CN107999267B - A flotation separation process of high-sulfur lead-zinc ore in a high-concentration environment - Google Patents
A flotation separation process of high-sulfur lead-zinc ore in a high-concentration environment Download PDFInfo
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- CN107999267B CN107999267B CN201711313393.1A CN201711313393A CN107999267B CN 107999267 B CN107999267 B CN 107999267B CN 201711313393 A CN201711313393 A CN 201711313393A CN 107999267 B CN107999267 B CN 107999267B
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- 238000005188 flotation Methods 0.000 title claims abstract description 44
- 239000011593 sulfur Substances 0.000 title claims abstract description 41
- 229910052717 sulfur Inorganic materials 0.000 title claims abstract description 41
- JQJCSZOEVBFDKO-UHFFFAOYSA-N lead zinc Chemical compound [Zn].[Pb] JQJCSZOEVBFDKO-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 238000000926 separation method Methods 0.000 title claims abstract description 21
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical compound [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 0.000 claims abstract description 90
- 238000000034 method Methods 0.000 claims abstract description 48
- 239000003112 inhibitor Substances 0.000 claims abstract description 30
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 20
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 20
- 239000004571 lime Substances 0.000 claims abstract description 20
- 239000012190 activator Substances 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 83
- 239000011701 zinc Substances 0.000 claims description 83
- 229910052725 zinc Inorganic materials 0.000 claims description 83
- 239000012141 concentrate Substances 0.000 claims description 73
- 230000002000 scavenging effect Effects 0.000 claims description 40
- 238000010408 sweeping Methods 0.000 claims description 24
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
- TUZCOAQWCRRVIP-UHFFFAOYSA-N butoxymethanedithioic acid Chemical compound CCCCOC(S)=S TUZCOAQWCRRVIP-UHFFFAOYSA-N 0.000 claims description 19
- 238000000227 grinding Methods 0.000 claims description 18
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 16
- 239000002002 slurry Substances 0.000 claims description 16
- 229910000365 copper sulfate Inorganic materials 0.000 claims description 12
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 12
- 239000004088 foaming agent Substances 0.000 claims description 11
- 238000003756 stirring Methods 0.000 claims description 9
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 238000005065 mining Methods 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 5
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 5
- 229960001763 zinc sulfate Drugs 0.000 claims description 5
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 4
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 claims description 4
- 229950004394 ditiocarb Drugs 0.000 claims description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 4
- 238000007670 refining Methods 0.000 claims description 4
- 235000010265 sodium sulphite Nutrition 0.000 claims description 4
- CJSZLPWCFGHOPN-UHFFFAOYSA-N triazanium dioxido-sulfanylidene-sulfido-lambda5-phosphane Chemical compound P([O-])([O-])(=S)[S-].[NH4+].[NH4+].[NH4+] CJSZLPWCFGHOPN-UHFFFAOYSA-N 0.000 claims description 4
- CONMNFZLRNYHIQ-UHFFFAOYSA-N 3-methylbutoxymethanedithioic acid Chemical compound CC(C)CCOC(S)=S CONMNFZLRNYHIQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract description 33
- 229910052737 gold Inorganic materials 0.000 abstract description 33
- 239000010931 gold Substances 0.000 abstract description 33
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract description 32
- 239000011707 mineral Substances 0.000 abstract description 32
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 29
- 229910052709 silver Inorganic materials 0.000 abstract description 29
- 239000004332 silver Substances 0.000 abstract description 29
- 238000011084 recovery Methods 0.000 abstract description 22
- 229910001739 silver mineral Inorganic materials 0.000 abstract description 12
- 239000002184 metal Substances 0.000 abstract description 10
- 229910052751 metal Inorganic materials 0.000 abstract description 10
- 239000005083 Zinc sulfide Substances 0.000 abstract description 7
- 229910052984 zinc sulfide Inorganic materials 0.000 abstract description 7
- 238000007667 floating Methods 0.000 abstract description 4
- 230000002209 hydrophobic effect Effects 0.000 abstract description 2
- 229910001656 zinc mineral Inorganic materials 0.000 abstract description 2
- PQTCMBYFWMFIGM-UHFFFAOYSA-N gold silver Chemical compound [Ag].[Au] PQTCMBYFWMFIGM-UHFFFAOYSA-N 0.000 abstract 3
- 229910020218 Pb—Zn Inorganic materials 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- BFUPQMKQJRHLRA-UHFFFAOYSA-N [Pb]=S.[Zn] Chemical compound [Pb]=S.[Zn] BFUPQMKQJRHLRA-UHFFFAOYSA-N 0.000 abstract 1
- 230000007547 defect Effects 0.000 abstract 1
- 238000004134 energy conservation Methods 0.000 abstract 1
- 230000007613 environmental effect Effects 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 239000011133 lead Substances 0.000 description 106
- 229910052949 galena Inorganic materials 0.000 description 6
- XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 6
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 6
- 229910052683 pyrite Inorganic materials 0.000 description 6
- 239000011028 pyrite Substances 0.000 description 6
- 229910052950 sphalerite Inorganic materials 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229910052946 acanthite Inorganic materials 0.000 description 4
- 238000005265 energy consumption Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229940056910 silver sulfide Drugs 0.000 description 4
- DVRDHUBQLOKMHZ-UHFFFAOYSA-N chalcopyrite Chemical compound [S-2].[S-2].[Fe+2].[Cu+2] DVRDHUBQLOKMHZ-UHFFFAOYSA-N 0.000 description 3
- 229910052951 chalcopyrite Inorganic materials 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229910021532 Calcite Inorganic materials 0.000 description 2
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 2
- 229910001919 chlorite Inorganic materials 0.000 description 2
- 229910052619 chlorite group Inorganic materials 0.000 description 2
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 2
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUARKZBEFFVFRG-UHFFFAOYSA-N silver sulfide Chemical compound [S-2].[Ag+].[Ag+] XUARKZBEFFVFRG-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 229940116411 terpineol Drugs 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- KOVPITHBHSZRLT-UHFFFAOYSA-N 2-methylpropoxymethanedithioic acid Chemical compound CC(C)COC(S)=S KOVPITHBHSZRLT-UHFFFAOYSA-N 0.000 description 1
- CETBSQOFQKLHHZ-UHFFFAOYSA-N Diethyl disulfide Chemical compound CCSSCC CETBSQOFQKLHHZ-UHFFFAOYSA-N 0.000 description 1
- VXLCNTLWWUDBSO-UHFFFAOYSA-N Ethiazide Chemical compound ClC1=C(S(N)(=O)=O)C=C2S(=O)(=O)NC(CC)NC2=C1 VXLCNTLWWUDBSO-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- NWXHSRDXUJENGJ-UHFFFAOYSA-N calcium;magnesium;dioxido(oxo)silane Chemical compound [Mg+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O NWXHSRDXUJENGJ-UHFFFAOYSA-N 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- -1 compound xanthate Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052637 diopside Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229950007164 ethiazide Drugs 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 229910052892 hornblende Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- LWUVWAREOOAHDW-UHFFFAOYSA-N lead silver Chemical compound [Ag].[Pb] LWUVWAREOOAHDW-UHFFFAOYSA-N 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910052969 tetrahedrite Inorganic materials 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
Classifications
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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
- 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
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
-
- 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
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- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
技术领域technical field
本发明涉及有色金属矿石浮选技术领域,尤其涉及一种回收高硫铅锌矿中有价金属矿物的选矿工艺。The invention relates to the technical field of non-ferrous metal ore flotation, in particular to a beneficiation process for recovering valuable metal minerals in high-sulfur lead-zinc ore.
