CN114000069B - Preparation method of continuous SiC fiber reinforced metal matrix composite lattice structure - Google Patents
Preparation method of continuous SiC fiber reinforced metal matrix composite lattice structure Download PDFInfo
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- 239000000835 fiber Substances 0.000 title claims abstract description 19
- 239000011156 metal matrix composite Substances 0.000 title claims abstract description 13
- 238000002360 preparation method Methods 0.000 title claims description 11
- 239000002243 precursor Substances 0.000 claims abstract description 83
- 229910052751 metal Inorganic materials 0.000 claims abstract description 24
- 239000002184 metal Substances 0.000 claims abstract description 24
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims abstract description 24
- 239000004926 polymethyl methacrylate Substances 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 14
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- 239000000956 alloy Substances 0.000 claims description 7
- 239000010410 layer Substances 0.000 claims description 7
- 238000004321 preservation Methods 0.000 claims description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
- 239000002356 single layer Substances 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 238000005520 cutting process Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- 238000007731 hot pressing Methods 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 238000004804 winding Methods 0.000 claims description 2
- 238000002791 soaking Methods 0.000 claims 1
- 239000011229 interlayer Substances 0.000 abstract description 4
- 238000005336 cracking Methods 0.000 abstract description 3
- 238000007711 solidification Methods 0.000 abstract 1
- 230000008023 solidification Effects 0.000 abstract 1
- 239000011800 void material Substances 0.000 abstract 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 5
- 239000002131 composite material Substances 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 229910010293 ceramic material Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
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- 230000017525 heat dissipation Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 239000006262 metallic foam Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/02—Pretreatment of the fibres or filaments
- C22C47/04—Pretreatment of the fibres or filaments by coating, e.g. with a protective or activated covering
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/02—Pretreatment of the fibres or filaments
- C22C47/06—Pretreatment of the fibres or filaments by forming the fibres or filaments into a preformed structure, e.g. using a temporary binder to form a mat-like element
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/14—Making alloys containing metallic or non-metallic fibres or filaments by powder metallurgy, i.e. by processing mixtures of metal powder and fibres or filaments
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C49/00—Alloys containing metallic or non-metallic fibres or filaments
- C22C49/02—Alloys containing metallic or non-metallic fibres or filaments characterised by the matrix material
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C49/00—Alloys containing metallic or non-metallic fibres or filaments
- C22C49/14—Alloys containing metallic or non-metallic fibres or filaments characterised by the fibres or filaments
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Abstract
本发明涉及一种连续SiC纤维增强金属基复合材料点阵结构的制备方法,利用聚甲基丙酸甲酯(PMMA)在中低温(~270℃)下可以软化、熔融‑凝固及在中温(~400℃)可完全裂解为气体的特性,以PMMA熔融液浸泡SiCf‑金属先驱丝带,固化后可得到均匀排布的先驱丝带,将先驱丝带交替排布后升温加压,使得先驱丝相互接触且在压力作用下相对位置固定,进一步升温使PMMA裂解气化,同时多空结构有利于裂解气体的挥发,然后升温至一定温度,加压使先驱丝之间相互扩散连接形成整体,得到点阵结构。该方法制备的点阵结构,先驱丝间距均匀可控,层间先驱丝的相对角度可根据位置实时调整,可满足更多的设计结构需求。
The invention relates to a method for preparing a lattice structure of a continuous SiC fiber reinforced metal matrix composite material. Polymethyl methacrylate (PMMA) can be softened, melted-solidified at medium and low temperatures (~270° C.) ~400℃) can be completely cracked into gas, soak SiCf-metal precursor ribbons in PMMA melt, and obtain uniformly arranged precursor ribbons after solidification. The precursor ribbons are alternately arranged and then heated and pressurized, so that the precursor ribbons are in contact with each other And the relative position is fixed under the action of pressure, further heating makes PMMA cracking and gasifying, and the multi-void structure is conducive to the volatilization of the cracking gas, and then the temperature is raised to a certain temperature, and the pressure is applied to make the precursor filaments diffuse and connect to each other to form a whole, and a lattice is obtained. structure. The lattice structure prepared by the method has uniform and controllable spacing of the precursor wires, and the relative angle of the interlayer precursor wires can be adjusted in real time according to the position, which can meet more design structure requirements.
