CN102189007A - Alumina coating slurry and preparation method thereof - Google Patents
Alumina coating slurry and preparation method thereof Download PDFInfo
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- CN102189007A CN102189007A CN2010101162772A CN201010116277A CN102189007A CN 102189007 A CN102189007 A CN 102189007A CN 2010101162772 A CN2010101162772 A CN 2010101162772A CN 201010116277 A CN201010116277 A CN 201010116277A CN 102189007 A CN102189007 A CN 102189007A
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- slurry
- alumina
- agent
- alumina slurry
- weight percentage
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title claims abstract description 92
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 239000006255 coating slurry Substances 0.000 title description 2
- 239000002002 slurry Substances 0.000 claims abstract description 84
- 238000000576 coating method Methods 0.000 claims abstract description 45
- 239000011248 coating agent Substances 0.000 claims abstract description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000005187 foaming Methods 0.000 claims abstract description 20
- 239000002245 particle Substances 0.000 claims abstract description 17
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 14
- 230000003750 conditioning effect Effects 0.000 claims abstract description 14
- 239000000084 colloidal system Substances 0.000 claims abstract description 11
- 238000000227 grinding Methods 0.000 claims abstract description 6
- 238000003756 stirring Methods 0.000 claims abstract description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 21
- 239000004411 aluminium Substances 0.000 claims description 21
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 21
- 239000004604 Blowing Agent Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 15
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- -1 magnesium aluminate Chemical class 0.000 claims description 7
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 235000012241 calcium silicate Nutrition 0.000 claims description 5
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 claims description 5
- ICAKDTKJOYSXGC-UHFFFAOYSA-K lanthanum(iii) chloride Chemical compound Cl[La](Cl)Cl ICAKDTKJOYSXGC-UHFFFAOYSA-K 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 229920000136 polysorbate Polymers 0.000 claims description 5
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 claims description 4
- NWXHSRDXUJENGJ-UHFFFAOYSA-N calcium;magnesium;dioxido(oxo)silane Chemical compound [Mg+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O NWXHSRDXUJENGJ-UHFFFAOYSA-N 0.000 claims description 4
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052637 diopside Inorganic materials 0.000 claims description 4
- 238000004945 emulsification Methods 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- 239000010451 perlite Substances 0.000 claims description 4
- 235000019362 perlite Nutrition 0.000 claims description 4
- 239000010456 wollastonite Substances 0.000 claims description 4
- 229910052882 wollastonite Inorganic materials 0.000 claims description 4
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 claims description 3
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 claims description 3
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 3
- 239000001119 stannous chloride Substances 0.000 claims description 3
- 235000011150 stannous chloride Nutrition 0.000 claims description 3
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 2
- 239000001110 calcium chloride Substances 0.000 claims description 2
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 2
- 239000008367 deionised water Substances 0.000 claims description 2
- 229910021641 deionized water Inorganic materials 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims description 2
- 235000001055 magnesium Nutrition 0.000 claims description 2
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000391 magnesium silicate Substances 0.000 claims description 2
- 235000019792 magnesium silicate Nutrition 0.000 claims description 2
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 239000006260 foam Substances 0.000 abstract description 14
- 239000002131 composite material Substances 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000004088 foaming agent Substances 0.000 abstract 2
- 230000001804 emulsifying effect Effects 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 description 15
- 235000019580 granularity Nutrition 0.000 description 13
- 230000000694 effects Effects 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 6
- 229910052878 cordierite Inorganic materials 0.000 description 5
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 229910000510 noble metal Inorganic materials 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000009828 non-uniform distribution Methods 0.000 description 3
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- 241000264877 Hippospongia communis Species 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000010433 feldspar Substances 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 206010013786 Dry skin Diseases 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007613 slurry method Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
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- Catalysts (AREA)
Abstract
The invention relates to foam alumina slurry and a preparation method thereof, which mainly solve the problems that production efficiency is low and the prepared coating has low uniformity and firmness because alumina slurry has a large particle size and low uniformity and stability, is easy to precipitate and greatly changes when stored for a long time in the prior art. The foam alumina slurry comprises water, alumina sol, alumina, a coating property auxiliary agent, an anionic-cationic conditioning agent and a foaming agent. The preparation method comprises the following steps of: dissolving the alumina sol, the alumina, the coating property auxiliary agent and the anionic-cationic conditioning agent in the water with stirring, and fully mixing to obtain slurry I; foaming a certain amount of foaming agent and water by using a foaming machine, and adding foam into the slurry I; and quickly emulsifying and grinding the slurry added with the foam in a colloid mill. Through the technical scheme, the problems are well solved, and the invention can be used for preparing the alumina slurry in the process of producing a layered composite carrier.
