CN114011582B - Flotation method for improving beneficiation index of gold-bearing copper sulfide ore - Google Patents
Flotation method for improving beneficiation index of gold-bearing copper sulfide ore Download PDFInfo
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- 239000010931 gold Substances 0.000 title claims abstract description 72
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 title claims abstract description 70
- 229910052737 gold Inorganic materials 0.000 title claims abstract description 69
- 238000000034 method Methods 0.000 title claims abstract description 38
- 238000005188 flotation Methods 0.000 title claims abstract description 31
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 title claims abstract description 18
- 239000003112 inhibitor Substances 0.000 claims abstract description 48
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229910052802 copper Inorganic materials 0.000 claims abstract description 44
- 239000010949 copper Substances 0.000 claims abstract description 44
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 17
- 239000011707 mineral Substances 0.000 claims abstract description 17
- 239000012141 concentrate Substances 0.000 claims abstract description 14
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000000926 separation method Methods 0.000 claims abstract description 10
- 229920002472 Starch Polymers 0.000 claims abstract description 8
- 235000019698 starch Nutrition 0.000 claims abstract description 8
- 239000008107 starch Substances 0.000 claims abstract description 8
- 230000002000 scavenging effect Effects 0.000 claims abstract 13
- 238000003756 stirring Methods 0.000 claims description 62
- 239000006260 foam Substances 0.000 claims description 40
- 239000004088 foaming agent Substances 0.000 claims description 40
- 229910052979 sodium sulfide Inorganic materials 0.000 claims description 22
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 claims description 22
- 230000008569 process Effects 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 10
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 9
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 9
- 238000000227 grinding Methods 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000011084 recovery Methods 0.000 abstract description 27
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 abstract description 14
- 229910052683 pyrite Inorganic materials 0.000 abstract description 13
- 239000011028 pyrite Substances 0.000 abstract description 13
- BWFPGXWASODCHM-UHFFFAOYSA-N copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052569 sulfide mineral Inorganic materials 0.000 abstract description 7
- XEIPQVVAVOUIOP-UHFFFAOYSA-N [Au]=S Chemical compound [Au]=S XEIPQVVAVOUIOP-UHFFFAOYSA-N 0.000 abstract description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract description 4
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 abstract description 4
- 238000001556 precipitation Methods 0.000 abstract description 3
- 230000008878 coupling Effects 0.000 abstract description 2
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- 235000008733 Citrus aurantifolia Nutrition 0.000 description 13
- 235000011941 Tilia x europaea Nutrition 0.000 description 13
- 239000004571 lime Substances 0.000 description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- DVRDHUBQLOKMHZ-UHFFFAOYSA-N chalcopyrite Chemical compound [S-2].[S-2].[Fe+2].[Cu+2] DVRDHUBQLOKMHZ-UHFFFAOYSA-N 0.000 description 8
- 229910052951 chalcopyrite Inorganic materials 0.000 description 8
- 229910001779 copper mineral Inorganic materials 0.000 description 8
- 239000011593 sulfur Substances 0.000 description 8
- 229910052717 sulfur Inorganic materials 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 239000003513 alkali Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000012991 xanthate Substances 0.000 description 5
- 229910052947 chalcocite Inorganic materials 0.000 description 4
- 239000000306 component Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
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- 238000010408 sweeping Methods 0.000 description 4
- 238000011161 development Methods 0.000 description 3
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 229910021532 Calcite Inorganic materials 0.000 description 2
- 229910052948 bornite Inorganic materials 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011573 trace mineral Substances 0.000 description 2
- 235000013619 trace mineral Nutrition 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910001919 chlorite Inorganic materials 0.000 description 1
- 229910052619 chlorite group Inorganic materials 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- QUQFTIVBFKLPCL-UHFFFAOYSA-L copper;2-amino-3-[(2-amino-2-carboxylatoethyl)disulfanyl]propanoate Chemical compound [Cu+2].[O-]C(=O)C(N)CSSCC(N)C([O-])=O QUQFTIVBFKLPCL-UHFFFAOYSA-L 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- IUMKBGOLDBCDFK-UHFFFAOYSA-N dialuminum;dicalcium;iron(2+);trisilicate;hydrate Chemical compound O.[Al+3].[Al+3].[Ca+2].[Ca+2].[Fe+2].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IUMKBGOLDBCDFK-UHFFFAOYSA-N 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 229910052869 epidote Inorganic materials 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052960 marcasite Inorganic materials 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
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- 239000007790 solid phase Substances 0.000 description 1
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- 150000004763 sulfides Chemical class 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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- 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
- 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
- B03D2201/04—Frothers
-
- 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
- B03D2203/025—Precious metal ores
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- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/52—Mechanical processing of waste for the recovery of materials, e.g. crushing, shredding, separation or disassembly
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
技术领域technical field
本发明涉及冶金选矿技术领域,特别涉及一种提高含金硫化铜矿石选矿指标的浮选方法。The invention relates to the technical field of metallurgical beneficiation, in particular to a flotation method for improving the beneficiation index of gold-bearing copper sulfide ore.