背景技术Background technique
铅锌多金属硫化矿矿石中常伴生贵金属金银矿物的存在,其中铅、锌、硫主要分别以方铅矿、(铁)闪锌矿、(磁)黄铁矿形式存在,金矿物以方铅矿包裹金、黄铁矿包裹金以及少量自然金形式存在,银矿物主要以硫化银和自然银形式存在。矿石中可综合回收的有价金属矿物有铅、锌、硫及伴生金银,金银矿物主要富集在铅精矿中得到综合回收。该类矿石分选过程中普遍存在铅、锌、硫分离难度大,金属互含严重,主金属及伴生金银矿物回收率偏低,浮选药耗、水耗、能耗高等问题,特别是高硫铅锌矿石的浮选过程中,存在浮选pH过高,浮选药剂用量大、浮选流程不稳定、选矿成本高等突出问题。The presence of precious metal gold and silver minerals is often associated with lead-zinc polymetallic sulfide ores, in which lead, zinc, and sulfur mainly exist in the form of galena, (iron) sphalerite, and (magnetic) pyrite, and the gold minerals are in the form of galena Ore-wrapped gold, pyrite-wrapped gold and a small amount of natural gold exist, and silver minerals mainly exist in the form of silver sulfide and natural silver. The valuable metal minerals that can be comprehensively recovered in the ore include lead, zinc, sulfur and associated gold and silver. The gold and silver minerals are mainly enriched in the lead concentrate for comprehensive recovery. In the sorting process of this kind of ore, there are generally problems such as difficult separation of lead, zinc and sulfur, serious metal intercontainment, low recovery rate of main metal and associated gold and silver minerals, high consumption of chemicals, water and energy in flotation, especially During the flotation process of high-sulfur lead-zinc ore, there are outstanding problems such as high flotation pH, large amount of flotation reagents, unstable flotation process, and high beneficiation cost.
专利号为CN103041924B的中国发明专利“铅锌银硫化矿中回收伴生银的选矿工艺”公开了一种从含高硫的铅锌银硫化矿中回收伴生银的选矿工艺,其提出在磨矿细度72%,浮选浓度30%的条件下,采用石灰作矿浆pH调整剂及硫矿物抑制剂,碳酸钠+硫酸锌为锌矿物抑制剂,乙硫氮为铅矿物主要捕收剂,复合黄药为辅助捕收剂,松醇油为起泡剂优先浮选铅银矿物;选锌时采用硫酸铜为活化剂,异丁基黄药为捕收剂,松醇油为起泡剂。此方法虽然获得了含铅大于52%、含银2382g/t,铅回收率88.43%、银回收率75.86%的铅银精矿,但存在银回收率偏低,铅浮选回路石灰用量过大(15kg/t)等问题,捕收剂乙硫氮+复合黄药用量也达到了210g/t,选矿成本、能耗依然偏高。Patent No. CN103041924B Chinese invention patent "Ore dressing process for recovering associated silver from lead-zinc-silver sulfide ore" discloses a mineral processing process for recovering associated silver from high-sulfur lead-zinc-silver sulfide ore. Under the conditions of 72% concentration and 30% flotation concentration, lime is used as slurry pH adjuster and sulfur mineral inhibitor, sodium carbonate + zinc sulfate is zinc mineral inhibitor, ethyl disulfide is the main collector of lead mineral, and compound yellow Medicine is used as an auxiliary collector, terpineol oil is used as a foaming agent to preferentially float lead and silver minerals; copper sulfate is used as an activator when zinc is selected, isobutyl xanthate is used as a collector, and terpineol oil is used as a foaming agent. Although this method has obtained a lead-silver concentrate with a lead content of more than 52%, a silver content of 2382g/t, a lead recovery rate of 88.43%, and a silver recovery rate of 75.86%, the silver recovery rate is low and the lime consumption in the lead flotation circuit is too large (15kg/t) and other issues, the amount of collector ethiazide + compound xanthate also reached 210g/t, and the cost of mineral processing and energy consumption are still high.
发明内容Contents of the invention
本发明要解决的技术问题是针对高硫含伴生金银的铅锌硫化矿石,采用传统选矿工艺选别难度大、分选效率低、选矿综合指标差、伴生金银回收率低,选矿成本及能耗高、浮选过程不稳定等问题,提供一种高效、稳定、节能、环保、分选效率高、适应能力强、选别指标好的高浓度浮选环境下回收高硫铅锌矿中有价金属矿物的选矿工艺,使这类铅锌硫化矿石中有价金属资源得以高效综合回收利用。The technical problem to be solved in the present invention is that for high-sulfur lead-zinc sulfide ores containing associated gold and silver, it is difficult to select by traditional mineral processing technology, the separation efficiency is low, the comprehensive index of mineral processing is poor, the recovery rate of associated gold and silver is low, and the cost and cost of mineral processing are low. To solve the problems of high energy consumption and unstable flotation process, provide a high-efficiency, stable, energy-saving, environmentally friendly, high-separation efficiency, strong adaptability, and high-concentration flotation environment to recover high-sulfur lead-zinc ore. The beneficiation process of valuable metal minerals enables efficient and comprehensive recycling of valuable metal resources in such lead-zinc sulfide ores.
