CN101117550A - High temperature binding agent and preparation method thereof - Google Patents
High temperature binding agent and preparation method thereof Download PDFInfo
- Publication number
- CN101117550A CN101117550A CNA2007101128248A CN200710112824A CN101117550A CN 101117550 A CN101117550 A CN 101117550A CN A2007101128248 A CNA2007101128248 A CN A2007101128248A CN 200710112824 A CN200710112824 A CN 200710112824A CN 101117550 A CN101117550 A CN 101117550A
- Authority
- CN
- China
- Prior art keywords
- making
- temperature agglomerant
- weight
- temperature
- powder
- 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.)
- Pending
Links
Images
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Abstract
A high-temperature adhesive and preparation method thereof belongs to the inorganic component adhesive technical field, and is characterized in that the preparation method comprises the following steps: preparing water solution of polyvinyl alcohol firstly, then adding silica sol, ceramic fiber cotton, coal gangue fine powder, aluminum hydroxide, zirconium-containing silicon fine powder, corundum fine powder and preservative and dispersing uniformly. The invention has simple manufacture method, low cost and applicability below 1500 DEG C.
Description
Technical field
The invention belongs to tamanori technical field, be specifically related to a kind of high-temperature agglomerant and method for making thereof based on inorganic components.
Background technology
After the energy dilemma, the cry of worldwide save energy is more and more surging, and each state all begins to be devoted to energy-conservation and consumption reduction work.The eighties of last century ceramic fiber forties is developed success, because of it has excellent performances such as refractory heat-insulating, is promoted being applied on the various Thermal Equipments, has brought into play the great energy-conservation and effect that lowers consumption, also by the 5th energy that is called of people's cordiality.Along with continuous advancement in technology and maturation, the application of ceramic fiber is constantly expansion also now, especially various fibre modules, and quilts such as fiber tangent plane piece are directly used in the fiery face of quilt of Thermal Equipment, and energy conservation and consumption reduction effects is obvious day by day, and use properties also obtains to such an extent that promote.
But, as ceramic fiber, itself be that pore and solid get combination, void content have up to more than 90%, this also is its reason with excellent heat-insulating capability.But loose relatively structure also restricted ceramic fibre and air-flow situation more complicated higher in internal gas flow speed Thermal Equipment on application.On the other hand, product all is to be fixed on the wall liner of equipment by resistant to elevated temperatures metal anchorage in the general module, yet for the less module class product of some sizes, traditional anchorage style difficulty is bigger, constructional difficulties, and effect is poor.
At above problem, the development high-temperature agglomerant is proposed, this binding agent is mainly used in bonding between ceramic fibre and the ceramic fibre or the bonding between the non-ceramic fiber fire resistant insulation products of ceramic fibre, adopt this product can effectively improve the bulk strength of product insulation construction, and alleviated difficulty of construction greatly.
Summary of the invention
The purpose of this invention is to provide a kind of high-temperature agglomerant, be mainly used in the bonding of ceramic fiber module, it has makes simple, low, the use temperature advantages of higher of cost.
The following technical scheme of the concrete employing of the present invention
A kind of method for making of high-temperature agglomerant is characterized in that, comprises the steps:
1) the polyethylene alcohol and water is mixed according to weight ratio 1: 9~11, stir and be warming up to 75 ℃, under this temperature, stirred 1.5~2.5 hours, to polyvinyl alcohol formation water white transparency uniform solution, cooling blowing below 50 ℃;
2) then according to per 7.5~9.0 weight account polyethylene alcohol, add 20-27 weight part silicon sol, 3-5 weight part ceramic fiber suede, 40~45 weight part coal gangue fine powders, 4~6 parts of weight aluminium hydroxides, 5-6 part weight successively and contain the corundum fine powder of zirconium silicon powder, 3-5 part weight, 0.2% the sanitas that adds said mixture weight then, stir 5~10min, be uniformly dispersed until all powders, and do not have the particle of reunion, goods are made.
Dispersion of the present invention be by stir ceramic fiber suede uniformly branch be sprinkling upon in the water, stirring operation can realize by various whipping devices, for example agitated pool.