Description
Technical field
The present invention relates to a kind of foamed alumina slurry and preparation method thereof.
Background technology
Noble metal is widely used in chemical industry, oil refining and vehicle exhaust processing as the loaded catalyst of active component at present.Active component non-uniform Distribution in carrier can reduce the consumption of noble metal, improves the utilization rate of noble metal; Simultaneously, the catalyst of non-uniform Distribution also showed than the better activity of equally distributed catalyst, selectivity and life-span in many reactions.Often reach the effect of non-uniform Distribution in early days, but often be difficult to control the distribution of catalyst by control to dipping.This just need provide a kind of special carrier, and this carrier is made up of inert core and coating, has only coating absorption metal and coating layer thickness controlled, Here it is lamellar composite carrier.Just made thickness and the controlled heterogeneity catalyst of distribution flooding catalyst on this carrier, ZL02100598.2 has reported cleaning catalyst for tail gases of automobiles as patent.This invention cleaning catalyst for tail gases of automobiles is first carrier with the cordierite honeycomb ceramic matrix, is second carrier with aluminum oxide coating layer slurries (salic, noble metal).By with first carrier impregnation in the coating slurries, disposable spray finishing is made catalyst.In ethylbenzene catalytic dehydrogenation～H 2 selective oxidation process, patent US6177381 and CN1479649A have reported lamellar composite carrier for another example.Carrier has for example coating gama-alumina for example of Alpha-alumina and an inorganic oxide of a kernel.And for example patent US6858769 and CN1705510A have reported that a kind of is the H 2 selective oxidation catalyst of carrier with the lithium aluminate.This catalyst is a kernel with the cordierite, is coating with the lithium aluminate.
The common feature of above-mentioned catalyst is to use an inert material on the one hand, is the kernel of carrier as ceramic honey comb, cordierite, α～aluminium oxide, and the coating material that applies one deck bigger serface on the other hand on carrier is to enlarge the carrier effective surface area.But the figure layer carrier rate of wear of prior art for preparing is bigger, strength of coating and coating and carrier to combine firmness relatively poor, coating is easy to wear or come off, thereby influences catalyst performance, the long period that has limited catalyst uses.Influence factor during the preparation coating is a lot, but slurry is undoubtedly one of crucial influence factor.Patent CN101491776A provides a kind of prescription and preparation method who prepares coating paste, and this slurry is made up of at the aluminium colloidal sol below 10 microns, activated alumina, organic adhesive, inorganic adhesive, surfactant, pH conditioning agent particle mean size.The preparation method is dissolved in aluminium colloidal sol, organic adhesive, surfactant, pH conditioning agent in the water, under 500～5000 rev/mins high-speed stirred, mix, then add inorganic binder, active oxidation aluminium powder, high speed dispersion 10～180 minutes, the gained alumina slurry ground 10 minutes～10 hours in ball mill, sand mill, ball mill or colloid mill again, made alumina coats pulp.The slurry that makes has improved the stability of coating to a certain extent, has reduced rate of wear, but this method prepares pulp preparation process complexity, and the cycle is long; The slurry that is worth disperses to make fully that inadequately the slurry granularity is bigger; Slurry is stable poor, places for a long time that granularity changes greatly even generation precipitates, and in addition, with the coated carrier that this slurry makes, rate of wear is bigger than normal, and the firmness of coating is also relatively poor.Need improve formula of size and preparation method, obtain when enhancing productivity one scattered, the slurry of the little and good stability of granularity, thus improve the firmness of the coating of preparation, reduce the rate of wear of coating.
