SU108917A1 - A method of processing nepheline concentrate on alumina and caustic alkali - Google Patents
A method of processing nepheline concentrate on alumina and caustic alkaliInfo
- Publication number
- SU108917A1 SU108917A1 SU10608A SU455577A SU108917A1 SU 108917 A1 SU108917 A1 SU 108917A1 SU 10608 A SU10608 A SU 10608A SU 455577 A SU455577 A SU 455577A SU 108917 A1 SU108917 A1 SU 108917A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alumina
- solution
- caustic alkali
- aluminate
- nepheline concentrate
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title description 9
- 239000010434 nepheline Substances 0.000 title description 9
- 229910052664 nepheline Inorganic materials 0.000 title description 9
- 239000003513 alkali Substances 0.000 title description 6
- 239000003518 caustics Substances 0.000 title description 4
- 238000012545 processing Methods 0.000 title description 4
- 239000012141 concentrate Substances 0.000 title description 3
- 239000000243 solution Substances 0.000 description 16
- 150000004645 aluminates Chemical class 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000013049 sediment Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 238000012958 reprocessing Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- DEPUMLCRMAUJIS-UHFFFAOYSA-N dicalcium;disodium;dioxido(oxo)silane Chemical compound [Na+].[Na+].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O DEPUMLCRMAUJIS-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 210000003405 ileum Anatomy 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Description
Отличительной особенностью предлагаемого способа вл етс обработка нефелинового концентрата раствором целочи в автоклавах при температуре не ниже 230° в присутствии извести, с целью получени алюминатных растворов.A distinctive feature of the proposed method is the treatment of nepheline concentrate with a solution of an intact autoclave at a temperature not lower than 230 ° in the presence of lime, in order to obtain aluminate solutions.
Сог.часно предлагаемому способу, производитс автоклавное разложение нефелина П1елочными раствора1 1И в присутствии окиси кальци , в результате чего образуетс твердьи водный матриево-кальциевый силикат , а освободив иа с окись алюмини переходит в раствор, образу алюминатный раствор по схеме:According to the proposed method, autoclave decomposition of nepheline is carried out by pulping solution 1 1 in the presence of calcium oxide, resulting in the formation of solid aqueous matrix calcium silicate, and by releasing alumina from the solution, it will form an aluminate solution according to the scheme:
(Na.KjzOAlaOapSiOa--- пСаО + нефелин(Na.KjzOAlaOapSiOa --- pCaO + nepheline
4- xNaOH + уНзО ,К) А1, + (х - т) NaOH + алюмпнатиый раствор4- xNaOH + уНзО, К) А1, + (х - т) NaOH + alumina solution
(у-К) НоО + + mNa2O пСаО pSiO. КН.О (y-K) Noo + + mNa2O pSaO pSiO. Kn.O
т 5ердый осадокt hard sediment
Экснерпмептально в лаборатор ых ус.тови х устаиов.чено, что дл Excerptal in laboratory instruments. Manuals and stats.
практически полного перехода окиси алюмини в раст1юр (на уровне 92-95 о) необходимы следуюп1пе рел имные услови проведенп процесса выщелачивани :An almost complete transition of alumina to a solution (at a level of 92-95 o) requires the following relevant conditions for the leaching process:
1.Продо.тжите.чьность вьпце.тачи1 аи11Я приблизнте.тьно 10 мин.1.Prod.tzhite.chnost vttce.tachi1 ai11YA about 10 minutes.
2.Давление 25-40 атм. что соответствует TeNuie)aType 230-- 250 2. The pressure is 25-40 atm. which corresponds to TeNuie) aType 230-- 250
3.Мол рное oTiiouieHHe3.Molar oTiiouieHHe
Ха/ . 9.Ha / 9.
AUO:iAUO: i
4..1 риое отпоп1еипе4..1 of this type
СаОCao
SiOoSiOo
5. Ко .щентрацп И1елочн 300-450 г 1.1.5. The conference center Ilochn 300-450 g 1.1.
Окись ка.чьци . вводима в процессе выи1елачиван11 пефелинл, способствует раз;1оже1П11() нефе.тпн;. п практически приемлемому обсск )емниванию алюлшнатных растворов , св зыва кремнезем.Oxide ka.tstsi. introduced in the process izhelachivan 11 pepelline, contributes once; 1o1P11 () nef.tpn ;. Practically acceptable obstetting of alumina-rich solutions, bonding silica.
