CN1296278C - Production of acqueous talc from brine - Google Patents
Production of acqueous talc from brine Download PDFInfo
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- CN1296278C CN1296278C CNB2004100734533A CN200410073453A CN1296278C CN 1296278 C CN1296278 C CN 1296278C CN B2004100734533 A CNB2004100734533 A CN B2004100734533A CN 200410073453 A CN200410073453 A CN 200410073453A CN 1296278 C CN1296278 C CN 1296278C
- Authority
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- China
- Prior art keywords
- solution
- bittern
- hydrotalcite
- salt
- carbonate
- Prior art date
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- Expired - Fee Related
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- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000012267 brine Substances 0.000 title description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 title description 2
- 239000000454 talc Substances 0.000 title 1
- 229910052623 talc Inorganic materials 0.000 title 1
- 241001131796 Botaurus stellaris Species 0.000 claims abstract description 63
- 229910001701 hydrotalcite Inorganic materials 0.000 claims abstract description 53
- 229960001545 hydrotalcite Drugs 0.000 claims abstract description 53
- 229910001570 bauxite Inorganic materials 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000002994 raw material Substances 0.000 claims abstract description 24
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000001035 drying Methods 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 238000005406 washing Methods 0.000 claims abstract description 7
- 150000002500 ions Chemical class 0.000 claims abstract description 5
- 239000002440 industrial waste Substances 0.000 claims abstract description 3
- 239000000243 solution Substances 0.000 claims description 63
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 45
- 239000011777 magnesium Substances 0.000 claims description 45
- 235000002639 sodium chloride Nutrition 0.000 claims description 40
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 39
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 33
- 238000003756 stirring Methods 0.000 claims description 31
- 239000000126 substance Substances 0.000 claims description 27
- 239000011259 mixed solution Substances 0.000 claims description 23
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 22
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 21
- 239000011780 sodium chloride Substances 0.000 claims description 21
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 20
- 238000000227 grinding Methods 0.000 claims description 18
- 238000002156 mixing Methods 0.000 claims description 17
- 238000001914 filtration Methods 0.000 claims description 16
- 235000017550 sodium carbonate Nutrition 0.000 claims description 16
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 15
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 13
- 239000011504 laterite Substances 0.000 claims description 13
- 229910001710 laterite Inorganic materials 0.000 claims description 13
- 239000011734 sodium Substances 0.000 claims description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 12
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052749 magnesium Inorganic materials 0.000 claims description 12
- 239000000725 suspension Substances 0.000 claims description 12
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 10
- 239000001099 ammonium carbonate Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 9
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 9
- 238000004140 cleaning Methods 0.000 claims description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 8
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 claims description 7
- 229910052593 corundum Inorganic materials 0.000 claims description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 7
- 235000010755 mineral Nutrition 0.000 claims description 7
- 239000011707 mineral Substances 0.000 claims description 7
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 7
- 229910052681 coesite Inorganic materials 0.000 claims description 6
- 229910052906 cristobalite Inorganic materials 0.000 claims description 6
- 239000013078 crystal Substances 0.000 claims description 6
- 229910001679 gibbsite Inorganic materials 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 229910052682 stishovite Inorganic materials 0.000 claims description 6
- 229910052905 tridymite Inorganic materials 0.000 claims description 6
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims description 5
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 5
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims description 5
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 5
- 229920000875 Dissolving pulp Polymers 0.000 claims description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 4
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 claims description 4
- 238000001354 calcination Methods 0.000 claims description 4
- 229910001623 magnesium bromide Inorganic materials 0.000 claims description 4
- 239000013535 sea water Substances 0.000 claims description 4
- 229910001388 sodium aluminate Inorganic materials 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 3
- 230000032683 aging Effects 0.000 claims description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 3
- 229910001648 diaspore Inorganic materials 0.000 claims description 3
- 239000010446 mirabilite Substances 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 238000004131 Bayer process Methods 0.000 claims description 2
- 229910001593 boehmite Inorganic materials 0.000 claims description 2
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- PWZFXELTLAQOKC-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O PWZFXELTLAQOKC-UHFFFAOYSA-A 0.000 claims 11
- 150000004677 hydrates Chemical class 0.000 claims 2
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 claims 2
- 238000007865 diluting Methods 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 abstract description 42
- 239000000047 product Substances 0.000 abstract description 25
- 239000003054 catalyst Substances 0.000 abstract description 6
- 230000007613 environmental effect Effects 0.000 abstract description 6