为解决上述技术问题,本发明采用如下技术方案:一种高浓度环境下高硫铅锌矿浮选分离工艺,其特征在于:按以下步骤进行,In order to solve the above-mentioned technical problems, the present invention adopts the following technical scheme: a high-sulfur lead-zinc ore flotation separation process in a high-concentration environment, which is characterized in that: it is carried out according to the following steps,
(1)磨矿:将矿石磨细,得到磨矿矿浆;其中原矿磨细的磨矿细度为-0.074mm粒度级别含量占原矿总重量的60~80%;(1) Ore grinding: grind the ore finely to obtain the ore grinding slurry; wherein the grinding fineness of the raw ore is -0.074mm, and the particle size grade content accounts for 60-80% of the total weight of the raw ore;
(2)将步骤(1)得到的磨矿矿浆调整好浮选浓度后进行铅粗选,得到铅粗精矿和铅粗选尾矿;其中铅粗选作业工艺条件为:先加入锌硫抑制剂XKY012为500~1000g/t,作用时间为3~5min,再加入捕收剂XK712为50~80g/t,作用时间为2~3min;(2) After adjusting the flotation concentration of the grinding slurry obtained in step (1), carry out lead roughing to obtain lead rough concentrate and lead roughing tailings; wherein the lead roughing operation process conditions are: first add zinc sulfur to inhibit The agent XKY012 is 500-1000g/t, and the action time is 3-5min, and the collector XK712 is added at 50-80g/t, and the action time is 2-3min;
(3)将步骤(2)得到的铅粗选尾矿进行铅扫选两次,即铅扫选Ⅰ和铅扫选Ⅱ,得到铅扫选尾矿和两个铅扫选中矿,两个铅扫选中矿分别顺序返回到上一层作业;其中铅扫选两次作业工艺条件为:铅扫选Ⅰ作业加入捕收剂XK712为20~30g/t,作用时间为2~3min;铅扫选Ⅱ作业加入捕收剂XK712为10~20g/t,作用时间为2~3min;(3) The lead roughing tailings obtained in step (2) are subjected to lead scavenging twice, i.e. lead scavenging I and lead scavenging II, to obtain lead scavenging tailings and two lead scavenging ores, two lead scavenging Sweeping and mining return to the previous layer of operations in sequence; the process conditions for the two operations of lead sweeping are as follows: lead sweeping I operation adds collector XK712 at 20-30g/t, and the action time is 2-3min; lead sweeping In operation II, add collector XK712 at 10-20g/t, and the action time is 2-3min;
(4)将步骤(2)得到的铅粗精矿进行铅精选二次,即铅精Ⅰ和铅精Ⅱ,得到铅精矿和二个铅精选中矿,二个铅精选中矿分别顺序返回到上一层作业;铅精选二次作业工艺条件为:铅精Ⅰ作业加入锌硫抑制剂XKY012为300~500g/t,作用时间为3~5min,铅精Ⅱ作业加入锌硫抑制剂XKY012为200~300g/t,作用时间为3~5min;(4) Carry out the lead concentrate that step (2) obtains to lead beneficiation twice, i.e. lead concentrate I and lead concentrate II, obtain lead concentrate and two lead concentrate middle ores, two lead concentrate middle ore Respectively return to the previous layer of operations in sequence; the process conditions of the secondary operation of lead selection are: the zinc-sulfur inhibitor XKY012 is added at 300-500g/t for the operation of lead concentration I, and the action time is 3-5min; The inhibitor XKY012 is 200-300g/t, and the action time is 3-5min;
(5)将步骤(3)得到的铅扫选尾矿进行锌硫第一次混合粗选,得到锌硫混合粗精矿Ⅰ和锌硫混合粗选Ⅰ尾矿;锌硫第一次混合粗选作业工艺条件为:加入矿浆调整剂石灰500~1000g/t,作用时间为3~5min,活化剂硫酸铜300~400g/t,作用时间为3~5min,捕收剂丁基黄药60~100g/t,作用时间为2~3min,起泡剂2#油10~20g/t,作用时间为1~2min;(5) The lead scavenging tailings obtained in step (3) are subjected to zinc-sulfur mixed roughing for the first time to obtain zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rougher I tailings; The technological conditions of the beneficiation operation are as follows: add the pulp regulator lime 500-1000g/t, the action time is 3-5min, the activator copper sulfate is 300-400g/t, the action time is 3-5min, the collector butyl xanthate 60- 100g/t, the action time is 2~3min, foaming agent 2# oil 10~20g/t, the action time is 1~2min;
(6)将步骤(5)得到的锌硫混合粗选Ⅰ尾矿进行锌硫第二次混合粗选,得到锌硫混合粗精矿Ⅱ和锌硫混合粗选Ⅱ尾矿;其中锌硫第二次混合粗选作业工艺条件为:加入活化剂硫酸铜50~80g/t,作用时间为3~5min,捕收剂丁基黄药20~30g/t,作用时间为2~3min;(6) Carry out the zinc-sulfur mixed roughing I tailings obtained in step (5) for the second mixed roughing of zinc and sulfur to obtain zinc-sulfur mixed rough concentrate II and zinc-sulfur mixed roughing II tailings; wherein the zinc-sulfur first The technical conditions of the secondary mixing and roughing operation are as follows: activator copper sulfate 50-80g/t is added, and the action time is 3-5 minutes; collector butyl xanthate is 20-30g/t, and the action time is 2-3 minutes;
(7)将步骤(6)得到的锌硫混合粗选Ⅱ尾矿进行锌硫混合扫选一次,得到锌硫混合浮选尾矿和锌硫混合扫选中矿,锌硫混合扫选中矿顺序返回到上一层作业;其中锌硫混合扫选作业工艺条件为:加入捕收剂丁基黄药20~30g/t,作用时间为2~3min;(7) The zinc-sulfur mixed roughing II tailings obtained in step (6) are subjected to zinc-sulfur mixed scavenging for one time to obtain zinc-sulfur mixed flotation tailings and zinc-sulfur mixed scavenging ore, and the zinc-sulfur mixed scavenging ore is returned in sequence Go to the upper layer for operation; the technological conditions for the zinc-sulfur mixed sweeping operation are: add collector butyl xanthate 20-30g/t, and the action time is 2-3min;
(8)将步骤(5)和将步骤(6)分别得到的锌硫混合粗精矿Ⅰ和锌硫混合粗精矿Ⅱ合并进行锌硫分离粗选,得到锌粗精矿和锌粗选尾矿;其中锌硫分离粗选作业工艺条件为:加入抑制剂石灰3000~5000g/t,作用时间为3~5min,活化剂硫酸铜30~50g/t,作用时间为3~5min,捕收剂丁基黄药10~20g/t,作用时间为2~3min;(8) Combine the zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rough concentrate II obtained in step (5) and step (6) respectively and carry out zinc-sulfur separation and roughing to obtain zinc rough concentrate and zinc roughing tailings ore; among them, zinc-sulfur separation and roughing process conditions are as follows: add inhibitor lime 3000-5000g/t, action time is 3-5min, activator copper sulfate 30-50g/t, action time is 3-5min, collector Butyl xanthate 10~20g/t, the action time is 2~3min;
(9)将步骤(8)得到的锌粗选尾矿进行一次锌扫选,得到硫精矿和一个锌扫选中矿,锌扫选中矿顺序返回到上一层作业;其中锌扫选工艺条件为:锌扫选作业加入捕收剂丁基黄药10~15g/t,作用时间为2~3min;(9) Zinc roughing tailings obtained in step (8) are carried out a zinc sweep to obtain sulfur concentrate and a zinc sweep, and the sequence of zinc sweep is returned to the previous layer of operation; wherein the zinc sweep process conditions For: adding collector butyl xanthate 10~15g/t to zinc sweeping operation, the action time is 2~3min;
(10)将步骤(9)得到的锌粗精矿进行锌精选二次,得到锌精矿和二个锌精选中矿,二个锌精选中矿分别顺序返回到上一层作业;其中锌精选二次作业工艺条件为:锌精Ⅰ作业加入抑制剂石灰1000~2000g/t,作用时间为3~5min;锌精Ⅱ作业加入抑制剂石灰500~1000g/t,作用时间为3~5min。(10) Carry out zinc concentration secondary to the zinc rough concentrate that step (9) obtains, obtain zinc concentrate and two zinc concentration medium ores, and two zinc concentration medium ores return to the operation of upper layer respectively sequentially; Among them, the process conditions for the secondary operation of zinc refining are: adding inhibitor lime 1000-2000g/t in zinc refining Ⅰ operation, and the action time is 3-5min; ~5min.
