Eeva Jernström

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.

Detection of Novel Carbohydrate-Related Compounds in Aqueous Samples Using a Capillary Electrophoretic Profiling Method

The aim of this research was to extend an existing capillary electrophoresis (CE) method, originally developed for the determination of mono- and disaccharides, to the determination of alternative carbohydrate compounds, namely furfural and polydatin. Empirical validation confirms that this novel method can be applied for the determination of analyte concentrations from complex matrices, and the evaluation of their carbohydrate composition. It is concluded that the approach has validity as an analytical procedure and has the ability to determine industrially important analytes from a heterogeneous biological sample matrix, and thus, the method adds value to the development of large scale separation processes. However, some additional optimization is required before online applications.

Types of connections between plant location selection and the long term corporate level value creation and methods for their identification. Case study; the pulp and paper industry

Many engineers see plant location selection only as an interesting task and a minor part of process and plant engineering. At the same time plant location selection is an important part of the corporate level strategic management and decision making. This paper discusses the types of interactions between plant location selection and strategic long term value creation at the corporate level. The research approach used in this case study is a combination of the classic value chain model and the core elements of plant location selection methods. The most important findings are that the plant location selection and the chosen technology are the core internal elements at the corporate level for long term value creation.

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.

Removal of hazardous trace elements from green liquor dregs by mechanical separation methods

Abstract Green liquor dregs represent the most important inorganic residue of chemical pulp mills. The dregs are usually settled in thickeners, washed and deliquored with lime mud precoat filters, and transported to the landfill. The utilization of dregs is challenging, due to the high concentration of hazardous trace elements (HTE) in their solid phase. There are basically two potential strategies for the reduction of the HTE content of dregs: mechanical classification according to differences in the size and density of particles, and removal of HTE by various chemical treatments. The objective of this study was to evaluate the applicability of straightforward mechanical separation methods for the purification of dregs from HTE. The evaluated separation methods included particle size–based classification by sieving, and classification on the basis of differences in the settling properties of particles in gravitational and centrifugal separation. It can be concluded that all the evaluated separation methods could be used to reduce the HTE content of dregs, although the separation efficiency was not very high in most cases. Centrifugation had clearly the best performance of the investigated techniques. The fractions consisting of large particles contained consistently lower concentrations of HTE, compared to fractions containing a lot of fines.

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.