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1.
The effects of partial substitution of light rare earths for Sm in (Sm1-xRx)2 (Co,Fe,Cu,Zr)17 have been investigated where R=Ce, Pr, Nd, Pr0.5Nd 0.5, Ce0.2Pr0.4Nd0.4 and x=0-0.5. Experiments show that both remanence and maximum energy product are improved for x=0.1-0.2, depending upon compositions and heat treatments. For a composition Sm0.8R0.2(Co0.633Fe0.286 Cu0.061Zr0.020)7.59 with R =Ce0.2Pr0.4Nd0.4, the authors obtained Br=11.57 kG, MHc =15.5 kOe, BHc=10.33 kOe, Hk=10.03 kOe, and (BH)max=30 MGOe  相似文献   

2.
Electron microscopic studies of as-cast Sm(Co,Fe,Cu,Zr)9 magnets revealed a hexagonal phase of the type Sm2(Co,Fe,Cu,Zr)17 with crystal lattice parameters of a=0.84 nm and c=3.2 nm. After a solid solution treatment, only rhombohedral (3R) and hexagonal (2H) grains were found. After an additional annealing treatment at 800°C, grains with a microcellular precipitation structure similar to the one found in Sm(Co,Fe,Cu,Zr)7.5 magnets occurred. In addition, in the as-cast and after-aged samples, other, partly unidentified Cu- or (Co,Fe)-enriched phases were detected  相似文献   

3.
寻求具有良好热物理性能的新型陶瓷材料是热障涂层领域的研究热点之一.本研究采用固相反应法制备了(Sm0.2Gd0.2Dy0.2Y0.2Yb0.2)3TaO7高熵陶瓷材料,对其晶体结构、显微组织、元素分布、结构稳定性和热物理性能进行了研究.结果表明:制备的高熵陶瓷具有单一的缺陷萤石结构,元素分布均匀,晶粒尺寸在0.2~3μ...  相似文献   

4.
The structure and magnetic properties of Sm3(Fe1-x Cox)27.7Ti1.3 compounds, with x ranging from 0 to 0.4, have been investigated by means of X-ray powder diffraction and magnetic measurements. The main phase formed was that of Nd3(Fe, Ti)29-type structure (3:29) with a relatively small amount of the ThMn12-type structure (1:12) as a secondary phase (7-13 wt.%). The lattice parameters and the unit-cell volume decrease with increasing Co content x. It is found that substitution of Co for Fe leads to a significant increase in the Curie temperature from 488 K for x=0 to 941 K for x=0.4. Saturation magnetization gradually increases with increasing Co. All compounds show easy cone-type anisotropy  相似文献   

5.
The mechanically alloyed (Al + 12.5 at.% Cu)3Zr powders were consolidated by cold isostatic pressing (CIP) and subsequent sintering. Effects of CIP pressure and sintering temperature on the stability of metastable L12 phase and nanocrystalline structure were investigated. Before sintering, the powders were CIPed at 138, 207, 276, and 414 MPa. The relative densities of the CIP compacts were not greatly affected by the CIP pressure. However, the L12 phase of the specimen CIPed at pressures greater than 276 MPa was partially transformed into D023. The optimum consolidation conditions for maintaining L12 phase and nanocrystalline microstructure were determined to be CIP at 207 MPa and sintering at 800 °C for 1 h for which the grain size was 34.2 nm and the relative density was 93.8%. Full density specimens could be prepared by sintering above 900 °C, however, these specimens consisted of L12 and D023 phases. The grain sizes of all the specimens were confirmed by TEM and XRD, and were found to be less than 40 nm. This is one of the smallest grain sizes ever reported in trialuminide intermetallic compounds.  相似文献   

6.
采用水热法在温度为503 K,反应时间为12 h的条件下制备了纺锤型磷灰石相Y4.67(SiO4)3O微晶,该微晶由粒径约为50 nm的颗粒组成。首次报道了纺锤型磷灰石相Y4.67(SiO4)3O微晶的热性能,同时研究了其相组成,微观结构及合成机理。结果表明,水热温度对所制备粉体的相组成及形貌有较大影响。此外,对应的陶瓷具有较低的热导率和较高的热膨胀系数,有望用作热障/环障涂层材料。  相似文献   

