CN1896005A - Container for producing aluminum hydroxide aggregate - Google Patents
Container for producing aluminum hydroxide aggregate Download PDFInfo
- Publication number
- CN1896005A CN1896005A CN 200610093599 CN200610093599A CN1896005A CN 1896005 A CN1896005 A CN 1896005A CN 200610093599 CN200610093599 CN 200610093599 CN 200610093599 A CN200610093599 A CN 200610093599A CN 1896005 A CN1896005 A CN 1896005A
- Authority
- CN
- China
- Prior art keywords
- container
- sodium aluminate
- aqueous solution
- aluminate aqueous
- aluminium
- 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.)
- Granted
Links
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
Aluminum hydroxide aggregated particles which have an average particle diameter of not less than 40 mu m, an average particle diameter as determined after pressing at 1,000 kg/cm<2> of not more than 35 mu m, and an L value of slurry obtained by mixing 20 ml of glycerol and 10 g of the aluminum hydroxide aggregated particles of not more than 69, are obtained by a process comprising the steps of: feeding a supersaturated aqueous sodium aluminate solution to a vessel, adding aluminum hydroxide seeds to the supersaturated aqueous sodium aluminate solution, stirring the seed-added solution in the vessel while continuously feeding an additional supersaturated aqueous sodium aluminate solution into the vessel to hydrolyze the supersaturated aqueous sodium aluminate solution, separating the aluminum hydroxide aggregated particles from the aqueous sodium aluminate solution, and continuously discharging the aqueous sodium aluminate solution out of the vessel.
Description
The application submitted on November 7th, 2002, and application number is 02149840.7, and name is called the dividing an application of application for a patent for invention of " aluminum hydroxide aggregate and method for making, used container and production process of aluminium hydroxide powder ".
Technical field
The present invention relates to a kind of method of aluminium-hydroxide powder of resin-filled composition of the transparency of to be improved that is used to produce, relate to aluminum hydroxide aggregate, its production method and used container thereof as its material therefor.
Background technology
Aluminium-hydroxide powder usually is used as the filler of resin such as unsaturated polyester resin in the production of artificial marble etc.When aluminium-hydroxide powder during as the filler of artificial marble etc., require powder to have excellent resin filling properties, do not damage the transparency of gained resin combination simultaneously.
As for the commercial run of producing aluminium hydroxide, known up to now method is included under the existence of seed crystal and makes the hydrolysis of supersaturation sodium aluminate aqueous solution.For example, JP 63-23131B discloses a kind of method, it comprises a plurality of containers is connected in series, the supersaturation sodium aluminate aqueous solution is sent into first container continuously, make the hydrolysis in the presence of seed crystal of supersaturation sodium aluminate aqueous solution, hydrolysis can be carried out and this solution is sent into second container and the 3rd container successively, obtain aluminium hydroxide.
But,, also can not obtain resin combination with enough transparencys even the aluminium hydroxide that obtains by aforesaid method is filled in the resin.
The purpose of this invention is to provide a kind of aluminum hydroxide aggregate, it can be used to produce aluminium-hydroxide powder suitably, this powder can obtain to present the resin combination of high transparent in being filled into resin etc. the time, a kind of method of producing described agglomerating particles is provided, a kind of its used container, and a kind of method of using described agglomerating particles to produce aluminium-hydroxide powder.
Description of drawings
Fig. 1 is the schematic section of expression according to a kind of embodiment of container of the present invention.
Fig. 2 is the schematic cross section of container shown in Figure 1.
Reference number among the figure is represented following meaning.
1 expression enrichment region, 2 expression settling sections, 3 expression containers, 4 expression baffle plates, 5 expression agitating vanes, 6 expression turning axles, 7 expression agitators, 8 expression swabbing pigs, 9 expression relief outlets, 10 expression impregnating material, 11 expression guide vanes
Summary of the invention
In order to address the above problem, the inventor has carried out extensive studies, has therefore finished the present invention.
