纳米CeO2掺杂对烧结钕铁硼磁体表面Zn-Al涂层性能的影响

采用喷涂工艺在烧结钕铁硼磁体表面制备了不同纳米 CeO₂ 掺杂量的 CeO₂ / Zn-Al 复合涂层。 利用扫描电子显微镜、显微硬度仪、盐雾试验箱和电化学工作站对 CeO₂ / Zn-Al 复合涂层的微观结构、力学性能及耐腐蚀性能进行表征分析。 结果表明:CeO₂ 纳米颗粒较均匀弥散分布于 Zn-Al 涂层中,不仅能够增加 Zn-Al 涂层的硬度,而且可以提高 Zn-Al 涂层的屏蔽性能,CeO₂ / Zn-Al 复合涂层耐中性盐雾试验能力高达 720 h。 添加的 CeO₂ 颗粒能够隔绝 Zn-Al 涂层中的锌铝薄片之间的直接接触,起到绝缘作用,延长了腐蚀介质渗入钕铁硼基体的腐蚀通道。     

煤油流量对NiCrBSi-CrSi2涂层微观结构及高温磨损性能的影响

在12CrMoVG基体上通过超音速火焰喷涂(HVOF)技术,分别采用不同煤油流量制备了NiCrBSi-CrSi₂复合涂层。利用 XRD、SEM、EDS、Raman、维氏显微硬度计、电子拉伸试验机和高温旋转式摩擦磨损试验机分别表征了不同煤油流量下涂层物相、组织结构、力学性能和高温摩擦磨损性能。结果表明: 不同煤油流量涂层的物相组成基本相同,均有γ-Ni、Ni₃B、Cr₂B、CrSi₂和Cr₅Si₃,但随着煤油流量升高,涂层中的CrSi₂和Cr₂B的部分会分别转变为Cr₅Si₃和CrB相。涂层显微硬度和结合强度随着煤油流量的升高均呈现先增后减的趋势,孔隙率和磨损率表现出先减后增的趋势。当煤油流量为30 L/h时,粉末熔融效果最好,涂层的孔隙率最低为0.17 %,显微硬度较高达到569 HV_0.3,结合强度较高为59 MPa,磨损率最低为2.84×10_-14 m₃^/(N.m)。磨痕表面产生的 Cr₂O₃、SiO₂和NiCr₂O₄等氧化物以及较高的涂层硬度使得30 L/h的涂层显示出最优的耐高温摩擦磨损性能。涂层的磨损机制以氧化磨损和黏着磨损为主。     

功率对激光熔覆(Fe0.25Co0.25Ni0.25Cr0.125Mo0.125)86B14涂层组织均质性及磨损性能的影响*

目前激光熔覆缺少对涂层组织、相结构纵向均质性与性能关联的研究。采用激光熔覆技术,选取不同的激光功率,制备(Fe_0.25Co_0.25Ni_0.25Cr_0.125Mo_0.125)₈₆B₁₄ 高熵合金涂层;借助电子探针(EPMA)、扫描电子显微镜(SEM)、能谱仪(EDS)和 X 射线衍射仪(XRD)等观察涂层微观组织与物相纵向分布,利用显微硬度计和摩擦磨损试验机测试涂层不同深度部位显微硬度及磨损性能,分析激光功率对熔覆(Fe_0.25Co_0.25Ni_0.25Cr_0.125Mo_0.125)₈₆B₁₄ 涂层纵向组织、物相分布影响规律及磨损性能。结果表明：三种功率下,涂层均由 BCC+FCC 相、硬质相 Mo₂B 组成,Mo₂B 在枝晶间富集。随着功率的增加,涂层中底部显微组织由细枝晶向粗大的柱状晶转变。三种涂层硬度均由表及里先增加后降低,摩擦因数先降低后增加;但是当激光功率为 1.6 kW 时,涂层呈现以 BCC 相为主的 FCC+BCC 双相结构,且由表及里 BCC 相含量不断增加、Mo₂B 含量逐渐减少,涂层组织均质化最高,摩擦因数变化梯度最小,耐磨损性能最佳。激光功率会影响熔覆高熵合金耐磨涂层均质性,进而影响摩擦性能的稳定性。     

激光重熔Al2O3-TiO2涂层的强韧性能

采用等离子喷涂和激光重熔复合工艺在Ti-6Al-4V基体上制备了Al₂O₃-TiO₂涂层,通过X射线衍射(XRD)、扫描电镜(SEM)、显微硬度试验和压痕试验等方法研究了激光重熔对涂层的组织及强韧性能的影响.结果表明,等离子喷涂Al₂O₃-TiO₂涂层中的主相为γ-Al₂O₃,而相应重熔涂层中的主相为α-Al₂O₃.激光重熔可消除喷涂态涂层内部的孔隙、微裂纹和层状堆垛等微观缺陷,获得致密化的组织,并使涂层与基体形成良好冶金结合.重熔涂层的硬度比相应喷涂态涂层约提高了50%,裂纹扩展抗力相比喷涂态涂层提高了近两倍.激光重熔纳米涂层中的未熔增强颗粒和纳米结构特性等对涂层起到了协同强化和韧化作用.     