Description
技术领域technical field
本发明属于材料制备技术领域,具体涉及一种连续SiC纤维增强金属基复合材料点阵结构的制备方法。The invention belongs to the technical field of material preparation, and in particular relates to a preparation method of a lattice structure of a continuous SiC fiber reinforced metal matrix composite material.
背景技术Background technique
点阵材料是一种具有规则孔形和孔穴周期排布的一类新型多孔材料,它与传统材料最大的不同之处在于其具有千变万化的有序微结构与高孔隙率,还具有轻质高强、高效散热、吸收电磁波及声音、抗爆炸冲击等优异的性能,在同等重量下比无序微结构的金属泡沫具有更好的力学性能,因此在很多领域都有很大的应用潜力,如航空航天、交通运输、武器装备、建筑等。点阵材料常用的材质有金属材料、陶瓷材料及碳纤维增强树脂基复合材料等。金属材料具有较好的成型性但无法在较高温度下使用,碳纤维增强树脂基复合材料同样受限于服役温度且其抗压缩性能较差,陶瓷材料虽可在高温下服役但成型性较差,尤其是“阵点”之间的连接。Lattice material is a new type of porous material with regular pore shape and periodic arrangement of holes. The biggest difference from traditional materials is that it has ever-changing ordered microstructure and high porosity, as well as light weight and high strength. , efficient heat dissipation, absorption of electromagnetic waves and sound, anti-explosive shock and other excellent properties, under the same weight, it has better mechanical properties than metal foam with disordered microstructure, so it has great application potential in many fields, such as aviation Aerospace, transportation, weapons and equipment, construction, etc. Commonly used materials for lattice materials include metal materials, ceramic materials and carbon fiber reinforced resin matrix composite materials. Metal materials have good formability but cannot be used at higher temperatures. Carbon fiber reinforced resin matrix composites are also limited by service temperature and their compression resistance is poor. Although ceramic materials can be used at high temperatures, they have poor formability. , especially the connections between "dots".
因此,要满足较高温度使用且具有较好成型性的需求,需要利用好金属成型性好、陶瓷耐高温的特点,陶瓷/金属复合材料具有很好的设计空间,其中连续单丝SiC纤维陶瓷纤维具有优良的室高温拉伸、压缩及剪切强度,适用于作为金属基复合材料的增强体,且其直径较大,可操作性好,便于成型,而钛合金的中高温性能也较为优异,成型性较好,与SiC纤维具有好的化学相容性,因此连续SiC纤维增强钛基复合材料点阵结构具有较好的应用潜力。目前制备连续SiC纤维增强钛基复合材料点阵结构的工艺主要是通过设计先驱丝排布辅助模具,铺放先驱丝后真空热压成型。该方法是所需模具较为复杂,且每层先驱丝与其上下层相邻的先驱丝只有一个固定的相对角度。Therefore, in order to meet the needs of higher temperature use and better formability, it is necessary to make good use of the characteristics of metal formability and high temperature resistance of ceramics. Ceramic/metal composite materials have a good design space. Among them, continuous monofilament SiC fiber ceramics The fiber has excellent tensile, compressive and shear strength at room temperature, and is suitable for use as a reinforcement for metal matrix composites. It has a large diameter, good operability, and is easy to form. Titanium alloys also have excellent medium and high temperature properties. , good formability and good chemical compatibility with SiC fibers, so the lattice structure of continuous SiC fiber reinforced titanium matrix composites has good application potential. At present, the process of preparing the lattice structure of continuous SiC fiber reinforced titanium matrix composites is mainly by designing an auxiliary mold for the arrangement of precursor wires, and vacuum hot pressing after laying the precursor wires. In this method, the required mold is relatively complicated, and each layer of precursor wire has only a fixed relative angle with the adjacent precursor wire of the upper and lower layers.