Therefore, according to the present invention, provide aluminum hydroxide aggregate, its average particulate diameter is not less than 40 microns, 1, and 000kg/cm
2The average particulate diameter that the pressurization back is measured is not more than 35 microns, is not more than 69 by the L value of this aluminum hydroxide aggregate of 20ml glycerine and 10g being mixed the slurry that obtains.
According to the present invention, a kind of method of producing aluminum hydroxide aggregate also is provided, it may further comprise the steps:
(a) in a container, send into the supersaturation sodium aluminate aqueous solution,
(b) in this supersaturation sodium aluminate aqueous solution, add the aluminium hydroxide seed crystal, so that in described container, form the solution that adds seed crystal,
(c) stir the solution of the adding seed crystal in this container, in this container, send into the supersaturation sodium aluminate aqueous solution continuously simultaneously, come hydrolysis supersaturation sodium aluminate aqueous solution, obtaining aluminum hydroxide aggregate and sodium aluminate aqueous solution,
(d) this sodium hydroxide agglomerating particles is separated with sodium aluminate aqueous solution and
(e) sodium aluminate aqueous solution is discharged this container continuously.
According to the present invention, a kind of method of producing aluminium-hydroxide powder also is provided, it comprises the aluminum hydroxide aggregate fragmentation that is as above obtained.
According to the present invention, a kind of used container of aforesaid method of producing aluminum hydroxide aggregate also is provided, promptly a kind of container with the cavity that limits by leg and bottom, wherein, described container has:
Inlet in described wall bottom,
Two or more baffle plates that are installed on the described wall internal surface, make described baffle plate in cavity outstanding and along the internal surface of described wall promptly begin to extend to from the top, bottom apart from the bottom predetermined height and
An agitating vane that is positioned at cavity and the space below the predetermined height of baffle plate.
Embodiment
The average particulate diameter of aluminum hydroxide aggregate of the present invention (hereinafter referred to as " agglomerating particles ") is 40 microns or bigger, preferably 50 microns or bigger, and more preferably 60 microns or bigger, and 1,000kg/cm
2The average particulate diameter that following pressurization back is measured is not more than 35 microns.Each agglomerating particles is at least 2, preferably 8 or the more set of primary particle.For poly-admittedly particle, the average particulate diameter of measuring after pressurization is less than the average particulate diameter before pressurizeing, and the average particulate diameter difference before and after the pressurization is not less than 5 microns usually.The littler fact of average particulate diameter that the pressurization back is measured shows that a little less than the bounding force of agglomerating particles, and the easy fragmentation of described particle forms primary particle.Above-mentioned average particulate diameter can be measured with laser light scattering type size distribution metering facility.
In agglomerating particles of the present invention, by the slurry of 20ml glycerine and 10g agglomerating particles mixing acquisition is being not more than 69 by the L value in the laboratory characterization system of Commission International de l ' Eclairage explanation.Even their are broken also to be filled in the resin, the L value is higher than the resin combination that 69 agglomerating particles can not obtain having high transparent.The L value of agglomerating particles is the smaller the better, for example preferably is not more than 65, more preferably is not more than 63.
For example, the agglomerating particles of the present invention of characteristic shown in can obtaining above having by the method that may further comprise the steps: (a) in a container, send into the supersaturation sodium aluminate aqueous solution, (b) in this supersaturation sodium aluminate aqueous solution, add aluminium hydroxide seed crystal (hereinafter being abbreviated as " seed crystal "), so that in described container, form the solution that adds seed crystal, (c) be stirred in the solution of the adding seed crystal in this container, in this container, send into simultaneously other supersaturation sodium aluminate aqueous solution continuously, so that make the hydrolysis of supersaturation sodium aluminate aqueous solution, obtain agglomerating particles, (d) agglomerating particles is separated with sodium aluminate aqueous solution and (e) sodium aluminate aqueous solution is discharged this container continuously.