背景技术Background technique
铜广泛应用于军工、电力、通讯、交通、运输、轻工、建筑、机械等行业。最新统计数据表明:我国已拥有查明铜矿资源储量为9553.8万吨,其中铜品位低于0.7%的铜矿资源储量占比约为56%,斑岩型铜矿床平均品位为0.5%左右。我国铜矿资源矿床的工业类型比较齐全,有工业价值的铜矿石中80%的铜矿物属于硫化物。随着开采的深入和易选矿石的减少,硫化铜矿石资源的贫、细、杂等特点日益突出,此类资源的高效加工一直是矿物加工领域研究的热点。Copper is widely used in military, electric power, communications, transportation, transportation, light industry, construction, machinery and other industries. The latest statistics show that my country has 95.538 million tons of proven copper resources, of which copper ore reserves with a copper grade below 0.7% account for about 56%, and the average grade of porphyry copper deposits is about 0.5%. . The industrial types of copper ore deposits in my country are relatively complete, and 80% of copper minerals in copper ore with industrial value belong to sulfides. With the deepening of mining and the reduction of easy-to-separate ores, the characteristics of copper sulfide ore resources such as lean, fine, and miscellaneous have become increasingly prominent. The efficient processing of such resources has always been a research hotspot in the field of mineral processing.
含金铜硫矿石是硫化矿中比较普遍的一类矿石,一般铜以黄铜矿为主、硫以黄铁矿为主的形式存在,金主要以自然金的形式存在,硫化铜矿物和黄铁矿都是金的主要载体矿物。浮选是从此类矿石中获取金、铜金属和硫资源的重要粗加工环节,而实现铜、硫选择性分离和金的综合回收是该类矿石浮选的关键。Gold-bearing copper-sulfur ore is a relatively common type of sulfide ores. Generally, copper is mainly in the form of chalcopyrite, sulfur is mainly in the form of pyrite, gold mainly exists in the form of natural gold, and copper sulfide minerals and Pyrite is the main carrier mineral for gold. Flotation is an important rough processing link to obtain gold, copper metal and sulfur resources from such ores, and the realization of selective separation of copper and sulfur and comprehensive recovery of gold is the key to flotation of such ores.
目前含金铜硫矿石生产普遍采用石灰高碱浮选工艺(pH>11),通过添加大量的石灰抑制黄铁矿,然后在高碱条件下添加硫化矿捕收剂黄药、黑药、起泡剂松醇油进行铜、金与硫的分离浮选。但该工艺方法存在以下问题:(1)在高碱(pH>11)条件下铜、金矿物会受到一定程度的抑制,导致铜、金回收率较低。原因在于在高碱(pH>11)条件下,大量的OH-将促使黄铜矿的表面形成亲水性的氢氧化铁薄膜,黄铜矿的可浮性变差,导致铜、金回收率较低。同时,含金载体矿物黄铁矿在高碱条件下将受到严重的抑制,金的单体矿物表面被污染导致可浮性变差。这是石灰高碱浮选工艺中铜、金回收率较低的根本原因;(2)大量的石灰的使用容易造成严重的矿泥夹带,影响精矿质量;(3)存在着石灰用量大,不易控制,管道易结垢堵塞,腐蚀设备、矿山废水污染严重等问题;(4)黄药、黑药作为含金铜硫矿石的捕收剂时,存在选择性较差的问题,进而造成抑制剂的消耗增加。由此可见,石灰高碱浮选工艺中铜、金回收率较低,铜精矿的品质较差,资源浪费严重,较难实现含金铜硫矿石资源的经济、高效、清洁开发利用。At present, the production of gold-bearing copper-sulfur ore generally adopts the lime high-alkali flotation process (pH>11), by adding a large amount of lime to suppress the pyrite, and then adding the sulfide ore collectors xanthate, black medicine, Separation and flotation of copper, gold and sulfur using terpineol oil as a foaming agent. However, this process method has the following problems: (1) Under the condition of high alkali (pH>11), copper and gold minerals will be inhibited to a certain extent, resulting in low recovery rates of copper and gold. The reason is that under the condition of high alkali (pH>11), a large amount of OH - will promote the formation of a hydrophilic iron hydroxide film on the surface of chalcopyrite, and the floatability of chalcopyrite will deteriorate, resulting in the recovery rate of copper and gold. lower. At the same time, the gold-bearing carrier mineral pyrite will be seriously inhibited under high alkali conditions, and the surface of the gold monomer mineral will be polluted, resulting in poor floatability. This is the fundamental reason for the low recovery rate of copper and gold in the lime high-alkali flotation process; (2) the use of a large amount of lime is likely to cause serious sludge entrainment, which affects the quality of the concentrate; (3) there is a large amount of lime, It is not easy to control, the pipeline is easy to scale and block, the equipment is corroded, and the mine wastewater is seriously polluted. Increased consumption of agents. It can be seen that the recovery rate of copper and gold in the lime high-alkali flotation process is low, the quality of copper concentrate is poor, and the waste of resources is serious, and it is difficult to realize the economical, efficient and clean development and utilization of gold-bearing copper-sulfur ore resources.
