高速电弧喷涂FeCrNiB/Cr3C2涂层的热腐蚀行为

采用高速电弧喷涂工艺在45钢基体上制备FeCrNiB/Cr3C2涂层。采用光学显微镜、扫描电镜和X射线衍射等手段分析了涂层微观组织和相组成。在650℃下研究了涂层的涂盐热腐蚀行为,腐蚀介质选用质量比为75∶25的Na2SO4+NaCl混合盐,并与20G钢作对比研究。结果表明,涂层具有典型的层状结构特征,致密且连续,涂层的抗热腐蚀性能都要优于20G钢。在650℃下涂层表面形成了Fe2O3、Cr2O3和FeCr2O4等致密的氧化膜,阻碍了熔盐的侵入,提高了涂层抗热腐蚀性能。     

Al/Cr复合涂层对Ti2AlNb合金抗热腐蚀性能的影响

目的改善Ti2AlNb合金在高温腐蚀盐环境中的耐热腐蚀性能。方法在Ti2AlNb合金表面通过双层辉光等离子渗铬及磁控溅射镀铝技术制备Al/Cr复合涂层,分析涂层热腐蚀前后的微观形貌和物相组成,并探究涂覆Na2SO4盐膜的试样在不同温度下(750、850、950℃)的热腐蚀行为。结果Al/Cr复合涂层组织均匀致密,且与基体结合良好,厚度约73μm,由表及里依次由Al沉积层、Al/Cr合金层、Cr沉积层、Cr扩散层四部分组成。经不同温度Na2SO4盐热腐蚀后,Al/Cr复合涂层腐蚀程度均显著小于合金基体。涂层试样经750~850℃Na2SO4盐热腐蚀后质量变化较小,850℃腐蚀增重仅0.525 mg/cm^2,而经历950℃、40 h熔盐热腐蚀后失重达到73.571 mg/cm^2,且试样截面出现剥离、脱落现象,Al/Cr复合涂层抵抗热腐蚀能力减弱。结论具有涂层保护的试样抗热腐蚀性能明显优于合金基体。Al/Cr复合涂层在750~850℃Na2SO4盐环境中具有良好的热腐蚀抗力,而更高温度段(850~950℃)的热腐蚀抗力下降。Al/Cr复合涂层在Na2SO4盐环境中良好的抗热腐蚀性得益于涂层中Al、Cr元素氧化形成以Al2O3、Cr2O3为主的混合氧化膜,有效阻碍外界氧气及腐蚀性介质侵入基体。     

渗铝改性离子镀NiCrAlY涂层的高温热腐蚀行为

为了进一步改善离子镀NiCrAlY涂层的抗热腐蚀性能,采用粉末包埋法在离子镀NiCrAlY涂层表面上进行渗铝,研究了涂层渗铝前后在850℃含氯硫酸盐膜下的热腐蚀行为.结果表明:在25%NaCl 75%Na2SO4熔盐中850℃热腐蚀40h时,未渗铝的NiCrAlY涂层生成的是外层以Cr2O3为主的氧化膜,渗铝后的NiCrAlY涂层仅生成一层Al2O3膜;未渗铝的NiCrAlY涂层在腐蚀50h后失去保护作用,而渗铝涂层在腐蚀100h后表面仍形成以Al2O3为主的保护膜.因此,渗铝处理可以明显提高原涂层的抗热腐蚀性能.     

渗铝镍基高温合金热腐蚀行为研究

采用低压气相渗铝工艺制备铝化物涂层 ,在涂层表面涂敷不同NaCl+Na2 SO4 含量的熔盐进行 90 0℃热腐蚀实验 .结果表明 ,涂层对NaCl含量不敏感 ,这与涂层表面生成Al2 O3 氧化膜有关 .涂层能有效提高合金抗热腐蚀性能 .     

纳米 NiCrBSi-TiB2 涂层在硫酸熔盐中的热腐蚀行为研究

目的研究纳米NiCrBSi-TiB2涂层在800℃下的Na2SO4-30%(质量分数)K2SO4熔盐中的热腐蚀行为。方法采用超音速火焰技术在中碳钢表面喷涂纳米NiCrBSi-TiB2涂层,以饱和Na2SO4-30%K2SO4溶液为腐蚀介质,研究该涂层在800℃时的热腐蚀行为。结果微米涂层晶粒粗大,Si的扩散系数低,易出现贫Si富Cr层,形成的Cr2O3膜在碱性熔盐中具有较低的溶解度,对涂层具有良好的保护作用。结论微米涂层在Na2SO4-30%K2SO4熔盐中具有更优的抗热腐蚀性能。     

