Chromium occurs in nature in various oxidation states, of which +3 and +6 are the most common. The most stable oxidation state of chromium is represented by Cr(III), and therefore most of the chromium in the soils is present in this form. Cr(VI) is considered to be the most toxic chemical species of chromium, as it is both carcinogenic and mutagenic, and is regarded as a serious threat to the environment and human health. In my diploma thesis, the sorption of both chemical species of chromium on apatites was investigated. Aqueous solutions of potassium chromate and chromium(III) nitrate of various concentrations were used as sources of Cr(VI) and Cr(III), while hydroxyapatite (HAp) and animal biochar (BC) were employed as examples of apatite species. Suspensions of each apatite species with chromium solutions were prepared at a solid-liquid ratio of 1:100 and extracted for 24 hours at room temperature under continuous shaking. The total chromium concentrations in the extracts, determined by inductively coupled plasma optical emission spectroscopy (ICP-OES), showed that the sorption of Cr(VI) to BC and HAp was negligible, while BC and HAp proved to be effective sorbents for Cr(III). The concentrations of Cr(VI) in BC and HAp extracts with potassium chromate were determined spectrophotometrically. To investigate the potential leaching of carbon species from BC, the concentration of inorganic and total carbon in the extracts were measured by TOC analysis. As expected, concentrations above the detection limit were observed only in samples with added BC, which was identified as the main source of the inorganic form of carbon.
|