WO2023077881A1 - 一种纳米颗粒铜铁复合合金及其制备与应用 - Google Patents

一种纳米颗粒铜铁复合合金及其制备与应用 Download PDF

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WO2023077881A1
WO2023077881A1 PCT/CN2022/108137 CN2022108137W WO2023077881A1 WO 2023077881 A1 WO2023077881 A1 WO 2023077881A1 CN 2022108137 W CN2022108137 W CN 2022108137W WO 2023077881 A1 WO2023077881 A1 WO 2023077881A1
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nanoparticles
copper
preparation
alloy
iron
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French (fr)
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冯科
徐诗鑫
何元媛
关小石
李坤
张芝民
白书霞
朱科
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中冶赛迪工程技术股份有限公司
中冶赛迪技术研究中心有限公司
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/02Making non-ferrous alloys by melting
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C30/00Alloys containing less than 50% by weight of each constituent
    • C22C30/02Alloys containing less than 50% by weight of each constituent containing copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/001Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0047Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
    • C22C32/0052Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0047Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
    • C22C32/0052Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides
    • C22C32/0063Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides based on SiC
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0047Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
    • C22C32/0073Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only borides
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper

Definitions

  • the invention relates to the technical field of preparation of nonferrous metal alloys, in particular to a nano-particle copper-iron composite alloy and its preparation and application.
  • Copper-iron alloys (5-50% iron content) have excellent thermal conductivity and bending resistance. When the iron content is greater than 30%, they have very good magnetic and electromagnetic shielding properties. In addition, they have good low thermal expansion coefficient and wear resistance. and antibacterial properties. According to analysis, this product will have huge application prospects, such as copper and iron strips can be used for 5G mobile phone heat sinks, shielding covers, large-size OLED backplane materials, large-size LED display heat sinks (already used in Japan), electrical connection connectors, wireless charging circuit boards, air-conditioning condensers, etc.; CuFe alloy rods, rods, wires, and wires can be used for electromagnetic shielding wires, high-fidelity audio cables, electromagnetic shielding wires for high-speed motors of drones, high-voltage cables, and robots.
  • CuFe alloy powder can be used in brake pads, wave-absorbing shielding coatings, 3D printing, medical antibacterial aspects (such as diabetic wound healing), etc. ; CuFe alloys also have potential application prospects in three-phase asynchronous motors, injection molds, EDM, electric soldering iron heads, and electrical contacts.
  • the solid solubility of iron in copper is extremely low, almost completely immiscible at room temperature, the solubility is still zero at 300°C, and the solid solubility is still less than 5% at 1100°C.
  • the density difference between iron and copper is large, and stratification is easy to occur during the smelting process; with the increase of iron content, the smelting temperature of the master alloy is very high, and when the Fe content>wt.20%, the Cu-Fe phase diagram liquid The phase line temperature exceeds 1400°C.
  • the melting points of copper and iron are very different, about 500 ° C, so segregation is easy to occur during casting, resulting in uneven composition and enrichment of iron ( Figure 1 shows the phase diagram of Cu-Fe binary alloy)
  • the object of the present invention is to provide a nano-particle copper-iron composite alloy and its preparation and application, which are used to solve the problem of uneven distribution of Fe precipitates in the copper-iron alloy produced by the existing process.
  • the present invention provides a method for preparing a nanoparticle copper-iron composite alloy, comprising the following steps:
  • the physical addition method is to wrap the nanoparticles with metal foil.
  • the metal foil is iron foil or copper foil.
  • the chemical addition method is a molten salt assisted method
  • the molten salt assisted method is: mixing the nanoparticles and the molten salt and then adding them to the Cu/Fe alloy solution.
  • the molten salt is at least one selected from alkali metals or alkaline earth metals and halides, silicates, carbonates, nitrates and phosphates.
  • the selection principle of molten salt is:
  • Molten salt should be matched with corresponding nanoparticles, where the molten salt is transformed into an ionic liquid after entering the liquid, which can change the surface charge distribution of the corresponding nanoparticles, thereby facilitating the stable dispersion and non-agglomeration of the nanoparticles.
  • the mixing and dispersing method is mechanical stirring or high-energy ultrasonic stirring.
  • the nanoparticles are evenly distributed in the alloy solution by high-energy dispersion methods such as high-power ultrasonic dispersion or high-speed mechanical stirring.
  • the post-treatment method is one or more deformation-aging treatments.