In step (a), send into the preferably effective Na of supersaturation sodium aluminate aqueous solution of described container
2O (causticity Na
2O) concentration is about 120-180g/l, Al
2O
3Concentration is about 120-180g/l, mol ratio (Na
2O/Al
2O
3) be about 1.2-1.8.Term " effective Na
2O " be meant by the total Na from sodium aluminate aqueous solution
2Deduct Na in the O content
2CO
3Content (is used Na
2O represents) value of gained.The supersaturation sodium aluminate aqueous solution for example can prepare by a kind of following method: promptly bauxitic clay is mixed with aqueous sodium hydroxide solution, the mixture of gained 120 ℃ or the heating of higher temperature, to extract the alumina composition in the bauxitic clay, make this mixture through separating then, for example use thickening material, filter the sodium aluminate aqueous solution that is obtained, and cooling filtrate; Perhaps by the preparation of a kind of following method: aluminium hydroxide is mixed with sodium hydroxide, and this mixture of heating makes this mixture through separating with the dissolved hydrogen aluminum oxide under 120 ℃ or higher temperature, for example filtration, and cool off the sodium aluminate solution of gained.The supersaturation sodium aluminate aqueous solution also can prepare by the following method: aluminium hydroxide is mixed with saturated sodium aluminate aqueous solution or unsaturated sodium aluminate aqueous solution after the hydrolysis, this mixture of heating is with the dissolved hydrogen aluminum oxide under 120 ℃ or higher temperature, filter then, and the sodium aluminate aqueous solution of cooling gained.
The seed crystal that adds in step (b) preferably average particulate diameter is about the 1-2 micron.With compare by grinding the seed crystal that thick aluminium hydroxide obtains, take not to grind by comprising that acid aluminium salt such as Tai-Ace S 150 are joined the seed crystal that the method that causes hydrolysis in the sodium aluminate aqueous solution prepares is preferred.The adding of seed crystal can shorten until the hydrolysis by the supersaturation sodium aluminate aqueous solution form aluminium hydroxide the induction time of process, and the particle diameter of the final aluminium-hydroxide powder that obtains of control.The amount of seed crystal can be as requested the particle diameter of aluminium-hydroxide powder determine suitably.
Stirring in step (c) for example can use mechanical stirrer to carry out.The circumferential speed of agitating vane is 0.1m/s or bigger preferably.This circumferential speed preferably is not more than 5m/s.
Separation in step (d) for example can be undertaken by the method for utilizing the difference in specific gravity between agglomerating particles and the sodium aluminate aqueous solution.By separating, agglomerating particles is usually to the motion of container bottom, and sodium aluminate aqueous solution moves to container top.Therefore, agglomerating particles is deposited on the container bottom, obtains to have the slurry of high solid concentration.The solid of this slurry (agglomerating particles) concentration is 600g/l or bigger preferably, 700g/l or bigger more preferably, and preferably be not more than 1000g/l, more preferably be not more than 900g/l.
In step (e), the sodium aluminate aqueous solution of discharging described container preferably has effective Na of about 120-180g/l
2O (causticity Na
2O) concentration, the Al of about 60-80g/l
2O
3Concentration, mol ratio (Na
2O/Al
2O
3) be about 2-3.5.
