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Hollow Microspheres (hollow + microsphere)
Selected AbstractsCreation of calcite hollow microspheres with attached bundles of aragonite needlesCRYSTAL RESEARCH AND TECHNOLOGY, Issue 5 2008Hua Tang Abstract Novel calcite hollow microspheres attached with bundles of aragonite needles have been synthesized via a simple precipitation reaction of aqueous solutions of CaClB2B and NaB2BCOB3B in the presence of MgP2+P ions at room temperature. The experimental results revealed that an appropriate molar ratio of [MgP2+P]/[CaP2+P], pH value of the solution and aging time are crucial for the formation of the unusual hierarchical CaCOB3B superstructure. A possible growth mechanism is proposed. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Electrochemical Immunoassay for Carbohydrate Antigen-125 Based on Polythionine and Gold Hollow Microspheres Modified Glassy Carbon ElectrodesELECTROANALYSIS, Issue 17 2007Xiao-Hong Fu Abstract A new electrochemical immunosensor for the detection of carbohydrate antigen-125 (CA125), a carcinoma antigen, was developed by immobilization CA125 antibody (anti-CA125) on gold hollow microspheres and porous polythionine (PTH) modified glassy carbon electrodes (GCE). The gold hollow microspheres provided a biocompatible microenvironment for proteins, and greatly amplified the coverage of anti-CA125 molecules on the electrode surface. The performance and factors influencing the immunosensor were investigated in detail. The detection is based on the current change before and after the antigen-antibody interaction. Under optimal conditions, the amperometric changes were proportional to CA125 concentration ranging from 4.5 to 36.5,U/mL with a detection limit of 1.3,U/mL (at 3,). The CA125 immunosensor exhibited good precision, high sensitivity, acceptable stability, accuracy and reproducibility. The as-prepared immunosensors were used to analyze CA125 in human serum specimens. Analytical results suggest that the developed immunoassay has a promising alternative approach for detecting CA125 in the clinical diagnosis. [source] Controllable Synthesis of Cu2O Microcrystals via a Complexant-Assisted Synthetic RouteEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 7 2010Wanqun Zhang Abstract A novel method using Cu(AC)2·H2O and dimethylglyoxime as reagents has been successfully developed for the controllable synthesis of Cu2O microcrystals with distinctive morphologies, including porous hollow microspheres, octahedral microcages, and microcrystals with truncated corners and edges and octahedral microcrystals. These structures can be fine-tuned by varying reaction temperature, reaction time, and concentration. The products were characterized by X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectra, and UV/Vis diffuse reflectance spectra. This is the first report of the preparation of the novel microcage structure of Cu2O through a simple solution-based route. By investigating the intermediate products which resemble the final crystal structures, a possible growth mechanism is proposed. Moreover, the investigations showed that the various 3D architectures of the as-made products exhibit different abilities to catalytically degrade rhodamine-B. Our work shows that octahedral Cu2O crystals with entirely {111} faces are photocatalytically more active than octahedral microcrystals with truncated corners and edges, suggesting the {111} faces of Cu2O nanostructures are catalytically more active than the {100} and {110} faces. Due to dual effect of the cavity structure and the {111} surfaces, the octahedral microcages with truncated corners and edges exhibit a higher extent of the photodecomposition reaction. As a result of very slow photocorrosion rate of the Cu2O microcrystal, it is expected that these microcrystals with different surfaces may find more applications in photocatalysis. [source] Reactive Template Method to Synthesize Gold Nanoparticles with Controllable Size and Morphology Supported on Shells of Polymer Hollow Microspheres and Their Application for Aerobic Alcohol Oxidation in WaterADVANCED FUNCTIONAL MATERIALS, Issue 7 2009Jie Han Abstract A novel method has been developed to synthesize gold nanoparticles with tunable size and morphology supported on both inner and outer surfaces of poly(o -phenylenediamine) (PoPD) hollow microspheres, which act as both reductant and template/stabilizer. The size of gold nanoparticles supported on shells of PoPD hollow microspheres can be tuned from 3 to 15,nm by changing the concentration of the gold source, HAuCl4. Gold nanorods supported on shells of PoPD hollow microspheres can also be fabricated by introducing a well-known seed-growth strategy. In addition, silver nanoparticles supported on shells of PoPD hollow microspheres can also be successfully fabricated using the same strategy, which indicates the diversity of this proposed method for polymer hollow microspheres supporting noble metal nanoparticles. The products are characterized by X-ray diffraction and contact angle analysis. Furthermore, the catalytic activity of the obtained PoPD-microsphere-supported gold nanoparticles for aerobic alcohol oxidation is investigated. The results demonstrate that such polymer-supported gold nanoparticles can be used as reusable catalysts with high catalytic activity for aerobic alcohol oxidation in water. [source] TiO2 -Coated Multilayered SnO2 Hollow Microspheres for Dye-Sensitized Solar CellsADVANCED MATERIALS, Issue 36 2009Jiangfeng Qian TiO2 -coated multilayered SnO2 hollow microspheres exhibit a high overall photoconversion efficiency of ,5.65% when used for dye-sensitized solar-cell photoelectrodes due to multiple reflecting and scattering of incident light in the hierarchical