  • the mass fraction of Fe in the liquid Cu/Fe alloy is 5-50wt.%.
  • the volume ratio of the nanoparticles to the alloy solution is 1-20%.
  • the selection principle of nanoparticles is:
  • Nanoparticles have thermal stability and chemical stability, and nanoparticles should not decompose or react with matrix elements (Fe, Cu) during the preparation process.
  • the nanoparticles (NP) should be thermodynamically stable at the interface between the growth phase (Fe) and the matrix phase (Cu). Ideally, the NP/Fe and NP/Cu interfacial free energies should be close to each other to obtain a great reduction in the total interfacial energy of the system.
  • the nanoparticles should move quickly to the growth interface (Fe/Cu interface).
  • the nanoparticles should have a small size (50-100 nm) as simulated by model calculations.
  • nanoparticles are selected from at least one of nano-carbide ceramic particles, nano-nitride ceramic particles, nano-oxide ceramic particles, and nano-boride ceramic particles.
  • the size of the nanoparticles is 50-100nm.
  • the nanoparticles are selected from at least one of SiC, MoC, WC, Al 2 O 3 , BN, and TiB 2 .
  • the second aspect of the present invention provides a nano-particle copper-iron composite alloy prepared by the method described in the first aspect.
  • the third aspect of the present invention provides the application of the method described in the first aspect in the preparation of copper-iron alloy.
  • nano-particle copper-iron composite alloy of the present invention and its preparation and application have the following beneficial effects:
  • the nano-particle copper-iron composite alloy billet prepared by the method of the invention has stable chemical composition, uniform composition in the upper, middle and lower parts of the ingot, uniform distribution of Fe elements, no segregation, and no enrichment of Fe particles.
  • the invention not only effectively solves the problem of inhomogeneous distribution of Fe precipitates in the copper-iron alloy, but also realizes uniform distribution of Fe precipitates in the copper matrix at submicron or even nanometer scale.
  • the preparation process of the nano-particle copper-iron composite alloy of the present invention is simpler in operation, lower in cost, and more suitable for large-scale and industrial production.
  • Figure 1 shows the Cu-Fe binary alloy phase diagram.
  • Fig. 2 is a schematic diagram of the nano-particle copper-iron composite alloy of the present invention.
  • the invention provides a method for preparing a nanoparticle copper-iron composite alloy, comprising the following steps:
  • the physical addition method is to wrap the nanoparticles with metal foil, and the metal foil is iron foil or copper foil.
  • the chemical addition method is a molten salt assisted method
  • the molten salt assisted method is: mixing nanoparticles and molten salt and then adding them to the Cu/Fe alloy solution.
  • the molten salt is selected from at least one of alkali metals or alkaline earth metals and halides, silicates, carbonates, nitrates and phosphates.
  • the selection principle of molten salt is:
  • Molten salt should be matched with corresponding nanoparticles, where the molten salt is transformed into an ionic liquid after entering the liquid, which can change the surface charge distribution of the corresponding nanoparticles, thereby facilitating the stable dispersion and non-agglomeration of the nanoparticles.
  • the post-treatment method is one or more deformation-aging treatments.
  • the mass fraction of Fe in the liquid Cu/Fe alloy is 5-50 wt.%, and the volume ratio of the nanoparticles to the alloy solution is 1-20%.
  • the selection principle of nanoparticles is:
  • Nanoparticles have thermal stability and chemical stability, and nanoparticles should not decompose or react with matrix elements (Fe, Cu) during the preparation process.
  • the nanoparticles (NP) should be thermodynamically stable at the interface between the growth phase (Fe) and the matrix phase (Cu). Ideally, the NP/Fe and NP/Cu interfacial free energies should be close to each other to obtain a great reduction in the total interfacial energy of the system.
  • nanoparticles should move quickly to the growth interface (Fe/Cu interface). Through model calculation simulations, nanoparticles should have small size and lower density.
  • the nanoparticles are selected from at least one of nano-carbide ceramic particles, nano-nitride particles, nano-oxide ceramic particles, and nano-boride ceramic particles.
  • the nanoparticles are selected from at least one of SiC, MoC, WC, Al 2 O 3 , BN, and TiB 2 .
