Li^+ extraction/adsorption properties of Li-Sb-Mn composite oxides in aqueous medium

Series Li-Sb-Mn composite oxides with different Sb/Mn molar ratios were obtained by solid state reaction.Their structure,morphology and Li^＋ extraction/adsorption properties were characterized by X-ray diffractometry （XRD）,scanning electron microscopy （SEM） and atomic absorption spectrophotometry （AAS）,respectively.XRD and SEM analyses reveal that the crystal of the products transfers from spinel to orthorhombic phase with the increase of molar ratio of Sb to Mn from 0.05 to 1.00.The Li^＋ extraction and adsorption experiments for these Li-Sb-Mn composite oxides demonstrate that the composite oxides can all be used as lithium inorganic adsorbents.The acid treated spinel Li-Sb-Mn composite oxide with Sb/Mn molar ratio of 0.05 has a high Li^＋ adsorption capacity of 33.23mg/g in lithium solution.The Sb/Mn molar ratio of these Li-Sb-Mn composite oxides should be a crucial factor in determining their structure and Li^＋ extraction and adsorption properties.

Catalytic performance of Ag/Co-Ce composite oxides during soot combustion in O_2 and NO_x:Insights into the effects of silver

The composite oxides xAg/Co_（0.93）Ce_（0.07）（x=Ag/（Co＋Ce） molar ratio）,intended for use as high performance catalytic materials,were successfully prepared via citric acid complexation.The effects of silver on the performance of these substances during soot combustion were subsequently investigated.Under O_2,the 0.3Ag/Co_（0.93）Ce_（0.07） catalyst resulted in the lowest ignition temperature,T_（10）,of197 ℃,while the minimum light-off temperature was obtained from both 0.2Ag/Co_（0.93）Ce_（0.07） and0.3Ag/Co_（0.93）Ce_（0.07） in the NO_x atmosphere.These materials were also characterized by various techniques,including H_2,soot and NO_x temperature programmed reduction,X-ray diffraction,and electron paramagnetic resonance,Raman,X-ray photoelectron,and Fourier transform infrared spectroscopic analyses.The results demonstrated that silver significantly alters the catalytic behavior under both O_2 and NO_x,even though the lattice structure of the mixed oxide is not affected.Surface silver oxides generated under the O_2 atmosphere favor soot combustion by participating in the redox cycles between soot and the silver oxide,whereas the AgNO_3 that forms in a NO_x-rich atmosphere facilitates soot abatement at a lower temperature.The inferior activity of AgNO_3 relative to that of Ag_2O results in the different catalytic performance in the presence of NO_x or O_2.

Higher alcohol synthesis over Cu-Fe composite oxides with high selectivity to C_(2+)OH

Cu-Fe composite oxides were prepared by co-precipitation method and tested for higher alcohol synthesis from syngas. The selectivity to C2＋OH and C6＋OH in alcohol distribution was very high while the methane product fraction in hydrocarbon distribution was rather low, demonstrating a promising potential in higher alcohols synthesis from syngas. The distribution of alcohols and hydrocarbons approximately obeyed Anderson-Schulz-Flory distribution with similar chain growth probability, indicating alcohols and hydrocarbons derived from the same intermediates. The effects of Cu/Fe molar ratio, reaction temperature and gas hourly space velocity （GHSV） on catalytic performance were studied in detail. The sample with a Cu/Fe molar ratio of 10/1 exhibited the best catalytic performance. Higher reaction temperature accelerated water-gas-shift reaction and led to lower total alcohols selectivity. GHSV showed great effect on catalytic performance and higher GHSV increased the total alcohol selectivity, indicating there existed visible dehydration reaction of alcohol into hydrocarbon.

Solvothermal synthesis and characterization of nanocrystalline vanadium-chromium composite oxides and catalytic ammoxidation of 2,6-dichlorotoluene