7.
We measured dielectric, magnetic, and microwave properties of Co 2U hexaferrite (Ba4Co2Fe36O 60) polycrystalline bulk and composite thick film samples, and studied the effect of annealing temperature on phase formation and microstructure. We synthesized the bulk samples from a precursor prepared by the citrate method. The values of dielectric constant at radio frequencies (50 Hz-1 MHz) of the bulk Co2U12 sample sintered at 1200degC are much higher, and the resistivities are lower, compared to M-type barium hexaferrites. Coercivity is also low, having a value of 5 G for the Co2U12 sample, whereas the saturation magnetization value is 59 emu/g, which is comparable to that of M-type hexaferrites. We also measured the complex permittivity and permeability for Co2U12 samples at microwave frequencies and found the values high compared to M-type barium hexaferrite at these frequencies. Thick composite films were prepared from a ferrite-polymer mix, and all the above properties were studied for these films. We observed that these thick films have lower values of dielectric and magnetic parameters both at low and microwave frequencies. We measured microwave-absorbing properties for the ferrite-polymer sample (ferrite to polymer ratio 70/30) which showed a maximum reflection loss of -37.5 dB at 11.5 GHz for the 3.5-mm-thick sample  相似文献   

8.
The coercivity of the melt-spun pseudobinary (NdFe10Cr 2)1-x (Nd2B)x alloys, in which Nd2B represents a composition of Nd0.67B0.33, was systematically studied. It was found that significant coercivities are possible with optimal additions of the Nd-B composition at x=0.5-0.7. The as-spun (substrate velocity=10 m/s) coercivity increased from 0.1 kOe at x=0.0 to maxima of 7.0 and 7.5 kOe at x=0.5 and 0.7, due to the Nd2 Fe14B and a new Fe-Nd phase, respectively, as evidenced from thermomagnetic analysis and X-ray diffraction. Annealing the overquenched amorphous x=0.7 alloy led to the crystallization of the Nd2Fe14B phase, and a coercivity of 8.5 kOe was obtained  相似文献   

9.
Co3O4 nanoparticles and cobalt (fcc-Co) powders were successfully synthesized by solvothermal process from a single precursor. The reaction of Co(Ac)2 with sodium dodecylbenzenesulfonate (SDBS) shows evident-dependent temperature effect. At 180 °C, Co(Ac)2 reacts with SDBS to produce precursor CoCO3 plate structures, which are assembled by small nanoparticles. At the temperature of 250 °C, the precursor CoCO3 can be gradually decomposed to form Co3O4 nanoparticles with diameter of ca. 70 nm. While, at 250 °C, the reaction of Co(Ac)2 with SDBS also produce precursor CoCO3 nanoparticles/plates, but the CoCO3 nanoparticles/plates would only decompose to give metal Co. In this process, SDBS acts as not only a surfactant but also a reagent. Magnetic measurements reveal that the as-prepared Co3O4 nanoparticles exhibit weak ferromagnetic properties and Co powders show ferromagnetic properties. In addition, a possible formation mechanism was elaborately discussed.  相似文献   

10.
采用静电纺丝技术结合高温煅烧方法,以乙酰丙酮钴(Co(C5H7O2)3)为前驱物,制备了由Co3O4纳米颗粒组成的多孔纳米纤维(Co3O4 NFs),其比表面积高达83 m2·g?1,并将制得的多孔Co3O4 NFs用于锂-空气电池催化剂。多孔Co3O4 NFs为电池反应提供了充足的活性位点及反应物的传输通道,有利于电池反应的顺利进行,使电池的放电容量得到极大地提高。另外,Co3O4催化剂的加入提高了电极的催化活性,较大程度降低了电池的过电位。值得注意的是,Co3O4催化剂的加入同时调控了锂-空气电池放电产物Li2O2的形貌,得到的放电产物Li2O2尺寸更小,在电极表面分布更为均匀,该形态的Li2O2在充电过程中更容易被分解,有利于提高电池的充电效率,同时电极的体积效应也可得到极大缓解。得益于以上优势,基于多孔Co3O4 NFs/炭黑Super P (Co3O4 NFs/SP)正极的锂-空气电池的电化学性能得到较大提高,50 mA·g?1电流密度下Co3O4 NFs/SP的放电容量高达10600 mA·h·g?1,电池可实现100次的充放电循环。   相似文献   

11.
Sodium potassium niobate, (Na0.5K0.5)NbO3, fine powder has been successfully synthesized at the low temperature of 550degC through a modified solid-state reaction method, in which urea [CO(NH2)2] plays an important role. High-density (Na0.5K0.5)NbO3 ceramics could be obtained by conventional sintering of the synthesized (Na0.5K0.5)NbO3 fine powder with the addition of 0.03 mol% Co3O4 as a sintering additive. The crystal structure, microstructure, and dielectric and piezoelectric properties were characterized. The (Na0.5K0.5)NbO3 ceramic showed a comparatively saturated P-E hysteresis loop. The (Na0.5K0.5)NbO3 ceramic also displayed piezoelectricity with a piezoelectric constant d33 of 126 pC/N and a planar electromechanical coupling factor kp of 33%.  相似文献   

