等离子喷涂纳米Al2O3/TiO2陶瓷复合涂层高温氧化和热震性能研究

采用等离子喷涂设备在H13热作模具钢表面制备含有不同质量分数TiO2的Al2O3纳米陶瓷复合涂层。采用X射线衍射仪(XRD)、高温氧化试验、热震试验等手段研究等离子喷涂纳米涂层的相组成及其性能。结果表明,等离子喷涂使α-Al2O3转变为亚稳态的γ-Al2O3相,喷涂后涂层中Al2O3由α-Al2O3相和γ-Al2O3相组成,TiO2仍以金红石相存在。纳米AT20涂层比其他涂层具有更好的抗氧化性能;与其他涂层相比,纳米AT13涂层具有最佳的抗热震性能。     

大气等离子喷涂Al2O3-40%TiO2涂层的组织与性能

为提高舰船关重部件的耐磨损、抗腐蚀性能,开展了大气等离子喷涂氧化铝复合涂层技术研究。在45钢表面制备Al2O3-40%TiO2陶瓷涂层,通过扫描电子显微镜、显微硬度计、电子天平、摩擦磨损试验机等仪器设备,分析该涂层的显微结构,测其显微硬度、孔隙率等性能,研究其在干摩擦条件下的摩擦磨损性能。结果表明:涂层均匀致密,孔隙率为1.86%,涂层与粘结层之间有明显的倒钩镶嵌结构;Al2O3-40%TiO2涂层的平均硬度为687.2 HV0.1,同时粘结层起到了硬度梯度作用;在干摩擦条件下,45钢主要为严重的黏着磨损,而涂层的磨损主要以层状剥离为主,伴随着少量磨粒磨损,且磨损量低于45钢。在某舰艇主机正时齿轮密封失效部位表面使用Al2O3-40%TiO2涂层,大大提高了正时齿轮的使用寿命,为舰船关重部件的维修与再制造提供了技术支持和理论参考。     

水环境中等离子喷涂纳米/微米喂料Al2O3/TiO2涂层的摩擦学行为

利用纳米结构和常规喂料用大气等离子喷涂方法制备了Al2O3/TiO2涂层,研究了水环境中两种涂层与不锈钢对磨时的摩擦磨损性能.结果表明：水环境中,两种涂层摩擦因数变化不大,但是纳米喂料涂层耐磨性能明显优于常规涂层,同时其对偶的磨损率仅为常规涂层对偶磨损率的1/3～1/5,磨损率随载荷的增加不断增加.讨论了水环境中两种涂层的磨损机制.     

等离子喷涂复合涂层磨损性能及机理

对Ni60、Al2O3 40％TiO2及Ni／Al2O3三种复合涂层与T10钢在不同载荷、不同时间下的干磨摩擦磨损的曲线进行了测试，探讨了磨损机制。研究发现，干磨时Ni60涂层具有较好的耐磨性。涂层的干磨性能与涂层的致密度、孔隙率等密切相关。     

等离子喷涂氧化铝基陶瓷涂层的性能研究

通过对45钢基体表面等离子喷涂Al2O3-13wt%TiO2(AT13)涂层和Al2O3涂层进行对比试验。结果表明:涂层组织呈明显的层片状结构,并含有孔隙、微裂纹及未熔颗粒等缺陷,基体与粘结层以及陶瓷层与粘结层之间形成良好的机械结合界面;TiO2的添加使AT13涂层孔隙减少,致密度提高;AT13涂层与Al2O3涂层相比硬度较低,但其硬度分布的分散性较小;在相同的摩擦磨损试验条件下,AT13涂层比Al2O3涂层耐磨性更好。     

Al2O3-TiO2对铝合金表面激光熔覆NiAl涂层组织性能的影响

目的 进一步提高6061铝合金表面的硬度、耐磨性。方法 应用脉冲Nd:YAG激光器在6061铝合金表面制备了NiAl合金涂层和NiAl/Al2O3-TiO2复合涂层。通过SEM、X射线衍射仪系统研究了Al2O3-TiO2陶瓷相添加对NiAl熔覆层组织形貌、成分分布、物相组成的影响。利用HVS-1000硬度测试仪及HSR-2M高速摩擦磨损机,对熔覆层硬度分布及耐磨性进行测试分析。结果 Al2O3-TiO2陶瓷颗粒加入使涂层宏观成形质量明显提高,表面平整光滑、波纹均匀,熔覆层枝晶间距减小,组织结构明显细化。与NiAl熔覆层相比,在NiAl/Al2O3-TiO2复合涂层中,具有较高硬度的Al3Ni、Al3Ni2硬质相含量增大。同时,高硬度Al2O3和良好韧性的TiO2、NiTi金属间化合物在复合涂层内部形成。NiAl/Al2O3-TiO2复合涂层的显微硬度平均可达650HV0.2,相比NiAl涂层提高了300HV0.2;磨损体积仅为铝合金基体的1/9,相比NiAl涂层降低了35%。干摩擦条件下,NiAl/Al2O3-TiO2复合涂层的犁削、剥落现象显著降低。结论 在细晶强化、硬质相弥散强化及良好韧性的NiTi金属间化合物共同作用下,6061铝合金表面硬度和耐磨性得到显著提高。     

