碳环氧蒙皮铝蜂窝夹心结构缺陷红外热波成像检测研究

针对人造卫星碳环氧蒙皮铝蜂窝夹心结构承力筒典型缺陷对无损检测技术的迫切需求,提出采用正弦调制热流激励的红外锁相热波成像检测技术对该类型材料开展检测试验研究。建立了调制热流作用于材料的三维热波扩散模型,并采用有限元方法分析了缺陷尺度对热波特征的影响。研制了红外锁相热波成像检测系统,针对预制平顶孔模拟脱粘缺陷的碳环氧蒙皮铝蜂窝夹心结构开展试验研究。分析了调制参数与缺陷尺度对热波幅频-相频特性的影响。制定了红外锁相热波成像针对于碳环氧蒙皮蜂窝夹心结构缺陷识别判据,根据判据可得,锁相热波成像检测方法的相位特征可以准确识别大于等于Φ10mm的预制缺陷,同时当环氧板蒙皮厚度小于1.0mm时,可以识别Φ5mm的脱粘缺陷。

Behavior of titanium dioxide in alumina carbothermic reduction-chlorination process in vacuum

Behaviors of TiO2 in the alumina carbothermic reduction and chlorination process in vacuum at different temperatures were investigated experimentally by means of XRD,SEM and EDS.In the preparation of materials,the molar ratio of Al2O3 to C was 1：4,and 10% TiO2 and excess AlCl3 were added.The results show that TiC is produced by C and TiO2 after TiO2 transforms from anatase into rutile gradually.In the temperature range of 1 763？1 783 K,the compounds of Ti and Al are not found in slags and condensate.The purity of aluminum reaches 98.35%,and TiO2 does not participate in alumina carbothermic reduction process and chlorination process in vacuum.

Sulfur phase and sulfur removal in high sulfur-containing bauxite

The sulfur phase in high sulfur-containing bauxite was studied by an X-ray diffraction analysis and a chemistry quantitative analysis.The methods for the removal of different shaped sulfur were also discussed.The results show that sulfur phases in high sulfur-containing bauxites exist in the main form of sulfide sulfur （pyrite） or sulfate sulfur,and the main sulfur forms of bauxites from different regions are not the same.Through a combination of an X-ray diffraction analysis and a chemistry quantitative analysis,the sulfur phases of high sulfur-containing bauxite could be accurately investigated.Deciding the main sulfur form of high sulfur-containing bauxite could provide theoretical instruction for choosing methods for the removal of sulfur from bauxite,and an oxidizing-roasting process is an effective way to remove sulfide sulfur from high sulfur-containing bauxite,the content of S^2-in crude ore in the digestion liquor is above 1.7 g/L,but in the roasted ore digestion liquor,it is below 0.18 g/L.Using the sodium carbonate solution washing technology to wash bauxite can effectively remove sulfate sulfur,the content of the total sulfur in ore is lowered to below 0.2% and can meet the production requirements for the sulfur content.

Enhanced catalytic activities and selectivities in preferential oxidation of CO over ceria-promoted Au/Al_2O_3 catalysts

The preferential oxidation of CO （CO‐PROX） is a hot topic because of its importance in pro‐ton‐exchange membrane fuel cells （PEMFCs）. Au catalysts are highly active in CO oxidation. Howev‐er, their activities still need to be improved at the PEMFC operating temperatures of 80–120 ＆#176;C. In the present study, Au nanoparticles of average size 2.6 nm supported on ceria‐modified Al2O3 were synthesized and characterized using powder X‐ray diffraction, nitrogen physisorption, transmission electron and scanning transmission electron microscopies, temperature‐programmed hydrogen reduction （H2‐TPR）, Raman spectroscopy, and in situ diffuse‐reflectance infrared Fourier‐transform spectroscopy. Highly dispersed Au nanoparticles and strong structures formed by Au–support in‐teractions were the main active species on the ceria surface. The Raman and H2‐TPR results show that the improved catalytic performance of the Au catalysts can be attributed to enhanced strong metal–support interactions and the reducibility caused by ceria doping. The formation of oxygen vacancies on the catalysts increased their activities in CO‐PROX. The synthesized Au catalysts gave excellent catalytic performances with high CO conversions （＆gt;97%） and CO2 selectivities （＆gt;50%） in the temperature range 80–150 ＆#176;C.

