CN102277089A - High temperature binder for inorganic non-metallic materials used in bulk curing barn and preparation method thereof - Google Patents

High temperature binder for inorganic non-metallic materials used in bulk curing barn and preparation method thereof Download PDF

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Publication number
CN102277089A
CN102277089A CN2011101395993A CN201110139599A CN102277089A CN 102277089 A CN102277089 A CN 102277089A CN 2011101395993 A CN2011101395993 A CN 2011101395993A CN 201110139599 A CN201110139599 A CN 201110139599A CN 102277089 A CN102277089 A CN 102277089A
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component
powder
bulk curing
polyvinyl alcohol
curing barn
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CN102277089B (en
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熊吉
程金树
袁红涛
汤李缨
梅东海
陆平
程曦
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HUBEI TOBACCO LEAF CO Ltd
Wuhan University of Technology WUT
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HUBEI TOBACCO LEAF CO Ltd
Wuhan University of Technology WUT
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Abstract

The invention relates to a high temperature binder for inorganic non-metallic materials used in bulk curing barns and a preparation method thereof. The high temperature binder for inorganic non-metallic materials used in bulk curing barns is characterized in that: the binder is obtained by mixing component A and component B, and the mass ratio of component A to component B is 1:2; component A is prepared by heating and mixing an aluminum dihydrogen phosphate solution, a thermocuring phenolic resin and a polyvinyl alcohol solution, wherein, mass percentage of the aluminum dihydrogen phosphate solution in component A is 55 to 75%, mass percentage of the thermocuring phenolic resin is 15 to 30% and mass percentage of the polyvinyl alcohol solution is 10 to 15%; component B is prepared by mixing copper oxide powder, spodumene powder and Zimujie powder, wherein, mass percentage of copper oxide powder in component B is 55 to 75%, mass percentage of spodumene powder is 15 to 25% and mass percentage of Zimujie powder is 10 to 20%. The high temperature binder has the characteristics of high working temperature, good thermal shock resistance, good water resistance, excellent corrosion resistance and good gas tightness.