Summary of the invention
One of technical problem to be solved by this invention is that the slurry that exists in the prior art disperses problem inhomogeneous, poor stability, a kind of new foamed alumina slurry is provided, that this foamed slurry has is scattered, granularity is little, good stability, the coating that makes in conjunction with firmly, advantage that rate of wear is low.Two of technical problem to be solved by this invention provides preparation method a kind of and one of technical solution problem corresponding slurry.
In order to solve the problems of the technologies described above, the technical solution used in the present invention is as follows: a kind of foamed alumina slurry comprises following component by weight percentage:
A) 1～25% aluminium colloidal sol;
B) 5～50% aluminium oxide;
C) 0.1～10% blowing agent;
D) 0.01～1% zwitterion conditioning agent;
E) 0.1～5.0% coating performance auxiliary agent;
F) 10～90% water;
Wherein: the zwitterion conditioning agent is selected from least a in aluminium oxide, aluminum nitrate, lanthanum chloride, stannic chloride, cerous nitrate, magnesium chloride, stannous chloride, lanthanum nitrate, calcium chloride, hydrochloric acid, nitric acid or the ammoniacal liquor; The coating performance auxiliary agent is selected from least a in wollastonite, diopside, perlite, magnesium silicate, calcium silicates, magnesium aluminate, zirconium aluminate or the kaolin; Blowing agent is selected from least two kinds in PVA, HPC, MC, EMC, tween, sapn or the polyethylene glycol.
In the technique scheme, aluminium colloidal sol consumption preferable range by weight percentage is 5～25%, and more preferably scope is 5～20%; The aluminium oxide preferred version is γ-Al
2O
3, δ-Al
2O
3Or θ-Al
2O
3In at least a and granularity be controlled at below 10 microns, consumption is 10%～40% by weight percentage; The blowing agent preferred version is by at least a material I that is selected among PVA, HPC or the EMC, mix with at least a material II that is selected from tween, sapn, the polyethylene glycol, the part by weight of material I and material II is 1: 5～10: 1, and blowing agent consumption by weight percentage is 0.5～10%; The zwitterion conditioning agent is at least a or several in aluminium oxide, lanthanum chloride, stannic chloride, cerous nitrate or the magnesium chloride, and consumption is 0.05～1% by weight percentage; The coating performance auxiliary agent is at least a in wollastonite, diopside, perlite, calcium silicates or the magnesium aluminate, and consumption is 0.5～5% by weight percentage; Water is deionized water, and consumption is 40～70% by weight percentage.
For two of technical solution problem, technical scheme provided by the invention is as follows: a kind of preparation method who is used for the foamed alumina slurry of one of technical solution problem may further comprise the steps:
1) pulverize: by breaking method control aluminium oxide and auxiliary agent particle diameter below 10 microns;
2) mix: with aluminium colloidal sol, aluminium oxide, zwitterion conditioning agent, the coating performance auxiliary agent of aequum, under condition of stirring, be dissolved in the water and fully and mix, obtain slurry I;
3) foaming; After the blowing agent process foaming machine foaming with aequum, join among the slurry I and mix;
4) emulsification and grinding: with alumina slurry emulsification in colloid mill, the grinding of gained, make the particle mean size of alumina coats pulp, make foamed alumina slurry II below 5 microns;
Aluminium oxide and performance auxiliary agent are pulverized by comminution by gas stream; With aluminium colloidal sol, aluminium oxide, zwitterion conditioning agent, the coating performance auxiliary agent of aequum, under 2000 rev/mins stirring, be dissolved in the water and mixed 0.5～1 hour, obtain slurry I; Blowing agent and water join in the blowing agent and foam, and obtain the foam of requirement and join to mix among the slurry I 10～30 minutes, join then and carry out colloidal grinding in the colloid mill, and the colloid mill time was controlled at 0.5～1 hour, obtained the slurry that needs.
