EP3071719A1 - Procédé pour la récupération de métaux terres rares à partir de déchets sulfates - Google Patents

Procédé pour la récupération de métaux terres rares à partir de déchets sulfates

Info

Publication number
EP3071719A1
EP3071719A1 EP14863833.1A EP14863833A EP3071719A1 EP 3071719 A1 EP3071719 A1 EP 3071719A1 EP 14863833 A EP14863833 A EP 14863833A EP 3071719 A1 EP3071719 A1 EP 3071719A1
Authority
EP
European Patent Office
Prior art keywords
sulphate
waste
rare earth
precipitate
metal
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.)
Withdrawn
Application number
EP14863833.1A
Other languages
German (de)
English (en)
Other versions
EP3071719A4 (fr
Inventor
Pertti Koukkari
Jarno MÄKINEN
Malin BOMBERG
Anna LEHTONEN
Mona Arnold
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Valtion Teknillinen Tutkimuskeskus
Original Assignee
Valtion Teknillinen Tutkimuskeskus
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Valtion Teknillinen Tutkimuskeskus filed Critical Valtion Teknillinen Tutkimuskeskus
Publication of EP3071719A1 publication Critical patent/EP3071719A1/fr
Publication of EP3071719A4 publication Critical patent/EP3071719A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B59/00—Obtaining rare earth metals
    • 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
    • B03C1/002—High gradient magnetic separation
    • 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
    • B03C1/02—Magnetic separation acting directly on the substance being separated
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00—Compounds of rare earth metals
    • C01F17/20—Compounds containing only rare earth metals as the metal element
    • C01F17/288—Sulfides
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00—Treatment of water, waste water, or sewage
    • C02F1/48—Treatment of water, waste water, or sewage with magnetic or electric fields
    • C02F1/488—Treatment of water, waste water, or sewage with magnetic or electric fields for separation of magnetic materials, e.g. magnetic flocculation
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/18—Extraction of metal compounds from ores or concentrates by wet processes with the aid of microorganisms or enzymes, e.g. bacteria or algae
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00—Technologies related to metal processing
    • Y02P10/20—Recycling

