EP2470306B1 - Verfahren zur kontinuierlichen magnetischen erztrennung und/oder -aufbereitung sowie zugehörige anlage - Google Patents
Verfahren zur kontinuierlichen magnetischen erztrennung und/oder -aufbereitung sowie zugehörige anlage Download PDFInfo
- Publication number
- EP2470306B1 EP2470306B1 EP10720630.2A EP10720630A EP2470306B1 EP 2470306 B1 EP2470306 B1 EP 2470306B1 EP 10720630 A EP10720630 A EP 10720630A EP 2470306 B1 EP2470306 B1 EP 2470306B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pulp
- magnetisable
- recoverable
- particulate material
- magnetite
- 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.)
- Not-in-force
Links
- 238000000034 method Methods 0.000 title claims description 66
- 238000000926 separation method Methods 0.000 title claims description 17
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 claims description 40
- 239000000463 material Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 16
- 239000011435 rock Substances 0.000 claims description 11
- 239000002283 diesel fuel Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 238000007885 magnetic separation Methods 0.000 claims description 5
- 239000012991 xanthate Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 239000011236 particulate material Substances 0.000 claims 8
- 239000000725 suspension Substances 0.000 claims 2
- 238000005054 agglomeration Methods 0.000 claims 1
- 230000002776 aggregation Effects 0.000 claims 1
- -1 and the magnetisable Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- 239000006194 liquid suspension Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 239000002245 particle Substances 0.000 description 15
- 239000012141 concentrate Substances 0.000 description 9
- 230000002209 hydrophobic effect Effects 0.000 description 9
- 239000010949 copper Substances 0.000 description 7
- 229910001779 copper mineral Inorganic materials 0.000 description 7
- 238000001035 drying Methods 0.000 description 5
- 238000005188 flotation Methods 0.000 description 5
- 230000005021 gait Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 230000008021 deposition Effects 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 239000006148 magnetic separator Substances 0.000 description 3
- 238000005065 mining Methods 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 238000012958 reprocessing Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004890 Hydrophobing Agent Substances 0.000 description 1
- 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 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229910052948 bornite Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 229910052947 chalcocite Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- BUGICWZUDIWQRQ-UHFFFAOYSA-N copper iron sulfane Chemical compound S.[Fe].[Cu] BUGICWZUDIWQRQ-UHFFFAOYSA-N 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 230000005226 mechanical processes and functions Effects 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 210000002023 somite Anatomy 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C1/00—Magnetic separation
- B03C1/005—Pretreatment specially adapted for magnetic separation
- B03C1/015—Pretreatment specially adapted for magnetic separation by chemical treatment imparting magnetic properties to the material to be separated, e.g. roasting, reduction, oxidation
-
- 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
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C1/00—Magnetic separation
- B03C1/005—Pretreatment specially adapted for magnetic separation
- B03C1/01—Pretreatment specially adapted for magnetic separation by addition of magnetic adjuvants
-
- 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
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C2201/00—Details of magnetic or electrostatic separation
- B03C2201/18—Magnetic separation whereby the particles are suspended in a liquid
Definitions
- the invention relates to a method for continuous magnetic ore separation and / or treatment according to the preamble of claim 1. It should also be possible in particular a treatment of the substances used and a re-introduction into the process process.
- ore is understood to mean a metal-containing rock from which the metal-containing constituents are to be separated as valuable substances.
- the valuable substances are in particular sulfidic copper materials which are to be enriched, for example - but not exclusively - Cu 2 S.
- the Cu-free rock surrounding the material grains is referred to as matrix rock or gangue, in the professional world after grinding the rock also as tailing or hereinafter referred to as sand for short.
- Magnetically assisted ore deposition methods have also been proposed, but are discontinuous in the related art. By performing as a batch batch process, the yield and the associated efficiency is limited, which affects the cost. Other methods work continuously, such. B. drum, but have low mass flow rates because of the high mechanical complexity and maintenance requirements and are therefore not suitable for many of the mining operations used in mining.
- the new method described below can be used in addition to the magnetic ore deposition, where appropriate, for the treatment of water by means of the magnetic separation.
- the object of the present invention is an overall process for the continuous magnetic ore deposition and in particular for the subsequent reprocessing indicate the substances used.
- a suitable system is to be created, which can be realized on a large scale in practice.
