群弱直积合成

用换位函数给出群的弱直积合成的方法

积合成模型是唯一保序合成模型的条件

在层次分析(AHP)中,积合成模型是保序的,如果想得到只有积合成模型保序的结论,还必须限定属性个数大于2.

某些附有自由积群的无限次元Cayley图的谱分解

主要研究附有两个巡回群的自由积G=Zn%Zm(n,m≥2)的Cayley图的离散邻接作用素A的谱分解。Gr,(Zn%Zm)是由un=vm=1这样两个Unitary作用素u,v生成的C,-环,它的构造是已知的。若令n≥3时,T1=u+u,T2=v+v,;n=m=2时,T1=u,T2=v,那么A=T1+T2,T1,T2在(Cr,(G),τG)上是自由独立的,利用T1,T2各自的分布,使用自由合成积,就可以求出T1+T2的分布。

Research on 3D marine electromagnetic interferometry with synthetic sources for suppressing the airwave interference

In order to suppress the airwave noise in marine controlled-source electromagnetic （CSEM） data, we propose a 3D deconvolution （3DD） interferometry method with a synthetic aperture source and obtain the relative anomaly coefficient （RAC） of the EM field reflection responses to show the degree for suppressing the airwave. We analyze the potential of the proposed method for suppressing the airwave, and compare the proposed method with traditional methods in their effectiveness. A method to select synthetic source length is derived and the effect of the water depth on RAC is examined via numerical simulations. The results suggest that 3DD interferometry method with a synthetic source can effectively suppress the airwave and enhance the potential of marine CSEM to hydrocarbon exploration.

In-situ homogeneous synthesis of carbon nanotubes on aluminum matrix and properties of their composites

Using nickel catalyst supported on aluminum powders, carbon nanotubes （CNTs） were successfully synthesized in aluminum powders by in-situ chemical vapor deposition at 650 ℃. Structural characterization revealed that the as-grown CNTs possessed higher graphitization degree and straight graphite shell. By this approach, more homogeneous dispersion of CNTs in aluminum powders was achieved compared with the traditional mechanical mixture methods. Using the in-situ synthesized CNTs/Al composite powders and powder metallurgy process, CNTs/Al bulk composites were prepared. Performance testing showed that the mechanical properties and dimensional stability of the composites were improved obviously, which was attributed to the superior dispersion of CNTs in aluminum matrix and the strong interfacial bonding between CNTs and matrix.

PROCESSING PARAMETER OPTIMIZATION OF FDM BASED ON ROBUST DESIGN

The influence of processing parameters on the precision of parts fabricated by fused deposition modeling （FDM） technology is studied based on a series of performed experiments. Processing parameters of FDM in terms of wire-width compensation, extrusion velocity, filing velocity, and layer thickness are chosen as the control fac- tors. Robust design analysis and multi-index fuzzy comprehensive assessment method are used to obtain the opti- mal parameters. Results show that the influencing degrees of these four factors on the precision of as-processed parts are different. The optimizations of individual parameters and their combined effects are of the same impor- tance for a high precision manufacturing.

Morphology effect of zirconia support on the catalytic performance of supported Ni catalysts for dry reforming of methane

