CN1114364A - Method and equipment for producing titanium-rich material - Google Patents
Method and equipment for producing titanium-rich material Download PDFInfo
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- CN1114364A CN1114364A CN 94111054 CN94111054A CN1114364A CN 1114364 A CN1114364 A CN 1114364A CN 94111054 CN94111054 CN 94111054 CN 94111054 A CN94111054 A CN 94111054A CN 1114364 A CN1114364 A CN 1114364A
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- leaching
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- ilmenite
- fluidization
- titanium material
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- 239000000463 material Substances 0.000 title claims abstract description 36
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims abstract description 27
- 239000010936 titanium Substances 0.000 title claims abstract description 27
- 229910052719 titanium Inorganic materials 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000002386 leaching Methods 0.000 claims abstract description 29
- 238000005243 fluidization Methods 0.000 claims abstract description 22
- YDZQQRWRVYGNER-UHFFFAOYSA-N iron;titanium;trihydrate Chemical compound O.O.O.[Ti].[Fe] YDZQQRWRVYGNER-UHFFFAOYSA-N 0.000 claims abstract description 22
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000005406 washing Methods 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 238000010298 pulverizing process Methods 0.000 claims abstract description 4
- 230000003647 oxidation Effects 0.000 claims abstract description 3
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 230000001590 oxidative effect Effects 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 7
- 239000007789 gas Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 238000000605 extraction Methods 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 239000000919 ceramic Substances 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 239000012452 mother liquor Substances 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims 1
- 239000004576 sand Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 229910010413 TiO 2 Inorganic materials 0.000 description 7
- 238000006253 efflorescence Methods 0.000 description 7
- 206010037844 rash Diseases 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 241000282326 Felis catus Species 0.000 description 3
- 241000628997 Flos Species 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000003034 coal gas Substances 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 210000003953 foreskin Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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- Manufacture And Refinement Of Metals (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The invention relates to a method and equipment for producing a titanium-rich material by treating ilmenite with dilute hydrochloric acid.
The method adopts primary ilmenite or ilmenite sand with low weathering degree, and adopts 18-20% hydrochloric acid to carry out multistage countercurrent normal-pressure leaching and washing in a fluidized leaching device consisting of two fluidization towers and two circulating grooves after oxidation roasting treatment, wherein the pulverization rate is less than 1%, and the primary ilmenite with maintained granularity and TiO content is obtained2More than 90 percent of titanium-rich material, the yield is higher than 94 percent, the fluidized leaching device has simple structure, easy manufacture, convenient operation, high running efficiency and good working environment.
Description
What the present invention relates to is a kind of method and device thereof of producing rich titanium material with dilute hydrochloric acid processing ilmenite.
Method and equipment thereof that existing dilute hydrochloric acid is handled the rich titanium material of ilmenite production are ilmenite to be carried out reducing roasting handle.In pressure is boiled the ball cylinder, press and soak, 0.5～2.5% of adding ore deposit amount sulfuric acid or vitriol in leaching process.When this method was used for the low placer of the abundantest primary ilmenite of reserves or rate of decay, efflorescence was serious, and process has some setbacks, and product is not popular with users.Pressure is soaked equipment and material is required high, presses and soaks that hydrogen chloride gas leaks in the process, contaminate environment, etching apparatus and buildings.(see United States Patent (USP) 4019898, Lammartion, N.R, ChemicalEnginering 1976, V83, No.11,100～101) and for example the metallurgical office of Zigong City coal wait unit directly to boil the leaching of ball cylinder with pressure with the Flos Bombacis Malabarici concentrated ilmenite, produce 4～7 microns fine powders in the process, take out of with mother liquor and wash water, therefrom reclaim these fine powders again, make titanium yellow powder, drag-out accounts for 26.86% of total rich titanium material, makes in the coarse fodder remaining fine powder amount reduce to 4.15%.This method, efflorescence is serious, and the thickness material separates bad, particularly reclaims the fine powder difficulty from solution and wash water, adds and press the problem of soaking equipment itself that the industrialization difficulty is big.(see the pressurization of choosing-smelting associating dilute hydrochloric acid leach the Flos Bombacis Malabarici ilmenite concentrate and produce artificial rutile, commerical test report, the metallurgical office of Zigong City coal etc., 1984.11).
