Preparation of magnetic chitosan nanoparticles and immobilization of laccase

The magnetic chitosan nanoparticles were prepared by reversed-phase suspension method using Span-80 as an emulsifier, glutaraldehyde as cross-linking reagent. And the nanoparticles were characterized by TEM, FT-IR and hysteresis loop. The results show that the nanoparticles are spherical and almost superparamagnetic. The laccase was immobilized on nanoparticles by adsorption and subsequently by cross-linking with glutaraldehyde. The immobilization conditions and characterizations of the immobilized laccase were investigated. The optimal immobilization conditions were as follows: 10 mL of phosphate buffer (0.1 M, pH 7.0) containing 50 mg of magnetic chitosan nanoparticles, 1.0 mg · mL⁻1 of laccase and 1% (v/v) glutaraldehyde, immobilization temperature of 4°C and immobilization time of 4 h. The immobilized laccase exhibited an appreciable catalytic capability (480 units · g⁻¹ support) and had good storage stability and operation stability. The K _m of immobilized and free laccase for ABTS were 140.6 and 31.1 μM in phosphate buffer (0.1 M, pH 3.0) at 37 °C, respectively. The immobilized laccase is a good candidate for the research and development of biosensors based on laccase catalysis. Funded by Key Project of National Science Foundation of China (No. 60537050) and the National Science Foundation of China (No. 60377032)     

Effect of Thermal Treatment and Acid Leaching Process on Pore Characteristics of Nanometer Porous Glass

Porous glass was prepared by thermally treating sodium borosilicate glass for different time, the effect of thermal treatment on pore size distribution was discussed and the pore size of the prepared porous glass was measured by scanning electron microscopy （SEM） and differential thermal analysis （DTA）. The results show that the optimum porous glass with an average diameter of 80 nm can be prepared by thermal treatment at 600℃ for 12 h and then acid treatment for 12 h in 2 mol·L^-1 hydrochloric acid solution.     

Synthesis and structural characterization of macroporous bioactive glass

Porous sol-gel glass of CaO-SiO2-P2O5 system with macropores larger than 100 μm was prepared by adding stearic acid as pore former when the sintering was carried out at 700 ℃ for 3 h. The sol-gel porous glass shows an amorphous structure. The diameter of the pore created by pore former varies from 100 to 300 μm, and macroporous glass has a narrow and small pore size distribution in mesoporous scale. The porosity and pore size ofmacroporous bioactive glass can be controlled.     

Relationship between Liquid Phase Content and the Orientation of PMNT Ceramics by TGG Method

The effects of glass frit on the sintering and electric properties of PMN-PT textured ceramics were investigated. The glass frits, including PbO, Bi2O3 and ZnO, were selected since liquid phase sintering lowered the PMN-PT sintering temperature. The piezoelectric properties of PMN-PT ceramics with glass frit addition are strongly dependent on the densification. The addition of glass frits into PMN-PT matrix reduced the sintering temperature to 1 100 ℃ instead of 1 150 ℃ for samples without glass. The piezoelectric coefficients (d33) of PMN-PT textured ceramics achieved 568 pc/N with 1 wt% excess PbO.     

Microstructure and Properties of CePO4 Ceramic

Cerium phosphate powders were synthesized by direct solid liquid reaction of cerium dioxide and phosphate acid at the Ce ： P ratio of 1 ： 1. Phase-pure and fine grain size CePO4 powers could be obtained by calcining the as received powders at the temperature higher than 600 ℃ . It is demonstrated that the grain size and morphology of the CePO4 powders were calcined at various temperatures. An interesting layered crystal structure and a series of microcracks that cross and occur along the extrusion stress direction on the extruded surface inside CePO4 were observed. The ductility and machinabililty of CePO4 ceramic are attributed to the layered structure. Continuous machining debris was observed on the turned surface.     