发明内容SUMMARY OF THE INVENTION
针对上述技术问题,本发明的目的在于提供一种提高含金硫化铜矿石选矿指标的浮选方法。通过“硫代硫酸盐溶蚀-硫化沉淀-双氧水+淀粉耦合抑制-铜硫选择浮选分离”的技术路线,将载体矿物中的金转化为独立硫化金矿物,避免赋存在黄铁矿中的金向尾矿中的流失,充分发挥组合抑制剂的协同效益,提高金、铜精矿的品质和回收率,在低碱度下实现含金铜硫矿石经济、高效、清洁开发利用。In view of the above technical problems, the purpose of the present invention is to provide a flotation method for improving the beneficiation index of gold-bearing copper sulfide ore. Through the technical route of "thiosulfate dissolution-sulfide precipitation-hydrogen peroxide+starch coupling inhibition-copper-sulfur selective flotation separation", the gold in carrier minerals is converted into independent gold sulfide minerals, avoiding the occurrence of gold in pyrite The loss to tailings can give full play to the synergistic benefits of combined inhibitors, improve the quality and recovery rate of gold and copper concentrates, and realize economical, efficient and clean development and utilization of gold-bearing copper-sulfur ore under low alkalinity.
为实现上述目的,本发明提供了如下技术方案:For achieving the above object, the present invention provides the following technical solutions:
一种提高含金硫化铜矿石选矿指标的浮选方法,步骤包括:A flotation method for improving beneficiation index of gold-bearing copper sulfide ore, comprising the steps of:
(1)粗选:向矿浆中加入组合抑制剂,搅拌,加入硫化钠,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行粗选,得到粗选泡沫和粗选底流;(1) Roughing: adding combined inhibitor to the pulp, stirring, adding sodium sulfide, stirring, then adding combined collector and foaming agent, and performing roughing after stirring to obtain roughing foam and roughing underflow;
(2)扫选I:向粗选底流中加入组合抑制剂,搅拌,加入硫化钠,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行扫选I,得到扫选I泡沫和扫选I底流,扫选I泡沫返回到粗选作业;(2) sweep selection 1: add combined inhibitor in rough selection underflow, stir, add sodium sulfide, stir, then add combination collector and foaming agent, carry out sweep selection 1 after stirring, obtain sweep selection 1 foam and sweep selection 1 Select I underflow, sweep and select I foam to return to the roughing operation;
(3)精选I:向粗选泡沫中加入组合抑制剂,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行精选I,得到精选I泡沫和精选I底流,精选I底流返回到粗选作业;(3) Selection I: add the combined inhibitor to the rough selection foam, stir, then add the combined collector and foaming agent, and perform selection I after stirring to obtain selection I foam and selection I underflow, and select I underflow returns to roughing operation;
(4)扫选Ⅱ:向扫选I底流中加入组合抑制剂,搅拌,加入硫化钠,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行扫选Ⅱ,得到扫选Ⅱ泡沫和尾矿,扫选Ⅱ泡沫返回到扫选I作业;(4) Sweeping II: Add the combined inhibitor to the underflow of sweeping I, stir, add sodium sulfide, stir, then add the combined collector and foaming agent, and carry out sweeping II after stirring to obtain sweeping II foam and For tailings, sweep II foam returns to sweep I operation;
(5)精选Ⅱ:向精选I泡沫中加入组合抑制剂,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行精选Ⅱ,得到精选Ⅱ泡沫和精选Ⅱ底流,精选Ⅱ底流返回到精选I作业;(5) Selection II: Add the combined inhibitor to the selected I foam, stir, and then add the combined collector and foaming agent. After stirring, carry out the selection II to obtain the selected II foam and the selected II underflow. Select II underflow to return to Select I operation;
(6)精选Ⅲ:向精选Ⅱ泡沫中加入组合抑制剂,搅拌,再加入组合捕收剂和起泡剂,搅拌后进行精选Ⅲ,得到含金铜精矿和精选Ⅲ底流,精选Ⅲ底流返回到精选Ⅱ作业;(6) Selection III: Add the combined inhibitor to the selection II foam, stir, and then add the combined collector and foaming agent. After stirring, carry out the selection III to obtain the gold-containing copper concentrate and the selection III underflow. The selection III underflow returns to the selection II operation;
所述组合抑制剂的组分按质量份数计包括:双氧水30~50份和淀粉50~70份;所述组合捕收剂的组分按质量份数计包括:捕收剂Z-20050~70份和捕收剂BK91630~50份。The components of the combined inhibitor include, in parts by mass: 30-50 parts of hydrogen peroxide and 50-70 parts of starch; the components of the combined collector include, in parts by mass: collector Z-20050~ 70 copies and collector BK91630 to 50 copies.
优选的,所述步骤(1)中矿浆的制备步骤为:将原矿磨矿至粒径≤74μm的矿粉含量占原矿总质量75%~90%,磨矿过程中加入碳酸钠调节原浆pH至8~9,并加入原矿质量0.03%~0.05%的硫代硫酸钠,磨矿完成后,将所得原浆调浆至矿粉质量浓度为25%~35%,制得矿浆。Preferably, the preparation step of the pulp in the step (1) is as follows: grinding the raw ore to a particle size of ≤ 74 μm, the content of which accounts for 75% to 90% of the total mass of the raw ore, and adding sodium carbonate during the grinding process to adjust the pH of the raw pulp To 8-9, and adding 0.03%-0.05% sodium thiosulfate of raw ore mass, after grinding, the obtained raw pulp is slurried to the ore powder mass concentration of 25%-35% to prepare ore pulp.