进一步地,在步骤(2)、(4)中,所述锌硫抑制剂XKY012是以硫酸锌、亚硫酸钠、羟乙基纤维素为原料,按质量比1.0:(0.5~1.0):(0.1~0.2)的配比混合,在常压下以烧杯作为容器,60℃以上的热水为溶剂,以磁力搅拌器搅拌20~30分钟制取得到。Further, in steps (2) and (4), the zinc-sulfur inhibitor XKY012 is made of zinc sulfate, sodium sulfite, and hydroxyethyl cellulose, and the mass ratio is 1.0:(0.5~1.0):(0.1~ The ratio of 0.2) is mixed under normal pressure with a beaker as a container, hot water above 60°C as a solvent, and stirred with a magnetic stirrer for 20 to 30 minutes to obtain it.
进一步地,在步骤(2)、(3)中,所述捕收剂XK712是以二烃基二硫代磷酸盐、二苯胺基二硫代磷酸铵、二乙基二硫代氨基甲酸钠、异戊基黄药为原料,按质量比4:3:2:1的配比混合,在常温常压下以烧杯作为容器,10%浓度碳酸钠溶液为溶剂,以磁力搅拌器搅拌40~60分钟制取得到。Further, in steps (2), (3), the collector XK712 is based on dihydrocarbyl dithiophosphate, dianilino ammonium dithiophosphate, sodium diethyldithiocarbamate, isoamyl Base xanthate as raw material, mixed according to the mass ratio of 4:3:2:1, under normal temperature and pressure, use a beaker as a container, 10% sodium carbonate solution as a solvent, and stir with a magnetic stirrer for 40 to 60 minutes. get it.
优选地,在步骤(2)中,所述浮选浓度为45~50%。Preferably, in step (2), the flotation concentration is 45-50%.
进一步地,在步骤(5)中,锌硫第一次混合粗选作业加入矿浆调整剂石灰500~1000g/t,调整矿浆pH值为8.5~9.5。Further, in step (5), 500-1000 g/t of lime, a slurry regulator, is added to the zinc-sulfur first mixed roughing operation to adjust the pH value of the slurry to 8.5-9.5.
进一步地,所述捕收剂XK712兼作为起泡剂,同时具有起泡剂的功能。Further, the collector XK712 doubles as a foaming agent and has the function of a foaming agent.
本发明的主要优点在于,第一,针对高硫含伴生金银的铅锌硫化矿石,传统选矿工艺选别难度大、分选效率低、选矿综合指标差、伴生金银回收率低,石灰用量、矿浆pH值高、选矿成本及能耗高、浮选过程不稳定等突出问题。本发明创造性提出铅及伴生金银浮选在高浓度、自然pH介质环境下进行,高浓度浮选环境打破了常规浮选浓度(30~35%)条件下捕收剂用量大,生产处理量小的弊端,高浓度浮选工艺增加了矿浆中药剂浓度,强化了药剂与矿物的作用能力,并有效强化了气泡对有用疏水颗粒的拱抬效应,缩短了有用矿物矿化气泡浮升距离,减小了颗粒(特别是粗颗粒)从气泡上脱落的概率;自然pH介质矿浆条件下优先浮铅,有效克服了高碱环境下浮选泡沫发粘、泡沫流动性差、铅捕收剂种类单一及用量大等问题,同时自然pH矿浆环境为伴生金银矿物的浮选回收创造了良好的条件。The main advantages of the present invention are that, firstly, for high-sulfur lead-zinc sulfide ores containing associated gold and silver, the traditional mineral processing technology is difficult to sort, the sorting efficiency is low, the comprehensive index of mineral processing is poor, the recovery rate of associated gold and silver is low, and the amount of lime used , high pH value of pulp, high cost and energy consumption of beneficiation, unstable flotation process and other prominent problems. The invention creatively proposes that the flotation of lead and associated gold and silver is carried out in a high-concentration, natural pH medium environment, and the high-concentration flotation environment breaks the conventional flotation concentration (30-35%) condition where the amount of collector is large and the production capacity is large. Minor disadvantages, high-concentration flotation process increases the concentration of reagents in the slurry, strengthens the interaction between reagents and minerals, and effectively strengthens the arching effect of air bubbles on useful hydrophobic particles, shortening the buoyancy distance of useful mineral mineralized bubbles. Reduces the probability of particles (especially coarse particles) falling off from the air bubbles; under the condition of natural pH medium ore slurry, lead is preferentially floated, effectively overcoming the stickiness of flotation foam, poor foam fluidity and single type of lead collector in high alkali environment At the same time, the natural pH slurry environment creates good conditions for the flotation recovery of associated gold and silver minerals.
第二,对于高硫铅锌矿,铅浮选过程锌、硫容易上浮进入铅精矿中,导致铅精矿品位不高,含杂严重,为此,针对性地研制了锌、硫矿物高效抑制剂XKY012,实现优先浮铅工艺下对锌、硫矿物的深度抑制,提高铅精矿质量,有效降低杂质含量。Second, for high-sulfur lead-zinc mines, zinc and sulfur are easy to float into the lead concentrate during the lead flotation process, resulting in low-grade lead concentrate and serious impurities. Inhibitor XKY012 realizes the deep suppression of zinc and sulfur minerals under the priority floating process, improves the quality of lead concentrate, and effectively reduces the impurity content.
第三,发明铅金银高效选择性捕收剂,有效强化细粒铅矿物及伴生金银矿物的高效上浮,特别是提高金的部分载体矿物黄铁矿的疏水能力,提高主金属铅及伴生金银矿物的选矿回收率。Third, the invention of high-efficiency selective collectors for lead, gold and silver can effectively strengthen the high-efficiency flotation of fine-grained lead minerals and associated gold and silver minerals. The beneficiation recovery rate of gold and silver minerals.