Description

A kind of bulk curing barn ceramic high-temperature agglomerant and preparation method thereof
Technical field
The present invention relates to a kind of bulk curing barn ceramic high-temperature agglomerant and preparation method thereof.
Background technology
Bulk curing barn has following principal feature with the Working environment of ceramic: thermograde is big, and flue gas is acid strong, and the temperature height requires high to resistance to air loss.The subject matter of traditional cupric oxide-phosphate-based binding agent is that corrosion resistance is general, and water tolerance is relatively poor, and thermal shock resistance is poor, and thermal expansivity is bigger, is unfavorable for bonding bulk curing barn ceramic.
Summary of the invention
The purpose of this invention is to provide a kind of bulk curing barn with ceramic high-temperature agglomerant and preparation method thereof, this high-temperature agglomerant has that working temperature height, thermal shock resistance are good, water-tolerant, characteristics that resistance to corrosion is strong.
For achieving the above object, the technical solution used in the present invention is: a kind of bulk curing barn ceramic high-temperature agglomerant, it is characterized in that it is mixed by A component and B component, and A component and B component mass ratio are 1: 2;
Described A component (base fluid) is mixed by phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution heating; The mass percent of the shared A component of each raw material is: phosphate dihydrogen aluminum solution 55~75%, thermoset phenolic resin 15~30%, polyvinyl alcohol solution 10~15%;
Described B component (solidifying agent and filler) is formed by cupric oxide powder, triphane powder and camwood knag powder mixes, and the mass percent of the shared B component of each raw material is: cupric oxide powder 55~75%, triphane powder 15~25%, camwood knag powder 10~20%.
The density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
Described cupric oxide powder granularity is 240~300 orders, and the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
A kind of bulk curing barn is characterized in that with the preparation method of ceramic high-temperature agglomerant it comprises the steps:
1) preparation of A component (base fluid): the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 55~75%, thermoset phenolic resin 15~30%, polyvinyl alcohol solution 10~15%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 80~100 ℃ of hybrid reaction 20~35min, obtain A component (base fluid);
2) preparation of B component (solidifying agent and filler): the mass percent by the shared B component of each raw material is: cupric oxide powder 55~75%, triphane powder 15~25%, camwood knag powder 10~20%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain B component (solidifying agent and filler);
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn with ceramic high-temperature agglomerant (can use).
After with the gained binding agent test specimen bonding being finished, need be cured by following thermal system: 40 ℃ of insulation 1h, be warming up to 80 ℃ of insulation 3h then, be warming up to 150 ℃ of insulation 1h at last, be cooled to normal temperature, the thermofixation stage finishes.
Cupric oxide-phosphate-bonded dose is base fluid with the phosphate dihydrogen aluminum solution traditionally, and cupric oxide powder is a solidifying agent.The present invention adds polyvinyl alcohol solution to strengthen its plasticity-, makes the modulation of binding agent and construction thereof use more convenient; Add thermoset phenolic resin, utilize the fine and close macromolecule network and the high thermal resistance of its formation, improve the high-temperature thermal stability performance and the erosion resistance of binding agent; Add triphane as filler, can improve the thermal shock resistance of caking agent, effectively improved its working life in the bigger environment of internal-external temperature difference; The interpolation camwood knag is a filler, can improve the plasticity-of caking agent, and utilizes its stickiness to make the sealing-in slots close, and resistance to air loss and water resistance are strengthened.
The invention has the beneficial effects as follows: the bulk curing barn that is provided has effectively overcome the shortcoming (solved that existing cupric oxide-phosphate system high-temperature agglomerant thermal expansivity is big, corrosion resistance is general, the problem of thermal shock resistance difference and poor water resistance) of conventional oxidation copper-phosphate-based high temperature adhesive with the ceramic high-temperature agglomerant.The present invention has working temperature height (reaching as high as 1200 ℃), and thermal shock resistance is good, water-tolerant, series of advantages such as resistance to corrosion is strong, but also can regulate prescription according to different requirements, and make it to adapt to better Working environment, reach the ideal adhesive effect.
Embodiment
In order to understand the present invention better, further illustrate content of the present invention below in conjunction with embodiment, but content of the present invention not only is confined to the following examples.
Embodiment 1:
A kind of bulk curing barn preparation method of ceramic high-temperature agglomerant, it comprises the steps:
1) preparation of A component (base fluid): the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 75%, thermoset phenolic resin 15%, polyvinyl alcohol solution 10%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 90 ℃ of hybrid reaction 25min, obtain A component (base fluid);
The density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
2) preparation of B component (solidifying agent and filler): the mass percent by the shared B component of each raw material is: cupric oxide powder 65%, triphane powder 15%, camwood knag powder 20%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain B component (solidifying agent and filler);
Described cupric oxide powder granularity is 240~300 orders, and the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn with ceramic high-temperature agglomerant (can use).
After with the gained binding agent alumina-ceramic test specimen bonding being finished, need be cured by following thermal system: 40 ℃ of insulation 1h, be warming up to 80 ℃ of insulation 3h then, be warming up to 150 ℃ of insulation 1h at last, be cooled to normal temperature, the thermofixation stage finishes.
Bonding alumina-ceramic test specimen is carried out performance test, and the result is as follows:
1) working temperature test: working temperature test: will solidify rear oxidation aluminium ceramic test piece and be elevated in the hot environment of differing temps with the temperature rise rate of 6~10 ℃/min, insulation 30~120min, take out its adhesive shear strength of test, the results are shown in Table 1, illustrate that the present invention has the characteristics of working temperature height (reaching as high as 1200 ℃).
2) thermal shock resistance test: bonding test specimen is tested according to the YB/T376.3 standard, met this standard-required, illustrate that thermal shock resistance of the present invention is good.
3) water resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature distilled water, take out behind the 24h, and the oven dry weighing, rate of weight loss is 0.49wt%, and water-tolerant of the present invention is described.
4) erosion resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature sulphuric acid solns (concentration is 2wt%), take out behind the 24h, and the oven dry weighing, rate of weight loss is 1.2wt%, illustrates that resistance to corrosion of the present invention is strong.