发明内容SUMMARY OF THE INVENTION
为了克服制备连续SiC纤维增强金属基复合材料点阵结构所需先驱丝铺放辅助模具复杂、先驱丝排布角度相对单一等缺点,本发明的目的在于提供一种可简化制备过程所需辅助模具,先驱丝排布角度可调、可变的SiC纤维增强金属基复合材料点阵结构制备工艺。In order to overcome the disadvantages of complex precursor wire laying auxiliary mold and relatively single distribution angle of precursor wire required for the preparation of continuous SiC fiber-reinforced metal matrix composite lattice structure, the purpose of the present invention is to provide an auxiliary mold that can simplify the preparation process. , Pioneering wire arrangement angle adjustable, variable SiC fiber reinforced metal matrix composite material lattice structure preparation process.
为了实现上述目的,本发明采用以下技术方案:In order to achieve the above object, the present invention adopts the following technical solutions:
一种连续SiC纤维增强金属基复合材料点阵结构的制备方法,其特征在于,制备过程按以下步骤进行:A preparation method of continuous SiC fiber reinforced metal matrix composite material lattice structure, characterized in that, the preparation process is carried out according to the following steps:
步骤一、裁剪连续SiCf-金属先驱丝,得到由一组平行排布,间隔均匀的先驱丝组成的先驱丝带,具体地,可通过将连续SiCf-金属先驱丝缠绕在圆筒外侧,将先驱丝的相对间距进行固定后沿圆筒母线裁剪得到所述先驱丝带,这样可以提高均匀性及效率。相邻先驱丝之间的中心距离可根据设计要求通过控制缠绕节距控制在0.2mm~3mm之间,并且可根据具体设计要求调整。其中所述连续SiCf-金属先驱丝为表面带有20μm~100μm厚的金属或其合金的涂层的SiC纤维。所述金属可以选自钛、铜、铁、镍、铝、镁或钨等。Step 1, cutting the continuous SiC f -metal precursor wire to obtain a precursor ribbon composed of a group of parallel arranged precursor wires with uniform spacing . The relative spacing of the precursor wires is fixed, and then the precursor ribbons are obtained by cutting along the cylindrical bus bar, which can improve the uniformity and efficiency. The center distance between adjacent precursor wires can be controlled between 0.2 mm and 3 mm by controlling the winding pitch according to design requirements, and can be adjusted according to specific design requirements. The continuous SiC f -metal precursor wire is a SiC fiber with a coating of metal or its alloy with a thickness of 20 μm to 100 μm on the surface. The metal may be selected from titanium, copper, iron, nickel, aluminum, magnesium or tungsten, among others.
步骤二、用聚甲基丙酸甲酯熔融液浸泡步骤一制得的先驱丝带固化后得到单层先驱丝板;具体地,可以将步骤一中的先驱丝带置于深度为预定深度的凹槽内并固定;将聚甲基丙酸甲酯(PMMA)加热至熔融状态后倒入凹槽直至完全浸没先驱丝带,冷却后聚甲基丙酸甲酯固化将所述先驱丝的相对位置固定,制得所述单层先驱丝板。当所述连续SiCf-金属先驱丝为表面带有20μm~100μm厚的金属或其合金的涂层的直径100μm的SiC纤维时,所述凹槽的预定深度可以为0.15~0.5mm。Step 2, soak the precursor ribbon prepared in step 1 with polymethyl methacrylate melt and solidify to obtain a single-layer precursor ribbon; specifically, the precursor ribbon in step 1 can be placed in a groove with a predetermined depth inside and fixed; polymethyl methacrylate (PMMA) is heated to a molten state and poured into the groove until the pioneer ribbon is completely immersed, and the polymethyl methacrylate solidifies after cooling to fix the relative position of the pioneer silk, The single-layer precursor silk sheet was prepared. When the continuous SiC f -metal precursor wire is a SiC fiber with a diameter of 100 μm with a coating of 20 μm to 100 μm thick metal or its alloy on the surface, the predetermined depth of the groove may be 0.15 to 0.5 mm.
