Effect of carbon fibre on properties of TiB2/C composite cathode coating for aluminum electrolysis

The tensile strength, compressive strength and electrical resistivity of TiB₂/C composite cathode coating were measured with a hydraulic pressure universal test machine and an electrical resistivity test device, and the effects of carbon fibre content and carbon fibre length on tensile strength, compressive strength and electrical resistivity were investigated. The results show that the tensile strength of coating increases at the beginning and then reduces with the increase of carbon fibre content when the carbon fibre (length of 3 mm) content ranges from 0 to 4.0%; at the carbon fibre content of 1.5%, the tensile strength of coating reaches the maximum, 25.6 MPa. For the coating with carbon fibre content of 1.5%, the carbon fibre length has a great influence on tensile strength and compressive strength of coating; when the carbon fibre length is 6 mm, the tensile strength and compressive strength of coating reach the maximum, 27.6 MPa and 39.2 MPa, respectively. The electrical resistivity of coating reduces with the rise of temperature and the length of carbon fibre, and the influence of carbon fibre length on electrical resistivity of coating at low temperature (30–200 °C) is more obvious than that at high temperature (960 °C). Foundation item: Project(2005CB623703) supported by the Major State Basic Research Development Program of China     

Preparation and properties of 4.25Cu-0.75Ni／NiFe2O4 cermet

4.25Cu-0.75Ni/NiFe₂O₄ cermets were prepared by doping NiFe₂O₄ ceramic matrix with the mixed powders of Cu and Ni or Cu-Ni alloy powder as the electrical conducting metallic elements. The effects of technological parameters, such as the adding modes of metallic elements, the ball milling time, the sintering time and the sintering temperature, on the relative density and resistivity of the cermets were studied. The results show that the resistivity of 4.25Cu-0.75Ni/NiFe₂O₄ cermets decreases with increasing temperature, and has a turning point at 590 °C, which is similar to that of NiFe₂O₄ ceramic. The sintering temperature and adding modes of metallic elements have a great influence on the properties of 4.25Cu-0.75Ni/NiFe₂O₄ cermets. When the sintering temperature increases from 1200 °C to 1300 °C, the relative density increases from 89.86% to 95.33%, and the resistivity at 960 °C decreases from 0.11 Ω · cm to 0.03 Ω · cm, respectively. When the metallic elements are added with the mixed powders of Cu and Ni, the cermets of finely and uniformly dispersed metallic phase, high density and electric conductivity are obtained. The relative density and resistivity at 960 °C are 90.23% and 0.04 Ω · cm respectively for the cermet samples sintered at 1200 °C for 2 h, which are both better than those of the cermets prepared under the same technique conditions but with the metallic elements added as 85Cu-15Ni alloy powders. Foundation item: Project (G1999064903) supported by the National Key Fundamental Research and Development Program of China; project(2001AA335013) supported by the National High Technology Research and Development Program of China; project (50204014) supported by the National Natural Science Foundation of China     

Combustion Synthesis and Densification of NiAl／TiB2 Composites

A suitable combustion synthesis and densification process was designed to fabricate dense NiAl/TiB2 composites from Ni-Al-Ti-B system. Combustion synthesis processing and microstructure characteristies of products were studied in detail. The results show that the amount of TiB2 ceramics has a great influence on the combustion synthesis processing and microstructure; with the increase of the amount of TiB2 ceramics, the combus-tion temperature and combustion velocity increase rapidly. The volume of synthesized products and the grain size of ceramics particle size are also affected by the amount of TiB2 ceramics. TiB2 ceramics fiber can be produced in this synthesis system. The dense NiAl/TiB2 composites with residual porosity of no more than 1% are fabricated by the combustion synthesis and hot pressing, the mechanical properties of the dense NiAl/TiB2 composites increase with increase of the amount of TiB2 ceramics.     

Forming regularity and relation between composition and property of B2O3-BaO-ZnO glass

B2O3-BaO-ZnO glass was prepared by using conventional melt quenching technology. The forming regularity and the relationship between the composition and the property of B2O3-BaO-ZnO glass were investigated. The results show that the composition range for forming B2O3-BaO-ZnO glass is very wide, but the content of B2O3 has a limit within mole fraction of 25%-75%. When the content of B2O3 is over the limit, the melt will be divided into two phases with different compositions and structures, whereas too low content of B2O3 will result in the crystallization of the melt during the cooling process. The thermal expansion coefficient, the transition temperature and the resistivity of the glass at room temperature are (5-10)×10-6 ℃-1, 480-620 ℃ and (1.5-3.0)×1010 Ω·m, respectively.     

Preparation and electrical properties of BaPbO3 thin film

BaPbO3 thin films were deposited on Al2O3 substrates by sol-gel spin-coating and rapid thermal annealing. The microstructure and phase of BaPbO3 thin films were determined by X-ray diffractometry, scanning electrons microscopy and energy dispersive X-ray spectrometry. The influence of annealing temperature and annealing time on sheet resistance of the thin films was investigated. The results show that heat treatment, including annealing temperature and time, causes notable change in molar ratio of Pb to Ba, resulting in the variations of sheet resistance. The variation of electrical properties demonstrates that the surface state of the film changes from two-dimensional behavior to three-dimensional behavior with the increase of film thickness. Crack-free BaPbO3 thin films with grain size of 90 nm can be obtained by a rapid thermal annealing at 700 ℃ for 10 min. And the BaPbO3 films with a thickness of 2.5 μm has a sheet resistance of 35 Ω·-1.     

Influence of TiX (<Emphasis Type="Italic">X</Emphasis>=B<Subscript>2</Subscript> or N) addition on the interfacial microstructure features of CBN grains and AgCuTi composite filler

Joining experiments of CBN grains to AISI 1045 steel were conducted using Ag-Cu-Ti composite fillers containing TiX (X=B₂ or N) particles at 920 °C for 5 min. The influences of TiB₂ and TiN particles on the interfacial microstructure features between CBN and filler were investigated comparatively. The experimental results show that TiN particles are more effective than TiB₂ ones to control the interfacial reaction and particularly the resultants. Thermodynamic analysis reveals that the varied interfacial reaction induced by the addition of TiB₂ and TiN particles is mainly atttributed to the activity change of the B and Ti elements in the brazing reaction system.     

Synthesis of 3D ordered macroporous indium tin oxide using polymer colloidal crystal template

Three-dimensional (3D) ordered macroporous indium tin oxide (ITO) is pre- pared using a polymer colloidal crystal template that is formed by self-assembly of the monodisperse poly(methyl methacrylate) (PMMA) microspheres. The morphologies and BET surface area of the macroporous material is examined by scanning electron micro- scope, transmission electron microscopy and N2 adsorption/desorption. Results indicate that the macroporous material has highly ordered arrays of the uniform pores replicated from the PMMA colloidal crystal template when the polymer colloidal crystal template is removed by calcinations at 500℃. The pore diameter (about 450 nm) of macroporous ITO slightly shrank to the PMMA microspheres. The BET surface area and pore volume of the macroporous material are 389 m2·g-1 and 0.36 cm3·g-1, respectively. Moreover, the macroporous ITO, containing 5 mol% Sn and after annealing under vacuum, shows the minimum resistivity of ρ = 8.2×10-3 Ω· cm. The conductive mechanism of macroporous ITO is discussed, and it is believed that the oxygen vacancies are the major factor for excellent electrical properties.     

Combustion Synthesis of TiB2 Ceramics Powder from B2O3-TiO2-Mg System in Air Atmosphere

TiB2 ceramics powder was syuthesized from B2O3 - TiO2 - Mg system. The effects of TiB2 addition as diluent on the conbustion synthesis process were investigated. The results of thermodynanmic calculation and experiments stow that the increase of TiBz content ranging from 0 to 20wt% can reduce the adiabatic temperature Tad from 3100 Kto 2896 K and combustion temperature T,. from 2139 K to 1621 K respectively. The particle size and half width of the particle distributhm are also increased with the addition of TiB2 increasing from 0 to 20wt% . The combustion product is a mixture of TiB2 , MgO , and other intermediate phases. The leached produet contains mairdy TiBz, TiOz and TiN, and its oxygen content is 7.77wt% .     

Electronic Structure and Chemical Bond of Titanium Diboride

1　IntroductionTitaniumdiboride (TiB2 )hasattractedmuchatten tionrecentlybecauseofitshighmeltingpoint,hardnessandchemicalstability .Ontheotherhand ,TiB2 hasfineelectricalproperty ,soitmaybeusedinwide rangingfields[1-3 ] .Aswellknown ,thepropertiesofmaterialsaredecidedbythestructures .Obviously ,thespecialpropertyofTiB2 isrelatedtoitsstructuresofcrystalandelectrons .However ,thereislessstudyonstructuresofvalenceelec tronsandtypeofchemicalbondofTiB2 .JiJia mingetal[4] studiedtheelectronicst…     

黄磷生产炭质还原剂的选用

电热法制磷选用的炭质还原剂有煤炭和焦炭两种,相同条件下,炭质还原剂性能的选择决定了炉况的好坏及生产经济技术指标的高低.炭质还原剂的质量影响炉内最佳电炉熔池的形成.无烟煤化学活性差,常温下与高温下的电阻率相差2 500倍,不宜作为电热法制磷电炉的炭质还原剂.炭质还原剂的粒度15mm时炉料电阻最大,此时液固两相间接触面积大,有利于还原反应速度加快,是黄磷生产炭质还原剂规定粒度为3~16mm的理论依据.科学合理地选择炭质还原剂,使黄磷生产在最佳工艺条件下稳定运行,能创造好的经济效益.     

Influence of thickness on the properties of solution-derived LiMn<Subscript>2</Subscript>O<Subscript>4</Subscript> thin films

LiMn₂O₄ thin films of different thickness were derived from solution deposition and heat treated by rapid thermal annealing. The phase identification and surface morphology were studied by X-ray diffraction and scanning electron microscopy. The electrochemical properties of the films were examined by galvanostatic charge-discharge experiments and electrochemical impedance spectroscopy. LiMn₂O₄ thin films of different thickness derived from solution deposition and rapid thermal annealing are homogeneous and crack free with the grain size between 20 nm and 50 nm. The specific capacity of these films is between 42 and 47 μAh·cm²·μm⁻¹. The capacity decreases with the increase of discharge current density. The capacity loss per cycle increases from 0.012% to 0.16% after being cycled 50 times as the film thickness increases from 0.18 μm to 1.04 μm. The lithium diffusion coefficients of these films are in the same order of 10⁻¹¹ cm²·s⁻¹.     

Preparation of Bauxite Ceramic Microsphere

Ceramic microspheres were prepared by using Chinese bauxite as raw materials through the centrifugal spray drying method. The control technology of microsphere size, degree of sphericity was researched. The ceramic microspheres were sintered by a double sintering process. The microstructure and composition of ceramic microsphere were investigated by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and X-ray energy spectroscopy. The results show that the degree of sphericity of the ceramic microsphere was good and the particle size was 10-100 μm. The XRD analysis reveals that the main crystalline phase of the ceramic microsphere was a-Al2O3 and mullite （3Al2O3·2SiO2）. The product can be used as reinforced material for composite material, especially for antiskid and hard wearing aluminum alloy coating.     

Manufacture of high-dispersed W-Cu composite powder by mechano-thermal process

In order to improve the process of co-reduction of oxide powder, a new mechano-thermal process was designed to produce high-dispersed W-Cu composite powder by high temperature oxidation, short time high-energy milling and reduction at lower temperature. The particle size, oxygen content and their sintering abilities of W-Cu composite powder in different conditions were analyzed. The results show that after a quick milling of the oxide powder for about 3-10 h, the reduction temperature of the W-Cu oxide powder can be lowered to about 650 ℃ from 700-750 ℃ owning to the lowering of particle size of the oxide powder. The average particle size of W-Cu powder after reduction at 650 ℃ is about 0. 5μm smaller than that reduced at 750 ℃. After sintering at 1 200℃ for 1 h in hydrogen atmosphere, the relative density and thermal conductivity of final products (W-20Cu) can attain 99. 5% and 210 W ·m-1· K-1 respectively.     

Effect of baking processes on properties of TiB2/C composite cathode material

Pitch and TiB₂/C green composite cathode material were respectively analyzed with simultaneous DSC-TGA, and effects of three baking processes of TiB₂/C composite cathode material, i.e. K25, K5 and M5, on properties of TiB₂/C composite cathode material were investigated. The results show that thermogravimetric behavior of pitch and TiB₂/C green composite cathode is similar, and appears the largest mass loss rate in the temperature range from 200 to 600°C. The bulk density variation of sample K5 before and after baking is the largest (11.9%), that of sample K25 is the second, and that of sample M5 is the smallest (6.7%). The crushing strength of sample M5 is the biggest (51.2 MPa), that of sample K25 is the next, and that of sample K5 is the smallest (32.8 MPa). But, the orders of the electrical resistivity and electrolysis expansion of samples are just opposite with the order of crushing strength. The heating rate has a great impact on the microstructure of sample. The faster the heating rate is, the bigger the pore size and porosity of sample are. Compared with the heating rate between 200 and 600° of samples K25 and K5, that of sample M5 is slower and suitable for baking process of TiB₂/C composite cathode material. Foundation item: Project (2005CB623703) supported by the Major State Basic Research and Development Program of China; Project (2008AA030502) supported by the National High-Tech Research and Development Program of China     

Thermochemical Study of Mixed Ligand Complexes of Rare Earths with Glycine and L-alanine

In order to obtain the standard molar enthalpies of formation of Rare-Earth amino acid coordination compounds, precise isothermal solution-reaction calorimetric method was used. The value of Δ_rH _m ^Θ of two coordination reactions was determined at T=298.2 K. From the experimental results and other auxiliary values, the standard molar enthalpies of formation of Ln(Gly)_5/2(Ala)_3/2(ClO₄)₃·H₂O(s) [Ln=La, Yb] at T=298.2 K were obtained. The values of them is to be Δ_rH _m ^Θ [La(Gly)_5/2(Ala)_3/2(ClO₄)₃·H₂O(s)]=−3545.45 kJ/mol and Δ_rH _m ^Θ [Yb(Gly)_5/2(Ala)_3/2)(ClO₄)₃·H₂O(s)]=−3793.81 kJ/mol, respectively. QU Jing-nian: Born in 1954 Funded by the Teaching and Research Award Program for Outstanding Young Professors in High Education Institute, Ministry of Education, P. R. China     

Effect of the sputtering parameters on the structure and properties of Cu<Subscript>3</Subscript>N thin film materials

Copper nitride (Cu₃N) thin films were successfully deposited on glass substrates by reactive radio frequency magnetron sputtering. The effects of sputtering parameters on the structure and properties of the films were studied. The experimental results show that with increasing of RF power and nitrogen partial pressure, the preferential crystalline orientation of Cu₃N film is changed from (111) to (100). With increasing of substrate temperature from 70 °C to 200 °C, the film phase is changed from Cu₃N phase to Cu. With increasing sputtering power from 80 W to 120 W, the optical energy decreases from 1.85 eV to 1.41 eV while the electrical resistivity increases from 1.45 ×10² Ω · cm to 2.99 × 10³ Ω · cm, respectively.     

Simultaneous determination of adenine, uridine and adenosine in cordyceps sinensis and its substitutes by LC／ESI-MS

A simple, sensitive and reproducible high performance liquid chromatography-mass spectrometry coupled with electrospray ionization method for simultaneous separation and determination of adenine, adenosine and uridine was developed. The analytical column is a 2.0 mm× 150 mm Shimadzu VP-ODS column and volume fraction of the mobile phase is 86.5 %water, 12.0%methanol and 1.5%formic acid. 2-chloroadenosine was used as internal standard. Selective ion monitoring mode and selective ion monitoring ions at ratio of mass to electric charge of 136 for adenine, 268 for adenosine and 267 for uridine were chosen for quantitative analysis of the three active components. The results show that the regression equations and linear range are Y=0. 062X 0. 005 and 2.0 - 140.0μg · mL 1for adenine, Y=0. 049X 0. 004 and 4. 0 - 115.0 μg · mL-1 for uridine, Y=0. 154X 0. 014 and 1.0 - 125.0 μg · mL 1 for adenosine. The limits of detection are 0.6 μg · mL 1 for adenine, 1.0μg · mL-1 for uri dine and 0.2 μg · mL 1 for adenosine.The recoveries of the three constituents are from 96.6% to 103.2%.     

Adsorption of Pb^2＋ on macroporous weak acid adsorbent resin from aqueous solutions： Batch and column studies

The adsorption properties of a novel macroporous weak acid resin (D152) for Pb²⁺ were investigated with chemical methods. The optimal adsorption condition of D152 resin for Pb²⁺ is at pH 6.00 in HAc-NaAc medium. The statically saturated adsorption capacity is 527 mg/g at 298 K. Pb²⁺ adsorbed on D152 resin can be eluted with 0.05 mol/L HCl quantitatively. The adsorption rate constants determined under various temperatures are k _{288 K}=2.22×10⁻⁵ s^t-1, k _{298 K}=2.51×10⁻⁵ s⁻¹, and k _{308 K}= 2.95×10⁻⁵ s⁻¹, respectively. The apparent activation energy, E _a is 10.5 kJ/mol, and the adsorption parameters of thermodynamics are ΔH ^Θ=13.3 kJ/mol, ΔS ^Θ=119 J/(mol·K), and ΔG ^Θ 298 K =−22.2 kJ/mol, respectively. The adsorption behavior of D152 resin for Pb²⁺ follows Langmuir model. Foundation item: Project(2008F70059) supported by the Scientific and Technological Research Planning of Zhejiang Province, China     

Preparation and Properties of IrO2 Thin Films Grown by Pulsed Laser Deposition Technique

Highly conductive IrO2 thin films were prepared on Si （100） substrates by means of pulsed laser deposition technique from an iridium metal target in an oxygen ambient atmosphere. Emphasis was put on the effect of oxygen pressure and substrate temperature on the structure, morphology and resistivity of IrO2 films. It was found that the above properties were strongly dependent on the oxygen pressure and substrate temperature. At 20 Pa oxygen ambient pressure, pure polycrystalline IrO2 thin films were obtained at substrate temperature in the 300-500℃ range with the preferential growth orientation of IrO2 films changed with the substrate temperature. IrO2 films exhibited a uniform and densely packed granular morphology with an average feature size increasing with the substrate temperature. The room-temperature resistivity variations of IrO2 films correlated well with the corresponding film morphology changes. IrO2 films with the minimum resistivity of （42 ±6）μΩ·cm was obtained at 500℃.     

Preparation of MWNTs/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composites and their mechanical and electrical properties

Since their discovery by Iijima[1], carbon nanotubes (CNTs) have been the focus in novel materials research. Theoretical and experimental studies show[2-9] that CNTs have extraordinary mechanical and electrical properties. Krishnan et al.[2] have reported that the mean value of Young’s modulus of single-wall nanotubes (SWNTs) is 1.25 TPa. Yu et al.[3] measured Yang’s modulus of multi-wall nanotubes (MWNTs) between 270 and 950 GPa and breaking strength between 11 and 63 GPa. The ele…