  • Nanoparticle copper-iron composite alloy preparation principle of the present invention is as follows:
  • nanoparticles are introduced into the binary alloy (Cu/Fe), and the growth of crystal nuclei is controlled by rapidly surrounding the nucleation phase with thermally stable nanoparticles; when suitable nanoparticles When uniformly dispersed in the alloy solution, the nanoparticles will spontaneously gather at the interface between a small number of crystal nuclei (Fe) and the liquid matrix (Cu/Fe) during cooling into the immiscible zone, and rapidly in a small number of A nanoparticle wall forms around the nuclei (Fe), which hinders the diffusion transport between the nuclei and the liquid matrix, thereby greatly limiting nuclei growth and allowing new nuclei to continue to form throughout the cooling period.
  • the first nucleated Fe grows rapidly to consume the supersaturated solute (Fe) in the surrounding liquid matrix (Cu/Fe), and release latent heat to increase the surrounding liquid matrix. temperature, resulting in a lack of sufficient undercooling to form new nuclei; the initially formed nuclei (Fe) continue to grow, and finally segregate, resulting in uneven composition and enrichment of Fe.
  • the chemical composition of the nano-particle copper-iron composite alloy prepared by the method of the invention is stable, the composition of the upper, middle and lower parts of the ingot is uniform, and the Fe element is evenly distributed without segregation.
  • the present embodiment prepares a kind of nanoparticle copper-iron composite alloy, and its preparation method steps are as follows:
  • wrap SiC nanoparticles with iron foil, and the SiC nanoparticles account for 1% of the volume ratio of the copper-iron solution. into the alloy solution;
  • a nano-particle copper-iron composite alloy sample is obtained by casting into a billet and performing cold rolling and aging.
  • the present embodiment prepares a kind of nanoparticle copper-iron composite alloy, and its preparation method steps are as follows:
  • a nano-particle copper-iron composite alloy sample is obtained by die-casting a billet and performing multiple deformation aging treatments.
  • the present embodiment prepares a kind of nanoparticle copper-iron composite alloy, and its preparation method steps are as follows:
  • a nano-particle copper-iron composite alloy sample is obtained by die-casting a billet and performing multiple deformation aging treatments.

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Abstract

本发明属于有色金属合金制备技术领域,具体公开了一种纳米颗粒铜铁复合合金及其制备与应用,包括如下步骤:在高温保护气氛下,通过物理或化学方式向液态Cu/Fe合金中加入纳米颗粒,混合并将其分散均匀,然后将混合均匀的具有纳米颗粒的Cu/Fe熔体铸造成坯,再将铸坯进行后处理。采用本发明方法制得的纳米颗粒铜铁复合合金铸坯化学成分稳定,Fe元素分布均匀、不偏析。本发明能解决铜铁合金中Fe析出相分布不均匀的问题,可实现铜基体内Fe析出相的亚微米级乃至纳米级的均匀分布,另外,本发明工艺相较于传统快冷工艺、粉末冶金工艺更简单,更适合规模化生产。

Description

一种纳米颗粒铜铁复合合金及其制备与应用 技术领域
本发明涉及有色金属合金制备技术领域,特别是涉及一种纳米颗粒铜铁复合合金及其制备与应用。
背景技术
铜铁合金(铁含量为5~50%)具有优良的导热性、抗弯折性能,铁含量大于30%时具有非常优良的磁性、电磁屏蔽性能,另外还有良好的低热膨胀系数,耐磨性和抑菌性等特性。据分析,该产品将具有巨大的应用前景,如铜铁板带可用于5G手机散热板、屏蔽罩、大尺寸OLED背板材料、大尺寸LED显示屏散热板(在日本已经应用)、电连接器接插件、无线充电线路板、空调冷凝管等;CuFe合金杆、棒、线、丝材可用于电磁屏蔽线、高保真音频线、无人机高速电机用电磁屏蔽电线、高压电缆线、机器人通讯控制线、射频线、编织电磁屏蔽网/带、海水养殖网箱、焊接丝材等;CuFe合金粉末可用于刹车片、吸波屏蔽涂料、3D打印,医用抗菌方面(如糖尿病伤口愈合)等;CuFe合金在三相异步电机、注塑模具、电火花加工、电烙铁头、电工触头等方面也具有潜在的应用前景。
目前制备高含量铜铁合金存在以下难题:铁在铜中的固溶度极低,室温时几乎完全不互溶,300℃时溶解度仍然为零,在1100℃时固溶度仍小于5%。铁和铜的密度相差较大,在熔炼过程中易发生分层;随着铁含量的升高,中间合金的熔炼温度很高,Fe含量>wt.20%时,Cu-Fe相图中液相线温度超过1400℃。而且铜和铁的熔点相差很大,约500℃,所以在浇铸时很容易发生偏析,导致成分不均和铁的富集(图1所示为Cu-Fe二元合金相图)
因此,通过在生产Cu-Fe二元合金过程中采用特定的纳米颗粒辅助工艺,以期改变所制备Cu-Fe二元合金的固溶性,优化其性能及拓展应用范围,对于高铁含量铜铁合金的规模化生产非常必要。
发明内容
鉴于以上所述现有技术的缺点,本发明的目的在于提供一种纳米颗粒铜铁复合合金及其制备与应用,用于解决现有工艺生产的铜铁合金中Fe析出相分布不均匀的问题。
为实现上述目的及其他相关目的,本发明提供一种纳米颗粒铜铁复合合金的制备方法,包括如下步骤:
在高温保护气氛下,通过物理或化学方式向液态Cu/Fe合金中加入纳米颗粒,混合并将 其分散均匀,然后将混合均匀的具有纳米颗粒的Cu/Fe熔体铸造成坯,再将铸坯进行后处理。
进一步,物理加入方式为金属箔包裹纳米颗粒。
进一步,所述金属箔为铁箔或铜箔。
进一步,化学加入方式为熔盐辅助法,熔盐辅助法为:将纳米颗粒与熔盐混匀后加入到Cu/Fe合金溶液中。
进一步,所述熔盐选自碱金属或碱土金属与卤化物、硅酸盐、碳酸盐、硝酸盐以及磷酸盐组成中的至少一种。
本发明中,熔盐的选取原则为:
a.由碱金属或碱土金属与卤化物、硅酸盐、碳酸盐、硝酸盐以及磷酸盐组成;
b.熔盐应搭配对应的纳米颗粒,其中熔盐进入液体以后转变成离子液体,能改变相应纳米颗粒表面电荷分布,从而利于纳米颗粒之间稳定分散且不团聚。