Embodiment 2:
A kind of bulk curing barn preparation method of ceramic high-temperature agglomerant, it comprises the steps:
1) preparation of A component (base fluid): the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 60%, thermoset phenolic resin 25%, polyvinyl alcohol solution 15%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 80 ℃ of hybrid reaction 30min, obtain A component (base fluid);
The density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
2) preparation of B component (solidifying agent and filler): the mass percent by the shared B component of each raw material is: cupric oxide powder 55%, triphane powder 25%, camwood knag powder 20%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain B component (solidifying agent and filler);
Described cupric oxide powder granularity is 240~300 orders, and the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn with ceramic high-temperature agglomerant (can use).
After with the gained binding agent alumina-ceramic test specimen bonding being finished, need be cured by following thermal system: 40 ℃ of insulation 1h, be warming up to 80 ℃ of insulation 3h then, be warming up to 150 ℃ of insulation 1h at last, be cooled to normal temperature, the thermofixation stage finishes.
Bonding alumina-ceramic test specimen is carried out performance test, and the result is as follows:
1) working temperature test: will solidify rear oxidation aluminium ceramic test piece and be elevated in the hot environment of differing temps with the temperature rise rate of 6~10 ℃/min, insulation 30~120min, take out its adhesive shear strength of test, the results are shown in Table 1, illustrate that the present invention has the characteristics of working temperature height (reaching as high as 1200 ℃).
2) thermal shock resistance test: bonding test specimen is tested according to the YB/T376.3 standard, met this standard-required, illustrate that thermal shock resistance of the present invention is good.
3) water resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature distilled water, take out behind the 24h, and the oven dry weighing, rate of weight loss is 0.36wt%, and water-tolerant of the present invention is described.
4) erosion resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature sulphuric acid solns (concentration is 2wt%), take out behind the 24h, and the oven dry weighing, rate of weight loss is 0.88wt%, illustrates that resistance to corrosion of the present invention is strong.
Embodiment 3:
A kind of bulk curing barn preparation method of ceramic high-temperature agglomerant, it comprises the steps:
1) preparation of A component (base fluid): the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 70%, thermoset phenolic resin 15%, polyvinyl alcohol solution 15%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 100 ℃ of hybrid reaction 20min, obtain A component (base fluid);
The density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
2) preparation of B component (solidifying agent and filler): the mass percent by the shared B component of each raw material is: cupric oxide powder 55%, triphane powder 25%, camwood knag powder 20%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain B component (solidifying agent and filler);
Described cupric oxide powder granularity is 240~300 orders, and the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn with ceramic high-temperature agglomerant (can use).
After with the gained binding agent alumina-ceramic test specimen bonding being finished, need be cured by following thermal system: 40 ℃ of insulation 1h, be warming up to 80 ℃ of insulation 3h then, be warming up to 150 ℃ of insulation 1h at last, be cooled to normal temperature, the thermofixation stage finishes.
Bonding alumina-ceramic test specimen is carried out performance test, and the result is as follows:
1) working temperature test: working temperature test: will solidify rear oxidation aluminium ceramic test piece and be elevated in the hot environment of differing temps with the temperature rise rate of 6~10 ℃/min, insulation 30~120min, take out its adhesive shear strength of test, the results are shown in Table 1, illustrate that the present invention has the characteristics of working temperature height (reaching as high as 1200 ℃).
2) thermal shock resistance test: bonding test specimen is tested according to the YB/T376.3 standard, met this standard-required, illustrate that thermal shock resistance of the present invention is good.
3) water resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature distilled water, take out behind the 24h, and the oven dry weighing, rate of weight loss is 0.78wt%, and water-tolerant of the present invention is described.
4) erosion resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature sulphuric acid solns (concentration is 2wt%), take out behind the 24h, and the oven dry weighing, rate of weight loss is 1.68wt%, illustrates that resistance to corrosion of the present invention is strong.
Embodiment 4:
A kind of bulk curing barn preparation method of ceramic high-temperature agglomerant, it comprises the steps:
1) preparation of A component (base fluid): the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 55%, thermoset phenolic resin 30%, polyvinyl alcohol solution 15%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 90 ℃ of hybrid reaction 35min, obtain A component (base fluid);
The density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
2) preparation of B component (solidifying agent and filler): the mass percent by the shared B component of each raw material is: cupric oxide powder 75%, triphane powder 15%, camwood knag powder 10%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain B component (solidifying agent and filler);
Described cupric oxide powder granularity is 240~300 orders, and the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn with ceramic high-temperature agglomerant (can use).
After with the gained binding agent alumina-ceramic test specimen bonding being finished, need be cured by following thermal system: 40 ℃ of insulation 1h, be warming up to 80 ℃ of insulation 3h then, be warming up to 150 ℃ of insulation 1h at last, be cooled to normal temperature, the thermofixation stage finishes.
Bonding alumina-ceramic test specimen is carried out performance test, and the result is as follows:
1) working temperature test: working temperature test: will solidify rear oxidation aluminium ceramic test piece and be elevated in the hot environment of differing temps with the temperature rise rate of 6~10 ℃/min, insulation 30~120min, take out its adhesive shear strength of test, the results are shown in Table 1, illustrate that the present invention has the characteristics of working temperature height (reaching as high as 1200 ℃).
2) thermal shock resistance test: bonding test specimen is tested according to the YB/T376.3 standard, met this standard-required, illustrate that thermal shock resistance of the present invention is good.
3) water resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature distilled water, take out behind the 24h, and the oven dry weighing, rate of weight loss is 0.69wt%, and water-tolerant of the present invention is described.
4) erosion resistance test: the caking agent ball milling after will solidifying obtains powder, crosses 100 mesh sieves, is soaked in 20 ℃ of constant temperature sulphuric acid solns (concentration is 2wt%), take out behind the 24h, and the oven dry weighing, rate of weight loss is 1.39wt%, illustrates that resistance to corrosion of the present invention is strong.
Table 1
Figure BDA0000064231280000051

