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Narrow Size Distribution (narrow + size_distribution)
Selected AbstractsMicrowave-Assisted Synthesis of Water-Dispersed CdTe Nanocrystals with High Luminescent Efficiency and Narrow Size Distribution.CHEMINFORM, Issue 18 2007Yao He Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Thermally Stable Nanocrystalline Mesoporous Gallium Oxide PhasesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 22 2009Chinmay A. Deshmane Abstract Semicrystalline and fully crystalline mesoporous galliumoxide phases were synthesized in the presence of ionic and non-ionic structure directing agents via Evaporation-Induced Self-Assembly (EISA) and Self-Assembly Hydrothermal-Assisted (SAHA) methods respectively. EISA led to partially crystalline mesoporous gallium oxide phases displaying unimodal pore size distribution in the range of ca. 2,5 nm and surface areas as high as 300 m2/g. SAHA led to nanocrystalline mesoporous uniform micron-sized gallium oxide spheres (ca. 0.3,6.5 ,m) with narrow size distribution displaying cubic spinel type structure. These mesophases displayed surface areas as high as ca. 221 m2/g and unimodal pore size distribution in the 5,15 nm range. Textural properties such as surface areas and pore sizes were effectively fine-tuned by the nature and relative concentration of the structure directing agents. Due to their high surface areas, tunability of pore sizes and the nature of the wall structure, these gallium oxide mesophases could find potential applications as heterogeneous catalysts.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Comparative Sol,Hydro(Solvo)thermal Synthesis of TiO2 NanocrystalsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 11 2006Xianfeng Yang Abstract Three small inorganic compounds [acetic acid (CH3COOH), nitric acid (HNO3), and hydrochloric acid (HCl)] andfive small organic compounds [n -butyl alcohol (CH3CH2CH2CH2OH), 1,2-propanediol (CH2OHCHOHCH3), propane-1,3-dicarboxylic acid (HOOCCH2COOH), butane-1,4-dicarboxylic acid (HOOCCH2CH2COOH), and ethylenediamine (H2NCH2CH2NH2)] with different donors (Cl,, NO3,, OH, COO,, and NH2) are used respectively and comparatively in different reaction media for tailoring the sol,hydrothermal synthesis of TiO2 nanocrystals at a specific reaction temperature and/or for different reaction times. Both anatase and rutile with a variety of nanostructures such as nanocubes, nanorods, nanoneedles, and their self-assembled nanospheres are selectively grown. Well-defined and crystalline anatase nanocrystals with a narrow size distribution are prepared in the presence of n -butyl alcohol. With the use of HCl, nanoneedles and their assembled nanospheres of phase-pure rutile are obtained under much less drastic conditions, even at 100 °C and for only two hours. The effects of the reaction media, synthesis temperatures, and aging times on the structures and shapes of the products are investigated in detail by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Sugar Balls: Synthesis and Supramolecular Assembly of [60]Fullerene GlycoconjugatesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 16 2007Haruhito Kato Abstract The synthesis and characterization of fully deprotected C60 glycoconjugates 4 and 17 is reported. Bis(,- D -mannopyranosyl)malonamide 4 was obtained by using nucleophilic cyclopropanation chemistry, which in general is a very versatile method for fullerene functionalization. Fullerene sugar 17 contains two dendritic ,- D -mannopyranosides that are connected through two adjacent imino bridges to the all-carbon framework. In this adduct-type of C60, which represents a 1,9-dihydro-1a-aza-1(2)a-homo(C60 - Ih)[5,6]fullerene derivative, the entire 60-,-electron system of the fullerene core is retained. This architecture allows the basic cleavage of the acetyl protection groups of precursor adduct 16 without destruction of the core structure of the fullerene sugar. Dendritic glycoconjugate 17 containing six deprotected sugar building blocks is very soluble in water. The amphiphilic nature of 17 with its cone-shaped structure forces the formation of small supramolecular aggregates in aqueous solutions to shield the hydrophobic fullerene units from the water subphase. DOSY NMR spectroscopy and TEM investigation reveal micellar sugar balls with an extremely narrow size distribution of around 4 nm.