- 238000002425 crystallisation Methods 0.000 abstract description 5
- 230000008025 crystallization Effects 0.000 abstract description 5
- 238000001179 sorption measurement Methods 0.000 abstract description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003063 flame retardant Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
- 230000008901 benefit Effects 0.000 abstract description 3
- 238000003889 chemical engineering Methods 0.000 abstract description 3
- 239000008204 material by function Substances 0.000 abstract description 3
- 239000010865 sewage Substances 0.000 abstract description 3
- 239000003513 alkali Substances 0.000 abstract description 2
- 230000002265 prevention Effects 0.000 abstract description 2
- 238000010521 absorption reaction Methods 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000004888 barrier function Effects 0.000 abstract 1
- 231100000614 poison Toxicity 0.000 abstract 1
- 230000007096 poisonous effect Effects 0.000 abstract 1
- 239000002002 slurry Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 description 13
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- 229940001593 sodium carbonate Drugs 0.000 description 10
- 239000002184 metal Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 238000000643 oven drying Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000005303 weighing Methods 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-O azanium;hydron;hydroxide Chemical compound [NH4+].O VHUUQVKOLVNVRT-UHFFFAOYSA-O 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000004679 hydroxides Chemical class 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000006077 pvc stabilizer Substances 0.000 description 2
- 238000005067 remediation Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 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 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 229910052598 goethite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 239000000413 hydrolysate Substances 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000001027 hydrothermal synthesis Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- AEIXRCIKZIZYPM-UHFFFAOYSA-M hydroxy(oxo)iron Chemical compound [O][Fe]O AEIXRCIKZIZYPM-UHFFFAOYSA-M 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- XZPVPNZTYPUODG-UHFFFAOYSA-M sodium;chloride;dihydrate Chemical compound O.O.[Na+].[Cl-] XZPVPNZTYPUODG-UHFFFAOYSA-M 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
The present invention discloses a method for preparing hydrotalcite from raw materials of salt producing bittern. In the present invention, bittern is mixed with ore slurry dissolved in bauxite acid or alkali or discarded red mud of a plant for preparing alumina by a Bayer method; crystallization is carried out under proper conditions, and hydrotalcite is obtained through water washing and drying. The method has the advantages of simple technical flow and little equipment investment. Natural resources and industrial waste are used as raw materials; consequently, cost and consumption are greatly reduced on one hand; on the other hand, the problems of the stacking of a large amount of red mud and the harm of the red mud to the environment are solved. Hydrotalcite as the obtained product can be used as a catalyst and a catalyst carrier in the field of chemistry and chemical engineering, a barrier material for the absorption of infrared and ultraviolet in the field of functional materials, and a flame retardant and a PVC stabilizing agent in plastic industry; hydrotalcite performs the strong adsorption action on a plurality of poisonous and harmful negative ions in the field of environmental protection so that hydrotalcite can also be used for sewage treatment, pollution prevention and environment repair.
Description
Technical Field
The invention relates to a method for preparing hydrotalcite by taking salt-making bittern as a raw material.
Background
The salt-making bittern is prepared by evaporating and concentrating seawater, salt lake water and underground bittern to obtain salt (NaCl) or mirabilite (Na)2SO4·10H2Solution remaining after O) containing dissolved components predominantly MgCl2And secondly MgSO4NaCl and KCl, and MgBr2Equal trace components, see references [1-3]]. After NaCl is obtained from seawater or brine water from other sources through solarization and evaporation, the NaCl solution is difficultto be further concentrated through solarization and evaporation due to high viscosity and strong hygroscopicity. Although many technical schemes for comprehensive utilization are available at present [1-4]]However, due to the factors of cost and benefit, considerable amount of bittern is still not reasonably utilized.
Hydrotalcite is also known as Layered Double Hydroxides, abbreviated as LDH. It has a layered structure, structured layers consisting of hydroxides of divalent and trivalent metals, filled with carbonate or other anions between the structured layers, and is therefore also referred to as anionic clay. Hydrotalcite is converted into a Double metal oxide, abbreviated as LDO, after dehydration by heating and loss of hydroxyl groups. It partially retains the original layered structure, and can recover and rebuild the crystal structure of hydrotalcite by absorbing water molecules, anions and hydroxide radicals in aqueous solution.
LDH and LDO are artificial synthetic layered mineral materials which are popular in recent years and can be used as catalysts and catalyst carriers in the fields of chemistry and chemical engineering; in the field of functional materials, as infrared and ultraviolet absorbing and blocking materials; in the plastic industry, can be used as a flame retardant and a PVC stabilizer; in the field of environmental protection, the compounds have strong adsorption effect on a plurality of toxic and harmful anions, so the compounds have wide application prospect in the aspects of sewage treatment, pollution prevention, environmental remediation and the like.
Reference to the literature
[1]Relief, roof beam Yuhua, Tangwenxia, Zhang Changxin, old new feelings, comprehensive utilization of salt-making bittern. Marine lake salt and chemical engineering, 1993, 22 (2): 4-7.
