V2O5-CaCo3-Nb2O5掺杂对低损耗功率Mn-Zn铁氧体的影响

Effect of the content of dopants in the manganese-zinc ferrites on the low power loss is studied by measuring magnetic properties and observing the grain boundary structures. The Mn0.738Zn0.206Fe2.066O4 composition powders were prepared by using conventional ceramic powder processing technique. The microstructure of grain boundary was observed by scanning electron microscope （SEM）. It has been found that power loss is greatly dependent upon the content of the additives.     

Catalytic properties of CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 in NO＋CO reaction

Using SnxTi1-xO2 as carriers, CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 catalysts with different loading amounts of copper oxide (CuO) were prepared by an impregnation method. The catalytic properties of CuO/Sn0.9Ti0.1O2 and CuO/Sn0.7Ti0.3O2 were examined using a microreactor-gas chromatography (GC) NO CO reaction system and the methods of BET (Brun- auer-Emmett-Teller), TG-DTA (themogravimetric and differential thermal analysis), X-ray diffraction (XRD) and H2-temperature programmed reduction (TPR). The results showed that NO conversions of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 were 47.2% and 43.6% respectively, which increased to 95.3% and 90.9% at 6 wt% CuO loading. However, further increase in CuO loading caused a decrease in the catalytic activity. The nitrogen adsorption-desorption isotherm and pore-size distribution curve of Sn0.9Ti0.1O2 and Sn0.7Ti0.3O2 represented type IV of the BDDT (Brunauer, Deming, Deming and Teller) system and a typical mesoporous sample. There were two CuO diffraction peaks (2θ 35.5° and 38.7°), and the diffraction peak areas increased with increasing CuO loading. TPR analysis also detected three peaks (α, β and γ) from the CuO-loaded catalysts, suggesting that the α peak was the reduction of the highly dispersed copper oxide, the β peak was the reduction of the isolated copper oxide, and the γ peak was the reduction of crystal phase copper oxide. In addition, a fourth peak (δ) of the catalysts meant that the SnxTi1-xO2 mixed oxides could be reductive.     

A novel reduction of diketones with i-RMgBr catalyzed by Cp<Subscript>2</Subscript>TiCl<Subscript>2</Subscript> and deoxygenation of sulfoxides by Cp<Subscript>2</Subscript>TiCl<Subscript>2</Subscript>/Al system

α-diketones and β-diketones react with Grignard reagents in the presence of a catalytic amount of Cp₂TiCl₂ to yield α-ketols and corresponding ketones respectively. Sulfoxides can be deoxygenated by Cp₂TiCl₂/Al system. The possible mechanisms are also discussed. Project (No. 20072033) supported by the National Natural Science Foundation of China and the Specialized Research Fund for the Doctoral Program of Higher Education Ministry, China     

Fall and rise of a D<Subscript>2</Subscript>O ice cube in liquid H<Subscript>2</Subscript>O

In this section of Resonance, we invite readers to pose questions likely to be raised in a classroom situation. We may suggest strategies for dealing with them, or invite responses, or both. “Classroom” is equally a forum for raising broader issues and sharing personal experiences and viewpoints on matters related to teaching and learning science.The demonstration described in this article is to show that while H₂O ice floats in water, D₂O ice sinks in water, proving the higher density of ‘heavy water’. This experiment can be done in a classroom or in an auditoriam.     

A SISO mixed<Emphasis Type="Italic">H</Emphasis><Subscript>2</Subscript>/l<Subscript>1</Subscript> optimal control problem and its solution

Study of the SISO mixedH ₂/l₁ problem for discrete time systems showed that there exists a unique optimal solution which can be approximated within any prescribed missing error bound inl ₂ norm with solvable suboptimal solutions and solvable superoptimal solutions. Project supported by the National Natural Science Foundation of China (No. 60174026) and the Scientific Research Foundation for Returned Overseas Chinese Scholars of Zhejiang Province (No. J20020546)     

The Electrochemical Performance of Ml0.7Mm0.3Ni3.7Co0.7Mn0.4Al0.2 Nanocrystalline Hydrogen Storage Alloy as Metal Hydride Electrode

Ml0.7Mm0.3Ni3.7Co0.7Mn0.4Al0.2 nanocrystalline hydrogen storage materials are prepared by melt-spinning(MS).X-ray diffraction is used for the measurement of the nanocrystalline size.Compared to the electrode of polycrystalline alloys,the property of activation MH9metal hydride)electrode of the alloys with nanometer scale became worse and the inital discharge capacity decreased.It may be ascribed to the decrease of the total amount of rare earth metals and the increase of oxygen on the surface from the analysis of components of the alloys.After heat-treatment,the electrochemical performance of MH electrode of as-spun alloys could be improved,which could be attributed to the alleviation of the lattice strain.     