环境障涂层用纳米结构Yb2SiO5粉体喂料的制备与表征

纳米结构稀土硅酸盐涂层被认为是未来新型环境障涂层的发展方向,其中 Yb₂ SiO₅ 由于与中间层莫来石的热物性能匹配良好、优异的抗水氧腐蚀能力成为非常有发展前景的环境障涂层面层候选材料。 从材料制备的角度出发, 探索纳米结构 Yb₂ SiO₅ 喂料制备工艺并对喂料进行物相、组织结构和性能表征。 采用喷雾造粒加固相烧结的方法制备了纳米结构 Yb₂ SiO₅ 喷涂粉体喂料,探索了制备高纯度 Yb₂ SiO₅ 的固相烧结工艺,后续通过等离子处理改善粉体喂料的喷涂性能。 借助 X 射线衍射仪研究了粉体喂料的物相,采用扫描电镜、透射电镜研究了粉体喂料的形貌与微观结构。 结果显示,固相烧结工艺采用在 1500 ℃下保温 4 h,再将得到的粉体喂料等离子处理可得到高纯度的 Yb₂ SiO₅ 喷涂粉体喂料,等离子处理之后的喂料为纳米结构,喂料粒度分布均符合等离子喷涂要求,喂料具有良好的流动性和致密性。     

转移等离子弧熔敷TiC-MoSi2 增强复合涂层显微组织及抗氧化性

为了提高AISI 304不锈钢的高温抗氧化性及耐磨性,利用转移等离子弧熔敷技术在AISI 304基材表面制备了TiC-MoSi₂复合相增强复合涂层。对比分析了氧化前后复合涂层的显微组织,测试了复合涂层的显微硬度分布,测试并拟合了复合涂层的氧化动力学曲线,探讨了复合涂层的氧化机理。结果表明：复合涂层典型显微组织由TiC-MoSi₂复合相、初生TiC枝晶和γ-(Ni,Fe)/NiSi₂共晶构成,TiC-MoSi₂复合相和初生TiC枝晶作为复合涂层的增强相均匀分布在γ-(Ni,Fe)/NiSi₂共晶基体上。由于TiC-MoSi₂复合相的增强作用以及超细γ-(Ni,Fe)/NiSi₂共晶基体的粘结和支撑作用,复合涂层具有高且均匀的硬度分布、良好的强度和韧性。得益于独特的显微组织,复合涂层表现出良好的高温抗氧化性。     

煤油流量对HVOF喷涂WC-12Co/NiCrBSi复合涂层显微组织与性能的影响

在 CrZrCu 基体上电镀 Ni 粘结层,通过超音速火焰喷涂(HVOF)技术,采用不同煤油流量在电镀 Ni 粘结层上制备了 WC-12Co / NiCrBSi 复合涂层。 利用 XRD、SEM、Raman、维氏显微硬度计、电子拉伸试验机和球盘式摩擦磨损试验机考察了不同煤油流量下涂层相组成、组织结构、力学性能和高温摩擦磨损性能。 结果表明:不同涂层的物相组成基本相同,喷涂过程中发生了一定程度的分解脱碳生成了 W2C,以及少量的 Cr₇C₃ 和 Co₃W₃C 相;随着煤油流量升高,涂层硬度提高,涂层孔隙率和耐磨性表现出先降低后升高趋势,致密的结构与较高的硬度有利于提高涂层的耐磨性;煤油流量为 26 L/ h 的工艺下制备的涂层孔隙率最低,为 0. 11%,硬度较高达到 927. 0 HV_{0. 3} ,摩擦因数最低约为 0. 46,磨损率最低为 2. 83×10^-15 m³ / (N·m),抗粘着磨损性能最好。     

