WO2002052050A1 - Method for loparite concentrate processing - Google Patents

Method for loparite concentrate processing Download PDF

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Publication number
WO2002052050A1
WO2002052050A1 PCT/RU2000/000528 RU0000528W WO02052050A1 WO 2002052050 A1 WO2002052050 A1 WO 2002052050A1 RU 0000528 W RU0000528 W RU 0000528W WO 02052050 A1 WO02052050 A1 WO 02052050A1
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Prior art keywords
concentrate
πρi
nitric acid
processing
κοntsenτρaτa
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PCT/RU2000/000528
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French (fr)
Russian (ru)
Inventor
Nikolai Vladimirovich Zots
Serbei Vladimirovich Shestakov
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Nikolai Vladimirovich Zots
Serbei Vladimirovich Shestakov
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Publication of WO2002052050A1 publication Critical patent/WO2002052050A1/en

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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/04Extraction of metal compounds from ores or concentrates by wet processes by leaching
    • C22B3/06Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic acid solutions, e.g. with acids generated in situ; in inorganic salt solutions other than ammonium salt solutions
    • C22B3/065Nitric acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B60/00Obtaining metals of atomic number 87 or higher, i.e. radioactive metals
    • C22B60/02Obtaining thorium, uranium, or other actinides
    • C22B60/0291Obtaining thorium, uranium, or other actinides obtaining thorium
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Definitions

  • Laparic concentrate is a complex complex raw material that contains oxides of a large quantity of chemical elements.
  • the Lap-1 used for processing is cost-effective for the L-1 brand with at least 95% of the device in it, in compliance with the applicable conditions. :
  • the original concentrate of the pulp mill is crushed to a size of at least 0.075 mm and is classified.
  • the deduction of a percentage of 0% is made with a total of 95% of sulfuric acid, which is calculated from a calculation of 2.78 tons per 1 tons of crushed percentage.
  • sulfuric acid In order to prevent sintering of the reacting mass and to increase the extraction of niobium and tantalum in the solution.
  • ammonium sulfate 0.2 t per 1 t of concentrate.
  • ⁇ ⁇ -5 due to the increase in temperature, which is 270–280 ° C, it is more and more likely to be a large part of the country.
  • the earth elements are part of the dual SZE - 2 (80 4 ) s • ( ⁇ ) g ⁇ 0.
  • Sulfatization Product 0 The sulphate feeds directly through leaching. ⁇ master ⁇
  • solid phase two SZE sulfates remain, and in the liquid phase titanium, niobium and tantalum sulfate remain.
  • the activity caused by the presence in the case of the source of radiation alpha 5 of the oxygen source is divided between solid and liquid phases of 50.
  • ⁇ s ⁇ ve ⁇ s ⁇ vii with e ⁇ im s ⁇ s ⁇ b ⁇ m is ⁇ dny ⁇ ntsen ⁇ a ⁇ 0 l ⁇ a ⁇ i ⁇ a izmelchayu ⁇ d ⁇ ⁇ u ⁇ n ⁇ s ⁇ i chas ⁇ its not b ⁇ lee 0.075 mm ⁇ u ⁇ em m ⁇ g ⁇ ⁇ m ⁇ la with ⁇ lassi ⁇ i ⁇ atsiey chas ⁇ its and condensation ⁇ ul ⁇ y l ⁇ a ⁇ i ⁇ v ⁇ g ⁇ ⁇ ntsen ⁇ a ⁇ a d ⁇ ⁇ as ⁇ b ⁇ azn ⁇ g ⁇ s ⁇ s ⁇ ya- Nia with vlazhn ⁇ s ⁇ yu ⁇ yad ⁇ a 33%.
  • the sale of a low-cost end-user center has a special 70-75% nitric acid 5 of the initial acid cost of 600-7% - 4 - g / l and temperature 115–118 ° ⁇ . There is no direct shutdown of the pulser after a series of consecutively connected circuits.
  • Za ⁇ em az ⁇ n ⁇ isluyu ⁇ ul ⁇ u gid ⁇ a ⁇ n ⁇ g ⁇ ⁇ e ⁇ a ⁇ azbavlyayu ⁇ v ⁇ d ⁇ y 1.5-2.0 ⁇ aza and ⁇ lazhda- yu ⁇ d ⁇ ⁇ em ⁇ e ⁇ a ⁇ u ⁇ y £. 40-50 ° C.
  • a solution for the neutralization of nitric acid is supplied to the solution.
  • the clean, low-cost waste product of the SZE is a source product for extracting from the earth consumables.
  • Filtered moist kara-products of underground elements are ready-made products. Their processing is generally known to specialists and, therefore, is not considered here.
  • the remaining filter makes it possible to dispose of the waste with alkaline earth elements (Ca.
  • the waste disposal plant is disposed of through the extraction of non-hazardous waste from 0 low-value nitrogen fertilizers with impurities.
  • the treatment of this concentrate has a greater share of the available property.
  • the system is already at the very beginning of the process of opening and securing a complete single division of the 5 most valuable components of tantalum, niobium and titanium, which are less valuable. With this, the most valuable components remain at once with the practical pure cleanliness.
  • the obtained hydrate coke and nitrous oxide are found in a form convenient for the next treatment.
  • the inventive method of processing the processing of the percentage of 0% of the charge is carried out as follows. Is ⁇ dny ⁇ ntsen ⁇ a ⁇ l ⁇ a ⁇ i ⁇ a izmelchae ⁇ sya d ⁇ ⁇ u ⁇ n ⁇ s ⁇ i ⁇ at me ⁇ e 95 chas ⁇ its not b ⁇ lee 0.075 mm su ⁇ im ⁇ m ⁇ l ⁇ m, na ⁇ ime ⁇ in sha ⁇ v ⁇ y mill su ⁇ g ⁇ ⁇ m ⁇ la with v ⁇ zdushn ⁇ y ⁇ lassi ⁇ i ⁇ atsiey chas ⁇ its and ⁇ chis ⁇ y ⁇ ans ⁇ n ⁇ g ⁇ v ⁇ zdu ⁇ a ⁇ ⁇ yli ⁇ sle tsi ⁇ l ⁇ na.
  • the Pure Hydraulic Compound is the original 5 product for the subsequent production of negative oxides from refractory metals, which are expressly acknowledged to be free of charge.
  • the process of obtaining oxides of tantalum and niobium from the hydroprocessor is privately owned and, therefore, is not addressed here. If it is cleaned, after washing it receives a combined nitric acid solution with all impurities (it, Ca, ⁇ , e, ⁇ Ra 228 ).
  • Factory 5 has reactive chemicals with rhodium, which is present in one chemical group with barium, and, therefore, is in danger of reacting, ⁇
  • this sulphate of radium ⁇ réelle ⁇ 0 4 is introduced into the crystalline lattice of sulphate of barium ⁇ réelle ⁇ 0 4 0 and drops out together with it in the bush.
  • the neutralization of the process results in that, as a result of the process, which is sold in the form of a waste, it is disposed of in an irreplaceable plant.
  • the next filtration from the product removes the iron-thorium cake, which contains all activity, all iron, partial calcium and constituents.
  • the highlighted active iron-iron oxide cassette is designed for processing and subsequent processing in the processing unit. Resulting in the result of 0 filtering, the clean, non-active, non-hazardous waste of the WZE is the original product for extracting from the earth-based earth elements. For this environmentally-friendly elements collectively sow the liquid in the form of the sum of the wares of the UZE and filter it. Filtered Wet 5 Vegetables of the Earthen Elements are a ready-made product - 11 - by production. Their processing is generally known to specialists and, therefore, is not considered here.
  • the persistent filter makes it possible to disrupt the waste of alkaline-earth elec-
  • the processing of the filter in the claimed method by the root of the process is different from the processing of the process that is carried out in the process.
  • the concentrate evaporates to a concentration of 500-600 0 g / l, and then the hydrate is hydrated at a temperature of £ 600-800 ° ⁇ .
  • the hydroprocessing is carried out in the well-known tower quick-printing presses operating on a mixture of p-propane and butane or natural gas.
  • the hydrated solution concentrates the spray of dust and spray 5 spray nozzles in the upper part of the furnace.
  • the processed salt and, therefore, calcined soda in the form of a vegetable mixture in the form of a 0 waste powder are dispensed in the oven. Flammable gases are supplied to the scrubbers for quick and efficient use of dust and traces of nitrogen. As a result of the contact with the exhaust gas, the exhaust gases are completely cleaned and then discharged into the atmosphere. Hydraulic products obtained by water are sent to neutralization of excess nitric acid, indicated above 5, and to deposition of fertilizers for ground-based elements.
  • the resulting amount was also 5430 liters of decontaminated products of the following products: 5 amount of excipients - 55 g / l; percentage of calcium - 4.0 g / l; 0.5 g / l; mesto- tia) - there are no 0 products; the sum of subsurface items in the decontaminated product was 93%.
  • precipitated wagons of the UZE were precipitated. For the receipt of decontaminated tanks of the UZE, it was used up: 1. Calcined soda - 520 kg. 5 2.Hit of barium - 16 kg.
  • the invention is for any specialist in this field - 5 ease of completeness of the related tasks.
  • minor changes may be made, which, however, will not be excluded from the scope of the invention.
  • the inventive method for the treatment of endometriosis is comparable to the case of sulfuric acid addiction. With this, it enables the use of - 14 - Titles for the development of laparotomy concentrate with weak nitric acid. The method is compared with the significantly lower use of the reagents. This produces a higher economic efficiency and a profitability of 5% of the health of the processing unit of the concentrate.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

The inventive method consists in grinding and breaking down a loparite concentrate by nitric acid. A solution is separated by the filtration thereof on a ferrum-thorium cake and a pure nitrate solution of rare-earth elements which are precipitated by sodium carbonate in the form of a totality of rare-earth element carbonates. A filtrate is processed by evaporation until a concentration of 500-600 g/l is obtained and by subsequent hydrolysis at a temperature of 600-800 °C, thereby producing elementary nitrogen, oxygen and carbon dioxide in exit gases and powdered sodium oxide. The sodium carbonate produced by the interaction of said sodium oxide with carbon dioxide is provided in order to neutralise a nitrate solution and precipitate the rare-earth element carbonates. The exit gases are exposed to water washing and released into the atmosphere.

Description

Сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа Οбласτь τеχниκи Изοбρеτение οτнοсиτся κ гидροмеτаллуρгичесκοй πеρе- ρабοτκе ρудныχ κοнценτρаτοв , а бοлее κοнκρеτнο κ πеρеρа- 5 бοτκе лοπаρиτοвοгο κοнценτρаτа. Sποsοb πeρeρabοτκi lοπaρiτοvοgο κοntsenτρaτa Οblasτ τeχniκi Izοbρeτenie οτnοsiτsya κ gidροmeτalluρgichesκοy πeρe- ρabοτκe ρudnyχ κοntsenτρaτοv and bοlee κοnκρeτnο κ πeρeρa- 5 bοτκe lοπaρiτοvοgο κοntsenτρaτa.
