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1.
陶瓷颗粒增强型金属基复合涂层在诸多工业领域都有需求,其中包括炼钢工业。本文中,MCr Al Y-Al2O3复合粉末通过球磨法制备,并且通过等离子喷涂、超音速火焰喷涂和冷喷涂分别制备了MCr Al Y-Al2O3复合涂层。实验结果显示,可以选用不优先使基体与Al2O3结合的复合粉末控制涂层中的Al2O3含量。涂层粉末的微结构在冷喷涂涂层和超音速火焰喷涂涂层中得到了良好的保留,这是因为喷涂粒子未熔化或部分熔化。然而,对于等离子喷涂的涂层,大多数Al2O3颗粒被隔离在层状界面,在条状界面上形成连续的氧化皮。经退火处理后,由元素扩散引起的条状界面的强化使得超音速火焰喷涂和大气等离子喷涂的涂层硬度增大。此外,冷喷涂涂层由于退火后加工硬化效果的消除,硬度增加不像超音速火焰喷涂和等离子喷涂涂层那样明显。  相似文献   

2.
介绍了基于激光重熔技术的纳米陶瓷颗粒改性热喷涂耐磨涂层复合加工方法.以SiC纳米颗粒和WC-Co及Al2O3-TiO2热喷涂涂层为研究对象,进行了涂层改性加工试验.使用扫描电镜分析了纳米颗粒改性重熔涂层微观组织结构,并分别对热喷涂涂层、激光重熔喷涂涂层和纳米颗粒改性涂层进行了耐磨性测试.结果表明:SiC纳米颗粒能有效改善热喷涂涂层组织,并能显著提高涂层耐磨损性能.  相似文献   

3.
《Acta Metallurgica Materialia》1990,38(11):2283-2286
Precipitation and hardening were investigated in cobalt-tungsten alloys containing 5–13 at.% W. A significant hardening up to 860 HV in alloys aged at 600°C is caused by discontinuous precipitation. Transmission electron microscopy shows that as-quenched alloys consist of f.c.c. α-Co grains with frequent twins and martensitic plates. During ageing L12-type order develops within α-Co and simultaneously discontinuous precipitation starts at a grain boundaries. The microstructure consists of hexagonal ε-Co and Co3W lamellae as found during in situ high temperature studies in the electron microscope. High resolution electron microscopy reveals coherency strains within a few atomic layers at the ε-Co/Co3W interface and nonhomogeneous D19 ordering within the Co3W lamellae, resembling in some places nonstoichiometric B19 ordering.  相似文献   

4.
采用燃烧合成法成功制备了CoCr Mo合金。燃烧合成的合金是由钴的两种固溶体组成,分别为密排六方的ε-CoCr Mo相和面心立方的γ-CoCr Mo相;渣相主要为Al2O3;合金的微观结构为铸态树枝晶,并且存在枝晶偏析现象,枝晶上富钴,枝晶间富钼,铬分布比较均匀;此外,燃烧合成过程中可能产生马氏体相变使γ-Co相转变为ε-Co相,并且在马氏体片中出现了带状亚结构。  相似文献   

5.
The SiCp (20%) reinforced cobalt-based alloy composite coatings deposited by lasercladding on IF steel were introduced. The microstructure across the whole section of such coat-ings was examined using optical microscope, scanning electron microscope (SEM) and X-raydiffractometer (XRD), and the wear resistance of the coatings was measured by MM-200 typewear testing machine. The results show that the SiCp is completely dissolved during laser clad-ding and the primary phase in the coatings is r-Co. The other phases, such as SizW, CoWSi,Cr3Si and CoSi2, are formed by carbon, silicon reacting with other elements existing in themelting pool. There are various crystallization morphologies in different zones, such as planarcrystallization at the interface, followed by cellular and dendrite crystallization from interface tothe surface. The direction of solidification changes from one direction perpendicular to interfaceto multi-directions at the central and upper regions of the clad. The wear resistance of the cladis improved by adding SiCp.  相似文献   

6.
以铝粉和氧化铁粉作原料,采用等离子反应合成技术制备出了金属颗粒增韧的FeAl2O4-Al2O3-Fe复合陶瓷涂层。研究分析了复合涂层的组织及其性能。结果表明:等离子反应合成得到了以层状基体相FeAl2O4与硬质相Al2O3为骨架,球状Fe相弥散分布于基体相上的复合涂层。复合涂层的断裂韧性和结合强度明显优于普通Al2O3涂层,特别是复合涂层的具有较高的耐磨性能。  相似文献   