Above-mentioned steps (a) and (b), (c), (d) and (e) preferably in single container, carry out.A case representation of container used herein is in Fig. 1.Container 3 has inlet (not shown) and baffle plate 4 in its underpart.As shown in Figure 2, baffle plate 4 is outstanding from the inner circumferential surface of the wall of container 3, and provides many (for example 2-10) with predetermined space in the circumferential direction of container 3.Each of baffle plate 4 is promptly extended along the vertical direction (direction of turning axle) of container 3 from the top, bottom of container 3.By so provided baffle plate, improve stirring efficiency, and when stirring, form upwelling along the internal surface of the wall of container 3, Gu this slurry in the enrichment region 1 that the height by baffle plate 4 shows can be realized admixture substantially completely.Owing to, can obtain only to have weak bounding force and broken easily agglomerating particles with complete admixture hydrolysis sodium aluminate aqueous solution in enrichment region 1.The height that upwelling can reach is subjected to the effect of altitude of baffle plate 4.The height of baffle plate 4 increases many more, and the point that upwelling reaches is high more, and enrichment region 1 size increases.Usually the upper end of baffle plate 4 and the upper end of enrichment region 1 are similar on identical horizontal plane.With respect to the total height of container 3, baffle plate 4 it is highly preferred that 50% or bigger, more preferably 70% or bigger, most preferably 75% or bigger, and preferably be no more than 90%, more preferably be no more than 80%.Container 3 has agitator 7, and agitator 7 is made up of the turning axle 6 of agitating vane 5 and driven vane 5.For example, agitating vane 5 is a kind of agitating vanes and is provided in the enrichment region 1.Turning axle 6 is provided at the kernel of section of container 3 usually, perpendicular to the longitudinal axis (perpendicular to the longitudinal direction) of container.By the rotation of agitating vane 5, stir the slurry of enrichment region 1.At the end portion of turning axle 6, provide swabbing pig 8.By means of swabbing pig 8, can prevent that agglomerating particles is deposited to container 3 bottoms.
When the agglomerating particles that uses container 3 to produce, in container 3, form enrichment region and at the settling section 2 of enrichment region more than 1.With container 3 itself,, also can carry out concentrating of agglomerating particles except the separating of the hydrolysis of supersaturation sodium aluminate aqueous solution and agglomerating particles and sodium aluminate aqueous solution.
The internal surface and the bottom inside surface of the wall of the container 3 below the height that is not higher than baffle plate 4 preferably are lined with impregnating material 10.Used impregnating material for example can be metallic substance such as stainless steel, nickel, nickelalloy and titanium; Inorganic materials such as pottery; Organic materials such as fluoro-resin.Lining for example can be undertaken by flame plating or the method for toasting above-mentioned metallic substance or inorganic materials; Be 1 millimeter or bigger by welding or bonding thickness perhaps, preferably 2 millimeters or bigger, and preferably be not more than 10, the method that preferably is not more than the plate that 3 millimeters metallic substance makes is carried out; Perhaps undertaken by the method for bonding organic materials.With the impregnating material 10 of lining like this, can prevent the corrosion of internal surface of the wall of the container 3 that contacts with enrichment region 1, and can reduce aluminium-hydroxide powder painted of final acquisition.For example, when mixing the aluminium-hydroxide powder that 10g methyl methacrylate and 18g obtained, in the Lab characterization system that is shown by CommissionInternational de 1 ' Eclairage, the slurry of gained presents and is not more than 3, preferably is not more than 2 b value.More little b value shows painted low approximately.
Outstanding a plurality of (for example 2-8) guide vane 11 is provided on the inner circumferential surface of the wall of the container 3 that contacts with settling section 2.These guide vanes 11 play promotion and are separated from each other in enrichment region 1 by sodium aluminate aqueous solution and the agglomerating particles that hydrolysis forms, and improve the clarity of sodium aluminate aqueous solution.The quantity of guide vane 11 and size be restriction especially, only otherwise the clarifying effect of infringement liquid gets final product.Because agglomerating particles is not present in the settling section 2 substantially, the internal surface of the container 3 that contacts with settling section 2 does not need to serve as a contrast impregnating material 10.Sodium aluminate aqueous solution in settling section 2 is discharged to outside the container 3 from the relief outlet (not shown) that provides on container 3 tops.
