Determination of Fe 2+

In the presented article, oxide forms of iron catalysts with the wustite structure and with a R = Fe2+/Fe3+ molar ratio in the range from 3.78 to 8.16 were investigated. The chemical composition of the tested catalyst precursors was determined by inductively coupled plasma optical emission spectrometry (ICP-OES). The X-ray diffraction (XRD) technique was used to determine the phase composition and location of reflections characteristic of the Fe1−xO phase. The molar ratio of iron ions R = Fe2+/Fe3+ was determined by manganometric titration. The distribution of promoters in the structure of iron catalyst precursors with different R = Fe2+/Fe3+ ratio was determined by a selective etching method. The dependence of the lattice parameter ao value in the crystal structure Fe1−xO on the molar ratio R = Fe2+/Fe3+ was determined. On the basis of the determined dependence, R can easily be calculated in catalyst precursors of the wustite structure

Determination of Fe2+/Fe3+ mole ratio based on the change of precursor lattice parameters of wustite based iron catalysts for the ammonia synthesis

In the presented article, oxide forms of iron catalysts with the wustite structure and with a R = Fe2+/Fe3+ molar ratio in the range from 3.78 to 8.16 were investigated. The chemical composition of the tested catalyst precursors was determined by inductively coupled plasma optical emission spectrometry (ICP-OES). The X-ray diffraction (XRD) technique was used to determine the phase composition and location of reflections characteristic of the Fe1−xO phase. The molar ratio of iron ions R = Fe2+/Fe3+ was determined by manganometric titration. The distribution of promoters in the structure of iron catalyst precursors with different R = Fe2+/Fe3+ ratio was determined by a selective etching method. The dependence of the lattice parameter ao value in the crystal structure Fe1−xO on the molar ratio R = Fe2+/Fe3+ was determined. On the basis of the determined dependence, R can easily be calculated in catalyst precursors of the wustite structure

Determination of the Content of Promoters in Magnetite and Wustite Phases in the Fused Iron Catalyst

Taking advantage of differences in etching rates of crystallographic phases, forming an oxidized form of the fused iron catalyst, a content of promoters in main phases, magnetite and wustite, was determined. A calcium oxide content in magnetite and wustite was 0.54 wt% and 3.59 wt%, respectively. Aluminum oxide was found in the magnetite phase, and its content was 4.5 wt%. The third promoter, potassium oxide, was almost completely located outside these phases. XRD and ICP-OES instrumental methods were used in the investigations

Studies on the recrystalization of nanocrystalline metals

The influence of the promoters such as CaO, Al2O3 and K2O on the specific surface area of the nanocrystalline cobalt was determined. The recrystalization process of the nanocrystalline cobalt was determined and compared with the examinations conducted on the iron catalyst for ammonia synthesis. The triply promoted nanocrystalline obtained cobalt after the annealing process, has got greater specific surface area than the triply promoted iron

The activity of fused-iron catalyst doped with lithium oxide for ammonia synthesis

The iron catalyst precursor promoted with Al2O3, CaO, and Li2O was obtained applying the fusing method. Lithium oxide forms two phases in this iron catalyst: a chemical compound with iron oxide (Li2Fe3O4) and a solid solution with magnetite. The catalyst promoted with lithium oxide was not fully reduced at 773 K, while the catalyst containing potassium was easily reducible at the same conditions. After reduction at 873 K the activity of the catalyst promoted with lithium oxide was 41% higher per surface than the activity of the catalyst promoted with potassium oxide. The concentration of free active sites on the surface of the catalyst containing lithium oxide after full reduction was greater than the concentration of free active sites on the surface of the catalyst promoted with potassium oxide

Characterization of FeCo based catalyst for ammonia decomposition. The effect of potassium oxide

FeCo fused catalyst was obtained by fusing iron and cobalt oxides with an addition of calcium, aluminium, and potassium oxides (CaO, Al2O3, K2O). An additional amount of potassium oxide was inserted by wet impregnation. Chemical composition of the prepared catalysts was determined with an aid of the XRF method. On the basis of XRD analysis it was found that cobalt was built into the structure of magnetite and solid solution of CoFe2O4 was formed. An increase in potassium content develops surface area of the reduced form of the catalyst, number of adsorption sites for hydrogen, and the ammonia decomposition rate. The nitriding process of the catalyst slows down the ammonia decomposition

Microwave-Reactor-Based Preparation of Red Iron Oxide Pigment from Waste Iron Sulfate

This article presents a two-step method of iron red synthesis based on waste long-term deposited iron(II) sulfate. The first step is the purification of waste iron sulfate, and then the pigment is synthesized by precipitation using a microwave reactor. The newly developed method of purification allows for quick and thorough purification of iron salt. The use of a microwave reactor in the synthesis of iron red makes it possible to reduce the temperature of the goethite–hematite phase transition from 500 °C to 170 °C and skip the calcination process. A temperature reduction in the synthesis decreases the formation of agglomerates of synthesized materials compared to commercial ones. The results of the research showed a change in the physicochemical properties of the obtained pigments depending on the conditions of synthesis. Waste iron(II) sulfate is a promising raw material for the synthesis of iron red pigments. Laboratory pigments are found to be differ from commercial pigments. The difference in properties speaks in favor of synthesized materials

Characterization of FeCo based catalyst for ammonia decomposition. The effect of potassium oxide

FeCo fused catalyst was obtained by fusing iron and cobalt oxides with an addition of calcium, aluminium, and potassium oxides (CaO, Al2O3, K2O). An additional amount of potassium oxide was inserted by wet impregnation. Chemical composition of the prepared catalysts was determined with an aid of the XRF method. On the basis of XRD analysis it was found that cobalt was built into the structure of magnetite and solid solution of CoFe2O4 was formed. An increase in potassium content develops surface area of the reduced form of the catalyst, number of adsorption sites for hydrogen, and the ammonia decomposition rate. The nitriding process of the catalyst slows down the ammonia decomposition

TiO2-Modified Magnetic Nanoparticles (Fe3O4) with Antibacterial Properties

This paper presents the synthesis and characteristics of Fe3O4/C/TiO2 hybrid magnetic nanomaterials with antibacterial properties. The materials used were obtained using a microwave-assisted two-stage precipitation method. In the first stage, magnetite nanoparticles (Fe3O4) were prepared with the precipitation method, during which an additional glucose layer was placed on them. Next, the surface of Fe3O4 nanoparticles was covered by TiO2. It was observed that the addition of carbon and titanium dioxide caused a decrease in the average size of magnetite crystallites from 15.6 to 9.2 nm. Materials with varying contents of anatase phase were obtained. They were characterized in terms of phase composition, crystallite size, specific surface area, surface charge and the kinds of function groups on the surface. The results show a successful method of synthesizing hybrid magnetic nanoparticles, stable in a solution, with antibacterial properties under direct solar light irradiation. Compared to classical materials based on TiO2 and used for water disinfection, the obtained photocatalytic nanomaterials have magnetic properties. Owing to this fact, they can be easily removed from water once their activity under direct irradiance in a given process has completed