![]() Method of producing phosphoric acid
专利摘要:
Concentrated phosphoric acid and calcium sulfate hemihydrate are directly produced by sulfuric acid attack upon calcium phosphate, the improvements comprising (i) continuously conducting the acid attack reaction, with concomitant formation of crystalline calcium sulfate hemihydrate, in but a single, homogeneous liquid reaction medium comprising the products of reaction, (ii) maintaining constant the temperature of the reaction medium as to effect formation of hemihydrated calcium sulfate, (iii) controlling the amount of reactants introduced to the reaction medium such as to maintain essentially constant, in liquid phase, a determined sulfate ion content, said content being at least 5 g/l and said determined content increasing with decreasing concentrations of P2O5 at a given temperature, and (iv) withdrawing a fraction of reaction effluent, including the concentrated phosphoric acid, and individually separating and recovering hemihydrated calcium sulfate from said reaction effluent fraction. Advantageously, the hemihydrate is recrystallized into a marketable gypsum by means of a treatment liquid which is subsequently recycled, preferably first to wash the hemihydrate and thence for purposes of the phosphate attack. 公开号:SU1223838A3 申请号:SU782683951 申请日:1978-11-14 公开日:1986-04-07 发明作者:Биго Бернар 申请人:Рон-Пуленк Эндюстри (Фирма); IPC主号:
专利说明:
The invention relates to the process of phosphoric acid supply by the sulfuric acid decomposition of phosphate raw material in the hemihydrate-dehydrate mode and can be used in the production of concentrated phosphoric acid without evaporation. The aim of the invention is to increase the yield of PaOg in the product and the stability of calcium sulfate hemihydrate. Example 3. The reactor is injected 13.1 t / h of Morocco phosphate, containing 75% g of tricalcium phosphate, a recycled hemihydrate suspension and a mixture of 11.6 tons / h of sulfuric acid and 32 tons / h of circulating acid (37.5% PrOy). The temperature of the reaction suspension is maintained in the range of 95-100 ° C by circulating the suspension through a vacuum evaporator. In the liquid phase, the suspension maintains a phosphoric acid concentration of 50% PjOfH sulfate ion of 12 g / l by controlling the amount of recycled acid. The amount of solids in the suspension is maintained at 35%, A portion of the suspension circulating through a vacuum evaporator, equivalent to the phosphate introduced, is directed to a horizontal filter. The temperature of the filter suspension is 70 ° C, which reduces the risk of corrosion. The phosphate decomposition time is 3 hours and 5 minutes. As a result of filtration, phosphoric acid with a content of 50% PrO $ is obtained. Semi calcium sulfate hydrate on the filter is successively washed with mother liquor from recrystallization of subhydrate to calcium sulfate dihydrate and water. The yield of FjOs is 96.9%. The wash water as recycled phosphoric acid is directed to the processing of the raw material. The washed calcium sulfate hemihydrate is sent to recrystallization in the dihydra in the presence of a seed. This stage allows the captured acid to be extracted from the sediment and the remaining amount of phosphate is decomposed. The table presents the data on the effect of the final treatment of the raw material on the yield of Pg05- at the hemihydrate stage. The data in the table shows that the yield of PaOj of more than 96% is observed in the proposed concentration regime for phosphoric and sulfuric acids. The stability of the hemihydrate obtained can be determined by the substance of the precipitate and the shape of the crystals. The precipitate washed and dried at 60 ° C is then heated at 120 ° C to remove the water. It was determined that the water molecule is removed. The ratio of the weight of the dewatered sludge to its original weight is 1.056-1.063 (the theoretical ratio is 1.06) by a known method the ratio is higher. The precipitate itself consists of small crystals, there are no calcium sulfate dihydrate crystals. In addition, during a long (3-5 days) stand, the scales of calcium sulfate hemihydrate fall out of it. Example 2, In a reactor volume. 