7.
利用激光熔覆技术在Q235钢基体表面分别制备出添加不同质量分数Y2O3的AlCoCrFeNi高熵合金涂层。采用X射线衍射仪、扫描电子显微镜、显微硬度计和摩擦磨损试验机对AlCoCrFeNi高熵合金涂层的微观组织、硬度及摩擦磨损性能进行了分析。结果表明:AlCoCrFeNi高熵合金涂层由面心立方结构(FCC)和体心立方结构(BCC)两相构成;随着Y2O3质量分数的提高,其体心立方结构相体积分数增加,而面心立方结构相的体积分数变化呈相反趋势。AlCoCrFeNi高熵合金涂层组织由等轴晶构成,加入Y2O3后,促进了熔池流动,使气孔逐渐消失,致密性提高,晶粒明显细化。添加质量分数5%Y2O3的涂层组织呈树枝晶状,形成弥散分布的YAl2和Y2O3相;涂层的显微硬度可达HV 350,约为AlCoCrFeNi高熵合金涂层硬度的2倍,强化效果明显。Y2O3的添加有利于促进涂层中体心立方相的形成和YAl2相的析出,能有效提高高熵合金涂层的硬度及耐磨性能。  相似文献   

8.
Ni-P-nano Al2O3 composite coatings were deposited by electroless plating,and their microstructures were observed by SEM(scanning electron microscope).The microhardness and the wear resistance of the Ni-P-nano Al2O3 composite coatings were measured using microhardness tester and block-on-ring tribometer,respectively,and the comparison with those of Ni-P coatings or Ni-P-micro Al2O3 coating was given.The influences of aging temperature on their hardness and wear resistance were analyzed.The results showed that the nano Al2O3 particles were distributed uniformly in the Ni-P-Al2O3 coatings.Among three kinds of Ni-P based coatings,the hardness and wear resistance of Ni-P-nano Al2O3 coatings were largest,and the maximum values could be obtained at 400 ℃.This indicated that the precipitation of nano Al2O3 particles would improve the hardness and wear resistance of the Ni-P coatings.  相似文献   

9.

The macroscopic multiphase flow and the growth of the solidification microstructures in the mushy zone of a direct chill (DC) casting are closely coupled. These couplings are the key to the understanding of the formation of the macrosegregation and of the non-uniform microstructure of the casting. In the present paper we use a multiphase and multiscale model to provide a fully coupled picture of the links between macrosegregation and microstructure in a DC cast billet. The model describes nucleation from inoculant particles and growth of dendritic and globular equiaxed crystal grains, fully coupled with macroscopic transport phenomena: fluid flow induced by natural convection and solidification shrinkage, heat, mass, and solute mass transport, motion of free-floating equiaxed grains, and of grain refiner particles. We compare our simulations to experiments on grain-refined and non-grain-refined industrial size billets from literature. We show that a transition between dendritic and globular grain morphology triggered by the grain refinement is the key to the explanation of the differences between the macrosegregation patterns in the two billets. We further show that the grain size and morphology are strongly affected by the macroscopic transport of free-floating equiaxed grains and of grain refiner particles.

  相似文献   

10.
TiB2 and Dy2O3 were used as codeposited particles in the preparation of Ni-TiB2-Dy2O3 composite coatings to improve its per-formance. Ni-TiB2-Dy2O3 composite coatings were prepared by electrodeposition method with a nickel cetyltrimethylanunonium bromide and hexadecylpyridinium bromide solution containing TiB2 and Dy2O3 particles. The content of codeposited TiB2 and Dy2O3 in the compos-ite coatings was controlled by adding TiB2 and Dy2O3 particles of different concentrations into the solution, respectively. The effects of TiB2 and Dy2O3 content on microhardness, wear mass loss and friction coefficients of composite coatings were investigated. The composite coat-ings were characterized by X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometer (ICP-AES) and scanning electron microscopy (SEM) techniques. Ni-TiB2-Dy2O3 composite coatings showed higher microhardness, lower wear mass loss and friction coefficient compared with those of the pure Ni coating and Ni-TiB2 composite coatings. The wear mass loss of Ni-TiB2-Dy2O3 composite coatings was 9 and 1.57 times lower than that of the pure Ni coating and Ni-TiB2 composite coatings, respectively. The friction coefficient of pure Ni coating, Ni-TiB2 and Ni-TiB2-Dy2O3 composite coatings were 0.723, 0.815 and 0.619, respectively. Ni-TiB2-Dy2O3 composite coat-ings displayed the least friction coefficient among the three coatings. DY2O3 particles in composite coatings might serve as a solid lubricant between contact surfaces to decrease the friction coefficient and abate the wear of the composite coatings. The loading-bearing capacity and the wear-reducing effect of the Dy2O3 particles were closely related to the content of Dy2O3 particles in the composite coatings.  相似文献   

