CeO_2对铝化物涂层高温氧化膜生长应力的影响(英文)

采用改进的双面氧化弯曲法,原位测定了900℃下 CeO_2及其含量对 Al 化物涂层上的氧化膜生长应力的影响,并计算出了含 CeO_2的复合涂层与两种简单渗 Al 涂层的生长应力差值。实验表明:涂层中添加 CeO_2可细化 Al_2O_3膜的晶粒,增加了氧化膜的塑性,使复合涂层在900℃氧化45h 后的氧化膜内的生长应力同 NiAl 涂层和M38G 合金渗 Al 层相比分别降低了约2000MPa 和500MPa。此外,试样在升温过程中的弯曲行为表明,三种涂层的线膨胀系数间关系为 α_(NiAl)>α_(NiAl+CeO(?))>α_(渗 Al M38G 合金)。     

等离子喷涂CNTs/Al2O3复合涂层力学性能研究

通过等离子喷涂工艺制备了不同碳纳米管含量的CNTs/Al2O3复合涂层,系统研究了碳纳米管含量对涂层孔隙率、洛氏硬度和断裂韧性的影响规律。实验结果表明:采用喷雾干燥工艺制备的CNTs/Al2O3颗粒为球形,CNTs均匀分布在团聚颗粒的表面;部分CNTs经等离子喷涂后保留在沉积涂层内部并且与Al2O3基体形成冶金结合,起到一定桥接作用。涂层孔隙率和洛氏硬度值均随CNTs含量的增加呈现降低的趋势。随CNTs含量从6%(质量分数)增加到12%(质量分数),CNTs增韧效果的增强和涂层孔隙率的降低导致涂层断裂韧性值从48MPa增加到90MPa。     

重力分离SHS法制备钢管Al2O3内衬耐热耐磨涂层的研究

采用重力分离SHS制备了钢管内衬Al2O3涂层,进行了力学、抗热震、耐蚀等性能测试,研究了管径、装料密度及不同含量SiO2、CrO3添加剂对涂层组织与性能的影响。研究结果表明,涂层主要物相结构为α-Al2O3+FeAl2O4相,添加剂SiO2和CrO3不改变涂层的主要相组成。反应过程中熔融金属Fe在钢管基体和内衬陶瓷层之间形成了一层金属过渡层。当添加2%SiO2+6%CrO3时,涂层孔隙率最小,硬度最大,抗热震性能最好,耐蚀性也较好,具有良好的综合性能。实验条件下,管径25cm、装料密度1.5g/cm3的内衬涂层硬度为1917HV,孔隙率为9.0%。     

掺杂型固态电解质Li1.4Al0.4ZrxTi1.6-x(PO4)3的制备及其在锂硫电池中的应用

以LiNO_3、Al(NO_3)_3、ZrO(NO_3)_2、NH_4H_2PO_4、Ti(OC_4H_9)_4为原料,采用修饰的溶胶凝胶法制备出NASICON型固态电解质Li_(1.4)Al_(0.4)Zr_xTi_(1.6-x)(PO_4)_3(LAZTP),通过烧结得到固态电解质片。研究了Zr~(4+)掺杂取代Ti~(4+)对固态电解质性能的影响。分别采用X射线衍射仪(XRD)、场发射扫描电子显微镜(FE-SEM)、电化学阻抗谱(EIS)表征了固态电解质的结构和电化学性能。结果表明,固体电解质Li_(1.4)Al_(0.4)Zr_xTi_(1.6-x)(PO_4)_3在掺Zr量为x=0.1时具有最高的纯度、好的致密度(98%)和高的离子电导率(体电导率和总电导率分别为2.8×10~(-3)S/cm、1.4×10~(-3)S/cm)。将该样品用作锂硫电池的电解质并采用恒流充放电法测试电池的电化学性能,电池在50mA/g的电流密度下首次可逆容量为1187mAh/g,循环40次后可逆容量仍达990mAh/g,显示出比液态锂硫电池更好的充放电性能和循环稳定性。     

射频磁控溅射制备 HA(+ZrO2+Y2O3)/Ti6Al4V 复合生物活性涂层

采用射频磁控溅射法制备了HA（＋ZrO2＋Y2O3）／Ti6Al4V生物复合涂层．借助于XRD、SEM、FTIR和AFM等对溅射涂层的相组成、微观形貌和界面结合进行了研究，并以模拟体液试验探讨了涂层的生物活性．实验结果表明：磁控溅射的复合涂层呈非晶态，经过退火处理，可以使其转化为晶态；复合涂层的微观表面凹凸不平，并呈现网状结构和较多的孔隙，其孔隙直径约为0．5-2．0μm，孔隙面积占涂层表面积的30％-40％；HA（＋ZrO2＋Y2O3）／Ti6Al4V复合涂层的界面结合强度随（ZrO2＋Y2O3）复合颗粒含量的增大和溅射功率的提高而增强，最高可达59．6MPa．复合涂层在模拟体液中浸泡一段时间后，表面覆盖一层新生物质—含有CO^2-3的类骨磷灰石，其晶粒非常小，它与自然骨中无机相的结构成分相似，表明复合涂层具有良好的生物活性．     

