Among the elements that compose steel slags and blast furnace slags, metallic precipitates occur alongside the dominant glass and crystalline phases. Their main component is metallic iron, the content of which varies from about 90% to 99% in steel slags, while in blast furnace slags the presence of precipitates was identified with the proportion of metallic iron amounting to 100%. During observations using scanning electron microscopy and X-ray spectral microanalysis it has been found that the form of occurrence of metallic precipitates is varied. There were fine drops of metal among them, surrounded by glass, larger, single precipitates in a regular, spherical shape, and metallic aggregates filling the open spaces between the crystalline phases. Tests carried out for: slags resulting from the open-hearth process, slags that are a by-product of smelting in electric arc furnaces, blast furnace slags and waste resulting from the production of ductile cast iron showed that depending on the type of slag, the proportion and form of metallic precipitates is variable and the amount of Fe in the precipitates is also varied. Research shows that in terms of quality, steel and blast furnace slag can be a potential source of iron recovery. However, further quantitative analyses are required regarding the percentage of precipitates in the composition of slags in order to determine the viability of iron recovery. This paper is the first part of a series of publications aimed at understanding the functional properties of steel and blast furnace slags in the aspect of their destructive impact on the components of devices involved in the process of their processing, which is a significant operational problem.
Height, frequency and spatial differentiation of atmospheric precipitation of the summer season for the period 1975-1982 are presented. Results of the respective investigations are compared with atmospheric precipitation in other areas of the western coast of Spitsbergen.
Magnetite nanoparticles have become a promising material for scientific research. Among numerous technologies of their synthesis, co-precipitation seems to be the most convenient, less time-consuming and cheap method which produces fine and pure iron oxide particles applicable to environmental issues. The aim of the work was to investigate how the co-precipitation synthesis parameters, such as temperature and base volume, influence the magnetite nanoparticles ability to separate heavy metal ions. The synthesis were conducted at nine combinations of different ammonia volumes - 8 cm3, 10 cm3, 15 cm3 and temperatures - 30°C, 60°C, 90°C for each ammonia volume. Iron oxides synthesized at each combination were examined as an adsorbent of seven heavy metals: Cr(VI), Pb(II), Cr(III), Cu(II), Zn(II), Ni(II) and Cd(II). The representative sample of magnetite was characterized using XRD, SEM and BET methods. It was observed that more effective sorbent for majority of ions was produced at 30°C using 10 cm3 of ammonia. The characterization of the sample produced at these reaction conditions indicate that pure magnetite with an average crystallite size of 23.2 nm was obtained (XRD), the nanosized crystallites in the sample were agglomerated (SEM) and the specific surface area of the aggregates was estimated to be 55.64 m2·g-1 (BET). The general conclusion of the work is the evidence that magnetite nanoparticles have the ability to adsorb heavy metal ions from the aqueous solutions. The effectiveness of the process depends on many factors such as kind of heavy metal ion or the synthesis parameters of the sorbent.
This work presents the results of a study whose aim was to determine the influence of algal blooms on precipitation of heavy metals. The scope of the study covered culture of a mixed population made up of Scenedesmus and Pseudokirchneriella algae in experimental conditions and initiating a metal biosorption process with the use of culture biomass by administering ions of Zn(II) and Ni(II). The process was controlled by assessing the level of biosorption of metals entered at a one-off basis in the form of Zn(II) and Ni(II) salts or in the form of mixture of both ions, in comparison to the control sample, at different exposure times (2 hours and 24 hours). The presence of metals was determined both in the biomass and in the culture medium. The presented results of the study confirm the effectiveness of Chlorophyta in the process of zinc and nickel biosorption. A phenomenon of competitiveness between the metals was observed when they were administered at the same time.