Vanadium‐chromium oxides(VCrO)were usually prepared by high‐temperature solid‐state reactions;however,mixed phases were frequently produced and the morphology of the products was not well controlled.In this work,we prepared amorphous VCrO precursors by using V2O5 and CrO3 and alcohols or mixtures of alcohol and water via solvothermal reaction at 180°C.The precursors were then calcined under nitrogen at various temperatures.The products were characterized by powder X‐ray diffraction,transmission electron microscopy,and X‐ray photoelectron spectroscopy.It was revealed that pure‐phase nanocrystalline orthorhombic CrVO4 was obtained when methanol or methanol/water was used as the solvothermal medium and the precursor was calcined at 700°C.The size of the CrVO4 crystals was around 500 nm when methanol was used,whereas it reduced significantly to less than 50 nm when a mixture of methanol and water was used.The sizes could be effectively tuned from 10 to 50 nm by varying the methanol/water volume ratio.To the best of our knowledge,this is the first report on the synthesis of pure‐phase CrVO4 nanocrystals.The nano‐CrVO4 showed almost the highest catalytic activity for the ammoxidation of 2,6‐dichlorotoluene to 2,6‐dichlorobenzonitrile among the reported bi‐component composite oxides,owing to its smaller particle size,larger specific surface area,and more exposed active centers.

Efficiency and Mechanism of Phosphorus Removal by Coagulation of Iron-manganese Composited Oxide

Iron-manganese composited oxide（FeMnO） was prepared with potassium permanganate and ferrous salt. Interface performance, charge property and structure topography of the FeMnO were investigated. Coagulation efficiency and pollution removal mechanism of the FeMnO were approached. Results show that the main compositions of the FeMnO are δ-manganese dioxide and ferric hydroxide. The specific surface area is about 146.22 m^2/g. The FeMnO contains rich hydroxyl with extremely strong adsorption action and chemical adsorption activity. The zero charge point of the oxide in pure water is about 8.0 of pH value. Under neutral pH value conditions, the FeMnO particle surface carried positive charges. The FeMnO particles are quasi-spherical micro-particles with irregular sizes adjoined each other to form net construction. Phosphorus removal efficiency of the FeMnO is remarkable, the total dissoluble phosphorus of settled water can be reduced below detecting level（0.3 μtg/L） at a FeMnO dosage of 6 mg/L, and total phosphorus below detecting level at a FeMnO dosage of 10 mg/L, for water samples containing total phos- phorus of 1281.70 μg/L and total dissoluble phosphorus of 1187.91 μtg/L. The mechanism of effective coagulation for phosphorus removal is combined results of multiple actions of adsorption, charge neutralization, adsorption/bridging and so on.

Formation and capacitance properties of Ti-Al composite oxide film on aluminum

Al specimens were covered with TiO2 film by sol-gel dip-coating and then anodized in ammonium adipate solution.The structure,composition and capacitance properties of the anodic oxide film were investigated by transmission electron microscopy (TEM),Auger electron spectroscopy (AES),X-ray diffractometry (XRD) and electrochemical impedance spectroscopy (EIS).It was found that an anodic oxide film with a dual-layer structure formed between TiO2 coating and Al substrate.The film consisted of an inner Al2O3 layer and an outer Ti-Al composite oxide layer.The thickness of layers varied with the number of times of sol-gel dip-coating.The capacitance of anodic oxide films formed on coated specimens was at most 80% higher than that without TiO2.In film formation mechanism,it was claimed that the formation of composite oxide film was mainly affected by the structure of micro-pores network in TiO2 coating which had an influence on Al3+ and O2? ions transport during the anodizing.

Influence of La precursors on structure and properties of CeO_2-ZrO_2-Al_2O_3 composite oxides

Three La-doped CeO2-ZrO2-Al2O3(CZA)composite oxide samples,namely,CZA-I,CZA-II and CZA-III,were prepared following a co-precipitation method in the presence of La2O3,La(NO3)3-6H2O and H[La(EDTA)]-16H2O precursors,respectively.When the precursor samples are sintered at 1000°C,the as-prepared composite oxides mainly exhibit the CeO2-ZrO2 cubic fluorite phase,while theγ-Al2O3 andδ-Al2O3 phases appear when the precursor samples are subjected to sintering at 1100 and 1200°C.CZA-III exhibits improved redox properties after high-temperature treatment compared with CZA-I and CZA-II.CZA-III presents the largest surface area of 97.46 m2/g among the three CZAs when the CZA-III precursor sample is sintered at 1000°C.Furthermore,the corresponding oxygen storage capacity(OSC)is the largest with value of 400.27μmol/g when CZA-III precursor sample is sintered at 1000°C.Additionally,CZA-III exhibits the best thermal stability and the highest reduction temperature.However,by increasing the sintering temperature to 1200°C,there is a dramatic decline in the properties of surface area and OSC.And a decrease for CZA-III in surface area by 58.94%and a decrease of the OSC value by 74.56%are observed.