One aspect of the present invention has been optimized the alumina slurry prescription, the zwitterion conditioning agent that adds provides enough electrolyte and must acid or alkali environment on the one hand for the system of slurry is stable, in suspension system, blowing agent and particle can reach high dispersive and stable effect by the repulsive force between the surperficial adsorption charge, and the auxiliary element that also can be used as coated carrier or catalyst on the other hand is through playing the effect of stable coatings with the effect of coating oxidation aluminium after the high-temperature roasting; The coating performance auxiliary agent, thus mainly be that the stable composition that utilizes itself and aluminium oxide at high temperature to generate helps coating; On the other hand, blowing agent is by the foaming of blowing agent, it is more abundant to make that blowing agent disperses, and the foam quality that obtains is good, bubble diameter is little, the foam yardstick is even, after joining among the alumina slurry like this, a large amount of vesicle foams have uniformly stoped the gathering of alumina particle, and granularity increases because assemble can either to prevent aluminium oxide particles, can make that again dispersion of nano-particles is more even, the blowing agent of high dispersive can be at shell of the peripheral formation of particle simultaneously, increased intergranular distance, reduced the effect of Van der Waals force, thereby the electro kinetic potential that has increased suspension makes dispersion reach stable state.In addition, by the dispersion efficiency of blowing agent foaming raising blowing agent, production efficiency also can improve greatly.The slurry that makes is when spraying, because granularity is little, and good dispersion, atomizing effect improves, and can increase the compactness of coating, thereby improves the firmness of coating, the rate of wear of reduction figure layer.The foamed alumina slurry that uses the inventive method to make, slurry granularity d
50All less than 4um, place 15 days disposed slurry granularities and still maintain about 4um, in the time of 30 days, the slurry granularity is still about 5 microns; Making coating 1000 with this slurry changes rate of wear less than 0.15%, and loss late can be controlled at below 0.3% in ultrasonic 30 minutes.It is little to illustrate that slurry that the present invention makes has granularity, and it is low that the advantage of good stability, the coating that makes with this slurry have a rate of wear, and the advantage that firmness is high has obtained better technical effect.
The present invention is further elaborated below by embodiment.
The specific embodiment
[embodiment 1]
With 300 gram water, the aluminium colloidal sol of 1200 grams 10%, 40 gram concentration are 20% lanthanum chloride solution, 800 gram gamma oxidation aluminium powders, 8 gram calcium silicates, add successively and mix 60 minutes in the mixer, get 10 gram HPC, 5 gram sapns add water 300 gram and place the foaming machine foaming to make foam, join in the above-mentioned slurry, mixed 30 minutes, add in the colloid mill and ground 40 minutes, make the slurry A that needs.
[embodiment 2]
With 500 gram water, the aluminium colloidal sol of 1000 grams 20%, 70 gram concentration are 50% tin chloride solution, 1200 gram δ-alumina powders, 50 gram magnesium aluminates, 60 gram diopsides add successively and mix 30 minutes in the mixer, get 50 gram PVA, 10 gram tweens add water 600 gram and place the foaming machine foaming to make foam, join in the above-mentioned slurry, mixed 10 minutes, add in the colloid mill and ground 50 minutes, make the slurry B that needs.
[embodiment 3]
With 300 gram water, the aluminium colloidal sol of 2000 grams 40%, 40 gram concentration are 10% magnesium chloride solution, and 40 gram concentration are 20% stannous chloride solution, 300 gram 0-alumina powders, 30 gram wollastonites add successively and mix 40 minutes in the mixer, get 50 gram HPMC, 10 gram polyethylene glycol add water 500 gram and place the foaming machine foaming to make foam, join in the above-mentioned slurry, mixed 20 minutes, add in the colloid mill and ground 30 minutes, make the slurry C that needs.
[embodiment 4]
With 800 gram water, the aluminium colloidal sol of 1000 grams 40%, 50 grams, 10% aluminum nitrate solution, 50 grams, 10% cerous nitrate, 300 gram 0-alumina powders, 300 gram gamma oxidation aluminium powders, 20 gram kyanites once add and mix 50 minutes in the mixer, get 30 gram EMC, molten Sha Mujia water 700 grams of 4 gram pools place the foaming machine foaming to make foam, join to mix in the above-mentioned slurry 15 minutes, add in the colloid mill and ground 60 minutes, make slurry D.