- the invention thus relates to a continuous process for magnetic ore separation or treatment, including a reprocessing of the most important substances used. This results in a particularly environmentally friendly and economical overall process for the continuous separation of ores, in particular non-magnetic ores with the aid of magnetic particles, which can replace the conventional, complex flotation process as a whole.
- the new process has a lower energy requirement and a higher extraction yield than the known processes and can in particular separate ore particles in a further particle size range than is possible according to the prior art. It is advantageous that an entire system can be largely composed of already available technical devices or facilities.
- Magnetite Fe 3 O 4
- Magnetite is already hydrophobic in finely ground form, ie, it preferentially binds to hydrophobic particles in aqueous solutions.
- the magnetite to be used is further treated in finely ground form with a surface modifying agent which makes the surfaces of the particles much more hydrophobic, i. water repellent, power.
- Hydrophobic particles agglomerate in aqueous suspension to minimize interfacial water. This is exploited to the extent that the ore particles are also selectively hydrophobized, but the gangue remains hydrophilic; This results in larger agglomerates of Werterzpellen and magnetite, which are magnetizable as a whole because of Magnetitanteils.
- the magnetic properties of the magnetite are exploited by: can be separated from the nonmagnetic materials (gait) by means of defined magnetic fields or fields that can be activated by the magnetite with the value ore particles bound thereto.
- the following are examples of sulfidic copper minerals, the method can also be used for other sulfidic minerals such as molybdenum sulfide, zinc sulfide.
- the functional group of the hydrophobing agent for other minerals the method described here can also be used for minerals of other chemical composition.
- a major additive at the beginning of the process chain of the process is a long chain potassium or sodium alkylxanthate (hereinafter referred to simply as "xanthate”), an agent that is known to selectively adsorb to and render hydrophobic the surfaces of sulfidic copper minerals.
- xanthate usually consists of a carbon chain with typically 5 to 12 carbon atoms and a functional head group that selectively binds to the copper mineral. In the present case, this results in a hydrophobization of the value ore particles.
- the ore in finely ground form and water and diesel oil are used as input materials for the process described below.
- a mixture of the input materials takes place in a first process step.
- the ore stream which consists of the ground rock (ore), water and - depending on the application - different chemicals, mixed with the required already hydrophobized magnetite and the other water repellents, especially the xanthate.
- the ore stream has a solids content of about 40 to 70 percent by mass, making the stream pumpable and accordingly FIG. 2 can be passed by means of a pump 25 in a mixing vessel or stirred tank 26.
- the aim is that in an aqueous suspension (pulp), which in addition to the ore particles still contains the gangue, the Xanthat hydrophobized copper minerals, such as chalcocite (Cu 2 S), bornite (Cu 5 FeS 4 ) or chalcopyrite (CuFeS 2 ) with the hydrophobic magnetite (Fe 3 O 4 h ) agglomerates due to their water-repellent properties.
- This process step is referred to below as "load” process 2.
- the hydrophobizing agent is used for the hydrophobization of the valuable material contained in the ore stream.
- the ore stream, the hydrophobizing agent and the magnetite are mixed together ("load process").
- a mixing device or a stirred tank 26 is necessary, which must be carried out so that enough shear forces and residence time are available so that the hydrophobization reaction and the bringing together of magnetite and ore particles can take place.
- a possible embodiment is a stirred tank 26, in which such a stirrer is used, which has high shear forces.
- the chemicals and the magnetite are metered in the vicinity of the stirrer.
- Such a stirrer must also be capable of ensuring not only local but also global mixing. It can alternatively be used an additional mixer, which also circulates the fluid. This produces large particles (agglomerates), which consist of hydrophobized resin and hydrophobized magnetite.
- Box 3 is then followed by a separation of the ore into two streams, in particular the sulfidischen Werterzanmaschine the gait.
- this step in addition to the Stöffstrom "Tailing” (ie the largely freed from the Werterzan heating gait) of the recyclable material "raw concentrate” generated. While tailing, as in the flotation processes used today, can be disposed of directly, the raw concentrate must be further processed in order to recover in particular the magnetite used and to prepare the copper mineral fraction accordingly for the subsequent further processing steps.
- the magnetite stream of recycled magnetite obtained in this way is additionally supplemented with fresh, hydrophobized magnetite in order to supplement the substance losses that are unimaginable in the overall process.