An immature pinecone shaped hierarchically structured zirconia （ZrO2-ipch） and a cobblestone-like zirconia nanoparticulate （ZrO2-cs）, both with the monoclinic phase （m-phase）, were synthesized by the facile hydrothermal method and used as the support for a Ni catalyst for the dry reforming of methane （DRM） with CO2. ZrO2-ipch is a much better support than ZrO2-cs and the traditional ZrO2 irregular particles made by a simple precipitation method （ZrO2-ip）. The supported Ni catalyst on ZrO2-ipch （Ni/ZrO2-ipch） exhibited outstanding catalytic activity and coke-resistant stability compared to the ones on ZrO2-cs （Ni/ZrO2-cs） and ZrO2-ip （Ni/ZrO2-ip）. Ni/ZrO2-ip exhibited the worst catalytic performance. The origin of the significantly enhanced catalytic performance was revealed by characterization including XRD, N2 adsorption measurement （BET）, TEM, H2-TPR, CO chemisorption, CO2-TPD, XPS and TGA. The superior catalytic activity of Ni/ZrO2-ipch to Ni/ZrO2-cs or Ni/ZrO2-ip was ascribed to a higher Ni dispersion, increased reducibility, enhanced oxygen mo- bility, and more basic sites with a higher strength, which were due to the unique hierarchically structural morphology of the ZrO2-ipch support. Ni/ZrO2-ipch exhibited better stability for the DRM reaction than Ni/ZrO2-ip, which was ascribed to its higher resistance to Ni sintering due to a strengthened metal-support interaction and the confinement effect of the mesopores and coke deposition resistance. The higher coking resistance of Ni/ZrO2-ipch for the DRM reaction in comparison with Ni/ZrOz-ip orignated from the coke-removalabitity of the higher amount of lattice oxygen and more basic sites, confirmed by XPS and CO2-TPD analysis, and the stabilized Ni on the Ni/ZrO2-ipch catalyst by the confinement effect of the mesopores of the hierarchical ZrO2-ipch sup- port. The superior catalytic performance and coking resistance of the Ni/ZrO2-ipch catalyst makes it a promising candidate for synthesis gas production from the DRM reaction.

Nucleation and growth mechanism of electrodeposited Ni−W alloy

The nucleation and growth mechanism of electrodeposited Ni−W alloy were investigated.Cyclic voltammetry(CV)and chronoamperometry(CA)were used to examine the electrochemical behavior and nucleation mechanism of the electrodeposited Ni−W alloy.The nucleation type and kinetic parameters of the electrodeposited Ni−W alloy were obtained from the CA analysis results.SEM,AFM,and TEM were also used to investigate the nucleation and growth process of the electrodeposition of Ni−W alloy.The results demonstrate that the nucleation and initial stages of the growth phase of the Ni−W alloy undergo the formation,movement,and aggregation of atoms,single crystals,and nanoclusters.When the size of single crystal increases up to approximately 10 nm and the average size of the crystal granules is approximately 68 nm,they no longer grow.Increasing the applied potential increases the number of nuclei but does not affect the size of the final crystal granules.Therefore,the electrodeposited Ni−W alloy shows a nanocrystalline structure.

Low temperature induces oocytes p34^(cdc2) synthesis and accumulation-the acquisition of competence to resume meiosis in toad oocytes

Full grown oocytes derived from Bufo Bufo gargarizans rearing at high temperature environment (24℃),never underwent GVBD after progesterone treatment. No p34cdc2, H1 kinase activity was detected in the oocytes after progesterone stimulation or OA microinjection; Western blotting analysis showed that the level of p3cdc2, and p33 in the oocytes are significantly lower than those in the oocytes derived from the hibernating toads (below 10 ℃). 25S-Met incorporation analysis showed that when the oocytes were incubated at 6℃, synthesis of about thirty defferent polypeptides was promoted or induced, including p34cdc2 and some other p13suc1-binding proteins. All these results indicated that a low temperature environment is essential for the oocytes of Bufo Bufo gargarizans to express and store some cell cycle drivers and its regulators, and to gain the maturation competence. These results will also provide a new clue for explaining the molecular mechanisms why gametogenesis of some organisms depends on a relative low temperature and how to maintain the geographical distribution of some animals.

Biosynthesis of copper nanoparticles supported on manganese dioxide nanoparticles using Centella asiatica L. leaf extract for the efficient catalytic reduction of organic dyes and nitroarenes