[comparative example 1]
With 1200 gram water, the aluminium colloidal sol of 1000 gram concentration 10%, 10 gram PVA, 7.5 gram CMC, 30 gram sorbester p17s are made slurries, with 2000 rev/mins of high-speed stirred 30 minutes, add 2.5 ml concns again and be 8% nitric acid, 37.5 gram potassic feldspar, 20 gram diatomite, 1000 gram gamma oxidation aluminium powders continue to stir 60 minutes, ball milling 4 hours at room temperature makes alumina slurry E again.
[comparative example 2]
Prescription according to patent CN101491776 embodiment 1, with 750 gram water, the aluminium colloidal sol of 1000 gram concentration 10%, 2.5 ml concn is 8% nitric acid, 37.5 gram potassic feldspar, 20 gram diatomite, 1000 gram gamma oxidation aluminium powders once join and mix 30 minutes in the mixer, get 10 gram PVA, 7.5 gram CMC, 30 gram sorbester p17s, foaming makes foam in the 500 gram water adding foaming machines, joins to mix in the above-mentioned slurry 10 minutes, join in the colloid mill and ground 40 minutes, make slurry F.
[embodiment 5]
With the slurry A of prepared fresh, B, C, D, E, F measures its granule size and distribution with laser particle analyzer, the results are shown in Table 1.With particle diameter is that 4 millimeters cordierite bead joins in the cylinder, cylinder is heated to 200 ℃, the index drum temperature is 200 rev/mins, slurry A～F is sprayed to respectively on the cordierite bead, dry in the shade under the room temperature, with 80 ℃ of dryings 2 hours, then be warmed up to 120 ℃ dry 2 hours once more, 1000 ℃ of roastings 12 hours obtain lamellar composite carrier A
0～F
0The rate of wear of carrier and ultrasonic loss late the results are shown in Table 2.
The particle diameter of table 1 slurry and distribution
| Particle diameter/um | A | B | C | D | E | F |
| d 50 | 3.4 | 3.5 | 3.3 | 3.7 | 8.3 | 5.2 |
| d 90 | 8.9 | 9.1 | 8.6 | 10.2 | 24.5 | 14.9 |
As can be seen from Table 1, the slurry A that adopts prescription of the present invention and preparation technology to obtain, B, C, D and slurry E, F compares, and particle diameter is littler, and the particle size distribution of slurry is narrower, illustrates that the slurry that adopts this patent method to make disperses more even.Contrast E and F and F and A～D this patent as can be seen all have facilitation with prescription to slurry.
The physical and chemical performance test result of table 2 carrier
| A 0 | B 0 | C 0 | D 0 | E 0 | F 0 | |
| 1000 change rate of wear/% | 0.11 | 0.13 | 0.13 | 0.12 | 0.28 | 0.16 |
| Ultrasonic 30min loss late a/％ | 0.23 | 0.23 | 0.25 | 0.22 | 0.45 | 0.30 |
A gets carrier 30 as one kind and restrains ultrasonic 30min in the 20kHz ultrasonic wave, and oven dry is weighed, and calculates ultrasonic front and back loss late.
As shown in Table 2, the coating A that adopts the slurry of this patent method to make
0～D
0, its rate of wear and ultrasonic loss late are starkly lower than the E of reference
0, F
0, the coating rate of wear is all below 0.15%, and ultrasonic loss late is all less than 0.3%; Contrast E0 and F0 as can be seen, under the situation of prescription unanimity, its rate of wear of coating and the ultrasonic loss late of the pulp preparation that employing this patent method obtains are lower, illustrate that coating is more firm; Contrast A
0～D
0With F0, adopt this patent prescription also more favourable as can be seen for coating.
[embodiment 6]
Slurry D and slurry E were placed respectively 7 days, and 15 days, after 30 days, laser particle analyzer was measured its granularity, sprayed according to embodiment 5 modes and was prepared into carrier, corresponded to D
1, D
2, D
3And E
1, E
2, E
3The thing of slurry and coating sees Table 2.