与现有技术相比,本发明的优点在于:针对高硫含伴生金银的铅锌硫化矿,创造性的提出了高浓度、自然pH环境下优先浮铅,解决了选矿流程长、药剂用量大、能耗高、浮选过程不稳定、金银对矿浆pH敏感的问题;其次,发明了高效锌硫矿物抑制剂XKY012和铅金银高效选择性捕收剂XK712,实现了对锌硫矿物的深度抑制,改善了铅精矿质量,并降低了精矿中杂质含量,还实现了捕收剂、抑制剂与高浓度、自然pH矿浆环境的良好匹配,为铅-锌、铅-硫矿物的浮选分离创造了良好条件,提高了铅及伴生金银回收率,实现了铅锌硫矿物的高效分选及伴生金银矿物的综合回收,同时该技术还具有节能、环保、流程短、流程稳定等显著优势。Compared with the prior art, the present invention has the advantages of: for high-sulfur lead-zinc sulfide ores containing associated gold and silver, it creatively proposes high-concentration and preferential floating lead in natural pH environment, which solves the problem of long beneficiation process and large dosage of chemicals. , high energy consumption, unstable flotation process, gold and silver are sensitive to the pH of the ore pulp; secondly, the high-efficiency zinc-sulfur mineral inhibitor XKY012 and the high-efficiency lead-gold-silver selective collector XK712 were invented to realize the protection of zinc-sulfur minerals Deep suppression improves the quality of lead concentrate and reduces the impurity content in the concentrate. It also realizes a good match between collectors and inhibitors and high-concentration and natural pH slurry environment. It is the lead-zinc and lead-sulfur minerals Flotation separation creates good conditions, improves the recovery rate of lead and associated gold and silver, and realizes the efficient separation of lead, zinc and sulfur minerals and the comprehensive recovery of associated gold and silver minerals. Stability and other significant advantages.
附图说明Description of drawings
图1为本发明工艺流程图。Fig. 1 is process flow chart of the present invention.
具体实施方式Detailed ways
下面结合图1通过具体实施例对本发明做进一步说明:The present invention will be further described below in conjunction with Fig. 1 by specific embodiment:
实施例1,一、高效锌硫矿物抑制剂XKY012的制备Embodiment 1, one, the preparation of efficient zinc-sulfur mineral inhibitor XKY012
将100克硫酸锌、50克亚硫酸钠、10克羟乙基纤维素混合,在常压下以烧杯做容器,60℃以上的热水为溶剂,以磁力搅拌器搅拌20~30分钟得到XKY012溶液。Mix 100 grams of zinc sulfate, 50 grams of sodium sulfite, and 10 grams of hydroxyethyl cellulose, use a beaker as a container under normal pressure, use hot water above 60°C as a solvent, and stir with a magnetic stirrer for 20 to 30 minutes to obtain XKY012 solution.
二、高效铅金银矿物捕收起泡剂XK712的制备2. Preparation of high-efficiency lead, gold and silver mineral collection foaming agent XK712
(1)将100克无水碳酸钠、1000克清水,在常温常压下以烧杯做容器,以磁力搅拌器搅拌5~10分钟得到10%浓度碳酸钠溶液。(1) With 100 grams of anhydrous sodium carbonate, 1000 grams of clear water, under normal temperature and pressure, use a beaker as a container, and stir with a magnetic stirrer for 5 to 10 minutes to obtain a 10% concentration sodium carbonate solution.
(2),将40克二烃基二硫代磷酸盐、30克二苯胺基二硫代磷酸铵、20克二乙基二硫代氨基甲酸钠、10克异戊基黄药混合,在常压下以烧杯做容器,上述10%浓度碳酸钠为溶剂,以磁力搅拌器搅拌40~60分钟得到XK712溶液。(2), 40 grams of dihydrocarbyl dithiophosphate, 30 grams of dianilino ammonium dithiophosphate, 20 grams of sodium diethyldithiocarbamate, and 10 grams of isoamyl xanthate were mixed, and the A beaker is used as a container, the above-mentioned 10% sodium carbonate is used as a solvent, and the XK712 solution is obtained by stirring with a magnetic stirrer for 40-60 minutes.
三、选矿过程3. Mining process
选别的矿石为某含方铅矿、铁闪锌矿、黄铁矿,并伴生金银的铅锌硫化矿石,其中金主要为黄铁矿包裹金及少量自然金,银主要为硫化银和自然银;原矿含铅2.94%、含锌4.03%、含硫19.16%、含金0.37g/t、含银42.18g/t;主要的金属矿物是黄铁矿,铁闪锌矿、方铅矿,其次为磁铁矿、菱锰矿、胶状黄铁矿,少量黄铜矿、菱锌矿等;主要的脉石矿物是石英、方解石、透辉石、绿泥石等。采用传统的铅锌优先浮选工艺处理该矿石,获得的铅精矿含铅72.54%、含锌3.68%、含金2.56g/t、含银867.65g/t,铅回收率91.34%、金回收率26.48%、银回收率78.71%;获得的锌精矿含锌46.24%、锌回收率92.86%;获得的硫精矿含硫40.52%、硫回收率70.43%。The selected ore is a lead-zinc sulfide ore containing galena, sphalerite, pyrite, and associated gold and silver. The gold is mainly pyrite-wrapped gold and a small amount of natural gold, and the silver is mainly silver sulfide and Natural silver; raw ore contains 2.94% lead, 4.03% zinc, 19.16% sulfur, 0.37g/t gold and 42.18g/t silver; the main metal minerals are pyrite, sphalerite and galena , followed by magnetite, rhodochrosite, colloidal pyrite, a small amount of chalcopyrite, smithsonite, etc.; the main gangue minerals are quartz, calcite, diopside, chlorite, etc. The ore is treated with the traditional lead-zinc priority flotation process, and the obtained lead concentrate contains 72.54% lead, 3.68% zinc, 2.56g/t gold, and 867.65g/t silver, with a lead recovery rate of 91.34% and gold recovery The obtained zinc concentrate contains 46.24% zinc and the zinc recovery rate is 92.86%; the obtained sulfur concentrate contains 40.52% sulfur and the sulfur recovery rate is 70.43%.