本发明通过通过硫代硫酸盐溶蚀-硫化沉淀将赋存在硫化矿中的金转化为独立的硫化金矿物,通过组合捕收剂实现金的高效回收,有效地避免了赋存在黄铁矿中的金向尾矿中的流失。The invention converts the gold hosted in sulfide ore into independent gold sulfide minerals through thiosulfate dissolution-sulfide precipitation, realizes high-efficiency recovery of gold by combining collectors, and effectively avoids the occurrence of gold in pyrite. Loss of gold to tailings.
优选的,所述起泡剂为2#油。Preferably, the foaming agent is 2 # oil.
优选的,所述步骤(1)中组合抑制剂的加入量为原矿质量的0.06%~0.08%,硫化钠的加入量为原矿质量的0.02%~0.04%,组合捕收剂的加入量为原矿质量的0.004%~0.008%,起泡剂的加入量为原矿质量的0.0005%~0.0012%。Preferably, in the step (1), the added amount of the combined inhibitor is 0.06% to 0.08% of the raw ore mass, the added amount of sodium sulfide is 0.02% to 0.04% of the raw ore mass, and the added amount of the combined collector is the raw ore mass. 0.004% to 0.008% of the mass, and the added amount of the foaming agent is 0.0005% to 0.0012% of the original ore mass.
优选的,所述步骤(2)中组合抑制剂的加入量为原矿质量的0.06%~0.08%,硫化钠的加入量为原矿质量的0.02%~0.04%,组合捕收剂的加入量为原矿质量的0.004%~0.008%,起泡剂的加入量为原矿质量的0.0005%~0.0012%。Preferably, in the step (2), the added amount of the combined inhibitor is 0.06% to 0.08% of the raw ore mass, the added amount of sodium sulfide is 0.02% to 0.04% of the raw ore mass, and the added amount of the combined collector is the raw ore mass. 0.004% to 0.008% of the mass, and the added amount of the foaming agent is 0.0005% to 0.0012% of the original ore mass.
优选的,所述步骤(3)中组合抑制剂的加入量为原矿质量的0.01%~0.03%,组合捕收剂的加入量为原矿质量的0.002%~0.004%,起泡剂的加入量为原矿质量的0.0003%~0.0006%。Preferably, in the step (3), the added amount of the combined inhibitor is 0.01% to 0.03% of the raw ore mass, the added amount of the combined collector is 0.002% to 0.004% of the raw ore mass, and the added amount of the foaming agent is 0.0003% to 0.0006% of the quality of the original ore.
优选的,所述步骤(4)中组合抑制剂的加入量为原矿质量的0.015%~0.02%,硫化钠的加入量为原矿质量的0.005%~0.01%,组合捕收剂的加入量为原矿质量的0.001%~0.002%,起泡剂的加入量为原矿质量的0.0002%~0.004%。Preferably, in the step (4), the added amount of the combined inhibitor is 0.015% to 0.02% of the raw ore mass, the added amount of sodium sulfide is 0.005% to 0.01% of the raw ore mass, and the added amount of the combined collector is the raw ore mass. 0.001% to 0.002% of the mass, and the added amount of the foaming agent is 0.0002% to 0.004% of the original ore mass.
优选的,所述步骤(5)中组合抑制剂的加入量为原矿质量的0.005%~0.015%,组合捕收剂的加入量为原矿质量的0.0005%~0.001%,起泡剂的加入量为原矿质量的0.0001%~0.0003%。Preferably, in the step (5), the added amount of the combined inhibitor is 0.005% to 0.015% of the raw ore mass, the added amount of the combined collector is 0.0005% to 0.001% of the raw ore mass, and the added amount of the foaming agent is 0.0001% to 0.0003% of the original ore quality.
优选的,所述步骤(6)中组合抑制剂的加入量为原矿质量的0.007%~0.01%,组合捕收剂的加入量为原矿质量的0.0002%~0.0005%,起泡剂的加入量为原矿质量的0.0001%~0.0003%。Preferably, in the step (6), the added amount of the combined inhibitor is 0.007% to 0.01% of the raw ore mass, the added amount of the combined collector is 0.0002% to 0.0005% of the raw ore mass, and the added amount of the foaming agent is 0.0001% to 0.0003% of the original ore quality.
优选的,所述搅拌的搅拌时间为2~4min。Preferably, the stirring time of the stirring is 2-4 min.
本发明的有益技术效果如下:The beneficial technical effects of the present invention are as follows:
本发明在低碱度下(pH=7~9)实现了含金铜硫矿石经济、高效、清洁开发利用,避免了传统的石灰高碱-黄药类工艺中,石灰用量大、设备和矿浆输送管道的结垢和矿山废水的环境污染等问题。The invention realizes economical, efficient and clean development and utilization of gold-containing copper-sulfur ore under low alkalinity (pH=7-9), and avoids the large amount of lime, equipment and pulp in the traditional lime high alkali-xanthate process. Scaling of pipelines and environmental pollution of mine wastewater.
