Synthesis of Y_2O_3 particle enhanced Ni/TiC composite on TC4 Ti alloy by laser cladding

A Y2O3 particle enhanced Ni/TiC composite coating was fabricated in-situ on a TC4 Ti alloy by laser surface cladding. The phase component, microstructure, composition distribution and properties of the composite layer were investigated. The composite layer has graded microstructures and compositions, due to the fast melting followed by rapid solidification and cooling during laser cladding. The TiC powders are completely dissolved into the melted layer during melting and segregated as fine dendrites when solidified. The size of TiC dendrites decreases with increasing depth. Y2O3 fine particles distribute in the whole clad layer. The Y2O3 particle enhanced Ni/TiC composite layer has a quite uniform hardness along depth with a maximum value of HV1380, which is 4 times higher than the initial hardness. The wear resistance of the Ti alloy is significantly improved after laser cladding due to the high hardness of the composite coating.

Microstructure evolution and nitrides precipitation in in-situ Ti_2 AlN/TiAl composites during isothermal aging at 900°C

Microstructures of Ti2AlN/TiAl composites prepared by in-situ method were characterized in in-situ and aging treatment conditions and the nitride precipitation was investigated in Ti2AlN/TiAl composites aged at 900 ℃ for 24 h after being heat treated at 1400 ℃ for 0.5 h. The in-situ composites consist of γ＋α2 lamellar colonies, equiaxed y grains and Ti2AlN reinforcements. Matrix with nearly fully lamellar structure formed after solution and subsequently aging treatment. With the increase of Ti2AlN content, the nearly fully lamellar structure becomes instable for the aged composites. According to TEM study, fine Ti2AlN precipitates are found to distribute at the grain boundaries of lamellar colony. Needle-like Ti3AlN precipitates arrange in line with growing axis parallel to [001] direction of the γ-TiAl matrix and another needle-like Ti3AlN precipitates with lager size distribute at the dislocations. Key words：

Microstructure stability of Ti_2Al N/Ti-48Al-2Cr-2Nb composite at 900 °C

Microstructure stability of in situ synthesized Ti2AlN/Ti-48Al-2Cr-2Nb composite during aging at 900 ℃ was investigated by XRD, OM and TEM, and the unreinforced Ti-48Al-2Cr-2Nb alloy was also examined for comparison. The result showed that in the TiAl alloy,α2 lamellae thinned and were broken down, and became discontinuous with increasing aging time. The decomposition ofα2 lamella toγ which was characterized by parallel decomposition and breakdown ofα2 lamellae led to the degradation of the lamellar structure. While in the composite, lamellar structure remained relatively stable even after aging at 900 ℃ for 100 h. No breakdown ofα2 lamellae except parallel decomposition and precipitation of fine nitride particles was observed. The better microstructural stability of the composite was mainly attributed to the precipitation of Ti2AlN particles at theα2/γ interface which played an important role in retarding the coarsening of lamellar microstructure in the matrix of composite.

Fabrication and Magnetic Properties of Composite Ni_(0.5)Zn_(0.5)Fe_2O_4/Pb(Zr_(0.52)Ti_(0.48))O_3 Nanofibers by Electrospinning

One-dimensional and quasi-one-dimensional nanostructure materials are promising building blocks for electromagnetic devices and nanosystems.In this work,the composite Ni0.5Zn0.5Fe2O4（NZFO）/ Pb（Zr0.52Ti0.48）O3（PZT） nanofibers with average diameters about 65 nm are prepared by electrospinning from poly（vinyl pyrrolidone） （PVP） and metal salts.The precursor composite NZFO/PZT/PVP nanofibers and the subsequent calcined NZFO/PZT nanofibers are investigated by Fourier transform infrared spectroscopy （FT- IR） ,X-ray diffraction （XRD）,scanning electron microscopy （SEM）.The magnetic properties for nanofibers are measured by vibrating sample magnetometer（VSM）.The NZFO/PZT nanofibers obtained at calcination temperature of 900 °C for 2 h consist of the ferromagnetic spinel NZFO and ferroelectric perovskite PZT phases,which are constructed from about 37 nm NZFO and 17 nm PZT grains.The saturation magnetization of these NZFO/PZT nanofibers increases with increasing calcination temperature and contents of NZFO in the composite.