[2]Chenghaihao, which is the potassiummagnesium salt extracted from bitter bittern of Gaotai salt lake. Gansu chemical 1997, fourth phase, 14-17.
[3]The comprehensive utilization process of recovery, long source of poplar, treyide and bittern. Fujian chemical, 1992, first phase, 42-45.
[4]Study on the production of magnesium sulfate by Hechunbao, Zulixiang, Tantan sun-drying. Sea lake salt and chemical, 1994, 23 (3): 18-19.
[5]Yangshuang, Caozaihua, the current situation of comprehensive utilization and development of red mud produced by alumina. Mineral protection and utilization, 1999 (6): 46-49.
[6]Removing Sulfur (SO) from brine by using Song Kuiyuan, Song Yulin, Yangyongzhen, Chenhong Wei and calcium chloride method4 2-) The study of (1). Shenyang chemical industry, 1989 (1): 4-9.
Disclosure of Invention
The invention aims to provide a method for preparing hydrotalcite by taking salt-making bittern as a raw material.
The chemical components of the salt-making bittern are as follows: MgCl2=11.0~45.0%,MgSO4=4.0~8.5%,NaCl=2.0~8.5%,KCl=0.2~2.0%,MgBr20.2-0.8%, (for details see reference)[1-3])。
The method for preparing the hydrotalcite comprises the following steps:
1) mixing the salt-making bittern with acid-soluble pulp of laterite-type bauxite to make Mg/(Al + Fe) in the solution3+) The molar ratio of the Mg to the Mg is 1: 1-5: 1, and the Mg is diluted by adding water to ensure that the Mg is in the solution2+The concentration of ions is not more than 0.3mol/L, and the solution is marked as solution A;
2) preparing a mixed solution of NaOH and carbonate or bicarbonate, wherein the molar number of the carbonate or the bicarbonate is 35 to 50 percent of that of magnesium in the solution A, the molar number of the NaOH is 60 to 100 percent of that of the magnesium, and the total concentration of the solution is not more than 1mol/L and is marked as solution B.
3) Rapidly mixing the solution A and the solution B while strongly stirring, and continuously stirring for 5-10 minutes;
4) crystallizing the mixed solution at the constant temperature of 50-80 ℃ for 6-48 hours, dehydrating, filtering, cleaning, drying at the temperature lower than 90 ℃, grinding to less than 200 meshes, and bagging. The obtained product is hydrotalcite, and the chemical structure general formula is as follows: [ Mg1-x(Al,Fe3+)x(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; Mg/(Al + Fe)3+)=1~5。
The laterite bauxite refers to bauxite with gibbsite as a main mineral component, and the laterite bauxite has the following representative chemical components: al (Al)2O3=40~50%,Fe2O3=10~20%,SiO2=3~10%,TiO22-5% of crystal water, 22-28%; the acid-soluble ore pulp of the laterite-type bauxite refers to a solution obtained by dissolving the laterite-type bauxite in hydrochloric acid or nitric acid with the concentration of 1-5N and removing residues; the carbonate or bicarbonate is one or more of sodium carbonate, ammonium carbonate, sodium bicarbonate, ammonium bicarbonate or hydrate thereof.
The method for preparing the hydrotalcite comprises the following two steps:
1) mixing the salt-making bittern with bauxite alkali-soluble ore pulp to make Mg/Al molar ratio in the solution be 11-5: 1, and adding water for dilution if necessary toensure that Mg is contained in the solution2+The concentration of the ions is not more than 0.3 mol/L;
2) adding a pre-prepared carbonate or bicarbonate solution with the concentration of 0.5-2 mole/L into the mixed solution, wherein the weight ratio of the carbonate or bicarbonate to (Mg + Al) in the mixed solution is 1: 1-1: 1.5;
3) crystallizing the mixed solution at the constant temperature of 50-80 ℃ for 6-48 hours, dehydrating, filtering, cleaning, drying at the temperature lower than 90 ℃, grinding to less than 200 meshes, and bagging. The obtained product is hydrotalcite,the chemical structural general formula is as follows: [ Mg1-xAlx(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; 1-5 Mg/Al.
The bauxite refers to a general name of ores which can be utilized industrially and are composed of gibbsite, boehmite, diaspore or a mixture of the gibbsite and the diaspore as main minerals; the alkaline dissolving pulp of the bauxite is caustic soda (commonly used Na)2O), sodium aluminate (Al is commonly used)2O3Represented by general formula (II) and soda ash (Na)2CO3) The mixed solution of (a) and (b) contains the following representative components: na (Na)2O=250~300g/L,Al2O3=280~350g/L,Na2CO310-50 g/L; the carbonate or bicarbonate is one or more of sodium carbonate, ammonium carbonate, sodium bicarbonate, ammonium bicarbonate or hydrate thereof.