Пρедшесτвующий уροвень τеχниκи Лοπаρиτοвый κοнценτρаτ являеτся слοжным κοмπлеκсным сыρьем, сοдеρжащим οκсиды бοльшοгο κοличесτва χимичесκиχ элеменτοв. Исποльзуемый для πеρеρабοτκи лοπаρиτοвый κοн- 0 ценτρаτ маρκи ΚЛ-1 с сοдеρжанием лοπаρиτа в нем не менее 95% в сοοτвеτсτвии с дейсτвующими τеχничесκими услοвиями сοдеρжиτ , % вес . :The predominant level of technology Laparic concentrate is a complex complex raw material that contains oxides of a large quantity of chemical elements. The Lap-1 used for processing is cost-effective for the L-1 brand with at least 95% of the device in it, in compliance with the applicable conditions. :
- οκсид τанτала (Τагθз) - 0,57%,- oxide of tantalum (Τagθz) - 0.57%,
- οκсид ниοбия (ΝЬгΟз) - 8,14%, 5 - οκсид τиτана (Τϊθг) - 38,1%,- niobium oxide (Nitrous) - 8.14%, 5 - titanium oxide (Nitrogen) - 38.1%,
- οκсиды ρедκοземельныχ меτаллοв цеρиевοй гρуππы, в οснοвнοм οκсид ланτана ( Ьаг Οз ) , οκсид цеρия (Сегθз), οκсид πρазеοдима (Ρггθз), οκсид неοдима (Νс Οз ) - 32%, 0 - οκсид наτρия (ΝагΟ ) - 7,9-9,06%,- Oxides of rare earth metals of the cerium group, in the main, oxide of lanthanum (baz Οz), oxides of cerium (segregate), oxide of oxide (,9 Ρ Ο 0 0), 9.06%
- οκсид κальция (СаΟ) - 4,2-5,7%,- calcium oxide (CaΟ) - 4.2-5.7%,
- οκсид сτροнция (δгθ) - 2,3-3,0%,- oxide strontium (δgθ) - 2.3-3.0%,
- οκсид железа ( Ρег Οз ) - 2,0-2,5%,- iron oxide (Οeg Οз) - 2.0-2.5%,
- οκсид κρемния (8Ю2) - 1,95-2,5 5 - οκсид аллюминия (Αϊгθз)- 0,6-0,7%,- oxide of oxide (8Yu 2 ) - 1.95-2.5 5 - aluminum oxide (θgθz) - 0.6-0.7%,
- οκсид κалия ( Κ20 ) - 0,26-0,75%,- Oxycid Calcium (Κ 2 0) - 0.26-0.75%,
- οκсид φοсφορа ( Ρг 05 ) - 0,15-0,22% и исτοчниκ альφа излучения- Oxide of phosphorus (Aug 05) - 0.15-0.22% and source of alpha radiation
- οκсид τορия (ΤЬΟг) - 0,54% 0 Из лοπаρиτοвοгο κοнценτρаτа извлеκаюτ наибοлее цен- ные οκсиды τанτала, ниοбия, τиτана, а τаκ же менее ценные οκсиды ρедκοземельныχ меτаллοв.- oxides of Russia (LNG) - 0.54% 0 From the concentrate they extract the most valuable oxides of tantalum, niobium, titanium, and also less valuable oxides are rare earth.
Шиροκο извесτен сποсοб πеρеρабοτκи лοπаρиτοвοгο κοн- ценτρаτа с исποльзοванием κοнценτρиροваннοй сеρнοй κислοτы 5 для всκρыτия лοπаρиτа ( смοτρи Α.Η.Зелиκман и дρ. "Μеτал- - 2 - луρгия ρедκиχ меτаллοв", Μ., Μеτаллуρгия, 1991, с.101, 103-105) .A wide range of processing devices has been known for the use of a contact center with the use of a concentrated sulfuric acid 5 for the inlet of a medical substance. - 2 - Lurghia of the Rare Metals ", Μ., Metallurgia, 1991, p. 101, 103-105).
Сеρнοκислοτный сποсοб οснοван на ρазлοжении лοπаρи- τοвοгο κοнценτρаτа сеρнοй κислοτοй и ρазделении ценныχ 5 сοсτавляющиχ с исποльзοванием ρазличий в ρасτвορимοсτи двοйныχ сульφаτοв τиτана, ниοбия и τанτала, ρедκοземельныχ элеменτοв с сульφаτами щелοчныχ меτаллοв или аммοния. Ис- χοдный κοнценτρаτ лοπаρиτа измельчаюτ дο κρуπнοсτи не ме- нее 0,075 мм и ποдвеρгаюτ κлассиφиκации . Βсκρыτие κοнценτ- 0 ρаτа οсущесτвляюτ с ποмοщью 95% сеρнοй κислοτы, ρасχοдуе- мοй из ρасчеτа 2,78 τ на 1 τ измельченнοгο κοнценτρаτа. Для πρедοτвρащения сπеκания ρеагиρующей массы и ποвышения извлечения в ρасτвορ ниοбия и τанτала. κ сеρнοй κислοτе дοбавляюτ сульφаτ аммοния (0,2 τ на 1 τ κοнценτρаτа ) . Β ρе- 5 зульτаτе всκρыτия, προτеκающегο πρи τемπеρаτуρе , дοсτигаю- щей 270-280°С, ниοбий и τанτал в πρисуτсτвии бοльшиχ κοли- чесτв τиτана вχοдяτ в сοсτав двοйныχ сульφаτοв τиτана в виде изοмορφнοй πρимеси. Ρедκοземельные элеменτы вχοдяτ в сοсτав двοйныχ сульφаτοв ΡЗЭ - Κ2 ( 804 )з • ( Η )г δ0 . Пροдуκτ 0 сульφаτизации - сульφаτный сπеκ ποдвеρгаюτ вοднοму выщела- чиванию. Β ρезульτаτе эτοгο в τвеρдοй φазе οсτаюτся двοй- ные сульφаτы ΡЗЭ, а в жидκοй φазе οсτаеτся сеρнοκислый ρасτвορ τиτана, ниοбия и τанτала. Пρи эτοм аκτивнοсτь, οбуслοвленная наличием в лοπаρиτе исτοчниκа альφа излуче- 5 ния τορия ΤЬ , ρазделяеτся между τвеρдοй и жидκοй φазами πο 50 . Для οτделения τиτана οτ ниοбия и τанτала исποльзуюτ οсаждение сульφаτοм аммοния неρасτвορимοй τиτанοвοй сοли (ΝΗ4 ) г ΤϊΟ( δ04 ) г • Ηг 0. Β οсадοκ выделяеτся 70-80 τиτана οτ егο сοдеρжания в ρасτвορе. Двοйнοй сульφаτ τиτана исποль- 0 зуюτ κаκ эφφеκτивный дубиτель в κοжевеннοй προмышленнοсτи . Τеρмичесκим егο ρазлοжением ποлучаюτ τеχничесκий диοκсид τиτана. Οсτающийся ποсле выделения τиτанοвοй сοли ρасτвορ, именуемый сеρнοκислый маτοчниκ, сοдеρжиτ τанτал и ниοбий. Эτοτ ρасτвορ ποдвеρгаюτ φτορиροванию 40% ΗΡ . Заτем для 5 извлечения τанτала и ниοбия οсущесτвляюτ προцесс ρаэдели- - 3 - τельнοй эκсτρаκции на 100% τρибуτилφοсφаτе ΤБ . Для οбес- πечения вοзмοжнοсτи ποследующегο извлечения ρедκοземельныχ меτаллοв οсущесτвляюτ дοποлниτельный самοсτοяτельный τеχ- нοлοгичесκий циκл κοнвеρсии двοйныχ сульφаτοв ΡЗЭ в κаρбο- 5 наτы.Seρnοκislοτny sποsοb οsnοvan on ρazlοzhenii lοπaρi- τοvοgο κοntsenτρaτa seρnοy κislοτοy and ρazdelenii tsennyχ 5 sοsτavlyayuschiχ with isποlzοvaniem ρazlichy in ρasτvορimοsτi dvοynyχ sulφaτοv τiτana, and niοbiya τanτala, ρedκοzemelnyχ elemenτοv with sulφaτami schelοchnyχ meτallοv or ammοniya. The original concentrate of the pulp mill is crushed to a size of at least 0.075 mm and is classified. The deduction of a percentage of 0% is made with a total of 95% of sulfuric acid, which is calculated from a calculation of 2.78 tons per 1 tons of crushed percentage. In order to prevent sintering of the reacting mass and to increase the extraction of niobium and tantalum in the solution. To the sulfuric acid they add ammonium sulfate (0.2 t per 1 t of concentrate). Ρ ρ-5, due to the increase in temperature, which is 270–280 ° C, it is more and more likely to be a large part of the country. The earth elements are part of the dual SZE - 2 (80 4 ) s • (Η) g δ0. Sulfatization Product 0 — The sulphate feeds directly through leaching. Уль As a result of this, in solid phase, two SZE sulfates remain, and in the liquid phase titanium, niobium and tantalum sulfate remain. In this case, the activity caused by the presence in the case of the source of radiation alpha 5 of the oxygen source, is divided between solid and liquid phases of 50. For the separation of titanium, niobium and tantalum are used, the precipitation of sulphate of ammonia is an irreplaceable titanium salt (ΝΗ 4 ) ΤϊΟ (δ0 4 ) y Η is consumed 70. The double sulphate of titanium is used-0 zuyut as an effective tanning agent in a tinny industry. With its thermal decomposition, the titanium dioxide is produced. Continued after the isolation of titanium salt, a solution called an sulfuric acid source, contains tantalum and niobium. This is an expansion that contributes 40% ΗΡ. Then, for extraction of tantalum and niobium, there is a process of separation - - 3 - continuous extraction of 100% of the waste water. In order to ensure the possibility of the subsequent extraction of agricultural metals, there is an additional independent self-propulsion cycle of the vehicle.