步骤三、重复步骤二或采用多个凹槽同步进行先驱丝板的制备,制备多个先驱丝板;Step 3, repeating Step 2 or using multiple grooves to simultaneously prepare the precursor silk sheets to prepare multiple pioneer silk sheets;
步骤四、将步骤三中制得的先驱丝板进行堆叠,相邻两层先驱丝板中的先驱丝呈一定角度排布;所述角度一般为20°~90°,取决于设计要求。Step 4. Stack the precursor wire plates prepared in step 3, and the precursor wires in the adjacent two layers of precursor wire plates are arranged at a certain angle; the angle is generally 20° to 90°, depending on design requirements.
步骤五、将步骤四中堆垛在一起的先驱丝板置于真空热压炉,施加0.01MPa~0.5MPa的压力,抽真空至10-2Pa,升温至180℃~200℃,升温时间为2h~3h,升温过程中PMMA会软化、熔融,保温保压1h~3h,压力作用使得层间的SiCf-金属先驱丝达到相互接触的状态;升温至270℃~400℃,保温保压4h~6h,在该温度下PMMA完全裂解为气体;然后升温至金属熔点的0.4~0.8倍的温度(当金属为钛时,700℃~1000℃(由钛合金牌号决定)),加压至0.5MPa~40MPa,保温保压2h~10h,使得相接触的先驱丝之间相互扩散连接成为整体,炉冷至低于200℃后卸压取出,得到连续SiC纤维增强金属基复合材料点阵结构。Step 5. Place the stacking precursor wire plates in step 4 in a vacuum hot-pressing furnace, apply a pressure of 0.01 MPa to 0.5 MPa, evacuate to 10 -2 Pa, and heat up to 180 ℃ to 200 ℃, and the heating time is 2h ~ 3h, PMMA will soften and melt during the heating process, keep the heat preservation and pressure for 1h ~ 3h, the pressure will make the SiC f -metal precursor wires between the layers reach the state of mutual contact; increase the temperature to 270℃ ~ 400℃, keep the heat preservation and pressure for 4h ~6h, at this temperature, PMMA is completely cracked into gas; then it is heated to a temperature of 0.4 to 0.8 times the melting point of the metal (when the metal is titanium, 700 ° C ~ 1000 ° C (determined by the titanium alloy grade)), pressurized to 0.5 MPa ~ 40MPa, heat preservation and pressure for 2h ~ 10h, so that the mutual diffusion connection between the contacting precursor filaments becomes a whole, and the furnace is cooled to less than 200 ℃, and then the pressure is relieved and taken out, and the continuous SiC fiber reinforced metal matrix composite material lattice structure is obtained.
本发明的优点:(1)本发明制备过程不需要复杂的先驱丝铺放模具,同时能实现先驱丝间距均匀可控,且PMMA具有良好的透光性,可以目视检查、筛选制备的先驱丝板排布均匀性及缺陷;(2)金属基复合材料点阵结构大量的孔隙便于PMMA裂解后气体的挥发;(3)本发明突破了现有的模具方法对层间先驱丝固定、单一角度的限制,层间先驱丝的排布角度更为灵活,能更灵活地满足设计需求;(4)本方法得到的金属基复合材料点阵结构最表层为金属或其合金,便于通过焊接与其他构件/结构连接,连接位置具有耐高温、强度高的优势。The advantages of the present invention: (1) the preparation process of the present invention does not require a complex precursor wire laying die, and at the same time, the spacing of the precursor wires can be uniform and controllable, and the PMMA has good light transmittance, which can be visually inspected and screened. The uniformity and defects of the silk plate arrangement; (2) the large number of pores in the lattice structure of the metal matrix composite material facilitates the volatilization of the gas after the PMMA cracking; Due to the limitation of the angle, the arrangement angle of the interlayer precursor wires is more flexible, which can more flexibly meet the design requirements; (4) the outermost layer of the lattice structure of the metal matrix composite material obtained by this method is metal or its alloy, which is convenient for welding and welding. For other component/structural connections, the connection position has the advantages of high temperature resistance and high strength.