The method for preparing the hydrotalcite comprises the following three steps:
1) mixing the salt-making bittern from which sulfate radicals are removed with Bayer red mud of an alumina plant, and adding the mixture into a stirrer to ensure that Mg/(Al + Fe) in the mixture3+) The molar ratio is 1: 1-5: 1, water is added for dilution if necessary to ensure that the solid-to-liquid ratio of the ore pulp is not more than 1: 10, the mixture is uniformly stirred to prepare suspension, and the suspension is aged for 6-48 hours;
2) dehydrating the suspension, airing or drying at a temperature lower than 90 ℃, calcining for 2-5 hours at a temperature of 450-750 ℃, and grinding to a particle size of less than 200 meshes for later use; the obtained product is a bimetal oxide, and the chemical junction of the bimetal oxideThe general formula is Mgm·(Al,Fe3+)n·OxWherein x is m +3 n/2;
3) preparing soluble carbonate or bicarbonate into a solution with the concentration of 0.5-2 mole/L, adding the product obtained in the step 2) into the solution according to the proportion of adding 200-300 g of bimetallic oxide into each gram of carbonate or bicarbonate, uniformly mixing, continuously stirring for 5-10 minutes, crystallizing at the constant temperature of 50-90 ℃ for 6-48 hours, filtering or centrifugally dewatering, washing with clean water for 2-3 times, dewatering, airing or drying at the temperature lower than 90 ℃, and grinding to less than 200 meshes for later use, wherein the obtained product is hydrotalcite, and the general chemical structure formula of the obtained product is as follows: [ Mg1-x(Al,Fe3+)x(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; Mg/(Al + Fe)3+)=1~5。
The Bayer red mud is industrial waste formed in the process of preparing alumina and aluminum hydroxide by using a Bayer method, the granularity of the Bayer red mud is micron-submicron grade, and the Bayer red mud has the following representative chemical components: fe2O3=30~60%,Al2O3=10~25%,SiO2=3~50%,Na2O=2~15%,CaO=0~8%,TiO20-10%, (see reference 5 for details)]) (ii) a The soluble carbonate or bicarbonate is one or more of sodium carbonate, ammonium carbonate, sodium bicarbonate, ammonium bicarbonate or hydrate thereof.
The invention has the advantages of simple process flow and less equipment investment; the main raw materials have wide sources and low price. If the salt-making bittern and the Bayer red mud are adopted as raw materials to synthesize the hydrotalcite, the problems of stacking of the red mud and environmental harm can be solved at the same time. The obtained product hydrotalcite can be used as a catalyst and a catalyst carrier in the fields of chemistry and chemical industry; in the field of functional materials, as infrared and ultraviolet absorbing and blocking materials; in the plastic industry, can be used as an antibacterial additive, a flame retardant and a PVC stabilizer; in the field of environmental protection, they have a strong adsorption effect on many toxic and harmful anions, and thus can be used for water purification, sewage treatment, pollution control and environmental remediation.
Detailed Description
The first method for preparing hydrotalcite provided by the invention is to synthesize hydrotalcite by taking salt-making bittern as a source of divalent metal elements, namely magnesium, and laterite type bauxite acid-soluble ore pulp as a source of trivalent metal elements, namely aluminum and iron, through chemical reaction and crystallization. The main mineral composition of the laterite bauxite is gibbsite, and then goethite and hematite. The bauxite has a loose structure and strong chemical activity, is easily dissolved by inorganic acids such as hydrochloric acid, nitric acid, sulfuric acid and the like, and is recommended to use hydrochloric acid in consideration of environment and cost. Due to the existence of ferric iron, hydrotalcite synthesized by taking laterite type bauxite as a raw material is reddish. The ratio of the divalent metal element and the trivalent metal element in the additive has certain influence on the performance of the final product. Generally, when the former is used in a higher amount, the crystal structure of the product is more stable; when the latter is used in high amount, the product has better adsorption performance. The molar ratio of the divalent to trivalent metal elements is preferably controlled to be in the range of 1: 1 to 5: 1. In practical application, the dosage of the bittern can be calculated according to the dosage of the bauxite, and the content of magnesium element in the added bittern is 0.5-2.5 times of the dry weight of the bauxite.