Preparation and Microstructure of a Si-Mo Fused Slurry Coating on Carbon/Carbon Composites for Oxidation Protection

A coating of composition Si-40Mo (wt pct) was prepared by fused slurry coating method on the two-dimensional carbon/carbon (2D-C/C) composite to improve oxidation resistance. In the procedure of the fabrication, pure St slurry inner layer in the pre-coating was necessary to apply because of infiltration of liquid Si into the substrate during the sintering. The coating consists of Si continuous phase and MoSi2 particles. In addition, the infiltration of Si into the substrate and the SiC reaction layer between the coating and the C/C composite were observed. Oxidation behavior of coated and uncoated C/C composites was studied in cyclic mode. The oxidation resistance and the thermal shock resistance of the Si-Mo fused slurry coating were quite excellent at 1370℃.

Bacterial Cellulose Templated p-Co3O4/n-ZnO Nanocomposite with Excellent VOCs Response Performance

In this work,p-type Co3O4 decorated n-type ZnO(Co3O4/ZnO)nanocomposite was designed with the assistance of bacterial cellulose template.Phase composition,morphology and element distribution were investigated by XRD,SEM,HRTEM,EDS mapping and XPS.Volatile organic compounds(VOCs)sensing measurements indicated a noticeable improvement of response and decrease of working temperature for Co3O4/ZnO sensor,in comparison with pure ZnO,i.e.,the response towards 100 ppm acetone was 63.7(at a low working temperature of 180℃),which was 26 times higher than pure ZnO(response of 2.3 at 240℃).Excellent VOCs response characteristics could be ascribed to increased surface oxygen vacancy concentration(revealed by defect characterizations),catalytic activity of Co3O4 and the special p-n heterojunction structure,and bacterial cellulose provides a facile template for designing diverse functional heterojunctions for VOCs detection and other applications.

Novel Ni/CeO_2-Al_2O_3 composite catalysts synthesized by one-step citric acid complex and their performance in catalytic partial oxidation of methane

A series of novel Ni/CeOe-Al2O3 composite catalysts were synthesized by one-step citric acid complex method, The as-synthesized catalysts were characterized by N2 physical adsorption/desorption, X-ray diffraction （XRD）, Fourier transform infrared （FT-IR） spectroscopy, hydrogen temperature-programmed reduction （Hz-TPR）, X-ray photoelectron spectroscopy （XPS） and thermogravimetry analysis （TGA）. The effects of nickel content, calcination and reaction temperatures, gas hourly space velocity （GHSV） and inert gas dilution of N2 on their performance of catalytic partial oxidation of methane （CPOM） were investigated. Catalytic activity test results show that the highest methane conversion （〉85%）, the best selectivities to carbon monoxide （〉87%） and to hydrogen （〉95%）, the excellent stability and perfect Hz/CO ratio （2.0） can be obtained over Ni/CeO2-Al2O3 with 8 wt% Ni content calcined at 700 ℃ under the reaction condition of 750 ℃, CH4/O2 ratio of 2 ： 1 and gas hourly space velocity of 12000 mL.h-1 .g-1. Characterization results show that the good catalytic performance of this composite catalyst can be contributed to its large specific surface area （~108 m2.g-1）, small crystallite size, easy reducibility and low coking rate.

Synthesis and Characterization of Worm-shaped Tubular Lanthanum Aluminum Composite Mesoporous Materials

The lanthanum aluminum mesoporous materials were synthesized using sodium dodecyl sulfate as a template agent by ultrasonic hydrothermal method.The resulting samples were characterized by low angle X-ray diffraction（XRD）,N2 adsorption-desorption studies,transmission electron microscopy（TEM）and surface morphology analysis（SEM）,surface acid（NH3-TPD）,reducibility properties（TPR）,X-ray energy dispersive spectrometer（EDS）and thermogravimetric analysis（TG/DTG）.A l/La composite mesoporous material were synthesized with n（Al）︰n（La）=70︰1.0,80°C of reaction temperature,20 h of reaction time,12 h of crystallization time,650°C of calcination temperature.The specific surface area of the sample is 273.90 m 2 ·g ？1 ,with the average diameter 5.642 nm and pore volume 0.2354 cm 3 ·g ？1 .The samples have mesoporous structure and its particles are similar to a worm-shaped tubular structure.The influence of calcination temperature on the surface physical and chemical properties of Al/La composited mesoporous materials was examined,and the results showed that the acid strength was increased but the amount of acidic sites is decreased as the calcination temperature increased.It was found that the sample calcined at 650°C had appropriate acid content,acid strength and better reducibility.