Purpose of the present invention is exactly to be that seeking a kind of efflorescence normal pressure that prevents for primary ilmenite and the low ferrotianium placer dilute hydrochloric acid method of rate of decay leaches method and the equipment thereof of producing rich titanium material.
For achieving the above object, technical scheme of the present invention is: the ferrotianium placer that primary ilmenite or rate of decay is low, through oxidizing roasting handle, cooling, the hydrochloric acid with 18～20%, in fluidization leaching device, carry out the multistage counter current normal pressure and leach, wash, filter, dry or be sintered into rich titanium material product based on two fluidization column.The percentage composition of its raw material is: TiO
240～53, ∑ Fe28～37, Fe
2+22～32%, MgO0.1～7, CaO0.1～1.4, SiO
2L～3, Al
2O
30.25～1.5, size composition is 0.04～0.6 millimeter.
Technical process of the present invention as shown in Figure 1.The drawing label is 1-oxidizing roasting, 2-fluidization leaching, 3-filtration washing, 4-oven dry or calcining.Key step division of the present invention is as follows:
One, oxidizing roasting is handled.
For making ilmenite have stronger anti-efflorescence ability, can suppress the chemical atomizing that titanium causes because of homogeneous nucleation effectively in hydrolytic process, and for to make the titanium on the ore particle in the hydrolysis settled layer, have stronger intensity, alleviate efflorescence because of mechanical effect, this technology is at first carried out raw material oxidizing roasting and is handled in rotary kiln or fluidizing furnace, fuel can be oils or coal gas, its maturing temperature is 425～875 ℃, furnace exhaust gas oxygen is 5～20%, it is left alone without help that to stay the time be 3～30 minutes, can make 5～35% ferrous oxidation defend ferric iron, roasting material is cooled to 85 ℃ in air, carry out acidleach to send into the hypomere operation.
Two, the fluidization of multistage counter current normal pressure is leached.
Multistage counter current can be strengthened leaching process, leaching velocity that also can satisfaction guaranted under normal pressure, in whole process, can keep than the isostatic speed of response simultaneously, particularly the ore deposit contacts with acid for the first time, to be unlikely decomposition rate too fast because acidity is low, the matrix of titanium hydrolyzate destroyed easily cause the settling efflorescence that comes off.In addition, in the fluidization bed of certain voidage, the impact that titanium hydrolysis settled layer is subjected to, collision mechanical effect such as mill is little and alleviate its efflorescence effectively.So this technology will be cooled to the oxidizing roasting material below 85 ℃, directly add in the fluidized bed from cat head, solution is gone into from column bottoms pump, and solution leaches by the fluidization bed continuously, and the bed porosity is 0.61～0.74.Use mother liquor that the final stage of batch of material leached as leach liquor, form the dense multistage counter current in earlier rare back and leach mode.With three sections is example, every section leach liquor concentration of hydrochloric acid is followed successively by 5～10%, 10～18%, 18～20%, and the temperature in the bed is hanged down 2～5 ℃ than the boiling point of solution under this state, and leaching intrasystem vapour pressure is normal pressure, total extraction time is 6～9 hours, and liquid-solid ratio is 2.8～4.0 (V: W).Pulverization ratio is less than 1%, and rich titanium material keeps the granularity of ilmenite, TiO
2Greater than 90%, be to produce TiCe
4, the high quality raw material of titanium yellow powder, welding electrode foreskin and ceramic industry.Yield from ilmenite to rich titanium material is greater than 94%.
The present invention aims at the structural representation of device shown in Fig. 2 a that multistage fluidization extract technology provides, and it is mainly constructed and is: two fluidization column are formed by connecting by two groups of pumps, two heat exchangers and pipe valve and two circulation grooves.Switching effect by some valves, each tower all can be formed the same form two cover leaching systems with each groove, this tower, groove alternately connect, form multistage counter current and leach and wash, and two cover system commissure effects have joint to finish leaching process one by one again and again with beating.Its drawing label is 1,6-fluidization column, 2,5-interchanger, 3,4-pump, 7,8-circulation groove, 9～16-valve.