In this study we designed a novel,cost‐efficient and green method for the synthesis of copper nanoparticles(Cu NPs)supported on manganese dioxide(MnO2)NPs,using Centella asiatica L.leaf extract as a naturally‐sourced reducing agent,without stabilizers or surfactants.This synthetic process is environmentally‐friendly and avoids the use of toxic reducing agents.Phenolic hydroxyl groups in the leaf extract are believed to reduce Cu2+in solution to generate Cu NPs that are subsequently stabilized on the MnO2NP surfaces.The resulting Cu/MnO2nanocomposite was fully characterized using X‐ray diffraction,transmission electron microscopy,field emission scanning electron microscopy,energy‐dispersive X‐ray spectroscopy and Fourier transform infrared spectroscopy.This material was found to function as a highly active,efficient and recyclable heterogeneous catalyst for the reduction of Congo red,rhodamine B and methylene blue as well as nitro compounds such as2,4‐dinitrophenylhydrazine and4‐nitrophenol in the presence of NaBH4in aqueous media at ambient temperature.The high stability of the Cu/MnO2nanocomposite also allows the catalyst to be separated and reused several times without any significant loss of activity.?2018,Dalian Institute of Chemical Physics,Chinese Academy of Sciences.Published by Elsevier B.V.All rights reserved.

Preparation and characterization of Cu-doped mesoporous CeO_2 for CO oxidation

Mesoporous CeO2 was first synthesized by hydrothermal method,and then used to synthesize different contents of CuO)x/CeO2(x:molar ratio of Cu to Ce) by deposition-precipitation method.These materials were characterized by X-ray diffraction(XRD),N2 adsorption and desorption,H2 temperature programmed reduction(H2-TPR) and O2 temperature programmed desorption(O2-TPD) to study the crystal structure,surface area,and the mechanism of CO oxidation.The results show that,on XRD patterns,no evidence of CuO diffraction peaks is present until Cu loading is increased to 20%.The BET surface area decreases noticeably with the increase of Cu content.Compared with other samples,the better reducibility and activity oxygen species of(CuO)10%/CeO2coincide with its better catalytic activity.

Enhanced Property of Thin Cuprous Oxide Film Prepared through Green Synthetic Route

Thin cuprous oxide films have been prepared by chemical vapor deposition(pulsed spray evaporation-chemical vapor deposition)method without post-treatment.The synthesis of cuprous oxide was produced by applying a water strategy effect.Then,the effect of water on the morphology,topology,structure,optical properties and surface composition of the obtained films has been comprehensively investigated.The results reveal that a pure phase of Cu2O was obtained.The introduction of a small quantity of water in the liquid feedstock lowers the band gap energy from 2.16 eV to 2.04 eV.This finding was mainly related to the decrease of crystallite size due to the effect of water.The topology analyses,by using atomic force microscope,also revealed that surface roughness decreases with water addition,namely more uniform covered surface.Moreover,theoretical calculations based on density functional theory method were performed to understand the adsorption and reaction behaviors of water and ethanol on the Cu2O thin film surface.Formation mechanism of the Cu2O thin film was also suggested and discussed.

Synthesis of Macro-Mesostructured γ-Al_2O_3 with Large Pore Volume and High Surface Area by a Facile Secondary Reforming Method

Through improving the aging process during synthesis of the support, γ-Al2O3 with large pore volume and high surface area was synthesized by a facile secondary reforming method. The synthesis parameters, such as the reaction temperature, the first aging temperature and the second aging temperature, were investigated. The textural properties of γ-Al2O3 were characterized by means of N2 adsorption-desorption isotherms, X-ray powder diffractometry （XRD）, scanning electron microscopy （SEM）, Fourier transform infrared （FTIR） spectroscopy and thermogravimetry （TG）. The experimental results indicated that AACH and amorphous A1OOH were the precursors of alumina, which were formed via precipitation from solutions after reaction of aluminum sulphate with ammonium hydrogen carbonate. The precursor nanocrystallites grew and re-assembled during the secondary reforming process, which resulted in an increased pore size and pore volume and a decreased bulk density. The as-synthesized γ-Al2O3 materials featured meso/macroporosity, large pore volume （2.175 cm^3/g）, high surface area （237.8 m^2/g）, and low bulk density （0.284 g/mL）.