11.
 Microstructure and tensile properties of the Ti-23Al-17Nb alloy sheets rolling at (α2+B2+O)phase field with the various heat treatments were studied. Before rolling the microstructure of B2 phase particles embedded in O phase continuity matrix is acquired. The B2 phases deform more greatly and recrystallize more easily than α2/ O phases during the same rolling step. The (α2+B2) two-phase equiaxed microstructure is obtain by solution treatment at (α2+B2) phase field. The B2 phases become the continuity matrix by recrystallization and growing up of B2 grains and the anisotropy caused by rolling disappears. The microstructure obtained by solution treatment has more excellent tensile properties than the microstructure gained by subsequent aging treatment at (O+B2) phase field because the O phases precipitate as the block structure during aging and the B2 matrix continuity is broken down.  相似文献   

12.
激光熔敷合金层组织和腐蚀磨损特性的研究   总被引:4,自引:0,他引:4  
郑世安  张一民 《钢铁》1996,31(9):47-51,14
研究了在45钢表面进行激光熔敷镍基合金,镍基Cr2O3合金和镍基WC合金的熔敷层的组织结构、耐蚀性及不同冲击速度和不同浓度的腐蚀介质下的腐蚀磨损特性。结果表明,激光熔敷合金层不论耐性还是抗腐蚀磨损性能都优于不锈钢,产根据组织分析,显微硬度测试及腐蚀磨损后的表面形貌观察,探讨了熔敷合金层的腐蚀磨损过程。  相似文献   

13.
With the development of microwave integratedsystem for wireless communication, requirements ofthe microwave device are combined with high dielec tric constants (εr), low dielectric losses (Q = 1/tanδ) and near zero temperature coefficient for stabili ty and frequency selectivity[1,2]. But it is hard to findmaterials that satisfy all above mentioned requiredcharacteristics. In general, a ceramic with a high di electric constant has a larger positive temperature coef fi…  相似文献   

14.
Sm2O3 and TiB2 were used as codeposited particles in electrodeposition Ni-TiB2-Sm2O3 composite coatings to improve its performance. Ni-TiB2-Sm2O3 composite coatings were electrodeposited in the nickel sulfate,hexadecylpyridinium bromide and cetyltrimethylammonium bromide solution containing TiB2 and Sm2O3 particles. The content of codeposited Sm2O3 in the composite coating was controlled by changing the concentrations of Sm2O3 particles in the solution. The composite coatings were characterized with X-ray diffraction(XRD) and inductively coupled plasma-atomic emission spectrometer(ICP-AES) . The effects of Sm2O3 content on microhardness,wear weight loss and friction coefficient of composite coatings were investigated,respectively. The microhardness of the Ni-TiB2-Sm2O3 composite coatings was 19.35%,16.58%,2.03% higher than that of the Ni coating,Ni-Sm2O3 and Ni-TiB2 composite coatings,respectively. The wear weight loss of the Ni-TiB2-Sm2O3 composite coatings was 7,2.33,1.22 times lower than that of the Ni coating,Ni-Sm2O3 and Ni-TiB2 composite coatings,respectively. The friction coefficient of the Ni coating,Ni-Sm2O3,Ni-TiB2 and Ni-TiB2-Sm2O3 composite coatings were 0.712,0.649,0.850 and 0.788,respectively. The loading-bearing capacity and the wear-reducing effect of the Sm2O3 particles were closely related to the content of Sm2O3 particles in the composite coatings.  相似文献   