汽轮机超音速火焰喷涂 NiCr-Cr3C2涂层

目的 通过热喷涂涂层,解决 350 MW 超临界机组再热第一级静叶栅的高温冲蚀问题。 方法 采用超音速火焰喷涂制备了 NiCr-Cr₃C₂ 涂层,测试了涂层的显微组织、孔隙率、显微硬度、结合强度及高温冲蚀性能,并对涂层在冲蚀条件下的失效机理进行分析。 结果 实验室条件下, NiCr-Cr₃C₂ 涂层孔隙率为 0 . 98% ,显微硬度达到 1061 . 2 HV0 . 3 ,结合强度约为 80 MPa。 装机试车时,0 . 22 mm 厚的 NiCr-Cr₃C₂涂层可使再热第一级静叶的寿命延长 3 倍左右。 结论 采用 NiCr-Cr₃C₂ 涂层可显著延长静叶寿命,小角度粒子犁削冲蚀是涂层加速失效的主要原因。     

氩弧熔敷原位合成TiC-TiB2/Ti基复合涂层组织及性能分析

利用氩弧熔敷技术,在TC4合金表面原位合成了TiC-TiB₂增强镍基复合材料涂层,利用SEM和XRD等方法分析了涂层的显微组织并测试了涂层的显微硬度.结果表明,熔敷组织主要由TiC,TiB₂和Ti(Ni,Cr)组成,TiB₂主要以棒状形式存在;在所形成的TiC-TiB₂/Ti复合材料层中,TiC和TiB₂颗粒分布均匀且尺寸细小;熔敷涂层由表及里组织不同;熔敷层与基体呈冶金结合,无气孔、裂纹等缺陷;涂层的显微硬度达到13.8 GPa,较基体提高了4.5倍.     

硅对高硅奥氏体不锈钢析出相的影响

采用XRD、TEM和压痕变形等方法研究了Si含量（4%~8%,质量分数）对高硅奥氏体不锈钢（ZeCorn）显微组织的影响。结果表明,Si含量的增加会导致ZeCor合金的相组成发生变化：ZeCor-4%Si合金组织为单相奥氏体（γ相）,ZeCor-6%Si合金主要含γ相和少量σ相,在ZeCor-8%Si合金中主要析出Cr₃Ni₅Si₂相和少量σ相。此外,Cr₃Ni₅Si₂与σ相相比具有更高的硅、镍含量。显微硬度HV高达7840 MPa的Cr₃Ni₅Si₂相是典型的硬脆相,该相的析出将大大提高ZeCor-8%Si合金中γ基体的显微硬度。ZeCor合金中γ基体的强化机制如下：固溶强化是ZeCor-6%Si合金的主要强化机制,而Si的固溶强化和Cr₃Ni₅Si₂的析出强化机制都大大提高ZeCor-8%Si合金中的γ基体的显微硬度。在ZeCor-8%Si合金中,Cr₃Ni₅Si₂相起显著作用。     

Effects of Mo and Al Additions on the Sulfidation Behavior of 310 Stainless Steel

The high-temperature sulfidation behavior of 310stainless steel (310SS) with Mo and Al additions (up to10 at.%) was studied over the temperature range700-900°C in pure-sulfur vapor over the range of 10^-3 to 10^-1 atm. Thecorrosion kinetics followed the parabolic rate law inall cases and the sulfidation rates increased withincreasing temperature and sulfur pressure. Thesulfidation rates decreased with increasing Mo and Al contents and it wasfound that the addition of 10 at.% Mo resulted in themost pronounced reduction among the alloys studied. Thescales formed on 310SS with Mo additions were complex, consisting of an outer layer of ironsulfide (with dissolved Cr), (Fe,Ni)₉S₈, andCr₂S₃/Cr₃S₄(with dissolved Fe), and an inner heterophasic layer ofFe_1-xS,Cr₂S₃/Cr₃S₄,NiCr₂S₄,Fe_1.25Mo₆S_7.7, FeMo₂S₄, andMoS₂. The scales formed on 310SS with Mo andAl additions had a similar mixture as above, except thatAl_0.55Mo₂S₄ was alsoobserved in the inner layer. The formation ofMoS₂ andAl_0.55Mo₂S₄ partly blocked the transport of cations throughthe inner scale, resulting in the reduction of thesulfidation rates compared to 310SS.     

