CN101182022B - Preparation method of powder aluminum hydroxide - Google Patents

Preparation method of powder aluminum hydroxide Download PDF

Info

Publication number
CN101182022B
CN101182022B CN2007101161636A CN200710116163A CN101182022B CN 101182022 B CN101182022 B CN 101182022B CN 2007101161636 A CN2007101161636 A CN 2007101161636A CN 200710116163 A CN200710116163 A CN 200710116163A CN 101182022 B CN101182022 B CN 101182022B
Authority
CN
China
Prior art keywords
aluminium hydroxide
sodium aluminate
aluminate solution
hours
solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN2007101161636A
Other languages
Chinese (zh)
Other versions
CN101182022A (en
Inventor
张蕾
孙丽菊
栾福森
崔兰浩
苏爱玲
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aluminum Corp of China Ltd
Original Assignee
Aluminum Corp of China Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aluminum Corp of China Ltd filed Critical Aluminum Corp of China Ltd
Priority to CN2007101161636A priority Critical patent/CN101182022B/en
Publication of CN101182022A publication Critical patent/CN101182022A/en
Application granted granted Critical
Publication of CN101182022B publication Critical patent/CN101182022B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention relates to a preparation method of micro powder aluminum hydroxide, which is used for preparing the micro powder aluminum hydroxide. Sodium aluminate solution with the alumina content of 80-130g/l and liquor caustic ratio Alpha k equal to 1.4-1.6 is used as raw material and added with aluminum hydroxide seeds under the temperature of 40-65 DEG C. The method is characterized in that CO2 gas with mass concentration of 30-40 percent is fed into the solution for 2-6 hours after the solution is stirred for 0.5-2 hours, with the dissolution rate controlled at 85-95 percent, so as to obtain slurry which is then treated with conventional liquid-solid separation, washing and drying to finally obtain the micro powder aluminum hydroxide with d 50 of 0.6-4.5 Mum. The preparation method has simple technology, easy control, high dissolution rate, high yield and good crystallization of the products.

