WO2020057096A1 - In-situ silicon carbide-iron silicon composite material and preparation method therefor - Google Patents

In-situ silicon carbide-iron silicon composite material and preparation method therefor Download PDF

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WO2020057096A1
WO2020057096A1 PCT/CN2019/080546 CN2019080546W WO2020057096A1 WO 2020057096 A1 WO2020057096 A1 WO 2020057096A1 CN 2019080546 W CN2019080546 W CN 2019080546W WO 2020057096 A1 WO2020057096 A1 WO 2020057096A1
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silicon carbide
iron
composite material
situ
raw materials
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马北越
任鑫明
苏畅
于景坤
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东北大学
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Definitions

  • the invention belongs to the technical field of composite material preparation, and particularly relates to an in-situ silicon carbide-iron-silicon composite material and a preparation method thereof.
  • Silicon carbide ceramics have excellent mechanical properties, such as low friction coefficient, high bending strength, and excellent thermal and electrical properties. Excellent mechanical properties make silicon carbide one of the important structural materials, such as bearings, mechanical seal rings, and armored vehicle bulletproof plates. Outstanding thermal and electrical properties make SiC useful in the fabrication of certain functional materials, such as catalyst carriers, electronic heat sinks, and sensitive resistors, with great application potential.
  • silicon carbide because of its poor wettability with common metals such as Fe and Al, the interface between the metal and ceramic is poor, which affects the final performance of the material. This is also one of the difficulties of the current silicon carbide-metal composite materials. With the rapid development of high-tech industries such as aerospace, automotive, and atomic energy, the demand for low-cost and high-performance silicon carbide-based composite materials will increase.
  • the purpose of the present invention is to overcome the shortcomings of the prior art described above, and to solve the defects of poor interface bonding and complex preparation process of silicon carbide-metal composite materials, and provide an in-situ silicon carbide-iron silicon composite material and preparation thereof.
  • method Using silicon carbide and iron oxide as raw materials, an iron-silicon reinforcing phase is formed in situ at high temperatures. Because the intermetallic compound iron-silicon and silicon carbide have better wetting properties, and at the same time, when the iron-silicon is formed in situ, a part of the liquid phase is generated, and liquid-phase sintering is initiated to promote sintering.
  • the present invention adopts the following technical solutions:
  • An in-situ silicon carbide-iron-silicon composite material includes a raw material and a binder, wherein the raw material components and their mass percentages are: 35-73% of silicon carbide, 5-12% of carbon powder, and iron oxide 22 -53%, and the added mass of the binder is 1 to 5% of the total mass of the raw materials.
  • the silicon carbide is industrial silicon carbide powder with a purity of ⁇ 98%.
  • the carbon powder is one or more of activated carbon, carbon black, graphite or charcoal.
  • iron oxide is chemically or industrially pure Fe 2 O 3 , and the added amount and carbon powder follow the following chemical formula ratio: 3C (s) + Fe 2 O 3 (s) ⁇ 2Fe (s) + 3CO (g).
  • the binder is one or more of a solid phenolic resin, a liquid phenolic resin, asphalt, or water glass.
  • the in-situ silicon carbide-iron-silicon composite material phase is ⁇ -SiC, SiO 2 , FexSiy (FeSi, FeSi 2 , Fe 3 Si, Fe 5 Si 3 ) and C, and the apparent porosity is 42-68%.
  • the bulk density is 1.3 to 1.8 g ⁇ cm -3
  • the compressive strength at room temperature is 6.4 to 15.8 MPa
  • the number of air-cooled thermal shock cycles from room temperature to 1000 ° C reaches 50 to 66 times.
  • a method for preparing an in-situ silicon carbide-iron-silicon composite material includes the following steps:
  • the pressed green body is fully dried in a drying box or a tunnel drying kiln;
  • the dried sample is put into a high-temperature furnace, and sintering is completed under the protection of high-purity argon. After the furnace is cooled, an in-situ silicon carbide-iron-silicon composite material is prepared.
  • the mixing method in the step (1) is high-energy ball milling.
  • the high-energy ball milling is mixed at a 2: 1 ball-to-material ratio, the ball milling speed is 200-400 r ⁇ min -1 , and the ball milling time is 1-8 h.
  • the press forming operation is performed in a stainless steel mold.
  • the molding method in the step (2) is one of compression molding or isostatic pressing, and the molding pressure is 50 to 300 MPa, and the holding time is 3 to 5 minutes.
  • the drying temperature in the step (3) is 70 to 120 ° C, and the drying and holding time is 8 to 12 hours.
  • the high temperature furnace in the step (4) is one of a box resistance furnace, a tube resistance furnace, and a tunnel kiln; the sintering temperature is 1400 to 1600 ° C, and the sintering holding time is 2 to 10 hours.
  • the ferro-silicon phase is generated in situ by the carbothermal reduction method, and the compound with the silicon carbide interface is better, and the problem of poor interface bonding of the traditional silicon carbide-metal composite material is solved.
  • iron oxide can also be used as an iron source and a pore-forming agent
  • carbon powder can be used as a reducing agent and a pore-forming agent.
  • the porous silicon carbide-iron-silicon composite material can be made by adjusting the addition amount to expand the carbonization. Applications of silicon-iron-silicon composites.
  • FIG. 1 is a process flowchart of the present invention
  • FIG. 2 is an XRD pattern of the silicon carbide-iron-silicon composite material prepared in Example 3.
  • FIG. 2 is an XRD pattern of the silicon carbide-iron-silicon composite material prepared in Example 3.
  • the silicon carbide used in the examples is commercially available industrial silicon carbide powder with a purity of ⁇ 98%.
  • An in-situ silicon carbide-iron-silicon composite material includes a raw material and a solid phenolic resin, wherein the raw material components and their mass percentages are: 73% silicon carbide, 5% carbon powder, and 22% iron oxide; The added mass of solid phenolic resin is 3% of the total mass of the raw materials.
  • FIG. 1 A method for preparing an in-situ silicon carbide-iron-silicon composite material.
  • the process flow chart is shown in FIG. 1 and is made by the following specific steps:
  • the phase of the obtained silicon carbide-iron-silicon composite was 6H-SiC and Fe 3 Si; the apparent porosity was 42%; the bulk density was 1.8g ⁇ cm -3 ; the compressive strength at room temperature was 15.8MPa; room temperature The number of air-cooled thermal shock cycles to 1000 ° C reached 55.
  • An in-situ silicon carbide-iron-silicon composite material includes a raw material and a solid phenolic resin, wherein the raw material components and their mass percentages are: 57% industrial silicon carbide powder, 8% carbon powder, and ferric oxide 35 %, The added mass of the solid phenolic resin is 5% of the total mass of the raw materials, wherein the carbon powder is a 1: 1 mixture of graphite and activated carbon.
  • FIG. 1 A method for preparing an in-situ silicon carbide-iron-silicon composite material.
  • the process flow chart is shown in FIG. 1 and is made by the following specific steps:
  • the phase of the obtained silicon carbide-iron-silicon composite is 6H-SiC, Fe 3 Si, and SiO 2 ; the apparent porosity is 50%; the bulk density is 1.74 g ⁇ cm -3 ; the compressive strength at room temperature is 10.9 MPa; Shock test: The number of air-cooled thermal shock cycles from room temperature to 1000 has reached 50 times.
  • An in-situ silicon carbide-iron-silicon composite material includes a raw material and a liquid phenolic resin, wherein the raw material components and their mass percentages are: industrial silicon carbide powder silicon carbide 35%, carbon powder 12%, and trioxide The iron is 53%, and the added mass of the liquid phenolic resin is 5% of the total mass of the raw materials.
  • FIG. 1 A method for preparing an in-situ silicon carbide-iron-silicon composite material.
  • the process flow chart is shown in FIG. 1 and is made by the following specific steps:
  • the phase of the obtained silicon carbide-iron-silicon composite is 6H-SiC, Fe 3 Si, Fe 5 Si 3 , SiO 2 , C; the apparent porosity is 68%; the bulk density is 1.37 g ⁇ cm -3 ; The compressive strength is 6.4 MPa; the number of air-cooled thermal shock cycles from room temperature to 1000 ° C reaches 66 times.

Abstract

An in-situ silicon carbide-iron silicon composite material and a preparation method therefor, the composite material comprising raw materials and a binder; the raw material components and the mass percentages thereof are as follows: 35-73% of silicon carbide, 5-12% of carbon powder, and 22-53% of iron oxide; the added mass of the binder is 1-5% of the total mass of the raw materials. The method steps are as follows: (1) according to mass percentage, mixing the raw materials uniformly, and adding a corresponding amount of the binder according to mass so that the binder and the raw materials are uniformly mixed to form mixed raw materials; (2) pressing and molding the mixed raw materials; (3) fully drying a pressed and molded green body in a drying box or a tunnel drying kiln; (4) placing a dried sample into a high-temperature furnace, completing sintering under the protection of high-purity argon, and fabricating an in-situ silicon carbide-iron silicon composite material after cooling in the furnace. A carbothermal reduction method is used to generate a ferro-silicon phase in situ, and thus compounding with a silicon carbide interface is better, and the sintering temperature of the material is reduced to save energy consumption; in addition, a porous silicon carbide-iron silicon composite material may be fabricated.

Description

一种原位碳化硅-铁硅复合材料及其制备方法In-situ silicon carbide-iron-silicon composite material and preparation method thereof 技术领域：Technical field:
本发明属于复合材料制备技术领域，具体涉及一种原位碳化硅-铁硅复合材料及其制备方法。The invention belongs to the technical field of composite material preparation, and particularly relates to an in-situ silicon carbide-iron-silicon composite material and a preparation method thereof.
背景技术：Background technique:
碳化硅陶瓷具有优异的机械性能，如：摩擦系数低，抗弯强度高，且其热学和电学性能也非常出众。优异的机械性能使得碳化硅成为重要的结构材料之一，如轴承、机械密封环、装甲车防弹板等。出众的热学性能和电性能又使得碳化硅可用于制作某些功能材料，如催化剂载体、电子散热板、敏感电阻等，应用潜力巨大。Silicon carbide ceramics have excellent mechanical properties, such as low friction coefficient, high bending strength, and excellent thermal and electrical properties. Excellent mechanical properties make silicon carbide one of the important structural materials, such as bearings, mechanical seal rings, and armored vehicle bulletproof plates. Outstanding thermal and electrical properties make SiC useful in the fabrication of certain functional materials, such as catalyst carriers, electronic heat sinks, and sensitive resistors, with great application potential.
但是，本征脆性是陶瓷材料一种天然的缺陷，碳化硅也不例外。同时，因为碳化硅是强共价键化合物，常规烧结时扩散系数很低，一般需要很高的烧结温度才能最终成型。因此，可选用有较好韧性的金属(Fe、Al、Cu等)与之复合，以解决脆性和强度不足的缺陷，同时在烧结过程中加入一些烧结助剂(Al 2O 3+Y 2O 3、V 2O 5、MgO等)引发液相烧结，促进碳化硅的结晶过程和致密化行为。但对碳化硅而言，因为其与Fe、Al等常见金属的润湿性很差，导致金属与陶瓷之间的界面结合很差，影响了材料的最终性能。这也是目前碳化硅-金属复合材料的难点之一。随着航空航天、汽车、原子能等高精尖行业的迅猛发展，对低成本高性能碳化硅基复合材料的需求将日益增加。 However, intrinsic brittleness is a natural defect of ceramic materials, and silicon carbide is no exception. At the same time, because silicon carbide is a strong covalent bond compound, the diffusion coefficient is low during conventional sintering. Generally, a high sintering temperature is required for final molding. Therefore, a metal with better toughness (Fe, Al, Cu, etc.) can be used to compound it to solve the defects of brittleness and insufficient strength. At the same time, some sintering aids (Al 2 O 3 + Y 2 O) are added during the sintering process. 3 , V 2 O 5 , MgO, etc.) initiate liquid phase sintering, promote the crystallization process and densification behavior of silicon carbide. But for silicon carbide, because of its poor wettability with common metals such as Fe and Al, the interface between the metal and ceramic is poor, which affects the final performance of the material. This is also one of the difficulties of the current silicon carbide-metal composite materials. With the rapid development of high-tech industries such as aerospace, automotive, and atomic energy, the demand for low-cost and high-performance silicon carbide-based composite materials will increase.
发明内容：Summary of the invention:
本发明的目的是克服上述现有技术存在的不足，旨在解决碳化硅-金属复合材料界面结合差、制备过程复杂等缺陷，并提供了一种原位碳化硅-铁硅复合材料及其制备方法。以碳化硅和氧化铁为原料，高温原位形成铁硅增强相。因为金属间化合物铁硅与碳化硅有更好的润湿性能，同时在原位形成铁硅时会生成部分液相，引发液相烧结以促进烧结。The purpose of the present invention is to overcome the shortcomings of the prior art described above, and to solve the defects of poor interface bonding and complex preparation process of silicon carbide-metal composite materials, and provide an in-situ silicon carbide-iron silicon composite material and preparation thereof. method. Using silicon carbide and iron oxide as raw materials, an iron-silicon reinforcing phase is formed in situ at high temperatures. Because the intermetallic compound iron-silicon and silicon carbide have better wetting properties, and at the same time, when the iron-silicon is formed in situ, a part of the liquid phase is generated, and liquid-phase sintering is initiated to promote sintering.
为实现上述目的，本发明采用以下技术方案：To achieve the above objective, the present invention adopts the following technical solutions:
一种原位碳化硅-铁硅复合材料，包括原料和粘结剂，其中，所述的原料组分及其质量百分比为，碳化硅35～73％，碳粉5～12％和氧化铁22～53％，所述的粘结剂添加质量为原料总质量的1～5％。An in-situ silicon carbide-iron-silicon composite material includes a raw material and a binder, wherein the raw material components and their mass percentages are: 35-73% of silicon carbide, 5-12% of carbon powder, and iron oxide 22 -53%, and the added mass of the binder is 1 to 5% of the total mass of the raw materials.
进一步地，所述的碳化硅为纯度≥98％的工业碳化硅粉。Further, the silicon carbide is industrial silicon carbide powder with a purity of ≧ 98%.
进一步地，所述的碳粉为活性炭、炭黑、石墨或木炭的一种或多种。Further, the carbon powder is one or more of activated carbon, carbon black, graphite or charcoal.
进一步地，所述的氧化铁为化学纯或工业纯Fe 2O 3，并且加入量与碳粉遵循如下化学式 配比：3C(s)+Fe 2O 3(s)→2Fe(s)+3CO(g)。 Further, the iron oxide is chemically or industrially pure Fe 2 O 3 , and the added amount and carbon powder follow the following chemical formula ratio: 3C (s) + Fe 2 O 3 (s) → 2Fe (s) + 3CO (g).
进一步地，所述的粘结剂为固态酚醛树脂、液态酚醛树脂、沥青或水玻璃中的一种或多种。Further, the binder is one or more of a solid phenolic resin, a liquid phenolic resin, asphalt, or water glass.
所述的原位碳化硅-铁硅复合材料物相为α-SiC、SiO 2、FexSiy(FeSi、FeSi 2、Fe 3Si、Fe 5Si 3)和C，显气孔率为42～68％，体积密度为1.3～1.8g·cm -3，常温抗压强度为6.4～15.8MPa，室温至1000℃的空冷热震循环次数达到50～66次。 The in-situ silicon carbide-iron-silicon composite material phase is α-SiC, SiO 2 , FexSiy (FeSi, FeSi 2 , Fe 3 Si, Fe 5 Si 3 ) and C, and the apparent porosity is 42-68%. The bulk density is 1.3 to 1.8 g · cm -3 , the compressive strength at room temperature is 6.4 to 15.8 MPa, and the number of air-cooled thermal shock cycles from room temperature to 1000 ° C reaches 50 to 66 times.
一种原位碳化硅-铁硅复合材料的制备方法，包括以下步骤：A method for preparing an in-situ silicon carbide-iron-silicon composite material includes the following steps:
(1)配料：(1) ingredients:
按质量百分比：碳化硅35～73％，碳粉5～12％，氧化铁22～53％，将原料混合均匀，并按质量添加原料1～5％的粘结剂，使粘结剂与原料均匀混合，形成混合原料；By mass percentage: 35 ~ 73% of silicon carbide, 5 ~ 12% of carbon powder, 22 ~ 53% of iron oxide, mix the raw materials uniformly, and add 1 ~ 5% of the binder of the raw materials by mass to make the binder and raw materials Mix evenly to form mixed raw materials;
(2)成型：(2) Forming:
将混合原料压制成型；Press molding the mixed raw materials;
(3)干燥：(3) Drying:
将压制成型的生坯在干燥箱或隧道干燥窑中充分干燥；The pressed green body is fully dried in a drying box or a tunnel drying kiln;
(4)烧结：(4) Sintering:
将经过干燥的试样放入高温炉，并在高纯氩气保护下完成烧结，随炉冷却后制得原位碳化硅-铁硅复合材料。The dried sample is put into a high-temperature furnace, and sintering is completed under the protection of high-purity argon. After the furnace is cooled, an in-situ silicon carbide-iron-silicon composite material is prepared.
进一步地，所述步骤(1)中的混合方式为高能球磨，所述的高能球磨按2∶1球料比混合，球磨转速为200～400r·min -1，球磨时间为1～8h。 Further, the mixing method in the step (1) is high-energy ball milling. The high-energy ball milling is mixed at a 2: 1 ball-to-material ratio, the ball milling speed is 200-400 r · min -1 , and the ball milling time is 1-8 h.
进一步地，所述步骤(2)中，压制成型操作在不锈钢模具中进行。Further, in the step (2), the press forming operation is performed in a stainless steel mold.
进一步地，所述步骤(2)中的成型方式为模压成型或等静压成型的一种，成型压力为50～300MPa，保压时间为3～5min。Further, the molding method in the step (2) is one of compression molding or isostatic pressing, and the molding pressure is 50 to 300 MPa, and the holding time is 3 to 5 minutes.
进一步地，所述步骤(3)中的干燥温度为70～120℃，干燥保温时间为8～12h。Further, the drying temperature in the step (3) is 70 to 120 ° C, and the drying and holding time is 8 to 12 hours.
进一步地，所述步骤(4)中的高温炉为箱式电阻炉、管式电阻炉、隧道窑中的一种；烧结温度为1400～1600℃，烧结保温时间为2～10h。Further, the high temperature furnace in the step (4) is one of a box resistance furnace, a tube resistance furnace, and a tunnel kiln; the sintering temperature is 1400 to 1600 ° C, and the sintering holding time is 2 to 10 hours.
本发明的有益效果：The beneficial effects of the present invention:
(1)本发明采用碳热还原法原位生成铁硅相，与碳化硅界面复合更好，解决了传统碳化硅-金属复合材料界面结合差的问题。(1) In the present invention, the ferro-silicon phase is generated in situ by the carbothermal reduction method, and the compound with the silicon carbide interface is better, and the problem of poor interface bonding of the traditional silicon carbide-metal composite material is solved.
(2)在高温原位形成铁硅相的过程中，会有液相生成，少量液相将促进烧结过程，降低了材料的烧结温度，节约能耗。(2) During the in-situ formation of the iron-silicon phase at high temperature, a liquid phase is generated. A small amount of liquid phase will promote the sintering process, reduce the sintering temperature of the material, and save energy.
(3)在制备过程中氧化铁还可作为铁源和造孔剂，碳粉可作为还原剂和造孔剂，可通过调 整其添加量制成多孔碳化硅-铁硅复合材料，扩大了碳化硅-铁硅复合材料的应用范围。(3) In the preparation process, iron oxide can also be used as an iron source and a pore-forming agent, and carbon powder can be used as a reducing agent and a pore-forming agent. The porous silicon carbide-iron-silicon composite material can be made by adjusting the addition amount to expand the carbonization. Applications of silicon-iron-silicon composites.
附图说明：Brief description of the drawings:
图1为本发明的工艺流程图；FIG. 1 is a process flowchart of the present invention;
图2为实施例3制备的碳化硅-铁硅复合材料的XRD图。FIG. 2 is an XRD pattern of the silicon carbide-iron-silicon composite material prepared in Example 3. FIG.
具体实施方式：detailed description:
下面结合实施例对本发明作进一步的详细说明。The present invention will be further described in detail with reference to the following embodiments.
以下通过实施例对本发明的技术方案做更详细的说明，但本发明并不局限于以下实施例，所述只是适用本发明的部分实例。The technical solutions of the present invention will be described in more detail through the following examples, but the present invention is not limited to the following examples, and the descriptions are only some examples to which the present invention is applicable.
实施例中采用的碳化硅为市购纯度≥98％的工业碳化硅粉。The silicon carbide used in the examples is commercially available industrial silicon carbide powder with a purity of ≧ 98%.
实施例1Example 1
一种原位碳化硅-铁硅复合材料，包括原料和固态酚醛树脂，其中，所述的原料组分及其质量百分比为，碳化硅73％，碳粉5％和氧化铁22％；所述的固态酚醛树脂添加质量为原料总质量的3％。An in-situ silicon carbide-iron-silicon composite material includes a raw material and a solid phenolic resin, wherein the raw material components and their mass percentages are: 73% silicon carbide, 5% carbon powder, and 22% iron oxide; The added mass of solid phenolic resin is 3% of the total mass of the raw materials.
一种原位碳化硅-铁硅复合材料的制备方法，其工艺流程图如图1所示，由以下具体步骤制成：A method for preparing an in-situ silicon carbide-iron-silicon composite material. The process flow chart is shown in FIG. 1 and is made by the following specific steps:
(1)按质量分数为73％工业碳化硅粉、22％三氧化二铁，5％活性炭配料，另外加3％的固态酚醛树脂(与酒精一起使用)，并球磨转速为200～400r·min -1，球磨2h，形成混合原料； (1) According to the mass fraction of 73% industrial silicon carbide powder, 22% ferric oxide, 5% activated carbon, add 3% solid phenolic resin (used with alcohol), and the ball milling speed is 200 ～ 400r · min -1 , ball milling for 2h to form mixed raw materials;
(2)将混合原料装入不锈钢模具，用单轴手动压样机在100MPa压力下保压5min制成φ20mm×20mm的素坯；(2) Put the mixed raw materials into a stainless steel mold, and use a single-axis manual sample press to hold the pressure for 5 minutes at a pressure of 100 MPa to make a plain φ20mm × 20mm;
(3)将素坯在恒温干燥箱中100℃保温6h充分干燥；(3) The plain blank is fully dried in a constant temperature drying box at 100 ° C for 6 hours;
(4)将干燥后的素坯放入真空管式炉中以5℃/min升温至1400℃保温2h，随炉冷却，便可制得碳化硅-铁硅复合材料。(4) Put the dried blank into a vacuum tube furnace and raise the temperature to 5400 ° C / min to 1400 ° C for 2h, and then cool the furnace to obtain a silicon carbide-iron-silicon composite material.
本实施例相关性能指标如下：The relevant performance indicators of this embodiment are as follows:
经检测，制得碳化硅-铁硅复合材料的物相为6H-SiC、Fe 3Si；显气孔率为42％；体积密度为1.8g·cm -3；常温耐压强度为15.8MPa；室温至1000℃的空冷热震循环次数达到55次。 After testing, the phase of the obtained silicon carbide-iron-silicon composite was 6H-SiC and Fe 3 Si; the apparent porosity was 42%; the bulk density was 1.8g · cm -3 ; the compressive strength at room temperature was 15.8MPa; room temperature The number of air-cooled thermal shock cycles to 1000 ° C reached 55.
实施例2Example 2
一种原位碳化硅-铁硅复合材料，包括原料和固态酚醛树脂，其中，所述的原料组分及其质量百分比为，工业碳化硅粉57％，碳粉8％和三氧化二铁35％，所述的固态酚醛树脂添加质量为原料总质量的5％，其中，碳粉为石墨与活性炭1∶1混合的料。An in-situ silicon carbide-iron-silicon composite material includes a raw material and a solid phenolic resin, wherein the raw material components and their mass percentages are: 57% industrial silicon carbide powder, 8% carbon powder, and ferric oxide 35 %, The added mass of the solid phenolic resin is 5% of the total mass of the raw materials, wherein the carbon powder is a 1: 1 mixture of graphite and activated carbon.
一种原位碳化硅-铁硅复合材料的制备方法，其工艺流程图如图1所示，由以下具体步骤制成：A method for preparing an in-situ silicon carbide-iron-silicon composite material. The process flow chart is shown in FIG. 1 and is made by the following specific steps:
(1)按质量分数为工业碳化硅粉57％，碳粉8％和三氧化二铁35％配料，另外加5％的固态酚醛树脂(与酒精一起使用)，并球磨转速为200～400r·min -1，球磨2h，形成混合原料； (1) According to the mass fraction of 57% of industrial silicon carbide powder, 8% of carbon powder and 35% of ferric oxide, add 5% solid phenolic resin (used with alcohol), and the ball milling speed is 200 ～ 400r · min -1 , ball milling for 2h to form mixed raw materials;
(2)将混合原料装入不锈钢模具，用单轴手动压样机在100MPa压力下保压5min制成φ20mm×20mm的素坯；(2) Put the mixed raw materials into a stainless steel mold, and use a single-axis manual sample press to hold the pressure for 5 minutes at a pressure of 100 MPa to make a plain φ20mm × 20mm;
(3)将素坯在恒温干燥箱中100℃保温6h充分干燥；(3) The plain blank is fully dried in a constant temperature drying box at 100 ° C for 6 hours;
(4)将干燥后的素坯放入真空管式炉中以5℃/min升温至1500℃保温4h，随炉冷却，便可制得碳化硅-铁硅复合材料。(4) Put the dried blank into a vacuum tube furnace and raise the temperature to 5 ° C / min to 1500 ° C for 4h, and then cool the furnace to obtain a silicon carbide-iron-silicon composite material.
本实施例相关性能指标如下：The relevant performance indicators of this embodiment are as follows:
制得碳化硅-铁硅复合材料的物相为6H-SiC、Fe 3Si、SiO 2；显气孔率为50％；体积密度为1.74g·cm -3；常温耐压强度为10.9MPa；热震试验：室温至1000的空冷热震循环次数达到50次。 The phase of the obtained silicon carbide-iron-silicon composite is 6H-SiC, Fe 3 Si, and SiO 2 ; the apparent porosity is 50%; the bulk density is 1.74 g · cm -3 ; the compressive strength at room temperature is 10.9 MPa; Shock test: The number of air-cooled thermal shock cycles from room temperature to 1000 has reached 50 times.
实施例3Example 3
一种原位碳化硅-铁硅复合材料，包括原料和液态酚醛树脂，其中，所述的原料组分及其质量百分比为，工业碳化硅粉碳化硅35％，碳粉12％和三氧化二铁53％，所述的液态酚醛树脂添加质量为原料总质量的5％。An in-situ silicon carbide-iron-silicon composite material includes a raw material and a liquid phenolic resin, wherein the raw material components and their mass percentages are: industrial silicon carbide powder silicon carbide 35%, carbon powder 12%, and trioxide The iron is 53%, and the added mass of the liquid phenolic resin is 5% of the total mass of the raw materials.