The SiO of described silicon sol
2Content is 30.0-31.0%, viscosity≤7.0mPas, and the pH value is 8.0~10.0; Described polyethylene solution is a commercially available polyvinyl alcohol one-level powder and the secondary powder is a kind of or two kinds of compound uses; The concentration of described polyvinyl alcohol solution is 8.5-11%; Described coal gangue powder particle size 〉=325 orders; The described zirconium silicon powder particle diameter≤5mm that contains.
A kind of high-temperature agglomerant is characterized in that, described high-temperature agglomerant physical and chemical index is:
Appearance white thick-pasty or sky blue thick-pasty
1500 ℃ of use temperatures
Viscosity, mPas 4000~6000
Al
2O
3Content 70~75%.
Prior aries such as the present invention can be widely used in bonding between ceramic fibre and the ceramic fibre or the bonding between the non-ceramic fiber fire resistant insulation products of ceramic fibre, and binding agent of the present invention can adopt spray, be coated with, brush, smear are used.The present invention has and makes simple, low, the use temperature advantages of higher of cost.
Description of drawings
Fig. 1 is a process flow diagram of the present invention.
Embodiment
Embodiment 1
The polyethylene alcohol and water is added in the reactor according to 1: 9 ratio, starts stirrer, and feed steam and be warming up to 75 ℃, under this temperature, stirred 1.5 hours, form the water white transparency uniform solution to polyvinyl alcohol after, the 50 ℃ of blowings of lowering the temperature.Add 27 parts of silicon sol according to per 7.5 weight account polyethylenes alcohol then, add 3 parts of fine suedes of making pottery, add 40 parts of coal gangue fine powders, add 4 parts of ρ-Al
2O
3, add 4 parts of aluminium hydroxides, add 6 parts and contain the zirconium silicon powder.All add agitated pool, stir on one side the limit adds above raw material, behind the stirring 5min, be uniformly dispersed until all powders, and do not have the particle of reunion, goods are made.
Goods have following technical indicator:
Outward appearance: white thick-pasty;
Use temperature: 1500 ℃;
Viscosity (mPas): 45000;
Al
2O
3Content: 73%
Embodiment 2
The polyethylene alcohol and water added to send out according to 1: 10 ratio answers in the still, start stirrer, and feed steam and be warming up to 80 ℃, under this temperature, stirred 2.0 hours, form the water white transparency uniform solution to polyvinyl alcohol after, cooling blowing below 50 ℃.According to per 27 parts of silicon sol, add 8.5 parts of polyvinyl alcohol then, add 5 parts of fine suedes of making pottery, add 1.5 parts of aluminum oxide fine suede of making pottery, add 49 parts of coal gangue fine powders, add 3.5 parts of ρ-Al
2O
3, add 4 parts of aluminium hydroxides, add 5.5 parts and contain the zirconium silicon powder, add 0.2% sanitas, all add agitated pool, stir while add above raw material, behind the stirring 5min, be uniformly dispersed until all powders, there is not the particle of reunion, goods are made.
The goods product have following technical indicator:
Outward appearance: white thick paste;
Use temperature: 1500 ℃;
Viscosity (mPas): 4700;
Al
2O
3Content: 76%
Embodiment 3
The polyethylene alcohol and water added to send out according to 1: 11 ratio answers in the still, start stirrer, and feed steam and be warming up to 80 ℃, under this temperature, stirred 2.5 hours, form the water white transparency uniform solution to polyvinyl alcohol after, cooling blowing below 50 ℃.According to per 27 parts of silicon sol, add 7.9 parts of polyvinyl alcohol then, add 4 parts of standards fine suede of making pottery, add 3 parts of fine suedes of making pottery, add 45 parts of coal gangue fine powders, add .4.5 part aluminium hydroxide, add 5.6 parts and contain the zirconium silicon powder, add 0.2% sanitas, all add agitated pool, stir on one side the limit adds above raw material, after stirring 5min, be uniformly dispersed until all powders, do not have the particle of reunion, goods are made.
The goods product have following technical indicator:
Outward appearance: white thick paste;
Use temperature: 1500 ℃;
Viscosity (mPas): 4900;
Al
2O
3Content: 75%.