15.
Al_2O_3等氧化物对YSZ热障涂层的高温使用性能有一定的影响。本文用HVOF喷涂Ni Co Cr Al Y合金粘结层,APS喷涂YSZ陶瓷面层,制备了Al_2O_3含量为0.01~0.64wt%的YSZ涂层。比较了不同Al_2O_3含量的YSZ涂层在1100℃下的热震性能和抗烧结性能,并探讨Al_2O_3对涂层的影响机理。结果表明相较于高纯YSZ涂层,随着涂层中Al_2O_3含量升高,涂层的抗热震性能降低,且Al_2O_3促进YSZ涂层的烧结。Al_2O_3含量在小于0.01wt%-0.12wt%区间内时,对涂层抗热震和抗烧结性能有显著影响,含量继续增加至0.64%时,对性能影响减缓。显微组织观察与EDS检测结果表明涂层中Al_2O_3并未在熔融颗粒界面处偏聚,但在颗粒内部有局部偏析。由此推测,含Al_2O_3的YSZ涂层热震失效的原因可能是Al_2O_3在YSZ颗粒内部偏析,并影响涂层的烧结性能,导致裂纹容易萌生和扩展。  相似文献   

16.
 采用直流放电压缩电弧等离子束表面冶金技术,在Q235钢表面制备了添加La2O3和CeO2的铁基冶金涂层。研究了冶金涂层开裂的主要形式、稀土氧化物对冶金涂层组织及抗裂性的影响,初步探讨了稀土氧化物改善界面显微结构、抑制冶金涂层开裂的机制。结果表明:稀土除可与氧、硫、硼等反应外,还可固溶于晶内、晶界或晶界附近;添加适量的稀土氧化物可有效改善冶金涂层的组织和性能,抑制等离子束表面冶金涂层中的裂纹和孔洞。  相似文献   

17.
本文采用高能高速等离子喷涂方法制备了纳米Al2O3-13%TiO2(质量分数)涂层.通过X射线衍射法(XRD)分析了涂层物相成分,利用电子扫描显微镜(SEM)观察涂层截面组织形貌,并测量涂层显微硬度与结合强度.结果表明:该涂层具有独特的显微组织结构;涂层的维氏显微硬度达到了1134HV0.1;结合强度超过64MPa.  相似文献   

18.
采用直流电沉积技术在45#钢基体上制备Ni-W-Al2O3复合镀层,通过显微硬度计、摩擦磨损试验机、划痕仪等研究Al2O3颗粒含量对复合镀层的力学性能及摩擦磨损性能等的影响,并用SEM、XRD对复合镀层的表面断面形貌、物相结构进行分析.结果表明,Ni-W-Al2O3复合镀层为晶态结构,其耐磨性能明显优于Ni-W镀层,且随着Al2O3颗粒含量的增加,复合镀层的摩擦系数呈现出先减小后增大趋势.磨损形式主要表现为粘着磨损与磨粒磨损.复合镀层与基体之间结合牢固,结合力大小约为70~80 N.当Al2O3含量为5 g/L时,复合镀层的综合性能最优.  相似文献   

19.
将30MnB5热成形钢进行淬火和回火处理,利用扫描电镜、透射电镜、能谱仪和拉伸性能检测等方法研究了不同回火温度后的显微组织和力学性能变化.经200℃保温2 min回火后热成形钢的综合力学性能最佳,抗拉强度为1774 MPa,总伸长率为8%,强塑积达14 GPa·%以上,该性能满足热成形后作为汽车结构件的使用要求;并且随着回火温度的升高,力学性能呈非单调性变化.200℃低温回火后,主要为板条马氏体和ε碳化物,位错密度略有降低,析出的ε碳化物粒子呈针状分布在马氏体板条内,长度方向大小为100 nm左右,并与位错发生钉扎作用.随着回火温度的升高,板条马氏体发生回复和再结晶,板条边界逐渐模糊,并向等轴状铁素体转变,位错密度显著降低,ε碳化物逐渐向低能态的近球形渗碳体转变并粗化至200 nm左右,对位错的钉扎作用也随之减弱.   相似文献   

20.
CeO2-Co3O4 Catalysts for CO Oxidation   总被引:1,自引:0,他引:1  
CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction (TPR), and FT-IR, the influence of the cerium content on the catalytic performance of CeO2-Co3O4 was investigated. The results indicate that the prepared CeO2-Co3O4 catalysts exhibit a better activity than that of pure CeO2 or pure Co3O4. The catalyst with the Ce/Co atomic ratio 1 : 16 exhibits the best activity, which converts 77% of CO at room temperature and completely oxidizes CO at 45 ℃.  相似文献   

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