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Synthesis of Magnetic, Up-Conversion Luminescent, and Mesoporous Core,Shell-Structured Nanocomposites as Drug CarriersADVANCED FUNCTIONAL MATERIALS, Issue 7 2010Shili Gai Abstract The synthesis (by a facile two-step sol,gel process), characterization, and application in controlled drug release is reported for monodisperse core,shell-structured Fe3O4@nSiO2@mSiO2@NaYF4: Yb3+, Er3+/Tm3+ nanocomposites with mesoporous, up-conversion luminescent, and magnetic properties. The nanocomposites show typical ordered mesoporous characteristics and a monodisperse spherical morphology with narrow size distribution (around 80,nm). In addition, they exhibit high magnetization (38.0,emu g,1, thus it is possible for drug targeting under a foreign magnetic field) and unique up-conversion emission (green for Yb3+/Er3+ and blue for Yb3+/Tm3+) under 980,nm laser excitation even after loading with drug molecules. Drug release tests suggest that the multifunctional nanocomposites have a controlled drug release property. Interestingly, the up-conversion emission intensity of the multifunctional carrier increases with the released amount of model drug, thus allowing the release process to be monitored and tracked by the change of photoluminescence intensity. This composite can act as a multifunctional drug carrier system, which can realize the targeting and monitoring of drugs simultaneously. [source] Delivery of Nucleic Acids through the Controlled Disassembly of Multifunctional NanocomplexesADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Mahmoud Elsabahy Abstract In this study, novel pH-responsive polyion complex micelles (PICMs) were developed for the efficient delivery of nucleic acid drugs, such as antisense oligonucleotide (AON) and short interfering RNA (siRNA). The PICMs consisted of a poly(amidoamine) (PAMAM) dendrimer,nucleic acid core and a detachable poly(ethylene glycol)- block -poly(propyl methacrylate- co -methacrylic acid) (PEG- b -P(PrMA- co -MAA)) shell. The micelles displayed a mean hydrodynamic diameter ranging from 50 to 70,nm, a narrow size distribution, and a nearly neutral surface charge. They could be lyophilized without any additives and stored in dried form. Upon redispersion in water, no change in complexation efficiency or colloidal properties was observed. Entry of the micelles into cancers cells was mediated by a monoclonal antibody fragment positioned at the extremity of the PEG segment via a disulfide linkage. Upon cellular uptake and protonation of the MAA units in the acidic endosomal environment, the micelles lost their corona, thereby exposing their positively charged endosomolytic PAMAM/nucleic acid core. When these pH-responsive targeted PICMs were loaded with AON or siRNAs that targeted the oncoprotein Bcl-2, they exhibited a greater transfection activity than nontargeted PICMs or commercial PAMAM dendrimers. Moreover, their nonspecific cytotoxicity was lower than that of PAMAM. The pH-responsive PICMs reported here appear as promising carriers for the delivery of nucleic acids. [source] One-Pot Preparation of Polymer,Enzyme,Metallic Nanoparticle Composite Films for High-Performance Biosensing of Glucose and GalactoseADVANCED FUNCTIONAL MATERIALS, Issue 11 2009Yingchun Fu Abstract New polymer,enzyme,metallic nanoparticle composite films with a high-load and a high-activity of immobilized enzymes and obvious electrocatalysis/nano-enhancement effects for biosensing of glucose and galactose are designed and prepared by a one-pot chemical pre-synthesis/electropolymerization (CPSE) protocol. Dopamine (DA) as a reductant and a monomer, glucose oxidase (GOx) or galactose oxidase (GaOx) as the enzyme, and HAuCl4 or H2PtCl6 as an oxidant to trigger DA polymerization and the source of metallic nanoparticles, are mixed to yield polymeric bionanocomposites (PBNCs), which are then anchored on the electrode by electropolymerization of the remaining DA monomer. The prepared PBNC material has good biocompatibility, a highly uniform dispersion of the nanoparticles with a narrow size distribution, and high load/activity of the immobilized enzymes, as verified by transmission/scanning electron microscopy and electrochemical quartz crystal microbalance. The thus-prepared enzyme electrodes show a largely improved amperometric biosensing performance, e.g., a very high detection sensitivity (99 or 129,µA cm,2 mM,1 for glucose for Pt PBNCs on bare or platinized Au), a sub-micromolar limit of detection for glucose, and an excellent durability, in comparison with those based on conventional procedures. Also, the PBNC-based enzyme electrodes work well in the second-generation biosensing mode. The proposed one-pot CPSE protocol may be extended to the preparation of many other functionalized PBNCs for wide applications. [source] Natural convection of a water-fine particle suspension in a rectangular cell heated and cooled from opposing vertical walls: The effect of distribution of particle sizeHEAT TRANSFER - ASIAN RESEARCH (FORMERLY HEAT TRANSFER-JAPANESE RESEARCH), Issue 8 2001Masashi Okada Abstract A water-fine particle suspension with a uniform initial temperature and concentration in a rectangular cell was heated from a vertical wall and cooled from the opposing vertical wall. The dispersed particles had a distribution in size. In this natural convection, many layers separated by almost-horizontal sharp interfaces were observed. In the beginning many layers appear, and each interface of the layers falls gradually with a constant velocity, and finally all layers vanish. To clarify this phenomenon, concentrations and mean diameters of the particles in each layer and temperature distributions were measured. Moreover, natural convection of the other suspension with particles which had a narrow size distribution was also investigated. © 2001 Scripta Technica, Heat Trans Asian Res, 30(8): 636,647, 2001 [source] Bottom-Imprint Method for VSS Growth of Epitaxial Silicon Nanowire Arrays with an Aluminium CatalystADVANCED MATERIALS, Issue 46 2009Zhang Zhang A bottom-imprint method to fabricate high-quality Si [100] nanowire arrays is described (see figure). This new approach combines the functions of a highly ordered anodic aluminum oxide (AAO) template that acts as both a stamp and a template. Vertically aligned, Al-catalyzed Si nanowire (NW) arrays are grown epitaxially on the Si substrate with a narrow size distribution. [source] Ordered High-Density Si [100] Nanowire Arrays Epitaxially Grown by Bottom Imprint MethodADVANCED MATERIALS, Issue 27 2009Zhang Zhang A novel bottom imprint method to fabricate high-quality Si [100] nanowire arrays is demonstrated. This new approach combines the functions of a high-ordering AAO template as a stamp and template simultaneously. By the protective polymer layer in the hot imprint, the vertical 40,nm Si nanowire arrays grow epitaxially on the Si substrate with a narrow size distribution [source] Facile Synthesis and Characterization of Luminescent TiO2 Nanocrystals,ADVANCED MATERIALS, Issue 16 2005D. Pan A simple, two-phase approach using an autoclave is taken to synthesize high-quality anatase TiO2 nanocrystals with a narrow size distribution (see Figure). The size-tunable luminescence of the TiO2 nanocrystals is dominated by band-edge luminescence at room temperature. The nanocrystals could be readily dispersed in toluene after capping with stearic or oleic acid. [source] Controlled size chitosan nanoparticles as an efficient, biocompatible oligonucleotides delivery systemJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2010Romila Manchanda Abstract Polymeric nanoparticles of chitosan crosslinked with glutaraldehyde have been prepared using reverse micellar system. An optically clear solution was obtained on redispersing these nanoparticles in aqueous buffer. The nanoparticles were characterized for their size and surface morphology employing dynamic laser scattering (DLS) and transmission electron microscopy (TEM). The TEM images showed spherical particles with smooth surface and narrow size distribution of about 90 nm, which was also supported by DLS data. Size and morphology of the particles remains the same on redispersing the lyophilized powder of these nanoparticles in aqueous buffer. Further, these nanoparticles were loaded with different synthetic oligonucleotides (ODNs). In vitro pH dependent release of the adsorbed oligonucleotides from these nanoparticles was also studied. At basic pH the release of oligonucleotides was found higher as compared with neutral and acidic medium. Cytotoxicity studies done on HEK 293 cells reveals that oligonucleotide loaded nanoparticles have high cell viability of nearly 76,88% whereas those of lipofectamine was about 35%. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Synthesis by a single-step swelling process and characterization of micrometer-sized polychloromethylstyrene/poly(butyl methacrylate) hemispherical composite particles of narrow size distributionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Sigal Baruch-Sharon Abstract Polychloromethylstyrene (PCMS) micrometer-sized particles of narrow size distribution were prepared by the dispersion polymerization of chloromethylstyrene in a mixture of ethanol and dimethyl sulfoxide. Micrometer-sized PCMS/poly(butyl methacrylate) hemispherical composite particles of narrow size distribution were prepared by a single-step swelling process of the uniform PCMS template particles with emulsion droplets of butyl methacrylate (BMA) containing benzoyl peroxide, followed by the polymerization of BMA at 73°C within the swollen template particles. The effects of various polymerization parameters, for example, BMA volume, initiator type and concentration, and toluene as the swelling solvent, on the properties (size and size distribution, morphology, polymerization yield, and composition) of the hemispherical composite particles were elucidated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] In situ thermo-TOF-SIMS study of thermal decomposition of zinc acetate dihydrateJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 10 2004Anil Vithal Ghule Abstract Time-of-flight secondary ion mass spectrometry (TOF-SIMS) was used for an in situ thermal decomposition study of Zn(CH3COO)2·2H2O forming ZnO nanoparticles. TOF-SIMS spectra were recorded at regular temperature intervals of 25 °C in positive and negative detection modes in a dynamic thermal process. Controlled heating (5 °C min,1) of Zn(CH3COO)2·2H2O was also carried out using thermogravimetric analysis (TGA) in an oxygen atmosphere (20 ml min,1). Nearly spherical ZnO nanoparticles with no agglomeration and a narrow size distribution (diameter ,50 nm) were observed, which were characterized using scanning electron microscopy, transmission electron microscopy and x-ray diffraction. In situ thermo-TOF-SIMS was used to monitor the 64Zn+ and 66Zn+ ion abundances as a function of temperature, which showed a similar profile to that observed for weight loss in TGA during decomposition. Based on the experimental results, a possible decomposition mechanism for the formation of ZnO is proposed. Copyright © 2004 John Wiley & Sons, Ltd. [source] Effect of pH and generation of dendron on single-step synthesis of gold nanoparticles using PEGylated polyamidoamine dendron in aqueous mediumJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2010Atsushi Harada Abstract Three types of PEGylated polyamidoamine (PAMAM) dendrons were synthesized through PEGylation of primary amines at the periphery of second, third, and fourth generation dendrons. Au(III) precursors and the synthesized PEGylated PAMAM dendrons were mixed at various pHs to evaluate the effect of pH on gold nanoparticle (Au NP) synthesis by monitoring the change in surface plasmon resonance. The Au NP synthesis reaction was controlled by pH through the balance between protonated and deprotonated tertiary amines and the reactivity of Au(III) precursors. By using PEGylated PAMAM dendrons with higher generation, the obtained Au NPs had narrow size distribution with small average size because of the limitation of intermolecular space among PEGylated PAMAM dendrons for the growth to Au NP. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1391,1398, 2010 [source] Microencapsulation of a functional dye and its UV crosslinking controlled releasing behaviorJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2009Gangqiang Li Abstract A new family of microcapsules containing photopolymerizable tripropylene glycol diacrylate (TPGDA) was synthesized by using interfacial polymerization. The release behavior of encapsulated dye could be controlled easily by changing the crosslink density of network formed from TPGDA. The chemical structure and properties of microcapsules were characterized by Fourier Transform infrared spectroscopy, scanning electron microscope, differential scanning calorimetry, optical microscope, wide angle X-ray diffraction and UV-visible spectrophotometer. The results demonstrate that the higher agitation rate results in a smaller particle size with a narrow size distribution. When core/shell ratio is low, the surface of the microcapsules becomes smooth. Additionally, it was found that UV radiation time is most effective factor to change the CC double bond conversion ratio. After microcapsules were synthesized, the release speed could be changed according to requirement by exposing them to UV light for minutes. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3630,3639, 2009 [source] Photoinitiated dispersion polymerization of methyl methacrylate: A quick approach to prepare polymer microspheres with narrow size distributionJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2008Jia Chen Abstract Photoinitiated dispersion polymerization of methyl methacrylate was carried out in a mixture of ethanol and water as dispersion medium in the presence of poly(N -vinylpyrrolidone) (PVP) as the steric stabilizer and Darocur 1173 as photoinitiator. 93.7% of conversion was achieved within 30 min of UV irradiation at room temperature, and microspheres with 0.94 ,m number,average diameter and 1.04 polydispersity index (PDI) were obtained. X-ray photoelectron spectroscope (XPS) analysis revealed that only parts of surface of the microspheres were covered by PVP. The particle size decreased from 2.34 to 0.98 ,m as the concentration of PVP stabilizer increased from 2 to 15%. Extra stabilizer (higher than 15%) has no effect on the particle size and distribution. Increasing medium polarity or decreasing monomer and photoinitiator concentration resulted in a decrease in the particle size. Solvency of reaction medium toward stabilizer, which affects the adsorption of stabilizer on the particle surface, was shown to be crucial for controlling particle size and uniformity because of the high reaction rate in photoinitiated dispersion polymerization. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1329,1338, 2008 [source] Developing a hybrid emulsion polymerization system to synthesize Fe3O4/polystyrene latexes with narrow size distribution and high magnetite contentJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2007Longlan Cui Abstract A hybrid emulsion polymerization was formulated for synthesizing Fe3O4/polystyrene composite latex. This system, containing binary droplets that are magnetic (Mag)-droplets with a diameter of 100,200 nm and styrene (St)-droplets with a diameter of 3,4 ,m, was obtained by mixing Mag-miniemulsion and St-macroemulsion. With extremely low surfactants concentration (,critical micelle concentration, CMC), the nucleated loci are selectively controlled in the Mag-droplets, as the result of smaller droplet size and larger surface ratio. Both water-soluble potassium persulfate (KPS) and oil-soluble 2,2,-azobis(2-isobutyronitrile) was adopted to initiate the polymerization. In the presence of KPS, magnetic polystyrene latices with particles size of 60,200 nm, narrow size distribution, and high magnetite content (86 wt % measured by TGA) were attained successfully. The synthesized magnetic Fe3O4/polystyrene latices assembled into well-ordered hexagonal structure in the surface of a carbon supported copper grid. The influence of various parameters on various aspects of the as-synthesized Fe3O4/polystyrene was investigated in detail: type of initiator on composite morphology, feed ratio of Mag-miniemulsion and St-macroemulsion on magnetite content, and hydrophobic agent or amount of surfactant on size and size distribution. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5285,5295, 2007 [source] Polycarbonate particles and dye-labeled particles by miniemulsion polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 8 2004Frédéric Tronc Abstract We describe the synthesis of several different polycarbonate particles by miniemulsion polymerization. The monomers were allylmethyl carbonate (AlMeC), di(ethylene glycol) bisallylcarbonate (DBAC), and 4-vinyl-1,3-dioxan-2-one [vinyl ethylene carbonate (VEC)]. For these polymerizations, higher monomer conversions were obtained with oil-soluble initiators (azobisisobutyronitrile and benzoyl peroxide) than with a water-soluble initiator (potassium persulfate). Benzoyl peroxide was particularly effective in yielding particles with a narrow size distribution. Although increasing amounts of a surfactant (sodium dodecyl sulfate) led to smaller particles, the choice of the monomer was the major determinant. For example, in polymerization reactions carried out at 85 °C with benzoyl peroxide as the initiator and with otherwise identical recipes, we obtained particle sizes of 181 nm with AlMeC, 296 nm with VEC, and 203 nm with DBAC. Fluorescent particles were synthesized with comonomers based on the benzothioxanthene nucleus. Because the dyes had poor solubility in the monomers, it was necessary to include typically 20 wt % bromobenzene or dichlorobenzene based on the monomer in the miniemulsion reaction mixture. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1999,2009, 2004 [source] Nanosized CdSe Particles Synthesized by an Air Pressure Solution Process Using Ethylene-Glycol-Based SolventJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2010Tao Wang Nanosized CdSe particles were synthesized at a temperature of 115°,175°C by a solution method with air pressure condition. Ethylene glycol (EG) was used as the main solvent and sodium selenite and cadmium nitrate-tetrahydrate as inorganic sources. The influence of refluxing temperature and time on growth morphology and crystallization was investigated by transmission electron microscope, high-resolution transmission electron microscope, and X-ray diffraction. The chemical reaction was deducted based on X-ray photoelectron spectra. The optical absorption property was measured by UV-vis. The CdSe nanoparticles synthesized through this EG solvent system was single wurtzite crystallization and had a nanoscale size below 15 nm diameter with a narrow size distribution. The reduction of Se4+,Se0,Se2,and the disproportionation of Se0 occurred during the synthetic process and dominated the chemical reaction. [source] Synthesis of Nano-sized BaTiO3 Powders by the Rotary-Hydrothermal ProcessJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2009Takashi Kubo Nano-sized BaTiO3 powders with narrow size distribution and high tetragonality were attempted to be synthesized by the rotary-hydrothermal process in a water system as a novel technique, using a mixture of anatase-type TiO2 and Ba(OH)2 as starting material. The rotary-hydrothermal syntheses were performed under conditions with a rotary-speed of 20 revolutions per minute at 423,523 K for 3,96 h. Highly- and mono-dispersed BaTiO3 powders mainly composed of coarse-faceted particles with the tetragonal phase were successfully synthesized by controlling the conditions for rotary-hydrothermal treatments. TEM and TG results revealed that these coarse-faceted BaTiO3 particles contained very few structural defects such as hydroxyl content. Thus, the rotary-hydrothermal process was a useful method to synthesize very high-quality BaTiO3 particles, and the further control of various conditions of the rotary-hydrothermal treatment is expected to control the crystalline phase and microstructures of final BaTiO3 powders. [source] Synthesis and Investigation of Submicrometer Spherical Indium Oxide ParticlesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2008Sung-En Lin Spherical indium (In) oxide in submicrometer size is considered as a practical material in photonic bandgap applications. To obtain narrow size distribution, systematic studies of different conditions such as precursor concentration, reaction temperature, and other parameters have been carried out and are reported here. Tri- or dicarboxylic acid of citric acid (CA), malic acid, and tartaric acid were introduced into the reaction system and In-precipitates of spherical shape were produced. The particle size and internal morphology were observed by scanning electron microscopy and transmission electron microscopy. X-ray diffraction and thermal analysis were performed. The reaction kinetics analysis shows that the reaction rate depends on the reaction temperature, urea, and In concentration rather than on CA. [source] Photoluminescent Properties of SrTiO3:Pr, Al Nanophosphors Synthesized by Microemulsion,Microwave HeatingJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2007Qi Pang A novel approach for the preparation of SrTiO3:Pr, Al nanophosphors by microemulsion,microwave heating is reported in this paper. In comparison with the conventional solid-state sintering processes, this novel method provides a limited small space in a micelle for the formation of nanosized precursors and requires a very short heating time, thus reducing the energy consumption. As a result, small-sized particles with a narrow size distribution and high purity were produced. Transmission electron microscopy characterizations indicated that the synthesized particles were almost spherical with an averaging diameter of ,24 nm and agglomerates slightly. The X-ray diffraction analysis revealed the perovskite cubic structure of SrTiO3:Pr3+ nanoparticles. The luminescent of SrTiO3:Pr, Al phosphors were investigated by photoluminescence. Under 350 nm excitation, SrTiO3:Pr, Al showed a strong red emission, peaking at around 615 nm. The photoluminescence excitation intensity was enhanced by the addition of Al3+ ions. [source] Preparation of a Monodispersed Suspension of Barium Titanate Nanoparticles and Electrophoretic Deposition of Thin FilmsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2004Juan Li A transparent and stable monodispersed suspension of nanocrystalline barium titanate was prepared by dispersing a piece of BaTiO3 gel into a mixed solvent of 2-methoxyethanol and acethylacetone. The results of high-resolution transmission electron microscopy (HR-TEM) and size analyzer confirmed that the BaTiO3 nanoparticles in the suspension had an average size of ,10 nm with a narrow size distribution. Crystal structure characterization via TEM and X-ray diffraction indicated BaTiO3 nanocrystallites to be a perovskite cubic phase. BaTiO3 thin films of controlled thickness from 100 nm to several micrometers were electrophoretic deposited compactly on Pt/Ti/SiO2/Si substrates. The deposited thin film had uniform nanostructure with a very smooth surface. [source] Synthesis of BaTiO3 Particles with Tailored Size by Precipitation from Aqueous SolutionsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2004Andrea Testinon Well-defined and stoichiometric spherical particles of BaTiO3 of narrow size distribution were produced at 82° and 92°3C by precipitation from chloride solutions in a strong alkaline environment. The size of the particles can be tailored in the range from ,103 to 70,80 nm by increasing the barium concentration from ,0.07 to 0.7 mol/L. The particles are composed of tight aggregates resulting from the assembly of several nanocrystals. The size of the nanocrystals decreases from 200,300 to 30,40 nm by increasing reactant concentration. At low barium concentration (,0.07 mol/L at 82°3C, ,0.06 mol/L at 92°3C), formation of BaTiO3 is strongly slowed down and nonstoichiometric, Ti-rich powders are produced. Under these conditions, the particles have the tendency to develop a dendritic-like morphology. [source] Kinetics of Electrophoretic Deposition for Nanocrystalline Zinc Oxide CoatingsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2004Yuan-Chung Wang An integrated process combining the preparation of ZnO nanoparticles and the formation of ZnO coatings using electrophoretic deposition (EPD) is reported. The work focuses on the deposition kinetics of nanocrystalline ZnO coatings on copper electrodes during EPD by direct measurement of the thickness of the deposited layer. The experimental results show that the EPD process is a powerful route to fabricate uniform coatings with desired thickness and excellent surface smoothness, which might be attributed to small particle size and narrow size distribution. On the other hand, the deposition kinetics changes with applied voltage and deposition time. The deposition thickness increases with increasing applied voltage and deposition time. In a short deposition time, the deviation of deposition rate between the theoretical and experimental values is caused by voltage drops during deposition, and the discrepancy increases with the applied voltage. Moreover, the increasing voltage drop and depletion of the suspension lead to decreasing current and lower deposition rate after longer deposition time. The critical transition time of deposition kinetics is found to exponentially decrease with increasing applied voltage. [source] Microwave-Hydrothermal Synthesis of Nanocrystalline Zirconia PowdersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2001Federica Bondioli Nanosized zirconium oxide (ZrO2) powders were prepared by adding NaOH to a zirconyl chloride aqueous solution under microwave-hydrothermal conditions. The obtained results showed that the tetragonal polymorph increased with increasing NaOH concentration in the starting solution and reached the maximum value by using 1M ZrOCl2. The microwave-assisted hydrothermal synthesis is expected to be able to process continuously, and may lead to energy savings because of rapid heating to temperature and increased kinetics of crystallization. This method is very simple and can lead to powders with desirable characteristics such as very fine size, narrow size distribution, and good chemical homogeneity. [source] Conversion of silver nanoprisms into colloidal nanoparticles induced by femtosecond laser pulsesLASER PHYSICS LETTERS, Issue 3 2004Qitao Zhao Abstract Shape transformation of silver nanoprisms in aqueous solution was studied using femtosecond laser pulses. Irradiation of a pulsed Ti:Sapphire laser at 800 nm caused the shape change of the nanoprisms from triangle into sphere, forming a stable colloid of a narrow size distribution with the particle diameters having ,10 nm. The effects of laser fluence on fragmentation and conversion were investigated using UV-vis absorption spectroscopy and transmission electron microscopy. The mechanism of laser-induced colloid formation is discussed. (© 2004 by HMS Consultants. Inc. Published exclusively by WILEY-VCH Verlag GmbH & Co.KGaA) [source] Fabrication of Silver Nanoparticles in Hydrogel Networks,MACROMOLECULAR RAPID COMMUNICATIONS, Issue 16 2006Y. Murali Mohan Abstract Summary: This paper describes a simple and facile approach to fabricate well dispersed silver nanoparticles (AgNPs) in poly[N -isopropylacrylamide- co -(sodium acrylate)] hydrogels. The silver nanoparticles formed are spherical in shape with a narrow size distribution in the hydrogel networks in which the nanoparticles are stabilized by the polymer network. Uniformly dispersed silver nanoparticles were obtained with poly[N -isopropylacrylamide- co -[sodium acrylate)] hydrogels, whereas a poly(N -isopropylacrylamide)/poly(sodium acrylate) IPN gel showed aggregated nanoparticles. It is demonstrated that the hydrogel network structure determines the size and shape of the nanoparticles. These particles are more stable in the gel networks compared to other reduction methods. The hydrogel/silver nanohybrids were well characterized by XRD, UV-vis spectrometry, scanning electron microscopy and transmission electron microscopy. Schematic representation of the preparation of Ag nanoparticles in hydrogel networks. [source] Nanogel-Templated Mineralization: Polymer-Calcium Phosphate Hybrid NanomaterialsMACROMOLECULAR RAPID COMMUNICATIONS, Issue 6 2006Ayae Sugawara Abstract Summary: We report novel organic-inorganic hybrid nanomaterials that consist of polymer hydrogel nanoparticles (nanogels) and calcium phosphate. Hybrid nanoparticles that measure ca. 40 nm are synthesized from a dilute solution of hydroxyapatite using nanogels as templates for calcium phosphate mineralization. These nanoparticles show a narrow size distribution and high colloidal stability. Nanogel-adsorbed liposomes act as templates for hierarchical hybrid nanostructures. These nanohybrids can potentially be used as biocompatible drug carriers with controlled-release properties. TEM images of calcium phosphate nanoparticles formed in the presence of CHP nanogels (0.5 mg,·,mL,1) (left) and nanogel-liposomes (CHP 0.05 mg,·,mL,1, DPPC 0.08 mg,·,mL,1)(right). [source] | |||||||||||||||||||||||||||||||