本发明所用组合抑制剂中的双氧水能氧化黄铁矿的表面,诱导黄铁矿表面钝化改性,形成亲水性铁组元的稳定罩盖。其中的淀粉因富含羟基可与黄铁矿的富铁表面发生强烈的吸附,造成黄铁矿表面的亲水性增加,而组合抑制剂对黄铜矿表面的影响较少,这是实现铜、硫选择性浮选分离的重要原因。The hydrogen peroxide in the combined inhibitor used in the invention can oxidize the surface of the pyrite, induce the passivation modification of the pyrite surface, and form a stable cover of the hydrophilic iron component. Among them, starch can be strongly adsorbed on the iron-rich surface of pyrite due to its rich hydroxyl groups, resulting in an increase in the hydrophilicity of the pyrite surface, while the combined inhibitor has less effect on the chalcopyrite surface, which is the realization of copper , An important reason for sulfur selective flotation separation.
本发明通过硫代硫酸盐溶蚀-硫化沉淀的方式,提高了金的回收率。其原理在于:在碳酸钠的弱碱矿浆体系中,硫代硫酸钠可将赋存在硫化矿物中的固相金(Au)转变为溶液中的液相金组([Au(S2O3)3]3-),硫化钠进一步将液相金组分沉淀为独立的硫化金矿物(Au2S)。通过捕收剂的作用将实现独立硫化金矿物的有效回收。The invention improves the recovery rate of gold by means of thiosulfate corrosion-sulfide precipitation. The principle is: in the weak alkaline slurry system of sodium carbonate, sodium thiosulfate can convert the solid-phase gold (Au) hosted in the sulfide minerals into the liquid-phase gold group ([Au(S 2 O 3 ) 3 ] 3- ), sodium sulfide further precipitates the liquid-phase gold component as an independent gold sulfide mineral (Au 2 S). The effective recovery of independent gold sulfide minerals will be achieved through the action of collectors.
本发明所用组合捕收剂能降药制组分溶解的胶束溶度,改善药剂的溶解性能,因而对硫化铜矿的浮选具有较强的选择性,能有效地避免矿泥夹带,提高了铜精矿的品质和回收率。与传统的石灰高碱-黄药类工艺相比,铜品位提高1~2%,铜回收率提高3~5%,金的品位提高2~3%,金回收率提高10~15%。The combined collector used in the invention can reduce the solubility of the dissolved micelles of the pharmaceutical components and improve the solubility of the pharmaceuticals, so it has strong selectivity for the flotation of copper sulfide ore, can effectively avoid the entrainment of ore slime, and improve the quality and recovery of copper concentrates. Compared with the traditional lime high alkali-xanthate process, the copper grade is increased by 1-2%, the copper recovery rate is increased by 3-5%, the gold grade is increased by 2-3%, and the gold recovery rate is increased by 10-15%.
附图说明Description of drawings
图1为本发明含金硫化铜矿石浮选的工艺流程图。Fig. 1 is the process flow chart of the flotation of gold-bearing copper sulfide ore of the present invention.
具体实施方式Detailed ways
现详细说明本发明的多种示例性实施方式,该详细说明不应认为是对本发明的限制,而应理解为是对本发明的某些方面、特性和实施方案的更详细的描述。应理解本发明中所述的术语仅仅是为描述特别的实施方式,并非用于限制本发明。Various exemplary embodiments of the present invention will now be described in detail, which detailed description should not be construed as a limitation of the invention, but rather as a more detailed description of certain aspects, features, and embodiments of the invention. It should be understood that the terms described in the present invention are only used to describe particular embodiments, and are not used to limit the present invention.
另外,对于本发明中的数值范围,应理解为还具体公开了该范围的上限和下限之间的每个中间值。在任何陈述值或陈述范围内的中间值以及任何其他陈述值或在所述范围内的中间值之间的每个较小的范围也包括在本发明内。这些较小范围的上限和下限可独立地包括或排除在范围内。Additionally, for numerical ranges in the present disclosure, it should be understood that each intervening value between the upper and lower limits of the range is also specifically disclosed. Every smaller range between any stated value or intervening value in a stated range and any other stated value or intervening value in that stated range is also encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included or excluded in the range.
除非另有说明,否则本文使用的所有技术和科学术语具有本发明所述领域的常规技术人员通常理解的相同含义。虽然本发明仅描述了优选的方法和材料,但是在本发明的实施或测试中也可以使用与本文所述相似或等同的任何方法和材料。Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention relates. Although only the preferred methods and materials are described herein, any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention.
关于本文中所使用的“包含”、“包括”、“具有”、“含有”等等,均为开放性的用语,即意指包含但不限于。As used herein, "comprising," "including," "having," "containing," and the like, are open-ended terms, meaning including but not limited to.
本发明实施例及对比例所用捕收剂Z-200购自铁岭选矿药剂有限公司;所用捕收剂BK916购自北京矿冶研究总院。The collector Z-200 used in the examples and comparative examples of the present invention was purchased from Tieling Mineral Processing Chemicals Co., Ltd.; the used collector BK916 was purchased from Beijing General Research Institute of Mining and Metallurgy.
本发明实施例及对比例中所加入的硫代硫酸钠、硫化钠、组合抑制剂、组合捕收剂和起泡剂的量,均是以原矿质量为基准值,加入对应质量的各物质。The amounts of sodium thiosulfate, sodium sulfide, combined inhibitor, combined collector and foaming agent added in the examples and comparative examples of the present invention are all based on the quality of raw ore, and each substance of corresponding quality is added.