State in the use in the container production aluminium-hydroxide powder process, at first, the supersaturation sodium aluminate aqueous solution of predetermined amount is sent into container 3, the feasible content that can stir this container.In container 3, add seed crystal, drive agitator 7, then the supersaturation sodium aluminate aqueous solution is sent in the container 3 continuously, and when stirring described content, hydrolysis supersaturation sodium aluminate aqueous solution.When continuing to send into the supersaturation sodium aluminate aqueous solution in container 3, liquid level rises and reaches the upper end of baffle plate 4, when continuing feeding again, reaches the relief outlet that provides on container 3 tops.In container 3,, obtain agglomerating particles and sodium aluminate aqueous solution owing to separate.Solid in enrichment region 1 (agglomerating particles) concentration increases gradually.On the other hand, sodium aluminate aqueous solution is discharged to outside the container 3 from the relief outlet that container 3 tops provide.After this, comprise the operation of sending into the sodium aluminate aqueous solution of supersaturation sodium aluminate aqueous solution and discharge equivalent from container 3 bottoms continuously.By this operation, the solids concn in enrichment region 1 increases with the amount of the supersaturation sodium aluminate aqueous solution of sending into continuously.In above-mentioned series operation, the temperature of container 3 remain on 45 ℃ or more than, preferably 50 ℃ or more than, and remain on 80 ℃ or following, preferably 60 ℃ or following.When the average particulate diameter of agglomerating particles reaches preset value (for example 80 microns), end sending into of supersaturation sodium aluminate aqueous solution, and reaction mixture is kept preset time under agitation condition.At this moment, the solids concn of enrichment region 1 is 600g/l or bigger preferably, 700g/l or bigger more preferably, and preferably be not more than 1,000g/l more preferably is not more than 900g/l.Send into the time of supersaturation sodium aluminate aqueous solution process, though its on the estimation particle diameter and change, preferably be not less than 500 hours, and preferably be not more than 1,000 hour.The relief outlet 9 that agglomerating particles in the enrichment region 1 is provided from container 3 bottoms is discharged, and by centrifugal, filtration etc. and liquid separation, washs as required then.
Then, the agglomerating particles fragmentation, obtain aluminium-hydroxide powder.Preferably by can destroy between a primary particle and another primary particle combine and the method for not destroying the primary particle itself that constitutes agglomerating particles is substantially carried out described fragmentation, and preferably for example carry out with muller, mixing machine, forcing machine etc.As required, this aluminium-hydroxide powder can be through super-dry or surface treatment.So the average particulate diameter of the aluminium-hydroxide powder that obtains preferably is not less than 10 microns, and preferably is not more than 35 microns, and can be used as the filler of resin such as unsaturated polyester resin, acrylic resin and Resins, epoxy suitably.
Embodiment 1
The preparation of agglomerating particles
Is temperature 58 ℃, Na
2O concentration is 125g/l, Al
2O
3Concentration be 125g/l and mol ratio be 1.65 supersaturation sodium aluminate aqueous solution with 100 weight parts/hour flow send in the structure container 3 as shown in Figure 1.The inwall of container 3 provides the height of each baffle plate to be equivalent to 75% baffle plate 4 of container 3 total heights.Have two up and down during the lower end of the last agitating vane of the blade 5 of agitating vane when the liquid level of supersaturation sodium aluminate aqueous solution reaches, begin the rotation of agitator 7, and the average particulate diameter that adds 150 weight parts is 1.1 microns a seed crystal.When revolving stirrer 7 makes that the circumferential speed of agitating vane 5 is 0.5m/s, continue to send into the supersaturation sodium aluminate aqueous solution to the enrichment region 1 of container 3, make hydrolysis in enrichment region, to carry out, and sodium aluminate aqueous solution is discharged from container 3 upper ends.The Na of the sodium aluminate aqueous solution of being discharged
2O concentration is 125g/l, Al
2O
3Concentration is that 65g/l and mol ratio are 3.2.When the average particulate diameter of the agglomerating particles in the enrichment region 1 reaches 80 microns, end to send into the supersaturation sodium aluminate aqueous solution, and reaction system is remained under this state.Solids concn when ending feeding in the enrichment region 1 is 800g/l.After maintenance, content is extracted out from the relief outlet 9 of container 3, use centrifuge separator to make described content through solid-liquid separation, the solid of gained is through washing to obtain agglomerating particles.
