The possibility of Cu(II), Ni(II) and Sn(II) removal from model solutions and real wastewater from the production of PCBs using Na2 CS3 for precipitation was presented in this paper. The testing was carried out on a laboratory scale using model and real industrial wastewater containing additives in the form of complexing compounds used in the production of PCBs (Na2 EDTA, NH3(aq), thiourea) and recommended by the USEPA (Na3 MGDA, Na4 GLDA). Application of Na2 CS3 in optimal conditions of conducting precipitation process was connected with obtaining wastewater containing low concentrations of metals (Cu 0.02 mg/L, Sn <0.01 mg/L, Ni <0.005 mg/L at pH 9.39 and Cu 0.07 mg/L, Sn <0.01 mg/L, Ni 0.006 mg/L at pH 7.79). Controlled application of Na2 CS3 by the use of a platinum redox electrode was also connected with obtaining treated wastewater containing low concentrations of metals (Cu 0.019 mg/L, Sn <0.05 mg/L, Ni <0.0098 mg/L at pH 9–9.5 and E= -142 mV in the laboratory scale and Cu 0.058 mg/L, Sn <0.005 mg/L, Ni 0.011 mg/L at pH 9.14 and E= +10 mV in the industrial scale). Changing the value of redox potential of treated wastewater by dosing Na2 CS3 made it possible to control the precipitation process on laboratory and industrial scale by the use of a platinum redox electrode. Controlled application of Na2 CS3 can be used to remove Cu(II), Ni(II) and Sn(II) from industrial effl uent containing chelating compounds like Na2 EDTA, NH3(aq), thiourea, Na3 MGDA and Na4 GLDA.
The possibility of removing organic compounds from wastewater originating from the photochemical production of printed circuit boards by use of waste acidification and disposal of precipitated photopolymer in the first stage and the UV-Fenton method in a second stage has been presented. To optimize the process of advanced oxidation, the RSM (Response Surface Methodology) for three independent factors was applied, i.e. pH, the concentration of Fe(II) and H2O2 concentration. The use of optimized values of individual parameters in the process of wastewater treatment caused a decrease in the concentration of the organic compounds denoted as COD by approx. 87% in the first stage and approx. 98% after application of both processes. Precipitation and the decomposition of organic compounds was associated with a decrease of wastewater COD to below 100 mg O2/L whereas the initial value was 5550 mg O2/L. Decomposition of organic compounds and verification of the developed model of photopolymers removal was also carried out with use of alternative H2O2 sources i.e. CaO2, MgO2, and Na2CO3·1,5H2O2.
Rare earth elements are characterized by the high risk of their shortage resulting from limited resources. From this reason REE constitute a group of elements of special importance for the European Union. The aim of this study was to evaluate ashes from the burning of coal in fluidized bed boilers as an potential source of REY . Twelve samples of fly ash and bottom ash taken from power plants in Poland were analyzed. Tests have shown that despite some differences in chemical composition, the fly ash and bottom ash from fluidized beds could be classified as the calsialic, low acid type. It was found that fly ashes contained more REY than bottom ashes. Among REY , the light elements (LREY ) had the highest share in the total REY content in both fly ashes and bottom ashes. Heavy elements (HREY ) had the lowest content. The normalized curves plotted for fly ash samples within almost all of their entire range were positioned above the reference level and these curves were of the L-M or H-M type. The content of the individual REY in these samples was even twice as high as in UCC . The normalized curves plotted for bottom ash samples were classified as of L, L-M or H type. They were positioned on the reference level or above it. The content of the individual REY in these samples was the same or up to about 4 times lower than in UCC. It was found that the content of critical elements and of excessive elements in fly ash and bottom ash differs, which has an effect on the value of the outlook coefficient Coutl, and which is always higher in the case of fly ash than in the case of bottom ash. Nevertheless, the computed values of the outlook coefficient Coutl allow both fly ash and bottom ash from fluidized beds to be regarded as promising REY raw materials.
Fly ash which has been separated from the flue gas stream as a result of fossil fuels combustion constitutes a huge amount of waste generated worldwide. Due to environmental problems, many directions of their rational use have been developed. Various attempts to convert fly ash into sorption materials, mainly synthetic zeolites, are conducted successfully. In this paper, an attempt was made to convert fly ash from lignite combustion from one of the Polish power plants, using alkaline hydrothermal synthesis. The primary phases in the fly ash were: quartz, gehlenite, mullite, hematite, feldspar, lime, anhydrite, occasionally grains of ZnO phase and pyrrhotite, glass and unburned fuel grains. As a result of hydrothermal synthesis a material containing new phases – pitiglianoite and tobermorite was obtained. Among the primary ash constituents, only gehlenite with an unburned organic substance, on which tobermorite with crystallized pitiglianoite was present. As a result of detailed testing of products after synthesis, it was found that among the tested grains: • two populations can be distinguished – grains containing MgO and Fe2O3 as well as grains containing Fe2O3 or MgO or containing none of these components, • the main quantitative component was pitiglianoite, • pitiglianoite was present in larger amounts in grains containing Fe2O3 or MgO or in the absence of both components than in grains in which Fe2O3 and MgO were found. The results of the study indicate that in post-synthesis products, the contribution of components were as follows: pitiglianoite – 39.5% mas., tobermorite – 54% mas., gehlenite – 3% mas. and organic substance – 3.5% mas.