When caustic soda and sodium carbonate or sodium bicarbonate are used to prepare the solution B, the molar concentrations of the caustic soda and the sodium carbonate or sodium bicarbonate in the solution are in a 2: 1 relationship. The molar number of sodium carbonate or sodium bicarbonate in the solution B is 35 to 50 percent of that of magnesium element in the solution A, the molar number of NaOH is 60 to 100 percent of that of magnesium element, and the total concentration of the solution is not more than 3 mol/L. The mixed solution of bittern and acid-soluble laterite ore pulp (solution A) and solution B needs to be intensively stirred before being mixed, and the two solutions are quickly mixed while being stirred. Stirring should be continued for 5-10 minutes to ensure uniform mixing. The optimal crystallization condition is 60-70 ℃ and 10-16 hours.
The crystallized suspension can be dehydrated by filtration, filter pressing or centrifugation, and dried naturally as far as possible, or dried at a temperature not higher than 90 deg.C, or spray dried.
The second method for preparing hydrotalcite of the invention,salt-making bittern is used as a source of divalent metal element magnesium, alkaline ore pulp of bauxite is used as a source of trivalent metal element aluminum, and hydrotalcite is synthesized through hydrothermal reaction. The alkaline dissolving pulp is an intermediate product of Bayer process for preparing alumina and aluminum hydroxide, can be obtained from alumina plant, and is caustic soda (common Na)2O), sodium aluminate (Al is commonly used)2O3Represented by general formula (II) and soda ash (Na)2CO3) The mixed solution of (a) and (b) contains the following representative components: na (Na)2O=250~300g/L,Al2O3=280~350g/L,Na2CO310-50 g/L. The hydrotalcite product is pure white due to the absence of iron in the raw materials.
The dosage of the bittern is controlled to keep the molar ratio of the divalent and trivalent metal elements in the mixed solution within 1: 1-5: 1. After sodium carbonate or sodium bicarbonate is added into the solution, the conditions of crystallization, dehydration and drying are the same as the former method.
The third method for preparing hydrotalcite provided by the invention is to synthesize hydrotalcite by taking salt-making bittern as a source of magnesium as a divalent metal element and Bayer red mud of an alumina plant as a source of aluminum as a trivalent metal element through chemical reaction and crystallization. Because the Bayer red mud contains high impurity components, the product obtained by the method is only suitable for applications with low requirements on purity and color, such as wastewater treatment, flame retardant additives of dark plastic products and the like.
The sulfate radical in bittern is first eliminated in the presentprocess, and this is because red mud contains calcium in different amount and the sulfate radical in bittern is easy to react with calcium to form gypsum and reduce the relative content of hydrotalcite in reactant. The removal of sulphate from bittern is a well-known technique [6]]. Adding appropriate amount of CaCl into bittern2Then the following reactions occur:
the gypsum precipitate formed is easily separated from the bittern. After the sulfur-free bittern is mixed with the red mud, the calcium in the red mud and the magnesium chloride in the bittern can have the following reactions:
that is, calcium in the raw material favors Mg (OH)2Precipitation of CaCl formed2Will be removed during dewatering and washing. The large amount of NaOH in the red mud also promotes the magnesium ions in the bittern to precipitate out:
the result of the reaction is that magnesium is transferred to the solid phase, while sodium and calcium are brought into solution and will be removed in the next step.
The ratio of the divalent metal element in the additive to the trivalent metal element in the red mud has certain influence on the performance of the final product. Generally, when the former is used in a higher amount, the crystal structure of the product is more stable; when the latter is used in high amount, the product has better adsorption performance. In practical application, the dosage of the bittern can be calculated according to the dosage of the red mud, and the content of magnesium element in the bittern added is 0.5-3 times of the dry weight of the red mud.
The water adding amount can be adjusted according to the drying degree of the red mud, so that the product after stirring is a viscous and flowable suspension. The water consumption is too low, and the raw materials are difficult to stir uniformly; the water consumption is too high, which greatly increases the energy consumption of the subsequent process and the equipment abrasion.
The suspension after stirring can be dehydrated by methods such as filtration, filter pressing or centrifugation, and natural drying is adopted as far as possible, or drying is carried out at the temperature of not more than 90 ℃ so as to further age in the drying process.
The intermediate product is calcined for the purpose of converting the divalent and trivalent element oxides (hydroxides) in the mixture into a solid solution. The calcined product is a bimetal oxide, can be directly put on the market as a product, and can also be used as a raw material for further synthesizing the hydrotalcite.
And (3) hydrolyzing the bimetallic oxide in a carbonate solution to obtain the hydrotalcite. Representative chemical reactions in solution are:
The present invention is further illustrated by the following examples.
Example 1: hydrotalcite is prepared from salt lake bittern and bauxite acid-soluble pulp.
Raw material 1: the salt lake bittern in certain area comprises the following chemical components: MgSO (MgSO)4=70g/L,MgCl2165g/L, 90g/L NaCl, 20g/L KCl. Raw material 2: the laterite type bauxite comprises the following chemical components: al (Al)2O3=48%;Fe2O3=16;SiO2=7%,TiO23%, crystal water 24%, and other impurities 2%.