Definitions

  • the present invention relates to recovery of rare earth metals from waste sulphate materials.
  • the invention relates to reductive fractionation of waste gypsum, comprising sulphate salts of calcium and other metals to their dispersed sulphides, in which form the metal components with high magnetic susceptibility can be recovered by using magnetic separation.
  • Sulphate reducing bacteria are preferably used for the reductive fractionation.
  • Igneous apatite minerals are a known secondary source of rare earth metals.
  • the rare earth (RE) content of apatites varies between 0,5 to 1 % as oxides.
  • Several pilot processes to recover the valuable rare earth metals in connection with the adjacent fertiliser production have been developed, so far without economic success (Jorjani et ah, 2011; Al-Shawi et ah, 2002).
  • the for long time leading fertilizer manufacturing process includes the leaching of the ore with sulphuric acid, which includes formation of phosphogypsum as CaSC"42H 2 0
  • the rare earth metals are present in the gypsum as their respective sulphates, even though particulates of monazite, non-dissolved in the sulphuric acid process may also appear.
  • Typical techniques for the chemical fractionation of rare earths from phosphogypsum usually include leaching with dilute sulphuric acid solution, separation of rare earth concentrates from leaching sulphuric acid by pre-concentration via evaporation, liquid- liquid extraction or precipitation method and anhydrite production from purified phosphogypsum by recrystallization of concentrated sulphuric acid solution. All such methods have so far rendered complex and uneconomical (Preston et al., 1996; WO 2011/008137 A3), due to ineffectiveness of the multi-stage procedures and low initial concentration of rare earths in the phosphogypsum.
  • a combined mechanical-magnetic separation method (FI 101787 B) has been proposed to purify phosphogypsum waste from its heavy metal impurities.
  • WO 2009/125064 Al discloses a respective method for purification of flue gas desulfurization (FGD) gypsum. In such techniques gypsum is subjected to grinding in various degrees of fineness, then slurried by water addition and finally led to high gradient magnetic separation (HGMS) to collect the magnetized fraction.
  • FGD flue gas desulfurization
  • HGMS high gradient magnetic separation
  • the main goal of the method has been to purify waste gypsum for its possible future use as contaminant free filler in various components such as boards in construction industry or as pigment in paper-making, but the method has shown potential in using the magnetic separation to recover metals from waste gypsum. Yet the recovery of such metals is highly dependent on the consistency of the slurry as well as of the fineness of the gypsum stock and in average but 35 % of the rare earth metals such as La, Nd, Ce and Y could be recovered.
  • SRB sulphate reducing bacteria
  • a mixed culture of sulfate-reducing bacteria utilizes inexpensive carbon sources, such as sewage digestor synthesis gas, to reduce FGD gypsum to hydrogen sulfide.
  • the sulphide is further oxidized to elemental sulfur via reaction with ferric sulfate, and accumulating calcium ions are precipitated as calcium carbonate using carbon dioxide.
  • AD-MSS anaerobically digested municipal sewage sludge
  • EP 0844981 Bl proposes a biomagnetic separation method for the recovery of metals from an influent liquid containing e.g. radioactive heavy metal contaminants from waste water of a nuclear plant.
  • the technique involves adding specific adsorbent material to the contaminated solution to attach the contaminants by chemical or electrostatic adsorption.
  • bacterially generated ferrous sulphide from the respective sulphate is preferably used (Watson et al., 1996). The method is targeted to remove toxic heavy metals from the influent solution, and proved successful in dropping the
  • concentrations of e.g. mercury, cadmium, chromium and lead contents of the solution by several orders of magnitude.
  • WO 2013/044376 Al relates to magnetic separation of different rare earth compounds, wherein a quantitative fractionation of various rare earth metal compounds is described in terms of their magnetic susceptibilities by using a separation channel rigged with magnets arranged progressively from weakest to strongest along the length axis and respective output channels to fractionate compounds with various susceptibilities and specific gravities.
  • This publication shows the feasibility of separating and refining rare individual rare earth compounds by HGMS techniques, yet chemical formulation of the rare earth compounds as a necessary pre-treatment before magnetic fractionation is not disclosed.
  • the present invention is based on reductive and enriching treatment of sulphate materials combined with magnetic separation to recover rare earth metals.
