学 | Lead-zinc oxide ore flotation inhibitor and application thereof |
| CN109482352A (en) * | 2018-09-28 | 2019-03-19 | 昆明理工大学 | A kind of irony zinc oxide ore beneficiation method of sulfuric acid preactivating |
Non-Patent Citations (2)
| Title |
|---|
| 朱玉霜,朱建光: "《浮选药剂的化学原理 修订版》", 31 December 1996, 长沙:中南工业大学出版社 * |
| 龚明光: "《浮选技术问答》", 31 October 2012, 北京:冶金工业出版社 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116116568A (en) * | 2023-01-10 | 2023-05-16 | 保山金厂河矿业有限公司 | Beneficiation method for efficiently recycling valuable components from low-grade zinc oxide ores |
| CN116116568B (en) * | 2023-01-10 | 2023-08-18 | 保山金厂河矿业有限公司 | Beneficiation method for efficiently recycling valuable components from low-grade zinc oxide ores |
| CN116899742A (en) * | 2023-08-08 | 2023-10-20 | 昆明理工大学 | A foam controlled flotation method for fine-grained zinc oxide ore |
Also Published As
| Publication number | Publication date |
|---|---|
| CN111940146B (en) | 2022-07-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104084315B (en) | Beneficiation method for separating fluorite and tungsten through flotation | |
| CN110976097B (en) | Flotation method for zinc oxide in sulfide ore tailings | |
| CN106179761B (en) | Beneficiation method for zinc oxide ore | |
| CN109701736B (en) | Complex ore dressing process containing magnetite and pyrrhotite | |
| CN113680534B (en) | Fine iron mineral collector and method for asynchronous flotation of coarse and fine iron ore containing carbonate | |
| CN111330741A (en) | A kind of simultaneous flotation method of oxidation-sulfide mixed zinc ore | |
| CN1285416C (en) | Flotation method for mixed lead-zinc sulfide-oxide ores | |
| CN111940146B (en) | Low-temperature-resistant zinc oxide ore flotation composite reagent and preparation method and application thereof | |
| CN116586196A (en) | Flotation method of cobalt oxide copper ore | |
| CN113976331B (en) | Method for preparing high-purity pyrite through flotation mass transfer dynamics regulation and control | |
| LU505782B1 (en) | Efficient flotation method for talc-type secondary copper-molybdenum mixed concentrate | |
| CN116727110B (en) | Preparation method and application of a collector for simultaneous removal of fluorine and sulfur from magnetite concentrate | |
| CN113751203A (en) | Beneficiation method for copper-molybdenum ore in alpine region | |
| CN115945299B (en) | A method for enhanced flotation of zinc sulfide ore based on copper-lead coupling activation | |
| CN115155820B (en) | A method for strengthening zinc-sulfur separation flotation | |
| CN110076006A (en) | A method of extracting pyrite from phosphorus tailing | |
| CN113856911A (en) | Beneficiation method for high-sulfur copper gold silver ore | |
| CN113058748A (en) | Method for improving grade of low-grade spodumene rough concentrate | |
| CA1212788A (en) | Process for the selective separation of base metal sulfides and oxides contained in an ore | |
| CN118385028A (en) | Low-alkali asynchronous separation method for copper sulfide ore containing arsenic | |
| CN119016207A (en) | A method for extracting valuable metals from gold cyanide tailings | |
| CN113289764B (en) | Beneficiation method for recycling fine-particle ilmenite | |
| CN115090421A (en) | A method for eliminating copper ions to activate sphalerite and sphalerite flotation | |
| CN112705354A (en) | Beneficiation method for high-calcium scheelite | |
| CN114011582A (en) | A flotation method for improving beneficiation index of gold-bearing copper 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 | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |