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 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

We have studied poly(methyl methacrylate)-grafted(PMMA) particle monolayer systems at the air-water interface. In previous papers, we reported that PMMA chains grafted from particles (silica particle and polystyrene latex) were extended on water surfaces. Through observing deposited particle monolayers on substrates using SEM, we have confirmed that PMMA of large molecular weights were either dispersed or arrayed in structure with long inter-particle distances approximately 500 nm. In contrast, low molecular weight PMMA were observed to aggregate upon deposition. We speculated that the difference in morphology in deposited particle monolayers would be attributed to the affinity between the grafted polymer and the substrate. To examine the effect of this affinity three new polymer-grafted silica particles were synthesized with a fairly high graft density of about 0.14 approximately 0.43 nm(-2). As well as PMMA-grafted silica particles (SiO2-PMMA), poly(2-hydroxyethyl methacrylate) and poly(t-butyl methacrylate)--grafted silica particles (SiO2-PHEMA and SiO2-PtBuMA) were also prepared and subjected to pi-A isotherm measurements and SEM observations. These pi-A isotherms indicated that polymer-grafted silica formed monolayer at the air-water interface, and the onset area of increasing surface pressure suggests that the polymer chains are extended on a water surface. However, the morphology of the deposited monolayer is highly dependent on polymer species: SiO2-PHEMA showed that the dispersed particle monolayer structure was independent of grafted molecular weight while SiO2-tBuMA showed an aggregated structure that was also independent of grafted moleculer weight. SiO2-PMMA showed intermediate tendencies: dispersed structure was observed with high grafted molecular weight and aggregated structure was observed with low grafted molecule weight. The morphology on glass substrate would be explaiened by hydrophilic interaction between grafted polymer and hydrophilic glass substrate.
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PMID:Effect of grafted polymer species on particle monolayer structure at the air-water interface. 2144 11

Aligned CNT mats were prepared by thermal chemical vapor deposition (CVD) method by exposing a mixture of ferrocene and xylene vapor to the SiO2/Si substrates. Aligned CNT mats functionalized with reactive chemicals without disturbing CNT alignment were characterized by SEM, XRD, FT-IR, FT-Raman and XPS. The thermal stability of the CNT, CNT-OH and CNT-NaCIO4 are investigated using TG-DSC analysis. Oxidation and combustion temperatures of CNT mats were found to be decreased by functionalizing the CNT mats with NaClO4.
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PMID:Thermal decomposition properties of NaClO4 functionalized CNT arrays. 2145 47

Strength development, leachability and microstructure of heavy metals from the solidified waste using synthesis rice husk ash (sRHA) and lime blended at the weight ratio of 1:1 were used as binders. The heavy metal-containing sludge was used at the level of 0 wt.%, 30 wt.%, and 50 wt.% dry weight, respectively. The sample specimens with and without 1.5 wt.% of sodium silicate (SiO2/Na2O = 1.0) were cured under the ambient condition and elevated temperature curing at 50 degrees C for 24 hr. Experimental results showed that the introduction of sodium silicate solution and elevated temperature curing to sRHA-based solidified waste containing 30 wt.% of heavy metal sludge gave one day strength of 20 kg/cm2 compared to 0.9 kg/cm2 for the control sample. XRD patterns indicated that most metal-sulfides present in the sludge were appeared in the solidified waste and SEM coupled with EDX techniques reveal these metal-sulfide particles were trapped within the lime-sRHA matrices. In addition, cumulative leaching behavior by tank test (EA NEN 7375:2004) showed that solidified waste containing up to 30 wt.% of heavy metal sludge was suitable to dispose in a secured landfill.
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PMID:Effect of chemical and thermal activations on the properties of rice husk ash-based solidified wastes. 2146 21

Novel inorganic-organic hybrid hollow nanospheres, acrylated SiO2 and SiO2@TiO2, were synthesized via a sol-gel polymerization, using crown-appended sugar gelator 1 as an organic template for the unique nanospherical structures in demand for a fast expanding area in nanomaterial research. In this work, hollow SiO2 nanospheres were obtained by a simple sol-gel method followed by calcination and rather rough TiO2 nanolayers were coated onto the highly dispersed surface of SiO2 nanospheres and further copolymerization of MPA on the surface of SiO2 and SiO2@TiO2 nanosphseres was successfully conducted. The morphological properties of those hollow nanospheres were characterized by TEM, SEM and powder-XRD. Furthermore, the physical and chemical properties of the synthesized nanocomposites were characterized by the analysis of EDX, FT-IR, TGA and ESCA.
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PMID:Preparation and characterization of acrylated-SiO2@TiO2 hollow hybrid nanospheres. 2177 57

Fractal structures were formed on silicon substrates from SiO2 nanoparticles homogeneously synthesized in low temperature atmospheric pressure plasma from tetraethoxysilane (TEOS). RF discharge (power absorbed was about 10 W) sustained between two parallel mesh electrodes was used to generate plasma. The average size of nanoparticles was in the range of 8-20 nm and was determined by process parameters. The obtained products were analyzed by SEM (scanning electron microscopy) and XPS (X-ray photoelectron spectroscopy). Values of fractal dimension parameter of bidimensionals agglomerates formed on the substrate surface from nanoparticles were calculated with the use of Gwyddion and others. It was found that values of this parameter of the deposited structures varied in the range of 1.48-2 and were determined by combination of the process parameters. An empirical model explaining mechanism of the fractal structures formation and variation of the fractal dimension parameter with the process parameters was proposed.
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PMID:Formation of fractal structures from silicon dioxide nanoparticles synthesized by RF atmospheric pressure plasma enhanced chemical vapor deposition. 2209 14