  • the present invention relates to a method for recovering rare earth metal enrichment from waste sulphates by first reducing rare earth metal sulphates to a metal sulphide precipitate and then separating a highly magnetized fraction of the metal sulphide precipitate with a magnetic separator.
  • sulphate reduction may be carried out for example by utilizing sulphate reducing bacteria, by applying thermal treatment or by using hydrometallurgical reduction with H 2 S.
  • the method according to the present invention is characterized by what is stated in the characterizing part of claim 1.
  • the use of said method is characterized in claim 16.
  • Figure 1 is a schematic description of a process according to the present invention.
  • Numbers 1-5 are process steps, which are explained in the detailed description below.
  • Characterizing to the method of the present invention is to combine a reductive treatment of a waste sulphate material and a following magnetic separation to recover valuable rare earth metals.
  • the waste sulphate material is waste gypsum, for example waste phosphogypsum.
  • waste sulphates containing rare earth metal compounds are reduced in a liquid phase e.g. by sulphate reducing bacteria (SRB) to form a finely divided rare earth metal precipitate, followed by separation of the magnetized fraction of the precipitate by a magnetic separator, such as high grade magnetic separator (HGMS).
  • SRB sulphate reducing bacteria
  • HGMS high grade magnetic separator
  • the present invention is based on an enrichment of the rare earth metal content of e.g. waste gypsum into a metal sulphide precipitate, and to a higher magnetic susceptibility of the RE compounds in the precipitate compared to other substances present in said precipitate (such as calcium sulphate/sulphide/phosphate).
  • the method relates to a recovery of a rare earth metal enrichment, which comprises rare earth metals as their corresponding sulphides, oxides or phosphates, or as a combination thereof.
  • Said enrichment may also comprise small amounts of other compounds than rear earth metals compounds, for example K, Fe, Ca, Mg and Al sulphides.
  • the magnetized fraction of the metal sulphide precipitate comprises rare earth metals and has a higher magnetic susceptibility compared to other substances, such as calcium compounds, present in said precipitate. It has been discovered that he magnetic susceptibility of e.g. rare earth metal sulphides is often exceptionally high, whereas that of calcium sulphide is low. The same applies to corresponding oxides and sulphates.
  • the process comprises the following steps (numbers 1 to 5 are also correspondingly marked into Figure 1):
  • One suitable sulphate reducing bacteria for use in the present method originate from genus Desulfovibrio.
  • Desulfovibrio desulfuricans can be used.
  • SRB belonging to the genera Desulfobulbus and Desulfotomaculum have shown to be promising.
  • SRB need some organic nutrients for their metabolism.
  • SRB may use carbon sources, such as sewage digests, alcohol or synthesis gas, as microbial nutrients, and, also as electron donors.
  • This biological reduction, i.e. bioreduction is preferably carried out in anaerobic reaction conditions and at temperatures between 20 °C and 50 °C, more preferably between 30 and 40 °C and particularly about 37 °C.
  • the steps 1 to 3 in the above process example by a thermal treatment of the gypsum by using e.g. syngas produced by gasification of biomass or by using hydrometallurgical reduction with hydrogen sulphide H 2 S.
  • the sulphate reduction is thus performed with calcium sulphide received from thermal roasting or sulphidisation of waste gypsum.
  • the waste sulphate material is reduced to a finely divided precipitate having a maximum particle size of below 0,50 ⁇ , such as between 0,10 and 0,50 ⁇ .
  • the precipitate is typically formed as an ultimately fine sludge, with low or negligible degree of co -precipitated granules.
  • the sulphides have higher magnetic susceptibility than the corresponding sulphates.
  • the enriched sludge of such rare earth metal sulphides which have potentially high magnetic susceptibility, can be subjected to an effective fractionation process by applying high magnetic fields.
  • the metal precipitate obtained by the bioreduction or such reductive treatment of waste gypsum consists of elements, which are selected from the group of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Ga, Ge, Ho, Nb, Sc, Ta, Th, U, Y, In, Al, Ca, Fe, K, Mg, Mn, Na, P and S, as their corresponding sulphides, phosphates or oxides, or as any combination thereof.
  • the formed non-rear earth metal comprising substances (i.e. nonmagnetic e.g.
  • calcium sulphate fraction from step 5 can be used for the treatment of acid mine waters to precipitate heavy metal sulphates or it may be recycled in a thermal process to recycle sulphur as sulphuric acid and calcium as quicklime.
