电热爆炸喷涂法原位合成MoSi2涂层的试验研究

利用电热爆炸喷涂设备,在低碳钢基体上制备了MoSi:涂层.对涂层进行了显微组织、相结构、元素分布及显微硬度分析.结果表明,涂层中存在树枝晶、柱状晶和等轴晶,晶粒细小致密均匀.涂层主要由MoSi2相组成,并含有微量的Mo5si3相.涂层与基体间存在着原子扩散现象,为冶金结合.涂层显微硬度为1000～1400 HV0.1.     

电火花沉积法在铜电极表面制备TiB2/Ni涂层

为了提高镀锌钢板用点焊电极的使用寿命,在铜电极表面涂覆过渡层Ni后沉积了TiB2涂层。通过SEM和XRD分析了Ni和TiB2涂层的物相和微观结构,并测试了其显微硬度。结果表明：由于材料具有良好的塑性,预涂覆的Ni涂层结构致密无裂纹,与基体Cu无分层;而TiB2涂层内存在裂纹和孔洞。通过过渡层Ni将TiB2涂层和基体Cu粘结起来,获得了较理想的涂层。随着电火花放电电容和电压的增加,TiB2的氧化程度增强,Cu和Ni大量扩散进入涂层表面,使TiB2/Ni涂层的硬度降低。由于TiB2良好的导电和导热性能及高的硬度,TiB2/Ni涂层电极在点焊时的塑性变形降低,寿命比无涂层电极和TiC涂层电极得到了明显提高。     

TC4合金氩弧熔覆Ni60+B4C复合涂层组织及耐磨性

利用氩弧熔覆技术在TC4合金表面成功制备出TiC、TiB、TiB2增强Ti基复合涂层.利用SEM、XRD和EDS分析了熔覆涂层的显微组织;利用显微硬度仪测试了复合涂层的显微硬度;利用摩擦磨损试验机测试了涂层在室温干滑动磨损条件下的耐磨性能.结果表明:氩弧熔覆涂层组织均匀致密,熔覆层与基体呈冶金结合,TC4合金表面有颗粒状TiC、粗大棒状相TiB2、细小棒状相TiB生成;复合涂层明显改善了TC4合金的表面硬度,涂层的最高显微硬度可达1300 HV0.2;复合涂层在室温干滑动磨损试验条件下具有优异的耐磨性,磨损机制主要是魔力磨损,其耐磨性较TC4合金基体提高近10倍.     

大气等离子喷涂制备Ni基TiB_2复合涂层的研究

采用化学镀Ni-B合金包覆TiB2粉,Metco-7M等离子喷涂制备TiB2/Ni-5%Al金属陶瓷涂层,研究TiB2含量对涂层的微观组织、结合强度、显微硬度的影响。用X射线衍射、SEM扫描电镜分析涂层物相组成和形貌;用线扫描能谱分析涂层与基体的界面元素分布;采用对偶件拉伸法测试涂层结合强度,用显微硬度仪测试涂层硬度。结果显示,TiB2以原始颗粒形态存在于涂层中,无TiB2的氧化产物TiO2,其他氧化产物Al2O3、NiO含量较低;涂层与低碳钢基体存在微观冶金结合;结合强度高达40 MPa,随TiB2含量增加,涂层显微硬度增大,结合强度变化不大。     

反应磁控溅射法制备(Ti,Al)N薄膜的力学性能

以WF6和H2为原料,采用化学气相沉积法在纯铜基体上沉积出难熔金属钨涂层。分析研究了不同沉积温度(500℃,600℃,700℃)沉积层显微组织、表面形貌、表面粗糙度及相关机制。试验分析表明:随沉积温度升高,沉积速率加快,涂层组织柱状晶生长取向趋于杂乱;沉积层表面形貌发生明显改变,表面粗糙度显著增加。杂质颗粒对沉积组织有显著的影响,造成沉积表面粗糙度显著增加。     