SiO_2添加剂对等离子喷涂ZrO_2涂层结构和性能的影响

本文研究 SiO_2添加剂对 ZrO_2涂层结构和性能的影响。结果表明,在增加过渡层的同时,添加3wt-%左右的 SiO_2,可使涂层的粘结强度和熱冲击寿命提高4—5倍。添加剂改善涂层寿命的原因是等离子喷涂时,SiO_2熔化渗入 ZrO_2颗粒之间和孔隙中,首先起到液相烧结作用;随后在涂层内汽化(蒸发)增加其孔隙率,使涂层的应力易于松弛,而且,SiO_2以石英相形态沿平行于表面方向塞积在涂层孔隙处,隔绝氧化气氛的进入,起到“自封孔”的作用。在粘结层和 ZrO_2层之间增加过渡层,有利于涂层应力的延缓过渡。     

Al2O3/Al2O3-ZrO2（3Y）层状纳米复合材料的制备与性能优化

为优化Al2O3层状复合材料的制备工艺及力学性能,选用不同初始粉体为原料制备了系列Al2O3/Al2O3-ZrO2(3Y)层状复合材料。借助X射线衍射、冷场发射扫描电镜和万能试验机等手段,系统考察了粉体结构和形貌对层状复合材料显微结构和性能的影响。结果表明:初始粉体的颗粒尺寸及尺寸分布会显著影响层状复合材料的显微结构及力学性能,以球磨微-纳米复合粉体为原料制备的层状复合材料具有最佳的力学性能,其抗弯强度和断裂功分别可达740MPa及3892J.m-2。同时,材料具有较高的层间结合强度,平行于层方向的抗弯强度高达436MPa。     

Ni-Cr2O3复合等离子喷涂层热处理改性前后的结构及性能

等离子喷涂层经热处理后可进一步改进其结构及性能,以往对其改性机理研究不多。采用等离子喷涂技术在20钢表面制备了Ni-Cr2O3复合涂层,经500℃、6 h热处理后随炉冷却。通过金相显微分析、X射线衍射、盐雾腐蚀、电化学试验等方法,对比研究了热处理前后Ni-Cr2O3复合涂层的组织形貌、相组成以及耐蚀性的变化。结果表明:Ni-Cr2O3复合涂层热处理前后物相组成未发生改变,经热处理后,孔隙率减小,组织更致密,耐蚀性大幅提高。     

纳米Cr2O3对环氧涂层耐腐蚀性的影响

利用燃烧法制备粒径为10-20 nm的球状纳米Cr2O3。将纳米Cr2O3粉体添加到环氧涂层中,根据电化学阻抗谱和盐雾试验研究Nano-Cr2O3对环氧涂层耐蚀性的影响。结果表明,Nano-Cr2O3可显著提高环氧涂层耐蚀性。Nano-Cr2O3主要在涂层中提高涂层耐蚀性起到两方面作用:一是减少了孔隙率,增加了涂层的物理屏蔽作用;二是Cr3+离子直接与溶液中腐蚀热镀锌所产生的Zn2+、OH-离子反应,生成了不溶性的Zn Cr2O4隔离层。     

Fe/Al2O3陶瓷梯度涂层的微观结构与性能

采用喷涂法和溶胶-凝胶法相结合的工艺,以FeAlNi混合粉体为过渡层材料在钢基体表面制备了Fe/Al2O3梯度涂层,并对其微观结构与性能进行分析.结果表明:当烧结温度为1220℃时,梯度涂层与钢基体的界面结合强度达到25.3MPa,涂层主要由α-Al2O3,AlFeO3和NiFe2O4等物相组成.Fe/Al2O3梯度涂层与钢基体的结合主要通过吸附与扩散化合两种方式共同起作用.涂层中没有明显的孔洞和平整的界面,且有树枝状组织生成,涂层与钢基体实现良好的结合,这表明涂层成分的梯度化设计能够有效地缓和界面处的应力集中,改善涂层与钢基体的界面结合状态,提高涂层材料的使用性能.     

Al对热压MoSi2材料显微结构的影响

本文研究了添加Al对热压MoSi     

Syntheses and structures of Ta2(WO2)0.87H0.26(PO4)4 and Ta2(MoO2)(PO4)4

Tantalum hydrogen phosphate, β-TaH(PO₄)₂, has a three-dimensional structure that is stable to remarkably high temperature (∼600 °C) presumably due to the presence of strong hydrogen bonds. Impedance measurements indicate a low conductivity, 2.0 × 10⁻⁶ S/cm at 200 °C in 5% H₂. In further studies aimed at enhancing the conductivity by aliovalent doping, we have investigated systematically the synthesis of compounds in the TaH(PO₄)₂-W₂P₂O₁₁ system at 380 °C. As a result, a new phase, Ta₂(WO₂)_0.87H_0.26(PO₄)₄, was identified and subsequently the molybdenum analog Ta₂(MoO₂)(PO₄)₄ was also prepared. The structures were determined by single crystal X-ray diffraction techniques. The structures of Ta₂(WO₂)_0.87H_0.26(PO₄)₄ and Ta₂(MoO₂)(PO₄)₄ can be formally derived from the structure of β-TaH(PO₄)₂ by the replacement of two P-OH protons with an MO₂²⁺ (M = Mo and W) group together with a change in the orientation of some phosphate tetrahedra.     

Corrosion resistance of the Al2O3+ZrO2 thermal barrier coatings on stainless steel substrates

Al₂O₃ + ZrO₂ composite thermal barrier coatings (TBCs) were deposited on SUS304 substrates using the gas tunnel type plasma spraying method. Groups of coating samples with different mixing ratios of Al₂O₃ and different thicknesses were respectively obtained. The graded microstructure of the coatings was examined using optical microscopy (OM) and a scanning electron microscope (SEM). It is well known that the thermal oxidation of interfaces is the main reason for the spallation of TBC coatings, because sprayed TBCs contain micropores and microcracks. The anodic polarization characterization of sprayed TBCs provides a way, to some extent, to investigate the mechanism of the interface oxidation. In this research, anodic polarization was performed to investigate the effect of coatings on the corrosion resistance. The results showed that a higher alumina mixing ratio and thicker coatings lead to higher corrosion resistance. The corrosion potential and deactivated corrosion current of the samples were correlated and analyzed according to the coating porosity, because the through pores in the coatings provided the way for the oxidants of the ambient solution to access the interface. The analysis indicated that lowering the porosity and increasing the gradient of coating porosity help lowering the oxidation.     

Preparation of (NH4)Zr2(PO4)3 and HZr2(PO4)3

(NH₄)Zr₂(PO₄)₃ has been prepared, hydrothermally, from α-zirconium phosphate in three different ways; (1) from amine intercalates at 300°C, (2) from mixtures of ZrOCl₂·8H₂O in excess (NH₄)H₂PO₄ and (3) reaction of NH₄Cl with Zr(NaPO₄)₂. Ammonium dizirconium triphosphate is rhombohedral with a = 8.676(1) and $\text{c}\text{= 24.288(5)}\text{A}\text{?}$. It decomposed on heating to HZr₂(PO₄)₃. Below 600°C a complex, as yet unindexed, X-ray pattern was obtained. A very similar X-ray pattern was obtained by washing LiTi_0.1Zr_1.9(PO₄)₃ with 0.3N HCl. Heating this phase or NH₄Zr₂(PO₄)₃, above 600°C resulted in the appearance of a rhombohedral phase of HZr₂(PO₄)₃ with cell dimensions a = 8.803(5) and $\text{c}\text{= 23.23(1)}\text{A}\text{?}$. The protons were not completely removed until about 1150°C. Decomposition of (NH₄)Zr₂(PO₄)₃ at 450°C yielded an acidic gas whereas at 700°C NH₃ was evolved. A possible explanation for this behavior is presented.     

Hydrothermal synthesis, characterization and magnetic properties of (N4C6H21)·(Co(H2PO4)(HPO4)2)

The title compound, (N₄C₆H₂₁)·(Co(H₂PO₄)(HPO₄)₂), was prepared hydrothermally (473 K, 10 days, autogenous pressure), in the presence of the tris(2-aminoethyl)amine as organic template. Its structure is built up from a network of four membered-rings, formed by the vertex linkages between [CoO₄] and [H₂PO₄] tetrahedra with [HPO₄] moieties hanging from the Co center. Hydrogen bonds involving the cobalt phosphate units and the triply protonated amine molecule, contribute to the stability of the structure. The IR spectrum shows bands characteristic of the (N₄C₆H₂₁)³⁺ cations and the (H₂PO₄)⁻ and (HPO₄)²⁻ phosphate anions. The UV-Visible-NIR spectrum confirms the tetrahedral coordination of Co²⁺ ions. The TGA analysis indicates that the dehydration of (N₄C₆H₂₁)·(Co(H₂PO₄)(HPO₄)₂) occurs in one step. Magnetic measurements from 4.5 to 305 K show a weak antiferromagnetic character of this compound.     

Diagramme d'equilibre du systeme binaire Ba(PO3)2  CsPO3; donnees cristallographiques sur BaCs4(PO3)6, Ba2Cs(PO3)5 et BaCsP3O9, H2O

Equilibrium diagram of Ba(PO₃)₂  CsPO₃ system is given. Two compounds are identified: BaCs₄(PO₃)₆, Ba₂Cs(PO³₃)₅  BaCsP₃O₉.H₂O was also prepared and characterized.     

Improvement of alkali corrosion resistance of mullite ceramics at high temperature by depositing Ca0.3Mg0.2Zr2(PO4)3 coating

Ca_0.3Mg_0.2Zr₂(PO₄)₃ coating was deposited on the mullite ceramic to improve its alkali corrosion resistance at high temperatures, using sol–gel method and dip-coating technique. The phase composition and microstructure of the coating were characterized by X-ray diffraction and scanning electron microscopy (SEM). Results show that homogeneous, dense and single-phase Ca_0.3Mg_0.2Zr₂(PO₄)₃ coating was successfully deposited on mullite ceramics. SEM microstructural examination revealed the excellent bonding between Ca_0.3Mg_0.2Zr₂(PO₄)₃ coating and mullite ceramics. The effectiveness of the prepared coating to improve the alkali corrosion resistance of mullite ceramics was assessed through the measurements of mass loss and flexural strength degradation after 96 h and longer exposure time at alkali corrosion condition at 1000 °C. A significant enhancement of the alkali corrosion resistance for Ca_0.3Mg_0.2Zr₂(PO₄)₃-coated mullite samples was observed. Therefore, the effectiveness of the Ca_0.3Mg_0.2Zr₂(PO₄)₃ material as protection coating for mullite ceramic is confirmed.     

SiO2 and Al2O3/SiO2 coatings for increasing emissivity of Cu(In, Ga)Se2 thin-film solar cells for space applications

In this study, optical coatings were investigated as substitutes for the coverglass on flexible thin-film space solar cells. The inherent low emissivity of copper-indium-gallium-diselenide (CIGS) thin-film solar cells was increased using optical coatings for thermal balance in space. Evaporated silicon dioxide (SiO₂) and an additional aluminum oxide (Al₂O₃) coating on the CIGS solar cell increased the emissivity from 0.18 to 0.77. Higher emissivity was realized with the Al₂O₃/SiO₂ double-layer coating than with the SiO₂ single-layer coating. The straightforward double-layer coating gives the CIGS solar cells appropriate radiative properties for keeping the cell within a permissible temperature range in space.     

On the proton conductor (H3O)Zr2(PO4)3

The compound HZr₂(PO₄)₃ was converted to (H₃O)Zr₂(PO₄)₃ by refluxing in water for 12 or more hours. The water is lost above 150°C to regenerate the original triphosphate. The hydronium ion phase is rhombohedral with hexagonal axes of a = 8.760(1) and $\text{c}\text{= 23.774(4)}\text{A}\text{?}$. Proton conduction in these compounds was investigated by an ac impedance method over the frequency range 5Hz – 10MHz. The activation energy for (H₃O)Zr₂(PO₄)₃ in the temperature range of 25 to 150°C was 0.56eV while the corresponding value for HZr₂(PO₄)₃ (125 – 300°C) was 0.44eV.     

Flower-like microparticles and novel superparamagnetic properties of new binary Co1/2Fe1/2(H2PO4)2·2H2O obtained by a rapid solid state route at ambient temperature

A new binary Co_1/2Fe_1/2(H₂PO₄)₂·2H₂O was synthesized by a simple, rapid and cost-effective method using CoCO₃-Fe(c)-H₃PO₄ system at ambient temperature. Thermal treatment of the obtained Co_1/2Fe_1/2(H₂PO₄)₂·2H₂O at 600 °C yielded as a binary cobalt iron cyclotetraphosphate CoFeP₄O₁₂. The FTIR and XRD results of the synthesized Co_1/2Fe_1/2(H₂PO₄)₂·2H₂O and its final decomposed product CoFeP₄O₁₂ indicate the monoclinic phases with space group P2₁/n and C2/c, respectively. The particle morphologies of both binary metal compounds appear the flower-like microparticle shapes. Room temperature magnetization results show novel superparamagnetic behaviors of the Co_1/2Fe_1/2(H₂PO₄)₂·2H₂O and its final decomposed product CoFeP₄O₁₂, having no hysteresis loops in the range of ±10,000 Oe with the specific magnetization values of 0.045 and 12.502 emu/g at 10 kOe, respectively. The dominant physical properties of the obtained binary metal compounds (Co_1/2Fe_1/2(H₂PO₄)₂·2H₂O and CoFeP₄O₁₂) are compared with the single compounds (M(H₂PO₄)₂·2H₂O and M₂P₄O₁₂; where M = Co, Fe), indicating the presence of Co ions in substitution position of Fe ions.