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71.
The goal of this work was the development of a novel type of heterogeneous catalyst, consisting of bare metal nanoparticles
on stainless steel foils, which can be shaped to any kind of architecture and, if necessary, heated electrically. Solutions
of pre-prepared, ligand protected and monodispersed gold, palladium, platinum and rhodium nanoparticles were sprayed onto
stainless steel foils, followed by the careful removal of the ligand molecules by an oxygen plasma treatment. Due to this,
bare particles become irreversibly fixed on the steel support. It could be shown that the original particle sizes do not change
during the plasma treatment. Foils, densely coated with the nanoparticles, were used for gas phase catalyses in a self-made
reactor at room temperature or at 60 °C. Hydrogenation of 1,3-butadiene at 15 nm Pd and 2 nm Pt, CO oxidation at 16 nm, 8 nm
and 1.4 nm gold and NO reduction with NH3 at 2 nm Rh particles were performed, indicating that the novel catalysts might in principle be applicable in technical processes
if the experimental conditions like form and temperature would be optimized.
Dedicated to Professor Dieter Fenske on the occassion of his 65th birthday. 相似文献
72.
The synthesis of goethite by oxidation of Fe2+in presence of metallic iron was undertaken in an aqueous medium containing indifferent salts such as Na2SO4, (NH4)2SO4, NaCl, and NH4Cl. Temperature and bubbling air rate were maintained, respectively, at 70°C and 1 L/min. The influence of anions and cations on the kinetics of each step of the process has been followed distinctly, the iron dissolution rate has been determined by the variation of the medium acidity, and the precipitation of goethite has been determined by gravimetric measurements. With respect to Cl−, the SO42−anion decreases the rate of the two reactions. NH4+acts as an inhibitor when it is present at low concentrations and as an accelerator for higher concentrations; the limit corresponding to the change of NH4+behavior depends on the nature of the counter ion. The reaction product is composed of pure goethite in the presence of sulfate salts, whereas a mixture of goethite and lepidocrocite, respectively, 60–70 and 40–30%, was observed in the presence of chloride salts. 相似文献
73.
GangWEI HaiYahHUANG RongChunXIONG 《中国化学快报》2003,14(8):877-880
TiO2 nanoparticles were synthesized by using micro-reactors. The shape and size of the nanoparticles produced from the original micro-reactors and the five times recycled micro-reactorsmother liquor were investigated on transmission electron microscopy (TEM) by using the original sample, freeze prepared sample, and dyeing treated sample, respectively. UV-VIS spectrometry was used to study the growth process of TiO2 nanoparticles in main reactors. The results showed that micro-reactors with nanometer magnitude had spherical or oval structures, and could restore to their original structure after they were destroyed. The products prepared in the original micro-reactors were similar to that in the micro-reactors recycled for many times, suggesting that the micro-reactors had memory function. 相似文献
74.
A novel sensitive and simple method for rapid and selective extraction, preconcentration and determination of iron (as its
bathophenanthroline complex) and copper (as its neocuproine complex) using octadecyl silica cartridges and dual wavelength
spectrophotometry is presented. The dual wavelength method (533 nm for the iron-bathophenanthroline and 454 nm for the copper-neocuproine
as the analytical wavelength) is used to eliminate spectral interferences. Extraction efficiency and the influence of flow
rates of sample solution and eluent, pH, amount of neocuproine, bathophenanthroline and hydroxylamine hydrochloride, type
and least amount of eluent for elution of iron and copper complexes from cartridge, break-through volume and limit of detection
are evaluated. The effects of various cationic and anionic interferences on percent recovery of iron and copper are also studied.
Extraction efficiencies >95% are obtained by elution of cartridges with minimal amount of organic solvent. Iron and copper
were determined in the range of 3–100 ng mL−1. The limits of detection are 0.98 and 1.13 ng mL−1 for iron and copper, respectively. The proposed method is applied successfully to the determination of both analytes in river,
tap and well water samples.
Author for correspondence. E-mail: yyamini@modares.ac.ir
Received September 18, 2002; accepted December 12, 2002
Published online May 5, 2003 相似文献
75.