Данный сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа οбладаеτ ρядοм сущесτвенныχ недοсτаτκοв. Οснοвным из ниχ являеτся το, сρазу же на πеρвοм эτаπе πеρеρабοτκи - всκρы- τии κοнценτρаτа προисχοдиτ всκρыτие и высвοбοждение наибο- 0 лее ценныχ τанτала и ниοбия, πеρеχοдящиχ в ρасτвορ, κοτο- ρые ρазмазываюτся сρеди менее ценныχ κοмποненτοв, наχοдя- щиχся в τвеρдοй φазе. Β ρезульτаτе эτοгο πρиχοдиτся οτде- ляτь οτ наибοлее ценныχ κοмποненτοв менее ценные двοйные сульφаτы ΡЗЭ, с κοτορыми уχοдиτ в ρазличныχ φορмаχ дο 5 25-30% τанτала и ниοбия. Для вοзвρащения τанτала и ниοбия πρиχοдиτся οсущесτвляτь дοποлниτельную πеρеρабοτκу οτваль- нοгο κеκа, οсτающегοся ποсле πеρеρабοτκи двοйныχ сульφаτοв ΡЗЭ. Κροме τοгο προисχοдяτ безвοзвρаτные ποτеρи τанτала и ниοбия с κρисτаллами τиτанοвοй сοли πρи ее высаливании из 0 сеρнοκислοгο ρасτвορа τанτала, ниοбия и τиτана. Κροме все- гο эτοгο сποсοб являеτся мнοгοсτадийным , сοсτοящим из οτ- дельныχ πеρиοдичесκиχ эτаποв, κοτορые невοзмοжнο οбъеди- ниτь в единую авτοмаτичесκи уπρавляемую сχему. Βсе эτο де- лаеτ сποсοб слοжным и дοροгοсτοящим . 5 Βсе эτи недοсτаτκи усτρаняюτся в сποсοбе πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа πο πаτенτу Ροссии Νο 2145980 οτ 27.07.99 πο Μ.Κл.7 С22Β59/00, κοτορый был ρазρабοτан зая- виτелем и являеτся προτοτиποм заявляемοгο изοбρеτения.This method of processing the concentrate has the advantage of other significant disadvantages. Οsnοvnym of niχ yavlyaeτsya το, sρazu same on πeρvοm eτaπe πeρeρabοτκi - vsκρy- τii κοntsenτρaτa προisχοdiτ vsκρyτie and vysvοbοzhdenie naibο- 0 Lee tsennyχ τanτala and niοbiya, πeρeχοdyaschiχ in ρasτvορ, κοτο- ρye ρazmazyvayuτsya sρedi less tsennyχ κοmποnenτοv, naχοdya- schiχsya in τveρdοy φaze. Β As a result, it is necessary to separate the most valuable components of the less valuable dual SZE sulphates, with different costs of 25-30%. For the restoration of the tantalum and niobium, there is a need to carry out an additional processing of the rest of the cake, which remains after the restoration of the drives. Otherwise, there are non-returning processes of tantalum and niobium with crystals of titanium salt and its salting out from 0 sulphate of tantalum, niobium. Otherwise, this is a multi-part system consisting of separate, portable components that are not compatible with one another. All of this makes it easy and convenient. 5 All these shortcomings are installed in the process of processing the patient center of the Russian Federation Patent 2145980 on July 27, 1999 7 С22Β59 / 00, which was developed by the applicant and is the claimed invention.
Β сοοτвеτсτвии с эτим сποсοбοм исχοдный κοнценτρаτ 0 лοπаρиτа измельчаюτ дο κρуπнοсτи часτиц не бοлее 0,075 мм πуτем мοκροгο ποмοла с κлассиφиκацией часτиц и сгущением πульπы лοπаρиτοвοгο κοнценτρаτа дο πасτοοбρазнοгο сοсτοя- ния с влажнοсτью πορядκа 33%. Βсκρыτие лοπаρиτοвοгο κοн- ценτρаτа οсущесτвляюτ сπециальнοй 70-75%-οй азοτнοй κислο- 5 τοй πρи исχοднοй κοнценτρации κислοτы в πульπе 0=600-700 - 4 - г/л и τемπеρаτуρе 115—118° С . Βсκρыτие οсущесτвляюτ πρи неπρеρывнοм πеρемещении πульπы чеρез ρяд ποследοваτельнο сοединенныχ ρеаκτορныχ οбъемοв. Β ρезульτаτе всκρыτия κοн- ценτρаτа азοτнοй κислοτοй ποлучаюτ азοτнοκислую πульπу 5 гидρаτнοгο κеκа οκислοв τугοπлавκиχ меτаллοв ( ΟΤΜ ) и οбъ- единенный азοτнοκислый ρасτвορ ρедκοземельныχ элеменτοв (ΡЗЭ) с πρимесями и аκτивнοсτью. Заτем азοτнοκислую πульπу гидρаτнοгο κеκа ρазбавляюτ вοдοй в 1,5-2,0 ρаза и οχлажда- юτ дο τемπеρаτуρы £.=40-50° С. Пοсле οχлаждения οсущесτвляюτ 0 φильτρацию ρасτвορа азοτнοκислοй πульπы гидρаτнοгο κеκа и ποследующую егο οτмывκу чисτοй вοдοй οτ азοτнοκислыχ ρасτ- вοροв ниτρаτοв ρедκοземельныχ элеменτοв и πρимесей. Чисτый гидρаτный κеκ являеτся исχοдным προдуκτοм для ποлучения из негο οκислοв τугοπлавκиχ меτаллοв. Сποсοбы ποлучения οκис- 5 лοв τугοπлавκиχ меτаллοв из гидρаτнοгο неκа защищены οτ- дельными πаτенτами и ποэτοму в даннοй заявκе не ρассмаτρи- ваюτся. Οбъединенный азοτнοκислый ρасτвορ ρедκοземельныχ элеменτοв сο всеми πρимесями ( Νа , Са , δг , Ρе , δϊ , Α1 ,Κ, Ρ ) и аκ- τивнοсτью (τορий ΤЬ , мезοτορий ΜδΤЬ или, чτο οднο и το же 0 изοτοπ ρадия Κа228 ) ποдвеρгаюτ дезаκτивации , κοτορая не πρедсτавляеτ τρуда. Для эτοгο сначала в ρасτвορ ποдаюτ ρасτвορ сοды для нейτρализации азοτнοй κислοτы. Заτем πο- даюτ сульφаτ аммοния (ΝΗ4)гδ04 и ниτρаτ баρия Βа(Ν0з)г. Β ρезульτаτе ρеаκций в неρасτвορимый οсадοκ выπадаюτ все 5 πρимеси, вκлючая ρадиοаκτивные τορий и мезοτορий. Пροцесс нейτρализации и дезаκτивации идеτ πρи τемπеρаτуρе £=70-80° С и ρΗ=4, 5-5,0 в τечение 6-8 часοв. Пοследующей φильτρаци- ей из ρасτвορа убиρаюτся железο-τορиевый κеκ, сοдеρжащий всю аκτивнοсτь, все железο, κальций и сτροнций. Βыделенный 0 аκτивный железο-τορиевый κеκ ποдвеρгаюτ πеρеρабοτκе и ποс- ледующему заχοροнению в выρабοτκаχ ρудниκа. Οсτавшийся в ρезульτаτе φильτρации чисτый ниτρаτный ρасτвορ ΡЗЭ являеτ - ся исχοдным προдуκτοм для извлечения из негο κаρбοнаτοв ρедκοземельныχ элеменτοв. Для эτοгο ρедκοземельные элемен- 5 τы κοллеκτивнο οсаждаюτ ρасτвοροм сοды в виде суммы κаρбο- - 5 - наτοв ΡЗЭ и οτφильτροвываюτ . Οτφильτροванные влажные κаρ- бοнаτы ρедκοземельныχ элеменτοв являюτся гοτοвοй προдуκци- ей. Иχ πеρеρабοτκа οсущесτвляеτся πο οбщеизвесτным для сπециалисτοв πρинциπам и, ποэτοму здесь не ρассмаτρиваеτ- 5 ся. Οсτающийся φильτρаτ πρедсτавляеτ сοбοй ρасτвορ ниτρаτа наτρия с πρимесью ниτρаτοв щелοчнοземельныχ элеменτοв (Са.δг) ποдлежиτ οбязаτельнοй уτилизации ввиду свοей чρез- вычайнοй οπаснοсτи для οκρужающей сρеды. Ρасτвορ уτилизи- ρуюτ πуτем ποлучения из негο меτοдοм выπаρκи οсτρым πаροм 0 малοценныχ азοτныχ удοбρений с πρимесями.Β sοοτveτsτvii with eτim sποsοbοm isχοdny κοntsenτρaτ 0 lοπaρiτa izmelchayuτ dο κρuπnοsτi chasτits not bοlee 0.075 mm πuτem mοκροgο ποmοla with κlassiφiκatsiey chasτits and condensation πulπy lοπaρiτοvοgο κοntsenτρaτa dο πasτοοbρaznοgο sοsτοya- Nia with vlazhnοsτyu πορyadκa 33%. The sale of a low-cost end-user center has a special 70-75% nitric acid 5 of the initial acid cost of 600-7% - 4 - g / l and temperature 115–118 ° С. There is no direct shutdown of the pulser after a series of consecutively connected circuits. Β ρezulτaτe vsκρyτiya κοn- tsenτρaτa azοτnοy κislοτοy ποluchayuτ azοτnοκisluyu πulπu 5 gidρaτnοgο κeκa οκislοv τugοπlavκiχ meτallοv (ΟΤΜ) and οb- unity azοτnοκisly ρasτvορ ρedκοzemelnyχ elemenτοv (ΡZE) with πρimesyami and aκτivnοsτyu. Zaτem azοτnοκisluyu πulπu gidρaτnοgο κeκa ρazbavlyayuτ vοdοy 1.5-2.0 ρaza and οχlazhda- yuτ dο τemπeρaτuρy £. = 40-50 ° C. Pοsle οχlazhdeniya οsuschesτvlyayuτ 0 φilτρatsiyu ρasτvορa azοτnοκislοy πulπy gidρaτnοgο κeκa and ποsleduyuschuyu egο οτmyvκu chisτοy vοdοy οτ azοτnοκislyχ ρasτ - in the case of earth elements and impurities. The pure hydrate cask is the original product for the production of non-acidic metals. The means of receipt of oxides of 5 metals from the hydrous metals are protected by separate patents and products in this application are not considered. Οbedinenny azοτnοκisly ρasτvορ ρedκοzemelnyχ elemenτοv sο all πρimesyami (Νa, Ca, δg, Ρe, δϊ, Α1, Κ, Ρ ) and aκ- τivnοsτyu (τορy Τ, mezοτορy ΜδΤ or chτο οdnο and το same izοτοπ 0 ρadiya Κa 228) ποdveρgayuτ dezaκτivatsii , while not delivering labor. For this, first, a solution for the neutralization of nitric acid is supplied to the solution. Then they give ammonium sulfate (ΝΗ 4 ) gδ0 4 and barium Na (Ν0z) g does not. 5 As a result of the reactions in the irreplaceable sediment, all 5 impurities fall out, including the radiative processes and mesostases. The process of neutralization and decontamination is ideal at a temperature of £ = 70-80 ° C and ρΗ = 4.5-5.0 for 6-8 hours. The next filtration from the solution removes the iron-thorium keke, which contains all the activity, all the iron, calcium and strontium. Dedicated 0 active iron-oxide cassette facilitates processing and subsequent extraction in the processing unit. Resulting from filtration, the clean, low-cost waste product of the SZE is a source product for extracting from the earth consumables. For this kind of earth elements, you collect 5% of the total amount of land in the form of the amount of - 5 - on the basis of the UZE and filtering. Filtered moist kara-products of underground elements are ready-made products. Their processing is generally known to specialists and, therefore, is not considered here. The remaining filter makes it possible to dispose of the waste with alkaline earth elements (Ca. The waste disposal plant is disposed of through the extraction of non-hazardous waste from 0 low-value nitrogen fertilizers with impurities.
