Electronic Microscopy (electronic + microscopy)

Distribution by Scientific Domains

Kinds of Electronic Microscopy

  • scanning electronic microscopy
  • transmission electronic microscopy


  • Selected Abstracts


    Two-Dye Core/Shell Zeolite Nanoparticles: A New Tool for Ratiometric pH Measurements

    ADVANCED FUNCTIONAL MATERIALS, Issue 1 2009
    Tristan Doussineau
    Abstract The preparation of core/shell nanoparticles that enable ratiometric pH measurement is described. The core of the nanoparticles consists of a zeolite- , matrix that exhibits a 3-hydroxyflavone reference dye within the porous network. Coating an amorphous silica shell containing a fluorosensor around the zeolite through the Stöber process provides pH sensitivity to the nanoparticles. Morphological characterization (dynamic light scattering, transmission electronic microscopy) demonstrates the control of the sensing silica shell around the zeolite cores, leading to highly monodisperse spherical nanoparticles, while structural characterization (wide-angle X-ray diffraction, nitrogen adsorption) shows the amorphous character of the shell. Spectral characterization via UV/Vis absorption and steady-state fluorescence shows good pH sensitivity of the resulting nanosensors with a pKa suitable for bioanalytical applications. [source]


    Cell wall modifications during osmotic stress in Lactobacillus casei

    JOURNAL OF APPLIED MICROBIOLOGY, Issue 1 2005
    M. Piuri
    Abstract Aims:, To study the modification of the cell wall of Lactobacillus casei ATCC 393 grown in high salt conditions. Methods and Results:, Differences in the overall structure of cell wall between growth in high salt (MRS + 1 mol l,1 NaCl; N condition) and control (MRS; C condition) conditions were determined by transmission electronic microscopy and analytical procedures. Lactobacillus casei cells grown in N condition were significantly larger than cells grown under unstressed C condition. Increased sensitivity to mutanolysin and antibiotics with target in the cell wall was observed in N condition. Purified cell wall also showed the increased sensitivity to lysis by mutanolysin. Analysis of peptidoglycan (PG) from stressed cells showed that modification was at the structural level in accordance with a decreased PG cross-link involving penicillin-binding proteins (PBP). Nine PBP were first described in this species and these proteins were expressed in low percentages or presented a modified pattern of saturation with penicillin G (Pen G) during growth in high salt. Three of the essential PBP were fully saturated in N condition at lower Pen G concentrations than in C condition, suggesting differences in functionality in vivo. Conclusions:, The results show that growth in high salt modified the structural properties of the cell wall. Significance and Impact of Study:, Advances in understanding the adaptation to high osmolarity, in particular those involving sensitivity to lysis of lactic acid bacteria. [source]


    Polymer-acid solutions: Their use for the enhancement of oil reservoir stimulation

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008
    Mohammed M. Amro
    Abstract A reduction in permeability occurring around the wellbore resulting from drilling, completion and/or workover fluids increases the flow resistance to the petroleum reservoir fluids and is defined as formation damage. Acidizing process removes near-wellbore damage and enhances hydrocarbon production from producing wells. This study investigates the effect of adding polymer as a retarding agent to acid solutions to slow and control the reaction in matrix acidizing treatment of carbonate rocks. Two different polymers, polyacrylamide (PAA) and polysaccharide (xanthan) and two different acids, acetic acid and formic acid, were used through this study. The results revealed that the presence of PAA did not change the viscosity of the acid solution significantly, while the viscosity of xanthan-acid solutions was decreased with increasing the acid concentration. Additionally, the reaction of polymer-acid solutions with the rock material was monitored under microscope. Original rock samples obtained from Saudi reservoirs containing mainly carbonate were used in the reaction. The PAA-acid solution did not show any decrease in the reaction rate compared to that of acid solution. Thus, the PAA solution applied in this study is not recommended as a retarder. However, xanthan-acid solutions showed a significant decrease in the reaction time. Therefore, xanthan was selected to perform further investigations in Rotating Disk Reactor at different pressures. Scanning electronic microscopy (SEM) was conducted on pretreated and posttreated rock samples. This provides the opportunity to perform a detailed description of the rock surface and facilitates the identification of the changes occurring due to polymer-acid treatment. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]


    Synthesis and characterization of cobalt nano-particles through microwave polyol process

    AICHE JOURNAL, Issue 6 2009
    Wen-Tung Cheng
    Abstract This article aims to synthesize and character cobalt nano-particles through microwave polyol process. At first, cobalt acetate is used as precursor to synthesize cobalt nano-particles by microwave assisted ethylene glycol in the presence of polyvinylpyrrolidone (PVP) as capping agent. As measured from ion-coupled plasma (ICP) and thermo-gravimetric analysis (TGA), the yields of as-synthesized cobalt particles in average diameters of 40 and 81 nm verified by transmission electronic microscopy (TEM), are 71 and 85%, respectively; and the structure of as-synthesized cobalt nano-particle is a face-center cubic structure analyzed by X-ray diffraction (XRD). Finally, the as-synthesized cobalt nano-particle modified by oleic acid is dispersed in kerosene to character magnetic property. As measured by vibration sample magnetometer (VSM), the saturation magnetisms of cobalt nano-particles with average diameters of 40 and 81 nm are 39.1 and 29.5 emu/g, respectively, in solution. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source]


    Molecular modeling of H2 purification on Na-LSX zeolite and experimental validation

    AICHE JOURNAL, Issue 1 2005
    B. Weinberger
    Analysis of hydrogen purification process by adsorption in the dehydrated Na-LSX zeolite is described. New measurements of hydrogen and nitrogen adsorption selectivity of this zeolite have been performed up to a pressure of 20 MPa and at temperatures of 273, 293 and 313 K, by using a gravimetric-volumetric method. Structural characterizations were realized by helium density displacement, nuclear magnetic resonance, X-ray diffraction and scanning electronic microscopy. Furthermore, Monte Carlo simulations of gas adsorption were performed in a zeolite model of Na-LSX, using pair potentials to represent the interaction between gas molecules and zeolite atoms. Comparison of simulation results and experimental data enabled testing of the validity of such a modeling of the gas-zeolite interaction. © 2004 American Institute of Chemical Engineers AIChE J, 51:142,148, 2005 [source]


    Effects of surface treatments on bond strength of glass-infiltrated ceramic

    JOURNAL OF ORAL REHABILITATION, Issue 9 2001
    Y.-C. Lu
    The purpose of this study was to evaluate the effects of various surface treatments on the bond strength at the In-Ceram/resin composite interface. Ninety-eight In-Ceram specimens were divided into seven groups and exposed to various surface treatments as follows: (A) control (B) saliva contamination (C) saliva contamination plus aluminum oxide sandblasting (D) glove powder contamination (E) glove powder contamination plus aluminum oxide sandblasting (F) rough aluminum oxide sandblasting and (G) excess glass infiltration. A resin composite cylinder was cemented to each In-Ceram specimen with Panavia 21 resin luting cement. Half of the cemented specimens in each group were stored in water for 24 h, and the other half were stored in water for 2 weeks and then were thermo-cycled for 2000 cycles. Shear bond strengths (SBS) of seven specimens in each subgroup were determined and analysed using analysis of variance (ANOVA) and Tukey HSD test as well as Student,s t -test. Scanning electronic microscopy was used to identify the type of bond failure. Shear bond strength was significantly decreased by saliva and glove powder contaminations (P < 0·05). Sandblasting treatment did not improve the saliva-contaminated specimens. However, the glove powder plus sandblasting group showed no significant difference in SBS compared with the control group. There was no significant difference in SBS between the excess glass-infiltrating group and the control group. The SBS was significantly decreased by rough aluminum oxide sandblasting (P < 0·05). The SBS values of groups without thermocycling were significantly greater than those of groups with thermocycling (P < 0·05). There were no significant differences among SBS values of the seven groups with thermocycling. Combined cohesive and adhesive bond failures were seen in every group. Various surface treatments or contaminants may significantly influence the bond strength of In-Ceram restorative in clinical use. [source]


    A novel thermotropic liquid crystalline copolyester containing phosphorus and aromatic ether moity toward high flame retardancy and low mesophase temperature

    JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2010
    Xiang-Cheng Bian
    Abstract A series of thermotropic liquid crystalline polyesters containing phosphorus and aromatic ether groups (TLCP-AEs) were synthesized from p -acetoxybenzoic acid (p -ABA), terephthalic acid (TPA), 4,4,-oxybis(benzoic acid) (OBBA), and acetylated 2-(6-oxid-6H-dibenz(c,e) (1,2) oxaphosphorin 6-yl) 1,4-benzenediol (DOPO-AHQ). The chemical structure and the properties of TLCP-AEs were characterized by Fourier-transform spectroscopy (FTIR), proton nuclear magnetic resonance spectroscopy (1H NMR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), thermogravimetry analysis (TGA), scanning electronic microscopy (SEM), polarizing optical microscopy (POM), limiting oxygen index, and UL-94 tests, respectively. The results showed that TLCP-AEs had low and broad mesophase temperatures (230,400 °C). TLCP-AEs also showed excellent thermal stability; their 5%-weight-loss temperatures were above 440 °C and the char yields at 700 °C were higher than 45 wt %. All TLCP-AE polyesters exhibited high flame retardancy with a LOI value of higher than 70 and UL-94 V-0 rating. The SEM observation revealed that TLCP-AEs had good fibrillation ability. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1182,1189, 2010 [source]


    Fatigue and Fluoride Corrosion on Streptococcus mutans Adherence to Titanium-Based Implant/Component Surfaces

    JOURNAL OF PROSTHODONTICS, Issue 5 2009
    Cassia Bellotto Correa DDS
    Abstract Purpose: The influence of fatigue and the fluoride ion corrosion process on Streptococcus mutans adherence to commercially pure Titanium (Cp Ti) implant/component set surfaces were studied. Materials and Methods: Thirty Nobel implants and 30 Neodent implants were used. Each commercial brand was divided into three groups. Group A: control, Group B: sets submitted to fatigue (105 cycles, 15 Hz, 150 N), and Group C: sets submitted to fluoride (1500 ppm, pH 5.5) and fatigue, simulating a mean use of 5 years in the oral medium. Afterward, the sets were contaminated with standard strains of S. mutans (NTCC 1023) and analyzed by scanning electronic microscopy (SEM) and colony-forming unit counts (CFU/mL). Results: By SEM, bacterial adherence was verified only in group C in both brands. By CFU/mL counts, S. mutans was statistically higher in both brands in group C than in groups A and B (p < 0.05, ANOVA). Conclusion: The process of corrosion by fluoride ions on Cp Ti implant/component sets allowed greater S. mutans adherence than in the absence of corrosion and with the fatigue process in isolation. [source]


    A Potential Red-Emitting Phosphor BaGd2(MoO4)4:Eu3+ for Near-UV White LED

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2009
    Chongfeng Guo
    Red-emitting phosphor BaGd2,xEux(MoO4)4 has been successfully synthesized by a simple sol,gel method. The process of phosphor formation is characterized by thermogravimetric-differential thermal analysis and X-ray diffraction. Field-emission scanning electronic microscopy is used to characterize the size and the shape of the phosphor particles. Photo-luminescent property of the phosphor is also performed at the room temperature. The effects of firing temperature and Eu3+ activator concentration on the photoluminescence (PL) properties are elaborated in detail. PL characterization reveals that the sample with the firing temperature at 800°C and the concentration of Eu3+ at 0.7 shows the most intense emission, and its intensity is about three times stronger than that of phosphor prepared by solid-state method with the same composition and firing temperature. The new red-emitting phosphor shows an intense absorption at 396 nm, which matches well with commercial near-UV light-emitting diode (LED) chips, therefore, it is a good candidate of red phosphor used for near-UV white LEDs. [source]


    Phase Separation Inducing Controlled Crystallization of GeSe2,Ga2Se3,CsI Glasses for Fabricating Infrared Transmitting Glass,Ceramics

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2009
    Cunming Liu
    Infrared transmitting glass,ceramics based on the selected glass of 65GeSe2,25Ga2Se3,10CsI were obtained by a two-stage heat-treatment method. Results of X-ray diffraction and scanning electronic microscopy indicated that droplet-like nanoparticles containing cubic Ga2,,Ge,Se3 crystals are homogeneously generated in the glass,ceramics and that the whole glass,ceramic process is composed of phase separation, nucleation, and crystal growth. Evolutions of the optical and mechanical properties of glass,ceramics versus annealing time at the first-stage heat treatment were also investigated. Compared with the parent glass, the fabricated glass,ceramics show considerably enhanced fracture toughness, practicable infrared transparence, and microhardness, which confer them with considerable competitive advantages over currently used infrared materials. [source]


    An environmentally-relevant mixture of organochlorines and its vehicle control, dimethylsulfoxide, induce ultrastructural alterations in porcine oocytes

    MOLECULAR REPRODUCTION & DEVELOPMENT, Issue 1 2006
    Céline Campagna
    Abstract Organochlorine chemicals accumulate in the environment, particularly in the Arctic, and constitute potential developmental hazards to wildlife and human health. Although some of their harmful effects are recognized, their mechanisms of action within the target cells need to be better understood. This study was designed to test the hypothesis that an environmentally-relevant organochlorine mixture alters oocyte ultrastructure in the porcine model. Immature cumulus,oocyte complexes (COCs), partially cultured (18 hr) COCs without treatment or exposed to the organochlorine mixture or its vehicle (0.1% dimethysulfoxide; DMSO) during culture were processed for light and transmission electronic microscopy (TEM). The organochlorines induced major ultrastructural changes in the COCs: decreased density of the lipid droplets, increased smooth endoplasmic reticulum (SER) volume and increased interactions among SER, mitochondria, lipid droplets and vesicles. We suggest that these ultrastructural changes facilitate energy formation necessary to produce metabolizing enzymes. Other ultrastructural changes may reflect some degree of organochlorine toxicity: fewer gap junctions and decreased electron density of the cortical granules. Unexpectedly, the DMSO control treatment also induced similar ultrastructural changes, but to a lesser degree than the organochlorine mixture. This study is the first to demonstrate the effect of environmental contaminants on mammalian oocyte ultrastructure. Mol. Reprod. Dev. © 2005 Wiley-Liss, Inc. [source]


    Control synthesis of iron oxide nanospheres using solution chemistry

    PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 12 2007
    M. Z. Wu
    Abstract A facile solution chemistry approach to the batch synthesis of magnetite nanocrystals is developed. By using different starting materials, the control of particle size and size distribution can be achieved. Detailed investigations into the morphology and size distribution of the final products were carried out with the aid of field emission scanning electronic microscopy (FESEM). The crystal structure was studied by powder X ray diffraction (XRD). Vibrating sample magnetometer (VSM) was used to study the magnetic properties of these sphere-like products. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


    Observations on surface morphologies and dislocations of a-plane GaN grown by metal organic chemical vapor deposition

    PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 7 2007
    T. S. Ko
    Abstract In this study, we grew non-polar a-plane GaN thin films on r-plane sapphire using a series of growth conditions by metal-organic chemical vapor deposition. The results showed that high temperature and low-pressure conditions benefited two-dimension growth could lead to a fully coalesced a-plane GaN layer with a very smooth surface. The best surface morphology with an excellent mean roughness of 10.5 Å was obtained. The different thickness AlN as a nucleation layer and the different ,/, ratio were also considered. The results revealed that the surface morphology would get worse when the thickness of nucleation layer and ,/, ratio were away from the values of optimal condition. The observation of transmission electronic microscopy shown the lowest density of threading dislocations was 1.85×1010/cm2. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


    Synthesis of exfoliated polyamide 6,6/organically modified montmorillonite nanocomposites by in situ interfacial polymerization

    POLYMER COMPOSITES, Issue 6 2007
    M. Tarameshlou
    Polyamide 6,6 (PA 6,6)/organically modified montmorillonite (OMMT) nanocomposites were prepared by a novel method, using direct interfacial polymerization of an aqueous hexamethylene diamine and a nonaqueous adipoyl chloride in dichloromethane solution containing different amounts of OMMT dispersed nanoparticles. The state of dispersion of OMMT in the PA 6,6 matrix was investigated by means of X-ray diffraction, as well as transmission electronic microscopy. The results indicated that the OMMT nanoparticles were dispersed homogeneously and nearly exfoliated in the PA 6,6 matrix. The random arrangement of clay platelets in the PA 6,6 matrix, exfoliation, and intercalation of clays between the PA 6,6 matrix were distinguished. The amount of the incorporated OMMT in the PA 6,6 matrix was determined by means of TGA technique. Furthermore it was found that addition of a small amount of OMMT dramatically improved the thermal stability of PA 6,6. The TGA thermograms of all the synthesized nanocomposite samples showed an interesting unexpected lag in the weight loss at high temperatures, which could be another evidence for formation of fully exfoliated nanocomposites structures, with improved thermal stability. Nucleating effect of the OMMT nanoparticles and their influence on crystallization behavior of PA 6,6 was confirmed by DSC. Finally it is concluded that the in situ interfacial polycondensation is a suitable method for synthesis of nanocomposites with well dispersed structures and enhanced properties. POLYM. COMPOS., 28:733,738, 2007. © 2007 Society of Plastics Engineers [source]


    The occurrence of surface roughness in gas assist injection molded nylon composites

    POLYMER COMPOSITES, Issue 2 2000
    Shih-Jung Liu
    Gas assist injection molding has increasingly become an important industrial process because of its tremendous flexibility in the design and manufacture of plastic parts. However, there are some unsolved problems that limit the overall success of this technique. The purpose of this report was to study the surface roughness phenomenon occurring in gas assist injection molded thermoplastic composities. The materials used were 15 % and 35% glass-fiber filled nylon-6 composites. Experiments were carried out on an 80-ton injection molding machine equipped with a high-pressure nitrogen-gas injection unit. Two "float-shape" axisymmetric cavities were used. After molding, the surface quality of molded parts was measured by a roughness meter. Various processing variables were studied in terms of their influence on formation of surface roughness: melt temperature, mold temperature, melt filling speed, short-shot size, gas pressure, and gas injection delay time. Scanning electronic microscopy was also employed to characterize the composites. It was found that the surface roughness results mainly from the exposure of glass fiber in the matrix. The jetting and irregular flows of the polymer melt during the filling process might be factors causing the fiber exposure. [source]


    Synthesis, characterization and properties of organoclay-modified polyurethane/epoxy interpenetrating polymer network nanocomposites

    POLYMER INTERNATIONAL, Issue 3 2006
    Qingming Jia
    Abstract organoclay-modified polyurethane/epoxy interpenetrating network nanocomposites (oM-PU/EP nanocomposites) were prepared by adding organophilic montmorillonite (oMMT) to interpenetrating polymer networks (IPNs) of polyurethane and epoxy resin (PU/EP) which had been prepared by a sequential polymerization technique. Wide-angle X-ray diffraction (WAXD) and transmission electronic microscopy (TEM) analysis showed that the interpenetrating process of PU and EP improved the exfoliation and dispersion degree of oMMT. The effects of the NCO/OH ratio (isocyanate index), the weight ratio of PU/EP and oMMT content on the phase structure and the mechanical properties of the oM-PU/EP nanocomposites were studied by tensile testing and scanning electronic microscopy (SEM). Water absorption tests showed that the PU/EP interpenetrating networks and oMMT had synergistic effects on improvement in the water resistance of the oM-PU/EP nanocomposites. Differential scanning calorimetry (DSC) analysis showed that PU was compatible with EP and that the glass transition temperature (Tg) of the oM-PU/EP nanocomposites increased with the oMMT content up to 3 wt%, and then decreased with further increasing oMMT content. The thermal stability of these nanocomposites with various oMMT contents was studied by thermogravimetric analysis (TGA), and the mechanism of thermal stability improvement was discussed according to the experimental results. Copyright © 2005 Society of Chemical Industry [source]


    Synthesis and characterization of nanocomposites of silicon dioxide and polyurethane and epoxy resin interpenetrating network

    POLYMER INTERNATIONAL, Issue 9 2003
    Hongwen Zhang
    Abstract Nanocomposites with varying concentrations of nanosized silicon dioxide particles were prepared by adding nanosilica to interpenetrating polymer networks (IPN)s of polyurethane and epoxy resin (PU/EP). The PU/EP IPNs and nanocomposites were studied by dynamic mechanical analysis, scanning electronic microscopy, wide-angle X-ray diffraction and small-angle X-ray scattering. The result showed that adding nanosize silicon dioxide can improve the properties of compatibility, damping and phase structure of IPN matrices. Copyright © 2003 Society of Chemical Industry [source]


    Flammability and thermal stability studies of ABS/Montmorillonite nanocomposite

    POLYMER INTERNATIONAL, Issue 6 2003
    Shaofeng Wang
    Abstract Acrylonitrile,butadiene,styrene (ABS)/montmorillonite nanocomposites have been prepared using a direct melt intercalation technique by blending ABS and organophilic clay of two different particle sizes: OMTa (5 µm) and OMTb (38 µm). Their structure and flammability properties were characterized by X-ray diffraction, high resolution electronic microscopy (HREM), thermogravimetric analysis (TGA) and cone calorimeter experiments. The results of HREM showed that ABS/5 wt% OMTa nanocomposite was a kind of intercalated,delaminated structure, while ABS/5 wt% OMTb nanocomposite was mainly an intercalated structure. The nanocomposites showed a lower heat release rate peak and higher thermal stability than the original ABS by TGA and cone calorimeter experiments. Also, the intercalated nanocomposite was more effective than an exfoliated,intercalated nanocomposite in fire retardancy. Copyright © 2003 Society of Chemical Industry [source]


    OC1 Effects of Cryopreservation on the Expression of Glut-3, Glut-5 and As-A Proteins in Iberian Boar Sperm Membranes

    REPRODUCTION IN DOMESTIC ANIMALS, Issue 2006
    S Sancho
    In order to determine the injure produced in boar spermatozoa through cryopreservation process, we analyzed the expression of the hexose transporters Glut-3 and Glut-5 and the zona pellucida binding protein As-A (P68) in three different steps of the freezing-thawed protocol: at 17°C (fresh BTS-diluted semen, 1 : 2 v/v, step 1), at 5°C (after glycerol addition; step 2), and post-thawing (step 3). All sperm analyses were carried out with immunogold techniques under electronic microscopy. For this study eight healthy post-pubertal Iberian boars were submitted to a collection of twice per week through 3 months, evaluating two ejaculates from each boar. Glut-3 maintains the expression in the acrosome region post-thawing but not along the tail where is reduced. The expression of Glut-5 and As-A is majority located at the post-acrosome region of the spermatozoa at step 1, but in step 2 and step 3 this expression is relocated to sperm tail area. In conclusion, while cryopreservation affects the localization and the expression of Glut-3 and Glut-5, its fertilizing capacity is not significantly reduced. The stabilization of boar semen at 5°C was found to be the most crucial step for sperm survival. [source]


    Novel Flower-Like Ag-SiO2 -MgO-Al2O3 Material: Preparation, Characterization and Catalytic Application in Methanol Dehydrogenation

    CHINESE JOURNAL OF CHEMISTRY, Issue 6 2008
    Jing-Xia LI
    Abstract Catalytic direct dehydrogenation of methanol to formaldehyde was carried out over Ag-SiO2 -MgO-Al2O3 catalysts prepared by sol-gel method. The optimal preparation mass fractions were determined as 8.3% MgO, 16.5% Al2O3 and 20% silver loading. Using this optimum catalyst, excellent activity and selectivity were obtained. The conversion of methanol and the selectivity to formaldehyde both reached 100%, which were much higher than other previously reported silver supported catalysts. Based on combined characterizations, such as X-ray diffraction (XRD), scanning electronic microscopy (SEM), diffuse reflectance ultraviolet-visible spectroscopy (UV-Vis, DRS), nitrogen adsorption at low temperature, temperature programmed desorption of ammonia (NH3 -TPD), desorption of CO2 (CO2 -TPD), etc., the correlation of the catalytic performance to the structural properties of the Ag-SiO2 - MgO-Al2O3 catalyst was discussed in detail. This perfect catalytic performance in the direct dehydrogenation of methanol to formaldehyde without any side-products is attributed to its unique flower-like structure with a surface area less than 1 m2/g, and the strong interactions between neutralized support and the nano-sized Ag particles as active centers. [source]