CN114437504B - Totally-enclosed fireproof bus and manufacturing process thereof - Google Patents
Totally-enclosed fireproof bus and manufacturing process thereof Download PDFInfo
- Publication number
- CN114437504B CN114437504B CN202111655433.7A CN202111655433A CN114437504B CN 114437504 B CN114437504 B CN 114437504B CN 202111655433 A CN202111655433 A CN 202111655433A CN 114437504 B CN114437504 B CN 114437504B
- Authority
- CN
- China
- Prior art keywords
- silicate
- bus
- scandium
- parts
- yttrium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/16—Solid spheres
- C08K7/18—Solid spheres inorganic
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02G—INSTALLATION OF ELECTRIC CABLES OR LINES, OR OF COMBINED OPTICAL AND ELECTRIC CABLES OR LINES
- H02G5/00—Installations of bus-bars
- H02G5/06—Totally-enclosed installations, e.g. in metal casings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/202—Applications use in electrical or conductive gadgets use in electrical wires or wirecoating
Abstract
The invention discloses a totally-enclosed fire-resistant bus, which comprises a bus body and a fire-resistant pouring layer arranged on the surface of the bus body; the refractory pouring layer comprises the following components in parts by weight: 50-60 parts of epoxy resin, 40-65 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 22-30 parts of alumina powder, 12-27 parts of quartz powder, 1-3 parts of dispersing agent and 20-30 parts of curing agent. The invention discloses a totally-enclosed fire-resistant bus, wherein a fire-resistant casting layer is arranged on the surface of the bus, and the fire-resistant casting layer is prepared from epoxy resin and a fire-resistant material, can bear high-temperature baking and has strong heat dissipation performance, so that the totally-enclosed fire-resistant bus prepared by the invention has better applicability and is recommended to be popularized and used.
Description
Technical Field
The invention relates to the field of fire-resistant buses, in particular to a totally-enclosed fire-resistant bus and a manufacturing process thereof.
Background
At present, the fire-resistant bus used in the domestic market has two types, namely a common fire-resistant bus duct and a pouring type fire-resistant bus. The common fire-resistant bus duct is a common intensive bus duct or an air bus duct, is coated with high-temperature-resistant fireproof asbestos of 10-20 cm, is coated with a steel plate shell, and is coated with fire-resistant paint outside the shell, so that the common fire-resistant bus duct is called as the common fire-resistant bus duct with fire resistance. The pouring type fire-resistant bus is a pouring type fire-resistant bus duct which is formed by wrapping a pouring type bus with about 20cm of fire-resistant asbestos or a fire-resistant plate, and additionally coating a layer of metal shell with a fire-resistant coating by some manufacturers.
The fire-resistant bus mainly depends on the fire-resistant asbestos to realize fire resistance, the required thickness of the fire-resistant asbestos is generally more than 20cm due to the heat resistance of the fire-resistant asbestos, and the bus can generate a large amount of heat in the using process, so that the heat generated by the operation of the bus cannot be timely dissipated, and the current-carrying capacity of the medium-voltage bus to current is influenced, so that the current-carrying capacity of the current can be met only by increasing the diameter of a conductor bus, and the bus with the increased diameter has higher manufacturing cost and larger volume and occupies too much space. Therefore, a fire-resistant bus bar having good fire resistance and high thermal conductivity is urgently required in the market.
Disclosure of Invention
The invention aims to provide a fully-closed fire-resistant bus and a manufacturing process thereof, aiming at the problems that the heat resistance of fire-resistant asbestos in the prior art causes the required thickness to be generally more than 20 centimeters, and a bus can generate a large amount of heat in the use process, so that the heat generated by the operation of the bus can not be dissipated in time, and the current carrying capacity of a medium-voltage bus is influenced.
The purpose of the invention is realized by adopting the following technical scheme:
the invention discloses a totally-enclosed fire-resistant bus, which comprises a bus body and a fire-resistant pouring layer arranged on the surface of the bus body, wherein the bus body is provided with a plurality of grooves; the refractory pouring layer comprises the following components in parts by weight:
50-60 parts of epoxy resin, 40-65 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 22-30 parts of alumina powder, 12-27 parts of quartz powder, 1-3 parts of dispersing agent and 20-30 parts of curing agent.
Preferably, the bus body is a copper-clad aluminum bus.
Preferably, the thickness of the refractory casting layer is 10 to 20mm.
Preferably, the epoxy resin is a bisphenol a type epoxy resin.
Preferably, the scandium silicate/yttrium silicate coated aluminum nitride microspheres are shell-core microspheres prepared by using scandium silicate/yttrium silicate as a shell and aluminum nitride as a core.
Preferably, the alumina powder has a particle size of 100 to 150 mesh, and the quartz powder has a particle size of 50 to 100 mesh.
Preferably, the dispersant is an epoxy organosilane coupling agent.
Preferably, the curing agent is an acid anhydride curing agent, and comprises one of diphenyl ether tetracarboxylic dianhydride, cyclopentanetetracarboxylic dianhydride and tetrachlorophthalic anhydride.
Preferably, the preparation method of the scandium silicate/yttrium silicate coated aluminum nitride microspheres comprises the following steps:
s1, weighing ethyl orthosilicate, mixing the ethyl orthosilicate with an ethanol solution, dispersing the ethyl orthosilicate and the ethanol solution uniformly, dropwise adding a mixed solution of scandium chloride and yttrium chloride while stirring, and continuously stirring for 6-10 hours after dropwise adding is finished to obtain a scandium silicate/yttrium silicate precursor;
wherein the mass fraction of the ethanol solution is 35-55%; the mixed solution of scandium chloride and yttrium chloride is obtained by mixing scandium chloride, yttrium chloride and deionized water according to the mass ratio of 1; the mass ratio of the ethyl orthosilicate and the ethanol solution to the mixed solution of scandium chloride and yttrium chloride is 1.2-1.6;
s2, dispersing aluminum nitride nanoparticles into an ethanol solution, adding a silane coupling agent KH550, performing ultrasonic dispersion uniformly, then dropwise adding the mixture into a scandium silicate/yttrium silicate precursor which is continuously stirred, stirring the mixture for 24-48 hours at the temperature of 45-55 ℃ after dropwise adding, filtering, washing and drying a filter cake, and thus obtaining a composite microsphere precursor;
wherein, the mass fraction of the ethanol solution is 35-55%, and the mass ratio of the aluminum nitride nanoparticles, the silane coupling agent KH550 and the ethanol solution is 1; the mass ratio of the aluminum nitride nanoparticles to the scandium silicate/yttrium silicate precursor is 1;
s3, placing the composite microsphere precursor into a reaction furnace, heating to 900-1000 ℃, performing heat preservation treatment for 1-3 h, heating to 1250-1400 ℃, performing heat preservation treatment for 2-4 h, and naturally cooling to room temperature to obtain the scandium silicate/yttrium silicate coated aluminum nitride microspheres.
Preferably, the invention discloses a manufacturing process of a totally-enclosed fire-resistant bus, which comprises the following steps:
step 1, weighing epoxy resin, a dispersing agent, aluminum oxide, silicon oxide and scandium silicate/yttrium silicate coated aluminum nitride microspheres of a refractory pouring layer according to parts by weight, mixing the materials into a stirrer, and stirring and mixing the materials uniformly to obtain a first mixture;
step 2, adding a curing agent into the first mixture, and uniformly stirring and mixing to obtain a second mixture;
step 3, taking a casting mold, placing the clean bus in the casting mold, and slowly injecting a second mixture;
and 4, placing the casting mold in a reaction furnace, heating and curing, and demolding to obtain the totally-enclosed refractory bus.
Preferably, in the step 1, the aluminum nitride microspheres coated with aluminum oxide, silicon oxide and scandium silicate/yttrium silicate are added after the epoxy resin and the dispersant are fully mixed.
Preferably, in the step 3, the bus bar is placed after the mold release agent is coated inside the casting mold.
Preferably, in step 3, the clean bus bar is obtained by cleaning the bus bar with ethanol or acetone.
Preferably, in the step 4, the temperature for heating and curing in the reaction furnace is firstly increased to 110-120 ℃, and the heat preservation treatment is carried out for 2-3 h, and then increased to 140-150 ℃, and the heat preservation treatment is carried out for 1-2 h.
The invention has the beneficial effects that:
the invention discloses a totally-enclosed fire-resistant bus, wherein a fire-resistant pouring layer is arranged on the surface of the bus, and the fire-resistant pouring layer is prepared from epoxy resin and a fire-resistant material, can bear high-temperature baking and has strong heat dissipation, so that the totally-enclosed fire-resistant bus prepared by the invention has better applicability and is suggested to be popularized and used.
The preparation method disclosed by the invention has the advantages that the thermal conductivity and other mechanical properties of the aluminum nitride can be utilized, the aluminum nitride can be protected, the contact of the aluminum nitride with external moisture is reduced, the hydrolysis effect of the aluminum nitride is reduced, in addition, the preparation method also has the effect of relieving thermal stress and pressure stress to a certain extent, and the prepared refractory material has longer usability.
The scandium silicate/yttrium silicate prepared by the invention is different from the conventional single metal silicate preparation, and the combination of scandium and yttrium can compensate each other, so that the effect which can not be achieved by any single metal can be achieved, for example, the scandium silicate/yttrium silicate has higher strength or stability. In addition, the silicate can be used as a silicon flame retardant and is excellent in performance, and the scandium silicate/yttrium silicate prepared by the invention has better flame retardance.
Detailed Description
For the purpose of more clearly illustrating the present invention and more clearly understanding the technical features, objects and advantages of the present invention, the technical solutions of the present invention will now be described in detail below, but the present invention should not be construed as being limited to the implementable scope of the present invention.
The aluminum nitride has the characteristics of high strength, high volume resistivity, high insulation and pressure resistance, good thermal conductivity and the like, is not only used as a sintering aid or a reinforcing phase of structural ceramics, but also has the performance far higher than that of aluminum oxide particularly in the field of ceramic electronic substrates and packaging materials of intense fire in recent years. However, aluminum nitride is very easy to hydrolyze in a humid environment, forms aluminum hydroxide with hydroxyl in water, forms an aluminum oxide layer on the surface of the aluminum nitride powder, dissolves a large amount of oxygen in aluminum oxide lattices, and reduces the nitrogen content after hydrolysis, thereby obviously reducing the thermal conductivity and other physical and chemical properties of the aluminum nitride.
The invention is further described below with reference to the following examples.
Example 1
A totally-enclosed refractory bus comprises a bus body and a refractory pouring layer arranged on the surface of the bus body; the bus body is a copper clad aluminum bus, and the thickness of the refractory casting layer is 15mm.
The refractory pouring layer comprises the following components in parts by weight:
55 parts of bisphenol A epoxy resin, 52 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 28 parts of alumina powder, 21 parts of quartz powder, 2 parts of epoxy organosilane coupling agent and 25 parts of diphenyl ether tetracarboxylic dianhydride.
The grain size of the alumina powder is 100-150 meshes, and the grain size of the quartz powder is 50-100 meshes.
The preparation method of the scandium silicate/yttrium silicate coated aluminum nitride microspheres comprises the following steps:
s1, weighing ethyl orthosilicate, mixing the ethyl orthosilicate with an ethanol solution, uniformly dispersing, dropwise adding a mixed solution of scandium chloride and yttrium chloride while stirring, and continuously stirring for 8 hours after dropwise adding is finished to obtain a scandium silicate/yttrium silicate precursor;
wherein the mass fraction of the ethanol solution is 45 percent; the mixed solution of scandium chloride and yttrium chloride is obtained by mixing scandium chloride, yttrium chloride and deionized water according to the mass ratio of 1; the mass ratio of the ethyl orthosilicate and the ethanol solution to the mixed solution of scandium chloride and yttrium chloride is 1.4;
s2, dispersing aluminum nitride nanoparticles into an ethanol solution, adding a silane coupling agent KH550, after uniform ultrasonic dispersion, dropwise adding the aluminum nitride nanoparticles into a scandium silicate/yttrium silicate precursor which is continuously stirred, after dropwise adding, stirring at 50 ℃ for 36 hours, filtering, washing and drying a filter cake, and obtaining a composite microsphere precursor;
wherein the mass fraction of the ethanol solution is 45%, and the mass ratio of the aluminum nitride nanoparticles, the silane coupling agent KH550 and the ethanol solution is 1; the mass ratio of the aluminum nitride nanoparticles to the scandium silicate/yttrium silicate precursor is 1;
s3, placing the composite microsphere precursor in a reaction furnace, heating to 1000 ℃, carrying out heat preservation treatment for 2 hours, then heating to 1350 ℃ again, carrying out heat preservation treatment for 3 hours, and naturally cooling to room temperature to obtain the scandium silicate/yttrium silicate coated aluminum nitride microspheres.
The manufacturing process of the totally-enclosed fire-resistant bus comprises the following steps:
step 1, weighing epoxy resin, epoxy organosilane coupling agent, aluminum oxide, silicon oxide and scandium silicate/yttrium silicate coated aluminum nitride microspheres of a refractory casting layer according to parts by weight, fully mixing the epoxy resin and the epoxy organosilane coupling agent in a stirrer, adding the aluminum oxide, the silicon oxide and the scandium silicate/yttrium silicate coated aluminum nitride microspheres, mixing the mixture in the stirrer, and stirring and mixing the mixture uniformly to obtain a first mixture;
step 2, adding diphenyl ether tetracid dianhydride into the first mixture, and stirring and mixing uniformly to obtain a second mixture;
step 3, taking a casting mold, coating a release agent inside the casting mold, placing a clean bus obtained by cleaning the bus with ethanol or acetone into the casting mold, and slowly injecting a second mixture;
and step 4, placing the casting mold in a reaction furnace, heating to 120 ℃, carrying out heat preservation treatment for 2.5 hours, heating to 150 ℃, carrying out heat preservation treatment for 1.5 hours, cooling to room temperature, and demolding to obtain the totally-enclosed refractory bus.
Example 2
A totally-enclosed fire-resistant bus comprises a bus body and a fire-resistant pouring layer arranged on the surface of the bus body; the bus body is a copper-clad aluminum bus, and the thickness of the refractory pouring layer is 10mm.
The refractory pouring layer comprises the following components in parts by weight:
50 parts of bisphenol A epoxy resin, 40 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 22 parts of aluminum oxide powder, 12 parts of quartz powder, 1 part of epoxy organosilane coupling agent and 20 parts of cyclopentanetetracarboxylic dianhydride.
The grain size of the alumina powder is 100-150 meshes, and the grain size of the quartz powder is 50-100 meshes.
The preparation method of the scandium silicate/yttrium silicate coated aluminum nitride microspheres comprises the following steps:
s1, weighing tetraethoxysilane and mixing with an ethanol solution, after uniform dispersion, dropwise adding a mixed solution of scandium chloride and yttrium chloride while stirring, and after dropwise adding, continuously stirring for 6 hours to obtain a scandium silicate/yttrium silicate precursor;
wherein the mass fraction of the ethanol solution is 35 percent; the mixed solution of scandium chloride and yttrium chloride is obtained by mixing scandium chloride, yttrium chloride and deionized water according to the mass ratio of 1; the mass ratio of the ethyl orthosilicate and the ethanol solution to the mixed solution of scandium chloride and yttrium chloride is 1.2;
s2, dispersing aluminum nitride nanoparticles into an ethanol solution, adding a silane coupling agent KH550, after uniform ultrasonic dispersion, dropwise adding the aluminum nitride nanoparticles into a scandium silicate/yttrium silicate precursor which is continuously stirred, after dropwise adding, stirring at 45 ℃ for 24 hours, filtering, washing and drying a filter cake, and obtaining a composite microsphere precursor;
wherein the mass fraction of the ethanol solution is 35%, and the mass ratio of the aluminum nitride nanoparticles to the silane coupling agent KH550 to the ethanol solution is 1; the mass ratio of the aluminum nitride nanoparticles to the scandium silicate/yttrium silicate precursor is 1;
s3, placing the composite microsphere precursor into a reaction furnace, heating to 900 ℃, performing heat preservation treatment for 1 hour, heating to 1250 ℃, performing heat preservation treatment for 2 hours, and naturally cooling to room temperature to obtain the scandium silicate/yttrium silicate coated aluminum nitride microspheres.
The manufacturing process of the totally-enclosed fire-resistant bus comprises the following steps:
step 1, weighing epoxy resin, epoxy organosilane coupling agent, aluminum oxide, silicon oxide and scandium silicate/yttrium silicate coated aluminum nitride microspheres of a refractory pouring layer according to parts by weight, fully mixing the epoxy resin and the epoxy organosilane coupling agent in a stirrer, adding the aluminum oxide, the silicon oxide and the scandium silicate/yttrium silicate coated aluminum nitride microspheres, mixing the mixture in the stirrer, and stirring and mixing the mixture uniformly to obtain a first mixture;
step 2, adding cyclopentanetetracarboxylic dianhydride into the first mixture, and uniformly stirring and mixing to obtain a second mixture;
step 3, taking a casting mold, coating a release agent inside the casting mold, placing a clean bus obtained by cleaning the bus with ethanol or acetone into the casting mold, and slowly injecting a second mixture;
and 4, placing the casting mold in a reaction furnace, heating to 110 ℃, carrying out heat preservation treatment for 2 hours, heating to 140 ℃, carrying out heat preservation treatment for 1 hour, cooling to room temperature, and demolding to obtain the totally-enclosed refractory bus.
Example 3
A totally-enclosed fire-resistant bus comprises a bus body and a fire-resistant pouring layer arranged on the surface of the bus body; the bus body is a copper-clad aluminum bus, and the thickness of the refractory pouring layer is 20mm.
The refractory pouring layer comprises the following components in parts by weight:
60 parts of bisphenol A epoxy resin, 65 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 30 parts of alumina powder, 27 parts of quartz powder, 3 parts of epoxy organosilane coupling agent and 30 parts of tetrachlorophthalic anhydride.
The grain size of the alumina powder is 100-150 meshes, and the grain size of the quartz powder is 50-100 meshes.
The preparation method of the scandium silicate/yttrium silicate coated aluminum nitride microspheres comprises the following steps:
s1, weighing ethyl orthosilicate, mixing the ethyl orthosilicate with an ethanol solution, uniformly dispersing, dropwise adding a mixed solution of scandium chloride and yttrium chloride while stirring, and continuously stirring for 10 hours after dropwise adding is finished to obtain a scandium silicate/yttrium silicate precursor;
wherein the mass fraction of the ethanol solution is 55%; the mixed solution of scandium chloride and yttrium chloride is obtained by mixing scandium chloride, yttrium chloride and deionized water according to the mass ratio of 1; the mass ratio of the ethyl orthosilicate and the ethanol solution to the mixed solution of scandium chloride and yttrium chloride is 1.6;
s2, dispersing aluminum nitride nanoparticles into an ethanol solution, adding a silane coupling agent KH550, performing ultrasonic dispersion uniformly, then dropwise adding the mixture into a scandium silicate/yttrium silicate precursor which is continuously stirred, stirring at 55 ℃ for 48 hours after dropwise adding, filtering, washing and drying a filter cake, and thus obtaining a composite microsphere precursor;
wherein the mass fraction of the ethanol solution is 55%, and the mass ratio of the aluminum nitride nanoparticles to the silane coupling agent KH550 to the ethanol solution is 1; the mass ratio of the aluminum nitride nanoparticles to the scandium silicate/yttrium silicate precursor is 1;
s3, placing the composite microsphere precursor in a reaction furnace, heating to 1000 ℃, performing heat preservation treatment for 3 hours, heating to 1400 ℃ again, performing heat preservation treatment for 4 hours, and naturally cooling to room temperature to obtain the scandium silicate/yttrium silicate coated aluminum nitride microspheres.
The manufacturing process of the totally-enclosed fire-resistant bus comprises the following steps:
step 1, weighing epoxy resin, epoxy organosilane coupling agent, aluminum oxide, silicon oxide and scandium silicate/yttrium silicate coated aluminum nitride microspheres of a refractory pouring layer according to parts by weight, fully mixing the epoxy resin and the epoxy organosilane coupling agent in a stirrer, adding the aluminum oxide, the silicon oxide and the scandium silicate/yttrium silicate coated aluminum nitride microspheres, mixing the mixture in the stirrer, and stirring and mixing the mixture uniformly to obtain a first mixture;
step 2, adding tetrachlorophthalic anhydride into the first mixture, and uniformly stirring and mixing to obtain a second mixture;
step 3, taking a casting mold, coating a release agent inside the casting mold, placing a clean bus obtained by cleaning the bus with ethanol or acetone into the casting mold, and slowly injecting a second mixture;
and 4, placing the casting mold in a reaction furnace, heating to 120 ℃, carrying out heat preservation treatment for 3 hours, heating to 150 ℃, carrying out heat preservation treatment for 2 hours, cooling to room temperature, and demolding to obtain the totally-enclosed refractory bus.
Comparative example
The preparation process of the totally-enclosed refractory bus is the same as that of the embodiment 1, and the difference is that:
the refractory pouring layer comprises the following components in parts by weight:
55 parts of bisphenol A epoxy resin, 52 parts of aluminum nitride microspheres, 28 parts of aluminum oxide powder, 21 parts of quartz powder, 2 parts of epoxy organosilane coupling agent and 25 parts of diphenyl ether tetracarboxylic dianhydride.
The grain size of the alumina powder is 100-150 meshes, and the grain size of the quartz powder is 50-100 meshes.
In order to more clearly illustrate the invention, the performance of the refractory casting layers prepared in examples 1 to 3 of the invention and comparative examples is tested and compared, and reference is made to GA/T537-2005 test method for flame retardant, fire retardant and fire resistant performance of busbar trunk system (bus duct) and requirements of 8.2.14 and 7.1.1.6 in GB 7251.2-2006.
Fire resistance detection: the examples 1-3 and the comparative example are placed in flame at 1000 ℃ for a period of time, and the refractory pouring layer is stripped to observe whether each refractory bus is burned black or is sintered. The bending strength and the compressive strength are detected for the refractory pouring layer. The salt spray corrosion resistance is detected by adopting a manual salt spray test of standard ISO 3768-1976 to observe whether the surface is corroded.