12.
The fabrication process and the head material properties for shielded magnetoresistive heads with planarized lower shields using a tri-layered MR element are described in detail. Applying the etch-back process with low molecular weight polystyrene and CF4/O2 reactive ion etching, the residual step height for a lower shield is dramatically decreased to less than 5% of the initial step height. The tri-layered MR element consists of an MR layer, a magnetic separation layer (MSL), and a soft adjacent layer (SAL). 40-nm thick Ni 81Fe19 (wt.%) films were deposited by evaporation for use as an MR layer. Evaporated Ti MSL thickness was experimentally determined to be 20 nm. Amorphous Co82Zr6Mo12 SAL films exhibited preferable magnetic properties as an SAL material. The fabricated shielded MR heads, using the tri-layered MR element with these NiFe, Ti, and CoZrMo films, provide superior capability to realize high recording density  相似文献   

13.
对物理法制备的再生铜合金粉末进一步合金化,通过机械合金化(MA)结合放电等离子烧结(SPS)的方法制备了(Fe_(40)Ni_(40)Mn_(20))_(50)Cu_(50),(Fe_(38)Ni_(38)Ni_(38)Mn_(19)Al_(5))_(50)Cu_(50),(Fe_(36)Ni_(36)Mn_(18)Al_(10))50 Cu_(50)和(Fe_(32)Ni_(32)Mn_(16)Al_(20))_(50)Cu_(50)四种中熵合金块体,并研究了Al元素的含量对中熵合金微观组织与力学性能的影响。结果表明:在高能球磨60 h之后合金粉末完成合金化,四种中熵合金粉末均形成单一FCC相的过饱和固溶体且有微量WC杂质。经SPS烧结后,(Fe_(40)Ni_(40)Mn_(20))_(50)Cu_(50),(Fe_(38)Ni_(38)Mn_(19)Al_(5))_(50)Cu_(50)和(Fe_(36)Ni_(36)Mn_(18)Al_(10))50 Cu_(50)形成了由富Cu的FCC1相和富Fe-Ni的FCC2相组成的双相FCC结构,并具有超细晶+微米晶的多尺度结构;而(Fe_(32)Ni_(32)Mn_(16)Al_(20))_(50)Cu_(50)由富Cu的FCC主相和少量富Fe-Mn的FCC2相及富Ni-Al的BCC相(B2)组成。随着Al含量的提高,四种中熵合金的塑性逐渐降低,而强度和硬度逐渐提高。(Fe_(40)Ni_(40)Mn_(20))_(50)Cu_(50)合金的压缩屈服强度、抗压强度和维氏硬度分别为878 MPa,1257 MPa和248.5HV。与(Fe_(40)Ni_(40)Mn_(20))_(50)Cu_(50)相比,(Fe_(32)Ni_(32)Mn_(16)Al_(20))_(50)Cu_(50)的压缩屈服强度和硬度分别提高了50.1%和50.4%,断裂应变由19.55%下降至8.31%。  相似文献   

14.
Sm5Fe17 bulk materials, one of the newer permanent magnetic materials, were successfully produced by the spark plasma sintering method. The resultant bulk materials had high densities of 85–98%. When obtained by sintering at relatively lower temperatures, the Sm5Fe17 bulk materials consisted of the Sm5Fe17 and SmFe3 phases, whereas they contained some -Fe phase together with the Sm5Fe17 and SmFe3 phases when obtained by sintering at relatively high temperatures. High coercivity values, exceeding 2 MAm−1, were found in the Sm5Fe17 bulk materials consisting of the Sm5Fe17 and SmFe3 phases.  相似文献   

15.
Several alloys in the SmFe11Ti-Sm2TM17 (TM=Co/Fe/Cu/Zr) pseudobinary system containing O-90 wt.% Sm2TM17 were prepared by the melt spinning technique. A maximum as-spun coercivity of 4.6 kOe was obtained for the alloy containing 10 wt.% Sm2TM17 at a substrate velocity of 15 m/s. The coercivity is enhanced to 5.3 kOe after annealing at 800°C for 1 h. XRD (X-ray diffractometry) and TEM (transmission electron microscopy) were used to investigate the microstructure of the alloys. It is suggested that the grain refinement, doping of the 1-12 phase with Sm and other elements, and reduced free iron might be the main causes coercivity enhancement  相似文献   