1) Weighing 175 g of laterite type bauxite, grinding the laterite type bauxite into powder, adding 6.5L of hydrochloric acid with the concentration of 1N, stirring until the ore powder is basically dissolved, filtering to remove residues, adding 1.3L of bittern, and stirring uniformly to obtain a solution A;
2) 90g NaOH and 120 g Na were weighed out2CO3Dissolving 2 liters of water, and stirring until the solute is completely dissolved, and marking as solution B;
3) stirring the solution A intensely, pouring the solution B into the solution A quickly while stirring, and continuing to stir for 5 minutes;
4) crystallizing the mixed solution at 60 deg.C for 12 hr, filtering, dewatering, cleaning, oven drying at 80 deg.C, grinding to less than 200 meshes, and bagging. The product obtained is hydrotalcite.
Example 2: hydrotalcite is prepared from sea salt bittern and bauxite acid-dissolved pulp.
Raw material 1: the sea salt bittern comprises the following chemical components: MgSO (MgSO)4=116g/L,MgCl2311g/L, 52g/L NaCl, 5g/L KCl. Raw material 2: the chemical composition of the ore of the laterite type bauxite is the same as that of the ore in example 1.
1) Weighing 175 g of laterite type bauxite, grinding the laterite type bauxite into powder, adding 1.5L of hydrochloric acid with the concentration of 4N, stirring until the ore powder is basically dissolved, filtering to remove residues, adding 0.7L of bittern, adding 15L of water, and stirring uniformly to obtain a solution A;
2) 100 g NaOH and 100 g NaHCO were weighed3Dissolving 4 liters of water, and stirring until the solute is completely dissolved, and marking as solution B;
3) stirring the solution A intensely, pouring the solution B into the solution A quickly while stirring, and continuing to stir for 5 minutes;
4) crystallizing the mixed solution at 80 deg.C for 10 hr, filtering, dewatering, cleaning, oven drying at 60 deg.C, grinding to less than 200 meshes, and bagging. The product obtained is hydrotalcite.
Example 3: hydrotalcite is prepared from sea salt bittern and bauxite alkali-soluble pulp.
Raw material 1: the sea salt bittern comprises the following chemical components: MgSO (MgSO)4=72g/L,MgCl2570g/L, 3.5g/L NaCl, 2.0g/L KCl. Raw material 2: the alkali dissolving pulp of an alumina factory in a certain place comprises the following components: na (Na)2O=260g/L,Al2O3=310g/L,Na2CO3=30g/L。
1) Mixing 1L of bauxite alkali-soluble ore pulp with 2L of bittern, adding 20L of water, and stirring uniformly;
2) adding 25 liters of pre-prepared sodium carbonate solution with the concentration of 1mole/L into the mixed solution, and uniformly stirring;
3) crystallizing the mixed solution at 60 deg.C for 12 hr, dehydrating, filtering, cleaning, oven drying at 70 deg.C, grinding to less than 200 meshes, and packaging. The obtained product is hydrotalcite.
Example 4: hydrotalcite is prepared from sea salt bittern and bauxite alkali-soluble pulp.
The starting materials used were the same as in example 3.
1) Mixing 1L of bauxite alkali-soluble ore pulp with 2L of bittern, adding 20L of water, and stirring uniformly;
2) adding 28 liters of pre-prepared sodium bicarbonate solution with the concentration of 1mole/L into the mixed solution, and uniformly stirring;
3) crystallizing the mixed solution at 70 deg.C for 10 hr, dehydrating, filtering, cleaning, oven drying at 80 deg.C, grinding to less than 200 meshes, and packaging. The obtained product is hydrotalcite.
Example 5: hydrotalcite is prepared from sea salt bittern and bayer red mud.
Raw material 1: the sea salt bittern comprises the following chemical components: MgSO (MgSO)4=80g/L,MgCl2430g/L, 16.0g/L NaCl, 5.0g/L KCl, as per reference [6]before use]The method of (3) removing sulfate radicals. Raw material 2: bayer red mud discharged from an alumina plant in a certain place comprises the following chemical components: al (Al)2O3=24.6%;Fe2O3=34.2%;SiO2=16.5%,CaO=3.7%,Na2O=9.8%,TiO2=6.8%。
1) Taking 1.5 liters of bittern from which sulfate radicals are removed, weighing 0.5 kg of dried red mud, mixing, adding 5 liters of water, stirring uniformly to prepare suspension, and aging for 12 hours;
2) dehydrating the suspension, drying at 80 ℃, calcining at 500 ℃ for 3 hours, and grinding to less than 200 meshes for later use;
3) taking 2 liters of sodiumcarbonate solution with the concentration of 1mole/L, adding the product obtained in the step 2) into the solution, uniformly mixing, continuously stirring for 5 minutes, crystallizing at the constant temperature of 60 ℃ for 12 hours, filtering, dehydrating, washing with clean water for 2-3 times, drying at the temperature of 80 ℃ after dehydrating, and grinding to less than 200 meshes for later use, wherein the obtained product is hydrotalcite.