The evaluation of agglomerating particles
Measure the L value that agglomerating particles that 10g is obtained above and 20ml glycerine mix the slurry of acquisition with color difference meter (Nippon Denshoku Kogyo K.K. make trade(brand)name A-300 type).The result of gained is illustrated in the table 1.Individually, the above-mentioned agglomerating particles of 5g is placed in the circular die of 20 millimeters of diameters and 000kg/cm 1
2Down pressurization 1 minute of pressure, the disk of gained is broken with hand and roller rod, measures the average particulate diameter of gained powder then.The result of gained is illustrated in the table 2.Term in the table 2 " velocity of variation " is illustrated in average particulate diameter the reducing of observing the pressurization back with respect to the average particulate diameter before pressurizeing.
The preparation of aluminium-hydroxide powder and evaluation
Use the above agglomerating particles that obtains of mixing machine fragmentation, dry then to obtain aluminium-hydroxide powder.In unsaturated polyester resin, fill this aluminium-hydroxide powder and obtain the excellent artificial marble of the transparency.
The comparative example 1
In first container of the equipment that comprises 8 containers that are connected in series (each container is equipped with agitator) with 100 weight parts/hour flow to send into temperature continuously be 58 ℃, Na
2O concentration is 125g/l, Al
2O
3Concentration is that 121g/l and mol ratio are 1.7 supersaturation sodium aluminate aqueous solution.In this container, make a part of sodium aluminate aqueous solution hydrolysis to obtain (aluminium hydroxide) agglomerating particles.The sodium aluminate aqueous solution that contains agglomerating particles transferred in second container hydrolysis is proceeded.Make the hydrolysis in the 3rd to the 8th container successively of this sodium aluminate aqueous solution, to obtain agglomerating particles.The mol ratio of the sodium aluminate aqueous solution of discharging from the 8th container is 3.3.The agglomerating particles that is obtained is estimated under the condition identical with " evaluation of agglomerating particles " described in the embodiment 1.The result who is obtained is illustrated in table 1 and 2.
Table 1
The L value | |
Embodiment 1 | 63 |
The comparative example 1 | 70 |
Table 2
Average particulate diameter (μ m) | Velocity of variation (%) | ||
Before the pressurization | After the pressurization | ||
Embodiment 1 | 68 | 30 | 55.9 |
The comparative example 1 | 56 | 44 | 21.4 |
The agglomerating particles of above acquisition use with " preparation of aluminium-hydroxide powder and the evaluation " described in the embodiment in identical method handle.So the artificial marble that obtains does not have enough transparencys.
Embodiment 2
The preparation of aluminium-hydroxide powder
By repeating the process acquisition aluminium-hydroxide powder identical with embodiment 1, be lined with thick 2 millimeters SUS 304 stainless steel plates that are welded on the container inner wall container but be to use as impregnating material, the upper end of welding scope from the container bottom to the baffle plate of stainless steel plate, and the average particulate diameter of the agglomerating particles in enrichment region 1 is ended sending into of supersaturation sodium aluminate aqueous solution when reaching 40 microns.
The evaluation of aluminium-hydroxide powder
Measure by mixing the b value of the slurry that powder that 18g obtains above and 10g methyl methacrylate obtain with color difference meter (making trade(brand)name Z-1001DP by Nippon Denshoku Kogyo K.K.).So the result who obtains is illustrated in the table 3.
Embodiment 3
Repeat the process identical and prepared aluminium-hydroxide powder, but do not add stainless steel lining for described container with " preparation of aluminium-hydroxide powder " described in the embodiment 2.Under the condition identical, estimate the aluminium-hydroxide powder that so obtains with " evaluation of aluminium-hydroxide powder " described in the embodiment 2.Gained is the result be illustrated in the table 3.