- the other necessary chemicals are added in dissolved form.
- the chemicals are preferably added in dissolved form, because the metering and transport of liquids within the plant can be made more homogeneous, faster and more precise than the metering of solids.
- the separation of the copper sulfide-magnetite mixture In the lower part of the FIG. 1 is illustrated by the boxes 6 to 9, the separation of the copper sulfide-magnetite mixture.
- a non-polar liquid must be supplied to the mixture of sulphidic copper minerals, magnetite and gangue, as can be achieved, for example, by diesel oil.
- the box 6 includes the supply of diesel oil to the final product according to box 5 and a related mixture of both substances.
- the diesel oil on the one hand and the magnetite on the other hand are regenerated for further use. According to the dashed line with associated arrow, the magnetite, a part of the remaining in the raw concentrate gait, and diesel oil are returned to the input step.
- FIG. 2 The operation of the plant for carrying out the method is in FIG. 2 illustrated by the sequence of all devices / devices.
- Reference numeral 20 here denotes the container ("big bag") for the magnetite with a metering device 21.
- the magnetite is mixed in a stirring device 22 with water and recycled magnetite.
- the mixture passes via a metering pump 23 into a stirring device 26, wherein the mixture Xanthat is supplied via a second metering pump 24.
- the valuable materials in the form of the pulp are fed with ore via a further metering pump 25 to the stirring device 26.
- the pulp and the mixture with xanthate are mixed in the agitator 46.
- the stirring device 26 is designed as a reactor and in this the "load" process is performed.
- the magnetic separators 30, 40 operate on the same physical principles. They each have a metering pump 27 and 39 assigned, which ensures the transport of the pulp. The aim of the magnetic separators 30 and 40 is to win a concentrate with a higher proportion of copper.
- the latter intermediate product stream is subsequently passed with the aid of at least one metering pump 31 to a drying step.
- the drying can, if necessary, be carried out in two steps. In the first, indispensable step, most of the water is extracted by means of a mechanical process, in particular by centrifugal forces. Depending on the process, this water can be returned to the process, resulting in a largely closed water cycle with little impact on the environment. However, the separated water can also be fed back directly into the pulp preparation.
- One possible embodiment for the first dewatering step is the use of the decanter unit 32 according to FIG. 2 , This produces the already mentioned intermediate product stream which still has at most 10 to 30% by mass residual moisture content.
- This stream can, if necessary, for. B. be brought by means of a flexible screw conveyor 33 or a conveyor belt to a second drying step.
- This is, for example, a thermal dryer 34, which evaporates the remaining moisture.
- This dryer may e.g. operated by process steam or gas or oil burner. This creates steam that can be used elsewhere for preheating.
- the latter step may become superfluous depending on the application and process management.
- From the dryer comes a stream of solids with a residual moisture of less than 1%.
- This stream is cooled in a solid heat exchanger 36 and added, for example by means of a screw conveyor 37 to another stirred tank 38.
- the three process steps: coarse dehumidification-drying-heat dissipation are integrated in a single process unit, so that the number of apparatuses to be used in this step is reduced from three to one.
- the other chemicals in particular the non-polar liquid such as diesel are admixed to the solids flow. It is necessary to choose chemicals that neutralize the hydrophobic bond between the recyclable material and the magnetite, which is ideally met by diesel.
- the diesel stream that is mixed in each case contains the recycled diesel oil and a fresh portion of diesel oil, which is necessary to compensate for material losses in the overall process.
- the diesel content must be at least 40 percent by mass in order to make the mixture flowable and pumpable.
- the diesel-containing mixture is passed with the aid of at least one metering pump 39 to the subsequent separation step, in which the magnetite particles are separated from the ore.
- the "unload process” involves another magnetic separation.
- the magnetite is separated from the material flow, in order subsequently to be fed back to the "load process”.
- the one stream contains the valuable material (ore) and is dehumidified with the help of the decanter 44.
- another thermal dryer can be used. Thereafter, this mass flow is given by means of conveyors 44 in a stirred tank 46, mixed with water and output as a final product "concentrate" via a pump 47.
- the magnetite stream is also dehumidified by means of a decanter 42.
- additional thermal drying steps may be added.
- Recovered diesel oil in turn is fed to the actual process, e.g. via the tank for diesel oil 50.