16.
以Co(NO3)2·6H2O为钴源, NH4F和尿素作为添加剂, 通过水热法在粘胶基活性炭纤维(ACF)的表面生长了Co3O4纳米线, 制备了Co3O4@ACF复合材料并进行了结构形貌表征及电化学性能测试。结果表明: 针状的Co3O4纳米线阵列均匀地垂直生长在活性炭纤维表面, 形成了丰富的介孔结构。通过改变Co(NO3)2·6H2O的用量, 可以获得不同负载量的Co3O4@ACF复合材料。当Co3O4负载量为47wt%时, Co3O4@ACF复合材料在1 A/g电流密度下的比电容高达566.9 F/g, 几乎是纯Co3O4的2倍; 在15 A/g的电流密度下, 其比电容仍可达到393.3 F/g, 表现了较好的倍率特性; 经过5000次循环充放电后, 其比电容仍可保持84.2%, 展现了优良的循环稳定性。  相似文献   

17.
预先在酵母菌模板表面沉积Co(OH)3, 经高温煅烧后成功制得Co3O4空心微球, 并作为前驱体催化NaBH4水解制氢。通过场发射扫描电镜(FE-SEM)和X射线衍射(XRD)进行样品的微观形貌和物相分析。研究结果表明, 当反应液中NaBH4含量为10wt%时, 模板法制备的Co3O4空心微球催化产氢速率高达2140 mL/(min•g) (25℃), 约是同等条件下无模板制备Co3O4活性的9倍, 且所制备的Co3O4空心微球长期储存性能良好。  相似文献   

18.
The (1 − x) La0.67Ca0.33MnO3/xCuFe2O4 (x = 0, 0.04, 0.07, 0.10 and 0.15) composites have been prepared and investigated systematically for their microstructure, electrical and magnetic properties. The X-ray diffraction and scanning electronic microscopy analysis reveal that both La0.67Ca0.33MnO3 (LCMO) and CuFe2O4 phases are distributed in the composites. Compared with pure LCMO, an obvious enhancement of magnetoresistance is observed over a wide temperature range for the composites. Under 3 T field, the magnetoresistance rises from a base value 44.5% for pure LCMO, to a maximum value of 66.7% for x = 0.1 composite. Meanwhile, a weak temperature-dependent MR platform is observed in the temperature range from 210 K to 240 K. The MR enhancement is discussed in terms of spin-polarized intergrain tunneling due to enhanced magnetic disorder and magnetic coupling near boundaries between LCMO and CuFe2O4 grains.  相似文献   

19.
以AlN粉末为原料, 添加稀土氧化物(Sm2O3、Y2O3), 在氮气气氛下, 采用SPS烧结方法制备AlN陶瓷, 研究稀土氧化物的掺杂对AlN烧结试样相组成、微观结构和电性能的影响。实验表明: Sm2O3、Y2O3与Al2O3反应生成的液相稀土金属铝酸盐会提高AlN陶瓷致密度, 且在晶界处形成导电通路降低了AlN陶瓷电阻率。随着Sm2O3掺杂量的增加, 晶界相逐渐由Sm4Al2O9过渡到SmAlO3, 且Sm4Al2O9对电阻率贡献最大。其中, 3wt% Sm2O3掺杂AlN陶瓷电阻率最低, 为   相似文献   

20.
通过高温固相合成方法制备了烧绿石结构Gd2Zr2O7陶瓷材料,研究了其高温相稳定性和热物理性能。采用电子束物理气相沉积方法制备了Gd2Zr2O7-8YSZ(8%Y2O3-ZrO2)双陶瓷层结构热障涂层,分析了涂层顶层的晶体结构和原子数量比。结果表明,Gd2Zr2O7在室温至1500℃范围内具有良好的相稳定性,比第一代热障涂层8YSZ的高温相稳定区间提高250℃以上。Gd2Zr2O7块材的热膨胀系数在100~1500℃范围内介于8.8×10-6~11.0×10-6 K-1之间,与8YSZ接近; 在1000~1400℃高温区间,热导率约为1.0 W(m·K)-1,比8YSZ降低一半左右。沉积制得的Gd2Zr2O7涂层化学成分符合化学计量比,为烧绿石结构,涂层呈现典型的柱状晶结构。  相似文献   

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