废旧锂离子电池中Li, Fe和V的回收及xLiFePO4-yLi3V2(PO4)3的制备

由于LiFePO_4和Li_3V_2(PO_4)_3材料的特征相近,制备方法类似,提供了一种从废旧LiFePO_4和Li_3V_2(PO_4)_3混合电池中回收Li、Fe和V,再制备xLiFePO_4-yLi_3V_2(PO_4)_3的方法。在空气气氛中600℃热处理1h后,去除粘结剂PVDF使活性物质与集流体分离。调节Li、Fe、V和P摩尔比,球磨、锻烧,配制不同比例的xLiFePO_4-yLi_3V_2(PO_4)_3(x:y=5:1,7:1,9:1)复合电极材料。表征了其形貌、结构和电化学性能,结果表明,回收制备的复合材料将同时具备LiFePO_4和Li_3V_2(PO_4)_3两种材料的电化学性能,能显著改善LiFePO_4的倍率性能。     

LaSrCuO4粉体微结构对Ag/LSCO电接触材料性能的影响

以硝酸镧、硝酸铜、硝酸锶等为原料,分别采用固相法、溶胶-凝胶法和共沉淀法合成了不规则颗粒状(LSCO_g)、介孔状(LSCOm)和片层状(LSCOl)的LaSrCuO_4(LSCO)粉体。采用高能球磨并结合初压-初烧-热压工艺制备出Ag/LSCO电接触材料。利用X射线衍射(XRD)、扫描电镜(SEM)、金属电导率仪、维氏硬度计和电寿命试验机等对粉体形貌及电接触材料的物理和电学性能进行了表征。结果表明:与Ag/LSCO_(m)、Ag/LSCO_l材料相比,Ag/LSCO_(g)电接触材料表现出更加优异的物理性能,其电阻率为2.37μΩ·cm,硬度为800MPa,密度为9.32g/cm~3;但电学性能差异较小,其在AC220V12A开断状态下的燃弧能量为400 mJ、燃弧时间为23 ms,关合状态下的燃弧能量为1500 mJ,燃弧时间为68ms。Ag/LSCO电接触材料的主要失效形式是液滴喷溅,微裂纹和孔洞。     

Synthesis of lanthanum carbonate nanoparticles via sonochemical method for preparation of lanthanum hydroxide and lanthanum oxide nanoparticles

Lanthanum carbonate nanoparticles were synthesized from the reaction of lanthanum acetate and Na₂CO₃ under sonication via sonochemical method. Lanthanum hydroxide nanoparticles were prepared by facial hydrothermal processing from the resulted product at 110 °C for 24 h. The role of surfactant, calcination temperature and sonication time were investigated on the morphology and particle size of the products. Products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectrum (XPS), and Fourier transform infrared (FT-IR) spectra. La₂O₃ nanoparticles were obtained by calcinations of the nanoparticles of lanthanum carbonate at 600 °C.     

Effects of sulfur pressure on the sulfidation behavior of 310 stainless steel

High-temperature sulfidation behavior of 310 stainless steel was studied over the temperature range of 700–900°C above a pure sulfur pool with the sulfurvapor range of 10^–4–10^–1 atm. The corrosion kinetics followed the parabolic rate law in all cases. The corrosion rates increased with increasing temperature and sulfur pressure. The scales formed on 310 stainless steel were complex and multilayered. The outer scale consisted of iron sulfide (with dissolved Cr), (Fe, Ni)₉S₈ and chromium sulfides (Cr₂S₃ and Cr₃S₄ with dissolved Fe), while the inner layer was a heterophasic mixture of Cr₂S₃, Cr₃S₄, NiCr₂S₄, and Fe₁–_xS. Platinum markers were found to be located at the interface between the inner and outer scales, suggesting that the outer scale grew by the outward transport of cations (Fe, Ni, and Cr), and the inner scale grew by the inward transport of sulfur. The formation of Cr₂S₃, Cr₃S₄, and NiCr₂S₄ partly blocked the transport of iron through the inner scale, resulting in a reduction of the corrosion rates as compared with the results in the literature.     

Improved capacity and rate capability of Ru-doped and carbon-coated Li4Ti5O12 anode material

Pure Li₄Ti₅O₁₂, modified Li₄Ti₅O₁₂/C, Li₄Ru_0.01Ti_4.99O₁₂ and Li₄Ru_0.01Ti_4.99O₁₂/C were successfully prepared by a modified solid-state method and its electrochemical properties were investigated. From the XRD patterns, the added sugar or doped Ru did not affect the spinel structure. The results of electrochemical properties revealed that Li₄Ru_0.01Ti_4.99O₁₂/C showed 120 and 110 mAh/g at 5 and 10 C rate after 100 charge/discharge cycles. Li₄Ru_0.01Ti_4.99O₁₂/C exhibited the best rate capability and the highest capacity at 5 and 10 C charge/discharge rate owing to the increase of electronic conductivity and the reduction of interface resistance between particles of Li₄Ti₅O₁₂.It is expected that the Li₄Ru_0.01Ti_4.99O₁₂/C will be a promising anode material to be used in high-rate lithium ion battery.     