hollow spherical structure. [source] Use of Enzymes for the Processing of BiomaterialsINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 1 2007Hidero Unuma Ceramic/polymer composites and hollow ceramic microspheres are receiving attention as biomaterials as a bone/tissue substitute and cancer remedy. This article describes the advantages of the use of enzymes as "controllable precipitant supplier" in the processing of such biomaterials. It has been demonstrated that hydroxyapatite (HA)/polymer composites and hollow microspheres of Y2O3, Fe3O4, and HA may be fabricated in a shorter time and using a simpler operation. [source] Synthesis and characterization of uniform-sized hollow chitosan microspheresADVANCES IN POLYMER TECHNOLOGY, Issue 1 2009Shan Wang Abstract Hollow chitosan (CS) microspheres were obtained using an inverse-emulsion crosslinking method. The temperature and viscosity of the CS emulsion affected the characteristics of the derived microspheres. The microspheres were characterized by differential scanning calorimetry, Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy, optical microscopy, scanning electron microscopy (SEM), and laser particle size analysis. FT-IR indicated the sequence of transformations taking place before, during, and after the crosslinking of CS. Optical microscopy and SEM confirmed the spherical morphology of the gel. The formation of hollow microspheres with a single cavity was identified by SEM. The CS microspheres exhibited a narrow particle size distribution. Furthermore, particle size could be controlled by changing the stirring speed. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:40,47, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20145 [source] Synthesis of Yttrium,Aluminum,Garnet Hollow Microspheres by Reverse-Emulsion TechniqueJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2006Minati Chatterjee Yttrium,aluminum,garnet (YAG, Y3Al5O12) hollow microspheres were synthesized by reverse-emulsion (w/o) technique starting with aqua-based precursors of oxides. The non-ionic surfactant was used as the emulsifying agent. The gel powders were calcined at 700°,1200°C. The synthesized powders were characterized by differential thermal analysis (DTA), thermogravimetry, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The appearance of an exothermic peak at 932°C in the DTA curve revealed the crystallization of YAG, which was further confirmed by XRD and FTIR studies. SEM confirmed the formation of hollow microspheres. [source] Mechanical properties of particulate-filler/woven-glass-fabric-filled vinyl ester compositesJOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 1 2010L. Yusriah Studies of the effect of particulate fillers on specific mechanical properties of vinyl ester epoxy (VE) reinforced with woven glass fiber composites were carried out with different filler types and particulate filler contents (1%, 3%, and 5% by weight). Two types of particulate filler were used, i.e., calcium carbonate (CC) and phenolic hollow microspheres (PHMS). The composites were prepared by using a hand lay-up and vacuum bagging method. Woven glass fabric composites filled with particulate PHMS were observed to have better specific flexural strength and specific impact strength, as well as lower density, than those filled with particulate CC. Morphological features determined by scanning electron microscope (SEM) proved that the PHMS filler experienced good bonding in the VE matrix, a feature which contributed to the improvement in the properties of the composites. The incorporation of particulate fillers into the composites also influenced the storage modulus with a minimal effect on Tg. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers [source] Interfacial polymerization of morphologically modified polyaniline: from hollow microspheres to nanowiresPOLYMER INTERNATIONAL, Issue 2 2008Jinbo Li Abstract BACKGROUND: Polyaniline (PANI) has attracted much attention in many fields due to its chemical and physical properties, and different nanostructures of PANI changing from one-dimensional to three-dimensional have been obtained. By changing the concentration of cetyltrimethylammonium bromide (CTAB), the morphology of hydrochloric acid-doped polyaniline could be changed from one-dimensional nanoneedles or nanowires with a network structure (50,100 nm in diameter) to three-dimensional hollow microspheres (ca 400 nm in outer diameter) via combining interfacial polymerization and self-assembly process. RESULTS These different nanostructures of PANI were proved using scanning electron and transmission electron microscopies. A plausible mechanism of the formation of the changeable nanostructures of PANI may be different from that of interfacial polymerization without surfactant or a traditional homogenous reaction system using CTAB as surfactant. CONCLUSION The results obtained from Fourier transform infrared spectrometry, X-ray diffraction and the four-probe method showed that the molecular structure of PANI does not change with increasing CTAB concentration, but crystallinity and conductivity of PANI increase with surfactant concentration. Copyright © 2007 Society of Chemical Industry [source] Sonochemical Method for the Preparation of Hollow SnO2 MicrospheresCHINESE JOURNAL OF CHEMISTRY, Issue 7 2006Xia Zhang Abstract A simple sonochemical route has been successfully developed to synthesize SnO2 hollow microspheres. The obtained sample is characterized by XRD, TEM, XPS and UV-visible spectrophotometer. The TEM image of the sample at high magnification shows that the shell of the hollow sphere is composed of 3,5 nm SnO2 nanoparticles. A possible formation mechanism of the hollow spheres is briefly discussed. [source] | |||||||||||||||||||||||||