Claims (9)
1. the method for making of a high-temperature agglomerant is characterized in that, comprises the steps:
1) the polyethylene alcohol and water is mixed according to weight ratio 1: 9~11, stir and be warming up to 75 ℃, under this temperature, stirred 1.5~2.5 hours, to polyvinyl alcohol formation water white transparency uniform solution, cooling blowing below 50 ℃;
2) then according to per 7.5~9.0 weight account polyethylene alcohol, add 20-27 weight part silicon sol, 3-5 weight part ceramic fiber suede, 40~45 weight part coal gangue fine powders, 4~6 parts of weight aluminium hydroxides, 5-6 part weight successively and contain zirconium silicon powder, 3-5 part weight corundum fine powder, the water of 5-8 part weight, stir 5~10min, be uniformly dispersed until all powders, and do not have the particle of reunion, goods are made.
2. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, the SiO of described silicon sol
2Content is 30.0-31.0%, viscosity≤7.0mPas, and the pH value is 8.0~10.0.
3. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, described polyethylene solution is commercially available polyvinyl alcohol one-level powder and a kind of or two kinds of compound uses in the secondary powder.
4. the method for making of high-temperature agglomerant according to claim 3 is characterized in that, the concentration of described polyvinyl alcohol solution is 8.5-11%.
5. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, described coal gangue powder particle size 〉=600 orders.
6. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, describedly contains zirconium silicon powder particle diameter 〉=300 orders, and SiO
2〉=90%.
7. a high-temperature agglomerant is characterized in that, described high-temperature agglomerant physical and chemical index is:
Appearance white thick-pasty or sky blue thick-pasty
1500 ℃ of use temperatures
Viscosity, mPas 4000~6000
Al
2O
3Content 70~75%.
8. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, described corundum fine powder particle diameter 〉=200 orders, and Al
2O
3〉=99%.
9. the method for making of high-temperature agglomerant according to claim 1 is characterized in that, described ceramic fiber suede, its staple length<5mm, and slag ball content<5%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNA2007101128248A CN101117550A (en) | 2007-09-10 | 2007-09-10 | High temperature binding agent and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNA2007101128248A CN101117550A (en) | 2007-09-10 | 2007-09-10 | High temperature binding agent and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101117550A true CN101117550A (en) | 2008-02-06 |
Family
ID=39053813
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2007101128248A Pending CN101117550A (en) | 2007-09-10 | 2007-09-10 | High temperature binding agent and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101117550A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102584253A (en) * | 2012-02-15 | 2012-07-18 | 广东道氏技术股份有限公司 | Ceramic green body reinforcing agent and application thereof |
CN103011861A (en) * | 2012-12-18 | 2013-04-03 | 山西高科耐火材料股份有限公司 | Glass kiln-used dry type micro-expansion heat preservation coating |
CN103333618A (en) * | 2013-05-28 | 2013-10-02 | 苏州绿科环保新材料有限公司 | Silicate inorganic aqueous binder |
CN103966630A (en) * | 2014-04-28 | 2014-08-06 | 沈阳化工大学 | Method for treating waste electrolyte generated in production of electrolytic aluminium |
CN105462300A (en) * | 2015-12-25 | 2016-04-06 | 山东鲁阳节能材料股份有限公司 | Paint and preparation method thereof |
CN105665617A (en) * | 2014-11-18 | 2016-06-15 | 中国科学院金属研究所 | Adhesive for ceramic cores, preparation method and application of adhesive |
CN105859311A (en) * | 2016-04-06 | 2016-08-17 | 遵义市恒新化工有限公司 | High-temperature adhesive |
CN113603460A (en) * | 2021-08-27 | 2021-11-05 | 郑州瑞泰耐火科技有限公司 | Micro-pore magnesia-hercynite brick for cement rotary kiln burning zone and preparation method thereof |
-
2007
- 2007-09-10 CN CNA2007101128248A patent/CN101117550A/en active Pending
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102584253B (en) * | 2012-02-15 | 2013-09-11 | 广东道氏技术股份有限公司 | Ceramic green body reinforcing agent and application thereof |