进一步,纳米颗粒加入到加入液态Cu/Fe合金中后,混合分散方式为机械搅拌分散或高能超声搅拌。通过大功率超声分散或者大转速机械搅拌等高能分散方式使得纳米颗粒均匀分布在合金溶液中。
进一步,所述后处理方式为一次或多次变形-时效处理。
进一步,所述液态Cu/Fe合金中Fe的质量分数为5~50wt.%。
进一步,所述纳米颗粒占合金溶液体积比为1~20%。
本发明中,纳米颗粒的选取原则为:
a.纳米颗粒具有热稳定性以及化学稳定性,在制备过程中纳米颗粒不应分解或与基体元素(Fe、Cu)反应。
b.纳米颗粒(NP)在生长相(Fe)和基体相(Cu)之间的界面上应具有热力学稳定性。理想情况下,NP/Fe和NP/Cu界面自由能应相互接近,以获得系统总界面能的极大减少。
c.纳米颗粒应快速移动到生长界面(Fe/Cu界面)。通过模型计算模拟,纳米颗粒应该具有小的尺寸(50-100nm)。
进一步,所述纳米颗粒选自纳米碳化物陶瓷颗粒、纳米氮化物陶瓷颗粒、纳米氧化物陶瓷颗粒、纳米硼化物陶瓷颗粒中的至少一种。
进一步,所述纳米颗粒的尺寸为50-100nm。
进一步,所述纳米颗粒选自SiC、MoC、WC、Al 2O 3、BN、TiB 2中的至少一种。
本发明第二方面提供一种由第一方面所述的方法制备得到的纳米颗粒铜铁复合合金。
本发明第三方面提供由第一方面所述的方法在制备铜铁合金上的应用。
如上所述,本发明的纳米颗粒铜铁复合合金及其制备与应用,具有以下有益效果:
采用本发明方法制得的纳米颗粒铜铁复合合金铸坯化学成分稳定,铸锭上、中、下成分均匀,Fe元素分布均匀、不偏析,无Fe颗粒的富集。本发明不仅有效解决了铜铁合金中Fe析出相分布不均匀的问题,还能够实现铜基体内Fe析出相的亚微米级乃至纳米级的均匀分布。同时,相较于传统快冷工艺、粉末冶金工艺,本发明的纳米颗粒铜铁复合合金制备工艺操作更加简单,成本低,更适合规模化、工业化生产。
附图说明
图1显示为Cu-Fe二元合金相图。
图2显示为本发明的纳米颗粒铜铁复合合金的原理图。
具体实施方式
以下通过特定的具体实例说明本发明的实施方式,本领域技术人员可由本说明书所揭露的内容轻易地了解本发明的其他优点与功效。本发明还可以通过另外不同的具体实施方式加以实施或应用,本说明书中的各项细节也可以基于不同观点与应用,在没有背离本发明的精神下进行各种修饰或改变。
本发明提供了一种纳米颗粒铜铁复合合金的制备方法,包括如下步骤:
在高温保护气氛下,通过物理或化学方式向液态Cu/Fe合金中加入纳米颗粒,通过机械搅拌分散或高能超声搅拌混合均匀,然后将混合均匀的具有纳米颗粒的Cu/Fe熔体铸造成坯,再将铸坯进行后处理。
具体的,物理加入方式为金属箔包裹纳米颗粒,所述金属箔为铁箔或铜箔。
具体的,化学加入方式为熔盐辅助法,熔盐辅助法为:将纳米颗粒与熔盐混匀后加入到Cu/Fe合金溶液中。可选地,所述熔盐选自碱金属或碱土金属与卤化物、硅酸盐、碳酸盐、硝酸盐以及磷酸盐组成中的至少一种。
本发明中,熔盐的选取原则为:
a.由碱金属或碱土金属与卤化物、硅酸盐、碳酸盐、硝酸盐以及磷酸盐组成;
b.熔盐应搭配对应的纳米颗粒,其中熔盐进入液体以后转变成离子液体,能改变相应纳米颗粒表面电荷分布,从而利于纳米颗粒之间稳定分散且不团聚。
具体的,所述后处理方式为一次或多次变形-时效处理。
具体的,所述液态Cu/Fe合金中Fe的质量分数为5~50wt.%,所述纳米颗粒占合金溶液体积比为1~20%。
本发明中,纳米颗粒的选取原则为:
a.纳米颗粒具有热稳定性以及化学稳定性,在制备过程中纳米颗粒不应分解或与基体元素(Fe、Cu)反应。
b.纳米颗粒(NP)在生长相(Fe)和基体相(Cu)之间的界面上应具有热力学稳定性。理想情况下,NP/Fe和NP/Cu界面自由能应相互接近,以获得系统总界面能的极大减少。
c.纳米颗粒应快速移动到生长界面(Fe/Cu界面)。通过模型计算模拟,纳米颗粒应该具有小的尺寸和更低的密度。
具体的,所述纳米颗粒选自纳米碳化物陶瓷颗粒、纳米氮化物颗粒、纳米氧化物陶瓷颗粒、纳米硼化物陶瓷颗粒中的至少一种。优选地,所述纳米颗粒选自SiC、MoC、WC、Al 2O 3、BN、TiB 2中的至少一种。
本发明的纳米颗粒铜铁复合合金制备原理如下:
如图2所示,在二元合金(Cu/Fe)中引入分布均匀且稳定的纳米颗粒,通过用热稳定的纳米颗粒快速包围住形核相来控制晶核的增长;当合适的纳米颗粒均匀分散在合金溶液中时,冷却进入到不混溶区过程中,纳米颗粒会自发地聚集在少数的晶核(Fe)和液体基体(Cu/Fe)之间的界面上,迅速在少数的晶核(Fe)周围形成一层纳米颗粒墙,阻碍晶核与液体基体之前的扩散运输,从而大大限制晶核生长,并使新的晶核在整个冷却期间持续形成。在没有纳米颗粒纯体系(Cu/Fe)的冷却过程中,首先形核的Fe快速长大会消耗周围液体基体(Cu/Fe)中的过饱和溶质(Fe),并释放潜热提高周围液体基体的温度,从而造成缺乏足够的过冷度,无法形成新的晶核;最初形成的晶核(Fe)不断长大,最后发生偏析,导致成分不均和Fe的富集。