TABLE 1 Performance of different refractory buses
Example 1 | Example 2 | Example 3 | Comparative example | |
Fire resistance | >240min | >240min | >240min | <240min |
Thermal conductivity (W/(m.K)) | 1.16 | 1.15 | 1.18 | 1.23 |
Bending strength(MPa) | 117 | 109 | 118 | 97 |
Compressive strength (MPa) | 192 | 185 | 197 | 171 |
Resistance to salt spray corrosion | >1000h | >1000h | >1000h | <800h |
As can be seen from Table 1 above, the refractory times of the refractory castable layers prepared according to inventive examples 1-3 were above 240min, whereas the comparative examples did not reach 240min. Furthermore, although examples 1 to 3 are somewhat inferior to the comparative examples in thermal conductivity, the difference is not so large and the refractory castable layer of examples 1 to 3 is more excellent in flexural strength, compressive strength and salt spray corrosion resistance as a whole.
Finally, it should be noted that the above embodiments are only used for illustrating the technical solutions of the present invention, and not for limiting the protection scope of the present invention, although the present invention is described in detail with reference to the preferred embodiments, it should be understood by those skilled in the art that modifications or equivalent substitutions can be made on the technical solutions of the present invention without departing from the spirit and scope of the technical solutions of the present invention.
Claims (9)
1. A totally-enclosed fire-resistant bus is characterized by comprising a bus body and a fire-resistant pouring layer arranged on the surface of the bus body; the refractory pouring layer comprises the following components in parts by weight:
50-60 parts of epoxy resin, 40-65 parts of scandium silicate/yttrium silicate coated aluminum nitride microspheres, 22-30 parts of alumina powder, 12-27 parts of quartz powder, 1-3 parts of dispersing agent and 20-30 parts of curing agent;
the preparation method of the scandium silicate/yttrium silicate coated aluminum nitride microspheres comprises the following steps:
s1, weighing tetraethoxysilane and mixing with an ethanol solution, after uniform dispersion, dropwise adding a mixed solution of scandium chloride and yttrium chloride while stirring, and after dropwise adding, continuously stirring for 6-10 hours to obtain a scandium silicate/yttrium silicate precursor;
wherein the mass fraction of the ethanol solution is 35-55%; the mixed solution of scandium chloride and yttrium chloride is obtained by mixing scandium chloride, yttrium chloride and deionized water according to the mass ratio of 1; the mass ratio of the ethyl orthosilicate and the ethanol solution to the mixed solution of scandium chloride and yttrium chloride is 1.2-1.6;
s2, dispersing aluminum nitride nanoparticles into an ethanol solution, adding a silane coupling agent KH550, performing ultrasonic dispersion uniformly, then dropwise adding the mixture into a scandium silicate/yttrium silicate precursor which is continuously stirred, stirring the mixture for 24-48 hours at the temperature of 45-55 ℃ after dropwise adding, filtering, washing and drying a filter cake, and thus obtaining a composite microsphere precursor;
wherein, the mass fraction of the ethanol solution is 35-55%, and the mass ratio of the aluminum nitride nanoparticles, the silane coupling agent KH550 and the ethanol solution is 1; the mass ratio of the aluminum nitride nanoparticles to the scandium silicate/yttrium silicate precursor is 1;
s3, placing the composite microsphere precursor into a reaction furnace, heating to 900-1000 ℃, performing heat preservation treatment for 1-3 h, then heating to 1250-1400 ℃, performing heat preservation treatment for 2-4 h, and naturally cooling to room temperature to obtain the scandium silicate/yttrium silicate coated aluminum nitride microspheres.
2. The fully-enclosed refractory bus bar according to claim 1, wherein the bus bar body is a copper-clad aluminum bus bar.
3. The fully enclosed refractory busbar according to claim 1, wherein said refractory castable layer has a thickness of 10 to 20mm.
4. The totally enclosed refractory busbar according to claim 1, wherein said epoxy resin is bisphenol a epoxy resin.
5. The fully-enclosed refractory busbar of claim 1, wherein the scandium silicate/yttrium silicate coated aluminum nitride microspheres are shell-core microspheres prepared from scandium silicate/yttrium silicate as a shell and aluminum nitride as a core.
6. The fully-closed refractory bus bar according to claim 1, wherein the alumina powder has a particle size of 100 to 150 mesh, and the quartz powder has a particle size of 50 to 100 mesh.