附图说明Description of drawings
图1是本发明的先驱丝板的制备及堆垛过程示意图;Fig. 1 is the preparation and stacking process schematic diagram of the pioneer silk plate of the present invention;
图2为本发明方法制备的点阵结构的示意图。FIG. 2 is a schematic diagram of a lattice structure prepared by the method of the present invention.
具体实施方式Detailed ways
为了更清楚地理解本发明的目的、技术方案及优点,以下结合附图及实施例,对本发明进行进一步详细说明。In order to understand the objectives, technical solutions and advantages of the present invention more clearly, the present invention will be further described in detail below with reference to the accompanying drawings and embodiments.
本发明提供一种连续SiC纤维增强金属基复合材料点阵结构的制备方法,图1是本发明的先驱丝板的制备及堆垛过程示意图,图2为本发明方法制备的点阵结构的示意图。The present invention provides a method for preparing a continuous SiC fiber reinforced metal matrix composite material lattice structure. .
在圆筒工装外的外圆柱面的母线方向贴上双面胶,将SiCf-TC17先驱丝(表面带有25μm厚的TC17钛合金涂层的直径100μm的SiC纤维)的一端垂直于双面胶固定在圆筒工装表面,沿着圆筒工装的中心轴将其顺时针旋转,圆筒的直径和高度均可调节,圆筒的周长即SiCf-TC17先驱丝带的长度,先驱丝缠绕间距设为0.5mm,缠绕至指定的宽度后缠绕的SiCf-TC17先驱丝由双面胶固定,示意图如图1(a)。将所有缠绕的SiCf-TC17先驱丝沿着双面胶的方向(即,外圆柱面的母线方向)切断,得到SiCf-TC17先驱丝带,采用这种方式,SiCf-TC17先驱丝带的先驱丝排布均匀,并且效率高。Put double-sided tape on the busbar direction of the outer cylindrical surface outside the cylindrical tooling, and place one end of the SiC f -TC17 precursor wire (a SiC fiber with a diameter of 100 μm with a TC17 titanium alloy coating of 25 μm on the surface) perpendicular to the double-sided The glue is fixed on the surface of the cylinder tooling, and it is rotated clockwise along the central axis of the cylinder tooling. The diameter and height of the cylinder can be adjusted. The circumference of the cylinder is the length of the SiC f -TC17 precursor ribbon, and the precursor wire is wound. The spacing is set to 0.5mm, and the SiC f -TC17 precursor wire wound to the specified width is fixed by double-sided tape, as shown in Figure 1(a). Cut all the wound SiC f -TC17 precursor wires along the direction of the double-sided tape (i.e., the busbar direction of the outer cylindrical surface) to obtain SiC f -TC17 precursor ribbons, in this way, the precursors of SiC f -TC17 precursor ribbons The filaments are evenly distributed and the efficiency is high.
将先驱丝带置于深度为0.3mm的凹槽内并固定,如图1(b);将PMMA加热至200℃呈熔融状态,将熔液倒入凹槽直至完全浸没先驱丝带,冷却后PMMA固化将SiCf-TC17先驱丝的相对位置固定,制得单层SiCf-TC17先驱丝板;Place the precursor ribbon in a groove with a depth of 0.3mm and fix it, as shown in Figure 1(b); heat the PMMA to 200 °C to melt, pour the melt into the groove until the precursor ribbon is completely immersed, and the PMMA solidifies after cooling The relative position of the SiC f -TC17 precursor wire was fixed to obtain a single-layer SiC f -TC17 precursor wire plate;
重复上一步骤或采用多个凹槽制备多个SiCf-TC17先驱丝板。Repeat the previous step or use multiple grooves to prepare multiple SiC f -TC17 precursor silk sheets.