PIEZOSPECTROSCOPIC STUDY OF RESIDUAL STRESSES AROUND INDENTATIONS IN SiC/Al_O_3 NANOCOMPOSITE

A new experimental measurement of residual stresses around Vickers′ indentations on the surface of the SiC/Al 2O 3 nanocomposites is proposed with the aid of a Raman microprobe. Results s how that the shifts of R lines in the fluorescence spectra va ry with the distance from the centre of indentation. The magnitude of load appli ed on the surface of the materials through the indenter influences the shifts of R lines to great extent. The luminescence of R lines of the materials before indenting is used to determine the residual stresses around the indentation in the materials, assuming that the stress tensor is transversely isotropic. Final ly, the term of hydrostatic stress is adopted to explain and compare different residual stresses around indentations with the increase of the indenting load an d the distance from the centre of indentations. <

Separation of aluminosilicates and diaspore from diasporic-bauxite by selective flocculation

The flocculation tests of four pure minerals(diaspore,kaolinite,illite,pyrophyllite)and bauxite ore were investigated by the sedimentation.The dispersion behavior of the four pure minerals shows a very good consistency with the variation of zeta potential.The concentrate with the mass ratio of Al2O3 to SiO2(m(Al2O3)/m(SiO2))8.90 and the recovery of Al2O3 86.98%is obtained from bauxite ore(m(Al2O3)/m(SiO2)=5.68)in pH range of 9.5-10.0 by using sodium carbonate(5 kg/t)and sodium polyacrylate(7 g/t)as dispersant and flocculant respectively.Sodium carbonate acts as both pH modifier and favorable dispersant for aluminosilicates.The high performance of sodium polyacrylate on flocculation for diaspore is contributed to the carboxyl of sodium polyacrylate that interacts with active Al sites on diaspore by chemical absorption,and the hydrogen bond effects between hydroxyl group of macromolecule and surface Al—OH on diaspore to accelerate the sedimentation of diaspore.

Rod-shaped porous alumina-supported Cr_2O_3 catalyst with low acidity for propane dehydrogenation

Direct catalytic propane dehydrogenation(PDH)to obtain propylene is a more economical and environmentally friendly route for propylene production.In particular,alumina-supported Cr2O3 catalysts can have better potential applications if the acidic properties could be tuned.Herein,a series of rod-shaped porous alumina were prepared through a hydrothermal route,followed by calcination.It was found that the acidity of the synthesized alumina was generally lower than that of the commercial alumina and could be adjusted well by varying the calcination temperature.Such alumina materials were used as supports for active Cr2O3,and the obtained catalysts could enhance the resistance to coke formation associated with similar activity in PDH reaction compared to the commercial alumina.The amount of coke deposited on a self-made catalyst(Cr-Al-800)was 3.6%,which was much lower than that deposited on the reference catalyst(15.7%).The lower acidity of the catalyst inhibited the side reactions and coke formation during the PDH process,which was beneficial for its high activity and superior anti-coking properties.

Preparation of Pseudo-boehmite and y-Al_2O_3 Support by Neutralization of NaAlO_2 Solution with CO_2

Pseudo-boehmite (PB) and γ-Al2O3 support are prepared by neutralization ofNaAlO2 solution with CO2(mixed gases) on bench scale. PB, typically loosely packed, fibrous particle/aggregate, is obtained by adjustingconcentration and flow rate of CO2 and concentration of NaAlO2 solution at a pH level lower than that commonlyassumed during neutralization. After calcination at different temperatures, γ-Al2O3 supports with different pore vol-ume and different pore size are prepared at different conditions.

Effects of SiC interfacial coating on mechanical properties of carbon fiber needled felt reinforced sol-derived Al2O3 composites

3D carbon fiber needled felt and polycarbosilane-derived SiC coating were selected as reinforcement and interfacial coating,respectively,and the sol-impregnation-drying-heating(SIDH)route was used to fabricate C/Al2O3 composites.The effects of Si C interfacial coating on the mechanical properties,oxidation resistance and thermal shock resistance of C/Al2O3 composites were investigated.It is found that the fracture toughness of C/Al2O3 composites was remarkably superior to that of monolithic Al2O3 ceramics.The introduction of SiC interfacial coating obviously improved the strengths of C/Al2O3 composites although the fracture work diminished to some extent.Owing to the tight bonding between SiC coating and carbon fiber,the C/SiC/Al2O3 composites showed much better oxidation and thermal shock resistance over C/Al2O3 composites under static air.

Ultradurable fluorinated V_(2)AlC for peroxymonosulfate activation in organic pollutant degradation processes

Vanadium‐based catalysts are considered the most promising materials to replace cobalt‐based catalysts for the activation of peroxymonosulfate(PMS)to degrade organic pollutants.However,these traditional vanadium species easily leak out metal ions that can affect the environment,even though the of vanadium is much less than that of cobalt.Compared to other vanadium‐based cata‐lysts,e.g.,V_(2)O_(3),fluorinated V_(2)AlC shows a high and constant activity and reusability regarding PMS activation.Furthermore,it features extremely low ion leakage.Active oxygen species scavenging and electron spin resonance measurements reveal that the main reactive oxygen species was 1O_(2),which was induced by a two‐dimensional confinement effect.More importantly,for the real‐life application of tetracycline(TC)degradation,the introduction of fluorine changed the adsorption mode of TC over the catalyst,thereby changing the degradation path.The intermediate products were detected by liquid‐chromatography mass spectroscopy(LC‐MS),and a possible degradation path was proposed.The environmental impact test of the decomposition products showed that the toxicity of the degradation intermediates was greatly reduced.Therefore,the investigated ultradu‐rable catalyst material provides a basis for the practical application of advanced PMS oxidation technology.

Fabrication of cobalt aluminum-layered double hydroxide nanosheets/carbon spheres composite as novel electrode material for supercapacitors

A new design route was presented to fabricate cobalt aluminum-layered double hydroxide(CoAl-LDH)thin layers whichgrow on carbon spheres(CSs)through a growth method.The CoAl-LDH thin layers consist of nanoflakes with a thickness of20nm.The galvanostatic charge-discharge test of the CoAl-LDH/CSs composite shows a great specific capacitance of1198F/g at1A/g(based on the mass of the CoAl-LDH/CSs composite)in6mol/L KOH solution,and the composite displays an impressive specificcapacitance of920F/g even at a high current density of10A/g.Moreover,the composite remains a specific capacitance of928F/gafter1000cycles at2A/g,and the specific capacitance retention is84%,indicating that the composite has high specific capacitance,excellent rate capability and good cycling stability in comparison to pristine CoAl-LDH.

Promotion effects of nickel-doped Al2O3-nanosheet-supported Au catalysts for CO oxidation

Supported gold catalysts show high activity toward CO oxidation, and the nature of the support significantly affects the catalytic activity. Herein, serial Ni doping of thin porous Al2 O3 nanosheets was performed via a precipitation-hydrothermal method by varying the amount of Ni during the precipitation step. The prepared nanosheets were subsequently used as supports for the deposition of Au nanoparticles(NPs). The obtained Au/Nix Al catalysts were studied in the context of CO oxidation to determine the effect of Ni doping on the supports. Enhanced catalytic performances were obtained for the Au/Nix Al catalysts compared with those of the Au supported on bare Al2 O3. The Ni content and pretreatment atmosphere were both shown to influence the catalytic activity. Pretreatment under a reducing atmosphere was beneficial for improving catalytic activity. The highest activity was observed for the catalysts with a Ni/Al molar ratio of 0.05, achieving complete CO conversion at 20 °C with a gold loading of 1 wt%. The in-situ FTIR results showed that the introduction of Ni strengthened CO adsorption on the Au NPs. The H2-TPR and O2-TPD results indicated that the introduction of Ni produced new oxygen vacancies and allowed the oxygen molecules to be adsorbed and activated more easily. The improved catalytic performance after doping Ni was attributed to the smaller size of the Au NPs and more active oxygen species.

