CN115433011A - 一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 - Google Patents
一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 Download PDFInfo
- Publication number
- CN115433011A CN115433011A CN202211235921.7A CN202211235921A CN115433011A CN 115433011 A CN115433011 A CN 115433011A CN 202211235921 A CN202211235921 A CN 202211235921A CN 115433011 A CN115433011 A CN 115433011A
- Authority
- CN
- China
- Prior art keywords
- sic
- complex phase
- vnbtamow
- phase ceramic
- mpa
- 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.)
- Granted
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/5607—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/565—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/64—Burning or sintering processes
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3839—Refractory metal carbides
- C04B2235/3847—Tungsten carbides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/66—Specific sintering techniques, e.g. centrifugal sintering
- C04B2235/666—Applying a current during sintering, e.g. plasma sintering [SPS], electrical resistance heating or pulse electric current sintering [PECS]
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/74—Physical characteristics
- C04B2235/77—Density
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/74—Physical characteristics
- C04B2235/78—Grain sizes and shapes, product microstructures, e.g. acicular grains, equiaxed grains, platelet-structures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/30—Nuclear fission reactors
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Ceramic Products (AREA)
Abstract
本发明属于高熵碳化物复相陶瓷技术领域,具体涉及一种高熵碳化物(VNbTaMoW)C5‑SiC复相陶瓷。本发明复相陶瓷是以金属碳化物和碳化硅(SiC)粉末为原料,采用放电等离子烧结,在较低温度下制得。本发明复相陶瓷的基体(VNbTaMoW)C5为面心立方结构,第二相SiC均匀分布。本发明中SiC的引入细化了高熵相的晶粒,所得复相陶瓷的高熵相的晶粒得到了细化,复相陶瓷的硬度可达17‑18 GPa,且断裂韧性好,同时还具有优异的耐磨性,其平均比磨损率为(5.7‑8.1)×10‑8 mm³/N•m。
Description
技术领域
本发明属于高熵碳化物复相陶瓷技术领域,具体涉及一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷。
背景技术
高熵碳化物复相陶瓷(High-Entropy Ceramics)一般是至少有一套晶格点阵由四种或四种以上等摩尔比或近似等摩尔比的金属元素组成的碳化物陶瓷。高熵碳化物往往具有简单晶体结构,相稳定,高熔点、高硬度、耐磨等特性。
高熵碳化物可通过金属碳化物固溶反应、单质化合、氧化物碳热还原、机械球磨辅助等方法制备。固溶反应法因其高的普适性,被广泛用于陶瓷材料制备。以金属一元碳化物为原料,经球磨混合,而后热压烧结或放电等离子烧结(SPS)。烧结过程中金属原子间相互扩散,形成了金属原子随机占据阳离子位点的多主元单相固溶体碳化物。金属高熵碳化物具有远高于其组元一元碳化物按照混合法则预测的硬度和杨氏模量。高的硬度使得高熵碳化物具有良好的耐磨损性能,金属元素摩擦氧化产物则因具有润滑作用而使高熵碳化物具有相对较低的摩擦系数。
