SU1247343A1 - Method of isolating sodium,kainite and carnallite - Google Patents
Method of isolating sodium,kainite and carnallite Download PDFInfo
- Publication number
- SU1247343A1 SU1247343A1 SU843749110A SU3749110A SU1247343A1 SU 1247343 A1 SU1247343 A1 SU 1247343A1 SU 843749110 A SU843749110 A SU 843749110A SU 3749110 A SU3749110 A SU 3749110A SU 1247343 A1 SU1247343 A1 SU 1247343A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- solution
- cainite
- carnallite
- separation
- evaporation
- Prior art date
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- BMQVDVJKPMGHDO-UHFFFAOYSA-K magnesium;potassium;chloride;sulfate;trihydrate Chemical compound O.O.O.[Mg+2].[Cl-].[K+].[O-]S([O-])(=O)=O BMQVDVJKPMGHDO-UHFFFAOYSA-K 0.000 title claims description 6
- PALNZFJYSCMLBK-UHFFFAOYSA-K magnesium;potassium;trichloride;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-].[Cl-].[K+] PALNZFJYSCMLBK-UHFFFAOYSA-K 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 title description 3
- 239000011734 sodium Substances 0.000 title description 3
- 229910052708 sodium Inorganic materials 0.000 title description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- 239000000725 suspension Substances 0.000 claims description 11
- 238000000926 separation method Methods 0.000 claims description 8
- 238000001704 evaporation Methods 0.000 claims description 7
- 230000008020 evaporation Effects 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
- 239000011591 potassium Substances 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 2
- 239000001110 calcium chloride Substances 0.000 claims description 2
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 2
- 238000006477 desulfuration reaction Methods 0.000 claims description 2
- 230000023556 desulfurization Effects 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
- 239000006260 foam Substances 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 229910001425 magnesium ion Inorganic materials 0.000 claims 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000001103 potassium chloride Substances 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- -1 sulphate ions Chemical class 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229940072033 potash Drugs 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000015320 potassium carbonate Nutrition 0.000 description 2
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 description 2
- 235000011151 potassium sulphates Nutrition 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- WZISDKTXHMETKG-UHFFFAOYSA-H dimagnesium;dipotassium;trisulfate Chemical compound [Mg+2].[Mg+2].[K+].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O WZISDKTXHMETKG-UHFFFAOYSA-H 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000001120 potassium sulphate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
Classifications
-
- 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
- C01F5/00—Compounds of magnesium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Fertilizers (AREA)
Description
Изобретение относитс к перерабоТ ке рассолов, содержащих хлориды и сульфаты кали , магни и натри , с получением растворов хлорида маг- 1ШЯ и может быть использовано при пе- реработке полиминеральных руд на бесхлорные калийные удобрени .The invention relates to the treatment of brines containing chlorides and sulphates of potassium, magnesium and sodium, with the production of solutions of magnesium chloride and can be used in the processing of polymineral ores into chlorine-free potash fertilizers.
Целью изобретени вл етс повышение выхода и чистоты каинита,The aim of the invention is to increase the yield and purity of Cainite,
Согласно предлагаемому способу выделени хлорида натри , каинита и карналлита из растворов, включающему упарива ше раствора, отделение выкристаллизовавшегос при этом хлорида натри , дополнительное упаривание оставшегос раствора при 60-80 С, выделение нз образовавшейс суспензии каинита, обуссульфачивание оставшегос раствора : лоридом кальци и повторное упаривание этого раствора с последуюпртм выделением карналлита, полученную каинитовую суспензию перед .отделением каинита нагревают до 90- при.переме1Ш1вании и конвертируют в течение 10-60 мин, из полученной суспензии отдел ют каинит, а раствор о:шаж;дают и после отделени рвда кали подают на обессульфачи- ваиие.According to the proposed method of separating sodium chloride, kainit and carnallite from solutions, including evaporation of the solution, separating the sodium chloride that crystallized out at the same time, additional evaporation of the remaining solution at 60-80 ° C, separation of the resulting suspension of kainite, extinguishing the remaining solution with calcium chloride. of this solution, followed by the release of carnallite, the resulting kainitic suspension is heated to 90– before the separation of the kainit, at a cross-section of 1 ° C, and converted into After 10–60 minutes, Cainite is separated from the resulting suspension, and the solution is about: a step, and after the separation, potassium is supplied to potassium sulfate.
Подогрев до температуры 90-100°С и конверси полученных ранее при 60- 80°С каинитовых суспензий приводит к значительному увеличению выхода каинита из раствора и повышению его чистоты. Это достигаетс в резуль- тате растворени хлорида кали при более высоких температурах (90-100°С) и кристаллизации дополнительного количества каинита KCF-MgSO ЗЫ20 и леонита K SO -MgSO -4Н О.Heated to a temperature of 90-100 ° C and the conversion of Cainite suspensions obtained previously at 60-80 ° C leads to a significant increase in the yield of Cainite from the solution and an increase in its purity. This is achieved as a result of dissolution of potassium chloride at higher temperatures (90-100 ° C) and crystallization of an additional amount of kainite KCF-MgSO ЗЫ20 and leonite K SO -MgSO-4H O.