选别步骤为:The selection steps are:
(1)将矿石磨细,得到磨矿矿浆;其中原矿磨细的磨矿细度为-0.074mm粒度级别含量占原矿总重量的60%;(1) Grinding the ore to obtain a grinding slurry; wherein the grinding fineness of the raw ore grinding is -0.074mm, and the particle size level content accounts for 60% of the total weight of the raw ore;
(2)将步骤(1)得到的磨矿矿浆调整浮选浓度45%后进行铅粗选,得到铅粗精矿和铅粗选尾矿;其中铅粗选作业工艺条件为:先加入锌硫抑制剂XKY012为1000g/t,作用时间为5min,再加入捕收剂XK712为80g/t,作用时间为3min;(2) carry out lead roughing after adjusting the flotation concentration 45% of the grinding ore slurry obtained in step (1), obtain lead coarse concentrate and lead roughing tailings; wherein the lead roughing operation process condition is: first add zinc sulfur Inhibitor XKY012 is 1000g/t, and the action time is 5min, and the collector XK712 is added at 80g/t, and the action time is 3min;
(3)将步骤(2)得到的铅粗选尾矿进行铅扫选两次,即铅扫选Ⅰ和铅扫选Ⅱ,得到铅扫选尾矿和两个铅扫选中矿,两个铅扫选中矿分别顺序返回到上一层作业;其中铅扫选两次作业工艺条件为:铅扫选Ⅰ作业加入捕收剂XK712为30g/t,作用时间为3min;铅扫选Ⅱ作业加入捕收剂XK712为20g/t,作用时间为3min;(3) The lead roughing tailings obtained in step (2) are subjected to lead scavenging twice, i.e. lead scavenging I and lead scavenging II, to obtain lead scavenging tailings and two lead scavenging ores, two lead scavenging Sweeping and mining return to the previous layer of operations in sequence; the process conditions of the two operations of lead sweeping are as follows: lead sweeping I operation adds collector XK712 at 30g/t, and the action time is 3min; lead sweeping II operation adds capture The receiving agent XK712 is 20g/t, and the action time is 3min;
(4)将步骤(2)得到的铅粗精矿进行铅精选二次,即铅精Ⅰ和铅精Ⅱ,得到铅精矿和二个铅精选中矿,二个铅精选中矿分别顺序返回到上一层作业;铅精选二次作业工艺条件为:铅精Ⅰ作业加入锌硫抑制剂XKY012为500g/t,作用时间为5min,铅精Ⅱ作业加入锌硫抑制剂XKY012为300g/t,作用时间为5min;(4) Carry out the lead concentrate that step (2) obtains to lead beneficiation twice, i.e. lead concentrate I and lead concentrate II, obtain lead concentrate and two lead concentrate middle ores, two lead concentrate middle ore Return to the previous operation in sequence; the process conditions for the secondary operation of lead selection are as follows: 500g/t of zinc-sulfur inhibitor XKY012 is added to the lead fine Ⅰ operation, and the action time is 5min; the zinc-sulfur inhibitor XKY012 is added to the lead fine Ⅱ operation 300g/t, the action time is 5min;
(5)将步骤(3)得到的铅扫选尾矿进行锌硫第一次混合粗选,得到锌硫混合粗精矿Ⅰ和锌硫混合粗选Ⅰ尾矿;锌硫第一次混合粗选作业工艺条件为:加入矿浆调整剂石灰500g/t,作用时间为5min,活化剂硫酸铜400g/t,作用时间为5min,捕收剂丁基黄药100g/t,作用时间为3min,起泡剂2#油20g/t,作用时间为2min;(5) The lead scavenging tailings obtained in step (3) are subjected to zinc-sulfur mixed roughing for the first time to obtain zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rougher I tailings; The technological conditions of the beneficiation operation are as follows: add 500g/t of pulp regulator lime, and the action time is 5min; Foaming agent 2# oil 20g/t, action time is 2min;
(6)将步骤(5)得到的锌硫混合粗选Ⅰ尾矿进行锌硫第二次混合粗选,得到锌硫混合粗精矿Ⅱ和锌硫混合粗选Ⅱ尾矿;其中锌硫第二次混合粗选作业工艺条件为:加入活化剂硫酸铜80g/t,作用时间为5min,捕收剂丁基黄药30g/t,作用时间为3min;(6) Carry out the zinc-sulfur mixed roughing I tailings obtained in step (5) for the second mixed roughing of zinc and sulfur to obtain zinc-sulfur mixed rough concentrate II and zinc-sulfur mixed roughing II tailings; wherein the zinc-sulfur first The technical conditions of the secondary mixing and roughing operation are as follows: activator copper sulfate 80g/t is added, and the action time is 5min; collector butyl xanthate is 30g/t, and the action time is 3min;
(7)将步骤(6)得到的锌硫混合粗选Ⅱ尾矿进行锌硫混合扫选一次,得到锌硫混合浮选尾矿和锌硫混合扫选中矿,锌硫混合扫选中矿顺序返回到上一层作业;其中锌硫混合扫选作业工艺条件为:加入捕收剂丁基黄药30g/t,作用时间为3min;(7) The zinc-sulfur mixed roughing II tailings obtained in step (6) are subjected to zinc-sulfur mixed scavenging for one time to obtain zinc-sulfur mixed flotation tailings and zinc-sulfur mixed scavenging ore, and the zinc-sulfur mixed scavenging ore is returned in sequence Go to the upper layer for operation; the zinc-sulfur mixed sweeping operation process conditions are: add collector butyl xanthate 30g/t, and the action time is 3min;
(8)将步骤(5)和将步骤(6)分别得到的锌硫混合粗精矿Ⅰ和锌硫混合粗精矿Ⅱ合并进行锌硫分离粗选,得到锌粗精矿和锌粗选尾矿;其中锌硫分离粗选作业工艺条件为:加入抑制剂石灰3000g/t,作用时间为5min,活化剂硫酸铜50g/t,作用时间为5min,捕收剂丁基黄药20g/t,作用时间为3min;(8) Combine the zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rough concentrate II obtained in step (5) and step (6) respectively and carry out zinc-sulfur separation and roughing to obtain zinc rough concentrate and zinc roughing tailings ore; among them, zinc-sulfur separation and roughing process conditions are as follows: add inhibitor lime 3000g/t, action time is 5min, activator copper sulfate 50g/t, action time is 5min, collector butyl xanthate 20g/t, The action time is 3 minutes;
(9)将步骤(8)得到的锌粗选尾矿进行一次锌扫选,得到硫精矿和一个锌扫选中矿,锌扫选中矿顺序返回到上一层作业;其中锌扫选工艺条件为:锌扫选作业加入捕收剂丁基黄药15g/t,作用时间为3min;(9) Zinc roughing tailings obtained in step (8) are carried out a zinc sweep to obtain sulfur concentrate and a zinc sweep, and the sequence of zinc sweep is returned to the previous layer of operation; wherein the zinc sweep process conditions For: adding collector butyl xanthate 15g/t to zinc sweeping operation, the action time is 3min;
(10)将步骤(9)得到的锌粗精矿进行锌精选二次,得到锌精矿和二个锌精选中矿,二个锌精选中矿分别顺序返回到上一层作业;其中锌精选二次作业工艺条件为:锌精Ⅰ作业加入抑制剂石灰2000g/t,作用时间为5min;锌精Ⅱ作业加入抑制剂石灰1000g/t,作用时间为5min。(10) Carry out zinc concentration secondary to the zinc rough concentrate that step (9) obtains, obtain zinc concentrate and two zinc concentration medium ores, and two zinc concentration medium ores return to the operation of upper layer respectively sequentially; Among them, the process conditions of the secondary operation of zinc concentration are: adding 2000g/t of inhibitor lime to the zinc concentration I operation, and the action time is 5 minutes; adding 1000g/t inhibitor lime to the zinc concentration II operation, and the action time is 5 minutes.
选矿结果如下表1所示:The beneficiation results are shown in Table 1 below:
表1浮选指标(%)Table 1 Flotation index (%)
续:continued:
实施例2,一、高效锌硫矿物抑制剂XKY012的制备Embodiment 2, one, the preparation of efficient zinc-sulfur mineral inhibitor XKY012
将50克硫酸锌、50克亚硫酸钠、10克羟乙基纤维素混合,在常温常压下以烧杯做容器,60℃以上的热水为溶剂,磁力搅拌器搅拌20~30分钟得到XKY012溶液。Mix 50 grams of zinc sulfate, 50 grams of sodium sulfite, and 10 grams of hydroxyethyl cellulose, use a beaker as a container at normal temperature and pressure, use hot water above 60°C as a solvent, and stir with a magnetic stirrer for 20 to 30 minutes to obtain XKY012 solution.