7. The fully enclosed refractory bus of claim 1, wherein the dispersant is an epoxy-based organosilane coupling agent.
8. The fully-enclosed fire resistant busbar according to claim 1, wherein the curing agent is an anhydride curing agent comprising one of diphenyl ether tetracarboxylic dianhydride, cyclopentanetetracarboxylic dianhydride, and tetrachlorophthalic anhydride.
9. A process for manufacturing a totally enclosed refractory busbar according to any one of claims 1 to 8, comprising the steps of:
step 1, weighing epoxy resin, a dispersing agent, aluminum oxide, silicon oxide and scandium silicate/yttrium silicate coated aluminum nitride microspheres of a refractory pouring layer according to parts by weight, mixing the materials into a stirrer, and stirring and mixing the materials uniformly to obtain a first mixture;
step 2, adding a curing agent into the first mixture, and uniformly stirring and mixing to obtain a second mixture;
step 3, taking a casting mold, placing the clean bus in the casting mold, and slowly injecting a second mixture;
and 4, placing the casting mold in a reaction furnace, heating and curing, and demolding to obtain the totally-enclosed refractory bus.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111655433.7A CN114437504B (en) | 2021-12-30 | 2021-12-30 | Totally-enclosed fireproof bus and manufacturing process thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111655433.7A CN114437504B (en) | 2021-12-30 | 2021-12-30 | Totally-enclosed fireproof bus and manufacturing process thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN114437504A CN114437504A (en) | 2022-05-06 |
CN114437504B true CN114437504B (en) | 2022-11-08 |
Family
ID=81365851
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111655433.7A Active CN114437504B (en) | 2021-12-30 | 2021-12-30 | Totally-enclosed fireproof bus and manufacturing process thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN114437504B (en) |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4713302A (en) * | 1982-12-22 | 1987-12-15 | Tokyo Shibaura Denki Kabushiki Kaisha | Sintered ceramic body |
US5589714A (en) * | 1992-06-08 | 1996-12-31 | The Dow Chemical Company | Epoxy polymer filled with aluminum nitride-containing polymer and semiconductor devices encapsulated with a thermosetting resin containing aluminum nitride particles |
JP2004083334A (en) * | 2002-08-27 | 2004-03-18 | Toyo Aluminium Kk | Aluminum nitride powder |
JP2014001286A (en) * | 2012-06-15 | 2014-01-09 | Toshiba Corp | Fluophor and manufacturing method of the same, and light-emitting device using the same |
CN103618273A (en) * | 2013-10-10 | 2014-03-05 | 江苏江城电气有限公司 | Waterproof bus duct used in high temperature environment |
CN104946028A (en) * | 2015-06-02 | 2015-09-30 | 金海新源电气江苏有限公司 | Coating process of insulating material for bus ducts |
CN108462130A (en) * | 2018-04-08 | 2018-08-28 | 江苏银庆电气有限公司 | Fireproof bus duct and preparation method thereof |
CN108963926A (en) * | 2018-06-06 | 2018-12-07 | 荣马电器有限公司 | A kind of high-strength bus duct and preparation method thereof |
CN110233454A (en) * | 2019-06-05 | 2019-09-13 | 辰亮科技信息服务(江苏)有限公司 | A kind of high heat dissipation bus duct and preparation method thereof |
CN110669316A (en) * | 2019-10-24 | 2020-01-10 | 瑞鑫集团有限公司 | Insulating material for bus duct |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1278995C (en) * | 2005-04-07 | 2006-10-11 | 上海交通大学 | Method for preventing hydrolysis of aluminium nitride |
EP2894126B1 (en) * | 2012-09-07 | 2018-08-01 | Tokuyama Corporation | Method for producing water-resistant aluminum nitride powder |
WO2017098566A1 (en) * | 2015-12-07 | 2017-06-15 | 株式会社日立製作所 | Electrical insulating material for high-voltage devices |
KR20190097602A (en) * | 2018-02-12 | 2019-08-21 | 주식회사 케이씨씨 | Powder coating composition |
US11401599B2 (en) * | 2018-06-18 | 2022-08-02 | Applied Materials, Inc. | Erosion resistant metal silicate coatings |
JP6687818B1 (en) * | 2018-08-24 | 2020-04-28 | 昭和電工株式会社 | Method for producing silicon-containing oxide-coated aluminum nitride particles and silicon-containing oxide-coated aluminum nitride particles |
CN109326405A (en) * | 2018-09-26 | 2019-02-12 | 合肥博微田村电气有限公司 | A kind of preparation method and soft magnetic metal powder of high heat conductive insulating soft magnetic metal powder |
-
2021
- 2021-12-30 CN CN202111655433.7A patent/CN114437504B/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4713302A (en) * | 1982-12-22 | 1987-12-15 | Tokyo Shibaura Denki Kabushiki Kaisha | Sintered ceramic body |