Pt-Al涂层在两种熔盐中的高温热腐蚀行为

采用表面涂盐法研究了镍基高温合金上Pt-Al涂层在Na2SO4和Na2SO4+NaCl两种熔盐中的高温热腐蚀行为.结果表明,在Na2SO4熔盐中,Pt-Al涂层具有很好的抗热腐蚀性能,表面只生成一层致密的氧化膜.在Na2SO4+NaCl混合熔盐中,它的抗热蚀性下降,涂层发生了内氧化和内硫化,并且内层NiAl相的腐蚀比外层富Pt相的更严重     

高速电弧喷涂FeNiCrAl/Cr_3C_2涂层的高温氧化性能和氧化机理

选用两种不同外皮的Fe Ni Cr Al/Cr3C2金属陶瓷粉芯丝材,采用高速电弧喷涂技术在45钢基体上制备涂层.采用增重法研究Fe Ni Cr Al/Cr3C2涂层在750℃时的氧化动力学曲线,利用金相显微镜、扫描电镜、X射线衍射仪研究涂层的显微组织结构和氧化产物,分析涂层在750℃时的抗高温氧化性能和氧化机理.结果表明,Fe NiCr Al/Cr3C2涂层的氧化动力学曲线呈抛物线型,涂层的增重明显低于20G钢,并且以304不锈钢为外皮的涂层的抗高温氧化性能明显优于以430不锈钢为外皮的涂层;涂层氧化后表面生成致密的氧化膜,阻塞氧的扩散通道,抑制氧化,起到保护作用.     

低碳钢表面电弧喷涂层FeNiCr/Cr_3C_2与NiCrTi的热腐蚀性能

采用高速电弧喷涂工艺在低碳钢基体表面制备了FeNiCr/Cr3C2和NiCrTi两种电弧喷涂涂层。通过光学显微镜对涂层的显微组织进行了观察研究。试验选用摩尔比为7：3的Na2SO4＋K2SO4饱和水溶液涂刷在涂层表面,在700℃的条件下进行了156 h的热腐蚀试验。通过腐蚀动力学测试对电弧喷涂涂层的抗热腐蚀性能进行了评估。采用了X射线衍射,扫描电镜和能谱分析技术对热腐蚀机理进行了探讨。结果表明,两种电弧喷涂涂层具有致密的层状结构,涂层中含有少量空隙。在涂层表面生成的连续致密的氧化膜使得NiCrTi涂层具有良好的抗热腐蚀性能。FeNiCr/Cr3C2涂层则遭受了较严重的氧化腐蚀和硫化腐蚀,并且有内硫化物析出,抗热腐蚀性能较差。     

电弧离子镀NiCrAlY涂层900℃的热腐蚀行为

采用电弧离子镀技术在镍基单晶合金上沉积Ni28Cr11Al0.5Y涂层,并研究了镍基单晶合金及有Ni28Cr11Al0.5Y涂层镍基单晶合金在900℃的75%Na2SO4+25%K2SO4熔盐中的热腐蚀行为。结果表明,镍基单晶合金遭受了破坏性的热腐蚀,出现了严重的内硫化和内氧化;而由于Ni28Cr11Al0.5Y涂层在熔盐中生成连续的Al2O3氧化膜,阻止了熔盐对单晶合金的腐蚀,有涂层镍基单晶合金表现出优良的抗热腐蚀性能。     

退火处理对离子镀NiCrAlY涂层热腐蚀性能的影响

为了进一步改善离子镀NiCrAlY涂层的抗热腐蚀性能,对NiCrAlY涂层在1050℃进行真空退火2h,研究了涂层退火前后的热腐蚀行为.结果表明,退火处理消除了离子镀NiCrAlY涂层的一些孑L洞,涂层形成了γ/γ' β多相平衡组织,使涂层组织更致密;在25%NaCl 75%Na2SO4(质量分数)盐膜下850℃热腐蚀20h时,未退火的NiCrAlY涂层生成的是外层Cr2O3、内层Al2O3的双层氧化膜,退火后的NiCrAlY涂层仅生成一层Al2O3膜,孕育期增长,在一定程度上提高了抗热腐蚀寿命.     

X-ray diffraction study of Ba0.985Na0.015Ti0.985Nb0.015O3, Ba0.6Na0.4Ti0.6Nb0.4O3 and Ba0.3Na0.7Ti0.3Nb0.7O3 compositions

The Ba_0.985Na_0.015Ti_0.985Nb_0.015O₃, Ba_0.6Na_0.4Ti_0.6Nb_0.4O₃ and Ba_0.3Na_0.7Ti_0.3Nb_0.7O₃ compositions of the (1 − x) BaTiO₃–xNaNbO₃ (BTNNx) system have been studied by X-ray diffraction and by measurements of dielectric properties. The specimens with composition BTNN (x = 0.015, 0.40 and 0.70) have been refined by the JANA program from X-ray powder diffraction data. Ceramic samples with composition (1 − x) BaTiO₃ + xNaNbO₃ (where x = 0.015, 0.40 and 0.70) were prepared by calcinations from appropriate mixture of BaCO₃, TiO₂, Na₂CO₃ and Nb₂O₅. The calcined powder was sintered at temperature range 1200–1400 °C. As the composition x increased from 0.015 (and 0.70), the ferroelectric ceramics (x = 0.015, FE) with tetragonal phase changed to the ferroelectric relaxors (RFE, x = 0.40). RFE ceramics showed a peculiar diffuse phase transition and dielectric relaxation at the low temperature (down to 180 K) due to a frustration between RFE and FE state. These ceramics present the classical ferroelectric character when 0 ≤ x < 0.075 and 0.55 < x ≤ 1 and relaxor character when 0.075 ≤ x ≤ 0.55.     

Magnetic, electrical and plastic properties of Fe76Nb2Si13B9, Fe75Ag1Nb2Si13B9 and Fe75Cu1Nb2Si13B9 amorphous alloys

Influence of 1 h annealing in vacuum on magnetic, electrical and plastic properties of Fe₇₆Nb₂Si₁₃B₉, Fe₇₅Ag₁Nb₂Si₁₃B₉ and Fe₇₅Cu₁Nb₂Si₁₃B₉ melt spun ribbons were carefully investigated. It was shown that in all cases soft magnetic properties can be significantly enhanced by applying 1-h annealing at characteristic temperatures T_op. This optimization annealing causes that permeability increases more than 15-times and magnetic losses (tangent of loss angle) achieves a minimum in relation to the as quenched state. Using structural examinations (X-ray and HRTEM) it was shown that for the Fe₇₅Cu₁Nb₂Si₁₃B₉ alloy the optimized microstructure corresponds to a nanocrystalline αFe(Si) phase whereas in other alloys to a relaxed amorphous phase free of iron nanograins. As a consequence of this fact the Fe₇₆Nb₂Si₁₃B₉ and Fe₇₅Ag₁Nb₂Si₁₃B₉ alloys show higher plasticity in comparison to the nanocrystalline Fe₇₅Cu₁Nb₂Si₁₃B₉ alloy. Temperatures of the first stage of crystallization, and related diffusion parameters were determined using measurements of resistivity versus temperature with different heating rates.     

Fe2+-Ni2+-NH3-NH4+-C2O42-H2O体系的沉淀配合平衡热力学

针对草酸盐配位共沉淀热分解还原法制备超细铁镍合金粉过程中Fe2+-Ni2+-NH3-NH4+-C2O42--H2O体系的溶液平衡建立热力学分析模型,并根据模型进行相关计算,揭示反应体系中各物质随pH值、氨及草酸浓度的变化关系。结果表明:溶液中的Fe主要以[Fe(C2O4)n]2 2n络合物形式存在,而铁氨络合物含量很低。当氨含量较低时,溶液中的Ni主要以[Ni(C2O4)n]2 2n存在;氨含量较高时,在酸性条件下,溶液中的Ni主要以[Ni(C2O4)n]2 2n存在,在碱性条件下,则主要以[Ni(NH3)n]2+存在。低pH值下,Ni的沉淀率较Fe的高,而高pH值下,Ni的沉淀率则较Fe的低。     

Al2O3-Sm2O3-CeO2电解质的性能（英文）

采用溶胶-凝胶法和低温燃烧技术制备Ce1-xSmxO2（x=0,0.1,0.2,0.3）和掺杂Sm和（2%-8%）Al2O3的二氧化铈;研究其合成、结构、致密化、导电性和热膨胀等性能,并利用XRD研究其结构和相组成。结果表明,于1300°C烧结球团,获得致密的陶瓷,于1250°C在Ce0.8Sm0.2O0.2中加入2%和4%的Al2O3以促进烧结。利用扫描电子显微镜观察烧结后球团的表面形貌,使用双探针交流阻抗谱研究总离子电导率。     

Sinterability and dielectric properties of Ba0.55Sr0.4Ca0.05TiO3-CaTiSiO5-Mg2TiO4 composite ceramics

The composite ceramics of Ba_0.55Sr_0.4Ca_0.05TiO₃-CaTiSiO₅-Mg₂TiO₄ (BSCT-CTS-MT) were prepared by the conventional solid-state route. The sintering performance, phase structures, morphologies, and dielectric properties of the composite ceramics were investigated. The BSCT-CTS-MT ceramics were sintered at 1100 °C and possessed dense microstructure. The dielectric constant was tailored from 1196 to 141 as the amount of Mg₂TiO₄ increased from 0 to 50 wt%. The dielectric constant and dielectric loss of 40 wt% Ba_0.55Sr_0.4Ca_0.05TiO₃-10 wt% CaTiSiO₅-50 wt% Mg₂TiO₄ was 141 and 0.0020, respectively, and the tunability was 8.64% under a DC electric field of 8.0 kV/cm. The Curie peaks were broadened and depressed after the addition of CaTiSiO₅. The optimistic dielectric properties made it a promising candidate for the application of tunable capacitors and phase shifters.     

Synthesis and electrochemical properties of LiNi0.4Mn1.5Cr0.1O4 and Li4Ti5O12

Spinel compound LiNi_0.4Mn_1.5Cr_0.1O₄ (LNMCO) and Li₄Ti₅O₁₂ (LTO) were synthesized by the sol-gel method and the solid-state method, respectively. The particle sizes of the products LiNi_0.4Mn_1.5Cr_0.1O₄ and Li₄Ti₅O₁₂ were 0.5 to 2 um and 0.5 to 0.8 um, respectively. All samples exhibited excellent electrochemical properties. A LiNi_0.4Mn_1.5Cr_0.1O₄/Li₄Ti₅O₁₂ (LNMCO/LTO) cell was fabricated and was demonstrated to exhibit good electrochemical properties at the high current rate of 1 C. When the specific capacity was determined based on the mass of the LNMCO cathode, the LNMCO/LTO cell delivered 125 mAh g⁻¹ at 1 C and 77 mAh g⁻¹ at 5 C. The capacity retentions after 30 cycles were 94.4 % and 83.1 %, respectively.     

Phase transition and piezoelectric properties of K0.48Na0.52NbO3-LiTa0.5Nb0.5O3-NaNbO3 lead-free ceramics

Plate-like NaNbO₃ (NN) particles were used as the raw material to fabricate (1 − x)[0.93 K_0.48Na_0.52Nb O₃-0.07Li(Ta_0.5Nb_0.5)O₃]-xNaNbO₃ lead-free piezoelectric ceramics using a conventional ceramic process. The effects of NN on the crystal structure and piezoelectric properties of the ceramics were investigated. The results of X-ray diffraction suggest that the perovskite phase coexists with the K₃Li₂Nb₅O₁₅ phase, and the tilting of the oxygen octahedron is probably responsible for the evolution of the tungsten-bronze-typed K₃Li₂Nb₅O₁₅ phase. The Curie temperature (T_C) is shifted to lower temperature with increasing NN content. (1 − x)[0.93 K_0.48Na_0.52NbO₃-0.07Li(Ta_0.5Nb_0.5)O₃]-xNaNbO₃ ceramics show obvious dielectric relaxor characteristics for x > 0.03, and the relaxor behavior of ceramics is strengthened by increasing NN content. Both the electromechanical coupling factor (k_p) and the piezoelectric constant (d₃₃) decrease with increasing amounts of NN. 0.01-0.03 mol of plate-like NaNbO₃ in 0.93 K_0.48Na_0.52NbO₃-0.07Li(Ta_0.5Nb_0.5)O₃ gives the optimum content for preparing textured ceramics by the RTGG method.     

AB3 型 Mm0.78 Mg0.22 Ni2.48 Mn0.09 Al0.23 Co0.47储氢合金的表面氟化处理

目的提高AB3型储氢合金的电化学性能,扩大其应用范围。方法运用HF和NaF组成的溶液对AB3型合金Mm0.78Mg0.22Ni2.48Mn0.09Al0.23Co0.47(Mm由82.3%La和17.7%Nd(均为原子数分数)组成)进行表面处理,考察改性处理对合金相结构、电化学性能以及动力学性能的影响。结果氟化处理后有MgF2相生成,合金电极的最大放电容量得到提高,50次循环后的容量保持率由83.3%提高到92.8%。此外,合金的动力学性能也得到一定改善。结论氟化处理改变了合金的表面结构,提高了其电化学性能。