等离子喷涂Al_2O_3-TiO_2陶瓷涂层摩擦学性能研究

针对超声电机摩擦驱动的特性,利用大气等离子喷涂技术在45钢表面设计制备不同配比的Al2O3/Ti O2陶瓷涂层。采用X射线衍射仪分析相结构,用扫描电镜表征磨损后涂层表面特征,探讨其磨损机理,在直线型超声电机上测试其磨损性能。结果表明:在高温条件下,Ti O2和Al2O3形成固溶体,而XRD测试时,只能检测到Al2O3的特征峰而Ti O2相消失。五种配比材料中,Al2O3-16%Ti O2涂层的磨损性能优于其他涂层,使用寿命更长。Al2O3-10%Ti O2和Al2O3-13%Ti O2涂层表现出轻微的疲劳磨损机制,Al2O3-16%Ti O2涂层则是轻微的磨粒磨损,而Al2O3-19%Ti O2和Al2O3-22%Ti O2涂层的磨损机制是轻微的脆性断裂。     

Lu2O3/TiO2/Nb2O5共稳定ZrO2热障涂层材料研究

采用Lu2O3/TiO2/Nb2O5作为ZrO2热障涂层材料的稳定剂,研究Lu2O3/TiO2/Nb2O5共稳定ZrO2(15%LTNSZ)热障涂层材料在900℃、40 mol%V2O5+60 mol%Na2SO4熔盐中的热腐蚀行为。结果表明:8%YSZ热障涂层材料热腐蚀2 h后,t相ZrO2全部相变为m相ZrO2,热腐蚀产物为尺寸较大的YVO4晶体;15%LTNSZ热障涂层材料热腐蚀20 h后,m相ZrO2的比例仅为5.5%,热腐蚀产物为尺寸较小的LuVO4晶体。与Y2O3稳定剂相比,Lu2O3/TiO2/Nb2O5稳定剂使ZrO2在40 mol%V2O5+60 mol%Na2SO4熔盐中的抗热腐蚀性能提高1个量级以上。     

Al2O3–TiB2复合陶瓷涂层制备及耐液锌腐蚀性能

针对连续热镀锌生产线中浸锌零部件表面的腐蚀磨损问题,应用高能高速等离子喷涂设备制备了Al2O3-TiB2复合陶瓷涂层。测试了涂层的显微组织、显微硬度、结合强度及耐熔融锌液腐蚀性能。结果表明涂层显微组织中不存在相互贯通的孔隙、微裂纹和未熔化颗粒,孔隙分布均匀且孔径较小,孔隙率<3%。涂层与基体结合状态良好,结合强度达到56 MPa。经过30天的熔融锌液浸泡,涂层表面未见有点蚀、裂纹或剥落现象。Al2O3-TiB2复合陶瓷涂层高的致密性和较好的抗热震性能对涂层力学性能和耐熔融锌液腐蚀性能提高起到了重要作用。     

AZ91D镁合金等离子喷涂Ni-Al/陶瓷涂层的组织和性能

以Ni-Al为粘结层,在AZ91D镁合金基体上等离子喷涂Ni-Al/Al2O3、Ni-Al/Al2O3-13%TiO2(Ni-Al/AT13)、Ni-Al/Al2O3-20%TiO2(Ni-Al/AT20)复合涂层及Ni-Al/Al2O3/Al2O3-13%TiO2/Al2O3-20%TiO2(Ni-Al/Al2O3/AT13/AT20)梯度涂层,利用SEM、EDS和XRD分析涂层的微观组织特征,通过硬度、拉伸和热震实验研究涂层硬度、结合强度和抗热震性能,并与直接喷涂Al2O3、AT20的涂层进行比较。结果表明:Ni-Al粘结层因"自粘结"效应与基体形成较为致密并具有冶金结合的界面,且与Al2O3、AT13和AT20陶瓷层互有渗透、交叉和啮合,涂层致密性及结合力大为提高,表现出优良的抗热震性能。Al2O3涂层主要由亚稳态γ-Al2O3组成,AT20涂层以Al2O3和Al2TiO5为主。镁合金表面喷涂Al2O3陶瓷层后硬度大幅提高,由于加入TiO2,AT13和AT20涂层的硬度略低于Al2O3涂层的。Ni-Al/Al2O3-TiO2复合陶瓷的涂层结合强度高于Ni-Al/Al2O3单一陶瓷涂层的,而Ni-Al/Al2O3/AT13/AT20梯度涂层的结合强度比Ni-Al/AT20涂层的更高。     

Crystal structures and structural relationships of KFe2(SeO2OH)(SeO3)3 and SrCo2(SeO2OH)2(SeO3)2

The new phases KFe₂(SeO₂OH)(SeO₃)₃ and SrCo₂(SeO₂OH)₂(SeO₃)₂ have been synthesized under low-hydrothermal conditions and their structures were determined by single-crystal X-ray methods. Both compounds are monoclinic; KFe₂(SeO₂OH)(SeO₃)₃: space group P2, A = 9.983(4), B = 5.270(1), C = 10.614(4) Å, β = 97.42(2)°, V = 553.7 ų, Z = 2; SrCo₂(SeO₂OH)₂(SeO₃)₂: space group P2ln, A = 14.984(2), B = 5.286(1), C = 13.790(2) Å, β = 94.72(1)°, V = 1088.5 ų , Z = 4. The refinements converged to R-values of 2.9 and 3.6% respectively.

The atomic arrangement in KFe₂(SeO₂OH)(SeO₃)₃ and SrCo₂(SeO₂OH)₂(SeO₃)₂ is based on isolated MO₆ octahedra (M = Fe³⁺, Co²⁺), which are corner-linked via trigonal pyramidal selenite groups to a framework structure. Interstitials are occupied by potassium or strontium atoms in ten- or eight-coordination respectively, and by the lone-pair electrons of the Se⁴⁺ atoms. Both compounds are not isotypic but are closely related and may be interpreted as different distortions of an idealized structure type in space group P2/m, which was modelled for a theoretical compound SrFe₂(SeO₃)₄ by distance least squares refinement (program ).     

Sm2Zr2O7-ZrB2/SiC复合材料的制备及力学性能研究

运用共沉淀法制备Sm2Zr2O7原料粉末,利用放电等离子烧结技术(SPS)制备锆酸钐质量分数分别为25%、50%、75%的Sm2Zr2O7-ZrB2/SiC复合材料,对材料进行相成分、微观形貌、力学性能测试表征。结果表明,采用SPS在1600℃下可制备出高致密度的Sm2Zr2O7-ZrB2/SiC三相复合材料。随着复合材料中Sm2Zr2O7含量的增加力学性能显著降低,主要是Sm2Zr2O7材料本身的力学性能较低,且烧结过程中易形成连续相以及烧结应力共同作用的结果。     

Magnetic properties of CeAg2Ge2

A.c. susceptibility and magnetization measurements of CAg₂Ge₂ are reported. Two phase transitions at T = 7 and 11 K are detected. The magnetization curve at T = 4.2 K has a two-step character.     

孔道Al2O3/SiO2对NaAlH4-Tm2O3体系储氢性能的影响

以机械球磨法制备具有可逆吸放氢性能的NaAlH4-Tm2O3储氢材料体系。利用相同制备方法进一步研究两种不同孔道材料(大孔Al2O3与介孔SiO2)对NaAlH4-Tm2O3体系储氢性能的影响,测试样品的循环吸放氢性能,并对样品吸放氢前后的结构进行表征。结果表明:大孔Al2O3材料的添加并不能明显改善NaAlH4-Tm2O3体系的放氢速率和放氢量,而介孔SiO2的加入使NaAlH4-Tm2O3体系在150℃条件下5 h内的首次放氢量(质量分数)达到4.61%,高于NaAlH4-Tm2O3体系的4.27%,增加了约8.0%。此外,添加介孔SiO2的NaAlH4-Tm2O3体系放氢速率也有所提高。     

氧化钠对CaO-Al2O3-SiO2三元系铝酸钙形成规律的影响（英文）

利用XRD、SEMEDS和DSCTG技术研究了添加Na2O的CaO-Al2O3-SiO2体系中铝酸钙的形成规律。结果表明,当Al2O3与SiO2的质量比为3.0、CaO与Al2O3的摩尔比为1.0时,在1350°C烧结后的熟料主要由12CaO·7Al2O3、2CaO·Al2O3·SiO2和2CaO·SiO2组成。熟料中12CaO·7Al2O3的含量随着Na2O的增加而增加,2CaO·Al2O3·SiO2的含量随着Na2O的增加而降低。Na2O在12CaO·7Al2O3中形成固溶体,增加了其单位晶胞体积。DSC分析表明,Na2O不仅促进了12CaO·7Al2O3的形成,而且使C12A7的形成温度降低了30°C。烧结熟料中的氧化铝溶出性能随着Na2O的增加而大幅度提高。     

Y2Cu2O5光催化剂的制备及模拟太阳光催化产氢

分别用固相法和液相法制备Y2Cu2O5光催化剂,利用热重差热分析(TG-DTA)、X射线衍射(XRD)、扫描电子显微镜(SEM)、紫外可见光漫反射光谱(UV-Vis DRS)等技术对光催化剂进行表征。在模拟太阳光照射条件下,以草酸(H2C2O4)为牺牲剂对所制得的光催化剂制氢性能进行评价,考察制备方法和牺牲剂类型等因素对其产氢性能的影响以及光催化剂的稳定性能。结果表明:溶胶凝胶法所得样品中含有Y2O3杂质,为Y2Cu2O5与Y2O3的混合物;固相法所得样品为纯净的Y2Cu2O5,具备较高的光催化产氢活性。用固相法制备的光催化剂Y2Cu2O5,当其用量为0.8 g/L、草酸为牺牲剂且初始浓度为0.05 mol/L时,表现出最佳光催化产氢活性,其产氢量为3.78mmol/(h.g)。但Y2Cu2O5在草酸溶液中不稳定,会与草酸反应生成Y2(C2O4)3.2H2O,导致产氢活性降低。     

Al2O3包覆改善P2型Na2/3Fe1/2Mn1/2O2正极材料的存储性能

采用超声喷雾热解与高温固相烧结相结合的方法合成P2型Na_2/3Fe_1/2Mn_1/2O₂材料。通过X射线衍射仪、扫描电子显微镜和电化学充放电设备对材料的结构、形貌和电化学性能进行全面的表征。此外,在Na_2/3Fe_1/2Mn_1/2O₂表面包覆Al₂O₃薄层,该包覆层可以抑制Na₂CO₃·H₂O的形成,提高Na_2/3Fe_1/2Mn_1/2O₂材料的存储性能,从而改善其电化学性能。这种简单的表面改性方法为合成高性能钠离子电池正极材料提供了新思路。     

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.     

Cu/Y2O3掺杂MgB2的组织控制及动力学分析

观察并研究了不同Y2O3含量的Cu/Y2O3共掺杂MgB2的体系,样品通过传统的固相烧结法制备。结合扫描电镜和X射线衍射技术的分析发现,只有在5%Y2O3掺杂的样品中获得了层状组织。选择5%Y2O3含量的体系结合热分析曲线对固相反应阶段进行了动力学分析,得出最概然机理函数为Avrami-Erofeev,n=2,表达式为2[-ln(1-α)]1/2。其意义是随机形核和随后的瞬时生长。最后对动力学参数进行了计算,结果表明反应的活化能和指前因子均先趋于稳定后减小。     

Self-propagating High-temperature Synthesis of Al2O3-TiB2 Coatings by Aluminothermic Reactions

The Al2O3-TiB2 coatings were fabricated on Q235 steel by self-propagating high-temperature synthesis(SHS)process using aluminothermic reactions with aluminum,titania,boron oxide and ferric oxide powders.The effect of the content of excessive aluminum in the reactants on Al2O3-TiB2 coatings was studied when only Al-TiO2-B2O3 system was used for preparation of the coatings.The results indicate that the combustion reaction cannot occur when excessive aluminum is over 40wt%and the coating has good quality when excessive aluminum is 20wt%.In order to improve the bonding of the coating and substrate and optimize the ratio of Al2O3/TiB2,composite reaction systems Al-TiO2-B2O3 and Al-Fe2O3 were used for the preparation of Al2O3-TiB2 coatings.The XRD result shows that the coatings contain FeAl intermetallic compound which can improve efficiently the interface bonding of the coating and substrate.The percentage of Al-Fe2O3 system in reactants has only a small effect on the hardness of Al2O3-TiB2 coating,which is about 22000 MPa(Hv),but has an obvious effect on the morphology and interface bonding of the coatings.