实施例1Example 1
本实施例所选用的原矿品位为铜0.75%、硫24.50%、铁25.32%,金0.28g/t。其物质组成为:矿石中主要金属矿物以黄铁矿、黄铜矿为主,少量及微量矿物有白铁矿、斑铜矿、辉铜矿、蓝辉铜矿;脉石矿物有辉石、白云石、石英、方解石、长石、绿泥石、绿帘石等。原矿铜物相分析结果表明,铜矿物以原生铜矿物为主(占92%),原生铜矿物中黄铜矿占95%。The selected raw ore grades in this embodiment are copper 0.75%, sulfur 24.50%, iron 25.32%, and gold 0.28g/t. Its material composition is: the main metal minerals in the ore are mainly pyrite and chalcopyrite, and a small amount of and trace minerals include marcasite, bornite, chalcocite, and blue chalcocite; gangue minerals include pyroxene, Dolomite, quartz, calcite, feldspar, chlorite, epidote, etc. The results of phase analysis of copper in the original ore show that the copper minerals are mainly primary copper minerals (accounting for 92%), and chalcopyrite accounts for 95% of the primary copper minerals.
本实施例所用组合抑制剂由双氧水45份和淀粉65份混合得到。The combined inhibitor used in this example is obtained by mixing 45 parts of hydrogen peroxide and 65 parts of starch.
本实施例所用组合捕收剂由捕收剂Z-20060份和捕收剂BK91640份混合得到。The combined collector used in this example is obtained by mixing 60 parts of collector Z-2000 with 40 parts of collector BK91640.
具体选矿步骤如下:The specific beneficiation steps are as follows:
(1)原矿磨矿过程中加入碳酸钠调节原浆pH=8.5和硫代硫酸钠400g/t,并磨矿至粒径≤74μm的矿粉含量占原矿质量的80%;对原浆调浆至矿粉浓度为30wt%,得到矿浆,加入组合抑制剂800g/t,搅拌3min,硫化钠300g/t,搅拌3min,组合捕收剂60g/t,起泡剂2#油10g/t,搅拌3min,进行粗选,得到泡沫和底流;(1) During the grinding process of raw ore, add sodium carbonate to adjust pH=8.5 and sodium thiosulfate 400g/t, and grind the ore to a particle size of ≤74μm, which accounts for 80% of the raw ore mass; When the concentration of mineral powder is 30wt%, obtain mineral pulp, add combined inhibitor 800g/t, stir for 3min, sodium sulfide 300g/t, stir for 3min, combined collector 60g/t, foaming agent 2 # oil 10g/t, stir 3min, carry out rough selection to obtain foam and underflow;
(2)向步骤(1)粗选得到的底流加入组合抑制剂400g/t,搅拌3min,硫化钠150g/t,搅拌3min,组合捕收剂30g/t,起泡剂2#油6g/t,搅拌3min,进行扫选I,得到泡沫和底流,扫选I泡沫返回到粗选作业;向步骤(1)粗选得到的泡沫加入组合抑制剂200g/t,搅拌3min,组合捕收剂30g/t,起泡剂2#油4g/t,搅拌3min,进行精选I,得到泡沫和底流,底流返回到粗选作业;(2) Add 400g/t of combined inhibitor to the underflow obtained by rough selection in step (1), stir for 3min, 150g/t of sodium sulfide, stir for 3min, combined collector 30g/t, foaming agent 2 # oil 6g/t , stir for 3min, carry out sweep selection I, obtain foam and underflow, sweep selection I foam back to rough selection operation; add combined inhibitor 200g/t to the foam obtained in step (1) rough selection, stir for 3min, combined collector 30g /t, foaming agent 2 # oil 4g/t, stirs 3min, carries out selection 1, obtains foam and underflow, underflow returns to rough selection operation;
(3)向步骤(2)扫选I得到的底流加入组合抑制剂200g/t,搅拌3min,硫化钠80g/t,搅拌3min,组合捕收剂15g/t,起泡剂2#油4g/t,搅拌3min,进行扫选II,得到泡沫和尾矿,扫选II泡沫返回到扫选I作业;向步骤(2)精选I得到的泡沫加入组合抑制剂100g/t,搅拌3min,组合捕收剂15g/t,起泡剂2#油2g/t,搅拌3min,进行精选II,得到泡沫和底流,底流返回到精选I作业;(3) add combined inhibitor 200g/t to the underflow obtained by step (2) sweep selection 1, stir 3min, sodium sulfide 80g/t, stir 3min, combined collector 15g/t, foaming agent 2 #oil 4g/ t, stir for 3min, carry out sweep II to obtain foam and tailings, sweep II foam and return to sweep I operation; add 100 g/t of combined inhibitor to the foam obtained in step (2) selection I, stir for 3min, combine Collecting agent 15g/t, foaming agent 2 # oil 2g/t, stir for 3min, carry out selection II, obtain foam and underflow, and underflow returns to selection I operation;
(4)向步骤(2)精选II得到泡沫加入组合抑制剂70g/t,搅拌3min,组合捕收剂4g/t,起泡剂2#油2g/t,搅拌3min,进行精选III,得到含金铜精矿和底流,底流返回到精选II作业。(4) Add 70g/t of combined inhibitor to step (2) selection II to obtain foam, stir for 3min, combine collector 4g/t, foaming agent 2 # oil 2g/t, stir for 3min, carry out selection III, A gold-bearing copper concentrate and underflow are obtained, and the underflow is returned to the Select II operation.