Three sections adverse currents of this technology leach and the function mode of first wash is: Open valve (13) and (9) are valve-off (14) simultaneously, (15), (10) and (11), ejector priming (3), the solution of groove (7) [last consignment of carries out second section solution that leached in tower (6)] is through heat exchanger (2), pump into fluidization column (1), material adds from cat head, solution carries out first section leaching by the fluidization bed, meanwhile, tower (6), groove (8), the system that pump (4) and interchanger (5) are formed carries out the 3rd section leaching to the last consignment of ore deposit, soaks two systems of certain hour and finishes this section leaching simultaneously; Open valve (15) and (11), shut-off valve (13) and (9), use the 3rd section solution that leached in last consignment of ore deposit instead and carry out second section leaching, meanwhile, open the water valve (not marking among the figure) that leads to pump (4), open the bleed valve (not marking) of tower (6) upflow tube, carry out washing in the tower, washing wash water acidity reduces to below 0.1%, material in the tower (6) is put into storage tank (not marking), and used for filtering, groove (7) is 18～22% in complex acid concentration, treat that tower (1) leaches into to give and fix time open valve (13) and (9), close (15) and (11), groove (7) solution pumps into tower (1) and carries out the 3rd section leaching.Meanwhile, open valve (16) and (12), groove (8) solution pump into tower (6), and next batch of material is carried out first section leaching, after treating that two systems have leached certain hour to two batch of materials, change washing and second section leaching respectively over to, arrive this, finished one and embathed the cycle.By the switching of valve, the tower groove is alternately connected like this, both formed multistage counter current and leached and washing, make two to embathe system's commissure operation again, finished the process of embathing one by one rhythmically again and again.
Accompanying drawing 2b is the fluidization column structural representation, and its drawing label is:
20-nozzle, the 21-awl end, 22-tower body, 23-troclia, 24-upflow tube, 25-overflow weir, 26-charge cavity, 27-guide ring.The material of this technology adds from cat head, the nozzle (20) of leach liquor at the bottom of the tower pumps into, passed through (21) at the bottom of the awl of sieve plate effect, after adjusting the cross section flow velocity, enter tower body (22), leach by the fluidization bed, in troclia (23), clarify through guide ring (27), after compiling by overflow weir (25), flow to circulation groove by upflow tube (24), the nozzle bore be on the tower body diameter 4～12%, tower body (22) is up big and down small garden tube, cone angle is 0～10 °, the cone angle at the awl end is 10～40 °, the overflow weir diameter is 1～4 times of diameter on the tower body, and 0～3 guide ring is installed in the tower body troclia, ring spacing be on the tower body diameter 1/15～1/6, whole tower is made by general steel plate, is lined with acid proof offset plate or acid-proof ceramic tile in the tower.
Embathe device with this fluidization and the high reduced ilmenite of rate of decay is carried out three sections adverse current normal pressures of dilute hydrochloric acid leach and first wash, Pulverization ratio is less than 0.3%, rich titanium material TiO
2Greater than 95%.Acidleach of the present invention and washing process all do not have hydrogen chloride gas leakage, good operational environment, convenience, equipment operation normal, leach containing mineral material 1 such as chromium, manganese, barium, iron～section, leaching and washing is same is suitable for.
Embodiment one
With the Flos Bombacis Malabarici concentrated ilmenite is raw material, and its percentage composition is TiO
246.43, ∑ Fe32.06, Fe
2+25.30, Mg5.95, CaO1.17, SiO
22.32, Al
2O
31.25, sreen analysis sees Table 1.This raw material in rotary kiln under 750 ℃ the temperature condition, oxidizing roasting 10 minutes, fuel is 7% for the coal gas of heating up water, tail gas oxygen level, Fe
2+19.20%, when roasting material is cooled to 85 ℃ in air, utilizes fluidization of the present invention to leach device and carry out three sections adverse current normal pressures leachings, it is 2 listed that its condition sees Table, leach product behind washing and filtering, calcination becomes rutile under 960 ℃ of conditions, and its product percentage composition is TiO
292.27, TFe2.78, MgO+CaO0.56, Al
2O
30.13, SiO22.15, the loss that fine powder causes is 0.17%, direct yield is 94.5%, the rutile of table 1 is listed in the screen analysis of rutile in.
With the Guangxi beach placer is raw material, and its percentage composition is: TiO
258.73, ∑ Fe26.35, Fe
2+6.24, Mg0.1, CaO0.28, SiO
21.02, Al
2O
31.25 sreen analysis is as shown in table 3.Oxidizing roasting under 900 ℃ condition makes Fe
2+Reach its roasting condition of 25.95%. and leaching condition with embodiment one, behind washing and filtering, be sintered into rutile under 960 ℃, its composition is TiO
292.27%, TFe2.78%, MgO+CaO0.56%, Al
2O
30.13%, SiO
22.15%, the loss that fine powder causes is that 0.17% direct yield is 94.50%, and the screening of rutile is torn open and listed table 3 in.