非晶态镍磷合金空心微球的制备及其催化加氢性能

以空心玻璃微球作为模板材料,采用化学镀法在模板表面沉积了均匀的非晶态Ni-P合金镀层,用化学溶解法去除内部的空心玻璃微球模板,制备出非晶态Ni-P合金空心微球。分别利用EDS、SEM、XRD等手段对制品进行表征,以硝基苯液相加氢为探针反应,考察了非晶态Ni-P合金空心微球的催化加氢性能。结果表明,非晶态Ni-P合金空心微球具有良好的催化活性和循环使用性能。     

Study on the protection of Er-doped phosphate glass waveguide surface in ion-exchange processing

A novel method, sputtering K9 glass film, is proposed to solve the surface corrosion of Er-doped phosphate glass during ion-exchange processing for optical waveguide fabrication. The corrosion causes are analyzed to be the intrinsically weak stabilization of phosphate glass structure, hydrophile and weakly acidic property of phosphate radical. Experimental results show that the K9 glass film could not only protect the Er-doped phosphate glass surface from being corroded but also give no influence on the waveguide fabrication. The effect of thickness of K9 glass film on the optical property of waveguide is also investigated and the optimal thickness is found to be 60–80 nm. It provides a good base for further fabrication of active phosphate glass optical waveguide devices. Supported by the Optical Science and Technology Foundation of Shanghai Technology Committee (Grant No. 022261009), the Young Teacher Cultivation Foundation of Dalian University of Technology (Grant No. 893210), and the Doctor Startup Foundation of Dalian University of Technology (Grant No. 893322)     

Synthesis ofNanocrystalline RuO2（60%）-SnO2（40%） Powders by Amorphous Citrate Route

Nanometer RuO2-SnO2 was synthesized by the citrate-gel method using RuCl3, SnCl4 as cation sources, citric acid as complexing agent and anhydrous ethanol as solvent. The structures of the derived powders were characterized by thermogravimetric and differential thermal analysis, X-ray diffraction, transmission electron microscope, and Brunauer-Emmett-Teller surface area measurement. The pure, fine and amorphous powders was obtained at 160℃. The materials calcined at above 400 ℃ were composed of rutile-type oxide phases having particle sizes of fairly narrow distribution and good thermal resistant properties. By adding SnO2 to RuO2, the Ru metallic phase can be effectively controlled under a traditional temperature of preparation for dimensional stable anode.     

Preparation of Fe-Al Intermetallie /TiC-Al2O3 Ceramie Composites from llmenite by SHS

Fe-Al intermetallic/TiC-Al2O3 ceramic composites were successfully prepared by selfpropagating high-temperature synthesis （SHS） from natural ilmenite, aluminium and carbon as the raw materials. The effects of carbon sources, preheating time and heat treatment temperature on synthesis process and products were investigated in detail, and the reaction process of the FeTiO3-Al-C system was also discussed. It is shown that the temperature and velocity of the combustion wave are higher when graphite is used as the carbon source, which can reflect the effect of the carbon source structure on the combustion synthesis; Prolonging the preheating time or heat treatment temperature is beneficial to the formation of the ordered intermetallics; The temperature and velocity of the combustion wave are improved, but the disordered alloys are difficult to eliminate with the preheating time prolonged. The compound powders mainly containing ordered Fe3Al intermetallic can be prepared through heat treatment at 750 ℃.     

Preparation of conducting poly N-methylaniline microsphere and its antibacterial performance to sulfate reducing bacteria

Microspheres of conducting polymers poly N-methylaniline （PNMA） were successfully synthesized through oxidation of N-methylaniline without any template. The average diameter of the microspheres with a smooth surface was about 0.40 μm when 0.2 M N-methylanUine was oxidized with 0.2 M ammonium persulfate in 0.2 M of HClO4 solution. The size of microspheres can be controlled by changing reaction time and temperature. The acid concentration was critical for the formation of microspheres with smooth surfaces. The excellent antibacterial performance of PNMA in novolac epoxy coating to sulfate reducing bacteria was demonstrated. Moreover, in API media, PNMA inhibited growth of SRB and then reduced the corrosion rate of carbon steel remarkably.     

Coating of Fe, Ni on α-alumina microspheres by heterogeneous precipitation

1INTRODUCTION Themagneticmetal coatedceramicoxides,core shellstructuralcompositematerials,inwhichthinmetallicfilmsarecoatedonaceramicoxide matrixwithmicrometerparticlesizes,areattrac tiveduetothecombinationofthefunctionalchar acteristicsofmetalsandmechanicalpropertiesoftheceramicmatrix.Theceramic basedtransition metal coated,core shellcompositessuchasNi coatedAl2O3[1],Fe coatedAl2O3[2],FeNi coated Al2O3[3]orCoFe coatedSiO2[4],havebeenfoundtoexhibitinterestingfunctionalperformancesdue…     