基体温度对磁控溅射CrN涂层微观结构和性能的影响

采用直流反应磁控溅射技术在1Cr18Ni9Ti奥氏体不锈钢表面沉积Cr N涂层,利用SEM、XRD、显微硬度仪、划痕仪和摩擦磨损试验仪研究了基体温度对涂层组织结构、力学性能和摩擦磨损性能的影响。结果表明,Cr N涂层主要呈现出fcc结构,并存在(111)晶面择优取向,基本温度为100℃时制备的涂层(111)和(220)取向竞争生长,300℃时制备的涂层(200)晶面生长增强;涂层的表面晶粒主要呈现三棱锥形貌;基体温度对涂层的力学性能影响较大,300℃时制备的涂层显微硬度和结合力的最高值分别达到1900 HV和50 N;涂层磨损率随基体温度的升高而降低。     

TiB2对Ni基合金激光熔覆层组织与性能的影响

采用5 kW CO2激光器在低碳钢表面熔覆Ni基合金层及TiB2/Ni基合金金属陶瓷涂层,研究了两种涂层的组织、显微硬度以及滑动磨损特性.结果表明,Ni基合金层主要组成相为γ-(Ni,Fe),Cr23C6等,TiB2/Ni基合金复合涂层组成相主要有γ-(Ni,Fe),Ni3B,TiB2和TiC等;Ni基合金层由发达γ-(Ni,Fe)枝晶和其间共晶组织所组成,TiB2/Ni基合金复合涂层典型组织为等轴固溶体以及其间细小共晶组织;TiB2对熔覆层的组织有显著的影响,使熔覆层组织细化,并由树枝晶转变为等轴晶;加入TiB2可显著提高Ni基合金涂层的显微硬度及耐磨性能.     

稀土对氩弧熔覆复合涂层组织和性能的影响

以Ti,B4C,Y2O3和Ni60A粉末为原料,利用氩弧熔覆技术在Q235钢基材表面成功制备出镍基增强相复合涂层,运用 XRD,SEM等分析手段研究了复合涂层的显微组织,利用显微硬度仪测试了复合涂层的显微硬度,并用磨损试验机分析了其在室温干滑动磨损条件下的耐磨性能. 结果表明,复合涂层与基体界面无气孔、裂纹,呈冶金结合. 复合涂层由TiC,TiB2,Cr23C6和γ-Ni组成. 稀土加入改变了TiC和TiB2的长大形态,呈颗粒状均匀、细小的分布在熔覆涂层中. 显微硬度和耐磨性测试结果表明,稀土加入后提高其显微硬度和磨损性能.     

沉积温度对CrB_2涂层结构与性能的影响

为了研究沉积温度对涂层微结构与力学性能的影响,采用直流磁控溅射技术制备了CrB_2涂层。通过XPS、XRD、SPM、SEM、HRTEM、纳米压痕仪和维氏压痕仪分别分析了涂层的成分、结构、微观形貌和力学性能。结果表明:在不同沉积温度下,CrB_2涂层均由CrB_2和少量Cr相组成。涂层具有致密的纳米柱状结构,其直径大约为7nm,且沿着生长方向贯穿整个涂层截面。随沉积温度升高,涂层晶体取向由(101)和(001)的混合取向逐渐转变为(001)择优取向,涂层由纤维状结构转变为柱状晶结构,且柱状晶尺寸随沉积温度的增加逐渐细化,致密化程度增加。涂层的力学性能随沉积温度的升高而显著增加;当沉积温度达到400℃时,涂层具有最高硬度(50.7±2)GPa和最高弹性模量(513.6±10)GPa。微观结构和力学性能随沉积温度的演变归因于沉积原子运动的逐渐增强和结构的致密化。     