一种原位碳化硅-铁硅复合材料的制备方法，其工艺流程图如图1所示，由以下具体步骤制成：A method for preparing an in-situ silicon carbide-iron-silicon composite material. The process flow chart is shown in FIG. 1 and is made by the following specific steps:
(1)按质量分数为工业碳化硅粉57％，碳粉8％和三氧化二铁35％配料，另外加5％的固态酚醛树脂(与酒精一起使用)，并球磨转速为200～400r·min -1，球磨2h，形成混合原料； (1) According to the mass fraction of 57% of industrial silicon carbide powder, 8% of carbon powder and 35% of ferric oxide, add 5% solid phenolic resin (used with alcohol), and the ball milling speed is 200 ～ 400r · min -1 , ball milling for 2h to form mixed raw materials;
(2)将混合原料装入不锈钢模具，用单轴手动压样机在100MPa压力下保压5min制成φ20mm×20mm的素坯；(2) Put the mixed raw materials into a stainless steel mold, and use a single-axis manual sample press to hold the pressure for 5 minutes at a pressure of 100 MPa to make a plain φ20mm × 20mm;
(3)将素坯在恒温干燥箱中100℃保温6h充分干燥；(3) The plain blank is fully dried in a constant temperature drying box at 100 ° C for 6 hours;
(4)将干燥后的素坯放入真空管式炉中以5℃/min升温至1600℃保温4h，随炉冷却，便可制得碳化硅-铁硅复合材料，其XRD图如图2所示。(4) Put the dried blank into a vacuum tube furnace and heat it to 1600 ℃ at 5 ℃ / min for 4h. After the furnace is cooled, the silicon carbide-iron-silicon composite material can be prepared. Show.
本实施例相关性能指标如下：The relevant performance indicators of this embodiment are as follows:
制得碳化硅-铁硅复合材料的物相为6H-SiC、Fe 3Si、Fe 5Si 3、SiO 2、C；显气孔率为68％；体积密度为1.37g·cm -3；常温耐压强度为6.4MPa；室温至1000℃的空冷热震循环次数达到66次。 The phase of the obtained silicon carbide-iron-silicon composite is 6H-SiC, Fe 3 Si, Fe 5 Si 3 , SiO 2 , C; the apparent porosity is 68%; the bulk density is 1.37 g · cm -3 ; The compressive strength is 6.4 MPa; the number of air-cooled thermal shock cycles from room temperature to 1000 ° C reaches 66 times.

Claims (10)

  1. 一种原位碳化硅-铁硅复合材料，其特征在于，包括原料和粘结剂，其中，所述的原料组分及其质量百分比为，碳化硅35～73％，碳粉5～12％和氧化铁22～53％，所述的粘结剂添加质量为原料总质量的1～5％。An in-situ silicon carbide-iron-silicon composite material, comprising a raw material and a binder, wherein the raw material components and their mass percentages are: 35-73% of silicon carbide, and 5-12% of carbon powder. And iron oxide are 22 to 53%, and the added mass of the binder is 1 to 5% of the total mass of the raw materials.
  2. 根据权利要求1所述的原位碳化硅-铁硅复合材料，其特征在于，所述的碳化硅为纯度≥98％的工业碳化硅粉。The in-situ silicon carbide-iron-silicon composite material according to claim 1, wherein the silicon carbide is an industrial silicon carbide powder having a purity of ≥98%.
  3. 根据权利要求1所述的原位碳化硅-铁硅复合材料，其特征在于，所述的碳粉为活性炭、炭黑、石墨或木炭的一种或多种。The in-situ silicon carbide-iron-silicon composite material according to claim 1, wherein the carbon powder is one or more of activated carbon, carbon black, graphite, or charcoal.
  4. 根据权利要求1所述的原位碳化硅-铁硅复合材料，其特征在于，所述的粘结剂为固态酚醛树脂、液态酚醛树脂、沥青或水玻璃中的一种或多种。The in-situ silicon carbide-iron-silicon composite material according to claim 1, wherein the binder is one or more of a solid phenolic resin, a liquid phenolic resin, asphalt, or water glass.
  5. 根据权利要求1所述的原位碳化硅-铁硅复合材料，其特征在于，所述的原位碳化硅-铁硅复合材料物相为α-SiC、SiO 2、Fe xSi y(FeSi、FeSi 2、Fe 3Si、Fe 5Si 3)和C，显气孔率为42～68％，体积密度为1.3～1.8g·cm -3，常温抗压强度为6.4～15.8MPa，室温至1000℃的空冷热震循环次数达到50～66次。 The in-situ silicon carbide-iron-silicon composite material according to claim 1, wherein the in-situ silicon carbide-iron-silicon composite material phase is α-SiC, SiO 2 , Fe x Si y (FeSi, FeSi 2 , Fe 3 Si, Fe 5 Si 3 ) and C. The apparent porosity is 42 to 68%, the bulk density is 1.3 to 1.8 g · cm -3 , the compressive strength at room temperature is 6.4 to 15.8 MPa, and the temperature is from room temperature to 1000 ° C. The number of air-cooled heat shock cycles reached 50 to 66 times.