Example 6: hydrotalcite is prepared from sea salt bittern and bayer red mud.
The starting material was the same as in example 5, and the sulfate group was removed by the method described in reference [6]before use.
1) Taking 2 liters of bittern from which sulfate radicals are removed, weighing 0.8 kg of dried red mud, mixing, adding 6 liters of water, stirring uniformly to prepare suspension, and aging for 8 hours;
2) dehydrating the suspension, drying at 70 ℃, calcining at 600 ℃ for 2 hours, and grinding to less than 200 meshes for later use;
3) taking 4 liters of sodium bicarbonate solution with the concentration of 1mole/L, adding the obtained substance in the step 2) into the solution, uniformly mixing, continuously stirring for 10 minutes, crystallizing at the constant temperature of 80 ℃ for 8 hours, filtering, dehydrating, washing with clean water for 2-3 times, drying at the temperature of 80 ℃ after dehydrating, and grinding to less than 200 meshes for later use, wherein the obtained product is hydrotalcite.
Claims (10)
1. A method for preparing hydrotalcite by taking salt-making bittern as raw material is characterized by comprising the following steps:
1) mixing the salt-making bittern with acid-soluble pulp of laterite-type bauxite to make Mg/(Al + Fe) in the solution3+) The molar ratio of the Mg to the Mg is 1: 1 to 5: 1, and the Mg is diluted by adding water to lead the Mg in the solution to be2+The concentration of ions is not more than 0.3mol/L, and the solution is marked as solution A;
2) preparing a mixed solution of NaOH and carbonate or NaOH and bicarbonate, wherein the molar number of the carbonate or the bicarbonate is 35 to 50 percent of that of magnesium in the solution A, the molar number of the NaOH is 60 to 100 percent of that of the magnesium, the total concentration of the solution is not more than 1mol/L, and the solution is marked as solution B;
3) mixing the solution A and the solution B while stirring, and continuously stirring for 5-10 minutes;
4) crystallizing the mixed solution at the constant temperature of 50-80 ℃ for 6-48 hours, dehydrating, filtering and cleaning the mixed solution, drying at the temperature lower than 90 ℃, grinding to less than 200 meshes, and bagging to obtain a product, namely hydrotalcite, wherein the chemical structural formula of the product is as follows: [ Mg1-x(Al,Fe3+)x(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; Mg/(Al + Fe)3+)=1~5。
2. The method for preparing hydrotalcite from bittern used for salt production as claimed in claim 1, wherein said bittern used for salt production is seawater, salt lake water, or underground bittern, and is prepared by evaporating and concentrating to obtain salt (NaCl) or mirabilite (Na)2SO4·10H2Solution remaining after O) containing the dissolved components: MgCl2=11.0~45.0%,MgSO4=4.0~8.5%,NaCl=2.0~8.5%,KCl=0.2~2.0%,MgBr2=0.2~0.8%。
3. The method for preparing hydrotalcite from bittern used for making salt as raw material as claimed in claim 1, wherein said laterite type bauxite is bauxite with gibbsite as main mineral component, and its representative chemical composition is: al (Al)2O3=40~50%,Fe2O3=10~20%,SiO2=3~10%,TiO22-5% of crystal water, 22-28%; the acid-soluble ore pulp of the laterite-type bauxite refers to a solution obtained by dissolving the bauxite in hydrochloric acid or nitric acid with the concentration of 1-5N and removing residues.
4. The method for preparing hydrotalcite from bittern for salt production as claimed in claim 1, wherein the carbonate or bicarbonate is one or more of sodium carbonate, ammonium carbonate, sodium bicarbonate, ammonium bicarbonate or their hydrates.
5. A method for preparing hydrotalcite by taking salt-making bittern as raw material is characterized by comprising the following steps:
1) mixing salt-making bittern with bauxite alkali-soluble ore pulp to make Mg/Al molar ratio in the solution be 1: 1-5: 1, adding water to dilute to make Mg in the solution2+The concentration of the ions is not more than 0.3 mol/L;
2) adding a pre-prepared carbonate or bicarbonate solution with the concentration of 0.5-2 mole/L into the mixed solution, wherein the weight ratio of the carbonate or bicarbonate to (Mg + Al) in the mixed solution is 1: 1 to 1: 1.5;
3) crystallizing the mixed solution at the constant temperature of 50-80 ℃ for 6-48 hours, dehydrating, filtering and cleaning the mixed solution, drying at the temperature lower than 90 ℃, grinding to less than 200 meshes, and bagging to obtain a product, namely hydrotalcite, wherein the chemical structural formula of the product is as follows: [ Mg1-xAlx(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; 1-5 Mg/Al.