  • the sulphate reduction may also be performed by a chemical reaction or reactions in aqueous sulphate slurry by using hydrogen sulphide.
  • Sulphate waste material can also be treated thermally to produce metal precipitates.
  • HGMS equipment is preferred for an efficient separation of the finely dispersed magnetic REs.
  • the equipment itself is usually rather simple and provides an easy flushing of magnetics.
  • the maintenance cost is low as well as the power consumption.
  • HGMS equipment capable of recovering rare earth metals having a magnetic susceptibility ⁇ of at least 1 000, more preferably at least 5 000.
  • the separator should preferably be adjustable or able to perform within a wide magnetic susceptibility scale.
  • the present invention wherein sulphate reduction is combined with magnetic separation provides an environmentally friendly and an efficient method for recovering valuable rare earth metals from waste sulphate materials. The said method is targeted to metal companies and is usable around the world, especially in areas where industrial phosphate production takes place.
  • the present invention is illustrated by a non-limiting working example. It should be understood, however, that the embodiments given in the description above and in the example are for illustrative purposes only, and that various changes and
  • Phosphogypsum samples were first dried in oven (105 °C, 20 h). Gypsum leachate was then prepared by adding dry phosphogypsum powder to water (50 g/L), followed by 24 h mixing in Erlenmeyer glass. Obtained solution was filtered (0,45 ⁇ ) to remove solid phosphogypsum particles. Clear solution was used for sulphate reducing bacteria (SRB) studies. The phosphogypsum filtrate was rendered anaerobic by flushing with N 2 gas through a 0,22 ⁇ pore size filter for 1 hour, after which the flask containing the gypsum leachate was sealed with a gas tight butyl rubber stopper and open top screw cap.
  • SRB sulphate reducing bacteria
  • the phosphogypsum leachate was amended with 0,2 g yeast extract and 3,75 ml lactate L "1 .
  • Pre-grown Desulfovibrio desulfuricans bacteria were added to the 2,5 L volume of phosphogypsum leachate.
  • the culture developed a precipitation, which was collected on a 0,22 ⁇ pore size filter funnel by vacuum suction.
  • the precipitate was rinsed from the filter with sterile double distilled water, collected in 50 ml cone tubes and dried prior to analysis.
  • the formed precipitate was analysed by using standard ICM-MS and ICP-OES methods.
  • the contents of La, Ce and Y in the SRB precipitate were observed as 30 400, 66 200 and 8 800 ppm (mg/kg), respectively.
  • the Nd-content of the SRB precipitate was 45 000 ppm. The result indicates substantial enrichment of the said metals and also of other rare earth metals in the formed SRB precipitate.
  • HGMS high grade magnetic separation
  • Phosphogypsum samples of the same origin as used in the aforementioned patent FI 101787 B were dried in oven (105 °C, 20 h).
  • Gypsum leachate was prepared by adding dry phosphogypsum powder to water (50 g/L), followed by 24 h mixing in Erlenmeyer glass. Obtained solution was filtered (0,45 ⁇ ) to remove solid phosphogypsum particles. Clear solution was used for sulphate reducing bacteria (SRB) studies.
  • the continuously operated sulphate reduction and REE precipitation experiment was done in 0,7-liter UASB (upflow anaerobic sludge blanket) column, equipped also with solution recycling line with a powerful pump to adjust the sludge fluidization and, if needed, to mix and homogenize the sludge in column.
  • the column was inoculated with 500 ml of anaerobic granular sludge from an operating waste water treatment plant, and filled up to a total volume of 700 ml with sulphate rich water. Microbial activity was ensured by continuing the sulphate rich water, ethanol and substrates pumping.
  • the phosphogypsum filtrate used in the experiment was rendered anaerobic by flushing with N2 gas for 1 hour and pumped then to 0,7-liter column with the speed of 27 ml/h for 20 days. Simultaneously, substrate-nutrition solution was pumped to the column with the speed of 1,75 ml/h for providing following concentrations to the total feed: ethanol (0,16 v-%), KH 2 PO 4 (13,8 mg/1), (NH 4 ) 2 S0 4 (33,7 mg/1), ascorbic acid (2,7 mg/1), thioglycolic acid (2,7 mg/1) and yeast extract (2,7 mg/1). With these parameters, the hydraulic retention time (HRT) was maintained at 24 hours.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Geology (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Biochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Water Supply & Treatment (AREA)
  • Hydrology & Water Resources (AREA)
  • Analytical Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Removal Of Specific Substances (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