Table 3 standing time is to the influence of the coating of slurry and preparation
| Time/sky | Container name | Corresponding slurry d 50/um | 1000 change rate of wear/% | Ultrasonic 30min loss late/% |
| 0 | D 0 | 3.7 | 0.12 | 0.22 |
| 7 | D 1 | 4.0 | 0.12 | 0.22 |
| 15 | D 2 | 4.3 | 0.12 | 0.23 |
| 30 | D 3 | 5.0 | 0.16 | 0.29 |
| 0 | E 0 | 8.3 | 0.28 | 0.45 |
| 7 | E 1 | 10.0 | 0.32 | 0.47 |
| 15 | E 2 | 13.5 | 0.46 | 0.55 |
| 30 | E 3 | 17.1 | 0.65 | 0.72 |
By table 3, contrast standing time is to the influence of the coating of the slurry of two kinds of methods preparation and preparation thereof, as can be seen, the foamed slurry and the coating thereof that adopt this method to obtain, prolongation along with standing time, though slurry granularity, coating rate of wear and ultrasonic loss late slightly increase, substantially all control scope in, show that the slurry dispersion that adopts this method to obtain is more stable.
Claims (8)
1. foamed alumina slurry comprises following component by weight percentage:
A) 1～25% aluminium colloidal sol;
B) 5～50% aluminium oxide;
C) 0.1～10% blowing agent;
D) 0.01～1% zwitterion conditioning agent;
E) 0.1～5.0% coating performance auxiliary agent;
F) 10～90% water;
Wherein: the zwitterion conditioning agent is selected from least a in aluminium oxide, aluminum nitrate, lanthanum chloride, stannic chloride, cerous nitrate, magnesium chloride, stannous chloride, lanthanum nitrate, calcium chloride, hydrochloric acid, nitric acid or the ammoniacal liquor; The coating performance auxiliary agent is selected from least a in wollastonite, diopside, perlite, magnesium silicate, calcium silicates, magnesium aluminate, zirconium aluminate or the kaolin; Blowing agent is selected from least two kinds in PVA, HPC, MC, EMC, tween, sapn or the polyethylene glycol.
2. according to the described foamed alumina slurry of claim 1, it is characterized in that aluminium colloidal sol by weight percentage consumption be 5～25%.
3. according to the described foamed alumina slurry of claim 1, it is characterized in that aluminium oxide is γ-Al
2O
3, δ-Al
2O
3Or θ-Al
2O
3In at least a and granularity be controlled at below 10 microns, consumption is 10～40% by weight percentage.
4. according to the described foamed alumina slurry of claim 1, it is characterized in that blowing agent is by at least a material I that is selected among PVA, HPC or the EMC, mix with at least a material II that is selected from tween, sapn, the polyethylene glycol, the part by weight of material I and material II is 1: 10～10: 1, and blowing agent consumption by weight percentage is 0.5～10%.
5. according to the described foamed alumina slurry of claim 1, it is characterized in that the zwitterion conditioning agent is selected from least a in aluminium oxide, lanthanum chloride, stannic chloride, cerous nitrate, the magnesium chloride, consumption is 0.05～1% by weight percentage.
6. according to the described foamed alumina slurry of claim 1, it is characterized in that the coating performance auxiliary agent is selected from least a in wollastonite, diopside, perlite, calcium silicates, the magnesium aluminate, consumption is 0.5～5.0% by weight percentage.
7. according to the described foamed alumina slurry of claim 1, it is characterized in that water is deionized water, consumption is 40～70% by weight percentage.
8. the preparation method of the described foamed alumina slurry of claim 1 may further comprise the steps:
1) pulverize: by breaking method control aluminium oxide and auxiliary agent particle diameter below 10 microns;
2) mix: with aluminium colloidal sol, aluminium oxide, zwitterion conditioning agent, the coating performance auxiliary agent of aequum, under condition of stirring, be dissolved in the water and fully and mix, obtain slurry I;
3) foaming; After the blowing agent process foaming machine foaming with aequum, join among the slurry I and mix;
4) emulsification and grinding: with alumina slurry emulsification in colloid mill, the grinding of gained, make the particle mean size of alumina coats pulp, make foamed alumina slurry II below 5 microns.
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| CN103447099A (en) * | 2013-09-27 | 2013-12-18 | 上海第二工业大学 | Method for manufacturing block photocatalytic material by using foaming method |
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