6. The method of claim 5, wherein the bauxite is a general term for an industrially available ore comprising gibbsite, boehmite, diaspore or a mixture thereof as a main mineral; the alkaline dissolving pulp of bauxite is a mixed solution of caustic soda, sodium aluminate and soda ash, and uses Na2O、Al2O3And Na2CO3Respectively represent caustic soda, sodium aluminate and soda ash, and the representative components are as follows: na (Na)2O=250~300g/L,Al2O3=280~3S0g/L,Na2CO3=10~50g/L。
7. A method for preparing hydrotalcite by taking salt-making bittern as raw material is characterized by comprising the following steps:
1) mixing bittern from which sulfate radical is removed with Bayer red mud of alumina plant, adding into a stirrer to make Mg/(Al + Fe) in the mixture3+) Diluting with water until the ratio of the ore pulp to the solid to the liquid is not more than 1: 10, uniformly stirring to prepare a suspension, and aging for 6-48 hours, wherein the molar ratio is 1: 1 to 5: 1;
2) dehydrating the suspension, airing or drying at a temperature lower than 90 ℃, calcining for 2-5 hours at a temperature of 450-750 ℃, and grinding to a particle size of less than 200 meshes for later use; the obtained product is a bimetal oxide with the chemical structural general formula of Mgm·(Al,Fe3+)n·OxWherein x is m +3 n/2;
3) preparing carbonate or bicarbonate into a solution with the concentration of 0.5-2 mole/L, adding the product obtained in the step 2) into the solution according to the proportion of adding 200-300 g of bimetallic oxide into each gram of carbonate or bicarbonate, uniformly mixing, continuously stirring for 5-10 minutes, crystallizing at the constant temperature of 50-90 ℃ for 6-48 hours, filtering or centrifugally dewatering, washing with clean water for 2-3 times, dewatering, airing or at the temperature lower than 90 DEG CDrying at a certain temperature, grinding to less than 200 meshes for later use, wherein the obtained product is hydrotalcite, and the chemical structural general formula is as follows: [ Mg1-x(Al,Fe3+)x(OH)2]x+[(CO3)x/2·nH2O]Wherein X is 0.5-0.17; Mg/(Al + Fe)3+)=1~5。
8. The method for preparing hydrotalcite from bittern used for salt production as claimed in claim 5 or 7, wherein said bittern used for salt production is seawater, salt lake water, or underground bittern, and is prepared by evaporating and concentrating to obtain salt (NaCl) or mirabilite (Na)2SO4·10H2Solution remaining after O) containing the dissolved components: MgCl2=11.0~45.0%,MgSO4=4.0~8.5%,NaCl=2.0~8.5%,KCl=0.2~2.0%,MgBr2=0.2~0.8%。
9. The method of claim 7, wherein the Bayer red mud is industrial waste from the Bayer process of preparing alumina and aluminum hydroxide, and has a particle size of micrometer to submicron, and the representative chemical components are as follows: fe2O3=30~60%,Al2O3=10~25%,SiO2=3~50%,Na2O=2~15%,CaO=0~8%,TiO2=0~10%。
10. The method for preparing hydrotalcite from bittern for salt production as claimed in claim 5 or 7, wherein the carbonate or bicarbonate is one or more of sodium carbonate, ammonium carbonate, sodium bicarbonate, ammonium bicarbonate or their hydrates.
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CN101353815B (en) * | 2008-08-19 | 2011-05-18 | 浙江大学 | Method for preparing basic magnesium chloride whisker from dolomite and bittern |
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CN111285383A (en) * | 2018-12-07 | 2020-06-16 | 华东理工大学 | Method for preparing hydrotalcite by desalting strong brine from seawater |
CN114573034B (en) * | 2021-12-31 | 2024-03-22 | 武汉工程大学 | Method for preparing layered iron-aluminum double metal hydroxide from Bayer red mud |
CN115745003B (en) * | 2022-12-02 | 2024-06-14 | 华北科技学院 | Iron-magnesium-aluminum carbonate hydrotalcite material prepared from red mud, and preparation method and application thereof |
CN117735507A (en) * | 2023-11-30 | 2024-03-22 | 南京联塑科技实业有限公司 | Preparation method of bitter marinated hydrotalcite and application of bitter marinated hydrotalcite in PVC heat stabilizer |
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