La présente invention porte sur un procédé pour la récupération de métaux terre rares à partir de déchets sulfates, tels que des déchets de type gypse, qui sont une ressource secondaire connue de métaux terres rares et largement présents par exemple dans des endroits où a lieu la production de phosphates industriels. La présente invention combine un traitement de réduction des sulfates, tel qu'une bioréduction avec des bactéries sulfatoréductrices, et une séparation magnétique, qui est basée sur une susceptibilité magnétique exceptionnellement élevée des composés de terres rares par rapport par exemple au composé du calcium dans un tel précipité de gypse prétraité par réduction.
EP14863833.1A 2013-11-22 2014-11-21 Procédé pour la récupération de métaux terres rares à partir de déchets sulfates Withdrawn EP3071719A4 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI20136167A FI125550B (en) 2013-11-22 2013-11-22 Method for recovering rare earth metals from waste sulphates
PCT/FI2014/050891 WO2015075317A1 (fr) 2013-11-22 2014-11-21 Procédé pour la récupération de métaux terres rares à partir de déchets sulfates

Publications (2)

Publication Number Publication Date
EP3071719A1 true EP3071719A1 (fr) 2016-09-28
EP3071719A4 EP3071719A4 (fr) 2017-08-09

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP14863833.1A Withdrawn EP3071719A4 (fr) 2013-11-22 2014-11-21 Procédé pour la récupération de métaux terres rares à partir de déchets sulfates

Country Status (5)

Country Link
EP (1) EP3071719A4 (fr)
CN (1) CN105765091B (fr)
CA (1) CA2930349A1 (fr)
FI (1) FI125550B (fr)
WO (1) WO2015075317A1 (fr)

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Publication number Priority date Publication date Assignee Title
CN110184460A (zh) * 2019-06-28 2019-08-30 四川省乐山锐丰冶金有限公司 一种氯化镨钕料液中除铝离子的方法

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DE102017008035A1 (de) 2016-09-05 2018-03-08 Technische Universität Ilmenau Vorrichtung und Verfahren zur Separation von magnetisch anziehbaren Teilchen aus Fluiden
CN108117224B (zh) * 2016-11-29 2021-01-05 中国石油化工股份有限公司 一种脱硫废水的预处理方法
CN109425549B (zh) * 2017-08-21 2021-03-02 北新集团建材股份有限公司 一种分析石膏品位的方法
CN109957523B (zh) * 2017-12-25 2021-02-23 有研工程技术研究院有限公司 一株寡营养硫酸盐还原菌及其用于河道底泥重金属污染修复的工艺
DE102018113358B4 (de) 2018-06-05 2022-12-29 Technische Universität Ilmenau Vorrichtung und Verfahren zur kontinuierlichen separaten Entnahme von magnetisch anziehbaren und magnetisch abstoßbaren Teilchen aus einem strömenden Fluid
CN110028258A (zh) * 2019-05-16 2019-07-19 西南科技大学 一种钛石膏中铁硫资源分别利用的方法
US10954582B2 (en) * 2019-07-17 2021-03-23 West Virginia University Systems and processes for recovery of high-grade rare earth concentrate from acid mine drainage
CN110918251B (zh) * 2019-10-31 2021-08-03 昆明理工大学 高梯度磁场脱除磷石膏中杂质的方法和装置
CN110961248B (zh) * 2019-11-29 2022-03-04 南华大学 一种含钪铀矿中分离钪、铀的方法
CN115572740A (zh) * 2022-09-30 2023-01-06 武汉工程大学 一种利用硫酸盐还原菌群分解磷石膏生成硫化钙的方法

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Publication number Priority date Publication date Assignee Title
CN110184460A (zh) * 2019-06-28 2019-08-30 四川省乐山锐丰冶金有限公司 一种氯化镨钕料液中除铝离子的方法

Also Published As

Publication number Publication date
EP3071719A4 (fr) 2017-08-09
CN105765091A (zh) 2016-07-13
CA2930349A1 (fr) 2015-05-28
WO2015075317A1 (fr) 2015-05-28
CN105765091B (zh) 2018-10-09
FI125550B (en) 2015-11-30
FI20136167A (fi) 2015-05-23

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