- the dry magnetite can be transported via a transport screw 43 to the stirring device 22. There, the recycled magnetite is mixed with fresh magnetite and water and returned to the material flow.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Paper (AREA)
- Lubricants (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL10720630T PL2470306T3 (pl) | 2009-08-24 | 2010-05-31 | Sposób ciągłego magnetycznego rozdzielania i/lub wzbogacania rudy oraz przynależna instalacja |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102009038666A DE102009038666A1 (de) | 2009-08-24 | 2009-08-24 | Verfahren zur kontinuierlichen magnetischen Erztrennung und/oder -aufbereitung sowie zugehörige Anlage |
PCT/EP2010/057542 WO2011023426A1 (de) | 2009-08-24 | 2010-05-31 | Verfahren zur kontinuierlichen magnetischen erztrennung und/oder -aufbereitung sowie zugehörige anlage |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2470306A1 EP2470306A1 (de) | 2012-07-04 |
EP2470306B1 true EP2470306B1 (de) | 2013-10-02 |
Family
ID=42395028
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP10720630.2A Not-in-force EP2470306B1 (de) | 2009-08-24 | 2010-05-31 | Verfahren zur kontinuierlichen magnetischen erztrennung und/oder -aufbereitung sowie zugehörige anlage |
Country Status (14)
Country | Link |
---|---|
US (1) | US8584862B2 (ru) |
EP (1) | EP2470306B1 (ru) |
CN (1) | CN102596415B (ru) |
AR (1) | AR077893A1 (ru) |
AU (1) | AU2010288822B2 (ru) |
CA (1) | CA2771797C (ru) |
CL (1) | CL2012000242A1 (ru) |
DE (1) | DE102009038666A1 (ru) |
ES (1) | ES2433645T3 (ru) |
PE (1) | PE20121367A1 (ru) |
PL (1) | PL2470306T3 (ru) |
RU (1) | RU2539474C2 (ru) |
WO (1) | WO2011023426A1 (ru) |
ZA (1) | ZA201200507B (ru) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2537591B1 (de) * | 2011-06-21 | 2014-06-18 | Siemens Aktiengesellschaft | Verfahren zur Gewinnung von nichtmagnetischen Erzen aus einer Erzpartikel-Magnetpartikel-Agglomerate enthaltenden Suspension |
WO2016083491A1 (en) * | 2014-11-27 | 2016-06-02 | Basf Corporation | Improvement of concentrate quality |
RU2693203C1 (ru) * | 2017-12-27 | 2019-07-01 | Общество с ограниченной ответственностью "Научно-производственное региональное объединение "Урал" (ООО НПРО "Урал") | Линия трехстадийного измельчения магнетито-гематитовых руд |
CN112566725A (zh) * | 2018-08-13 | 2021-03-26 | 巴斯夫欧洲公司 | 用于矿物加工的载体-磁力分离与其他分离的组合 |
EP3880853A4 (en) * | 2018-11-14 | 2022-08-31 | IB Operations Pty Ltd | METHOD AND DEVICE FOR PROCESSING MAGNETITE |
CN109530079B (zh) * | 2018-11-21 | 2022-05-20 | 中南大学 | 磁重联合分选工艺 |
CN110090731B (zh) * | 2019-05-20 | 2021-05-25 | 大连地拓环境科技有限公司 | 一种低品位菱镁矿采用磁流体选矿的工艺方法 |
CN115259459B (zh) * | 2022-05-05 | 2024-02-02 | 中国矿业大学(北京) | 一种选矿厂分段分质分支废水流程内循环利用的方法 |
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SU109529A1 (ru) * | 1957-07-25 | 1957-11-30 | И.Д. Ремесников | Способ обессеривани углей |
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DE2528137C3 (de) * | 1975-04-04 | 1980-06-26 | Financial Mining - Industrial And Shipping Corp., Athen | Verfahren zur Gewinnung von Nickelkonzentrat aus nickelhaltigen Erzen |
SU899137A1 (ru) * | 1980-01-23 | 1982-01-23 | за витель 899137 о | Устройство дл мокрого разделени производственных и бытовых отходов |
ATE25595T1 (de) * | 1981-10-26 | 1987-03-15 | Wsr Pty Ltd | Magnetisches flotationsverfahren. |