目前,由多种金属元素固溶反应制备的高熵碳化物虽然具有高的硬度和模量,但是仍然存在很多问题,如:1、韧性并没有得到较大改善;2、以碳化物为原料,通过固溶反应制备高熵碳化物,往往需要在较高的SPS温度下(>2000 oC)才能实现致密化(相对密度>97%);3、无法避免高温下晶粒生长过快和尺寸过大的问题。而由这类高熵碳化物制备的高熵碳化物复相陶瓷也普遍存在相应的问题暨待解决。
发明内容
针对现有技术中制备的高熵碳化物复相陶瓷存在的问题,克服现有技术的不足,本发明的目的是提供一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷。本发明高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷是以金属碳化物和碳化硅(SiC)粉末为原料,采用放电等离子烧结,在较低温度下制得。本发明高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷的高熵相的晶粒得到了细化,复相陶瓷的硬度得到了提高,可达17-18 GPa,且断裂韧性好,同时还具有优异的耐磨性,其平均比磨损率为(5.7-8.1)×10-8 mm³/N•m。
为实现上述目的,本发明采用的技术方案是:一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,主要成分为(VNbTaMoW)C5和SiC。其中,SiC 的质量分数为5%-30%。
本发明一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其制备方法包括以下步骤。
S01. 称料:按照等摩尔比称量金属碳化物VC、NbC、TaC、Mo2C和WC,加入质量分数为5%-30%的SiC,混合。
S02. 球磨:将步骤S01混合得到的原料装入硬质合金球磨罐,加入无水乙醇,加入硬质合金球,球料比为(5-10):1,球磨混合8-12 h。
S03. 干燥:将步骤S02球磨混合得到的物料置于100 ℃真空干燥箱中,充分干燥。
S04. 烧结:将步骤S03干燥后的粉末装入石墨模具中,在压力30-40 MPa以及真空25-50 Pa条件下在SPS中烧结;以100-160℃/min从室温升至650 ℃,同时压力上升为24MPa;再以80-140 ℃/min升温至1600 ℃,同时压力由24 MPa上升至30 MPa;最后以60 ℃/min升温至烧结温度1700 – 2100 ℃,同时压力保持30 MPa或上升至30 - 40 MPa,保温保压5-15 min。
S05. 卸压冷却:待步骤S04烧结结束后,卸压至初始压力,随炉冷却。
由上述方法所得复相陶瓷的基体(VNbTaMoW)C5为面心立方结构,SiC为第二相。
由上述方法所得复相陶瓷SiC含量5-30%。
由上述方法所得复相陶瓷相对密度为89.4 - 100 %,其维氏硬度和断裂韧性分别为 17 - 18.3 GPa 和 4.5 - 5.7 MPa•m1/2。
本发明的发明人团队以金属碳化物和SiC为原料,采用SPS制备了高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,研究SiC含量对复相陶瓷相对密度,微结构,力学和摩擦磨损性能的影响,研究结果对高韧性高熵碳化物耐磨材料的制备具有很好的指导作用。
本发明与现有技术相比具有如下突出的实质性特点和显著进步。
(1)本发明在1700-2100 oC,30-40 MPa下采用放电等离子烧结制备了(VNbTaMoW)C5-SiC复相陶瓷。复相陶瓷的基体(VNbTaMoW)C5为面心立方结构,SiC为第二相。SiC的引入细化了高熵相的晶粒。当SiC含量至20%以上,复相陶瓷相对密度达到99.2%以上。复相陶瓷的断裂方式随SiC含量增加由穿晶断裂转变为混合断裂。
(2)本发明所得复相陶瓷的硬度约为17-18 GPa;当SiC含量为20% 时,复相陶瓷的相对密度为99.2%,其维氏硬度和断裂韧性分别为18.2 GPa和5.7 MPa•m1/2。
(3)本发明所得复相陶瓷具有优异的耐磨性能,其平均比磨损率仅为(5.7-8.1)×10-8 mm³/N·m。
附图说明
图1:HEC-SiC复相陶瓷的XRD图。
图2:HEC-SiC复相陶瓷的抛光面的SEM图。
图3:HEC-SiC断面的SEM图。
图4:HEC-SiC复相陶瓷的摩擦系数随时间的变化图。
图5:HEC10磨痕的SEM图(a)和三维表面轮廓图(b)。
具体实施方式
下面结合附图对本发明的技术方案进行详细说明,但本发明的内容并不局限于此。
在实施例中通过制备复相陶瓷,然后对其性能进行检测,同时将所得结果与纯(VNbTaMoW)C5进行对比分析,进一步证明本发明所得复相陶瓷具有优异的性能。
实施例1:
一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷的制备:
本试验所使用的原料包括α-SiC,(D50,0.69 μm,纯度>98.5%,O含量<1.5%,德国H.C. Starck)和VC,NbC,TaC,Mo2C,WC,其平均粒径,杂质成分如表1所示。
各金属碳化物按照等摩尔比称量,分别加入质量分数为0%、5%、10%、20%、30%的SiC。将混合原料装入硬质合金球磨罐,加入无水乙醇,加入硬质合金球,球料比为(5-10):1,球磨混合8-12 h。而后置于100 ℃真空干燥箱中,充分干燥。将干燥后粉末装入石墨模具中,在压力30 - 40 MPa以及真空条件下(25-50 Pa)在SPS中烧结。以100-160 ℃/min从室温升至650 ℃,同时压力上升为24 MPa。再以80-140 ℃/min升温至1600 ℃,同时压力由24MPa上升至30 MPa。最后以60 ℃/min升温至烧结温度(1700-2100 ℃),同时压力保持30MP或上升至30-40 MPa。保温保压5-15 min。烧结结束后,卸压至初始压力,随炉冷却。
