This application is a national stage application of PCT Application No. PCT/CZ2019/00004 filed under 35 U.S.C. § 371 on Jan. 22, 2019, which in turn claimed priority to Czech Patent Application No. PV 2018-45 filed on Jan. 30, 2018.
This invention relates to/concerns technology of alunite ore processing resulting in the production of γ-Al2O3 with the production of fertilizer potassium sulfate, kitchen salt, metallurgical aluminum oxide and quartz sand.
Alunite is a raw material for the aluminum and chemical industries. Industrial alunite ore deposits are common in the USA, China, Azerbaijan, Iran, Mexico, Kazakhstan, Ukraine, Russia and other countries. The presented invention concerns the processing of alunite ore with the production of fertilizer potassium sulphate, kitchen salt, metallurgical alumina and quartz sand.
An alkaline reduction method for processing alunite ore [1] is known. This method was used in the Ganja Aluminum Combine (GGC). Due to significant technological drawbacks (such as low alumina yield of less than 70 pollution of the environment by dust and gas, a need for rare and expensive raw materials, large quantities of solid waste from 5 tons per 1 ton of alumina and an undesirable by-product sulfuric acid) GGC ceased its operations in 1992 and to this date does not operate.
A method for processing of alunite ore was developed for the production of potassium fertilizers (SOP), sulfuric acid, alumina and quartz sand in Utah (USA) [2]. In this method, the alunite ore is roasted at 600° C. or lower with the release of SO2, which leads to the production of sulfuric acid, and the roasted alunite is extracted with hot water to produce K2SO4(SOP). A reducing agent (excess oil or elemental sulfur vapors) should be introduced during roasting in order to acquire entire SO2 aluminium sulphate. The combustion temperature of 600° C. allows to preserve γ-Al2O3 in an active form. However, leaching (in hot water at 80 to 99° C.) of the alunite T≤600° C. results in the loss of SOPs due to the formation of water-insoluble basic salts. The yield of SOP in the solution does not exceed 65 to 70%. Roasting of the alunite at 800 to 900° C. improves SOP yield to almost 100%, while γ-Al2O3 is converted into an insoluble form of α-Al2O3. There is no floatation method that can divide α-Al2O3 and quartz the insoluble residue in order to obtain metallurgical alumina.
The drawbacks were eliminated by the potash-alkaline method (Liner-Taghiyev) [3, 4, 5, 7], where the alunite roasted at the temperature of T≤550° C. was leached with potassium carbonate solution according to the reaction:
K2SO4·Al2(SO4)3·2Al2O3+nn+3K2CO3=4K2SO4+3Al2O3+nn+3CO2(nn−waste rock).
Up to 4 times more SOP and alumina (γ-Al2O3) is transferred into the solution, the metallurgical-Al2O3 remains in the insoluble residue. The SOP is obtained from the solution and the insoluble residue is processed by the Bayer method by means of leaching with the recycled solution of aluminate at T=80-90° C. to obtain metallurgical alumina and quartz sand. The disadvantage of this method is the use of a rare and expensive (including USA) potassium carbonate.
The foregoing drawbacks are addressed by the invention below.
The state of the art is further described in the following literature:
The processing of the alunite ore (alunite) consists first of the known steps: crushing, grinding and flotation of alunite ore. Flotation of the alunite ore proceeds with a flotoreagent and is proposed in the method according to the state of the art, point 2. The enriched alunite ore containing 25-95% preferably 60% of mineral alunite is further roasted at a temperature of 520 to 620° C., the roasting time is 1 to 3 hours. The roasted alunite, in accordance with the present invention, is further leached with 5 to 20% sodium carbonate solution, which is added in an amount of 100 to 110% of the stoichiometric amount required to bond the SO3 aluminium sulphate in the alunite, that is Na2CO3 is added in an excess of 0 to 10% over the calculated stoichiometric coefficients of the reaction equation 1, at 70-100° C. for 0.5 to 2.0 hours. The obtained slurry solution contains all potassium sulphate from alunite and sodium sulphate obtained from sodium carbonate. In the insoluble residue remains all of aluminium oxide from alunite and waste rock, where the waste rock is silica-SiO2 and clay (aluminum) aluminosilicate. The sulfate solution is further separated by either filtration or precipitation from an insoluble residue and is converted with potassium chloride to potassium sulphate (fertilizer) and kitchen salt. The insoluble residue is processed by the Bayer method without autoclaving and at a temperature of less than 100° C. to form aluminium oxide (alumina) and quartz sand.