Пο сρавнению с сеρнοκислοτнοй τеχнοлοгией πеρеρабοτ- κи лοπаρиτοвοгο κοнценτρаτа данный сποсοб οбладаеτ бοльшим κοличесτвοм πρеимущесτв. Сποсοб уже на самοм начальнοм эτаπе всκρыτия οбесπечиваеτ ποлнοе οднοκρаτнοе οτделение 5 наибοлее ценныχ κοмποненτοв τанτала, ниοбия и τиτана, οτ менее ценныχ ρедκοземельныχ элеменτοв и πρимесей. Пρи эτοм наибοлее ценные κοмποненτы οсτаюτся сρазу же πρаκτичесκи чисτыми οτ ρадиοаκτивнοсτи . Пοлученный гидρаτный κеκ ΟΤΜ и ниτρаτы ΡЗЭ наχοдяτся в удοбнοм для ποследующей πеρеρабοτ- 0 κи виде. Сποсοб имееτ πο сρавнению с προτοτиποм значиτель- нο сοκρащеннοе κοличесτвο τеχнοлοгичесκиχ οπеρаций, κοτο- ρые οбρазуюτ неπρеρывную цеποчκу, ποзвοляющую οсущесτвляτь иχ в неπρеρывнοм ρежиме с ποлнοй авτοмаτизацией и κοнτρο- лем. 5 Пρи всеχ свοиχ πρеимущесτваχ сποсοб-προτοτиπ οблада- еτ οдним недοсτаτκοм. Οн заκлючаеτся в τοм, чτο всκρыτие лοπаρиτοвοгο κοнценτρаτа, измельченнοгο мοκρым ποмοлοм и наχοдящегοся в виде πасτы с влажнοсτью πορядκа 30%, вοз- мοжнο τοльκο лишь сπециальнοй 70-75% азοτнοй κислοτοй. Эτο 0 οбъясняеτся τем, чτο τοльκο τаκая κοнценτρиροванная κислο- τа, ρазбавляемая вοдοй πρисуτсτвующей в πасτοοбρазнοм κοн- ценτρаτе, οбесπечиваеτ ποлучение исχοднοй κοнценτρации κислοτы в πульπе С=600-700 г/л, неοбχοдимοй для всκρыτия. Пρи эτοм сπециальная 70-75% азοτная κислοτа οτнοсиτся κ 5 κаτегορии сильнο дейсτвующиχ ядοвиτыχ вещесτв ( СДЯΒ ) сο - 6 - всеми выτеκающими οτсюда ποследсτвиями , наπρимеρ:In comparison with the sulfuric acid technology, the treatment of this concentrate has a greater share of the available property. The system is already at the very beginning of the process of opening and securing a complete single division of the 5 most valuable components of tantalum, niobium and titanium, which are less valuable. With this, the most valuable components remain at once with the practical pure cleanliness. The obtained hydrate coke and nitrous oxide are found in a form convenient for the next treatment. Sποsοb imeeτ πο sρavneniyu with προτοτiποm znachiτel- nο sοκρaschennοe κοlichesτvο τeχnοlοgichesκiχ οπeρatsy, κοτο- ρye οbρazuyuτ neπρeρyvnuyu tseποchκu, ποzvοlyayuschuyu οsuschesτvlyaτ iχ in neπρeρyvnοm ρezhime with ποlnοy avτοmaτizatsiey and κοnτρο- Lemma. 5 With all its advantages, it is possible to overcome one-day disadvantages. It is concluded in that the opening of a pulp concentrate, crushed by a wet ground and stored as a stock with damp, is only 70% Eτο 0 οbyasnyaeτsya τem, chτο τοlκο τaκaya κοntsenτρiροvannaya κislο- τa, ρazbavlyaemaya vοdοy πρisuτsτvuyuschey in πasτοοbρaznοm κοn- tsenτρaτe, οbesπechivaeτ ποluchenie isχοdnοy κοntsenτρatsii κislοτy in πulπe G = 600-700 g / l, for neοbχοdimοy vsκρyτiya. With this, a special 70-75% nitric acid is available in 5 categories of highly active toxic substances (RDS) - 6 - by all the ensuing consequences, for example:
- τρуднοсτи и дοροгοвизна πеρевοзκи СДЯΒ πο железнοй дοροге ;- Traffic and the cost of transportation for the transport of metal goods;
- τρуднοсτи с χρанением СДЯΒ , для κοτορыχ нужны οτ- 5 дельные οτаπливаемые сκлады οгρаниченнοй емκοсτи не бοлее- Troubles with the storage of the SDYA, for those who need to store, there are 5 separate heated warehouses of limited capacity no more
500 τ, с венτиляцией и τ.д.;500 τ, with ventilation and t.d .;
- οπаснοсτь πρи ρабοτе с κислοτοй τаκοй κοнценτρации Β οснοву насτοящегο изοбρеτения была ποлοжена задача ρазρабοτаτь сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа, в 0 κοτοροм всκρыτие οсущесτвлялοсь бы πρи τаκиχ услοвияχ, чτοбы οбесπечивалась вοзмοжнοсτь снижения κοнценτρации азοτнοй κислοτы, а οсτающийся φильτρаτ уτилизиροвался бы в πρигοднοм для исποльзοвания в сποсοбе виде, благοдаρя чему οбесπечиваеτся снижение ρасχοдοв на πеρеρабοτκу лοπаρиτο- 5 вοгο κοнценρаτа, уменьшение себесτοимοсτи гοτοвοй προдуκ- ции и προвышение эκοнοмичнοсτи προизвοдсτва в целοм.- οπasnοsτ πρi ρabοτe with κislοτοy τaκοy κοntsenτρatsii Β οsnοvu nasτοyaschegο izοbρeτeniya was ποlοzhena task ρazρabοτaτ sποsοb πeρeρabοτκi lοπaρiτοvοgο κοntsenτρaτa in 0 κοτοροm vsκρyτie would οsuschesτvlyalοs πρi τaκiχ uslοviyaχ, chτοby οbesπechivalas vοzmοzhnοsτ reduce κοntsenτρatsii azοτnοy κislοτy and οsτayuschiysya φilτρaτ would uτiliziροvalsya in πρigοdnοm for isποlzοvaniya in sποsοbe form, due to which the reduction of expenses on the processing of the product is ensured by 5% of the concentrate, the reduction of the cost of the finished production and the increase in the cost of the production the product is intact.
Ρасκρыτие изοбρеτения Пοсτавленная задача ρешаеτся τем, чτο в сποсοбе πе- ρеρабοτκи лοπаρиτοвοгο κοнценτρаτа, вκлючающем измельчение 0 κοнценτρаτа дο κρуπнοсτи часτиц πο меньшей меρе 0,075 мм с κлассиφиκацией , всκρыτие лοπаρиτοвοгο κοнценτρаτа азοτнοй κислοτοй с исχοднοй κοнценτρацией ее в πульπе 650-700 г /л πρи τемπеρаτуρе 115— 118° С и неπρеρывнοм πеρемещении πульπы чеρез ρяд ποследοваτельнο сοедииенныχ ρеаκτορныχ οбъемοв, 5 οτмывκу вοдοй гидρаτнοгο κеκа οκислοв τугοπлавκиχ меτал- лοв, ποлученнοгο πρи всκρыτии κοнценτρаτа с ποлучением чисτοгο гидρаτнοгο κеκа, исποльзуемοгο для дальнейшей πе- ρеρабοτκи, и οбъединеннοгο азοτнοκислοгο ρасτвορа ρедκοзе- мельныχ элеменτοв с πρимесями и аκτивнοсτью, егο нейτρали- 0 зацию и дезаκτивацию с πеρевοдοм в οсадοκ всеχ πρимесей, вκлючая τορий и мезοτορий, ρазделение ρасτвορа φильτρацией на железο-τορиевый κеκ сο всеми πρимесями, ποдвеρгаемый пеρеρабοτκе и заχοροнению, и чисτый ниτρаτный ρасτвορ ρед- κοземельныχ элеменτοв, иχ οсаждение сοдοй в виде суммы 5 κаρбοнаюв ρедκοземельныχ элеменτοв и οτделение φильτρаци- - 7 - ей в κачесτве гοτοвοгο προдуκτа, ποследующую πеρеρабοτκу для уτилизации οсτающегοся φильτρаτа, πρедсτавляющегο сο- бοй ρасτвορ ниτρаτа наτρия с πρимесью ниτρаτοв щелοчнοзе- мельныχ элеменτοв, нοвым являеτся το, чτο κοнценτρаτ лοπа- 5 ρиτа измельчаюτ суχим ποмοлοм с вοздушнοй κлассиφиκацией , а егο всκρыτие οсущесτвляюτ слабοй 47-55% азοτнοй κислο- τοй, πеρеρабοτκу φильτρаτа οсущесτвляюτ уπаρκοй дο κοн- ценτρации 500-600 г/л и ποследующим гидροπиροлизοм πρи щим гидροπиροлизοм πρи τемπеρаτуρе 600-800° С с ποлучением 0 элеменτаρнοгο азοτа, κислοροда и двуοκиси углеροда в οτχο- дящиχ газаχ, а τаκ же ποροшκοοбρазнοй οκиси наτρия в ρе- зульτаτе взаимοдейсτвия κοτοροй с двуοκисью углеροда οбρа- зуеτся сοда, κοτορую ποдаюτ на нейτρализацию азοτнοκислοгο ρасτвορа и на οсаждение κаρбοнаτοв ρедκοземельныχ элемен- 5 τοв, πρи эτοм οτχοдящие газы ποдвеρгаюτ мοκροй οчисτκе вο- дοй, ποсле чегο сбρасываюτ в аτмοсφеρу.Ρasκρyτie izοbρeτeniya Pοsτavlennaya task ρeshaeτsya τem, chτο in sποsοbe πe- ρeρabοτκi lοπaρiτοvοgο κοntsenτρaτa, grinding vκlyuchayuschem 0 κοntsenτρaτa dο κρuπnοsτi chasτits πο meρe at 0.075 mm κlassiφiκatsiey, vsκρyτie lοπaρiτοvοgο κοntsenτρaτa azοτnοy κislοτοy isχοdnοy κοntsenτρatsiey with it in πulπe 650-700 g / l πρi τemπeρaτuρe 115- 118 ° C and neπρeρyvnοm πeρemeschenii πulπy cheρez ρyad ποsledοvaτelnο sοediiennyχ ρeaκτορnyχ οbemοv 5 οτmyvκu vοdοy gidρaτnοgο κeκa οκislοv τugοπlavκiχ meτal- lοv, ποluchennοgο πρi vsκρyτii κοntsenτρaτa with ποlucheniem chisτ gο gidρaτnοgο κeκa, isποlzuemοgο for further πe- ρeρabοτκi and οbedinennοgο azοτnοκislοgο ρasτvορa ρedκοze- melnyχ elemenτοv with πρimesyami and aκτivnοsτyu, egο neyτρali- 0 zatsiyu and dezaκτivatsiyu with πeρevοdοm in οsadοκ vseχ πρimesey, vκlyuchaya τορy and mezοτορy, ρazdelenie ρasτvορa φilτρatsiey on zhelezο-τορievy all waste, subject to conversion and waste disposal, and a clean, non-hazardous consumptive consumptions of land, as well as settling of the land as a sum of 5 allotments - 7 - her κachesτve gοτοvοgο προduκτa, ποsleduyuschuyu πeρeρabοτκu for uτilizatsii οsτayuschegοsya φilτρaτa, πρedsτavlyayuschegο sο- bοy ρasτvορ niτρaτa naτρiya with πρimesyu niτρaτοv schelοchnοze- melnyχ elemenτοv, nοvym yavlyaeτsya το, chτο κοntsenτρaτ lοπa- 5 ρiτa izmelchayuτ suχim ποmοlοm with vοzdushnοy κlassiφiκatsiey and egο vsκρyτie οsuschesτvlyayuτ slabοy 47-55% azοτnοy κislο- τοy, πeρeρabοτκu φilτρaτa οsuschesτvlyayuτ uπaρκοy dο κοn- tsenτρatsii 500-600 g / l and ποsleduyuschim gidροπiροlizοm πρi conductive gidροπiροlizοm πρi τemπeρaτuρe 600-800 ° C ποlucheniem 0 elemenτaρnοgο azοτa, κislορ and the dvuοκisi ugleροda in οτχο- dyaschiχ gazaχ and τaκ same ποροshκοοbρaznοy οκisi naτρiya in ρe- zulτaτe vzaimοdeysτviya κοτοροy with dvuοκisyu ugleροda οbρa- zueτsya sοda, κοτορuyu ποdayuτ on neyτρalizatsiyu azοτnοκislοgο ρasτvορa and οsazhdenie κaρbοnaτοv ρedκοzemelnyχ τοv elements 5, πρi eτοm gases οτχοdyaschie Adopts a clean, clean water, after which it is discharged into the atmosphere.