Claims (4)

1. a bulk curing barn ceramic high-temperature agglomerant is characterized in that it is mixed by A component and B component, and A component and B component mass ratio are 1: 2;
Described A component is mixed by phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution heating; The mass percent of the shared A component of each raw material is: phosphate dihydrogen aluminum solution 55~75%, thermoset phenolic resin 15~30%, polyvinyl alcohol solution 10~15%;
Described B component is formed by cupric oxide powder, triphane powder and camwood knag powder mixes, and the mass percent of the shared B component of each raw material is: cupric oxide powder 55~75%, triphane powder 15~25%, camwood knag powder 10~20%.
2. a kind of bulk curing barn ceramic high-temperature agglomerant according to claim 1 is characterized in that: the density of described phosphate dihydrogen aluminum solution is 1.8~2.2g/cm 3, the concentration of polyvinyl alcohol solution is 7.5wt%.
3. a kind of bulk curing barn ceramic high-temperature agglomerant according to claim 1, it is characterized in that: described cupric oxide powder granularity is 240~300 orders, the triphane powder size is 300 orders~400 orders, and the camwood knag powder size is 240~270 orders.
4. a kind of bulk curing barn as claimed in claim 1 is characterized in that with the preparation method of ceramic high-temperature agglomerant it comprises the steps:
1) preparation of A component: the mass percent by the shared A component of each raw material is: phosphate dihydrogen aluminum solution 55~75%, thermoset phenolic resin 15~30%, polyvinyl alcohol solution 10~15%, choose phosphate dihydrogen aluminum solution, thermoset phenolic resin and polyvinyl alcohol solution, place reactor to be heated to 80~100 ℃ of hybrid reaction 20~35min, obtain the A component;
2) preparation of B component: the mass percent by the shared B component of each raw material is: cupric oxide powder 55~75%, triphane powder 15~25%, camwood knag powder 10~20%, choose cupric oxide powder, triphane powder and camwood knag powder, mix, obtain the B component;
When 3) using, be 1: 2, choose A component and B component, mix stirring, obtain grey black ointment shape material by A component and B component mass ratio, leave standstill 10min after, obtain bulk curing barn ceramic high-temperature agglomerant.
CN 201110139599 2011-05-27 2011-05-27 High temperature binder for inorganic non-metallic materials used in bulk curing barn and preparation method thereof Expired - Fee Related CN102277089B (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634626A (en) * 2016-11-02 2017-05-10 黑龙江省科学院石油化学研究院 Preparation method for phenolic resin modified high-temperature-resistant alcohol-soluble phosphate adhesive
CN112142417A (en) * 2020-11-24 2020-12-29 佛山市建通混凝土制品有限公司 Plastering anti-crack waterproof mortar and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1094269A (en) * 1993-04-26 1994-11-02 张文池 A kind of cooking white sand pot of tool high thermal stability
CN101724352A (en) * 2009-12-11 2010-06-09 北京工业大学 Inorganic adhesive for artificial board and preparation method thereof
CN101875830A (en) * 2009-11-23 2010-11-03 黑龙江省科学院石油化学研究院 Phenolic resin/phosphate hybrid adhesive and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1094269A (en) * 1993-04-26 1994-11-02 张文池 A kind of cooking white sand pot of tool high thermal stability
CN101875830A (en) * 2009-11-23 2010-11-03 黑龙江省科学院石油化学研究院 Phenolic resin/phosphate hybrid adhesive and preparation method thereof
CN101724352A (en) * 2009-12-11 2010-06-09 北京工业大学 Inorganic adhesive for artificial board and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
鲍光辉: "磷酸盐胶粘涂层制备及结合性能研究", 《中国优秀硕士学位论文全文数据库工程科技I辑》, 15 December 2007 (2007-12-15) *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634626A (en) * 2016-11-02 2017-05-10 黑龙江省科学院石油化学研究院 Preparation method for phenolic resin modified high-temperature-resistant alcohol-soluble phosphate adhesive
CN106634626B (en) * 2016-11-02 2020-01-10 黑龙江省科学院石油化学研究院 Preparation method of phenolic resin modified high-temperature-resistant alcohol-soluble phosphate adhesive
CN112142417A (en) * 2020-11-24 2020-12-29 佛山市建通混凝土制品有限公司 Plastering anti-crack waterproof mortar and preparation method thereof
CN112142417B (en) * 2020-11-24 2021-03-23 佛山市建通混凝土制品有限公司 Plastering anti-crack waterproof mortar and preparation method thereof

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