Preparation method of anhydrous yttrium chloride

A technology of yttrium chloride and ammonium chloride, applied in chemical instruments and methods, inorganic chemistry, rare earth metal chlorides, etc., can solve the problems that it is difficult to obtain pure anhydrous rare earth chloride, unfavorable for industrial production, unsuitable for industrial production, etc. , to achieve the effect of safe and effective production method, high yield of reaction product and easy operation

Active Publication Date: 2018-07-20
上海泰坦科技股份有限公司
View PDF10 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, the method for preparing anhydrous rare earth chloride can be prepared by tetrahydrofuran complex method through metal exchange reaction in THF solution to prepare anhydrous rare earth chloride, starting from the rare earth metal and reacting with mercuric chloride to prepare THF of anhydrous rare earth chloride Complexes, but the reaction involves toxic and harmful substances, which is not conducive to industrial production; the ammonium chloride sublimation method converts rare earth oxides into rare earth chlorides, but it is difficult to obtain high-purity anhydrous Rare earth chloride: Anhydrous rare earth chloride prepared by chlorination of rare earth oxides is prone to residual impurities and water-insoluble substances. The chlorination temperature requires high requirements and the process is complicated.
Yttrium chloride has strong water absorption and is prone to oxidation-reduction reactions to form yttrium oxychloride, which affects industrial applications
[0004] The new preparation method of anhydrous rare earth chlorides prepares anhydrous rare earth chlorides from rare earth oxides (Ding Zongbiao, Cheng Kejun, Chemical Journal, 1997, 55:1004-1008) discloses a method using trimethylchlorosilane as a scavenger The method of preparing anhydrous rare earth chloride by aqueous solution is carried out at room temperature and in THF under a dry nitrogen atmosphere. Both methanol and trimethylchlorosilane are excessive. The reaction is stopped after 15 hours, and a fine crystalline white solid is precipitated. Flow down and heat to reflux for 3 hours, remove volatile substances under reduced pressure, wash the product with dry n-pentane, and dry it in vacuum to obtain a white solid which is the target product. Although the method has mild conditions, the procedure is complicated and involves toxic and harmful reagents, so it is not suitable for industrial production.
CN107827140A discloses a method for preparing anhydrous rare earth chlorides. The heptahydrate rare earth chlorides are divided into three stages for fluidized dehydration, and the dehydration is carried out under a hydrogen chloride gas atmosphere. The dehydration method needs to undergo three times of fluidized dehydration, and strict temperature control is required. and wind speed, not suitable for industrial production

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of anhydrous yttrium chloride
  • Preparation method of anhydrous yttrium chloride

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] (1) pretreatment: yttrium oxide is pulverized through a 150-mesh sieve, and ammonium chloride is pulverized through a 150-mesh sieve;

[0055] (2) The ammonium chloride is tiled on the bottom of the reaction device, the tile thickness is 10cm, and the yttrium oxide is tiled on the ammonium chloride solid, and the mass ratio of the yttrium oxide to the ammonium chloride is 1:1.5;

[0056] (3) Gradient heating, the heating rate is 20°C / min, stop heating when the temperature reaches 240°C, constant temperature reaction, constant temperature reaction time is 4.5h;

[0057] (4) Feed dry hydrogen chloride gas after 2 hours from the start of the constant temperature reaction, and the ventilation rate is 0.7L / min;

[0058] (5) The reaction product obtained in step (4) is fluidized and dried under an argon atmosphere, and the inlet air temperature is 180° C., and fluidized and dried for 3 hours;

[0059] (6) Dry the product obtained in step (5) for 6 hours at a temperature of 2...

Embodiment 2

[0061] (1) pretreatment: yttrium oxide is pulverized through a 160 mesh sieve, and ammonium chloride is pulverized through a 140 mesh sieve;

[0062] (2) The ammonium chloride is tiled on the bottom of the reaction device, the tile thickness is 12cm, and the yttrium oxide is tiled on the ammonium chloride solid, and the mass ratio of the yttrium oxide to the ammonium chloride is 1:1.2;

[0063] (3) Gradient heating, the heating rate is 22 ° C / min, stop heating when the temperature reaches 250 ° C, constant temperature reaction, constant temperature reaction time is 5h;

[0064] (4) Pass into dry hydrogen chloride gas after the constant temperature reaction starts 3h, and the ventilation rate is 0.8L / min;

[0065] (5) The reaction product obtained in step (4) is fluidized and dried under a nitrogen atmosphere, and the inlet air temperature is 190° C., and fluidized and dried for 2 hours;

[0066] (6) Dry the product obtained in step (5) for 5 hours at a temperature of 230° C...

Embodiment 3

[0068] (1) pretreatment: yttrium oxide is pulverized through a 140 mesh sieve, and ammonium chloride is pulverized through a 130 mesh sieve;

[0069] (2) The ammonium chloride is tiled on the bottom of the reaction device, the tile thickness is 8cm, and the yttrium oxide is tiled on the ammonium chloride solid, and the mass ratio of the yttrium oxide to the ammonium chloride is 1:0.5;

[0070] (3) Gradient heating, the heating rate is 15°C / min, stop heating when the temperature reaches 220°C, constant temperature reaction, constant temperature reaction time is 4h;

[0071] (4) 1 hour after the start of the constant temperature reaction, dry hydrogen chloride gas is introduced, and the ventilation rate is 0.5L / min;

[0072] (5) The reaction product obtained in step (4) is fluidized and dried under a helium atmosphere, and the inlet air temperature is 160° C., and fluidized and dried for 1 hour;

[0073] (6) Dry the product obtained in step (5) for 4 hours at a temperature of 2...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
thicknessaaaaaaaaaa
Login to view more

Abstract

The invention provides a preparation method of anhydrous yttrium chloride. The preparation method includes the steps that yttrium oxide is used as a raw material to react with solid ammonium chloride,then dry hydrogen chloride gas is introduced, heating is performed until the reaction is complete, and a product is fluidized, dried, baked and dewatered to obtain anhydrous yttrium chloride. Throughcombined use of ammonium chloride and hydrogen chloride gas and combination with the proportion amount of the reactants, a synergistic effect of ammonium chloride and hydrogen chloride is achieved; the positional relationship of all the reactants is adjusted, so that the reaction is more complete, and the yield of the reaction product is high; fluidized drying and baking are sequentially performed, so that the occurrence of redox side reactions is prevented, the product purity is improved, the production method is safe and effective, and the product is pure.

Description

technical field [0001] The invention belongs to the field of rare earth material preparation, and mainly relates to a preparation method of anhydrous rare earth yttrium chloride. Background technique [0002] Rare earth elements are the general term for group IIIB yttrium and lanthanide elements in the periodic table. They are active metals with very similar properties. They have important biological activity and pharmacological effects. They can be used in two salt systems of chloride and fluoride. Anhydrous rare earth chlorides are basic reagents for the preparation of rare earth-containing organic compounds. [0003] At present, the method for preparing anhydrous rare earth chloride can be prepared by tetrahydrofuran complex method, through metal exchange reaction in THF solution to prepare anhydrous rare earth chloride, starting from the rare earth metal and reacting with mercuric chloride to prepare THF of anhydrous rare earth chloride Complexes, but the reaction invol...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C01F17/00
CPCC01F17/271C01P2006/80
Inventor 谢应波张庆张华徐肖冰罗桂云张维燕
Owner 上海泰坦科技股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products