Description

The preparation method of aluminium hydroxide micropowder
Technical field
The present invention relates to a kind of preparation method of aluminium hydroxide micropowder, be used to produce aluminium hydroxide micropowder.
Background technology
Patent documentation about the preparation method of aluminium hydroxide micropowder is a lot, as: adopt kind of a point-score to prepare aluminium hydroxide micropowder, in sodium aluminate solution, add superfine aluminium hydroxide seed, stir to decompose and obtain aluminium hydroxide micropowder, equipment is simple, and quality product is easy to control, and rate of decomposition can reach 40~60%, lower, most of manufacturer adopts this method to produce.
As: adopt carbon decomposition aluminium hydroxide micropowder under the hypergravity situation, rate of decomposition can reach about 90%, but application apparatus equipment more complicated, equipment is difficult to maximize the industrial application difficulty.
As: adopt the acid-base neutralisation legal system to be equipped with aluminium hydroxide micropowder, obtain unformed aluminium hydroxide micropowder, product is unformed non-crystalline state.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of aluminium hydroxide micropowder, process is simple, control easily, rate of decomposition height, productive rate height, product advantages of good crystallization.
The preparation method of aluminium hydroxide micropowder of the present invention, with the sodium aluminate solution is raw material, alumina content is 80~130g/l in the sodium aluminate solution, solution caustic ratio α k=1.4~1.6, under 40~65 ℃ of temperature, add the aluminium hydroxide seed, it is characterized in that stirring 0.5~2 hour, feed mass concentration then and be 30~40% CO 2Gas was ventilated 2~6 hours, and rate of decomposition is controlled at 85~95%, and the slurries of gained are carried out liquid-solid separation, washing and the oven dry of routine, obtained aluminium hydroxide micropowder at last, its d 50Be 0.6~4.5 μ m.
Wherein: the common particle diameter of aluminium hydroxide seed is 0.6~0.8 μ m, can be sand-blast aluminium hydroxide seed for the aluminium hydroxide seed, add-on be in the sodium aluminate solution aluminium hydroxide quality 4~8%, or neutralisation aluminium hydroxide seed, add-on be in the sodium aluminate solution aluminium hydroxide quality 0.2~4.0%.
Whole production flow process of the present invention is divided into two operations, and plant branch process and carbon and divide process, with the sodium aluminate solution raw material, add superfine aluminium hydroxide seed, stir and decompose; After planting decomposition, feed CO 2The gas neutralization, rate of decomposition is controlled at below 95%, obtains aluminium hydroxide micropowder, d 50Be 0.6~4.5 μ m.Technological process is simple, and operating process is easy to control, rate of decomposition height, productive rate height, product advantages of good crystallization.
Description of drawings
Fig. 1, process flow diagram of the present invention.
Embodiment
The invention will be further described below in conjunction with embodiment.
Embodiment 1
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 100g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 10m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.815 μ m, its analytical results sees Table 1.
Embodiment 2
Soda-lime sintering process gained refined sodium aluminate solution, its composition are that aluminum oxide contains 80g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 8.5m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 95%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.809 μ m, its analytical results sees Table 1.
Embodiment 3
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 130g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 11.5m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 80%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.803 μ m, its analytical results sees Table 1.
Embodiment 4
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 100g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 20m 3/ hour m 3Solution, carbon divided 2 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 1.408 μ m, its analytical results sees Table 1.
Embodiment 5
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 80g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 4m 3/ hour m 3Solution, carbon divided 8 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.807 μ m, its analytical results sees Table 1.
Embodiment 6
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 130g/l, and α k1.44 under 60 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 4%, stirred 0.5 hour, feed concentration then and be 38% CO 2Gas, ventilation speed are 13m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 2.328 μ m, its analytical results sees Table 1.
Embodiment 7
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 100g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 4 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 10m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.801 μ m, its analytical results sees Table 1.
Embodiment 8
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 80g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 4%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 8m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 1.26 μ m, its analytical results sees Table 1.
Embodiment 9
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 130g/l, and α k1.44 under 55 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 16%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 13m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.659 μ m, its analytical results sees Table 1.
Embodiment 10
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 100g/l, and α k1.44 under 65 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 4%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 10m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 4.283 μ m, its analytical results sees Table 1.
Embodiment 11
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 80g/l, and α k1.44 under 45 ℃, adds d 50Be the sand-blast aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 8%, stirred 1.0 hours, feed concentration then and be 35% CO 2Gas, ventilation speed are 8m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.626 μ m, its analytical results sees Table 1.
Embodiment 12
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 130g/l, and α k1.45 under 55 ℃, adds d 50Be the neutralisation aluminium hydroxide seed of 0.4 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 1%, stirred 1.0 hours, feed concentration then and be 37% CO 2Gas, ventilation speed are 13m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.834 μ m, its analytical results sees Table 1.
Embodiment 13
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 100g/l, and α k1.5 under 55 ℃, adds d 50Be the neutralisation aluminium hydroxide seed of 0.2 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 4%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 10m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 0.609 μ m, its analytical results sees Table 1.
Embodiment 14
Soda-lime sintering process gained refined sodium aluminate solution, its composition are alumina content 80g/l, and α k1.44 under 65 ℃, adds d 50Be the neutralisation aluminium hydroxide seed of 0.6 μ m, quality be in the sodium aluminate solution aluminium hydroxide quality 0.2%, stirred 1.0 hours, feed concentration then and be 38% CO 2Gas, ventilation speed are 8m 3/ hour m 3Solution, carbon divided 4 hours, and rate of decomposition is 90%, and the slurries of gained carry out liquid-solid separation, washing and oven dry, the aluminium hydroxide micropowder that obtains, d 50Be 4.327 μ m, its analytical results sees Table 1.
(table 1 vides infra)
Table 1 product analysis result (weight percent)
Figure S2007101161636D00051

Claims (3)

1. the preparation method of an aluminium hydroxide micropowder, with the sodium aluminate solution is raw material, alumina content is 80~130g/l in the sodium aluminate solution, solution caustic ratio α k=1.4~1.6, under 40~65 ℃ of temperature, add the aluminium hydroxide seed, it is characterized in that stirring 0.5~2 hour, feed mass concentration then and be 30~40% CO 2Gas was ventilated 2~6 hours, and rate of decomposition is controlled at 85~95%, and the slurries of gained are carried out liquid-solid separation, washing and the oven dry of routine, obtained aluminium hydroxide micropowder at last, its d 50Be 0.6~4.5 μ m.
2. the preparation method of aluminium hydroxide micropowder according to claim 1 is characterized in that the aluminium hydroxide seed is a sand-blast aluminium hydroxide seed, add-on be in the sodium aluminate solution aluminium hydroxide quality 4~8%.
3. the preparation method of aluminium hydroxide micropowder according to claim 1 is characterized in that the aluminium hydroxide seed is a neutralisation aluminium hydroxide seed, add-on be in the sodium aluminate solution aluminium hydroxide quality 0.2~4.0%.
CN2007101161636A 2007-12-11 2007-12-11 Preparation method of powder aluminum hydroxide Active CN101182022B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2007101161636A CN101182022B (en) 2007-12-11 2007-12-11 Preparation method of powder aluminum hydroxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2007101161636A CN101182022B (en) 2007-12-11 2007-12-11 Preparation method of powder aluminum hydroxide