Table 3
Average particulate diameter (micron) | The b value | |
Embodiment 2 | 29 | 1.5 |
Embodiment 3 | 27 | 3.3 |
According to aluminum hydroxide aggregate of the present invention and production method thereof, obtaining can provide the resin combination with high transparent as the aluminum hydroxide aggregate of producing the material that aluminium-hydroxide powder uses again when described aluminium-hydroxide powder is filled in the resin.Method according to production aluminium-hydroxide powder of the present invention is a kind of method of using above-mentioned aluminum hydroxide aggregate, according to this method, can easily obtain aluminium-hydroxide powder.In addition, use is produced aluminum hydroxide aggregate according to the method that container of the present invention can be easy.
Claims (2)
1. a container has the cavity that is limited by leg and bottom, and wherein, described container has:
Inlet in described wall bottom,
Two or more baffle plates that are installed on the described wall internal surface, make described baffle plate towards described cavity outstanding and promptly begin from the bottom along the internal surface of described wall extend in vertical direction on the predetermined height in bottom and
Be positioned at described cavity and be positioned at the agitating vane in the following space of the predetermined height of described baffle plate.
2. according to the container of claim 1, wherein, the internal surface of the internal surface of described bottom and the wall below the height of described baffle plate is lined with impregnating material.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP342359/2001 | 2001-11-07 | ||
JP2001342358A JP4097418B2 (en) | 2001-11-07 | 2001-11-07 | Method for producing aluminum hydroxide aggregate, method for producing aluminum hydroxide powder using the same, and precipitation tank |
JP342358/2001 | 2001-11-07 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB021498407A Division CN1301907C (en) | 2001-11-07 | 2002-11-07 | Agglomerate aluminium hgdroxide grain and its production process and container and the production process of aluminium hydroxide powder |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1896005A true CN1896005A (en) | 2007-01-17 |
CN100478060C CN100478060C (en) | 2009-04-15 |
Family
ID=19156233
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2006100935993A Expired - Fee Related CN100478060C (en) | 2001-11-07 | 2002-11-07 | Container for producing aluminum hydroxide aggregate |
CN 200710002162 Pending CN100999622A (en) | 2001-11-07 | 2002-11-07 | Aluminum hydroxide aggregate |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 200710002162 Pending CN100999622A (en) | 2001-11-07 | 2002-11-07 | Aluminum hydroxide aggregate |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP4097418B2 (en) |
CN (2) | CN100478060C (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102172487A (en) * | 2011-01-26 | 2011-09-07 | 浙江港龙新材料有限公司 | Nano material dispersing device for spray painting and method for preparing ink absorption layer paint by using same |
CN102527276A (en) * | 2010-12-07 | 2012-07-04 | 沈阳铝镁设计研究院有限公司 | Upper-layer paddle for high-performance agitating tank |
CN102527275A (en) * | 2010-12-07 | 2012-07-04 | 沈阳铝镁设计研究院有限公司 | Agitating device of high-performance agitating tank |
CN102921365A (en) * | 2011-08-08 | 2013-02-13 | 四川西陇化工有限公司 | Enamel flat-bottom concentration reaction vessel |
CN102989379A (en) * | 2011-09-09 | 2013-03-27 | 曲靖师范学院 | Gas-solid phase reactor |
CN103657570A (en) * | 2012-09-25 | 2014-03-26 | 昆山尚达智机械有限公司 | Reaction kettle convenient to clean |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4518465B2 (en) * | 2003-07-07 | 2010-08-04 | 月島機械株式会社 | Crystallization method and apparatus |
JP6163457B2 (en) * | 2014-06-12 | 2017-07-12 | 日軽産業株式会社 | Waste liquid treatment tank and waste liquid treatment method for waste liquid containing sodium aluminate |