Осадок водного натриево-ка,1ьц11еBOiO силиката, получаемый после 1зЫП1елачиваии нефелина, пмеет кристаллическую структур) п хороню отдел етс фи.тьтрацие и-Л,; отстапlUIHHC .VI. Повторной обработкой -лосо осадка известковым MIJ.TOKO. содержлдца с в осадке ше.чочь переходит 15 раствор, заме1ца с окисью киЬ;)ци по схеме: mNa.O пСаО pSiO, Ki ЬО осадок иосле 1-го Р,ы1целачи15аин + ) СаО + Н,() р(2Са(2 SK2. -.О) lи;Ia t - 2niNaO l + Н,.() це.точи() ) При продо.чжите.тьности иовто,)ной обработки 1 час и да1.тении 10-12 агм, что соо1т етствует ) 120-200, практически I;CH илслочь переходит is раствор. На основании ироведеиных эксиериментальиых работ но автоклавному вьинелачива1И-ио иефе.тииа И1е .точными растворами, повто)иой обработке получаемого осадка известковьв мо,токолг, а также работ ио выделению окиси а.тюмини из по.тучаемых алюмииатных растворов может быть предложена следующа технологическа схема переработки нефелина. Нефелиновый концентрат в смеси с окисью ка.тьци вьпиелачиваетс в автоклавах оборотным И1елочным раствором (с небольнли.м содержа1И1ем глинозема), полученным после отделени выкристаллизова вшегос твердого алюмината И1елочей. Осадок водного натриево-кальциевого силиката отде.ч ете от алюминатного раствора фильтрацией или отста1П5анием , промываетс и поступает повторную обработку известковы .м молоком с целью извлечени щелочей . Шлам, еосто п.шй после повторной обработки в основном нз водного двухкаль 1,иевого силиката, отдел етс от н елочиого раствора, промываетс н служит сырьем дл по.чучени цемента. Алюминатный раствор, ио.чученный выщелачиванием нефелина в автоклаве, а также промывные воды luxMi- их унаргшании до коицеитрации - 500 г/.1 Na/) иаправ.ч ютс па кр11стал,чнза1и1К) твердого алюмината щелочей состава (Na,K)2O А12Оз-2,5Н2О. Откристаллизованный а,ч1ом1П1ат 1целочей отде.ч ете от маточного щелочного раствора с каустическим отношением мол рным АЬОз paiiHbiM 25-40, направ.ч емою затем на 5ьпцелачир ание li го.чову процесса , раствор етс к нромывных водах , и полученный илюминатный раствор с каустическнм oTHOHJcimeM 1,4--1,6 иерерабатываеч-с аналогично способу Байера при переработке бокенто, т. е. )учиваетс с выде .чением в твердую фазу гидрата окиси а.чюмиии , котора затем oiдел ечх , промываечс и кальцинч )уетс . Маточный расчвор пос..че отделени гидрата окиси алюмини с каустическим . отноигением 3.5-4,0 также поступает иа упаривание и кристаллизацию а.чю.мипата И1,елочей . HacTii маточного П1,елочного раствора после кристаллизации алюмината е концентрацией 640 г/-} NaOH и 18-22 г/л АЬОз выводитс из процесса, вл сь товарным щелочным раствором, а остальна часть с 15ыкристаллизовавшнмс алюминачом )це.чочей (в виде алюминатпой пульпы) поступает в процессе криста .ч.1изации алюминатных pacTisoров , иолучениых выще чачиваь ием нефелина, и служит затравкой д.ч интенсификации этого процесса. Г1ромы15ные воды промывки продукционного гидрата направл ютс на растворение алюмината щелочей. Изложенна выше схема полностью замкнута и состоит только из гидрохимических операций (за исключением кальцинации глинозема). В результате такой обработки иефелииа могут быть получены три продукта: глннозем, концентрироваиый целочной раствор, который моет быть использован в г.чиноземой промышленности, и цементный шлам. Извлечение цепных жомпонепов - глинозема н Н1,елочей - .может ыть обеспечено в колнчестве 90ЧоThe precipitate of aqueous sodium silicate, silicate obtained after crystallization of nepheline, drank crystalline structures) separates the fritration of the organic substance by the coronary; otstaplUIHHC .VI. By reprocessing the precipitate is lime with MIJ.TOKO. contains in the sediment she.chochek passes 15 solution, replaces with oxide ki;) chi according to the scheme: mNa.O pSaO pSiO, Ki bO sediment and after 1st P, s1 celachine 15 + CaO + H, () p (2Ca (2 SK2. -.O) land; Ia t - 2niNaO l + H,. () T.tochi ()) When you go through it, and) Noah processing for 1 hour and give 10-12 agm, which is ) 120-200, practically I; CH or alobum is transferred solution. On the basis of irovedeynyi experimental work of autoclave refining and fine treatment, followed by treatment of the resulting sediment limestone, as well as the extraction of oxide of aluminum from spent aluminumate solutions, it can be proposed to proceed. processing nepheline. The nepheline concentrate mixed with potassium oxide is heated in autoclaves with recycled Ileloch solution (with a small amount of alumina), obtained after separation crystallized into the solid Ileum aluminate. The precipitate of aqueous sodium-calcium silicate is separated from the aluminate solution by filtration or sedimentation, washed and re-treated with lime milk to extract alkalis. After