CN102584253A (en) * | 2012-02-15 | 2012-07-18 | 广东道氏技术股份有限公司 | Ceramic green body reinforcing agent and application thereof |
CN103011861B (en) * | 2012-12-18 | 2014-07-16 | 山西高科耐火材料股份有限公司 | Glass kiln-used dry type micro-expansion heat preservation coating |
CN103011861A (en) * | 2012-12-18 | 2013-04-03 | 山西高科耐火材料股份有限公司 | Glass kiln-used dry type micro-expansion heat preservation coating |
CN103333618B (en) * | 2013-05-28 | 2014-09-03 | 苏州绿科环保新材料有限公司 | Silicate inorganic aqueous binder |
CN103333618A (en) * | 2013-05-28 | 2013-10-02 | 苏州绿科环保新材料有限公司 | Silicate inorganic aqueous binder |
CN103966630A (en) * | 2014-04-28 | 2014-08-06 | 沈阳化工大学 | Method for treating waste electrolyte generated in production of electrolytic aluminium |
CN105665617A (en) * | 2014-11-18 | 2016-06-15 | 中国科学院金属研究所 | Adhesive for ceramic cores, preparation method and application of adhesive |
CN105665617B (en) * | 2014-11-18 | 2018-02-16 | 中国科学院金属研究所 | A kind of ceramic core bonding agent, preparation method and applications |
CN105462300A (en) * | 2015-12-25 | 2016-04-06 | 山东鲁阳节能材料股份有限公司 | Paint and preparation method thereof |
CN105462300B (en) * | 2015-12-25 | 2017-12-01 | 山东鲁阳节能材料股份有限公司 | A kind of coating and preparation method thereof |
CN105859311A (en) * | 2016-04-06 | 2016-08-17 | 遵义市恒新化工有限公司 | High-temperature adhesive |
CN113603460A (en) * | 2021-08-27 | 2021-11-05 | 郑州瑞泰耐火科技有限公司 | Micro-pore magnesia-hercynite brick for cement rotary kiln burning zone and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101117550A (en) | High temperature binding agent and preparation method thereof | |
CN109020370B (en) | Interface mortar with anticorrosive coating for steel structure exterior wall | |
CN106882947B (en) | A kind of environmentally protective phase-transition heat-preserving cracking resistance coagulates the preparation method of spraying mortar fastly | |
CN105367032B (en) | A kind of preparation method of nano thermal insulation plate | |
CN103086657A (en) | Interface-enhanced anti-crack mortar and production technology thereof | |
CN102219465A (en) | Formula design of novel cement-based insulation dry powder | |
CN107987601A (en) | A kind of two-component insulation putty for architectural exterior wall and preparation method thereof | |
CN102040899B (en) | Outer-wall thermal insulating paint and preparation method thereof | |
CN108623268A (en) | A kind of self-heat-insulating bearing concrete and preparation method thereof based on 3D printing performance | |
CN105541313A (en) | Nano heat-insulating material and preparation method of nano heat-insulating board | |
CN105153827A (en) | Thermal insulation coating material | |
CN104804674A (en) | Environment-friendly building adhesive and preparation method thereof | |
CN103396129B (en) | Light-weight hot-blast furnace pipeline spray paint and application method thereof | |
CN115259702A (en) | Slag fly ash-based alkali-activated cementing material and preparation method thereof | |
CN105777037A (en) | Fluorine-gypsum-based machine-spraying thermal insulation mortar and preparation method thereof | |
CN101028968A (en) | Production of unshaped thermal-insulating material | |
CN102352204B (en) | Preparation method for bonding material for energy-saving lamp | |
CN106927839A (en) | A kind of micropore insulation brick | |
CN102219450A (en) | Waterproof crack-resistant fireproof internal and external wall heat-preserving heat-insulating coating and preparation method thereof | |
CN108727036A (en) | A kind of efficient energy-saving heat-preservation brick and preparation method thereof | |
CN102352202B (en) | Method for preparing bonding material | |
CN107162625A (en) | A kind of fireproof insulation brick and preparation method thereof | |
CN105130284A (en) | Thermal-insulation mortar with high waste utilization comprehensive performance and preparation method thereof | |
CN101509066A (en) | High-efficiency energy-conservation sintering additive | |
CN106927858A (en) | A kind of environment protecting thermal insulating mortar and its preparation technology |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C12 | Rejection of a patent application after its publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20080206 |