二、高效铅金银矿物捕收起泡剂XK712的制备2. Preparation of high-efficiency lead, gold and silver mineral collection foaming agent XK712
(1)将100克无水碳酸钠、1000克清水,在常温常压下以烧杯做容器,以磁力搅拌器搅拌5~10分钟得到10%浓度碳酸钠溶液。(1) With 100 grams of anhydrous sodium carbonate, 1000 grams of clear water, under normal temperature and pressure, use a beaker as a container, and stir with a magnetic stirrer for 5 to 10 minutes to obtain a 10% concentration sodium carbonate solution.
(2),将40克二烃基二硫代磷酸盐、30克二苯胺基二硫代磷酸铵、20克二乙基二硫代氨基甲酸钠、10克异戊基黄药混合,在常压下以烧杯做容器,上述10%浓度碳酸钠为溶剂,以磁力搅拌器搅拌40~60分钟得到XK712溶液。(2), 40 grams of dihydrocarbyl dithiophosphate, 30 grams of dianilino ammonium dithiophosphate, 20 grams of sodium diethyldithiocarbamate, and 10 grams of isoamyl xanthate were mixed, and the A beaker is used as a container, the above-mentioned 10% sodium carbonate is used as a solvent, and the XK712 solution is obtained by stirring with a magnetic stirrer for 40-60 minutes.
三、选矿过程3. Mining process
选别的矿石为含黄铁矿、方铅矿、闪锌矿并伴生银的高硫复杂低品位铅锌硫化矿石,银矿物主要以伴生银的形式伴生于方铅矿、闪锌矿、黄铁矿和黄铜矿等矿物中,嵌布特征极为复杂;原矿含铅1.30%、含锌3.15%、含硫22.49%、含银79.65g/t;主要金属矿物有方铅矿、闪锌矿、黄铁矿、黄铜矿、银黝铜矿等,脉石矿物主要为石英、绿泥石、绢云母、角闪石、方解石、长石等。采用传统的铅锌优先浮选工艺处理该矿石,获得的铅精矿含铅45.28%、含锌4.52%、含银1620g/t,铅回收率83.23%、银回收率50.60%;获得的锌精矿含锌50.13%、锌回收率84.77%;获得的硫精矿含硫42.37%、硫回收率67.38%。The selected ores are high-sulfur complex low-grade lead-zinc sulfide ores containing pyrite, galena, sphalerite and associated silver. In minerals such as iron ore and chalcopyrite, the distribution characteristics are extremely complex; the raw ore contains 1.30% lead, 3.15% zinc, 22.49% sulfur, and 79.65g/t silver; the main metal minerals are galena and sphalerite , pyrite, chalcopyrite, silver tetrahedrite, etc., gangue minerals are mainly quartz, chlorite, sericite, hornblende, calcite, feldspar, etc. The ore was processed by the traditional lead-zinc priority flotation process, and the obtained lead concentrate contained 45.28% lead, 4.52% zinc, and 1620g/t silver, with a lead recovery rate of 83.23% and a silver recovery rate of 50.60%; the obtained zinc concentrate The ore contains 50.13% zinc and the zinc recovery rate is 84.77%; the obtained sulfur concentrate contains 42.37% sulfur and the sulfur recovery rate is 67.38%.
选别步骤为:The selection steps are:
(1)将矿石磨细,得到磨矿矿浆;其中原矿磨细的磨矿细度为-0.074mm粒度级别含量占原矿总重量的80%;(1) Grinding the ore to obtain a grinding slurry; wherein the grinding fineness of the raw ore grinding is -0.074mm, and the particle size level content accounts for 80% of the total weight of the raw ore;
(2)将步骤(1)得到的磨矿矿浆调整好浮选浓度为50%后进行铅粗选,得到铅粗精矿和铅粗选尾矿;其中铅粗选作业工艺条件为:先加入锌硫抑制剂XKY012为500g/t,作用时间为3min,再加入捕收剂XK712为50g/t,作用时间为2min;(2) carry out lead roughing after adjusting the flotation concentration of the grinding slurry obtained in step (1) to be 50%, to obtain lead rough concentrate and lead roughing tailings; wherein the lead roughing operation process conditions are: first add The zinc-sulfur inhibitor XKY012 is 500g/t, and the action time is 3min, and the collector XK712 is added at 50g/t, and the action time is 2min;
(3)将步骤(2)得到的铅粗选尾矿进行铅扫选两次,即铅扫选Ⅰ和铅扫选Ⅱ,得到铅扫选尾矿和两个铅扫选中矿,两个铅扫选中矿分别顺序返回到上一层作业;其中铅扫选两次作业工艺条件为:铅扫选Ⅰ作业加入捕收剂XK712为20g/t,作用时间为2min;铅扫选Ⅱ作业加入捕收剂XK712为10g/t,作用时间为2min;(3) The lead roughing tailings obtained in step (2) are subjected to lead scavenging twice, i.e. lead scavenging I and lead scavenging II, to obtain lead scavenging tailings and two lead scavenging ores, two lead scavenging Sweeping and mining returns to the previous layer in sequence; the process conditions for the two operations of lead sweeping are as follows: lead sweeping I operation adds collector XK712 at 20g/t, and the action time is 2min; lead sweeping II operation adds capture The receiving agent XK712 is 10g/t, and the action time is 2min;
(4)将步骤(2)得到的铅粗精矿进行铅精选二次,即铅精Ⅰ和铅精Ⅱ,得到铅精矿和二个铅精选中矿,二个铅精选中矿分别顺序返回到上一层作业;铅精选二次作业工艺条件为:铅精Ⅰ作业加入锌硫抑制剂XKY012为300g/t,作用时间为3min,铅精Ⅱ作业加入锌硫抑制剂XKY012为200g/t,作用时间为3min;(4) Carry out the lead concentrate that step (2) obtains to lead beneficiation twice, i.e. lead concentrate I and lead concentrate II, obtain lead concentrate and two lead concentrate middle ores, two lead concentrate middle ore Respectively return to the previous layer of operation in sequence; the process conditions of the secondary operation of lead selection are as follows: the zinc sulfur inhibitor XKY012 is added to the lead fine Ⅰ operation at 300g/t, and the action time is 3min; the lead fine Ⅱ operation adds the zinc sulfur inhibitor XKY012 to 200g/t, the action time is 3min;
(5)将步骤(3)得到的铅扫选尾矿进行锌硫第一次混合粗选,得到锌硫混合粗精矿Ⅰ和锌硫混合粗选Ⅰ尾矿;锌硫第一次混合粗选作业工艺条件为:加入矿浆调整剂石灰1000g/t,作用时间为3min,活化剂硫酸铜300g/t,作用时间为3min,捕收剂丁基黄药60g/t,作用时间为2min,起泡剂2#油10g/t,作用时间为1min;(5) The lead scavenging tailings obtained in step (3) are subjected to zinc-sulfur mixed roughing for the first time to obtain zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rougher I tailings; The technological conditions of the beneficiation operation are as follows: add the slurry regulator lime 1000g/t, the action time is 3min, the activator copper sulfate is 300g/t, the action time is 3min, the collector butyl xanthate is 60g/t, the action time is 2min, Foaming agent 2# oil 10g/t, action time is 1min;