reprocessing, the sludge, which is obtained mainly from the aqueous dicalcium 1, silicic acid, is separated from the scum, washed and serves as a raw material for extracting the cement. Aluminate solution, obtained by leaching nepheline in an autoclave, as well as luxMi washings before coititration - 500 g / .1 Na /) and applied by a pair of solid, alkali aluminate of composition (Na, K) 2O А12Оз -2.5H2O. Crystallized carbon dioxide from the mother liquor with a caustic molar HVOC3 paiiHbiM 25-40 molar caustic ratio, which is then directed to the melting point of the process, dissolves to the washing water, and the resulting alkali liquor is discharged into the cistern of the process, dissolves into the washing water, and the resulting alkali liquor is discharged into the molten water of the process, dissolves into the washing water, and the resulting alkali liquor is discharged into the cistern. oTHOHJcimeM 1,4--1,6 irerabotyvaetch-s, similar to the Bayer method, in the processing of bokento, i.e., is taken into account with the release of chyumium oxide in the solid phase, which is then otech, washed, and calcined). The uterine solution is the separation of alumina hydrate with caustic. A ratio of 3.5–4.0 also comes from the evaporation and crystallization of the cymipata I1, herpes. After crystallization of aluminate E with a concentration of 640 g / -} NaOH and 18-22 g / l HOCO, the HacTii uterine P1, 18-22 g / l, is removed from the process as a commercial alkaline solution, and the remainder with 15% crystallized aluminum)) (in the form of aluminate pulp ) enters the process of crista. 1 of the aluminate pacTisors, and the results of nepheline cleavage, and serves as seed for the intensification of this process. The hydrothermal waters of the washing of the production hydrate are directed to the dissolution of alkali aluminate. The scheme outlined above is completely closed and consists only of hydrochemical operations (with the exception of alumina calcination). As a result of this treatment, three products can be obtained: ground oil, concentrated healing solution, which can be used in the city and the earth industry, and cement slurry. Extraction of chain jomonepes - alumina and H1, woods - can be provided in quality 90%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU10608A SU108917A1 (en) | 1954-09-06 | 1954-09-06 | A method of processing nepheline concentrate on alumina and caustic alkali |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU10608A SU108917A1 (en) | 1954-09-06 | 1954-09-06 | A method of processing nepheline concentrate on alumina and caustic alkali |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU108917A1 true SU108917A1 (en) | 1956-11-30 |
Family
ID=48381983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU10608A SU108917A1 (en) | 1954-09-06 | 1954-09-06 | A method of processing nepheline concentrate on alumina and caustic alkali |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU108917A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3998927A (en) * | 1975-10-20 | 1976-12-21 | Aluminum Company Of America | Recovery of sodium aluminate from high-silica aluminous materials |
| US4044095A (en) | 1975-10-20 | 1977-08-23 | Aluminum Company Of America | Process for recovery of alumina from high-silica ore |
| US4159195A (en) | 1977-01-24 | 1979-06-26 | Exxon Research & Engineering Co. | Hydrothermal alkali metal recovery process |
| US4193772A (en) | 1978-06-05 | 1980-03-18 | Exxon Research & Engineering Co. | Process for carbonaceous material conversion and recovery of alkali metal catalyst constituents held by ion exchange sites in conversion residue |
| US4219338A (en) | 1978-05-17 | 1980-08-26 | Exxon Research & Engineering Co. | Hydrothermal alkali metal recovery process |
-
1954
- 1954-09-06 SU SU10608A patent/SU108917A1/en active
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3998927A (en) * | 1975-10-20 | 1976-12-21 | Aluminum Company Of America | Recovery of sodium aluminate from high-silica aluminous materials |
| US4044095A (en) | 1975-10-20 | 1977-08-23 | Aluminum Company Of America | Process for recovery of alumina from high-silica ore |
| US4159195A (en) | 1977-01-24 | 1979-06-26 | Exxon Research & Engineering Co. | Hydrothermal alkali metal recovery process |
| US4219338A (en) | 1978-05-17 | 1980-08-26 | Exxon Research & Engineering Co. | Hydrothermal alkali metal recovery process |
| US4193772A (en) | 1978-06-05 | 1980-03-18 | Exxon Research & Engineering Co. | Process for carbonaceous material conversion and recovery of alkali metal catalyst constituents held by ion exchange sites in conversion residue |
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