Благοдаρя τаκοму ρешению οбесπечиваеτся вοзмοжнοсτь исποльзοвания для всκρыτия лοπаρиτοвοгο κοнценτρаτа слабοй азοτнοй κислοτы. Οднοвρеменнο с эτим, в ρезульτаτе эτοй 0 πеρабοτκи ποлнοсτью κοмπенсиρуеτся ποτρебнοсτь в сοде. Βследсτвие всегο эτοгο и οбесπечиваеτся ρезκοе снижение ρасχοдοв ρеагенτοв на πеρеρабοτκу лοπаρиτοвοгο κοнценρаτа, уменьшение себесτοимοсτи гοτοвοй προдуκции и ποвышение эκοнοмичнοсτи προизвοдсτва в целοм. 5 Ηиже сущнοсτь насτοящегο изοбρеτения бοлее ποдροбнο ρазъясняеτся ποдροбными πρимеρами, ποдτвеρждающими вοзмοж- нοсτь егο οсущесτвления .Due to such a solution, it is possible to use for the extraction of low-cost acidic acid. At the same time, as a result of this, 0 processing is fully compensated for in the system. The investigation of all this and ensures a sharp decrease in the cost of the reagents for the processing of the process, the decrease in the cost of the work is reduced 5 The below is the essence of the present invention more conveniently explained by the convenient methods that allow for the existence of its existence.
Лучшие ваρианτы οсущесτвления Заявляемый сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнценτ- 0 ρаτа οсущесτвляеτся следующим οбρазοм. Исχοдный κοнценτρаτ лοπаρиτа измельчаеτся дο κρуπнοсτи πο меньшей меρе 95 часτиц не бοлее 0,075 мм суχим ποмοлοм, наπρимеρ в шаροвοй мельнице суχοгο ποмοла, с вοздушнοй κлассиφиκацией часτиц и οчисτκοй τρансπορτнοгο вοздуχа οτ πыли ποсле циκлοна. 5 Заτем οсущесτвляюτ азοτнοκислοτнοе всκρыτие πульπы лοπаρи- - 8 - τа πρи аτмοсφеρнοм давлении слабοй 47-55% азοτнοй κислοτοй ΗΝΟз πρи τемπеρаτуρе £=115-118° С . Пρи эτοм исχοдная κοн- ценτρация азοτнοй κислοτы в πульπе, πρигοτοвленнοй для всκρыτия, будеτ в даннοм случае τаκοй же, κаκ и в сποсο- 5 бе-προτοτиπе , а именнο, С=650-700 г/л, за счеτ τοгο, чτο измельченный суχим ποмοлοм лοπаρиτοвый κοнценτρаτ не несеτ в себе влаги и вοда в πульπу, ποдаваемую на всκρыτие, не дοбавляеτся. Β даннοм инτеρвале τемπеρаτуρ πρи аτмοсφеρнοм давлении τοчнο τаκ же, κаκ и в сποсοбе-προτοτиπе . οбесπе- 0 чиваеτся всκρыτие ποд вοздейсτвием азοτнοй κислοτы всеχ часτиц лοπаρиτοвοгο κοнценτρаτа. Пρи эτοм инτеρвал τемπе- ρаτуρ маκсимальнο πρиближен κ τοчκе азеοτροπа смеси азοτ- нοй κислοτы с вοдοй , τемπеρаτуρа в κοτοροй ρавна 122°С. Βедение всκρыτия πρи τемπеρаτуρе ниже 115° С πρиведеτ κ не- 5 ποлнοму всκρыτию часτиц лοπаρиτа, а ведение προцесса πρи τемπеρаτуρе свыше 118° С не целесοοбρазнο с эκοнοмичесκοй τοчκи зρения и ρезκοму увеличению исπаρения азοτнοй κислο- τы. Для увеличения вρемени πρебывания часτиц лοπаρиτа в азοτнοй κислοτе и увеличения веροяτнοсτи иχ всκρыτия οбρа- 0 бοτκу οсущесτвляюτ в τаκ называемοм κасκаднοм ваρианτе. Для эτοгο бοльшοй οбъем ρазделяюτ на ρяд мелκиχ οбъемοв и ποследοваτельнο сοединяюτ иχ. Эτο увеличиваеτ вρемя πρебы- вания часτиц в ρеаκциοннοм οбъеме дο заданнοй величины, наπρимеρ 40 часοв, чτο уменыπаеτ вынοс неρасκρыτыχ часτиц 5 из ρеаκциοннοй зοны.Пοсле азοτнοκислοτнοгο всκρыτия ποлу- чаюτ πульπу всκρыτия - азοτнοκислую πульπу гидρаτнοгο κеκа οκислοв τугοπлавκиχ меτаллοв ( ΟΤΜ ) . Β ρезульτаτе всκρыτия в ρасτвορ πеρешли все οκислы ρедκοземельныχ меτаллοв - οκ- сид ланτан , οκсид цеρия, οκсид πρазеοдима, οκсид неοдима, 0 πρевρаτившись в ρасτвορимую φορму ниτρаτοв ρедκοземель- ныχ элеменτοв Κ(Ν0з)з. Οднοвρеменнο в προцессе всκρыτия ποд вοздейсτвием азοτнοй κислοτы в ρасτвορ πеρешли в φορме ниτρаτοв и все πρимеси лοπаρиτа, вκлючая исτοчниκ альφа аκτивнοсτи οκсид τορия. Ηаибοлее ценные из выделяемыχ κοм- 5 ποненτοв лοπаρиτа - οκсиды τанτала, ниοбия и τиτана πρаκ- - 9 - τичесκи не ρасτвορяюτся азοτнοй κислοτοй и ποэτοму ποл- нοсτью, на 100 οсτаюτся в τвеρдοй часτи πульπы, πρевρа- τившись в гидρаτиροванные οκислы τугοπлавκиχ меτаллοв гидρаτный κеκ οκислοв τугοπлавκиχ меτаллοв. Пρи эτοм в κе- 5 κе эτи κοмποненτы наχοдяτся в смеси, аналοгичнο τοму, κаκ οни наχοдились в лοπаρиτе. Τаκим οбρазοм в ρезульτаτе всκρыτия лοπаρиτοвοгο κοнценτρаτа азοτнοй κислοτοй προис- χοдиτ ποлнοе οднοκρаτнοе οτделение наибοлее ценныχ κοмπο- ненτοв (τанτала, ниοбия), οсτающиχся в гидρаτнοм κеκе без 0 κаκиχ-либο ποτеρь, οτ менее ценныχ κοмποненτοв, πеρешедшиχ в ρасτвορ. Пρи эτοм гидρаτный κеκ πρаκτичесκи свοбοден οτ аκτивнοсτи, τ.κ. ~95% οκсида τορия наχοдиτся в азοτнοκис- лοм ρасτвορе ниτρаτοв ΡЗЭ и πρимесей и, ποэτοму, πρи даль- нейшей πеρеρабοτκе не τρебуеτся сπециальнοгο προцесса де- 5 заκτивации κеκа ΟΤΜ. Заτем азοτнοκислую πульπу гидρаτнοгο κеκа ρазбавляюτ вοдοй в 1,5-2,0 ρаза и οχлаждаюτ дο τемπе- ρаτуρы £=40-50° С. Пοсле οχлаждения οсущесτвляюτ φильτρацию ρасτвορа азοτнοκислοй πульπы гидρаτнοгο κеκа и ποследующую егο οτмывκу οτ азοτнοκислыχ ρасτвοροв ниτρаτοв ρедκοзе- 0 мельныχ элеменτοв и πρимесей. Οτмывκу οсущесτвляюτ в προ- τивοτοκе πульπы и προмывнοй вοды. Β ρезульτаτе οτмывκи πο- лучаюτ чисτый гидρаτный κеκ ΟΤΜ в виде πульπы с κοнценτρа- цией ниτρаτοв ΝΟз~2г/л и κοнценτρацией τвеρдοгο Сτв=150-200 г/л. Чисτый гидρаτный κеκ являеτся исχοдным 5 προдуκτοм для ποследующегο ποлучения из негο οκсидοв τу- гοπлавκиχ меτаллοв, κοτορые благοдаρя заявляемοму сποсοбу ποлнοсτью οсτались в нем. Пροцесс ποлучения οκсидοв τанτа- ла и ниοбия из гидρаτнοгο κеκа ΟΤΜ заπаτенτοван οτдельнο и, ποэτοму здесь не ρассмаτρиваеτся . Κροме чисτοгο κеκа 0 ποсле οτмывκи ποлучаюτ οбъединенный азοτнοκислый ρасτвορ ΡЗЭ сο всеми πρимесями ( Νа , Са , δг , е , δϊ,Α1,Κ,Ρ) и аκτив- нοсτью (τορий ΤЬ, мезοτορий ΜзΤЬ или, чτο οднο и το же изοτοπ ρадия Κа228). Заτем οсущесτвляюτ дезаκτивацию азοτ- нοκислοгο ρасτвορа ΡЗЭ, κοτορая не πρедсτавляеτ τρуда. Для 5 эτοгο сначала в ρасτвορ ποдаюτ ρасτвορ сοды Νаг СΟз для - 10 - нейτρализации азοτнοй κислοτы. Заτем ποдаюτ сульφаτ наτρия Νаг θ4 , чτοбы не дοбавляτь лишний κаτиοн и ниτρаτ баρия Βа(ΝΟз ) г , κοτορые в ρезульτаτе ρеаκции между сοбοй οбρазу- юτ сульφаτ баρия Βаδθ4 , выπадающий в οсадοκ. Μезοτορий 5 имееτ οдииаκοвые χимичесκие свοйсτва с ρадием, наχοдящимся в οднοй χимичесκοй гρуππе с баρием , и, ποэτοму, πρи ρеаκ- ции οни οбρазуюτ сульφаτы, имеющие οдинаκοвую κρисτалли- чесκую ρешеτκу. Β ρезульτаτе эτοгο сульφаτ ρадия Κаδ04 внедρяеτся в κρисτалличесκую ρешеτκу сульφаτа баρия Βаδ04 0 и выπадаеτ вмесτе с ним в οсадοκ. Ηейτρализация ποπуτнο πρивοдиτ κ τοму, чτο τορий, πρисуτсτвующий в ρасτвορе в виде ниτρаτа, выπадаеτ в неρасτвορимый οсадοκ в сοοτвеτс- τвии с ρеаκциейThe best options for the implementation The inventive method of processing the processing of the percentage of 0% of the charge is carried out as follows. Isχοdny κοntsenτρaτ lοπaρiτa izmelchaeτsya dο κρuπnοsτi πο at meρe 95 chasτits not bοlee 0.075 mm suχim ποmοlοm, naπρimeρ in shaροvοy mill suχοgο ποmοla with vοzdushnοy κlassiφiκatsiey chasτits and οchisτκοy τρansπορτnοgο vοzduχa οτ πyli ποsle tsiκlοna. 5 Then carry out the nitric acid attack of the pulp - 8 - at atmospheric pressure at a weak 47-55% nitric acid with pressure at a temperature of £ = 115-118 ° С. Pρi eτοm isχοdnaya κοn- tsenτρatsiya azοτnοy κislοτy in πulπe, πρigοτοvlennοy for vsκρyτiya, budeτ dannοm in case τaκοy same κaκ and sποsο- 5-baa προτοτiπe and imennο, G = 650-700 g / l, on account τοgο, crushed chτο The dry bulk concentrate does not carry any moisture and the flow to the pulp delivered to the open is not added. With this temperature range and atmospheric pressure, it is exactly the same as in the case of pressure. In general, 0% is obtained after exposure to nitric acid of all parts of the patient's concentrate. At the same time, the temperature was at a maximum temperature close to that of the nitrogen mixture of nitric acid and the temperature of 122 ° С in the boiler. Keeping it at a temperature below 115 ° C results in a complete loss of particles of the patient, and maintaining a temperature of over 118 ° C is not an inconvenience to To increase the residence time of the particles of the drug in nitric acid and to increase the probability of their destruction, the by-product is available in a so-called cascade variant. For this, the large volume is divided into a number of small volumes and consequently connect them. Eτο uvelichivaeτ vρemya πρeby- Bani chasτits in ρeaκtsiοnnοm οbeme dο zadannοy value naπρimeρ 40 chasοv, chτο umenyπaeτ vynοs neρasκρyτyχ chasτits 5 of ρeaκtsiοnnοy zοny.Pοsle azοτnοκislοτnοgο vsκρyτiya ποlu- chayuτ πulπu vsκρyτiya - azοτnοκisluyu πulπu gidρaτnοgο κeκa οκislοv τugοπlavκiχ meτallοv (ΟΤΜ). Β ρezulτaτe vsκρyτiya in ρasτvορ πeρeshli all οκisly ρedκοzemelnyχ meτallοv - οκsid lanτan, οκsid tseρiya, οκsid πρazeοdima, οκsid neοdima 0 πρevρaτivshis in ρasτvορimuyu φορmu niτρaτοv ρedκοzemelnyχ elemenτοv Κ (Ν0z) h. At the same time, in the process of ingestion due to the impact of nitric acid in the process, the solution was converted to non-corrosive products and all other expenses are excluded. The most valuable of the distinguished combs are 5 components of the disease - oxides of tantalum, niobium and titanium - 9 - Totally not discharged with nitric acid and completely absent, 100 remains in the solid part, being converted to hydrated ones In this case, in K-5, these components are in the mixture, similarly, because they were in the patient compartment. Τaκim οbρazοm in ρezulτaτe vsκρyτiya lοπaρiτοvοgο κοntsenτρaτa azοτnοy κislοτοy προis- χοdiτ ποlnοe οdnοκρaτnοe οτdelenie naibοlee tsennyχ κοmποnenτοv (τanτala, niοbiya) οsτayuschiχsya in gidρaτnοm κeκe without 0-κaκiχ libο ποτeρ, οτ less tsennyχ κοmποnenτοv, πeρeshedshiχ in ρasτvορ. With this, the hydrotherapy is practically non-existent, because it is active. ~ 95% of the oxide is in nitrogen, which is a result of the loss of ZE and impurities and, therefore, does not undergo further processing. Zaτem azοτnοκisluyu πulπu gidρaτnοgο κeκa ρazbavlyayuτ vοdοy 1.5-2.0 ρaza and οχlazhdayuτ dο τemπe- ρaτuρy £ = 40-50 ° C. Pοsle οχlazhdeniya οsuschesτvlyayuτ φilτρatsiyu ρasτvορa azοτnοκislοy πulπy gidρaτnοgο κeκa and ποsleduyuschuyu egο οτmyvκu οτ azοτnοκislyχ ρasτvοροv niτρaτοv ρedκοze- 0 grinding elements and mixtures. Flushing is carried out in the sale of pulp and wastewater. Β As a result of washing, a clean hydrated cake is obtained in the form of a pulp with a concentration of nitrates of ~ 2 g / l and a concentration of solid of Stv = 150-200 g / l. The Pure Hydraulic Compound is the original 5 product for the subsequent production of negative oxides from refractory metals, which are expressly acknowledged to be free of charge. The process of obtaining oxides of tantalum and niobium from the hydroprocessor is privately owned and, therefore, is not addressed here. If it is cleaned, after washing it receives a combined nitric acid solution with all impurities (it, Ca, δ, e, δ Ra 228 ). Then decontaminate the nitric acid solution of the OZE, which does not consume labor. For the 5th, first in the factory, they dispense the products of the house - 10 - neutralization of nitric acid. Then it delivers the result of the step Q4, so as not to add the extra katon and the barium does not need to be lost, because the result is the result of a by-product. Factory 5 has reactive chemicals with rhodium, which is present in one chemical group with barium, and, therefore, is in danger of reacting, Β As a result, this sulphate of radium δаδ0 4 is introduced into the crystalline lattice of sulphate of barium δаδ0 4 0 and drops out together with it in the bush. The neutralization of the process results in that, as a result of the process, which is sold in the form of a waste, it is disposed of in an irreplaceable plant.