Synthesis, Characterization of Mesoporous Al-Mg Composite Oxide and Catalytic Performance for Oxyethylation of Fatty Alcohol

A mesoporous Al-Mg composite oxide with a hexagonal structure was synthesized with aluminium nitrate and magnesium nitrate as the reagents and sodium dodecyl sulfate（SDS） as the template in the presence of ethylenediamine. The XRD, nitrogen adsorption-desorption and TEM studies indicate that the composite has a hexagonal framework structure and an average pore diameter of 2. 6 nm. The TG/DTA spectra indicate that the decomposition and the removal of the occluded surfactant of the sample take place in a range of 230-550 ℃. The mesoporous Al-Mg composite oxide exhibites a highly catalytic activity for the oxyethylation of fatty alcohols. Narrow-range distributed ethoxylates are formed in the presence of the mesoporous Al-Mg composite oxide catalyst. The distribution selectivity coefficient（Cx） is 24 when the mesoporous Al-Mg composite oxide was used as a catalyst for the oxyethylation of octanol and the average adduct degree of ethoxylates is 6. 4.

Application of CO_2-TPD in the Synthesis of Composite Oxides from Metal-Organic Precursors

CO2-TPD was demonstrated an effective way to investigate the phase formation during pyrolysis for the preparation of composite oxides using metal-organic molecules as precursors.Based on the CO2-TPD results, it was found that calcination condition had deep effect on the carbonate formation and the minimum firing temperature to acquire pure phase composite oxide.An optimized calcination schedule was then developed.

Synthesis of optically active lactide catalyzed by nanocrystals of La-Ti composite oxides

With sol-gel method,nanometer La-Ti composite oxides were prepared.By means of atomic force microscope,the surface pattern,particle size distribution and specific surface area were studied.The newly prepared nanocrystals of La-Ti composite oxides were used as the catalysts to catalyze the dehydration of external compensated lactic acid to lactide.The lactide product was measured by polarimeter and micropolariscope.The results demonstrate that the ratio between D-lactide and L-lactide will not be equal to 1-1 if nanocrystals of La-Ti composite oxides are used as the catalysts,which implies,that nanocrystals of La-Ti composite oxides may be potential catalysts with a good selectivity.

Efficient Thickness of Solid Oxide Fuel Cell Composite Electrode

The efficient thickness of a composite electrode for solid oxide fuel cells was directly calculated by developing a physical model taking into account of the charge transfer process, the oxygen ion and electron transportation, and the microstructure characteristics of the electrode. The efficient thickness, which is defined as the electrode thickness corresponding to the minimum electrode polarization resistance, is formulated as a function of charge transfer resistivity, effective resistivity to ion and electron transport, and three-phase boundary length per unit volume. The model prediction is compared with the experimental reports to check the validity. Simulation is performed to show the effect of microstructure, intrinsic material properties, and electrode reaction mechanism on the efficient thickness. The results suggest that when an electrode is fabricated, its thickness should be controlled regarding its composition, particle size of its components, the intrinsic ionic and electronic conductivities,and its reaction mechanisms as well as the expected operation temperatures. The sensitivity of electrode polarization resistance to its thickness is also discussed.

Effects of SiC amount on phase compositions and properties of Ti_3SiC_2-based composites

The phase compositions and properties of Ti3SiC2-based composites with SiC addition of 5%-30% in mass fraction fabricated by in-situ reaction and hot pressing sintering were studied. SiC addition effectively prevented TiC synthesis but facilitated SiC synthesis. The Ti3SiC2/Ti C-SiC composite had better oxidation resistance when SiC added quantity reached 20% but poorer oxidation resistance with SiC addition under 15% than Ti3SiC2/TiC composite at higher temperatures. There were more than half of the original SiC and a few Ti3SiC2 remaining in Ti3SiC2/Ti C-SiC with 20% SiC addition, but all constituents in Ti3Si2/TiC composite were oxidized after 12 h in air at 1500 °C. The oxidation scale thickness of TS30, 1505.78 μm, was near a half of that of T,2715 μm, at 1500 °C for 20 h. Ti3SiC2/Ti C composite had a flexural strength of 474 MPa, which was surpassed by Ti3SiC2/TiC-SiC composites when SiC added amount reached 15%. The strength reached the peak of 518 MPa at 20% SiC added amount.