High-temperature corrosion of Co-15Mo alloys containing ternary additions of Al in mixed-gas environments

The corrosion behavior of Co-15 at.% Mo alloys containing up to 20at.% Al in gaseous H ₂ -H ₂ O-H ₂ S mixtures was studied over the temperature range of 600–900°C. The corrosion kinetics of all alloys followed the parabolic rate law over the temperature range of interest. Corrosion resistance increased with increasing aluminum content. Complex scales formed on the alloys, consisting of an outer layer of cobalt sulfide and a heterophasic inner layer. Al ₂ O ₃ formed only at high temperatures in alloys having aluminum additions of 15at.% or more. The absence of Al ₂ O ₃ in some cases is due to the small volume fraction of the intermetallic phase CoAl in the alloys and the nature of the slow growth rate of Al ₂ O ₃.Improvement in corrosion resistance is attributed to the presence of a ternary sulfide, Al _0.55 Mo ₂ S ₄,and Al ₂ O ₃ in the inner layer.     

The combined effect of refractory coatings containing reactive elements on high temperature oxidation behavior of chromia-forming alloys

The high temperature oxidation behaviors of chromia-forming alloys (F17Ti and Fe-30Cr alloys) have been studied at 1273 K under isothermal conditions and at 1223 K under cyclic conditions, in air under the atmospheric pressure. To extend the oxidation lifetime, coatings have been applied onto the alloy surfaces. Al₂O₃ and Cr₂O₃ films doped with Sm₂O₃ or Nd₂O₃ were prepared via the metal-organic chemical vapor deposition technique. Single Cr₂O₃, Al₂O₃, Nd₂O₃ and codeposited Cr₂O₃-Nd₂O₃, Al₂O₃-Nd₂O₃, Al₂O₃-Sm₂O₃ coatings drastically improved the chromia-forming alloy high temperature oxidation behavior, since they decreased the oxidation rate and enhanced the oxide scale adhesion. Results showed that a critical amount of reactive element (Nd or Sm) in chromia or alumina coatings (11-18 at.%) was needed to observe the most effective effect. The fast precipitation of NdCrO₃ or NdTi₂₁O₃₈ and the segregation of reactive elements at the chromia grain boundaries slowing down outward cation transport and consequently blocking the chromia grain growth, was supposed to be the main reasons of the beneficial effect ascribed to the reactive elements in chromia scales.     

Effect of Y2O3 additions on the plasticity of sintered Cr2O3

We have carried our constant strain-rate compression tests on polycrystalline Cr₂O₃ and Cr₂O₃ doped with 0.09 wt. % Y₂O₃ to establish whether there exists an effect of Y₂O₃ on the plasticity of Cr₂O₃. This study is motivated by previous work on the oxidation of alloys containing reactive-element additions. In that work, it has been observed that the addition of oxygen-active elements, such as Y to alloys that form Cr₂O₃ or Al₂O₃ oxide layers upon exposure at high temperature, strongly enhances the adhesion of the oxide layer to the base alloy as compared with alloys without reactive-element additions. We have found that at 1200°C (1) chromia exhibits limited plasticity at high temperatures, and (2) the presence of Y in the oxides does not enhance plasticity compared with addition-free oxides.     

The high-temperature corrosion behavior of Co-Nb alloys in mixed-gas atmospheres

The corrosion of Co-Nb alloys containing up to 30 wt.% Nb in H₂-H₂S-H₂O gas mixtures was studied over the temperature range of 600–800°C. The gas composition falls in the stability region of cobalt sulfide and Nb₂O₅ in the phase diagrams of the Co-O-S and Nb-O-S systems at all temperatures studied. Duplex scales, consisting of an outer layer of cobalt sulfide and a complex, heterophasic inner layer, were formed at all temperatures studied. In addition to cobalt sulfide and CoNb₃S₆, a small amount of NbO₂ was found in the inner layer. The reason for the formation of NbO₂ over that of Nb₂O₅ in the scale is that the outer sulfide scale lowers the oxygen activity within the scale into the NbO₂-stability region. Two-stage kinetics were observed for all alloys, including an initial irregular stage usually followed by a steady-state parabolic stage. The steady-state parabolic rate constants decreased with increasing amounts of Nb, except for Co-20Nb corroded at 700°C. Nearly identical kinetics were observed for Co-20Nb corroded at 600°C and 700°C. The presence of NbO₂ particles leads only to a limited decrease of the available cross-section area for the outward-diffusing metal ions. The activation energies for all alloys are similar and are in agreement with those obtained in a study of the sulfidation of the same alloys. The primary corrosion mechanism involves an outward Co transport.