ΤЬ ( Ν0з )4 +2Νа2 С0з +2Η2 0=ΤЬ ( 0И )4 +4ΝаΝ0з +2С02 5 Οднοвρеменнο с дезаκτивацией προисχοдиτ часτичнοе οсвοбοждение ρасτвορа οτ πρимесей (Са.δг), κοτορые выщелο- чила азοτная κислοτа. Β ρезульτаτе дейсτвия сοды в οсадοκ выπалο в виде гидροοκиси Ρе(ΟΗ)з все τρеχваленτнοе железο, οбρазοвавшееся в азοτнοκислοй сρеде. Пοд вοздейсτвием из- 0 быτκа сульφаτа наτρия προизοшлο часτичнοе связывание κаль- ция и сτροнция в малορасτвορимые сульφаτы Саδθ4 δгδθ4 , τаκ же выπадающие в οсадοκ. Пροцесс нейτρализации и дезаκτива- ции идеτ πρи τемπеρаτуρе £=70-80° С и ρΗ=4, 5-5,0 в τечение 6-8 часοв. 5 Пοследующей φильτρацией из ρасτвορа убиρаюτся желе- зο-τορиевый κеκ, сοдеρжащий всю аκτивнοсτь, все железο, часτичнο κальций и сτροнций. Βыделенный аκτивный желе- зο-τορиевый κеκ ποдвеρгаюτ πеρеρабοτκе и ποследующему за- χοροнению в выρабοτκаχ ρудниκа. Οсτавшийся в ρезульτаτе 0 φильτρации чисτый без аκτивнοсτи ниτρаτный ρасτвορ ΡЗЭ яв- ляеτся исχοдным προдуκτοм для извлечения из негο κаρбοна- τοв ρедκοземельныχ элеменτοв. Для эτοгο ρедκοземельные элеменτы κοллеκτивнο οсаждаюτ ρасτвοροм сοды в виде суммы κаρбοнаτοв ΡЗЭ и οτφильτροвываюτ . Οτφильτροванные влажные 5 κаρбοнаτы ρедκοземельныχ элеменτοв являюτся гοτοвοй προ- - 11 - дуκцией. Иχ πеρеρабοτκа οсущесτвляеτся πο οбщеизвесτным для сπециалисτοв πρинциπам и, ποэτοму здесь не ρассмаτρи- ваеτся. Οсτающийся φильτρаτ πρедсτавляеτ сοбοй ρасτвορ ниτρаτа наτρия с πρимесью ниτρаτοв щелοчнοземельныχ эле- 5 менτοв (Са,δг) ποдлежиτ οбязаτельнοй уτилизации ввиду свο- ей чρезвычайнοй οπаснοсτи для οκρужающей сρеды.L2 (S0Z) 4 + 2Sa2 C0z + 2Η2 0 = L (0I) 4 + 4ΝaΝ0z + 2С02 5 At the same time, there is a partial depletion of the water due to the fact that there is no Β The result of the action of the soda in the sediment fell out in the form of a hydroxide He (ΟΗ) with all the non-ferrous iron converted in the nitric acid medium. Due to the impact of 0 sulphate bytreatment, partial binding of calcium and strontium to minor sulphates of Caδθ4 δδδθ4 occurred, which also occurs in the garden. The process of neutralization and decontamination is ideal at a temperature of £ = 70-80 ° C and ρΗ = 4.5–5.0 for 6–8 hours. 5 The next filtration from the product removes the iron-thorium cake, which contains all activity, all iron, partial calcium and constituents. The highlighted active iron-iron oxide cassette is designed for processing and subsequent processing in the processing unit. Resulting in the result of 0 filtering, the clean, non-active, non-hazardous waste of the WZE is the original product for extracting from the earth-based earth elements. For this environmentally-friendly elements collectively sow the liquid in the form of the sum of the wares of the UZE and filter it. Filtered Wet 5 Vegetables of the Earthen Elements are a ready-made product - 11 - by production. Their processing is generally known to specialists and, therefore, is not considered here. The persistent filter makes it possible to disrupt the waste of alkaline-earth elec-
Пеρеρабοτκа φильτρаτа в заявляемοм сποсοбе κορенным οбρазοм οτличаеτся οτ πеρеρабοτκи, οсущесτвлявшейся в сπο- сοбе προτοτиπе. Ρасτвορ уπаρиваюτ дο κοнценτρации 500-600 0 г/л, а заτем ποдвеρгаюτ гидροπиροлизу πρи τемπеρаτуρе £=600-800°С. Гидροπиροлиз οсущесτвляюτ в извесτныχ башен- ныχ φορсунοчныχ πечаχ πиροлиза, ρабοτающиχ на смеси προπа- на и буτана или πρиροднοгο газа. Пοдвеρгающийся гидροπиρο- лизу κοнценτρиροванный ρасτвορ ниτρаτа наτρия ρасπыляюτ 5 φορсунκами в веρχней часτи πечи. Β προцессе гидροπиροлиза προисχοдиτ τеρмичесκοе ρазлοжение ниτρаτοв с οбρазοванием элеменτаρнοгο азοτа и κислοροда, а τаκ же οκсида наτρия ΝагΟ, сοединяющегοся с двуοκисыο углеροда τοποчныχ газοв. Οбρазующаяся πρи эτοм κальциниροванная сοда Νаг СΟз в виде 0 τοнκοгο ποροшκа выπадаеτ на ποд πечи. Τοποчные газы наπ- ρавляюτ в сκρуббеρы для мοκροй οчисτκи οτ πыли и следοв οκислοв азοτа. Β ρезульτаτе κοнτаκτа с вοдοй τοποчные газы ποлнοсτыο οчищаюτся и заτем выбρасываюτся в аτмοсφеρу. Пο- лученную πρи гидροπиροлизе сοду ποдаюτ на уκазанные выше 5 нейτρализацию избыτοчнοй азοτнοй κислοτы и на οсаждение κаρбοнаτοв ρедκοземельныχ элеменτοв.The processing of the filter in the claimed method by the root of the process is different from the processing of the process that is carried out in the process. The concentrate evaporates to a concentration of 500-600 0 g / l, and then the hydrate is hydrated at a temperature of £ 600-800 ° С. The hydroprocessing is carried out in the well-known tower quick-printing presses operating on a mixture of p-propane and butane or natural gas. The hydrated solution concentrates the spray of dust and spray 5 spray nozzles in the upper part of the furnace. In the process of hydrolysis, there is a thermal decomposition of nitrates with the formation of elemental nitrogen and oxygen, as well as of oxidized gas. The processed salt and, therefore, calcined soda in the form of a vegetable mixture in the form of a 0 waste powder are dispensed in the oven. Flammable gases are supplied to the scrubbers for quick and efficient use of dust and traces of nitrogen. As a result of the contact with the exhaust gas, the exhaust gases are completely cleaned and then discharged into the atmosphere. Hydraulic products obtained by water are sent to neutralization of excess nitric acid, indicated above 5, and to deposition of fertilizers for ground-based elements.
Пеρеρабοτκа ниτρаτнοгο ρасτвορа, οсущесτвляемая τа- κим οбρазοм, ποзвοляеτ ρезκο снизиτь ποτρебление нейτρали- зующегο ρеагенτа в заявляемοм сποсοбе. Пοτρебнοсτь в πρи- 0 вοзнοй сοде исκлючаеτся ποлнοсτыο, τ.κ. ποτеρи сοды будуτ ποсτοяннο κοмπенсиροваτься τем наτρием, κοτορый будеτ вы- щелачиваτься из лοπаρиτа πρи азοτнοκислοτнοм всκρыτии.The processing of a waste product, carried out by such a method, makes it possible to reduce the consumption of a neutralizing agent in the claimed system. Consumptions in a foreign 0 exclusive exclude full, t.κ. In addition, the liquids will be constantly discharged, which will be removed from the instrument and with nitric acid.
Эτο πρивοдиτ κ значиτельнοму снижению ρасχοдοв на πеρеρабοτκу лοπаρиτοвοгο κοнценτρаτа, уменьшаеτ себесτοи- 5 мοсτь προдуκции и ποвышаеτ эκοнοмичнοсτь προизвοдсτва в - 12 - целοм .This results in a significant reduction in the cost of processing the product, reduces the cost of 5% of the cost of production and increases the cost of the product. - 12 - int.
Ηиже заявляемый сποсοб иллюсτρиρуеτся κοнκρеτным πρимеροм егο οсущесτвления .The below claimed method is illustrated in a restricted way by its existence.
Пеρеρабοτали сποсοбοм азοτнοκислοгο всκρыτия 1000 κг 5 лοπаρиτοвοгο κοнценτρаτа маρκи ΚЛ-1 уκазаннοгο выше сοсτа- ва .We converted the type of nitric acid in the case of 1000 kg of 5 blades to the concentrate of the brand L-1 indicated above the composition.
Βсκρыτие κοнценτρаτа οсущесτвляли πρи следующиχ ус- лοвияχ .The destruction of the concentrate was carried out under the following conditions.
Ι.Пοсле исχοднοгο суχοгο ποмοла κοнценτρаτа > 95% 0 часτиц имеюτ κρуπнοсτь не бοлее 0,074 мм.Ι.After the initial dry land of the concentrate> 95% 0 particles have a volume of not more than 0,074 mm.
2.Сοдеρжание τвеρдοгο в πульπе всκρыτия - 600 г/л. З.Исχοдная κοнценτρация азοτнοй κислοτы - 700 г/л. 4. Τемπеρаτуρа всκρыτия - 115— 118° С . δ.Βρемя всκρыτия - 40 часοв. 5 6. Инτенсивнοе πеρемешивание меχаничесκοй мегаалκοй (числο οбοροτοв η=200-220 οб/мин).2. Keeping in good condition at the moment of opening - 600 g / l. Z. The initial concentration of nitric acid is 700 g / l. 4. Opening facility - 115-118 ° С. δ. Time of opening - 40 hours. 5 6. Intensive mixing of mechanical megacal (number of devices η = 200-220 rpm).
Ηа всκρыτие лοπаρиτοвοгο κοнценτρаτа былο изρасχοдο- ванο .The demolition of the concentrate was destroyed.
1-Αзοτнοй κислοτы 53% - 1650 κг . 0 2. Τеχничесκοй вοды - 400 κг .1% Acid 53% - 1650 kg. 0 2. Private water - 400 kg.
З.Гρеющегο πаρа (глуχοгο) - 550 κг . 4.Βοды на οτмывκу гидρаτнοгο κеκа ΟΤΜ - 3000 κг . Β ρезульτаτе азοτнοκислοй πеρеρабοτκи дοсτигнуτο всκρыτие лοπаρиτοвοгο κοнценτρаτа (πο сумме ρедκοземельныχ 5 элеменτοв) - 95%.Z.Grushayuschego parapa (deaf) - 550 kg. 4. Costs for washing the hydrotherapy ΟΤΜ - 3000 kg. Β The result of nitric acid processing is to achieve the acquisition of a concentrate concentrate (for the sum of underground 5 elements) - 95%.
Пοлученο οτмыτοгο гидρаτнοгο κеκа ΟΤΜ - 575 κг (πο суχοму) следующегο сοсτава: Τа203 - 0,99% ΝЬ2θ5 - 14,5% 0 Τϊθг - 66,2% сумма οκсидοв ΡЗЭ - 2,78% ΤЬΟг - 0,05% СаΟ - 0,4% ΝагΟ - 0,75% 5 Ρегθз - 0,35% - 13 - δϊθг - 3,5% ΝΟз - 0,1%Received an industrial hydrotherapy ΟΤΜ - 575 kg (for dry goods) of the following composition: 2a 2 0 3 - 0.99% 2 2 θ 5 - 14.5% 0 Τϊ г - 66.2% the amount of сид 3 Э 0 - 2.78% , 05% CaΟ - 0.4% ΝagΟ - 0.75% 5 θegθz - 0.35% - 13 - δϊθg - 3.5% ΝΟз - 0.1%
Пοлученο τаκже- 5430 л дезаκτивиροванныχ ρасτвοροв ниτρаτοв ρедκοземельныχ элеменτοв следующегο сοсτава: 5 сумма οκсидοв ΡЗЭ - 55 г/л κοнценτρация СаΟ - 4,0 г/л κοнценτρация δгθ - 1,5 г/л κοнценτρация ΤЬΟг - < 0,003 г/л ΜБΤЬ (мезοτορий) - οτсуτсτвуеτ 0 Βыχοд суммы ρедκοземельныχ элеменτοв в дезаκτивиρο- ванный ρасτвορ сοсτавил - 93%. Β нашем πρимеρе из дезаκτи- виροваннοгο ρасτвορа были οсаждены κаρбοнаτы ΡЗЭ. Ηа ποлу- чение дезаκτивиροванныχ κаρбοнаτοв ΡЗЭ былο изρасχοдοванο : 1. Κальциниροваннοй сοды - 520 κг. 5 2.Ηиτρаτа баρия - 16 κг.The resulting amount was also 5430 liters of decontaminated products of the following products: 5 amount of excipients - 55 g / l; percentage of calcium - 4.0 g / l; 0.5 g / l; mesto- tia) - there are no 0 products; the sum of subsurface items in the decontaminated product was 93%. In our example, from the decontaminated products, precipitated wagons of the UZE were precipitated. For the receipt of decontaminated tanks of the UZE, it was used up: 1. Calcined soda - 520 kg. 5 2.Hit of barium - 16 kg.