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SU1717231A1 (ru) * | 1986-03-12 | 1992-03-07 | Государственный проектно-конструкторский институт "Гипромашуглеобогащение" | Магнитный сепаратор |
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RU2131304C1 (ru) * | 1997-05-15 | 1999-06-10 | Открытое акционерное общество "Иргиредмет" | Способ флотации тонковкрапленных бедных медных и золотосодержащих руд |
RU2123389C1 (ru) * | 1998-01-20 | 1998-12-20 | Научно-производственное предприятие "Экология-сервис" | Способ мокрого магнитного обогащения слабомагнитных тонковкрапленных железных руд |
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RU2307710C2 (ru) * | 2004-07-20 | 2007-10-10 | Марат Азатович Бикбов | Способ обогащения железных руд |
US8033398B2 (en) * | 2005-07-06 | 2011-10-11 | Cytec Technology Corp. | Process and magnetic reagent for the removal of impurities from minerals |
RU2284221C1 (ru) * | 2006-01-10 | 2006-09-27 | Закрытое Акционерное Общество "Уралкалий-Технология" | Способ получения коллективного концентрата для извлечения благородных металлов |
UA99623C2 (ru) | 2007-07-17 | 2012-09-10 | Басф Се | Способ обогащения руды с помощью гидрофобной поверхности и использование гидрофобной поверхности |
BRPI0816189A2 (pt) | 2007-09-03 | 2015-04-14 | Basf Se | Processo para a separação de pelo menos um primeiro material de uma mistura |
DE102008047842A1 (de) | 2008-09-18 | 2010-04-22 | Siemens Aktiengesellschaft | Vorrichtung und Verfahren zum Abscheiden ferromagnetischer Partikel aus einer Suspension |
DE102008047841B4 (de) | 2008-09-18 | 2015-09-17 | Siemens Aktiengesellschaft | Vorrichtung zum Abschneiden ferromagnetischer Partikel aus einer Suspension |
-
2009
- 2009-08-24 DE DE102009038666A patent/DE102009038666A1/de not_active Ceased
-
2010
- 2010-05-31 US US13/392,504 patent/US8584862B2/en active Active
- 2010-05-31 WO PCT/EP2010/057542 patent/WO2011023426A1/de active Application Filing
- 2010-05-31 PL PL10720630T patent/PL2470306T3/pl unknown
- 2010-05-31 ES ES10720630T patent/ES2433645T3/es active Active
- 2010-05-31 EP EP10720630.2A patent/EP2470306B1/de not_active Not-in-force
- 2010-05-31 PE PE2012000252A patent/PE20121367A1/es active IP Right Grant
- 2010-05-31 AU AU2010288822A patent/AU2010288822B2/en not_active Ceased
- 2010-05-31 RU RU2012111223/03A patent/RU2539474C2/ru not_active IP Right Cessation
- 2010-05-31 CA CA2771797A patent/CA2771797C/en not_active Expired - Fee Related
- 2010-05-31 CN CN201080037729.6A patent/CN102596415B/zh not_active Expired - Fee Related
- 2010-08-20 AR ARP100103048A patent/AR077893A1/es not_active Application Discontinuation
-
2012
- 2012-01-20 ZA ZA2012/00507A patent/ZA201200507B/en unknown
- 2012-01-30 CL CL2012000242A patent/CL2012000242A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
ES2433645T3 (es) | 2013-12-12 |
AR077893A1 (es) | 2011-09-28 |
RU2539474C2 (ru) | 2015-01-20 |
CN102596415A (zh) | 2012-07-18 |
CN102596415B (zh) | 2014-11-05 |
PL2470306T3 (pl) | 2014-02-28 |
WO2011023426A1 (de) | 2011-03-03 |
CL2012000242A1 (es) | 2012-09-07 |
DE102009038666A1 (de) | 2011-03-10 |
RU2012111223A (ru) | 2013-10-10 |
CA2771797C (en) | 2014-08-19 |
EP2470306A1 (de) | 2012-07-04 |
CA2771797A1 (en) | 2011-03-03 |
AU2010288822A1 (en) | 2012-03-01 |
US8584862B2 (en) | 2013-11-19 |
AU2010288822B2 (en) | 2013-06-06 |
PE20121367A1 (es) | 2012-10-20 |
US20120189512A1 (en) | 2012-07-26 |
ZA201200507B (en) | 2012-09-26 |
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