采用本发明方法制备得到的纳米颗粒铜铁复合合金化学成分稳定,铸锭上、中、下成分均匀,Fe元素分布均匀、不偏析。
下面具体的例举实施例以详细说明本发明。同样应理解,以下实施例只用于对本发明进行具体的说明,不能理解为对本发明保护范围的限制,本领域的技术人员根据本发明的上述内容作出的一些非本质的改进和调整均属于本发明的保护范围。下述示例具体的工艺参数等也仅是合适范围中的一个示例,即本领域技术人员可以通过本文的说明做合适的范围内选择,而并非要限定于下文示例的具体数值。
实施例1
本实施例制备一种纳米颗粒铜铁复合合金,其制备方法步骤如下:
(1)通过加热炉在氧化铝坩埚中熔化纯铜(400g)、纯铁(100g),得铜铁合金溶液;
(2)在氮气保护氛围中,通过铁箔包裹SiC纳米颗粒,SiC纳米颗粒占铜铁溶液体积比 为1%,以棒状(棒状的铁箔包裹的SiC纳米颗粒)喂食的方法将纳米颗粒送入合金溶液中;
(3)在溶液中进行机械搅拌分散纳米颗粒,转速200rpm;
(4)通过浇铸成坯,并进行冷轧时效得到纳米颗粒铜铁复合合金样品。
实施例2
本实施例制备一种纳米颗粒铜铁复合合金,其制备方法步骤如下:
(1)通过加热炉在氧化铝坩埚中熔化纯铜(250g)、纯铁(250g),得铜铁合金溶液;
(2)在氮气保护氛围中,通过熔盐辅助法加入MoC纳米颗粒,具体方式为:将占铜铁溶液体积比为20%的MoC纳米颗粒与NaCl混匀以后直接加入到Cu/Fe合金溶液中;
(3)在溶液中进行高能超声搅拌分散纳米颗粒,超声振幅120μm,频率20kHz;
(4)通过压铸成坯,并进行多次形变时效处理得到纳米颗粒铜铁复合合金样品。
实施例3
本实施例制备一种纳米颗粒铜铁复合合金,其制备方法步骤如下:
(1)通过加热炉在氧化铝坩埚中熔化纯铜(375g)、纯铁(125g),得铜铁合金溶液;
(2)在惰性气体(氩气)保护氛围中,通过熔盐辅助法加入TiB 2纳米颗粒,具体方式为:将占铜铁溶液体积比为10%的TiB 2纳米颗粒与CaF 2混匀以后直接加入到Cu/Fe合金溶液中;
(3)在溶液中进行高能超声搅拌分散纳米颗粒,超声振幅120μm,频率20kHz;
(4)通过压铸成坯,并进行多次形变时效处理得到纳米颗粒铜铁复合合金样品。
上述实施例仅例示性说明本发明的原理及其功效,而非用于限制本发明。任何熟悉此技术的人士皆可在不违背本发明的精神及范畴下,对上述实施例进行修饰或改变。因此,举凡所属技术领域中具有通常知识者在未脱离本发明所揭示的精神与技术思想下所完成的一切等效修饰或改变,仍应由本发明的权利要求所涵盖。

Claims (10)

  1. 一种纳米颗粒铜铁复合合金的制备方法,其特征在于,包括如下步骤:在高温保护气氛下,通过物理和/或化学方式向液态Cu/Fe合金中加入纳米颗粒,混合并将其分散均匀,然后将混合均匀的具有纳米颗粒的Cu/Fe熔体铸造成坯,再将铸坯进行后处理。
  2. 根据权利要求1所述的制备方法,其特征在于:物理加入方式为金属箔包裹纳米颗粒;
    和/或,化学加入方式为熔盐辅助法,熔盐辅助法为:将纳米颗粒与熔盐混匀后加入到Cu/Fe合金溶液中;
    和/或,纳米颗粒加入到加入液态Cu/Fe合金中后,混合分散方式为机械搅拌分散或高能超声搅拌。
  3. 根据权利要求2所述的制备方法,其特征在于:所述金属箔为铁箔或铜箔。
  4. 根据权利要求1所述的制备方法,其特征在于:所述后处理方式为一次或多次变形-时效处理。
  5. 根据权利要求1所述的制备方法,其特征在于:所述液态Cu/Fe合金中Fe的质量分数为5~50wt.%。
  6. 根据权利要求1所述的制备方法,其特征在于:所述纳米颗粒占合金溶液体积比为1~20%。
  7. 根据权利要求1所述的制备方法,其特征在于:所述纳米颗粒选自纳米碳化物陶瓷颗粒、纳米氮化物颗粒、纳米氧化物陶瓷颗粒、纳米硼化物陶瓷颗粒中的至少一种。
  8. 根据权利要求7所述的制备方法,其特征在于:所述纳米颗粒选自SiC、MoC、WC、Al 2O 3、BN、TiB 2中的至少一种。
  9. 一种根据权利要求1-8任一项所述的方法制备得到的纳米颗粒铜铁复合合金。
  10. 根据权利要求1-8任一项所述的方法在制备铜铁合金上的应用。
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