过冷液相区内轧制温度对Zr52.5Al10Ni10Cu15Be12.5大块金属玻璃表面形貌的影响

Surface morphologies of Zr52.5 Al10 Ni10 Cu15 Be12.5 bulk metallic glass after being rolled at both a temperature around T9 and near （ Tx - 50） K were investigated with a scanning electron microscopy. Macroscopic and microscopic observation results show that squamae, cracks, steps and wedges exist on the surface when the samples were rolled at temperatures around Ty. However, a smooth and fiat surface appears when the samples were rolled at temperatures near （ Tx - 50） K. These results indicate that the mode of deformation in the supercooled liquid region is a partially homogeneous flow at a temperature around T9, and a fully homogeneous one at temperatures near （ Tx - 50） K. According to the results, it is more feasible to roll the amorphous alloys at temperatures near （ Tx - 50） K to obtain parts with smooth and fiat surface.     

Integrated direct air capture and CO<Subscript>2</Subscript> utilization of gas fertilizer based on moisture swing adsorption

A new concept of low-cost direct air capture technology integrated with a fertilization system is proposed, as an alternative to the application of air derived CO₂. A moisture swing sorbent can elevate the CO₂ concentration from 400 parts per million (ppm) to several thousand ppm, and this can be used to cultivate plants. Desorption isotherms were determined and are described well by a Langmuir model. The adsorption rate constant and the desorption rate constant were gained at 25 °C, 35 °C, and 45 °C under 1000 ppm concentration of CO₂. In accelerated cultivation experiments, the effects of CO₂ concentration, light intensity, and spectrum on the CO₂ uptake rate of the plants were investigated. A multi-bed desorption system which is capable of providing a continuous and stable CO₂ supply for a greenhouse is demonstrated based on the desorption characteristic and CO₂ uptake feature of plants. An energy and cost assessment for the integrated system was performed and the results indicated that minimum energy requirements and cost estimate of CO₂ are 35.67 kJ/mol and 34.68 USD/t, respectively. This makes direct air capture a competitive and sustainable carbon source for agriculture.     

Green epoxidation of cyclooctene with molecular oxygen over an ecofriendly heterogeneous polyoxometalate-gold catalyst Au/BW<Subscript>11</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript>

An ecofriendly heterogeneous polyoxometalate (POM)-gold catalyst Au/BW₁₁/Al₂O₃ was synthesized and used for solvent-free epoxidation of cyclooctene under mild reaction conditions using molecular oxygen as an oxidant and t-butyl hydroperoxide (TBHP) as an initiator. The catalyst was characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD), induced coupled plasma optical emission spectrometry (ICP-OES), and Brunauer-Emmett-Teller (BET). The catalyst showed good conversion and high selectivity without use of solvents or environmentally harmful oxidants. Moreover, the catalyst is recyclable up to three cycles with no significant loss in selectivity towards epoxide.     

高能球磨法制备的含铁TiO2的穆斯堡尔谱研究

1Introduction Oxide dilutedmagneticsemiconductors(O DMS)havedrawnmuchattentioninthelastdecadebecause thesematerialsappeartohavegreatpotentialforuse inspin dependentelectronicdevices[1].Recently,iron cobalt dopedtitaniumdioxideswithroomtemperature ferromagnetismhavebeenreported[2].Specially,the resultsofmagneticpropertiesofFexTi1-xO2(x=0.065and0.250)indicatethatferromagnetismwitha Femagneticmomentislargerthantheonereported forCo[3].ThefabricationmethodsofFe Co doped TiO2includepulsedlaser…     

Study of transport behavior for Fe-doping La<Subscript>0.67</Subscript>Ca<Subscript>0.33</Subscript>MnO<Subscript>3</Subscript> perovskite manganese

Systematic studies of the transport properties of La_0.67Ca_0.33Mn_1?xFe _x O₃ (x=0–0.3) systems showed that with increasing Fe-doping contentx the resistance increases and the insulator-metal transition temperature moves to lower temperature. For small doping content, the transport property satisfies metal transport behavior below the transition temperature, and above the transition temperature it satisfies the small polaron model. This behavior can be explained by Fe³⁺ doping, which easily forms Fe³⁺?O^2??Mn⁴⁺ channel, suppressing the double exchange Mn³⁺?O^2??Mn⁴⁺ channel and enhancing the spin scattering of Mn ions induced by antiferromagnetic clusters of Fe ions.     

Synthesis of TiO<Subscript>2</Subscript> supported on activated carbon by MOCVD: operation parameters study

A novel metallo-organic chemical vapor deposition (MOCVD) technique has been applied to the preparation of the photocatalytic titanium dioxide supported on activated carbon. The effects of various condition parameters such as carrier gas flow rate, source temperature and deposition temperature on the deposition rate were investigated. The maximum deposition rate of 8.2 mg/(g·h) was obtained under conditions of carrier gas flow rate of 400 ml/min, source temperature of 423 K and deposition temperature of 913 K. The deposition rate followed Arrhenius behavior at temperature of 753 K to 913 K, corresponding to activation energy E _a of 51.09 kJ/mol. TiO₂ existed only in anatase phase when the deposition temperature was 773 K to 973 K. With increase of deposition temperature from 1073 K to 1273 K, the rutile content sharply increased from 7% to 70%. It was found that a deposition temperature of 773 K and a higher source temperature of 448 K resulted in finely dispersed TiO₂ particles, which were mainly in the range of 10–20 nm. Project (No. 90206007) supported by the National Natural Science Foundation of China     

Theoretical study of NO adsorbed on the surface of TiO<Subscript>2</Subscript> (110) cluster model

The chemisorption properties of N¹⁸O adsorption on TiO₂(110) surface were investigated by experimental and theoretical methods. The results of temperature programmed desorption (TPD) indicated that the temperatures of the three desorption peaks of the main N₂ molecules were at (low) temperature of 230 K, 450 K and (high) temperature of 980 K. This meant that N¹⁸O decomposed and recombined during the process of N₂ desorption after N¹⁸O was exposed. Analysis of the stable combination and orbital theory calculation of the surface reaction of NO adsorption on the TiO₂(110) cluster model showed that there was clear preference for the Ti-NO orientation.     

Mixed G<Emphasis Type="Italic">l</Emphasis><Subscript>2</Subscript>/G<Emphasis Type="Italic">H</Emphasis><Subscript>2</Subscript> multi-channel multi-objective control synthesis for discrete time systems

This paper proposes a new approach for multi-objective robust control. The approach extends the standard generalizedl ₂ (Gl ₂) and generalizedH ₂ (GH ₂) conditions to a set of new linear matrix inequality (LMI) constraints based on a new stability condition. A technique for variable parameterization is introduced to the multi-objective control problem to preserve the linearity of the synthesis variables. Consequently, the multi-channel multi-objective mixed Gl ₂/GH ₂ control problem can be solved less conservatively using computationally tractable algorithms developed in the paper. Project supported by the National Natural Science Foundation of China (No. 60374028), and the Scientific Research Foundation for Returned Overseas Chinese Scholars, Ministry of Education (No. [2004]176)     

Preparation and electrochemical application of praseodymium modified TiO<Subscript>2</Subscript>-NTs/SnO<Subscript>2</Subscript>-Sb anode by cyclic voltammetry method