铜合金表面激光改性研究

利用500WYAG固体激光器在紫铜表面原位合成TiB2/Cu复合涂层,用扫描电镜分析了复合涂层的组织形貌以及熔覆层和基底之间的结合界面,测试了复合涂层的显微硬度和磨损性能。结果表明,采用激光熔覆表面改性技术可在紫铜表面合成厚度为100μm的TiB2/Cu复合涂层;涂层与铜基底形成了较好的冶金结合;TiB2分布均匀、颗粒细小,颗粒尺寸约为300～500nm;熔覆层显微硬度最高达380HV,平均硬度约240HV,是铜基底的3～4倍;TiB2/Cu复合涂层耐磨性能为紫铜的5～8倍。     

改进型镁扩散法制备高临界电流密度MgB2超导体性能研究

本文采用一种改进型镁扩散法成功制备出密度达到1.95g/cm₃的MgB₂超导块材。论文研究了不同的热处理条件对MgB₂块材的超导转变温度(T_c)和临界电流密度(J_c)性能的影响。采用最佳热处理条件制备的MgB₂超导体T_c和J_c分别达到了38.1K和0.53MA/cm₂(10K,自场)。为了改进镁扩散法MgB₂超导体中弱的高场磁通钉扎性能,本文还研究了nano-Pr₆O₁₁和C掺杂对MgB₂超导体的临界电流密度和不可逆场(H_irr)的影响。结果表明C掺杂的MgB₂超导体临界电流密度在10K,6T下达到了10₄A/cm₂,该结果比未掺杂MgB₂超导体在同样条件下性能提高了两个量级,甚至比固态反应法制备的nano-C掺杂MgB₂超导体性能更好。利用该方法制备的nano-Pr₆O₁₁掺杂的MgB₂超导体在10K,2T下也比未掺杂样品J_c提高达9.4倍。根据大量的实验结果和理论分析我们提出基于改进型镁扩散法和化学掺杂,包括纳米粒子和C掺杂,很有可能是一种制备高性能MgB₂超导体非常有效的途径。     

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。     

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.     

The high-temperature corrosion behavior of Nb-Al alloys in a H2/H2S/H2O gas mixture

The corrosion behavior of pure Nb and three Nb Al alloys containing 12.5, 25, and 75 at.% Al was studied over the temperature range of 800–1000°C in a H₂/H₂S/H₂O gas mixture. Except for the Nb-12.5Al alloy consisting of a two phase structure of -Nb and Nb₃Al, other alloys studied were single phase. The corrosion kinetics followed the parabolic rate law in all cases, regardless of temperature and alloy composition. The parabolic rate constants increased with increasing temperature, but fluctuated with increasing Al content. The Nb-75Al alloy exhibited the best corrosion resistance among all alloys studied, whose corrosion rates are 1.6–2.2 orders of magnitude lower than those of pure-Nb (depending on temperature). An exclusive NbO₂ layer was formed on pure Nb, while heterophasic scales were observed on Nb-Al alloys whose compositions and amounts strongly depended on Al content and temperature. The scales formed on Nb-12.5Al consisted of mostly NbO₂ and minor amounts of Nb₂O₅, NbS2, and -Al₂O₃, while the scales formed on Nb-25Al consisted of mostly Nb₂O₅ and some -Al₂O₃. The scales formed on Nb-75Al consisted of mostly -Al₂O₃ and Nb₃S₄ atT 900°C, and mostly -Al₂O₃ , Nb₃S₄ and some AlNbO₄ at 1000°C. The formation of -Al₂O₃ and Nb₃S₄ resulted in a significant reduction of the corrosion rates.     

Preparation and characteristic of spherical Li3V2(PO4)3

Spherical Li₃V₂(PO₄)₃ was synthesized by using N₂H₄ as reducer. The products were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results show that single-phase, spherical and well-dispersed Li₃V₂(PO₄)₃ has been successfully synthesized in our experimental process. Electrochemical behaviors have been characterized by charge/discharge measurements. The initial discharge capacities of Li₃V₂(PO₄)₃ were 123 mAh g⁻¹ in the voltage range of 3.0–4.3 V and 132 mAh g⁻¹ in the voltage range of 3.0–4.8 V.     

Effects of K2O-Li2O doping on surface and catalytic properties of Fe2O3/Cr2O3 system

The effects of K₂O and Li₂O-doping (0.5, 0.75 and 1.5 mol%) of Fe₂O₃/Cr₂O₃ system on its surface and the catalytic properties were investigated. Pure and differently doped solids were calcined in air at 400-600 °C. The formula of the un-doped calcined solid was 0.85Fe₂O₃:0.15Cr₂O₃. The techniques employed were TGA, DTA, XRD, N₂ adsorption at −196 °C and catalytic oxidation of CO oxidation by O₂ at 200-300 °C. The results revealed that DTA curves of pure mixed solids consisted of one endothermic peak and two exothermic peaks. Pure and doped mixed solids calcined at 400 °C are amorphous in nature and turned to α-Fe₂O₃ upon heating at 500 and 600 °C. K₂O and Li₂O doping conducted at 500 or 600 °C modified the degree of crystallinity and crystallite size of all phases present which consisted of a mixture of nanocrystalline α- and γ-Fe₂O₃ together with K₂FeO₄ and LiFe₅O₈ phases. However, the heavily Li₂O-doped sample consisted only of LiFe₅O₈ phase. The specific surface area of the system investigated decreased to an extent proportional to the amount of K₂O and Li₂O added. On the other hand, the catalytic activity was found to increase by increasing the amount of K₂O and Li₂O added. The maximum increase in the catalytic activity, expressed as the reaction rate constant (k) measured at 200 °C, attained 30.8% and 26.5% for K₂O and Li₂O doping, respectively. The doping process did not modify the activation energy of the catalyzed reaction but rather increased the concentration of the active sites without changing their energetic nature.     

Alloyed W–(Co,Ni,Fe)–C phases for reaction sintering of hardmetals

It has been shown that W–Co–C phases could dissolve a substantial amount of metals such as V, Cr and Ta, which are known to positively influence the microstructure of hardmetals with respect to uniform grain size distribution and fine grain size. This offers a tool to circumvent the conventional doping of hardmetals with individual carbides. In the present study we used double- and triple-alloyed κ-W₉Co₃C₄ (i.e. κ-(W,V,Cr)₉Co₃C₄ and κ-(W,V,Cr,Ta)₉Co₃C₄) and applied a variety of sintering experiments to obtain WC–Co, WC–(Ti,Ta,Nb)C–Co and WC–(Ti,Ta,Nb)(C,N)–Co hardmetals. We also prepared κ-W₉Fe₃C₄, alloyed κ-W₉Ni₃C₄, and κ-W₉(Fe/Ni)₃C₄, and used the latter for sintering.     

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.     

锂离子电池正极材料LiNi0.8Co0.15Al0.05O2的制备及电化学性能

首先以AlO2-为铝源,采用三元共沉淀法制备前驱体Ni_(0.8)Co_(0.15)Al_(0.05)(OH)_2。对前驱体进行500℃高温处理,随后与过量的锂盐混合均匀,在氧气气氛下700℃煅烧12 h制得LiNi_(0.8)Co_(0.15)Al_(0.05)O_2(NCA)材料。采用X射线衍射仪(XRD)测试可知,所得的NCA材料呈典型的α-NaFeO_2层状结构,属于R-3m空间群。扫描电子显微镜(SEM)测试显示,NCA为粒径5～6μm的球状颗粒。材料在电流倍率为0.1C下首次放电容量为167.1mAh/g,循环200次以后容量保持率为96.2%。倍率测试表明,0.1、10 C下NCA的容量分别为184.0、112.7 mAh/g,到恢复到0.1 C时,容量仍可达179.7mAh/g,具有比较好的倍率性能。     

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.