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It is of high priority to capture the extent of microplastics (MP) contamination for understanding its impact and consequences to our environment. However, due to a lack of standardized methods, MP analysis as well as its quality assurance, is still a challenge. The thermal extraction desorption-gas chromatography/-mass spectrometry (TED-GC/MS) as a novel innovative thermoanalytic method can detect MP particles in environmental samples based on their decomposition products. According to MP analysis, a distinctively larger polyethylene (PE) content in comparison to other synthetic polymers was detected in environmental samples. Various substances within the matrix which have a similar molecular structure to PE, like fats and oils, might interfere with its marker and lead to an overestimation. In this investigation an automated extraction method, the accelerated solvent extraction (ASE), is introduced as quality control tool before TED-GC/MS measurement. Thereby, not the extract like usually used, but the solid filtrate is analyzed. The aim is to clean the environmental samples from solvent removable compounds which could lead to false positive signals and thus receive a more accurate PE mass. Consequently, a sample mimicking environmental samples with a defined matrix and a known polymer mass was generated. The common polymers polyethylene, polypropylene, polystyrene and styrene-butadiene rubber, used as an indication for tire wear, were added to the matrix. Different parameters for ASE extraction were varied such as different solvents, filters and purge time. Finally, a PE recovery rate of 91 % after extraction could be reached.
Ein drastisch hoher Polyethylene Massenanteil wurde bei der Analytik der Umweltproben im Vergleich zu weiteren Polymeren festgestellt. Zu einem Überbefund des Polyethylene können strukturell verwandte Verbindungen wie z.B. Fette durch Signalüberlagerung führen. Mithilfe von beschleunigter Lösemittelextraktion soll die störende Komponente entfernt werden.
Background and aims
Olive mill wastewater (OMW) generated in Mediterranean countries is partly disposed of on soil. Its underlying fate mechanisms and influences on plant growth are still largely unknown. Our goal was to understand OMW organic matter (OMW-OM) degradation in soil and its phytotoxic effects. We hypothesized that OMW phytotoxicity decreased with degradation of its phenolic components.
Methods
In a 60 day incubation study, we monitored soil respiration, extractable total phenolic content (TPC) and carbon isotope ratio (δ13C) of OMW treated Israeli soil. The soil was extracted using accelerated solvent extraction (ASE) and its extracts were exemplarily analyzed for four phenolic substances by LC/MS. Phytotoxicity of soil and soil extracts were tested using a Lepidium sativum seed germination bioassay.
Results
Soil respiration was 2.5 times higher for OMW treated soil with two respiration maxima and indicated a degradation of up to 27 % of the added OMW-OM. Four phases of OMW-OM degradation were identified: (i) degradation of easily degradable OMW-OM and transformation of phenolic compounds, (ii) intermediate suppression of phytotoxicity, (iii) degradation of phytotoxic phenolic compounds and (iv) significant physical immobilization of phytotoxic compounds.
Conclusion
Environmental conditions during and after OMW disposal on soil ought to favor fast degradation of OMW-OM, minimizing their physical immobilization and phytotoxic effects.