Fibrous activated alumina prepared through phase transformation using dawsonite as a template

Fibrous activated alumina is widely applied in catalysts,adsorbents,and composite materials.This work presents a green approach in preparing the fibrous activated Al_(2)O_(3) with high purity and specific surface area through multistep phase transformation of aluminum-bearing substances using intermediate dawsonite as a template.Thermodynamic calculations and experimental results show that increasing the concentration of Na_(2)CO_(3) and(NH_(4))_(2)CO_(3) is remarkably beneficial to the formation of dawsonite and ammonium aluminum carbonate hydroxide,respectively.Based on determination of dissolution and precipitation mechanism,the ultrafine granular gibbsite is converted to the uniform fibrous dawsonite with a ratio of length to diameter over 50,and the fibrous dawsonite changes into the long fibrous ammonium aluminum carbonate hydroxide with a ratio of length to diameter is about 80 in above 70 g/L(NH_(4))_(2)CO_(3) solution.Furthermore,the activated alumina remains fibrous morphology after roasting ammonium aluminum carbonate hydroxide at a slow heating rate,plentiful open mesopore and weak aggregation of particles,which contributes to the high specific surface area of 159.37 m^(2)/g at 1273 K for the activated alumina.The complete transformation of dawsonite to ammonium aluminum carbonate hydroxide and high specific surface area contribute to the purity of the activated fibrous alumina above 99.9%with low Na and Fe content.

Recycling of waste residue in aluminum production process

The preparation of crystal form of Al（OH）3 from the deposited residues of anodizing lines in the process of producing aluminum was studied. Alkali is used to dissolve the residue, and then blow CO2 is bellowed in, finally a kind of useful crystal Al（OH）3 is accessed by hydrolysis. The yield of the crystal Al（OH）3 was affected by temperature, pH and flow rate of CO2. The experimental results showed that under constant stirring, the optimized conditions was to control the temperature of 75-85℃, pH 7.5-9.0, CO/flow rate 60-80 mL/min. Using this method, the purpose of recovering valuable resources of Al, cleaning up the environment, and recycling of the by-product of Na2CO3 was achieved. It was of good economic and social benefits.

Depolarised gas anodes for aluminium electrowinning

Consumable carbon anodes are used in the electrowinning of aluminium by the Hall-Heroult process. Emissions of CO2 may be eliminated by introducing an inert oxygen evolving anode, which however will require a higher anode potential. An alternative approach is to use a natural gas or hydrogen gas anode to reduce the CO2 emissions and lower the anode potential. Preliminary laboratory experiments were carried out in an alternative molten salt electrolyte consisting of CaCl2-CaO-NaCl at 680℃ Porous anodes of platinum and tin oxide were tested during electrolysis at constant current. The behaviour of inert anode candidate materials such as tin oxide and nickel ferrite were also studied.

Carbothermic reduction of alumina with carbon in vacuum

Carbothermic reduction alumina in vacuum was conducted, and the products were analysed by means of XRD and gas chromatography. Thermodynamic analysis shows that in vacuum the initial carbothermic reduction reaction temperature reduces compared with that under normal pressure, and the preferential order of products is Al404C, Al4C3, Al2OC, Al20 and A1. Experiment results show that the carbothermic reduction products of alumina are A1404C and A14C3, and neither A12OC, Al20 or Al was found. During the carbothermic reduction process, the reaction rate of Al203 and carbon decreases gradually with increasing time. Meanwhile, lower system pressure or higher temperature is beneficial to the carbothermic reduction of alumina process. A1404C is firstly formed in the carbothermic reaction, and then A14C3 is formed in lower system pressure or at higher temperature.