所得复相陶瓷(VNbTaMoW)C5-SiC样品根据SiC质量分数含量分别命名为HEC、HEC5、HEC10、HEC20、HEC30,分别表示加入了0%、5%、10%、20%、30%。
实施例2:
性能检测:在实施例1的基础上,对实施例1所得复相陶瓷采用以下方法进行检测,同时将所得结果与纯(VNbTaMoW)C5进行对比,进一步证明本发明所得复相陶瓷具有优异的性能。
1、检测方法:
采用X射线衍射仪(XRD,XRD-6000,日本岛津)测定复相陶瓷的物相。采用 Cu-Kα射线(λ=0.15405 nm ),加速电压为40 kV,电流为30 mA,扫描测试范围为10°-80°,扫描速率为1 °/min。采用场发射扫描电子显微镜(FESEM,Zeiss supra55, 德国卡尔蔡司)分析复相陶瓷的显微结构和磨损面形貌。高熵陶瓷的晶粒尺寸由抛光面的FESEM照片通过线截距法计算得到,测量的晶粒个数大于150。根据复相陶瓷中高熵陶瓷的各衍射峰角度,计算高熵陶瓷的理论密度,进而根据混合法则计算复相陶瓷的理论密度。采用阿基米德法测量烧结体的实际密度,并结合理论密度计算复相陶瓷的致密度。
采用摩擦磨损试验机(HT-1000,兰州凯华)测试材料的摩擦系数和磨损率,摩擦试验机为球-盘试接触方式,试样单向滑动。复相陶瓷样品固为盘,硬质合金球为对偶。线速度为0.3 m/s,载荷为15 N、实验时间为300 min、摩擦半径为3 mm。磨损率计算采用公式(1)。
W=V/(F∙L) (1)
其中,V为磨损体积,F为载荷,L为滑动距离。
采用显微维氏硬度计(432SVD,上海沃伯特)测试材料的维氏硬度。压入载荷为10kgf (98 N),保压10 s。每个样品取10个不同测试点,对测得值取平均值。采用压痕法测试复相陶瓷的断裂韧性。利用维氏硬度计,在测量显微硬度(H)的同时,测量压痕四角裂纹的长度(c)。根据混合法则,由(VNbTaMoW)C5和SiC的弹性模量计算复相陶瓷的弹性模量(E)。根据Antis公式(式2),计算复相陶瓷的断裂韧性(K 1c )。P为压入载荷。
2、检测结果
2.1 物相组成
HEC-SiC复相陶瓷的XRD如图1所示。由图1可见,混合粉末中金属碳化物TaC (PDF:35-0801)、VC (PDF: 73-0476)、WC (PDF: 51-0939)、NbC (PDF: 38-1364)、Mo2C (PDF:35-0787)和SiC (PDF: 49-1428)的峰值清晰可辨,说明原料粉末经过球磨混合后,保持了原有的晶型,未发生反应。经烧结得到的HEC-SiC复相陶瓷中,高熵碳化物(VNbTaMoW)C5为立方相(fcc),SiC的衍射峰与高熵相的衍射峰重叠,在图1中不可见。
2.2 致密度
HEC-SiC复相陶瓷的相对密度如表2所示。由表2可知,HEC的相对密度为97.5%。加入SiC后,复相陶瓷的相对密度先减小(HEC5,89.4%;HEC10,93.1%),后增大(HEC20,99.2%;HEC30,100%)。
2.3 显微结构
HEC-SiC复相陶瓷的抛光面和断面的形貌分别如图2和图3所示。 由图2可见,复相陶瓷基体中SiC分布较为均匀。HEC5的晶界处和晶粒内部均存在较多气孔,与样品致密度较单相高熵陶瓷小的结果一致。随着SiC含量增加,HEC-SiC复相陶瓷中气孔数量逐渐减少。由图3可见,HEC5和HEC10中晶粒的断裂方式以穿晶断裂为主,HEC20和HEC30中晶粒断裂方式为穿晶断裂和沿晶断裂。断裂方式的转变主要是因为SiC含量增加,HEC/SiC界面数量增加,其强度小于HEC/HEC界面的强度。
HEC-SiC复相陶瓷的平均晶粒尺寸如表2所示。随SiC含量的增加,HEC-SiC复相陶瓷中高熵相的平均晶粒尺寸(表2)由5.1 μm(HEC)逐渐减小至2.5 μm。由此,SiC能够抑制高温下晶粒的长大,从而细化了高熵相的晶粒。
2.4 力学性能
HEC-SiC复相陶瓷的力学性能如表2所示。由表2可见,向HEC中引入SiC,复相陶瓷(HEC5)的硬度由19.6 GPa减小至17.1 GPa,断裂韧性略减小。这主要是因为HEC5相对密度较小(89.4%)。由HEC5至HEC30,复相陶瓷的硬度略有增大后基本保持不变,而断裂韧性先增大后减小。HEC20的断裂韧性高达5.7±1.2 MPa·m。SiC含量增大,复相陶瓷的致密度明显增大,晶粒尺寸持续减小,复相陶瓷的硬度和断裂韧性增大。SiC含量进一步增大,弱的HEC/SiC界面数增大,复相陶瓷中裂纹扩展阻力减小,裂纹长度增大,根据Antis公式(式2),复相陶瓷的断裂韧性减小。
2.5 摩擦磨损性能
图4为HEC-SiC复相陶瓷的摩擦系数随时间的变化。由图4可见,复相陶瓷经历了短暂的磨合阶段后,摩擦过程进入了稳定阶段。HEC10和HEC20的摩擦系数波动很小,但HEC30的摩擦系数随时间波动较大。HEC-SiC复相陶瓷的平均摩擦系数和平均比磨损率如表3所示。复相陶瓷的平均摩擦系数随SiC含量的增加,由0.51增大至0.66。HEC的平均比磨损率由5.7×10-8 mm³/Nm增大至8.1×10-8 mm³/Nm。摩擦系数和磨损率的增大主要是由于SiC与高熵相结合较弱,易拔出,导致磨损率增大。HEC10磨痕的SEM图(a)和三维表面轮廓(b) 见图5。由以上可见,复相陶瓷的摩擦损率比(VNbTaMoW)C5和一元金属碳化物,低二至四个数量级,表现出优异的耐磨性能。