  6. 权利要求1所述的原位碳化硅-铁硅复合材料的制备方法，其特征在于，包括以下步骤：The method for preparing an in-situ silicon carbide-iron-silicon composite material according to claim 1, comprising the following steps:
    (1)配料：(1) ingredients:
    按质量百分比：碳化硅35～73％，碳粉5～12％，氧化铁22～53％，将原料混合均匀，并按质量添加原料1～5％的粘结剂，使粘结剂与原料均匀混合，形成混合原料；By mass percentage: 35 ~ 73% of silicon carbide, 5 ~ 12% of carbon powder, 22 ~ 53% of iron oxide, mix the raw materials uniformly, and add 1 ~ 5% of the binder of the raw materials by mass to make the binder and raw materials Mix evenly to form mixed raw materials;
    (2)成型：(2) Forming:
    将混合原料压制成型；Press molding the mixed raw materials;
    (3)干燥：(3) Drying:
    将压制成型的生坯在干燥箱或隧道干燥窑中充分干燥；The pressed green body is fully dried in a drying box or a tunnel drying kiln;
    (4)烧结：(4) Sintering:
    将经过干燥的试样放入高温炉，并在高纯氩气保护下完成烧结，随炉冷却后制得原位碳化硅-铁硅复合材料。The dried sample is put into a high-temperature furnace, and sintering is completed under the protection of high-purity argon. After the furnace is cooled, an in-situ silicon carbide-iron-silicon composite material is prepared.
  7. 根据权利要求6所述的原位碳化硅-铁硅复合材料的制备方法，其特征在于，所述步骤(1)中的混合方式为高能球磨，所述的高能球磨按2:1球料比混合，球磨转速为200～400r·min -1，球磨时间为1～8h。 The method for preparing an in-situ silicon carbide-iron-silicon composite material according to claim 6, wherein the mixing method in the step (1) is high-energy ball milling, and the high-energy ball milling is based on a 2: 1 ball-material ratio Mixing, ball milling speed is 200 ～ 400r · min -1 , and ball milling time is 1 ～ 8h.
  8. 根据权利要求6所述的原位碳化硅-铁硅复合材料的制备方法，其特征在于，进一步地，所述步骤(2)中的成型方式为模压成型或等静压成型的一种，成型压力为50～300MPa，保压时间为3～5min。The method for preparing an in-situ silicon carbide-iron-silicon composite material according to claim 6, characterized in that, further, the molding method in the step (2) is one of compression molding or isostatic pressing, and molding The pressure is 50 ~ 300MPa, and the holding time is 3 ~ 5min.
  9. 根据权利要求6所述的原位碳化硅-铁硅复合材料的制备方法，其特征在于，所述步骤(3)中的干燥温度为70～120℃，干燥保温时间为8～12h。The method for preparing an in-situ silicon carbide-iron-silicon composite material according to claim 6, wherein the drying temperature in the step (3) is 70 to 120 ° C, and the drying and holding time is 8 to 12 hours.
  10. 根据权利要求6所述的原位碳化硅-铁硅复合材料的制备方法，其特征在于，所述步骤(4)中的高温炉为箱式电阻炉、管式电阻炉、隧道窑中的一种；烧结温度为1400～1600℃，烧结保温时间为2～10h。The method for preparing an in-situ silicon carbide-iron-silicon composite material according to claim 6, wherein the high temperature furnace in step (4) is one of a box resistance furnace, a tube resistance furnace, and a tunnel kiln. Sintering temperature is 1400 ～ 1600 ℃, sintering holding time is 2 ～ 10h.
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109160814A (en) * 2018-09-20 2019-01-08 东北大学 A kind of in-situ carbon SiClx-iron silicon composite and preparation method thereof
CN110918997A (en) * 2019-11-20 2020-03-27 内蒙古科技大学 Method for preparing porous stainless steel from iron scale

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60005096T2 (en) * 1999-07-21 2004-08-26 Institut Français Du Petrole Monolithic honeycomb structure made of porous ceramic material, and use as a particle filter
CN101863668A (en) * 2010-05-24 2010-10-20 北京科技大学 Method for synthesizing SiC/FexSiy composite material by using iron ore tailings
CN107686353A (en) * 2017-08-22 2018-02-13 东北大学 A kind of preparation method of high-strength conducting carbonization ferrosilicon composite porous ceramic
CN109160814A (en) * 2018-09-20 2019-01-08 东北大学 A kind of in-situ carbon SiClx-iron silicon composite and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60005096T2 (en) * 1999-07-21 2004-08-26 Institut Français Du Petrole Monolithic honeycomb structure made of porous ceramic material, and use as a particle filter
CN101863668A (en) * 2010-05-24 2010-10-20 北京科技大学 Method for synthesizing SiC/FexSiy composite material by using iron ore tailings
CN107686353A (en) * 2017-08-22 2018-02-13 东北大学 A kind of preparation method of high-strength conducting carbonization ferrosilicon composite porous ceramic
CN109160814A (en) * 2018-09-20 2019-01-08 东北大学 A kind of in-situ carbon SiClx-iron silicon composite and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112646989A (en) * 2020-12-08 2021-04-13 昆明理工大学 Method for preparing copper-based composite material by in-situ generation of carbonaceous reinforcement

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