Copper-Ti_3SiC_2 composite powder prepared by electroless plating under ultrasonic environment

In this article, a new type of Cu-Ti3SiC2 composite powder prepared using the electroless plating technique was introduced. The initial Ti3SiC2 particles are 11 μm in diameter on an average. The Cu plating was carried out at middle temperature （62-65℃） with the application of ultrasonic agitation. The copper deposition rate was determined by measuring the weight gain of the powder after plating. It has been found that the pretreatment of Ti3SiC2 powder is very important to obtain copper nanoparticles on the surface of Ti3SiC2 The optimum procedure before plating aimed to add activated sites and the adjustment of the traditional composition of the electroless copper plating bath could decelerate the copper deposition rate to 0.8 gm/h. X-ray diffraction （XRD） indicates that the chemical composition of the plating layer is copper. SEM images show that the surface of the Ti3SiC2 particles is successfully coated with continuous copper layer. The wetting property between the copper matrix and Ti3SiC2 can be improved so as to increase the interfacial strength.

Effect of Ti/B Additions on the Formation of Al_3 Ti of in situ TiB_2/Al Composites

A novel technique for fabricating TiB_2/Al composites in molten aluminum was introduced. The formation mechanism of brittleAl,Ti particulates up to 30 m in size produced in the composites was studied and a method of eliminating them was proposed. The resultsshow that (l) the brittle Al,Ti particulates are always present in the composites when the molar ratio of Ti to B 'T,:nB is l:2; and (2) theformation of the brittle Al,Ti phase can be avoided entirely from the final product by using a proper 'T,:nB of l:4 in the Ti-B-Al preforms.In the former case, the tensile elongation of the composite is only 4%, much lower than the value of pure aluminum (20%). In the latercase, the tensile elongation of this composite is 10%, higher than the value of the composite with a lot ofAl,Ti (4%), whereas the ultimatetensile stfength of the former is nearly that of the later.

Friction and Wear Properties of TiAl and Ti_2AlN/TiAl Composites at High Temperature

The high-temperature friction and wear properties of TiAl alloys and Ti2AlN/TiAl composites （TTC） in contact with nickel-based superalloy were studied. The results showed that, at 800 and 1 000 ℃, the coefficient of the friction （COF） decreased with the increase of sliding velocity and the wear loss of the TTC decreased with the increase of volume fraction of Ti2AlN. The wear mechanisms of the pairs are adhesive wear and the wear debris mainly comes from the contacting nickel-based superalloy. The intergranular fracture and the cracking of the phase boundary in the lamellar structure are the wear mode of TiAl alloy. The wear mode of TTC is phase boundary fracture and adhesive spalling. The abrasive resistance of TTC is slightly higher than that of TiAl alloy.

Fabrication and Mechanical Properties of Sm2O3 Doped CeO2 Reinforced Ti3AlC2 Nano Composite

The fabrication process of Sm2O3 doped CeO2 reinforced Ti3AlC2 nano composites including the nano particle dispersion process by a hetero-coagulation process was developed using in-situ synthesis and densification process of Ti3AlC2. The effects of Sm2O2 doped CeO2 nano particles on mechanical properties of Ti3AlC2 were investigated. It was found that the presence of 20SDC nano particles in Ti3AlC2 was very effective to improve the mechanical properties of Ti3AlC2 without spoiling the unique characteristics of Ti3AlC2temary carbide.

Physical, Antioxidant and Thermal Shock Properties of Cu/Ti_2AlC Conductive Composites

Cu/Ti2AlC composites were fabricated by vacuum hot-pressing technique. Phase composition was analyzed by XRD and morphology of fracture was observed by SEM. Physical performance such as density, resistivity, hardness and friction coefficient with different volume fraction of Cu/Ti2AlC composites were studied. When the content of Ti2AlC increased from 10% to 70%, the relative density reduced from 99.38% to 90.56% and the resistivity increased significantly. Hardness reached the maximum value when Ti2AlC was at 60% and friction coefficient declined with the increasing of Ti2AlC. Cu/Ti2AlC composites, showing good conductivity properties and friction performance. Oxidation resistance enhanced obviously with the content of Ti2AlC increasing. Cu-60%Ti2AlC sample possessed optimum thermal shock resistance, and no cracking was found at 600 ℃ cycled for 10 times and 900 ℃ cycled for 1 time.

Rheological behavior of semi-solid TiB_2/7075 composites and simulation of their rheocasting processes

In the present study, in-situ Ti B2 particle-reinforced 7075 aluminum alloy was produced by adding a mixture of K2 Ti F6 and KBF4 to the molten base alloy. The effects of the addition of 4.5wt.% and 9wt.%Ti B2 on the apparent viscosity and microstructure were investigated. The results showed that adding Ti B2 is effective for optimizing primary α-Al, but compared with the 4.5wt.%Ti B2/7075 composite, the addition of 9wt.%Ti B2 had no further significant refinement role in the 9wt.%Ti B2/7075 composite due to particle aggregation. The viscosities of semi-solid 7075 alloy and Ti B2/7075 composite slurries increased with an increase in solid fraction, but decreased with an increase in shear rate. The viscosity of 4.5wt.% Ti B2/7075 was the lowest among the three samples, and that of 7075 alloy was the highest under the same conditions. The primary α-Al grain size was decreased, and the dendritic grains grew into spherical shapes after shearing. Based on the experimental results, viscosity models of the semi-solid 7075 alloy and 4.5wt.% and 9wt.%Ti B2/7075 composites were formulated. According to the simulation results, the shrinkage porosity of the 4.5wt.%Ti B2/7075 wheel was lower than those of the 7075 alloy and 9wt.%Ti B2/7075 wheels.

Preparation and characterization of SnO_2-Li_4Ti_5O_(12) composite by sol-gel technique

SnO2-Li4Ti5O12 was prepared by sol-gel method using tin tetrachloride,lithium acetate,tetrabutylorthotitanate and aqueous ammonia as starting materials.The composite was characterized by thermogravimertric(TG)analysis and differential thermal analysis(DTA),X-ray diffractometry(XRD)and transmission electron microscopy(TEM)combined with electrochemical tests.The results show that SnO2-Li4Ti5O12 composite derived by sol-gel technique is a nanocomposite with core-shell structure, and the amorphous Li4Ti5O12 layer with 20?40 nm in thickness is coated on the surface of SnO2 particles.Electrochemical tests show that SnO2-Li4Ti5O12 composite delivers a reversible capacity of 688.7 mA·h/g at 0.1C and 93.4%of that is retained after 60 cycles at 0.2C.The amorphous Li4Ti5O12 in composite can accommodate the volume change of SnO2 electrode and prevent the small and active Sn particles from aggregating into larger and inactive Sn clusters during the cycling effectively,and enhance the cycling stability of SnO2 electrode significantly.

Preparation and Microstructural Analysis of Ti_2AlC/TiAl(Nb) Composite

By using the spark plasma sintering process, Ti2AlC/TiAlcomposite with the addition of Niobium （Nb） was prepared in-situ and the microstructure of Ti2AlC/TiAl （Nb） composite was investigated by means of transmission electron microscopy （TEM） and high-resolution electron microscopy （HREM）. The results indicate that new-formed Ti2AIC particles disperse with a high degree of uniformity and well combine with the matrix. In the area of phase interface the d-spaces of Ti2AlC （100） and TiAI （110） were measured as 0.2648 nm and 0.2991 nm,respectively. The atom arrangement beside the interface was only partly corresponding, existing in semicoherent state. On the contrary, in the area of grain interface the d-spaces of TiAl （100） and TiAl （110） were measured as 0.2462 nm and 0.2631 nm,respectively and the atom arrangement beside the interface was almost corresponding, existing in coherent state.

Antibacterial Activity of TiO₂/Ti Composite Photocatalyst Films Treated by Ultrasonic Cleaning

In this work, TiO2/Ti composite films were fabricated by 2-setp MCT and the following high temperature oxidation. Antibacterial activity of the composite films treated by ultrasonic cleaning to increase the performance reliability was examined. The prepared TiO2/Ti composite films showed high photocatalytic activity in the degradation of methylene blue solution. It is obvious that? TiO2/Ti composite films have antibacterial activity under UV irradiation.

时效转变与Ti/(Ti,Zr)_2Si复合材料的制备

通过真空自耗电极炉熔炼得到硅锆比为 1/2的Ti Zr Si合金材料 ,对合金材料进行了 12 0 0℃ ,3 .5h的固溶处理和 85 0℃不同时间的时效处理 ,通过时效析出反应制备Ti/(Ti,Zr) 2 Si复合材料。利用光学显微镜、扫描电镜、X射线衍射、EDX分析了Ti Zr Si合金的铸造、固溶和不同时效阶段的显微组织及其相组成。分析结果表明 ,硅锆比为 1/2 (重量百分比 )的Ti Zr Si合金 ,铸造组织为块状 β Ti、晶界由块状β Ti和条状的 5 3型硅化物组成 ;Ti Zr Si合金经过 85 0℃ ,480min的时效处理 ,5 3型硅化物转变为 2 1型硅化物 ;尺寸细小、分布均匀的 2 1型硅化物使制备高性能的Ti/(Ti,Zr) 2

Preparation of TiAl/Ti_2AlC Composites with Ti/Al/C Powders by In-situ Hot Pressing

TiAl/Ti2AlC composites were prepared by in-situ hot pressing of TilAl/C powders mixtures and sintered at different temperatures were investigated by X- ray diffraction （ XRD ） of samples. The reaction procedure of Ti-Al-C system could be divided into three stnges. Below 900℃ , Ti reacts with Al to form TiAl intermetallics ; above 900 ℃ , C reacts with remain Ti to form TiC triggered by the exothermal reaction of Ti and Al ; TiAl reacts with TiC to produce dense TiAl/Ti2AlC compasites.In the holding stage, ternary Ti2AlC develops to layered polycrystal and composites pyknosis in the meanwhile. The mechanism of synthesis and microstructure was especially discussed.

The Influence of Mo Additive on the Microstructure and Property of Ti/Al_2O_3 Composite

The influence of Mo on the microstructure,bending strength and HV of Ti/Al 2O 3 composite was studied,and the influence mechanism was analyzed.The results indicate that after the addition of Mo,the composite organization is finer and phases distribution is better-proportioned which make the microstructure denser,the bending strength and HV of composite are also increased to a degree.But the bending strength increases first then decreases with the increasing of Mo content,so the appropriate Mo content for the Ti/Al 2O 3 composite is to be further confirmed.

Effect of Nb on the Mechanical Properties of Ti/Al_2O_3 Composite

Ti/Al 2O 3 composite with improved mechanical properties was synthesized by th e spark plasma sintering. The effect of Nb on the microstructure of the composit e was analyzed by TEM, SEM and so on. The experimental results indicate that the bending strength, fracture toughness, micro-hardness and relative density of t he composite are 897.29MPa, 17.38MPa·m 1/2, 17.13GPa and 99.24% respec tively when adding 1.5vol%Nb. The bending strength is improved by reason of form ing dislocation ring and transfering fracture mode from intergranular to mixture fracture of intergranular and transgranular. The crack propagating is mainly th e deflection bridging. It indicates a reduction of crack driving force and an in crease in crack growth resistance,which results in toughness enhanced.

Synthesis and electrochemical properties of LiMn_2O_4/Li_4Ti_5O_(12) composite

LiMn2O4/Li4Ti5O12 composite was synthesized by in-situ composite technique using LiMn2O4,lithium acetate,tetrabutyl titanate as starting materials and characterized by various electrochemical methods in combination with X-ray diffractometry(XRD), infrared(IR)spectroscopy and scanning electron microscopy(SEM).The results show that Li4Ti5O12 is coated on the surface of crystalline LiMn2O4 to form LiMn2O4/Li4Ti5O12 composite.The structure of LiMn2O4 does not change due to the introduction of Li4Ti5O12.By being coated with Li4Ti5O12,the rate capability and high temperature cyclability of LiMn2O4 is improved greatly.At room temperature,the discharge capacity of LiMn2O4/Li4Ti5O12 composite is more than 108.4 mA·h/g and the capacity loss per cycle is only 0.053%after 20 cycles at 2.0C.While at 55℃,the discharge capacity of LiMn2O4/Li4Ti5O12 composite is more than 109.9 mA·h/g and the capacity loss per cycle is only 0.036%after 60 cycles at 1.0C.

Photocatalytic Hydrogen Evolution from the Splitting of Water over Cd_(1-x)Zn_xS/K_2La_2Ti_3O_(10) Composites under Visible Light Irradiation

A series of Cd1-xZnxS/K2La2Ti3O10 composites were synthesized via a simple co-precipitation method. The prepared samples were characterized by X-ray diffraction(XRD), scanning electron microscopy(SEM), X-ray energy dispersive spectroscopy(EDX), ultraviolet-visible diffuse reflection(UV-Vis), X-ray photoelectron spectroscopy(XPS) and photoluminescence(PL) measurements. The composite structures consisted of Cd1-xZnxS nanoparticles evenly distributed on the surface of K2La2Ti3O10. The absorption edge of K2La2Ti3O10 shifted to the visible light region upon introduction of the Cd1-xZnxS nanoparticles. The photocatalytic activities of the catalysts were evaluated by hydrogen production under visible light irradiation. The prepared Cd0.8Zn0.2S(30wt%)/K2La2Ti3O10 exhibited higher photocatalytic activity, evolving 6.92 mmol/g H2 under visible light irradiation for 3 h. The promoted photocatalytic activity of the composites was attributed to the synergistic effect between Cd1-xZnxS and K2La2Ti3O10, which resulted in enhanced separation of photogenerated electrons and holes.

新型Ti/Zr-SnO_(2)/β-PbO_(2)电极的构筑及高效降解亚甲基蓝

该文采用热分解法先制备Zr-SnO_(2)中间层,再电沉积β-PbO_(2)层,成功制备了Ti/Zr-SnO_(2)/β-PbO_(2)电极。利用扫描电镜(SEM)、能量散射谱(EDS)、X射线衍射(XRD)、X射线光电子能谱(XPS)技术对电极形貌、晶体结构、元素组成等进行了分析。通过循环伏安法(CV)、电化学交流阻抗法(EIS)、加速寿命实验等测试其电化学性能,考察其电催化降解亚甲基蓝(Methylene Blue,MB)活性,优化电流密度和初始MB浓度。结果表明:Ti/Zr-SnO_(2)/β-PbO_(2)电极的表面为致密四棱锥结构,形成了非化学计量比的β-PbO_(2);与传统的Ti/β-PbO_(2)电极相比,Zr-SnO_(2)中间层可有效提高钛基涂层电极的析氧过电位;修饰电极阻抗为87.64Ω/cm2,电极加速寿命为439 min,是Ti/β-PbO_(2)电极的219.5倍,是Ti/SnO_(2)/β-PbO_(2)电极的1.71倍;在50 mA/cm2的电流密度下降解初始浓度为50.00 mg/L的MB时,180 min内MB去除率可达97%。