Formation mechanisms of Ni-Al intermetallics during heat treatment of Ni coating on 6061 Al substrate

The formation mechanisms and growth kinetics of Al3 Ni and Al3Ni2 in Ni-Al diffusion couple prepared by electrodeposition of Ni on Al substrate were investigated. The nickel coating with 20 μm thickness was applied on 6061 aluminum alloy by direct current electroplating. The samples were then heat-treated for different durations at 450, 500 and 550 °C under argon atmosphere. The intermetallic phases were identified by means of scanning electron microscopy（SEM）, energy dispersive spectrometry（EDS） and X-ray diffraction（XRD）. The results showed that the formation of intermetallic phases consisted of two important steps. The first step was the lateral growth of intermetallic phase from separate sites, resulting in the formation of a continuous layer. The second step was the growth of the continuous intermetallic layer in the direction perpendicular to the interface. However, excessive increase in thickness of intermetallic phases led to the detachment of reaction products, i.e., Al3 Ni and Al3Ni2, from the substrate. It was also observed that aluminum was the dominant diffusing element during Al3 Ni growth, while nickel diffusion was dominant during Al3Ni2 growth. The growth kinetics of both Al3 Ni and Al3Ni2 phases obeyed a parabolic law.

Synthesis and Photocatalytic Property of ZnO/TiO2 Inverse Opals Films with Controllable Composition and Topology

A novel method to fabricate composition- （IO） films using a positive sacrificial ZnO and topology-controlled ZnO/TiO2 inverse opals IO template has been developed. This method includes a two-step process, preparation of ZnO IO by a simple electrochemical deposition using a self-assembly polystyrene colloidal crystal template and preparation of ZnO/TiO2 IO by a liquid phase deposition （LPD） process at room temperature. The composition and topology of ZnO/TiO2 IO can be easily controlled by changing the duration of the LPD. After 20 min LPD process, a ZnO/TiO2 composite IO with non-close-packed face-centered cubic air sphere array was obtained. Prolonging the duration to 60 min, a pure TiO2 IO （TIO-LPD60） with obviously thickened walls was formed. The formation mechanism for the compositional and topological variation was discussed. A preliminary study on UV photocatalytic property of the samples for degradation of methylene blue reveals that the composition and topology significantly influenced the photocatalytic activity of the IO film. The ZnO/TiO2 composite IO demonstrates a higher degree of activity than both pure ZnO and pure TiO2 IO, although they have a similar IO wall thickness. Moreover, with increasing IO wall thickness from -52 nm to -90 nm, TIO-LPD60 exhibits the highest level of photocatalytic performance.

Electrochemical synthesis of catalytic materials for energy catalysis

Electrocatalysis is a process dealing with electrochemical reactions in the interconversion of chemical energy and electrical energy.Precise synthesis of catalytically active nanostructures is one of the key challenges that hinder the practical application of many important energy‐related electrocatalytic reactions.Compared with conventional wet‐chemical,solid‐state and vapor deposition synthesis,electrochemical synthesis is a simple,fast,cost‐effective and precisely controllable method for the preparation of highly efficient catalytic materials.In this review,we summarize recent progress in the electrochemical synthesis of catalytic materials such as single atoms,spherical and shaped nanoparticles,nanosheets,nanowires,core‐shell nanostructures,layered nanomaterials,dendritic nanostructures,hierarchically porous nanostructures as well as composite nanostructures.Fundamental aspects of electrochemical synthesis and several main electrochemical synthesis methods are discussed.Structure‐performance correlations between electrochemically synthesized catalysts and their unique electrocatalytic properties are exemplified using selected examples.We offer the reader with a basic guide to the synthesis of highly efficient catalysts using electrochemical methods,and we propose some research challenges and future opportunities in this field.