Конверси каинитовых суспензий при температурах выше сопровож .даетс кристаллизацией труднорастворимого лангбейнита, не пригодного дл переработки в бесхлорные калий- ные удобрени , а при температурахConversion of kainitic suspensions at temperatures above is accompanied by the crystallization of poorly soluble langbeinite, which is not suitable for processing into chlorine-free potassium fertilizers, and at temperatures
По известному способу16,07By a known method 16,07
По предлагаемомуAccording to the proposed
85 60 20,1585 60 20.15
ниже 90 С снижаетс выход и чистота каинита.below 90 ° C, the yield and purity of Cainite are reduced.
Продолжительность конверсии каинитовых суспензий практически заканчиваетс в течение 45-60 мин.The duration of the conversion of the kainitic suspensions almost ends within 45-60 minutes.
Качество полученных проконверти- рованных каинитовых суспензий по сравнению с непроконвертированными улучшаетс в результате получени при повьппенных температурах более крупных кристаллов.The quality of the resulting converted kainitic suspensions is improved compared to the non-converted ones, resulting in larger crystals at higher temperatures.
Каинитовый раствор после вьщеле- ни каинита подают на охлаждение до с целью выделени хлорида кали .Cainite solution after crushing kainit is fed to cooling to release potassium chloride.
Пример, Шенитовый раствор после вьщелени из него хлорида натри , содержащий %: калий 4,56; магний 4,74; натрий 3,05; сульфат-ионы 5,35; хлор 18,72 и вода 63,58, упаривают при 70 С с удельной интенсивностью удалени воды 100 кг/( ч) до содержани в растворе 5,49% сульфат-ионов и 6,5% магни . Полученную при 70 С каинитовую суспензию нагревают до и при этой температуре её конвертируют при перемешивании в течение 30 мин. После конверсии суспензию сразу же (без охлаж 1;ени ) раздел ют на каинит и каинитовый раствор отстаиванием и фильтрацией. Каинит направл ю на получение бесхлорных калийных удобрений, а каинитовый раствор охлаждают и после отде леш1 хлорида кали подают на обес- сульфачивание.An example is a Shenit solution after precipitating sodium chloride from it containing%: potassium 4.56; magnesium 4.74; sodium 3.05; sulphate ions 5.35; chlorine 18.72 and water 63.58, evaporated at 70 ° C with a specific removal rate of water 100 kg / (h) to contain 5.49% sulphate ions and 6.5% magnesium in solution. The kainitic suspension obtained at 70 ° C is heated to and converted at this temperature with stirring for 30 minutes. After conversion, the suspension is immediately (without cooling 1; h) separated into kainite and kainitic solution by settling and filtration. Cainite was sent to obtain chlorine-free potash fertilizers, and the kainitic solution was cooled and, after separation, potassium chloride was supplied for desulfurization.
Результаты опьи-ов представлены в таблице.The results of opi-s are presented in the table.
Как следует из результатов таблицы , при предлагаемой технологии обработки повышаетс выход и чистота каинита за счет более полного извлечени из раствора сульфат-ионов (сульфата магни и сульфата кали ), вход щих в каинит KC.G-MgSO и леонит KjSO MgSO 4HjO.As the results of the table show, with the proposed processing technology, the yield and purity of kainite are increased due to more complete extraction from the solution of sulphate ions (magnesium sulphate and potassium sulphate), included in kainitum KC.G-MgSO and leonite KjSO MgSO 4HjO.
4,074.07
36,2436.24
41,6541.65
5,105.10
46,6946.69
52,2552.25
Примечание: Выход каинита определ ют по степени извлечени Note: Cainite yield is determined by recovery.
сульфат-ионов из раствора в твердую фазу. Чистота каинита - содержание KCE-MgS04- в твердой фазе. Упаривание производ т при 70 С.sulfate ions from solution to the solid phase. Cainite purity is the content of KCE-MgS04- in the solid phase. Evaporation is carried out at 70 C.
Составитель Л.Темирова:Compiled by L. Temirova:
Редактор Л.Повхан Техред-Д.Бонкало Корректор М.МаксимишинецEditor L.Povkhan Tehred-D.Bonkalo Proofreader M.Maksiminshynets
Заказ 4072/22 Тираж 450ПодписноеOrder 4072/22 Circulation 450 Subscription
ВНИИПИ Государственного комитета СССРVNIIPI USSR State Committee
по делам изобретений и открытий 113035, Москва, Ж-35, Раушска наб., д. 4/5for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab., 4/5
Производственно-полиграфическое предпри тие, г.Ужгород, ул.Проектна , 4Production and printing company, Uzhgorod, Projecto st., 4
Продолжение таблицыTable continuation
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU843749110A SU1247343A1 (en) | 1984-04-16 | 1984-04-16 | Method of isolating sodium,kainite and carnallite |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU843749110A SU1247343A1 (en) | 1984-04-16 | 1984-04-16 | Method of isolating sodium,kainite and carnallite |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1247343A1 true SU1247343A1 (en) | 1986-07-30 |
Family
ID=21122221
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU843749110A SU1247343A1 (en) | 1984-04-16 | 1984-04-16 | Method of isolating sodium,kainite and carnallite |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU1247343A1 (en) |
-
1984
- 1984-04-16 SU SU843749110A patent/SU1247343A1/en active
Non-Patent Citations (1)
| Title |
|---|
| Авторское свидетельство СССР № 882915, кл. С 01 D 3/08, 1981. * |
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