50 m of 2 t / h of milled Togo phosphorite (36.8% PjO) and a mixture of 9 t / h are introduced 98% sulfuric acid and 15 m / h of recycled phosphoric acid containing 500 g / l of PjOj- and 70 g / l of sulfuric acid. The temperature is heated by circulating the suspension through a vacuum evaporator. The decomposition time of the raw material is 2 hours and 10 minutes. A part of the suspension cooled to 70 ° C is filtered on a vacuum filter of 12 m. The calcium sulfate hemihydrate precipitate is washed from the recrystallization with a liquor hemihydrate to calcium sulfate dihydrate, containing 150 g / l of PgO 5 and 180 g / l of sulfuric acid, and then with water, 9.4 tons / h of phosphoric acid containing 48% of PaOs and 0.6% of sulfuric acid are obtained. Promvodnye water and part of the product is directed to the processing of phosphate. Yield 96,4%, Calcium sulfate hemihydrate precipitate, consisting of 17 tons / h of solid, 6 tons; water, 1.8 g of PgOj, of which 0.25% is trapped acid, and 1.2 tons of sulfuric acid are introduced into the hydration reactor (80 m), where the seed is located and where 1 t / h of sulfuric acid, pre-mixed with 14 m / h wash water from the washing of gypsum, having a concentration of 100 g / l and sulfuric acid 125 g / l. The hydration time is 2 h 50 min, the temperature is 60 C. The hemihydrate is completely converted into calcium sulfate dihydrate. The dihydrate suspension is filtered on a vacuum filter of 7 m. The precipitate of the dihydrate on the filter is countercurrently washed with a mild whistle and water. The mother liquor is used to give the hemihydrate washes, and the washings are sent to the hydration reactor. Washed gaps contain less than 0.2% P 0s- and less than OD% fluorine. The overall yield of 1 Of two stages is 99.1%, Example 3, Togo and Morocco phosphorites containing 78 and 75% tricalcium phosphate, respectively, are processed under the same conditions, 10 t / h of phosphorite and a mixture of 11.2 t / h of 93% sulfuric acid and circulating 4x) sforic acid are fed to the reactor. The temperature of the process at the hemihydrate stage is maintained at 100 ° C, the concentration in the liquid phase of the suspension is 50% PsOs, the process time is 4 h. The suspension slurry is filtered at and washed. An acid containing 50% PgOg is obtained. The washed calcium sulfate hemihydrate is hydrated in the presence of a 60 ° C seed in a solution containing 10% PjOs- and 100 g / l of sulfuric acid. The hydration time is 2 hours. The dihydrate suspension is filtered and washed. The resulting calcium sulfate dihydrate consists of flat white crystals and contains the RE Of, wt%: Neprorea- rastvu- capturing him 37 25 1,801.20 5,102,0 40-47 (known) The yield of PjOf in the product is 99% (phosphate Togo). The proposed method allows to obtain phosphoric acid of increased concentration, which can exclude the operation of evaporation of BaiffH acid. Pj Of yield in the product reaches 99%. The resulting calcium sulfate creep is quite stable and can be washed with water, which increases the yield to the hemihydrate stage. Gypsum obtained in the process of hydration of calcium sulfate half-excess, contains harmful impurities in insignificant amounts (phosphorus and fluorine) and can be used in other industries. Phosphate grain blocking Also 97.5 97.0 96.7 96.5 92.9 Slow filtration due to high viscosity 92.5
权利要求:
Claims (2) [1] 1. METHOD FOR PRODUCING PHOSPHORIC ACID, including the processing of phosphate feedstock with reverse phosphoric and sulfuric acids at 80 - lOcf С, crystallization of the precipitate of calcium sulfate hemihydrate, separation of it from the product by filtration, countercurrent washing of the precipitate with the mother liquor from recrystallization of the hemihydrate to calcium sulfate dihydrate, direction as recycled phosphoric acid for processing raw materials, recrystallization of semi-guides. calcium sulfate to dihydrate in a solution containing 10% P a O 5 and 9% sulfuric acid, in the presence of a seed, followed by separation of the precipitate of calcium sulfate dihydrate from the mother liquor by filtration, countercurrent washing with water and the direction of the wash water for recrystallization, which that, in order to increase the output P r Os into the product and increase the stability of calcium sulphate hemihydrate, raw phosphate processing while maintaining the lead in the liquid phase of the slurry concentration Pr O y equal to 40-55%, and the concentration of sulfate ion equal 5- 20 g / l, while the concentration of sulfate ion is maintained inversely proportional to the concentration of PjOy in the indicated intervals, and the precipitate of calcium sulfate hemihydrate is additionally washed with water. [2] 2. The method of pop. 1, characterized in that the processing of raw materials is carried out for 1-8 hours.