In order to overcome the disadvantages of the prior art, it is proposed to replace the solution of potassium carbonate with a solution of calcined soda (1) and then to convert right after the first leaching the obtained sodium sulphate by the conversion method with KCl to potassium sulphate (fertilizer) and sodium chloride NaCl (2), which is the basic/fundamental inventive idea of this invention.
K2SO4·Al2(SO4)3·2Al2O3+nn+3Na2CO3=K2SO4+3Na2SO4+3Al2O3+nn+3CO2 Reaction (1):
K2SO4+3Na2SO4+6KCl=4K2SO4+6NaCl, Reaction (2):
3Al2O3+nn is the insoluble residue, which is processed by the Bayer method without autoclaving to form aluminium oxide (alumina) and quartz sand. Alunite is roasted at 520 to 620° C., the time of roasting is 1 to 3 hours.
The roasted alunite is leached with 5 to 20% sodium carbonate solution in an amount of 100 to 110% of the stoichiometric amount required to bond the SO3 aluminium sulphate in the alunite, that is Na2CO3 is added in an excess of 0 to 10% over the calculated stoichiometric coefficients of the reaction equation at 70 to 100° C. for 0.5 to 2.0 hours.
The products of this process are: K2SO4— fertilizer, NaCl—kitchen salt, Al2O3— metallurgical, SiO2— quartz sand and coagulant for water purification [6].
Note: The United States is the second largest producer of sodium carbonate in the world, and Canada is the world's largest producer of potassium chloride (KCl).
We take an alunite ore with an alunite content of 60% by weight, with the following composition, % by weight:
100 g of alunite (alumina) is crushed. Alunite (alunite ore) is further grinded, after the flotation enrichment it is roasted in an oven at T=550° C. for 1 hour and then leached in the solution of Na2CO3.
A sodium salt solution is prepared: 22.2 g of Na2CO3 is dissolved in 350 ml of water, the amount of soda is 105% wt. from stoichiometric. The leaching time is 1.5 hours at Tleach 90° C.
Into solution are transferred: K2O—99% by weight; Na2CO3-100% by weight; Al2O3— 0.5% wt.; SO3—9 8% wt. or K2O=6.8 g, Na2O=13 g, SO3=2.3 g, Al2O3=0.1 g.
In the insoluble residue remains 62.2 g. CO2 gas is formed.
The suspension is filtered and washed.
The filtrate with the washing water is evaporated.
We obtain a mixture of sulphates K, Na, where the sulphate K is 12.5 g, Na sulphate—29.8 g, the total of 42.3 g of the mixture. This is a mixture of sulphates obtained from the evaporated mixture of the filtrate and washed water.
It is required 23.7 g of KCl to produce 29.8 g of Na2SO4. This is reaction number 2: K2SO4+3Na2SO4+6KCl=4K2SO4+6NaCl, with K2SO4 already present in the alunite in the amount of 12.5 g.
The result is 36.6 g of K2SO4 plus 12.5 g of K2SO4 from alunite. Total of 49 g of K2SO4 and NaCl of 16.8 g.
The method of treating the alunite ore consists of the following steps:
1.19 t of KCl is used for the conversion.
Aluminium oxide (alumina) is formed and remains unchanged “waste rock”, i.e. silica sand (SiO2) and aluminosilicate.
16. One ton of γ-Al2O3 is formed by calcination of Al(OH)3.
Diagram in
According to the present invention, the method for the treatment of alunite is used to treat alunite ores with the production of Al2O3, as well as potassium sulphate, quartz sand, utility and potable water purification coagulant and kitchen salt as a by-product.
Number | Date | Country | Kind |
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CZ2018-45 | Jan 2018 | CZ | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CZ2019/000004 | 1/22/2019 | WO |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2019/149293 | 8/8/2019 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
1338428 | Downs | Apr 1920 | A |
4024087 | Lainer | May 1977 | A |
4230678 | Hartman | Oct 1980 | A |
Number | Date | Country |
---|---|---|
271816 | Jun 1927 | CA |
104313346 | Jan 2015 | CN |
106800015 | Jun 2017 | CN |
307974 | Sep 2019 | CZ |
1 375 996 | Dec 1972 | GB |
819060 | Jul 1981 | SU |
Entry |
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International Search Report, PCT App. No. PCT/CZ2019/000004, ISA: EPO; dated Aug. 4, 2020. |
Search Report of the Industrial Property Office of the Czech Republic, CZ App. No. PV 2018-45; dated Oct. 26, 2018. |
Communication from Eurasian Patent Office, 2020. |
Communication from Eurasian Patent Office, 2019. |
Allowed Czech claims in Czech. |
Allowed Czech claims in English. |
PCT search results in Czech. |
Search report from CZ IPO. |
Number | Date | Country | |
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20210071281 A1 | Mar 2021 | US |