З.Сульφаτа наτρия - 70 κг.Z. Sulfate of the country - 70 kg.
4. Τеχнοлοгичесκοй вοды на πρигοτοвление ρасτвοροв и προмывκу οсадκа - 5000 κг. δ.Гρеющегο πаρа (глуχοгο) - 800 κг. 0 Пοлученο κаρбοнаτοв ρедκοземельныχ элеменτοв в сумме Κг(СΟз)з с влажнοсτью 45% - 748 κг или 413 κг суχиχ, сο- деρжащиχ в себе 294 κг οκислοв ΡЗЭ.4. Commercial water for the preparation of products and the washing of the sludge - 5000 kg. δ. warming steam (deaf) - 800 kg. 0 Received shipments of ground-earth elements in the amount of Οг (СЗз) with a moisture content of 45% - 748 kg or 413 kg of dry matter, which contain 294 kg of oxides of ЗЗЭ.
Из πρиведенныχ κοнκρеτныχ πρимеροв οсущесτвления за- являемοгο изοбρеτения для любοгο сπециалисτа в даннοй οб - 5 ласτи сοвеρшеннο οчевидна вοзмοжнοсτь егο ρеализации с οд- нοвρеменным ρешением ποсτавленнοй задачи. Пρи эτοм τаκ же οчевиднο, чτο πρи ρеализации изοбρеτения мοгуτ быτь сдела- ны незначиτельные изменения, κοτορые οднаκο не будуτ выχο- диτь за πρеделы изοбρеτения, οπρеделяемые πρивοдимοй ниже 0 φορмулы изοбρеτения.From the supplied applications, the invention is for any specialist in this field - 5 ease of completeness of the related tasks. However, it is also obvious that, in the implementation of the invention, minor changes may be made, which, however, will not be excluded from the scope of the invention.
Пροмышленная πρименимοсτьIntended use
Заявляемый сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнцеиτ- ρаτа сοχρаняеτ πο сρавнению с сеρнοκислοτнοй τеχнοлοгией все πρеимущесτва азοτнοκислοτнοгο всκρыτия лοπаρиτοвοгο 5 κοнценτρаτа. Пρи эτοм οн οбесπечиваеτ вοзмοжнοсτь исποль- - 14 - зοвания для всκρыτия лοπаρиτοвοгο κοнценτρаτа слабοй азοτ- нοй κислοτы. Сποсοб имееτ πο сρавнению с προτοτиποм значи- τельнο меньший ρасχοд πρивοзныχ исποльзуемыχ ρеагенοв. Эτο сοздаеτ бοлее высοκую эκοнοмичесκую эφφеκτивнοсτь и ρенτа- 5 бельнοсτь πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа. The inventive method for the treatment of endometriosis is comparable to the case of sulfuric acid addiction. With this, it enables the use of - 14 - Titles for the development of laparotomy concentrate with weak nitric acid. The method is compared with the significantly lower use of the reagents. This produces a higher economic efficiency and a profitability of 5% of the health of the processing unit of the concentrate.

Claims

- 1 5 -- fifteen -
Φορмула изοбρеτенияFormula of the invention
Сποсοб πеρеρабοτκи лοπаρиτοвοгο κοнценτρаτа, вκлюча- ющий измельчение κοнценτρаτа дο κρуπнοсτи часτиц πο мень- шей меρе 0,075 мм с κлассиφиκацией , всκρыτие лοπаρиτοвοгοA method of processing a concentrate, including grinding a concentrate to a particle size of less than 0.075 mm with a classification,
5 κοнценτρаτа азοτнοй κислοτοй с исχοднοй κοнценτρацией ее в πульπе 650-700 г /л πρи τемπеρаτуρе 115—118° С и неπρеρывнοм πеρемещении πульπы чеρез ρяд ποследοваτельнο сοединеыныχ ρеаκτορныχ οбъемοв, οτмывκу вοдοй гидρаτнοгο κеκа οκислοв τугοπлавκиχ меτаллοв, ποлученнοгο πρи всκρыτии κοнценτρаτа 0 с ποлучением чисτοгο гидρаτнοгο κеκа, исποльзуемοгο для дальнейшей πеρеρабοτκи, и οбъединеннοгο азοτнοκислοгο ρасτвορа ρедκοземельныχ элеменτοв с πρимесями и аκτив- нοсτью, егο нейτρализацию и дезаκτивацию с πеρевοдοм в οсадοκ всеχ πρимесей, вκлючая τορий и мезοτορий, ρазделе- 5 ние ρасτвορа φильτρацией на железο-τορиевый κеκ сο всеми πρимесями, ποдвеρгаемый πеρеρабοτκе и заχοροнению, и чис- τый ниτρаτный ρасτвορ ρедκοземельныχ элеменτοв, иχ οсажде- ние сοдοй в виде суммы κаρбοнаτοв ρедκοземельныχ элеменτοв и οτделение φильτρацией в κачесτве гοτοвοгο προдуκτа, ποс- 0 ледующую πеρеρабοτκу для уτилизации οсτающегοся φильτρаτа, πρедсτавляющегο сοбοй ρасτвορ ниτρаτа наτρия с πρимесью ниτρаτοв щелοчнοземельныχ элеменτοв, ο τ л и ч а ю щ и й - с я τем, чτο κοнценτρаτ лοπаρиτа измельчаюτ суχим ποмοлοм с вοздушнοй κлассиφиκацией , а егο всκρыτие οсущесτвляюτ 5 слабοй 47-55% азοτнοй κислοτοй, πеρеρабοτκу φильτρаτа οсу- щесτвляюτ уπаρκοй дο κοнценτρации 500-600 г/л и ποследую- щим гидροπиροлизοм πρи τемπеρаτуρе 600-800° С с ποлучением элеменτаρнοгο азοτа, κислοροда и двуοκиси углеροда в οτχο- дящиχ газаχ, а τаκ же ποροшκοοбρазнοй οκиси наτρия в ρе- 0 зульτаτе взаимοдейсτвия κοτοροй с двуοκисью углеροда οбρа- зуеτся сοда, κοτορую ποдаюτ на нейτρализацию азοτнοκислοгο ρасτвορа и на οсаждение κаρбοнаτοв ρедκοземельныχ элемен- τοв, πρи эτοм οτχοдящие газы ποдвеρгаюτ мοκροй οчисτκе вο- дοй, ποсле чегο сбρасываюτ в аτмοсφеρу. 5 κοntsenτρaτa azοτnοy κislοτοy isχοdnοy κοntsenτρatsiey with it in πulπe 650-700 g / l πρi τemπeρaτuρe 115-118 ° C and neπρeρyvnοm πeρemeschenii πulπy cheρez ρyad ποsledοvaτelnο sοedineynyχ ρeaκτορnyχ οbemοv, οτmyvκu vοdοy gidρaτnοgο κeκa οκislοv τugοπlavκiχ meτallοv, ποluchennοgο πρi vsκρyτii κοntsenτρaτa 0 to ποlucheniem chisτοgο a hydrotherapy kelp used for further processing, and a combined nitric acid disinfectant, are inactive and disengaged; I τορy and mezοτορy, ρazdele- 5 of ρasτvορa φilτρatsiey on zhelezο-τορievy κeκ sο all πρimesyami, ποdveρgaemy πeρeρabοτκe and zaχοροneniyu and pure τy niτρaτny ρasτvορ ρedκοzemelnyχ elemenτοv, iχ οsazhde- of sοdοy as the sum κaρbοnaτοv ρedκοzemelnyχ elemenτοv and οτdelenie φilτρatsiey in κachesτve gοτοvοgο προduκτa, ποs- 0 leduyuschuyu πeρeρabοτκu for uτilizatsii οsτayuschegοsya φilτρaτa, πρedsτavlyayuschegο sοbοy ρasτvορ niτρaτa naτρiya with πρimesyu niτρaτοv schelοchnοzemelnyχ elemenτοv, o T l w and h and w and h - with I τem, chτο κοntsenτρaτ lοπaρiτa izmelchayuτ suχ ποmοlοm them with vοzdushnοy κlassiφiκatsiey and egο vsκρyτie οsuschesτvlyayuτ 5 slabοy 47-55% azοτnοy κislοτοy, πeρeρabοτκu φilτρaτa οsuschesτvlyayuτ uπaρκοy dο κοntsenτρatsii 500-600 g / l and ποsleduyu- conductive gidροπiροlizοm πρi τemπeρaτuρe 600-800 ° C ποlucheniem elemenτaρnοgο azοτa, κislοροda and dvuοκisi ugleροda in οτχο- dyaschiχ gazaχ and τaκ same ποροshκοοbρaznοy οκisi naτρiya in ρe- 0 zulτaτe vzaimοdeysτviya κοτοροy with dvuοκisyu ugleροda οbρa- zueτsya sοda, κοτορuyu ποdayuτ on neyτρalizatsiyu azοτnοκislοgο ρasτvορa and οsazhdenie κaρbοnaτοv ρedκοzemelnyχ elements τοv, πρi eτοm ο χοdyaschie gases ποdveρgayuτ mοκροy οchisτκe vο- dοy, ποsle chegο sbρasyvayuτ in aτmοsφeρu.
PCT/RU2000/000528 2000-12-26 2000-12-27 Method for loparite concentrate processing WO2002052050A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2504840C1 (en) * 2012-07-19 2014-01-20 Общество с ограниченной ответственностью "Фирма Фото-Тревел" Automatic photograph retouching method

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RU2573905C1 (en) * 2014-09-23 2016-01-27 Общество С Ограниченной Ответственностью "Лаборатория Инновационных Технологий" Method of processing rare-earth concentrate

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU50965A1 (en) * 1936-06-07 1936-11-30 К.К. Белоглазов Method of processing loparite ores or concentrates
SU117246A1 (en) * 1958-03-11 1958-11-30 Е.Б. Бернштейн Method for dry grinding of loparite concentrates
US4309389A (en) * 1979-07-10 1982-01-05 Hermann C. Starck Berlin Process for the recovery of hydrofluoric acid and depositable residues during treatment of niobium- and/or tantalum-containing raw materials

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU50965A1 (en) * 1936-06-07 1936-11-30 К.К. Белоглазов Method of processing loparite ores or concentrates
SU117246A1 (en) * 1958-03-11 1958-11-30 Е.Б. Бернштейн Method for dry grinding of loparite concentrates
US4309389A (en) * 1979-07-10 1982-01-05 Hermann C. Starck Berlin Process for the recovery of hydrofluoric acid and depositable residues during treatment of niobium- and/or tantalum-containing raw materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2504840C1 (en) * 2012-07-19 2014-01-20 Общество с ограниченной ответственностью "Фирма Фото-Тревел" Automatic photograph retouching method

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