Extraction of hazardous metals from green liquor dregs by ethylenediaminetetraacetic acid.

Green liquor dregs are the major inorganic solid side stream of kraft pulp mills which contain environmentally hazardous metals. The presence of hazardous metals in this industrial residue brings statutory limits for its landfilling, although they are not easily mobilized from the solid phase. In this study, the chelating agent ethylenediaminetetraacetic acid (EDTA) is utilized to extract hazardous metals such as Cd, Pb and Zn from green liquor dregs. Furthermore, the influence of EDTA on the removal of Ca as the main mineral nutrient present in the green liquor dregs is studied. The effect of parameters such as EDTA dosage, L/S ratio and contact time on the removal rate of the elements is investigated. In addition, the experimental data are fitted to the Elovich model and the pseudo-first-order model to describe the desorption kinetics. The results show that 59 wt% of Cd, 13 wt% of Co, 62 wt% of Cu, 3 wt% of Mn, 12 wt% of Ni, 43 wt% of Pb, 16 wt% of Zn, and less than 1 wt% of Ca were extracted from green liquor dregs with EDTA dosage of 0.035 gEDTA salt/gdregs and the L/S ratio of 6.25 ml/g. The current study opens up new possibilities to use the green liquor dregs for improving the soil fertility instead of landfilling.

Effective removal of hazardous trace metals from recovery boiler fly ashes.

The objective of this study is to introduce a treatment sequence enabling straightforward and effective recovery of hazardous trace elements from recovery boiler fly ash (RBFA) by a novel method, and to demonstrate the subsequent removal of Cl and K with the existing crystallization technology. The treatment sequence comprises two stages: dissolution of most other RBFA components than the hazardous trace elements in water in Step 1 of the treatment, and crystallization of the process chemicals in Step 2. Solid-liquid separation has an important role in the treatment, due to the need to separate first the small solid residue containing the trace elements, and to separate the valuable crystals, containing Na and S, from the liquid rich in Cl and K. According to the results, nearly complete recovery of cadmium, lead and zinc can be reached even without pH adjustment. Some other metals, such as Mg and Mn, are removed together with the hazardous metals. Regarding the removal of Cl and K from the process, in this non-optimized case the removal efficiency was satisfactory: 60-70% for K when 80% of sodium was recovered, and close to 70% for Cl when 80% of sulfate was recovered.

Determination of statins by gas chromatography - EI/MRM - Tandem mass spectrometry: fermentation of pine samples with Pleurotus ostreatus.

Statins were separated and quantified with gas chromatography-mass spectrometry (GC-EI-MS/MS) using total ion monitoring (TIC) and multiple reactions monitoring (MRM). The MRM method in statins determination has a novelty value, since there are no previous studies on their simultaneous analysis in environmental or plant samples. The method development and optimization was challenging due to the physicochemical similarities of the silylated lovastatin, simvastatin, pravastatin, fluvastatin, and atorvastatin. The results showed that the use of MRM decreased their detection and quantification limits by factors of 2-10 compared to that obtained in TIC monitoring. The concentration calibration was made between 247.5ng/L and 9900ng/L. Limits of detection and quantification were between 50ng/L (lovastatin)-500ng/L (pravastatin) and 250ng/L (lovastatin)-1000ng/L (pravastatin), respectively. Based on the MRM results, the wood bark and phloem samples contained lovastatin, lovastatin-lactone, simvastatin, simvastatin-lactone, and pravastatin. Their concentrations were 250-3000µg/L, i.e. 4.2-50mg/kg in phloem and bark. However, they were not detected in fluids made with Pleurotus ostreatus fermentation of wood core.