Porous Structure, Salt Component Distribution and Catalytic Preference of Zinc Acetate Catalysts for Vinylacetate Synthesis on Modified Carbon Supports

The main problem in an efficient Zn（CH3COO）2/AC （AC-activated carbon） catalyst preparation is the achievement of uniform distribution of highly dispersed salt component on the activated carbon （AC） surface. The solution of this problem is modification of the AC by hydrogen peroxide （H202） oxidation of the surface and treatment of AC with acetic acid as well as special methods of salt deposition and catalyst drying. The investigations of these ways of AC surface modification （treatment of AC with acetic acid and H2O2） have demonstrated the obtained AC to have both an increased adsorption capacity as to Zn（OAc）2 and optimum volumes of meso- and micro-pores as well as high catalyst activity in vinyl acetate （VA） synthesis. The characteristics of supports and catalysts were found out by benzene, water and acetic acid vapors adsorption. The distribution of the salt on the AC surface was studied by small-angle X-ray scattering （SAXS）, by scanning electron microscopy （SEM） and X-ray micro-analysis （XMA）. The catalysts were tested in vinyl acetate synthesis in flow-bed isothermal reactor by cyclic method at 175, 205 and 230℃.

Novel synthesis of nickel oxide microsphere with high surface area and its catalytic application for carbon dioxide reforming of methane

Nickel oxide(NiO)microsphere with a large surface area was novelly synthesized through nickel bicarbonate(Ni(HCO3)2)precursor.The obtained nickel oxide(NiO)microsphere was characterized by X-ray pattern diffraction,scanning electron microscopy,CO2 temperature-programmed desorption,H2 temperature-programmed reduction,N2 adsorption/desorption and laser scattering particle size distribution analyzer.It was found that nickel oxide(NiO)synthesized by the thermal decomposition of Ni(HCO3)2through area hydrolysis,presented very nice microsphere with high surface area.The catalytic properties of obtained nickel oxide(NiO)microsphere were studied in the reaction of carbon dioxide reforming of methane where 91.3% conversion of CH4 with 93% conversion of CO2 was observed.Besides,the catalyst maintained high stability over 200 h on the stream.

Synthesis and Separation Performance of Y-type Zeolite Membranes by Pre-Seeding Using Electrophoresis Deposition Method

Y-type zeolite membranes were synthesized by a two-step approach in which a particle seed layer was prepared by electrophoresis deposition(EPD) at first, followed by densification through secondary growth. The pre-seeding adopted the directing agent for Y-type zeolite synthesis serving as seeds. The effects of aging time of the directing agent, electrophoresis voltage and electrophoresis deposition time on seed layers quality as well as the quality of zeolite membranes were investigated. The results indicated that the zeolite seeds derived from the directing agent could be evenly deposited on substrate under certain EPD conditions. The XRD patterns of the seeded substrates after the secondary growth showed that the pure as-synthesized Y-type zeolite membranes had successfully grown on the substrates. The SEM images indicated that the substrate was covered by the highly intergrown zeolite crystals when the seeding solution employed the directing agent with an aging time of 2 days. The separation performance of zeolite membrane was evaluated using a CO_2/N2 mixture(with a mole ratio of 1:1) at different temperatures. Furthermore, the pervaporation measurements were carried out for the dehydration of isopropanol aqueous solutions with different mass fractions. The as-synthesized Y-type zeolite membranes exhibited a relatively high selectivity of water from isopropanol and sustainable permeation flux.

Hydrogen Adsorption Study upon Ni/AI203 Nano-composite Synthesized by MOCVD Technique

The hydrogen adsorption （storage） studies upon Ni/A1203 nano-composite prepared by metal organic chemical vapor deposition technique （MOCVD） exploiting single source molec ular precursor （SSP） approach were carried out. The Ni/A1203 nano-composite is prepared in cold walled MOCVD reactor by the decomposition of SSP, [H2AI（OtBu）]2, on a substrate holding Ni（acac）2 powder. The SSP is a reducing agent which reduces Ni＋2 to Ni0 and works as source for Al203 matrix in which the Ni0 is dispersed. The resulting Ni/A1203 nano-composite is characterized by XRD, SEM, TEM, and EDX. The hydrogen adsorption （storage） studies are performed using home-made Sievert＇s type apparatus. The hydrogen storage studies reveal that approximately 2.9% （mass ratio） hydrogen can be stored in the Ni/A1203 nano-composite. The results show that Ni/A1203 nano-composite can be a po- tential candidate for hydrogen storage which can be used for onboard fuel purposes.