Publications (2)

Publication Number Publication Date
CN101182022A CN101182022A (en) 2008-05-21
CN101182022B true CN101182022B (en) 2010-11-10

Family

ID=39447466

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2007101161636A Active CN101182022B (en) 2007-12-11 2007-12-11 Preparation method of powder aluminum hydroxide

Country Status (1)

Country Link
CN (1) CN101182022B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011137481A1 (en) * 2010-05-03 2011-11-10 Bhp Billiton Worsley Alumina Pty Ltd Process for recovery of alumina using tricalcium aluminate
WO2011137480A1 (en) * 2010-05-03 2011-11-10 Bhp Billiton Worsley Alumina Pty Ltd Sequestration of carbon dioxide using tricalcium aluminate
CN102303881A (en) * 2011-08-18 2012-01-04 中国铝业股份有限公司 Preparation method of aluminum hydroxide for titanium white
CN112028095A (en) * 2020-08-12 2020-12-04 中铝山东有限公司 Superfine aluminum hydroxide seed crystal and preparation method thereof, submicron aluminum hydroxide and preparation method and application thereof
CN112960682B (en) * 2021-03-03 2022-10-11 杭州智华杰科技有限公司 Method for increasing regeneration times of chromatographic alumina
CN114873619B (en) * 2022-06-03 2024-02-13 中铝中州铝业有限公司 Preparation method of amorphous aluminum hydroxide
CN115231596A (en) * 2022-08-05 2022-10-25 洛阳中超新材料股份有限公司 Industrial preparation method of bayer stone
CN116239134A (en) * 2022-12-07 2023-06-09 雅安百图高新材料股份有限公司 Treatment method of aluminum oxide calcined powder for heat conduction field

Also Published As

Publication number Publication date
CN101182022A (en) 2008-05-21

Similar Documents

Publication Publication Date Title
CN101182022B (en) Preparation method of powder aluminum hydroxide
US20080022997A1 (en) Process and apparatus for the conversion of biomass
CN104291350B (en) A kind of technique of K-feldspar powder hydro-thermal alkaline process synthesis analcime
CN101020579A (en) Process of preparing high purity light calcium carbonate fine powder with carbide residue
CN102275957B (en) Process for producing high purity magnesium oxide with dolomite
CN108928834B (en) MCM-41 mesoporous molecular sieve, and preparation method and application thereof
CN104529562A (en) Method used for preparing potash magnesium sulphate fertilizer and potassium chloride fertilizer from carnallite
CN101886180A (en) Method for preparing high-activity zinc oxide from electrolytic zinc leaching slag and lead smelting granulated slag
CN106219586A (en) A kind of be raw material production nanometer grade calcium carbonate with carbide slag device and method
CN105969977A (en) Method for extracting tungsten from scheelite
CN105384669A (en) Preparation method of xanthate
CN110844928B (en) Method for preparing micro-nano aluminum oxide from aluminum alloy hydrolysate
CN108726518A (en) A kind of method that alkali activation method prepares active carbon with high specific surface area
CN102757072B (en) Process for preparing magnesium sulfate heptahydrate
CN104386752A (en) Method for preparing chromium sulfate basic by utilizing residual liquor obtained during menadione production
CN103112875B (en) Process for preparing agricultural potassium nitrate by utilizing potassium-enriched rock
CN105197957A (en) Synthetic method of zeolite 4A
CN106350870B (en) A kind for the treatment of and use method of sulfuric acid waste
CN105755297B (en) A kind of method that high pressure carbonization carries magnesium
CN1226276C (en) Extraction of natural capsaicine
CN109627183B (en) Preparation method of chloroacetaldehyde oxime
CN111704149A (en) Process for producing sodium bicarbonate
CN107500800B (en) Porous ceramic material containing copper tailings and preparation method thereof
CN108238609B (en) Preparation method of sodium octaborate tetrahydrate
CN104860344A (en) Preparation method of spherical strontium carbonate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant