203 resultados para Fe-Rh alloy
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本文以EDTA溶胶凝胶法合成K2NiF4型稀土复合氧化物La2Ni1-xMxO4(M=Cu,Fe),并对反应生成粉体分别进行SEM表征与XRD测试。结果表明,选取合适的制备工艺,可以形成La2Ni1-xMxO4(M=Cu,Fe)稀土复合氧化物材料;随着掺杂离子半径增大,生成材料晶格常数a增大同时,c减少,粉体颗粒粒径较大,同时少量杂相存在。
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本文设计并制备了具有优良的强韧性能和高温性能的激光熔覆涂层。利用 SEM、TEMEY X-射线衍射仪等研究了涂层的化学成分、宏微观结构及其转变机制,同时研究了涂层强韧性及耐高温磨损性能及其影响机制。对激光溶覆涂层进行了合金化、微观组织、强韧化机制、加工工艺性能设计。合金系为 Fe-Cr-C-W-Ni,成分配比(质量分数),Fe:52-60%, Cr:24-30%, C:5-6%, W:4.5-7.5%, Ni:5-6%。强化机制为两相强化、亚结构强化及固溶强化,其中强化相为合金碳化物,基体相为合金元素过饱和度极高的韧性奥氏体。亚共晶及过共晶组织的领先凝固相分别为奥氏体及 M_7C_3 合金碳化物,两相共晶组织均为韧性相奥氏体和强化相 M_7C_3 合金碳化物。加工工艺控制领先凝固相的结构、组织演化及力学性能。熔覆组织在高温时效过程中形成大量新的碳化物。在过饱和奥氏体内部,可弥散析出细小的 Mc、M_2C 及 M_(23)C_6碳化物;在奥氏体与 M_7C_3 相界面,亚稳相M_7C_3发生原位转变,形成 M_(23)C_6 及 M_6C碳化物。激光熔覆合金具有较高的综合力学性能,熔覆涂层有高的显微硬度、优良的抗回火稳定性、显著的二次硬化特征、优异的抗磨粒磨损和冲击磨损性能。Fe-Cr-C-W-Ni 激光熔覆合金具有较低的裂纹形成倾向和良好的表面成形性能,这与奥氏体较高的高温韧塑性及合金的低熔点共晶特征密切相关;实验及理论分析表明,通过调整合金成分、激光工艺参数和后续热处理工艺,可获得具有不同强韧性能的熔覆涂层。
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Metal-alumina joints have found various practical applications in electronic devices and high technology industry. However, making of sound metal ceramic brazed couple is still a challenge in terms of its direct application in the industry. In this work we successfully braze copper with Al2O3 ceramic using Zr52.5Cu17.9Ni14.6Al10Ti5 bulk metallic glass forming alloy as filler alloy. The shear strength of the joints can reach 140 MPa, and the microstructrural analysis confirms a reliable chemical boning of the interface. The results show that the bulk metallic glass forming alloys with high concentration of active elements are prospective for using as filler alloy in metal-ceramic bonding.
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A process of laser cladding Ni-CF-C-CaF2 mixed powders to form a multifunctional composite coatingd on gamma-TiAl substrate was carried out. The microstructure of the coating was examined using XRD, SEM and EDS. The coating has a unique microstructure consisting of primary dendrite or short-stick TiC and block Al4C3 carbides reinforcement as well as fine isolated spherical CaF2 solid lubrication particles uniformly dispersed in the NiCrAlTi (gamma) matrix. The average microhardness of the composite coatings is approximately HV 650 and it is 2-factor greater than that of the TiAl substrate. (C) 2008 Elsevier B.V. All rights reserved.
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The effects of constitution of precursor mixed powders and scan speed on microstructure and wear properties were designed and investigated during laser clad gamma/Cr7C3/TiC composite coatings on gamma-TiAl intermetallic alloy substrates with NiCr-Cr3C2 precursor mixed powders. The results indicate that both the constitution of the precursor mixed powders and the beam scan rate have remarkable influence on microstructure and attendant hardness as well as wear resistance of the formed composite coatings. The wear mechanisms of the original TiAl alloy and laser clad composite coatings were investigated. The composite coating with an optimum compromise between constitution of NiCr-Cr3C2 precursor mixed powders as well as being processed under moderate scan speed exhibits the best wear resistance under dry sliding wear test conditions. (C) 2008 Elsevier Ltd. All rights reserved.
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在光折变过程中,光波对掺杂中心的激发系数S是一个重要的物理量。为了求出光激发系数S对波长A的依赖,研究了在不同的擦除波长条件下,记录在光折变晶体LiNbO3:Fe中的光栅衰减特性。实验结果表明lnP(P为光擦除灵敏度)与擦除波长λ呈线性关系,即波长越短,光栅擦除越快,光擦除灵敏度越高。在单中心电子带传输模型的基础上,理论计算也证实了实验结果。利用带传输模型,给出了理论上光激发系数S对波长的指数依赖关系。同时微观量φμγ(φ为量子效率)也可由光栅擦除实验求出。
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针对90°全息记录结构的特殊性,在记录和读出阶段分别施加不同极性的外加电场,实现了Fe:LiNbO3晶体中高衍射效率的全息记录和读出。在库赫塔列夫(Kukhtarev)方程基础上引人两维耦合波理论,对组合外加电场提高掺铁铌酸锂晶体光折变特性的机理进行了探讨。实验和理论计算结果都表明这种分别在记录和读出过程施加不同极性组合的外加电场是在Fe:LiNbO3中实现高衍射效率90°记录结构体全息的有效技术方案。
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采用三种不同的双光记录方案进行了LiNbO3:Fe:Ni晶体全息存储实验.详细研究了饱和衍射效率、固定衍射效率、动态范围和记录灵敏度,以及退火条件对记录的影响。结果表明,氧化LiNbO3:Fe:Ni晶体的饱和衍射效率、固定衍射效率和记录灵敏度比其他报道的双掺杂LiNbO3晶体高。结合掺杂能级图,理论分析了LiNbO3双掺杂晶体深陷阱中心能级的相对位置及其微观光学参量对全息记录性能的影响。LiNbO3:Fe:Ni晶体有望成为一种新的高效率非挥发全息存储材料。
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为了解决读出过程中全息数据的擦除问题,研究了新型双掺杂LiNbOa:Fe:Ru晶体的全息读出特性。分析了双中心和单中心记录方案光栅的读出特性,并联立双中心物质方程和耦合波方程进行了模拟计算。结果表明,双中心记录所得到的饱和全息的读出时间常数远低于LiNbO2:Fe:Mn晶体的读出时间常数;单色光记录可以实现有效的全息,且其读出时间常数远大于记录时间常数,表现为准态非挥发读出。分析表明,这可能由于Ru的能级比Mn更靠近Fe,更易被红光激发,从而使得双中心记录所得饱和光栅的存贮持久性降低;单色光记录中红光能够
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观察到了双掺杂LiNbO3:Ru:Fe晶体中电色效应伴随畴反转而发生,且与畴反转一样也具有可逆性,两者相辅相成,畴反转导致了晶体变色,电色效应促进了畴反转,系统的实验结果证明了两者的相辅相成性.基于铌酸锂铁电微结构模型,简要解释了其机理.而且发现在极化过程中电色效应促使了畴核的形成,使之不同于非掺杂同成分比铌酸锂晶体的矫顽场大于击穿电场,用恒定直流电场代替脉冲电场也能实现畴反转,这将为周期性极化铌酸锂的制备提供一种新的技术改进.
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We report our observation of a bleaching effect under an ultraviolet exposure in LiNbO3:Fe:Cu crystals. Two three-step recording-transferring-fixing schemes are proposed to record nonvolatile photorefractive holograms in such crystals. In the schemes two red laser beams and an ultraviolet illumination are used selectively to write the charge grating in the shallow-level Fe centers, to develop the charge grating in the deep-level Cu centers by transferring the charge grating in the Fe centers, and to fix only the charge grating in the Cu centers for unerasable read-out. Experimental results, verifications, and an optimal recording scheme are given. A comparison of the lithium niobate crystals of the same double-doping system of Fe:Mn, Ce:Mn, Ce:Cu, and Fe:Cu is outlined. (C) 2002 Optical Society of America.
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The photorefractive holographic dynamics of grating formation in photochromic doubly doped LiNbO3:Fe:Mn crystal is studied numerically and analytically in terms of the two-center model of Kukhtarev Et al. [Ferroelectrics 22, 949 (1979)]. The relations among the recorded and fixed space-charge fields and the doping densities, the oxidation-reduction states of the fields, and the intensities of UV-sensitizing and red recording beams are studied. Important conditions and effects are feued, and an optimal prescription for material doping and oxidation-reduction processing is suggested in which the crystal can be strongly oxidized and the Mn-doping density is smaller than the Fe-doping density. (C) 2000 Optical Society of America. OCIS codes: 050.7330, 190.5330, 090.2900.
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In this paper the saturated diffraction efficiency has been optimized by considering the effect of the absorption of the recording light on a crossed-beam grating with 90 degrees recording geometry in Fe:LiNbO3 crystals. The dependence of saturated diffraction efficiency on the doping levels with a known oxidation-reduction state, as well as the dependence of saturated diffraction efficiency on oxidation-reduction state with known doping levels, has been investigated. Two competing effects on the saturated diffraction efficiency were discussed, and the intensity profile of the diffracted beam at the output boundary has also been investigated. The results show that the maximal saturated diffraction efficiency can be obtained in crystals with moderate doping levels and modest oxidation state. An experimental verification is performed and the results are consistent with those of the theoretical calculation.
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A reversible electrochromic effect accompanying domain-inversion during the electrical poling process in LiNbO3: Ru: Fe crystals at room temperature has been observed. In electrode area, both electrochromism and domain-inversion occur alternately, and electrochromism is also reversible during back-switch poling, which is experimentally verified and whose mechanism is briefly explained using a microstructure ferroelectric model. In addition, because of the enhancing elcctrochromic effect, different from the undoped LiNbO3 crystals, the coercive riled (21.0 kV/mm or so) measured in LiNbO3: Ru: Fe is lower than its breakdown field, thus providing a possible new technique for realizing the domain-inversion by constant electric field rather than a pulsed one.
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A reversible electrochromic effect during the electrical poling process in LiNbO3:Ru:Fe crystals at room temperature is observed. In electrode area, both electrochromism and domain-inversion occur mutually and electrochromism is reversible during back-switch poling, which are experimentally verified, and a microstructure model to explain the mechanism is proposed. In addition, different from the undoped LiNbO3 crystals, the breakdown field (> 25.0 kV/mm) is higher than the coercive (21.0 kV/mm) measured in LiNbO3:Ru:Fe, which proves a possible new technique to realize domain-inversion by constant electric field rather than pulsed one. (c) 2005 American Institute of Physics.