Table 1
| Sieve mesh | +60 | -60 +90 | -90 +110 | -110 +130 | -130 +150 | -150 +190 | -190 |
| Ilmenite | 4.5 | 28.51 | 9.5 | 20.7 | 9.6 | 16.0 | 17.0 |
| Rutile | 0.4 | 19.8 | 12.6 | 28.1 | 10.0 | 10.7 | 18.2 |
Table 2
| Job step | Strength of solution % | Extraction temperature ℃ | Apparent velocity cm/s | Extraction time (hour) |
| First section second section the 3rd section | 8.75 12.69 20.00 | 117 112 106 | 0.4～0.45 0.3～0.4 0.2～0.3 | 3 3 3 |
Table 3
| Sieve mesh | +40 | -40 +60 | -60 +80 | -80 +100 | -100 +140 | -140 +200 | -200 |
| Ilmenite | 1.84 | 31.91 | 49.85 | 12.35 | 3.16 | 0.81 | 0.07 |
| Rutile | 0.20 | 30.89 | 51.63 | 13.77 | 3.03 | 0.44 | 0.04 |
Acidleach and washing process all do not have hydrogen chloride gas to leak, good operational environment, and it is intact, easy to operate to leach device, works well.
Claims (7)
1. handle method and the device thereof that ilmenite is produced rich titanium material with dilute hydrochloric acid for one kind, it is characterized in that: adopt the low titanium placer of primary ilmenite or rate of decay, handle, cool off through oxidizing roasting, hydrochloric acid with 18～20% leaches and carries out the fluidization of multistage counter current normal pressure in the device and leach, wash, dry or be sintered into rich titanium material product following fluidization that groove forms with two fluidization column and two.
2. the method for the rich titanium material of production according to claim 1 is characterized in that: ∑ Fe28～37%, Fe in the content of the ferrotianium placer that primary ilmenite or rate of decay are low
2+22～32%, mineral granularity is 0.04～0.6 millimeter.
3. the method for the rich titanium material of production according to claim 1, it is characterized in that: raw material oxidizing roasting in rotary kiln or fluidizing furnace is handled, its temperature is that 425～875 ℃, the content of furnace exhaust gas oxygen are 5～20%, roasting 3～30 minutes, after making 5～35% ferrous oxidation become ferric iron, roasting material is cooled to 85 ℃ in air.
4. the method for the rich titanium material of production according to claim 1, it is characterized in that: the step that multistage counter current normal pressure fluidised form leaches is: use mother liquor that the final stage of batch of material leached as leach liquor, having formed every batch of material is repeatedly leached by the solution that free acid concentration increases, 2～4 times (promptly 2～4 sections) of general leaching, with three sections is example, the solution salt acid concentration of every section leaching is followed successively by: 5～10%, 10～18%, 18～20%, the voidage of fluidization bed is 0.61～0.74, extraction temperature is than low 2～5 ℃ of the solution boiling point under this state, liquid-solid ratio (V: be 2.8～4.0 W), carry out washing in the tower after the 3rd section leaching, total extraction time is 6～9 hours, and Pulverization ratio is less than 1%.
5. the device of the rich titanium material of production according to claim 1, it is characterized in that: two fluidization column are formed by connecting by two groups of pumps, two interchanger and pipe valve and two circulation grooves, switch by several valves, each tower all can be formed the same form two cover leaching systems with each groove, form alternately through tower, groove that multistage counter current leaches and washing, two cover system commissure operations, finish one by one leaching process again and again rhythmically.
6. the device of the rich titanium material of production according to claim 5, it is characterized in that: fluidization column mainly is made up of parts such as tower body, nozzle mouth, the awl end, overflow weir, guide ring, overflow weirs, tower body is that up big and down small garden tube, cone angle is 0～10 °, nozzle directly for bore on the tower body 4～12%, the cone angle at the awl end is 10～40 °, the overflow weir diameter is that tower body back cut diameter 1～4 beta body troclia is installed 0～3 guide ring, hoop apart from being 1/15～1/6 of tower body back cut diameter, tower is surrounded by general steel plate, and the tower liner is acidproof offset plate or acid-proof ceramic tile.