类似技术:
公开号 | 公开日 | 专利标题 US4299804A|1981-11-10|Removal of magnesium and aluminum impurities from wet process phosphoric acid US3421845A|1969-01-14|Production of sodium phosphates SU1223838A3|1986-04-07|Method of producing phosphoric acid IL26076A|1970-07-19|Method for the manufacture of phosphoric acid and calcium sulphate hemihydrate GB1205122A|1970-09-16|Process for the production of phosphoric acid DE2625248A1|1976-12-23|METHOD FOR TREATMENT OF BRINE SLUDGE US4325927A|1982-04-20|Purified monoammonium phosphate process DE1947643B2|1979-11-15|Process for the production of potassium dihydrogen phosphate US3745208A|1973-07-10|Wet process manufacture of phosphoric acid and calcium sulphate US3984525A|1976-10-05|Manufacture of phosphoric acid US2730542A|1956-01-10|Process for preparing ethanol-2-aminophosphoric acid US3645677A|1972-02-29|Production of gypsum US4113835A|1978-09-12|Process for preparing pure synthetic calcium sulfate semihydrate US4039616A|1977-08-02|Process for the manufacture of stabilized, hardenable calcium sulphate by reacting crude phosphate with sulphuric acid SU551248A1|1977-03-25|The method of producing phosphoric acid SU582198A1|1977-11-30|Method of preparing phosphoric acid US3726660A|1973-04-10|Nitrophosphate fertilizer production SU1430342A1|1988-10-15|Method of producing phosphoric acid SU1586999A1|1990-08-23|Method of producing phosphoric acid SU945076A1|1982-07-23|Process for purifying phosphogypsum IL26394A|1970-02-19|Process for the preparation of phosphoric acid and gypsum from phosphate rock SU353396A1| US3226187A|1965-12-28|Method of obtaining insoluble basic aluminum ammonium alum SU1474082A1|1989-04-23|Method of producing phosphoric acid SU1527147A1|1989-12-07|Method of producing phosphoric acid
同族专利:
公开号 | 公开日 IL55956A|1981-09-13| ZA786430B|1979-10-31| BE872015A|1979-05-14| CA1103423A|1981-06-23| BR7807491A|1979-07-24| OA06104A|1981-06-30| IL55956D0|1979-01-31| US4524057A|1985-06-18| YU264078A|1982-06-30| FR2409230B1|1981-05-29| AU518965B2|1981-10-29| FR2409230A1|1979-06-15| AU4160978A|1979-05-24|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3632307A|1969-04-09|1972-01-04|Albatros Super Fosfaatfabrieke|Process for the preparation of phosphoric acid and gypsum from phosphate rock|US4424196A|1982-06-29|1984-01-03|United States Gypsum Company|Phosphohemihydrate process for purification of gypsum| LU84713A1|1983-03-25|1984-11-14|Prayon Soc|PROCESS AND PREPARATION OF PHOSPHORIC ACID AND CALCIUM HEMIHYDRATE ALPHA SULFATE| DE3583209D1|1984-11-05|1991-07-18|Prayon Dev Sa|CONTINUOUS PROCESS FOR PRODUCING PHOSPHORIC ACID AND CALCIUM SULFATE.| JPH044968B2|1986-12-08|1992-01-30| US20030224075A1|2002-02-21|2003-12-04|Jue-Chen Liu|Soy composition for balancing combination skin| BE1023754B1|2016-06-23|2017-07-12|Prayon Technologies|PROCESS FOR PRODUCING CALCIUM SULPHATE|
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申请号 | 申请日 | 专利标题 FR7734395A|FR2409230B1|1977-11-16|1977-11-16| 相关专利
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