A Pr-doped TiO₂-NTs/SnO₂-Sb electrode was prepared by a simple method, cyclic voltammetry(CV). The methyl orange(MO)aqueous solution was selected as a simulated wastewater. The ordered microstructural TiO₂-NTs substrate was synthesized by an electrochemical method to obtain large specific surface area and high space utilization. The phase structure, electrode surface morphology and electrochemical properties of electrodes were characterized by XRD, SEM and electrochemical technology, respectively. The results showed that praseodymium oxide was successfully doped into the SnO₂-Sb film by CV method. Due to the doped Pr, the oxygen evolution potential increased from 2.25 V to 2.40 V. The degradation of MO was investigated by UV-vis. The C _t /C ₀ (φ) was studied as a function to obtain the optimal parameters, such as the amount of doped Pr, current density and initial dye concentration. In addition, the degradation process followed pseudo-first-order reaction kinetics and the rate constant was 0.099 3 min^-1. The result indicated that the introduction of Pr reduced the formation of oxygen vacancies or enhanced the formation of adsorbed hydroxyl radical groups on the surface, thus leading to better activity and stability.     

Science Letters：Nitrogen doping of activated carbon loading Fe2O3 and activity in carbon-nitric oxide reaction

Nitrogen doping of activated carbon loading Fe2O3 was performed by annealing in ammonia, and the activity of the modified carbon for NO reduction was studied in the presence of oxygen. Results show that Fe2O3 enhances the amount of surface oxygen complexes and facilitates nitrogen incorporation in the carbon, especially in the form of pyridinic nitrogen. The modified carbon shows excellent activity for NO reduction in the low temperature regime (<500 °C) because of the cooperative effect of Fe2O3 and the surface nitrogen species.     

Preparation and Properties of TiNx-SiO2 Antireflective Coatings with Print Process

This paper describes the preparation and properties of TiNx-SiO2 double-layered antireflective(AR) coatings that were applied with print process. The coating material was analyzed and TiNx was used instead of TiO2 as high refractive material. The influence of solution concentration on AR property was studied. The testing result shows that the coatings using print process are featured with excellent mechanical property and the AR property is comparable to American Southwall AR product. It is expected that the study would promote the industrialization progress in AR coatings.     

Study of 2-Propanol Photocatalytic Degradation on Surface of Phase-Ratio-Controlled TiO<Subscript>2</Subscript> Nanoparticles

The crystal form of TiO₂ is a crucial focus of research on the photocatalytic degradation of gaseous pollutants by TiO₂-based composite photocatalysts. To explore the synergistic effect of mixed crystalline TiO₂ on gaseous organic-pollutant photocatalytic degradation, we synthesized a series of TiO₂ nanoparticles with controllable phase ratios. We explored the role of the TiO₂ phase ratio on the photocatalytic activity and degradation pathway in the photodegradation of 2-propanol (IPA). We estimated the crystallite size and crystal proportions of anatase and rutile by X-ray diffraction. We used the Brunauer–Emmett–Teller method to calculate the specific surface area and Fourier transform infrared spectroscopy to characterize the surface chemistry of the samples. Our results show the photocatalytic activities of pure anatase and the sample with 8.6% rutile to be much better than those of the samples with a phase junction and pure rutile. As such, anatase is the better option for the study of photodegradation design and preparation of gas-phase organic pollutants.     

在室温和常压下用机械合金化方法制备Fe5C2金属间化合物

Single phase Fe5C2 intermetallic compound was prepared by mechanical alloying method. The phase and crystal structure of sample were analyzed with X-ray differaction spectrum. The decomposing temperature of the Fe5C2 compound is 596.4℃ determined by the DSC curve. It is further shown that the size of nanometer crystal grain is an important condition for carrying out the solid state reaction at room temperature and normal pressure.     

Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> as indicator of heavy metal enrichment in Zhujiang (Pearl River) estuary sediments

A part of the heavy metals in estuary and coastal zone occurs naturally in the environment; the other part is due to human activity; so the directly measured concentration of heavy metal does not automatically indicate anthropogenic enrichment. Fe₂O₃ was used in this study as conservative tracer to distinguish natural components from anthropogenic components of heavy metal sediment concentration in the Zhujiang estuary. Compared with clay and Al₂O₃, Fe₂O₃ is more suitable as reference element. The final results showed that two zones in the Zhujiang estuary were seriously contaminated by heavy metals. One nearby the Humen mouth; the other around the west coast of the estuary. The horizontal distribution of heavy metals indicates that Zn, Ni and Cu have wider contaminating areas than TiO₂, V and Cr in the estuary.