SummaryMn-doped zinc oxide nanoparticles were prepared by using the microwave solvothermal synthesis (MSS) technique. The nanoparticles were produced from a solution of zinc acetate dihydrate and manganese(II) acetate tetrahydrate using ethylene glycol as solvent. The content of Mn2+ in Zn1− xMnxO ranged from 1 to 25 mol %. The following properties of the nanostructures were investigated: skeleton density, specific surface area (SSA), phase purity (XRD), lattice parameters, dopant content, average particle size, crystallite size distribution, morphology. The average particle size of Zn1− xMnxO was determined using Scherrer’s formula, the Nanopowder XRD Processor Demo web application and by converting the specific surface area results. X-ray diffraction of synthesized samples shows a single-phase wurtzite crystal structure of ZnO without any indication of additional phases. Spherical Zn1− xMnxO particles were obtained with monocrystalline structure and average particle sizes from 17 to 30 nm depending on the content of dopant. SEM images showed an impact of the dopant concentration on the morphology of the nanoparticles.
The aim of the present work is to compare two methods of synthesis of nanocrystallline zinc oxide doped with iron oxide. The synthesis was carried out using microwave asssisted hydrothermal synthesis and traditional wet chemistry method followed by calcination. The phase composition of the samples was determined using X-ray diffraction measurements. Depending on the chemical composition of the samples, hexagonal ZnO, and/or cubic ZnFe2O4 were identified. The morphology of the received materials was characterized using scanning electron microscopy. Two different structures of agglomerates were observed: a hexagonal structure (corresponding to zinc oxide) and spherical (corresponding to spinel phase). The effect of the iron oxide concentration on specific surface area and density of the samples was determined.
Industrially relevant nanopowder was synthesised by microwave hydrothermal synthesis to obtain wellcontrolled composition (ZrO 2 -AlO(OH) system) which was found to determine a number of physical and thermal characteristics. This study reports variation of particle size, density, specific surface area (SSA BET ), as well as thermal behaviour of nanopowder mixtures of ZrO 2 -AlO(OH) in the whole range of compositions. It was found that the onset temperature (T on ) of physically and chemically bounded water desorption depends on the Al 3? /or AlO(OH) content. The lower content of Al 3? in the ZrO 2 -AlO(OH) system, the higher T on of physically bound water desorption. There are three distinct temperature regions for water decomposition for nanomaterials investigated in air (at approximately 50, 250 and 450°C). These temperature ranges depend on particle size and chemical composition of ZrO 2 -AlO(OH) nanopowders. Materials were divided into three groups characterised by different properties: (1) ZrO 2 with 2-12% of Al 3? , where particle sizes are from 4 to 8 nm, (2) ZrO 2 with 30-67% of AlO(OH), where particle sizes are from 10 to 13 nm, and (3) ZrO 2 with 80-99% of AlO(OH), where particle sizes are from 13 to 23 nm. AlO(OH) content determines thermal and physico-chemical properties of synthesised ZrO 2 -AlO(OH) nanopowders.
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