This investigation was undertaken to determine the optimum conditions for physical-chemical treatment of waste water contaminated with heavy metals in the industry of metallic coatings. The industry uses substances such as: inorganic acids, alkalis, acidic and alkaline metal salts, that has a high water demand in the processes of flushing and cleaning the parts to be coated. According to the preliminary characterization of samples and reported in the literature theory, physico-chemical process was implemented for the removal of contaminants that consisted in chemical oxidation of CN-ions, followed by chemical precipitation made next to a coagulation/flocculation and subsequent adsorption on activated coal. Laboratory scale tests showed the optimal conditions of treatment including chemical oxidation by the addition of 4.15 cm3 of H2O2(30%) per gram of CN, chemical precipitation with NaOH to a pH of 12, followed by coagulation/flocculation with Fe2(SO4)3 at a speed of 135 rpm for 3 min and 20 rpm for 20 min and finally the addition of 1.0 g of adsorbent previously activated at 700°C. From this study, it is clear that the adsorption on activated carbon is highly efficient in the removal ofheavy metals from industrial waste water from electroplating. However, it is also clear that the parallel application of the treatments, shown here, is more effective to completely remove contaminants such as lead, nickel, silver, and copper at la-boratory scale, so it is recommended the simultaneous use of these physico-chemical processes.
Because of excellent properties, similar to natural bone minerals, and variety of possible biomedical applications, hydroxyapatite (HAp) is a valuable compound among the calcium phosphate salts. A number of synthesis routes for producing HAp powders have been reported. Despite this fact, it is important to develop new methods providing precise control over the reaction and having potential to scale-up. The main motivation for the current paper is a view of continuous synthesis methods toward medical application of produced hydroxyapatite, especially in the form of nanoparticles.
One type of spheroidal cast iron, with additions of 0.51% Cu and 0.72% Ni, was subjected to precipitation hardening. Assuming that the
greatest increase in hardness after the shortest time of ageing is facilitated by chemical homogenisation and fragmentation of cast iron
grain matrix, precipitation hardening after pre-normalisation was executed. Hardness (HB), microhardness (HV), qualitative and
quantitative metalographic (LM, SEM) and X-ray structural (XRD) tests were performed. The acquired result of 13.2% increase in
hardness after ca. 5-hour ageing of pre-normalised cast iron confirmed the assumption.
In the present investigation, the morphology of Ti inclusions in high strength tire cord steel was investigated and their precipitation behavior was discussed using a precipitation and growth model. The results show that Ti inclusions mainly exist in the form of TiN. The two-dimensional characterization of Ti inclusions is square-like with sharp edges and corners, while its three-dimensional shape exhibits a cubic or rectangular-prism morphology. The Ti inclusions do not precipitate when the solid fraction of tire cord during solidification is less than 0.987, and their final radius is closely related to the cooling rate and initial concentration product. The higher the cooling speed, the smaller the final radius, when the cooling speed is constant, the final radius of Ti inclusions is mainly determined by the initial concentration product, w[N]0×w[Ti]0. In order to retard the precipitation and growth of Ti inclusions in tire cord steel, the cooling rate and initial concentration product can be taken into consideration.
The scope of this work is to investigate the precipitation of two Al-Mg-Si alloys with and without Cu and excess Si by using the differential scanning calorimetry (DSC), transmission electron microscopic (TEM), Vickers hardness measurement and X-ray diffraction. The analysis of the DSC curves found that the excess Si accelerate the precipitation and the alloy contain the excess Si and small addition of copper has higher aging-hardness than that of free alloy (without excess Si and Cu) at the same heat treatment condition. The sufficient holding time for the precipitation of the β'' phase was estimated to be 6 hours for the alloy aged at 100°C and 10 hours for the alloy aged at 180°C. The low Copper containing Al-Mg-Si alloy gives rise to the forming a finer distribution of β (Mg2Si) precipitates which increases the hardness of the alloy. In order to know more about the precipitation reactions, concern the peaks on the DSC curve transmission electron microscopy observation were made on samples annealed at temperatures (250°C, 290°C and 400°C) just above the corresponding peaks of the three phases β'', β' and β respectively.