7. according to the method and the device thereof of claim 4,5, the rich titanium material of 6 described productions, it is characterized in that: same being suitable for of 1～4 section leaching, leaching and washing that contains mineral materials such as chromium, manganese, barium, iron.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN94111054A CN1041114C (en) | 1994-06-29 | 1994-06-29 | Method and equipment for producing titanium-rich material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN94111054A CN1041114C (en) | 1994-06-29 | 1994-06-29 | Method and equipment for producing titanium-rich material |
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| Publication Number | Publication Date |
|---|---|
| CN1114364A true CN1114364A (en) | 1996-01-03 |
| CN1041114C CN1041114C (en) | 1998-12-09 |
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ID=5034961
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|---|---|---|---|
| CN94111054A Expired - Fee Related CN1041114C (en) | 1994-06-29 | 1994-06-29 | Method and equipment for producing titanium-rich material |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1320141C (en) * | 2005-06-16 | 2007-06-06 | 昆明理工大学 | Method for preparing rutile type titanium-rich material from primary titanium-rich material |
| WO2011026434A1 (en) * | 2009-09-02 | 2011-03-10 | 沙立林 | Titaniumrich hydrochloric acid leaching residue,use thereof and preparation method of titanium dioxide |
| CN102765750A (en) * | 2012-05-19 | 2012-11-07 | 河南佰利联化学股份有限公司 | Preparation method of titanium-rich material |
| CN103352129A (en) * | 2013-06-17 | 2013-10-16 | 中国船舶重工集团公司第七二五研究所 | Method for improving quality of titanium concentrate |
| CN101723448B (en) * | 2009-12-29 | 2013-11-06 | 攀钢集团研究院有限公司 | Method for preparing titaniferous solution |
| CN103482696A (en) * | 2013-09-02 | 2014-01-01 | 攀钢集团攀枝花钢铁研究院有限公司 | Method and device for preparing titanium solution from fluidized acidolysis titanium-containing material |
| CN103910382A (en) * | 2014-04-01 | 2014-07-09 | 攀钢集团攀枝花钢铁研究院有限公司 | Method for preparing artificial rutile |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4119696A (en) * | 1977-11-14 | 1978-10-10 | Uop Inc. | Production of titanium metal values |
-
1994
- 1994-06-29 CN CN94111054A patent/CN1041114C/en not_active Expired - Fee Related
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1320141C (en) * | 2005-06-16 | 2007-06-06 | 昆明理工大学 | Method for preparing rutile type titanium-rich material from primary titanium-rich material |
| WO2011026434A1 (en) * | 2009-09-02 | 2011-03-10 | 沙立林 | Titaniumrich hydrochloric acid leaching residue,use thereof and preparation method of titanium dioxide |
| RU2518860C2 (en) * | 2009-09-02 | 2014-06-10 | ША Лилинь | Titanium-enriched ilmenite residue, its application and method of obtaining titanium pigment |
| US9206055B2 (en) | 2009-09-02 | 2015-12-08 | Lilin Sha | Titaniumrich hydrochloric acid leaching residue, use thereof and preparation method of titanium dioxide |
| CN101723448B (en) * | 2009-12-29 | 2013-11-06 | 攀钢集团研究院有限公司 | Method for preparing titaniferous solution |
| CN102765750A (en) * | 2012-05-19 | 2012-11-07 | 河南佰利联化学股份有限公司 | Preparation method of titanium-rich material |
| CN103352129A (en) * | 2013-06-17 | 2013-10-16 | 中国船舶重工集团公司第七二五研究所 | Method for improving quality of titanium concentrate |
| CN103482696A (en) * | 2013-09-02 | 2014-01-01 | 攀钢集团攀枝花钢铁研究院有限公司 | Method and device for preparing titanium solution from fluidized acidolysis titanium-containing material |
| CN103910382A (en) * | 2014-04-01 | 2014-07-09 | 攀钢集团攀枝花钢铁研究院有限公司 | Method for preparing artificial rutile |
| CN103910382B (en) * | 2014-04-01 | 2015-07-22 | 攀钢集团攀枝花钢铁研究院有限公司 | Method for preparing artificial rutile |
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