Preparation of TiO<Subscript>2</Subscript> thin film by the LPD method on functionalized organic self-assembled monolayers

In this paper, uniform titania (TiO₂) films have been formed at 50° on silanol SAMs by the liquid-phase deposition (LPD) method at a temperature below 100°C. OTS (Octadecyltrichloro-Silane) self-assembled monolayers (SAMs) on glass wafers were used as substrates for the deposition of titanium dioxide thin films. This functionalized organic surface has shown to be effective for promoting the growth of films from titanic aqueous solutions by the LPD method at a low temperature below 100°C. The crystal phase composition, microstructure and topography of the as-prepared films were characterized by various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The results indicate that the as-prepared thin films are purely crystallized anatase TiO₂ constituted by nanorods after being annealed at 500°. The pH values, concentration of reactants, and deposition temperatures play important roles in the growth of TiO₂ thin films. Support by the National Natural Science Foundation of China (Grant No. 50672055) and National Key Technology R&D Program (Grant No. 2006BAF02A28)     

Preparation and characterization of nanocomposite MgFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/SiO<Subscript>2</Subscript>

Nanocomposites MgFe₂O₄/SiO₂ were successfully synthesized by the sol-gel method in the presence of N, N-dimethylformamide (DMF). The formation of pure MgFe₂O₄ was confirmed by powder X-ray diffraction (XRD) and electron diffraction. The structural evolution of MgFe₂O₄ nanocrystals was followed by powder X-ray diffraction and IR absorption spectroscopy. The formation of spinel structure of MgFe₂O₄ started at 800 °C, and completed at 900 °C. The transmission electron microscopy (TEM) measurements suggest that the particle sizes increase with the increasing annealing temperature, and the mean particle sizes of the spherical samples annealed at 800 °C, 900 °C and 1 050 °C are ca. 3 nm, 8 nm and 11 nm, respectively. Magnetization measurements at room temperature and 78 K indicate superparamagnetic nature of these MgFe₂O₄ nanocrystals. Funded by the National Natural Science Foundation of China(No. 30771676), the Natural Science Foundation of Jiangsu Province (No. BK20081842), and the Foundation of Nanjing Bureau of Personal for the Returned Overseas Chinese Excellent Scholars     

Preparation and Properties of Dip-coated CeO2-TiO2 Thin Golden Glass Film

The golden and ultraviolet-absorbed CeO2-TiO2 film was prepared on soda-lime glass substrate with the thickness of 2 mm via the sol-gel method. The transmission spectra in range of 200 nm-800 nm were measured, and the crystallization, the abrasion and acid resistance were also investigated. The appropriate sol contents and heat-treatment schedule were determined. The results indicate that the appropriate molar ratio of Ce/Ti was 3：5 to 5：6. The ultraviolet-absorbance ability increased with the increase of the Ce/Ti molar ratio, but when the Ce/Ti molar ratio was higher than 1.5, the homogeneity of the film was deteriorated. With the increase of heat-treatment temperature, the main wavelengths of the color of the coated glasses were equal, but the color＇ s saturation decreased; the transmission peaks were the same, while the intensity of the peaks decreased. The roughness, abrasion and acid resistance of the film were also enhanced at the same time. The appropriate heat- treatment temperature may be 340℃.     

Study on the most early glass eye-beads in China unearthed from Xu Jialing Tomb in Xichuan of Henan Province,China

The eye-beads dating to the early Warring States Period unearthed from Xu Jialing Tomb in Xichuan County of Henan Province, China are studied. The structure and the chemical composition of the samples are analysed by the undestructive methods of X-ray diffraction (XRD) and the Proton Induced X-ray Emission (PIXE) technique. The results show that these eye-beads are of glass state. Its chemical composition indicates that they belong to the glass of soda lime silicate system (Na₂O-CaO-SiO₂). By comparing the decorative design and the chemical composition of the samples with those from ancient Babylon and ancient Egypt, we think that these ancient eye-beads in Xichuan were most possibly imported from the West. Supported by the National Natural Science Foundation of China (Grant No. 50672106) and the Intellectual Innovation Project of the Chinese Academy of Sciences (Grant No. KJCX3-SYW.No.12)     

Preparation of bioactive calcium phosphate coating on porous C/C substrate by a novel deposition technique

A novel heat substrate technique, high frequency inductive heat deposition （IHD）, was introduced to coat porous carbon materials, C/C and carbon felt to improve their bioactivity. The morphologies, composition and microstructure of the resulting coatings were examined by scanning electron microscopy （SEM）, energy dispersive spectra （EDS）, X-ray diffractometer （XRD） and Fourier transform infrared spectroscopy （FTIR）. The results show that, the calcium phosphate consisted of non-stoichiometric, CO3-containing and plate- like octacalcium phosphate （Ca8-xH2（PO4）6, OCP） could uniformly cover the entire porous surfaces of carbon materials. Good adhesion of the coating to carbon material substrates was observed.     