Deposits of individual diamond grains and continuous polycrystalline diamond layers have been generated by means of a HFCVD technique onto different types of untreated or seeded NbN surfaces. To test the feasibility of using diamond layers as protective coatings for aerospace applications, we carried out diamond deposition onto the lithographically defined NbN microelectrodes of a NbN/SiO2 multifinger device. The morphological and structural features of the diamond deposits and of the substrates were characterized by FE-SEM, XRD and Raman spectroscopy. The preferential growth of diamond on the superconductive NbN enables the selective coating of the NbN microstripes sputtered on the insulating SiO2. Moreover the diamond coating procedure is able to preserve the structural integrity of the substrate material and to retain the shaped architecture of the device. For the polycrystalline diamond layers grown on NbN a residual stress of -9.8 GPa, largely due to thermal stress, has been estimated by Raman analysis. The diamond coatings of the NbN-based architectures result to be mechanically stable.
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PMID:Diamond layers grown by chemical vapor deposition on NbN systems and NbN/SiO2-based devices. 2209 52

Large-scale beta-MnO2/SiO2 core-shell nanorods were synthesized by hydrolysis process. The product was characterized by XRD, EDS, SEM and TEM. The thickness of the SiO2 shell layer is about 3 nm approximately 5 nm, which can be tuned by changing the amount of tetraethyl orthosilicate (TEOS) and the reaction time. The dielectric properties of the synthesized core-shell nanorods at the temperature range from 373 K to 773 K in X-band were investigated in detail and the mechanism of the dielectric response was discussed. The dielectric loss of the SiO2-coated MnO2 nanorods at 773 K was about twice than that at 373 K. The high dielectric loss is mainly attributed to the interfacial polarization and the electromagnetic impedance match between the SiO2 shell layer and MnO2 core layer. The quantitative formula between the permittivity of beta-MnO2/SiO2 core-shell nanorods and the thickness of the SiO2 shell is established, which can be used to tune the dielectric properties of the core-shell nanorods through controlling the thickness of the SiO2 shell layer.
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PMID:Beta-MnO2/SiO2 core-shell nanorods: synthesis and dielectric properties. 2210 4

Hexamethyldisilazane (HMDS, [(CH3)3Si]2NH) was used as a precursor to form SiO2 protective coatings on IN738LC alloys by combustion chemical vapor deposition (CCVD). SEM and XPS showed that the processed coatings were composed mainly of SiO2. The amount of HMDS had the largest effect on the size of the SiO2 agglomerates and the thickness of the deposited coatings. The specimens coated with SiO2 using the 0.05 mol/l HMDS solution showed a significantly higher temperature oxidation resistance than those deposited under other conditions.
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PMID:Processing of SiO2 protective layer using HMDS precursor by combustion CVD. 2210 73

An aerogel of silica gel dopeyd with 2.86 wt% Fe was prepared by an alkoxide sol-gel method and using tetraethyl orthosilicate as a precursor material. The synthesized aerogel was calcined at 500 degress C to produce nanoparticle solids, and was characterized by XRD, FT-IR and SEM. The nanosized iron-silica gel mixed oxide was tested in the photooxidation of the azo dye Acid Red 14 (AR 14) using 30% aqueous hydrogen peroxide as oxidant and UV light. The 2.86 wt% Fe-loaded SiO2 showed very good efficiency in the decolorization of AR 14. The effects of various parameters including solution pH, catalyst, oxidant and initial dye concentrations on photodegradation were investigated and the optimum conditions were determined. The catalyst was resistant to leaching and could be recycled several times without appreciable loss of activity.
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PMID:Photo-assisted hetero-fenton decolorization of azo dye from contaminated water by Fe-Si mixed oxide nanocomposite. 2232 54

Zinc oxide [ZnO] thin films are deposited using a radiofrequency magnetron sputtering method under room temperature. Its crystalline quality, surface morphology, and composition purity are characterized by X-ray diffraction [XRD], atomic force microscopy [AFM], field-emission scanning electron microscopy [FE-SEM], and energy-dispersive X-ray spectroscopy [EDS]. XRD pattern of the ZnO thin film shows that it has a high c-axis-preferring orientation, which is confirmed by a FE-SEM cross-sectional image of the film. The EDS analysis indicates that only Zn and O elements are contained in the ZnO film. The AFM image shows that the film's surface is very smooth and dense, and the surface roughness is 5.899 nm. The microcantilever (Au/Ti/ZnO/Au/Ti/SiO2/Si) based on the ZnO thin film is fabricated by micromachining techniques. The dynamic characterizations of the cantilever using a laser Doppler vibrometer show that the amplitude of the cantilever tip is linear with the driving voltage, and the amplitude of this microcantilever's tip increased from 2.1 to 13.6 nm when the driving voltage increased from 0.05 to 0.3 Vrms. The calculated transverse piezoelectric constant d31 of the ZnO thin film is -3.27 pC/N. This d31 is high compared with other published results. This ZnO thin film will be used in smart slider in hard disk drives to do nanoactuation in the future.
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PMID:Preparation and characterization of ZnO microcantilever for nanoactuation. 2240 Nov 38


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