(6)将步骤(5)得到的锌硫混合粗选Ⅰ尾矿进行锌硫第二次混合粗选,得到锌硫混合粗精矿Ⅱ和锌硫混合粗选Ⅱ尾矿;其中锌硫第二次混合粗选作业工艺条件为:加入活化剂硫酸铜50g/t,作用时间为3min,捕收剂丁基黄药20g/t,作用时间为2min;(6) Carry out the zinc-sulfur mixed roughing I tailings obtained in step (5) for the second mixed roughing of zinc and sulfur to obtain zinc-sulfur mixed rough concentrate II and zinc-sulfur mixed roughing II tailings; wherein the zinc-sulfur first The technical conditions of the secondary mixing and roughing operation are as follows: activator copper sulfate 50g/t is added, and the action time is 3min; collector butyl xanthate is 20g/t, and the action time is 2min;
(7)将步骤(6)得到的锌硫混合粗选Ⅱ尾矿进行锌硫混合扫选一次,得到锌硫混合浮选尾矿和锌硫混合扫选中矿,锌硫混合扫选中矿顺序返回到上一层作业;其中锌硫混合扫选作业工艺条件为:加入捕收剂丁基黄药20g/t,作用时间为2min;(7) The zinc-sulfur mixed roughing II tailings obtained in step (6) are subjected to zinc-sulfur mixed scavenging for one time to obtain zinc-sulfur mixed flotation tailings and zinc-sulfur mixed scavenging ore, and the zinc-sulfur mixed scavenging ore is returned in sequence Go to the upper layer for operation; the technological conditions for the zinc-sulfur mixed sweeping operation are: add collector butyl xanthate 20g/t, and the action time is 2min;
(8)将步骤(5)和将步骤(6)分别得到的锌硫混合粗精矿Ⅰ和锌硫混合粗精矿Ⅱ合并进行锌硫分离粗选,得到锌粗精矿和锌粗选尾矿;其中锌硫分离粗选作业工艺条件为:加入抑制剂石灰5000g/t,作用时间为3min,活化剂硫酸铜30g/t,作用时间为3min,捕收剂丁基黄药10g/t,作用时间为2min;(8) Combine the zinc-sulfur mixed rough concentrate I and zinc-sulfur mixed rough concentrate II obtained in step (5) and step (6) respectively and carry out zinc-sulfur separation and roughing to obtain zinc rough concentrate and zinc roughing tailings ore; among them, zinc-sulfur separation and roughing process conditions are as follows: add inhibitor lime 5000g/t, action time is 3min, activator copper sulfate 30g/t, action time is 3min, collector butyl xanthate 10g/t, The action time is 2 minutes;
(9)将步骤(8)得到的锌粗选尾矿进行一次锌扫选,得到硫精矿和一个锌扫选中矿,锌扫选中矿顺序返回到上一层作业;其中锌扫选工艺条件为:锌扫选作业加入捕收剂丁基黄药10g/t,作用时间为2min;(9) Zinc roughing tailings obtained in step (8) are carried out a zinc sweep to obtain sulfur concentrate and a zinc sweep, and the sequence of zinc sweep is returned to the previous layer of operation; wherein the zinc sweep process conditions For: adding collector butyl xanthate 10g/t to zinc sweeping operation, the action time is 2min;
(10)将步骤(9)得到的锌粗精矿进行锌精选二次,得到锌精矿和二个锌精选中矿,二个锌精选中矿分别顺序返回到上一层作业;其中锌精选二次作业工艺条件为:锌精Ⅰ作业加入抑制剂石灰1000g/t,作用时间为3min;锌精Ⅱ作业加入抑制剂石灰500g/t,作用时间为3min。(10) Carry out zinc concentration secondary to the zinc rough concentrate that step (9) obtains, obtain zinc concentrate and two zinc concentration medium ores, and two zinc concentration medium ores return to the operation of upper layer respectively sequentially; Among them, the process conditions of the secondary operation of zinc concentration are: 1000g/t of inhibitor lime is added to the zinc concentration Ⅰ operation, and the action time is 3 minutes; 500g/t of inhibitor lime is added to the zinc concentration Ⅱ operation, and the action time is 3 minutes.
选矿结果如下表2所示:The beneficiation results are shown in Table 2 below:
表2:浮选指标(%)Table 2: Flotation Index (%)
续:continued:
以上已将本发明做一详细说明,以上所述,仅为本发明之较佳实施例而已,当不能限定本发明实施范围,即凡依本申请范围所作均等变化与修饰,皆应仍属本发明涵盖范围内。The present invention has been described in detail above. The foregoing description is only a preferred embodiment of the present invention, and should not limit the implementation scope of the present invention. within the scope of the invention.
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Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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CN115945299B (en) * | 2022-12-13 | 2024-04-30 | 昆明理工大学 | A method for enhanced flotation of zinc sulfide ore based on copper-lead coupling activation |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1562492A (en) * | 2004-04-06 | 2005-01-12 | 南京栖霞山锌阳矿业有限公司 | Technique for fast selecting plumbum and zinc for sulphidic ore of plumbum-zinc |
CN1943870A (en) * | 2006-08-23 | 2007-04-11 | 青海西部矿业科技有限公司 | Process for increasing complicated sulfurized-lead-zinc ore dressing recovery rate |
CN101195110A (en) * | 2007-12-31 | 2008-06-11 | 南京银茂铅锌矿业有限公司 | High concentration energy-saving environment protection beneficiation method for plumbum and zincium sulfuration mine |
CN101417266A (en) * | 2008-11-19 | 2009-04-29 | 湖南有色金属股份有限公司黄沙坪矿业分公司 | New flotation technique of lead zinc sulphur ore |
-
2017
- 2017-12-12 CN CN201711313393.1A patent/CN107999267B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1562492A (en) * | 2004-04-06 | 2005-01-12 | 南京栖霞山锌阳矿业有限公司 | Technique for fast selecting plumbum and zinc for sulphidic ore of plumbum-zinc |
CN1943870A (en) * | 2006-08-23 | 2007-04-11 | 青海西部矿业科技有限公司 | Process for increasing complicated sulfurized-lead-zinc ore dressing recovery rate |
CN101195110A (en) * | 2007-12-31 | 2008-06-11 | 南京银茂铅锌矿业有限公司 | High concentration energy-saving environment protection beneficiation method for plumbum and zincium sulfuration mine |
CN101417266A (en) * | 2008-11-19 | 2009-04-29 | 湖南有色金属股份有限公司黄沙坪矿业分公司 | New flotation technique of lead zinc sulphur ore |
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