US5589714A (en) * | 1992-06-08 | 1996-12-31 | The Dow Chemical Company | Epoxy polymer filled with aluminum nitride-containing polymer and semiconductor devices encapsulated with a thermosetting resin containing aluminum nitride particles |
JP2004083334A (en) * | 2002-08-27 | 2004-03-18 | Toyo Aluminium Kk | Aluminum nitride powder |
JP2014001286A (en) * | 2012-06-15 | 2014-01-09 | Toshiba Corp | Fluophor and manufacturing method of the same, and light-emitting device using the same |
CN103618273A (en) * | 2013-10-10 | 2014-03-05 | 江苏江城电气有限公司 | Waterproof bus duct used in high temperature environment |
CN104946028A (en) * | 2015-06-02 | 2015-09-30 | 金海新源电气江苏有限公司 | Coating process of insulating material for bus ducts |
CN108462130A (en) * | 2018-04-08 | 2018-08-28 | 江苏银庆电气有限公司 | Fireproof bus duct and preparation method thereof |
CN108963926A (en) * | 2018-06-06 | 2018-12-07 | 荣马电器有限公司 | A kind of high-strength bus duct and preparation method thereof |
CN110233454A (en) * | 2019-06-05 | 2019-09-13 | 辰亮科技信息服务(江苏)有限公司 | A kind of high heat dissipation bus duct and preparation method thereof |
CN110669316A (en) * | 2019-10-24 | 2020-01-10 | 瑞鑫集团有限公司 | Insulating material for bus duct |
Non-Patent Citations (1)
Title |
---|
DC link bus design for high frequency, high temperature converters;Joshua Stewart;《2017 IEEE Applied Power Electronics Conference and Exposition (APEC)》;20170518;全文 * |
Also Published As
Publication number | Publication date |
---|---|
CN114437504A (en) | 2022-05-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111303636B (en) | Low-heat-conductivity flame-retardant fireproof silicone rubber composite material and preparation method thereof | |
CN101468906B (en) | SiO2 enriched nano composite inorganic flame-retardant heat insulating thermal preserving board and manufacturing process thereof | |
CN108189520A (en) | A kind of production method of modified polytetrafluoroethylcopper copper clad plate | |
CN108117811B (en) | Graphene-silicon electromagnetic shielding filler and electromagnetic shielding coating | |
CN105859306A (en) | Flexible flame-retardant incrusted fireproof refractory porcelainized mixture | |
CN106046684B (en) | A kind of hot-face insulation bus duct | |
CN109285685A (en) | A kind of preparation method of high magnetic permeability aerosolization Fe-Si-Al magnetic core | |
CN112266648B (en) | Steel structure with fireproof coating layer and preparation method thereof | |
CN112279685A (en) | MTaO with environmental thermal barrier coating4Graphite-based composite material and preparation method thereof | |
CN114437504B (en) | Totally-enclosed fireproof bus and manufacturing process thereof | |
CN111533486A (en) | Graphene modified resin packaging material and preparation method thereof | |
CN106882922A (en) | A kind of seal glass of resistance to 550 DEG C of high temperature and preparation method thereof | |
CN108587290A (en) | A kind of steady weather-proof high insulating property wire enamel and preparation method thereof of property | |
CN104650597A (en) | Preparation method of fire-preventing and fire-resisting silicon rubber capable of being ceramized | |
US6699522B2 (en) | Inorganic insulation coating material | |
CN113527892A (en) | Ceramizable silicone rubber and preparation method and application thereof | |
CN111902036A (en) | Electromagnetic wave noise suppression sheet and high-frequency electronic equipment | |
CN105776256A (en) | Preparation method for moisture-proof magnesium oxide powder for insulated cables | |
WO2022095597A1 (en) | Alumina composite ceramic, preparation method therefor, and application therefor | |
CN107057365B (en) | Flame-retardant ceramifiable silicon rubber for fire-resistant cable and preparation method thereof | |
CN114437497B (en) | Energy-saving heat-resistant corrosion-resistant high-voltage tube bus | |
CN114974684A (en) | Wear-resistant tear-resistant silicone rubber wire cable and preparation method thereof | |
CN112142485B (en) | Ceramic fiber material and preparation method thereof | |
CN107746576A (en) | A kind of silica/micro- swollen graphite/graphite composite heat-conducting silicone grease and preparation method thereof | |
CN113817196A (en) | Polyimide film having improved alkali resistance and method for preparing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |