李萨如图形形状相同的基本定理

本文建立并证明了关于两个李萨如图形在什么条件下形状相同的基本定理,澄清了以往关于这个问题的模糊认识。     

电弧喷涂铝、锌涂层防腐研究

对金属热喷涂层(Al和Zn)的防腐性能进了行研究,重点讨论了电弧喷涂层(Al和Zn)的防腐性能。研究认为:电弧喷涂铝涂层与基体结合,强度明显优于气喷铝涂层,且涂层经封闭处理后,其防腐效果亦明显优于气喷涂层。     

Subcritical crack growth behavior of a perovskite‐structured Ba0.5Sr0.5Co0.8Fe0.2O3−δ oxygen transport membrane

This paper herein studies subcritical crack growth (SCG) behavior of a perovskite‐structured Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3?δ (BSCF) as an oxygen transport membrane material. The SCG behavior of BSCF is evaluated by a constant load method and constant stress rate method at room temperature (RT) and 800°C in air, respectively. The low crack velocity measurements are carried out by ring‐on‐ring bending tests while the high crack velocity measurements by compact tension tests. The stress rates vary approximately from 0.1012 to 101.2 MPa/min. The fracture stress increases with increasing stress rate at 800°C. The SCG parameter, n, of BSCF is determined to be 24.32 and 13.83 at RT and 800°C in air, respectively. This indicates that BSCF is more susceptible to SCG at 800°C. The strength‐probability‐time (SPT) diagram is constructed for design proposes. The stress for a lifetime of 40 years should not exceed 27.21 MPa at RT or 4.53 MPa at 800°C to assure a failure probability below 1%.     

基于镁铝水滑石的Mo/Al2O3-MgO催化剂制备及其加氢脱硫性能

生产低硫或无硫柴油是当今世界范围内清洁燃料发展的趋势,加氢脱硫（HDS）是大规模生产清洁柴油最为有效的技术之一,而研制高活性的HDS催化剂成为该技术的关键。以镁铝水滑石与氧化铝的复合氧化物为载体,通过等体积浸渍法制备了一系列Mo/Al₂O₃-MgO催化剂,以二苯并噻吩（DBT）的正庚烷溶液为原料,在固定床反应器上评价所得催化剂的HDS活性,考察了不同镁铝比的水滑石、焙烧温度和添加量对催化剂物化性质和催化性能的影响。研究结果表明,镁铝比、焙烧温度和添加量均影响催化剂的酸性、金属还原性、硫化性能和MoS₂片晶的堆垛度等,当镁铝摩尔比为3、焙烧温度为800℃、成型时水滑石加入量为10%（质量分数）时,所制备催化剂的HDS活性最高,其脱硫率可达96.2%。这是由于该催化剂的酸性较适宜,活性组分与载体间的相互作用力适中,活性组分更易硫化,有助于提高MoS₂片晶的堆垛度进而改善催化剂的HDS性能。     

Influence of LiBO2 addition on the microstructure and lithium-ion conductivity of Li1+xAlxTi2−x(PO4)3(x = 0.3) ceramic electrolyte

Concerning the safety problems of conventional Li-ion batteries with liquid electrolytes, it is crucial to develop reliable solid-state electrolytes with high ionic conductivity. Li_1+xAl_xTi_2?x(PO₄)₃ (LATP, x = 0.3) is regarded as one of the most promising solid electrolytes due to its high ionic conductivity and excellent chemical stability to humidity.Herein, a new strategy is proposed for improving the sintering behavior and enhancing the ionic conductivity of LATP by using LiBO₂ as the sintering aid via liquid phase sintering. The as-prepared sample LATP with homogeneous microstructure and high relative density of 97.1% was successfully synthesized, yielding high total ionic conductivity of 3.5 × 10^?4 S cm^?1 and low activation energy of 0.39 eV at room temperature. It was found that the addition of LiBO₂ could effectively enhance the densification and increase the ionic conductivity of LATP electrolyte, proving an effective way to synthesis LATP ceramics by a simple and reliable route.     

Fabrication and properties of Y2Ti2O7 transparent ceramics with excess Y content

Transparent Y₂Ti₂O₇ ceramics with excess Y content were fabricated by solid state reactive sintering in vacuum using Y₂O₃ and TiO₂ powders as the starting materials. Phase composition, microstructure, density and in-line transmittance of the Y₂Ti₂O₇ ceramics were investigated. The detailed results indicated that as Y content increased, the density and in-line transmittance increased at first and then decreased. And the highest in-line transmittance of Y₂Ti₂O₇ ceramics is 49.9% at 1100?nm when the excess amount of Y to Ti is 2%. The effect of Y content on densification process of Y₂Ti₂O₇ ceramics was discussed based on an assumption that oxygen vacancy defects were the dominated defects.     

Two-step method to deposit ZrO2 coating on carbon fiber: Preparation,characterization, and performance in SiC composites

Recently, ceramic matrix composites reinforced by short carbon fibers (CFs) attracted increasing attentions. To further improve mechanical properties and oxidation resistances, CFs were subjected to oxidation and acidification followed by sol-gel dip-coating to deposit ZrO₂ on their surfaces. ZrO₂-C_f/SiC composites were fabricated by joint hot compression molding and sintering, compared to C_f/SiC and SiC prepared by the same method. Microstructural analyses indicated that ZrO₂ coatings were successfully deposited on CF surfaces, formed strong bonding and interfaces between CF and the matrix. Meanwhile, CFs were found uniformly distributed in SiC matrix with random orientations. Flexural curves of ZrO₂-C_f/SiC and C_f/SiC revealed the presence of “false plasticity” regions after sharp drops, which were quite different from brittle flexural behavior of SiC ceramic. Compression strength of the three samples showed step-up growth. ZrO₂-C_f/SiC exhibited the highest value, indicating the introduction of CFs and ZrO₂ coatings do have great influence on mechanical performances. After heat treatment, ZrO₂-C_f/SiC exhibited better oxidation resistance than C_f/SiC, with weight loss ratios estimated to ??3.76% and ??6.43%, respectively. These improved properties indicated that ZrO₂-C_f/SiC would be excellent alternatives to other existence materials under ultra-high temperature environments.     

High spin polarization induced by the interface hybridization in Co/C composite films

Co/C composite films with 10 at.% Co were fabricated by facing-target sputtering and postannealed in vacuum at 300–650 °C for 1.5 h. Co nanoparticles are dispersed in amorphous carbon matrix and Co–C compounds exist at the interface between Co nanoparticles and carbon matrix. Negative magnetoresistance was observed in the Co/C films and its maximum value of ?19% was measured at 3.98 × 10⁶ A/m and 5 K for the as-deposited film. Besides cotunneling effect, higher interfacial spin polarization, which is probably induced by the hybridization between Co 3d and C 2p electrons and consequently the preferred d-electron conduction and interfacial spin-filtering effect, also contributes to the large negative magnetoresistance. Postannealing treatment damages the interface hybridization, and thus leads to the disappearance of the higher interfacial spin polarization and large negative magnetoresistance.     

Adsorption of butanol from aqueous solution onto a new type of macroporous adsorption resin: Studies of adsorption isotherms and kinetics simulation

BACKGROUND: Owing to the rapid depletion of petroleum fuel, the production of bio‐butanol has attracted much attention. However, low butanol productivity severely limits its potential industrial application. It is important to establish an approach for recovering low‐concentration butanol from fermentation broth. Experiments were conducted using batch adsorption mode under different conditions of initial butanol concentration and temperature. Batch adsorption data were fitted to Langmuir and Freundlich isotherms and the macropore diffusion, pseudo‐first‐ and second‐order models for kinetic study. RESULTS: The maximum adsorption capacity of butanol onto KA‐I resin increase with increasing temperature, ranged from 139.836 to 304.397 mg g^?1. The equilibrium adsorption data were well fitted by the Langmuir isotherm. The adsorption kinetics was more accurately represented by the macropore diffusion model, which also clearly predicted the intraparticle distribution of the concentration. The effective pore diffusivity (D_p) was dependent upon temperature, but independent of initial butanol concentration, and was 0.251 × 10^?10, 0.73 × 10^?10, 1.32 × 10^?10 and 4.31 × 10^?10 m² s^?1 at 283.13, 293.13, 303.13 and 310.13 K, respectively. CONCLUSION: This work demonstrates that KA‐I resin is an efficient adsorbent for the removal of butanol from aqueous solutions and available for practical applications for future in situ product recovery of butanol from ABE fermentation broth. Copyright © 2012 Society of Chemical Industry     

Effect of TiO2 nanoparticles on the antibacterial and physical properties of polyethylene-based film

TiO₂ nanoparticles and their application in packaging systems have attracted a lot of attention because of its antimicrobial activity. In this work, effect of TiO₂ nanoparticles on the antibacterial and physical properties of polyethylene (PE)-based film was investigated. Results indicated that the antibacterial activity of TiO₂-incorporated PE films should be due to the killing effect property of TiO₂ nanoparticles against microorganisms. The TiO₂-incorporated PE film exhibited more effective antibacterial activity for Staphylococcus aureus. The antibacterial activity to inactivate Escherichia coli or S. aureus was improved by UV irradiation. The inhibition ratio of TiO₂-incorporated PE films sample irradiated for 60 min by UV light was improved significantly, which were 89.3% for E. coli and 95.2% for S. aureus, respectively, compared to that of TiO₂-PE film without UV irradiation. The analysis of physical properties revealed that TiO₂ nanoparticles increased the tensile strength and elongation at break of PE-based film. The climate resistance of nano-TiO₂ films is greatly enhanced, compared to that of the blank PE film. Water vapor transmission increased from 18.1 to 24.6 g/m²·24 h with the incorporation of TiO₂ nanoparticles. Results revealed that PE based film incorporating with TiO₂ nanoparticles have a good potential to be used as active food packaging system.