CN109310977A (en) * | 2016-06-14 | 2019-02-05 | 住友金属矿山株式会社 | Chemical reaction equipment and used chemical reaction equipment particle manufacturing method |
CN112546946B (en) * | 2020-12-08 | 2021-08-13 | 山东瑞尚机械有限公司 | Aluminum oxide seed precipitation decomposer |
-
2001
- 2001-11-07 JP JP2001342358A patent/JP4097418B2/en not_active Expired - Fee Related
-
2002
- 2002-11-07 CN CNB2006100935993A patent/CN100478060C/en not_active Expired - Fee Related
- 2002-11-07 CN CN 200710002162 patent/CN100999622A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102527276A (en) * | 2010-12-07 | 2012-07-04 | 沈阳铝镁设计研究院有限公司 | Upper-layer paddle for high-performance agitating tank |
CN102527275A (en) * | 2010-12-07 | 2012-07-04 | 沈阳铝镁设计研究院有限公司 | Agitating device of high-performance agitating tank |
CN102172487A (en) * | 2011-01-26 | 2011-09-07 | 浙江港龙新材料有限公司 | Nano material dispersing device for spray painting and method for preparing ink absorption layer paint by using same |
CN102921365A (en) * | 2011-08-08 | 2013-02-13 | 四川西陇化工有限公司 | Enamel flat-bottom concentration reaction vessel |
CN102989379A (en) * | 2011-09-09 | 2013-03-27 | 曲靖师范学院 | Gas-solid phase reactor |
CN102989379B (en) * | 2011-09-09 | 2014-07-23 | 曲靖师范学院 | Gas-solid phase reactor |
CN103657570A (en) * | 2012-09-25 | 2014-03-26 | 昆山尚达智机械有限公司 | Reaction kettle convenient to clean |
Also Published As
Publication number | Publication date |
---|---|
JP4097418B2 (en) | 2008-06-11 |
CN100999622A (en) | 2007-07-18 |
CN100478060C (en) | 2009-04-15 |
JP2003146653A (en) | 2003-05-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1301907C (en) | Agglomerate aluminium hgdroxide grain and its production process and container and the production process of aluminium hydroxide powder | |
CN100434182C (en) | Continuous colloid mixer and its application | |
CN1896005A (en) | Container for producing aluminum hydroxide aggregate | |
WO2011070218A1 (en) | Method and equipment for separating solids from slurry and use of the method and/or equipment | |
CN101972624A (en) | Combined stirred tank reactor | |
CN1990508A (en) | Methods for preparing alkali cellulose and cellulose ether | |
CN102836656A (en) | Horizontal stirring apparatus | |
CN212578876U (en) | Aerated concrete pouring agitating unit | |
CN211303055U (en) | Special forced turbulence double-acting reactor for molybdenum disulfide production | |
CN110237578B (en) | Can handle concentrated machine of high concentration ore pulp | |
CN202212139U (en) | Toothpaste powder mixer | |
CN102765728A (en) | Precipitation reactor for producing highly dispersed silicon dioxide | |
CN202826052U (en) | Mixing device for solid concrete admixture | |
CN1265045A (en) | Process for selection of particles of preselected size from particulate pharmaceutical product | |
CN105964213A (en) | Fertilizer reaction device | |
CN207342689U (en) | A kind of reaction kettle with even distributor | |
CN214262309U (en) | Device for removing large particles of micro powder | |
CN205495579U (en) | Reation kettle for chemical industry with solid reducing mechanism | |
CN220110913U (en) | Liquid coating stirring device | |
CN217418636U (en) | Dosing treatment mixing device for biodiesel low-saponification-value raw oil | |
CN217450074U (en) | Feeding and throwing device of double-body cyclopentadiene cracking kettle | |
CN220633899U (en) | Raw material mixing device for suspending agent production | |
CN220835097U (en) | Stirrer for lithium battery production | |
CN220696445U (en) | Multistage stirring piece for solid-liquid mixing system | |
CN218452076U (en) | Raw material mixing equipment for producing potash fertilizer |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090415 Termination date: 20201107 |
|
CF01 | Termination of patent right due to non-payment of annual fee |