以上所述,仅是本发明的较佳实施例,并非用以限制本发明的权利范围。任何以本申请专利范围所涵盖的权利范围实施的技术方案,或者任何熟悉本领域的技术人员,利用上述揭示的方法内容做出许多可能的变动和修饰的方案,均属于本发明的保护范围。
Claims (8)
1.一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:主要成分为(VNbTaMoW)C5和SiC,所述SiC 的质量分数为5%-30%。
2.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述复相陶瓷,其制备方法包括以下步骤:
S01. 称料:按照等摩尔比称量金属碳化物VC、NbC、TaC、Mo2C和WC,加入质量分数为5%-30%的SiC,混合;
S02. 球磨:将步骤S01混合得到的原料装入硬质合金球磨罐,加入无水乙醇,加入硬质合金球,球料比为(5- 10):1,球磨混合8-12 h;
S03. 干燥:将步骤S02球磨混合得到的物料置于100 ℃真空干燥箱中,充分干燥;
S04. 烧结:将步骤S03干燥后的粉末装入石墨模具中,在压力 30 - 40 MPa以及真空25 -50 Pa条件下在SPS中烧结;以100-160 ℃/min从室温升至650 ℃,同时压力上升为24MPa;再以 80 - 140 ℃/min升温至1600 ℃,同时压力由24 MPa上升至30 MPa;最后以60℃/min升温至烧结温度 1700 - 2100 ℃,同时压力保持30 MPa或上升至40 MPa,保温保压5-15 min;
S05. 卸压冷却:待步骤S04烧结结束后,卸压至初始压力,随炉冷却。
3.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述复相陶瓷的基体(VNbTaMoW)C5为面心立方结构,SiC为第二相。
4.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述SiC含量5-30%。
5. 如权利要求 1 所述的一种高熵碳化物(VNbTaMoW)C5 -SiC复相陶瓷,其特征在于:所述复相陶瓷相对密度为89.4 - 100 %,其维氏硬度和断裂韧性分别为 17 - 18.3 GPa和 4.5 - 5.7 MPa•m1/2。
6.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述SiC含量为20%。
7.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述复相陶瓷相对密度为99.2%,其维氏硬度和断裂韧性分别为18.2 GPa和5.7 MPa•m1/2。
8.如权利要求1所述的一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷,其特征在于:所述复相陶瓷具有优异的耐磨性能,平均比磨损率为(5.7-8.1)×10-8 mm³/N·m。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211235921.7A CN115433011B (zh) | 2022-10-10 | 2022-10-10 | 一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211235921.7A CN115433011B (zh) | 2022-10-10 | 2022-10-10 | 一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115433011A true CN115433011A (zh) | 2022-12-06 |
CN115433011B CN115433011B (zh) | 2023-08-18 |
Family
ID=84250158
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202211235921.7A Active CN115433011B (zh) | 2022-10-10 | 2022-10-10 | 一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN115433011B (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116283296A (zh) * | 2023-02-22 | 2023-06-23 | 广东工业大学 | 一种碳化硅增硬增韧高熵碳化物的复相陶瓷及其制备方法和应用 |
CN117986028A (zh) * | 2024-04-07 | 2024-05-07 | 山东硅苑新材料科技股份有限公司 | 碳化硅晶须增韧高熵氮化物陶瓷刀具材料及其制备方法 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109180189A (zh) * | 2018-10-08 | 2019-01-11 | 中南大学 | 一种高熵碳化物超高温陶瓷粉体及其制备方法 |
CN110205533A (zh) * | 2019-07-12 | 2019-09-06 | 南方科技大学 | 一种硬质合金及其制备方法与应用 |
CN110627508A (zh) * | 2019-08-28 | 2019-12-31 | 广东工业大学 | 一种高熵硼化物基陶瓷及其制备方法和应用 |