Kojima Kunihiko Miyazaki Mitsuharu Mizukami Fujio Maeda Kazuyuki 《Journal of Sol-Gel Science and Technology》1997,8(1-3):77-81
The structure of iron oxide was controlled by regulating the hydrolytic polymerization of aquo iron complexes with organic
polydentate ligands such as diols. Iron oxides were prepared by calcining the precursor polymers obtained from iron nitrate
nonahydrate and diols. When the diols were 1,2-pentanediol, 1,2-hexanediol and 1,2-octanediol, α-Fe2O3 with corundum structure appeared exclusively or as the main crystalline phase, in spite of the amount of diol used and the
calcination temperature. In the case of 1,2-decanediol and 1,2-dodecanediol, when five moles of the diols were used to one
mole of iron nitrate and the calcination temperatures were below 400°C, ψ-Fe2O3 with spinel structure appeared as the main phase and, when less than five moles of the diols were used, α-Fe2O3 appeared exclusively or as the main phase, irrespective of the calcination temperature. This tendency was also observed in
thin films. Thus, a transparent magnetic film composed of γ-Fe2O3 could be prepared by applying a benzene solution of the iron polymer, obtained with 5 equivalents of 1,2-decanediol, on quartz
and calcining the gel film at 350°C. 相似文献
76.
单分散磁性纳米颗粒的制备及生物高分子在其上的组装 总被引:3,自引:0,他引:3
磁性纳米颗粒因其潜在的生物医学应用价值而成为纳米生物材料领域研究的前沿。本文综述了单分散磁性纳米颗粒的制备方法以及生物高分子在磁性纳米颗粒上的组装的研究进展。 相似文献
77.
Summary Thermomagnetometry has been applied to mineralized archaeological iron samples and samples from accelerated corrosion tests. It has successfully quantified the degree of corrosion, measured by the loss of iron, as well as the amount of magnetite formed and water held in the corrosion and adhered soil layers. Thermomagnetometry, thermogravimetric analysis and differential scanning calorimetry have been applied to the reported corrosion products from archaeological iron. Fourier transform infra-red and Raman spectroscopies and X-ray diffraction analyses were undertaken on the residues and at intermediate heating stages, where the thermal analyses indicated, to identify the reaction products. 相似文献
78.
Carbonylation of benzyl halides to phenylacetic acid was studied in a two-phase system with iron pentacarbonyl as the catalyst precursor. The solutions consisted of a benzyl halide and iron pentacarbonyl in benzene and tetrabutylammonium hydrogen sulfate in aqueous sodium hydroxide. Stirring under carbon monoxide readily produced phenylacetic salts in aqueous phase which were then acidified and extracted with ether. The yields of phenylacetic acid from benzyl iodide and from benzyl bromide were similar at a evel of about 50percnt;, that of the latter being higher by 1%. The yield from benzyl chloride was far less, at a level of only 21%. The rate as studied with gas chromatography was found to decrease in the order benzyl iodide>benzyl bromide>benzyl chloride. 相似文献
79.
Noble metal nanoparticles were prepared by the in situ reduction of the respective metal salt precursors in the presence
of various protective polymers. Transmission electron microscopy (TEM) has been used to determine the particle shapes and
morphologies. These are strongly influenced by the reduction methods and conditions chosen, but the choice of the protective
polymer is equally important for controlling the particle morphologies and for the stabilization of the colloids. A whole
spectrum of nanoparticle morphologies and shapes was obtained, ranging from nanoagglomerates which are nevertheless well-defined
and well-stabilized to nanosized single crystals with triangular shape.
Received: 2 February 1998 Accepted: 29 May 1998 相似文献
80.
铅系弛豫铁电陶瓷钨铁酸铅Pb(Fe2/3W1/3)O3(PFW)是一种重要的介电材料,具有较大的介电常数(8000)和较低的烧结温度(小于900℃),适用于制备低烧高介的多层陶瓷电容器犤1~4犦。在传统氧化物法合成PFW的过程中,易生成恶化介电性能的钨酸铅(PbWO4或Pb2WO5)或焦绿石相(Pb2FeWO6)等其他相犤3,4犦。尽管通过加入过量5%的Fe2O3可以消除这些其他相,但因含较多的变价铁离子(Fe3+和Fe2+)而产生介电老化的缺点犤5犦。虽然二次合成法被广泛用于制备铅系弛豫铁电陶瓷犤6犦,但对制备PFW陶瓷的效果并不明显,仍有少量的钨酸铅PbWO4存在,并且预烧… 相似文献