将SiCf-TC17先驱丝板在真空热压炉内进行堆叠,铺放角度呈现0°/45°/90°交替分布,示意图如图1(c)。施加0.1MPa的载荷进行预加压,抽真空至10-2Pa,升温至200℃之间,升温时间为2h,保温保压3h,升温过程中PMMA开始软化、熔融,压力作用下使得层间的SiCf-TC17先驱丝达到相接触的状态,即先驱丝之间的相对位置已被固定;升温至400℃,保温保压6h,在该温度下PMMA完全裂解为气体,只剩位置被固定的先驱丝;然后升温至900℃,加压至10MPa,保温保压5h,使得相接触的先驱丝之间相互扩散连接形成整体,然后炉冷至低于200℃后卸压取出,制得连续SiC纤维增强TC17复合材料点阵结构,示意图如图2。The SiC f -TC17 precursor wire plates were stacked in a vacuum hot pressing furnace, and the laying angles were alternately distributed at 0°/45°/90°, as shown in Figure 1(c). Apply a load of 0.1 MPa for pre-pressurization, evacuate to 10 -2 Pa, heat up to 200 °C, heat up for 2 hours, and keep the pressure for 3 hours. During the heating process, PMMA begins to soften and melt. Under the action of pressure, the interlayer is formed. The SiC f -TC17 precursor filaments reached a state of contact, that is, the relative positions between the precursor filaments have been fixed; the temperature was raised to 400 °C, and the temperature was maintained for 6 hours. At this temperature, PMMA was completely decomposed into gas, and only the position was fixed. Then the temperature was raised to 900°C, pressurized to 10MPa, and kept under pressure for 5h, so that the contacting precursor wires were connected to each other by diffusion to form a whole. The lattice structure of SiC fiber reinforced TC17 composite is shown in Figure 2.
尽管上面以TC17钛合金为例进行了说明,不过,可以采用钛或其他钛合金来替代,或者甚至替换为其他金属或其合金,这种情况下,使相接触的先驱丝之间相互扩散连接形成整体所需的温度一般为对应金属或其合金熔点的0.4~0.8倍的温度。Although the TC17 titanium alloy is used as an example for the above description, it can be replaced by titanium or other titanium alloys, or even replaced by other metals or their alloys. In this case, the contacting precursor wires are interdiffused The temperature required to form the whole is generally 0.4 to 0.8 times the melting point of the corresponding metal or its alloy.
本发明利用聚甲基丙酸甲酯(PMMA)在中低温(~270℃)下可以软化、熔融-凝固及在中温(~400℃)可完全裂解为气体的特性,以PMMA熔融液浸泡SiCf-金属先驱丝带,固化后可得到均匀排布的先驱丝带,将先驱丝带交替排布后升温加压,使得先驱丝相互接触且在压力作用下相对位置固定,进一步升温使PMMA裂解气化,同时多空结构有利于裂解气体的挥发,然后升温至一定温度,加压使先驱丝之间相互扩散连接形成整体,得到点阵结构。该方法制备的点阵结构,先驱丝间距均匀可控,层间先驱丝的相对角度可根据位置实时调整,可满足更多的设计结构需求。The present invention utilizes the characteristics that polymethyl methacrylate (PMMA) can be softened, melted and solidified at medium and low temperature (~270°C) and can be completely cracked into gas at medium temperature (~400°C), and the SiCf is soaked in PMMA melt. -Metal precursor ribbons, uniformly arranged precursor ribbons can be obtained after curing. The precursor ribbons are alternately arranged and then heated and pressurized, so that the precursor ribbons are in contact with each other and their relative positions are fixed under the action of pressure. Further heating causes the PMMA to crack and gasify. The multi-empty structure is conducive to the volatilization of the pyrolysis gas, and then the temperature is raised to a certain temperature, and the pressure is applied to make the precursor filaments diffuse and connect to each other to form a whole to obtain a lattice structure. The lattice structure prepared by the method has uniform and controllable spacing of the precursor wires, and the relative angle of the interlayer precursor wires can be adjusted in real time according to the position, which can meet more design structure requirements.
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