The Mechanism of Sol-Gel Synthesis of Normal Spinel LiMn2O4 with Chelation of Citric Acid

The sol-gel process of citric acid chelating with metal cations for the synthesis of normol spinel LiMn2O4 and the reaction mechanion mechavism were investigated by means of XRD,TG-DTA,and SEM ,the results show that at the beginning lithium citrate and chelate compound of citic acid with manganese ions formed ,and then with heating the esterification and condensation reacions occured between them and glyol ,The products obtained are polymers in which metal cations are distibuted homogeneously on atomic scale that ensur hight reacivity to cations of Li^ and Mn^2 ,Firing the gel grepared by this process ,the lattice diffusions of solid reactant ions caused by non-homogeneity of reactants are elinimated and avoided .At 400℃ phase-pure LiMn2O4 with nanometer scale crystallization having precise stoichiometry and perfect crystallization can be obtained ,The model of chelate coordinated of double -molecule between citric acid and Mn^2 in the gel network is proosed ,It is important for explaining the dispersion state of Mn^2 and the formaiton process of gel by this model.     

Optical Characteristics of Porous Glasses Matrix and Its Light-conducted Mechanism

The optical properties of matrix of porous glasses and phase separated glasses were investigated by visible spectroscopy and infrared spectroscopy.The experimental results show that.both the porous glasses and phase-separated glasses hare very good light transmission in visible ligth region that wavelenth is longer than 560nm.The micropores of porous glasses and the boron-rich phase of phase-separated glasses have strong Rayleigh scatter effects on the visible light.the largest scatter occurrs at 360-370nm;the thicker the glasses.the larger the light scattering.Thus .the pore size disribution and thed size of heterogeneous micro zone in boron-rich phase of phase-separated glasses can be measured .After coupled into porours glasses.the most intense absorption of hydrated ious of [Co(H2O) 6]^2 shifts from 508 nm to 515nm.The production of the most intense absorption and the red shift were owde to Jahn-Teller of octahedral field formed by six H2O moleculur and perturbation effect resulted by microporous of porous glasses for its physics-chemical cirumstance.As a result.the porous glasses are perfect optical function materials in risible region.ichich can be assembled by chenvical method.     

Effect of the Cool System on Internal Stress of CaO-Al203-SiO2 Glass-ceramic System

The samples were attained through altering the cooling system of producing glass-ceramics. The X-ray diffraction was used to test the stress value of different samples. The relation of the cooling system and internal stress were also investigated. The experimental results show that the stress of glass-ceramic had a close relation with starting cool temperature. Above 800 ~C, glass-ceramic could be accelerated cooling and did not bring stress. Temperature between 500 ℃ and 800℃ was an important temperature range of the formation of stress in glass-ceramic, in which the glass-ceramic stress would change obviously. Cool system was the key on how to control and eliminate internal stress in order to reduce the destroy of materials crated by internal stress. In addition, glass particles size increase, glass-ceramic stress increase in consequent.     

Preparation of TiAl/Ti2AlC Composites with Ti/Al/C Powders by In-situ Hot Pressing

TiAl/Ti2AlC composites were prepared by in-situ hot pressing of TilAl/C powders mixtures and sintered at different temperatures were investigated by X- ray diffraction （ XRD ） of samples. The reaction procedure of Ti-Al-C system could be divided into three stnges. Below 900℃ , Ti reacts with Al to form TiAl intermetallics ; above 900 ℃ , C reacts with remain Ti to form TiC triggered by the exothermal reaction of Ti and Al ; TiAl reacts with TiC to produce dense TiAl/Ti2AlC compasites.In the holding stage, ternary Ti2AlC develops to layered polycrystal and composites pyknosis in the meanwhile. The mechanism of synthesis and microstructure was especially discussed.