试验结果:铜精矿品位21.88%,铜的回收率93.12%,金品位5.8g/t,金回收率83.15%。与传统的石灰高碱-黄药工艺相比(采用与实施例1相同的浮选流程,区别在于利用石灰取代组合抑制剂并控制粗选pH=12,乙基黄药取代组合捕收剂,每次作业的用量与组合捕收剂相同,无硫代硫酸钠和硫化钠添加),铜品位提高1.8%,铜回收率提高3.2%,金品位提高1.5g/t,金回收率提高14%。Test results: the copper concentrate grade is 21.88%, the copper recovery rate is 93.12%, the gold grade is 5.8g/t, and the gold recovery rate is 83.15%. Compared with the traditional lime high alkali-xanthate process (using the same flotation process as in Example 1, the difference is that lime is used to replace the combined inhibitor and control the roughing pH=12, ethyl xanthate replaces the combined collector, The dosage of each operation is the same as that of the combined collector, without the addition of sodium thiosulfate and sodium sulfide), the copper grade is increased by 1.8%, the copper recovery rate is increased by 3.2%, the gold grade is increased by 1.5g/t, and the gold recovery rate is increased by 14% .
实施例2Example 2
本实施例所选用的原矿品位为铜0.58%、硫22.50%、铁23.32%,金0.21g/t。其物质组成为:矿石中主要金属矿物为黄铁矿、黄铜矿,少量及微量矿物有斑铜矿、辉铜矿、蓝辉铜矿;脉石矿物为白云石、石英、方解石。原矿铜物相分析结果表明,铜矿物包括原生铜矿物和次生铜矿物,以原生铜矿物为主(占92%),原生铜矿物中黄铜矿占95%,氧化铜占2%。The selected raw ore grades in this embodiment are copper 0.58%, sulfur 22.50%, iron 23.32%, and gold 0.21 g/t. Its material composition is: the main metal minerals in the ore are pyrite and chalcopyrite, and the minor and trace minerals are bornite, chalcocite and blue chalcocite; gangue minerals are dolomite, quartz and calcite. The phase analysis results of copper in the original ore show that the copper minerals include primary copper minerals and secondary copper minerals, mainly primary copper minerals (accounting for 92%), chalcopyrite accounting for 95%, and copper oxide 2%.
本实施例所用组合抑制剂由双氧水50份和淀粉50份混合得到。The combined inhibitor used in this example is obtained by mixing 50 parts of hydrogen peroxide and 50 parts of starch.
本实施例所用组合捕收剂由捕收剂Z-20050份和捕收剂BK91650份混合得到。The combined collector used in this example is obtained by mixing 50 parts of collector Z-2000 and 50 parts of collector BK91650.
具体选矿步骤如下:The specific beneficiation steps are as follows:
(1)原矿磨矿过程中加入碳酸钠调节原浆pH=9和硫代硫酸钠300g/t,并磨矿至粒径≤74μm的矿粉含量占原矿质量的90%;对原浆调浆至矿粉浓度为30wt%,得到矿浆,加入组合抑制剂600g/t,搅拌3min,硫化钠150g/t,搅拌3min,组合捕收剂50g/t,起泡剂2#油10g/t,搅拌3min,进行粗选,得到泡沫和底流;(1) During the grinding process of raw ore, add sodium carbonate to adjust pH=9 and sodium thiosulfate 300g/t, and grind the ore to a particle size of ≤74μm, which accounts for 90% of the raw ore quality; When the concentration of mineral powder is 30wt%, obtain mineral pulp, add combined inhibitor 600g/t, stir for 3min, sodium sulfide 150g/t, stir for 3min, combined collector 50g/t, foaming agent 2 # oil 10g/t, stir 3min, carry out rough selection to obtain foam and underflow;
(2)向步骤(1)粗选得到的底流加入组合抑制剂300g/t,搅拌3min,硫化钠80g/t,搅拌3min,组合捕收剂30g/t,起泡剂2#油5g/t,搅拌3min,进行扫选I,得到泡沫和底流,扫选I泡沫返回到粗选作业;向步骤(1)粗选得到的泡沫加入组合抑制剂150g/t,搅拌3min,组合捕收剂30g/t,起泡剂2#油5g/t,搅拌3min,进行精选I,得到泡沫和底流,底流返回到粗选作业;(2) Add 300g/t of combined inhibitor to the underflow obtained by rough selection in step (1), stir for 3min, sodium sulfide 80g/t, stir for 3min, combined collector 30g/t, foaming agent 2 # oil 5g/t , stir for 3min, carry out sweep selection I, obtain foam and underflow, sweep selection I foam and return to rough selection operation; add combined inhibitor 150g/t to the foam obtained in step (1) rough selection, stir for 3min, combined collector 30g /t, foaming agent 2 # oil 5g/t, stirs 3min, carries out selection 1, obtains foam and underflow, underflow returns to rough selection operation;