WO2020047278A1 (en) * | 2018-08-30 | 2020-03-05 | University Of Virginia Patent Foundation | Functional barrier coating and related methods thereof |
CN113185295A (zh) * | 2021-06-04 | 2021-07-30 | 合肥工业大学 | 一种制备max相高熵陶瓷材料的方法 |
CN113430443A (zh) * | 2021-06-18 | 2021-09-24 | 厦门钨业股份有限公司 | 一种超细wc硬质合金的制备方法 |
CN113817946A (zh) * | 2020-07-21 | 2021-12-21 | 中国人民解放军空军工程大学 | 一种HEA-SiC高温吸波材料及其制备方法 |
CN114315359A (zh) * | 2022-01-04 | 2022-04-12 | 哈尔滨工业大学 | 一种利用固溶耦合法制备高强韧复相高熵陶瓷的方法和应用 |
CN114850475A (zh) * | 2022-05-13 | 2022-08-05 | 北方民族大学 | 一种基于高熵合金粘结剂的高温抗氧化碳氮化钛金属陶瓷及其制备方法 |
-
2022
- 2022-10-10 CN CN202211235921.7A patent/CN115433011B/zh active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020047278A1 (en) * | 2018-08-30 | 2020-03-05 | University Of Virginia Patent Foundation | Functional barrier coating and related methods thereof |
CN109180189A (zh) * | 2018-10-08 | 2019-01-11 | 中南大学 | 一种高熵碳化物超高温陶瓷粉体及其制备方法 |
CN110205533A (zh) * | 2019-07-12 | 2019-09-06 | 南方科技大学 | 一种硬质合金及其制备方法与应用 |
CN110627508A (zh) * | 2019-08-28 | 2019-12-31 | 广东工业大学 | 一种高熵硼化物基陶瓷及其制备方法和应用 |
CN113817946A (zh) * | 2020-07-21 | 2021-12-21 | 中国人民解放军空军工程大学 | 一种HEA-SiC高温吸波材料及其制备方法 |
CN113185295A (zh) * | 2021-06-04 | 2021-07-30 | 合肥工业大学 | 一种制备max相高熵陶瓷材料的方法 |
CN113430443A (zh) * | 2021-06-18 | 2021-09-24 | 厦门钨业股份有限公司 | 一种超细wc硬质合金的制备方法 |
CN114315359A (zh) * | 2022-01-04 | 2022-04-12 | 哈尔滨工业大学 | 一种利用固溶耦合法制备高强韧复相高熵陶瓷的方法和应用 |
CN114850475A (zh) * | 2022-05-13 | 2022-08-05 | 北方民族大学 | 一种基于高熵合金粘结剂的高温抗氧化碳氮化钛金属陶瓷及其制备方法 |
Non-Patent Citations (2)
Title |
---|
HAO CHEN等: "Synthesis, microstructure and mechanical properties of high-entropy (VNbTaMoW)C5 ceramics", 《JOURNAL OF THE EUROPEAN CERAMIC SOCIETY》 * |
WENJIAN GUO等: "Ablation behavior of (TiZrHfNbTa)C high-entropy ceramics with the addition of SiC secondary under an oxyacetylene fame", 《CERAMICS INTERNATIONAL》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116283296A (zh) * | 2023-02-22 | 2023-06-23 | 广东工业大学 | 一种碳化硅增硬增韧高熵碳化物的复相陶瓷及其制备方法和应用 |
CN117986028A (zh) * | 2024-04-07 | 2024-05-07 | 山东硅苑新材料科技股份有限公司 | 碳化硅晶须增韧高熵氮化物陶瓷刀具材料及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN115433011B (zh) | 2023-08-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Qin et al. | A high entropy silicide by reactive spark plasma sintering | |
Asl et al. | Spark plasma sintering of TiC–SiCw ceramics | |
Guo | Densification of ZrB2-based composites and their mechanical and physical properties: a review | |