Research on Gelcasting Formation of SiC-Al_2O_3-Y_2O_3-La_2O_3 Systems

The rheological behavior and gelcasting of composite suspensions of SiC and synthesized Al 2O 3-Y 2O 3-La 2O 3 powder as sintering aid were investigated. It was found that the rheological behavior of SiC particles could be modified with a slightly oxidized surface that was similar to silica in colloidal behavior. The smaller the particles were, the more similar to silica the SiC powder was. The pH value of Al 2O 3-Y 2O 3-La 2O 3 synthesized powder slurry at isoelectric points (IEP) is higher than that of SiC powder. The dispersant PAA-NH 4 changes the IEP of both SiC and Al 2O 3-Y 2O 3-La 2O 3 powder slurry to higher pH values. The experimental results indicate that the composite suspension could possess satisfactory stability and lower viscosity at pH =10.1 and PAA-NH 4 as dispersant. The optimum solid loading was 550 0 in volume. Machinable green bodies with uniform complex shape are gained after molding.

Al_4O_4C的碳热还原合成及其反应动力学

以氧化铝(Al2O3)和石墨(C)为原料,采用碳热还原工艺合成铝氧碳(Al4O4C),借助于X射线衍射仪和场发射扫描电子显微镜研究了加热温度和保温时间对合成铝氧碳(Al4O4C)的影响。结果表明:提高加热温度,可加快Al2O3和C反应生成Al4O4C的反应速率;延长保温时间可增大Al2O3和C反应生成Al4O4C的反应程度。在反应初期主要为固-固反应,Al2O3和C直接接触反应生成Al4O4C和一氧化碳(CO);后期主要为气-固反应,Al2O3和CO气体反应生成Al4O4C和二氧化碳(CO2)。计算得到气-固反应的频率因子和活化能分别为338.66和264.19kJ/mol。

Fe2O3对天然原料合成Al4SiC4/Al4O4C复合耐火材料的影响(英文)

以焦宝石、活性炭和铝粉为原料并添加Fe2O3后制备了Al4SiC4/Al4O4C复合耐火材料。利用化学分析、X射线衍射和扫描电镜研究了Fe2O3对所制备复合材料的物相组成和显微结构的影响。结果表明:在烧结过程中,从1400℃开始,Fe2O3转变为低熔点物相Fe3Si,产生液相促进Al4SiC4成核、细化晶粒,同时包裹Al4SiC4。此外,未添加Fe2O3的样品中生成的Al4O4C短纤维,Fe2O3的加入使得Al4O4C相变为细小的晶粒。

氮气保护下镁砂对Al–刚玉体系物相的影响

以烧结刚玉、α-Al2O3微粉、金属铝粉、高纯镁砂[加入量分别为3%（质量分数）、6%、15%]为原料,酚醛树脂为结合剂,制备Al–MgO–Al2O3系复合材料。样品成型后经过200℃烘干后在1 300℃氮气气氛下烧结。结果表明：添加金属铝粉后样品常规物理性能显著改善。样品中的主晶相为α-Al2O3和Mg Al2O4,有金属铝残留。镁砂对金属铝–烧结刚玉耐火材料物相组成影响大,当镁砂加入量为3%时形成Al4O4C相,镁砂加入量为6%或15%时,新相为Al4C3,未检测到Al4O4C相,镁砂添加量为15%时能检测到方镁石相。镁砂加入量大于或等于6%时,α-Al2O3颗粒或细粉表面形成的镁铝尖晶石包裹刚玉结构,将α-Al2O3表面包覆,阻断Al4C3与α-Al2O3反应生成Al4O4C。最后建立了该体系中新相形成机理的反应模型。