(3)向步骤(2)扫选I得到的底流加入组合抑制剂150g/t,搅拌3min,硫化钠40g/t,搅拌3min,组合捕收剂15g/t,起泡剂2#油3g/t,搅拌3min,进行扫选II,得到泡沫和尾矿,扫选II泡沫返回到扫选I作业;向步骤(2)精选I得到的泡沫加入组合抑制剂80g/t,搅拌3min,组合捕收剂15g/t,起泡剂2#油2g/t,搅拌3min,进行精选II,得到泡沫和底流,底流返回到精选I作业;(3) add combined inhibitor 150g/t to the underflow obtained by step (2) sweep selection 1, stir 3min, sodium sulfide 40g/t, stir 3min, combined collector 15g/t, foaming agent 2 #oil 3g/ t, stir for 3min, carry out sweep II to obtain foam and tailings, sweep II foam and return to sweep I operation; add combined inhibitor 80g/t to the foam obtained in step (2) selection I, stir for 3min, combine Collecting agent 15g/t, foaming agent 2 # oil 2g/t, stir for 3min, carry out selection II, obtain foam and underflow, and underflow returns to selection I operation;
(4)向步骤(2)精选II得到泡沫加入组合抑制剂40g/t,搅拌3min,组合捕收剂8g/t,起泡剂2#油3g/t,搅拌3min,进行精选III,得到含金铜精矿和底流,底流返回到精选II作业。(4) Add 40g/t of combined inhibitor to step (2) selection II to obtain foam, stir for 3min, combine collector 8g/t, foaming agent 2 # oil 3g/t, stir for 3min, carry out selection III, A gold-bearing copper concentrate and underflow are obtained, and the underflow is returned to the Select II operation.
试验结果:铜精矿品位20.20%,铜的回收率91.32%,金品位5.3g/t,金回收率81.5%。与传统的石灰高碱-黄药工艺相比(采用与实施例2相同的浮选流程,区别在于利用石灰取代组合抑制剂并控制粗选pH=12,乙基黄药取代组合捕收剂,每次作业的用量与组合捕收剂相同,无硫代硫酸钠和硫化钠添加),铜品位提高1.3%,铜回收率提高2.8%,金品位提高1.2g/t,金回收率提高12%。Test results: the copper concentrate grade is 20.20%, the copper recovery rate is 91.32%, the gold grade is 5.3g/t, and the gold recovery rate is 81.5%. Compared with the traditional lime high alkali-xanthate process (using the same flotation process as in Example 2, the difference is that lime is used to replace the combined inhibitor and control the roughing pH=12, ethyl xanthate replaces the combined collector, The dosage of each operation is the same as that of the combined collector, without the addition of sodium thiosulfate and sodium sulfide), the copper grade is increased by 1.3%, the copper recovery rate is increased by 2.8%, the gold grade is increased by 1.2g/t, and the gold recovery rate is increased by 12% .
对比例1Comparative Example 1
采用与实施例1相同的原矿和浮选流程,区别在于利用等质量的淀粉替代各步骤中的组合抑制剂。The same raw ore and flotation process as in Example 1 are used, the difference is that the combined inhibitor in each step is replaced with starch of the same quality.
试验结果:铜精矿品位19.21%,铜的回收率91.2%,金品位4.2g/t,金回收率82.5%。Test results: the copper concentrate grade is 19.21%, the copper recovery rate is 91.2%, the gold grade is 4.2g/t, and the gold recovery rate is 82.5%.
对比例2Comparative Example 2
采用与实施例1相同的原矿和浮选流程,区别在于利用等质量的捕收剂BK916替代各步骤中的组合捕收剂。The same raw ore and flotation process as in Example 1 were used, except that the collector BK916 of the same quality was used to replace the combined collector in each step.
试验结果:铜精矿品位19.3%,铜的回收率91.45%,金品位4.8g/t,金回收率79.5%。Test results: the copper concentrate grade is 19.3%, the copper recovery rate is 91.45%, the gold grade is 4.8g/t, and the gold recovery rate is 79.5%.
对比例3Comparative Example 3
采用与实施例1相同的原矿和浮选流程,区别在于无硫代硫酸钠的添加。The same raw ore and flotation process as in Example 1 were adopted, except that no sodium thiosulfate was added.
试验结果:铜精矿品位19.5%,铜的回收率91.45%,金品位4.2g/t,金回收率61.5%。Test results: the grade of copper concentrate is 19.5%, the recovery rate of copper is 91.45%, the grade of gold is 4.2g/t, and the recovery rate of gold is 61.5%.
以上所述的实施例仅是对本发明的优选方式进行描述,并非对本发明的范围进行限定,在不脱离本发明设计精神的前提下,本领域普通技术人员对本发明的技术方案做出的各种变形和改进,均应落入本发明权利要求书确定的保护范围内。The above-mentioned embodiments are only to describe the preferred modes of the present invention, but not to limit the scope of the present invention. Without departing from the design spirit of the present invention, those of ordinary skill in the art can make various modifications to the technical solutions of the present invention. Variations and improvements should fall within the protection scope determined by the claims of the present invention.
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