CN115433011A (zh) | 一种高熵碳化物(VNbTaMoW)C5-SiC复相陶瓷 | |
Ghahremani et al. | Densification, microstructure and mechanical properties of mullite–TiC composites prepared by spark plasma sintering | |
Hu et al. | Developments in hot pressing (HP) and hot isostatic pressing (HIP) of ceramic matrix composites | |
Wang et al. | Effect of TiB2 content on microstructure and mechanical properties of in-situ fabricated TiB2/B4C composites | |
Ghadami et al. | Novel HfB2-SiC-MoSi2 composites by reactive spark plasma sintering | |
Liu et al. | Strong high-entropy diboride ceramics with oxide impurities at 1800° C | |
Guo | Effects of VC additives on densification and elastic and mechanical properties of hot-pressed ZrB2–SiC composites | |
Guo et al. | Low‐temperature hot pressing of ZrB2‐based ceramics with ZrSi2 additives | |
Zhang et al. | Pressureless densification, microstructure tailoring and properties of Ta0. 8Hf0. 2C-based composites | |
Demirskyi et al. | Fracture and property relationships in the double diboride ceramic composites by spark plasma sintering of TiB2 and NbB2 | |
Baharvandi et al. | Processing and mechanical properties of boron carbide–titanium diboride ceramic matrix composites | |
Perevislov et al. | Thermal conductivity of SiC-B4C materials obtained by reaction-sintering method | |
Lin et al. | Effect of ZrB2 and its oxide impurities (ZrO2 and B2O3) on hot-pressed Si3N4 ceramics at low temperature | |
Yu et al. | Enhanced mechanical properties of Si3N4 ceramics with ZrB2-B binary additives prepared at low temperature | |
JP2002003276A (ja) | 炭化ケイ素−窒化ホウ素複合材料の反応合成 | |
Zhao et al. | Fast preparation of ZTA-TiC-FeCrNi cermets by high-gravity combustion synthesis | |
CN112011717B (zh) | 一种高强度低膨胀复合材料及制备方法 | |
KR101723675B1 (ko) | 전기전도성 탄화규소-질화붕소 복합 소재 제조용 조성물 및 이를 이용한 전기전도성 탄화규소-질화붕소 복합 소재의 제조방법 | |
Pourali et al. | Microstructures and Mechanical Behavior of Ti 3 SiC 2/Al 2 O 3-Ni Composites Synthesized by Pulse Discharge Sintering | |
Kannan et al. | Densification, mechanical, and tribological properties of ZrB2‐ZrCx composites produced by reactive hot pressing | |
Cai et al. | Mechanical and thermal properties and microstructural evolution of Ta-doped Nb4AlC3 | |
Attia et al. | Hot Pressed Si 3 N 4 Ceramics Using MgO–Al 2 O 3 as Sintering Additive for Vehicle Engine Parts |
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 |