Effect of Oxidation on Fracture Toughness of a Carbon/Carbon Composite

The fracture toughness of a carbon/carbon composites oxidized at different temperature for 1 h was measured. The fracture surfaces were examined by scanning electron microscopy （SEM）. The results indicate that oxidation temperature has significant effects on the fracture toughness. Fracture toughness decreases with the increase of the weight loss. The SEM images reveal that the decrease of fracture toughness was mainly attributed to the oxidation of the interface in the composite.

Synthesis and characterization of Fe_3O_4@SiO_2 magnetic composite nanoparticles by a one-pot process

Fe3O4@SiO2 core–shell composite nanoparticles were successfully prepared by a one-pot process. Tetraethyl-orthosilicate was used as a surfactant to synthesize Fe3O4@SiO2 core–shell structures from prepared Fe3O4 nanoparticles. The properties of the Fe3O4 and Fe3O4@SiO2 composite nanoparticles were studied by X-ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. The prepared Fe3O4 particles were approximately 12 nm in size, and the thickness of the SiO2 coating was approximately 4 nm. The magnetic properties were studied by vibrating sample magnetometry. The results show that the maximum saturation magnetization of the Fe3O4@SiO2 powder（34.85 A·m^2·kg^–1） was markedly lower than that of the Fe3O4 powder（79.55 A·m^2·kg^–1）, which demonstrates that Fe3O4 was successfully wrapped by SiO2. The Fe3O4@SiO2 composite nanoparticles have broad prospects in biomedical applications; thus, our next study will apply them in magnetic resonance imaging.

Phase Evolution and Oxidation Resistance of YSZ/(Ni,Al) Composite Coatings in CH_4 Atmosphere

YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios were deposited on superalloy Inconel 600 by electrophoretic deposition（EPD） technique, followed by sintering in CH_4 atmosphere at 1 100 ℃for 2 h and isothermally oxidation at 1000 ℃ for 50 h. After sintering at 1100 ℃ for 2 h in CH_4 atmosphere, besides ZrC and t-ZrO_2 phases, the phase constitutes of Ni：Al mole ratios with 1：3, 1：2, and 1：1 were（Zr, Al）C, AlNi_3 and Ni phases, respectively. A remarkable difference in the oxidation behaviors of YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios was observed. For YSZ（Ni：Al=1：3） coated sample, oxidation at 1000 ℃ causes decomposition of the（Zr,Al）C solid solution to metallic Al, and then most of the Al is oxidized to Al_2O_3. For the YSZ（Ni：Al=1：2） coated sample, oxidation at 1000 ℃ mainly causes decomposition of the AlNi_3 phase. For YSZ（Ni：Al=1：1） coated sample, after oxidation at 1000 ℃, most of the Ni is oxidized to Ni O phase, and tolerated 50 h of oxidation and finally cracked and spalled from the specimen. YSZ（Ni：Al=1：3） and YSZ（Ni：Al=1：2） coated samples show superior oxidation resistance than that of YSZ coating. The different oxidation resistance mechanisms of YSZ/（Ni, Al） composite coatings sintered in CH_4 atmosphere were discussed.

Microstructure and abrasive wear behaviour of anodizing composite films containing Si C nanoparticles on Ti6Al4V alloy

Anodized composite films containing Si C nanoparticles were synthesized on Ti6Al4 V alloy by anodic oxidation procedure in C4O6H4Na2 electrolyte. Scanning electron microscopy(SEM), energy dispersive spectroscopy(EDS) and X-ray photoelectron spectroscopy(XPS) were employed to characterize the morphology and composition of the films fabricated in the electrolytes with and without addition of Si C nanoparticles. Results show that Si C particles can be successfully incorporated into the oxide film during the anodizing process and preferentially concentrate within internal cavities and micro-cracks. The ball-on-disk sliding tests indicate that Si C-containing oxide films register much lower wear rate than the oxide films without Si C under dry sliding condition. Si C particles are likely to melt and then are oxidized by frictional heat during sliding tests. Potentiodynamic polarization behavior reveals that the anodized alloy with Si C nanoparticles results in a reduction in passive current density to about 1.54×10-8 A/cm2, which is more than two times lower than that of the Ti O2 film(3.73×10-8 A/cm2). The synthesized composite film has good anti-wear and anti-corrosion properties and the growth mechanism of nanocomposite film is also discussed.